date generated: 2020-11-16
Mitch performs unidimensional and multidimensional gene set enrichment analysis. The concept behind this dates to work by Cox and Mann (https://doi.org/10.1186/1471-2105-13-S16-S12). This implementation is suited to R based workflows of multi-omics datasets. This software was developed by Antony Kaspi and Mark Ziemann. Learn more about Mitch at the website: https://github.com/markziemann/Mitch
Here is the first few lines of the input profile.
## FSHD hu_model Watt_m Jones_m
## A4GALT 2.81314560 -14.988939 0.8182771 5.5001019
## AAAS -0.15717628 -2.435804 0.3877972 0.7776159
## AACS 0.05482256 -1.581711 4.1420212 11.1737053
## AAED1 4.15163719 -1.286093 -0.8848853 -39.4294484
## AAGAB -2.32526173 -1.722220 -1.3839648 0.2777522
## AAK1 1.06457576 14.833940 0.4269837 -1.5398326
Here are some metrics about the input data profile:
Profile metrics | |
---|---|
num_genes_in_profile | 10538 |
duplicated_genes_present | 0 |
num_profile_genes_in_sets | 6164 |
num_profile_genes_not_in_sets | 4374 |
Here is a plot of the input profiles. Note the dynamic ranges.
Here is the contour plot of the profile including all detected genes.
Here are some metrics about the gene sets used: GMT file of genesets: ReactomePathways.gmt
Gene sets metrics | |
---|---|
num_genesets | 2408 |
num_genesets_excluded | 1179 |
num_genesets_included | 1229 |
FSHD | hu_model | Watt_m | Jones_m | Count | |
---|---|---|---|---|---|
1 | -1 | -1 | -1 | -1 | 1515 |
2 | 1 | -1 | -1 | -1 | 606 |
3 | -1 | 0 | -1 | -1 | 1 |
4 | -1 | 1 | -1 | -1 | 1083 |
5 | 1 | 1 | -1 | -1 | 417 |
6 | -1 | -1 | 1 | -1 | 383 |
7 | 1 | -1 | 1 | -1 | 300 |
8 | -1 | 1 | 1 | -1 | 659 |
9 | 1 | 1 | 1 | -1 | 340 |
10 | -1 | -1 | -1 | 0 | 1 |
11 | -1 | -1 | -1 | 1 | 400 |
12 | 0 | -1 | -1 | 1 | 1 |
13 | 1 | -1 | -1 | 1 | 598 |
14 | -1 | 1 | -1 | 1 | 357 |
15 | 1 | 1 | -1 | 1 | 337 |
16 | 1 | 1 | 0 | 1 | 1 |
17 | -1 | -1 | 1 | 1 | 437 |
18 | 1 | -1 | 1 | 1 | 1324 |
19 | -1 | 1 | 1 | 1 | 614 |
20 | 1 | 1 | 1 | 1 | 1164 |
s.FSHD | s.hu_model | s.Watt_m | s.Jones_m | Count | |
---|---|---|---|---|---|
1 | -1 | -1 | -1 | -1 | 46 |
2 | 1 | -1 | -1 | -1 | 12 |
3 | -1 | 1 | -1 | -1 | 20 |
4 | -1 | -1 | 1 | -1 | 14 |
5 | 1 | -1 | 1 | -1 | 6 |
6 | -1 | 1 | 1 | -1 | 142 |
7 | -1 | -1 | -1 | 1 | 2 |
8 | 1 | -1 | -1 | 1 | 44 |
9 | -1 | 1 | -1 | 1 | 2 |
10 | 1 | 1 | -1 | 1 | 4 |
11 | -1 | -1 | 1 | 1 | 3 |
12 | 1 | -1 | 1 | 1 | 135 |
13 | -1 | 1 | 1 | 1 | 139 |
14 | 1 | 1 | 1 | 1 | 41 |
All sets with FDR<0.05. Try hovering over the points.
Significance is the -log2(p.adjustMANOVA) and effect size is the s.dist which is the hypotenuse of the s scores.
Top N= 100 gene sets
set | setSize | pMANOVA | p.adjustMANOVA | s.dist | s.FSHD | s.hu_model | s.Watt_m | s.Jones_m | p.FSHD | p.hu_model | p.Watt_m | p.Jones_m |
---|---|---|---|---|---|---|---|---|---|---|---|---|
Interleukin-10 signaling | 11 | 1.12e-06 | 8.69e-06 | 1.310 | 0.7360 | -0.25200 | 0.74800 | 0.742 | 2.34e-05 | 1.48e-01 | 1.74e-05 | 2.03e-05 |
Citric acid cycle (TCA cycle) | 21 | 6.96e-09 | 8.14e-08 | 1.100 | -0.6690 | -0.24300 | -0.59700 | -0.585 | 1.09e-07 | 5.43e-02 | 2.21e-06 | 3.42e-06 |
Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell | 13 | 1.14e-05 | 6.63e-05 | 1.050 | 0.7670 | 0.11300 | 0.32400 | 0.622 | 1.66e-06 | 4.81e-01 | 4.30e-02 | 1.02e-04 |
Branched-chain amino acid catabolism | 20 | 9.57e-07 | 7.69e-06 | 1.000 | -0.6120 | -0.07400 | -0.53100 | -0.586 | 2.18e-06 | 5.67e-01 | 3.92e-05 | 5.68e-06 |
Pyruvate metabolism and Citric Acid (TCA) cycle | 49 | 3.58e-17 | 1.69e-15 | 0.990 | -0.5710 | -0.26300 | -0.55900 | -0.522 | 4.77e-12 | 1.46e-03 | 1.28e-11 | 2.63e-10 |
Signal regulatory protein family interactions | 10 | 6.38e-04 | 2.26e-03 | 0.988 | 0.5440 | -0.41200 | 0.50700 | 0.504 | 2.92e-03 | 2.42e-02 | 5.47e-03 | 5.77e-03 |
Glyoxylate metabolism and glycine degradation | 20 | 4.39e-07 | 3.83e-06 | 0.985 | -0.6690 | -0.17200 | -0.51100 | -0.481 | 2.24e-07 | 1.83e-01 | 7.56e-05 | 1.98e-04 |
The NLRP3 inflammasome | 10 | 2.77e-03 | 8.04e-03 | 0.978 | 0.5410 | -0.08910 | 0.49000 | 0.645 | 3.04e-03 | 6.26e-01 | 7.31e-03 | 4.11e-04 |
Prolactin receptor signaling | 10 | 3.91e-03 | 1.09e-02 | 0.957 | -0.4690 | -0.24600 | -0.53600 | -0.591 | 1.03e-02 | 1.78e-01 | 3.34e-03 | 1.22e-03 |
Post-chaperonin tubulin folding pathway | 15 | 3.49e-06 | 2.34e-05 | 0.923 | 0.3150 | -0.48300 | 0.55600 | 0.459 | 3.48e-02 | 1.22e-03 | 1.94e-04 | 2.10e-03 |
Inflammasomes | 12 | 1.05e-03 | 3.54e-03 | 0.922 | 0.4760 | -0.21800 | 0.44600 | 0.614 | 4.32e-03 | 1.90e-01 | 7.46e-03 | 2.30e-04 |
Mitochondrial tRNA aminoacylation | 18 | 2.69e-06 | 1.84e-05 | 0.913 | -0.6090 | 0.17900 | -0.56500 | -0.334 | 7.59e-06 | 1.89e-01 | 3.36e-05 | 1.42e-02 |
Complex I biogenesis | 52 | 8.57e-16 | 3.51e-14 | 0.913 | -0.5510 | -0.19600 | -0.40100 | -0.575 | 6.54e-12 | 1.46e-02 | 5.92e-07 | 7.40e-13 |
Mitochondrial Fatty Acid Beta-Oxidation | 29 | 2.61e-09 | 3.31e-08 | 0.903 | -0.5160 | -0.35100 | -0.53700 | -0.370 | 1.55e-06 | 1.06e-03 | 5.49e-07 | 5.68e-04 |
Degradation of cysteine and homocysteine | 12 | 5.19e-04 | 1.93e-03 | 0.902 | -0.2890 | -0.30200 | -0.40700 | -0.688 | 8.33e-02 | 7.00e-02 | 1.47e-02 | 3.64e-05 |
Regulation of pyruvate dehydrogenase (PDH) complex | 15 | 1.96e-04 | 8.14e-04 | 0.901 | -0.4690 | -0.16200 | -0.63100 | -0.411 | 1.67e-03 | 2.78e-01 | 2.34e-05 | 5.88e-03 |
Interferon alpha/beta signaling | 36 | 3.95e-10 | 5.72e-09 | 0.883 | 0.5950 | -0.00808 | 0.35000 | 0.551 | 6.56e-10 | 9.33e-01 | 2.78e-04 | 1.05e-08 |
Chondroitin sulfate biosynthesis | 13 | 3.80e-04 | 1.47e-03 | 0.875 | 0.7180 | -0.10600 | 0.28600 | 0.396 | 7.36e-06 | 5.07e-01 | 7.43e-02 | 1.33e-02 |
PECAM1 interactions | 10 | 5.25e-03 | 1.39e-02 | 0.873 | 0.5160 | -0.25000 | 0.28300 | 0.594 | 4.72e-03 | 1.70e-01 | 1.21e-01 | 1.15e-03 |
Defective B3GALT6 causes EDSP2 and SEMDJL1 | 14 | 1.06e-04 | 4.81e-04 | 0.865 | 0.6150 | -0.45400 | 0.21200 | 0.344 | 6.71e-05 | 3.25e-03 | 1.70e-01 | 2.61e-02 |
Pyruvate metabolism | 26 | 7.39e-07 | 6.05e-06 | 0.863 | -0.4910 | -0.22800 | -0.52200 | -0.423 | 1.48e-05 | 4.45e-02 | 4.18e-06 | 1.88e-04 |
HS-GAG degradation | 16 | 5.14e-06 | 3.39e-05 | 0.860 | 0.5730 | -0.43500 | -0.01360 | 0.471 | 7.20e-05 | 2.62e-03 | 9.25e-01 | 1.10e-03 |
Defective B3GAT3 causes JDSSDHD | 14 | 6.44e-05 | 3.10e-04 | 0.860 | 0.6190 | -0.49400 | 0.17500 | 0.285 | 6.16e-05 | 1.37e-03 | 2.58e-01 | 6.46e-02 |
Formation of Senescence-Associated Heterochromatin Foci (SAHF) | 10 | 1.86e-03 | 5.71e-03 | 0.857 | 0.1020 | 0.11500 | 0.47500 | 0.697 | 5.76e-01 | 5.31e-01 | 9.26e-03 | 1.36e-04 |
The citric acid (TCA) cycle and respiratory electron transport | 142 | 4.04e-38 | 1.24e-35 | 0.856 | -0.5290 | -0.20200 | -0.42300 | -0.482 | 1.42e-27 | 3.56e-05 | 3.80e-18 | 3.89e-23 |
Respiratory electron transport | 92 | 2.25e-24 | 2.31e-22 | 0.841 | -0.5490 | -0.17700 | -0.36700 | -0.490 | 9.03e-20 | 3.34e-03 | 1.22e-09 | 5.01e-16 |
tRNA Aminoacylation | 24 | 2.34e-06 | 1.63e-05 | 0.840 | -0.5880 | 0.18500 | -0.40500 | -0.402 | 6.22e-07 | 1.18e-01 | 5.97e-04 | 6.65e-04 |
Mucopolysaccharidoses | 11 | 4.04e-04 | 1.56e-03 | 0.834 | 0.4630 | -0.33500 | 0.00854 | 0.607 | 7.83e-03 | 5.44e-02 | 9.61e-01 | 4.86e-04 |
Defective B4GALT7 causes EDS, progeroid type | 14 | 1.58e-04 | 6.78e-04 | 0.828 | 0.5740 | -0.49300 | 0.13600 | 0.308 | 2.03e-04 | 1.40e-03 | 3.79e-01 | 4.58e-02 |
Activation of Matrix Metalloproteinases | 11 | 2.43e-03 | 7.24e-03 | 0.826 | 0.6550 | -0.30700 | 0.19300 | 0.349 | 1.69e-04 | 7.82e-02 | 2.68e-01 | 4.48e-02 |
Scavenging by Class A Receptors | 13 | 1.56e-03 | 4.93e-03 | 0.817 | 0.6000 | -0.19500 | 0.20400 | 0.478 | 1.80e-04 | 2.23e-01 | 2.04e-01 | 2.84e-03 |
rRNA processing in the mitochondrion | 11 | 1.03e-02 | 2.43e-02 | 0.814 | -0.5890 | -0.03730 | -0.36700 | -0.423 | 7.14e-04 | 8.30e-01 | 3.50e-02 | 1.52e-02 |
Carnitine metabolism | 11 | 3.97e-03 | 1.11e-02 | 0.813 | -0.2750 | -0.43400 | -0.56800 | -0.272 | 1.14e-01 | 1.28e-02 | 1.12e-03 | 1.18e-01 |
Cell recruitment (pro-inflammatory response) | 12 | 8.63e-03 | 2.09e-02 | 0.810 | 0.5180 | -0.02050 | 0.34700 | 0.517 | 1.89e-03 | 9.02e-01 | 3.72e-02 | 1.94e-03 |
Purinergic signaling in leishmaniasis infection | 12 | 8.63e-03 | 2.09e-02 | 0.810 | 0.5180 | -0.02050 | 0.34700 | 0.517 | 1.89e-03 | 9.02e-01 | 3.72e-02 | 1.94e-03 |
A tetrasaccharide linker sequence is required for GAG synthesis | 18 | 1.98e-05 | 1.07e-04 | 0.797 | 0.6000 | -0.41300 | 0.21000 | 0.246 | 1.06e-05 | 2.43e-03 | 1.24e-01 | 7.04e-02 |
Respiratory electron transport, ATP synthesis by chemiosmotic coupling, and heat production by uncoupling proteins. | 96 | 1.91e-22 | 1.47e-20 | 0.795 | -0.5080 | -0.17600 | -0.35800 | -0.464 | 8.80e-18 | 2.92e-03 | 1.41e-09 | 3.97e-15 |
Caspase activation via Death Receptors in the presence of ligand | 11 | 1.37e-02 | 3.06e-02 | 0.789 | 0.4890 | -0.23900 | 0.33900 | 0.458 | 4.96e-03 | 1.70e-01 | 5.15e-02 | 8.50e-03 |
Collagen degradation | 20 | 5.57e-06 | 3.58e-05 | 0.775 | 0.6020 | -0.27400 | 0.01500 | 0.403 | 3.18e-06 | 3.37e-02 | 9.07e-01 | 1.79e-03 |
Diseases associated with the TLR signaling cascade | 16 | 9.63e-04 | 3.29e-03 | 0.772 | 0.3580 | -0.17400 | 0.31800 | 0.580 | 1.33e-02 | 2.28e-01 | 2.78e-02 | 5.89e-05 |
Diseases of Immune System | 16 | 9.63e-04 | 3.29e-03 | 0.772 | 0.3580 | -0.17400 | 0.31800 | 0.580 | 1.33e-02 | 2.28e-01 | 2.78e-02 | 5.89e-05 |
Mitochondrial calcium ion transport | 21 | 7.14e-05 | 3.39e-04 | 0.772 | -0.5980 | -0.01110 | -0.33800 | -0.351 | 2.12e-06 | 9.30e-01 | 7.32e-03 | 5.33e-03 |
MET activates PTK2 signaling | 14 | 3.31e-04 | 1.31e-03 | 0.769 | 0.5870 | -0.43100 | 0.03610 | 0.244 | 1.44e-04 | 5.24e-03 | 8.15e-01 | 1.14e-01 |
Acyl chain remodelling of PS | 10 | 1.23e-02 | 2.79e-02 | 0.767 | 0.4140 | 0.21800 | 0.21500 | 0.568 | 2.33e-02 | 2.34e-01 | 2.38e-01 | 1.86e-03 |
Voltage gated Potassium channels | 11 | 1.04e-03 | 3.54e-03 | 0.767 | 0.2120 | -0.52800 | -0.36100 | -0.365 | 2.23e-01 | 2.43e-03 | 3.80e-02 | 3.59e-02 |
Mitochondrial translation | 87 | 1.59e-19 | 1.02e-17 | 0.764 | -0.5540 | 0.15900 | -0.31500 | -0.389 | 4.10e-19 | 1.07e-02 | 4.08e-07 | 3.59e-10 |
Syndecan interactions | 17 | 1.45e-03 | 4.64e-03 | 0.761 | 0.5440 | -0.04840 | 0.35700 | 0.392 | 1.04e-04 | 7.30e-01 | 1.08e-02 | 5.21e-03 |
N-Glycan antennae elongation | 12 | 6.08e-03 | 1.56e-02 | 0.759 | 0.2620 | -0.26000 | 0.42900 | 0.505 | 1.16e-01 | 1.18e-01 | 1.00e-02 | 2.47e-03 |
Other interleukin signaling | 13 | 7.41e-03 | 1.84e-02 | 0.757 | 0.5540 | -0.13100 | 0.26700 | 0.421 | 5.43e-04 | 4.12e-01 | 9.55e-02 | 8.60e-03 |
Biotin transport and metabolism | 10 | 3.96e-02 | 7.50e-02 | 0.757 | -0.3230 | -0.02010 | -0.53500 | -0.426 | 7.66e-02 | 9.12e-01 | 3.39e-03 | 1.98e-02 |
Mitochondrial translation termination | 81 | 1.65e-17 | 8.47e-16 | 0.754 | -0.5380 | 0.15600 | -0.29300 | -0.411 | 5.73e-17 | 1.52e-02 | 5.20e-06 | 1.77e-10 |
Mitochondrial translation elongation | 81 | 1.59e-17 | 8.47e-16 | 0.753 | -0.5420 | 0.15900 | -0.29700 | -0.399 | 3.57e-17 | 1.37e-02 | 3.81e-06 | 5.70e-10 |
Gluconeogenesis | 21 | 1.67e-05 | 9.17e-05 | 0.749 | -0.0701 | -0.55500 | -0.35200 | -0.352 | 5.78e-01 | 1.06e-05 | 5.28e-03 | 5.23e-03 |
Integrin cell surface interactions | 45 | 1.02e-11 | 1.98e-10 | 0.748 | 0.5990 | -0.23100 | 0.09650 | 0.372 | 3.67e-12 | 7.31e-03 | 2.63e-01 | 1.63e-05 |
CS/DS degradation | 10 | 2.00e-02 | 4.18e-02 | 0.746 | 0.4740 | -0.26500 | 0.16300 | 0.485 | 9.43e-03 | 1.47e-01 | 3.72e-01 | 7.89e-03 |
Sema3A PAK dependent Axon repulsion | 15 | 3.33e-03 | 9.54e-03 | 0.746 | 0.3150 | -0.18300 | 0.39200 | 0.520 | 3.46e-02 | 2.20e-01 | 8.57e-03 | 4.95e-04 |
Phase 0 - rapid depolarisation | 17 | 7.93e-05 | 3.75e-04 | 0.746 | -0.0740 | -0.62200 | -0.26000 | -0.310 | 5.98e-01 | 8.98e-06 | 6.35e-02 | 2.69e-02 |
Chondroitin sulfate/dermatan sulfate metabolism | 37 | 1.73e-08 | 1.82e-07 | 0.744 | 0.5660 | -0.22600 | 0.19400 | 0.380 | 2.58e-09 | 1.73e-02 | 4.15e-02 | 6.48e-05 |
Elastic fibre formation | 34 | 1.94e-07 | 1.82e-06 | 0.743 | 0.5880 | -0.04050 | 0.28000 | 0.356 | 2.98e-09 | 6.83e-01 | 4.82e-03 | 3.36e-04 |
SEMA3A-Plexin repulsion signaling by inhibiting Integrin adhesion | 14 | 5.36e-03 | 1.41e-02 | 0.743 | 0.4410 | -0.21500 | 0.25700 | 0.495 | 4.32e-03 | 1.63e-01 | 9.67e-02 | 1.34e-03 |
Regulation of Complement cascade | 13 | 3.47e-04 | 1.36e-03 | 0.741 | 0.6520 | 0.04740 | -0.00954 | 0.348 | 4.68e-05 | 7.67e-01 | 9.53e-01 | 2.97e-02 |
Mitochondrial translation initiation | 81 | 4.72e-17 | 2.15e-15 | 0.740 | -0.5400 | 0.15200 | -0.29100 | -0.385 | 4.46e-17 | 1.84e-02 | 6.38e-06 | 2.12e-09 |
Formation of tubulin folding intermediates by CCT/TriC | 17 | 1.34e-05 | 7.63e-05 | 0.739 | 0.0756 | -0.09460 | 0.68300 | 0.255 | 5.89e-01 | 5.00e-01 | 1.07e-06 | 6.91e-02 |
Binding and Uptake of Ligands by Scavenger Receptors | 23 | 3.26e-05 | 1.67e-04 | 0.737 | 0.5550 | -0.15200 | 0.15700 | 0.433 | 4.15e-06 | 2.08e-01 | 1.92e-01 | 3.30e-04 |
tRNA processing in the mitochondrion | 11 | 1.28e-02 | 2.88e-02 | 0.736 | -0.6160 | 0.02140 | -0.25900 | -0.307 | 4.00e-04 | 9.02e-01 | 1.37e-01 | 7.80e-02 |
Defects in vitamin and cofactor metabolism | 17 | 1.55e-03 | 4.92e-03 | 0.735 | -0.3460 | 0.10500 | -0.52300 | -0.368 | 1.35e-02 | 4.52e-01 | 1.89e-04 | 8.64e-03 |
Degradation of the extracellular matrix | 58 | 8.33e-14 | 2.38e-12 | 0.734 | 0.5400 | -0.30100 | 0.14100 | 0.370 | 1.11e-12 | 7.64e-05 | 6.28e-02 | 1.15e-06 |
Regulation of IFNA signaling | 12 | 2.77e-02 | 5.51e-02 | 0.732 | 0.4190 | -0.03780 | 0.34500 | 0.489 | 1.19e-02 | 8.21e-01 | 3.85e-02 | 3.35e-03 |
Metabolism of steroid hormones | 12 | 9.82e-03 | 2.32e-02 | 0.732 | 0.2180 | -0.11700 | 0.38700 | 0.569 | 1.90e-01 | 4.85e-01 | 2.02e-02 | 6.42e-04 |
Interleukin-4 and Interleukin-13 signaling | 64 | 4.20e-12 | 9.07e-11 | 0.731 | 0.4280 | -0.13000 | 0.40100 | 0.416 | 3.24e-09 | 7.28e-02 | 2.88e-08 | 8.56e-09 |
ECM proteoglycans | 37 | 9.76e-09 | 1.12e-07 | 0.730 | 0.5690 | -0.27000 | 0.14300 | 0.341 | 2.08e-09 | 4.58e-03 | 1.33e-01 | 3.40e-04 |
Collagen biosynthesis and modifying enzymes | 47 | 3.12e-11 | 5.48e-10 | 0.729 | 0.5000 | -0.35200 | 0.11700 | 0.379 | 3.16e-09 | 3.02e-05 | 1.67e-01 | 7.07e-06 |
TP53 Regulates Transcription of Genes Involved in G1 Cell Cycle Arrest | 12 | 1.16e-02 | 2.66e-02 | 0.726 | 0.2740 | -0.19300 | 0.50300 | 0.403 | 1.00e-01 | 2.47e-01 | 2.57e-03 | 1.58e-02 |
Synthesis of bile acids and bile salts via 7alpha-hydroxycholesterol | 10 | 6.13e-02 | 1.06e-01 | 0.725 | -0.3860 | -0.14100 | -0.46800 | -0.371 | 3.44e-02 | 4.42e-01 | 1.05e-02 | 4.20e-02 |
Laminin interactions | 19 | 1.99e-05 | 1.07e-04 | 0.724 | 0.5750 | -0.34400 | -0.06030 | 0.268 | 1.44e-05 | 9.38e-03 | 6.49e-01 | 4.34e-02 |
Defective EXT1 causes exostoses 1, TRPS2 and CHDS | 11 | 1.14e-02 | 2.64e-02 | 0.723 | 0.5370 | -0.36000 | 0.16200 | 0.280 | 2.04e-03 | 3.89e-02 | 3.52e-01 | 1.08e-01 |
Defective EXT2 causes exostoses 2 | 11 | 1.14e-02 | 2.64e-02 | 0.723 | 0.5370 | -0.36000 | 0.16200 | 0.280 | 2.04e-03 | 3.89e-02 | 3.52e-01 | 1.08e-01 |
rRNA modification in the nucleus and cytosol | 52 | 1.28e-15 | 4.91e-14 | 0.722 | -0.1810 | 0.60100 | 0.35700 | 0.011 | 2.44e-02 | 6.53e-14 | 8.81e-06 | 8.91e-01 |
RHO GTPases Activate WASPs and WAVEs | 31 | 2.90e-05 | 1.49e-04 | 0.718 | 0.3620 | 0.09060 | 0.42800 | 0.440 | 4.85e-04 | 3.83e-01 | 3.82e-05 | 2.24e-05 |
NF-kB activation through FADD/RIP-1 pathway mediated by caspase-8 and -10 | 10 | 9.89e-04 | 3.37e-03 | 0.717 | 0.1140 | -0.24500 | 0.05040 | 0.662 | 5.32e-01 | 1.80e-01 | 7.82e-01 | 2.88e-04 |
FCGR3A-mediated phagocytosis | 47 | 5.38e-08 | 5.42e-07 | 0.713 | 0.3840 | -0.01190 | 0.37700 | 0.467 | 5.20e-06 | 8.88e-01 | 8.09e-06 | 3.05e-08 |
Leishmania phagocytosis | 47 | 5.38e-08 | 5.42e-07 | 0.713 | 0.3840 | -0.01190 | 0.37700 | 0.467 | 5.20e-06 | 8.88e-01 | 8.09e-06 | 3.05e-08 |
Parasite infection | 47 | 5.38e-08 | 5.42e-07 | 0.713 | 0.3840 | -0.01190 | 0.37700 | 0.467 | 5.20e-06 | 8.88e-01 | 8.09e-06 | 3.05e-08 |
Cristae formation | 10 | 5.76e-02 | 1.02e-01 | 0.712 | -0.5120 | 0.05020 | -0.29300 | -0.395 | 5.03e-03 | 7.84e-01 | 1.09e-01 | 3.04e-02 |
Collagen formation | 63 | 7.69e-15 | 2.62e-13 | 0.711 | 0.5070 | -0.30900 | 0.08070 | 0.383 | 3.43e-12 | 2.29e-05 | 2.69e-01 | 1.45e-07 |
Extracellular matrix organization | 192 | 7.97e-44 | 3.27e-41 | 0.711 | 0.5450 | -0.25800 | 0.14200 | 0.348 | 9.51e-39 | 8.04e-10 | 7.16e-04 | 1.07e-16 |
Glycogen storage diseases | 11 | 2.64e-03 | 7.75e-03 | 0.709 | -0.3700 | -0.40700 | -0.06070 | -0.443 | 3.38e-02 | 1.95e-02 | 7.27e-01 | 1.09e-02 |
Diseases associated with glycosaminoglycan metabolism | 30 | 1.97e-06 | 1.41e-05 | 0.708 | 0.5650 | -0.21700 | 0.19300 | 0.311 | 8.36e-08 | 3.97e-02 | 6.70e-02 | 3.26e-03 |
Condensation of Prophase Chromosomes | 11 | 6.32e-04 | 2.24e-03 | 0.706 | -0.1530 | 0.37300 | 0.18800 | 0.548 | 3.80e-01 | 3.21e-02 | 2.79e-01 | 1.67e-03 |
Postmitotic nuclear pore complex (NPC) reformation | 24 | 1.70e-06 | 1.23e-05 | 0.705 | -0.1870 | 0.54400 | 0.35100 | 0.208 | 1.14e-01 | 4.01e-06 | 2.97e-03 | 7.72e-02 |
Processing of SMDT1 | 15 | 2.49e-03 | 7.38e-03 | 0.703 | -0.5840 | 0.14900 | -0.26800 | -0.244 | 9.01e-05 | 3.18e-01 | 7.29e-02 | 1.01e-01 |
GPVI-mediated activation cascade | 18 | 3.88e-03 | 1.09e-02 | 0.701 | 0.2350 | 0.16000 | 0.46100 | 0.444 | 8.40e-02 | 2.41e-01 | 7.03e-04 | 1.11e-03 |
Activation of PPARGC1A (PGC-1alpha) by phosphorylation | 10 | 4.97e-02 | 9.06e-02 | 0.700 | -0.1980 | -0.37900 | -0.42600 | -0.356 | 2.78e-01 | 3.82e-02 | 1.98e-02 | 5.12e-02 |
Heparan sulfate/heparin (HS-GAG) metabolism | 34 | 3.73e-07 | 3.32e-06 | 0.695 | 0.5370 | -0.27200 | 0.17300 | 0.300 | 5.94e-08 | 6.01e-03 | 8.04e-02 | 2.48e-03 |
Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs) | 65 | 2.15e-13 | 5.63e-12 | 0.694 | 0.5570 | -0.09370 | 0.16900 | 0.367 | 8.07e-15 | 1.92e-01 | 1.88e-02 | 3.29e-07 |
EGR2 and SOX10-mediated initiation of Schwann cell myelination | 20 | 6.74e-05 | 3.22e-04 | 0.689 | 0.1790 | -0.42200 | 0.31100 | 0.409 | 1.67e-01 | 1.08e-03 | 1.62e-02 | 1.55e-03 |
Assembly of collagen fibrils and other multimeric structures | 42 | 4.73e-10 | 6.68e-09 | 0.688 | 0.5060 | -0.28400 | 0.00267 | 0.370 | 1.42e-08 | 1.46e-03 | 9.76e-01 | 3.32e-05 |
Synthesis of bile acids and bile salts | 18 | 7.00e-03 | 1.76e-02 | 0.687 | -0.3920 | -0.09860 | -0.39500 | -0.391 | 4.00e-03 | 4.69e-01 | 3.70e-03 | 4.13e-03 |
Heme biosynthesis | 12 | 1.48e-02 | 3.23e-02 | 0.686 | -0.1320 | -0.12700 | -0.58000 | -0.317 | 4.29e-01 | 4.45e-01 | 4.99e-04 | 5.77e-02 |
Post-translational protein phosphorylation | 62 | 4.30e-12 | 9.12e-11 | 0.686 | 0.5430 | -0.07840 | 0.18700 | 0.367 | 1.48e-13 | 2.87e-01 | 1.10e-02 | 5.90e-07 |
set | setSize | pMANOVA | p.adjustMANOVA | s.dist | s.FSHD | s.hu_model | s.Watt_m | s.Jones_m | p.FSHD | p.hu_model | p.Watt_m | p.Jones_m |
---|---|---|---|---|---|---|---|---|---|---|---|---|
Interleukin-10 signaling | 11 | 1.12e-06 | 8.69e-06 | 1.3100 | 0.736000 | -0.252000 | 0.748000 | 0.742000 | 2.34e-05 | 1.48e-01 | 1.74e-05 | 2.03e-05 |
Citric acid cycle (TCA cycle) | 21 | 6.96e-09 | 8.14e-08 | 1.1000 | -0.669000 | -0.243000 | -0.597000 | -0.585000 | 1.09e-07 | 5.43e-02 | 2.21e-06 | 3.42e-06 |
Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell | 13 | 1.14e-05 | 6.63e-05 | 1.0500 | 0.767000 | 0.113000 | 0.324000 | 0.622000 | 1.66e-06 | 4.81e-01 | 4.30e-02 | 1.02e-04 |
Branched-chain amino acid catabolism | 20 | 9.57e-07 | 7.69e-06 | 1.0000 | -0.612000 | -0.074000 | -0.531000 | -0.586000 | 2.18e-06 | 5.67e-01 | 3.92e-05 | 5.68e-06 |
Pyruvate metabolism and Citric Acid (TCA) cycle | 49 | 3.58e-17 | 1.69e-15 | 0.9900 | -0.571000 | -0.263000 | -0.559000 | -0.522000 | 4.77e-12 | 1.46e-03 | 1.28e-11 | 2.63e-10 |
Signal regulatory protein family interactions | 10 | 6.38e-04 | 2.26e-03 | 0.9880 | 0.544000 | -0.412000 | 0.507000 | 0.504000 | 2.92e-03 | 2.42e-02 | 5.47e-03 | 5.77e-03 |
Glyoxylate metabolism and glycine degradation | 20 | 4.39e-07 | 3.83e-06 | 0.9850 | -0.669000 | -0.172000 | -0.511000 | -0.481000 | 2.24e-07 | 1.83e-01 | 7.56e-05 | 1.98e-04 |
The NLRP3 inflammasome | 10 | 2.77e-03 | 8.04e-03 | 0.9780 | 0.541000 | -0.089100 | 0.490000 | 0.645000 | 3.04e-03 | 6.26e-01 | 7.31e-03 | 4.11e-04 |
Prolactin receptor signaling | 10 | 3.91e-03 | 1.09e-02 | 0.9570 | -0.469000 | -0.246000 | -0.536000 | -0.591000 | 1.03e-02 | 1.78e-01 | 3.34e-03 | 1.22e-03 |
Post-chaperonin tubulin folding pathway | 15 | 3.49e-06 | 2.34e-05 | 0.9230 | 0.315000 | -0.483000 | 0.556000 | 0.459000 | 3.48e-02 | 1.22e-03 | 1.94e-04 | 2.10e-03 |
Inflammasomes | 12 | 1.05e-03 | 3.54e-03 | 0.9220 | 0.476000 | -0.218000 | 0.446000 | 0.614000 | 4.32e-03 | 1.90e-01 | 7.46e-03 | 2.30e-04 |
Mitochondrial tRNA aminoacylation | 18 | 2.69e-06 | 1.84e-05 | 0.9130 | -0.609000 | 0.179000 | -0.565000 | -0.334000 | 7.59e-06 | 1.89e-01 | 3.36e-05 | 1.42e-02 |
Complex I biogenesis | 52 | 8.57e-16 | 3.51e-14 | 0.9130 | -0.551000 | -0.196000 | -0.401000 | -0.575000 | 6.54e-12 | 1.46e-02 | 5.92e-07 | 7.40e-13 |
Mitochondrial Fatty Acid Beta-Oxidation | 29 | 2.61e-09 | 3.31e-08 | 0.9030 | -0.516000 | -0.351000 | -0.537000 | -0.370000 | 1.55e-06 | 1.06e-03 | 5.49e-07 | 5.68e-04 |
Degradation of cysteine and homocysteine | 12 | 5.19e-04 | 1.93e-03 | 0.9020 | -0.289000 | -0.302000 | -0.407000 | -0.688000 | 8.33e-02 | 7.00e-02 | 1.47e-02 | 3.64e-05 |
Regulation of pyruvate dehydrogenase (PDH) complex | 15 | 1.96e-04 | 8.14e-04 | 0.9010 | -0.469000 | -0.162000 | -0.631000 | -0.411000 | 1.67e-03 | 2.78e-01 | 2.34e-05 | 5.88e-03 |
Interferon alpha/beta signaling | 36 | 3.95e-10 | 5.72e-09 | 0.8830 | 0.595000 | -0.008080 | 0.350000 | 0.551000 | 6.56e-10 | 9.33e-01 | 2.78e-04 | 1.05e-08 |
Chondroitin sulfate biosynthesis | 13 | 3.80e-04 | 1.47e-03 | 0.8750 | 0.718000 | -0.106000 | 0.286000 | 0.396000 | 7.36e-06 | 5.07e-01 | 7.43e-02 | 1.33e-02 |
PECAM1 interactions | 10 | 5.25e-03 | 1.39e-02 | 0.8730 | 0.516000 | -0.250000 | 0.283000 | 0.594000 | 4.72e-03 | 1.70e-01 | 1.21e-01 | 1.15e-03 |
Defective B3GALT6 causes EDSP2 and SEMDJL1 | 14 | 1.06e-04 | 4.81e-04 | 0.8650 | 0.615000 | -0.454000 | 0.212000 | 0.344000 | 6.71e-05 | 3.25e-03 | 1.70e-01 | 2.61e-02 |
Pyruvate metabolism | 26 | 7.39e-07 | 6.05e-06 | 0.8630 | -0.491000 | -0.228000 | -0.522000 | -0.423000 | 1.48e-05 | 4.45e-02 | 4.18e-06 | 1.88e-04 |
HS-GAG degradation | 16 | 5.14e-06 | 3.39e-05 | 0.8600 | 0.573000 | -0.435000 | -0.013600 | 0.471000 | 7.20e-05 | 2.62e-03 | 9.25e-01 | 1.10e-03 |
Defective B3GAT3 causes JDSSDHD | 14 | 6.44e-05 | 3.10e-04 | 0.8600 | 0.619000 | -0.494000 | 0.175000 | 0.285000 | 6.16e-05 | 1.37e-03 | 2.58e-01 | 6.46e-02 |
Formation of Senescence-Associated Heterochromatin Foci (SAHF) | 10 | 1.86e-03 | 5.71e-03 | 0.8570 | 0.102000 | 0.115000 | 0.475000 | 0.697000 | 5.76e-01 | 5.31e-01 | 9.26e-03 | 1.36e-04 |
The citric acid (TCA) cycle and respiratory electron transport | 142 | 4.04e-38 | 1.24e-35 | 0.8560 | -0.529000 | -0.202000 | -0.423000 | -0.482000 | 1.42e-27 | 3.56e-05 | 3.80e-18 | 3.89e-23 |
Respiratory electron transport | 92 | 2.25e-24 | 2.31e-22 | 0.8410 | -0.549000 | -0.177000 | -0.367000 | -0.490000 | 9.03e-20 | 3.34e-03 | 1.22e-09 | 5.01e-16 |
tRNA Aminoacylation | 24 | 2.34e-06 | 1.63e-05 | 0.8400 | -0.588000 | 0.185000 | -0.405000 | -0.402000 | 6.22e-07 | 1.18e-01 | 5.97e-04 | 6.65e-04 |
Mucopolysaccharidoses | 11 | 4.04e-04 | 1.56e-03 | 0.8340 | 0.463000 | -0.335000 | 0.008540 | 0.607000 | 7.83e-03 | 5.44e-02 | 9.61e-01 | 4.86e-04 |
Defective B4GALT7 causes EDS, progeroid type | 14 | 1.58e-04 | 6.78e-04 | 0.8280 | 0.574000 | -0.493000 | 0.136000 | 0.308000 | 2.03e-04 | 1.40e-03 | 3.79e-01 | 4.58e-02 |
Activation of Matrix Metalloproteinases | 11 | 2.43e-03 | 7.24e-03 | 0.8260 | 0.655000 | -0.307000 | 0.193000 | 0.349000 | 1.69e-04 | 7.82e-02 | 2.68e-01 | 4.48e-02 |
Scavenging by Class A Receptors | 13 | 1.56e-03 | 4.93e-03 | 0.8170 | 0.600000 | -0.195000 | 0.204000 | 0.478000 | 1.80e-04 | 2.23e-01 | 2.04e-01 | 2.84e-03 |
rRNA processing in the mitochondrion | 11 | 1.03e-02 | 2.43e-02 | 0.8140 | -0.589000 | -0.037300 | -0.367000 | -0.423000 | 7.14e-04 | 8.30e-01 | 3.50e-02 | 1.52e-02 |
Carnitine metabolism | 11 | 3.97e-03 | 1.11e-02 | 0.8130 | -0.275000 | -0.434000 | -0.568000 | -0.272000 | 1.14e-01 | 1.28e-02 | 1.12e-03 | 1.18e-01 |
Cell recruitment (pro-inflammatory response) | 12 | 8.63e-03 | 2.09e-02 | 0.8100 | 0.518000 | -0.020500 | 0.347000 | 0.517000 | 1.89e-03 | 9.02e-01 | 3.72e-02 | 1.94e-03 |
Purinergic signaling in leishmaniasis infection | 12 | 8.63e-03 | 2.09e-02 | 0.8100 | 0.518000 | -0.020500 | 0.347000 | 0.517000 | 1.89e-03 | 9.02e-01 | 3.72e-02 | 1.94e-03 |
A tetrasaccharide linker sequence is required for GAG synthesis | 18 | 1.98e-05 | 1.07e-04 | 0.7970 | 0.600000 | -0.413000 | 0.210000 | 0.246000 | 1.06e-05 | 2.43e-03 | 1.24e-01 | 7.04e-02 |
Respiratory electron transport, ATP synthesis by chemiosmotic coupling, and heat production by uncoupling proteins. | 96 | 1.91e-22 | 1.47e-20 | 0.7950 | -0.508000 | -0.176000 | -0.358000 | -0.464000 | 8.80e-18 | 2.92e-03 | 1.41e-09 | 3.97e-15 |
Caspase activation via Death Receptors in the presence of ligand | 11 | 1.37e-02 | 3.06e-02 | 0.7890 | 0.489000 | -0.239000 | 0.339000 | 0.458000 | 4.96e-03 | 1.70e-01 | 5.15e-02 | 8.50e-03 |
Collagen degradation | 20 | 5.57e-06 | 3.58e-05 | 0.7750 | 0.602000 | -0.274000 | 0.015000 | 0.403000 | 3.18e-06 | 3.37e-02 | 9.07e-01 | 1.79e-03 |
Diseases associated with the TLR signaling cascade | 16 | 9.63e-04 | 3.29e-03 | 0.7720 | 0.358000 | -0.174000 | 0.318000 | 0.580000 | 1.33e-02 | 2.28e-01 | 2.78e-02 | 5.89e-05 |
Diseases of Immune System | 16 | 9.63e-04 | 3.29e-03 | 0.7720 | 0.358000 | -0.174000 | 0.318000 | 0.580000 | 1.33e-02 | 2.28e-01 | 2.78e-02 | 5.89e-05 |
Mitochondrial calcium ion transport | 21 | 7.14e-05 | 3.39e-04 | 0.7720 | -0.598000 | -0.011100 | -0.338000 | -0.351000 | 2.12e-06 | 9.30e-01 | 7.32e-03 | 5.33e-03 |
MET activates PTK2 signaling | 14 | 3.31e-04 | 1.31e-03 | 0.7690 | 0.587000 | -0.431000 | 0.036100 | 0.244000 | 1.44e-04 | 5.24e-03 | 8.15e-01 | 1.14e-01 |
Acyl chain remodelling of PS | 10 | 1.23e-02 | 2.79e-02 | 0.7670 | 0.414000 | 0.218000 | 0.215000 | 0.568000 | 2.33e-02 | 2.34e-01 | 2.38e-01 | 1.86e-03 |
Voltage gated Potassium channels | 11 | 1.04e-03 | 3.54e-03 | 0.7670 | 0.212000 | -0.528000 | -0.361000 | -0.365000 | 2.23e-01 | 2.43e-03 | 3.80e-02 | 3.59e-02 |
Mitochondrial translation | 87 | 1.59e-19 | 1.02e-17 | 0.7640 | -0.554000 | 0.159000 | -0.315000 | -0.389000 | 4.10e-19 | 1.07e-02 | 4.08e-07 | 3.59e-10 |
Syndecan interactions | 17 | 1.45e-03 | 4.64e-03 | 0.7610 | 0.544000 | -0.048400 | 0.357000 | 0.392000 | 1.04e-04 | 7.30e-01 | 1.08e-02 | 5.21e-03 |
N-Glycan antennae elongation | 12 | 6.08e-03 | 1.56e-02 | 0.7590 | 0.262000 | -0.260000 | 0.429000 | 0.505000 | 1.16e-01 | 1.18e-01 | 1.00e-02 | 2.47e-03 |
Other interleukin signaling | 13 | 7.41e-03 | 1.84e-02 | 0.7570 | 0.554000 | -0.131000 | 0.267000 | 0.421000 | 5.43e-04 | 4.12e-01 | 9.55e-02 | 8.60e-03 |
Biotin transport and metabolism | 10 | 3.96e-02 | 7.50e-02 | 0.7570 | -0.323000 | -0.020100 | -0.535000 | -0.426000 | 7.66e-02 | 9.12e-01 | 3.39e-03 | 1.98e-02 |
Mitochondrial translation termination | 81 | 1.65e-17 | 8.47e-16 | 0.7540 | -0.538000 | 0.156000 | -0.293000 | -0.411000 | 5.73e-17 | 1.52e-02 | 5.20e-06 | 1.77e-10 |
Mitochondrial translation elongation | 81 | 1.59e-17 | 8.47e-16 | 0.7530 | -0.542000 | 0.159000 | -0.297000 | -0.399000 | 3.57e-17 | 1.37e-02 | 3.81e-06 | 5.70e-10 |
Gluconeogenesis | 21 | 1.67e-05 | 9.17e-05 | 0.7490 | -0.070100 | -0.555000 | -0.352000 | -0.352000 | 5.78e-01 | 1.06e-05 | 5.28e-03 | 5.23e-03 |
Integrin cell surface interactions | 45 | 1.02e-11 | 1.98e-10 | 0.7480 | 0.599000 | -0.231000 | 0.096500 | 0.372000 | 3.67e-12 | 7.31e-03 | 2.63e-01 | 1.63e-05 |
CS/DS degradation | 10 | 2.00e-02 | 4.18e-02 | 0.7460 | 0.474000 | -0.265000 | 0.163000 | 0.485000 | 9.43e-03 | 1.47e-01 | 3.72e-01 | 7.89e-03 |
Sema3A PAK dependent Axon repulsion | 15 | 3.33e-03 | 9.54e-03 | 0.7460 | 0.315000 | -0.183000 | 0.392000 | 0.520000 | 3.46e-02 | 2.20e-01 | 8.57e-03 | 4.95e-04 |
Phase 0 - rapid depolarisation | 17 | 7.93e-05 | 3.75e-04 | 0.7460 | -0.074000 | -0.622000 | -0.260000 | -0.310000 | 5.98e-01 | 8.98e-06 | 6.35e-02 | 2.69e-02 |
Chondroitin sulfate/dermatan sulfate metabolism | 37 | 1.73e-08 | 1.82e-07 | 0.7440 | 0.566000 | -0.226000 | 0.194000 | 0.380000 | 2.58e-09 | 1.73e-02 | 4.15e-02 | 6.48e-05 |
Elastic fibre formation | 34 | 1.94e-07 | 1.82e-06 | 0.7430 | 0.588000 | -0.040500 | 0.280000 | 0.356000 | 2.98e-09 | 6.83e-01 | 4.82e-03 | 3.36e-04 |
SEMA3A-Plexin repulsion signaling by inhibiting Integrin adhesion | 14 | 5.36e-03 | 1.41e-02 | 0.7430 | 0.441000 | -0.215000 | 0.257000 | 0.495000 | 4.32e-03 | 1.63e-01 | 9.67e-02 | 1.34e-03 |
Regulation of Complement cascade | 13 | 3.47e-04 | 1.36e-03 | 0.7410 | 0.652000 | 0.047400 | -0.009540 | 0.348000 | 4.68e-05 | 7.67e-01 | 9.53e-01 | 2.97e-02 |
Mitochondrial translation initiation | 81 | 4.72e-17 | 2.15e-15 | 0.7400 | -0.540000 | 0.152000 | -0.291000 | -0.385000 | 4.46e-17 | 1.84e-02 | 6.38e-06 | 2.12e-09 |
Formation of tubulin folding intermediates by CCT/TriC | 17 | 1.34e-05 | 7.63e-05 | 0.7390 | 0.075600 | -0.094600 | 0.683000 | 0.255000 | 5.89e-01 | 5.00e-01 | 1.07e-06 | 6.91e-02 |
Binding and Uptake of Ligands by Scavenger Receptors | 23 | 3.26e-05 | 1.67e-04 | 0.7370 | 0.555000 | -0.152000 | 0.157000 | 0.433000 | 4.15e-06 | 2.08e-01 | 1.92e-01 | 3.30e-04 |
tRNA processing in the mitochondrion | 11 | 1.28e-02 | 2.88e-02 | 0.7360 | -0.616000 | 0.021400 | -0.259000 | -0.307000 | 4.00e-04 | 9.02e-01 | 1.37e-01 | 7.80e-02 |
Defects in vitamin and cofactor metabolism | 17 | 1.55e-03 | 4.92e-03 | 0.7350 | -0.346000 | 0.105000 | -0.523000 | -0.368000 | 1.35e-02 | 4.52e-01 | 1.89e-04 | 8.64e-03 |
Degradation of the extracellular matrix | 58 | 8.33e-14 | 2.38e-12 | 0.7340 | 0.540000 | -0.301000 | 0.141000 | 0.370000 | 1.11e-12 | 7.64e-05 | 6.28e-02 | 1.15e-06 |
Regulation of IFNA signaling | 12 | 2.77e-02 | 5.51e-02 | 0.7320 | 0.419000 | -0.037800 | 0.345000 | 0.489000 | 1.19e-02 | 8.21e-01 | 3.85e-02 | 3.35e-03 |
Metabolism of steroid hormones | 12 | 9.82e-03 | 2.32e-02 | 0.7320 | 0.218000 | -0.117000 | 0.387000 | 0.569000 | 1.90e-01 | 4.85e-01 | 2.02e-02 | 6.42e-04 |
Interleukin-4 and Interleukin-13 signaling | 64 | 4.20e-12 | 9.07e-11 | 0.7310 | 0.428000 | -0.130000 | 0.401000 | 0.416000 | 3.24e-09 | 7.28e-02 | 2.88e-08 | 8.56e-09 |
ECM proteoglycans | 37 | 9.76e-09 | 1.12e-07 | 0.7300 | 0.569000 | -0.270000 | 0.143000 | 0.341000 | 2.08e-09 | 4.58e-03 | 1.33e-01 | 3.40e-04 |
Collagen biosynthesis and modifying enzymes | 47 | 3.12e-11 | 5.48e-10 | 0.7290 | 0.500000 | -0.352000 | 0.117000 | 0.379000 | 3.16e-09 | 3.02e-05 | 1.67e-01 | 7.07e-06 |
TP53 Regulates Transcription of Genes Involved in G1 Cell Cycle Arrest | 12 | 1.16e-02 | 2.66e-02 | 0.7260 | 0.274000 | -0.193000 | 0.503000 | 0.403000 | 1.00e-01 | 2.47e-01 | 2.57e-03 | 1.58e-02 |
Synthesis of bile acids and bile salts via 7alpha-hydroxycholesterol | 10 | 6.13e-02 | 1.06e-01 | 0.7250 | -0.386000 | -0.141000 | -0.468000 | -0.371000 | 3.44e-02 | 4.42e-01 | 1.05e-02 | 4.20e-02 |
Laminin interactions | 19 | 1.99e-05 | 1.07e-04 | 0.7240 | 0.575000 | -0.344000 | -0.060300 | 0.268000 | 1.44e-05 | 9.38e-03 | 6.49e-01 | 4.34e-02 |
Defective EXT1 causes exostoses 1, TRPS2 and CHDS | 11 | 1.14e-02 | 2.64e-02 | 0.7230 | 0.537000 | -0.360000 | 0.162000 | 0.280000 | 2.04e-03 | 3.89e-02 | 3.52e-01 | 1.08e-01 |
Defective EXT2 causes exostoses 2 | 11 | 1.14e-02 | 2.64e-02 | 0.7230 | 0.537000 | -0.360000 | 0.162000 | 0.280000 | 2.04e-03 | 3.89e-02 | 3.52e-01 | 1.08e-01 |
rRNA modification in the nucleus and cytosol | 52 | 1.28e-15 | 4.91e-14 | 0.7220 | -0.181000 | 0.601000 | 0.357000 | 0.011000 | 2.44e-02 | 6.53e-14 | 8.81e-06 | 8.91e-01 |
RHO GTPases Activate WASPs and WAVEs | 31 | 2.90e-05 | 1.49e-04 | 0.7180 | 0.362000 | 0.090600 | 0.428000 | 0.440000 | 4.85e-04 | 3.83e-01 | 3.82e-05 | 2.24e-05 |
NF-kB activation through FADD/RIP-1 pathway mediated by caspase-8 and -10 | 10 | 9.89e-04 | 3.37e-03 | 0.7170 | 0.114000 | -0.245000 | 0.050400 | 0.662000 | 5.32e-01 | 1.80e-01 | 7.82e-01 | 2.88e-04 |
FCGR3A-mediated phagocytosis | 47 | 5.38e-08 | 5.42e-07 | 0.7130 | 0.384000 | -0.011900 | 0.377000 | 0.467000 | 5.20e-06 | 8.88e-01 | 8.09e-06 | 3.05e-08 |
Leishmania phagocytosis | 47 | 5.38e-08 | 5.42e-07 | 0.7130 | 0.384000 | -0.011900 | 0.377000 | 0.467000 | 5.20e-06 | 8.88e-01 | 8.09e-06 | 3.05e-08 |
Parasite infection | 47 | 5.38e-08 | 5.42e-07 | 0.7130 | 0.384000 | -0.011900 | 0.377000 | 0.467000 | 5.20e-06 | 8.88e-01 | 8.09e-06 | 3.05e-08 |
Cristae formation | 10 | 5.76e-02 | 1.02e-01 | 0.7120 | -0.512000 | 0.050200 | -0.293000 | -0.395000 | 5.03e-03 | 7.84e-01 | 1.09e-01 | 3.04e-02 |
Collagen formation | 63 | 7.69e-15 | 2.62e-13 | 0.7110 | 0.507000 | -0.309000 | 0.080700 | 0.383000 | 3.43e-12 | 2.29e-05 | 2.69e-01 | 1.45e-07 |
Extracellular matrix organization | 192 | 7.97e-44 | 3.27e-41 | 0.7110 | 0.545000 | -0.258000 | 0.142000 | 0.348000 | 9.51e-39 | 8.04e-10 | 7.16e-04 | 1.07e-16 |
Glycogen storage diseases | 11 | 2.64e-03 | 7.75e-03 | 0.7090 | -0.370000 | -0.407000 | -0.060700 | -0.443000 | 3.38e-02 | 1.95e-02 | 7.27e-01 | 1.09e-02 |
Diseases associated with glycosaminoglycan metabolism | 30 | 1.97e-06 | 1.41e-05 | 0.7080 | 0.565000 | -0.217000 | 0.193000 | 0.311000 | 8.36e-08 | 3.97e-02 | 6.70e-02 | 3.26e-03 |
Condensation of Prophase Chromosomes | 11 | 6.32e-04 | 2.24e-03 | 0.7060 | -0.153000 | 0.373000 | 0.188000 | 0.548000 | 3.80e-01 | 3.21e-02 | 2.79e-01 | 1.67e-03 |
Postmitotic nuclear pore complex (NPC) reformation | 24 | 1.70e-06 | 1.23e-05 | 0.7050 | -0.187000 | 0.544000 | 0.351000 | 0.208000 | 1.14e-01 | 4.01e-06 | 2.97e-03 | 7.72e-02 |
Processing of SMDT1 | 15 | 2.49e-03 | 7.38e-03 | 0.7030 | -0.584000 | 0.149000 | -0.268000 | -0.244000 | 9.01e-05 | 3.18e-01 | 7.29e-02 | 1.01e-01 |
GPVI-mediated activation cascade | 18 | 3.88e-03 | 1.09e-02 | 0.7010 | 0.235000 | 0.160000 | 0.461000 | 0.444000 | 8.40e-02 | 2.41e-01 | 7.03e-04 | 1.11e-03 |
Activation of PPARGC1A (PGC-1alpha) by phosphorylation | 10 | 4.97e-02 | 9.06e-02 | 0.7000 | -0.198000 | -0.379000 | -0.426000 | -0.356000 | 2.78e-01 | 3.82e-02 | 1.98e-02 | 5.12e-02 |
Heparan sulfate/heparin (HS-GAG) metabolism | 34 | 3.73e-07 | 3.32e-06 | 0.6950 | 0.537000 | -0.272000 | 0.173000 | 0.300000 | 5.94e-08 | 6.01e-03 | 8.04e-02 | 2.48e-03 |
Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs) | 65 | 2.15e-13 | 5.63e-12 | 0.6940 | 0.557000 | -0.093700 | 0.169000 | 0.367000 | 8.07e-15 | 1.92e-01 | 1.88e-02 | 3.29e-07 |
EGR2 and SOX10-mediated initiation of Schwann cell myelination | 20 | 6.74e-05 | 3.22e-04 | 0.6890 | 0.179000 | -0.422000 | 0.311000 | 0.409000 | 1.67e-01 | 1.08e-03 | 1.62e-02 | 1.55e-03 |
Assembly of collagen fibrils and other multimeric structures | 42 | 4.73e-10 | 6.68e-09 | 0.6880 | 0.506000 | -0.284000 | 0.002670 | 0.370000 | 1.42e-08 | 1.46e-03 | 9.76e-01 | 3.32e-05 |
Synthesis of bile acids and bile salts | 18 | 7.00e-03 | 1.76e-02 | 0.6870 | -0.392000 | -0.098600 | -0.395000 | -0.391000 | 4.00e-03 | 4.69e-01 | 3.70e-03 | 4.13e-03 |
Heme biosynthesis | 12 | 1.48e-02 | 3.23e-02 | 0.6860 | -0.132000 | -0.127000 | -0.580000 | -0.317000 | 4.29e-01 | 4.45e-01 | 4.99e-04 | 5.77e-02 |
Post-translational protein phosphorylation | 62 | 4.30e-12 | 9.12e-11 | 0.6860 | 0.543000 | -0.078400 | 0.187000 | 0.367000 | 1.48e-13 | 2.87e-01 | 1.10e-02 | 5.90e-07 |
p130Cas linkage to MAPK signaling for integrins | 10 | 1.29e-02 | 2.89e-02 | 0.6860 | 0.400000 | -0.141000 | 0.520000 | 0.140000 | 2.85e-02 | 4.39e-01 | 4.42e-03 | 4.42e-01 |
Plasma lipoprotein remodeling | 11 | 8.59e-03 | 2.09e-02 | 0.6820 | 0.507000 | -0.282000 | -0.051100 | 0.355000 | 3.62e-03 | 1.06e-01 | 7.69e-01 | 4.17e-02 |
Striated Muscle Contraction | 30 | 1.01e-07 | 9.91e-07 | 0.6800 | 0.030300 | -0.602000 | -0.187000 | -0.254000 | 7.74e-01 | 1.15e-08 | 7.60e-02 | 1.62e-02 |
CRMPs in Sema3A signaling | 12 | 3.79e-02 | 7.27e-02 | 0.6800 | 0.363000 | -0.202000 | 0.335000 | 0.422000 | 2.97e-02 | 2.26e-01 | 4.47e-02 | 1.14e-02 |
LDL clearance | 14 | 8.58e-03 | 2.09e-02 | 0.6750 | 0.305000 | 0.023000 | 0.219000 | 0.561000 | 4.82e-02 | 8.81e-01 | 1.56e-01 | 2.83e-04 |
Retinoid metabolism and transport | 19 | 1.61e-03 | 5.04e-03 | 0.6710 | 0.372000 | -0.262000 | 0.205000 | 0.449000 | 5.01e-03 | 4.81e-02 | 1.23e-01 | 7.08e-04 |
Class A/1 (Rhodopsin-like receptors) | 38 | 3.05e-07 | 2.73e-06 | 0.6710 | 0.557000 | -0.069400 | 0.233000 | 0.284000 | 2.86e-09 | 4.60e-01 | 1.32e-02 | 2.49e-03 |
Activation of IRF3/IRF7 mediated by TBK1/IKK epsilon | 10 | 6.38e-02 | 1.09e-01 | 0.6700 | 0.212000 | 0.109000 | 0.540000 | 0.318000 | 2.46e-01 | 5.49e-01 | 3.12e-03 | 8.18e-02 |
Transport of the SLBP Dependant Mature mRNA | 29 | 6.43e-07 | 5.41e-06 | 0.6670 | -0.141000 | 0.557000 | 0.307000 | 0.144000 | 1.89e-01 | 2.11e-07 | 4.18e-03 | 1.78e-01 |
Mitochondrial protein import | 55 | 7.63e-09 | 8.85e-08 | 0.6660 | -0.477000 | -0.007500 | -0.288000 | -0.365000 | 9.51e-10 | 9.23e-01 | 2.27e-04 | 2.92e-06 |
TNFR1-induced proapoptotic signaling | 11 | 4.27e-02 | 7.99e-02 | 0.6640 | 0.383000 | -0.322000 | 0.254000 | 0.354000 | 2.78e-02 | 6.44e-02 | 1.45e-01 | 4.21e-02 |
Metabolism of non-coding RNA | 45 | 2.13e-11 | 3.80e-10 | 0.6630 | -0.273000 | 0.557000 | 0.236000 | -0.010100 | 1.57e-03 | 1.03e-10 | 6.24e-03 | 9.06e-01 |
snRNP Assembly | 45 | 2.13e-11 | 3.80e-10 | 0.6630 | -0.273000 | 0.557000 | 0.236000 | -0.010100 | 1.57e-03 | 1.03e-10 | 6.24e-03 | 9.06e-01 |
NCAM1 interactions | 21 | 3.48e-05 | 1.77e-04 | 0.6620 | 0.367000 | -0.486000 | -0.142000 | 0.215000 | 3.60e-03 | 1.15e-04 | 2.61e-01 | 8.76e-02 |
Unwinding of DNA | 10 | 5.90e-02 | 1.04e-01 | 0.6590 | 0.135000 | -0.035000 | 0.473000 | 0.436000 | 4.59e-01 | 8.48e-01 | 9.56e-03 | 1.70e-02 |
N-glycan antennae elongation in the medial/trans-Golgi | 17 | 5.80e-03 | 1.50e-02 | 0.6580 | 0.239000 | -0.124000 | 0.339000 | 0.496000 | 8.88e-02 | 3.77e-01 | 1.55e-02 | 3.96e-04 |
Transport of the SLBP independent Mature mRNA | 28 | 1.53e-06 | 1.13e-05 | 0.6570 | -0.155000 | 0.557000 | 0.285000 | 0.128000 | 1.56e-01 | 3.43e-07 | 9.14e-03 | 2.41e-01 |
Defective B3GALTL causes Peters-plus syndrome (PpS) | 23 | 7.57e-06 | 4.68e-05 | 0.6560 | 0.455000 | -0.187000 | -0.082700 | 0.426000 | 1.58e-04 | 1.21e-01 | 4.92e-01 | 4.06e-04 |
Regulation of actin dynamics for phagocytic cup formation | 49 | 3.88e-07 | 3.43e-06 | 0.6550 | 0.309000 | -0.022400 | 0.373000 | 0.440000 | 1.85e-04 | 7.86e-01 | 6.21e-06 | 1.02e-07 |
O-glycosylation of TSR domain-containing proteins | 24 | 8.56e-06 | 5.18e-05 | 0.6550 | 0.459000 | -0.186000 | -0.053900 | 0.424000 | 9.87e-05 | 1.14e-01 | 6.48e-01 | 3.21e-04 |
FOXO-mediated transcription of oxidative stress, metabolic and neuronal genes | 20 | 5.18e-03 | 1.37e-02 | 0.6540 | -0.374000 | -0.168000 | -0.378000 | -0.342000 | 3.79e-03 | 1.94e-01 | 3.45e-03 | 8.09e-03 |
Transport of Ribonucleoproteins into the Host Nucleus | 25 | 5.49e-06 | 3.55e-05 | 0.6530 | -0.227000 | 0.542000 | 0.270000 | 0.095000 | 4.93e-02 | 2.75e-06 | 1.97e-02 | 4.11e-01 |
Leading Strand Synthesis | 14 | 5.61e-03 | 1.45e-02 | 0.6520 | -0.014900 | 0.228000 | 0.392000 | 0.469000 | 9.23e-01 | 1.40e-01 | 1.12e-02 | 2.40e-03 |
Polymerase switching | 14 | 5.61e-03 | 1.45e-02 | 0.6520 | -0.014900 | 0.228000 | 0.392000 | 0.469000 | 9.23e-01 | 1.40e-01 | 1.12e-02 | 2.40e-03 |
Collagen chain trimerization | 31 | 1.13e-06 | 8.69e-06 | 0.6510 | 0.464000 | -0.306000 | -0.010700 | 0.340000 | 7.92e-06 | 3.21e-03 | 9.18e-01 | 1.06e-03 |
Sulfur amino acid metabolism | 21 | 1.14e-03 | 3.78e-03 | 0.6500 | -0.298000 | -0.196000 | -0.236000 | -0.490000 | 1.83e-02 | 1.20e-01 | 6.16e-02 | 1.01e-04 |
Effects of PIP2 hydrolysis | 19 | 1.66e-05 | 9.15e-05 | 0.6490 | 0.375000 | -0.324000 | -0.389000 | -0.155000 | 4.62e-03 | 1.46e-02 | 3.37e-03 | 2.43e-01 |
Transcriptional activation of mitochondrial biogenesis | 47 | 1.58e-06 | 1.16e-05 | 0.6470 | -0.373000 | -0.044800 | -0.375000 | -0.370000 | 9.99e-06 | 5.96e-01 | 8.80e-06 | 1.17e-05 |
Mitochondrial biogenesis | 66 | 3.45e-09 | 4.24e-08 | 0.6470 | -0.368000 | -0.070800 | -0.363000 | -0.382000 | 2.34e-07 | 3.21e-01 | 3.54e-07 | 8.26e-08 |
Nuclear import of Rev protein | 26 | 5.46e-06 | 3.55e-05 | 0.6460 | -0.187000 | 0.534000 | 0.275000 | 0.148000 | 9.87e-02 | 2.45e-06 | 1.53e-02 | 1.91e-01 |
EPHB-mediated forward signaling | 32 | 1.73e-04 | 7.34e-04 | 0.6460 | 0.401000 | 0.019900 | 0.322000 | 0.390000 | 8.58e-05 | 8.46e-01 | 1.63e-03 | 1.34e-04 |
SUMOylation of SUMOylation proteins | 27 | 3.01e-06 | 2.05e-05 | 0.6440 | -0.211000 | 0.543000 | 0.254000 | 0.104000 | 5.76e-02 | 1.04e-06 | 2.26e-02 | 3.51e-01 |
Export of Viral Ribonucleoproteins from Nucleus | 26 | 7.57e-06 | 4.68e-05 | 0.6430 | -0.163000 | 0.543000 | 0.275000 | 0.129000 | 1.51e-01 | 1.64e-06 | 1.54e-02 | 2.55e-01 |
Interactions of Rev with host cellular proteins | 29 | 2.59e-06 | 1.80e-05 | 0.6360 | -0.153000 | 0.499000 | 0.318000 | 0.176000 | 1.55e-01 | 3.30e-06 | 3.02e-03 | 1.00e-01 |
Keratinization | 11 | 2.86e-02 | 5.64e-02 | 0.6350 | 0.369000 | -0.395000 | 0.270000 | 0.196000 | 3.42e-02 | 2.33e-02 | 1.21e-01 | 2.61e-01 |
Defective TPR may confer susceptibility towards thyroid papillary carcinoma (TPC) | 23 | 3.50e-05 | 1.77e-04 | 0.6350 | -0.202000 | 0.539000 | 0.235000 | 0.127000 | 9.31e-02 | 7.62e-06 | 5.09e-02 | 2.91e-01 |
Regulation of Glucokinase by Glucokinase Regulatory Protein | 23 | 3.50e-05 | 1.77e-04 | 0.6350 | -0.202000 | 0.539000 | 0.235000 | 0.127000 | 9.31e-02 | 7.62e-06 | 5.09e-02 | 2.91e-01 |
SUMOylation of DNA replication proteins | 35 | 2.18e-07 | 2.03e-06 | 0.6340 | -0.114000 | 0.499000 | 0.316000 | 0.200000 | 2.44e-01 | 3.19e-07 | 1.21e-03 | 4.08e-02 |
NGF-stimulated transcription | 30 | 1.25e-05 | 7.20e-05 | 0.6340 | 0.349000 | -0.032200 | 0.493000 | 0.188000 | 9.32e-04 | 7.61e-01 | 2.98e-06 | 7.42e-02 |
Non-integrin membrane-ECM interactions | 35 | 1.28e-06 | 9.57e-06 | 0.6340 | 0.503000 | -0.281000 | 0.093700 | 0.246000 | 2.60e-07 | 4.08e-03 | 3.38e-01 | 1.18e-02 |
Glycogen breakdown (glycogenolysis) | 14 | 7.44e-03 | 1.85e-02 | 0.6320 | -0.110000 | -0.537000 | -0.259000 | -0.177000 | 4.77e-01 | 4.99e-04 | 9.37e-02 | 2.52e-01 |
The role of Nef in HIV-1 replication and disease pathogenesis | 19 | 5.42e-03 | 1.42e-02 | 0.6320 | 0.209000 | -0.095900 | 0.377000 | 0.452000 | 1.15e-01 | 4.69e-01 | 4.43e-03 | 6.58e-04 |
Zinc transporters | 11 | 6.20e-02 | 1.07e-01 | 0.6310 | 0.372000 | 0.304000 | 0.288000 | 0.290000 | 3.25e-02 | 8.10e-02 | 9.85e-02 | 9.64e-02 |
Signaling by NODAL | 10 | 4.99e-02 | 9.06e-02 | 0.6290 | -0.322000 | -0.167000 | -0.136000 | -0.495000 | 7.81e-02 | 3.59e-01 | 4.57e-01 | 6.69e-03 |
Vpr-mediated nuclear import of PICs | 27 | 4.06e-06 | 2.71e-05 | 0.6280 | -0.252000 | 0.493000 | 0.286000 | 0.080800 | 2.35e-02 | 9.44e-06 | 1.01e-02 | 4.68e-01 |
EPH-ephrin mediated repulsion of cells | 37 | 8.71e-06 | 5.22e-05 | 0.6260 | 0.426000 | -0.125000 | 0.162000 | 0.411000 | 7.56e-06 | 1.89e-01 | 8.78e-02 | 1.51e-05 |
Peroxisomal protein import | 49 | 7.97e-07 | 6.44e-06 | 0.6240 | -0.414000 | -0.116000 | -0.319000 | -0.320000 | 5.45e-07 | 1.60e-01 | 1.15e-04 | 1.06e-04 |
TP53 Regulates Transcription of Death Receptors and Ligands | 11 | 4.10e-02 | 7.73e-02 | 0.6230 | 0.546000 | -0.007260 | 0.152000 | 0.259000 | 1.71e-03 | 9.67e-01 | 3.83e-01 | 1.37e-01 |
NEP/NS2 Interacts with the Cellular Export Machinery | 25 | 2.17e-05 | 1.15e-04 | 0.6230 | -0.194000 | 0.526000 | 0.245000 | 0.119000 | 9.40e-02 | 5.39e-06 | 3.37e-02 | 3.03e-01 |
Carboxyterminal post-translational modifications of tubulin | 21 | 8.96e-04 | 3.09e-03 | 0.6220 | 0.472000 | -0.153000 | 0.063800 | 0.370000 | 1.83e-04 | 2.26e-01 | 6.13e-01 | 3.34e-03 |
SUMOylation of ubiquitinylation proteins | 31 | 2.25e-06 | 1.60e-05 | 0.6190 | -0.127000 | 0.530000 | 0.270000 | 0.111000 | 2.22e-01 | 3.21e-07 | 9.23e-03 | 2.86e-01 |
GRB2:SOS provides linkage to MAPK signaling for Integrins | 10 | 3.71e-02 | 7.15e-02 | 0.6180 | 0.345000 | -0.202000 | 0.449000 | 0.144000 | 5.92e-02 | 2.69e-01 | 1.39e-02 | 4.31e-01 |
Peptide ligand-binding receptors | 22 | 9.19e-04 | 3.16e-03 | 0.6170 | 0.530000 | -0.071400 | 0.195000 | 0.238000 | 1.67e-05 | 5.63e-01 | 1.14e-01 | 5.36e-02 |
Rev-mediated nuclear export of HIV RNA | 28 | 1.15e-05 | 6.68e-05 | 0.6170 | -0.133000 | 0.490000 | 0.306000 | 0.170000 | 2.22e-01 | 7.09e-06 | 5.13e-03 | 1.21e-01 |
RORA activates gene expression | 17 | 2.33e-02 | 4.77e-02 | 0.6140 | -0.385000 | -0.105000 | -0.360000 | -0.297000 | 6.00e-03 | 4.52e-01 | 1.02e-02 | 3.38e-02 |
mRNA Splicing - Major Pathway | 161 | 7.65e-37 | 1.57e-34 | 0.6120 | -0.148000 | 0.509000 | 0.300000 | -0.059500 | 1.26e-03 | 8.41e-29 | 6.11e-11 | 1.95e-01 |
Antigen Presentation: Folding, assembly and peptide loading of class I MHC | 17 | 2.24e-02 | 4.61e-02 | 0.6120 | 0.266000 | 0.229000 | 0.316000 | 0.389000 | 5.76e-02 | 1.02e-01 | 2.43e-02 | 5.52e-03 |
Complement cascade | 14 | 4.23e-03 | 1.17e-02 | 0.6090 | 0.534000 | -0.008580 | -0.029600 | 0.291000 | 5.37e-04 | 9.56e-01 | 8.48e-01 | 5.97e-02 |
Mitotic Telophase/Cytokinesis | 10 | 5.08e-02 | 9.19e-02 | 0.6090 | -0.386000 | 0.399000 | -0.204000 | -0.145000 | 3.45e-02 | 2.90e-02 | 2.65e-01 | 4.28e-01 |
Molecules associated with elastic fibres | 25 | 5.00e-04 | 1.87e-03 | 0.6050 | 0.509000 | 0.033400 | 0.190000 | 0.264000 | 1.06e-05 | 7.73e-01 | 1.00e-01 | 2.24e-02 |
ADP signalling through P2Y purinoceptor 12 | 13 | 1.11e-02 | 2.60e-02 | 0.6030 | 0.518000 | 0.048400 | 0.020800 | 0.305000 | 1.23e-03 | 7.62e-01 | 8.97e-01 | 5.66e-02 |
G-protein activation | 13 | 1.11e-02 | 2.60e-02 | 0.6030 | 0.518000 | 0.048400 | 0.020800 | 0.305000 | 1.23e-03 | 7.62e-01 | 8.97e-01 | 5.66e-02 |
mRNA Splicing | 169 | 1.11e-37 | 2.73e-35 | 0.6020 | -0.161000 | 0.501000 | 0.283000 | -0.074400 | 3.36e-04 | 2.87e-29 | 2.52e-10 | 9.66e-02 |
Interactions of Vpr with host cellular proteins | 29 | 5.45e-06 | 3.55e-05 | 0.6020 | -0.228000 | 0.477000 | 0.280000 | 0.073100 | 3.37e-02 | 8.95e-06 | 9.19e-03 | 4.96e-01 |
Synaptic adhesion-like molecules | 12 | 1.75e-02 | 3.75e-02 | 0.6020 | 0.448000 | -0.343000 | -0.078200 | 0.194000 | 7.20e-03 | 3.94e-02 | 6.39e-01 | 2.45e-01 |
Cell surface interactions at the vascular wall | 71 | 1.78e-10 | 2.80e-09 | 0.6010 | 0.355000 | -0.262000 | 0.190000 | 0.361000 | 2.36e-07 | 1.39e-04 | 5.61e-03 | 1.51e-07 |
RIP-mediated NFkB activation via ZBP1 | 14 | 4.38e-02 | 8.15e-02 | 0.6000 | 0.149000 | 0.076800 | 0.361000 | 0.449000 | 3.34e-01 | 6.19e-01 | 1.94e-02 | 3.63e-03 |
Transport of Mature mRNA derived from an Intron-Containing Transcript | 59 | 3.66e-12 | 8.10e-11 | 0.6000 | -0.124000 | 0.527000 | 0.258000 | -0.020900 | 9.97e-02 | 2.61e-12 | 6.23e-04 | 7.82e-01 |
Role of LAT2/NTAL/LAB on calcium mobilization | 11 | 4.84e-02 | 8.88e-02 | 0.5980 | 0.000527 | 0.201000 | 0.497000 | 0.264000 | 9.98e-01 | 2.49e-01 | 4.32e-03 | 1.30e-01 |
EPHA-mediated growth cone collapse | 13 | 5.06e-02 | 9.17e-02 | 0.5970 | 0.435000 | -0.103000 | 0.325000 | 0.226000 | 6.57e-03 | 5.21e-01 | 4.23e-02 | 1.59e-01 |
Cobalamin (Cbl, vitamin B12) transport and metabolism | 11 | 7.70e-02 | 1.28e-01 | 0.5970 | -0.299000 | 0.149000 | -0.430000 | -0.243000 | 8.57e-02 | 3.91e-01 | 1.35e-02 | 1.63e-01 |
Processing of Capped Intron-Containing Pre-mRNA | 211 | 1.05e-45 | 6.43e-43 | 0.5960 | -0.154000 | 0.502000 | 0.274000 | -0.065400 | 1.24e-04 | 3.59e-36 | 8.70e-12 | 1.04e-01 |
Formation of Fibrin Clot (Clotting Cascade) | 13 | 3.48e-02 | 6.79e-02 | 0.5960 | 0.471000 | 0.073000 | 0.127000 | 0.334000 | 3.30e-03 | 6.49e-01 | 4.29e-01 | 3.69e-02 |
EPH-Ephrin signaling | 75 | 2.25e-09 | 2.88e-08 | 0.5950 | 0.396000 | -0.083300 | 0.274000 | 0.340000 | 3.10e-09 | 2.13e-01 | 4.17e-05 | 3.80e-07 |
ZBP1(DAI) mediated induction of type I IFNs | 17 | 2.16e-02 | 4.47e-02 | 0.5950 | 0.195000 | 0.095400 | 0.307000 | 0.461000 | 1.65e-01 | 4.96e-01 | 2.86e-02 | 1.01e-03 |
HIV Transcription Initiation | 40 | 1.16e-08 | 1.25e-07 | 0.5930 | -0.206000 | 0.453000 | 0.313000 | -0.075200 | 2.45e-02 | 7.25e-07 | 6.17e-04 | 4.11e-01 |
RNA Polymerase II HIV Promoter Escape | 40 | 1.16e-08 | 1.25e-07 | 0.5930 | -0.206000 | 0.453000 | 0.313000 | -0.075200 | 2.45e-02 | 7.25e-07 | 6.17e-04 | 4.11e-01 |
RNA Polymerase II Promoter Escape | 40 | 1.16e-08 | 1.25e-07 | 0.5930 | -0.206000 | 0.453000 | 0.313000 | -0.075200 | 2.45e-02 | 7.25e-07 | 6.17e-04 | 4.11e-01 |
RNA Polymerase II Transcription Initiation | 40 | 1.16e-08 | 1.25e-07 | 0.5930 | -0.206000 | 0.453000 | 0.313000 | -0.075200 | 2.45e-02 | 7.25e-07 | 6.17e-04 | 4.11e-01 |
RNA Polymerase II Transcription Initiation And Promoter Clearance | 40 | 1.16e-08 | 1.25e-07 | 0.5930 | -0.206000 | 0.453000 | 0.313000 | -0.075200 | 2.45e-02 | 7.25e-07 | 6.17e-04 | 4.11e-01 |
RNA Polymerase II Transcription Pre-Initiation And Promoter Opening | 40 | 1.16e-08 | 1.25e-07 | 0.5930 | -0.206000 | 0.453000 | 0.313000 | -0.075200 | 2.45e-02 | 7.25e-07 | 6.17e-04 | 4.11e-01 |
p75NTR signals via NF-kB | 13 | 4.76e-02 | 8.76e-02 | 0.5920 | 0.292000 | 0.002260 | 0.465000 | 0.222000 | 6.87e-02 | 9.89e-01 | 3.71e-03 | 1.66e-01 |
Activation of SMO | 12 | 1.13e-02 | 2.63e-02 | 0.5890 | 0.512000 | -0.189000 | -0.115000 | 0.190000 | 2.16e-03 | 2.58e-01 | 4.91e-01 | 2.55e-01 |
Viral Messenger RNA Synthesis | 35 | 1.12e-06 | 8.69e-06 | 0.5890 | -0.170000 | 0.467000 | 0.295000 | 0.112000 | 8.26e-02 | 1.78e-06 | 2.52e-03 | 2.51e-01 |
Caspase-mediated cleavage of cytoskeletal proteins | 11 | 1.14e-01 | 1.75e-01 | 0.5830 | 0.359000 | -0.257000 | 0.239000 | 0.297000 | 3.90e-02 | 1.40e-01 | 1.71e-01 | 8.86e-02 |
ABC transporters in lipid homeostasis | 11 | 5.74e-03 | 1.48e-02 | 0.5820 | 0.063300 | -0.122000 | -0.566000 | -0.004480 | 7.16e-01 | 4.82e-01 | 1.16e-03 | 9.79e-01 |
Nuclear Receptor transcription pathway | 37 | 2.08e-05 | 1.11e-04 | 0.5800 | -0.304000 | -0.341000 | -0.274000 | -0.229000 | 1.41e-03 | 3.39e-04 | 3.89e-03 | 1.62e-02 |
Interaction between L1 and Ankyrins | 14 | 1.13e-02 | 2.63e-02 | 0.5790 | -0.043300 | -0.512000 | -0.268000 | -0.021900 | 7.79e-01 | 9.19e-04 | 8.31e-02 | 8.87e-01 |
ROS and RNS production in phagocytes | 20 | 3.62e-03 | 1.02e-02 | 0.5790 | 0.172000 | -0.036200 | 0.224000 | 0.504000 | 1.83e-01 | 7.79e-01 | 8.28e-02 | 9.57e-05 |
Thrombin signalling through proteinase activated receptors (PARs) | 20 | 1.25e-02 | 2.82e-02 | 0.5790 | 0.431000 | -0.049600 | 0.187000 | 0.334000 | 8.45e-04 | 7.01e-01 | 1.47e-01 | 9.82e-03 |
Transport of Mature mRNAs Derived from Intronless Transcripts | 36 | 1.49e-06 | 1.10e-05 | 0.5780 | -0.146000 | 0.469000 | 0.290000 | 0.091500 | 1.31e-01 | 1.12e-06 | 2.62e-03 | 3.43e-01 |
Translation of Replicase and Assembly of the Replication Transcription Complex | 11 | 2.13e-02 | 4.41e-02 | 0.5780 | -0.495000 | 0.239000 | -0.178000 | -0.019400 | 4.51e-03 | 1.70e-01 | 3.06e-01 | 9.11e-01 |
Metabolism of fat-soluble vitamins | 22 | 4.60e-03 | 1.25e-02 | 0.5770 | 0.327000 | -0.235000 | 0.166000 | 0.379000 | 8.00e-03 | 5.69e-02 | 1.78e-01 | 2.07e-03 |
Ephrin signaling | 18 | 1.65e-02 | 3.56e-02 | 0.5770 | 0.365000 | -0.192000 | 0.321000 | 0.244000 | 7.37e-03 | 1.59e-01 | 1.83e-02 | 7.34e-02 |
Retrograde neurotrophin signalling | 11 | 1.07e-01 | 1.66e-01 | 0.5750 | 0.239000 | 0.022800 | 0.212000 | 0.478000 | 1.70e-01 | 8.96e-01 | 2.24e-01 | 6.03e-03 |
RNA Polymerase II Pre-transcription Events | 69 | 6.15e-14 | 1.84e-12 | 0.5750 | -0.199000 | 0.433000 | 0.321000 | -0.025800 | 4.37e-03 | 5.24e-10 | 4.25e-06 | 7.11e-01 |
Adrenaline,noradrenaline inhibits insulin secretion | 16 | 1.66e-03 | 5.16e-03 | 0.5730 | 0.506000 | -0.036900 | -0.104000 | 0.245000 | 4.56e-04 | 7.99e-01 | 4.73e-01 | 8.93e-02 |
Long-term potentiation | 10 | 3.94e-02 | 7.49e-02 | 0.5730 | 0.080000 | -0.507000 | -0.093600 | -0.237000 | 6.61e-01 | 5.50e-03 | 6.09e-01 | 1.94e-01 |
Class I peroxisomal membrane protein import | 20 | 2.63e-02 | 5.27e-02 | 0.5710 | -0.355000 | 0.040400 | -0.310000 | -0.320000 | 6.02e-03 | 7.55e-01 | 1.65e-02 | 1.33e-02 |
Glycosaminoglycan metabolism | 80 | 3.64e-10 | 5.33e-09 | 0.5710 | 0.404000 | -0.144000 | 0.174000 | 0.334000 | 4.35e-10 | 2.59e-02 | 7.38e-03 | 2.56e-07 |
Caspase activation via extrinsic apoptotic signalling pathway | 19 | 1.41e-02 | 3.10e-02 | 0.5700 | 0.310000 | -0.264000 | 0.212000 | 0.338000 | 1.93e-02 | 4.66e-02 | 1.10e-01 | 1.08e-02 |
Transport of Mature Transcript to Cytoplasm | 68 | 8.92e-13 | 2.24e-11 | 0.5690 | -0.118000 | 0.485000 | 0.271000 | -0.026200 | 9.34e-02 | 4.56e-12 | 1.16e-04 | 7.09e-01 |
Transport of Mature mRNA Derived from an Intronless Transcript | 35 | 3.41e-06 | 2.31e-05 | 0.5670 | -0.157000 | 0.467000 | 0.271000 | 0.076900 | 1.08e-01 | 1.80e-06 | 5.50e-03 | 4.31e-01 |
Interferon gamma signaling | 43 | 7.99e-06 | 4.91e-05 | 0.5670 | 0.470000 | -0.040300 | 0.211000 | 0.235000 | 1.01e-07 | 6.48e-01 | 1.70e-02 | 7.69e-03 |
Cardiac conduction | 60 | 2.02e-09 | 2.64e-08 | 0.5670 | -0.034600 | -0.459000 | -0.284000 | -0.168000 | 6.43e-01 | 7.70e-10 | 1.41e-04 | 2.45e-02 |
HS-GAG biosynthesis | 18 | 1.18e-02 | 2.70e-02 | 0.5660 | 0.392000 | -0.292000 | 0.201000 | 0.204000 | 4.01e-03 | 3.22e-02 | 1.40e-01 | 1.34e-01 |
Transcription of the HIV genome | 59 | 1.69e-11 | 3.19e-10 | 0.5660 | -0.177000 | 0.436000 | 0.310000 | -0.043800 | 1.86e-02 | 6.93e-09 | 3.91e-05 | 5.61e-01 |
Regulation of KIT signaling | 14 | 4.86e-02 | 8.89e-02 | 0.5650 | 0.401000 | -0.224000 | 0.252000 | 0.212000 | 9.39e-03 | 1.47e-01 | 1.03e-01 | 1.70e-01 |
Diseases associated with O-glycosylation of proteins | 32 | 1.51e-05 | 8.45e-05 | 0.5650 | 0.334000 | -0.220000 | -0.012700 | 0.399000 | 1.08e-03 | 3.15e-02 | 9.01e-01 | 9.44e-05 |
Platelet degranulation | 86 | 7.46e-11 | 1.27e-09 | 0.5650 | 0.387000 | -0.142000 | 0.158000 | 0.352000 | 6.00e-10 | 2.30e-02 | 1.12e-02 | 1.72e-08 |
AKT phosphorylates targets in the nucleus | 10 | 1.37e-01 | 2.00e-01 | 0.5650 | -0.219000 | -0.381000 | -0.282000 | -0.215000 | 2.30e-01 | 3.71e-02 | 1.23e-01 | 2.39e-01 |
Nef-mediates down modulation of cell surface receptors by recruiting them to clathrin adapters | 15 | 3.50e-02 | 6.82e-02 | 0.5640 | 0.141000 | -0.125000 | 0.332000 | 0.415000 | 3.45e-01 | 4.04e-01 | 2.59e-02 | 5.35e-03 |
NS1 Mediated Effects on Host Pathways | 31 | 2.17e-05 | 1.15e-04 | 0.5630 | -0.150000 | 0.452000 | 0.289000 | 0.077700 | 1.49e-01 | 1.33e-05 | 5.36e-03 | 4.54e-01 |
Prefoldin mediated transfer of substrate to CCT/TriC | 22 | 4.44e-04 | 1.68e-03 | 0.5610 | -0.015300 | 0.124000 | 0.520000 | 0.169000 | 9.01e-01 | 3.14e-01 | 2.39e-05 | 1.69e-01 |
Smooth Muscle Contraction | 31 | 5.74e-07 | 4.86e-06 | 0.5590 | 0.250000 | -0.470000 | 0.133000 | -0.107000 | 1.63e-02 | 6.03e-06 | 1.99e-01 | 3.05e-01 |
PINK1-PRKN Mediated Mitophagy | 17 | 1.39e-02 | 3.08e-02 | 0.5580 | -0.471000 | 0.134000 | -0.068000 | -0.259000 | 7.72e-04 | 3.40e-01 | 6.28e-01 | 6.43e-02 |
Glycogen metabolism | 23 | 1.16e-03 | 3.82e-03 | 0.5580 | -0.245000 | -0.414000 | -0.167000 | -0.229000 | 4.24e-02 | 5.88e-04 | 1.66e-01 | 5.74e-02 |
Keratan sulfate/keratin metabolism | 22 | 4.40e-03 | 1.20e-02 | 0.5550 | 0.263000 | -0.169000 | 0.146000 | 0.435000 | 3.26e-02 | 1.70e-01 | 2.38e-01 | 4.13e-04 |
WNT5A-dependent internalization of FZD2, FZD5 and ROR2 | 13 | 5.45e-02 | 9.74e-02 | 0.5530 | 0.068300 | 0.008600 | 0.322000 | 0.444000 | 6.70e-01 | 9.57e-01 | 4.41e-02 | 5.60e-03 |
Muscle contraction | 116 | 6.33e-20 | 4.32e-18 | 0.5520 | 0.056400 | -0.499000 | -0.159000 | -0.165000 | 2.95e-01 | 1.94e-20 | 3.13e-03 | 2.17e-03 |
Defects in cobalamin (B12) metabolism | 10 | 1.15e-01 | 1.76e-01 | 0.5510 | -0.243000 | 0.139000 | -0.436000 | -0.188000 | 1.83e-01 | 4.48e-01 | 1.69e-02 | 3.03e-01 |
DNA strand elongation | 30 | 2.73e-04 | 1.10e-03 | 0.5510 | 0.015200 | 0.136000 | 0.355000 | 0.399000 | 8.85e-01 | 1.97e-01 | 7.78e-04 | 1.54e-04 |
SUMOylation of intracellular receptors | 23 | 4.59e-03 | 1.25e-02 | 0.5490 | -0.340000 | -0.247000 | -0.178000 | -0.305000 | 4.81e-03 | 4.04e-02 | 1.39e-01 | 1.15e-02 |
Peroxisomal lipid metabolism | 22 | 5.99e-03 | 1.54e-02 | 0.5480 | -0.316000 | -0.094900 | -0.405000 | -0.166000 | 1.03e-02 | 4.41e-01 | 1.01e-03 | 1.78e-01 |
Ion homeostasis | 36 | 3.52e-05 | 1.77e-04 | 0.5470 | -0.016300 | -0.432000 | -0.282000 | -0.181000 | 8.65e-01 | 7.25e-06 | 3.40e-03 | 6.07e-02 |
Gap junction trafficking | 10 | 1.98e-01 | 2.74e-01 | 0.5460 | 0.415000 | 0.070200 | 0.174000 | 0.301000 | 2.30e-02 | 7.01e-01 | 3.42e-01 | 9.95e-02 |
Cyclin A/B1/B2 associated events during G2/M transition | 17 | 1.13e-02 | 2.63e-02 | 0.5430 | -0.011600 | 0.395000 | 0.361000 | 0.091200 | 9.34e-01 | 4.78e-03 | 9.98e-03 | 5.15e-01 |
Synthesis of PIPs at the late endosome membrane | 10 | 6.24e-03 | 1.59e-02 | 0.5430 | -0.367000 | 0.258000 | -0.116000 | 0.282000 | 4.43e-02 | 1.57e-01 | 5.27e-01 | 1.22e-01 |
Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding | 24 | 3.45e-04 | 1.35e-03 | 0.5420 | 0.003880 | 0.068100 | 0.510000 | 0.172000 | 9.74e-01 | 5.64e-01 | 1.56e-05 | 1.46e-01 |
mRNA 3'-end processing | 48 | 6.85e-09 | 8.09e-08 | 0.5420 | -0.120000 | 0.423000 | 0.304000 | -0.086900 | 1.50e-01 | 4.10e-07 | 2.68e-04 | 2.98e-01 |
Major pathway of rRNA processing in the nucleolus and cytosol | 134 | 5.95e-26 | 8.13e-24 | 0.5380 | -0.100000 | 0.359000 | 0.386000 | -0.041700 | 4.60e-02 | 8.19e-13 | 1.39e-14 | 4.06e-01 |
Semaphorin interactions | 53 | 1.12e-05 | 6.60e-05 | 0.5380 | 0.302000 | -0.173000 | 0.245000 | 0.329000 | 1.43e-04 | 2.96e-02 | 2.05e-03 | 3.57e-05 |
Nuclear Pore Complex (NPC) Disassembly | 27 | 1.55e-04 | 6.67e-04 | 0.5380 | -0.223000 | 0.428000 | 0.207000 | 0.117000 | 4.52e-02 | 1.21e-04 | 6.28e-02 | 2.91e-01 |
Fcgamma receptor (FCGR) dependent phagocytosis | 67 | 1.20e-06 | 9.14e-06 | 0.5370 | 0.304000 | -0.064900 | 0.256000 | 0.356000 | 1.78e-05 | 3.59e-01 | 3.02e-04 | 4.80e-07 |
Response to elevated platelet cytosolic Ca2+ | 89 | 2.55e-10 | 3.82e-09 | 0.5370 | 0.376000 | -0.138000 | 0.139000 | 0.330000 | 9.57e-10 | 2.45e-02 | 2.35e-02 | 7.95e-08 |
ATF6 (ATF6-alpha) activates chaperone genes | 10 | 7.48e-02 | 1.26e-01 | 0.5360 | 0.010100 | 0.117000 | 0.504000 | 0.139000 | 9.56e-01 | 5.21e-01 | 5.80e-03 | 4.46e-01 |
rRNA processing in the nucleus and cytosol | 143 | 1.65e-27 | 2.90e-25 | 0.5360 | -0.102000 | 0.368000 | 0.372000 | -0.053300 | 3.61e-02 | 3.72e-14 | 1.71e-14 | 2.73e-01 |
mRNA Splicing - Minor Pathway | 47 | 1.55e-08 | 1.66e-07 | 0.5350 | -0.201000 | 0.399000 | 0.275000 | -0.106000 | 1.74e-02 | 2.26e-06 | 1.11e-03 | 2.10e-01 |
RNA Polymerase II Transcription Termination | 56 | 5.85e-10 | 7.91e-09 | 0.5320 | -0.123000 | 0.413000 | 0.303000 | -0.074400 | 1.12e-01 | 9.23e-08 | 8.74e-05 | 3.36e-01 |
Lagging Strand Synthesis | 20 | 5.06e-03 | 1.35e-02 | 0.5310 | -0.044900 | 0.222000 | 0.295000 | 0.380000 | 7.28e-01 | 8.65e-02 | 2.26e-02 | 3.25e-03 |
SUMOylation of RNA binding proteins | 38 | 8.16e-06 | 4.99e-05 | 0.5300 | -0.112000 | 0.452000 | 0.247000 | 0.052400 | 2.32e-01 | 1.40e-06 | 8.35e-03 | 5.77e-01 |
Protein localization | 136 | 1.53e-13 | 4.26e-12 | 0.5290 | -0.360000 | -0.045500 | -0.245000 | -0.297000 | 4.58e-13 | 3.62e-01 | 8.54e-07 | 2.43e-09 |
Pausing and recovery of Tat-mediated HIV elongation | 25 | 5.80e-04 | 2.11e-03 | 0.5290 | -0.042100 | 0.300000 | 0.424000 | 0.088900 | 7.16e-01 | 9.34e-03 | 2.41e-04 | 4.42e-01 |
Tat-mediated HIV elongation arrest and recovery | 25 | 5.80e-04 | 2.11e-03 | 0.5290 | -0.042100 | 0.300000 | 0.424000 | 0.088900 | 7.16e-01 | 9.34e-03 | 2.41e-04 | 4.42e-01 |
Negative regulation of NMDA receptor-mediated neuronal transmission | 12 | 3.69e-02 | 7.13e-02 | 0.5270 | 0.179000 | -0.467000 | -0.079700 | -0.147000 | 2.83e-01 | 5.13e-03 | 6.33e-01 | 3.78e-01 |
Response of Mtb to phagocytosis | 18 | 6.62e-03 | 1.68e-02 | 0.5270 | 0.054800 | 0.273000 | 0.443000 | 0.062800 | 6.88e-01 | 4.47e-02 | 1.15e-03 | 6.45e-01 |
FOXO-mediated transcription of cell death genes | 14 | 4.44e-02 | 8.25e-02 | 0.5260 | -0.395000 | -0.128000 | -0.068100 | -0.315000 | 1.05e-02 | 4.07e-01 | 6.59e-01 | 4.14e-02 |
Signaling by FGFR2 IIIa TM | 16 | 7.98e-03 | 1.97e-02 | 0.5260 | -0.117000 | 0.306000 | 0.410000 | 0.034500 | 4.17e-01 | 3.43e-02 | 4.55e-03 | 8.11e-01 |
Attenuation phase | 20 | 7.79e-04 | 2.74e-03 | 0.5250 | -0.092300 | 0.329000 | 0.390000 | -0.075600 | 4.75e-01 | 1.08e-02 | 2.52e-03 | 5.58e-01 |
CLEC7A (Dectin-1) induces NFAT activation | 10 | 1.81e-01 | 2.54e-01 | 0.5240 | -0.011600 | -0.329000 | -0.299000 | -0.277000 | 9.50e-01 | 7.14e-02 | 1.01e-01 | 1.30e-01 |
Other semaphorin interactions | 14 | 1.16e-02 | 2.66e-02 | 0.5240 | 0.301000 | -0.182000 | -0.123000 | 0.368000 | 5.16e-02 | 2.38e-01 | 4.26e-01 | 1.72e-02 |
Unblocking of NMDA receptors, glutamate binding and activation | 10 | 9.52e-02 | 1.51e-01 | 0.5220 | 0.024500 | -0.440000 | -0.124000 | -0.253000 | 8.93e-01 | 1.61e-02 | 4.99e-01 | 1.67e-01 |
Metal ion SLC transporters | 17 | 9.88e-02 | 1.56e-01 | 0.5220 | 0.263000 | 0.096300 | 0.271000 | 0.348000 | 6.10e-02 | 4.92e-01 | 5.28e-02 | 1.31e-02 |
Insulin receptor recycling | 17 | 9.48e-03 | 2.26e-02 | 0.5220 | 0.085800 | 0.018500 | 0.161000 | 0.488000 | 5.40e-01 | 8.95e-01 | 2.52e-01 | 4.91e-04 |
Adherens junctions interactions | 11 | 9.29e-02 | 1.48e-01 | 0.5210 | 0.235000 | -0.213000 | 0.050100 | 0.410000 | 1.77e-01 | 2.21e-01 | 7.74e-01 | 1.84e-02 |
Activation of the pre-replicative complex | 27 | 2.09e-04 | 8.61e-04 | 0.5210 | -0.135000 | 0.274000 | 0.262000 | 0.332000 | 2.26e-01 | 1.38e-02 | 1.87e-02 | 2.86e-03 |
Infection with Mycobacterium tuberculosis | 19 | 8.34e-03 | 2.05e-02 | 0.5210 | 0.091300 | 0.255000 | 0.436000 | 0.092200 | 4.91e-01 | 5.46e-02 | 1.02e-03 | 4.87e-01 |
Glycosphingolipid metabolism | 32 | 4.96e-04 | 1.86e-03 | 0.5210 | 0.288000 | -0.107000 | 0.094000 | 0.410000 | 4.79e-03 | 2.93e-01 | 3.58e-01 | 6.07e-05 |
MET activates RAP1 and RAC1 | 10 | 2.18e-02 | 4.49e-02 | 0.5210 | -0.126000 | 0.046200 | 0.503000 | 0.008130 | 4.91e-01 | 8.00e-01 | 5.86e-03 | 9.65e-01 |
Integrin signaling | 20 | 1.44e-02 | 3.14e-02 | 0.5200 | 0.265000 | -0.074400 | 0.405000 | 0.173000 | 4.06e-02 | 5.65e-01 | 1.70e-03 | 1.80e-01 |
Cell-extracellular matrix interactions | 16 | 5.57e-02 | 9.94e-02 | 0.5190 | 0.313000 | -0.258000 | 0.238000 | 0.220000 | 3.03e-02 | 7.40e-02 | 9.88e-02 | 1.27e-01 |
Bile acid and bile salt metabolism | 20 | 6.01e-02 | 1.05e-01 | 0.5190 | -0.271000 | -0.116000 | -0.317000 | -0.287000 | 3.61e-02 | 3.71e-01 | 1.42e-02 | 2.62e-02 |
Potassium Channels | 32 | 2.25e-05 | 1.19e-04 | 0.5190 | 0.271000 | -0.344000 | -0.253000 | -0.112000 | 7.91e-03 | 7.52e-04 | 1.34e-02 | 2.72e-01 |
SLBP Dependent Processing of Replication-Dependent Histone Pre-mRNAs | 10 | 8.30e-02 | 1.36e-01 | 0.5180 | -0.220000 | 0.338000 | 0.322000 | 0.051300 | 2.29e-01 | 6.41e-02 | 7.83e-02 | 7.79e-01 |
G beta:gamma signalling through BTK | 10 | 5.93e-02 | 1.05e-01 | 0.5170 | 0.468000 | -0.051900 | -0.108000 | 0.183000 | 1.03e-02 | 7.76e-01 | 5.56e-01 | 3.16e-01 |
Sema4D induced cell migration and growth-cone collapse | 19 | 1.43e-02 | 3.13e-02 | 0.5140 | 0.352000 | -0.206000 | 0.286000 | 0.128000 | 7.90e-03 | 1.20e-01 | 3.10e-02 | 3.32e-01 |
Gap junction trafficking and regulation | 12 | 1.35e-01 | 1.97e-01 | 0.5140 | 0.427000 | 0.013100 | 0.119000 | 0.259000 | 1.05e-02 | 9.37e-01 | 4.77e-01 | 1.20e-01 |
Abortive elongation of HIV-1 transcript in the absence of Tat | 21 | 4.03e-03 | 1.12e-02 | 0.5130 | -0.064900 | 0.286000 | 0.406000 | 0.112000 | 6.07e-01 | 2.34e-02 | 1.27e-03 | 3.73e-01 |
STING mediated induction of host immune responses | 11 | 4.52e-02 | 8.40e-02 | 0.5130 | 0.256000 | 0.149000 | -0.020200 | 0.418000 | 1.42e-01 | 3.92e-01 | 9.08e-01 | 1.63e-02 |
Response of EIF2AK1 (HRI) to heme deficiency | 14 | 9.03e-04 | 3.11e-03 | 0.5110 | -0.200000 | 0.068500 | 0.366000 | -0.286000 | 1.95e-01 | 6.57e-01 | 1.78e-02 | 6.36e-02 |
Constitutive Signaling by Overexpressed ERBB2 | 10 | 2.31e-01 | 3.11e-01 | 0.5100 | 0.055300 | 0.093300 | 0.345000 | 0.359000 | 7.62e-01 | 6.09e-01 | 5.87e-02 | 4.92e-02 |
Transcriptional regulation by small RNAs | 39 | 1.02e-05 | 6.06e-05 | 0.5100 | -0.169000 | 0.406000 | 0.214000 | 0.144000 | 6.85e-02 | 1.15e-05 | 2.10e-02 | 1.20e-01 |
Regulated proteolysis of p75NTR | 11 | 2.21e-01 | 3.01e-01 | 0.5070 | 0.374000 | 0.058700 | 0.148000 | 0.304000 | 3.17e-02 | 7.36e-01 | 3.95e-01 | 8.14e-02 |
FGFR2 alternative splicing | 22 | 4.83e-03 | 1.30e-02 | 0.5060 | -0.095000 | 0.392000 | 0.291000 | 0.092300 | 4.41e-01 | 1.48e-03 | 1.83e-02 | 4.54e-01 |
Sema4D in semaphorin signaling | 23 | 4.68e-03 | 1.27e-02 | 0.5050 | 0.264000 | -0.246000 | 0.322000 | 0.146000 | 2.86e-02 | 4.15e-02 | 7.55e-03 | 2.25e-01 |
Downregulation of SMAD2/3:SMAD4 transcriptional activity | 19 | 6.93e-03 | 1.74e-02 | 0.5040 | -0.389000 | 0.171000 | 0.081400 | -0.258000 | 3.33e-03 | 1.96e-01 | 5.39e-01 | 5.19e-02 |
Platelet Aggregation (Plug Formation) | 21 | 2.43e-02 | 4.90e-02 | 0.5040 | 0.275000 | -0.087300 | 0.363000 | 0.196000 | 2.90e-02 | 4.89e-01 | 3.97e-03 | 1.21e-01 |
NCAM signaling for neurite out-growth | 38 | 1.78e-05 | 9.67e-05 | 0.5030 | 0.323000 | -0.350000 | -0.112000 | 0.118000 | 5.77e-04 | 1.92e-04 | 2.32e-01 | 2.08e-01 |
Activation of G protein gated Potassium channels | 13 | 1.88e-02 | 3.95e-02 | 0.5020 | 0.360000 | -0.207000 | -0.242000 | 0.145000 | 2.49e-02 | 1.96e-01 | 1.31e-01 | 3.65e-01 |
G protein gated Potassium channels | 13 | 1.88e-02 | 3.95e-02 | 0.5020 | 0.360000 | -0.207000 | -0.242000 | 0.145000 | 2.49e-02 | 1.96e-01 | 1.31e-01 | 3.65e-01 |
Inhibition of voltage gated Ca2+ channels via Gbeta/gamma subunits | 13 | 1.88e-02 | 3.95e-02 | 0.5020 | 0.360000 | -0.207000 | -0.242000 | 0.145000 | 2.49e-02 | 1.96e-01 | 1.31e-01 | 3.65e-01 |
tRNA processing in the nucleus | 48 | 1.12e-06 | 8.69e-06 | 0.5000 | -0.118000 | 0.445000 | 0.195000 | 0.006760 | 1.56e-01 | 9.66e-08 | 1.93e-02 | 9.35e-01 |
Triglyceride catabolism | 13 | 1.19e-01 | 1.81e-01 | 0.5000 | -0.005710 | -0.274000 | -0.347000 | -0.233000 | 9.72e-01 | 8.69e-02 | 3.01e-02 | 1.47e-01 |
Formation of RNA Pol II elongation complex | 50 | 1.77e-07 | 1.70e-06 | 0.5000 | -0.194000 | 0.371000 | 0.273000 | -0.002330 | 1.80e-02 | 5.62e-06 | 8.55e-04 | 9.77e-01 |
RNA Polymerase II Transcription Elongation | 50 | 1.77e-07 | 1.70e-06 | 0.5000 | -0.194000 | 0.371000 | 0.273000 | -0.002330 | 1.80e-02 | 5.62e-06 | 8.55e-04 | 9.77e-01 |
Interleukin-20 family signaling | 12 | 1.14e-01 | 1.75e-01 | 0.4990 | 0.328000 | -0.315000 | 0.003210 | 0.205000 | 4.89e-02 | 5.92e-02 | 9.85e-01 | 2.19e-01 |
HIV elongation arrest and recovery | 27 | 6.14e-04 | 2.19e-03 | 0.4980 | -0.074600 | 0.335000 | 0.360000 | 0.033600 | 5.03e-01 | 2.60e-03 | 1.22e-03 | 7.62e-01 |
Pausing and recovery of HIV elongation | 27 | 6.14e-04 | 2.19e-03 | 0.4980 | -0.074600 | 0.335000 | 0.360000 | 0.033600 | 5.03e-01 | 2.60e-03 | 1.22e-03 | 7.62e-01 |
Metabolism of cofactors | 16 | 9.32e-02 | 1.48e-01 | 0.4970 | -0.350000 | -0.151000 | -0.236000 | -0.213000 | 1.53e-02 | 2.95e-01 | 1.02e-01 | 1.40e-01 |
RNA polymerase II transcribes snRNA genes | 67 | 5.53e-10 | 7.72e-09 | 0.4960 | -0.215000 | 0.387000 | 0.198000 | -0.107000 | 2.38e-03 | 4.56e-08 | 5.11e-03 | 1.30e-01 |
Resolution of D-loop Structures through Synthesis-Dependent Strand Annealing (SDSA) | 16 | 1.77e-02 | 3.78e-02 | 0.4960 | 0.176000 | 0.238000 | 0.055800 | 0.394000 | 2.23e-01 | 9.88e-02 | 6.99e-01 | 6.38e-03 |
Amyloid fiber formation | 29 | 8.50e-03 | 2.09e-02 | 0.4960 | 0.253000 | -0.184000 | 0.246000 | 0.295000 | 1.83e-02 | 8.60e-02 | 2.22e-02 | 5.92e-03 |
MET promotes cell motility | 24 | 6.84e-03 | 1.73e-02 | 0.4950 | 0.320000 | -0.247000 | 0.247000 | 0.143000 | 6.67e-03 | 3.61e-02 | 3.60e-02 | 2.24e-01 |
Negative regulation of MET activity | 16 | 8.37e-02 | 1.36e-01 | 0.4950 | 0.045600 | 0.182000 | 0.353000 | 0.291000 | 7.52e-01 | 2.07e-01 | 1.45e-02 | 4.42e-02 |
rRNA processing | 154 | 1.49e-25 | 1.83e-23 | 0.4920 | -0.137000 | 0.339000 | 0.320000 | -0.080100 | 3.38e-03 | 4.47e-13 | 8.76e-12 | 8.74e-02 |
Synthesis of PIPs at the Golgi membrane | 15 | 4.75e-02 | 8.76e-02 | 0.4920 | 0.027400 | 0.327000 | 0.171000 | 0.324000 | 8.54e-01 | 2.85e-02 | 2.52e-01 | 2.98e-02 |
Nephrin family interactions | 17 | 1.21e-01 | 1.83e-01 | 0.4900 | 0.171000 | 0.137000 | 0.279000 | 0.339000 | 2.22e-01 | 3.29e-01 | 4.67e-02 | 1.57e-02 |
DNA Damage/Telomere Stress Induced Senescence | 26 | 1.14e-02 | 2.64e-02 | 0.4900 | 0.121000 | 0.225000 | 0.234000 | 0.345000 | 2.84e-01 | 4.69e-02 | 3.87e-02 | 2.32e-03 |
TRAF3-dependent IRF activation pathway | 12 | 5.38e-02 | 9.64e-02 | 0.4860 | 0.150000 | -0.114000 | 0.025100 | 0.448000 | 3.69e-01 | 4.96e-01 | 8.81e-01 | 7.26e-03 |
Polymerase switching on the C-strand of the telomere | 22 | 2.77e-02 | 5.51e-02 | 0.4860 | 0.094600 | 0.252000 | 0.248000 | 0.319000 | 4.43e-01 | 4.08e-02 | 4.42e-02 | 9.58e-03 |
Signal transduction by L1 | 20 | 2.99e-02 | 5.88e-02 | 0.4850 | 0.412000 | -0.130000 | 0.119000 | 0.186000 | 1.42e-03 | 3.13e-01 | 3.58e-01 | 1.50e-01 |
Late Phase of HIV Life Cycle | 112 | 1.97e-15 | 7.34e-14 | 0.4830 | -0.149000 | 0.359000 | 0.285000 | 0.031800 | 6.63e-03 | 5.38e-11 | 1.97e-07 | 5.62e-01 |
mRNA Capping | 26 | 1.26e-03 | 4.12e-03 | 0.4830 | -0.216000 | 0.370000 | 0.218000 | -0.043300 | 5.69e-02 | 1.09e-03 | 5.40e-02 | 7.03e-01 |
Pentose phosphate pathway | 12 | 1.90e-01 | 2.64e-01 | 0.4820 | 0.300000 | 0.167000 | 0.306000 | 0.142000 | 7.21e-02 | 3.16e-01 | 6.64e-02 | 3.94e-01 |
PERK regulates gene expression | 28 | 5.81e-04 | 2.11e-03 | 0.4810 | -0.164000 | 0.356000 | 0.277000 | -0.032600 | 1.33e-01 | 1.12e-03 | 1.13e-02 | 7.66e-01 |
GPCR ligand binding | 73 | 3.22e-09 | 3.99e-08 | 0.4790 | 0.432000 | -0.159000 | 0.034000 | 0.129000 | 1.86e-10 | 1.88e-02 | 6.17e-01 | 5.69e-02 |
Inhibition of replication initiation of damaged DNA by RB1/E2F1 | 12 | 7.16e-02 | 1.21e-01 | 0.4790 | -0.169000 | 0.220000 | 0.278000 | 0.274000 | 3.11e-01 | 1.87e-01 | 9.58e-02 | 1.00e-01 |
Mitophagy | 24 | 2.01e-02 | 4.18e-02 | 0.4780 | -0.340000 | 0.135000 | -0.087900 | -0.295000 | 3.90e-03 | 2.54e-01 | 4.56e-01 | 1.23e-02 |
Platelet activation, signaling and aggregation | 168 | 6.57e-15 | 2.31e-13 | 0.4770 | 0.353000 | -0.088900 | 0.150000 | 0.269000 | 3.56e-15 | 4.77e-02 | 8.56e-04 | 1.98e-09 |
Diseases of glycosylation | 95 | 3.08e-09 | 3.86e-08 | 0.4760 | 0.377000 | -0.113000 | 0.099500 | 0.249000 | 2.35e-10 | 5.86e-02 | 9.46e-02 | 2.84e-05 |
Metabolism of RNA | 566 | 1.13e-79 | 1.39e-76 | 0.4750 | -0.152000 | 0.371000 | 0.248000 | -0.064000 | 1.16e-09 | 1.78e-50 | 2.56e-23 | 1.03e-02 |
HIV Life Cycle | 122 | 2.62e-16 | 1.11e-14 | 0.4750 | -0.156000 | 0.350000 | 0.279000 | 0.036000 | 2.93e-03 | 2.77e-11 | 1.14e-07 | 4.94e-01 |
Telomere C-strand (Lagging Strand) Synthesis | 30 | 5.05e-03 | 1.35e-02 | 0.4730 | 0.061000 | 0.238000 | 0.242000 | 0.324000 | 5.64e-01 | 2.44e-02 | 2.17e-02 | 2.13e-03 |
p75NTR recruits signalling complexes | 10 | 3.19e-01 | 4.03e-01 | 0.4730 | 0.202000 | 0.112000 | 0.377000 | 0.167000 | 2.68e-01 | 5.40e-01 | 3.89e-02 | 3.60e-01 |
Peptide chain elongation | 53 | 1.89e-10 | 2.94e-09 | 0.4720 | -0.009730 | -0.068900 | 0.467000 | -0.000315 | 9.03e-01 | 3.86e-01 | 4.23e-09 | 9.97e-01 |
Lysosome Vesicle Biogenesis | 26 | 3.62e-02 | 7.01e-02 | 0.4720 | 0.199000 | 0.093200 | 0.239000 | 0.342000 | 7.92e-02 | 4.11e-01 | 3.49e-02 | 2.53e-03 |
RNA Pol II CTD phosphorylation and interaction with CE | 24 | 3.43e-03 | 9.77e-03 | 0.4720 | -0.188000 | 0.377000 | 0.201000 | -0.067800 | 1.10e-01 | 1.40e-03 | 8.85e-02 | 5.65e-01 |
RNA Pol II CTD phosphorylation and interaction with CE during HIV infection | 24 | 3.43e-03 | 9.77e-03 | 0.4720 | -0.188000 | 0.377000 | 0.201000 | -0.067800 | 1.10e-01 | 1.40e-03 | 8.85e-02 | 5.65e-01 |
Leishmania infection | 118 | 9.74e-10 | 1.30e-08 | 0.4710 | 0.335000 | -0.078700 | 0.170000 | 0.274000 | 3.62e-10 | 1.41e-01 | 1.48e-03 | 3.00e-07 |
Prostacyclin signalling through prostacyclin receptor | 12 | 7.82e-02 | 1.30e-01 | 0.4710 | 0.441000 | -0.089100 | -0.049100 | 0.131000 | 8.21e-03 | 5.93e-01 | 7.69e-01 | 4.34e-01 |
NF-kB is activated and signals survival | 10 | 1.97e-01 | 2.73e-01 | 0.4700 | 0.202000 | -0.141000 | 0.380000 | 0.127000 | 2.70e-01 | 4.40e-01 | 3.76e-02 | 4.88e-01 |
Basigin interactions | 17 | 6.46e-02 | 1.11e-01 | 0.4700 | 0.217000 | -0.317000 | 0.123000 | 0.241000 | 1.21e-01 | 2.38e-02 | 3.80e-01 | 8.55e-02 |
Response of EIF2AK4 (GCN2) to amino acid deficiency | 63 | 1.73e-13 | 4.72e-12 | 0.4700 | -0.069800 | -0.031400 | 0.461000 | -0.050800 | 3.39e-01 | 6.67e-01 | 2.62e-10 | 4.86e-01 |
Regulation of HSF1-mediated heat shock response | 65 | 2.09e-08 | 2.18e-07 | 0.4700 | -0.174000 | 0.362000 | 0.244000 | 0.006350 | 1.55e-02 | 4.77e-07 | 6.83e-04 | 9.30e-01 |
Processive synthesis on the lagging strand | 15 | 7.02e-02 | 1.19e-01 | 0.4650 | -0.038500 | 0.121000 | 0.283000 | 0.347000 | 7.96e-01 | 4.17e-01 | 5.80e-02 | 2.00e-02 |
Selenocysteine synthesis | 56 | 1.18e-11 | 2.27e-10 | 0.4640 | -0.041600 | -0.030400 | 0.458000 | -0.057100 | 5.90e-01 | 6.95e-01 | 3.19e-09 | 4.61e-01 |
SRP-dependent cotranslational protein targeting to membrane | 74 | 4.94e-12 | 1.03e-10 | 0.4620 | -0.017900 | 0.096700 | 0.452000 | 0.018100 | 7.90e-01 | 1.51e-01 | 1.94e-11 | 7.88e-01 |
Signal amplification | 20 | 6.32e-02 | 1.09e-01 | 0.4620 | 0.354000 | 0.059000 | 0.127000 | 0.261000 | 6.15e-03 | 6.48e-01 | 3.24e-01 | 4.34e-02 |
Interleukin-37 signaling | 16 | 1.73e-01 | 2.45e-01 | 0.4600 | 0.158000 | 0.027500 | 0.353000 | 0.247000 | 2.75e-01 | 8.49e-01 | 1.46e-02 | 8.68e-02 |
Transcriptional regulation of granulopoiesis | 23 | 6.67e-02 | 1.14e-01 | 0.4590 | 0.266000 | -0.007070 | 0.307000 | 0.214000 | 2.74e-02 | 9.53e-01 | 1.08e-02 | 7.57e-02 |
Sealing of the nuclear envelope (NE) by ESCRT-III | 20 | 1.07e-02 | 2.51e-02 | 0.4590 | 0.042400 | -0.279000 | 0.298000 | 0.205000 | 7.43e-01 | 3.08e-02 | 2.13e-02 | 1.13e-01 |
Activation of ATR in response to replication stress | 28 | 2.55e-03 | 7.50e-03 | 0.4580 | -0.125000 | 0.306000 | 0.238000 | 0.210000 | 2.52e-01 | 5.15e-03 | 2.92e-02 | 5.44e-02 |
Processing of Capped Intronless Pre-mRNA | 25 | 1.61e-03 | 5.04e-03 | 0.4570 | -0.198000 | 0.264000 | 0.316000 | -0.007290 | 8.71e-02 | 2.23e-02 | 6.35e-03 | 9.50e-01 |
Interleukin-6 signaling | 10 | 3.77e-01 | 4.60e-01 | 0.4560 | 0.304000 | -0.202000 | 0.159000 | 0.223000 | 9.62e-02 | 2.69e-01 | 3.85e-01 | 2.22e-01 |
Neutrophil degranulation | 290 | 6.15e-22 | 4.45e-20 | 0.4550 | 0.227000 | -0.060600 | 0.207000 | 0.330000 | 3.96e-11 | 7.81e-02 | 1.61e-09 | 6.47e-22 |
E2F mediated regulation of DNA replication | 19 | 6.94e-03 | 1.74e-02 | 0.4550 | -0.274000 | 0.241000 | 0.190000 | 0.194000 | 3.88e-02 | 6.91e-02 | 1.52e-01 | 1.43e-01 |
Processing of Intronless Pre-mRNAs | 17 | 1.41e-02 | 3.10e-02 | 0.4540 | -0.225000 | 0.223000 | 0.325000 | -0.011300 | 1.08e-01 | 1.11e-01 | 2.06e-02 | 9.36e-01 |
BMAL1:CLOCK,NPAS2 activates circadian gene expression | 24 | 7.02e-02 | 1.19e-01 | 0.4530 | -0.290000 | -0.063900 | -0.261000 | -0.221000 | 1.39e-02 | 5.88e-01 | 2.69e-02 | 6.08e-02 |
Viral mRNA Translation | 53 | 4.52e-10 | 6.46e-09 | 0.4520 | -0.017000 | -0.055300 | 0.448000 | -0.030100 | 8.30e-01 | 4.87e-01 | 1.76e-08 | 7.05e-01 |
HATs acetylate histones | 71 | 6.55e-09 | 7.86e-08 | 0.4520 | -0.336000 | 0.235000 | 0.123000 | -0.145000 | 1.02e-06 | 6.46e-04 | 7.28e-02 | 3.51e-02 |
Eukaryotic Translation Elongation | 56 | 8.23e-11 | 1.39e-09 | 0.4520 | -0.035200 | -0.088600 | 0.441000 | -0.024600 | 6.49e-01 | 2.52e-01 | 1.19e-08 | 7.50e-01 |
YAP1- and WWTR1 (TAZ)-stimulated gene expression | 11 | 5.05e-02 | 9.17e-02 | 0.4510 | -0.058600 | -0.299000 | -0.008970 | 0.333000 | 7.36e-01 | 8.56e-02 | 9.59e-01 | 5.62e-02 |
Inwardly rectifying K+ channels | 16 | 2.26e-02 | 4.64e-02 | 0.4510 | 0.269000 | -0.218000 | -0.284000 | -0.052900 | 6.25e-02 | 1.32e-01 | 4.93e-02 | 7.14e-01 |
Synthesis of PIPs at the early endosome membrane | 16 | 3.29e-02 | 6.44e-02 | 0.4510 | -0.084000 | 0.153000 | 0.199000 | 0.365000 | 5.61e-01 | 2.90e-01 | 1.68e-01 | 1.16e-02 |
Synthesis of IP3 and IP4 in the cytosol | 19 | 2.39e-02 | 4.84e-02 | 0.4500 | 0.168000 | -0.415000 | -0.028600 | -0.030300 | 2.05e-01 | 1.73e-03 | 8.29e-01 | 8.19e-01 |
Formation of HIV-1 elongation complex containing HIV-1 Tat | 36 | 1.93e-04 | 8.05e-04 | 0.4500 | -0.141000 | 0.307000 | 0.296000 | 0.010600 | 1.43e-01 | 1.43e-03 | 2.14e-03 | 9.13e-01 |
HIV Transcription Elongation | 36 | 1.93e-04 | 8.05e-04 | 0.4500 | -0.141000 | 0.307000 | 0.296000 | 0.010600 | 1.43e-01 | 1.43e-03 | 2.14e-03 | 9.13e-01 |
Tat-mediated elongation of the HIV-1 transcript | 36 | 1.93e-04 | 8.05e-04 | 0.4500 | -0.141000 | 0.307000 | 0.296000 | 0.010600 | 1.43e-01 | 1.43e-03 | 2.14e-03 | 9.13e-01 |
Formation of HIV elongation complex in the absence of HIV Tat | 38 | 1.16e-04 | 5.22e-04 | 0.4490 | -0.159000 | 0.332000 | 0.257000 | -0.024600 | 8.97e-02 | 4.08e-04 | 6.21e-03 | 7.93e-01 |
Calnexin/calreticulin cycle | 23 | 8.29e-02 | 1.36e-01 | 0.4490 | 0.137000 | 0.124000 | 0.291000 | 0.287000 | 2.56e-01 | 3.03e-01 | 1.56e-02 | 1.73e-02 |
Receptor Mediated Mitophagy | 11 | 2.63e-01 | 3.45e-01 | 0.4490 | -0.203000 | 0.205000 | -0.096900 | -0.330000 | 2.45e-01 | 2.39e-01 | 5.78e-01 | 5.81e-02 |
PKA activation | 15 | 6.81e-02 | 1.16e-01 | 0.4480 | 0.031000 | -0.438000 | -0.090000 | 0.017300 | 8.35e-01 | 3.34e-03 | 5.46e-01 | 9.08e-01 |
Glycogen synthesis | 12 | 7.58e-02 | 1.27e-01 | 0.4480 | -0.392000 | -0.144000 | 0.041000 | -0.156000 | 1.88e-02 | 3.87e-01 | 8.06e-01 | 3.48e-01 |
Aberrant regulation of mitotic G1/S transition in cancer due to RB1 defects | 16 | 1.49e-01 | 2.15e-01 | 0.4470 | 0.214000 | -0.013600 | 0.140000 | 0.367000 | 1.38e-01 | 9.25e-01 | 3.31e-01 | 1.12e-02 |
Defective binding of RB1 mutants to E2F1,(E2F2, E2F3) | 16 | 1.49e-01 | 2.15e-01 | 0.4470 | 0.214000 | -0.013600 | 0.140000 | 0.367000 | 1.38e-01 | 9.25e-01 | 3.31e-01 | 1.12e-02 |
Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC) | 57 | 1.06e-10 | 1.69e-09 | 0.4470 | -0.067400 | -0.018900 | 0.440000 | -0.036100 | 3.79e-01 | 8.06e-01 | 9.57e-09 | 6.38e-01 |
Influenza Infection | 107 | 3.60e-14 | 1.11e-12 | 0.4460 | -0.050500 | 0.169000 | 0.406000 | 0.055000 | 3.69e-01 | 2.54e-03 | 4.37e-13 | 3.27e-01 |
TGF-beta receptor signaling in EMT (epithelial to mesenchymal transition) | 11 | 2.20e-01 | 2.99e-01 | 0.4460 | 0.369000 | 0.059500 | 0.226000 | 0.088800 | 3.40e-02 | 7.33e-01 | 1.95e-01 | 6.10e-01 |
AMER1 mutants destabilize the destruction complex | 13 | 6.02e-02 | 1.05e-01 | 0.4460 | -0.344000 | 0.190000 | 0.194000 | -0.079700 | 3.16e-02 | 2.36e-01 | 2.27e-01 | 6.19e-01 |
APC truncation mutants have impaired AXIN binding | 13 | 6.02e-02 | 1.05e-01 | 0.4460 | -0.344000 | 0.190000 | 0.194000 | -0.079700 | 3.16e-02 | 2.36e-01 | 2.27e-01 | 6.19e-01 |
AXIN missense mutants destabilize the destruction complex | 13 | 6.02e-02 | 1.05e-01 | 0.4460 | -0.344000 | 0.190000 | 0.194000 | -0.079700 | 3.16e-02 | 2.36e-01 | 2.27e-01 | 6.19e-01 |
AXIN mutants destabilize the destruction complex, activating WNT signaling | 13 | 6.02e-02 | 1.05e-01 | 0.4460 | -0.344000 | 0.190000 | 0.194000 | -0.079700 | 3.16e-02 | 2.36e-01 | 2.27e-01 | 6.19e-01 |
Truncations of AMER1 destabilize the destruction complex | 13 | 6.02e-02 | 1.05e-01 | 0.4460 | -0.344000 | 0.190000 | 0.194000 | -0.079700 | 3.16e-02 | 2.36e-01 | 2.27e-01 | 6.19e-01 |
truncated APC mutants destabilize the destruction complex | 13 | 6.02e-02 | 1.05e-01 | 0.4460 | -0.344000 | 0.190000 | 0.194000 | -0.079700 | 3.16e-02 | 2.36e-01 | 2.27e-01 | 6.19e-01 |
Methylation | 10 | 2.68e-01 | 3.48e-01 | 0.4450 | -0.376000 | -0.047900 | -0.215000 | -0.091100 | 3.97e-02 | 7.93e-01 | 2.38e-01 | 6.18e-01 |
Regulation of RUNX1 Expression and Activity | 17 | 2.16e-02 | 4.46e-02 | 0.4450 | 0.343000 | 0.063900 | -0.074200 | 0.266000 | 1.44e-02 | 6.48e-01 | 5.96e-01 | 5.81e-02 |
Regulation of MECP2 expression and activity | 26 | 5.69e-02 | 1.01e-01 | 0.4440 | -0.207000 | -0.077800 | -0.320000 | -0.214000 | 6.73e-02 | 4.93e-01 | 4.75e-03 | 5.92e-02 |
G beta:gamma signalling through PLC beta | 12 | 9.95e-02 | 1.57e-01 | 0.4440 | 0.374000 | -0.119000 | -0.117000 | 0.171000 | 2.49e-02 | 4.76e-01 | 4.83e-01 | 3.06e-01 |
Presynaptic function of Kainate receptors | 12 | 9.95e-02 | 1.57e-01 | 0.4440 | 0.374000 | -0.119000 | -0.117000 | 0.171000 | 2.49e-02 | 4.76e-01 | 4.83e-01 | 3.06e-01 |
O-linked glycosylation | 50 | 9.63e-05 | 4.45e-04 | 0.4430 | 0.223000 | -0.183000 | 0.067200 | 0.329000 | 6.45e-03 | 2.53e-02 | 4.12e-01 | 5.71e-05 |
Listeria monocytogenes entry into host cells | 15 | 2.14e-01 | 2.93e-01 | 0.4430 | 0.143000 | 0.162000 | 0.338000 | 0.186000 | 3.38e-01 | 2.77e-01 | 2.33e-02 | 2.11e-01 |
Platelet calcium homeostasis | 17 | 4.83e-02 | 8.87e-02 | 0.4420 | 0.186000 | -0.366000 | -0.146000 | -0.076200 | 1.85e-01 | 8.99e-03 | 2.97e-01 | 5.87e-01 |
Ribosomal scanning and start codon recognition | 45 | 2.81e-07 | 2.54e-06 | 0.4420 | -0.212000 | 0.125000 | 0.366000 | -0.026800 | 1.40e-02 | 1.47e-01 | 2.23e-05 | 7.56e-01 |
RIPK1-mediated regulated necrosis | 22 | 9.22e-02 | 1.47e-01 | 0.4410 | 0.300000 | -0.130000 | 0.184000 | 0.231000 | 1.50e-02 | 2.91e-01 | 1.35e-01 | 6.04e-02 |
Regulated Necrosis | 22 | 9.22e-02 | 1.47e-01 | 0.4410 | 0.300000 | -0.130000 | 0.184000 | 0.231000 | 1.50e-02 | 2.91e-01 | 1.35e-01 | 6.04e-02 |
Regulation of necroptotic cell death | 22 | 9.22e-02 | 1.47e-01 | 0.4410 | 0.300000 | -0.130000 | 0.184000 | 0.231000 | 1.50e-02 | 2.91e-01 | 1.35e-01 | 6.04e-02 |
Removal of the Flap Intermediate | 14 | 1.06e-01 | 1.65e-01 | 0.4410 | -0.075500 | 0.168000 | 0.259000 | 0.306000 | 6.25e-01 | 2.77e-01 | 9.39e-02 | 4.76e-02 |
Eukaryotic Translation Termination | 55 | 2.98e-10 | 4.42e-09 | 0.4400 | -0.053800 | -0.048300 | 0.432000 | -0.042400 | 4.91e-01 | 5.36e-01 | 3.04e-08 | 5.87e-01 |
Negative epigenetic regulation of rRNA expression | 43 | 1.28e-04 | 5.70e-04 | 0.4390 | -0.054800 | 0.389000 | 0.197000 | 0.000917 | 5.35e-01 | 1.03e-05 | 2.58e-02 | 9.92e-01 |
Amplification of signal from unattached kinetochores via a MAD2 inhibitory signal | 57 | 5.65e-06 | 3.60e-05 | 0.4390 | -0.117000 | 0.354000 | 0.206000 | 0.107000 | 1.26e-01 | 3.89e-06 | 7.16e-03 | 1.62e-01 |
Amplification of signal from the kinetochores | 57 | 5.65e-06 | 3.60e-05 | 0.4390 | -0.117000 | 0.354000 | 0.206000 | 0.107000 | 1.26e-01 | 3.89e-06 | 7.16e-03 | 1.62e-01 |
Translation | 222 | 1.58e-22 | 1.30e-20 | 0.4380 | -0.360000 | 0.145000 | 0.003910 | -0.204000 | 3.43e-20 | 2.23e-04 | 9.20e-01 | 1.77e-07 |
Keratan sulfate biosynthesis | 17 | 1.07e-01 | 1.66e-01 | 0.4370 | 0.158000 | -0.197000 | 0.145000 | 0.325000 | 2.58e-01 | 1.59e-01 | 3.00e-01 | 2.03e-02 |
Neurexins and neuroligins | 26 | 3.99e-03 | 1.11e-02 | 0.4370 | 0.241000 | -0.105000 | 0.345000 | 0.051000 | 3.34e-02 | 3.56e-01 | 2.32e-03 | 6.53e-01 |
InlB-mediated entry of Listeria monocytogenes into host cell | 11 | 3.91e-01 | 4.74e-01 | 0.4360 | 0.085800 | 0.152000 | 0.326000 | 0.231000 | 6.22e-01 | 3.84e-01 | 6.15e-02 | 1.85e-01 |
Translesion Synthesis by POLH | 16 | 6.57e-02 | 1.12e-01 | 0.4340 | -0.219000 | 0.347000 | 0.136000 | 0.045200 | 1.30e-01 | 1.64e-02 | 3.45e-01 | 7.54e-01 |
B-WICH complex positively regulates rRNA expression | 28 | 2.50e-03 | 7.39e-03 | 0.4340 | -0.124000 | 0.227000 | 0.342000 | 0.068500 | 2.55e-01 | 3.78e-02 | 1.75e-03 | 5.31e-01 |
Tristetraprolin (TTP, ZFP36) binds and destabilizes mRNA | 15 | 9.61e-02 | 1.52e-01 | 0.4340 | -0.104000 | 0.369000 | 0.204000 | 0.005250 | 4.86e-01 | 1.35e-02 | 1.71e-01 | 9.72e-01 |
Formation of the ternary complex, and subsequently, the 43S complex | 38 | 4.71e-06 | 3.13e-05 | 0.4340 | -0.179000 | 0.096900 | 0.383000 | -0.018700 | 5.69e-02 | 3.02e-01 | 4.44e-05 | 8.42e-01 |
Sphingolipid metabolism | 63 | 4.94e-04 | 1.86e-03 | 0.4340 | 0.269000 | -0.025000 | 0.201000 | 0.274000 | 2.31e-04 | 7.32e-01 | 5.80e-03 | 1.76e-04 |
Recycling pathway of L1 | 23 | 9.88e-02 | 1.56e-01 | 0.4340 | 0.250000 | -0.041700 | 0.169000 | 0.309000 | 3.83e-02 | 7.30e-01 | 1.60e-01 | 1.04e-02 |
BBSome-mediated cargo-targeting to cilium | 18 | 3.97e-02 | 7.51e-02 | 0.4330 | -0.133000 | 0.401000 | 0.049900 | 0.078200 | 3.28e-01 | 3.20e-03 | 7.14e-01 | 5.66e-01 |
GTP hydrolysis and joining of the 60S ribosomal subunit | 73 | 5.05e-12 | 1.03e-10 | 0.4330 | -0.143000 | 0.076000 | 0.400000 | -0.026900 | 3.46e-02 | 2.62e-01 | 3.46e-09 | 6.91e-01 |
G beta:gamma signalling through CDC42 | 13 | 8.38e-02 | 1.36e-01 | 0.4330 | 0.340000 | -0.015900 | -0.091300 | 0.251000 | 3.39e-02 | 9.21e-01 | 5.69e-01 | 1.17e-01 |
NOTCH2 Activation and Transmission of Signal to the Nucleus | 16 | 5.22e-02 | 9.40e-02 | 0.4330 | 0.338000 | -0.176000 | -0.114000 | 0.169000 | 1.91e-02 | 2.22e-01 | 4.28e-01 | 2.43e-01 |
Influenza Viral RNA Transcription and Replication | 91 | 2.70e-12 | 6.25e-11 | 0.4320 | -0.096800 | 0.157000 | 0.390000 | 0.026300 | 1.11e-01 | 9.92e-03 | 1.42e-10 | 6.65e-01 |
Fatty acid metabolism | 101 | 1.23e-07 | 1.20e-06 | 0.4320 | -0.143000 | -0.226000 | -0.296000 | -0.166000 | 1.35e-02 | 9.33e-05 | 3.01e-07 | 3.94e-03 |
DARPP-32 events | 21 | 2.82e-02 | 5.58e-02 | 0.4310 | -0.130000 | -0.202000 | -0.090100 | -0.347000 | 3.04e-01 | 1.10e-01 | 4.75e-01 | 5.93e-03 |
Formation of a pool of free 40S subunits | 63 | 2.19e-10 | 3.32e-09 | 0.4310 | -0.090000 | 0.016600 | 0.421000 | -0.007050 | 2.18e-01 | 8.20e-01 | 7.50e-09 | 9.23e-01 |
Telomere Maintenance | 56 | 1.01e-04 | 4.62e-04 | 0.4310 | 0.021400 | 0.294000 | 0.236000 | 0.209000 | 7.82e-01 | 1.47e-04 | 2.33e-03 | 7.00e-03 |
Resolution of Sister Chromatid Cohesion | 66 | 6.82e-07 | 5.67e-06 | 0.4310 | -0.153000 | 0.363000 | 0.157000 | 0.072200 | 3.14e-02 | 3.47e-07 | 2.73e-02 | 3.11e-01 |
Glucagon-type ligand receptors | 11 | 1.35e-01 | 1.97e-01 | 0.4300 | 0.391000 | -0.096000 | -0.108000 | 0.107000 | 2.47e-02 | 5.82e-01 | 5.35e-01 | 5.39e-01 |
Formation of Incision Complex in GG-NER | 39 | 2.13e-03 | 6.42e-03 | 0.4300 | -0.321000 | 0.174000 | -0.034100 | -0.224000 | 5.20e-04 | 6.08e-02 | 7.13e-01 | 1.58e-02 |
ADP signalling through P2Y purinoceptor 1 | 15 | 1.20e-01 | 1.82e-01 | 0.4290 | 0.380000 | -0.036300 | 0.020400 | 0.195000 | 1.08e-02 | 8.08e-01 | 8.91e-01 | 1.92e-01 |
PRC2 methylates histones and DNA | 14 | 1.60e-01 | 2.29e-01 | 0.4280 | -0.062600 | 0.259000 | 0.300000 | 0.149000 | 6.85e-01 | 9.38e-02 | 5.23e-02 | 3.34e-01 |
Deposition of new CENPA-containing nucleosomes at the centromere | 14 | 1.24e-01 | 1.87e-01 | 0.4280 | -0.131000 | 0.309000 | 0.203000 | 0.171000 | 3.96e-01 | 4.57e-02 | 1.88e-01 | 2.69e-01 |
Nucleosome assembly | 14 | 1.24e-01 | 1.87e-01 | 0.4280 | -0.131000 | 0.309000 | 0.203000 | 0.171000 | 3.96e-01 | 4.57e-02 | 1.88e-01 | 2.69e-01 |
Acyl chain remodelling of PE | 11 | 1.43e-01 | 2.08e-01 | 0.4270 | 0.342000 | 0.179000 | -0.027900 | 0.180000 | 4.95e-02 | 3.03e-01 | 8.73e-01 | 3.02e-01 |
Extension of Telomeres | 43 | 1.70e-03 | 5.26e-03 | 0.4270 | 0.058300 | 0.282000 | 0.212000 | 0.233000 | 5.09e-01 | 1.41e-03 | 1.62e-02 | 8.28e-03 |
Selenoamino acid metabolism | 68 | 1.83e-12 | 4.32e-11 | 0.4260 | -0.027700 | -0.013600 | 0.415000 | -0.089400 | 6.93e-01 | 8.47e-01 | 3.30e-09 | 2.03e-01 |
Beta-catenin phosphorylation cascade | 15 | 6.05e-02 | 1.05e-01 | 0.4260 | -0.262000 | 0.248000 | 0.222000 | -0.042400 | 7.90e-02 | 9.59e-02 | 1.37e-01 | 7.76e-01 |
E3 ubiquitin ligases ubiquitinate target proteins | 39 | 1.36e-04 | 6.00e-04 | 0.4260 | -0.317000 | 0.198000 | 0.145000 | -0.143000 | 6.17e-04 | 3.23e-02 | 1.18e-01 | 1.23e-01 |
RAF-independent MAPK1/3 activation | 21 | 2.09e-02 | 4.35e-02 | 0.4250 | 0.318000 | -0.157000 | 0.233000 | 0.032500 | 1.17e-02 | 2.14e-01 | 6.46e-02 | 7.97e-01 |
G0 and Early G1 | 23 | 4.01e-02 | 7.58e-02 | 0.4250 | -0.032400 | 0.285000 | 0.262000 | 0.172000 | 7.88e-01 | 1.80e-02 | 2.94e-02 | 1.54e-01 |
Formation of TC-NER Pre-Incision Complex | 48 | 8.42e-05 | 3.96e-04 | 0.4250 | -0.258000 | 0.267000 | 0.064000 | -0.196000 | 2.02e-03 | 1.37e-03 | 4.44e-01 | 1.88e-02 |
Cell-Cell communication | 71 | 5.57e-05 | 2.71e-04 | 0.4250 | 0.272000 | -0.169000 | 0.162000 | 0.226000 | 7.57e-05 | 1.38e-02 | 1.83e-02 | 9.91e-04 |
Signaling by Leptin | 10 | 2.84e-01 | 3.66e-01 | 0.4240 | 0.065000 | -0.319000 | -0.157000 | -0.222000 | 7.22e-01 | 8.08e-02 | 3.91e-01 | 2.24e-01 |
Activation of kainate receptors upon glutamate binding | 17 | 4.98e-02 | 9.06e-02 | 0.4240 | 0.368000 | -0.180000 | -0.072300 | 0.079100 | 8.63e-03 | 1.98e-01 | 6.06e-01 | 5.73e-01 |
Translation initiation complex formation | 44 | 1.93e-06 | 1.40e-05 | 0.4220 | -0.195000 | 0.119000 | 0.355000 | -0.015000 | 2.56e-02 | 1.74e-01 | 4.61e-05 | 8.63e-01 |
Sphingolipid de novo biosynthesis | 31 | 1.77e-02 | 3.78e-02 | 0.4220 | 0.247000 | 0.060400 | 0.311000 | 0.131000 | 1.75e-02 | 5.61e-01 | 2.76e-03 | 2.05e-01 |
Activation of AMPK downstream of NMDARs | 10 | 4.29e-01 | 5.12e-01 | 0.4220 | -0.101000 | -0.281000 | -0.202000 | -0.220000 | 5.79e-01 | 1.24e-01 | 2.68e-01 | 2.30e-01 |
HCMV Early Events | 50 | 6.15e-05 | 2.98e-04 | 0.4220 | -0.099000 | 0.363000 | 0.144000 | 0.125000 | 2.27e-01 | 9.02e-06 | 7.81e-02 | 1.26e-01 |
Activation of BAD and translocation to mitochondria | 13 | 1.87e-01 | 2.61e-01 | 0.4210 | 0.074900 | -0.220000 | 0.200000 | 0.289000 | 6.40e-01 | 1.69e-01 | 2.12e-01 | 7.17e-02 |
Anti-inflammatory response favouring Leishmania parasite infection | 56 | 3.75e-05 | 1.87e-04 | 0.4210 | 0.357000 | -0.156000 | 0.007930 | 0.157000 | 3.79e-06 | 4.41e-02 | 9.18e-01 | 4.18e-02 |
Leishmania parasite growth and survival | 56 | 3.75e-05 | 1.87e-04 | 0.4210 | 0.357000 | -0.156000 | 0.007930 | 0.157000 | 3.79e-06 | 4.41e-02 | 9.18e-01 | 4.18e-02 |
L13a-mediated translational silencing of Ceruloplasmin expression | 71 | 4.16e-11 | 7.20e-10 | 0.4200 | -0.123000 | 0.059100 | 0.397000 | -0.023600 | 7.25e-02 | 3.90e-01 | 7.62e-09 | 7.32e-01 |
Formation of the Early Elongation Complex | 30 | 3.10e-03 | 8.93e-03 | 0.4200 | -0.143000 | 0.299000 | 0.257000 | 0.000435 | 1.74e-01 | 4.59e-03 | 1.48e-02 | 9.97e-01 |
Formation of the HIV-1 Early Elongation Complex | 30 | 3.10e-03 | 8.93e-03 | 0.4200 | -0.143000 | 0.299000 | 0.257000 | 0.000435 | 1.74e-01 | 4.59e-03 | 1.48e-02 | 9.97e-01 |
Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S | 45 | 2.13e-06 | 1.52e-05 | 0.4190 | -0.205000 | 0.113000 | 0.347000 | 0.004750 | 1.75e-02 | 1.91e-01 | 5.72e-05 | 9.56e-01 |
Cooperation of PDCL (PhLP1) and TRiC/CCT in G-protein beta folding | 25 | 2.88e-02 | 5.67e-02 | 0.4180 | 0.193000 | 0.294000 | 0.203000 | 0.101000 | 9.57e-02 | 1.09e-02 | 7.93e-02 | 3.82e-01 |
Synthesis of active ubiquitin: roles of E1 and E2 enzymes | 25 | 9.61e-03 | 2.28e-02 | 0.4180 | -0.276000 | 0.114000 | 0.062100 | -0.286000 | 1.71e-02 | 3.24e-01 | 5.91e-01 | 1.33e-02 |
Diseases of programmed cell death | 24 | 8.37e-02 | 1.36e-01 | 0.4170 | 0.152000 | -0.051700 | 0.206000 | 0.326000 | 1.99e-01 | 6.62e-01 | 8.12e-02 | 5.72e-03 |
RHO GTPases Activate ROCKs | 18 | 8.53e-02 | 1.38e-01 | 0.4170 | 0.257000 | -0.194000 | 0.248000 | 0.097000 | 5.96e-02 | 1.55e-01 | 6.87e-02 | 4.76e-01 |
Gene Silencing by RNA | 54 | 1.13e-05 | 6.60e-05 | 0.4170 | -0.204000 | 0.353000 | 0.058900 | 0.063600 | 9.45e-03 | 7.44e-06 | 4.55e-01 | 4.20e-01 |
HSP90 chaperone cycle for steroid hormone receptors (SHR) | 33 | 6.97e-04 | 2.46e-03 | 0.4170 | -0.222000 | 0.223000 | 0.271000 | 0.038600 | 2.76e-02 | 2.68e-02 | 7.14e-03 | 7.02e-01 |
Chromosome Maintenance | 68 | 1.04e-05 | 6.17e-05 | 0.4170 | -0.020700 | 0.301000 | 0.221000 | 0.184000 | 7.68e-01 | 1.80e-05 | 1.66e-03 | 8.96e-03 |
ATF4 activates genes in response to endoplasmic reticulum stress | 24 | 1.21e-02 | 2.76e-02 | 0.4160 | -0.174000 | 0.297000 | 0.230000 | -0.037000 | 1.40e-01 | 1.19e-02 | 5.10e-02 | 7.54e-01 |
NoRC negatively regulates rRNA expression | 40 | 8.21e-04 | 2.84e-03 | 0.4160 | -0.053200 | 0.367000 | 0.187000 | 0.012500 | 5.61e-01 | 5.96e-05 | 4.10e-02 | 8.91e-01 |
Gene and protein expression by JAK-STAT signaling after Interleukin-12 stimulation | 25 | 4.20e-02 | 7.88e-02 | 0.4150 | 0.240000 | 0.061900 | 0.314000 | 0.112000 | 3.81e-02 | 5.92e-01 | 6.61e-03 | 3.31e-01 |
HDMs demethylate histones | 19 | 1.59e-02 | 3.42e-02 | 0.4150 | -0.300000 | 0.161000 | 0.224000 | -0.079600 | 2.36e-02 | 2.26e-01 | 9.13e-02 | 5.48e-01 |
Translation of structural proteins | 25 | 5.24e-02 | 9.41e-02 | 0.4150 | 0.163000 | -0.193000 | 0.234000 | 0.231000 | 1.58e-01 | 9.47e-02 | 4.29e-02 | 4.60e-02 |
IRAK2 mediated activation of TAK1 complex upon TLR7/8 or 9 stimulation | 10 | 2.24e-01 | 3.03e-01 | 0.4140 | -0.140000 | 0.199000 | 0.332000 | 0.046400 | 4.44e-01 | 2.77e-01 | 6.95e-02 | 7.99e-01 |
TRAF6-mediated induction of TAK1 complex within TLR4 complex | 10 | 2.24e-01 | 3.03e-01 | 0.4140 | -0.140000 | 0.199000 | 0.332000 | 0.046400 | 4.44e-01 | 2.77e-01 | 6.95e-02 | 7.99e-01 |
Regulation of TP53 Activity through Methylation | 14 | 4.21e-02 | 7.88e-02 | 0.4130 | 0.148000 | 0.349000 | -0.078500 | -0.146000 | 3.39e-01 | 2.39e-02 | 6.11e-01 | 3.44e-01 |
Metalloprotease DUBs | 15 | 1.03e-01 | 1.61e-01 | 0.4130 | -0.342000 | 0.223000 | 0.045600 | -0.049200 | 2.20e-02 | 1.35e-01 | 7.60e-01 | 7.42e-01 |
RHO GTPases activate CIT | 17 | 1.18e-01 | 1.79e-01 | 0.4130 | 0.226000 | -0.151000 | 0.289000 | 0.115000 | 1.06e-01 | 2.81e-01 | 3.91e-02 | 4.13e-01 |
Interferon Signaling | 119 | 2.40e-07 | 2.20e-06 | 0.4130 | 0.225000 | 0.149000 | 0.240000 | 0.201000 | 2.37e-05 | 5.20e-03 | 6.46e-06 | 1.61e-04 |
IKK complex recruitment mediated by RIP1 | 14 | 5.69e-02 | 1.01e-01 | 0.4120 | -0.172000 | 0.130000 | 0.351000 | 0.016000 | 2.64e-01 | 3.99e-01 | 2.31e-02 | 9.17e-01 |
Processing of DNA double-strand break ends | 50 | 1.86e-04 | 7.86e-04 | 0.4120 | -0.085100 | 0.295000 | 0.226000 | 0.156000 | 2.99e-01 | 3.16e-04 | 5.78e-03 | 5.64e-02 |
RNA Polymerase III Transcription Initiation From Type 2 Promoter | 25 | 9.63e-03 | 2.28e-02 | 0.4120 | -0.284000 | 0.270000 | 0.122000 | 0.023700 | 1.39e-02 | 1.94e-02 | 2.89e-01 | 8.37e-01 |
EML4 and NUDC in mitotic spindle formation | 61 | 1.18e-05 | 6.79e-05 | 0.4120 | -0.119000 | 0.326000 | 0.197000 | 0.100000 | 1.09e-01 | 1.06e-05 | 7.99e-03 | 1.77e-01 |
Hemostasis | 346 | 7.09e-24 | 6.70e-22 | 0.4110 | 0.303000 | -0.136000 | 0.115000 | 0.213000 | 6.94e-22 | 1.63e-05 | 2.81e-04 | 1.34e-11 |
Pre-NOTCH Processing in Golgi | 14 | 1.03e-01 | 1.61e-01 | 0.4110 | 0.077600 | -0.398000 | 0.061900 | -0.026900 | 6.15e-01 | 1.00e-02 | 6.88e-01 | 8.62e-01 |
FGFR2 mutant receptor activation | 18 | 6.21e-02 | 1.07e-01 | 0.4100 | -0.058600 | 0.166000 | 0.356000 | 0.102000 | 6.67e-01 | 2.24e-01 | 8.88e-03 | 4.54e-01 |
Cap-dependent Translation Initiation | 79 | 6.07e-12 | 1.20e-10 | 0.4100 | -0.161000 | 0.068100 | 0.369000 | -0.037300 | 1.38e-02 | 2.96e-01 | 1.46e-08 | 5.67e-01 |
Eukaryotic Translation Initiation | 79 | 6.07e-12 | 1.20e-10 | 0.4100 | -0.161000 | 0.068100 | 0.369000 | -0.037300 | 1.38e-02 | 2.96e-01 | 1.46e-08 | 5.67e-01 |
SUMOylation of transcription factors | 14 | 9.20e-02 | 1.47e-01 | 0.4090 | 0.033000 | 0.134000 | 0.385000 | 0.016700 | 8.31e-01 | 3.86e-01 | 1.27e-02 | 9.14e-01 |
Constitutive Signaling by NOTCH1 HD Domain Mutants | 11 | 2.57e-01 | 3.38e-01 | 0.4090 | 0.314000 | -0.202000 | -0.075700 | 0.150000 | 7.19e-02 | 2.47e-01 | 6.64e-01 | 3.90e-01 |
Signaling by NOTCH1 HD Domain Mutants in Cancer | 11 | 2.57e-01 | 3.38e-01 | 0.4090 | 0.314000 | -0.202000 | -0.075700 | 0.150000 | 7.19e-02 | 2.47e-01 | 6.64e-01 | 3.90e-01 |
Chaperone Mediated Autophagy | 14 | 9.90e-02 | 1.56e-01 | 0.4090 | -0.086100 | -0.054700 | 0.292000 | 0.267000 | 5.77e-01 | 7.23e-01 | 5.87e-02 | 8.35e-02 |
PCNA-Dependent Long Patch Base Excision Repair | 21 | 5.44e-02 | 9.74e-02 | 0.4070 | -0.077600 | 0.190000 | 0.287000 | 0.205000 | 5.38e-01 | 1.33e-01 | 2.31e-02 | 1.05e-01 |
Regulation of IFNG signaling | 13 | 2.41e-01 | 3.21e-01 | 0.4070 | 0.276000 | 0.136000 | 0.255000 | 0.077400 | 8.47e-02 | 3.98e-01 | 1.12e-01 | 6.29e-01 |
Activation of GABAB receptors | 24 | 9.21e-03 | 2.20e-02 | 0.4070 | 0.224000 | -0.217000 | -0.149000 | 0.214000 | 5.76e-02 | 6.59e-02 | 2.07e-01 | 6.91e-02 |
GABA B receptor activation | 24 | 9.21e-03 | 2.20e-02 | 0.4070 | 0.224000 | -0.217000 | -0.149000 | 0.214000 | 5.76e-02 | 6.59e-02 | 2.07e-01 | 6.91e-02 |
PKA activation in glucagon signalling | 14 | 1.58e-01 | 2.26e-01 | 0.4060 | 0.042900 | -0.396000 | -0.070800 | -0.032800 | 7.81e-01 | 1.03e-02 | 6.46e-01 | 8.32e-01 |
CaM pathway | 27 | 1.40e-02 | 3.08e-02 | 0.4060 | 0.132000 | -0.381000 | -0.044100 | 0.023000 | 2.36e-01 | 6.21e-04 | 6.92e-01 | 8.36e-01 |
Calmodulin induced events | 27 | 1.40e-02 | 3.08e-02 | 0.4060 | 0.132000 | -0.381000 | -0.044100 | 0.023000 | 2.36e-01 | 6.21e-04 | 6.92e-01 | 8.36e-01 |
G alpha (z) signalling events | 28 | 1.83e-02 | 3.89e-02 | 0.4060 | 0.289000 | -0.212000 | -0.021000 | 0.190000 | 8.26e-03 | 5.28e-02 | 8.48e-01 | 8.22e-02 |
DAG and IP3 signaling | 33 | 4.43e-03 | 1.21e-02 | 0.4050 | 0.155000 | -0.353000 | -0.125000 | 0.009530 | 1.24e-01 | 4.48e-04 | 2.15e-01 | 9.25e-01 |
Transferrin endocytosis and recycling | 21 | 2.12e-02 | 4.40e-02 | 0.4050 | 0.081100 | 0.044800 | 0.059200 | 0.390000 | 5.20e-01 | 7.23e-01 | 6.39e-01 | 1.97e-03 |
Regulation of glycolysis by fructose 2,6-bisphosphate metabolism | 11 | 5.33e-01 | 6.13e-01 | 0.4040 | -0.211000 | -0.140000 | -0.219000 | -0.227000 | 2.27e-01 | 4.23e-01 | 2.09e-01 | 1.92e-01 |
Resolution of AP sites via the multiple-nucleotide patch replacement pathway | 24 | 1.55e-02 | 3.35e-02 | 0.4040 | -0.170000 | 0.207000 | 0.254000 | 0.164000 | 1.51e-01 | 7.98e-02 | 3.11e-02 | 1.65e-01 |
FCGR3A-mediated IL10 synthesis | 25 | 2.39e-02 | 4.83e-02 | 0.4030 | 0.251000 | -0.284000 | -0.075900 | 0.113000 | 2.97e-02 | 1.41e-02 | 5.11e-01 | 3.27e-01 |
Protein ubiquitination | 56 | 8.71e-06 | 5.22e-05 | 0.4030 | -0.298000 | 0.186000 | 0.124000 | -0.153000 | 1.17e-04 | 1.63e-02 | 1.08e-01 | 4.76e-02 |
TRAF6 mediated NF-kB activation | 19 | 8.32e-02 | 1.36e-01 | 0.4030 | 0.120000 | -0.134000 | 0.103000 | 0.345000 | 3.66e-01 | 3.13e-01 | 4.38e-01 | 9.18e-03 |
RNA Polymerase III Transcription Initiation From Type 1 Promoter | 26 | 9.15e-03 | 2.19e-02 | 0.3980 | -0.286000 | 0.246000 | 0.121000 | 0.039100 | 1.16e-02 | 2.97e-02 | 2.87e-01 | 7.31e-01 |
Signaling by FGFR3 fusions in cancer | 10 | 2.72e-01 | 3.53e-01 | 0.3980 | -0.319000 | 0.193000 | 0.124000 | -0.063400 | 8.06e-02 | 2.91e-01 | 4.96e-01 | 7.29e-01 |
Interleukin-12 family signaling | 34 | 2.34e-02 | 4.77e-02 | 0.3980 | 0.231000 | -0.002870 | 0.292000 | 0.140000 | 1.99e-02 | 9.77e-01 | 3.19e-03 | 1.58e-01 |
Class B/2 (Secretin family receptors) | 33 | 1.59e-03 | 5.02e-03 | 0.3970 | 0.271000 | -0.236000 | -0.155000 | -0.066100 | 7.02e-03 | 1.93e-02 | 1.23e-01 | 5.11e-01 |
Plasma lipoprotein assembly, remodeling, and clearance | 39 | 2.78e-03 | 8.05e-03 | 0.3970 | 0.220000 | -0.208000 | -0.005590 | 0.257000 | 1.76e-02 | 2.50e-02 | 9.52e-01 | 5.61e-03 |
GABA receptor activation | 26 | 8.71e-03 | 2.10e-02 | 0.3960 | 0.227000 | -0.226000 | -0.166000 | 0.161000 | 4.49e-02 | 4.59e-02 | 1.43e-01 | 1.55e-01 |
Acyl chain remodelling of PC | 11 | 1.82e-01 | 2.55e-01 | 0.3940 | 0.333000 | 0.073900 | -0.083200 | 0.180000 | 5.62e-02 | 6.71e-01 | 6.33e-01 | 3.01e-01 |
Activation of gene expression by SREBF (SREBP) | 40 | 2.97e-03 | 8.58e-03 | 0.3940 | -0.197000 | -0.215000 | -0.076600 | -0.254000 | 3.10e-02 | 1.89e-02 | 4.02e-01 | 5.51e-03 |
HIV Infection | 187 | 2.88e-18 | 1.69e-16 | 0.3940 | -0.153000 | 0.244000 | 0.265000 | 0.047500 | 3.19e-04 | 1.02e-08 | 4.94e-10 | 2.65e-01 |
tRNA processing | 98 | 1.59e-08 | 1.69e-07 | 0.3930 | -0.147000 | 0.347000 | 0.100000 | -0.051000 | 1.19e-02 | 3.06e-09 | 8.80e-02 | 3.84e-01 |
Assembly Of The HIV Virion | 12 | 5.60e-02 | 9.97e-02 | 0.3930 | 0.034900 | -0.146000 | 0.356000 | -0.070200 | 8.34e-01 | 3.80e-01 | 3.25e-02 | 6.74e-01 |
Activated NOTCH1 Transmits Signal to the Nucleus | 23 | 5.16e-02 | 9.32e-02 | 0.3920 | 0.334000 | -0.032500 | 0.004650 | 0.202000 | 5.60e-03 | 7.87e-01 | 9.69e-01 | 9.39e-02 |
Misspliced GSK3beta mutants stabilize beta-catenin | 14 | 1.28e-01 | 1.90e-01 | 0.3910 | -0.282000 | 0.203000 | 0.170000 | -0.057200 | 6.81e-02 | 1.88e-01 | 2.71e-01 | 7.11e-01 |
S33 mutants of beta-catenin aren't phosphorylated | 14 | 1.28e-01 | 1.90e-01 | 0.3910 | -0.282000 | 0.203000 | 0.170000 | -0.057200 | 6.81e-02 | 1.88e-01 | 2.71e-01 | 7.11e-01 |
S37 mutants of beta-catenin aren't phosphorylated | 14 | 1.28e-01 | 1.90e-01 | 0.3910 | -0.282000 | 0.203000 | 0.170000 | -0.057200 | 6.81e-02 | 1.88e-01 | 2.71e-01 | 7.11e-01 |
S45 mutants of beta-catenin aren't phosphorylated | 14 | 1.28e-01 | 1.90e-01 | 0.3910 | -0.282000 | 0.203000 | 0.170000 | -0.057200 | 6.81e-02 | 1.88e-01 | 2.71e-01 | 7.11e-01 |
T41 mutants of beta-catenin aren't phosphorylated | 14 | 1.28e-01 | 1.90e-01 | 0.3910 | -0.282000 | 0.203000 | 0.170000 | -0.057200 | 6.81e-02 | 1.88e-01 | 2.71e-01 | 7.11e-01 |
phosphorylation site mutants of CTNNB1 are not targeted to the proteasome by the destruction complex | 14 | 1.28e-01 | 1.90e-01 | 0.3910 | -0.282000 | 0.203000 | 0.170000 | -0.057200 | 6.81e-02 | 1.88e-01 | 2.71e-01 | 7.11e-01 |
RNA Polymerase III Transcription Initiation From Type 3 Promoter | 27 | 1.86e-02 | 3.93e-02 | 0.3910 | -0.185000 | 0.335000 | 0.071600 | 0.024800 | 9.63e-02 | 2.56e-03 | 5.20e-01 | 8.23e-01 |
Nuclear Envelope (NE) Reassembly | 59 | 4.09e-05 | 2.02e-04 | 0.3900 | -0.084900 | 0.174000 | 0.309000 | 0.138000 | 2.60e-01 | 2.12e-02 | 4.02e-05 | 6.74e-02 |
Stimuli-sensing channels | 42 | 1.08e-03 | 3.62e-03 | 0.3900 | 0.003200 | -0.279000 | -0.272000 | -0.013100 | 9.71e-01 | 1.76e-03 | 2.31e-03 | 8.84e-01 |
Protein-protein interactions at synapses | 41 | 4.97e-03 | 1.33e-02 | 0.3900 | 0.213000 | -0.198000 | 0.224000 | 0.131000 | 1.83e-02 | 2.84e-02 | 1.32e-02 | 1.47e-01 |
RHO GTPases activate PAKs | 19 | 7.60e-02 | 1.27e-01 | 0.3900 | 0.191000 | -0.292000 | 0.164000 | 0.055900 | 1.49e-01 | 2.75e-02 | 2.17e-01 | 6.73e-01 |
RHO GTPases Activate Formins | 80 | 1.62e-05 | 8.96e-05 | 0.3900 | 0.001930 | 0.223000 | 0.267000 | 0.175000 | 9.76e-01 | 5.82e-04 | 3.64e-05 | 6.94e-03 |
SUMOylation of chromatin organization proteins | 46 | 5.66e-04 | 2.08e-03 | 0.3890 | -0.125000 | 0.333000 | 0.155000 | -0.028600 | 1.43e-01 | 9.36e-05 | 6.94e-02 | 7.38e-01 |
PKA-mediated phosphorylation of CREB | 17 | 1.22e-01 | 1.85e-01 | 0.3870 | 0.072500 | -0.372000 | -0.072200 | 0.036200 | 6.05e-01 | 7.98e-03 | 6.06e-01 | 7.96e-01 |
Signaling by Non-Receptor Tyrosine Kinases | 42 | 3.01e-02 | 5.92e-02 | 0.3870 | 0.223000 | -0.050400 | 0.219000 | 0.222000 | 1.25e-02 | 5.72e-01 | 1.41e-02 | 1.28e-02 |
Signaling by PTK6 | 42 | 3.01e-02 | 5.92e-02 | 0.3870 | 0.223000 | -0.050400 | 0.219000 | 0.222000 | 1.25e-02 | 5.72e-01 | 1.41e-02 | 1.28e-02 |
Telomere C-strand synthesis initiation | 11 | 3.06e-01 | 3.89e-01 | 0.3860 | 0.146000 | 0.261000 | 0.047200 | 0.238000 | 4.01e-01 | 1.34e-01 | 7.86e-01 | 1.71e-01 |
Resolution of D-Loop Structures | 21 | 7.64e-02 | 1.28e-01 | 0.3860 | 0.135000 | 0.118000 | 0.081400 | 0.332000 | 2.85e-01 | 3.50e-01 | 5.19e-01 | 8.56e-03 |
Resolution of D-loop Structures through Holliday Junction Intermediates | 21 | 7.64e-02 | 1.28e-01 | 0.3860 | 0.135000 | 0.118000 | 0.081400 | 0.332000 | 2.85e-01 | 3.50e-01 | 5.19e-01 | 8.56e-03 |
Interleukin-12 signaling | 29 | 3.84e-02 | 7.35e-02 | 0.3850 | 0.228000 | -0.004150 | 0.293000 | 0.105000 | 3.41e-02 | 9.69e-01 | 6.42e-03 | 3.28e-01 |
IRE1alpha activates chaperones | 47 | 2.65e-03 | 7.77e-03 | 0.3850 | 0.130000 | 0.012600 | 0.335000 | 0.138000 | 1.24e-01 | 8.82e-01 | 7.28e-05 | 1.02e-01 |
Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC) | 75 | 5.85e-10 | 7.91e-09 | 0.3850 | -0.118000 | 0.065600 | 0.358000 | -0.041700 | 7.74e-02 | 3.27e-01 | 8.65e-08 | 5.33e-01 |
Nonsense-Mediated Decay (NMD) | 75 | 5.85e-10 | 7.91e-09 | 0.3850 | -0.118000 | 0.065600 | 0.358000 | -0.041700 | 7.74e-02 | 3.27e-01 | 8.65e-08 | 5.33e-01 |
Cellular response to heat stress | 82 | 6.21e-08 | 6.21e-07 | 0.3840 | -0.187000 | 0.231000 | 0.243000 | 0.007940 | 3.45e-03 | 3.04e-04 | 1.45e-04 | 9.01e-01 |
p38MAPK events | 12 | 2.75e-01 | 3.56e-01 | 0.3840 | 0.119000 | -0.365000 | -0.006560 | 0.008710 | 4.76e-01 | 2.87e-02 | 9.69e-01 | 9.58e-01 |
RUNX2 regulates osteoblast differentiation | 20 | 6.22e-02 | 1.07e-01 | 0.3820 | 0.342000 | -0.040800 | -0.041700 | 0.160000 | 8.07e-03 | 7.52e-01 | 7.47e-01 | 2.15e-01 |
Nuclear Envelope Breakdown | 42 | 1.44e-03 | 4.61e-03 | 0.3820 | -0.168000 | 0.303000 | 0.151000 | 0.055000 | 5.95e-02 | 6.77e-04 | 9.11e-02 | 5.38e-01 |
Translesion synthesis by POLI | 15 | 1.44e-01 | 2.09e-01 | 0.3820 | -0.107000 | 0.309000 | 0.089200 | 0.176000 | 4.74e-01 | 3.83e-02 | 5.50e-01 | 2.37e-01 |
Frs2-mediated activation | 10 | 1.20e-01 | 1.82e-01 | 0.3820 | -0.015700 | 0.139000 | 0.301000 | -0.190000 | 9.32e-01 | 4.48e-01 | 9.95e-02 | 2.99e-01 |
RNA Polymerase III Chain Elongation | 17 | 1.16e-01 | 1.77e-01 | 0.3820 | -0.200000 | 0.298000 | 0.119000 | 0.056400 | 1.54e-01 | 3.35e-02 | 3.98e-01 | 6.87e-01 |
Plasma lipoprotein clearance | 21 | 1.39e-01 | 2.02e-01 | 0.3810 | 0.184000 | -0.110000 | 0.088600 | 0.302000 | 1.45e-01 | 3.84e-01 | 4.82e-01 | 1.67e-02 |
Adenylate cyclase inhibitory pathway | 11 | 2.08e-01 | 2.85e-01 | 0.3800 | 0.063300 | -0.228000 | -0.038000 | 0.296000 | 7.16e-01 | 1.91e-01 | 8.28e-01 | 8.96e-02 |
Deadenylation of mRNA | 24 | 5.16e-02 | 9.32e-02 | 0.3800 | -0.179000 | 0.317000 | 0.047400 | -0.096700 | 1.28e-01 | 7.14e-03 | 6.88e-01 | 4.12e-01 |
SHC-mediated cascade:FGFR2 | 10 | 6.23e-01 | 6.98e-01 | 0.3800 | 0.180000 | -0.090900 | 0.213000 | 0.241000 | 3.25e-01 | 6.19e-01 | 2.43e-01 | 1.87e-01 |
Signaling by PDGF | 46 | 7.74e-03 | 1.91e-02 | 0.3780 | 0.261000 | -0.181000 | 0.118000 | 0.168000 | 2.20e-03 | 3.39e-02 | 1.67e-01 | 4.84e-02 |
Cell junction organization | 45 | 4.18e-03 | 1.16e-02 | 0.3780 | 0.264000 | -0.228000 | 0.052300 | 0.137000 | 2.21e-03 | 8.21e-03 | 5.44e-01 | 1.13e-01 |
Mitotic Prophase | 70 | 5.41e-06 | 3.55e-05 | 0.3780 | -0.180000 | 0.274000 | 0.171000 | 0.079000 | 9.15e-03 | 7.65e-05 | 1.37e-02 | 2.54e-01 |
TP53 Regulates Transcription of DNA Repair Genes | 51 | 5.55e-04 | 2.05e-03 | 0.3770 | -0.050000 | 0.323000 | 0.188000 | 0.018600 | 5.37e-01 | 6.76e-05 | 2.04e-02 | 8.18e-01 |
TP53 regulates transcription of additional cell cycle genes whose exact role in the p53 pathway remain uncertain | 19 | 1.31e-01 | 1.93e-01 | 0.3770 | 0.139000 | 0.191000 | 0.289000 | 0.055000 | 2.95e-01 | 1.49e-01 | 2.93e-02 | 6.79e-01 |
Interleukin-6 family signaling | 16 | 2.55e-01 | 3.37e-01 | 0.3770 | 0.231000 | -0.246000 | 0.059000 | 0.158000 | 1.10e-01 | 8.90e-02 | 6.83e-01 | 2.73e-01 |
RNA Polymerase III Transcription Initiation | 34 | 5.03e-03 | 1.34e-02 | 0.3760 | -0.241000 | 0.273000 | 0.089600 | 0.036500 | 1.51e-02 | 5.98e-03 | 3.67e-01 | 7.13e-01 |
SUMOylation of DNA damage response and repair proteins | 62 | 6.86e-05 | 3.27e-04 | 0.3760 | -0.132000 | 0.319000 | 0.146000 | 0.031400 | 7.17e-02 | 1.46e-05 | 4.75e-02 | 6.69e-01 |
Signalling to RAS | 16 | 1.28e-01 | 1.91e-01 | 0.3760 | 0.156000 | -0.327000 | 0.100000 | 0.001520 | 2.80e-01 | 2.37e-02 | 4.88e-01 | 9.92e-01 |
Translesion synthesis by POLK | 15 | 1.29e-01 | 1.91e-01 | 0.3750 | -0.166000 | 0.318000 | 0.003730 | 0.110000 | 2.67e-01 | 3.29e-02 | 9.80e-01 | 4.61e-01 |
MTOR signalling | 40 | 1.07e-02 | 2.51e-02 | 0.3750 | -0.311000 | -0.078900 | -0.145000 | -0.128000 | 6.79e-04 | 3.89e-01 | 1.12e-01 | 1.61e-01 |
Ca-dependent events | 29 | 2.30e-02 | 4.71e-02 | 0.3750 | 0.166000 | -0.334000 | -0.020600 | 0.028600 | 1.21e-01 | 1.88e-03 | 8.48e-01 | 7.90e-01 |
Meiotic recombination | 17 | 8.28e-02 | 1.36e-01 | 0.3740 | -0.011900 | 0.320000 | 0.009500 | 0.194000 | 9.32e-01 | 2.25e-02 | 9.46e-01 | 1.66e-01 |
Diseases associated with N-glycosylation of proteins | 16 | 1.88e-01 | 2.62e-01 | 0.3740 | 0.293000 | 0.130000 | 0.182000 | 0.064800 | 4.26e-02 | 3.67e-01 | 2.08e-01 | 6.54e-01 |
Degradation of AXIN | 47 | 1.62e-05 | 8.96e-05 | 0.3740 | -0.245000 | 0.101000 | 0.239000 | -0.113000 | 3.74e-03 | 2.30e-01 | 4.67e-03 | 1.81e-01 |
G alpha (q) signalling events | 78 | 2.30e-06 | 1.61e-05 | 0.3730 | 0.328000 | -0.141000 | -0.036100 | 0.103000 | 5.88e-07 | 3.21e-02 | 5.82e-01 | 1.16e-01 |
Transport of vitamins, nucleosides, and related molecules | 24 | 1.13e-01 | 1.74e-01 | 0.3720 | 0.212000 | -0.206000 | 0.069700 | 0.216000 | 7.25e-02 | 8.15e-02 | 5.55e-01 | 6.69e-02 |
Host Interactions of HIV factors | 102 | 5.04e-09 | 6.14e-08 | 0.3720 | -0.136000 | 0.179000 | 0.283000 | 0.089500 | 1.79e-02 | 1.87e-03 | 8.10e-07 | 1.19e-01 |
The role of GTSE1 in G2/M progression after G2 checkpoint | 48 | 3.55e-05 | 1.78e-04 | 0.3720 | -0.147000 | 0.107000 | 0.324000 | 0.018500 | 7.92e-02 | 1.98e-01 | 1.02e-04 | 8.24e-01 |
AUF1 (hnRNP D0) binds and destabilizes mRNA | 46 | 1.83e-05 | 9.93e-05 | 0.3720 | -0.219000 | 0.096900 | 0.273000 | -0.077700 | 1.02e-02 | 2.56e-01 | 1.35e-03 | 3.63e-01 |
PIWI-interacting RNA (piRNA) biogenesis | 13 | 2.29e-01 | 3.08e-01 | 0.3710 | -0.112000 | 0.246000 | 0.254000 | -0.006890 | 4.83e-01 | 1.25e-01 | 1.13e-01 | 9.66e-01 |
O-linked glycosylation of mucins | 21 | 1.62e-01 | 2.31e-01 | 0.3710 | 0.101000 | -0.140000 | 0.225000 | 0.239000 | 4.23e-01 | 2.67e-01 | 7.40e-02 | 5.86e-02 |
L1CAM interactions | 69 | 3.51e-04 | 1.36e-03 | 0.3700 | 0.268000 | -0.149000 | 0.054000 | 0.200000 | 1.19e-04 | 3.28e-02 | 4.39e-01 | 4.20e-03 |
SMAD2/SMAD3:SMAD4 heterotrimer regulates transcription | 28 | 1.23e-02 | 2.80e-02 | 0.3700 | -0.011700 | 0.174000 | 0.326000 | 0.004250 | 9.14e-01 | 1.12e-01 | 2.81e-03 | 9.69e-01 |
Glucagon-like Peptide-1 (GLP1) regulates insulin secretion | 27 | 8.54e-03 | 2.09e-02 | 0.3700 | 0.349000 | -0.100000 | -0.070100 | -0.002630 | 1.71e-03 | 3.68e-01 | 5.29e-01 | 9.81e-01 |
Triglyceride metabolism | 20 | 8.02e-02 | 1.32e-01 | 0.3700 | 0.107000 | -0.163000 | -0.295000 | -0.109000 | 4.07e-01 | 2.08e-01 | 2.26e-02 | 3.98e-01 |
Intrinsic Pathway for Apoptosis | 41 | 2.37e-02 | 4.81e-02 | 0.3690 | 0.133000 | -0.092200 | 0.252000 | 0.216000 | 1.41e-01 | 3.07e-01 | 5.25e-03 | 1.69e-02 |
ADORA2B mediated anti-inflammatory cytokines production | 38 | 5.38e-03 | 1.41e-02 | 0.3690 | 0.315000 | -0.139000 | -0.036200 | 0.129000 | 7.82e-04 | 1.40e-01 | 7.00e-01 | 1.70e-01 |
RNA Polymerase I Promoter Escape | 25 | 3.86e-02 | 7.37e-02 | 0.3680 | -0.087500 | 0.293000 | 0.202000 | -0.036300 | 4.49e-01 | 1.14e-02 | 8.11e-02 | 7.54e-01 |
Spry regulation of FGF signaling | 14 | 1.77e-01 | 2.49e-01 | 0.3670 | 0.211000 | 0.025500 | 0.299000 | 0.007260 | 1.71e-01 | 8.69e-01 | 5.25e-02 | 9.62e-01 |
CREB1 phosphorylation through the activation of Adenylate Cyclase | 10 | 2.69e-01 | 3.50e-01 | 0.3670 | 0.133000 | -0.311000 | 0.071400 | -0.123000 | 4.66e-01 | 8.82e-02 | 6.96e-01 | 5.01e-01 |
Antiviral mechanism by IFN-stimulated genes | 64 | 1.58e-04 | 6.78e-04 | 0.3660 | -0.017700 | 0.283000 | 0.227000 | 0.050100 | 8.07e-01 | 9.46e-05 | 1.69e-03 | 4.89e-01 |
Signaling by BMP | 22 | 3.11e-03 | 8.93e-03 | 0.3660 | 0.030200 | -0.055200 | 0.085100 | -0.351000 | 8.06e-01 | 6.54e-01 | 4.90e-01 | 4.42e-03 |
DAP12 interactions | 15 | 4.01e-01 | 4.84e-01 | 0.3650 | 0.133000 | 0.026900 | 0.161000 | 0.299000 | 3.72e-01 | 8.57e-01 | 2.81e-01 | 4.52e-02 |
DAP12 signaling | 15 | 4.01e-01 | 4.84e-01 | 0.3650 | 0.133000 | 0.026900 | 0.161000 | 0.299000 | 3.72e-01 | 8.57e-01 | 2.81e-01 | 4.52e-02 |
Downstream TCR signaling | 67 | 1.95e-07 | 1.82e-06 | 0.3650 | -0.262000 | 0.086900 | 0.220000 | -0.095900 | 2.16e-04 | 2.19e-01 | 1.91e-03 | 1.76e-01 |
Early Phase of HIV Life Cycle | 11 | 3.42e-01 | 4.29e-01 | 0.3650 | -0.124000 | 0.149000 | 0.264000 | 0.162000 | 4.76e-01 | 3.91e-01 | 1.30e-01 | 3.53e-01 |
Translesion synthesis by REV1 | 14 | 1.84e-01 | 2.56e-01 | 0.3650 | -0.140000 | 0.291000 | 0.061600 | 0.158000 | 3.65e-01 | 5.95e-02 | 6.90e-01 | 3.06e-01 |
SUMOylation of transcription cofactors | 38 | 6.73e-03 | 1.70e-02 | 0.3630 | -0.165000 | 0.229000 | 0.022800 | -0.227000 | 7.80e-02 | 1.47e-02 | 8.08e-01 | 1.54e-02 |
Mitotic Spindle Checkpoint | 74 | 1.69e-05 | 9.20e-05 | 0.3630 | -0.131000 | 0.302000 | 0.134000 | 0.071000 | 5.13e-02 | 7.15e-06 | 4.58e-02 | 2.92e-01 |
Inhibition of DNA recombination at telomere | 19 | 1.97e-01 | 2.73e-01 | 0.3630 | 0.022200 | 0.290000 | 0.192000 | 0.101000 | 8.67e-01 | 2.87e-02 | 1.47e-01 | 4.47e-01 |
Transport of bile salts and organic acids, metal ions and amine compounds | 32 | 1.10e-01 | 1.70e-01 | 0.3620 | 0.202000 | -0.099000 | 0.188000 | 0.213000 | 4.81e-02 | 3.33e-01 | 6.63e-02 | 3.74e-02 |
Recognition of DNA damage by PCNA-containing replication complex | 28 | 3.93e-02 | 7.49e-02 | 0.3620 | -0.105000 | 0.252000 | 0.200000 | 0.126000 | 3.36e-01 | 2.10e-02 | 6.65e-02 | 2.49e-01 |
CDT1 association with the CDC6:ORC:origin complex | 48 | 9.70e-05 | 4.46e-04 | 0.3610 | -0.280000 | 0.120000 | 0.182000 | -0.069100 | 8.11e-04 | 1.51e-01 | 2.93e-02 | 4.08e-01 |
Visual phototransduction | 37 | 2.35e-02 | 4.80e-02 | 0.3610 | 0.142000 | -0.217000 | 0.171000 | 0.183000 | 1.34e-01 | 2.23e-02 | 7.26e-02 | 5.41e-02 |
KSRP (KHSRP) binds and destabilizes mRNA | 16 | 2.33e-01 | 3.12e-01 | 0.3600 | -0.039600 | 0.317000 | 0.164000 | 0.027300 | 7.84e-01 | 2.83e-02 | 2.57e-01 | 8.50e-01 |
Regulation of activated PAK-2p34 by proteasome mediated degradation | 42 | 1.27e-04 | 5.67e-04 | 0.3600 | -0.233000 | 0.084700 | 0.255000 | -0.051800 | 9.02e-03 | 3.43e-01 | 4.23e-03 | 5.62e-01 |
Deregulated CDK5 triggers multiple neurodegenerative pathways in Alzheimer's disease models | 18 | 2.32e-01 | 3.11e-01 | 0.3590 | 0.066100 | -0.084100 | 0.190000 | 0.285000 | 6.27e-01 | 5.37e-01 | 1.62e-01 | 3.61e-02 |
Neurodegenerative Diseases | 18 | 2.32e-01 | 3.11e-01 | 0.3590 | 0.066100 | -0.084100 | 0.190000 | 0.285000 | 6.27e-01 | 5.37e-01 | 1.62e-01 | 3.61e-02 |
Vpu mediated degradation of CD4 | 43 | 1.44e-04 | 6.32e-04 | 0.3590 | -0.266000 | 0.081100 | 0.205000 | -0.099000 | 2.60e-03 | 3.58e-01 | 1.99e-02 | 2.62e-01 |
NOTCH3 Activation and Transmission of Signal to the Nucleus | 21 | 1.41e-01 | 2.06e-01 | 0.3590 | 0.283000 | -0.178000 | 0.003130 | 0.132000 | 2.49e-02 | 1.59e-01 | 9.80e-01 | 2.96e-01 |
XBP1(S) activates chaperone genes | 45 | 5.40e-03 | 1.41e-02 | 0.3590 | 0.124000 | -0.003280 | 0.319000 | 0.110000 | 1.52e-01 | 9.70e-01 | 2.20e-04 | 2.02e-01 |
tRNA modification in the nucleus and cytosol | 38 | 8.57e-03 | 2.09e-02 | 0.3580 | -0.032700 | 0.323000 | 0.152000 | -0.007180 | 7.27e-01 | 5.86e-04 | 1.05e-01 | 9.39e-01 |
Telomere Extension By Telomerase | 19 | 1.08e-01 | 1.67e-01 | 0.3580 | 0.126000 | 0.325000 | 0.075800 | 0.028800 | 3.40e-01 | 1.42e-02 | 5.68e-01 | 8.28e-01 |
G alpha (12/13) signalling events | 54 | 1.19e-03 | 3.89e-03 | 0.3580 | 0.232000 | -0.231000 | -0.029900 | 0.140000 | 3.20e-03 | 3.29e-03 | 7.04e-01 | 7.54e-02 |
Orc1 removal from chromatin | 59 | 7.51e-06 | 4.68e-05 | 0.3580 | -0.211000 | 0.115000 | 0.263000 | 0.034600 | 5.13e-03 | 1.27e-01 | 4.86e-04 | 6.47e-01 |
Rap1 signalling | 14 | 4.70e-01 | 5.54e-01 | 0.3570 | 0.260000 | 0.078800 | 0.177000 | 0.151000 | 9.23e-02 | 6.10e-01 | 2.51e-01 | 3.30e-01 |
Sialic acid metabolism | 23 | 9.05e-02 | 1.46e-01 | 0.3570 | 0.118000 | -0.301000 | 0.020900 | 0.149000 | 3.29e-01 | 1.25e-02 | 8.62e-01 | 2.16e-01 |
NIK-->noncanonical NF-kB signaling | 50 | 2.48e-05 | 1.29e-04 | 0.3560 | -0.254000 | 0.077900 | 0.232000 | -0.047700 | 1.91e-03 | 3.41e-01 | 4.57e-03 | 5.60e-01 |
Initiation of Nuclear Envelope (NE) Reformation | 17 | 1.08e-01 | 1.67e-01 | 0.3550 | -0.109000 | 0.196000 | 0.273000 | -0.037300 | 4.37e-01 | 1.61e-01 | 5.18e-02 | 7.90e-01 |
mRNA decay by 3' to 5' exoribonuclease | 15 | 1.65e-01 | 2.35e-01 | 0.3550 | -0.150000 | 0.233000 | 0.180000 | -0.130000 | 3.15e-01 | 1.19e-01 | 2.27e-01 | 3.85e-01 |
Aquaporin-mediated transport | 29 | 1.87e-02 | 3.95e-02 | 0.3540 | 0.228000 | -0.215000 | -0.164000 | -0.022300 | 3.40e-02 | 4.51e-02 | 1.27e-01 | 8.35e-01 |
DNA Replication Pre-Initiation | 70 | 3.44e-06 | 2.32e-05 | 0.3530 | -0.186000 | 0.140000 | 0.250000 | 0.090700 | 7.18e-03 | 4.37e-02 | 3.03e-04 | 1.90e-01 |
Vif-mediated degradation of APOBEC3G | 43 | 2.09e-04 | 8.61e-04 | 0.3530 | -0.259000 | 0.085600 | 0.210000 | -0.077700 | 3.35e-03 | 3.32e-01 | 1.72e-02 | 3.79e-01 |
Epigenetic regulation of gene expression | 79 | 1.42e-05 | 8.06e-05 | 0.3520 | -0.076200 | 0.279000 | 0.201000 | 0.007730 | 2.43e-01 | 1.85e-05 | 2.03e-03 | 9.06e-01 |
Regulation of Apoptosis | 45 | 1.51e-04 | 6.57e-04 | 0.3520 | -0.274000 | 0.078300 | 0.195000 | -0.068600 | 1.46e-03 | 3.64e-01 | 2.37e-02 | 4.26e-01 |
Glucagon signaling in metabolic regulation | 23 | 8.68e-02 | 1.41e-01 | 0.3520 | 0.199000 | -0.274000 | -0.091700 | 0.034500 | 9.84e-02 | 2.32e-02 | 4.47e-01 | 7.74e-01 |
PLC beta mediated events | 39 | 1.15e-02 | 2.65e-02 | 0.3520 | 0.207000 | -0.260000 | -0.044000 | 0.107000 | 2.51e-02 | 5.05e-03 | 6.35e-01 | 2.47e-01 |
FCERI mediated NF-kB activation | 65 | 1.19e-06 | 9.08e-06 | 0.3520 | -0.275000 | 0.045600 | 0.177000 | -0.120000 | 1.27e-04 | 5.26e-01 | 1.36e-02 | 9.39e-02 |
SCF-beta-TrCP mediated degradation of Emi1 | 45 | 1.07e-04 | 4.87e-04 | 0.3520 | -0.263000 | 0.061800 | 0.205000 | -0.092000 | 2.31e-03 | 4.74e-01 | 1.72e-02 | 2.86e-01 |
Dectin-1 mediated noncanonical NF-kB signaling | 51 | 2.82e-05 | 1.46e-04 | 0.3510 | -0.234000 | 0.084100 | 0.244000 | -0.039600 | 3.94e-03 | 2.99e-01 | 2.55e-03 | 6.26e-01 |
Processive synthesis on the C-strand of the telomere | 19 | 3.70e-01 | 4.54e-01 | 0.3500 | 0.113000 | 0.110000 | 0.195000 | 0.244000 | 3.95e-01 | 4.08e-01 | 1.40e-01 | 6.52e-02 |
Thromboxane signalling through TP receptor | 14 | 3.63e-01 | 4.49e-01 | 0.3500 | 0.270000 | 0.055300 | 0.037400 | 0.213000 | 8.09e-02 | 7.20e-01 | 8.09e-01 | 1.67e-01 |
Nuclear Events (kinase and transcription factor activation) | 52 | 3.61e-03 | 1.02e-02 | 0.3500 | 0.202000 | -0.110000 | 0.244000 | 0.100000 | 1.19e-02 | 1.69e-01 | 2.34e-03 | 2.12e-01 |
Synthesis of substrates in N-glycan biosythesis | 52 | 2.01e-02 | 4.18e-02 | 0.3500 | 0.217000 | -0.107000 | 0.164000 | 0.192000 | 6.77e-03 | 1.84e-01 | 4.09e-02 | 1.66e-02 |
Innate Immune System | 606 | 1.51e-26 | 2.32e-24 | 0.3500 | 0.166000 | -0.042800 | 0.165000 | 0.257000 | 6.72e-12 | 7.63e-02 | 7.54e-12 | 1.66e-26 |
ISG15 antiviral mechanism | 59 | 5.42e-04 | 2.01e-03 | 0.3490 | -0.050200 | 0.271000 | 0.213000 | 0.025400 | 5.05e-01 | 3.18e-04 | 4.80e-03 | 7.37e-01 |
Amino acid transport across the plasma membrane | 20 | 1.44e-01 | 2.09e-01 | 0.3490 | 0.096100 | -0.303000 | 0.071600 | 0.126000 | 4.57e-01 | 1.92e-02 | 5.80e-01 | 3.31e-01 |
PI-3K cascade:FGFR3 | 10 | 3.09e-01 | 3.92e-01 | 0.3490 | -0.215000 | 0.065600 | 0.133000 | -0.231000 | 2.39e-01 | 7.19e-01 | 4.66e-01 | 2.06e-01 |
HCMV Late Events | 43 | 1.98e-03 | 6.03e-03 | 0.3490 | -0.258000 | 0.221000 | 0.070600 | 0.033400 | 3.45e-03 | 1.23e-02 | 4.24e-01 | 7.05e-01 |
Regulation of signaling by CBL | 13 | 4.61e-01 | 5.44e-01 | 0.3480 | 0.097400 | 0.033900 | 0.304000 | 0.136000 | 5.43e-01 | 8.33e-01 | 5.80e-02 | 3.97e-01 |
Uptake and function of anthrax toxins | 11 | 3.29e-01 | 4.14e-01 | 0.3470 | 0.047800 | -0.224000 | -0.065900 | -0.253000 | 7.84e-01 | 1.99e-01 | 7.05e-01 | 1.47e-01 |
ATF6 (ATF6-alpha) activates chaperones | 12 | 3.76e-01 | 4.60e-01 | 0.3460 | -0.037100 | 0.107000 | 0.310000 | 0.104000 | 8.24e-01 | 5.23e-01 | 6.28e-02 | 5.35e-01 |
Prolonged ERK activation events | 12 | 2.13e-01 | 2.91e-01 | 0.3460 | -0.043500 | 0.220000 | 0.215000 | -0.152000 | 7.94e-01 | 1.87e-01 | 1.96e-01 | 3.63e-01 |
G beta:gamma signalling through PI3Kgamma | 15 | 2.54e-01 | 3.36e-01 | 0.3460 | 0.288000 | -0.061800 | -0.043900 | 0.175000 | 5.32e-02 | 6.79e-01 | 7.69e-01 | 2.40e-01 |
Ubiquitin Mediated Degradation of Phosphorylated Cdc25A | 43 | 2.87e-04 | 1.15e-03 | 0.3460 | -0.217000 | 0.101000 | 0.243000 | -0.056500 | 1.40e-02 | 2.52e-01 | 5.80e-03 | 5.22e-01 |
p53-Independent DNA Damage Response | 43 | 2.87e-04 | 1.15e-03 | 0.3460 | -0.217000 | 0.101000 | 0.243000 | -0.056500 | 1.40e-02 | 2.52e-01 | 5.80e-03 | 5.22e-01 |
p53-Independent G1/S DNA damage checkpoint | 43 | 2.87e-04 | 1.15e-03 | 0.3460 | -0.217000 | 0.101000 | 0.243000 | -0.056500 | 1.40e-02 | 2.52e-01 | 5.80e-03 | 5.22e-01 |
Regulation of insulin secretion | 46 | 3.72e-03 | 1.05e-02 | 0.3450 | 0.303000 | -0.116000 | -0.023900 | 0.115000 | 3.82e-04 | 1.72e-01 | 7.80e-01 | 1.79e-01 |
Disorders of Developmental Biology | 10 | 7.28e-01 | 7.80e-01 | 0.3450 | -0.217000 | -0.040800 | -0.158000 | -0.212000 | 2.34e-01 | 8.23e-01 | 3.86e-01 | 2.46e-01 |
Disorders of Nervous System Development | 10 | 7.28e-01 | 7.80e-01 | 0.3450 | -0.217000 | -0.040800 | -0.158000 | -0.212000 | 2.34e-01 | 8.23e-01 | 3.86e-01 | 2.46e-01 |
Loss of function of MECP2 in Rett syndrome | 10 | 7.28e-01 | 7.80e-01 | 0.3450 | -0.217000 | -0.040800 | -0.158000 | -0.212000 | 2.34e-01 | 8.23e-01 | 3.86e-01 | 2.46e-01 |
Pervasive developmental disorders | 10 | 7.28e-01 | 7.80e-01 | 0.3450 | -0.217000 | -0.040800 | -0.158000 | -0.212000 | 2.34e-01 | 8.23e-01 | 3.86e-01 | 2.46e-01 |
Ubiquitin-dependent degradation of Cyclin D | 44 | 1.98e-04 | 8.18e-04 | 0.3450 | -0.211000 | 0.087000 | 0.254000 | -0.046300 | 1.57e-02 | 3.19e-01 | 3.57e-03 | 5.96e-01 |
RHO GTPase Effectors | 173 | 2.34e-07 | 2.16e-06 | 0.3440 | 0.106000 | 0.072100 | 0.247000 | 0.203000 | 1.67e-02 | 1.03e-01 | 2.37e-08 | 4.40e-06 |
Peptide hormone metabolism | 39 | 5.61e-03 | 1.45e-02 | 0.3440 | 0.099500 | 0.011500 | 0.043900 | 0.326000 | 2.83e-01 | 9.01e-01 | 6.35e-01 | 4.25e-04 |
VEGFR2 mediated cell proliferation | 16 | 1.98e-01 | 2.74e-01 | 0.3440 | 0.261000 | -0.158000 | -0.105000 | 0.120000 | 7.11e-02 | 2.74e-01 | 4.66e-01 | 4.08e-01 |
Energy dependent regulation of mTOR by LKB1-AMPK | 29 | 1.03e-01 | 1.61e-01 | 0.3440 | -0.277000 | -0.077100 | -0.142000 | -0.124000 | 9.97e-03 | 4.73e-01 | 1.85e-01 | 2.46e-01 |
Assembly of the pre-replicative complex | 56 | 2.72e-05 | 1.41e-04 | 0.3440 | -0.212000 | 0.095100 | 0.252000 | 0.026100 | 6.10e-03 | 2.19e-01 | 1.13e-03 | 7.36e-01 |
Insertion of tail-anchored proteins into the endoplasmic reticulum membrane | 18 | 1.75e-01 | 2.48e-01 | 0.3430 | 0.122000 | -0.006560 | 0.315000 | 0.061500 | 3.69e-01 | 9.62e-01 | 2.09e-02 | 6.52e-01 |
mTORC1-mediated signalling | 23 | 7.73e-02 | 1.29e-01 | 0.3430 | -0.332000 | -0.021600 | -0.037800 | -0.075100 | 5.86e-03 | 8.58e-01 | 7.54e-01 | 5.33e-01 |
Metabolic disorders of biological oxidation enzymes | 13 | 2.67e-01 | 3.47e-01 | 0.3430 | -0.203000 | -0.180000 | 0.020700 | -0.209000 | 2.06e-01 | 2.62e-01 | 8.97e-01 | 1.92e-01 |
GPCR downstream signalling | 243 | 6.61e-14 | 1.94e-12 | 0.3420 | 0.234000 | -0.204000 | 0.016900 | 0.143000 | 3.85e-10 | 5.49e-08 | 6.53e-01 | 1.29e-04 |
Signaling by MET | 52 | 2.64e-02 | 5.29e-02 | 0.3420 | 0.127000 | 0.012700 | 0.251000 | 0.194000 | 1.14e-01 | 8.75e-01 | 1.73e-03 | 1.58e-02 |
NRAGE signals death through JNK | 43 | 7.38e-03 | 1.84e-02 | 0.3420 | 0.125000 | -0.300000 | -0.050800 | 0.092900 | 1.58e-01 | 6.72e-04 | 5.65e-01 | 2.93e-01 |
Homologous DNA Pairing and Strand Exchange | 30 | 2.69e-02 | 5.37e-02 | 0.3410 | 0.002620 | 0.253000 | 0.060700 | 0.220000 | 9.80e-01 | 1.63e-02 | 5.66e-01 | 3.73e-02 |
G-protein mediated events | 40 | 1.40e-02 | 3.08e-02 | 0.3410 | 0.177000 | -0.268000 | -0.042000 | 0.106000 | 5.25e-02 | 3.43e-03 | 6.46e-01 | 2.46e-01 |
Glutathione conjugation | 21 | 2.38e-01 | 3.19e-01 | 0.3400 | -0.101000 | -0.252000 | -0.155000 | -0.134000 | 4.25e-01 | 4.53e-02 | 2.18e-01 | 2.90e-01 |
PTK6 Regulates RHO GTPases, RAS GTPase and MAP kinases | 13 | 3.89e-01 | 4.72e-01 | 0.3400 | 0.097600 | -0.079100 | 0.295000 | 0.112000 | 5.43e-01 | 6.22e-01 | 6.55e-02 | 4.83e-01 |
DNA Damage Recognition in GG-NER | 34 | 3.52e-02 | 6.85e-02 | 0.3390 | -0.197000 | 0.170000 | 0.008250 | -0.218000 | 4.72e-02 | 8.60e-02 | 9.34e-01 | 2.81e-02 |
Retrograde transport at the Trans-Golgi-Network | 43 | 1.29e-02 | 2.89e-02 | 0.3390 | -0.243000 | 0.191000 | -0.120000 | -0.072100 | 5.93e-03 | 3.02e-02 | 1.73e-01 | 4.14e-01 |
Dual incision in TC-NER | 60 | 4.36e-04 | 1.66e-03 | 0.3390 | -0.190000 | 0.250000 | 0.124000 | -0.033800 | 1.09e-02 | 8.26e-04 | 9.85e-02 | 6.51e-01 |
FBXL7 down-regulates AURKA during mitotic entry and in early mitosis | 46 | 3.36e-04 | 1.32e-03 | 0.3390 | -0.258000 | 0.090900 | 0.183000 | -0.082400 | 2.53e-03 | 2.87e-01 | 3.16e-02 | 3.34e-01 |
G2/M Checkpoints | 106 | 1.90e-07 | 1.81e-06 | 0.3390 | -0.123000 | 0.171000 | 0.243000 | 0.106000 | 2.97e-02 | 2.35e-03 | 1.58e-05 | 5.93e-02 |
G alpha (s) signalling events | 51 | 1.65e-03 | 5.14e-03 | 0.3390 | 0.250000 | -0.161000 | -0.076400 | 0.143000 | 2.01e-03 | 4.70e-02 | 3.46e-01 | 7.87e-02 |
Metabolism of porphyrins | 18 | 2.64e-01 | 3.45e-01 | 0.3380 | -0.047800 | -0.143000 | -0.290000 | -0.085400 | 7.26e-01 | 2.93e-01 | 3.30e-02 | 5.31e-01 |
Signaling by GPCR | 268 | 4.92e-15 | 1.78e-13 | 0.3380 | 0.234000 | -0.208000 | 0.020100 | 0.125000 | 5.40e-11 | 6.15e-09 | 5.74e-01 | 4.55e-04 |
G alpha (i) signalling events | 125 | 1.06e-06 | 8.33e-06 | 0.3370 | 0.209000 | -0.221000 | 0.048200 | 0.138000 | 5.62e-05 | 2.16e-05 | 3.54e-01 | 7.83e-03 |
Transport of inorganic cations/anions and amino acids/oligopeptides | 56 | 1.15e-03 | 3.81e-03 | 0.3370 | 0.070300 | -0.315000 | -0.077500 | 0.055300 | 3.63e-01 | 4.60e-05 | 3.17e-01 | 4.75e-01 |
Nucleotide salvage | 18 | 1.79e-01 | 2.51e-01 | 0.3370 | 0.060300 | -0.307000 | 0.090900 | 0.084400 | 6.58e-01 | 2.42e-02 | 5.05e-01 | 5.35e-01 |
Nonhomologous End-Joining (NHEJ) | 30 | 4.56e-02 | 8.43e-02 | 0.3360 | -0.196000 | 0.271000 | -0.028000 | -0.017400 | 6.37e-02 | 1.01e-02 | 7.91e-01 | 8.69e-01 |
Negative regulation of FGFR2 signaling | 19 | 1.35e-01 | 1.97e-01 | 0.3360 | 0.208000 | -0.011200 | 0.263000 | 0.013100 | 1.17e-01 | 9.33e-01 | 4.73e-02 | 9.21e-01 |
SCF(Skp2)-mediated degradation of p27/p21 | 52 | 3.00e-04 | 1.19e-03 | 0.3350 | -0.118000 | 0.106000 | 0.292000 | 0.045400 | 1.42e-01 | 1.87e-01 | 2.73e-04 | 5.72e-01 |
Vasopressin regulates renal water homeostasis via Aquaporins | 27 | 4.86e-02 | 8.89e-02 | 0.3340 | 0.233000 | -0.208000 | -0.119000 | 0.001650 | 3.64e-02 | 6.10e-02 | 2.86e-01 | 9.88e-01 |
HSF1 activation | 22 | 4.15e-02 | 7.80e-02 | 0.3340 | -0.055600 | 0.179000 | 0.257000 | -0.102000 | 6.52e-01 | 1.46e-01 | 3.68e-02 | 4.09e-01 |
Signaling by high-kinase activity BRAF mutants | 27 | 1.62e-01 | 2.31e-01 | 0.3340 | 0.180000 | -0.087800 | 0.234000 | 0.128000 | 1.05e-01 | 4.30e-01 | 3.51e-02 | 2.52e-01 |
Regulation of expression of SLITs and ROBOs | 114 | 3.69e-12 | 8.10e-11 | 0.3340 | -0.153000 | 0.026000 | 0.291000 | -0.053300 | 4.86e-03 | 6.33e-01 | 8.98e-08 | 3.27e-01 |
Mitochondrial iron-sulfur cluster biogenesis | 12 | 6.73e-01 | 7.36e-01 | 0.3340 | -0.189000 | -0.074500 | -0.151000 | -0.217000 | 2.57e-01 | 6.55e-01 | 3.64e-01 | 1.93e-01 |
Presynaptic phase of homologous DNA pairing and strand exchange | 29 | 3.94e-02 | 7.49e-02 | 0.3330 | 0.014000 | 0.261000 | 0.051000 | 0.200000 | 8.96e-01 | 1.51e-02 | 6.35e-01 | 6.25e-02 |
Signaling by NTRK3 (TRKC) | 16 | 3.53e-01 | 4.40e-01 | 0.3330 | 0.179000 | -0.155000 | 0.027600 | 0.233000 | 2.15e-01 | 2.84e-01 | 8.49e-01 | 1.07e-01 |
Repression of WNT target genes | 11 | 6.28e-01 | 6.98e-01 | 0.3330 | 0.223000 | 0.058500 | 0.215000 | 0.106000 | 2.00e-01 | 7.37e-01 | 2.17e-01 | 5.42e-01 |
Separation of Sister Chromatids | 125 | 2.66e-08 | 2.74e-07 | 0.3320 | -0.176000 | 0.242000 | 0.145000 | 0.000534 | 7.28e-04 | 3.11e-06 | 5.17e-03 | 9.92e-01 |
Nucleotide Excision Repair | 102 | 1.24e-06 | 9.35e-06 | 0.3320 | -0.205000 | 0.219000 | 0.094800 | -0.107000 | 3.61e-04 | 1.38e-04 | 9.90e-02 | 6.16e-02 |
Nicotinamide salvaging | 12 | 4.03e-01 | 4.86e-01 | 0.3320 | 0.245000 | -0.069700 | -0.050900 | 0.206000 | 1.42e-01 | 6.76e-01 | 7.60e-01 | 2.16e-01 |
Maturation of nucleoprotein | 10 | 6.61e-01 | 7.26e-01 | 0.3320 | 0.279000 | -0.005380 | 0.084500 | 0.158000 | 1.27e-01 | 9.77e-01 | 6.44e-01 | 3.86e-01 |
Cross-presentation of soluble exogenous antigens (endosomes) | 40 | 7.92e-04 | 2.77e-03 | 0.3310 | -0.230000 | 0.058100 | 0.225000 | -0.051900 | 1.18e-02 | 5.26e-01 | 1.38e-02 | 5.70e-01 |
Negative regulation of FGFR3 signaling | 19 | 1.00e-01 | 1.58e-01 | 0.3310 | 0.158000 | 0.080000 | 0.278000 | -0.029400 | 2.34e-01 | 5.46e-01 | 3.60e-02 | 8.24e-01 |
Cell Cycle Checkpoints | 191 | 3.42e-12 | 7.79e-11 | 0.3310 | -0.121000 | 0.219000 | 0.197000 | 0.088900 | 4.02e-03 | 1.98e-07 | 2.95e-06 | 3.50e-02 |
Activation of NF-kappaB in B cells | 56 | 2.59e-05 | 1.35e-04 | 0.3310 | -0.212000 | 0.063000 | 0.243000 | -0.036400 | 6.06e-03 | 4.15e-01 | 1.69e-03 | 6.38e-01 |
Hh mutants that don't undergo autocatalytic processing are degraded by ERAD | 46 | 5.10e-04 | 1.90e-03 | 0.3300 | -0.210000 | 0.104000 | 0.232000 | -0.017700 | 1.40e-02 | 2.23e-01 | 6.59e-03 | 8.35e-01 |
Unfolded Protein Response (UPR) | 82 | 9.15e-05 | 4.24e-04 | 0.3280 | 0.044600 | 0.127000 | 0.291000 | 0.071000 | 4.86e-01 | 4.66e-02 | 5.44e-06 | 2.67e-01 |
HDR through Homologous Recombination (HRR) or Single Strand Annealing (SSA) | 76 | 2.88e-04 | 1.15e-03 | 0.3280 | -0.053600 | 0.195000 | 0.187000 | 0.178000 | 4.20e-01 | 3.37e-03 | 4.87e-03 | 7.34e-03 |
Hh mutants abrogate ligand secretion | 47 | 5.84e-04 | 2.11e-03 | 0.3270 | -0.189000 | 0.113000 | 0.242000 | -0.007230 | 2.51e-02 | 1.81e-01 | 4.15e-03 | 9.32e-01 |
RHO GTPases activate PKNs | 29 | 1.71e-01 | 2.42e-01 | 0.3270 | 0.101000 | -0.042000 | 0.251000 | 0.179000 | 3.45e-01 | 6.96e-01 | 1.96e-02 | 9.49e-02 |
TICAM1, RIP1-mediated IKK complex recruitment | 14 | 2.11e-01 | 2.88e-01 | 0.3260 | -0.197000 | 0.112000 | 0.235000 | -0.008000 | 2.02e-01 | 4.69e-01 | 1.28e-01 | 9.59e-01 |
Transcription-Coupled Nucleotide Excision Repair (TC-NER) | 73 | 1.35e-04 | 6.00e-04 | 0.3260 | -0.218000 | 0.206000 | 0.091800 | -0.089600 | 1.31e-03 | 2.37e-03 | 1.76e-01 | 1.86e-01 |
RAF activation | 34 | 7.36e-02 | 1.24e-01 | 0.3260 | -0.199000 | -0.015900 | -0.051900 | -0.252000 | 4.53e-02 | 8.72e-01 | 6.01e-01 | 1.09e-02 |
Defective CFTR causes cystic fibrosis | 50 | 3.38e-04 | 1.33e-03 | 0.3250 | -0.220000 | 0.099500 | 0.217000 | 0.007070 | 7.14e-03 | 2.24e-01 | 8.00e-03 | 9.31e-01 |
Signaling by Retinoic Acid | 29 | 1.66e-01 | 2.35e-01 | 0.3250 | -0.098900 | -0.176000 | -0.229000 | -0.110000 | 3.57e-01 | 1.00e-01 | 3.29e-02 | 3.06e-01 |
Signaling by Receptor Tyrosine Kinases | 354 | 1.35e-12 | 3.31e-11 | 0.3240 | 0.195000 | -0.043600 | 0.159000 | 0.200000 | 4.01e-10 | 1.63e-01 | 3.63e-07 | 1.36e-10 |
Signaling by NOTCH2 | 24 | 9.33e-02 | 1.48e-01 | 0.3240 | 0.279000 | -0.025700 | -0.048400 | 0.156000 | 1.81e-02 | 8.28e-01 | 6.82e-01 | 1.86e-01 |
Negative regulation of NOTCH4 signaling | 47 | 1.89e-04 | 7.96e-04 | 0.3240 | -0.206000 | 0.039500 | 0.244000 | -0.039100 | 1.45e-02 | 6.40e-01 | 3.87e-03 | 6.43e-01 |
Cytosolic sensors of pathogen-associated DNA | 52 | 1.04e-02 | 2.46e-02 | 0.3240 | 0.016300 | 0.191000 | 0.149000 | 0.215000 | 8.39e-01 | 1.74e-02 | 6.37e-02 | 7.46e-03 |
G2/M DNA damage checkpoint | 49 | 1.28e-02 | 2.89e-02 | 0.3240 | -0.037600 | 0.212000 | 0.188000 | 0.152000 | 6.49e-01 | 1.02e-02 | 2.29e-02 | 6.64e-02 |
Regulation of TNFR1 signaling | 26 | 7.62e-02 | 1.28e-01 | 0.3240 | 0.051200 | -0.242000 | 0.043800 | 0.204000 | 6.52e-01 | 3.25e-02 | 6.99e-01 | 7.23e-02 |
SHC1 events in ERBB2 signaling | 15 | 4.91e-01 | 5.73e-01 | 0.3240 | 0.217000 | -0.162000 | 0.125000 | 0.126000 | 1.47e-01 | 2.78e-01 | 4.01e-01 | 3.97e-01 |
Constitutive Signaling by AKT1 E17K in Cancer | 26 | 1.02e-01 | 1.60e-01 | 0.3230 | -0.228000 | -0.176000 | -0.046300 | -0.139000 | 4.45e-02 | 1.20e-01 | 6.83e-01 | 2.21e-01 |
TRAF6 mediated IRF7 activation | 14 | 3.11e-01 | 3.94e-01 | 0.3230 | 0.049200 | 0.037000 | 0.065300 | 0.310000 | 7.50e-01 | 8.11e-01 | 6.72e-01 | 4.45e-02 |
RNA Polymerase III Abortive And Retractive Initiation | 39 | 1.31e-02 | 2.93e-02 | 0.3230 | -0.253000 | 0.195000 | 0.049000 | -0.005440 | 6.39e-03 | 3.52e-02 | 5.97e-01 | 9.53e-01 |
RNA Polymerase III Transcription | 39 | 1.31e-02 | 2.93e-02 | 0.3230 | -0.253000 | 0.195000 | 0.049000 | -0.005440 | 6.39e-03 | 3.52e-02 | 5.97e-01 | 9.53e-01 |
Deadenylation-dependent mRNA decay | 53 | 4.33e-03 | 1.19e-02 | 0.3220 | -0.174000 | 0.248000 | 0.063100 | -0.089800 | 2.88e-02 | 1.79e-03 | 4.27e-01 | 2.59e-01 |
DDX58/IFIH1-mediated induction of interferon-alpha/beta | 52 | 1.83e-02 | 3.88e-02 | 0.3220 | 0.064200 | -0.053900 | 0.210000 | 0.230000 | 4.24e-01 | 5.02e-01 | 8.87e-03 | 4.23e-03 |
Circadian Clock | 63 | 8.90e-03 | 2.14e-02 | 0.3220 | -0.217000 | -0.091800 | -0.097800 | -0.197000 | 2.94e-03 | 2.08e-01 | 1.80e-01 | 6.95e-03 |
Myogenesis | 26 | 9.04e-02 | 1.46e-01 | 0.3220 | 0.088400 | -0.278000 | -0.066500 | 0.118000 | 4.36e-01 | 1.41e-02 | 5.57e-01 | 2.97e-01 |
MHC class II antigen presentation | 71 | 3.89e-03 | 1.09e-02 | 0.3210 | 0.125000 | 0.090800 | 0.120000 | 0.255000 | 6.99e-02 | 1.87e-01 | 8.00e-02 | 2.10e-04 |
Regulation of ornithine decarboxylase (ODC) | 44 | 8.21e-04 | 2.84e-03 | 0.3210 | -0.231000 | 0.067900 | 0.211000 | -0.016900 | 8.12e-03 | 4.36e-01 | 1.55e-02 | 8.46e-01 |
RHO GTPases activate KTN1 | 10 | 7.20e-01 | 7.75e-01 | 0.3210 | 0.045700 | 0.107000 | 0.211000 | 0.212000 | 8.02e-01 | 5.59e-01 | 2.49e-01 | 2.46e-01 |
Regulation of RUNX3 expression and activity | 47 | 4.07e-04 | 1.56e-03 | 0.3200 | -0.125000 | 0.104000 | 0.269000 | -0.060200 | 1.38e-01 | 2.19e-01 | 1.41e-03 | 4.76e-01 |
Erythropoietin activates RAS | 11 | 5.44e-01 | 6.23e-01 | 0.3200 | 0.030000 | 0.037800 | 0.297000 | 0.109000 | 8.63e-01 | 8.28e-01 | 8.80e-02 | 5.32e-01 |
GAB1 signalosome | 12 | 2.02e-01 | 2.78e-01 | 0.3200 | 0.024300 | -0.242000 | 0.160000 | -0.131000 | 8.84e-01 | 1.46e-01 | 3.38e-01 | 4.31e-01 |
Mitotic Anaphase | 171 | 8.63e-11 | 1.39e-09 | 0.3200 | -0.143000 | 0.204000 | 0.194000 | 0.049900 | 1.27e-03 | 4.75e-06 | 1.31e-05 | 2.63e-01 |
Mitotic Metaphase and Anaphase | 171 | 8.63e-11 | 1.39e-09 | 0.3200 | -0.143000 | 0.204000 | 0.194000 | 0.049900 | 1.27e-03 | 4.75e-06 | 1.31e-05 | 2.63e-01 |
WNT5A-dependent internalization of FZD4 | 13 | 5.48e-01 | 6.27e-01 | 0.3200 | 0.134000 | -0.195000 | 0.121000 | 0.177000 | 4.04e-01 | 2.23e-01 | 4.51e-01 | 2.68e-01 |
Macroautophagy | 98 | 8.71e-05 | 4.05e-04 | 0.3200 | -0.281000 | 0.076700 | -0.074600 | -0.108000 | 1.62e-06 | 1.91e-01 | 2.03e-01 | 6.42e-02 |
Hedgehog ligand biogenesis | 50 | 4.79e-04 | 1.81e-03 | 0.3200 | -0.168000 | 0.095100 | 0.255000 | 0.013200 | 4.06e-02 | 2.45e-01 | 1.87e-03 | 8.72e-01 |
Synthesis of very long-chain fatty acyl-CoAs | 10 | 7.23e-01 | 7.77e-01 | 0.3190 | 0.254000 | 0.003400 | 0.097500 | 0.167000 | 1.65e-01 | 9.85e-01 | 5.94e-01 | 3.60e-01 |
TP53 Regulates Transcription of Cell Cycle Genes | 42 | 8.02e-02 | 1.32e-01 | 0.3190 | 0.084900 | 0.061500 | 0.252000 | 0.166000 | 3.41e-01 | 4.91e-01 | 4.80e-03 | 6.31e-02 |
Positive epigenetic regulation of rRNA expression | 41 | 1.29e-02 | 2.90e-02 | 0.3190 | -0.053100 | 0.145000 | 0.273000 | 0.059300 | 5.57e-01 | 1.09e-01 | 2.51e-03 | 5.12e-01 |
Autodegradation of the E3 ubiquitin ligase COP1 | 44 | 1.04e-03 | 3.54e-03 | 0.3190 | -0.207000 | 0.094900 | 0.209000 | -0.078700 | 1.75e-02 | 2.77e-01 | 1.68e-02 | 3.67e-01 |
Transcription of E2F targets under negative control by DREAM complex | 17 | 2.90e-01 | 3.73e-01 | 0.3190 | -0.123000 | 0.231000 | 0.160000 | 0.086700 | 3.81e-01 | 9.96e-02 | 2.54e-01 | 5.36e-01 |
Membrane binding and targetting of GAG proteins | 10 | 2.21e-01 | 3.01e-01 | 0.3180 | -0.084600 | -0.032300 | 0.260000 | -0.159000 | 6.43e-01 | 8.60e-01 | 1.54e-01 | 3.84e-01 |
Synthesis And Processing Of GAG, GAGPOL Polyproteins | 10 | 2.21e-01 | 3.01e-01 | 0.3180 | -0.084600 | -0.032300 | 0.260000 | -0.159000 | 6.43e-01 | 8.60e-01 | 1.54e-01 | 3.84e-01 |
HSF1-dependent transactivation | 30 | 5.34e-03 | 1.41e-02 | 0.3180 | -0.155000 | 0.035900 | 0.256000 | -0.103000 | 1.42e-01 | 7.34e-01 | 1.55e-02 | 3.30e-01 |
Degradation of beta-catenin by the destruction complex | 72 | 7.58e-06 | 4.68e-05 | 0.3180 | -0.205000 | 0.108000 | 0.203000 | -0.079300 | 2.64e-03 | 1.14e-01 | 3.00e-03 | 2.46e-01 |
Cytosolic sulfonation of small molecules | 11 | 3.48e-01 | 4.35e-01 | 0.3180 | 0.288000 | 0.029900 | -0.101000 | 0.083600 | 9.83e-02 | 8.64e-01 | 5.62e-01 | 6.31e-01 |
Detoxification of Reactive Oxygen Species | 26 | 7.93e-02 | 1.31e-01 | 0.3180 | 0.033000 | -0.291000 | 0.084000 | 0.091500 | 7.71e-01 | 1.04e-02 | 4.59e-01 | 4.20e-01 |
JNK (c-Jun kinases) phosphorylation and activation mediated by activated human TAK1 | 16 | 3.66e-01 | 4.51e-01 | 0.3170 | -0.216000 | -0.074100 | -0.024600 | -0.219000 | 1.35e-01 | 6.08e-01 | 8.65e-01 | 1.29e-01 |
Synthesis of DNA | 106 | 6.65e-07 | 5.56e-06 | 0.3170 | -0.138000 | 0.147000 | 0.221000 | 0.106000 | 1.40e-02 | 9.19e-03 | 9.08e-05 | 5.98e-02 |
DNA Replication | 111 | 7.14e-07 | 5.89e-06 | 0.3170 | -0.120000 | 0.153000 | 0.220000 | 0.119000 | 3.00e-02 | 5.34e-03 | 6.26e-05 | 3.08e-02 |
Signaling by PDGFRA extracellular domain mutants | 11 | 5.20e-01 | 6.01e-01 | 0.3160 | -0.075200 | 0.099300 | 0.208000 | 0.202000 | 6.66e-01 | 5.69e-01 | 2.32e-01 | 2.45e-01 |
Signaling by PDGFRA transmembrane, juxtamembrane and kinase domain mutants | 11 | 5.20e-01 | 6.01e-01 | 0.3160 | -0.075200 | 0.099300 | 0.208000 | 0.202000 | 6.66e-01 | 5.69e-01 | 2.32e-01 | 2.45e-01 |
Transcriptional activity of SMAD2/SMAD3:SMAD4 heterotrimer | 40 | 5.56e-03 | 1.45e-02 | 0.3160 | -0.156000 | 0.170000 | 0.199000 | -0.084500 | 8.81e-02 | 6.36e-02 | 2.97e-02 | 3.55e-01 |
Platelet sensitization by LDL | 13 | 2.78e-01 | 3.59e-01 | 0.3160 | -0.130000 | 0.119000 | 0.261000 | -0.027000 | 4.18e-01 | 4.59e-01 | 1.04e-01 | 8.66e-01 |
Global Genome Nucleotide Excision Repair (GG-NER) | 78 | 2.47e-04 | 1.00e-03 | 0.3150 | -0.221000 | 0.194000 | 0.054900 | -0.101000 | 7.66e-04 | 3.17e-03 | 4.03e-01 | 1.24e-01 |
FOXO-mediated transcription of cell cycle genes | 16 | 1.81e-01 | 2.54e-01 | 0.3150 | -0.028400 | -0.163000 | -0.000119 | -0.268000 | 8.44e-01 | 2.59e-01 | 9.99e-01 | 6.36e-02 |
Homology Directed Repair | 82 | 2.21e-04 | 9.06e-04 | 0.3150 | -0.068000 | 0.186000 | 0.183000 | 0.162000 | 2.88e-01 | 3.61e-03 | 4.22e-03 | 1.12e-02 |
SHC-mediated cascade:FGFR4 | 10 | 7.30e-01 | 7.80e-01 | 0.3140 | 0.156000 | -0.088400 | 0.101000 | 0.237000 | 3.93e-01 | 6.28e-01 | 5.80e-01 | 1.94e-01 |
Degradation of GLI2 by the proteasome | 50 | 2.53e-04 | 1.02e-03 | 0.3140 | -0.231000 | 0.030500 | 0.186000 | -0.098700 | 4.84e-03 | 7.09e-01 | 2.33e-02 | 2.28e-01 |
SHC-mediated cascade:FGFR3 | 10 | 7.57e-01 | 8.06e-01 | 0.3130 | 0.084600 | 0.082200 | 0.242000 | 0.161000 | 6.43e-01 | 6.53e-01 | 1.85e-01 | 3.80e-01 |
IL-6-type cytokine receptor ligand interactions | 10 | 5.95e-01 | 6.71e-01 | 0.3120 | 0.121000 | -0.252000 | -0.122000 | -0.065700 | 5.08e-01 | 1.67e-01 | 5.05e-01 | 7.19e-01 |
RNA Polymerase I Transcription Termination | 25 | 1.16e-01 | 1.77e-01 | 0.3110 | -0.051700 | 0.248000 | 0.175000 | -0.040800 | 6.55e-01 | 3.18e-02 | 1.29e-01 | 7.24e-01 |
Signaling by VEGF | 83 | 4.23e-03 | 1.17e-02 | 0.3110 | 0.187000 | -0.120000 | 0.136000 | 0.169000 | 3.33e-03 | 5.95e-02 | 3.22e-02 | 7.78e-03 |
Activation of BH3-only proteins | 24 | 3.76e-01 | 4.59e-01 | 0.3100 | 0.133000 | -0.063700 | 0.177000 | 0.208000 | 2.59e-01 | 5.89e-01 | 1.34e-01 | 7.77e-02 |
TP53 Regulates Transcription of Cell Death Genes | 32 | 6.35e-02 | 1.09e-01 | 0.3100 | 0.278000 | -0.054900 | -0.019600 | 0.125000 | 6.55e-03 | 5.91e-01 | 8.48e-01 | 2.22e-01 |
SLC-mediated transmembrane transport | 119 | 6.99e-06 | 4.40e-05 | 0.3100 | 0.140000 | -0.244000 | 0.020400 | 0.130000 | 8.43e-03 | 4.72e-06 | 7.02e-01 | 1.50e-02 |
Purine ribonucleoside monophosphate biosynthesis | 12 | 5.76e-01 | 6.53e-01 | 0.3100 | -0.052400 | 0.024000 | -0.270000 | -0.140000 | 7.53e-01 | 8.85e-01 | 1.05e-01 | 4.00e-01 |
Regulation of mRNA stability by proteins that bind AU-rich elements | 75 | 2.35e-05 | 1.23e-04 | 0.3100 | -0.111000 | 0.150000 | 0.245000 | -0.034900 | 9.72e-02 | 2.47e-02 | 2.53e-04 | 6.02e-01 |
HCMV Infection | 68 | 5.69e-04 | 2.09e-03 | 0.3100 | -0.151000 | 0.240000 | 0.099800 | 0.076700 | 3.21e-02 | 6.43e-04 | 1.55e-01 | 2.75e-01 |
Interleukin receptor SHC signaling | 15 | 5.59e-01 | 6.37e-01 | 0.3100 | 0.130000 | -0.043500 | 0.239000 | 0.141000 | 3.83e-01 | 7.70e-01 | 1.09e-01 | 3.46e-01 |
Gap-filling DNA repair synthesis and ligation in TC-NER | 59 | 2.35e-03 | 7.02e-03 | 0.3100 | -0.146000 | 0.239000 | 0.129000 | -0.028200 | 5.25e-02 | 1.53e-03 | 8.62e-02 | 7.08e-01 |
Signaling by Interleukins | 275 | 8.52e-11 | 1.39e-09 | 0.3100 | 0.136000 | -0.053800 | 0.232000 | 0.143000 | 1.15e-04 | 1.27e-01 | 4.27e-11 | 5.00e-05 |
Protein folding | 75 | 1.22e-02 | 2.78e-02 | 0.3100 | 0.147000 | 0.084500 | 0.215000 | 0.145000 | 2.84e-02 | 2.07e-01 | 1.34e-03 | 2.97e-02 |
Selective autophagy | 51 | 3.93e-02 | 7.49e-02 | 0.3090 | -0.252000 | 0.033500 | -0.089500 | -0.151000 | 1.85e-03 | 6.80e-01 | 2.69e-01 | 6.16e-02 |
Degradation of DVL | 48 | 3.67e-04 | 1.42e-03 | 0.3090 | -0.219000 | 0.016400 | 0.188000 | -0.110000 | 8.85e-03 | 8.44e-01 | 2.45e-02 | 1.86e-01 |
G1/S Transition | 112 | 7.65e-07 | 6.22e-06 | 0.3080 | -0.122000 | 0.127000 | 0.228000 | 0.107000 | 2.62e-02 | 2.04e-02 | 3.09e-05 | 5.06e-02 |
VEGFA-VEGFR2 Pathway | 77 | 6.26e-03 | 1.59e-02 | 0.3080 | 0.165000 | -0.128000 | 0.157000 | 0.162000 | 1.23e-02 | 5.33e-02 | 1.73e-02 | 1.40e-02 |
Diseases of carbohydrate metabolism | 26 | 1.31e-01 | 1.93e-01 | 0.3080 | 0.005990 | -0.301000 | -0.055000 | -0.030400 | 9.58e-01 | 7.93e-03 | 6.27e-01 | 7.88e-01 |
activated TAK1 mediates p38 MAPK activation | 17 | 2.22e-01 | 3.01e-01 | 0.3070 | -0.133000 | -0.170000 | 0.019500 | -0.217000 | 3.43e-01 | 2.25e-01 | 8.90e-01 | 1.22e-01 |
trans-Golgi Network Vesicle Budding | 62 | 1.80e-02 | 3.82e-02 | 0.3060 | 0.043700 | 0.152000 | 0.183000 | 0.187000 | 5.52e-01 | 3.83e-02 | 1.26e-02 | 1.10e-02 |
Senescence-Associated Secretory Phenotype (SASP) | 45 | 1.14e-01 | 1.75e-01 | 0.3060 | 0.133000 | 0.046400 | 0.222000 | 0.156000 | 1.24e-01 | 5.91e-01 | 9.89e-03 | 7.05e-02 |
Regulation of cholesterol biosynthesis by SREBP (SREBF) | 53 | 2.56e-02 | 5.14e-02 | 0.3050 | -0.186000 | -0.089000 | -0.072000 | -0.213000 | 1.93e-02 | 2.63e-01 | 3.65e-01 | 7.30e-03 |
GLI3 is processed to GLI3R by the proteasome | 50 | 6.13e-04 | 2.19e-03 | 0.3050 | -0.229000 | 0.049100 | 0.173000 | -0.091200 | 5.11e-03 | 5.49e-01 | 3.46e-02 | 2.65e-01 |
Signaling by NTRKs | 111 | 1.60e-04 | 6.82e-04 | 0.3050 | 0.165000 | -0.086900 | 0.212000 | 0.115000 | 2.71e-03 | 1.15e-01 | 1.22e-04 | 3.75e-02 |
Chaperonin-mediated protein folding | 69 | 1.79e-02 | 3.81e-02 | 0.3040 | 0.147000 | 0.106000 | 0.207000 | 0.128000 | 3.47e-02 | 1.27e-01 | 2.96e-03 | 6.64e-02 |
Negative regulation of FGFR1 signaling | 19 | 1.34e-01 | 1.97e-01 | 0.3040 | 0.219000 | 0.027900 | 0.203000 | -0.045300 | 9.80e-02 | 8.33e-01 | 1.25e-01 | 7.33e-01 |
G-protein beta:gamma signalling | 20 | 2.06e-01 | 2.83e-01 | 0.3030 | 0.193000 | -0.076100 | -0.054900 | 0.214000 | 1.35e-01 | 5.56e-01 | 6.71e-01 | 9.80e-02 |
FCERI mediated Ca+2 mobilization | 18 | 3.07e-01 | 3.89e-01 | 0.3030 | 0.181000 | -0.223000 | -0.091600 | 0.031600 | 1.84e-01 | 1.02e-01 | 5.01e-01 | 8.17e-01 |
Gap-filling DNA repair synthesis and ligation in GG-NER | 23 | 2.27e-01 | 3.07e-01 | 0.3020 | -0.062600 | 0.155000 | 0.195000 | 0.159000 | 6.04e-01 | 1.97e-01 | 1.05e-01 | 1.87e-01 |
Inactivation, recovery and regulation of the phototransduction cascade | 12 | 3.83e-01 | 4.65e-01 | 0.3020 | -0.111000 | -0.074100 | 0.026400 | -0.270000 | 5.07e-01 | 6.57e-01 | 8.74e-01 | 1.06e-01 |
The phototransduction cascade | 12 | 3.83e-01 | 4.65e-01 | 0.3020 | -0.111000 | -0.074100 | 0.026400 | -0.270000 | 5.07e-01 | 6.57e-01 | 8.74e-01 | 1.06e-01 |
Ovarian tumor domain proteases | 30 | 3.00e-01 | 3.83e-01 | 0.3020 | 0.092400 | 0.083500 | 0.192000 | 0.197000 | 3.81e-01 | 4.29e-01 | 6.92e-02 | 6.17e-02 |
Cholesterol biosynthesis | 23 | 7.30e-02 | 1.23e-01 | 0.3020 | -0.025000 | -0.275000 | 0.107000 | -0.059000 | 8.36e-01 | 2.26e-02 | 3.75e-01 | 6.25e-01 |
Transcriptional Regulation by E2F6 | 29 | 1.09e-01 | 1.69e-01 | 0.3010 | -0.077100 | 0.268000 | 0.101000 | -0.049900 | 4.73e-01 | 1.25e-02 | 3.47e-01 | 6.42e-01 |
Fatty acyl-CoA biosynthesis | 18 | 1.74e-01 | 2.47e-01 | 0.3010 | 0.275000 | -0.061400 | 0.095800 | -0.041900 | 4.33e-02 | 6.52e-01 | 4.82e-01 | 7.59e-01 |
Metabolism of water-soluble vitamins and cofactors | 89 | 1.12e-03 | 3.74e-03 | 0.2990 | -0.054400 | -0.021500 | -0.258000 | -0.140000 | 3.77e-01 | 7.26e-01 | 2.67e-05 | 2.30e-02 |
DCC mediated attractive signaling | 13 | 5.90e-01 | 6.67e-01 | 0.2990 | 0.181000 | -0.156000 | 0.018200 | 0.179000 | 2.58e-01 | 3.30e-01 | 9.09e-01 | 2.65e-01 |
RUNX2 regulates bone development | 26 | 1.30e-01 | 1.93e-01 | 0.2990 | 0.288000 | -0.018700 | 0.009920 | 0.075900 | 1.10e-02 | 8.69e-01 | 9.30e-01 | 5.03e-01 |
Hyaluronan metabolism | 11 | 7.78e-01 | 8.22e-01 | 0.2990 | 0.150000 | -0.072600 | 0.152000 | 0.196000 | 3.90e-01 | 6.77e-01 | 3.82e-01 | 2.60e-01 |
CD209 (DC-SIGN) signaling | 17 | 5.32e-01 | 6.13e-01 | 0.2990 | 0.153000 | -0.048200 | 0.089600 | 0.236000 | 2.75e-01 | 7.31e-01 | 5.23e-01 | 9.28e-02 |
Switching of origins to a post-replicative state | 79 | 4.63e-05 | 2.26e-04 | 0.2990 | -0.181000 | 0.134000 | 0.194000 | 0.026200 | 5.52e-03 | 3.95e-02 | 2.87e-03 | 6.87e-01 |
Signaling by SCF-KIT | 32 | 2.88e-01 | 3.71e-01 | 0.2990 | 0.196000 | -0.043600 | 0.128000 | 0.181000 | 5.58e-02 | 6.70e-01 | 2.09e-01 | 7.72e-02 |
Apoptotic factor-mediated response | 13 | 6.27e-01 | 6.98e-01 | 0.2990 | 0.060500 | -0.014200 | 0.245000 | 0.159000 | 7.06e-01 | 9.30e-01 | 1.26e-01 | 3.21e-01 |
G1/S-Specific Transcription | 21 | 1.50e-01 | 2.16e-01 | 0.2980 | -0.155000 | 0.138000 | 0.138000 | 0.164000 | 2.20e-01 | 2.74e-01 | 2.75e-01 | 1.93e-01 |
Cell-cell junction organization | 22 | 3.71e-01 | 4.56e-01 | 0.2980 | 0.219000 | -0.139000 | 0.067500 | 0.130000 | 7.55e-02 | 2.58e-01 | 5.84e-01 | 2.92e-01 |
Golgi Associated Vesicle Biogenesis | 48 | 3.74e-02 | 7.19e-02 | 0.2970 | -0.016700 | 0.204000 | 0.163000 | 0.141000 | 8.41e-01 | 1.46e-02 | 5.08e-02 | 9.14e-02 |
Nucleobase biosynthesis | 15 | 5.56e-01 | 6.35e-01 | 0.2970 | -0.055700 | 0.031700 | -0.236000 | -0.168000 | 7.09e-01 | 8.32e-01 | 1.13e-01 | 2.59e-01 |
SARS-CoV-2 Infection | 56 | 5.95e-02 | 1.05e-01 | 0.2970 | 0.090200 | 0.014200 | 0.188000 | 0.211000 | 2.44e-01 | 8.54e-01 | 1.52e-02 | 6.45e-03 |
Butyrate Response Factor 1 (BRF1) binds and destabilizes mRNA | 15 | 4.54e-01 | 5.38e-01 | 0.2970 | -0.099500 | 0.255000 | 0.111000 | 0.026400 | 5.05e-01 | 8.76e-02 | 4.55e-01 | 8.60e-01 |
Signaling by FGFR2 | 52 | 1.43e-02 | 3.13e-02 | 0.2970 | -0.004790 | 0.201000 | 0.215000 | 0.035100 | 9.52e-01 | 1.23e-02 | 7.31e-03 | 6.62e-01 |
Arachidonic acid metabolism | 19 | 2.83e-01 | 3.65e-01 | 0.2960 | 0.229000 | -0.153000 | -0.074700 | 0.076700 | 8.43e-02 | 2.48e-01 | 5.73e-01 | 5.63e-01 |
Assembly and cell surface presentation of NMDA receptors | 13 | 4.76e-01 | 5.57e-01 | 0.2950 | -0.056200 | -0.279000 | -0.027400 | -0.072300 | 7.26e-01 | 8.13e-02 | 8.64e-01 | 6.52e-01 |
Phase I - Functionalization of compounds | 39 | 5.94e-02 | 1.05e-01 | 0.2950 | 0.050500 | -0.226000 | -0.126000 | -0.131000 | 5.86e-01 | 1.45e-02 | 1.74e-01 | 1.56e-01 |
Golgi Cisternae Pericentriolar Stack Reorganization | 11 | 5.64e-01 | 6.42e-01 | 0.2950 | -0.124000 | 0.189000 | 0.188000 | 0.024700 | 4.76e-01 | 2.78e-01 | 2.81e-01 | 8.87e-01 |
Degradation of GLI1 by the proteasome | 51 | 1.34e-03 | 4.32e-03 | 0.2940 | -0.223000 | 0.062200 | 0.156000 | -0.092800 | 5.87e-03 | 4.43e-01 | 5.44e-02 | 2.52e-01 |
Meiosis | 38 | 2.00e-02 | 4.18e-02 | 0.2940 | -0.030600 | 0.261000 | -0.009600 | 0.131000 | 7.45e-01 | 5.41e-03 | 9.19e-01 | 1.61e-01 |
Apoptotic cleavage of cellular proteins | 27 | 3.01e-01 | 3.84e-01 | 0.2940 | 0.170000 | -0.126000 | 0.075900 | 0.189000 | 1.26e-01 | 2.58e-01 | 4.95e-01 | 8.94e-02 |
Autophagy | 108 | 6.59e-05 | 3.17e-04 | 0.2930 | -0.272000 | 0.047500 | -0.043500 | -0.089800 | 1.14e-06 | 3.95e-01 | 4.36e-01 | 1.08e-01 |
APC:Cdc20 mediated degradation of cell cycle proteins prior to satisfation of the cell cycle checkpoint | 62 | 5.84e-04 | 2.11e-03 | 0.2930 | -0.206000 | 0.121000 | 0.169000 | -0.020400 | 5.09e-03 | 1.01e-01 | 2.18e-02 | 7.82e-01 |
Cdc20:Phospho-APC/C mediated degradation of Cyclin A | 62 | 5.84e-04 | 2.11e-03 | 0.2930 | -0.206000 | 0.121000 | 0.169000 | -0.020400 | 5.09e-03 | 1.01e-01 | 2.18e-02 | 7.82e-01 |
Cleavage of the damaged purine | 10 | 6.31e-01 | 6.98e-01 | 0.2930 | 0.265000 | 0.076200 | 0.033700 | 0.092500 | 1.47e-01 | 6.77e-01 | 8.54e-01 | 6.13e-01 |
Depurination | 10 | 6.31e-01 | 6.98e-01 | 0.2930 | 0.265000 | 0.076200 | 0.033700 | 0.092500 | 1.47e-01 | 6.77e-01 | 8.54e-01 | 6.13e-01 |
Recognition and association of DNA glycosylase with site containing an affected purine | 10 | 6.31e-01 | 6.98e-01 | 0.2930 | 0.265000 | 0.076200 | 0.033700 | 0.092500 | 1.47e-01 | 6.77e-01 | 8.54e-01 | 6.13e-01 |
MAP3K8 (TPL2)-dependent MAPK1/3 activation | 13 | 2.94e-01 | 3.76e-01 | 0.2920 | -0.243000 | -0.001910 | 0.159000 | -0.030700 | 1.29e-01 | 9.91e-01 | 3.22e-01 | 8.48e-01 |
Signaling by FGFR | 60 | 1.52e-02 | 3.30e-02 | 0.2920 | 0.033700 | 0.187000 | 0.211000 | 0.070000 | 6.53e-01 | 1.26e-02 | 4.85e-03 | 3.49e-01 |
Cargo concentration in the ER | 21 | 1.75e-01 | 2.48e-01 | 0.2920 | -0.182000 | 0.209000 | 0.019000 | 0.088500 | 1.49e-01 | 9.68e-02 | 8.80e-01 | 4.83e-01 |
Role of phospholipids in phagocytosis | 14 | 4.11e-01 | 4.94e-01 | 0.2920 | 0.169000 | -0.165000 | -0.170000 | -0.026600 | 2.75e-01 | 2.87e-01 | 2.71e-01 | 8.63e-01 |
Interleukin-3, Interleukin-5 and GM-CSF signaling | 28 | 3.09e-01 | 3.92e-01 | 0.2920 | 0.144000 | -0.078200 | 0.198000 | 0.138000 | 1.88e-01 | 4.74e-01 | 6.97e-02 | 2.07e-01 |
Stabilization of p53 | 48 | 3.42e-03 | 9.77e-03 | 0.2920 | -0.177000 | 0.121000 | 0.180000 | -0.081400 | 3.41e-02 | 1.48e-01 | 3.12e-02 | 3.30e-01 |
Nucleotide-binding domain, leucine rich repeat containing receptor (NLR) signaling pathways | 38 | 1.49e-01 | 2.15e-01 | 0.2910 | 0.124000 | -0.133000 | 0.147000 | 0.174000 | 1.88e-01 | 1.55e-01 | 1.16e-01 | 6.42e-02 |
Iron uptake and transport | 42 | 2.79e-02 | 5.55e-02 | 0.2910 | 0.059700 | -0.036800 | 0.065600 | 0.275000 | 5.03e-01 | 6.80e-01 | 4.62e-01 | 2.06e-03 |
TCR signaling | 79 | 1.57e-05 | 8.77e-05 | 0.2900 | -0.156000 | 0.057300 | 0.238000 | 0.016600 | 1.67e-02 | 3.80e-01 | 2.68e-04 | 7.99e-01 |
Insulin processing | 19 | 1.33e-01 | 1.96e-01 | 0.2900 | 0.027100 | 0.090700 | -0.022800 | 0.274000 | 8.38e-01 | 4.94e-01 | 8.64e-01 | 3.90e-02 |
HDR through Homologous Recombination (HRR) | 49 | 2.57e-02 | 5.15e-02 | 0.2900 | -0.026200 | 0.171000 | 0.131000 | 0.193000 | 7.52e-01 | 3.91e-02 | 1.14e-01 | 1.97e-02 |
Association of TriC/CCT with target proteins during biosynthesis | 36 | 8.77e-02 | 1.42e-01 | 0.2900 | -0.000577 | 0.211000 | 0.196000 | 0.032200 | 9.95e-01 | 2.87e-02 | 4.19e-02 | 7.38e-01 |
Transcription of E2F targets under negative control by p107 (RBL1) and p130 (RBL2) in complex with HDAC1 | 14 | 3.77e-01 | 4.60e-01 | 0.2890 | -0.210000 | 0.172000 | 0.054500 | 0.080900 | 1.74e-01 | 2.65e-01 | 7.24e-01 | 6.01e-01 |
Regulation of TP53 Activity through Phosphorylation | 74 | 2.03e-03 | 6.15e-03 | 0.2880 | -0.024400 | 0.248000 | 0.144000 | 0.004880 | 7.17e-01 | 2.31e-04 | 3.24e-02 | 9.42e-01 |
Cellular response to hypoxia | 62 | 5.30e-04 | 1.97e-03 | 0.2880 | -0.219000 | 0.034600 | 0.116000 | -0.142000 | 2.84e-03 | 6.38e-01 | 1.16e-01 | 5.42e-02 |
Transcriptional regulation of pluripotent stem cells | 11 | 3.21e-01 | 4.04e-01 | 0.2870 | -0.090900 | -0.120000 | 0.242000 | -0.037700 | 6.02e-01 | 4.93e-01 | 1.65e-01 | 8.29e-01 |
Mitotic Prometaphase | 137 | 1.05e-06 | 8.29e-06 | 0.2870 | -0.067600 | 0.243000 | 0.071500 | 0.118000 | 1.74e-01 | 1.03e-06 | 1.50e-01 | 1.77e-02 |
Signaling by NTRK1 (TRKA) | 95 | 1.18e-03 | 3.89e-03 | 0.2860 | 0.145000 | -0.075200 | 0.214000 | 0.098500 | 1.47e-02 | 2.06e-01 | 3.30e-04 | 9.79e-02 |
Regulation of PTEN stability and activity | 59 | 1.45e-03 | 4.64e-03 | 0.2850 | -0.214000 | 0.108000 | 0.143000 | -0.059800 | 4.50e-03 | 1.53e-01 | 5.81e-02 | 4.27e-01 |
Estrogen-dependent gene expression | 75 | 1.31e-03 | 4.24e-03 | 0.2850 | -0.111000 | 0.227000 | 0.128000 | -0.034800 | 9.84e-02 | 6.86e-04 | 5.64e-02 | 6.03e-01 |
APC/C:Cdc20 mediated degradation of mitotic proteins | 63 | 1.12e-03 | 3.74e-03 | 0.2850 | -0.193000 | 0.134000 | 0.158000 | -0.034600 | 8.20e-03 | 6.57e-02 | 3.07e-02 | 6.35e-01 |
Activation of APC/C and APC/C:Cdc20 mediated degradation of mitotic proteins | 63 | 1.12e-03 | 3.74e-03 | 0.2850 | -0.193000 | 0.134000 | 0.158000 | -0.034600 | 8.20e-03 | 6.57e-02 | 3.07e-02 | 6.35e-01 |
Regulation of APC/C activators between G1/S and early anaphase | 67 | 4.44e-04 | 1.68e-03 | 0.2850 | -0.211000 | 0.109000 | 0.155000 | -0.024200 | 2.83e-03 | 1.25e-01 | 2.81e-02 | 7.33e-01 |
Dopamine Neurotransmitter Release Cycle | 11 | 6.91e-01 | 7.51e-01 | 0.2830 | 0.012400 | -0.014800 | 0.178000 | 0.220000 | 9.43e-01 | 9.32e-01 | 3.08e-01 | 2.07e-01 |
Negative regulation of FGFR4 signaling | 19 | 2.98e-01 | 3.81e-01 | 0.2830 | 0.195000 | -0.009840 | 0.204000 | 0.010900 | 1.40e-01 | 9.41e-01 | 1.24e-01 | 9.35e-01 |
Infectious disease | 533 | 5.21e-18 | 2.91e-16 | 0.2820 | 0.046200 | 0.091700 | 0.231000 | 0.125000 | 7.20e-02 | 3.55e-04 | 2.03e-19 | 1.10e-06 |
MAP2K and MAPK activation | 31 | 2.34e-01 | 3.13e-01 | 0.2820 | 0.168000 | -0.073600 | 0.193000 | 0.093000 | 1.07e-01 | 4.78e-01 | 6.35e-02 | 3.70e-01 |
PI-3K cascade:FGFR1 | 10 | 6.14e-01 | 6.91e-01 | 0.2810 | -0.098100 | -0.033300 | -0.008620 | -0.261000 | 5.91e-01 | 8.55e-01 | 9.62e-01 | 1.53e-01 |
Transcriptional Regulation by MECP2 | 42 | 6.77e-02 | 1.15e-01 | 0.2810 | -0.115000 | -0.151000 | -0.203000 | -0.037100 | 1.98e-01 | 9.00e-02 | 2.27e-02 | 6.78e-01 |
RNA Polymerase III Transcription Termination | 22 | 2.55e-01 | 3.37e-01 | 0.2800 | -0.229000 | 0.155000 | 0.040100 | -0.022300 | 6.27e-02 | 2.09e-01 | 7.45e-01 | 8.56e-01 |
Signaling by Rho GTPases | 268 | 5.15e-07 | 4.39e-06 | 0.2800 | 0.125000 | 0.000868 | 0.179000 | 0.175000 | 4.48e-04 | 9.81e-01 | 5.02e-07 | 9.28e-07 |
Autodegradation of Cdh1 by Cdh1:APC/C | 58 | 1.24e-03 | 4.04e-03 | 0.2800 | -0.206000 | 0.082300 | 0.165000 | -0.046600 | 6.81e-03 | 2.79e-01 | 3.03e-02 | 5.40e-01 |
Signaling by FGFR2 in disease | 28 | 1.13e-01 | 1.74e-01 | 0.2800 | -0.124000 | 0.124000 | 0.213000 | 0.047600 | 2.55e-01 | 2.57e-01 | 5.14e-02 | 6.63e-01 |
Competing endogenous RNAs (ceRNAs) regulate PTEN translation | 10 | 4.40e-01 | 5.24e-01 | 0.2800 | -0.036400 | 0.042000 | -0.270000 | 0.048500 | 8.42e-01 | 8.18e-01 | 1.40e-01 | 7.91e-01 |
Interleukin-15 signaling | 11 | 4.73e-01 | 5.55e-01 | 0.2790 | 0.024900 | -0.247000 | 0.115000 | -0.058100 | 8.86e-01 | 1.57e-01 | 5.10e-01 | 7.39e-01 |
APC/C:Cdc20 mediated degradation of Securin | 59 | 2.50e-03 | 7.39e-03 | 0.2790 | -0.209000 | 0.108000 | 0.127000 | -0.079600 | 5.45e-03 | 1.53e-01 | 9.25e-02 | 2.91e-01 |
G1/S DNA Damage Checkpoints | 57 | 1.79e-03 | 5.50e-03 | 0.2780 | -0.140000 | 0.105000 | 0.216000 | -0.019500 | 6.89e-02 | 1.72e-01 | 4.85e-03 | 8.00e-01 |
Oxygen-dependent proline hydroxylation of Hypoxia-inducible Factor Alpha | 55 | 1.34e-03 | 4.32e-03 | 0.2780 | -0.202000 | 0.031700 | 0.143000 | -0.123000 | 9.79e-03 | 6.85e-01 | 6.75e-02 | 1.16e-01 |
Antigen processing-Cross presentation | 69 | 8.57e-03 | 2.09e-02 | 0.2770 | -0.010800 | 0.048700 | 0.233000 | 0.140000 | 8.77e-01 | 4.85e-01 | 8.27e-04 | 4.42e-02 |
Mitotic G1 phase and G1/S transition | 127 | 9.20e-06 | 5.49e-05 | 0.2760 | -0.073600 | 0.100000 | 0.219000 | 0.114000 | 1.53e-01 | 5.21e-02 | 2.14e-05 | 2.73e-02 |
TAK1 activates NFkB by phosphorylation and activation of IKKs complex | 22 | 1.78e-01 | 2.50e-01 | 0.2760 | -0.036800 | -0.089000 | 0.242000 | 0.090600 | 7.65e-01 | 4.70e-01 | 4.93e-02 | 4.62e-01 |
Metabolism of polyamines | 50 | 4.87e-03 | 1.31e-02 | 0.2760 | -0.173000 | 0.089900 | 0.196000 | 0.002780 | 3.49e-02 | 2.72e-01 | 1.68e-02 | 9.73e-01 |
Removal of the Flap Intermediate from the C-strand | 17 | 6.29e-01 | 6.98e-01 | 0.2760 | 0.090900 | 0.138000 | 0.129000 | 0.179000 | 5.17e-01 | 3.24e-01 | 3.56e-01 | 2.02e-01 |
Neddylation | 199 | 8.69e-08 | 8.61e-07 | 0.2750 | -0.234000 | -0.003930 | -0.018400 | -0.144000 | 1.42e-08 | 9.24e-01 | 6.57e-01 | 4.94e-04 |
CDK-mediated phosphorylation and removal of Cdc6 | 63 | 1.62e-03 | 5.06e-03 | 0.2750 | -0.172000 | 0.125000 | 0.174000 | -0.016400 | 1.84e-02 | 8.64e-02 | 1.69e-02 | 8.22e-01 |
Signaling by cytosolic FGFR1 fusion mutants | 17 | 6.76e-01 | 7.38e-01 | 0.2750 | -0.128000 | -0.003090 | -0.127000 | -0.208000 | 3.61e-01 | 9.82e-01 | 3.67e-01 | 1.37e-01 |
Ras activation upon Ca2+ influx through NMDA receptor | 13 | 6.34e-01 | 7.00e-01 | 0.2750 | 0.039500 | -0.208000 | -0.128000 | -0.120000 | 8.05e-01 | 1.94e-01 | 4.24e-01 | 4.54e-01 |
ER-Phagosome pathway | 61 | 4.81e-03 | 1.30e-02 | 0.2720 | -0.074500 | 0.063700 | 0.239000 | 0.087000 | 3.15e-01 | 3.90e-01 | 1.28e-03 | 2.41e-01 |
COPI-dependent Golgi-to-ER retrograde traffic | 62 | 6.19e-02 | 1.07e-01 | 0.2720 | 0.136000 | 0.137000 | 0.148000 | 0.121000 | 6.36e-02 | 6.23e-02 | 4.37e-02 | 9.91e-02 |
Negative regulation of the PI3K/AKT network | 69 | 3.74e-02 | 7.19e-02 | 0.2720 | 0.192000 | 0.015300 | 0.163000 | 0.101000 | 5.82e-03 | 8.27e-01 | 1.94e-02 | 1.47e-01 |
UCH proteinases | 74 | 1.52e-04 | 6.58e-04 | 0.2720 | -0.182000 | 0.071900 | 0.180000 | -0.053300 | 6.77e-03 | 2.86e-01 | 7.38e-03 | 4.29e-01 |
Nicotinate metabolism | 20 | 2.67e-01 | 3.48e-01 | 0.2710 | 0.138000 | -0.128000 | -0.195000 | -0.012500 | 2.84e-01 | 3.22e-01 | 1.32e-01 | 9.23e-01 |
Nervous system development | 392 | 1.70e-12 | 4.09e-11 | 0.2710 | 0.127000 | -0.116000 | 0.170000 | 0.123000 | 1.90e-05 | 9.98e-05 | 1.03e-08 | 3.44e-05 |
Metabolism of folate and pterines | 13 | 5.89e-01 | 6.66e-01 | 0.2710 | -0.017300 | -0.264000 | -0.043100 | -0.037900 | 9.14e-01 | 9.89e-02 | 7.88e-01 | 8.13e-01 |
Rho GTPase cycle | 103 | 5.19e-03 | 1.37e-02 | 0.2710 | 0.173000 | -0.107000 | 0.087200 | 0.156000 | 2.49e-03 | 6.10e-02 | 1.27e-01 | 6.21e-03 |
Dual Incision in GG-NER | 38 | 5.85e-02 | 1.03e-01 | 0.2710 | -0.212000 | 0.159000 | 0.055900 | 0.014900 | 2.42e-02 | 8.99e-02 | 5.51e-01 | 8.74e-01 |
SARS-CoV Infections | 121 | 2.74e-03 | 7.98e-03 | 0.2700 | 0.084600 | -0.001650 | 0.185000 | 0.178000 | 1.09e-01 | 9.75e-01 | 4.65e-04 | 7.34e-04 |
APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins in late mitosis/early G1 | 63 | 2.25e-03 | 6.72e-03 | 0.2700 | -0.191000 | 0.117000 | 0.149000 | -0.023300 | 8.82e-03 | 1.07e-01 | 4.15e-02 | 7.49e-01 |
FOXO-mediated transcription | 51 | 1.05e-01 | 1.64e-01 | 0.2700 | -0.117000 | -0.121000 | -0.103000 | -0.184000 | 1.49e-01 | 1.36e-01 | 2.02e-01 | 2.31e-02 |
Neurotransmitter release cycle | 22 | 3.64e-01 | 4.49e-01 | 0.2700 | 0.011300 | 0.005490 | 0.242000 | 0.119000 | 9.27e-01 | 9.64e-01 | 5.00e-02 | 3.33e-01 |
DNA Double-Strand Break Repair | 109 | 1.52e-04 | 6.58e-04 | 0.2690 | -0.071200 | 0.183000 | 0.120000 | 0.139000 | 2.00e-01 | 9.72e-04 | 3.04e-02 | 1.21e-02 |
p53-Dependent G1 DNA Damage Response | 56 | 2.68e-03 | 7.83e-03 | 0.2690 | -0.137000 | 0.091900 | 0.212000 | -0.023900 | 7.71e-02 | 2.35e-01 | 6.17e-03 | 7.57e-01 |
p53-Dependent G1/S DNA damage checkpoint | 56 | 2.68e-03 | 7.83e-03 | 0.2690 | -0.137000 | 0.091900 | 0.212000 | -0.023900 | 7.71e-02 | 2.35e-01 | 6.17e-03 | 7.57e-01 |
PI5P, PP2A and IER3 Regulate PI3K/AKT Signaling | 62 | 5.18e-02 | 9.34e-02 | 0.2690 | 0.194000 | -0.004790 | 0.163000 | 0.091400 | 8.50e-03 | 9.48e-01 | 2.63e-02 | 2.14e-01 |
S Phase | 144 | 1.03e-06 | 8.24e-06 | 0.2690 | -0.132000 | 0.143000 | 0.170000 | 0.072700 | 6.42e-03 | 3.11e-03 | 4.47e-04 | 1.33e-01 |
N-glycan trimming in the ER and Calnexin/Calreticulin cycle | 31 | 3.35e-01 | 4.21e-01 | 0.2690 | 0.033300 | 0.108000 | 0.180000 | 0.164000 | 7.49e-01 | 2.98e-01 | 8.23e-02 | 1.15e-01 |
Constitutive Signaling by Aberrant PI3K in Cancer | 38 | 1.16e-01 | 1.77e-01 | 0.2680 | 0.223000 | -0.122000 | 0.074600 | 0.044600 | 1.75e-02 | 1.95e-01 | 4.26e-01 | 6.35e-01 |
Endogenous sterols | 13 | 8.15e-01 | 8.52e-01 | 0.2680 | -0.116000 | -0.053800 | -0.159000 | -0.174000 | 4.70e-01 | 7.37e-01 | 3.21e-01 | 2.78e-01 |
Downregulation of TGF-beta receptor signaling | 24 | 1.27e-01 | 1.90e-01 | 0.2680 | -0.120000 | 0.116000 | 0.164000 | -0.130000 | 3.08e-01 | 3.27e-01 | 1.64e-01 | 2.71e-01 |
APC/C-mediated degradation of cell cycle proteins | 72 | 1.28e-03 | 4.15e-03 | 0.2680 | -0.180000 | 0.135000 | 0.146000 | -0.005610 | 8.49e-03 | 4.82e-02 | 3.29e-02 | 9.35e-01 |
Regulation of mitotic cell cycle | 72 | 1.28e-03 | 4.15e-03 | 0.2680 | -0.180000 | 0.135000 | 0.146000 | -0.005610 | 8.49e-03 | 4.82e-02 | 3.29e-02 | 9.35e-01 |
Vitamin B5 (pantothenate) metabolism | 15 | 3.92e-01 | 4.74e-01 | 0.2670 | 0.013100 | 0.120000 | -0.228000 | -0.069500 | 9.30e-01 | 4.20e-01 | 1.26e-01 | 6.41e-01 |
TNFR1-induced NFkappaB signaling pathway | 21 | 2.57e-01 | 3.38e-01 | 0.2670 | -0.005190 | -0.232000 | -0.030400 | 0.129000 | 9.67e-01 | 6.55e-02 | 8.09e-01 | 3.08e-01 |
Activation of the AP-1 family of transcription factors | 10 | 3.63e-01 | 4.49e-01 | 0.2670 | 0.097100 | -0.007010 | 0.182000 | -0.169000 | 5.95e-01 | 9.69e-01 | 3.19e-01 | 3.54e-01 |
Formation of the beta-catenin:TCF transactivating complex | 28 | 3.98e-01 | 4.81e-01 | 0.2660 | 0.054000 | 0.159000 | 0.151000 | 0.141000 | 6.21e-01 | 1.46e-01 | 1.67e-01 | 1.95e-01 |
Neurotransmitter receptors and postsynaptic signal transmission | 95 | 1.48e-03 | 4.72e-03 | 0.2660 | 0.166000 | -0.195000 | -0.015100 | 0.071800 | 5.28e-03 | 1.07e-03 | 7.99e-01 | 2.27e-01 |
M Phase | 275 | 2.13e-11 | 3.80e-10 | 0.2660 | -0.112000 | 0.196000 | 0.120000 | 0.074900 | 1.57e-03 | 2.81e-08 | 6.89e-04 | 3.36e-02 |
TP53 Regulates Transcription of Genes Involved in Cytochrome C Release | 15 | 6.58e-01 | 7.24e-01 | 0.2660 | 0.201000 | 0.092500 | 0.113000 | 0.094000 | 1.77e-01 | 5.35e-01 | 4.51e-01 | 5.28e-01 |
MicroRNA (miRNA) biogenesis | 22 | 2.39e-01 | 3.19e-01 | 0.2660 | -0.203000 | 0.161000 | -0.038500 | 0.042100 | 9.87e-02 | 1.91e-01 | 7.55e-01 | 7.32e-01 |
Interleukin-1 family signaling | 102 | 8.41e-06 | 5.11e-05 | 0.2660 | -0.071400 | 0.040300 | 0.252000 | 0.014100 | 2.14e-01 | 4.84e-01 | 1.13e-05 | 8.06e-01 |
Intraflagellar transport | 35 | 2.37e-02 | 4.81e-02 | 0.2640 | 0.156000 | 0.122000 | -0.107000 | 0.139000 | 1.11e-01 | 2.12e-01 | 2.74e-01 | 1.56e-01 |
Metabolism of nitric oxide: NOS3 activation and regulation | 13 | 4.71e-01 | 5.55e-01 | 0.2640 | -0.060000 | -0.141000 | 0.178000 | 0.120000 | 7.08e-01 | 3.79e-01 | 2.66e-01 | 4.55e-01 |
Signaling by Hippo | 18 | 6.38e-01 | 7.04e-01 | 0.2630 | 0.041400 | 0.106000 | 0.196000 | 0.134000 | 7.61e-01 | 4.35e-01 | 1.51e-01 | 3.23e-01 |
AKT phosphorylates targets in the cytosol | 14 | 3.20e-01 | 4.04e-01 | 0.2630 | -0.181000 | -0.147000 | 0.108000 | 0.059300 | 2.42e-01 | 3.40e-01 | 4.86e-01 | 7.01e-01 |
Neuronal System | 172 | 2.26e-06 | 1.60e-05 | 0.2630 | 0.143000 | -0.217000 | 0.009390 | 0.044800 | 1.30e-03 | 1.06e-06 | 8.32e-01 | 3.13e-01 |
Downstream signaling events of B Cell Receptor (BCR) | 67 | 2.22e-04 | 9.06e-04 | 0.2630 | -0.185000 | -0.008680 | 0.180000 | -0.048100 | 8.83e-03 | 9.02e-01 | 1.09e-02 | 4.97e-01 |
FCERI mediated MAPK activation | 23 | 4.49e-01 | 5.33e-01 | 0.2630 | 0.150000 | -0.005480 | 0.048400 | 0.210000 | 2.14e-01 | 9.64e-01 | 6.88e-01 | 8.07e-02 |
Cytokine Signaling in Immune system | 514 | 1.88e-13 | 5.02e-12 | 0.2620 | 0.139000 | -0.025100 | 0.188000 | 0.115000 | 9.11e-08 | 3.36e-01 | 5.43e-13 | 1.01e-05 |
RUNX1 regulates transcription of genes involved in differentiation of HSCs | 55 | 4.29e-03 | 1.18e-02 | 0.2620 | -0.146000 | 0.094800 | 0.190000 | -0.049900 | 6.21e-02 | 2.25e-01 | 1.52e-02 | 5.23e-01 |
Cell Cycle, Mitotic | 397 | 1.30e-14 | 4.10e-13 | 0.2620 | -0.067500 | 0.183000 | 0.145000 | 0.098000 | 2.23e-02 | 5.60e-10 | 9.85e-07 | 9.02e-04 |
Chromatin modifying enzymes | 179 | 4.83e-07 | 4.16e-06 | 0.2620 | -0.193000 | 0.138000 | 0.053000 | -0.096000 | 8.99e-06 | 1.49e-03 | 2.23e-01 | 2.75e-02 |
Chromatin organization | 179 | 4.83e-07 | 4.16e-06 | 0.2620 | -0.193000 | 0.138000 | 0.053000 | -0.096000 | 8.99e-06 | 1.49e-03 | 2.23e-01 | 2.75e-02 |
Synthesis of IP2, IP, and Ins in the cytosol | 12 | 5.14e-01 | 5.95e-01 | 0.2610 | -0.112000 | -0.032500 | 0.186000 | 0.141000 | 5.00e-01 | 8.46e-01 | 2.66e-01 | 3.98e-01 |
SHC-mediated cascade:FGFR1 | 10 | 8.62e-01 | 8.91e-01 | 0.2600 | 0.201000 | -0.016800 | 0.100000 | 0.130000 | 2.70e-01 | 9.27e-01 | 5.84e-01 | 4.75e-01 |
Interleukin-1 signaling | 84 | 4.01e-05 | 1.99e-04 | 0.2600 | -0.118000 | 0.036900 | 0.227000 | -0.027700 | 6.13e-02 | 5.59e-01 | 3.26e-04 | 6.61e-01 |
Biosynthesis of the N-glycan precursor (dolichol lipid-linked oligosaccharide, LLO) and transfer to a nascent protein | 66 | 7.60e-02 | 1.27e-01 | 0.2600 | 0.196000 | -0.037400 | 0.116000 | 0.120000 | 5.99e-03 | 6.00e-01 | 1.05e-01 | 9.12e-02 |
Reproduction | 44 | 3.17e-02 | 6.22e-02 | 0.2590 | 0.019600 | 0.213000 | -0.004110 | 0.147000 | 8.22e-01 | 1.48e-02 | 9.62e-01 | 9.16e-02 |
Cell Cycle | 484 | 1.92e-17 | 9.43e-16 | 0.2590 | -0.069700 | 0.193000 | 0.134000 | 0.084200 | 9.45e-03 | 6.31e-13 | 6.21e-07 | 1.73e-03 |
Signaling by RAF1 mutants | 32 | 1.45e-01 | 2.09e-01 | 0.2590 | 0.147000 | -0.175000 | 0.121000 | 0.010600 | 1.50e-01 | 8.67e-02 | 2.38e-01 | 9.17e-01 |
Cytochrome P450 - arranged by substrate type | 18 | 5.57e-01 | 6.36e-01 | 0.2590 | 0.020800 | -0.190000 | -0.159000 | -0.069800 | 8.78e-01 | 1.62e-01 | 2.42e-01 | 6.08e-01 |
Meiotic synapsis | 22 | 3.05e-01 | 3.88e-01 | 0.2580 | -0.032200 | 0.226000 | 0.019900 | 0.119000 | 7.94e-01 | 6.72e-02 | 8.72e-01 | 3.34e-01 |
Regulation of RAS by GAPs | 57 | 6.03e-03 | 1.55e-02 | 0.2560 | -0.139000 | 0.089100 | 0.196000 | 0.004400 | 7.00e-02 | 2.45e-01 | 1.05e-02 | 9.54e-01 |
Tie2 Signaling | 13 | 5.13e-01 | 5.95e-01 | 0.2560 | -0.164000 | 0.159000 | 0.036400 | 0.110000 | 3.06e-01 | 3.21e-01 | 8.20e-01 | 4.92e-01 |
Signaling by NOTCH3 | 38 | 2.18e-01 | 2.98e-01 | 0.2560 | 0.185000 | -0.115000 | 0.023200 | 0.132000 | 4.86e-02 | 2.20e-01 | 8.04e-01 | 1.58e-01 |
Trafficking of GluR2-containing AMPA receptors | 10 | 6.62e-01 | 7.27e-01 | 0.2560 | 0.000931 | -0.162000 | 0.184000 | 0.072500 | 9.96e-01 | 3.75e-01 | 3.14e-01 | 6.91e-01 |
Signaling by ROBO receptors | 151 | 2.05e-09 | 2.65e-08 | 0.2550 | -0.084100 | -0.020900 | 0.240000 | -0.016200 | 7.57e-02 | 6.59e-01 | 4.09e-07 | 7.32e-01 |
SUMOylation | 137 | 4.25e-05 | 2.08e-04 | 0.2550 | -0.127000 | 0.203000 | 0.086500 | -0.011500 | 1.02e-02 | 4.25e-05 | 8.15e-02 | 8.17e-01 |
eNOS activation | 10 | 7.07e-01 | 7.65e-01 | 0.2550 | 0.062300 | -0.182000 | 0.159000 | 0.051600 | 7.33e-01 | 3.18e-01 | 3.84e-01 | 7.78e-01 |
PPARA activates gene expression | 101 | 6.55e-03 | 1.66e-02 | 0.2550 | -0.204000 | 0.087700 | -0.055500 | -0.112000 | 4.18e-04 | 1.29e-01 | 3.37e-01 | 5.16e-02 |
Immune System | 1219 | 4.56e-25 | 5.09e-23 | 0.2550 | 0.128000 | -0.022900 | 0.133000 | 0.174000 | 3.20e-13 | 1.92e-01 | 4.49e-14 | 3.03e-23 |
Axon guidance | 375 | 2.09e-10 | 3.21e-09 | 0.2540 | 0.124000 | -0.101000 | 0.163000 | 0.112000 | 4.45e-05 | 8.27e-04 | 7.98e-08 | 2.27e-04 |
TGF-beta receptor signaling activates SMADs | 29 | 8.49e-02 | 1.38e-01 | 0.2540 | -0.109000 | 0.095500 | 0.179000 | -0.108000 | 3.12e-01 | 3.74e-01 | 9.58e-02 | 3.13e-01 |
Regulation of TP53 Activity | 134 | 8.50e-05 | 3.97e-04 | 0.2540 | -0.052600 | 0.229000 | 0.094700 | -0.010100 | 2.94e-01 | 4.92e-06 | 5.92e-02 | 8.40e-01 |
TP53 Regulates Transcription of Genes Involved in G2 Cell Cycle Arrest | 14 | 4.57e-01 | 5.42e-01 | 0.2540 | -0.083000 | 0.047800 | 0.086600 | 0.218000 | 5.91e-01 | 7.57e-01 | 5.75e-01 | 1.58e-01 |
Mismatch Repair | 14 | 4.58e-01 | 5.42e-01 | 0.2530 | -0.160000 | 0.170000 | -0.031200 | 0.094600 | 3.01e-01 | 2.72e-01 | 8.40e-01 | 5.40e-01 |
ER Quality Control Compartment (ERQC) | 18 | 6.30e-01 | 6.98e-01 | 0.2530 | 0.003950 | 0.101000 | 0.182000 | 0.143000 | 9.77e-01 | 4.58e-01 | 1.80e-01 | 2.95e-01 |
Tight junction interactions | 10 | 4.29e-01 | 5.12e-01 | 0.2520 | 0.138000 | -0.011700 | 0.076700 | -0.197000 | 4.51e-01 | 9.49e-01 | 6.74e-01 | 2.81e-01 |
Kinesins | 24 | 2.47e-01 | 3.28e-01 | 0.2520 | 0.225000 | 0.077700 | -0.022900 | 0.080700 | 5.66e-02 | 5.10e-01 | 8.46e-01 | 4.94e-01 |
Potential therapeutics for SARS | 66 | 8.06e-02 | 1.33e-01 | 0.2520 | 0.081800 | -0.026300 | 0.189000 | 0.143000 | 2.52e-01 | 7.12e-01 | 7.93e-03 | 4.53e-02 |
RAB geranylgeranylation | 41 | 7.92e-02 | 1.31e-01 | 0.2510 | 0.126000 | 0.206000 | 0.021900 | 0.066900 | 1.63e-01 | 2.27e-02 | 8.08e-01 | 4.59e-01 |
Antigen activates B Cell Receptor (BCR) leading to generation of second messengers | 19 | 6.00e-01 | 6.76e-01 | 0.2510 | 0.204000 | -0.004710 | 0.040200 | 0.141000 | 1.23e-01 | 9.72e-01 | 7.61e-01 | 2.89e-01 |
TNFR2 non-canonical NF-kB pathway | 63 | 3.48e-03 | 9.88e-03 | 0.2510 | -0.063900 | -0.024100 | 0.234000 | 0.059900 | 3.81e-01 | 7.42e-01 | 1.34e-03 | 4.12e-01 |
Cell death signalling via NRAGE, NRIF and NADE | 57 | 5.32e-02 | 9.54e-02 | 0.2510 | 0.130000 | -0.199000 | -0.005470 | 0.081300 | 9.11e-02 | 9.49e-03 | 9.43e-01 | 2.89e-01 |
Inositol phosphate metabolism | 38 | 1.44e-01 | 2.08e-01 | 0.2510 | 0.108000 | -0.216000 | -0.060900 | -0.029800 | 2.49e-01 | 2.15e-02 | 5.16e-01 | 7.51e-01 |
p75 NTR receptor-mediated signalling | 73 | 3.56e-02 | 6.91e-02 | 0.2510 | 0.149000 | -0.155000 | 0.053600 | 0.117000 | 2.79e-02 | 2.27e-02 | 4.29e-01 | 8.32e-02 |
Termination of translesion DNA synthesis | 28 | 3.43e-01 | 4.29e-01 | 0.2500 | -0.028400 | 0.092300 | 0.170000 | 0.157000 | 7.95e-01 | 3.98e-01 | 1.21e-01 | 1.51e-01 |
Oncogene Induced Senescence | 29 | 2.26e-01 | 3.06e-01 | 0.2500 | 0.210000 | 0.113000 | 0.058600 | 0.048200 | 5.05e-02 | 2.91e-01 | 5.85e-01 | 6.53e-01 |
COPII-mediated vesicle transport | 56 | 2.82e-02 | 5.58e-02 | 0.2500 | -0.156000 | 0.181000 | 0.066300 | 0.032200 | 4.32e-02 | 1.94e-02 | 3.91e-01 | 6.78e-01 |
Signaling by ERBB2 TMD/JMD mutants | 14 | 7.72e-01 | 8.19e-01 | 0.2500 | 0.118000 | -0.106000 | 0.096700 | 0.168000 | 4.46e-01 | 4.94e-01 | 5.31e-01 | 2.77e-01 |
Cyclin A:Cdk2-associated events at S phase entry | 77 | 1.92e-03 | 5.88e-03 | 0.2500 | -0.097100 | 0.094800 | 0.208000 | 0.029800 | 1.41e-01 | 1.51e-01 | 1.66e-03 | 6.52e-01 |
Inactivation of APC/C via direct inhibition of the APC/C complex | 19 | 4.81e-01 | 5.62e-01 | 0.2500 | -0.176000 | 0.172000 | -0.042700 | -0.012100 | 1.85e-01 | 1.95e-01 | 7.47e-01 | 9.28e-01 |
Inhibition of the proteolytic activity of APC/C required for the onset of anaphase by mitotic spindle checkpoint components | 19 | 4.81e-01 | 5.62e-01 | 0.2500 | -0.176000 | 0.172000 | -0.042700 | -0.012100 | 1.85e-01 | 1.95e-01 | 7.47e-01 | 9.28e-01 |
Fanconi Anemia Pathway | 24 | 3.73e-01 | 4.58e-01 | 0.2490 | -0.165000 | 0.176000 | 0.050900 | -0.037600 | 1.62e-01 | 1.37e-01 | 6.66e-01 | 7.50e-01 |
Antigen processing: Ubiquitination & Proteasome degradation | 264 | 6.59e-09 | 7.86e-08 | 0.2490 | -0.223000 | 0.019000 | -0.004210 | -0.109000 | 5.80e-10 | 5.98e-01 | 9.07e-01 | 2.42e-03 |
CLEC7A (Dectin-1) signaling | 80 | 8.44e-05 | 3.96e-04 | 0.2490 | -0.166000 | -0.017900 | 0.174000 | -0.063300 | 1.06e-02 | 7.83e-01 | 7.37e-03 | 3.29e-01 |
Opioid Signalling | 64 | 2.37e-02 | 4.81e-02 | 0.2480 | 0.119000 | -0.200000 | -0.087800 | 0.004290 | 1.01e-01 | 5.80e-03 | 2.25e-01 | 9.53e-01 |
Regulation of lipid metabolism by PPARalpha | 103 | 7.56e-03 | 1.87e-02 | 0.2480 | -0.195000 | 0.095200 | -0.048700 | -0.109000 | 6.34e-04 | 9.57e-02 | 3.94e-01 | 5.67e-02 |
ERK/MAPK targets | 22 | 4.48e-01 | 5.33e-01 | 0.2460 | 0.020000 | -0.228000 | -0.090900 | -0.002650 | 8.71e-01 | 6.41e-02 | 4.61e-01 | 9.83e-01 |
Nuclear signaling by ERBB4 | 20 | 5.22e-01 | 6.03e-01 | 0.2460 | 0.217000 | -0.072500 | 0.005570 | 0.089700 | 9.28e-02 | 5.75e-01 | 9.66e-01 | 4.88e-01 |
Negative regulators of DDX58/IFIH1 signaling | 29 | 3.42e-01 | 4.29e-01 | 0.2460 | 0.043600 | -0.112000 | 0.148000 | 0.155000 | 6.85e-01 | 2.96e-01 | 1.69e-01 | 1.49e-01 |
Ion channel transport | 89 | 8.12e-04 | 2.83e-03 | 0.2450 | 0.031400 | -0.190000 | -0.119000 | 0.095000 | 6.10e-01 | 1.98e-03 | 5.31e-02 | 1.22e-01 |
SUMO E3 ligases SUMOylate target proteins | 131 | 1.59e-04 | 6.78e-04 | 0.2450 | -0.126000 | 0.193000 | 0.083000 | -0.010800 | 1.30e-02 | 1.41e-04 | 1.02e-01 | 8.32e-01 |
Cyclin E associated events during G1/S transition | 75 | 2.03e-03 | 6.15e-03 | 0.2450 | -0.117000 | 0.087200 | 0.197000 | 0.015600 | 8.11e-02 | 1.93e-01 | 3.27e-03 | 8.16e-01 |
Activation of HOX genes during differentiation | 48 | 6.31e-02 | 1.09e-01 | 0.2450 | -0.166000 | 0.156000 | 0.088100 | -0.023800 | 4.68e-02 | 6.25e-02 | 2.92e-01 | 7.76e-01 |
Activation of anterior HOX genes in hindbrain development during early embryogenesis | 48 | 6.31e-02 | 1.09e-01 | 0.2450 | -0.166000 | 0.156000 | 0.088100 | -0.023800 | 4.68e-02 | 6.25e-02 | 2.92e-01 | 7.76e-01 |
MECP2 regulates neuronal receptors and channels | 10 | 7.48e-01 | 7.98e-01 | 0.2450 | -0.141000 | 0.154000 | 0.113000 | -0.059600 | 4.39e-01 | 3.99e-01 | 5.37e-01 | 7.44e-01 |
APC-Cdc20 mediated degradation of Nek2A | 21 | 4.75e-01 | 5.57e-01 | 0.2440 | -0.149000 | 0.192000 | 0.018800 | -0.020000 | 2.37e-01 | 1.28e-01 | 8.81e-01 | 8.74e-01 |
EGFR downregulation | 22 | 5.40e-01 | 6.19e-01 | 0.2440 | 0.104000 | 0.154000 | 0.148000 | 0.057500 | 3.98e-01 | 2.11e-01 | 2.31e-01 | 6.41e-01 |
PI-3K cascade:FGFR2 | 10 | 5.81e-01 | 6.59e-01 | 0.2440 | -0.120000 | -0.107000 | 0.105000 | -0.150000 | 5.12e-01 | 5.56e-01 | 5.67e-01 | 4.11e-01 |
Late endosomal microautophagy | 23 | 1.72e-01 | 2.45e-01 | 0.2430 | -0.190000 | -0.126000 | 0.082100 | 0.014700 | 1.15e-01 | 2.95e-01 | 4.96e-01 | 9.03e-01 |
mRNA decay by 5' to 3' exoribonuclease | 14 | 6.91e-01 | 7.51e-01 | 0.2410 | -0.187000 | 0.143000 | -0.036000 | -0.034000 | 2.25e-01 | 3.53e-01 | 8.16e-01 | 8.26e-01 |
Regulation of PTEN mRNA translation | 11 | 4.56e-01 | 5.40e-01 | 0.2410 | 0.017000 | 0.091200 | -0.198000 | 0.102000 | 9.22e-01 | 6.00e-01 | 2.56e-01 | 5.60e-01 |
Diseases of metabolism | 152 | 1.38e-04 | 6.07e-04 | 0.2400 | 0.181000 | -0.128000 | -0.015300 | 0.091800 | 1.26e-04 | 6.51e-03 | 7.46e-01 | 5.18e-02 |
Ub-specific processing proteases | 145 | 1.30e-05 | 7.43e-05 | 0.2400 | -0.188000 | 0.099200 | 0.088600 | -0.068200 | 9.82e-05 | 3.99e-02 | 6.66e-02 | 1.58e-01 |
Regulation of RUNX2 expression and activity | 61 | 8.65e-03 | 2.09e-02 | 0.2400 | -0.188000 | 0.041300 | 0.105000 | -0.096400 | 1.10e-02 | 5.78e-01 | 1.56e-01 | 1.93e-01 |
Asymmetric localization of PCP proteins | 55 | 7.20e-03 | 1.80e-02 | 0.2390 | -0.145000 | 0.044300 | 0.176000 | -0.057200 | 6.39e-02 | 5.70e-01 | 2.38e-02 | 4.64e-01 |
Ion transport by P-type ATPases | 33 | 2.46e-01 | 3.28e-01 | 0.2380 | 0.044000 | -0.225000 | -0.052300 | 0.042100 | 6.62e-01 | 2.57e-02 | 6.03e-01 | 6.76e-01 |
Mismatch repair (MMR) directed by MSH2:MSH6 (MutSalpha) | 13 | 5.05e-01 | 5.87e-01 | 0.2380 | -0.123000 | 0.117000 | 0.021300 | 0.166000 | 4.44e-01 | 4.66e-01 | 8.94e-01 | 2.99e-01 |
Miscellaneous transport and binding events | 16 | 3.46e-01 | 4.32e-01 | 0.2380 | -0.105000 | 0.150000 | -0.092400 | 0.121000 | 4.68e-01 | 2.98e-01 | 5.22e-01 | 4.04e-01 |
Death Receptor Signalling | 106 | 6.20e-03 | 1.58e-02 | 0.2370 | 0.117000 | -0.171000 | 0.039000 | 0.109000 | 3.86e-02 | 2.41e-03 | 4.89e-01 | 5.40e-02 |
Signaling by TGF-beta Receptor Complex | 66 | 5.90e-03 | 1.52e-02 | 0.2360 | -0.095100 | 0.119000 | 0.160000 | -0.082400 | 1.82e-01 | 9.52e-02 | 2.48e-02 | 2.48e-01 |
PI-3K cascade:FGFR4 | 10 | 7.96e-01 | 8.36e-01 | 0.2360 | -0.143000 | -0.105000 | -0.007770 | -0.154000 | 4.32e-01 | 5.66e-01 | 9.66e-01 | 3.98e-01 |
Factors involved in megakaryocyte development and platelet production | 80 | 2.41e-02 | 4.87e-02 | 0.2350 | 0.193000 | -0.114000 | 0.040200 | 0.058600 | 2.86e-03 | 7.98e-02 | 5.35e-01 | 3.66e-01 |
Signaling by KIT in disease | 17 | 6.28e-01 | 6.98e-01 | 0.2350 | 0.110000 | -0.139000 | -0.004830 | 0.155000 | 4.32e-01 | 3.23e-01 | 9.73e-01 | 2.70e-01 |
Signaling by phosphorylated juxtamembrane, extracellular and kinase domain KIT mutants | 17 | 6.28e-01 | 6.98e-01 | 0.2350 | 0.110000 | -0.139000 | -0.004830 | 0.155000 | 4.32e-01 | 3.23e-01 | 9.73e-01 | 2.70e-01 |
Growth hormone receptor signaling | 17 | 6.87e-01 | 7.48e-01 | 0.2350 | 0.187000 | -0.083400 | 0.097600 | 0.060600 | 1.82e-01 | 5.52e-01 | 4.86e-01 | 6.65e-01 |
RHO GTPases Activate NADPH Oxidases | 13 | 7.97e-01 | 8.36e-01 | 0.2350 | 0.141000 | -0.059100 | 0.163000 | 0.072500 | 3.80e-01 | 7.12e-01 | 3.09e-01 | 6.51e-01 |
Translocation of SLC2A4 (GLUT4) to the plasma membrane | 50 | 1.19e-02 | 2.73e-02 | 0.2350 | -0.066600 | -0.095700 | -0.184000 | 0.086700 | 4.16e-01 | 2.43e-01 | 2.43e-02 | 2.89e-01 |
Cyclin D associated events in G1 | 41 | 3.68e-01 | 4.53e-01 | 0.2340 | 0.088900 | 0.078400 | 0.175000 | 0.101000 | 3.25e-01 | 3.86e-01 | 5.30e-02 | 2.63e-01 |
G1 Phase | 41 | 3.68e-01 | 4.53e-01 | 0.2340 | 0.088900 | 0.078400 | 0.175000 | 0.101000 | 3.25e-01 | 3.86e-01 | 5.30e-02 | 2.63e-01 |
Glycolysis | 53 | 8.94e-02 | 1.44e-01 | 0.2340 | -0.198000 | 0.117000 | -0.016500 | -0.041400 | 1.28e-02 | 1.41e-01 | 8.35e-01 | 6.03e-01 |
Glycerophospholipid biosynthesis | 80 | 4.43e-03 | 1.21e-02 | 0.2340 | 0.080000 | -0.146000 | -0.159000 | 0.042700 | 2.17e-01 | 2.39e-02 | 1.43e-02 | 5.10e-01 |
Metabolism of amino acids and derivatives | 223 | 9.82e-09 | 1.12e-07 | 0.2330 | -0.162000 | -0.071100 | 0.039700 | -0.147000 | 3.37e-05 | 6.89e-02 | 3.10e-01 | 1.69e-04 |
Netrin-1 signaling | 37 | 2.27e-01 | 3.07e-01 | 0.2330 | 0.098500 | -0.209000 | -0.029400 | 0.004580 | 3.00e-01 | 2.78e-02 | 7.58e-01 | 9.62e-01 |
Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks | 36 | 1.25e-01 | 1.88e-01 | 0.2330 | -0.196000 | 0.085500 | 0.092200 | 0.001590 | 4.18e-02 | 3.75e-01 | 3.39e-01 | 9.87e-01 |
AURKA Activation by TPX2 | 62 | 1.54e-02 | 3.34e-02 | 0.2320 | 0.007660 | 0.121000 | 0.022700 | 0.197000 | 9.17e-01 | 9.93e-02 | 7.57e-01 | 7.45e-03 |
ABC transporter disorders | 56 | 1.39e-02 | 3.08e-02 | 0.2320 | -0.196000 | 0.035000 | 0.119000 | -0.011700 | 1.13e-02 | 6.51e-01 | 1.25e-01 | 8.80e-01 |
DNA Damage Bypass | 43 | 1.35e-01 | 1.97e-01 | 0.2310 | -0.094700 | 0.155000 | 0.101000 | 0.099400 | 2.83e-01 | 7.83e-02 | 2.53e-01 | 2.60e-01 |
Pre-NOTCH Transcription and Translation | 31 | 5.33e-01 | 6.13e-01 | 0.2300 | 0.101000 | 0.034500 | 0.096400 | 0.180000 | 3.30e-01 | 7.40e-01 | 3.53e-01 | 8.35e-02 |
DNA Repair | 241 | 2.81e-07 | 2.54e-06 | 0.2290 | -0.117000 | 0.183000 | 0.071800 | 0.016700 | 1.91e-03 | 1.16e-06 | 5.65e-02 | 6.57e-01 |
Transmission across Chemical Synapses | 123 | 2.22e-03 | 6.67e-03 | 0.2290 | 0.114000 | -0.184000 | -0.004960 | 0.074500 | 2.96e-02 | 4.52e-04 | 9.24e-01 | 1.55e-01 |
Ca2+ pathway | 45 | 3.54e-02 | 6.87e-02 | 0.2290 | 0.168000 | -0.022300 | -0.153000 | -0.002630 | 5.09e-02 | 7.96e-01 | 7.61e-02 | 9.76e-01 |
VLDLR internalisation and degradation | 11 | 7.75e-01 | 8.21e-01 | 0.2280 | 0.019900 | -0.169000 | 0.077200 | 0.131000 | 9.09e-01 | 3.31e-01 | 6.58e-01 | 4.53e-01 |
HDR through Single Strand Annealing (SSA) | 30 | 2.76e-01 | 3.57e-01 | 0.2280 | -0.055300 | 0.197000 | 0.024000 | 0.097200 | 6.00e-01 | 6.18e-02 | 8.20e-01 | 3.57e-01 |
RNA Polymerase I Promoter Clearance | 43 | 1.49e-01 | 2.15e-01 | 0.2280 | -0.041000 | 0.162000 | 0.155000 | -0.006470 | 6.42e-01 | 6.69e-02 | 7.95e-02 | 9.42e-01 |
Signaling by PDGFR in disease | 17 | 6.15e-01 | 6.91e-01 | 0.2270 | -0.061400 | 0.093400 | 0.185000 | 0.068000 | 6.61e-01 | 5.05e-01 | 1.86e-01 | 6.27e-01 |
Endosomal Sorting Complex Required For Transport (ESCRT) | 24 | 3.24e-01 | 4.07e-01 | 0.2260 | -0.183000 | 0.081100 | 0.105000 | 0.013500 | 1.21e-01 | 4.92e-01 | 3.72e-01 | 9.09e-01 |
Disassembly of the destruction complex and recruitment of AXIN to the membrane | 25 | 2.66e-01 | 3.46e-01 | 0.2260 | -0.161000 | 0.056900 | 0.148000 | 0.006840 | 1.63e-01 | 6.23e-01 | 2.00e-01 | 9.53e-01 |
DNA Double Strand Break Response | 37 | 1.55e-01 | 2.22e-01 | 0.2260 | -0.164000 | 0.110000 | 0.108000 | 0.018900 | 8.45e-02 | 2.46e-01 | 2.55e-01 | 8.42e-01 |
Regulation of TP53 Activity through Association with Co-factors | 12 | 9.06e-01 | 9.23e-01 | 0.2260 | 0.125000 | 0.018100 | 0.112000 | 0.150000 | 4.52e-01 | 9.14e-01 | 5.01e-01 | 3.70e-01 |
Notch-HLH transcription pathway | 24 | 3.63e-01 | 4.49e-01 | 0.2260 | -0.073400 | -0.205000 | 0.014100 | -0.056900 | 5.34e-01 | 8.18e-02 | 9.05e-01 | 6.30e-01 |
SLC transporter disorders | 51 | 1.15e-01 | 1.77e-01 | 0.2260 | -0.058600 | 0.104000 | 0.141000 | 0.129000 | 4.70e-01 | 2.01e-01 | 8.12e-02 | 1.11e-01 |
TP53 Regulates Metabolic Genes | 79 | 2.25e-02 | 4.63e-02 | 0.2250 | -0.197000 | -0.068400 | -0.069300 | -0.049900 | 2.54e-03 | 2.95e-01 | 2.88e-01 | 4.44e-01 |
ERCC6 (CSB) and EHMT2 (G9a) positively regulate rRNA expression | 15 | 8.05e-01 | 8.43e-01 | 0.2250 | 0.055100 | 0.061500 | 0.187000 | 0.091800 | 7.12e-01 | 6.80e-01 | 2.09e-01 | 5.39e-01 |
Translesion synthesis by Y family DNA polymerases bypasses lesions on DNA template | 34 | 2.50e-01 | 3.32e-01 | 0.2240 | -0.077500 | 0.113000 | 0.117000 | 0.134000 | 4.34e-01 | 2.56e-01 | 2.40e-01 | 1.76e-01 |
VEGFR2 mediated vascular permeability | 23 | 6.59e-01 | 7.24e-01 | 0.2240 | 0.077900 | -0.078700 | 0.119000 | 0.154000 | 5.18e-01 | 5.14e-01 | 3.23e-01 | 2.01e-01 |
Diseases associated with glycosylation precursor biosynthesis | 18 | 6.34e-01 | 7.00e-01 | 0.2240 | 0.199000 | 0.035800 | 0.087900 | 0.039200 | 1.44e-01 | 7.92e-01 | 5.19e-01 | 7.73e-01 |
Metabolism of carbohydrates | 202 | 1.04e-04 | 4.73e-04 | 0.2240 | 0.122000 | -0.149000 | 0.036300 | 0.108000 | 2.96e-03 | 2.81e-04 | 3.76e-01 | 8.25e-03 |
ABC-family proteins mediated transport | 76 | 4.90e-02 | 8.95e-02 | 0.2240 | -0.193000 | 0.051100 | -0.012600 | -0.100000 | 3.72e-03 | 4.42e-01 | 8.49e-01 | 1.31e-01 |
Paradoxical activation of RAF signaling by kinase inactive BRAF | 36 | 1.34e-01 | 1.97e-01 | 0.2230 | 0.082000 | -0.166000 | 0.122000 | -0.024300 | 3.95e-01 | 8.49e-02 | 2.05e-01 | 8.01e-01 |
Signaling by RAS mutants | 36 | 1.34e-01 | 1.97e-01 | 0.2230 | 0.082000 | -0.166000 | 0.122000 | -0.024300 | 3.95e-01 | 8.49e-02 | 2.05e-01 | 8.01e-01 |
Signaling by moderate kinase activity BRAF mutants | 36 | 1.34e-01 | 1.97e-01 | 0.2230 | 0.082000 | -0.166000 | 0.122000 | -0.024300 | 3.95e-01 | 8.49e-02 | 2.05e-01 | 8.01e-01 |
Signaling downstream of RAS mutants | 36 | 1.34e-01 | 1.97e-01 | 0.2230 | 0.082000 | -0.166000 | 0.122000 | -0.024300 | 3.95e-01 | 8.49e-02 | 2.05e-01 | 8.01e-01 |
Synthesis of PA | 21 | 4.83e-01 | 5.64e-01 | 0.2230 | 0.096000 | -0.132000 | -0.152000 | 0.004940 | 4.47e-01 | 2.95e-01 | 2.28e-01 | 9.69e-01 |
Integration of energy metabolism | 71 | 3.66e-02 | 7.07e-02 | 0.2230 | 0.111000 | -0.185000 | -0.052800 | -0.021300 | 1.07e-01 | 7.09e-03 | 4.43e-01 | 7.56e-01 |
Mismatch repair (MMR) directed by MSH2:MSH3 (MutSbeta) | 13 | 6.18e-01 | 6.94e-01 | 0.2230 | -0.159000 | 0.113000 | -0.096400 | 0.050000 | 3.22e-01 | 4.81e-01 | 5.47e-01 | 7.55e-01 |
Phosphorylation of the APC/C | 18 | 5.85e-01 | 6.62e-01 | 0.2230 | -0.161000 | 0.139000 | -0.066000 | 0.002330 | 2.36e-01 | 3.07e-01 | 6.28e-01 | 9.86e-01 |
RNA Polymerase I Transcription | 44 | 1.30e-01 | 1.92e-01 | 0.2230 | -0.022000 | 0.145000 | 0.167000 | -0.017900 | 8.01e-01 | 9.64e-02 | 5.57e-02 | 8.38e-01 |
Regulation of TP53 Degradation | 32 | 3.50e-01 | 4.36e-01 | 0.2220 | -0.061600 | 0.210000 | 0.037200 | -0.000708 | 5.47e-01 | 3.96e-02 | 7.16e-01 | 9.94e-01 |
Post NMDA receptor activation events | 44 | 1.16e-01 | 1.77e-01 | 0.2220 | 0.096100 | -0.187000 | -0.003140 | -0.071000 | 2.71e-01 | 3.18e-02 | 9.71e-01 | 4.16e-01 |
Protein methylation | 10 | 6.94e-01 | 7.53e-01 | 0.2220 | -0.185000 | -0.003720 | 0.123000 | 0.007660 | 3.12e-01 | 9.84e-01 | 5.01e-01 | 9.67e-01 |
RAS processing | 18 | 5.33e-01 | 6.13e-01 | 0.2210 | 0.112000 | -0.155000 | 0.109000 | -0.013600 | 4.12e-01 | 2.54e-01 | 4.23e-01 | 9.20e-01 |
Purine salvage | 13 | 7.17e-01 | 7.72e-01 | 0.2190 | 0.054400 | -0.207000 | 0.040100 | -0.025800 | 7.34e-01 | 1.96e-01 | 8.02e-01 | 8.72e-01 |
Signaling by ERBB2 | 37 | 3.75e-01 | 4.59e-01 | 0.2190 | 0.045800 | -0.070200 | 0.116000 | 0.166000 | 6.30e-01 | 4.60e-01 | 2.24e-01 | 8.14e-02 |
Regulation of TP53 Activity through Acetylation | 28 | 4.72e-01 | 5.55e-01 | 0.2180 | -0.030900 | 0.162000 | 0.138000 | 0.034200 | 7.77e-01 | 1.38e-01 | 2.08e-01 | 7.54e-01 |
Glucose metabolism | 67 | 1.83e-01 | 2.55e-01 | 0.2170 | -0.171000 | -0.013800 | -0.082300 | -0.105000 | 1.59e-02 | 8.46e-01 | 2.45e-01 | 1.37e-01 |
Signaling by FGFR4 in disease | 11 | 7.49e-01 | 7.99e-01 | 0.2170 | -0.188000 | -0.042000 | -0.098700 | 0.016200 | 2.81e-01 | 8.09e-01 | 5.71e-01 | 9.26e-01 |
Purine catabolism | 14 | 5.85e-01 | 6.62e-01 | 0.2160 | 0.041600 | -0.118000 | -0.129000 | 0.119000 | 7.88e-01 | 4.44e-01 | 4.02e-01 | 4.41e-01 |
alpha-linolenic (omega3) and linoleic (omega6) acid metabolism | 10 | 8.46e-01 | 8.78e-01 | 0.2150 | -0.062700 | -0.197000 | -0.034200 | -0.050900 | 7.32e-01 | 2.82e-01 | 8.51e-01 | 7.80e-01 |
alpha-linolenic acid (ALA) metabolism | 10 | 8.46e-01 | 8.78e-01 | 0.2150 | -0.062700 | -0.197000 | -0.034200 | -0.050900 | 7.32e-01 | 2.82e-01 | 8.51e-01 | 7.80e-01 |
Activated NTRK2 signals through FRS2 and FRS3 | 10 | 7.85e-01 | 8.28e-01 | 0.2150 | -0.101000 | 0.048200 | 0.174000 | 0.060300 | 5.80e-01 | 7.92e-01 | 3.42e-01 | 7.41e-01 |
Signaling by FGFR1 | 34 | 4.07e-01 | 4.89e-01 | 0.2140 | 0.108000 | 0.089500 | 0.158000 | 0.036200 | 2.76e-01 | 3.67e-01 | 1.12e-01 | 7.15e-01 |
Cellular responses to external stimuli | 410 | 9.01e-15 | 2.91e-13 | 0.2140 | -0.080800 | 0.050200 | 0.191000 | 0.012100 | 5.46e-03 | 8.46e-02 | 4.61e-11 | 6.78e-01 |
Cellular responses to stress | 406 | 8.22e-15 | 2.73e-13 | 0.2140 | -0.082700 | 0.049300 | 0.191000 | 0.007360 | 4.65e-03 | 9.18e-02 | 6.61e-11 | 8.01e-01 |
Budding and maturation of HIV virion | 22 | 4.32e-01 | 5.15e-01 | 0.2130 | -0.115000 | 0.047600 | 0.137000 | 0.106000 | 3.52e-01 | 6.99e-01 | 2.66e-01 | 3.88e-01 |
Activation of NMDA receptors and postsynaptic events | 52 | 1.26e-01 | 1.89e-01 | 0.2130 | 0.112000 | -0.180000 | 0.022700 | -0.009840 | 1.63e-01 | 2.53e-02 | 7.78e-01 | 9.02e-01 |
ERKs are inactivated | 13 | 8.53e-01 | 8.85e-01 | 0.2130 | 0.145000 | -0.081000 | 0.115000 | 0.065800 | 3.64e-01 | 6.13e-01 | 4.74e-01 | 6.82e-01 |
Glutamate binding, activation of AMPA receptors and synaptic plasticity | 19 | 5.01e-01 | 5.82e-01 | 0.2120 | 0.039100 | -0.189000 | 0.054100 | -0.068500 | 7.68e-01 | 1.54e-01 | 6.83e-01 | 6.06e-01 |
Trafficking of AMPA receptors | 19 | 5.01e-01 | 5.82e-01 | 0.2120 | 0.039100 | -0.189000 | 0.054100 | -0.068500 | 7.68e-01 | 1.54e-01 | 6.83e-01 | 6.06e-01 |
APC/C:Cdc20 mediated degradation of Cyclin B | 20 | 6.29e-01 | 6.98e-01 | 0.2120 | -0.135000 | 0.163000 | 0.000970 | -0.007480 | 2.98e-01 | 2.06e-01 | 9.94e-01 | 9.54e-01 |
NR1H3 & NR1H2 regulate gene expression linked to cholesterol transport and efflux | 29 | 4.00e-01 | 4.84e-01 | 0.2120 | -0.121000 | 0.021500 | -0.171000 | -0.019700 | 2.60e-01 | 8.41e-01 | 1.11e-01 | 8.54e-01 |
Interleukin-2 family signaling | 22 | 5.91e-01 | 6.67e-01 | 0.2110 | 0.078300 | -0.167000 | 0.087800 | 0.052000 | 5.25e-01 | 1.74e-01 | 4.76e-01 | 6.73e-01 |
WNT ligand biogenesis and trafficking | 12 | 8.22e-01 | 8.57e-01 | 0.2110 | -0.157000 | -0.103000 | -0.026000 | -0.093100 | 3.48e-01 | 5.38e-01 | 8.76e-01 | 5.77e-01 |
Gamma carboxylation, hypusine formation and arylsulfatase activation | 28 | 1.39e-01 | 2.02e-01 | 0.2110 | -0.070500 | -0.083800 | -0.082100 | 0.160000 | 5.19e-01 | 4.43e-01 | 4.52e-01 | 1.43e-01 |
Metabolism of vitamins and cofactors | 126 | 7.04e-03 | 1.76e-02 | 0.2100 | -0.025600 | -0.071000 | -0.186000 | -0.061800 | 6.21e-01 | 1.70e-01 | 3.17e-04 | 2.32e-01 |
FGFR1 mutant receptor activation | 23 | 6.73e-01 | 7.36e-01 | 0.2100 | -0.065400 | -0.003300 | -0.079200 | -0.183000 | 5.88e-01 | 9.78e-01 | 5.11e-01 | 1.28e-01 |
Deubiquitination | 211 | 2.62e-06 | 1.81e-05 | 0.2100 | -0.167000 | 0.085400 | 0.079500 | -0.050800 | 3.06e-05 | 3.35e-02 | 4.76e-02 | 2.06e-01 |
Transcriptional regulation by RUNX3 | 86 | 1.52e-02 | 3.29e-02 | 0.2100 | -0.001530 | 0.005910 | 0.203000 | 0.055100 | 9.80e-01 | 9.25e-01 | 1.19e-03 | 3.78e-01 |
Resolution of Abasic Sites (AP sites) | 36 | 2.55e-01 | 3.37e-01 | 0.2090 | -0.095500 | 0.083500 | 0.130000 | 0.104000 | 3.22e-01 | 3.86e-01 | 1.77e-01 | 2.80e-01 |
Regulation of TP53 Expression and Degradation | 33 | 3.72e-01 | 4.57e-01 | 0.2090 | -0.038400 | 0.205000 | 0.009130 | 0.001060 | 7.03e-01 | 4.13e-02 | 9.28e-01 | 9.92e-01 |
Programmed Cell Death | 143 | 1.57e-03 | 4.96e-03 | 0.2090 | 0.011700 | -0.046800 | 0.174000 | 0.105000 | 8.09e-01 | 3.36e-01 | 3.31e-04 | 3.13e-02 |
Negative regulation of MAPK pathway | 39 | 7.68e-02 | 1.28e-01 | 0.2090 | -0.057600 | 0.058500 | 0.158000 | -0.109000 | 5.34e-01 | 5.27e-01 | 8.78e-02 | 2.41e-01 |
Aberrant regulation of mitotic cell cycle due to RB1 defects | 35 | 3.55e-01 | 4.41e-01 | 0.2090 | 0.035300 | 0.074500 | 0.056100 | 0.183000 | 7.18e-01 | 4.46e-01 | 5.66e-01 | 6.08e-02 |
Diseases of mitotic cell cycle | 35 | 3.55e-01 | 4.41e-01 | 0.2090 | 0.035300 | 0.074500 | 0.056100 | 0.183000 | 7.18e-01 | 4.46e-01 | 5.66e-01 | 6.08e-02 |
Signaling by NOTCH4 | 70 | 1.38e-02 | 3.07e-02 | 0.2080 | -0.096700 | 0.025300 | 0.181000 | 0.024600 | 1.63e-01 | 7.15e-01 | 8.98e-03 | 7.23e-01 |
Cilium Assembly | 158 | 1.49e-05 | 8.41e-05 | 0.2080 | 0.082500 | 0.114000 | -0.038800 | 0.148000 | 7.47e-02 | 1.35e-02 | 4.02e-01 | 1.38e-03 |
Anchoring of the basal body to the plasma membrane | 83 | 2.72e-02 | 5.42e-02 | 0.2080 | 0.085300 | 0.122000 | 0.016300 | 0.144000 | 1.80e-01 | 5.55e-02 | 7.98e-01 | 2.32e-02 |
FRS-mediated FGFR3 signaling | 12 | 7.13e-01 | 7.70e-01 | 0.2080 | -0.043000 | 0.086200 | 0.179000 | -0.042000 | 7.96e-01 | 6.05e-01 | 2.83e-01 | 8.01e-01 |
PKMTs methylate histone lysines | 37 | 3.58e-01 | 4.44e-01 | 0.2070 | -0.124000 | 0.153000 | -0.057200 | -0.030600 | 1.91e-01 | 1.08e-01 | 5.47e-01 | 7.48e-01 |
Signalling to ERKs | 29 | 1.76e-01 | 2.49e-01 | 0.2070 | 0.084500 | -0.058400 | 0.167000 | -0.065700 | 4.31e-01 | 5.87e-01 | 1.19e-01 | 5.40e-01 |
Gene expression (Transcription) | 991 | 2.62e-23 | 2.30e-21 | 0.2070 | -0.086500 | 0.168000 | 0.068900 | -0.047700 | 7.04e-06 | 2.71e-18 | 3.45e-04 | 1.33e-02 |
Clathrin-mediated endocytosis | 108 | 8.07e-02 | 1.33e-01 | 0.2060 | 0.079300 | 0.095300 | 0.121000 | 0.112000 | 1.56e-01 | 8.78e-02 | 3.03e-02 | 4.57e-02 |
Extra-nuclear estrogen signaling | 53 | 2.42e-01 | 3.22e-01 | 0.2060 | 0.171000 | 0.041900 | 0.039900 | 0.097700 | 3.11e-02 | 5.98e-01 | 6.15e-01 | 2.19e-01 |
Loss of Nlp from mitotic centrosomes | 60 | 4.56e-02 | 8.43e-02 | 0.2050 | 0.000986 | 0.100000 | 0.014700 | 0.178000 | 9.89e-01 | 1.79e-01 | 8.44e-01 | 1.72e-02 |
Loss of proteins required for interphase microtubule organization from the centrosome | 60 | 4.56e-02 | 8.43e-02 | 0.2050 | 0.000986 | 0.100000 | 0.014700 | 0.178000 | 9.89e-01 | 1.79e-01 | 8.44e-01 | 1.72e-02 |
Disorders of transmembrane transporters | 107 | 2.01e-03 | 6.11e-03 | 0.2050 | -0.131000 | 0.068100 | 0.130000 | 0.055800 | 1.94e-02 | 2.25e-01 | 2.04e-02 | 3.20e-01 |
Glutamate Neurotransmitter Release Cycle | 12 | 8.35e-01 | 8.68e-01 | 0.2040 | -0.015100 | -0.024700 | 0.150000 | 0.136000 | 9.28e-01 | 8.82e-01 | 3.70e-01 | 4.14e-01 |
Apoptosis | 133 | 1.74e-03 | 5.37e-03 | 0.2040 | -0.008730 | -0.041600 | 0.177000 | 0.092800 | 8.63e-01 | 4.09e-01 | 4.52e-04 | 6.56e-02 |
Base Excision Repair | 43 | 3.24e-01 | 4.07e-01 | 0.2040 | -0.033900 | 0.110000 | 0.122000 | 0.115000 | 7.01e-01 | 2.13e-01 | 1.66e-01 | 1.91e-01 |
G2/M Transition | 153 | 1.14e-03 | 3.78e-03 | 0.2040 | -0.080800 | 0.145000 | 0.111000 | 0.041500 | 8.56e-02 | 2.10e-03 | 1.85e-02 | 3.77e-01 |
Uptake and actions of bacterial toxins | 21 | 5.00e-01 | 5.82e-01 | 0.2030 | 0.105000 | -0.127000 | 0.118000 | -0.021500 | 4.05e-01 | 3.15e-01 | 3.50e-01 | 8.65e-01 |
Cytochrome c-mediated apoptotic response | 10 | 9.17e-01 | 9.32e-01 | 0.2020 | 0.083800 | -0.009820 | 0.170000 | 0.071000 | 6.47e-01 | 9.57e-01 | 3.53e-01 | 6.98e-01 |
Signal Transduction | 1391 | 1.67e-19 | 1.02e-17 | 0.2020 | 0.131000 | -0.061600 | 0.103000 | 0.097200 | 3.38e-15 | 2.07e-04 | 6.46e-10 | 4.75e-09 |
RNA Polymerase I Transcription Initiation | 40 | 2.62e-01 | 3.44e-01 | 0.2020 | -0.065500 | 0.145000 | 0.119000 | -0.037000 | 4.74e-01 | 1.14e-01 | 1.94e-01 | 6.86e-01 |
C-type lectin receptors (CLRs) | 94 | 1.17e-03 | 3.86e-03 | 0.2010 | -0.140000 | -0.016300 | 0.141000 | -0.026200 | 1.92e-02 | 7.86e-01 | 1.81e-02 | 6.61e-01 |
Biological oxidations | 85 | 9.24e-02 | 1.47e-01 | 0.2010 | 0.002580 | -0.141000 | -0.118000 | -0.081000 | 9.67e-01 | 2.52e-02 | 5.96e-02 | 1.98e-01 |
Amino acids regulate mTORC1 | 45 | 1.03e-01 | 1.61e-01 | 0.2010 | -0.094600 | -0.044400 | 0.125000 | 0.117000 | 2.73e-01 | 6.07e-01 | 1.47e-01 | 1.74e-01 |
Developmental Biology | 582 | 1.14e-09 | 1.50e-08 | 0.2000 | 0.082000 | -0.070400 | 0.136000 | 0.100000 | 8.67e-04 | 4.27e-03 | 3.32e-08 | 4.81e-05 |
Signaling by FGFR3 | 29 | 3.85e-01 | 4.68e-01 | 0.2000 | 0.036100 | 0.099800 | 0.168000 | -0.021500 | 7.37e-01 | 3.53e-01 | 1.17e-01 | 8.41e-01 |
Interleukin-7 signaling | 12 | 8.55e-01 | 8.86e-01 | 0.2000 | 0.087500 | -0.167000 | -0.042600 | 0.050800 | 6.00e-01 | 3.17e-01 | 7.99e-01 | 7.61e-01 |
CREB1 phosphorylation through NMDA receptor-mediated activation of RAS signaling | 20 | 7.25e-01 | 7.79e-01 | 0.2000 | 0.026000 | -0.103000 | -0.116000 | -0.122000 | 8.41e-01 | 4.25e-01 | 3.69e-01 | 3.43e-01 |
Downstream signal transduction | 27 | 4.29e-01 | 5.12e-01 | 0.1990 | 0.048500 | -0.175000 | 0.080900 | -0.006370 | 6.63e-01 | 1.15e-01 | 4.67e-01 | 9.54e-01 |
PI3K Cascade | 23 | 5.69e-01 | 6.47e-01 | 0.1990 | -0.158000 | 0.015700 | 0.036000 | -0.115000 | 1.91e-01 | 8.97e-01 | 7.65e-01 | 3.42e-01 |
Apoptotic execution phase | 35 | 6.34e-01 | 7.00e-01 | 0.1990 | 0.083600 | -0.039200 | 0.105000 | 0.141000 | 3.93e-01 | 6.88e-01 | 2.84e-01 | 1.49e-01 |
Signaling by FGFR1 in disease | 30 | 7.34e-01 | 7.84e-01 | 0.1990 | -0.099100 | 0.012700 | -0.103000 | -0.137000 | 3.48e-01 | 9.04e-01 | 3.29e-01 | 1.94e-01 |
COPI-independent Golgi-to-ER retrograde traffic | 27 | 2.93e-01 | 3.76e-01 | 0.1980 | -0.187000 | 0.012000 | 0.006170 | 0.064400 | 9.32e-02 | 9.14e-01 | 9.56e-01 | 5.63e-01 |
Mitotic G2-G2/M phases | 155 | 1.61e-03 | 5.04e-03 | 0.1980 | -0.075900 | 0.137000 | 0.113000 | 0.042800 | 1.04e-01 | 3.34e-03 | 1.54e-02 | 3.60e-01 |
Cargo trafficking to the periciliary membrane | 42 | 1.18e-01 | 1.80e-01 | 0.1960 | 0.043000 | 0.138000 | -0.059600 | 0.118000 | 6.30e-01 | 1.22e-01 | 5.04e-01 | 1.85e-01 |
Asparagine N-linked glycosylation | 237 | 1.90e-03 | 5.83e-03 | 0.1960 | 0.049600 | 0.056000 | 0.114000 | 0.141000 | 1.91e-01 | 1.40e-01 | 2.66e-03 | 2.10e-04 |
Aberrant regulation of mitotic exit in cancer due to RB1 defects | 20 | 5.48e-01 | 6.27e-01 | 0.1960 | -0.133000 | 0.121000 | -0.000105 | 0.076900 | 3.03e-01 | 3.49e-01 | 9.99e-01 | 5.52e-01 |
Signaling by Insulin receptor | 48 | 2.01e-01 | 2.77e-01 | 0.1950 | -0.044700 | 0.042300 | 0.102000 | 0.155000 | 5.92e-01 | 6.13e-01 | 2.20e-01 | 6.42e-02 |
Downregulation of ERBB2 signaling | 18 | 7.54e-01 | 8.04e-01 | 0.1940 | -0.003720 | -0.026500 | 0.121000 | 0.149000 | 9.78e-01 | 8.46e-01 | 3.73e-01 | 2.73e-01 |
Regulation of PTEN gene transcription | 57 | 9.16e-02 | 1.47e-01 | 0.1940 | 0.080800 | 0.052300 | 0.168000 | -0.017300 | 2.92e-01 | 4.95e-01 | 2.88e-02 | 8.22e-01 |
Conversion from APC/C:Cdc20 to APC/C:Cdh1 in late anaphase | 19 | 7.87e-01 | 8.29e-01 | 0.1920 | -0.108000 | 0.116000 | -0.090300 | -0.059900 | 4.16e-01 | 3.80e-01 | 4.96e-01 | 6.52e-01 |
PCP/CE pathway | 79 | 1.38e-02 | 3.07e-02 | 0.1920 | -0.037400 | -0.013100 | 0.187000 | 0.008030 | 5.67e-01 | 8.41e-01 | 4.09e-03 | 9.02e-01 |
Signaling by BRAF and RAF fusions | 52 | 1.92e-01 | 2.66e-01 | 0.1910 | 0.046400 | -0.173000 | 0.063500 | 0.019900 | 5.63e-01 | 3.12e-02 | 4.29e-01 | 8.05e-01 |
Intra-Golgi traffic | 38 | 3.60e-01 | 4.46e-01 | 0.1910 | -0.119000 | 0.128000 | 0.073200 | 0.022400 | 2.05e-01 | 1.71e-01 | 4.35e-01 | 8.12e-01 |
Fc epsilon receptor (FCERI) signaling | 104 | 2.24e-03 | 6.72e-03 | 0.1910 | -0.143000 | 0.015500 | 0.119000 | -0.039100 | 1.17e-02 | 7.86e-01 | 3.67e-02 | 4.91e-01 |
Signaling by TGFB family members | 84 | 3.79e-03 | 1.07e-02 | 0.1910 | -0.042100 | 0.053600 | 0.111000 | -0.139000 | 5.05e-01 | 3.97e-01 | 7.83e-02 | 2.81e-02 |
VxPx cargo-targeting to cilium | 17 | 4.61e-01 | 5.44e-01 | 0.1900 | -0.027800 | -0.040700 | -0.118000 | 0.141000 | 8.43e-01 | 7.72e-01 | 3.99e-01 | 3.16e-01 |
Interconversion of nucleotide di- and triphosphates | 21 | 7.82e-01 | 8.26e-01 | 0.1900 | 0.112000 | -0.096000 | 0.099800 | 0.066500 | 3.75e-01 | 4.46e-01 | 4.29e-01 | 5.98e-01 |
NR1H2 and NR1H3-mediated signaling | 34 | 6.63e-01 | 7.27e-01 | 0.1900 | -0.086500 | -0.097800 | -0.112000 | -0.080600 | 3.83e-01 | 3.24e-01 | 2.60e-01 | 4.17e-01 |
Platelet homeostasis | 50 | 2.42e-01 | 3.23e-01 | 0.1900 | 0.155000 | -0.108000 | -0.004730 | 0.009030 | 5.75e-02 | 1.86e-01 | 9.54e-01 | 9.12e-01 |
Regulation of FZD by ubiquitination | 11 | 7.07e-01 | 7.65e-01 | 0.1880 | -0.030300 | -0.101000 | 0.118000 | -0.101000 | 8.62e-01 | 5.62e-01 | 4.97e-01 | 5.63e-01 |
Regulation of localization of FOXO transcription factors | 11 | 8.31e-01 | 8.64e-01 | 0.1870 | -0.100000 | -0.139000 | -0.063200 | 0.037100 | 5.65e-01 | 4.24e-01 | 7.17e-01 | 8.31e-01 |
PI Metabolism | 68 | 1.18e-01 | 1.80e-01 | 0.1870 | 0.022000 | 0.098900 | 0.037600 | 0.152000 | 7.54e-01 | 1.59e-01 | 5.93e-01 | 3.04e-02 |
Nucleobase catabolism | 21 | 6.29e-01 | 6.98e-01 | 0.1860 | 0.017000 | -0.146000 | -0.091700 | 0.068900 | 8.93e-01 | 2.49e-01 | 4.67e-01 | 5.85e-01 |
Signaling by WNT in cancer | 28 | 6.63e-01 | 7.27e-01 | 0.1860 | -0.167000 | 0.036600 | -0.038400 | -0.060300 | 1.26e-01 | 7.38e-01 | 7.25e-01 | 5.81e-01 |
NRIF signals cell death from the nucleus | 13 | 8.21e-01 | 8.57e-01 | 0.1850 | 0.131000 | 0.075700 | 0.106000 | -0.006480 | 4.12e-01 | 6.37e-01 | 5.06e-01 | 9.68e-01 |
Signaling by EGFR in Cancer | 18 | 7.87e-01 | 8.28e-01 | 0.1850 | -0.033100 | 0.112000 | 0.138000 | 0.038500 | 8.08e-01 | 4.10e-01 | 3.09e-01 | 7.77e-01 |
NOTCH3 Intracellular Domain Regulates Transcription | 18 | 8.64e-01 | 8.92e-01 | 0.1850 | 0.096500 | -0.045000 | 0.053900 | 0.142000 | 4.79e-01 | 7.41e-01 | 6.92e-01 | 2.99e-01 |
Transcriptional regulation of white adipocyte differentiation | 71 | 1.26e-01 | 1.89e-01 | 0.1850 | -0.105000 | 0.147000 | 0.034700 | 0.015600 | 1.25e-01 | 3.22e-02 | 6.14e-01 | 8.20e-01 |
Signaling by EGFR | 41 | 6.58e-01 | 7.24e-01 | 0.1850 | 0.073400 | 0.044000 | 0.129000 | 0.102000 | 4.17e-01 | 6.26e-01 | 1.55e-01 | 2.59e-01 |
CTLA4 inhibitory signaling | 17 | 8.07e-01 | 8.44e-01 | 0.1840 | -0.002820 | -0.027600 | 0.144000 | 0.112000 | 9.84e-01 | 8.44e-01 | 3.04e-01 | 4.25e-01 |
RUNX1 regulates genes involved in megakaryocyte differentiation and platelet function | 30 | 4.16e-01 | 5.00e-01 | 0.1840 | 0.007940 | 0.162000 | -0.026400 | 0.084600 | 9.40e-01 | 1.26e-01 | 8.02e-01 | 4.23e-01 |
Synthesis of glycosylphosphatidylinositol (GPI) | 15 | 6.74e-01 | 7.37e-01 | 0.1840 | -0.072900 | 0.131000 | -0.048700 | 0.095400 | 6.25e-01 | 3.80e-01 | 7.44e-01 | 5.22e-01 |
Glutathione synthesis and recycling | 10 | 7.77e-01 | 8.22e-01 | 0.1830 | -0.087900 | -0.061500 | 0.113000 | -0.096300 | 6.30e-01 | 7.36e-01 | 5.36e-01 | 5.98e-01 |
Golgi-to-ER retrograde transport | 89 | 2.07e-01 | 2.83e-01 | 0.1830 | 0.038300 | 0.099400 | 0.105000 | 0.104000 | 5.34e-01 | 1.06e-01 | 8.62e-02 | 8.95e-02 |
Transcriptional regulation by the AP-2 (TFAP2) family of transcription factors | 23 | 6.97e-01 | 7.56e-01 | 0.1830 | -0.017200 | 0.046300 | 0.164000 | 0.063400 | 8.86e-01 | 7.01e-01 | 1.74e-01 | 5.99e-01 |
Signaling by the B Cell Receptor (BCR) | 85 | 1.19e-02 | 2.72e-02 | 0.1820 | -0.102000 | 0.001340 | 0.151000 | 0.001180 | 1.05e-01 | 9.83e-01 | 1.63e-02 | 9.85e-01 |
TBC/RABGAPs | 39 | 2.00e-01 | 2.75e-01 | 0.1820 | -0.074200 | 0.057000 | 0.123000 | -0.096200 | 4.23e-01 | 5.38e-01 | 1.83e-01 | 2.99e-01 |
MAPK6/MAPK4 signaling | 73 | 3.48e-02 | 6.79e-02 | 0.1820 | -0.103000 | 0.034800 | 0.146000 | -0.009410 | 1.29e-01 | 6.08e-01 | 3.17e-02 | 8.90e-01 |
Regulation of gene expression in late stage (branching morphogenesis) pancreatic bud precursor cells | 12 | 8.90e-01 | 9.13e-01 | 0.1810 | -0.026500 | 0.032000 | 0.151000 | 0.090600 | 8.74e-01 | 8.48e-01 | 3.64e-01 | 5.87e-01 |
Disease | 1011 | 2.13e-11 | 3.80e-10 | 0.1810 | 0.058400 | 0.007850 | 0.134000 | 0.107000 | 2.21e-03 | 6.81e-01 | 2.51e-12 | 1.85e-08 |
CD28 co-stimulation | 25 | 8.18e-01 | 8.54e-01 | 0.1810 | 0.094600 | -0.060000 | 0.077600 | 0.119000 | 4.13e-01 | 6.04e-01 | 5.02e-01 | 3.03e-01 |
Post-translational modification: synthesis of GPI-anchored proteins | 35 | 3.19e-01 | 4.03e-01 | 0.1800 | 0.152000 | 0.041500 | -0.061300 | 0.062100 | 1.21e-01 | 6.71e-01 | 5.31e-01 | 5.26e-01 |
Toll-like Receptor Cascades | 115 | 9.43e-02 | 1.50e-01 | 0.1800 | 0.063000 | -0.029300 | 0.141000 | 0.086700 | 2.45e-01 | 5.88e-01 | 8.99e-03 | 1.09e-01 |
Metabolism | 1363 | 2.20e-16 | 9.65e-15 | 0.1780 | -0.071400 | -0.113000 | -0.091000 | -0.073600 | 2.00e-05 | 1.40e-11 | 5.59e-08 | 1.11e-05 |
Transport to the Golgi and subsequent modification | 136 | 1.40e-02 | 3.08e-02 | 0.1770 | -0.025700 | 0.066900 | 0.086000 | 0.137000 | 6.06e-01 | 1.79e-01 | 8.44e-02 | 5.93e-03 |
RNA Polymerase II Transcription | 883 | 1.17e-15 | 4.66e-14 | 0.1760 | -0.067700 | 0.140000 | 0.064700 | -0.051600 | 8.47e-04 | 5.38e-12 | 1.44e-03 | 1.10e-02 |
Class I MHC mediated antigen processing & presentation | 302 | 6.46e-06 | 4.09e-05 | 0.1760 | -0.164000 | 0.032000 | 0.024700 | -0.048600 | 1.13e-06 | 3.42e-01 | 4.65e-01 | 1.49e-01 |
MAP kinase activation | 59 | 1.55e-01 | 2.23e-01 | 0.1760 | -0.105000 | -0.091100 | 0.023400 | -0.104000 | 1.62e-01 | 2.27e-01 | 7.56e-01 | 1.66e-01 |
Signaling by FGFR3 in disease | 14 | 8.59e-01 | 8.89e-01 | 0.1740 | -0.147000 | 0.050300 | 0.033900 | -0.069700 | 3.40e-01 | 7.45e-01 | 8.26e-01 | 6.52e-01 |
Signaling by FGFR3 point mutants in cancer | 14 | 8.59e-01 | 8.89e-01 | 0.1740 | -0.147000 | 0.050300 | 0.033900 | -0.069700 | 3.40e-01 | 7.45e-01 | 8.26e-01 | 6.52e-01 |
Regulation of PLK1 Activity at G2/M Transition | 74 | 9.22e-02 | 1.47e-01 | 0.1740 | -0.043500 | 0.126000 | 0.024300 | 0.109000 | 5.19e-01 | 6.13e-02 | 7.18e-01 | 1.06e-01 |
Costimulation by the CD28 family | 39 | 6.26e-01 | 6.98e-01 | 0.1730 | 0.032500 | -0.009130 | 0.140000 | 0.095700 | 7.25e-01 | 9.22e-01 | 1.31e-01 | 3.02e-01 |
IRS-mediated signalling | 27 | 6.29e-01 | 6.98e-01 | 0.1730 | -0.157000 | 0.031700 | 0.028600 | -0.057500 | 1.58e-01 | 7.76e-01 | 7.97e-01 | 6.05e-01 |
Cleavage of the damaged pyrimidine | 14 | 9.02e-01 | 9.19e-01 | 0.1720 | 0.101000 | 0.054100 | 0.026900 | 0.125000 | 5.11e-01 | 7.26e-01 | 8.62e-01 | 4.17e-01 |
Depyrimidination | 14 | 9.02e-01 | 9.19e-01 | 0.1720 | 0.101000 | 0.054100 | 0.026900 | 0.125000 | 5.11e-01 | 7.26e-01 | 8.62e-01 | 4.17e-01 |
Recognition and association of DNA glycosylase with site containing an affected pyrimidine | 14 | 9.02e-01 | 9.19e-01 | 0.1720 | 0.101000 | 0.054100 | 0.026900 | 0.125000 | 5.11e-01 | 7.26e-01 | 8.62e-01 | 4.17e-01 |
Downstream signaling of activated FGFR3 | 17 | 7.87e-01 | 8.28e-01 | 0.1720 | -0.104000 | 0.093600 | 0.083800 | -0.054200 | 4.58e-01 | 5.04e-01 | 5.50e-01 | 6.99e-01 |
Depolymerisation of the Nuclear Lamina | 13 | 8.75e-01 | 9.01e-01 | 0.1720 | 0.038200 | 0.091700 | 0.140000 | -0.002110 | 8.12e-01 | 5.67e-01 | 3.83e-01 | 9.89e-01 |
FRS-mediated FGFR2 signaling | 12 | 8.66e-01 | 8.94e-01 | 0.1720 | 0.036300 | -0.058100 | 0.155000 | 0.025200 | 8.28e-01 | 7.28e-01 | 3.52e-01 | 8.80e-01 |
SUMOylation of DNA methylation proteins | 15 | 7.67e-01 | 8.16e-01 | 0.1710 | 0.084900 | 0.105000 | 0.093400 | -0.049200 | 5.69e-01 | 4.81e-01 | 5.32e-01 | 7.42e-01 |
TCF dependent signaling in response to WNT | 134 | 2.20e-03 | 6.61e-03 | 0.1700 | -0.107000 | 0.032700 | 0.096900 | -0.084700 | 3.32e-02 | 5.15e-01 | 5.36e-02 | 9.16e-02 |
Recruitment of NuMA to mitotic centrosomes | 70 | 5.61e-02 | 9.97e-02 | 0.1700 | 0.013300 | 0.075600 | -0.023600 | 0.150000 | 8.48e-01 | 2.75e-01 | 7.34e-01 | 3.00e-02 |
ESR-mediated signaling | 126 | 4.16e-02 | 7.82e-02 | 0.1690 | -0.011900 | 0.148000 | 0.080900 | 0.000338 | 8.19e-01 | 4.22e-03 | 1.18e-01 | 9.95e-01 |
Signaling by Erythropoietin | 19 | 7.67e-01 | 8.16e-01 | 0.1690 | -0.111000 | -0.085100 | 0.010200 | -0.094400 | 4.05e-01 | 5.21e-01 | 9.38e-01 | 4.77e-01 |
PTEN Regulation | 127 | 9.07e-03 | 2.18e-02 | 0.1680 | -0.070800 | 0.084400 | 0.123000 | -0.034200 | 1.69e-01 | 1.02e-01 | 1.74e-02 | 5.07e-01 |
Intra-Golgi and retrograde Golgi-to-ER traffic | 148 | 1.78e-02 | 3.80e-02 | 0.1670 | -0.045500 | 0.130000 | 0.057200 | 0.075200 | 3.41e-01 | 6.68e-03 | 2.32e-01 | 1.15e-01 |
RUNX3 regulates NOTCH signaling | 13 | 9.49e-01 | 9.53e-01 | 0.1660 | 0.027300 | 0.080800 | 0.110000 | 0.091000 | 8.65e-01 | 6.14e-01 | 4.92e-01 | 5.70e-01 |
Cellular Senescence | 117 | 2.00e-01 | 2.75e-01 | 0.1660 | 0.073200 | 0.075200 | 0.104000 | 0.074600 | 1.72e-01 | 1.61e-01 | 5.16e-02 | 1.64e-01 |
Centrosome maturation | 71 | 7.94e-02 | 1.31e-01 | 0.1650 | 0.010600 | 0.092000 | -0.018900 | 0.135000 | 8.77e-01 | 1.81e-01 | 7.84e-01 | 4.99e-02 |
Recruitment of mitotic centrosome proteins and complexes | 71 | 7.94e-02 | 1.31e-01 | 0.1650 | 0.010600 | 0.092000 | -0.018900 | 0.135000 | 8.77e-01 | 1.81e-01 | 7.84e-01 | 4.99e-02 |
Pre-NOTCH Expression and Processing | 45 | 6.29e-01 | 6.98e-01 | 0.1640 | 0.085100 | -0.089900 | 0.063900 | 0.087200 | 3.24e-01 | 2.97e-01 | 4.59e-01 | 3.12e-01 |
Transcriptional Regulation by TP53 | 304 | 1.26e-04 | 5.65e-04 | 0.1630 | -0.059000 | 0.128000 | 0.081400 | -0.008030 | 7.90e-02 | 1.38e-04 | 1.54e-02 | 8.11e-01 |
Transport of small molecules | 406 | 4.07e-07 | 3.57e-06 | 0.1630 | 0.005860 | -0.136000 | -0.072700 | 0.051500 | 8.41e-01 | 3.24e-06 | 1.28e-02 | 7.79e-02 |
Interleukin-17 signaling | 61 | 1.62e-01 | 2.31e-01 | 0.1610 | -0.094600 | -0.098800 | 0.041100 | -0.074800 | 2.02e-01 | 1.83e-01 | 5.79e-01 | 3.13e-01 |
Metabolism of nucleotides | 74 | 2.64e-01 | 3.45e-01 | 0.1580 | 0.026600 | -0.151000 | -0.035500 | 0.013400 | 6.93e-01 | 2.49e-02 | 5.98e-01 | 8.43e-01 |
Organelle biogenesis and maintenance | 224 | 4.20e-04 | 1.61e-03 | 0.1580 | -0.051700 | 0.060000 | -0.136000 | -0.009180 | 1.85e-01 | 1.24e-01 | 4.83e-04 | 8.14e-01 |
RET signaling | 28 | 6.85e-01 | 7.47e-01 | 0.1570 | 0.070700 | -0.137000 | 0.016900 | -0.025200 | 5.18e-01 | 2.09e-01 | 8.77e-01 | 8.17e-01 |
RUNX1 interacts with co-factors whose precise effect on RUNX1 targets is not known | 36 | 2.87e-01 | 3.69e-01 | 0.1570 | 0.066500 | 0.060600 | 0.070000 | -0.108000 | 4.90e-01 | 5.30e-01 | 4.68e-01 | 2.61e-01 |
Aggrephagy | 16 | 8.24e-01 | 8.58e-01 | 0.1560 | -0.086100 | 0.047100 | 0.121000 | 0.015900 | 5.51e-01 | 7.44e-01 | 4.04e-01 | 9.12e-01 |
Synthesis of PIPs at the plasma membrane | 44 | 4.76e-01 | 5.57e-01 | 0.1560 | 0.032700 | 0.096000 | 0.014900 | 0.118000 | 7.08e-01 | 2.71e-01 | 8.64e-01 | 1.76e-01 |
RAF/MAP kinase cascade | 188 | 1.09e-04 | 4.92e-04 | 0.1560 | 0.028600 | -0.069100 | 0.130000 | -0.044400 | 5.01e-01 | 1.04e-01 | 2.30e-03 | 2.96e-01 |
MAPK1/MAPK3 signaling | 193 | 1.48e-04 | 6.48e-04 | 0.1550 | 0.030800 | -0.071300 | 0.130000 | -0.034500 | 4.63e-01 | 8.91e-02 | 1.96e-03 | 4.11e-01 |
RA biosynthesis pathway | 11 | 9.01e-01 | 9.19e-01 | 0.1550 | -0.037400 | -0.068100 | 0.061200 | 0.119000 | 8.30e-01 | 6.96e-01 | 7.25e-01 | 4.95e-01 |
RMTs methylate histone arginines | 28 | 5.72e-01 | 6.50e-01 | 0.1550 | -0.079300 | -0.103000 | 0.048200 | -0.068800 | 4.68e-01 | 3.48e-01 | 6.59e-01 | 5.29e-01 |
Toll Like Receptor 4 (TLR4) Cascade | 102 | 7.17e-02 | 1.21e-01 | 0.1530 | 0.039100 | -0.046400 | 0.139000 | 0.016200 | 4.97e-01 | 4.20e-01 | 1.54e-02 | 7.78e-01 |
Signaling by ERBB2 ECD mutants | 15 | 7.74e-01 | 8.20e-01 | 0.1530 | -0.121000 | -0.054500 | 0.025200 | 0.071100 | 4.18e-01 | 7.15e-01 | 8.66e-01 | 6.34e-01 |
ER to Golgi Anterograde Transport | 114 | 4.67e-02 | 8.61e-02 | 0.1520 | -0.092400 | 0.091000 | 0.041400 | 0.068000 | 8.91e-02 | 9.41e-02 | 4.47e-01 | 2.11e-01 |
MyD88-independent TLR4 cascade | 83 | 4.31e-02 | 8.04e-02 | 0.1520 | -0.041100 | -0.070200 | 0.126000 | -0.023000 | 5.18e-01 | 2.70e-01 | 4.73e-02 | 7.18e-01 |
TRIF(TICAM1)-mediated TLR4 signaling | 83 | 4.31e-02 | 8.04e-02 | 0.1520 | -0.041100 | -0.070200 | 0.126000 | -0.023000 | 5.18e-01 | 2.70e-01 | 4.73e-02 | 7.18e-01 |
MAPK targets/ Nuclear events mediated by MAP kinases | 31 | 7.07e-01 | 7.65e-01 | 0.1510 | -0.004840 | -0.125000 | -0.024700 | -0.081300 | 9.63e-01 | 2.29e-01 | 8.12e-01 | 4.34e-01 |
SARS-CoV-1 Infection | 40 | 4.49e-01 | 5.33e-01 | 0.1510 | -0.062000 | -0.021600 | 0.085300 | 0.105000 | 4.98e-01 | 8.14e-01 | 3.51e-01 | 2.50e-01 |
Signaling by FGFR in disease | 47 | 4.72e-01 | 5.55e-01 | 0.1500 | -0.101000 | 0.079500 | 0.071100 | -0.027500 | 2.31e-01 | 3.46e-01 | 3.99e-01 | 7.45e-01 |
Constitutive Signaling by Ligand-Responsive EGFR Cancer Variants | 17 | 8.91e-01 | 9.13e-01 | 0.1480 | -0.050000 | 0.076900 | 0.087800 | 0.076500 | 7.21e-01 | 5.83e-01 | 5.31e-01 | 5.85e-01 |
Signaling by Ligand-Responsive EGFR Variants in Cancer | 17 | 8.91e-01 | 9.13e-01 | 0.1480 | -0.050000 | 0.076900 | 0.087800 | 0.076500 | 7.21e-01 | 5.83e-01 | 5.31e-01 | 5.85e-01 |
Hedgehog 'on' state | 71 | 1.84e-01 | 2.56e-01 | 0.1480 | -0.001990 | 0.048400 | 0.138000 | -0.018200 | 9.77e-01 | 4.81e-01 | 4.40e-02 | 7.92e-01 |
TNF signaling | 34 | 5.59e-01 | 6.37e-01 | 0.1480 | -0.036600 | -0.123000 | -0.000790 | 0.073900 | 7.12e-01 | 2.16e-01 | 9.94e-01 | 4.56e-01 |
Estrogen-dependent nuclear events downstream of ESR-membrane signaling | 19 | 8.68e-01 | 8.95e-01 | 0.1480 | -0.009410 | -0.101000 | -0.030800 | -0.103000 | 9.43e-01 | 4.46e-01 | 8.16e-01 | 4.39e-01 |
PI3K/AKT Signaling in Cancer | 65 | 3.11e-01 | 3.93e-01 | 0.1470 | 0.047700 | -0.133000 | 0.033200 | -0.019800 | 5.07e-01 | 6.39e-02 | 6.44e-01 | 7.83e-01 |
Transcriptional regulation by RUNX2 | 99 | 1.82e-01 | 2.55e-01 | 0.1460 | 0.012300 | -0.002200 | 0.138000 | 0.047100 | 8.33e-01 | 9.70e-01 | 1.80e-02 | 4.20e-01 |
Synthesis of PC | 21 | 9.02e-01 | 9.19e-01 | 0.1450 | 0.004070 | -0.095300 | -0.096000 | -0.053200 | 9.74e-01 | 4.50e-01 | 4.47e-01 | 6.73e-01 |
Oncogenic MAPK signaling | 68 | 2.51e-01 | 3.33e-01 | 0.1440 | 0.036200 | -0.110000 | 0.085200 | -0.001470 | 6.06e-01 | 1.16e-01 | 2.25e-01 | 9.83e-01 |
IRS-related events triggered by IGF1R | 29 | 7.13e-01 | 7.70e-01 | 0.1420 | -0.139000 | 0.001660 | 0.018300 | -0.023500 | 1.95e-01 | 9.88e-01 | 8.65e-01 | 8.27e-01 |
Transcriptional regulation by RUNX1 | 139 | 6.78e-02 | 1.15e-01 | 0.1420 | -0.015600 | 0.082300 | 0.114000 | 0.002200 | 7.51e-01 | 9.51e-02 | 2.04e-02 | 9.64e-01 |
Base-Excision Repair, AP Site Formation | 16 | 9.20e-01 | 9.34e-01 | 0.1410 | 0.099000 | 0.031500 | -0.000309 | 0.095500 | 4.93e-01 | 8.27e-01 | 9.98e-01 | 5.09e-01 |
FLT3 Signaling | 199 | 2.29e-04 | 9.31e-04 | 0.1410 | 0.005000 | -0.068300 | 0.109000 | -0.057800 | 9.04e-01 | 9.84e-02 | 8.39e-03 | 1.62e-01 |
Signaling by FGFR4 | 29 | 7.68e-01 | 8.16e-01 | 0.1400 | 0.060800 | 0.040800 | 0.120000 | 0.004900 | 5.71e-01 | 7.04e-01 | 2.65e-01 | 9.64e-01 |
Phase II - Conjugation of compounds | 46 | 7.16e-01 | 7.72e-01 | 0.1400 | -0.038100 | -0.067000 | -0.111000 | -0.037500 | 6.55e-01 | 4.32e-01 | 1.93e-01 | 6.61e-01 |
Metabolism of steroids | 93 | 2.66e-01 | 3.47e-01 | 0.1400 | -0.091200 | -0.071200 | -0.011600 | -0.077300 | 1.30e-01 | 2.37e-01 | 8.47e-01 | 1.99e-01 |
Toll Like Receptor 3 (TLR3) Cascade | 82 | 8.31e-02 | 1.36e-01 | 0.1390 | -0.042400 | -0.071300 | 0.109000 | -0.024900 | 5.08e-01 | 2.65e-01 | 8.79e-02 | 6.97e-01 |
MAPK family signaling cascades | 224 | 5.87e-04 | 2.11e-03 | 0.1380 | 0.037300 | -0.066300 | 0.113000 | -0.023900 | 3.39e-01 | 8.89e-02 | 3.75e-03 | 5.41e-01 |
PIP3 activates AKT signaling | 211 | 4.77e-03 | 1.29e-02 | 0.1370 | -0.008250 | 0.045900 | 0.129000 | -0.008350 | 8.37e-01 | 2.53e-01 | 1.34e-03 | 8.35e-01 |
Insulin receptor signalling cascade | 32 | 6.91e-01 | 7.51e-01 | 0.1360 | -0.120000 | 0.038000 | 0.050000 | -0.001800 | 2.40e-01 | 7.10e-01 | 6.25e-01 | 9.86e-01 |
Transcriptional Regulation by VENTX | 34 | 5.34e-01 | 6.13e-01 | 0.1350 | 0.050900 | 0.072600 | -0.068000 | 0.074900 | 6.07e-01 | 4.64e-01 | 4.93e-01 | 4.50e-01 |
Oxidative Stress Induced Senescence | 59 | 4.59e-01 | 5.43e-01 | 0.1340 | 0.062300 | 0.069200 | 0.095900 | -0.010600 | 4.09e-01 | 3.59e-01 | 2.03e-01 | 8.88e-01 |
Signaling by ERBB2 in Cancer | 18 | 9.28e-01 | 9.42e-01 | 0.1340 | -0.003380 | -0.011300 | 0.101000 | 0.087100 | 9.80e-01 | 9.34e-01 | 4.59e-01 | 5.23e-01 |
Gastrin-CREB signalling pathway via PKC and MAPK | 15 | 9.39e-01 | 9.48e-01 | 0.1340 | 0.109000 | 0.000310 | 0.076100 | 0.012900 | 4.64e-01 | 9.98e-01 | 6.10e-01 | 9.31e-01 |
Phospholipid metabolism | 147 | 1.63e-02 | 3.50e-02 | 0.1340 | 0.049500 | -0.039600 | -0.074500 | 0.091100 | 3.02e-01 | 4.09e-01 | 1.20e-01 | 5.76e-02 |
HDACs deacetylate histones | 30 | 7.95e-01 | 8.36e-01 | 0.1330 | -0.034600 | 0.094700 | 0.006780 | -0.086500 | 7.43e-01 | 3.70e-01 | 9.49e-01 | 4.12e-01 |
Cargo recognition for clathrin-mediated endocytosis | 72 | 5.21e-01 | 6.02e-01 | 0.1320 | 0.028100 | 0.111000 | 0.063400 | 0.022700 | 6.81e-01 | 1.05e-01 | 3.53e-01 | 7.39e-01 |
Signaling by NTRK2 (TRKB) | 21 | 9.47e-01 | 9.53e-01 | 0.1320 | 0.034100 | 0.010200 | 0.073200 | 0.104000 | 7.87e-01 | 9.36e-01 | 5.62e-01 | 4.11e-01 |
Constitutive Signaling by EGFRvIII | 15 | 8.78e-01 | 9.02e-01 | 0.1290 | -0.070900 | 0.036300 | 0.019000 | 0.099500 | 6.35e-01 | 8.08e-01 | 8.99e-01 | 5.05e-01 |
Signaling by EGFRvIII in Cancer | 15 | 8.78e-01 | 9.02e-01 | 0.1290 | -0.070900 | 0.036300 | 0.019000 | 0.099500 | 6.35e-01 | 8.08e-01 | 8.99e-01 | 5.05e-01 |
Metabolism of proteins | 1396 | 4.95e-13 | 1.27e-11 | 0.1280 | -0.074200 | 0.080700 | 0.064300 | 0.015600 | 7.77e-06 | 1.15e-06 | 1.06e-04 | 3.46e-01 |
NOTCH4 Intracellular Domain Regulates Transcription | 15 | 9.62e-01 | 9.65e-01 | 0.1280 | 0.008660 | 0.002240 | 0.108000 | 0.068400 | 9.54e-01 | 9.88e-01 | 4.70e-01 | 6.46e-01 |
Regulation of beta-cell development | 17 | 8.78e-01 | 9.02e-01 | 0.1240 | -0.068600 | -0.086600 | 0.044600 | 0.033300 | 6.24e-01 | 5.37e-01 | 7.51e-01 | 8.12e-01 |
IGF1R signaling cascade | 30 | 7.70e-01 | 8.17e-01 | 0.1230 | -0.112000 | 0.028500 | 0.040600 | 0.010300 | 2.88e-01 | 7.87e-01 | 7.01e-01 | 9.22e-01 |
Generic Transcription Pathway | 775 | 1.42e-06 | 1.06e-05 | 0.1220 | -0.050700 | 0.093100 | 0.034900 | -0.050300 | 1.87e-02 | 1.56e-05 | 1.06e-01 | 1.96e-02 |
COPI-mediated anterograde transport | 73 | 3.57e-01 | 4.43e-01 | 0.1200 | -0.050500 | 0.028000 | 0.039800 | 0.097100 | 4.56e-01 | 6.80e-01 | 5.57e-01 | 1.52e-01 |
NOTCH1 Intracellular Domain Regulates Transcription | 42 | 5.56e-01 | 6.35e-01 | 0.1200 | -0.078200 | -0.042300 | 0.077800 | -0.018800 | 3.81e-01 | 6.36e-01 | 3.84e-01 | 8.33e-01 |
MyD88 dependent cascade initiated on endosome | 77 | 2.62e-01 | 3.44e-01 | 0.1140 | -0.004450 | -0.047600 | 0.099000 | -0.029200 | 9.46e-01 | 4.71e-01 | 1.34e-01 | 6.59e-01 |
Toll Like Receptor 7/8 (TLR7/8) Cascade | 77 | 2.62e-01 | 3.44e-01 | 0.1140 | -0.004450 | -0.047600 | 0.099000 | -0.029200 | 9.46e-01 | 4.71e-01 | 1.34e-01 | 6.59e-01 |
Vesicle-mediated transport | 506 | 7.89e-04 | 2.76e-03 | 0.1140 | -0.002220 | 0.059700 | 0.034800 | 0.090200 | 9.33e-01 | 2.32e-02 | 1.85e-01 | 6.06e-04 |
Signaling by ERBB4 | 37 | 7.99e-01 | 8.38e-01 | 0.1130 | 0.096700 | 0.011200 | -0.022100 | 0.053400 | 3.09e-01 | 9.06e-01 | 8.16e-01 | 5.74e-01 |
TRAF6 mediated induction of NFkB and MAP kinases upon TLR7/8 or 9 activation | 76 | 2.76e-01 | 3.57e-01 | 0.1110 | -0.017500 | -0.050900 | 0.090100 | -0.036200 | 7.93e-01 | 4.44e-01 | 1.75e-01 | 5.86e-01 |
MyD88 cascade initiated on plasma membrane | 75 | 3.00e-01 | 3.83e-01 | 0.1110 | -0.027600 | -0.067200 | 0.070100 | -0.045900 | 6.80e-01 | 3.15e-01 | 2.95e-01 | 4.93e-01 |
Toll Like Receptor 10 (TLR10) Cascade | 75 | 3.00e-01 | 3.83e-01 | 0.1110 | -0.027600 | -0.067200 | 0.070100 | -0.045900 | 6.80e-01 | 3.15e-01 | 2.95e-01 | 4.93e-01 |
Toll Like Receptor 5 (TLR5) Cascade | 75 | 3.00e-01 | 3.83e-01 | 0.1110 | -0.027600 | -0.067200 | 0.070100 | -0.045900 | 6.80e-01 | 3.15e-01 | 2.95e-01 | 4.93e-01 |
Signaling by Type 1 Insulin-like Growth Factor 1 Receptor (IGF1R) | 31 | 8.17e-01 | 8.54e-01 | 0.1110 | -0.076800 | 0.026900 | 0.062400 | 0.042200 | 4.60e-01 | 7.96e-01 | 5.48e-01 | 6.85e-01 |
Membrane Trafficking | 484 | 7.76e-04 | 2.73e-03 | 0.1090 | -0.031000 | 0.069200 | 0.028500 | 0.072800 | 2.48e-01 | 1.00e-02 | 2.89e-01 | 6.76e-03 |
FRS-mediated FGFR1 signaling | 12 | 9.38e-01 | 9.48e-01 | 0.1060 | 0.054300 | 0.003670 | 0.060900 | -0.067200 | 7.45e-01 | 9.82e-01 | 7.15e-01 | 6.87e-01 |
Signaling by NOTCH | 148 | 2.65e-01 | 3.46e-01 | 0.1040 | 0.007420 | -0.060700 | 0.074400 | 0.039300 | 8.77e-01 | 2.04e-01 | 1.19e-01 | 4.11e-01 |
Signaling by ERBB2 KD Mutants | 17 | 9.39e-01 | 9.48e-01 | 0.1040 | -0.040400 | -0.061300 | 0.050700 | 0.052800 | 7.73e-01 | 6.62e-01 | 7.18e-01 | 7.06e-01 |
NOD1/2 Signaling Pathway | 27 | 8.97e-01 | 9.18e-01 | 0.1030 | -0.011700 | -0.097200 | 0.031000 | 0.000116 | 9.16e-01 | 3.82e-01 | 7.81e-01 | 9.99e-01 |
Post-translational protein modification | 996 | 4.14e-05 | 2.04e-04 | 0.1010 | -0.026200 | 0.061500 | 0.061200 | 0.045300 | 1.73e-01 | 1.38e-03 | 1.45e-03 | 1.85e-02 |
Intracellular signaling by second messengers | 243 | 3.97e-02 | 7.51e-02 | 0.0998 | 0.013400 | -0.011000 | 0.098200 | -0.003550 | 7.21e-01 | 7.70e-01 | 8.76e-03 | 9.25e-01 |
Toll Like Receptor 9 (TLR9) Cascade | 80 | 3.92e-01 | 4.74e-01 | 0.0987 | -0.032200 | -0.023200 | 0.087200 | -0.023500 | 6.20e-01 | 7.21e-01 | 1.78e-01 | 7.17e-01 |
Signaling by NOTCH1 | 62 | 8.86e-01 | 9.10e-01 | 0.0983 | 0.060900 | -0.037500 | 0.034700 | 0.057800 | 4.08e-01 | 6.11e-01 | 6.37e-01 | 4.32e-01 |
Downstream signaling of activated FGFR1 | 19 | 9.42e-01 | 9.48e-01 | 0.0977 | -0.004830 | 0.035800 | 0.088000 | -0.022200 | 9.71e-01 | 7.87e-01 | 5.07e-01 | 8.67e-01 |
Metabolism of lipids | 489 | 8.64e-03 | 2.09e-02 | 0.0957 | -0.018200 | -0.066400 | -0.066100 | 0.007150 | 4.97e-01 | 1.30e-02 | 1.35e-02 | 7.89e-01 |
MyD88:MAL(TIRAP) cascade initiated on plasma membrane | 81 | 4.21e-01 | 5.04e-01 | 0.0954 | 0.009180 | -0.054600 | 0.069900 | -0.034000 | 8.87e-01 | 3.97e-01 | 2.78e-01 | 5.98e-01 |
Toll Like Receptor 2 (TLR2) Cascade | 81 | 4.21e-01 | 5.04e-01 | 0.0954 | 0.009180 | -0.054600 | 0.069900 | -0.034000 | 8.87e-01 | 3.97e-01 | 2.78e-01 | 5.98e-01 |
Toll Like Receptor TLR1:TLR2 Cascade | 81 | 4.21e-01 | 5.04e-01 | 0.0954 | 0.009180 | -0.054600 | 0.069900 | -0.034000 | 8.87e-01 | 3.97e-01 | 2.78e-01 | 5.98e-01 |
Toll Like Receptor TLR6:TLR2 Cascade | 81 | 4.21e-01 | 5.04e-01 | 0.0954 | 0.009180 | -0.054600 | 0.069900 | -0.034000 | 8.87e-01 | 3.97e-01 | 2.78e-01 | 5.98e-01 |
Adaptive Immune System | 476 | 1.06e-02 | 2.49e-02 | 0.0935 | -0.034600 | 0.025200 | 0.068800 | 0.046800 | 2.02e-01 | 3.53e-01 | 1.11e-02 | 8.40e-02 |
Deactivation of the beta-catenin transactivating complex | 32 | 9.50e-01 | 9.54e-01 | 0.0933 | 0.018600 | -0.044600 | 0.047000 | 0.064500 | 8.56e-01 | 6.63e-01 | 6.46e-01 | 5.28e-01 |
Diseases of signal transduction by growth factor receptors and second messengers | 304 | 1.87e-02 | 3.95e-02 | 0.0887 | -0.034600 | -0.025900 | 0.077000 | -0.008660 | 3.04e-01 | 4.40e-01 | 2.20e-02 | 7.97e-01 |
Hedgehog 'off' state | 87 | 5.23e-01 | 6.04e-01 | 0.0878 | -0.031300 | 0.020300 | 0.072100 | -0.033500 | 6.14e-01 | 7.44e-01 | 2.46e-01 | 5.90e-01 |
Beta-catenin independent WNT signaling | 117 | 6.20e-01 | 6.95e-01 | 0.0877 | 0.038700 | -0.008010 | 0.076900 | 0.015000 | 4.71e-01 | 8.81e-01 | 1.52e-01 | 7.80e-01 |
FRS-mediated FGFR4 signaling | 12 | 9.89e-01 | 9.91e-01 | 0.0876 | 0.016500 | -0.056000 | 0.061600 | 0.021700 | 9.21e-01 | 7.37e-01 | 7.12e-01 | 8.96e-01 |
Downstream signaling of activated FGFR2 | 17 | 9.66e-01 | 9.69e-01 | 0.0830 | -0.047900 | -0.008300 | 0.067000 | -0.006740 | 7.33e-01 | 9.53e-01 | 6.33e-01 | 9.62e-01 |
Signaling by WNT | 202 | 2.27e-01 | 3.07e-01 | 0.0784 | -0.042400 | 0.014900 | 0.057100 | -0.029400 | 3.01e-01 | 7.17e-01 | 1.64e-01 | 4.73e-01 |
Signaling by Hedgehog | 114 | 7.17e-01 | 7.72e-01 | 0.0765 | 0.041500 | 0.004510 | 0.063900 | 0.004820 | 4.45e-01 | 9.34e-01 | 2.40e-01 | 9.29e-01 |
Constitutive Signaling by NOTCH1 HD+PEST Domain Mutants | 50 | 9.41e-01 | 9.48e-01 | 0.0741 | 0.030200 | -0.067500 | -0.005640 | 0.000637 | 7.13e-01 | 4.10e-01 | 9.45e-01 | 9.94e-01 |
Constitutive Signaling by NOTCH1 PEST Domain Mutants | 50 | 9.41e-01 | 9.48e-01 | 0.0741 | 0.030200 | -0.067500 | -0.005640 | 0.000637 | 7.13e-01 | 4.10e-01 | 9.45e-01 | 9.94e-01 |
Signaling by NOTCH1 HD+PEST Domain Mutants in Cancer | 50 | 9.41e-01 | 9.48e-01 | 0.0741 | 0.030200 | -0.067500 | -0.005640 | 0.000637 | 7.13e-01 | 4.10e-01 | 9.45e-01 | 9.94e-01 |
Signaling by NOTCH1 PEST Domain Mutants in Cancer | 50 | 9.41e-01 | 9.48e-01 | 0.0741 | 0.030200 | -0.067500 | -0.005640 | 0.000637 | 7.13e-01 | 4.10e-01 | 9.45e-01 | 9.94e-01 |
Signaling by NOTCH1 in Cancer | 50 | 9.41e-01 | 9.48e-01 | 0.0741 | 0.030200 | -0.067500 | -0.005640 | 0.000637 | 7.13e-01 | 4.10e-01 | 9.45e-01 | 9.94e-01 |
Signaling by Nuclear Receptors | 175 | 6.11e-01 | 6.88e-01 | 0.0707 | -0.019400 | 0.058500 | 0.022000 | -0.026700 | 6.60e-01 | 1.83e-01 | 6.17e-01 | 5.44e-01 |
CD28 dependent PI3K/Akt signaling | 17 | 9.92e-01 | 9.93e-01 | 0.0636 | -0.021900 | -0.055200 | 0.009660 | -0.020700 | 8.76e-01 | 6.94e-01 | 9.45e-01 | 8.83e-01 |
Downstream signaling of activated FGFR4 | 17 | 9.93e-01 | 9.93e-01 | 0.0629 | -0.061900 | -0.006840 | 0.000800 | -0.009200 | 6.59e-01 | 9.61e-01 | 9.95e-01 | 9.48e-01 |
RAB GEFs exchange GTP for GDP on RABs | 81 | 9.16e-01 | 9.32e-01 | 0.0628 | 0.016600 | 0.034000 | 0.009840 | 0.049200 | 7.96e-01 | 5.98e-01 | 8.79e-01 | 4.45e-01 |
Rab regulation of trafficking | 110 | 9.37e-01 | 9.48e-01 | 0.0454 | -0.032000 | 0.020700 | 0.023200 | 0.008320 | 5.64e-01 | 7.08e-01 | 6.75e-01 | 8.81e-01 |
Interleukin-10 signaling
metric | value |
---|---|
setSize | 11 |
pMANOVA | 1.12e-06 |
p.adjustMANOVA | 8.69e-06 |
s.dist | 1.31 |
s.FSHD | 0.736 |
s.hu_model | -0.252 |
s.Watt_m | 0.748 |
s.Jones_m | 0.742 |
p.FSHD | 2.34e-05 |
p.hu_model | 0.148 |
p.Watt_m | 1.74e-05 |
p.Jones_m | 2.03e-05 |
Gene | Watt_m | Jones_m |
---|---|---|
TIMP1 | 5188 | 4988 |
TNFRSF1B | 4548 | 5115 |
STAT3 | 5013 | 4348 |
CCL2 | 5061 | 3964 |
ICAM1 | 4128 | 4600 |
CSF1 | 4312 | 3814 |
TNFRSF1A | 3322 | 4778 |
IL1R1 | 3866 | 4015 |
IL10RB | 3206 | 4242 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
CCL2 | 4787 | 2597 | 5061 | 3964 |
CSF1 | 4653 | -4188 | 4312 | 3814 |
ICAM1 | 4641 | 1044 | 4128 | 4600 |
IL10RB | 4957 | 1225 | 3206 | 4242 |
IL1R1 | 4382 | -2979 | 3866 | 4015 |
JAK1 | 1002 | -1843 | 4184 | -1810 |
STAT3 | 850 | -3836 | 5013 | 4348 |
TIMP1 | 4933 | -1301 | 5188 | 4988 |
TNFRSF1A | 3907 | -4606 | 3322 | 4778 |
TNFRSF1B | 4174 | -866 | 4548 | 5115 |
TYK2 | 2357 | -3081 | -49 | 4512 |
Citric acid cycle (TCA cycle)
metric | value |
---|---|
setSize | 21 |
pMANOVA | 6.96e-09 |
p.adjustMANOVA | 8.14e-08 |
s.dist | 1.1 |
s.FSHD | -0.669 |
s.hu_model | -0.243 |
s.Watt_m | -0.597 |
s.Jones_m | -0.585 |
p.FSHD | 1.09e-07 |
p.hu_model | 0.0543 |
p.Watt_m | 2.21e-06 |
p.Jones_m | 3.42e-06 |
Gene | FSHD | Watt_m |
---|---|---|
DLD | -4923 | -4683 |
IDH3A | -5238 | -3782 |
SUCLA2 | -4446 | -4329 |
CS | -5372 | -3526 |
FAHD1 | -4055 | -4256 |
ACO2 | -3871 | -4378 |
SUCLG2 | -3363 | -4245 |
SDHA | -3097 | -4539 |
SDHC | -4613 | -2969 |
FH | -4577 | -2865 |
DLST | -3558 | -3488 |
SDHB | -3231 | -3667 |
NNT | -4770 | -2350 |
OGDH | -3051 | -3610 |
IDH2 | -2867 | -3813 |
IDH3B | -4107 | -2153 |
SUCLG1 | -3825 | -2116 |
ME3 | -2144 | -3679 |
MDH2 | -2694 | -2826 |
IDH3G | -896 | -3096 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
ACO2 | -3871 | -3773 | -4378 | -3916 |
CS | -5372 | 3624 | -3526 | -4669 |
DLD | -4923 | 1175 | -4683 | -2906 |
DLST | -3558 | -322 | -3488 | -1773 |
FAHD1 | -4055 | -1748 | -4256 | -2464 |
FH | -4577 | 284 | -2865 | -3264 |
IDH2 | -2867 | -5154 | -3813 | -2755 |
IDH3A | -5238 | -2126 | -3782 | -4519 |
IDH3B | -4107 | -2843 | -2153 | -4270 |
IDH3G | -896 | -4125 | -3096 | -3697 |
MDH2 | -2694 | -4307 | -2826 | -2711 |
ME2 | -3037 | -1766 | 3484 | 4800 |
ME3 | -2144 | 4173 | -3679 | -5302 |
NNT | -4770 | -3281 | -2350 | -261 |
OGDH | -3051 | -5206 | -3610 | -3542 |
SDHA | -3097 | -4713 | -4539 | -4393 |
SDHB | -3231 | 427 | -3667 | -3677 |
SDHC | -4613 | -3665 | -2969 | -3035 |
SUCLA2 | -4446 | 1500 | -4329 | -3679 |
SUCLG1 | -3825 | -31 | -2116 | -5153 |
SUCLG2 | -3363 | -1153 | -4245 | -4203 |
Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell
metric | value |
---|---|
setSize | 13 |
pMANOVA | 1.14e-05 |
p.adjustMANOVA | 6.63e-05 |
s.dist | 1.05 |
s.FSHD | 0.767 |
s.hu_model | 0.113 |
s.Watt_m | 0.324 |
s.Jones_m | 0.622 |
p.FSHD | 1.66e-06 |
p.hu_model | 0.481 |
p.Watt_m | 0.043 |
p.Jones_m | 0.000102 |
Gene | FSHD | Jones_m |
---|---|---|
IFITM1 | 5068 | 5021 |
ITGB2 | 4906 | 5102 |
VCAM1 | 4924 | 4588 |
ICAM1 | 4641 | 4600 |
C3 | 4737 | 4049 |
CD81 | 4123 | 4155 |
COLEC12 | 4753 | 3221 |
B2M | 3754 | 3232 |
NPDC1 | 4308 | 1392 |
ITGB1 | 891 | 4783 |
CD34 | 3598 | 1165 |
ITGA4 | 2431 | 1443 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
B2M | 3754 | -727 | 1576 | 3232 |
C3 | 4737 | 4276 | 1818 | 4049 |
CD34 | 3598 | 847 | 882 | 1165 |
CD81 | 4123 | -4615 | 886 | 4155 |
COLEC12 | 4753 | 4226 | 45 | 3221 |
ICAM1 | 4641 | 1044 | 4128 | 4600 |
ICAM2 | 1999 | -1485 | -3439 | -639 |
IFITM1 | 5068 | 1557 | 4767 | 5021 |
ITGA4 | 2431 | -2840 | -5085 | 1443 |
ITGB1 | 891 | 945 | 4567 | 4783 |
ITGB2 | 4906 | -107 | 4945 | 5102 |
NPDC1 | 4308 | -2095 | 1815 | 1392 |
VCAM1 | 4924 | 2842 | 4665 | 4588 |
Branched-chain amino acid catabolism
metric | value |
---|---|
setSize | 20 |
pMANOVA | 9.57e-07 |
p.adjustMANOVA | 7.69e-06 |
s.dist | 1 |
s.FSHD | -0.612 |
s.hu_model | -0.074 |
s.Watt_m | -0.531 |
s.Jones_m | -0.586 |
p.FSHD | 2.18e-06 |
p.hu_model | 0.567 |
p.Watt_m | 3.92e-05 |
p.Jones_m | 5.68e-06 |
Gene | FSHD | Jones_m |
---|---|---|
ALDH6A1 | -5168 | -5042 |
BCKDHB | -4880 | -5232 |
MCCC2 | -4989 | -4935 |
HIBADH | -5132 | -4793 |
BCKDK | -4926 | -4871 |
AUH | -4887 | -4708 |
DBT | -4678 | -4844 |
MCCC1 | -4819 | -4559 |
ACADSB | -5075 | -4291 |
BCAT2 | -3351 | -5043 |
DLD | -4923 | -2906 |
HIBCH | -4290 | -3311 |
IVD | -2675 | -5071 |
ACAT1 | -3241 | -3742 |
SLC25A44 | -2647 | -2544 |
ECHS1 | -1230 | -2015 |
PPM1K | -849 | -2608 |
ACAD8 | -3612 | -184 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
ACAD8 | -3612 | -1244 | -4983 | -184 |
ACADSB | -5075 | 3061 | -4881 | -4291 |
ACAT1 | -3241 | 466 | -1915 | -3742 |
ALDH6A1 | -5168 | -1380 | -5181 | -5042 |
AUH | -4887 | -1278 | -3145 | -4708 |
BCAT1 | 3603 | -3502 | 4012 | 4365 |
BCAT2 | -3351 | -4129 | -4904 | -5043 |
BCKDHB | -4880 | -4187 | -2605 | -5232 |
BCKDK | -4926 | -4633 | -3584 | -4871 |
DBT | -4678 | 1983 | 5157 | -4844 |
DLD | -4923 | 1175 | -4683 | -2906 |
ECHS1 | -1230 | -3845 | -4723 | -2015 |
HIBADH | -5132 | -3981 | -2535 | -4793 |
HIBCH | -4290 | 483 | -5021 | -3311 |
HSD17B10 | -201 | -1178 | -480 | 3967 |
IVD | -2675 | -4745 | -5058 | -5071 |
MCCC1 | -4819 | 3980 | -4638 | -4559 |
MCCC2 | -4989 | 2184 | -4913 | -4935 |
PPM1K | -849 | 2258 | -5158 | -2608 |
SLC25A44 | -2647 | 4803 | 2415 | -2544 |
Pyruvate metabolism and Citric Acid (TCA) cycle
metric | value |
---|---|
setSize | 49 |
pMANOVA | 3.58e-17 |
p.adjustMANOVA | 1.69e-15 |
s.dist | 0.99 |
s.FSHD | -0.571 |
s.hu_model | -0.263 |
s.Watt_m | -0.559 |
s.Jones_m | -0.522 |
p.FSHD | 4.77e-12 |
p.hu_model | 0.00146 |
p.Watt_m | 1.28e-11 |
p.Jones_m | 2.63e-10 |
Gene | FSHD | Watt_m |
---|---|---|
PDP1 | -5181 | -4550 |
DLD | -4923 | -4683 |
IDH3A | -5238 | -3782 |
SUCLA2 | -4446 | -4329 |
ME1 | -4907 | -3918 |
CS | -5372 | -3526 |
VDAC1 | -3918 | -4553 |
RXRA | -4228 | -4147 |
FAHD1 | -4055 | -4256 |
GLO1 | -4424 | -3844 |
ACO2 | -3871 | -4378 |
DLAT | -4452 | -3783 |
PDK1 | -5017 | -3198 |
L2HGDH | -4395 | -3601 |
SLC16A3 | -3677 | -4114 |
SUCLG2 | -3363 | -4245 |
SDHA | -3097 | -4539 |
SDHC | -4613 | -2969 |
MPC1 | -4270 | -3199 |
FH | -4577 | -2865 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
ACO2 | -3871 | -3773 | -4378 | -3916 |
ADHFE1 | -5136 | -3988 | -2451 | -4869 |
BSG | -1369 | -2217 | -2093 | -5147 |
CS | -5372 | 3624 | -3526 | -4669 |
D2HGDH | -1446 | -4830 | -5276 | -4528 |
DLAT | -4452 | -1933 | -3783 | -2572 |
DLD | -4923 | 1175 | -4683 | -2906 |
DLST | -3558 | -322 | -3488 | -1773 |
FAHD1 | -4055 | -1748 | -4256 | -2464 |
FH | -4577 | 284 | -2865 | -3264 |
GLO1 | -4424 | -675 | -3844 | -4433 |
GSTZ1 | -2505 | -2039 | -4578 | -3972 |
HAGH | -2311 | -4451 | 1234 | -3032 |
IDH2 | -2867 | -5154 | -3813 | -2755 |
IDH3A | -5238 | -2126 | -3782 | -4519 |
IDH3B | -4107 | -2843 | -2153 | -4270 |
IDH3G | -896 | -4125 | -3096 | -3697 |
L2HGDH | -4395 | -261 | -3601 | -5228 |
LDHA | -341 | -3208 | -2881 | -3674 |
LDHB | -1357 | -1472 | -1954 | -1554 |
MDH2 | -2694 | -4307 | -2826 | -2711 |
ME1 | -4907 | 1772 | -3918 | -4943 |
ME2 | -3037 | -1766 | 3484 | 4800 |
ME3 | -2144 | 4173 | -3679 | -5302 |
MPC1 | -4270 | -3634 | -3199 | 4240 |
MPC2 | -2780 | 819 | -1719 | -3784 |
NNT | -4770 | -3281 | -2350 | -261 |
OGDH | -3051 | -5206 | -3610 | -3542 |
PDHA1 | -2764 | -2373 | -4403 | -777 |
PDHB | -3237 | -133 | -3954 | -943 |
PDHX | -2958 | -126 | -3831 | -4229 |
PDK1 | -5017 | 4559 | -3198 | -4230 |
PDK2 | -3728 | -5386 | -3496 | -5057 |
PDK3 | 3897 | 4705 | 4816 | 4812 |
PDK4 | 2105 | -708 | -5180 | -789 |
PDP1 | -5181 | -2146 | -4550 | -4820 |
PDP2 | -4664 | -2585 | -2415 | -2584 |
PDPR | -614 | -629 | -4776 | 2790 |
PPARD | -1449 | -4159 | -2316 | -2644 |
RXRA | -4228 | -5455 | -4147 | -5038 |
SDHA | -3097 | -4713 | -4539 | -4393 |
SDHB | -3231 | 427 | -3667 | -3677 |
SDHC | -4613 | -3665 | -2969 | -3035 |
SLC16A1 | -2731 | -975 | 5026 | 1675 |
SLC16A3 | -3677 | -4691 | -4114 | 22 |
SUCLA2 | -4446 | 1500 | -4329 | -3679 |
SUCLG1 | -3825 | -31 | -2116 | -5153 |
SUCLG2 | -3363 | -1153 | -4245 | -4203 |
VDAC1 | -3918 | -2871 | -4553 | -5178 |
Signal regulatory protein family interactions
metric | value |
---|---|
setSize | 10 |
pMANOVA | 0.000638 |
p.adjustMANOVA | 0.00226 |
s.dist | 0.988 |
s.FSHD | 0.544 |
s.hu_model | -0.412 |
s.Watt_m | 0.507 |
s.Jones_m | 0.504 |
p.FSHD | 0.00292 |
p.hu_model | 0.0242 |
p.Watt_m | 0.00547 |
p.Jones_m | 0.00577 |
Gene | FSHD | Watt_m |
---|---|---|
SIRPA | 5077 | 4178 |
PTPN6 | 3645 | 4751 |
PTK2B | 3738 | 3819 |
FYB | 3409 | 3446 |
GRB2 | 2101 | 4449 |
CD47 | 3471 | 2654 |
SRC | 5021 | 1364 |
SKAP2 | 1349 | 3730 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
CD47 | 3471 | -2154 | 2654 | 4552 |
FYB | 3409 | -2205 | 3446 | 5133 |
GRB2 | 2101 | -3999 | 4449 | 3 |
PTK2 | 692 | -2465 | -1494 | -4001 |
PTK2B | 3738 | -2429 | 3819 | 4345 |
PTPN11 | -1703 | -1554 | -660 | -1108 |
PTPN6 | 3645 | -920 | 4751 | 5055 |
SIRPA | 5077 | -5563 | 4178 | 5226 |
SKAP2 | 1349 | 511 | 3730 | 4714 |
SRC | 5021 | -3860 | 1364 | 2269 |
Glyoxylate metabolism and glycine degradation
metric | value |
---|---|
setSize | 20 |
pMANOVA | 4.39e-07 |
p.adjustMANOVA | 3.83e-06 |
s.dist | 0.985 |
s.FSHD | -0.669 |
s.hu_model | -0.172 |
s.Watt_m | -0.511 |
s.Jones_m | -0.481 |
p.FSHD | 2.24e-07 |
p.hu_model | 0.183 |
p.Watt_m | 7.56e-05 |
p.Jones_m | 0.000198 |
Gene | FSHD | Watt_m |
---|---|---|
DLD | -4923 | -4683 |
LIAS | -4836 | -4645 |
DHTKD1 | -5034 | -4064 |
GRHPR | -4445 | -3989 |
DLAT | -4452 | -3783 |
PXMP2 | -4332 | -3793 |
PDHB | -3237 | -3954 |
BCKDHB | -4880 | -2605 |
DLST | -3558 | -3488 |
ALDH4A1 | -3609 | -3426 |
PDHA1 | -2764 | -4403 |
LIPT2 | -4571 | -2613 |
PDHX | -2958 | -3831 |
OGDH | -3051 | -3610 |
NDUFAB1 | -3229 | -3221 |
GOT2 | -3182 | -3058 |
DDO | -1496 | -4307 |
GCSH | -2911 | -1027 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
ALDH4A1 | -3609 | -2272 | -3426 | -5036 |
BCKDHB | -4880 | -4187 | -2605 | -5232 |
DBT | -4678 | 1983 | 5157 | -4844 |
DDO | -1496 | -3730 | -4307 | -2212 |
DHTKD1 | -5034 | -417 | -4064 | -3053 |
DLAT | -4452 | -1933 | -3783 | -2572 |
DLD | -4923 | 1175 | -4683 | -2906 |
DLST | -3558 | -322 | -3488 | -1773 |
GCSH | -2911 | -140 | -1027 | 3384 |
GOT2 | -3182 | -3657 | -3058 | -2419 |
GRHPR | -4445 | -4670 | -3989 | -5011 |
LIAS | -4836 | -1118 | -4645 | -3638 |
LIPT1 | -1830 | 3389 | 4611 | 3565 |
LIPT2 | -4571 | 296 | -2613 | -2943 |
NDUFAB1 | -3229 | 1139 | -3221 | -1911 |
OGDH | -3051 | -5206 | -3610 | -3542 |
PDHA1 | -2764 | -2373 | -4403 | -777 |
PDHB | -3237 | -133 | -3954 | -943 |
PDHX | -2958 | -126 | -3831 | -4229 |
PXMP2 | -4332 | -1718 | -3793 | -5187 |
The NLRP3 inflammasome
metric | value |
---|---|
setSize | 10 |
pMANOVA | 0.00277 |
p.adjustMANOVA | 0.00804 |
s.dist | 0.978 |
s.FSHD | 0.541 |
s.hu_model | -0.0891 |
s.Watt_m | 0.49 |
s.Jones_m | 0.645 |
p.FSHD | 0.00304 |
p.hu_model | 0.626 |
p.Watt_m | 0.00731 |
p.Jones_m | 0.000411 |
Gene | Jones_m | FSHD |
---|---|---|
NFKB2 | 5030 | 5031 |
PYCARD | 4818 | 4190 |
APP | 4891 | 3990 |
CASP1 | 4113 | 3545 |
NFKB1 | 3086 | 4613 |
TXN | 4226 | 3016 |
RELA | 1891 | 3940 |
PANX1 | 1607 | 1524 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
APP | 3990 | -2756 | 574 | 4891 |
CASP1 | 3545 | -1282 | 3136 | 4113 |
HSP90AB1 | -1913 | -636 | 4582 | 723 |
NFKB1 | 4613 | -4179 | 3276 | 3086 |
NFKB2 | 5031 | -3876 | 3297 | 5030 |
PANX1 | 1524 | 1130 | 1051 | 1607 |
PYCARD | 4190 | -2774 | 4656 | 4818 |
RELA | 3940 | 1766 | 4484 | 1891 |
SUGT1 | -1257 | 3113 | -4483 | 3225 |
TXN | 3016 | 1838 | 4743 | 4226 |
Prolactin receptor signaling
metric | value |
---|---|
setSize | 10 |
pMANOVA | 0.00391 |
p.adjustMANOVA | 0.0109 |
s.dist | 0.957 |
s.FSHD | -0.469 |
s.hu_model | -0.246 |
s.Watt_m | -0.536 |
s.Jones_m | -0.591 |
p.FSHD | 0.0103 |
p.hu_model | 0.178 |
p.Watt_m | 0.00334 |
p.Jones_m | 0.00122 |
Gene | Jones_m | Watt_m |
---|---|---|
STAT5B | -5297 | -5248 |
GHR | -5231 | -4592 |
JAK2 | -4773 | -5002 |
SKP1 | -4257 | -2481 |
STAT5A | -2292 | -4522 |
BTRC | -2884 | -2731 |
RBX1 | -4220 | -962 |
CUL1 | -1576 | -1522 |
PTPN11 | -1108 | -660 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
BTRC | -4959 | -1172 | -2731 | -2884 |
CUL1 | -4085 | -3079 | -1522 | -1576 |
GHR | -4796 | 3964 | -4592 | -5231 |
JAK2 | -732 | -2536 | -5002 | -4773 |
PTPN11 | -1703 | -1554 | -660 | -1108 |
RBX1 | -1602 | -729 | -962 | -4220 |
SH2B1 | -2444 | -3792 | -965 | 196 |
SKP1 | -3134 | 2010 | -2481 | -4257 |
STAT5A | 2168 | -4072 | -4522 | -2292 |
STAT5B | -5194 | -4960 | -5248 | -5297 |
Post-chaperonin tubulin folding pathway
metric | value |
---|---|
setSize | 15 |
pMANOVA | 3.49e-06 |
p.adjustMANOVA | 2.34e-05 |
s.dist | 0.923 |
s.FSHD | 0.315 |
s.hu_model | -0.483 |
s.Watt_m | 0.556 |
s.Jones_m | 0.459 |
p.FSHD | 0.0348 |
p.hu_model | 0.00122 |
p.Watt_m | 0.000194 |
p.Jones_m | 0.0021 |
Gene | Watt_m | hu_model |
---|---|---|
TUBB6 | 5153 | -4998 |
TUBA1B | 4866 | -5262 |
TUBA1C | 5075 | -4823 |
TUBB2B | 4912 | -4644 |
TUBB2A | 4401 | -4616 |
TUBA1A | 3672 | -5166 |
TUBA4A | 2049 | -5280 |
TBCA | 1786 | -2549 |
TBCE | 492 | -452 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
ARL2 | 714 | -4089 | -518 | -3571 |
TBCA | 375 | -2549 | 1786 | 3693 |
TBCB | 4295 | 1103 | 3212 | 3467 |
TBCC | 706 | 3004 | 4671 | 2735 |
TBCD | 1482 | -4080 | -590 | 3505 |
TBCE | -4318 | -452 | 492 | 781 |
TUBA1A | 4948 | -5166 | 3672 | 3786 |
TUBA1B | 4448 | -5262 | 4866 | 4967 |
TUBA1C | 3088 | -4823 | 5075 | 5010 |
TUBA4A | -2112 | -5280 | 2049 | -3253 |
TUBA8 | -2556 | -1103 | -882 | -2976 |
TUBB2A | 2970 | -4616 | 4401 | 4710 |
TUBB2B | 2381 | -4644 | 4912 | 4788 |
TUBB4B | 776 | 426 | 4848 | 2861 |
TUBB6 | 4937 | -4998 | 5153 | 5168 |
Inflammasomes
metric | value |
---|---|
setSize | 12 |
pMANOVA | 0.00105 |
p.adjustMANOVA | 0.00354 |
s.dist | 0.922 |
s.FSHD | 0.476 |
s.hu_model | -0.218 |
s.Watt_m | 0.446 |
s.Jones_m | 0.614 |
p.FSHD | 0.00432 |
p.hu_model | 0.19 |
p.Watt_m | 0.00746 |
p.Jones_m | 0.00023 |
Gene | Jones_m | FSHD |
---|---|---|
NFKB2 | 5030 | 5031 |
PYCARD | 4818 | 4190 |
APP | 4891 | 3990 |
CASP1 | 4113 | 3545 |
NFKB1 | 3086 | 4613 |
TXN | 4226 | 3016 |
BCL2L1 | 1941 | 4359 |
RELA | 1891 | 3940 |
PANX1 | 1607 | 1524 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
APP | 3990 | -2756 | 574 | 4891 |
BCL2 | -3161 | -4574 | -1100 | 2806 |
BCL2L1 | 4359 | -5119 | 3393 | 1941 |
CASP1 | 3545 | -1282 | 3136 | 4113 |
HSP90AB1 | -1913 | -636 | 4582 | 723 |
NFKB1 | 4613 | -4179 | 3276 | 3086 |
NFKB2 | 5031 | -3876 | 3297 | 5030 |
PANX1 | 1524 | 1130 | 1051 | 1607 |
PYCARD | 4190 | -2774 | 4656 | 4818 |
RELA | 3940 | 1766 | 4484 | 1891 |
SUGT1 | -1257 | 3113 | -4483 | 3225 |
TXN | 3016 | 1838 | 4743 | 4226 |
Mitochondrial tRNA aminoacylation
metric | value |
---|---|
setSize | 18 |
pMANOVA | 2.69e-06 |
p.adjustMANOVA | 1.84e-05 |
s.dist | 0.913 |
s.FSHD | -0.609 |
s.hu_model | 0.179 |
s.Watt_m | -0.565 |
s.Jones_m | -0.334 |
p.FSHD | 7.59e-06 |
p.hu_model | 0.189 |
p.Watt_m | 3.36e-05 |
p.Jones_m | 0.0142 |
Gene | FSHD | Watt_m |
---|---|---|
IARS2 | -4937 | -5169 |
SARS2 | -4125 | -4633 |
LARS2 | -4758 | -4016 |
DARS2 | -5377 | -3100 |
CARS2 | -4742 | -3294 |
NARS2 | -4447 | -3318 |
VARS2 | -2948 | -4902 |
HARS2 | -4878 | -2721 |
TARS2 | -2811 | -4285 |
FARS2 | -3653 | -2932 |
AARS2 | -1823 | -4573 |
MARS2 | -3770 | -2080 |
EARS2 | -4338 | -1492 |
YARS2 | -2279 | -2282 |
PPA2 | -4060 | -958 |
RARS2 | -891 | -2276 |
PARS2 | -1167 | -205 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
AARS2 | -1823 | -2636 | -4573 | -3348 |
CARS2 | -4742 | -2732 | -3294 | -89 |
DARS2 | -5377 | 1623 | -3100 | -2855 |
EARS2 | -4338 | -2461 | -1492 | -3698 |
FARS2 | -3653 | 2730 | -2932 | 707 |
HARS2 | -4878 | 4682 | -2721 | -4375 |
IARS2 | -4937 | 1933 | -5169 | -2267 |
LARS2 | -4758 | 2101 | -4016 | -678 |
MARS2 | -3770 | 4644 | -2080 | -2858 |
NARS2 | -4447 | 2027 | -3318 | -1778 |
PARS2 | -1167 | 2627 | -205 | -727 |
PPA2 | -4060 | -162 | -958 | -194 |
RARS2 | -891 | -56 | -2276 | 163 |
SARS2 | -4125 | -3536 | -4633 | -3521 |
TARS2 | -2811 | -523 | -4285 | -2628 |
VARS2 | -2948 | -2605 | -4902 | -2295 |
WARS2 | 33 | -880 | -2086 | 425 |
YARS2 | -2279 | 4816 | -2282 | -2242 |
Complex I biogenesis
metric | value |
---|---|
setSize | 52 |
pMANOVA | 8.57e-16 |
p.adjustMANOVA | 3.51e-14 |
s.dist | 0.913 |
s.FSHD | -0.551 |
s.hu_model | -0.196 |
s.Watt_m | -0.401 |
s.Jones_m | -0.575 |
p.FSHD | 6.54e-12 |
p.hu_model | 0.0146 |
p.Watt_m | 5.92e-07 |
p.Jones_m | 7.4e-13 |
Gene | Jones_m | FSHD |
---|---|---|
NDUFB8 | -5016 | -5381 |
NDUFA5 | -4652 | -4522 |
ECSIT | -5076 | -4087 |
NDUFC1 | -4731 | -3946 |
NDUFB4 | -5024 | -3689 |
NDUFAF5 | -4659 | -3655 |
NDUFS1 | -3922 | -4162 |
NDUFA12 | -5025 | -3042 |
NDUFAF6 | -5247 | -2865 |
NDUFS3 | -5085 | -2951 |
NDUFB6 | -4176 | -3531 |
TIMMDC1 | -4130 | -3514 |
NDUFA2 | -4015 | -3321 |
NDUFA10 | -2953 | -4377 |
NDUFA9 | -3839 | -3316 |
MT-ND5 | -2299 | -5424 |
NDUFS2 | -4544 | -2719 |
NDUFV1 | -4349 | -2739 |
NDUFAF4 | -3101 | -3816 |
NDUFS5 | -4714 | -2493 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
ACAD9 | -1110 | -4519 | -4508 | -3752 |
ECSIT | -4087 | -2621 | -2817 | -5076 |
MT-ND1 | -3295 | -352 | -2191 | -3418 |
MT-ND2 | -4198 | -1107 | -2067 | -2726 |
MT-ND4 | -4132 | -2057 | -1579 | -2517 |
MT-ND5 | -5424 | -3201 | -2302 | -2299 |
MT-ND6 | -4175 | 806 | -4540 | -2336 |
NDUFA1 | -2847 | -733 | 306 | -3258 |
NDUFA10 | -4377 | -1928 | -3087 | -2953 |
NDUFA11 | -332 | -1021 | -1127 | -4129 |
NDUFA12 | -3042 | -1299 | -653 | -5025 |
NDUFA13 | 527 | -2222 | -2529 | -4498 |
NDUFA2 | -3321 | -1274 | -1958 | -4015 |
NDUFA3 | -2414 | -3756 | -587 | -3680 |
NDUFA5 | -4522 | 527 | -1654 | -4652 |
NDUFA6 | -3995 | -77 | -3352 | 2209 |
NDUFA7 | -635 | -463 | -1807 | -4700 |
NDUFA8 | -3418 | -599 | -2482 | -3118 |
NDUFA9 | -3316 | -2830 | -2055 | -3839 |
NDUFAB1 | -3229 | 1139 | -3221 | -1911 |
NDUFAF1 | 159 | 1163 | -4219 | -4277 |
NDUFAF2 | -2538 | 3477 | -3212 | 1596 |
NDUFAF3 | -940 | -3534 | -1253 | -805 |
NDUFAF4 | -3816 | 3710 | -2000 | -3101 |
NDUFAF5 | -3655 | 28 | -971 | -4659 |
NDUFAF6 | -2865 | -2523 | -4052 | -5247 |
NDUFAF7 | -4823 | 2947 | -452 | -803 |
NDUFB10 | -2966 | -3327 | -2076 | -3543 |
NDUFB11 | -4516 | -2074 | -2831 | 2192 |
NDUFB2 | -1608 | -3685 | -956 | -3647 |
NDUFB3 | -3864 | 841 | -1914 | -2545 |
NDUFB4 | -3689 | -310 | -1508 | -5024 |
NDUFB5 | -4024 | -2010 | -1167 | -1274 |
NDUFB6 | -3531 | 917 | -305 | -4176 |
NDUFB7 | -2656 | -4168 | -1974 | -3224 |
NDUFB8 | -5381 | -2981 | -2887 | -5016 |
NDUFB9 | -1933 | -984 | -3396 | -4313 |
NDUFC1 | -3946 | -661 | -2874 | -4731 |
NDUFC2 | -3783 | 32 | -2407 | -2927 |
NDUFS1 | -4162 | -1524 | -4327 | -3922 |
NDUFS2 | -2719 | -2987 | -2787 | -4544 |
NDUFS3 | -2951 | -3520 | -2726 | -5085 |
NDUFS4 | -2602 | -1667 | -2421 | 914 |
NDUFS5 | -2493 | -1220 | -1904 | -4714 |
NDUFS6 | -1709 | -1316 | -973 | -5106 |
NDUFS7 | -2104 | -4811 | -1886 | -5006 |
NDUFS8 | -2071 | -4271 | -1979 | -3515 |
NDUFV1 | -2739 | -4172 | -2709 | -4349 |
NDUFV3 | -3600 | -2346 | -2565 | -1926 |
NUBPL | -4866 | -1521 | -3506 | 1659 |
TIMMDC1 | -3514 | 210 | -1099 | -4130 |
TMEM126B | -2313 | 1013 | 1849 | 2331 |
Mitochondrial Fatty Acid Beta-Oxidation
metric | value |
---|---|
setSize | 29 |
pMANOVA | 2.61e-09 |
p.adjustMANOVA | 3.31e-08 |
s.dist | 0.903 |
s.FSHD | -0.516 |
s.hu_model | -0.351 |
s.Watt_m | -0.537 |
s.Jones_m | -0.37 |
p.FSHD | 1.55e-06 |
p.hu_model | 0.00106 |
p.Watt_m | 5.49e-07 |
p.Jones_m | 0.000568 |
Gene | Watt_m | FSHD |
---|---|---|
ACOT2 | -5094.5 | -5376 |
ACAD10 | -4840.0 | -5223 |
PCCA | -5148.0 | -4767 |
ACOT11 | -5262.0 | -4614 |
DECR1 | -4729.0 | -4711 |
ACADM | -4490.0 | -4808 |
MCEE | -4700.0 | -4437 |
ACADL | -3889.0 | -4476 |
PCCB | -4099.0 | -3972 |
ACADVL | -4253.0 | -3225 |
HADHB | -3570.0 | -3639 |
ACOT1 | -5094.5 | -2456 |
ACOT13 | -3068.0 | -4036 |
HADH | -5130.0 | -2398 |
NDUFAB1 | -3221.0 | -3229 |
ACAA2 | -4939.0 | -2008 |
ECI1 | -3376.0 | -2823 |
ACADS | -3951.0 | -2371 |
HADHA | -2474.0 | -2458 |
ECHS1 | -4723.0 | -1230 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
ACAA2 | -2008 | -2298 | -4939.0 | -2039.0 |
ACAD10 | -5223 | -4506 | -4840.0 | -3561.0 |
ACADL | -4476 | -1009 | -3889.0 | 477.0 |
ACADM | -4808 | -1691 | -4490.0 | -853.0 |
ACADS | -2371 | -4603 | -3951.0 | -299.0 |
ACADVL | -3225 | -4891 | -4253.0 | -2940.0 |
ACOT1 | -2456 | 1570 | -5094.5 | -2933.5 |
ACOT11 | -4614 | -5198 | -5262.0 | -2557.0 |
ACOT13 | -4036 | -2955 | -3068.0 | -3439.0 |
ACOT2 | -5376 | -2874 | -5094.5 | -2933.5 |
ACOT7 | 4896 | -712 | 3007.0 | -929.0 |
ACOT9 | 2563 | 473 | 4922.0 | 3476.0 |
ACSF2 | -4841 | -5086 | 1447.0 | 496.0 |
DBI | -3650 | -2822 | 4352.0 | -2011.0 |
DECR1 | -4711 | -2583 | -4729.0 | -3467.0 |
ECHS1 | -1230 | -3845 | -4723.0 | -2015.0 |
ECI1 | -2823 | -3924 | -3376.0 | -4661.0 |
HADH | -2398 | -2750 | -5130.0 | -3996.0 |
HADHA | -2458 | -3160 | -2474.0 | -2529.0 |
HADHB | -3639 | -2006 | -3570.0 | -3514.0 |
MCAT | -1336 | -625 | -2788.0 | -3968.0 |
MCEE | -4437 | -809 | -4700.0 | -253.0 |
MECR | -1664 | -3148 | -1704.0 | -577.0 |
MMAA | -1319 | 2774 | -4281.0 | -833.0 |
NDUFAB1 | -3229 | 1139 | -3221.0 | -1911.0 |
PCCA | -4767 | -2564 | -5148.0 | -4743.0 |
PCCB | -3972 | -164 | -4099.0 | -5276.0 |
PCTP | -1922 | -321 | -1684.0 | 1390.0 |
THEM4 | -4300 | -3569 | -495.0 | -1003.0 |
Degradation of cysteine and homocysteine
metric | value |
---|---|
setSize | 12 |
pMANOVA | 0.000519 |
p.adjustMANOVA | 0.00193 |
s.dist | 0.902 |
s.FSHD | -0.289 |
s.hu_model | -0.302 |
s.Watt_m | -0.407 |
s.Jones_m | -0.688 |
p.FSHD | 0.0833 |
p.hu_model | 0.07 |
p.Watt_m | 0.0147 |
p.Jones_m | 3.64e-05 |
Gene | Jones_m | Watt_m |
---|---|---|
TST | -4978 | -5185 |
SUOX | -5294 | -4875 |
MPST | -5097 | -4337 |
SQRDL | -4169 | -4832 |
ADO | -4832 | -2693 |
GADL1 | -2788 | -4111 |
GOT2 | -2419 | -3058 |
CSAD | -349 | -2596 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
ADO | -1946 | 3176 | -2693 | -4832 |
CDO1 | 4487 | 2019 | 2545 | -3150 |
CSAD | 2625 | -2112 | -2596 | -349 |
CTH | -3203 | 4066 | 1061 | -4612 |
ETHE1 | -1297 | -1826 | 1186 | -3004 |
GADL1 | -1355 | -5065 | -4111 | -2788 |
GOT2 | -3182 | -3657 | -3058 | -2419 |
MPST | -4276 | -5135 | -4337 | -5097 |
SQRDL | -756 | -3997 | -4832 | -4169 |
SUOX | -5153 | -2856 | -4875 | -5294 |
TST | -2901 | -4455 | -5185 | -4978 |
TXN2 | -3464 | -2801 | 633 | -3212 |
Regulation of pyruvate dehydrogenase (PDH) complex
metric | value |
---|---|
setSize | 15 |
pMANOVA | 0.000196 |
p.adjustMANOVA | 0.000814 |
s.dist | 0.901 |
s.FSHD | -0.469 |
s.hu_model | -0.162 |
s.Watt_m | -0.631 |
s.Jones_m | -0.411 |
p.FSHD | 0.00167 |
p.hu_model | 0.278 |
p.Watt_m | 2.34e-05 |
p.Jones_m | 0.00588 |
Gene | Watt_m | FSHD |
---|---|---|
PDP1 | -4550 | -5181 |
DLD | -4683 | -4923 |
RXRA | -4147 | -4228 |
DLAT | -3783 | -4452 |
PDK1 | -3198 | -5017 |
PDK2 | -3496 | -3728 |
PDHB | -3954 | -3237 |
PDHA1 | -4403 | -2764 |
GSTZ1 | -4578 | -2505 |
PDHX | -3831 | -2958 |
PDP2 | -2415 | -4664 |
PPARD | -2316 | -1449 |
PDPR | -4776 | -614 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
DLAT | -4452 | -1933 | -3783 | -2572 |
DLD | -4923 | 1175 | -4683 | -2906 |
GSTZ1 | -2505 | -2039 | -4578 | -3972 |
PDHA1 | -2764 | -2373 | -4403 | -777 |
PDHB | -3237 | -133 | -3954 | -943 |
PDHX | -2958 | -126 | -3831 | -4229 |
PDK1 | -5017 | 4559 | -3198 | -4230 |
PDK2 | -3728 | -5386 | -3496 | -5057 |
PDK3 | 3897 | 4705 | 4816 | 4812 |
PDK4 | 2105 | -708 | -5180 | -789 |
PDP1 | -5181 | -2146 | -4550 | -4820 |
PDP2 | -4664 | -2585 | -2415 | -2584 |
PDPR | -614 | -629 | -4776 | 2790 |
PPARD | -1449 | -4159 | -2316 | -2644 |
RXRA | -4228 | -5455 | -4147 | -5038 |
Interferon alpha/beta signaling
metric | value |
---|---|
setSize | 36 |
pMANOVA | 3.95e-10 |
p.adjustMANOVA | 5.72e-09 |
s.dist | 0.883 |
s.FSHD | 0.595 |
s.hu_model | -0.00808 |
s.Watt_m | 0.35 |
s.Jones_m | 0.551 |
p.FSHD | 6.56e-10 |
p.hu_model | 0.933 |
p.Watt_m | 0.000278 |
p.Jones_m | 1.05e-08 |
Gene | FSHD | Jones_m |
---|---|---|
IFITM3 | 5070 | 5021 |
IFITM1 | 5068 | 5021 |
IFITM2 | 5066 | 5021 |
IFI35 | 4092 | 4715 |
PTPN6 | 3645 | 5055 |
SOCS3 | 5006 | 3580 |
EGR1 | 4895 | 3599 |
MX1 | 4230 | 3968 |
IRF4 | 4366 | 3509 |
OAS2 | 3638 | 3785 |
IRF7 | 4967 | 2598 |
PSMB8 | 4574 | 2736 |
IFI27 | 2940 | 4016 |
STAT2 | 2887 | 3818 |
ADAR | 2648 | 4124 |
TYK2 | 2357 | 4512 |
RNASEL | 2323 | 4286 |
IRF3 | 4486 | 2206 |
IRF9 | 3867 | 2491 |
IP6K2 | 2629 | 3621 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
ABCE1 | -871 | 4666 | 564 | -3086 |
ADAR | 2648 | -2975 | 414 | 4124 |
EGR1 | 4895 | 4131 | 5187 | 3599 |
IFI27 | 2940 | -1088 | -397 | 4016 |
IFI35 | 4092 | -3266 | 172 | 4715 |
IFIT2 | 2444 | -1322 | 794 | 3114 |
IFIT3 | 3294 | -785 | 1406 | 1365 |
IFITM1 | 5068 | 1557 | 4767 | 5021 |
IFITM2 | 5066 | -315 | 4767 | 5021 |
IFITM3 | 5070 | 377 | 4767 | 5021 |
IFNAR1 | -1724 | 3617 | 1074 | 4092 |
IFNAR2 | 1842 | -1300 | 2336 | 3705 |
IP6K2 | 2629 | 3377 | -655 | 3621 |
IRF1 | 4221 | -1544 | 974 | -68 |
IRF2 | 1399 | -3341 | 2237 | 2345 |
IRF3 | 4486 | -3021 | -113 | 2206 |
IRF4 | 4366 | -1152 | 2559 | 3509 |
IRF7 | 4967 | 765 | 3986 | 2598 |
IRF9 | 3867 | 1253 | 131 | 2491 |
ISG15 | 3286 | -3878 | 1717 | 1948 |
JAK1 | 1002 | -1843 | 4184 | -1810 |
MX1 | 4230 | -1841 | 3181 | 3968 |
OAS2 | 3638 | 209 | 2041 | 3785 |
PSMB8 | 4574 | -672 | 2043 | 2736 |
PTPN1 | 739 | 1514 | 4538 | 4669 |
PTPN11 | -1703 | -1554 | -660 | -1108 |
PTPN6 | 3645 | -920 | 4751 | 5055 |
RNASEL | 2323 | 2882 | 869 | 4286 |
SAMHD1 | 2145 | 46 | 3023 | 4231 |
SOCS1 | 4531 | 196 | 3989 | -56 |
SOCS3 | 5006 | -282 | 5053 | 3580 |
STAT1 | 2094 | 233 | -1721 | 2082 |
STAT2 | 2887 | -2568 | 275 | 3818 |
TYK2 | 2357 | -3081 | -49 | 4512 |
USP18 | 3625 | 43 | -2543 | 1934 |
XAF1 | 838 | -319 | -1145 | 1883 |
Chondroitin sulfate biosynthesis
metric | value |
---|---|
setSize | 13 |
pMANOVA | 0.00038 |
p.adjustMANOVA | 0.00147 |
s.dist | 0.875 |
s.FSHD | 0.718 |
s.hu_model | -0.106 |
s.Watt_m | 0.286 |
s.Jones_m | 0.396 |
p.FSHD | 7.36e-06 |
p.hu_model | 0.507 |
p.Watt_m | 0.0743 |
p.Jones_m | 0.0133 |
Gene | FSHD | Jones_m |
---|---|---|
BGN | 4348 | 5088 |
VCAN | 4971 | 4285 |
CHSY1 | 4080 | 3666 |
CHST11 | 4013 | 3364 |
CHPF2 | 4430 | 2836 |
CSGALNACT1 | 3780 | 3223 |
CHPF | 4271 | 2760 |
CHST15 | 4124 | 1275 |
CSGALNACT2 | 561 | 480 |
CHST12 | 125 | 1673 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
BGN | 4348 | -1456 | 3875 | 5088 |
CHPF | 4271 | -4389 | 1240 | 2760 |
CHPF2 | 4430 | -2038 | 2362 | 2836 |
CHST11 | 4013 | -183 | 2253 | 3364 |
CHST12 | 125 | -1250 | 1266 | 1673 |
CHST15 | 4124 | -4640 | -3177 | 1275 |
CHST7 | 3877 | 2707 | -1313 | -269 |
CHSY1 | 4080 | 3773 | 1890 | 3666 |
CSGALNACT1 | 3780 | -204 | 2536 | 3223 |
CSGALNACT2 | 561 | 1490 | 3991 | 480 |
CSPG4 | 3730 | -5557 | 531 | -99 |
DCN | 4452 | -1036 | -890 | -1620 |
VCAN | 4971 | 1662 | 4386 | 4285 |
PECAM1 interactions
metric | value |
---|---|
setSize | 10 |
pMANOVA | 0.00525 |
p.adjustMANOVA | 0.0139 |
s.dist | 0.873 |
s.FSHD | 0.516 |
s.hu_model | -0.25 |
s.Watt_m | 0.283 |
s.Jones_m | 0.594 |
p.FSHD | 0.00472 |
p.hu_model | 0.17 |
p.Watt_m | 0.121 |
p.Jones_m | 0.00115 |
Gene | Jones_m | FSHD |
---|---|---|
PTPN6 | 5055 | 3645 |
FYN | 4010 | 4466 |
INPP5D | 5167 | 2998 |
LYN | 4433 | 3429 |
SRC | 2269 | 5021 |
ITGB3 | 2921 | 3693 |
ITGAV | 4981 | 801 |
YES1 | 2958 | 1006 |
PLCG1 | 210 | 1995 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
FYN | 4466 | -2813 | 3642 | 4010 |
INPP5D | 2998 | -2401 | 4281 | 5167 |
ITGAV | 801 | -812 | 49 | 4981 |
ITGB3 | 3693 | -485 | 4867 | 2921 |
LYN | 3429 | 775 | 3940 | 4433 |
PLCG1 | 1995 | -3905 | -4884 | 210 |
PTPN11 | -1703 | -1554 | -660 | -1108 |
PTPN6 | 3645 | -920 | 4751 | 5055 |
SRC | 5021 | -3860 | 1364 | 2269 |
YES1 | 1006 | -175 | -2910 | 2958 |
Defective B3GALT6 causes EDSP2 and SEMDJL1
metric | value |
---|---|
setSize | 14 |
pMANOVA | 0.000106 |
p.adjustMANOVA | 0.000481 |
s.dist | 0.865 |
s.FSHD | 0.615 |
s.hu_model | -0.454 |
s.Watt_m | 0.212 |
s.Jones_m | 0.344 |
p.FSHD | 6.71e-05 |
p.hu_model | 0.00325 |
p.Watt_m | 0.17 |
p.Jones_m | 0.0261 |
Gene | FSHD | hu_model |
---|---|---|
CSPG4 | 3730 | -5557 |
AGRN | 3889 | -4843 |
SDC3 | 3721 | -4560 |
GPC6 | 4618 | -2353 |
HSPG2 | 2035 | -5289 |
SDC1 | 3944 | -2017 |
BGN | 4348 | -1456 |
B3GALT6 | 3823 | -1236 |
DCN | 4452 | -1036 |
SDC4 | 1095 | -2361 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
AGRN | 3889 | -4843 | -2922 | 760 |
B3GALT6 | 3823 | -1236 | 4092 | 3103 |
BGN | 4348 | -1456 | 3875 | 5088 |
CSPG4 | 3730 | -5557 | 531 | -99 |
DCN | 4452 | -1036 | -890 | -1620 |
GPC1 | -1704 | -5207 | -2934 | -1700 |
GPC4 | -587 | -5108 | -3461 | -1575 |
GPC6 | 4618 | -2353 | 156 | 804 |
HSPG2 | 2035 | -5289 | -401 | 2942 |
SDC1 | 3944 | -2017 | 209 | 2683 |
SDC2 | 4456 | 1739 | 4436 | 5008 |
SDC3 | 3721 | -4560 | 2780 | 4191 |
SDC4 | 1095 | -2361 | 5103 | 946 |
VCAN | 4971 | 1662 | 4386 | 4285 |
Pyruvate metabolism
metric | value |
---|---|
setSize | 26 |
pMANOVA | 7.39e-07 |
p.adjustMANOVA | 6.05e-06 |
s.dist | 0.863 |
s.FSHD | -0.491 |
s.hu_model | -0.228 |
s.Watt_m | -0.522 |
s.Jones_m | -0.423 |
p.FSHD | 1.48e-05 |
p.hu_model | 0.0445 |
p.Watt_m | 4.18e-06 |
p.Jones_m | 0.000188 |
Gene | Watt_m | FSHD |
---|---|---|
PDP1 | -4550 | -5181 |
DLD | -4683 | -4923 |
ME1 | -3918 | -4907 |
VDAC1 | -4553 | -3918 |
RXRA | -4147 | -4228 |
GLO1 | -3844 | -4424 |
DLAT | -3783 | -4452 |
PDK1 | -3198 | -5017 |
SLC16A3 | -4114 | -3677 |
MPC1 | -3199 | -4270 |
PDK2 | -3496 | -3728 |
PDHB | -3954 | -3237 |
PDHA1 | -4403 | -2764 |
GSTZ1 | -4578 | -2505 |
PDHX | -3831 | -2958 |
PDP2 | -2415 | -4664 |
MPC2 | -1719 | -2780 |
PPARD | -2316 | -1449 |
PDPR | -4776 | -614 |
BSG | -2093 | -1369 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
BSG | -1369 | -2217 | -2093 | -5147 |
DLAT | -4452 | -1933 | -3783 | -2572 |
DLD | -4923 | 1175 | -4683 | -2906 |
GLO1 | -4424 | -675 | -3844 | -4433 |
GSTZ1 | -2505 | -2039 | -4578 | -3972 |
HAGH | -2311 | -4451 | 1234 | -3032 |
LDHA | -341 | -3208 | -2881 | -3674 |
LDHB | -1357 | -1472 | -1954 | -1554 |
ME1 | -4907 | 1772 | -3918 | -4943 |
MPC1 | -4270 | -3634 | -3199 | 4240 |
MPC2 | -2780 | 819 | -1719 | -3784 |
PDHA1 | -2764 | -2373 | -4403 | -777 |
PDHB | -3237 | -133 | -3954 | -943 |
PDHX | -2958 | -126 | -3831 | -4229 |
PDK1 | -5017 | 4559 | -3198 | -4230 |
PDK2 | -3728 | -5386 | -3496 | -5057 |
PDK3 | 3897 | 4705 | 4816 | 4812 |
PDK4 | 2105 | -708 | -5180 | -789 |
PDP1 | -5181 | -2146 | -4550 | -4820 |
PDP2 | -4664 | -2585 | -2415 | -2584 |
PDPR | -614 | -629 | -4776 | 2790 |
PPARD | -1449 | -4159 | -2316 | -2644 |
RXRA | -4228 | -5455 | -4147 | -5038 |
SLC16A1 | -2731 | -975 | 5026 | 1675 |
SLC16A3 | -3677 | -4691 | -4114 | 22 |
VDAC1 | -3918 | -2871 | -4553 | -5178 |
HS-GAG degradation
metric | value |
---|---|
setSize | 16 |
pMANOVA | 5.14e-06 |
p.adjustMANOVA | 3.39e-05 |
s.dist | 0.86 |
s.FSHD | 0.573 |
s.hu_model | -0.435 |
s.Watt_m | -0.0136 |
s.Jones_m | 0.471 |
p.FSHD | 7.2e-05 |
p.hu_model | 0.00262 |
p.Watt_m | 0.925 |
p.Jones_m | 0.0011 |
Gene | FSHD | Jones_m |
---|---|---|
SDC2 | 4456 | 5008 |
GUSB | 4047 | 5097 |
SDC3 | 3721 | 4191 |
GLB1L | 4309 | 3448 |
GLB1 | 3757 | 3737 |
NAGLU | 3005 | 4335 |
SGSH | 3076 | 3931 |
SDC1 | 3944 | 2683 |
IDS | 1662 | 4417 |
HSPG2 | 2035 | 2942 |
GPC6 | 4618 | 804 |
AGRN | 3889 | 760 |
SDC4 | 1095 | 946 |
IDUA | 4027 | 75 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
AGRN | 3889 | -4843 | -2922 | 760 |
GLB1 | 3757 | -2214 | 915 | 3737 |
GLB1L | 4309 | -1803 | -412 | 3448 |
GPC1 | -1704 | -5207 | -2934 | -1700 |
GPC4 | -587 | -5108 | -3461 | -1575 |
GPC6 | 4618 | -2353 | 156 | 804 |
GUSB | 4047 | 1905 | 4109 | 5097 |
HSPG2 | 2035 | -5289 | -401 | 2942 |
IDS | 1662 | -2441 | -3581 | 4417 |
IDUA | 4027 | -3817 | -4684 | 75 |
NAGLU | 3005 | -3661 | -707 | 4335 |
SDC1 | 3944 | -2017 | 209 | 2683 |
SDC2 | 4456 | 1739 | 4436 | 5008 |
SDC3 | 3721 | -4560 | 2780 | 4191 |
SDC4 | 1095 | -2361 | 5103 | 946 |
SGSH | 3076 | 701 | -507 | 3931 |
Defective B3GAT3 causes JDSSDHD
metric | value |
---|---|
setSize | 14 |
pMANOVA | 6.44e-05 |
p.adjustMANOVA | 0.00031 |
s.dist | 0.86 |
s.FSHD | 0.619 |
s.hu_model | -0.494 |
s.Watt_m | 0.175 |
s.Jones_m | 0.285 |
p.FSHD | 6.16e-05 |
p.hu_model | 0.00137 |
p.Watt_m | 0.258 |
p.Jones_m | 0.0646 |
Gene | FSHD | hu_model |
---|---|---|
CSPG4 | 3730 | -5557 |
AGRN | 3889 | -4843 |
SDC3 | 3721 | -4560 |
B3GAT3 | 4055 | -4180 |
GPC6 | 4618 | -2353 |
HSPG2 | 2035 | -5289 |
SDC1 | 3944 | -2017 |
BGN | 4348 | -1456 |
DCN | 4452 | -1036 |
SDC4 | 1095 | -2361 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
AGRN | 3889 | -4843 | -2922 | 760 |
B3GAT3 | 4055 | -4180 | 1326 | -1191 |
BGN | 4348 | -1456 | 3875 | 5088 |
CSPG4 | 3730 | -5557 | 531 | -99 |
DCN | 4452 | -1036 | -890 | -1620 |
GPC1 | -1704 | -5207 | -2934 | -1700 |
GPC4 | -587 | -5108 | -3461 | -1575 |
GPC6 | 4618 | -2353 | 156 | 804 |
HSPG2 | 2035 | -5289 | -401 | 2942 |
SDC1 | 3944 | -2017 | 209 | 2683 |
SDC2 | 4456 | 1739 | 4436 | 5008 |
SDC3 | 3721 | -4560 | 2780 | 4191 |
SDC4 | 1095 | -2361 | 5103 | 946 |
VCAN | 4971 | 1662 | 4386 | 4285 |
Formation of Senescence-Associated Heterochromatin Foci (SAHF)
metric | value |
---|---|
setSize | 10 |
pMANOVA | 0.00186 |
p.adjustMANOVA | 0.00571 |
s.dist | 0.857 |
s.FSHD | 0.102 |
s.hu_model | 0.115 |
s.Watt_m | 0.475 |
s.Jones_m | 0.697 |
p.FSHD | 0.576 |
p.hu_model | 0.531 |
p.Watt_m | 0.00926 |
p.Jones_m | 0.000136 |
Gene | Jones_m | Watt_m |
---|---|---|
HMGA1 | 5094 | 5049 |
CDKN1A | 4230 | 5043 |
UBN1 | 3549 | 3626 |
TP53 | 2810 | 3708 |
LMNB1 | 3270 | 2914 |
ASF1A | 2994 | 2526 |
RB1 | 5214 | 1448 |
HIRA | 1964 | 678 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
ASF1A | -4236 | 2494 | 2526 | 2994 |
CABIN1 | 1225 | -2008 | -280 | 4525 |
CDKN1A | 5043 | -4867 | 5043 | 4230 |
EP400 | 989 | 2456 | -165 | 2669 |
HIRA | 2024 | 821 | 678 | 1964 |
HMGA1 | -3434 | 589 | 5049 | 5094 |
LMNB1 | 3424 | 3365 | 2914 | 3270 |
RB1 | -2663 | -2417 | 1448 | 5214 |
TP53 | 4943 | 566 | 3708 | 2810 |
UBN1 | -3751 | 2067 | 3626 | 3549 |
The citric acid (TCA) cycle and respiratory electron transport
metric | value |
---|---|
setSize | 142 |
pMANOVA | 4.04e-38 |
p.adjustMANOVA | 1.24e-35 |
s.dist | 0.856 |
s.FSHD | -0.529 |
s.hu_model | -0.202 |
s.Watt_m | -0.423 |
s.Jones_m | -0.482 |
p.FSHD | 1.42e-27 |
p.hu_model | 3.56e-05 |
p.Watt_m | 3.8e-18 |
p.Jones_m | 3.89e-23 |
Gene | FSHD | Jones_m |
---|---|---|
NDUFB8 | -5381 | -5016 |
CS | -5372 | -4669 |
ADHFE1 | -5136 | -4869 |
PDP1 | -5181 | -4820 |
ME1 | -4907 | -4943 |
IDH3A | -5238 | -4519 |
L2HGDH | -4395 | -5228 |
TRAP1 | -4514 | -4770 |
RXRA | -4228 | -5038 |
PDK1 | -5017 | -4230 |
NDUFA5 | -4522 | -4652 |
COX11 | -4859 | -4306 |
ECSIT | -4087 | -5076 |
VDAC1 | -3918 | -5178 |
SUCLG1 | -3825 | -5153 |
GLO1 | -4424 | -4433 |
PDK2 | -3728 | -5057 |
NDUFC1 | -3946 | -4731 |
NDUFB4 | -3689 | -5024 |
IDH3B | -4107 | -4270 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
ACAD9 | -1110 | -4519 | -4508 | -3752 |
ACO2 | -3871 | -3773 | -4378 | -3916 |
ADHFE1 | -5136 | -3988 | -2451 | -4869 |
BSG | -1369 | -2217 | -2093 | -5147 |
COQ10A | -4639 | -3506 | -2628 | -3276 |
COQ10B | 1437 | 4309 | 4211 | -578 |
COX11 | -4859 | -2823 | -1157 | -4306 |
COX14 | -4487 | -2736 | -4322 | -2319 |
COX16 | -1762 | -2228 | -1923 | -3012 |
COX18 | -3092 | -551 | 627 | -1582 |
COX19 | -4943 | 3027 | 3451 | -1012 |
COX20 | -868 | 1092 | -2255 | -2823 |
COX4I1 | -2361 | -2325 | -1278 | -2561 |
COX5A | -3222 | -2479 | -2526 | -3071 |
COX5B | -4740 | -2527 | 452 | -2519 |
COX6A1 | 3593 | 2239 | 2217 | 2153 |
COX6B1 | -2721 | -2201 | -849 | -1772 |
COX6C | -3899 | -18 | -839 | -1015 |
COX7B | -3033 | 141 | -723 | -359 |
COX7C | -5186 | -1476 | -175 | -1747 |
COX8A | -2248 | -4283 | 2616 | 2136 |
CS | -5372 | 3624 | -3526 | -4669 |
CYC1 | -2742 | -4094 | -3987 | -3200 |
D2HGDH | -1446 | -4830 | -5276 | -4528 |
DLAT | -4452 | -1933 | -3783 | -2572 |
DLD | -4923 | 1175 | -4683 | -2906 |
DLST | -3558 | -322 | -3488 | -1773 |
ECSIT | -4087 | -2621 | -2817 | -5076 |
ETFA | -3503 | 3133 | -2734 | -460 |
ETFB | -1680 | -3567 | -2713 | -4113 |
ETFDH | -4280 | 1866 | -4534 | -2682 |
FAHD1 | -4055 | -1748 | -4256 | -2464 |
FH | -4577 | 284 | -2865 | -3264 |
GLO1 | -4424 | -675 | -3844 | -4433 |
GSTZ1 | -2505 | -2039 | -4578 | -3972 |
HAGH | -2311 | -4451 | 1234 | -3032 |
IDH2 | -2867 | -5154 | -3813 | -2755 |
IDH3A | -5238 | -2126 | -3782 | -4519 |
IDH3B | -4107 | -2843 | -2153 | -4270 |
IDH3G | -896 | -4125 | -3096 | -3697 |
L2HGDH | -4395 | -261 | -3601 | -5228 |
LDHA | -341 | -3208 | -2881 | -3674 |
LDHB | -1357 | -1472 | -1954 | -1554 |
LRPPRC | -4980 | 1639 | -4343 | -3018 |
MDH2 | -2694 | -4307 | -2826 | -2711 |
ME1 | -4907 | 1772 | -3918 | -4943 |
ME2 | -3037 | -1766 | 3484 | 4800 |
ME3 | -2144 | 4173 | -3679 | -5302 |
MPC1 | -4270 | -3634 | -3199 | 4240 |
MPC2 | -2780 | 819 | -1719 | -3784 |
MT-CO1 | -4597 | -3125 | -4070 | -3652 |
MT-CYB | -4704 | -1339 | -2332 | -2471 |
MT-ND1 | -3295 | -352 | -2191 | -3418 |
MT-ND2 | -4198 | -1107 | -2067 | -2726 |
MT-ND4 | -4132 | -2057 | -1579 | -2517 |
MT-ND5 | -5424 | -3201 | -2302 | -2299 |
MT-ND6 | -4175 | 806 | -4540 | -2336 |
NDUFA1 | -2847 | -733 | 306 | -3258 |
NDUFA10 | -4377 | -1928 | -3087 | -2953 |
NDUFA11 | -332 | -1021 | -1127 | -4129 |
NDUFA12 | -3042 | -1299 | -653 | -5025 |
NDUFA13 | 527 | -2222 | -2529 | -4498 |
NDUFA2 | -3321 | -1274 | -1958 | -4015 |
NDUFA3 | -2414 | -3756 | -587 | -3680 |
NDUFA4 | -2936 | -391 | -676 | -3194 |
NDUFA5 | -4522 | 527 | -1654 | -4652 |
NDUFA6 | -3995 | -77 | -3352 | 2209 |
NDUFA7 | -635 | -463 | -1807 | -4700 |
NDUFA8 | -3418 | -599 | -2482 | -3118 |
NDUFA9 | -3316 | -2830 | -2055 | -3839 |
NDUFAB1 | -3229 | 1139 | -3221 | -1911 |
NDUFAF1 | 159 | 1163 | -4219 | -4277 |
NDUFAF2 | -2538 | 3477 | -3212 | 1596 |
NDUFAF3 | -940 | -3534 | -1253 | -805 |
NDUFAF4 | -3816 | 3710 | -2000 | -3101 |
NDUFAF5 | -3655 | 28 | -971 | -4659 |
NDUFAF6 | -2865 | -2523 | -4052 | -5247 |
NDUFAF7 | -4823 | 2947 | -452 | -803 |
NDUFB10 | -2966 | -3327 | -2076 | -3543 |
NDUFB11 | -4516 | -2074 | -2831 | 2192 |
NDUFB2 | -1608 | -3685 | -956 | -3647 |
NDUFB3 | -3864 | 841 | -1914 | -2545 |
NDUFB4 | -3689 | -310 | -1508 | -5024 |
NDUFB5 | -4024 | -2010 | -1167 | -1274 |
NDUFB6 | -3531 | 917 | -305 | -4176 |
NDUFB7 | -2656 | -4168 | -1974 | -3224 |
NDUFB8 | -5381 | -2981 | -2887 | -5016 |
NDUFB9 | -1933 | -984 | -3396 | -4313 |
NDUFC1 | -3946 | -661 | -2874 | -4731 |
NDUFC2 | -3783 | 32 | -2407 | -2927 |
NDUFS1 | -4162 | -1524 | -4327 | -3922 |
NDUFS2 | -2719 | -2987 | -2787 | -4544 |
NDUFS3 | -2951 | -3520 | -2726 | -5085 |
NDUFS4 | -2602 | -1667 | -2421 | 914 |
NDUFS5 | -2493 | -1220 | -1904 | -4714 |
NDUFS6 | -1709 | -1316 | -973 | -5106 |
NDUFS7 | -2104 | -4811 | -1886 | -5006 |
NDUFS8 | -2071 | -4271 | -1979 | -3515 |
NDUFV1 | -2739 | -4172 | -2709 | -4349 |
NDUFV3 | -3600 | -2346 | -2565 | -1926 |
NNT | -4770 | -3281 | -2350 | -261 |
NUBPL | -4866 | -1521 | -3506 | 1659 |
OGDH | -3051 | -5206 | -3610 | -3542 |
PDHA1 | -2764 | -2373 | -4403 | -777 |
PDHB | -3237 | -133 | -3954 | -943 |
PDHX | -2958 | -126 | -3831 | -4229 |
PDK1 | -5017 | 4559 | -3198 | -4230 |
PDK2 | -3728 | -5386 | -3496 | -5057 |
PDK3 | 3897 | 4705 | 4816 | 4812 |
PDK4 | 2105 | -708 | -5180 | -789 |
PDP1 | -5181 | -2146 | -4550 | -4820 |
PDP2 | -4664 | -2585 | -2415 | -2584 |
PDPR | -614 | -629 | -4776 | 2790 |
PPARD | -1449 | -4159 | -2316 | -2644 |
RXRA | -4228 | -5455 | -4147 | -5038 |
SCO1 | -4774 | 3550 | 1689 | 2341 |
SCO2 | 1818 | -1915 | -766 | 740 |
SDHA | -3097 | -4713 | -4539 | -4393 |
SDHB | -3231 | 427 | -3667 | -3677 |
SDHC | -4613 | -3665 | -2969 | -3035 |
SLC16A1 | -2731 | -975 | 5026 | 1675 |
SLC16A3 | -3677 | -4691 | -4114 | 22 |
SLC25A14 | 4243 | 3803 | 1851 | 2411 |
SLC25A27 | -336 | -2446 | -4809 | -4546 |
SUCLA2 | -4446 | 1500 | -4329 | -3679 |
SUCLG1 | -3825 | -31 | -2116 | -5153 |
SUCLG2 | -3363 | -1153 | -4245 | -4203 |
SURF1 | -696 | -1725 | -4055 | -1565 |
TACO1 | -3389 | 642 | -4216 | -4383 |
TIMMDC1 | -3514 | 210 | -1099 | -4130 |
TMEM126B | -2313 | 1013 | 1849 | 2331 |
TRAP1 | -4514 | -5203 | -2043 | -4770 |
UCP2 | 4768 | -4888 | 4991 | 5018 |
UCP3 | 65 | -681 | -5302 | -499 |
UQCR10 | -2766 | -3097 | -257 | 2827 |
UQCRB | -4203 | 400 | -3675 | -1445 |
UQCRC1 | -2421 | -3288 | -3627 | -4053 |
UQCRC2 | -4768 | 543 | -3866 | -3335 |
UQCRFS1 | -2561 | -150 | -3030 | -2834 |
UQCRH | -3396 | -1512 | -1736 | -1917 |
UQCRQ | -1949 | -1744 | -1837 | 0 |
VDAC1 | -3918 | -2871 | -4553 | -5178 |
Respiratory electron transport
metric | value |
---|---|
setSize | 92 |
pMANOVA | 2.25e-24 |
p.adjustMANOVA | 2.31e-22 |
s.dist | 0.841 |
s.FSHD | -0.549 |
s.hu_model | -0.177 |
s.Watt_m | -0.367 |
s.Jones_m | -0.49 |
p.FSHD | 9.03e-20 |
p.hu_model | 0.00334 |
p.Watt_m | 1.22e-09 |
p.Jones_m | 5.01e-16 |
Gene | FSHD | Jones_m |
---|---|---|
NDUFB8 | -5381 | -5016 |
TRAP1 | -4514 | -4770 |
NDUFA5 | -4522 | -4652 |
COX11 | -4859 | -4306 |
ECSIT | -4087 | -5076 |
NDUFC1 | -3946 | -4731 |
NDUFB4 | -3689 | -5024 |
NDUFAF5 | -3655 | -4659 |
MT-CO1 | -4597 | -3652 |
NDUFS1 | -4162 | -3922 |
UQCRC2 | -4768 | -3335 |
NDUFA12 | -3042 | -5025 |
COQ10A | -4639 | -3276 |
NDUFAF6 | -2865 | -5247 |
LRPPRC | -4980 | -3018 |
NDUFS3 | -2951 | -5085 |
TACO1 | -3389 | -4383 |
NDUFB6 | -3531 | -4176 |
TIMMDC1 | -3514 | -4130 |
SDHC | -4613 | -3035 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
ACAD9 | -1110 | -4519 | -4508 | -3752 |
COQ10A | -4639 | -3506 | -2628 | -3276 |
COQ10B | 1437 | 4309 | 4211 | -578 |
COX11 | -4859 | -2823 | -1157 | -4306 |
COX14 | -4487 | -2736 | -4322 | -2319 |
COX16 | -1762 | -2228 | -1923 | -3012 |
COX18 | -3092 | -551 | 627 | -1582 |
COX19 | -4943 | 3027 | 3451 | -1012 |
COX20 | -868 | 1092 | -2255 | -2823 |
COX4I1 | -2361 | -2325 | -1278 | -2561 |
COX5A | -3222 | -2479 | -2526 | -3071 |
COX5B | -4740 | -2527 | 452 | -2519 |
COX6A1 | 3593 | 2239 | 2217 | 2153 |
COX6B1 | -2721 | -2201 | -849 | -1772 |
COX6C | -3899 | -18 | -839 | -1015 |
COX7B | -3033 | 141 | -723 | -359 |
COX7C | -5186 | -1476 | -175 | -1747 |
COX8A | -2248 | -4283 | 2616 | 2136 |
CYC1 | -2742 | -4094 | -3987 | -3200 |
ECSIT | -4087 | -2621 | -2817 | -5076 |
ETFA | -3503 | 3133 | -2734 | -460 |
ETFB | -1680 | -3567 | -2713 | -4113 |
ETFDH | -4280 | 1866 | -4534 | -2682 |
LRPPRC | -4980 | 1639 | -4343 | -3018 |
MT-CO1 | -4597 | -3125 | -4070 | -3652 |
MT-CYB | -4704 | -1339 | -2332 | -2471 |
MT-ND1 | -3295 | -352 | -2191 | -3418 |
MT-ND2 | -4198 | -1107 | -2067 | -2726 |
MT-ND4 | -4132 | -2057 | -1579 | -2517 |
MT-ND5 | -5424 | -3201 | -2302 | -2299 |
MT-ND6 | -4175 | 806 | -4540 | -2336 |
NDUFA1 | -2847 | -733 | 306 | -3258 |
NDUFA10 | -4377 | -1928 | -3087 | -2953 |
NDUFA11 | -332 | -1021 | -1127 | -4129 |
NDUFA12 | -3042 | -1299 | -653 | -5025 |
NDUFA13 | 527 | -2222 | -2529 | -4498 |
NDUFA2 | -3321 | -1274 | -1958 | -4015 |
NDUFA3 | -2414 | -3756 | -587 | -3680 |
NDUFA4 | -2936 | -391 | -676 | -3194 |
NDUFA5 | -4522 | 527 | -1654 | -4652 |
NDUFA6 | -3995 | -77 | -3352 | 2209 |
NDUFA7 | -635 | -463 | -1807 | -4700 |
NDUFA8 | -3418 | -599 | -2482 | -3118 |
NDUFA9 | -3316 | -2830 | -2055 | -3839 |
NDUFAB1 | -3229 | 1139 | -3221 | -1911 |
NDUFAF1 | 159 | 1163 | -4219 | -4277 |
NDUFAF2 | -2538 | 3477 | -3212 | 1596 |
NDUFAF3 | -940 | -3534 | -1253 | -805 |
NDUFAF4 | -3816 | 3710 | -2000 | -3101 |
NDUFAF5 | -3655 | 28 | -971 | -4659 |
NDUFAF6 | -2865 | -2523 | -4052 | -5247 |
NDUFAF7 | -4823 | 2947 | -452 | -803 |
NDUFB10 | -2966 | -3327 | -2076 | -3543 |
NDUFB11 | -4516 | -2074 | -2831 | 2192 |
NDUFB2 | -1608 | -3685 | -956 | -3647 |
NDUFB3 | -3864 | 841 | -1914 | -2545 |
NDUFB4 | -3689 | -310 | -1508 | -5024 |
NDUFB5 | -4024 | -2010 | -1167 | -1274 |
NDUFB6 | -3531 | 917 | -305 | -4176 |
NDUFB7 | -2656 | -4168 | -1974 | -3224 |
NDUFB8 | -5381 | -2981 | -2887 | -5016 |
NDUFB9 | -1933 | -984 | -3396 | -4313 |
NDUFC1 | -3946 | -661 | -2874 | -4731 |
NDUFC2 | -3783 | 32 | -2407 | -2927 |
NDUFS1 | -4162 | -1524 | -4327 | -3922 |
NDUFS2 | -2719 | -2987 | -2787 | -4544 |
NDUFS3 | -2951 | -3520 | -2726 | -5085 |
NDUFS4 | -2602 | -1667 | -2421 | 914 |
NDUFS5 | -2493 | -1220 | -1904 | -4714 |
NDUFS6 | -1709 | -1316 | -973 | -5106 |
NDUFS7 | -2104 | -4811 | -1886 | -5006 |
NDUFS8 | -2071 | -4271 | -1979 | -3515 |
NDUFV1 | -2739 | -4172 | -2709 | -4349 |
NDUFV3 | -3600 | -2346 | -2565 | -1926 |
NUBPL | -4866 | -1521 | -3506 | 1659 |
SCO1 | -4774 | 3550 | 1689 | 2341 |
SCO2 | 1818 | -1915 | -766 | 740 |
SDHA | -3097 | -4713 | -4539 | -4393 |
SDHB | -3231 | 427 | -3667 | -3677 |
SDHC | -4613 | -3665 | -2969 | -3035 |
SURF1 | -696 | -1725 | -4055 | -1565 |
TACO1 | -3389 | 642 | -4216 | -4383 |
TIMMDC1 | -3514 | 210 | -1099 | -4130 |
TMEM126B | -2313 | 1013 | 1849 | 2331 |
TRAP1 | -4514 | -5203 | -2043 | -4770 |
UQCR10 | -2766 | -3097 | -257 | 2827 |
UQCRB | -4203 | 400 | -3675 | -1445 |
UQCRC1 | -2421 | -3288 | -3627 | -4053 |
UQCRC2 | -4768 | 543 | -3866 | -3335 |
UQCRFS1 | -2561 | -150 | -3030 | -2834 |
UQCRH | -3396 | -1512 | -1736 | -1917 |
UQCRQ | -1949 | -1744 | -1837 | 0 |
tRNA Aminoacylation
metric | value |
---|---|
setSize | 24 |
pMANOVA | 2.34e-06 |
p.adjustMANOVA | 1.63e-05 |
s.dist | 0.84 |
s.FSHD | -0.588 |
s.hu_model | 0.185 |
s.Watt_m | -0.405 |
s.Jones_m | -0.402 |
p.FSHD | 6.22e-07 |
p.hu_model | 0.118 |
p.Watt_m | 0.000597 |
p.Jones_m | 0.000665 |
Gene | FSHD | Watt_m |
---|---|---|
IARS2 | -4937 | -5169 |
SARS2 | -4125 | -4633 |
LARS2 | -4758 | -4016 |
DARS2 | -5377 | -3100 |
CARS2 | -4742 | -3294 |
NARS2 | -4447 | -3318 |
VARS2 | -2948 | -4902 |
HARS2 | -4878 | -2721 |
TARS2 | -2811 | -4285 |
FARS2 | -3653 | -2932 |
AIMP2 | -3584 | -2586 |
AARS2 | -1823 | -4573 |
MARS2 | -3770 | -2080 |
EARS2 | -4338 | -1492 |
YARS2 | -2279 | -2282 |
AIMP1 | -4862 | -866 |
PPA2 | -4060 | -958 |
RARS2 | -891 | -2276 |
PARS2 | -1167 | -205 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
AARS2 | -1823 | -2636 | -4573 | -3348 |
AIMP1 | -4862 | 1405 | -866 | -4104 |
AIMP2 | -3584 | -2692 | -2586 | -5021 |
CARS2 | -4742 | -2732 | -3294 | -89 |
DARS2 | -5377 | 1623 | -3100 | -2855 |
EARS2 | -4338 | -2461 | -1492 | -3698 |
EEF1E1 | 42 | 2819 | 2913 | -2589 |
FARS2 | -3653 | 2730 | -2932 | 707 |
FARSA | 126 | -1780 | -861 | -1287 |
FARSB | -4646 | 3318 | 2662 | -3177 |
HARS2 | -4878 | 4682 | -2721 | -4375 |
IARS2 | -4937 | 1933 | -5169 | -2267 |
LARS2 | -4758 | 2101 | -4016 | -678 |
MARS2 | -3770 | 4644 | -2080 | -2858 |
NARS2 | -4447 | 2027 | -3318 | -1778 |
PARS2 | -1167 | 2627 | -205 | -727 |
PPA1 | -4622 | 1505 | 822 | -3074 |
PPA2 | -4060 | -162 | -958 | -194 |
RARS2 | -891 | -56 | -2276 | 163 |
SARS2 | -4125 | -3536 | -4633 | -3521 |
TARS2 | -2811 | -523 | -4285 | -2628 |
VARS2 | -2948 | -2605 | -4902 | -2295 |
WARS2 | 33 | -880 | -2086 | 425 |
YARS2 | -2279 | 4816 | -2282 | -2242 |
Mucopolysaccharidoses
metric | value |
---|---|
setSize | 11 |
pMANOVA | 0.000404 |
p.adjustMANOVA | 0.00156 |
s.dist | 0.834 |
s.FSHD | 0.463 |
s.hu_model | -0.335 |
s.Watt_m | 0.00854 |
s.Jones_m | 0.607 |
p.FSHD | 0.00783 |
p.hu_model | 0.0544 |
p.Watt_m | 0.961 |
p.Jones_m | 0.000486 |
Gene | Jones_m | FSHD |
---|---|---|
GALNS | 4953 | 4194 |
GUSB | 5097 | 4047 |
GLB1 | 3737 | 3757 |
NAGLU | 4335 | 3005 |
SGSH | 3931 | 3076 |
GNS | 4550 | 2638 |
IDS | 4417 | 1662 |
ARSB | 3584 | 471 |
IDUA | 75 | 4027 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
ARSB | 471 | -989 | 2803 | 3584 |
GALNS | 4194 | -3909 | 4498 | 4953 |
GLB1 | 3757 | -2214 | 915 | 3737 |
GNS | 2638 | 98 | -972 | 4550 |
GUSB | 4047 | 1905 | 4109 | 5097 |
HGSNAT | 3140 | -4541 | -3490 | -30 |
HYAL1 | -5197 | -3796 | 1588 | 129 |
IDS | 1662 | -2441 | -3581 | 4417 |
IDUA | 4027 | -3817 | -4684 | 75 |
NAGLU | 3005 | -3661 | -707 | 4335 |
SGSH | 3076 | 701 | -507 | 3931 |
Defective B4GALT7 causes EDS, progeroid type
metric | value |
---|---|
setSize | 14 |
pMANOVA | 0.000158 |
p.adjustMANOVA | 0.000678 |
s.dist | 0.828 |
s.FSHD | 0.574 |
s.hu_model | -0.493 |
s.Watt_m | 0.136 |
s.Jones_m | 0.308 |
p.FSHD | 0.000203 |
p.hu_model | 0.0014 |
p.Watt_m | 0.379 |
p.Jones_m | 0.0458 |
Gene | FSHD | hu_model |
---|---|---|
CSPG4 | 3730 | -5557 |
AGRN | 3889 | -4843 |
SDC3 | 3721 | -4560 |
GPC6 | 4618 | -2353 |
HSPG2 | 2035 | -5289 |
SDC1 | 3944 | -2017 |
BGN | 4348 | -1456 |
DCN | 4452 | -1036 |
B4GALT7 | 746 | -4099 |
SDC4 | 1095 | -2361 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
AGRN | 3889 | -4843 | -2922 | 760 |
B4GALT7 | 746 | -4099 | -1523 | 513 |
BGN | 4348 | -1456 | 3875 | 5088 |
CSPG4 | 3730 | -5557 | 531 | -99 |
DCN | 4452 | -1036 | -890 | -1620 |
GPC1 | -1704 | -5207 | -2934 | -1700 |
GPC4 | -587 | -5108 | -3461 | -1575 |
GPC6 | 4618 | -2353 | 156 | 804 |
HSPG2 | 2035 | -5289 | -401 | 2942 |
SDC1 | 3944 | -2017 | 209 | 2683 |
SDC2 | 4456 | 1739 | 4436 | 5008 |
SDC3 | 3721 | -4560 | 2780 | 4191 |
SDC4 | 1095 | -2361 | 5103 | 946 |
VCAN | 4971 | 1662 | 4386 | 4285 |
Activation of Matrix Metalloproteinases
metric | value |
---|---|
setSize | 11 |
pMANOVA | 0.00243 |
p.adjustMANOVA | 0.00724 |
s.dist | 0.826 |
s.FSHD | 0.655 |
s.hu_model | -0.307 |
s.Watt_m | 0.193 |
s.Jones_m | 0.349 |
p.FSHD | 0.000169 |
p.hu_model | 0.0782 |
p.Watt_m | 0.268 |
p.Jones_m | 0.0448 |
Gene | FSHD | Jones_m |
---|---|---|
TIMP1 | 4933 | 4988 |
CTSK | 4644 | 4241 |
MMP17 | 2906 | 5161 |
COL18A1 | 4351 | 3090 |
MMP14 | 4687 | 2675 |
MMP2 | 4410 | 2240 |
TIMP2 | 4689 | 1606 |
MMP11 | 2889 | 1218 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
COL18A1 | 4351 | -2864 | 2677 | 3090 |
CTSK | 4644 | 2 | 259 | 4241 |
CTSV | -84 | 2189 | 34 | 331 |
FURIN | 1239 | -4167 | 4073 | -1204 |
MMP11 | 2889 | -3240 | -393 | 1218 |
MMP14 | 4687 | -1668 | 1618 | 2675 |
MMP15 | 1264 | -5090 | -5214 | -4505 |
MMP17 | 2906 | -2335 | 5119 | 5161 |
MMP2 | 4410 | -689 | -1983 | 2240 |
TIMP1 | 4933 | -1301 | 5188 | 4988 |
TIMP2 | 4689 | -1860 | -732 | 1606 |
Scavenging by Class A Receptors
metric | value |
---|---|
setSize | 13 |
pMANOVA | 0.00156 |
p.adjustMANOVA | 0.00493 |
s.dist | 0.817 |
s.FSHD | 0.6 |
s.hu_model | -0.195 |
s.Watt_m | 0.204 |
s.Jones_m | 0.478 |
p.FSHD | 0.00018 |
p.hu_model | 0.223 |
p.Watt_m | 0.204 |
p.Jones_m | 0.00284 |
Gene | FSHD | Jones_m |
---|---|---|
MSR1 | 5020 | 4999 |
APOE | 3947 | 4717 |
CALR | 3782 | 4356 |
COL3A1 | 4565 | 3575 |
HSP90B1 | 3464 | 4544 |
COLEC12 | 4753 | 3221 |
COL4A2 | 3851 | 3295 |
COL4A1 | 3805 | 3236 |
COL1A2 | 4681 | 1250 |
COL1A1 | 4847 | 676 |
SCARA5 | 4409 | 415 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
APOE | 3947 | -1411 | -88 | 4717 |
CALR | 3782 | 1517 | 4947 | 4356 |
COL1A1 | 4847 | -1617 | 7 | 676 |
COL1A2 | 4681 | -1689 | -375 | 1250 |
COL3A1 | 4565 | 2950 | 2503 | 3575 |
COL4A1 | 3805 | -4695 | 688 | 3236 |
COL4A2 | 3851 | -4973 | 861 | 3295 |
COLEC12 | 4753 | 4226 | 45 | 3221 |
FTH1 | -3005 | -1864 | -126 | 409 |
HSP90B1 | 3464 | 456 | 4896 | 4544 |
MASP1 | -5427 | -4170 | -1574 | -2446 |
MSR1 | 5020 | -3413 | 5009 | 4999 |
SCARA5 | 4409 | -2526 | -3487 | 415 |
rRNA processing in the mitochondrion
metric | value |
---|---|
setSize | 11 |
pMANOVA | 0.0103 |
p.adjustMANOVA | 0.0243 |
s.dist | 0.814 |
s.FSHD | -0.589 |
s.hu_model | -0.0373 |
s.Watt_m | -0.367 |
s.Jones_m | -0.423 |
p.FSHD | 0.000714 |
p.hu_model | 0.83 |
p.Watt_m | 0.035 |
p.Jones_m | 0.0152 |
Gene | FSHD | Jones_m |
---|---|---|
MT-CO1 | -4597 | -3652 |
TRMT10C | -4316 | -3659 |
MT-ND5 | -5424 | -2299 |
MT-CYB | -4704 | -2471 |
MT-ND2 | -4198 | -2726 |
MT-ND1 | -3295 | -3418 |
MT-ND4 | -4132 | -2517 |
NSUN4 | -1691 | -4928 |
TFB1M | -1773 | -3272 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
ELAC2 | -1785 | 1503 | 1552 | 116 |
HSD17B10 | -201 | -1178 | -480 | 3967 |
MT-CO1 | -4597 | -3125 | -4070 | -3652 |
MT-CYB | -4704 | -1339 | -2332 | -2471 |
MT-ND1 | -3295 | -352 | -2191 | -3418 |
MT-ND2 | -4198 | -1107 | -2067 | -2726 |
MT-ND4 | -4132 | -2057 | -1579 | -2517 |
MT-ND5 | -5424 | -3201 | -2302 | -2299 |
NSUN4 | -1691 | -822 | -4973 | -4928 |
TFB1M | -1773 | 1520 | -3331 | -3272 |
TRMT10C | -4316 | 4737 | -8 | -3659 |
Carnitine metabolism
metric | value |
---|---|
setSize | 11 |
pMANOVA | 0.00397 |
p.adjustMANOVA | 0.0111 |
s.dist | 0.813 |
s.FSHD | -0.275 |
s.hu_model | -0.434 |
s.Watt_m | -0.568 |
s.Jones_m | -0.272 |
p.FSHD | 0.114 |
p.hu_model | 0.0128 |
p.Watt_m | 0.00112 |
p.Jones_m | 0.118 |
Gene | Watt_m | hu_model |
---|---|---|
RXRA | -4147 | -5455 |
THRSP | -4589 | -4254 |
PRKAA2 | -5106 | -3176 |
SLC22A5 | -2909 | -4594 |
PRKAG2 | -3494 | -3194 |
PPARD | -2316 | -4159 |
PRKAB2 | -2793 | -2300 |
SLC25A20 | -1424 | -3464 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
CPT1A | 3750 | -356 | 324 | 4495 |
CPT2 | -3090 | 547 | -5234 | -3083 |
MID1IP1 | -5004 | 2039 | -1702 | 2896 |
PPARD | -1449 | -4159 | -2316 | -2644 |
PRKAA2 | -3931 | -3176 | -5106 | -4407 |
PRKAB2 | -2523 | -2300 | -2793 | -5257 |
PRKAG2 | -382 | -3194 | -3494 | 2548 |
RXRA | -4228 | -5455 | -4147 | -5038 |
SLC22A5 | -3713 | -4594 | -2909 | -2085 |
SLC25A20 | -683 | -3464 | -1424 | -2559 |
THRSP | 3306 | -4254 | -4589 | -1021 |
Cell recruitment (pro-inflammatory response)
metric | value |
---|---|
setSize | 12 |
pMANOVA | 0.00863 |
p.adjustMANOVA | 0.0209 |
s.dist | 0.81 |
s.FSHD | 0.518 |
s.hu_model | -0.0205 |
s.Watt_m | 0.347 |
s.Jones_m | 0.517 |
p.FSHD | 0.00189 |
p.hu_model | 0.902 |
p.Watt_m | 0.0372 |
p.Jones_m | 0.00194 |
Gene | FSHD | Jones_m |
---|---|---|
NFKB2 | 5031 | 5030 |
P2RX4 | 4810 | 4918 |
PYCARD | 4190 | 4818 |
C3 | 4737 | 4049 |
CASP1 | 3545 | 4113 |
NFKB1 | 4613 | 3086 |
TXN | 3016 | 4226 |
RELA | 3940 | 1891 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
C3 | 4737 | 4276 | 1818 | 4049 |
CASP1 | 3545 | -1282 | 3136 | 4113 |
ENTPD5 | -4867 | -3984 | -3379 | -1327 |
HSP90AB1 | -1913 | -636 | 4582 | 723 |
NFKB1 | 4613 | -4179 | 3276 | 3086 |
NFKB2 | 5031 | -3876 | 3297 | 5030 |
NT5E | 4703 | 1980 | -3594 | -2534 |
P2RX4 | 4810 | -1095 | 2834 | 4918 |
PYCARD | 4190 | -2774 | 4656 | 4818 |
RELA | 3940 | 1766 | 4484 | 1891 |
SUGT1 | -1257 | 3113 | -4483 | 3225 |
TXN | 3016 | 1838 | 4743 | 4226 |
Purinergic signaling in leishmaniasis infection
metric | value |
---|---|
setSize | 12 |
pMANOVA | 0.00863 |
p.adjustMANOVA | 0.0209 |
s.dist | 0.81 |
s.FSHD | 0.518 |
s.hu_model | -0.0205 |
s.Watt_m | 0.347 |
s.Jones_m | 0.517 |
p.FSHD | 0.00189 |
p.hu_model | 0.902 |
p.Watt_m | 0.0372 |
p.Jones_m | 0.00194 |
Gene | FSHD | Jones_m |
---|---|---|
NFKB2 | 5031 | 5030 |
P2RX4 | 4810 | 4918 |
PYCARD | 4190 | 4818 |
C3 | 4737 | 4049 |
CASP1 | 3545 | 4113 |
NFKB1 | 4613 | 3086 |
TXN | 3016 | 4226 |
RELA | 3940 | 1891 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
C3 | 4737 | 4276 | 1818 | 4049 |
CASP1 | 3545 | -1282 | 3136 | 4113 |
ENTPD5 | -4867 | -3984 | -3379 | -1327 |
HSP90AB1 | -1913 | -636 | 4582 | 723 |
NFKB1 | 4613 | -4179 | 3276 | 3086 |
NFKB2 | 5031 | -3876 | 3297 | 5030 |
NT5E | 4703 | 1980 | -3594 | -2534 |
P2RX4 | 4810 | -1095 | 2834 | 4918 |
PYCARD | 4190 | -2774 | 4656 | 4818 |
RELA | 3940 | 1766 | 4484 | 1891 |
SUGT1 | -1257 | 3113 | -4483 | 3225 |
TXN | 3016 | 1838 | 4743 | 4226 |
A tetrasaccharide linker sequence is required for GAG synthesis
metric | value |
---|---|
setSize | 18 |
pMANOVA | 1.98e-05 |
p.adjustMANOVA | 0.000107 |
s.dist | 0.797 |
s.FSHD | 0.6 |
s.hu_model | -0.413 |
s.Watt_m | 0.21 |
s.Jones_m | 0.246 |
p.FSHD | 1.06e-05 |
p.hu_model | 0.00243 |
p.Watt_m | 0.124 |
p.Jones_m | 0.0704 |
Gene | FSHD | hu_model |
---|---|---|
CSPG4 | 3730 | -5557 |
AGRN | 3889 | -4843 |
SDC3 | 3721 | -4560 |
B3GAT3 | 4055 | -4180 |
GPC6 | 4618 | -2353 |
HSPG2 | 2035 | -5289 |
SDC1 | 3944 | -2017 |
BGN | 4348 | -1456 |
B3GALT6 | 3823 | -1236 |
DCN | 4452 | -1036 |
B4GALT7 | 746 | -4099 |
SDC4 | 1095 | -2361 |
XYLT2 | 2228 | -1124 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
AGRN | 3889 | -4843 | -2922 | 760 |
B3GALT6 | 3823 | -1236 | 4092 | 3103 |
B3GAT3 | 4055 | -4180 | 1326 | -1191 |
B4GALT7 | 746 | -4099 | -1523 | 513 |
BGN | 4348 | -1456 | 3875 | 5088 |
CSPG4 | 3730 | -5557 | 531 | -99 |
DCN | 4452 | -1036 | -890 | -1620 |
GPC1 | -1704 | -5207 | -2934 | -1700 |
GPC4 | -587 | -5108 | -3461 | -1575 |
GPC6 | 4618 | -2353 | 156 | 804 |
HSPG2 | 2035 | -5289 | -401 | 2942 |
SDC1 | 3944 | -2017 | 209 | 2683 |
SDC2 | 4456 | 1739 | 4436 | 5008 |
SDC3 | 3721 | -4560 | 2780 | 4191 |
SDC4 | 1095 | -2361 | 5103 | 946 |
VCAN | 4971 | 1662 | 4386 | 4285 |
XYLT1 | 3695 | 2589 | 2917 | -2537 |
XYLT2 | 2228 | -1124 | 1315 | 1093 |
Respiratory electron transport, ATP synthesis by chemiosmotic coupling, and heat production by uncoupling proteins.
metric | value |
---|---|
setSize | 96 |
pMANOVA | 1.91e-22 |
p.adjustMANOVA | 1.47e-20 |
s.dist | 0.795 |
s.FSHD | -0.508 |
s.hu_model | -0.176 |
s.Watt_m | -0.358 |
s.Jones_m | -0.464 |
p.FSHD | 8.8e-18 |
p.hu_model | 0.00292 |
p.Watt_m | 1.41e-09 |
p.Jones_m | 3.97e-15 |
Gene | FSHD | Jones_m |
---|---|---|
NDUFB8 | -5381 | -5016 |
TRAP1 | -4514 | -4770 |
NDUFA5 | -4522 | -4652 |
COX11 | -4859 | -4306 |
ECSIT | -4087 | -5076 |
NDUFC1 | -3946 | -4731 |
NDUFB4 | -3689 | -5024 |
NDUFAF5 | -3655 | -4659 |
MT-CO1 | -4597 | -3652 |
NDUFS1 | -4162 | -3922 |
UQCRC2 | -4768 | -3335 |
NDUFA12 | -3042 | -5025 |
COQ10A | -4639 | -3276 |
NDUFAF6 | -2865 | -5247 |
LRPPRC | -4980 | -3018 |
NDUFS3 | -2951 | -5085 |
TACO1 | -3389 | -4383 |
NDUFB6 | -3531 | -4176 |
TIMMDC1 | -3514 | -4130 |
SDHC | -4613 | -3035 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
ACAD9 | -1110 | -4519 | -4508 | -3752 |
COQ10A | -4639 | -3506 | -2628 | -3276 |
COQ10B | 1437 | 4309 | 4211 | -578 |
COX11 | -4859 | -2823 | -1157 | -4306 |
COX14 | -4487 | -2736 | -4322 | -2319 |
COX16 | -1762 | -2228 | -1923 | -3012 |
COX18 | -3092 | -551 | 627 | -1582 |
COX19 | -4943 | 3027 | 3451 | -1012 |
COX20 | -868 | 1092 | -2255 | -2823 |
COX4I1 | -2361 | -2325 | -1278 | -2561 |
COX5A | -3222 | -2479 | -2526 | -3071 |
COX5B | -4740 | -2527 | 452 | -2519 |
COX6A1 | 3593 | 2239 | 2217 | 2153 |
COX6B1 | -2721 | -2201 | -849 | -1772 |
COX6C | -3899 | -18 | -839 | -1015 |
COX7B | -3033 | 141 | -723 | -359 |
COX7C | -5186 | -1476 | -175 | -1747 |
COX8A | -2248 | -4283 | 2616 | 2136 |
CYC1 | -2742 | -4094 | -3987 | -3200 |
ECSIT | -4087 | -2621 | -2817 | -5076 |
ETFA | -3503 | 3133 | -2734 | -460 |
ETFB | -1680 | -3567 | -2713 | -4113 |
ETFDH | -4280 | 1866 | -4534 | -2682 |
LRPPRC | -4980 | 1639 | -4343 | -3018 |
MT-CO1 | -4597 | -3125 | -4070 | -3652 |
MT-CYB | -4704 | -1339 | -2332 | -2471 |
MT-ND1 | -3295 | -352 | -2191 | -3418 |
MT-ND2 | -4198 | -1107 | -2067 | -2726 |
MT-ND4 | -4132 | -2057 | -1579 | -2517 |
MT-ND5 | -5424 | -3201 | -2302 | -2299 |
MT-ND6 | -4175 | 806 | -4540 | -2336 |
NDUFA1 | -2847 | -733 | 306 | -3258 |
NDUFA10 | -4377 | -1928 | -3087 | -2953 |
NDUFA11 | -332 | -1021 | -1127 | -4129 |
NDUFA12 | -3042 | -1299 | -653 | -5025 |
NDUFA13 | 527 | -2222 | -2529 | -4498 |
NDUFA2 | -3321 | -1274 | -1958 | -4015 |
NDUFA3 | -2414 | -3756 | -587 | -3680 |
NDUFA4 | -2936 | -391 | -676 | -3194 |
NDUFA5 | -4522 | 527 | -1654 | -4652 |
NDUFA6 | -3995 | -77 | -3352 | 2209 |
NDUFA7 | -635 | -463 | -1807 | -4700 |
NDUFA8 | -3418 | -599 | -2482 | -3118 |
NDUFA9 | -3316 | -2830 | -2055 | -3839 |
NDUFAB1 | -3229 | 1139 | -3221 | -1911 |
NDUFAF1 | 159 | 1163 | -4219 | -4277 |
NDUFAF2 | -2538 | 3477 | -3212 | 1596 |
NDUFAF3 | -940 | -3534 | -1253 | -805 |
NDUFAF4 | -3816 | 3710 | -2000 | -3101 |
NDUFAF5 | -3655 | 28 | -971 | -4659 |
NDUFAF6 | -2865 | -2523 | -4052 | -5247 |
NDUFAF7 | -4823 | 2947 | -452 | -803 |
NDUFB10 | -2966 | -3327 | -2076 | -3543 |
NDUFB11 | -4516 | -2074 | -2831 | 2192 |
NDUFB2 | -1608 | -3685 | -956 | -3647 |
NDUFB3 | -3864 | 841 | -1914 | -2545 |
NDUFB4 | -3689 | -310 | -1508 | -5024 |
NDUFB5 | -4024 | -2010 | -1167 | -1274 |
NDUFB6 | -3531 | 917 | -305 | -4176 |
NDUFB7 | -2656 | -4168 | -1974 | -3224 |
NDUFB8 | -5381 | -2981 | -2887 | -5016 |
NDUFB9 | -1933 | -984 | -3396 | -4313 |
NDUFC1 | -3946 | -661 | -2874 | -4731 |
NDUFC2 | -3783 | 32 | -2407 | -2927 |
NDUFS1 | -4162 | -1524 | -4327 | -3922 |
NDUFS2 | -2719 | -2987 | -2787 | -4544 |
NDUFS3 | -2951 | -3520 | -2726 | -5085 |
NDUFS4 | -2602 | -1667 | -2421 | 914 |
NDUFS5 | -2493 | -1220 | -1904 | -4714 |
NDUFS6 | -1709 | -1316 | -973 | -5106 |
NDUFS7 | -2104 | -4811 | -1886 | -5006 |
NDUFS8 | -2071 | -4271 | -1979 | -3515 |
NDUFV1 | -2739 | -4172 | -2709 | -4349 |
NDUFV3 | -3600 | -2346 | -2565 | -1926 |
NUBPL | -4866 | -1521 | -3506 | 1659 |
SCO1 | -4774 | 3550 | 1689 | 2341 |
SCO2 | 1818 | -1915 | -766 | 740 |
SDHA | -3097 | -4713 | -4539 | -4393 |
SDHB | -3231 | 427 | -3667 | -3677 |
SDHC | -4613 | -3665 | -2969 | -3035 |
SLC25A14 | 4243 | 3803 | 1851 | 2411 |
SLC25A27 | -336 | -2446 | -4809 | -4546 |
SURF1 | -696 | -1725 | -4055 | -1565 |
TACO1 | -3389 | 642 | -4216 | -4383 |
TIMMDC1 | -3514 | 210 | -1099 | -4130 |
TMEM126B | -2313 | 1013 | 1849 | 2331 |
TRAP1 | -4514 | -5203 | -2043 | -4770 |
UCP2 | 4768 | -4888 | 4991 | 5018 |
UCP3 | 65 | -681 | -5302 | -499 |
UQCR10 | -2766 | -3097 | -257 | 2827 |
UQCRB | -4203 | 400 | -3675 | -1445 |
UQCRC1 | -2421 | -3288 | -3627 | -4053 |
UQCRC2 | -4768 | 543 | -3866 | -3335 |
UQCRFS1 | -2561 | -150 | -3030 | -2834 |
UQCRH | -3396 | -1512 | -1736 | -1917 |
UQCRQ | -1949 | -1744 | -1837 | 0 |
Caspase activation via Death Receptors in the presence of ligand
metric | value |
---|---|
setSize | 11 |
pMANOVA | 0.0137 |
p.adjustMANOVA | 0.0306 |
s.dist | 0.789 |
s.FSHD | 0.489 |
s.hu_model | -0.239 |
s.Watt_m | 0.339 |
s.Jones_m | 0.458 |
p.FSHD | 0.00496 |
p.hu_model | 0.17 |
p.Watt_m | 0.0515 |
p.Jones_m | 0.0085 |
Gene | FSHD | Jones_m |
---|---|---|
CASP8 | 4576 | 4108.0 |
TLR4 | 3937 | 4750.0 |
TRADD | 4253 | 4079.0 |
FAS | 3526 | 3480.0 |
RIPK1 | 2917 | 2881.0 |
TICAM1 | 1746 | 3735.0 |
TNFRSF10B | 4919 | 1242.5 |
TNFRSF10A | 3009 | 1242.5 |
FADD | 588 | 4118.0 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
CASP8 | 4576 | -1624 | 3056.0 | 4108.0 |
CFLAR | -5410 | -5487 | -3552.0 | -2793.0 |
FADD | 588 | -568 | 4829.0 | 4118.0 |
FAS | 3526 | -4711 | 2867.0 | 3480.0 |
RIPK1 | 2917 | 322 | 711.0 | 2881.0 |
TICAM1 | 1746 | 1607 | 4325.0 | 3735.0 |
TLR4 | 3937 | 1053 | 4868.0 | 4750.0 |
TNFRSF10A | 3009 | -3886 | 1248.5 | 1242.5 |
TNFRSF10B | 4919 | -1590 | 1248.5 | 1242.5 |
TRADD | 4253 | -702 | -1459.0 | 4079.0 |
TRAF2 | 2276 | -1526 | 970.0 | -697.0 |
Collagen degradation
metric | value |
---|---|
setSize | 20 |
pMANOVA | 5.57e-06 |
p.adjustMANOVA | 3.58e-05 |
s.dist | 0.775 |
s.FSHD | 0.602 |
s.hu_model | -0.274 |
s.Watt_m | 0.015 |
s.Jones_m | 0.403 |
p.FSHD | 3.18e-06 |
p.hu_model | 0.0337 |
p.Watt_m | 0.907 |
p.Jones_m | 0.00179 |
Gene | FSHD | Jones_m |
---|---|---|
MMP19 | 4747 | 5126 |
COL14A1 | 4785 | 4769 |
CTSK | 4644 | 4241 |
COL18A1 | 4351 | 3090 |
CTSB | 2843 | 4639 |
MMP14 | 4687 | 2675 |
MMP2 | 4410 | 2240 |
COL16A1 | 3846 | 2475 |
ADAM10 | 2507 | 3455 |
COL12A1 | 5001 | 1626 |
COL23A1 | 3199 | 2418 |
MMP11 | 2889 | 1218 |
CTSD | 1329 | 2582 |
COL15A1 | 2478 | 1179 |
ADAM17 | 411 | 2726 |
ADAM9 | 261 | 3770 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
ADAM10 | 2507 | -1489 | -1018 | 3455 |
ADAM17 | 411 | 2385 | 2056 | 2726 |
ADAM9 | 261 | 342 | 148 | 3770 |
COL12A1 | 5001 | 1907 | 511 | 1626 |
COL13A1 | -180 | -2295 | -1942 | 1914 |
COL14A1 | 4785 | 831 | 1493 | 4769 |
COL15A1 | 2478 | -169 | 1436 | 1179 |
COL16A1 | 3846 | -2915 | 1643 | 2475 |
COL18A1 | 4351 | -2864 | 2677 | 3090 |
COL23A1 | 3199 | -4585 | -845 | 2418 |
CTSB | 2843 | -1183 | -789 | 4639 |
CTSD | 1329 | -4757 | -3993 | 2582 |
CTSK | 4644 | 2 | 259 | 4241 |
FURIN | 1239 | -4167 | 4073 | -1204 |
MMP11 | 2889 | -3240 | -393 | 1218 |
MMP14 | 4687 | -1668 | 1618 | 2675 |
MMP15 | 1264 | -5090 | -5214 | -4505 |
MMP19 | 4747 | -167 | 4806 | 5126 |
MMP2 | 4410 | -689 | -1983 | 2240 |
PHYKPL | 4956 | -4988 | -3912 | -2713 |
Diseases associated with the TLR signaling cascade
metric | value |
---|---|
setSize | 16 |
pMANOVA | 0.000963 |
p.adjustMANOVA | 0.00329 |
s.dist | 0.772 |
s.FSHD | 0.358 |
s.hu_model | -0.174 |
s.Watt_m | 0.318 |
s.Jones_m | 0.58 |
p.FSHD | 0.0133 |
p.hu_model | 0.228 |
p.Watt_m | 0.0278 |
p.Jones_m | 5.89e-05 |
Gene | Jones_m | FSHD |
---|---|---|
NFKB2 | 5030 | 5031 |
TLR4 | 4750 | 3937 |
MYD88 | 3583 | 4634 |
NFKB1 | 3086 | 4613 |
IRAK4 | 3193 | 3956 |
TLR6 | 4168 | 2753 |
TLR5 | 4899 | 1981 |
RELA | 1891 | 3940 |
TRAF3 | 2668 | 2612 |
TICAM1 | 3735 | 1746 |
TLR3 | 2981 | 2103 |
NFKBIA | 1289 | 204 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
CD36 | -653 | -579 | -3797 | 1232 |
CHUK | -5003 | 213 | 946 | 4752 |
IKBKB | -4380 | -4041 | 570 | 3732 |
IRAK4 | 3956 | -566 | 1954 | 3193 |
MYD88 | 4634 | 2702 | 4632 | 3583 |
NFKB1 | 4613 | -4179 | 3276 | 3086 |
NFKB2 | 5031 | -3876 | 3297 | 5030 |
NFKBIA | 204 | -4209 | 4052 | 1289 |
RELA | 3940 | 1766 | 4484 | 1891 |
TICAM1 | 1746 | 1607 | 4325 | 3735 |
TIRAP | -273 | -2904 | -3591 | -2727 |
TLR3 | 2103 | -309 | -3670 | 2981 |
TLR4 | 3937 | 1053 | 4868 | 4750 |
TLR5 | 1981 | -3191 | 918 | 4899 |
TLR6 | 2753 | 877 | 1284 | 4168 |
TRAF3 | 2612 | -3766 | 2438 | 2668 |
Diseases of Immune System
metric | value |
---|---|
setSize | 16 |
pMANOVA | 0.000963 |
p.adjustMANOVA | 0.00329 |
s.dist | 0.772 |
s.FSHD | 0.358 |
s.hu_model | -0.174 |
s.Watt_m | 0.318 |
s.Jones_m | 0.58 |
p.FSHD | 0.0133 |
p.hu_model | 0.228 |
p.Watt_m | 0.0278 |
p.Jones_m | 5.89e-05 |
Gene | Jones_m | FSHD |
---|---|---|
NFKB2 | 5030 | 5031 |
TLR4 | 4750 | 3937 |
MYD88 | 3583 | 4634 |
NFKB1 | 3086 | 4613 |
IRAK4 | 3193 | 3956 |
TLR6 | 4168 | 2753 |
TLR5 | 4899 | 1981 |
RELA | 1891 | 3940 |
TRAF3 | 2668 | 2612 |
TICAM1 | 3735 | 1746 |
TLR3 | 2981 | 2103 |
NFKBIA | 1289 | 204 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
CD36 | -653 | -579 | -3797 | 1232 |
CHUK | -5003 | 213 | 946 | 4752 |
IKBKB | -4380 | -4041 | 570 | 3732 |
IRAK4 | 3956 | -566 | 1954 | 3193 |
MYD88 | 4634 | 2702 | 4632 | 3583 |
NFKB1 | 4613 | -4179 | 3276 | 3086 |
NFKB2 | 5031 | -3876 | 3297 | 5030 |
NFKBIA | 204 | -4209 | 4052 | 1289 |
RELA | 3940 | 1766 | 4484 | 1891 |
TICAM1 | 1746 | 1607 | 4325 | 3735 |
TIRAP | -273 | -2904 | -3591 | -2727 |
TLR3 | 2103 | -309 | -3670 | 2981 |
TLR4 | 3937 | 1053 | 4868 | 4750 |
TLR5 | 1981 | -3191 | 918 | 4899 |
TLR6 | 2753 | 877 | 1284 | 4168 |
TRAF3 | 2612 | -3766 | 2438 | 2668 |
Mitochondrial calcium ion transport
metric | value |
---|---|
setSize | 21 |
pMANOVA | 7.14e-05 |
p.adjustMANOVA | 0.000339 |
s.dist | 0.772 |
s.FSHD | -0.598 |
s.hu_model | -0.0111 |
s.Watt_m | -0.338 |
s.Jones_m | -0.351 |
p.FSHD | 2.12e-06 |
p.hu_model | 0.93 |
p.Watt_m | 0.00732 |
p.Jones_m | 0.00533 |
Gene | FSHD | Jones_m |
---|---|---|
VDAC3 | -5295 | -4968 |
MICU3 | -4344 | -4758 |
VDAC1 | -3918 | -5178 |
PMPCA | -3040 | -4811 |
SPG7 | -3269 | -4377 |
PHB | -3242 | -4330 |
YME1L1 | -5076 | -2146 |
C2orf47 | -4691 | -2251 |
VDAC2 | -2987 | -3338 |
STOML2 | -2788 | -3383 |
SLC8A3 | -1730 | -4578 |
AFG3L2 | -4583 | -1568 |
AKAP1 | -4443 | -1523 |
PMPCB | -5065 | -1223 |
PHB2 | -3483 | -1389 |
LETM1 | -2627 | -145 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
AFG3L2 | -4583 | -1974 | -3074 | -1568 |
AKAP1 | -4443 | -5031 | -4236 | -1523 |
C2orf47 | -4691 | 4125 | -472 | -2251 |
LETM1 | -2627 | -552 | -4525 | -145 |
MCU | -820 | 416 | 1521 | 4976 |
MICU1 | -1998 | 4883 | 2372 | 3567 |
MICU2 | -4462 | -606 | 1264 | 3704 |
MICU3 | -4344 | 2577 | -2525 | -4758 |
PARL | 220 | 762 | -4126 | -2890 |
PHB | -3242 | -583 | -2096 | -4330 |
PHB2 | -3483 | 584 | -889 | -1389 |
PMPCA | -3040 | -92 | -4554 | -4811 |
PMPCB | -5065 | -824 | -3599 | -1223 |
SLC8A3 | -1730 | -5413 | -3845 | -4578 |
SMDT1 | -2173 | -3739 | -157 | 1060 |
SPG7 | -3269 | -4482 | -3652 | -4377 |
STOML2 | -2788 | 1967 | 314 | -3383 |
VDAC1 | -3918 | -2871 | -4553 | -5178 |
VDAC2 | -2987 | -1424 | -2473 | -3338 |
VDAC3 | -5295 | 524 | 3115 | -4968 |
YME1L1 | -5076 | 4303 | -2155 | -2146 |
MET activates PTK2 signaling
metric | value |
---|---|
setSize | 14 |
pMANOVA | 0.000331 |
p.adjustMANOVA | 0.00131 |
s.dist | 0.769 |
s.FSHD | 0.587 |
s.hu_model | -0.431 |
s.Watt_m | 0.0361 |
s.Jones_m | 0.244 |
p.FSHD | 0.000144 |
p.hu_model | 0.00524 |
p.Watt_m | 0.815 |
p.Jones_m | 0.114 |
Gene | FSHD | hu_model |
---|---|---|
ITGA3 | 4809 | -5450 |
LAMA5 | 3521 | -5520 |
SRC | 5021 | -3860 |
LAMB2 | 3450 | -4834 |
LAMC1 | 4113 | -3181 |
LAMA2 | 3038 | -3750 |
LAMB3 | 2231 | -4929 |
LAMA3 | 3451 | -999 |
PTK2 | 692 | -2465 |
LAMB1 | 2539 | -455 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
ITGA3 | 4809 | -5450 | 2976 | 557 |
ITGB1 | 891 | 945 | 4567 | 4783 |
LAMA2 | 3038 | -3750 | -756 | 2040 |
LAMA3 | 3451 | -999 | -4332 | -2201 |
LAMA4 | 4388 | 736 | -121 | 2343 |
LAMA5 | 3521 | -5520 | -2717 | -2028 |
LAMB1 | 2539 | -455 | -385 | 3101 |
LAMB2 | 3450 | -4834 | -3037 | -2486 |
LAMB3 | 2231 | -4929 | -4569 | 386 |
LAMC1 | 4113 | -3181 | 2501 | 4089 |
LAMC2 | 4587 | 1336 | 5102 | 4436 |
MET | -2044 | -3482 | 2897 | 4177 |
PTK2 | 692 | -2465 | -1494 | -4001 |
SRC | 5021 | -3860 | 1364 | 2269 |
Acyl chain remodelling of PS
metric | value |
---|---|
setSize | 10 |
pMANOVA | 0.0123 |
p.adjustMANOVA | 0.0279 |
s.dist | 0.767 |
s.FSHD | 0.414 |
s.hu_model | 0.218 |
s.Watt_m | 0.215 |
s.Jones_m | 0.568 |
p.FSHD | 0.0233 |
p.hu_model | 0.234 |
p.Watt_m | 0.238 |
p.Jones_m | 0.00186 |
Gene | Jones_m | FSHD |
---|---|---|
PLA2R1 | 4946 | 4029 |
OSBPL10 | 4344 | 4129 |
OSBPL8 | 4794 | 2879 |
PLA2G4A | 3078 | 4275 |
LPCAT4 | 2121 | 4462 |
PLA1A | 3458 | 1853 |
OSBPL5 | 2260 | 2610 |
MBOAT1 | 4267 | 1080 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
LPCAT3 | -672 | 4190 | -2687 | -1766 |
LPCAT4 | 4462 | -1170 | 3757 | 2121 |
MBOAT1 | 1080 | 3887 | 4795 | 4267 |
OSBPL10 | 4129 | 4 | 914 | 4344 |
OSBPL5 | 2610 | -4800 | -552 | 2260 |
OSBPL8 | 2879 | 4837 | 4358 | 4794 |
PLA1A | 1853 | -1363 | 2239 | 3458 |
PLA2G12A | -4644 | 2245 | -2020 | 2064 |
PLA2G4A | 4275 | 594 | 3662 | 3078 |
PLA2R1 | 4029 | 63 | -3602 | 4946 |
Voltage gated Potassium channels
metric | value |
---|---|
setSize | 11 |
pMANOVA | 0.00104 |
p.adjustMANOVA | 0.00354 |
s.dist | 0.767 |
s.FSHD | 0.212 |
s.hu_model | -0.528 |
s.Watt_m | -0.361 |
s.Jones_m | -0.365 |
p.FSHD | 0.223 |
p.hu_model | 0.00243 |
p.Watt_m | 0.038 |
p.Jones_m | 0.0359 |
Gene | hu_model | Jones_m |
---|---|---|
KCNC4 | -4849 | -5210 |
KCNA7 | -5080 | -4397 |
KCNB1 | -5055 | -4312 |
KCNQ5 | -3706 | -4990 |
KCNQ4 | -5558 | -1338 |
KCNC1 | -3294 | -2070 |
KCNC3 | -364 | -3280 |
KCNH2 | -3484 | -248 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
KCNA1 | 3484 | 4556 | 2104 | -2224 |
KCNA7 | -3572 | -5080 | -3447 | -4397 |
KCNAB2 | 3225 | -3156 | 4972 | 4840 |
KCNB1 | 484 | -5055 | -5008 | -4312 |
KCNC1 | -4268 | -3294 | -5258 | -2070 |
KCNC3 | 3323 | -364 | 1008 | -3280 |
KCNC4 | 3670 | -4849 | -5217 | -5210 |
KCNH2 | 982 | -3484 | -1469 | -248 |
KCNQ1 | 3848 | -3838 | 557 | 1681 |
KCNQ4 | 2223 | -5558 | -4977 | -1338 |
KCNQ5 | -3117 | -3706 | -4711 | -4990 |
Mitochondrial translation
metric | value |
---|---|
setSize | 87 |
pMANOVA | 1.59e-19 |
p.adjustMANOVA | 1.02e-17 |
s.dist | 0.764 |
s.FSHD | -0.554 |
s.hu_model | 0.159 |
s.Watt_m | -0.315 |
s.Jones_m | -0.389 |
p.FSHD | 4.1e-19 |
p.hu_model | 0.0107 |
p.Watt_m | 4.08e-07 |
p.Jones_m | 3.59e-10 |
Gene | FSHD | Jones_m |
---|---|---|
GFM1 | -5327 | -4196 |
PTCD3 | -5161 | -4052 |
DAP3 | -4837 | -4034 |
MRPL30 | -4564 | -4158 |
GFM2 | -3662 | -5127 |
MRPL42 | -3577 | -5202 |
MRPS36 | -5429 | -3208 |
MRPL32 | -4818 | -3602 |
MTRF1L | -5397 | -3157 |
MTIF2 | -4920 | -3415 |
MRPS18B | -4367 | -3831 |
MRPS5 | -3273 | -5089 |
CHCHD1 | -3980 | -3974 |
MRPL16 | -4392 | -3597 |
MRPL11 | -3720 | -4218 |
TUFM | -3802 | -4101 |
MRPS16 | -4590 | -3231 |
MRPS15 | -3628 | -4018 |
MRPS23 | -4659 | -3082 |
OXA1L | -4632 | -3044 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
AURKAIP1 | -3378 | -2276 | -1747 | -3524 |
CHCHD1 | -3980 | -540 | -1809 | -3974 |
DAP3 | -4837 | -461 | 2611 | -4034 |
ERAL1 | -3167 | 2585 | -858 | -3141 |
GADD45GIP1 | -1089 | -2386 | -3149 | -2950 |
GFM1 | -5327 | 4168 | -4357 | -4196 |
GFM2 | -3662 | 3786 | -5236 | -5127 |
MRPL1 | -3901 | -1280 | -4021 | -2985 |
MRPL10 | -2288 | -2374 | -4353 | -2443 |
MRPL11 | -3720 | 2077 | -2512 | -4218 |
MRPL12 | -1963 | -2623 | -2727 | -2667 |
MRPL13 | -3539 | 343 | 285 | -3672 |
MRPL14 | -1974 | -1679 | -1052 | 1359 |
MRPL15 | -3132 | 2448 | -2949 | -4325 |
MRPL16 | -4392 | 3057 | -3392 | -3597 |
MRPL17 | 595 | 1912 | 2816 | 4209 |
MRPL18 | -2407 | 2971 | -4191 | -3349 |
MRPL19 | -4475 | 4046 | -3671 | -1186 |
MRPL2 | -2747 | -435 | -1567 | -4868 |
MRPL20 | -3024 | 531 | 207 | -510 |
MRPL21 | -3086 | 1674 | -768 | -3347 |
MRPL22 | -2171 | 3326 | -2754 | -3733 |
MRPL23 | -3087 | -3178 | -776 | -1241 |
MRPL24 | -1464 | -1858 | -2181 | -1722 |
MRPL27 | -2722 | -1594 | -1652 | -1044 |
MRPL28 | -7 | -271 | -990 | -2552 |
MRPL3 | -3854 | 2949 | -3937 | -192 |
MRPL30 | -4564 | 3470 | -1084 | -4158 |
MRPL32 | -4818 | 3042 | 2692 | -3602 |
MRPL34 | -3944 | -2159 | -3284 | -2255 |
MRPL35 | -5028 | 800 | -2563 | -2768 |
MRPL36 | -2568 | -557 | -2264 | 625 |
MRPL37 | -2913 | 1590 | -2744 | -3921 |
MRPL38 | -490 | 368 | -1753 | -3644 |
MRPL39 | -3867 | 2569 | -947 | -1196 |
MRPL4 | -1740 | 2929 | -505 | -2748 |
MRPL40 | -2857 | -249 | 796 | 637 |
MRPL41 | -4483 | -4838 | -1856 | 1777 |
MRPL42 | -3577 | 2087 | -1650 | -5202 |
MRPL43 | -1019 | -1428 | -663 | 1286 |
MRPL44 | -3543 | 4365 | -2069 | -3706 |
MRPL46 | -2332 | 996 | -440 | 1568 |
MRPL47 | -1558 | 3146 | -1887 | -1504 |
MRPL48 | -3651 | -80 | 163 | -1871 |
MRPL49 | -468 | 4723 | -3219 | -2978 |
MRPL50 | -3974 | 3074 | -150 | -1267 |
MRPL51 | -2492 | -387 | -1581 | -4128 |
MRPL52 | -1075 | -2282 | 1466 | -1004 |
MRPL54 | 445 | -1970 | 2366 | -2983 |
MRPL55 | -932 | 1077 | -3210 | -3400 |
MRPL9 | -2162 | 3406 | -3593 | -1971 |
MRPS10 | -2227 | -3045 | -784 | -2392 |
MRPS11 | -3081 | 280 | -2798 | -1751 |
MRPS12 | -2364 | -146 | 616 | 1122 |
MRPS14 | -1834 | 1778 | -4387 | -4044 |
MRPS15 | -3628 | 1857 | -1464 | -4018 |
MRPS16 | -4590 | 1192 | -2229 | -3231 |
MRPS17 | -3181 | -131 | -1389 | 4388 |
MRPS18A | -2481 | 465 | -4081 | -4980 |
MRPS18B | -4367 | -1848 | 1877 | -3831 |
MRPS18C | -3506 | 4342 | -675 | -570 |
MRPS2 | -2046 | 1425 | 2175 | -19 |
MRPS22 | -4388 | 4344 | -1949 | -275 |
MRPS23 | -4659 | 1657 | -4044 | -3082 |
MRPS25 | -3226 | -3514 | -3925 | 431 |
MRPS26 | -646 | -610 | -1343 | -2703 |
MRPS27 | -4915 | 555 | -2134 | -2848 |
MRPS28 | -2816 | 1341 | -1288 | -4916 |
MRPS30 | -3672 | 3442 | 761 | -2570 |
MRPS31 | -4207 | 3479 | -1758 | -2995 |
MRPS33 | -4017 | 149 | -530 | -1199 |
MRPS34 | -2775 | -3797 | -2222 | -3830 |
MRPS35 | -4450 | 3080 | -2647 | 954 |
MRPS36 | -5429 | -2678 | 682 | -3208 |
MRPS5 | -3273 | -1161 | -2766 | -5089 |
MRPS6 | 1135 | -4408 | 2857 | -486 |
MRPS7 | -3579 | -1321 | 849 | 138 |
MRPS9 | -3785 | 1389 | -4076 | -1007 |
MRRF | -2365 | -2758 | -206 | -1218 |
MTFMT | -3046 | -1437 | -1940 | 1267 |
MTIF2 | -4920 | 1787 | -4751 | -3415 |
MTIF3 | -4258 | 276 | -1404 | 3305 |
MTRF1L | -5397 | 1502 | -3819 | -3157 |
OXA1L | -4632 | -2587 | -3906 | -3044 |
PTCD3 | -5161 | 3456 | -5112 | -4052 |
TSFM | -3801 | 1946 | -2884 | 3728 |
TUFM | -3802 | -2555 | -3791 | -4101 |
Syndecan interactions
metric | value |
---|---|
setSize | 17 |
pMANOVA | 0.00145 |
p.adjustMANOVA | 0.00464 |
s.dist | 0.761 |
s.FSHD | 0.544 |
s.hu_model | -0.0484 |
s.Watt_m | 0.357 |
s.Jones_m | 0.392 |
p.FSHD | 0.000104 |
p.hu_model | 0.73 |
p.Watt_m | 0.0108 |
p.Jones_m | 0.00521 |
Gene | FSHD | Jones_m |
---|---|---|
ACTN1 | 4991 | 4955 |
SDC2 | 4456 | 5008 |
THBS1 | 4954 | 3647 |
TNC | 5019 | 3460 |
TGFB1 | 4177 | 4099 |
SDC3 | 3721 | 4191 |
ITGB3 | 3693 | 2921 |
SDC1 | 3944 | 2683 |
CASK | 1599 | 3957 |
ITGB1 | 891 | 4783 |
ITGAV | 801 | 4981 |
SDC4 | 1095 | 946 |
TRAPPC4 | 41 | 1401 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
ACTN1 | 4991 | -673 | 3653 | 4955 |
CASK | 1599 | 2860 | 3171 | 3957 |
FGF2 | 1476 | 741 | -1087 | -3508 |
ITGA6 | 1799 | -990 | -5243 | -114 |
ITGAV | 801 | -812 | 49 | 4981 |
ITGB1 | 891 | 945 | 4567 | 4783 |
ITGB3 | 3693 | -485 | 4867 | 2921 |
ITGB5 | 3604 | -2545 | -4743 | -4839 |
PRKCA | -720 | -2900 | -2894 | -4160 |
SDC1 | 3944 | -2017 | 209 | 2683 |
SDC2 | 4456 | 1739 | 4436 | 5008 |
SDC3 | 3721 | -4560 | 2780 | 4191 |
SDC4 | 1095 | -2361 | 5103 | 946 |
TGFB1 | 4177 | -3070 | 4895 | 4099 |
THBS1 | 4954 | 752 | 4384 | 3647 |
TNC | 5019 | 793 | 4283 | 3460 |
TRAPPC4 | 41 | 3212 | 2700 | 1401 |
N-Glycan antennae elongation
metric | value |
---|---|
setSize | 12 |
pMANOVA | 0.00608 |
p.adjustMANOVA | 0.0156 |
s.dist | 0.759 |
s.FSHD | 0.262 |
s.hu_model | -0.26 |
s.Watt_m | 0.429 |
s.Jones_m | 0.505 |
p.FSHD | 0.116 |
p.hu_model | 0.118 |
p.Watt_m | 0.01 |
p.Jones_m | 0.00247 |
Gene | Jones_m | Watt_m |
---|---|---|
B4GALT5 | 5074 | 4122 |
ST8SIA2 | 4293 | 3919 |
B4GALT6 | 5160 | 3047 |
ST3GAL4 | 3256 | 3728 |
MGAT5 | 3834 | 2701 |
ST6GAL1 | 3388 | 1734 |
B4GALT2 | 2616 | 2193 |
B4GALT1 | 1643 | 2563 |
MGAT4A | 943 | 3278 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
B4GALT1 | 1688 | -1298 | 2563 | 1643 |
B4GALT2 | -256 | -4979 | 2193 | 2616 |
B4GALT3 | 624 | 963 | 1156 | -435 |
B4GALT4 | 140 | 1624 | -695 | 2909 |
B4GALT5 | -3265 | -4015 | 4122 | 5074 |
B4GALT6 | -3537 | 2681 | 3047 | 5160 |
MGAT4A | 2876 | 265 | 3278 | 943 |
MGAT4B | 3709 | -4647 | -1197 | -1234 |
MGAT5 | 4691 | 2988 | 2701 | 3834 |
ST3GAL4 | 3433 | -2907 | 3728 | 3256 |
ST6GAL1 | 72 | -5325 | 1734 | 3388 |
ST8SIA2 | 4218 | -5360 | 3919 | 4293 |
Other interleukin signaling
metric | value |
---|---|
setSize | 13 |
pMANOVA | 0.00741 |
p.adjustMANOVA | 0.0184 |
s.dist | 0.757 |
s.FSHD | 0.554 |
s.hu_model | -0.131 |
s.Watt_m | 0.267 |
s.Jones_m | 0.421 |
p.FSHD | 0.000543 |
p.hu_model | 0.412 |
p.Watt_m | 0.0955 |
p.Jones_m | 0.0086 |
Gene | FSHD | Jones_m |
---|---|---|
IL10RB | 4957 | 4242 |
CSF1 | 4653 | 3814 |
IL16 | 3962 | 2759 |
TYK2 | 2357 | 4512 |
SDC1 | 3944 | 2683 |
STX4 | 2959 | 3083 |
CASP3 | 1918 | 4110 |
STX1A | 2700 | 1638 |
IL34 | 3608 | 1009 |
TXLNA | 525 | 1982 |
VAMP2 | 835 | 1196 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
CASP3 | 1918 | 419 | 4968 | 4110 |
CSF1 | 4653 | -4188 | 4312 | 3814 |
IL10RB | 4957 | 1225 | 3206 | 4242 |
IL16 | 3962 | -1591 | -1353 | 2759 |
IL34 | 3608 | 3034 | -1526 | 1009 |
JAK1 | 1002 | -1843 | 4184 | -1810 |
SDC1 | 3944 | -2017 | 209 | 2683 |
STX1A | 2700 | -409 | 1596 | 1638 |
STX3 | 2125 | 4340 | -2442 | -877 |
STX4 | 2959 | -2315 | 77 | 3083 |
TXLNA | 525 | -3173 | 2681 | 1982 |
TYK2 | 2357 | -3081 | -49 | 4512 |
VAMP2 | 835 | -3250 | 1792 | 1196 |
Biotin transport and metabolism
metric | value |
---|---|
setSize | 10 |
pMANOVA | 0.0396 |
p.adjustMANOVA | 0.075 |
s.dist | 0.757 |
s.FSHD | -0.323 |
s.hu_model | -0.0201 |
s.Watt_m | -0.535 |
s.Jones_m | -0.426 |
p.FSHD | 0.0766 |
p.hu_model | 0.912 |
p.Watt_m | 0.00339 |
p.Jones_m | 0.0198 |
Gene | Watt_m | Jones_m |
---|---|---|
PCCA | -5148 | -4743 |
MCCC2 | -4913 | -4935 |
ACACB | -4941 | -4435 |
PCCB | -4099 | -5276 |
MCCC1 | -4638 | -4559 |
PC | -3656 | -4683 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
ACACB | -2494 | -5314 | -4941 | -4435 |
BTD | 2964 | 2543 | 2171 | -688 |
HLCS | -4775 | -754 | -3859 | 1637 |
MCCC1 | -4819 | 3980 | -4638 | -4559 |
MCCC2 | -4989 | 2184 | -4913 | -4935 |
PC | 929 | -5164 | -3656 | -4683 |
PCCA | -4767 | -2564 | -5148 | -4743 |
PCCB | -3972 | -164 | -4099 | -5276 |
PDZD11 | 1299 | 1661 | 484 | 4847 |
SLC5A6 | 1784 | -431 | -42 | 72 |
Mitochondrial translation termination
metric | value |
---|---|
setSize | 81 |
pMANOVA | 1.65e-17 |
p.adjustMANOVA | 8.47e-16 |
s.dist | 0.754 |
s.FSHD | -0.538 |
s.hu_model | 0.156 |
s.Watt_m | -0.293 |
s.Jones_m | -0.411 |
p.FSHD | 5.73e-17 |
p.hu_model | 0.0152 |
p.Watt_m | 5.2e-06 |
p.Jones_m | 1.77e-10 |
Gene | FSHD | Jones_m |
---|---|---|
PTCD3 | -5161 | -4052 |
DAP3 | -4837 | -4034 |
MRPL30 | -4564 | -4158 |
GFM2 | -3662 | -5127 |
MRPL42 | -3577 | -5202 |
MRPS36 | -5429 | -3208 |
MRPL32 | -4818 | -3602 |
MTRF1L | -5397 | -3157 |
MRPS18B | -4367 | -3831 |
MRPS5 | -3273 | -5089 |
CHCHD1 | -3980 | -3974 |
MRPL16 | -4392 | -3597 |
MRPL11 | -3720 | -4218 |
MRPS16 | -4590 | -3231 |
MRPS15 | -3628 | -4018 |
MRPS23 | -4659 | -3082 |
OXA1L | -4632 | -3044 |
MRPS27 | -4915 | -2848 |
MRPL35 | -5028 | -2768 |
MRPS28 | -2816 | -4916 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
AURKAIP1 | -3378 | -2276 | -1747 | -3524 |
CHCHD1 | -3980 | -540 | -1809 | -3974 |
DAP3 | -4837 | -461 | 2611 | -4034 |
ERAL1 | -3167 | 2585 | -858 | -3141 |
GADD45GIP1 | -1089 | -2386 | -3149 | -2950 |
GFM2 | -3662 | 3786 | -5236 | -5127 |
MRPL1 | -3901 | -1280 | -4021 | -2985 |
MRPL10 | -2288 | -2374 | -4353 | -2443 |
MRPL11 | -3720 | 2077 | -2512 | -4218 |
MRPL12 | -1963 | -2623 | -2727 | -2667 |
MRPL13 | -3539 | 343 | 285 | -3672 |
MRPL14 | -1974 | -1679 | -1052 | 1359 |
MRPL15 | -3132 | 2448 | -2949 | -4325 |
MRPL16 | -4392 | 3057 | -3392 | -3597 |
MRPL17 | 595 | 1912 | 2816 | 4209 |
MRPL18 | -2407 | 2971 | -4191 | -3349 |
MRPL19 | -4475 | 4046 | -3671 | -1186 |
MRPL2 | -2747 | -435 | -1567 | -4868 |
MRPL20 | -3024 | 531 | 207 | -510 |
MRPL21 | -3086 | 1674 | -768 | -3347 |
MRPL22 | -2171 | 3326 | -2754 | -3733 |
MRPL23 | -3087 | -3178 | -776 | -1241 |
MRPL24 | -1464 | -1858 | -2181 | -1722 |
MRPL27 | -2722 | -1594 | -1652 | -1044 |
MRPL28 | -7 | -271 | -990 | -2552 |
MRPL3 | -3854 | 2949 | -3937 | -192 |
MRPL30 | -4564 | 3470 | -1084 | -4158 |
MRPL32 | -4818 | 3042 | 2692 | -3602 |
MRPL34 | -3944 | -2159 | -3284 | -2255 |
MRPL35 | -5028 | 800 | -2563 | -2768 |
MRPL36 | -2568 | -557 | -2264 | 625 |
MRPL37 | -2913 | 1590 | -2744 | -3921 |
MRPL38 | -490 | 368 | -1753 | -3644 |
MRPL39 | -3867 | 2569 | -947 | -1196 |
MRPL4 | -1740 | 2929 | -505 | -2748 |
MRPL40 | -2857 | -249 | 796 | 637 |
MRPL41 | -4483 | -4838 | -1856 | 1777 |
MRPL42 | -3577 | 2087 | -1650 | -5202 |
MRPL43 | -1019 | -1428 | -663 | 1286 |
MRPL44 | -3543 | 4365 | -2069 | -3706 |
MRPL46 | -2332 | 996 | -440 | 1568 |
MRPL47 | -1558 | 3146 | -1887 | -1504 |
MRPL48 | -3651 | -80 | 163 | -1871 |
MRPL49 | -468 | 4723 | -3219 | -2978 |
MRPL50 | -3974 | 3074 | -150 | -1267 |
MRPL51 | -2492 | -387 | -1581 | -4128 |
MRPL52 | -1075 | -2282 | 1466 | -1004 |
MRPL54 | 445 | -1970 | 2366 | -2983 |
MRPL55 | -932 | 1077 | -3210 | -3400 |
MRPL9 | -2162 | 3406 | -3593 | -1971 |
MRPS10 | -2227 | -3045 | -784 | -2392 |
MRPS11 | -3081 | 280 | -2798 | -1751 |
MRPS12 | -2364 | -146 | 616 | 1122 |
MRPS14 | -1834 | 1778 | -4387 | -4044 |
MRPS15 | -3628 | 1857 | -1464 | -4018 |
MRPS16 | -4590 | 1192 | -2229 | -3231 |
MRPS17 | -3181 | -131 | -1389 | 4388 |
MRPS18A | -2481 | 465 | -4081 | -4980 |
MRPS18B | -4367 | -1848 | 1877 | -3831 |
MRPS18C | -3506 | 4342 | -675 | -570 |
MRPS2 | -2046 | 1425 | 2175 | -19 |
MRPS22 | -4388 | 4344 | -1949 | -275 |
MRPS23 | -4659 | 1657 | -4044 | -3082 |
MRPS25 | -3226 | -3514 | -3925 | 431 |
MRPS26 | -646 | -610 | -1343 | -2703 |
MRPS27 | -4915 | 555 | -2134 | -2848 |
MRPS28 | -2816 | 1341 | -1288 | -4916 |
MRPS30 | -3672 | 3442 | 761 | -2570 |
MRPS31 | -4207 | 3479 | -1758 | -2995 |
MRPS33 | -4017 | 149 | -530 | -1199 |
MRPS34 | -2775 | -3797 | -2222 | -3830 |
MRPS35 | -4450 | 3080 | -2647 | 954 |
MRPS36 | -5429 | -2678 | 682 | -3208 |
MRPS5 | -3273 | -1161 | -2766 | -5089 |
MRPS6 | 1135 | -4408 | 2857 | -486 |
MRPS7 | -3579 | -1321 | 849 | 138 |
MRPS9 | -3785 | 1389 | -4076 | -1007 |
MRRF | -2365 | -2758 | -206 | -1218 |
MTRF1L | -5397 | 1502 | -3819 | -3157 |
OXA1L | -4632 | -2587 | -3906 | -3044 |
PTCD3 | -5161 | 3456 | -5112 | -4052 |
Mitochondrial translation elongation
metric | value |
---|---|
setSize | 81 |
pMANOVA | 1.59e-17 |
p.adjustMANOVA | 8.47e-16 |
s.dist | 0.753 |
s.FSHD | -0.542 |
s.hu_model | 0.159 |
s.Watt_m | -0.297 |
s.Jones_m | -0.399 |
p.FSHD | 3.57e-17 |
p.hu_model | 0.0137 |
p.Watt_m | 3.81e-06 |
p.Jones_m | 5.7e-10 |
Gene | FSHD | Jones_m |
---|---|---|
GFM1 | -5327 | -4196 |
PTCD3 | -5161 | -4052 |
DAP3 | -4837 | -4034 |
MRPL30 | -4564 | -4158 |
MRPL42 | -3577 | -5202 |
MRPS36 | -5429 | -3208 |
MRPL32 | -4818 | -3602 |
MRPS18B | -4367 | -3831 |
MRPS5 | -3273 | -5089 |
CHCHD1 | -3980 | -3974 |
MRPL16 | -4392 | -3597 |
MRPL11 | -3720 | -4218 |
TUFM | -3802 | -4101 |
MRPS16 | -4590 | -3231 |
MRPS15 | -3628 | -4018 |
MRPS23 | -4659 | -3082 |
OXA1L | -4632 | -3044 |
MRPS27 | -4915 | -2848 |
MRPL35 | -5028 | -2768 |
MRPS28 | -2816 | -4916 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
AURKAIP1 | -3378 | -2276 | -1747 | -3524 |
CHCHD1 | -3980 | -540 | -1809 | -3974 |
DAP3 | -4837 | -461 | 2611 | -4034 |
ERAL1 | -3167 | 2585 | -858 | -3141 |
GADD45GIP1 | -1089 | -2386 | -3149 | -2950 |
GFM1 | -5327 | 4168 | -4357 | -4196 |
MRPL1 | -3901 | -1280 | -4021 | -2985 |
MRPL10 | -2288 | -2374 | -4353 | -2443 |
MRPL11 | -3720 | 2077 | -2512 | -4218 |
MRPL12 | -1963 | -2623 | -2727 | -2667 |
MRPL13 | -3539 | 343 | 285 | -3672 |
MRPL14 | -1974 | -1679 | -1052 | 1359 |
MRPL15 | -3132 | 2448 | -2949 | -4325 |
MRPL16 | -4392 | 3057 | -3392 | -3597 |
MRPL17 | 595 | 1912 | 2816 | 4209 |
MRPL18 | -2407 | 2971 | -4191 | -3349 |
MRPL19 | -4475 | 4046 | -3671 | -1186 |
MRPL2 | -2747 | -435 | -1567 | -4868 |
MRPL20 | -3024 | 531 | 207 | -510 |
MRPL21 | -3086 | 1674 | -768 | -3347 |
MRPL22 | -2171 | 3326 | -2754 | -3733 |
MRPL23 | -3087 | -3178 | -776 | -1241 |
MRPL24 | -1464 | -1858 | -2181 | -1722 |
MRPL27 | -2722 | -1594 | -1652 | -1044 |
MRPL28 | -7 | -271 | -990 | -2552 |
MRPL3 | -3854 | 2949 | -3937 | -192 |
MRPL30 | -4564 | 3470 | -1084 | -4158 |
MRPL32 | -4818 | 3042 | 2692 | -3602 |
MRPL34 | -3944 | -2159 | -3284 | -2255 |
MRPL35 | -5028 | 800 | -2563 | -2768 |
MRPL36 | -2568 | -557 | -2264 | 625 |
MRPL37 | -2913 | 1590 | -2744 | -3921 |
MRPL38 | -490 | 368 | -1753 | -3644 |
MRPL39 | -3867 | 2569 | -947 | -1196 |
MRPL4 | -1740 | 2929 | -505 | -2748 |
MRPL40 | -2857 | -249 | 796 | 637 |
MRPL41 | -4483 | -4838 | -1856 | 1777 |
MRPL42 | -3577 | 2087 | -1650 | -5202 |
MRPL43 | -1019 | -1428 | -663 | 1286 |
MRPL44 | -3543 | 4365 | -2069 | -3706 |
MRPL46 | -2332 | 996 | -440 | 1568 |
MRPL47 | -1558 | 3146 | -1887 | -1504 |
MRPL48 | -3651 | -80 | 163 | -1871 |
MRPL49 | -468 | 4723 | -3219 | -2978 |
MRPL50 | -3974 | 3074 | -150 | -1267 |
MRPL51 | -2492 | -387 | -1581 | -4128 |
MRPL52 | -1075 | -2282 | 1466 | -1004 |
MRPL54 | 445 | -1970 | 2366 | -2983 |
MRPL55 | -932 | 1077 | -3210 | -3400 |
MRPL9 | -2162 | 3406 | -3593 | -1971 |
MRPS10 | -2227 | -3045 | -784 | -2392 |
MRPS11 | -3081 | 280 | -2798 | -1751 |
MRPS12 | -2364 | -146 | 616 | 1122 |
MRPS14 | -1834 | 1778 | -4387 | -4044 |
MRPS15 | -3628 | 1857 | -1464 | -4018 |
MRPS16 | -4590 | 1192 | -2229 | -3231 |
MRPS17 | -3181 | -131 | -1389 | 4388 |
MRPS18A | -2481 | 465 | -4081 | -4980 |
MRPS18B | -4367 | -1848 | 1877 | -3831 |
MRPS18C | -3506 | 4342 | -675 | -570 |
MRPS2 | -2046 | 1425 | 2175 | -19 |
MRPS22 | -4388 | 4344 | -1949 | -275 |
MRPS23 | -4659 | 1657 | -4044 | -3082 |
MRPS25 | -3226 | -3514 | -3925 | 431 |
MRPS26 | -646 | -610 | -1343 | -2703 |
MRPS27 | -4915 | 555 | -2134 | -2848 |
MRPS28 | -2816 | 1341 | -1288 | -4916 |
MRPS30 | -3672 | 3442 | 761 | -2570 |
MRPS31 | -4207 | 3479 | -1758 | -2995 |
MRPS33 | -4017 | 149 | -530 | -1199 |
MRPS34 | -2775 | -3797 | -2222 | -3830 |
MRPS35 | -4450 | 3080 | -2647 | 954 |
MRPS36 | -5429 | -2678 | 682 | -3208 |
MRPS5 | -3273 | -1161 | -2766 | -5089 |
MRPS6 | 1135 | -4408 | 2857 | -486 |
MRPS7 | -3579 | -1321 | 849 | 138 |
MRPS9 | -3785 | 1389 | -4076 | -1007 |
OXA1L | -4632 | -2587 | -3906 | -3044 |
PTCD3 | -5161 | 3456 | -5112 | -4052 |
TSFM | -3801 | 1946 | -2884 | 3728 |
TUFM | -3802 | -2555 | -3791 | -4101 |
Gluconeogenesis
metric | value |
---|---|
setSize | 21 |
pMANOVA | 1.67e-05 |
p.adjustMANOVA | 9.17e-05 |
s.dist | 0.749 |
s.FSHD | -0.0701 |
s.hu_model | -0.555 |
s.Watt_m | -0.352 |
s.Jones_m | -0.352 |
p.FSHD | 0.578 |
p.hu_model | 1.06e-05 |
p.Watt_m | 0.00528 |
p.Jones_m | 0.00523 |
Gene | hu_model | Watt_m |
---|---|---|
SLC25A12 | -5285 | -4498 |
SLC37A4 | -4706 | -4997 |
GPI | -5148 | -4088 |
ALDOA | -5511 | -3443 |
PC | -5164 | -3656 |
SLC25A11 | -4056 | -3802 |
TPI1 | -3331 | -4427 |
ENO3 | -4611 | -2827 |
MDH2 | -4307 | -2826 |
GOT2 | -3657 | -3058 |
FBP2 | -3279 | -3190 |
PGK1 | -1397 | -3476 |
GOT1 | -3709 | -1241 |
G6PC3 | -3026 | -1478 |
MDH1 | -1078 | -3603 |
SLC37A1 | -2557 | -200 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
ALDOA | -3976 | -5511 | -3443 | -5047 |
ENO1 | 5029 | -4031 | 2449 | 4819 |
ENO2 | 4873 | -1995 | 892 | 3627 |
ENO3 | -2016 | -4611 | -2827 | -4496 |
FBP2 | -598 | -3279 | -3190 | -5287 |
G6PC3 | 1060 | -3026 | -1478 | -3910 |
GOT1 | -2290 | -3709 | -1241 | -66 |
GOT2 | -3182 | -3657 | -3058 | -2419 |
GPI | -4196 | -5148 | -4088 | -3489 |
MDH1 | -3312 | -1078 | -3603 | -1356 |
MDH2 | -2694 | -4307 | -2826 | -2711 |
PC | 929 | -5164 | -3656 | -4683 |
PCK2 | 4447 | -2285 | 369 | 3424 |
PGK1 | -2419 | -1397 | -3476 | -4681 |
SLC25A1 | 4153 | -2654 | 3689 | -1464 |
SLC25A11 | -3036 | -4056 | -3802 | -2638 |
SLC25A12 | -3491 | -5285 | -4498 | -4932 |
SLC25A13 | 1610 | 4248 | 3565 | 3923 |
SLC37A1 | 1964 | -2557 | -200 | 1128 |
SLC37A4 | -3004 | -4706 | -4997 | -4920 |
TPI1 | -1402 | -3331 | -4427 | -4455 |
Integrin cell surface interactions
metric | value |
---|---|
setSize | 45 |
pMANOVA | 1.02e-11 |
p.adjustMANOVA | 1.98e-10 |
s.dist | 0.748 |
s.FSHD | 0.599 |
s.hu_model | -0.231 |
s.Watt_m | 0.0965 |
s.Jones_m | 0.372 |
p.FSHD | 3.67e-12 |
p.hu_model | 0.00731 |
p.Watt_m | 0.263 |
p.Jones_m | 1.63e-05 |
Gene | FSHD | Jones_m |
---|---|---|
SPP1 | 4998 | 5215 |
ITGB2 | 4906 | 5102 |
CD44 | 4845 | 5080 |
ITGAM | 4572 | 5107 |
VCAM1 | 4924 | 4588 |
ICAM1 | 4641 | 4600 |
LUM | 4580 | 4537 |
FN1 | 4783 | 4002 |
ITGA5 | 4033 | 4594 |
THBS1 | 4954 | 3647 |
TNC | 5019 | 3460 |
ITGA9 | 4154 | 3909 |
CD47 | 3471 | 4552 |
FBN1 | 4504 | 2988 |
COL18A1 | 4351 | 3090 |
COL4A2 | 3851 | 3295 |
COL4A1 | 3805 | 3236 |
ITGB3 | 3693 | 2921 |
ITGAX | 1897 | 5125 |
COL16A1 | 3846 | 2475 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
AGRN | 3889 | -4843 | -2922 | 760 |
BSG | -1369 | -2217 | -2093 | -5147 |
CD44 | 4845 | 826 | 4939 | 5080 |
CD47 | 3471 | -2154 | 2654 | 4552 |
COL13A1 | -180 | -2295 | -1942 | 1914 |
COL16A1 | 3846 | -2915 | 1643 | 2475 |
COL18A1 | 4351 | -2864 | 2677 | 3090 |
COL23A1 | 3199 | -4585 | -845 | 2418 |
COL4A1 | 3805 | -4695 | 688 | 3236 |
COL4A2 | 3851 | -4973 | 861 | 3295 |
COL4A3 | -2253 | -3782 | -4833 | -1934 |
COL4A4 | -2804 | -2983 | -3940 | -28 |
COMP | 5024 | 275 | -1007 | -884 |
F11R | 3414 | -2271 | -667 | -1517 |
FBN1 | 4504 | 636 | 3601 | 2988 |
FN1 | 4783 | 33 | 3978 | 4002 |
HSPG2 | 2035 | -5289 | -401 | 2942 |
ICAM1 | 4641 | 1044 | 4128 | 4600 |
ICAM2 | 1999 | -1485 | -3439 | -639 |
ITGA1 | 1435 | 1740 | -4092 | -3028 |
ITGA10 | 4023 | -1852 | -979 | -1086 |
ITGA11 | 4615 | -1000 | -2691 | 1284 |
ITGA3 | 4809 | -5450 | 2976 | 557 |
ITGA4 | 2431 | -2840 | -5085 | 1443 |
ITGA5 | 4033 | -4692 | 5127 | 4594 |
ITGA6 | 1799 | -990 | -5243 | -114 |
ITGA7 | 580 | -4661 | 2121 | -4020 |
ITGA8 | 1156 | 4577 | 93 | 2702 |
ITGA9 | 4154 | -5185 | 3041 | 3909 |
ITGAM | 4572 | -2599 | 4997 | 5107 |
ITGAV | 801 | -812 | 49 | 4981 |
ITGAX | 1897 | -886 | 3808 | 5125 |
ITGB1 | 891 | 945 | 4567 | 4783 |
ITGB2 | 4906 | -107 | 4945 | 5102 |
ITGB3 | 3693 | -485 | 4867 | 2921 |
ITGB5 | 3604 | -2545 | -4743 | -4839 |
ITGB6 | -3832 | 471 | -3693 | 4890 |
ITGB8 | 4079 | 3217 | -2411 | 711 |
JAM2 | 3444 | -5266 | -4961 | -2840 |
JAM3 | 4578 | 1269 | -3928 | 1313 |
LUM | 4580 | -1815 | 2455 | 4537 |
SPP1 | 4998 | 1150 | 3009 | 5215 |
THBS1 | 4954 | 752 | 4384 | 3647 |
TNC | 5019 | 793 | 4283 | 3460 |
VCAM1 | 4924 | 2842 | 4665 | 4588 |
CS/DS degradation
metric | value |
---|---|
setSize | 10 |
pMANOVA | 0.02 |
p.adjustMANOVA | 0.0418 |
s.dist | 0.746 |
s.FSHD | 0.474 |
s.hu_model | -0.265 |
s.Watt_m | 0.163 |
s.Jones_m | 0.485 |
p.FSHD | 0.00943 |
p.hu_model | 0.147 |
p.Watt_m | 0.372 |
p.Jones_m | 0.00789 |
Gene | Jones_m | FSHD |
---|---|---|
BGN | 5088 | 4348 |
VCAN | 4285 | 4971 |
HEXB | 4889 | 2661 |
HEXA | 4440 | 2020 |
IDS | 4417 | 1662 |
ARSB | 3584 | 471 |
IDUA | 75 | 4027 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
ARSB | 471 | -989 | 2803 | 3584 |
BGN | 4348 | -1456 | 3875 | 5088 |
CSPG4 | 3730 | -5557 | 531 | -99 |
DCN | 4452 | -1036 | -890 | -1620 |
HEXA | 2020 | -220 | 1726 | 4440 |
HEXB | 2661 | 743 | 2355 | 4889 |
HYAL1 | -5197 | -3796 | 1588 | 129 |
IDS | 1662 | -2441 | -3581 | 4417 |
IDUA | 4027 | -3817 | -4684 | 75 |
VCAN | 4971 | 1662 | 4386 | 4285 |
Sema3A PAK dependent Axon repulsion
metric | value |
---|---|
setSize | 15 |
pMANOVA | 0.00333 |
p.adjustMANOVA | 0.00954 |
s.dist | 0.746 |
s.FSHD | 0.315 |
s.hu_model | -0.183 |
s.Watt_m | 0.392 |
s.Jones_m | 0.52 |
p.FSHD | 0.0346 |
p.hu_model | 0.22 |
p.Watt_m | 0.00857 |
p.Jones_m | 0.000495 |
Gene | Jones_m | Watt_m |
---|---|---|
CFL1 | 4792 | 4672 |
HSP90AA1 | 4248 | 5204 |
FES | 4746 | 4465 |
PAK2 | 3813 | 4757 |
LIMK1 | 3639 | 4130 |
FYN | 4010 | 3642 |
PLXNA3 | 2143 | 3020 |
SEMA3A | 4313 | 1054 |
HSP90AB1 | 723 | 4582 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
CFL1 | 3939 | -898 | 4672 | 4792 |
FES | 4554 | 551 | 4465 | 4746 |
FYN | 4466 | -2813 | 3642 | 4010 |
HSP90AA1 | -961 | 3627 | 5204 | 4248 |
HSP90AB1 | -1913 | -636 | 4582 | 723 |
LIMK1 | 260 | -4797 | 4130 | 3639 |
NRP1 | 3290 | -112 | -4213 | 1660 |
PAK1 | 181 | -5356 | -4830 | 1730 |
PAK2 | 648 | 1508 | 4757 | 3813 |
PLXNA1 | 1173 | -4429 | -533 | 4647 |
PLXNA2 | 1233 | -5329 | 3681 | -1661 |
PLXNA3 | 3786 | -5050 | 3020 | 2143 |
PLXNA4 | -1934 | -318 | -836 | 2286 |
RAC1 | -458 | 2502 | 1441 | -618 |
SEMA3A | 3892 | 2659 | 1054 | 4313 |
Phase 0 - rapid depolarisation
metric | value |
---|---|
setSize | 17 |
pMANOVA | 7.93e-05 |
p.adjustMANOVA | 0.000375 |
s.dist | 0.746 |
s.FSHD | -0.074 |
s.hu_model | -0.622 |
s.Watt_m | -0.26 |
s.Jones_m | -0.31 |
p.FSHD | 0.598 |
p.hu_model | 8.98e-06 |
p.Watt_m | 0.0635 |
p.Jones_m | 0.0269 |
Gene | hu_model | Jones_m |
---|---|---|
CACNG6 | -5214 | -5152 |
CAMK2B | -5433 | -4601 |
SCN1B | -4839 | -5072 |
SCN4A | -5537 | -4415 |
CACNB1 | -5223 | -4634 |
CAMK2A | -5463 | -4357 |
CALM1 | -4406 | -3365 |
RANGRF | -3968 | -3463 |
CAMK2G | -2068 | -5073 |
SCN3B | -3842 | -1746 |
SCN2B | -4214 | -656 |
CACNA1C | -758 | -673 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
CACNA1C | 2297 | -758 | -662 | -673 |
CACNB1 | -227 | -5223 | -5290 | -4634 |
CACNG6 | -798 | -5214 | -4502 | -5152 |
CALM1 | 591 | -4406 | 95 | -3365 |
CAMK2A | -839 | -5463 | -4382 | -4357 |
CAMK2B | -1020 | -5433 | -4185 | -4601 |
CAMK2D | 210 | -2193 | 4093 | 4423 |
CAMK2G | -5165 | -2068 | -4907 | -5073 |
FGF11 | 805 | -3846 | -3695 | 1142 |
FGF13 | -3421 | -836 | 608 | 3908 |
RANGRF | 2572 | -3968 | 155 | -3463 |
SCN1B | -2988 | -4839 | -5256 | -5072 |
SCN2B | -2156 | -4214 | -1901 | -656 |
SCN3A | 406 | 2417 | 4375 | 661 |
SCN3B | 889 | -3842 | 2946 | -1746 |
SCN4A | -3428 | -5537 | -5031 | -4415 |
SCN5A | 2570 | -5247 | 3478 | 4731 |
Chondroitin sulfate/dermatan sulfate metabolism
metric | value |
---|---|
setSize | 37 |
pMANOVA | 1.73e-08 |
p.adjustMANOVA | 1.82e-07 |
s.dist | 0.744 |
s.FSHD | 0.566 |
s.hu_model | -0.226 |
s.Watt_m | 0.194 |
s.Jones_m | 0.38 |
p.FSHD | 2.58e-09 |
p.hu_model | 0.0173 |
p.Watt_m | 0.0415 |
p.Jones_m | 6.48e-05 |
Gene | FSHD | Jones_m |
---|---|---|
SDC2 | 4456 | 5008 |
BGN | 4348 | 5088 |
VCAN | 4971 | 4285 |
SDC3 | 3721 | 4191 |
CHSY1 | 4080 | 3666 |
DSEL | 4639 | 3188 |
CHST11 | 4013 | 3364 |
HEXB | 2661 | 4889 |
CHPF2 | 4430 | 2836 |
CSGALNACT1 | 3780 | 3223 |
B3GALT6 | 3823 | 3103 |
CHPF | 4271 | 2760 |
DSE | 2330 | 4865 |
CHST14 | 3538 | 3049 |
SDC1 | 3944 | 2683 |
UST | 4297 | 2114 |
HEXA | 2020 | 4440 |
IDS | 1662 | 4417 |
HSPG2 | 2035 | 2942 |
CHST15 | 4124 | 1275 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
AGRN | 3889 | -4843 | -2922 | 760 |
ARSB | 471 | -989 | 2803 | 3584 |
B3GALT6 | 3823 | -1236 | 4092 | 3103 |
B3GAT3 | 4055 | -4180 | 1326 | -1191 |
B4GALT7 | 746 | -4099 | -1523 | 513 |
BGN | 4348 | -1456 | 3875 | 5088 |
CHPF | 4271 | -4389 | 1240 | 2760 |
CHPF2 | 4430 | -2038 | 2362 | 2836 |
CHST11 | 4013 | -183 | 2253 | 3364 |
CHST12 | 125 | -1250 | 1266 | 1673 |
CHST14 | 3538 | -3780 | 1229 | 3049 |
CHST15 | 4124 | -4640 | -3177 | 1275 |
CHST7 | 3877 | 2707 | -1313 | -269 |
CHSY1 | 4080 | 3773 | 1890 | 3666 |
CSGALNACT1 | 3780 | -204 | 2536 | 3223 |
CSGALNACT2 | 561 | 1490 | 3991 | 480 |
CSPG4 | 3730 | -5557 | 531 | -99 |
DCN | 4452 | -1036 | -890 | -1620 |
DSE | 2330 | 3355 | 2098 | 4865 |
DSEL | 4639 | 4198 | 923 | 3188 |
GPC1 | -1704 | -5207 | -2934 | -1700 |
GPC4 | -587 | -5108 | -3461 | -1575 |
GPC6 | 4618 | -2353 | 156 | 804 |
HEXA | 2020 | -220 | 1726 | 4440 |
HEXB | 2661 | 743 | 2355 | 4889 |
HSPG2 | 2035 | -5289 | -401 | 2942 |
HYAL1 | -5197 | -3796 | 1588 | 129 |
IDS | 1662 | -2441 | -3581 | 4417 |
IDUA | 4027 | -3817 | -4684 | 75 |
SDC1 | 3944 | -2017 | 209 | 2683 |
SDC2 | 4456 | 1739 | 4436 | 5008 |
SDC3 | 3721 | -4560 | 2780 | 4191 |
SDC4 | 1095 | -2361 | 5103 | 946 |
UST | 4297 | 988 | 1404 | 2114 |
VCAN | 4971 | 1662 | 4386 | 4285 |
XYLT1 | 3695 | 2589 | 2917 | -2537 |
XYLT2 | 2228 | -1124 | 1315 | 1093 |
Elastic fibre formation
metric | value |
---|---|
setSize | 34 |
pMANOVA | 1.94e-07 |
p.adjustMANOVA | 1.82e-06 |
s.dist | 0.743 |
s.FSHD | 0.588 |
s.hu_model | -0.0405 |
s.Watt_m | 0.28 |
s.Jones_m | 0.356 |
p.FSHD | 2.98e-09 |
p.hu_model | 0.683 |
p.Watt_m | 0.00482 |
p.Jones_m | 0.000336 |
Gene | FSHD | Jones_m |
---|---|---|
LOXL3 | 4563 | 4925 |
MFAP5 | 4668 | 4499 |
LOXL1 | 4187 | 4524 |
ITGA5 | 4033 | 4594 |
LOXL2 | 5054 | 3520 |
LOX | 4606 | 3765 |
TGFB1 | 4177 | 4099 |
FBLN2 | 3856 | 4216 |
FBN1 | 4504 | 2988 |
LOXL4 | 3456 | 3757 |
MFAP4 | 4643 | 2564 |
ITGB3 | 3693 | 2921 |
MFAP2 | 4871 | 2158 |
ELN | 4832 | 1614 |
EFEMP2 | 1698 | 4207 |
ITGB1 | 891 | 4783 |
ITGAV | 801 | 4981 |
ITGA8 | 1156 | 2702 |
ITGB8 | 4079 | 711 |
LTBP1 | 555 | 4963 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
BMP2 | 3157 | -4202 | 820 | -1673 |
BMP4 | 2116 | 329 | 908 | 307 |
EFEMP1 | 4878 | 1197 | 2548 | -562 |
EFEMP2 | 1698 | -4478 | 2866 | 4207 |
ELN | 4832 | -4996 | -384 | 1614 |
FBLN1 | 4502 | -1609 | 1591 | -376 |
FBLN2 | 3856 | -641 | 3313 | 4216 |
FBLN5 | 3811 | 1519 | -1289 | -1272 |
FBN1 | 4504 | 636 | 3601 | 2988 |
FURIN | 1239 | -4167 | 4073 | -1204 |
ITGA5 | 4033 | -4692 | 5127 | 4594 |
ITGA8 | 1156 | 4577 | 93 | 2702 |
ITGAV | 801 | -812 | 49 | 4981 |
ITGB1 | 891 | 945 | 4567 | 4783 |
ITGB3 | 3693 | -485 | 4867 | 2921 |
ITGB5 | 3604 | -2545 | -4743 | -4839 |
ITGB6 | -3832 | 471 | -3693 | 4890 |
ITGB8 | 4079 | 3217 | -2411 | 711 |
LOX | 4606 | 4062 | 3160 | 3765 |
LOXL1 | 4187 | -1569 | 3956 | 4524 |
LOXL2 | 5054 | -3017 | 2997 | 3520 |
LOXL3 | 4563 | -1100 | 1944 | 4925 |
LOXL4 | 3456 | 552 | 27 | 3757 |
LTBP1 | 555 | -67 | -1267 | 4963 |
LTBP3 | 2480 | -3134 | -2528 | -990 |
LTBP4 | 3682 | -1659 | 2214 | 400 |
MFAP1 | -2124 | 4892 | 3769 | -1986 |
MFAP2 | 4871 | 78 | 422 | 2158 |
MFAP3 | -1951 | 4029 | 2831 | 3634 |
MFAP4 | 4643 | -755 | -329 | 2564 |
MFAP5 | 4668 | -121 | 4486 | 4499 |
TGFB1 | 4177 | -3070 | 4895 | 4099 |
TGFB2 | 3078 | 4561 | 1841 | -2330 |
TGFB3 | 3860 | -5264 | -2015 | -4211 |
SEMA3A-Plexin repulsion signaling by inhibiting Integrin adhesion
metric | value |
---|---|
setSize | 14 |
pMANOVA | 0.00536 |
p.adjustMANOVA | 0.0141 |
s.dist | 0.743 |
s.FSHD | 0.441 |
s.hu_model | -0.215 |
s.Watt_m | 0.257 |
s.Jones_m | 0.495 |
p.FSHD | 0.00432 |
p.hu_model | 0.163 |
p.Watt_m | 0.0967 |
p.Jones_m | 0.00134 |
Gene | Jones_m | FSHD |
---|---|---|
FES | 4746 | 4554 |
FYN | 4010 | 4466 |
SEMA3A | 4313 | 3892 |
RRAS | 4281 | 3554 |
TLN1 | 4067 | 2279 |
PLXNA3 | 2143 | 3786 |
RND1 | 4014 | 2013 |
NRP1 | 1660 | 3290 |
PLXNA1 | 4647 | 1173 |
PIP5K1C | 2520 | 1931 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
FARP2 | 137 | -1317 | -3360 | -426 |
FES | 4554 | 551 | 4465 | 4746 |
FYN | 4466 | -2813 | 3642 | 4010 |
NRP1 | 3290 | -112 | -4213 | 1660 |
PIP5K1C | 1931 | -1891 | 384 | 2520 |
PLXNA1 | 1173 | -4429 | -533 | 4647 |
PLXNA2 | 1233 | -5329 | 3681 | -1661 |
PLXNA3 | 3786 | -5050 | 3020 | 2143 |
PLXNA4 | -1934 | -318 | -836 | 2286 |
RAC1 | -458 | 2502 | 1441 | -618 |
RND1 | 2013 | 3850 | 5209 | 4014 |
RRAS | 3554 | -4446 | 1337 | 4281 |
SEMA3A | 3892 | 2659 | 1054 | 4313 |
TLN1 | 2279 | -3868 | 2941 | 4067 |
Regulation of Complement cascade
metric | value |
---|---|
setSize | 13 |
pMANOVA | 0.000347 |
p.adjustMANOVA | 0.00136 |
s.dist | 0.741 |
s.FSHD | 0.652 |
s.hu_model | 0.0474 |
s.Watt_m | -0.00954 |
s.Jones_m | 0.348 |
p.FSHD | 4.68e-05 |
p.hu_model | 0.767 |
p.Watt_m | 0.953 |
p.Jones_m | 0.0297 |
Gene | FSHD | Jones_m |
---|---|---|
C1S | 5050 | 4323 |
C1R | 4829 | 4496 |
CFH | 5027 | 4077 |
SERPING1 | 4526 | 4253 |
C3 | 4737 | 4049 |
CD81 | 4123 | 4155 |
PROS1 | 3701 | 4200 |
C2 | 5030 | 2346 |
C7 | 4661 | 832 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
C1R | 4829 | -806 | -1012 | 4496 |
C1S | 5050 | -2395 | -2030 | 4323 |
C2 | 5030 | -555 | -1347 | 2346 |
C3 | 4737 | 4276 | 1818 | 4049 |
C7 | 4661 | -1115 | 1322 | 832 |
CD46 | 540 | 1526 | -3448 | -2924 |
CD55 | 1172 | 217 | -321 | -3953 |
CD59 | -5248 | 1620 | -4331 | 1749 |
CD81 | 4123 | -4615 | 886 | 4155 |
CFH | 5027 | -553 | -114 | 4077 |
CLU | 4108 | 1612 | 4120 | -4236 |
PROS1 | 3701 | 100 | 2906 | 4200 |
SERPING1 | 4526 | 75 | 281 | 4253 |
Mitochondrial translation initiation
metric | value |
---|---|
setSize | 81 |
pMANOVA | 4.72e-17 |
p.adjustMANOVA | 2.15e-15 |
s.dist | 0.74 |
s.FSHD | -0.54 |
s.hu_model | 0.152 |
s.Watt_m | -0.291 |
s.Jones_m | -0.385 |
p.FSHD | 4.46e-17 |
p.hu_model | 0.0184 |
p.Watt_m | 6.38e-06 |
p.Jones_m | 2.12e-09 |
Gene | FSHD | Jones_m |
---|---|---|
PTCD3 | -5161 | -4052 |
DAP3 | -4837 | -4034 |
MRPL30 | -4564 | -4158 |
MRPL42 | -3577 | -5202 |
MRPS36 | -5429 | -3208 |
MRPL32 | -4818 | -3602 |
MTIF2 | -4920 | -3415 |
MRPS18B | -4367 | -3831 |
MRPS5 | -3273 | -5089 |
CHCHD1 | -3980 | -3974 |
MRPL16 | -4392 | -3597 |
MRPL11 | -3720 | -4218 |
MRPS16 | -4590 | -3231 |
MRPS15 | -3628 | -4018 |
MRPS23 | -4659 | -3082 |
OXA1L | -4632 | -3044 |
MRPS27 | -4915 | -2848 |
MRPL35 | -5028 | -2768 |
MRPS28 | -2816 | -4916 |
MRPL15 | -3132 | -4325 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
AURKAIP1 | -3378 | -2276 | -1747 | -3524 |
CHCHD1 | -3980 | -540 | -1809 | -3974 |
DAP3 | -4837 | -461 | 2611 | -4034 |
ERAL1 | -3167 | 2585 | -858 | -3141 |
GADD45GIP1 | -1089 | -2386 | -3149 | -2950 |
MRPL1 | -3901 | -1280 | -4021 | -2985 |
MRPL10 | -2288 | -2374 | -4353 | -2443 |
MRPL11 | -3720 | 2077 | -2512 | -4218 |
MRPL12 | -1963 | -2623 | -2727 | -2667 |
MRPL13 | -3539 | 343 | 285 | -3672 |
MRPL14 | -1974 | -1679 | -1052 | 1359 |
MRPL15 | -3132 | 2448 | -2949 | -4325 |
MRPL16 | -4392 | 3057 | -3392 | -3597 |
MRPL17 | 595 | 1912 | 2816 | 4209 |
MRPL18 | -2407 | 2971 | -4191 | -3349 |
MRPL19 | -4475 | 4046 | -3671 | -1186 |
MRPL2 | -2747 | -435 | -1567 | -4868 |
MRPL20 | -3024 | 531 | 207 | -510 |
MRPL21 | -3086 | 1674 | -768 | -3347 |
MRPL22 | -2171 | 3326 | -2754 | -3733 |
MRPL23 | -3087 | -3178 | -776 | -1241 |
MRPL24 | -1464 | -1858 | -2181 | -1722 |
MRPL27 | -2722 | -1594 | -1652 | -1044 |
MRPL28 | -7 | -271 | -990 | -2552 |
MRPL3 | -3854 | 2949 | -3937 | -192 |
MRPL30 | -4564 | 3470 | -1084 | -4158 |
MRPL32 | -4818 | 3042 | 2692 | -3602 |
MRPL34 | -3944 | -2159 | -3284 | -2255 |
MRPL35 | -5028 | 800 | -2563 | -2768 |
MRPL36 | -2568 | -557 | -2264 | 625 |
MRPL37 | -2913 | 1590 | -2744 | -3921 |
MRPL38 | -490 | 368 | -1753 | -3644 |
MRPL39 | -3867 | 2569 | -947 | -1196 |
MRPL4 | -1740 | 2929 | -505 | -2748 |
MRPL40 | -2857 | -249 | 796 | 637 |
MRPL41 | -4483 | -4838 | -1856 | 1777 |
MRPL42 | -3577 | 2087 | -1650 | -5202 |
MRPL43 | -1019 | -1428 | -663 | 1286 |
MRPL44 | -3543 | 4365 | -2069 | -3706 |
MRPL46 | -2332 | 996 | -440 | 1568 |
MRPL47 | -1558 | 3146 | -1887 | -1504 |
MRPL48 | -3651 | -80 | 163 | -1871 |
MRPL49 | -468 | 4723 | -3219 | -2978 |
MRPL50 | -3974 | 3074 | -150 | -1267 |
MRPL51 | -2492 | -387 | -1581 | -4128 |
MRPL52 | -1075 | -2282 | 1466 | -1004 |
MRPL54 | 445 | -1970 | 2366 | -2983 |
MRPL55 | -932 | 1077 | -3210 | -3400 |
MRPL9 | -2162 | 3406 | -3593 | -1971 |
MRPS10 | -2227 | -3045 | -784 | -2392 |
MRPS11 | -3081 | 280 | -2798 | -1751 |
MRPS12 | -2364 | -146 | 616 | 1122 |
MRPS14 | -1834 | 1778 | -4387 | -4044 |
MRPS15 | -3628 | 1857 | -1464 | -4018 |
MRPS16 | -4590 | 1192 | -2229 | -3231 |
MRPS17 | -3181 | -131 | -1389 | 4388 |
MRPS18A | -2481 | 465 | -4081 | -4980 |
MRPS18B | -4367 | -1848 | 1877 | -3831 |
MRPS18C | -3506 | 4342 | -675 | -570 |
MRPS2 | -2046 | 1425 | 2175 | -19 |
MRPS22 | -4388 | 4344 | -1949 | -275 |
MRPS23 | -4659 | 1657 | -4044 | -3082 |
MRPS25 | -3226 | -3514 | -3925 | 431 |
MRPS26 | -646 | -610 | -1343 | -2703 |
MRPS27 | -4915 | 555 | -2134 | -2848 |
MRPS28 | -2816 | 1341 | -1288 | -4916 |
MRPS30 | -3672 | 3442 | 761 | -2570 |
MRPS31 | -4207 | 3479 | -1758 | -2995 |
MRPS33 | -4017 | 149 | -530 | -1199 |
MRPS34 | -2775 | -3797 | -2222 | -3830 |
MRPS35 | -4450 | 3080 | -2647 | 954 |
MRPS36 | -5429 | -2678 | 682 | -3208 |
MRPS5 | -3273 | -1161 | -2766 | -5089 |
MRPS6 | 1135 | -4408 | 2857 | -486 |
MRPS7 | -3579 | -1321 | 849 | 138 |
MRPS9 | -3785 | 1389 | -4076 | -1007 |
MTFMT | -3046 | -1437 | -1940 | 1267 |
MTIF2 | -4920 | 1787 | -4751 | -3415 |
MTIF3 | -4258 | 276 | -1404 | 3305 |
OXA1L | -4632 | -2587 | -3906 | -3044 |
PTCD3 | -5161 | 3456 | -5112 | -4052 |
Formation of tubulin folding intermediates by CCT/TriC
metric | value |
---|---|
setSize | 17 |
pMANOVA | 1.34e-05 |
p.adjustMANOVA | 7.63e-05 |
s.dist | 0.739 |
s.FSHD | 0.0756 |
s.hu_model | -0.0946 |
s.Watt_m | 0.683 |
s.Jones_m | 0.255 |
p.FSHD | 0.589 |
p.hu_model | 0.5 |
p.Watt_m | 1.07e-06 |
p.Jones_m | 0.0691 |
Gene | Watt_m | Jones_m |
---|---|---|
TUBB6 | 5153 | 5168 |
TUBA1C | 5075 | 5010 |
TUBA1B | 4866 | 4967 |
TUBB2B | 4912 | 4788 |
TUBB2A | 4401 | 4710 |
TUBA1A | 3672 | 3786 |
TUBB4B | 4848 | 2861 |
CCT4 | 3292 | 2174 |
CCT3 | 4860 | 1411 |
CCT8 | 3753 | 1167 |
CCT2 | 4163 | 506 |
TCP1 | 1199 | 59 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
CCT2 | -566 | 3774 | 4163 | 506 |
CCT3 | -62 | 2307 | 4860 | 1411 |
CCT4 | -1655 | 939 | 3292 | 2174 |
CCT5 | -813 | 3048 | 2610 | -2806 |
CCT6A | -3336 | 2908 | 3000 | -3352 |
CCT7 | -2416 | 432 | 3340 | -2045 |
CCT8 | -2093 | 4116 | 3753 | 1167 |
TCP1 | -4260 | 4443 | 1199 | 59 |
TUBA1A | 4948 | -5166 | 3672 | 3786 |
TUBA1B | 4448 | -5262 | 4866 | 4967 |
TUBA1C | 3088 | -4823 | 5075 | 5010 |
TUBA4A | -2112 | -5280 | 2049 | -3253 |
TUBA8 | -2556 | -1103 | -882 | -2976 |
TUBB2A | 2970 | -4616 | 4401 | 4710 |
TUBB2B | 2381 | -4644 | 4912 | 4788 |
TUBB4B | 776 | 426 | 4848 | 2861 |
TUBB6 | 4937 | -4998 | 5153 | 5168 |
Binding and Uptake of Ligands by Scavenger Receptors
metric | value |
---|---|
setSize | 23 |
pMANOVA | 3.26e-05 |
p.adjustMANOVA | 0.000167 |
s.dist | 0.737 |
s.FSHD | 0.555 |
s.hu_model | -0.152 |
s.Watt_m | 0.157 |
s.Jones_m | 0.433 |
p.FSHD | 4.15e-06 |
p.hu_model | 0.208 |
p.Watt_m | 0.192 |
p.Jones_m | 0.00033 |
Gene | FSHD | Jones_m |
---|---|---|
MSR1 | 5020 | 4999 |
APOE | 3947 | 4717 |
CALR | 3782 | 4356 |
COL3A1 | 4565 | 3575 |
LRP1 | 4481 | 3531 |
HSP90B1 | 3464 | 4544 |
COLEC12 | 4753 | 3221 |
COL4A2 | 3851 | 3295 |
COL4A1 | 3805 | 3236 |
SSC5D | 4794 | 2492 |
HYOU1 | 2212 | 4376 |
SPARC | 3820 | 1957 |
SCARB1 | 2518 | 2858 |
COL1A2 | 4681 | 1250 |
COL1A1 | 4847 | 676 |
SCARA5 | 4409 | 415 |
HSPH1 | 303 | 4044 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
APOE | 3947 | -1411 | -88.0 | 4717.0 |
APOL1 | 5079 | 1818 | -2495.5 | -690.5 |
CALR | 3782 | 1517 | 4947.0 | 4356.0 |
CD36 | -653 | -579 | -3797.0 | 1232.0 |
COL1A1 | 4847 | -1617 | 7.0 | 676.0 |
COL1A2 | 4681 | -1689 | -375.0 | 1250.0 |
COL3A1 | 4565 | 2950 | 2503.0 | 3575.0 |
COL4A1 | 3805 | -4695 | 688.0 | 3236.0 |
COL4A2 | 3851 | -4973 | 861.0 | 3295.0 |
COLEC12 | 4753 | 4226 | 45.0 | 3221.0 |
FTH1 | -3005 | -1864 | -126.0 | 409.0 |
HSP90AA1 | -961 | 3627 | 5204.0 | 4248.0 |
HSP90B1 | 3464 | 456 | 4896.0 | 4544.0 |
HSPH1 | 303 | 4110 | 5024.0 | 4044.0 |
HYOU1 | 2212 | -1426 | 4981.0 | 4376.0 |
LRP1 | 4481 | -3605 | 1744.0 | 3531.0 |
MASP1 | -5427 | -4170 | -1574.0 | -2446.0 |
MSR1 | 5020 | -3413 | 5009.0 | 4999.0 |
SCARA5 | 4409 | -2526 | -3487.0 | 415.0 |
SCARB1 | 2518 | -4393 | -1712.0 | 2858.0 |
SPARC | 3820 | -2638 | -565.0 | 1957.0 |
SSC5D | 4794 | -1669 | 13.0 | 2492.0 |
STAB2 | 2605 | -3211 | -3761.0 | -4791.0 |
tRNA processing in the mitochondrion
metric | value |
---|---|
setSize | 11 |
pMANOVA | 0.0128 |
p.adjustMANOVA | 0.0288 |
s.dist | 0.736 |
s.FSHD | -0.616 |
s.hu_model | 0.0214 |
s.Watt_m | -0.259 |
s.Jones_m | -0.307 |
p.FSHD | 4e-04 |
p.hu_model | 0.902 |
p.Watt_m | 0.137 |
p.Jones_m | 0.078 |
Gene | FSHD | Jones_m |
---|---|---|
MT-CO1 | -4597 | -3652 |
TRMT10C | -4316 | -3659 |
MT-ND5 | -5424 | -2299 |
MT-CYB | -4704 | -2471 |
MT-ND2 | -4198 | -2726 |
MT-ND1 | -3295 | -3418 |
MT-ND4 | -4132 | -2517 |
MT-ND6 | -4175 | -2336 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
ELAC2 | -1785 | 1503 | 1552 | 116 |
HSD17B10 | -201 | -1178 | -480 | 3967 |
MT-CO1 | -4597 | -3125 | -4070 | -3652 |
MT-CYB | -4704 | -1339 | -2332 | -2471 |
MT-ND1 | -3295 | -352 | -2191 | -3418 |
MT-ND2 | -4198 | -1107 | -2067 | -2726 |
MT-ND4 | -4132 | -2057 | -1579 | -2517 |
MT-ND5 | -5424 | -3201 | -2302 | -2299 |
MT-ND6 | -4175 | 806 | -4540 | -2336 |
TRMT10C | -4316 | 4737 | -8 | -3659 |
TRNT1 | -861 | 3291 | 2491 | 831 |
Defects in vitamin and cofactor metabolism
metric | value |
---|---|
setSize | 17 |
pMANOVA | 0.00155 |
p.adjustMANOVA | 0.00492 |
s.dist | 0.735 |
s.FSHD | -0.346 |
s.hu_model | 0.105 |
s.Watt_m | -0.523 |
s.Jones_m | -0.368 |
p.FSHD | 0.0135 |
p.hu_model | 0.452 |
p.Watt_m | 0.000189 |
p.Jones_m | 0.00864 |
Gene | Watt_m | Jones_m |
---|---|---|
MMAB | -5284 | -5244 |
PCCA | -5148 | -4743 |
MCCC2 | -4913 | -4935 |
PCCB | -4099 | -5276 |
MCCC1 | -4638 | -4559 |
PC | -3656 | -4683 |
MMACHC | -3319 | -3475 |
LMBRD1 | -1893 | -1908 |
MMAA | -4281 | -833 |
MMADHC | -1031 | -3128 |
CD320 | -720 | -2647 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
ABCD4 | 1546 | 472 | -3534 | 2703 |
BTD | 2964 | 2543 | 2171 | -688 |
CD320 | 2152 | -2400 | -720 | -2647 |
HLCS | -4775 | -754 | -3859 | 1637 |
LMBRD1 | -2102 | 307 | -1893 | -1908 |
MCCC1 | -4819 | 3980 | -4638 | -4559 |
MCCC2 | -4989 | 2184 | -4913 | -4935 |
MMAA | -1319 | 2774 | -4281 | -833 |
MMAB | -3438 | -5316 | -5284 | -5244 |
MMACHC | -3367 | 1913 | -3319 | -3475 |
MMADHC | -2916 | 3215 | -1031 | -3128 |
MTR | -4381 | 2915 | -4450 | 5095 |
MTRR | -4955 | 2157 | 3226 | -5080 |
PC | 929 | -5164 | -3656 | -4683 |
PCCA | -4767 | -2564 | -5148 | -4743 |
PCCB | -3972 | -164 | -4099 | -5276 |
TCN2 | 4160 | -1706 | -2150 | 4250 |
Degradation of the extracellular matrix
metric | value |
---|---|
setSize | 58 |
pMANOVA | 8.33e-14 |
p.adjustMANOVA | 2.38e-12 |
s.dist | 0.734 |
s.FSHD | 0.54 |
s.hu_model | -0.301 |
s.Watt_m | 0.141 |
s.Jones_m | 0.37 |
p.FSHD | 1.11e-12 |
p.hu_model | 7.64e-05 |
p.Watt_m | 0.0628 |
p.Jones_m | 1.15e-06 |
Gene | FSHD | Jones_m |
---|---|---|
SPP1 | 4998 | 5215 |
CD44 | 4845 | 5080 |
TIMP1 | 4933 | 4988 |
MMP19 | 4747 | 5126 |
COL14A1 | 4785 | 4769 |
LAMC2 | 4587 | 4436 |
CTSK | 4644 | 4241 |
CTSS | 3773 | 5148 |
CAPN2 | 3440 | 5001 |
LAMC1 | 4113 | 4089 |
MMP17 | 2906 | 5161 |
CAPNS1 | 2784 | 5062 |
BMP1 | 3427 | 4072 |
ADAM15 | 3824 | 3617 |
COL18A1 | 4351 | 3090 |
CTSB | 2843 | 4639 |
ADAM8 | 2510 | 5134 |
MMP14 | 4687 | 2675 |
ADAMTS1 | 4378 | 2787 |
NID1 | 3391 | 3576 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
ADAM10 | 2507 | -1489 | -1018 | 3455 |
ADAM15 | 3824 | -3547 | 4576 | 3617 |
ADAM17 | 411 | 2385 | 2056 | 2726 |
ADAM8 | 2510 | -2559 | 5057 | 5134 |
ADAM9 | 261 | 342 | 148 | 3770 |
ADAMTS1 | 4378 | -4528 | 4660 | 2787 |
ADAMTS4 | 4986 | -3118 | 4239 | 2378 |
ADAMTS5 | 3999 | 3508 | -591 | 939 |
ADAMTS9 | 2574 | -777 | -1141 | 3604 |
BMP1 | 3427 | -4914 | 43 | 4072 |
BSG | -1369 | -2217 | -2093 | -5147 |
CAPN1 | 338 | -5104 | -4377 | -1115 |
CAPN10 | 3254 | -2153 | -2849 | 237 |
CAPN15 | 1471 | -4608 | 1808 | 695 |
CAPN2 | 3440 | -3365 | 4883 | 5001 |
CAPN3 | -3909 | -4761 | -2650 | -4046 |
CAPN5 | 3967 | -2597 | -276 | 764 |
CAPN6 | 1229 | -4866 | 3231 | 4668 |
CAPN7 | -4421 | -522 | -4909 | -4965 |
CAPNS1 | 2784 | -1330 | 1730 | 5062 |
CASP3 | 1918 | 419 | 4968 | 4110 |
CAST | -2581 | -749 | 4823 | -93 |
CD44 | 4845 | 826 | 4939 | 5080 |
COL12A1 | 5001 | 1907 | 511 | 1626 |
COL13A1 | -180 | -2295 | -1942 | 1914 |
COL14A1 | 4785 | 831 | 1493 | 4769 |
COL15A1 | 2478 | -169 | 1436 | 1179 |
COL16A1 | 3846 | -2915 | 1643 | 2475 |
COL18A1 | 4351 | -2864 | 2677 | 3090 |
COL23A1 | 3199 | -4585 | -845 | 2418 |
CTSB | 2843 | -1183 | -789 | 4639 |
CTSD | 1329 | -4757 | -3993 | 2582 |
CTSK | 4644 | 2 | 259 | 4241 |
CTSS | 3773 | -338 | 5035 | 5148 |
CTSV | -84 | 2189 | 34 | 331 |
DCN | 4452 | -1036 | -890 | -1620 |
FURIN | 1239 | -4167 | 4073 | -1204 |
HSPG2 | 2035 | -5289 | -401 | 2942 |
HTRA1 | 4656 | -2558 | -2428 | -3749 |
LAMA3 | 3451 | -999 | -4332 | -2201 |
LAMA5 | 3521 | -5520 | -2717 | -2028 |
LAMB1 | 2539 | -455 | -385 | 3101 |
LAMB3 | 2231 | -4929 | -4569 | 386 |
LAMC1 | 4113 | -3181 | 2501 | 4089 |
LAMC2 | 4587 | 1336 | 5102 | 4436 |
MMP11 | 2889 | -3240 | -393 | 1218 |
MMP14 | 4687 | -1668 | 1618 | 2675 |
MMP15 | 1264 | -5090 | -5214 | -4505 |
MMP17 | 2906 | -2335 | 5119 | 5161 |
MMP19 | 4747 | -167 | 4806 | 5126 |
MMP2 | 4410 | -689 | -1983 | 2240 |
NCSTN | -1401 | -2472 | 1251 | 2905 |
NID1 | 3391 | -1249 | 709 | 3576 |
PHYKPL | 4956 | -4988 | -3912 | -2713 |
PSEN1 | 2583 | 2051 | 2038 | 1484 |
SPP1 | 4998 | 1150 | 3009 | 5215 |
TIMP1 | 4933 | -1301 | 5188 | 4988 |
TIMP2 | 4689 | -1860 | -732 | 1606 |
Regulation of IFNA signaling
metric | value |
---|---|
setSize | 12 |
pMANOVA | 0.0277 |
p.adjustMANOVA | 0.0551 |
s.dist | 0.732 |
s.FSHD | 0.419 |
s.hu_model | -0.0378 |
s.Watt_m | 0.345 |
s.Jones_m | 0.489 |
p.FSHD | 0.0119 |
p.hu_model | 0.821 |
p.Watt_m | 0.0385 |
p.Jones_m | 0.00335 |
Gene | Jones_m | FSHD |
---|---|---|
PTPN6 | 5055 | 3645 |
SOCS3 | 3580 | 5006 |
STAT2 | 3818 | 2887 |
TYK2 | 4512 | 2357 |
USP18 | 1934 | 3625 |
IFNAR2 | 3705 | 1842 |
STAT1 | 2082 | 2094 |
PTPN1 | 4669 | 739 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
IFNAR1 | -1724 | 3617 | 1074 | 4092 |
IFNAR2 | 1842 | -1300 | 2336 | 3705 |
JAK1 | 1002 | -1843 | 4184 | -1810 |
PTPN1 | 739 | 1514 | 4538 | 4669 |
PTPN11 | -1703 | -1554 | -660 | -1108 |
PTPN6 | 3645 | -920 | 4751 | 5055 |
SOCS1 | 4531 | 196 | 3989 | -56 |
SOCS3 | 5006 | -282 | 5053 | 3580 |
STAT1 | 2094 | 233 | -1721 | 2082 |
STAT2 | 2887 | -2568 | 275 | 3818 |
TYK2 | 2357 | -3081 | -49 | 4512 |
USP18 | 3625 | 43 | -2543 | 1934 |
Metabolism of steroid hormones
metric | value |
---|---|
setSize | 12 |
pMANOVA | 0.00982 |
p.adjustMANOVA | 0.0232 |
s.dist | 0.732 |
s.FSHD | 0.218 |
s.hu_model | -0.117 |
s.Watt_m | 0.387 |
s.Jones_m | 0.569 |
p.FSHD | 0.19 |
p.hu_model | 0.485 |
p.Watt_m | 0.0202 |
p.Jones_m | 0.000642 |
Gene | Jones_m | Watt_m |
---|---|---|
AKR1B1 | 5216.0 | 4722.0 |
TSPO | 5024.0 | 4058.0 |
HSD17B12 | 3986.0 | 5012.0 |
AKR1B15 | 4916.5 | 3817.5 |
STARD3NL | 3036.0 | 4478.0 |
SRD5A3 | 4314.0 | 2905.0 |
FDX1 | 2577.0 | 3995.0 |
STARD4 | 357.0 | 3522.0 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
AKR1B1 | -2349 | -3237 | 4722.0 | 5216.0 |
AKR1B15 | -564 | -4434 | 3817.5 | 4916.5 |
FDX1 | -4748 | 2316 | 3995.0 | 2577.0 |
FDXR | 4489 | -4083 | -3246.0 | 2748.0 |
HSD11B1 | 2224 | -1937 | -3005.0 | 1249.0 |
HSD17B11 | 3281 | 1287 | -621.0 | 3260.0 |
HSD17B12 | -799 | 2099 | 5012.0 | 3986.0 |
SRD5A3 | 3626 | 3434 | 2905.0 | 4314.0 |
STARD3 | 2626 | -137 | -1739.0 | -1167.0 |
STARD3NL | -319 | -860 | 4478.0 | 3036.0 |
STARD4 | 1850 | -287 | 3522.0 | 357.0 |
TSPO | 2295 | -5082 | 4058.0 | 5024.0 |
Interleukin-4 and Interleukin-13 signaling
metric | value |
---|---|
setSize | 64 |
pMANOVA | 4.2e-12 |
p.adjustMANOVA | 9.07e-11 |
s.dist | 0.731 |
s.FSHD | 0.428 |
s.hu_model | -0.13 |
s.Watt_m | 0.401 |
s.Jones_m | 0.416 |
p.FSHD | 3.24e-09 |
p.hu_model | 0.0728 |
p.Watt_m | 2.88e-08 |
p.Jones_m | 8.56e-09 |
Gene | FSHD | Jones_m |
---|---|---|
F13A1 | 4992 | 5143 |
ITGB2 | 4906 | 5102 |
TIMP1 | 4933 | 4988 |
IL4R | 4964 | 4939 |
VIM | 4833 | 5069 |
ANXA1 | 4781 | 4954 |
ITGAM | 4572 | 5107 |
HMOX1 | 4609 | 5052 |
VCAM1 | 4924 | 4588 |
TNFRSF1B | 4174 | 5115 |
ICAM1 | 4641 | 4600 |
CDKN1A | 5043 | 4230 |
FN1 | 4783 | 4002 |
CCL2 | 4787 | 3964 |
IL2RG | 4862 | 3754 |
SOCS3 | 5006 | 3580 |
TGFB1 | 4177 | 4099 |
CCND1 | 3783 | 4327 |
HSP90B1 | 3464 | 4544 |
JUNB | 4433 | 3511 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
AKT1 | -463 | -4893 | 336 | 4183 |
ANXA1 | 4781 | 530 | 4497 | 4954 |
BCL2 | -3161 | -4574 | -1100 | 2806 |
BCL2L1 | 4359 | -5119 | 3393 | 1941 |
BCL6 | -884 | -4956 | -4761 | -1050 |
CCL2 | 4787 | 2597 | 5061 | 3964 |
CCND1 | 3783 | 747 | 522 | 4327 |
CD36 | -653 | -579 | -3797 | 1232 |
CDKN1A | 5043 | -4867 | 5043 | 4230 |
COL1A2 | 4681 | -1689 | -375 | 1250 |
F13A1 | 4992 | -2030 | 3600 | 5143 |
FGF2 | 1476 | 741 | -1087 | -3508 |
FN1 | 4783 | 33 | 3978 | 4002 |
FOS | 4091 | 1847 | 5216 | 3111 |
FOXO1 | -5116 | -430 | 1290 | 69 |
FOXO3 | -5444 | -42 | -1123 | 140 |
FSCN1 | 3079 | 1688 | -926 | 3701 |
HIF1A | 3477 | -1004 | 4959 | 2917 |
HMOX1 | 4609 | -2806 | 5022 | 5052 |
HSP90AA1 | -961 | 3627 | 5204 | 4248 |
HSP90B1 | 3464 | 456 | 4896 | 4544 |
HSPA8 | -3074 | 3645 | 5039 | 1622 |
ICAM1 | 4641 | 1044 | 4128 | 4600 |
IL13RA1 | 1037 | -1823 | 4469 | 4910 |
IL2RG | 4862 | -1917 | 3687 | 3754 |
IL4R | 4964 | -3290 | 4887 | 4939 |
IL6R | 1481 | -5451 | 3229 | 3550 |
IRF4 | 4366 | -1152 | 2559 | 3509 |
ITGAM | 4572 | -2599 | 4997 | 5107 |
ITGAX | 1897 | -886 | 3808 | 5125 |
ITGB1 | 891 | 945 | 4567 | 4783 |
ITGB2 | 4906 | -107 | 4945 | 5102 |
JAK1 | 1002 | -1843 | 4184 | -1810 |
JAK2 | -732 | -2536 | -5002 | -4773 |
JUNB | 4433 | -2560 | 5170 | 3511 |
LAMA5 | 3521 | -5520 | -2717 | -2028 |
MAOA | 235 | -96 | 3883 | -4296 |
MCL1 | -1416 | 2813 | 4778 | 185 |
MMP2 | 4410 | -689 | -1983 | 2240 |
MYC | 4902 | 3961 | 4838 | 1869 |
NDN | 3836 | 1134 | 1857 | 3469 |
PIK3R1 | -5317 | 2872 | -3114 | 468 |
PIM1 | 4265 | -227 | 4249 | -1858 |
POU2F1 | 1218 | 2993 | -3297 | -1284 |
RHOU | -4158 | -4175 | -323 | -3781 |
RORA | -3256 | -4994 | -2672 | -2510 |
RORC | -2179 | -5186 | -4271 | 1876 |
S1PR1 | 3355 | 2666 | 1535 | 53 |
SOCS1 | 4531 | 196 | 3989 | -56 |
SOCS3 | 5006 | -282 | 5053 | 3580 |
SOCS5 | -2651 | 4112 | 1866 | 3851 |
STAT1 | 2094 | 233 | -1721 | 2082 |
STAT3 | 850 | -3836 | 5013 | 4348 |
STAT6 | 4720 | -5255 | -1252 | 3190 |
TGFB1 | 4177 | -3070 | 4895 | 4099 |
TIMP1 | 4933 | -1301 | 5188 | 4988 |
TNFRSF1B | 4174 | -866 | 4548 | 5115 |
TP53 | 4943 | 566 | 3708 | 2810 |
TWIST1 | 4751 | 2601 | 2929 | 89 |
TYK2 | 2357 | -3081 | -49 | 4512 |
VCAM1 | 4924 | 2842 | 4665 | 4588 |
VEGFA | -901 | -4512 | -5139 | -3096 |
VIM | 4833 | -2988 | 4724 | 5069 |
ZEB1 | -2231 | -4169 | -194 | -3440 |
ECM proteoglycans
metric | value |
---|---|
setSize | 37 |
pMANOVA | 9.76e-09 |
p.adjustMANOVA | 1.12e-07 |
s.dist | 0.73 |
s.FSHD | 0.569 |
s.hu_model | -0.27 |
s.Watt_m | 0.143 |
s.Jones_m | 0.341 |
p.FSHD | 2.08e-09 |
p.hu_model | 0.00458 |
p.Watt_m | 0.133 |
p.Jones_m | 0.00034 |
Gene | FSHD | Jones_m |
---|---|---|
BGN | 4348 | 5088 |
VCAN | 4971 | 4285 |
LUM | 4580 | 4537 |
ASPN | 4403 | 3985 |
TNC | 5019 | 3460 |
TGFB1 | 4177 | 4099 |
LAMC1 | 4113 | 4089 |
ITGA9 | 4154 | 3909 |
SERPINE1 | 4636 | 3333 |
TNXB | 4386 | 3472 |
NCAM1 | 3566 | 3898 |
ITGB3 | 3693 | 2921 |
LAMA4 | 4388 | 2343 |
ITGAX | 1897 | 5125 |
MUSK | 2918 | 3328 |
LAMB1 | 2539 | 3101 |
SPARC | 3820 | 1957 |
LAMA2 | 3038 | 2040 |
HSPG2 | 2035 | 2942 |
PTPRS | 1732 | 2695 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
AGRN | 3889 | -4843 | -2922 | 760 |
ASPN | 4403 | 4376 | 2320 | 3985 |
BGN | 4348 | -1456 | 3875 | 5088 |
COMP | 5024 | 275 | -1007 | -884 |
DAG1 | -4941 | -5174 | 2661 | 4271 |
DCN | 4452 | -1036 | -890 | -1620 |
FMOD | 4377 | -328 | -1283 | -1405 |
HSPG2 | 2035 | -5289 | -401 | 2942 |
ITGA7 | 580 | -4661 | 2121 | -4020 |
ITGA8 | 1156 | 4577 | 93 | 2702 |
ITGA9 | 4154 | -5185 | 3041 | 3909 |
ITGAV | 801 | -812 | 49 | 4981 |
ITGAX | 1897 | -886 | 3808 | 5125 |
ITGB1 | 891 | 945 | 4567 | 4783 |
ITGB3 | 3693 | -485 | 4867 | 2921 |
ITGB5 | 3604 | -2545 | -4743 | -4839 |
ITGB6 | -3832 | 471 | -3693 | 4890 |
LAMA2 | 3038 | -3750 | -756 | 2040 |
LAMA3 | 3451 | -999 | -4332 | -2201 |
LAMA4 | 4388 | 736 | -121 | 2343 |
LAMA5 | 3521 | -5520 | -2717 | -2028 |
LAMB1 | 2539 | -455 | -385 | 3101 |
LAMB2 | 3450 | -4834 | -3037 | -2486 |
LAMC1 | 4113 | -3181 | 2501 | 4089 |
LRP4 | -3904 | -5103 | -4823 | -2122 |
LUM | 4580 | -1815 | 2455 | 4537 |
MUSK | 2918 | -3675 | 4380 | 3328 |
NCAM1 | 3566 | -3904 | 4088 | 3898 |
PTPRS | 1732 | -4554 | -4143 | 2695 |
SERPINE1 | 4636 | -210 | 5117 | 3333 |
SPARC | 3820 | -2638 | -565 | 1957 |
TGFB1 | 4177 | -3070 | 4895 | 4099 |
TGFB2 | 3078 | 4561 | 1841 | -2330 |
TGFB3 | 3860 | -5264 | -2015 | -4211 |
TNC | 5019 | 793 | 4283 | 3460 |
TNXB | 4386 | -65 | 2484 | 3472 |
VCAN | 4971 | 1662 | 4386 | 4285 |
Collagen biosynthesis and modifying enzymes
metric | value |
---|---|
setSize | 47 |
pMANOVA | 3.12e-11 |
p.adjustMANOVA | 5.48e-10 |
s.dist | 0.729 |
s.FSHD | 0.5 |
s.hu_model | -0.352 |
s.Watt_m | 0.117 |
s.Jones_m | 0.379 |
p.FSHD | 3.16e-09 |
p.hu_model | 3.02e-05 |
p.Watt_m | 0.167 |
p.Jones_m | 7.07e-06 |
Gene | FSHD | Jones_m |
---|---|---|
COL14A1 | 4785 | 4769 |
COL8A1 | 4315 | 5058 |
PLOD3 | 4888 | 4301 |
PCOLCE2 | 4527 | 4379 |
PPIB | 4256 | 4403 |
COL5A2 | 4413 | 4122 |
PCOLCE | 4784 | 3588 |
ADAMTS2 | 4952 | 3395 |
COL3A1 | 4565 | 3575 |
COL6A3 | 4171 | 3393 |
BMP1 | 3427 | 4072 |
COL6A2 | 4692 | 2927 |
COL6A1 | 4823 | 2788 |
COL18A1 | 4351 | 3090 |
CRTAP | 3334 | 3958 |
COL5A1 | 4323 | 2999 |
PLOD2 | 3184 | 4022 |
COL4A2 | 3851 | 3295 |
COL4A1 | 3805 | 3236 |
SERPINH1 | 4694 | 2554 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
ADAMTS14 | 1835 | -4629 | 2211 | 2819 |
ADAMTS2 | 4952 | -2722 | 53 | 3395 |
BMP1 | 3427 | -4914 | 43 | 4072 |
COL11A1 | 4414 | 2113 | -2198 | -116 |
COL11A2 | -2800 | -2814 | -4013 | -1603 |
COL12A1 | 5001 | 1907 | 511 | 1626 |
COL13A1 | -180 | -2295 | -1942 | 1914 |
COL14A1 | 4785 | 831 | 1493 | 4769 |
COL15A1 | 2478 | -169 | 1436 | 1179 |
COL16A1 | 3846 | -2915 | 1643 | 2475 |
COL18A1 | 4351 | -2864 | 2677 | 3090 |
COL1A1 | 4847 | -1617 | 7 | 676 |
COL1A2 | 4681 | -1689 | -375 | 1250 |
COL22A1 | 2071 | -4805 | -3249 | -3090 |
COL23A1 | 3199 | -4585 | -845 | 2418 |
COL24A1 | -3035 | -5069 | -4749 | 5120 |
COL27A1 | 1066 | -5022 | 3972 | 2845 |
COL28A1 | -3227 | 2507 | -192 | 4214 |
COL3A1 | 4565 | 2950 | 2503 | 3575 |
COL4A1 | 3805 | -4695 | 688 | 3236 |
COL4A2 | 3851 | -4973 | 861 | 3295 |
COL4A3 | -2253 | -3782 | -4833 | -1934 |
COL4A4 | -2804 | -2983 | -3940 | -28 |
COL4A5 | -4216 | -4266 | -3428 | -289 |
COL5A1 | 4323 | -1537 | 2338 | 2999 |
COL5A2 | 4413 | -2991 | 3064 | 4122 |
COL5A3 | 3094 | -1534 | 3807 | 1554 |
COL6A1 | 4823 | -1919 | 2015 | 2788 |
COL6A2 | 4692 | -1812 | 2344 | 2927 |
COL6A3 | 4171 | -119 | 2648 | 3393 |
COL6A6 | 1139 | -2109 | -3933 | 45 |
COL7A1 | -425 | -3189 | -3985 | -2664 |
COL8A1 | 4315 | 881 | 4752 | 5058 |
COL8A2 | 4912 | -457 | -2292 | -563 |
COLGALT1 | 4647 | -3703 | -1269 | 2044 |
COLGALT2 | -1497 | -4412 | -1435 | -792 |
CRTAP | 3334 | -3815 | 1832 | 3958 |
P4HA1 | -1548 | -2913 | 4840 | -4372 |
P4HA2 | 2577 | -3906 | 2007 | -2091 |
P4HB | -184 | -2493 | 4004 | 3152 |
PCOLCE | 4784 | -618 | 2120 | 3588 |
PCOLCE2 | 4527 | 1723 | -52 | 4379 |
PLOD1 | 860 | -4628 | 381 | 2050 |
PLOD2 | 3184 | 3503 | 4833 | 4022 |
PLOD3 | 4888 | -4263 | 3018 | 4301 |
PPIB | 4256 | -428 | 3462 | 4403 |
SERPINH1 | 4694 | -3479 | 3725 | 2554 |
TP53 Regulates Transcription of Genes Involved in G1 Cell Cycle Arrest
metric | value |
---|---|
setSize | 12 |
pMANOVA | 0.0116 |
p.adjustMANOVA | 0.0266 |
s.dist | 0.726 |
s.FSHD | 0.274 |
s.hu_model | -0.193 |
s.Watt_m | 0.503 |
s.Jones_m | 0.403 |
p.FSHD | 0.1 |
p.hu_model | 0.247 |
p.Watt_m | 0.00257 |
p.Jones_m | 0.0158 |
Gene | Watt_m | Jones_m |
---|---|---|
CCNE1 | 4705 | 4959 |
E2F8 | 5076 | 4501 |
E2F1 | 4616 | 4809 |
CCNA2 | 4247 | 5048 |
CDKN1A | 5043 | 4230 |
ZNF385A | 3961 | 4690 |
CDK2 | 2660 | 4566 |
TP53 | 3708 | 2810 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
ARID3A | 4083 | -4363 | 1298 | -318 |
CCNA2 | 2177 | 3035 | 4247 | 5048 |
CCNE1 | 2834 | 4352 | 4705 | 4959 |
CCNE2 | 1263 | 4626 | 145 | -2482 |
CDK2 | 2466 | 838 | 2660 | 4566 |
CDKN1A | 5043 | -4867 | 5043 | 4230 |
CDKN1B | -3557 | -3241 | -2427 | -5070 |
E2F1 | 2820 | -526 | 4616 | 4809 |
E2F8 | 319 | -5556 | 5076 | 4501 |
PCBP4 | -3178 | -5459 | -1853 | -2745 |
TP53 | 4943 | 566 | 3708 | 2810 |
ZNF385A | -4082 | -5149 | 3961 | 4690 |
Synthesis of bile acids and bile salts via 7alpha-hydroxycholesterol
metric | value |
---|---|
setSize | 10 |
pMANOVA | 0.0613 |
p.adjustMANOVA | 0.106 |
s.dist | 0.725 |
s.FSHD | -0.386 |
s.hu_model | -0.141 |
s.Watt_m | -0.468 |
s.Jones_m | -0.371 |
p.FSHD | 0.0344 |
p.hu_model | 0.442 |
p.Watt_m | 0.0105 |
p.Jones_m | 0.042 |
Gene | Watt_m | FSHD |
---|---|---|
CYP27A1 | -5277 | -5269 |
SCP2 | -4882 | -5322 |
RXRA | -4147 | -4228 |
AMACR | -4008 | -3399 |
HSD17B4 | -3004 | -4299 |
NCOA2 | -4995 | -2521 |
NCOA1 | -1158 | -2128 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
ACOT8 | -2551 | -946 | 417 | 820 |
AMACR | -3399 | 4127 | -4008 | 40 |
CYP27A1 | -5269 | -4450 | -5277 | -5087 |
HSD17B4 | -4299 | 680 | -3004 | -3754 |
HSD3B7 | 4131 | -4317 | 1041 | 2290 |
NCOA1 | -2128 | 2605 | -1158 | -3029 |
NCOA2 | -2521 | 143 | -4995 | -4281 |
PTGIS | 3434 | -1895 | 927 | 1214 |
RXRA | -4228 | -5455 | -4147 | -5038 |
SCP2 | -5322 | -854 | -4882 | -3079 |
Laminin interactions
metric | value |
---|---|
setSize | 19 |
pMANOVA | 1.99e-05 |
p.adjustMANOVA | 0.000107 |
s.dist | 0.724 |
s.FSHD | 0.575 |
s.hu_model | -0.344 |
s.Watt_m | -0.0603 |
s.Jones_m | 0.268 |
p.FSHD | 1.44e-05 |
p.hu_model | 0.00938 |
p.Watt_m | 0.649 |
p.Jones_m | 0.0434 |
Gene | FSHD | hu_model |
---|---|---|
ITGA3 | 4809 | -5450 |
LAMA5 | 3521 | -5520 |
LAMB2 | 3450 | -4834 |
LAMC1 | 4113 | -3181 |
COL18A1 | 4351 | -2864 |
LAMA2 | 3038 | -3750 |
LAMB3 | 2231 | -4929 |
HSPG2 | 2035 | -5289 |
NID1 | 3391 | -1249 |
LAMA3 | 3451 | -999 |
ITGA7 | 580 | -4661 |
ITGA6 | 1799 | -990 |
LAMB1 | 2539 | -455 |
ITGAV | 801 | -812 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
COL18A1 | 4351 | -2864 | 2677 | 3090 |
HSPG2 | 2035 | -5289 | -401 | 2942 |
ITGA1 | 1435 | 1740 | -4092 | -3028 |
ITGA3 | 4809 | -5450 | 2976 | 557 |
ITGA6 | 1799 | -990 | -5243 | -114 |
ITGA7 | 580 | -4661 | 2121 | -4020 |
ITGAV | 801 | -812 | 49 | 4981 |
ITGB1 | 891 | 945 | 4567 | 4783 |
LAMA2 | 3038 | -3750 | -756 | 2040 |
LAMA3 | 3451 | -999 | -4332 | -2201 |
LAMA4 | 4388 | 736 | -121 | 2343 |
LAMA5 | 3521 | -5520 | -2717 | -2028 |
LAMB1 | 2539 | -455 | -385 | 3101 |
LAMB2 | 3450 | -4834 | -3037 | -2486 |
LAMB3 | 2231 | -4929 | -4569 | 386 |
LAMC1 | 4113 | -3181 | 2501 | 4089 |
LAMC2 | 4587 | 1336 | 5102 | 4436 |
NID1 | 3391 | -1249 | 709 | 3576 |
NID2 | 2587 | 177 | -1976 | 3644 |
Defective EXT1 causes exostoses 1, TRPS2 and CHDS
metric | value |
---|---|
setSize | 11 |
pMANOVA | 0.0114 |
p.adjustMANOVA | 0.0264 |
s.dist | 0.723 |
s.FSHD | 0.537 |
s.hu_model | -0.36 |
s.Watt_m | 0.162 |
s.Jones_m | 0.28 |
p.FSHD | 0.00204 |
p.hu_model | 0.0389 |
p.Watt_m | 0.352 |
p.Jones_m | 0.108 |
Gene | FSHD | hu_model |
---|---|---|
AGRN | 3889 | -4843 |
SDC3 | 3721 | -4560 |
GPC6 | 4618 | -2353 |
HSPG2 | 2035 | -5289 |
SDC1 | 3944 | -2017 |
SDC4 | 1095 | -2361 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
AGRN | 3889 | -4843 | -2922 | 760 |
EXT1 | 4706 | 3854 | 4979 | 3717 |
EXT2 | 2935 | 2055 | 910 | -1968 |
GPC1 | -1704 | -5207 | -2934 | -1700 |
GPC4 | -587 | -5108 | -3461 | -1575 |
GPC6 | 4618 | -2353 | 156 | 804 |
HSPG2 | 2035 | -5289 | -401 | 2942 |
SDC1 | 3944 | -2017 | 209 | 2683 |
SDC2 | 4456 | 1739 | 4436 | 5008 |
SDC3 | 3721 | -4560 | 2780 | 4191 |
SDC4 | 1095 | -2361 | 5103 | 946 |
Defective EXT2 causes exostoses 2
metric | value |
---|---|
setSize | 11 |
pMANOVA | 0.0114 |
p.adjustMANOVA | 0.0264 |
s.dist | 0.723 |
s.FSHD | 0.537 |
s.hu_model | -0.36 |
s.Watt_m | 0.162 |
s.Jones_m | 0.28 |
p.FSHD | 0.00204 |
p.hu_model | 0.0389 |
p.Watt_m | 0.352 |
p.Jones_m | 0.108 |
Gene | FSHD | hu_model |
---|---|---|
AGRN | 3889 | -4843 |
SDC3 | 3721 | -4560 |
GPC6 | 4618 | -2353 |
HSPG2 | 2035 | -5289 |
SDC1 | 3944 | -2017 |
SDC4 | 1095 | -2361 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
AGRN | 3889 | -4843 | -2922 | 760 |
EXT1 | 4706 | 3854 | 4979 | 3717 |
EXT2 | 2935 | 2055 | 910 | -1968 |
GPC1 | -1704 | -5207 | -2934 | -1700 |
GPC4 | -587 | -5108 | -3461 | -1575 |
GPC6 | 4618 | -2353 | 156 | 804 |
HSPG2 | 2035 | -5289 | -401 | 2942 |
SDC1 | 3944 | -2017 | 209 | 2683 |
SDC2 | 4456 | 1739 | 4436 | 5008 |
SDC3 | 3721 | -4560 | 2780 | 4191 |
SDC4 | 1095 | -2361 | 5103 | 946 |
rRNA modification in the nucleus and cytosol
metric | value |
---|---|
setSize | 52 |
pMANOVA | 1.28e-15 |
p.adjustMANOVA | 4.91e-14 |
s.dist | 0.722 |
s.FSHD | -0.181 |
s.hu_model | 0.601 |
s.Watt_m | 0.357 |
s.Jones_m | 0.011 |
p.FSHD | 0.0244 |
p.hu_model | 6.53e-14 |
p.Watt_m | 8.81e-06 |
p.Jones_m | 0.891 |
Gene | hu_model | Watt_m |
---|---|---|
UTP14A | 4734 | 4989.5 |
NOP58 | 4847 | 4297.0 |
DCAF13 | 4757 | 4119.0 |
GAR1 | 4099 | 4715.0 |
HEATR1 | 4867 | 3812.0 |
WDR3 | 4794 | 3504.0 |
WDR43 | 4839 | 3438.0 |
NOP2 | 3445 | 4776.0 |
WDR36 | 4503 | 3463.0 |
UTP3 | 4873 | 2896.0 |
UTP18 | 3820 | 3693.0 |
IMP4 | 2781 | 4269.0 |
NOP56 | 3072 | 3816.0 |
UTP15 | 4104 | 2746.0 |
MPHOSPH10 | 3895 | 2797.0 |
NOL6 | 3788 | 2734.0 |
FBL | 4199 | 2189.0 |
WDR75 | 3713 | 2350.0 |
WDR46 | 3308 | 2620.0 |
DDX49 | 2158 | 3982.0 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
BMS1 | -3925 | 3484 | -4173.0 | 2837.0 |
DCAF13 | 2329 | 4757 | 4119.0 | 2732.0 |
DDX47 | -2373 | 3705 | 1420.0 | -2733.0 |
DDX49 | -365 | 2158 | 3982.0 | 971.0 |
DHX37 | -764 | 2086 | 2942.0 | 1278.0 |
DIEXF | 1711 | 4833 | 1136.0 | -1945.0 |
DIMT1 | 892 | 2514 | 1435.0 | -1291.0 |
DKC1 | -2792 | 3601 | -170.0 | -5125.0 |
FBL | 2415 | 4199 | 2189.0 | 2712.0 |
FCF1 | -221 | 3276 | 2030.0 | 2653.0 |
GAR1 | 1686 | 4099 | 4715.0 | 1513.0 |
HEATR1 | 1655 | 4867 | 3812.0 | 2362.0 |
IMP3 | -1650 | 4497 | -955.0 | -1140.0 |
IMP4 | -1870 | 2781 | 4269.0 | 2864.0 |
KRR1 | -5216 | 3888 | 1101.0 | -3181.0 |
MPHOSPH10 | -5196 | 3895 | 2797.0 | 246.0 |
NAT10 | -2447 | 3614 | -1149.0 | 3217.0 |
NHP2 | 919 | 685 | 2650.0 | 2538.0 |
NOC4L | 683 | 1746 | 1992.0 | 588.0 |
NOL11 | -4496 | 4872 | -390.0 | -2059.0 |
NOL6 | -1455 | 3788 | 2734.0 | 3169.0 |
NOP10 | -89 | 1321 | 902.0 | -4543.0 |
NOP14 | -4062 | 1573 | 4346.0 | 95.0 |
NOP2 | 304 | 3445 | 4776.0 | -617.0 |
NOP56 | 1503 | 3072 | 3816.0 | -3435.0 |
NOP58 | 23 | 4847 | 4297.0 | 1374.0 |
PDCD11 | -714 | -1447 | 807.0 | 586.0 |
PNO1 | -1122 | 4582 | 326.0 | -4540.0 |
PWP2 | -2511 | 2440 | 737.0 | -4460.0 |
RCL1 | -4680 | 3230 | -47.0 | -3988.0 |
RPS14 | -996 | -1395 | 1309.0 | -278.0 |
RPS6 | -549 | -244 | 3507.0 | -947.0 |
RPS9 | 1112 | -1094 | 1563.0 | 1857.0 |
RRP36 | -3795 | 1515 | 1834.0 | 1655.0 |
RRP7A | 133 | 2118 | 3584.0 | 2547.0 |
RRP9 | -593 | 761 | 2301.0 | -3087.0 |
TBL3 | -369 | -1531 | 1052.0 | -1653.0 |
THUMPD1 | -5026 | 4625 | -2539.0 | -2560.0 |
TSR3 | -967 | -3564 | -3243.0 | -3970.0 |
UTP14A | -1437 | 4734 | 4989.5 | 4165.5 |
UTP14C | -5428 | 1548 | 4989.5 | 4165.5 |
UTP15 | -1506 | 4104 | 2746.0 | -667.0 |
UTP18 | -4246 | 3820 | 3693.0 | 4299.0 |
UTP20 | -3726 | 4140 | 236.0 | 3401.0 |
UTP3 | 2107 | 4873 | 2896.0 | 1100.0 |
UTP6 | 1200 | 4736 | -4463.0 | -4013.0 |
WBSCR22 | -478 | 1724 | -1524.0 | -2587.0 |
WDR3 | -1677 | 4794 | 3504.0 | 1578.0 |
WDR36 | -2967 | 4503 | 3463.0 | 5191.0 |
WDR43 | -2876 | 4839 | 3438.0 | -2273.0 |
WDR46 | 3761 | 3308 | 2620.0 | 1772.0 |
WDR75 | 1462 | 3713 | 2350.0 | -1228.0 |
RHO GTPases Activate WASPs and WAVEs
metric | value |
---|---|
setSize | 31 |
pMANOVA | 2.9e-05 |
p.adjustMANOVA | 0.000149 |
s.dist | 0.718 |
s.FSHD | 0.362 |
s.hu_model | 0.0906 |
s.Watt_m | 0.428 |
s.Jones_m | 0.44 |
p.FSHD | 0.000485 |
p.hu_model | 0.383 |
p.Watt_m | 3.82e-05 |
p.Jones_m | 2.24e-05 |
Gene | Jones_m | Watt_m |
---|---|---|
ABI2 | 5112 | 5000 |
ACTR3 | 4879 | 5086 |
ARPC5 | 4898 | 4796 |
ARPC1B | 4719 | 4808 |
ACTB | 4471 | 4929 |
BAIAP2 | 4353 | 4993 |
ARPC2 | 4615 | 4570 |
ACTR2 | 4894 | 3889 |
ARPC3 | 4579 | 3719 |
ACTG1 | 3342 | 4938 |
BRK1 | 4085 | 3060 |
ARPC4 | 4316 | 2543 |
NCKAP1 | 2872 | 3543 |
ABI1 | 3901 | 2528 |
WIPF1 | 3677 | 1663 |
WASF2 | 3899 | 1495 |
ARPC1A | 2218 | 2622 |
MAPK3 | 1133 | 3682 |
NCK1 | 3133 | 1276 |
WASL | 1120 | 3230 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
ABI1 | 2432 | 3761 | 2528 | 3901 |
ABI2 | 2698 | -307 | 5000 | 5112 |
ABL1 | 2719 | -4474 | -3505 | -1534 |
ACTB | 4268 | 929 | 4929 | 4471 |
ACTG1 | 4406 | -3035 | 4938 | 3342 |
ACTR2 | 290 | 3520 | 3889 | 4894 |
ACTR3 | 2481 | 1361 | 5086 | 4879 |
ARPC1A | 2458 | -120 | 2622 | 2218 |
ARPC1B | 4929 | 660 | 4808 | 4719 |
ARPC2 | 493 | 1342 | 4570 | 4615 |
ARPC3 | 2801 | 2849 | 3719 | 4579 |
ARPC4 | 4280 | 1681 | 2543 | 4316 |
ARPC5 | 4326 | 2275 | 4796 | 4898 |
BAIAP2 | 3612 | -638 | 4993 | 4353 |
BRK1 | -453 | 2008 | 3060 | 4085 |
CDC42 | 1017 | 3281 | 746 | 2621 |
CYFIP2 | 2025 | -3726 | -1121 | 722 |
GRB2 | 2101 | -3999 | 4449 | 3 |
MAPK1 | 2000 | 1970 | -642 | -2044 |
MAPK3 | 2715 | -1012 | 3682 | 1133 |
NCK1 | -2442 | 3688 | 1276 | 3133 |
NCKAP1 | -5051 | 3536 | 3543 | 2872 |
NCKIPSD | 1603 | -2784 | 696 | -791 |
PTK2 | 692 | -2465 | -1494 | -4001 |
RAC1 | -458 | 2502 | 1441 | -618 |
WASF2 | 3489 | -4597 | 1495 | 3899 |
WASF3 | -651 | -1003 | 710 | -451 |
WASL | -3955 | 2660 | 3230 | 1120 |
WIPF1 | 4205 | -2520 | 1663 | 3677 |
WIPF2 | 2810 | 3272 | -497 | -676 |
WIPF3 | 1526 | -5045 | -5000 | 1136 |
NF-kB activation through FADD/RIP-1 pathway mediated by caspase-8 and -10
metric | value |
---|---|
setSize | 10 |
pMANOVA | 0.000989 |
p.adjustMANOVA | 0.00337 |
s.dist | 0.717 |
s.FSHD | 0.114 |
s.hu_model | -0.245 |
s.Watt_m | 0.0504 |
s.Jones_m | 0.662 |
p.FSHD | 0.532 |
p.hu_model | 0.18 |
p.Watt_m | 0.782 |
p.Jones_m | 0.000288 |
Gene | Jones_m | hu_model |
---|---|---|
IKBKB | 3732 | -4041 |
TRIM25 | 4120 | -3200 |
RNF135 | 2448 | -3630 |
CASP8 | 4108 | -1624 |
FADD | 4118 | -568 |
MAVS | 423 | -4708 |
IFIH1 | 4801 | -203 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
CASP8 | 4576 | -1624 | 3056 | 4108 |
CHUK | -5003 | 213 | 946 | 4752 |
DDX58 | 909 | 1576 | -903 | 3117 |
FADD | 588 | -568 | 4829 | 4118 |
IFIH1 | 3035 | -203 | -3084 | 4801 |
IKBKB | -4380 | -4041 | 570 | 3732 |
MAVS | -4398 | -4708 | -4806 | 423 |
RIPK1 | 2917 | 322 | 711 | 2881 |
RNF135 | 3350 | -3630 | 979 | 2448 |
TRIM25 | 2601 | -3200 | -118 | 4120 |
FCGR3A-mediated phagocytosis
metric | value |
---|---|
setSize | 47 |
pMANOVA | 5.38e-08 |
p.adjustMANOVA | 5.42e-07 |
s.dist | 0.713 |
s.FSHD | 0.384 |
s.hu_model | -0.0119 |
s.Watt_m | 0.377 |
s.Jones_m | 0.467 |
p.FSHD | 5.2e-06 |
p.hu_model | 0.888 |
p.Watt_m | 8.09e-06 |
p.Jones_m | 3.05e-08 |
Gene | Jones_m | FSHD |
---|---|---|
ARPC1B | 4719 | 4929 |
ELMO1 | 4983 | 4381 |
ARPC5 | 4898 | 4326 |
MYH9 | 4498 | 4535 |
ACTB | 4471 | 4268 |
ARPC4 | 4316 | 4280 |
VAV2 | 3870 | 4713 |
MYO9B | 4853 | 3722 |
FYN | 4010 | 4466 |
BAIAP2 | 4353 | 3612 |
WIPF1 | 3677 | 4205 |
LYN | 4433 | 3429 |
ACTG1 | 3342 | 4406 |
VAV3 | 5070 | 2792 |
ABI2 | 5112 | 2698 |
WASF2 | 3899 | 3489 |
ARPC3 | 4579 | 2801 |
ACTR3 | 4879 | 2481 |
DOCK1 | 3013 | 3791 |
SRC | 2269 | 5021 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
ABI1 | 2432 | 3761 | 2528 | 3901 |
ABI2 | 2698 | -307 | 5000 | 5112 |
ABL1 | 2719 | -4474 | -3505 | -1534 |
ACTB | 4268 | 929 | 4929 | 4471 |
ACTG1 | 4406 | -3035 | 4938 | 3342 |
ACTR2 | 290 | 3520 | 3889 | 4894 |
ACTR3 | 2481 | 1361 | 5086 | 4879 |
ARPC1A | 2458 | -120 | 2622 | 2218 |
ARPC1B | 4929 | 660 | 4808 | 4719 |
ARPC2 | 493 | 1342 | 4570 | 4615 |
ARPC3 | 2801 | 2849 | 3719 | 4579 |
ARPC4 | 4280 | 1681 | 2543 | 4316 |
ARPC5 | 4326 | 2275 | 4796 | 4898 |
BAIAP2 | 3612 | -638 | 4993 | 4353 |
BRK1 | -453 | 2008 | 3060 | 4085 |
CDC42 | 1017 | 3281 | 746 | 2621 |
CRK | -421 | 2125 | 2238 | -3653 |
CYFIP2 | 2025 | -3726 | -1121 | 722 |
DOCK1 | 3791 | -225 | -40 | 3013 |
ELMO1 | 4381 | -2137 | 1433 | 4983 |
ELMO2 | -2210 | -353 | 410 | -2080 |
FYN | 4466 | -2813 | 3642 | 4010 |
GRB2 | 2101 | -3999 | 4449 | 3 |
LYN | 3429 | 775 | 3940 | 4433 |
MAPK1 | 2000 | 1970 | -642 | -2044 |
MAPK3 | 2715 | -1012 | 3682 | 1133 |
MYH2 | -3590 | -3040 | -851 | -2213 |
MYH9 | 4535 | -1853 | 4150 | 4498 |
MYO10 | -1902 | 1365 | 289 | 2204 |
MYO1C | 2172 | -4782 | 3479 | 3687 |
MYO5A | 981 | -875 | 3241 | 5027 |
MYO9B | 3722 | -1875 | 4011 | 4853 |
NCK1 | -2442 | 3688 | 1276 | 3133 |
NCKAP1 | -5051 | 3536 | 3543 | 2872 |
NCKIPSD | 1603 | -2784 | 696 | -791 |
PTK2 | 692 | -2465 | -1494 | -4001 |
RAC1 | -458 | 2502 | 1441 | -618 |
SRC | 5021 | -3860 | 1364 | 2269 |
VAV2 | 4713 | -4898 | -893 | 3870 |
VAV3 | 2792 | 184 | -1056 | 5070 |
WASF2 | 3489 | -4597 | 1495 | 3899 |
WASF3 | -651 | -1003 | 710 | -451 |
WASL | -3955 | 2660 | 3230 | 1120 |
WIPF1 | 4205 | -2520 | 1663 | 3677 |
WIPF2 | 2810 | 3272 | -497 | -676 |
WIPF3 | 1526 | -5045 | -5000 | 1136 |
YES1 | 1006 | -175 | -2910 | 2958 |
Leishmania phagocytosis
metric | value |
---|---|
setSize | 47 |
pMANOVA | 5.38e-08 |
p.adjustMANOVA | 5.42e-07 |
s.dist | 0.713 |
s.FSHD | 0.384 |
s.hu_model | -0.0119 |
s.Watt_m | 0.377 |
s.Jones_m | 0.467 |
p.FSHD | 5.2e-06 |
p.hu_model | 0.888 |
p.Watt_m | 8.09e-06 |
p.Jones_m | 3.05e-08 |
Gene | Jones_m | FSHD |
---|---|---|
ARPC1B | 4719 | 4929 |
ELMO1 | 4983 | 4381 |
ARPC5 | 4898 | 4326 |
MYH9 | 4498 | 4535 |
ACTB | 4471 | 4268 |
ARPC4 | 4316 | 4280 |
VAV2 | 3870 | 4713 |
MYO9B | 4853 | 3722 |
FYN | 4010 | 4466 |
BAIAP2 | 4353 | 3612 |
WIPF1 | 3677 | 4205 |
LYN | 4433 | 3429 |
ACTG1 | 3342 | 4406 |
VAV3 | 5070 | 2792 |
ABI2 | 5112 | 2698 |
WASF2 | 3899 | 3489 |
ARPC3 | 4579 | 2801 |
ACTR3 | 4879 | 2481 |
DOCK1 | 3013 | 3791 |
SRC | 2269 | 5021 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
ABI1 | 2432 | 3761 | 2528 | 3901 |
ABI2 | 2698 | -307 | 5000 | 5112 |
ABL1 | 2719 | -4474 | -3505 | -1534 |
ACTB | 4268 | 929 | 4929 | 4471 |
ACTG1 | 4406 | -3035 | 4938 | 3342 |
ACTR2 | 290 | 3520 | 3889 | 4894 |
ACTR3 | 2481 | 1361 | 5086 | 4879 |
ARPC1A | 2458 | -120 | 2622 | 2218 |
ARPC1B | 4929 | 660 | 4808 | 4719 |
ARPC2 | 493 | 1342 | 4570 | 4615 |
ARPC3 | 2801 | 2849 | 3719 | 4579 |
ARPC4 | 4280 | 1681 | 2543 | 4316 |
ARPC5 | 4326 | 2275 | 4796 | 4898 |
BAIAP2 | 3612 | -638 | 4993 | 4353 |
BRK1 | -453 | 2008 | 3060 | 4085 |
CDC42 | 1017 | 3281 | 746 | 2621 |
CRK | -421 | 2125 | 2238 | -3653 |
CYFIP2 | 2025 | -3726 | -1121 | 722 |
DOCK1 | 3791 | -225 | -40 | 3013 |
ELMO1 | 4381 | -2137 | 1433 | 4983 |
ELMO2 | -2210 | -353 | 410 | -2080 |
FYN | 4466 | -2813 | 3642 | 4010 |
GRB2 | 2101 | -3999 | 4449 | 3 |
LYN | 3429 | 775 | 3940 | 4433 |
MAPK1 | 2000 | 1970 | -642 | -2044 |
MAPK3 | 2715 | -1012 | 3682 | 1133 |
MYH2 | -3590 | -3040 | -851 | -2213 |
MYH9 | 4535 | -1853 | 4150 | 4498 |
MYO10 | -1902 | 1365 | 289 | 2204 |
MYO1C | 2172 | -4782 | 3479 | 3687 |
MYO5A | 981 | -875 | 3241 | 5027 |
MYO9B | 3722 | -1875 | 4011 | 4853 |
NCK1 | -2442 | 3688 | 1276 | 3133 |
NCKAP1 | -5051 | 3536 | 3543 | 2872 |
NCKIPSD | 1603 | -2784 | 696 | -791 |
PTK2 | 692 | -2465 | -1494 | -4001 |
RAC1 | -458 | 2502 | 1441 | -618 |
SRC | 5021 | -3860 | 1364 | 2269 |
VAV2 | 4713 | -4898 | -893 | 3870 |
VAV3 | 2792 | 184 | -1056 | 5070 |
WASF2 | 3489 | -4597 | 1495 | 3899 |
WASF3 | -651 | -1003 | 710 | -451 |
WASL | -3955 | 2660 | 3230 | 1120 |
WIPF1 | 4205 | -2520 | 1663 | 3677 |
WIPF2 | 2810 | 3272 | -497 | -676 |
WIPF3 | 1526 | -5045 | -5000 | 1136 |
YES1 | 1006 | -175 | -2910 | 2958 |
Parasite infection
metric | value |
---|---|
setSize | 47 |
pMANOVA | 5.38e-08 |
p.adjustMANOVA | 5.42e-07 |
s.dist | 0.713 |
s.FSHD | 0.384 |
s.hu_model | -0.0119 |
s.Watt_m | 0.377 |
s.Jones_m | 0.467 |
p.FSHD | 5.2e-06 |
p.hu_model | 0.888 |
p.Watt_m | 8.09e-06 |
p.Jones_m | 3.05e-08 |
Gene | Jones_m | FSHD |
---|---|---|
ARPC1B | 4719 | 4929 |
ELMO1 | 4983 | 4381 |
ARPC5 | 4898 | 4326 |
MYH9 | 4498 | 4535 |
ACTB | 4471 | 4268 |
ARPC4 | 4316 | 4280 |
VAV2 | 3870 | 4713 |
MYO9B | 4853 | 3722 |
FYN | 4010 | 4466 |
BAIAP2 | 4353 | 3612 |
WIPF1 | 3677 | 4205 |
LYN | 4433 | 3429 |
ACTG1 | 3342 | 4406 |
VAV3 | 5070 | 2792 |
ABI2 | 5112 | 2698 |
WASF2 | 3899 | 3489 |
ARPC3 | 4579 | 2801 |
ACTR3 | 4879 | 2481 |
DOCK1 | 3013 | 3791 |
SRC | 2269 | 5021 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
ABI1 | 2432 | 3761 | 2528 | 3901 |
ABI2 | 2698 | -307 | 5000 | 5112 |
ABL1 | 2719 | -4474 | -3505 | -1534 |
ACTB | 4268 | 929 | 4929 | 4471 |
ACTG1 | 4406 | -3035 | 4938 | 3342 |
ACTR2 | 290 | 3520 | 3889 | 4894 |
ACTR3 | 2481 | 1361 | 5086 | 4879 |
ARPC1A | 2458 | -120 | 2622 | 2218 |
ARPC1B | 4929 | 660 | 4808 | 4719 |
ARPC2 | 493 | 1342 | 4570 | 4615 |
ARPC3 | 2801 | 2849 | 3719 | 4579 |
ARPC4 | 4280 | 1681 | 2543 | 4316 |
ARPC5 | 4326 | 2275 | 4796 | 4898 |
BAIAP2 | 3612 | -638 | 4993 | 4353 |
BRK1 | -453 | 2008 | 3060 | 4085 |
CDC42 | 1017 | 3281 | 746 | 2621 |
CRK | -421 | 2125 | 2238 | -3653 |
CYFIP2 | 2025 | -3726 | -1121 | 722 |
DOCK1 | 3791 | -225 | -40 | 3013 |
ELMO1 | 4381 | -2137 | 1433 | 4983 |
ELMO2 | -2210 | -353 | 410 | -2080 |
FYN | 4466 | -2813 | 3642 | 4010 |
GRB2 | 2101 | -3999 | 4449 | 3 |
LYN | 3429 | 775 | 3940 | 4433 |
MAPK1 | 2000 | 1970 | -642 | -2044 |
MAPK3 | 2715 | -1012 | 3682 | 1133 |
MYH2 | -3590 | -3040 | -851 | -2213 |
MYH9 | 4535 | -1853 | 4150 | 4498 |
MYO10 | -1902 | 1365 | 289 | 2204 |
MYO1C | 2172 | -4782 | 3479 | 3687 |
MYO5A | 981 | -875 | 3241 | 5027 |
MYO9B | 3722 | -1875 | 4011 | 4853 |
NCK1 | -2442 | 3688 | 1276 | 3133 |
NCKAP1 | -5051 | 3536 | 3543 | 2872 |
NCKIPSD | 1603 | -2784 | 696 | -791 |
PTK2 | 692 | -2465 | -1494 | -4001 |
RAC1 | -458 | 2502 | 1441 | -618 |
SRC | 5021 | -3860 | 1364 | 2269 |
VAV2 | 4713 | -4898 | -893 | 3870 |
VAV3 | 2792 | 184 | -1056 | 5070 |
WASF2 | 3489 | -4597 | 1495 | 3899 |
WASF3 | -651 | -1003 | 710 | -451 |
WASL | -3955 | 2660 | 3230 | 1120 |
WIPF1 | 4205 | -2520 | 1663 | 3677 |
WIPF2 | 2810 | 3272 | -497 | -676 |
WIPF3 | 1526 | -5045 | -5000 | 1136 |
YES1 | 1006 | -175 | -2910 | 2958 |
Cristae formation
metric | value |
---|---|
setSize | 10 |
pMANOVA | 0.0576 |
p.adjustMANOVA | 0.102 |
s.dist | 0.712 |
s.FSHD | -0.512 |
s.hu_model | 0.0502 |
s.Watt_m | -0.293 |
s.Jones_m | -0.395 |
p.FSHD | 0.00503 |
p.hu_model | 0.784 |
p.Watt_m | 0.109 |
p.Jones_m | 0.0304 |
Gene | FSHD | Jones_m |
---|---|---|
APOOL | -5041 | -4307 |
HSPA9 | -4467 | -4245 |
IMMT | -4687 | -3966 |
CHCHD3 | -4596 | -3379 |
DNAJC11 | -4805 | -2021 |
TMEM11 | -1792 | -3773 |
SAMM50 | -2462 | -2001 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
APOOL | -5041 | -69 | -606 | -4307 |
CHCHD3 | -4596 | 120 | -1967 | -3379 |
CHCHD6 | 2185 | -2148 | -1823 | 2590 |
DNAJC11 | -4805 | -2120 | -2786 | -2021 |
HSPA9 | -4467 | 2321 | -1418 | -4245 |
IMMT | -4687 | -289 | -5001 | -3966 |
MTX1 | 781 | 2000 | 245 | -2260 |
MTX2 | -3900 | 50 | 193 | 2197 |
SAMM50 | -2462 | 1129 | -3622 | -2001 |
TMEM11 | -1792 | -1318 | 877 | -3773 |
Collagen formation
metric | value |
---|---|
setSize | 63 |
pMANOVA | 7.69e-15 |
p.adjustMANOVA | 2.62e-13 |
s.dist | 0.711 |
s.FSHD | 0.507 |
s.hu_model | -0.309 |
s.Watt_m | 0.0807 |
s.Jones_m | 0.383 |
p.FSHD | 3.43e-12 |
p.hu_model | 2.29e-05 |
p.Watt_m | 0.269 |
p.Jones_m | 1.45e-07 |
Gene | FSHD | Jones_m |
---|---|---|
COL14A1 | 4785 | 4769 |
LOXL3 | 4563 | 4925 |
COL8A1 | 4315 | 5058 |
PLOD3 | 4888 | 4301 |
LAMC2 | 4587 | 4436 |
PCOLCE2 | 4527 | 4379 |
CTSS | 3773 | 5148 |
LOXL1 | 4187 | 4524 |
PPIB | 4256 | 4403 |
COL5A2 | 4413 | 4122 |
CD151 | 4172 | 4305 |
LOXL2 | 5054 | 3520 |
LOX | 4606 | 3765 |
PCOLCE | 4784 | 3588 |
ADAMTS2 | 4952 | 3395 |
COL3A1 | 4565 | 3575 |
COL6A3 | 4171 | 3393 |
BMP1 | 3427 | 4072 |
COL6A2 | 4692 | 2927 |
COL6A1 | 4823 | 2788 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
ADAMTS14 | 1835 | -4629 | 2211 | 2819 |
ADAMTS2 | 4952 | -2722 | 53 | 3395 |
BMP1 | 3427 | -4914 | 43 | 4072 |
CD151 | 4172 | -5328 | -921 | 4305 |
COL11A1 | 4414 | 2113 | -2198 | -116 |
COL11A2 | -2800 | -2814 | -4013 | -1603 |
COL12A1 | 5001 | 1907 | 511 | 1626 |
COL13A1 | -180 | -2295 | -1942 | 1914 |
COL14A1 | 4785 | 831 | 1493 | 4769 |
COL15A1 | 2478 | -169 | 1436 | 1179 |
COL16A1 | 3846 | -2915 | 1643 | 2475 |
COL18A1 | 4351 | -2864 | 2677 | 3090 |
COL1A1 | 4847 | -1617 | 7 | 676 |
COL1A2 | 4681 | -1689 | -375 | 1250 |
COL22A1 | 2071 | -4805 | -3249 | -3090 |
COL23A1 | 3199 | -4585 | -845 | 2418 |
COL24A1 | -3035 | -5069 | -4749 | 5120 |
COL27A1 | 1066 | -5022 | 3972 | 2845 |
COL28A1 | -3227 | 2507 | -192 | 4214 |
COL3A1 | 4565 | 2950 | 2503 | 3575 |
COL4A1 | 3805 | -4695 | 688 | 3236 |
COL4A2 | 3851 | -4973 | 861 | 3295 |
COL4A3 | -2253 | -3782 | -4833 | -1934 |
COL4A4 | -2804 | -2983 | -3940 | -28 |
COL4A5 | -4216 | -4266 | -3428 | -289 |
COL5A1 | 4323 | -1537 | 2338 | 2999 |
COL5A2 | 4413 | -2991 | 3064 | 4122 |
COL5A3 | 3094 | -1534 | 3807 | 1554 |
COL6A1 | 4823 | -1919 | 2015 | 2788 |
COL6A2 | 4692 | -1812 | 2344 | 2927 |
COL6A3 | 4171 | -119 | 2648 | 3393 |
COL6A6 | 1139 | -2109 | -3933 | 45 |
COL7A1 | -425 | -3189 | -3985 | -2664 |
COL8A1 | 4315 | 881 | 4752 | 5058 |
COL8A2 | 4912 | -457 | -2292 | -563 |
COLGALT1 | 4647 | -3703 | -1269 | 2044 |
COLGALT2 | -1497 | -4412 | -1435 | -792 |
CRTAP | 3334 | -3815 | 1832 | 3958 |
CTSB | 2843 | -1183 | -789 | 4639 |
CTSS | 3773 | -338 | 5035 | 5148 |
CTSV | -84 | 2189 | 34 | 331 |
DST | -3834 | -1727 | -4289 | -4863 |
ITGA6 | 1799 | -990 | -5243 | -114 |
LAMA3 | 3451 | -999 | -4332 | -2201 |
LAMB3 | 2231 | -4929 | -4569 | 386 |
LAMC2 | 4587 | 1336 | 5102 | 4436 |
LOX | 4606 | 4062 | 3160 | 3765 |
LOXL1 | 4187 | -1569 | 3956 | 4524 |
LOXL2 | 5054 | -3017 | 2997 | 3520 |
LOXL3 | 4563 | -1100 | 1944 | 4925 |
LOXL4 | 3456 | 552 | 27 | 3757 |
P4HA1 | -1548 | -2913 | 4840 | -4372 |
P4HA2 | 2577 | -3906 | 2007 | -2091 |
P4HB | -184 | -2493 | 4004 | 3152 |
PCOLCE | 4784 | -618 | 2120 | 3588 |
PCOLCE2 | 4527 | 1723 | -52 | 4379 |
PLEC | -3017 | -5409 | -1604 | -3459 |
PLOD1 | 860 | -4628 | 381 | 2050 |
PLOD2 | 3184 | 3503 | 4833 | 4022 |
PLOD3 | 4888 | -4263 | 3018 | 4301 |
PPIB | 4256 | -428 | 3462 | 4403 |
PXDN | 3490 | -1421 | -3444 | 3436 |
SERPINH1 | 4694 | -3479 | 3725 | 2554 |
Extracellular matrix organization
metric | value |
---|---|
setSize | 192 |
pMANOVA | 7.97e-44 |
p.adjustMANOVA | 3.27e-41 |
s.dist | 0.711 |
s.FSHD | 0.545 |
s.hu_model | -0.258 |
s.Watt_m | 0.142 |
s.Jones_m | 0.348 |
p.FSHD | 9.51e-39 |
p.hu_model | 8.04e-10 |
p.Watt_m | 0.000716 |
p.Jones_m | 1.07e-16 |
Gene | FSHD | Jones_m |
---|---|---|
SPP1 | 4998 | 5215 |
ADAM12 | 5018 | 5038 |
ITGB2 | 4906 | 5102 |
ACTN1 | 4991 | 4955 |
CD44 | 4845 | 5080 |
TIMP1 | 4933 | 4988 |
MMP19 | 4747 | 5126 |
ITGAM | 4572 | 5107 |
COL14A1 | 4785 | 4769 |
VCAM1 | 4924 | 4588 |
LOXL3 | 4563 | 4925 |
SDC2 | 4456 | 5008 |
BGN | 4348 | 5088 |
COL8A1 | 4315 | 5058 |
ICAM1 | 4641 | 4600 |
VCAN | 4971 | 4285 |
PLOD3 | 4888 | 4301 |
MFAP5 | 4668 | 4499 |
LUM | 4580 | 4537 |
LAMC2 | 4587 | 4436 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
ACTN1 | 4991 | -673 | 3653 | 4955 |
ADAM10 | 2507 | -1489 | -1018 | 3455 |
ADAM12 | 5018 | 643 | 5019 | 5038 |
ADAM15 | 3824 | -3547 | 4576 | 3617 |
ADAM17 | 411 | 2385 | 2056 | 2726 |
ADAM19 | -535 | -4618 | -2690 | 2501 |
ADAM8 | 2510 | -2559 | 5057 | 5134 |
ADAM9 | 261 | 342 | 148 | 3770 |
ADAMTS1 | 4378 | -4528 | 4660 | 2787 |
ADAMTS14 | 1835 | -4629 | 2211 | 2819 |
ADAMTS2 | 4952 | -2722 | 53 | 3395 |
ADAMTS4 | 4986 | -3118 | 4239 | 2378 |
ADAMTS5 | 3999 | 3508 | -591 | 939 |
ADAMTS9 | 2574 | -777 | -1141 | 3604 |
AGRN | 3889 | -4843 | -2922 | 760 |
ASPN | 4403 | 4376 | 2320 | 3985 |
BGN | 4348 | -1456 | 3875 | 5088 |
BMP1 | 3427 | -4914 | 43 | 4072 |
BMP2 | 3157 | -4202 | 820 | -1673 |
BMP4 | 2116 | 329 | 908 | 307 |
BSG | -1369 | -2217 | -2093 | -5147 |
CAPN1 | 338 | -5104 | -4377 | -1115 |
CAPN10 | 3254 | -2153 | -2849 | 237 |
CAPN15 | 1471 | -4608 | 1808 | 695 |
CAPN2 | 3440 | -3365 | 4883 | 5001 |
CAPN3 | -3909 | -4761 | -2650 | -4046 |
CAPN5 | 3967 | -2597 | -276 | 764 |
CAPN6 | 1229 | -4866 | 3231 | 4668 |
CAPN7 | -4421 | -522 | -4909 | -4965 |
CAPNS1 | 2784 | -1330 | 1730 | 5062 |
CASK | 1599 | 2860 | 3171 | 3957 |
CASP3 | 1918 | 419 | 4968 | 4110 |
CAST | -2581 | -749 | 4823 | -93 |
CD151 | 4172 | -5328 | -921 | 4305 |
CD44 | 4845 | 826 | 4939 | 5080 |
CD47 | 3471 | -2154 | 2654 | 4552 |
COL11A1 | 4414 | 2113 | -2198 | -116 |
COL11A2 | -2800 | -2814 | -4013 | -1603 |
COL12A1 | 5001 | 1907 | 511 | 1626 |
COL13A1 | -180 | -2295 | -1942 | 1914 |
COL14A1 | 4785 | 831 | 1493 | 4769 |
COL15A1 | 2478 | -169 | 1436 | 1179 |
COL16A1 | 3846 | -2915 | 1643 | 2475 |
COL18A1 | 4351 | -2864 | 2677 | 3090 |
COL1A1 | 4847 | -1617 | 7 | 676 |
COL1A2 | 4681 | -1689 | -375 | 1250 |
COL22A1 | 2071 | -4805 | -3249 | -3090 |
COL23A1 | 3199 | -4585 | -845 | 2418 |
COL24A1 | -3035 | -5069 | -4749 | 5120 |
COL27A1 | 1066 | -5022 | 3972 | 2845 |
COL28A1 | -3227 | 2507 | -192 | 4214 |
COL3A1 | 4565 | 2950 | 2503 | 3575 |
COL4A1 | 3805 | -4695 | 688 | 3236 |
COL4A2 | 3851 | -4973 | 861 | 3295 |
COL4A3 | -2253 | -3782 | -4833 | -1934 |
COL4A4 | -2804 | -2983 | -3940 | -28 |
COL4A5 | -4216 | -4266 | -3428 | -289 |
COL5A1 | 4323 | -1537 | 2338 | 2999 |
COL5A2 | 4413 | -2991 | 3064 | 4122 |
COL5A3 | 3094 | -1534 | 3807 | 1554 |
COL6A1 | 4823 | -1919 | 2015 | 2788 |
COL6A2 | 4692 | -1812 | 2344 | 2927 |
COL6A3 | 4171 | -119 | 2648 | 3393 |
COL6A6 | 1139 | -2109 | -3933 | 45 |
COL7A1 | -425 | -3189 | -3985 | -2664 |
COL8A1 | 4315 | 881 | 4752 | 5058 |
COL8A2 | 4912 | -457 | -2292 | -563 |
COLGALT1 | 4647 | -3703 | -1269 | 2044 |
COLGALT2 | -1497 | -4412 | -1435 | -792 |
COMP | 5024 | 275 | -1007 | -884 |
CRTAP | 3334 | -3815 | 1832 | 3958 |
CTSB | 2843 | -1183 | -789 | 4639 |
CTSD | 1329 | -4757 | -3993 | 2582 |
CTSK | 4644 | 2 | 259 | 4241 |
CTSS | 3773 | -338 | 5035 | 5148 |
CTSV | -84 | 2189 | 34 | 331 |
DAG1 | -4941 | -5174 | 2661 | 4271 |
DCN | 4452 | -1036 | -890 | -1620 |
DDR1 | -292 | -4722 | -249 | -4038 |
DDR2 | 3328 | -1929 | 164 | 2397 |
DMD | -4135 | -2931 | -4460 | -5048 |
DST | -3834 | -1727 | -4289 | -4863 |
EFEMP1 | 4878 | 1197 | 2548 | -562 |
EFEMP2 | 1698 | -4478 | 2866 | 4207 |
ELN | 4832 | -4996 | -384 | 1614 |
F11R | 3414 | -2271 | -667 | -1517 |
FBLN1 | 4502 | -1609 | 1591 | -376 |
FBLN2 | 3856 | -641 | 3313 | 4216 |
FBLN5 | 3811 | 1519 | -1289 | -1272 |
FBN1 | 4504 | 636 | 3601 | 2988 |
FGF2 | 1476 | 741 | -1087 | -3508 |
FMOD | 4377 | -328 | -1283 | -1405 |
FN1 | 4783 | 33 | 3978 | 4002 |
FURIN | 1239 | -4167 | 4073 | -1204 |
HSPG2 | 2035 | -5289 | -401 | 2942 |
HTRA1 | 4656 | -2558 | -2428 | -3749 |
ICAM1 | 4641 | 1044 | 4128 | 4600 |
ICAM2 | 1999 | -1485 | -3439 | -639 |
ITGA1 | 1435 | 1740 | -4092 | -3028 |
ITGA10 | 4023 | -1852 | -979 | -1086 |
ITGA11 | 4615 | -1000 | -2691 | 1284 |
ITGA3 | 4809 | -5450 | 2976 | 557 |
ITGA4 | 2431 | -2840 | -5085 | 1443 |
ITGA5 | 4033 | -4692 | 5127 | 4594 |
ITGA6 | 1799 | -990 | -5243 | -114 |
ITGA7 | 580 | -4661 | 2121 | -4020 |
ITGA8 | 1156 | 4577 | 93 | 2702 |
ITGA9 | 4154 | -5185 | 3041 | 3909 |
ITGAM | 4572 | -2599 | 4997 | 5107 |
ITGAV | 801 | -812 | 49 | 4981 |
ITGAX | 1897 | -886 | 3808 | 5125 |
ITGB1 | 891 | 945 | 4567 | 4783 |
ITGB2 | 4906 | -107 | 4945 | 5102 |
ITGB3 | 3693 | -485 | 4867 | 2921 |
ITGB5 | 3604 | -2545 | -4743 | -4839 |
ITGB6 | -3832 | 471 | -3693 | 4890 |
ITGB8 | 4079 | 3217 | -2411 | 711 |
JAM2 | 3444 | -5266 | -4961 | -2840 |
JAM3 | 4578 | 1269 | -3928 | 1313 |
LAMA2 | 3038 | -3750 | -756 | 2040 |
LAMA3 | 3451 | -999 | -4332 | -2201 |
LAMA4 | 4388 | 736 | -121 | 2343 |
LAMA5 | 3521 | -5520 | -2717 | -2028 |
LAMB1 | 2539 | -455 | -385 | 3101 |
LAMB2 | 3450 | -4834 | -3037 | -2486 |
LAMB3 | 2231 | -4929 | -4569 | 386 |
LAMC1 | 4113 | -3181 | 2501 | 4089 |
LAMC2 | 4587 | 1336 | 5102 | 4436 |
LOX | 4606 | 4062 | 3160 | 3765 |
LOXL1 | 4187 | -1569 | 3956 | 4524 |
LOXL2 | 5054 | -3017 | 2997 | 3520 |
LOXL3 | 4563 | -1100 | 1944 | 4925 |
LOXL4 | 3456 | 552 | 27 | 3757 |
LRP4 | -3904 | -5103 | -4823 | -2122 |
LTBP1 | 555 | -67 | -1267 | 4963 |
LTBP3 | 2480 | -3134 | -2528 | -990 |
LTBP4 | 3682 | -1659 | 2214 | 400 |
LUM | 4580 | -1815 | 2455 | 4537 |
MFAP1 | -2124 | 4892 | 3769 | -1986 |
MFAP2 | 4871 | 78 | 422 | 2158 |
MFAP3 | -1951 | 4029 | 2831 | 3634 |
MFAP4 | 4643 | -755 | -329 | 2564 |
MFAP5 | 4668 | -121 | 4486 | 4499 |
MMP11 | 2889 | -3240 | -393 | 1218 |
MMP14 | 4687 | -1668 | 1618 | 2675 |
MMP15 | 1264 | -5090 | -5214 | -4505 |
MMP17 | 2906 | -2335 | 5119 | 5161 |
MMP19 | 4747 | -167 | 4806 | 5126 |
MMP2 | 4410 | -689 | -1983 | 2240 |
MUSK | 2918 | -3675 | 4380 | 3328 |
NCAM1 | 3566 | -3904 | 4088 | 3898 |
NCSTN | -1401 | -2472 | 1251 | 2905 |
NID1 | 3391 | -1249 | 709 | 3576 |
NID2 | 2587 | 177 | -1976 | 3644 |
NTN4 | 4620 | -1246 | -942 | 2808 |
P4HA1 | -1548 | -2913 | 4840 | -4372 |
P4HA2 | 2577 | -3906 | 2007 | -2091 |
P4HB | -184 | -2493 | 4004 | 3152 |
PCOLCE | 4784 | -618 | 2120 | 3588 |
PCOLCE2 | 4527 | 1723 | -52 | 4379 |
PDGFA | 1632 | -4274 | -4407 | -2948 |
PDGFB | 3143 | -603 | 3307 | -1238 |
PHYKPL | 4956 | -4988 | -3912 | -2713 |
PLEC | -3017 | -5409 | -1604 | -3459 |
PLOD1 | 860 | -4628 | 381 | 2050 |
PLOD2 | 3184 | 3503 | 4833 | 4022 |
PLOD3 | 4888 | -4263 | 3018 | 4301 |
PPIB | 4256 | -428 | 3462 | 4403 |
PRKCA | -720 | -2900 | -2894 | -4160 |
PSEN1 | 2583 | 2051 | 2038 | 1484 |
PTPRS | 1732 | -4554 | -4143 | 2695 |
PXDN | 3490 | -1421 | -3444 | 3436 |
SDC1 | 3944 | -2017 | 209 | 2683 |
SDC2 | 4456 | 1739 | 4436 | 5008 |
SDC3 | 3721 | -4560 | 2780 | 4191 |
SDC4 | 1095 | -2361 | 5103 | 946 |
SERPINE1 | 4636 | -210 | 5117 | 3333 |
SERPINH1 | 4694 | -3479 | 3725 | 2554 |
SH3PXD2A | -126 | -5007 | -3424 | 2652 |
SPARC | 3820 | -2638 | -565 | 1957 |
SPP1 | 4998 | 1150 | 3009 | 5215 |
TGFB1 | 4177 | -3070 | 4895 | 4099 |
TGFB2 | 3078 | 4561 | 1841 | -2330 |
TGFB3 | 3860 | -5264 | -2015 | -4211 |
THBS1 | 4954 | 752 | 4384 | 3647 |
TIMP1 | 4933 | -1301 | 5188 | 4988 |
TIMP2 | 4689 | -1860 | -732 | 1606 |
TNC | 5019 | 793 | 4283 | 3460 |
TNXB | 4386 | -65 | 2484 | 3472 |
TRAPPC4 | 41 | 3212 | 2700 | 1401 |
VCAM1 | 4924 | 2842 | 4665 | 4588 |
VCAN | 4971 | 1662 | 4386 | 4285 |
Glycogen storage diseases
metric | value |
---|---|
setSize | 11 |
pMANOVA | 0.00264 |
p.adjustMANOVA | 0.00775 |
s.dist | 0.709 |
s.FSHD | -0.37 |
s.hu_model | -0.407 |
s.Watt_m | -0.0607 |
s.Jones_m | -0.443 |
p.FSHD | 0.0338 |
p.hu_model | 0.0195 |
p.Watt_m | 0.727 |
p.Jones_m | 0.0109 |
Gene | Jones_m | hu_model |
---|---|---|
SLC37A4 | -4920 | -4706 |
GAA | -4456 | -4939 |
GYS1 | -3594 | -5321 |
G6PC3 | -3910 | -3026 |
PPP1R3C | -1008 | -4953 |
NHLRC1 | -1269 | -3408 |
EPM2A | -5218 | -576 |
GYG1 | -86 | -3826 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
EPM2A | -4545 | -576 | -4739 | -5218 |
G6PC3 | 1060 | -3026 | -1478 | -3910 |
GAA | 28 | -4939 | -3333 | -4456 |
GBE1 | -4951 | 525 | -3398 | -528 |
GYG1 | -3160 | -3826 | 4388 | -86 |
GYS1 | -2080 | -5321 | -4613 | -3594 |
NHLRC1 | -3337 | -3408 | 3873 | -1269 |
PPP1R3C | -4164 | -4953 | 4005 | -1008 |
RPS27A | 1292 | 773 | 1820 | 1913 |
SLC37A4 | -3004 | -4706 | -4997 | -4920 |
UBC | -537 | 2649 | 4433 | -2992 |
Diseases associated with glycosaminoglycan metabolism
metric | value |
---|---|
setSize | 30 |
pMANOVA | 1.97e-06 |
p.adjustMANOVA | 1.41e-05 |
s.dist | 0.708 |
s.FSHD | 0.565 |
s.hu_model | -0.217 |
s.Watt_m | 0.193 |
s.Jones_m | 0.311 |
p.FSHD | 8.36e-08 |
p.hu_model | 0.0397 |
p.Watt_m | 0.067 |
p.Jones_m | 0.00326 |
Gene | FSHD | Jones_m |
---|---|---|
SDC2 | 4456 | 5008 |
BGN | 4348 | 5088 |
VCAN | 4971 | 4285 |
LUM | 4580 | 4537 |
EXT1 | 4706 | 3717 |
SDC3 | 3721 | 4191 |
CHSY1 | 4080 | 3666 |
HEXB | 2661 | 4889 |
B3GALT6 | 3823 | 3103 |
CHST14 | 3538 | 3049 |
SDC1 | 3944 | 2683 |
HEXA | 2020 | 4440 |
OGN | 3168 | 2569 |
HSPG2 | 2035 | 2942 |
GPC6 | 4618 | 804 |
AGRN | 3889 | 760 |
B4GALT1 | 1688 | 1643 |
SLC26A2 | 826 | 1507 |
SDC4 | 1095 | 946 |
B4GALT7 | 746 | 513 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
AGRN | 3889 | -4843 | -2922 | 760 |
B3GALT6 | 3823 | -1236 | 4092 | 3103 |
B3GAT3 | 4055 | -4180 | 1326 | -1191 |
B4GALT1 | 1688 | -1298 | 2563 | 1643 |
B4GALT7 | 746 | -4099 | -1523 | 513 |
BGN | 4348 | -1456 | 3875 | 5088 |
CHST14 | 3538 | -3780 | 1229 | 3049 |
CHSY1 | 4080 | 3773 | 1890 | 3666 |
CSPG4 | 3730 | -5557 | 531 | -99 |
DCN | 4452 | -1036 | -890 | -1620 |
EXT1 | 4706 | 3854 | 4979 | 3717 |
EXT2 | 2935 | 2055 | 910 | -1968 |
FMOD | 4377 | -328 | -1283 | -1405 |
GPC1 | -1704 | -5207 | -2934 | -1700 |
GPC4 | -587 | -5108 | -3461 | -1575 |
GPC6 | 4618 | -2353 | 156 | 804 |
HEXA | 2020 | -220 | 1726 | 4440 |
HEXB | 2661 | 743 | 2355 | 4889 |
HSPG2 | 2035 | -5289 | -401 | 2942 |
KERA | 4979 | 519 | -844 | -956 |
LUM | 4580 | -1815 | 2455 | 4537 |
OGN | 3168 | 993 | -1826 | 2569 |
PAPSS2 | 951 | 1700 | 378 | 208 |
SDC1 | 3944 | -2017 | 209 | 2683 |
SDC2 | 4456 | 1739 | 4436 | 5008 |
SDC3 | 3721 | -4560 | 2780 | 4191 |
SDC4 | 1095 | -2361 | 5103 | 946 |
SLC26A2 | 826 | 1373 | 2008 | 1507 |
ST3GAL3 | -4430 | -4784 | -2254 | -2153 |
VCAN | 4971 | 1662 | 4386 | 4285 |
Condensation of Prophase Chromosomes
metric | value |
---|---|
setSize | 11 |
pMANOVA | 0.000632 |
p.adjustMANOVA | 0.00224 |
s.dist | 0.706 |
s.FSHD | -0.153 |
s.hu_model | 0.373 |
s.Watt_m | 0.188 |
s.Jones_m | 0.548 |
p.FSHD | 0.38 |
p.hu_model | 0.0321 |
p.Watt_m | 0.279 |
p.Jones_m | 0.00167 |
Gene | Jones_m | hu_model |
---|---|---|
SMC4 | 3733 | 4094 |
NCAPD3 | 4711 | 2977 |
SMC2 | 5025 | 2455 |
H2AFX | 4862 | 2335 |
CDK1 | 4727 | 1563 |
MCPH1 | 1875 | 2156 |
PHF8 | 435 | 3366 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
CDK1 | 346 | 1563 | 3225 | 4727 |
H2AFX | 1120 | 2335 | 5014 | 4862 |
MCPH1 | -5201 | 2156 | -1835 | 1875 |
NCAPD3 | 847 | 2977 | -4842 | 4711 |
NCAPG2 | 349 | -13 | 1143 | 4767 |
NCAPH2 | -561 | -1821 | -2801 | -1811 |
PHF8 | 526 | 3366 | 2113 | 435 |
RB1 | -2663 | -2417 | 1448 | 5214 |
SET | -1958 | 3653 | 2107 | -2226 |
SMC2 | -371 | 2455 | 3726 | 5025 |
SMC4 | -3282 | 4094 | 1087 | 3733 |
Postmitotic nuclear pore complex (NPC) reformation
metric | value |
---|---|
setSize | 24 |
pMANOVA | 1.7e-06 |
p.adjustMANOVA | 1.23e-05 |
s.dist | 0.705 |
s.FSHD | -0.187 |
s.hu_model | 0.544 |
s.Watt_m | 0.351 |
s.Jones_m | 0.208 |
p.FSHD | 0.114 |
p.hu_model | 4.01e-06 |
p.Watt_m | 0.00297 |
p.Jones_m | 0.0772 |
Gene | hu_model | Watt_m |
---|---|---|
NUP98 | 4201 | 5018 |
NUP54 | 4471 | 3788 |
TNPO1 | 3157 | 5079 |
NUP205 | 4401 | 3546 |
KPNB1 | 3591 | 3475 |
NUP43 | 4522 | 2192 |
NUP107 | 3205 | 2916 |
NUP188 | 2098 | 3787 |
SUMO1 | 4179 | 1384 |
SEH1L | 1073 | 4219 |
RAN | 2308 | 1918 |
NUP160 | 3965 | 1024 |
RCC1 | 986 | 3577 |
NUP35 | 4530 | 641 |
RANGAP1 | 478 | 4294 |
UBE2I | 1232 | 1203 |
SEC13 | 721 | 1683 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
AHCTF1 | -5298 | 4621 | -1774 | -4269 |
KPNB1 | -3838 | 3591 | 3475 | 1881 |
NDC1 | 618 | 1259 | -2329 | 470 |
NUP107 | 900 | 3205 | 2916 | 3187 |
NUP133 | -5319 | 878 | -4004 | -4497 |
NUP155 | -4100 | 4271 | -2213 | -1602 |
NUP160 | 571 | 3965 | 1024 | -107 |
NUP188 | 2427 | 2098 | 3787 | 3045 |
NUP205 | -4103 | 4401 | 3546 | 3230 |
NUP35 | -4243 | 4530 | 641 | 2545 |
NUP37 | -5311 | -326 | 189 | -1501 |
NUP43 | -1288 | 4522 | 2192 | 118 |
NUP54 | -3175 | 4471 | 3788 | 1839 |
NUP85 | 2367 | 3154 | -391 | -1193 |
NUP93 | 3230 | -1483 | 3860 | 4885 |
NUP98 | -2852 | 4201 | 5018 | 2583 |
RAN | 166 | 2308 | 1918 | 385 |
RANGAP1 | 2817 | 478 | 4294 | 3126 |
RCC1 | 2015 | 986 | 3577 | 2530 |
SEC13 | -607 | 721 | 1683 | 165 |
SEH1L | -254 | 1073 | 4219 | 2743 |
SUMO1 | -3179 | 4179 | 1384 | -466 |
TNPO1 | 296 | 3157 | 5079 | 3196 |
UBE2I | 253 | 1232 | 1203 | 3159 |
Processing of SMDT1
metric | value |
---|---|
setSize | 15 |
pMANOVA | 0.00249 |
p.adjustMANOVA | 0.00738 |
s.dist | 0.703 |
s.FSHD | -0.584 |
s.hu_model | 0.149 |
s.Watt_m | -0.268 |
s.Jones_m | -0.244 |
p.FSHD | 9.01e-05 |
p.hu_model | 0.318 |
p.Watt_m | 0.0729 |
p.Jones_m | 0.101 |
Gene | FSHD | Watt_m |
---|---|---|
PMPCB | -5065 | -3599 |
AFG3L2 | -4583 | -3074 |
PMPCA | -3040 | -4554 |
SPG7 | -3269 | -3652 |
MICU3 | -4344 | -2525 |
YME1L1 | -5076 | -2155 |
PHB | -3242 | -2096 |
PHB2 | -3483 | -889 |
C2orf47 | -4691 | -472 |
SMDT1 | -2173 | -157 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
AFG3L2 | -4583 | -1974 | -3074 | -1568 |
C2orf47 | -4691 | 4125 | -472 | -2251 |
MCU | -820 | 416 | 1521 | 4976 |
MICU1 | -1998 | 4883 | 2372 | 3567 |
MICU2 | -4462 | -606 | 1264 | 3704 |
MICU3 | -4344 | 2577 | -2525 | -4758 |
PARL | 220 | 762 | -4126 | -2890 |
PHB | -3242 | -583 | -2096 | -4330 |
PHB2 | -3483 | 584 | -889 | -1389 |
PMPCA | -3040 | -92 | -4554 | -4811 |
PMPCB | -5065 | -824 | -3599 | -1223 |
SMDT1 | -2173 | -3739 | -157 | 1060 |
SPG7 | -3269 | -4482 | -3652 | -4377 |
STOML2 | -2788 | 1967 | 314 | -3383 |
YME1L1 | -5076 | 4303 | -2155 | -2146 |
GPVI-mediated activation cascade
metric | value |
---|---|
setSize | 18 |
pMANOVA | 0.00388 |
p.adjustMANOVA | 0.0109 |
s.dist | 0.701 |
s.FSHD | 0.235 |
s.hu_model | 0.16 |
s.Watt_m | 0.461 |
s.Jones_m | 0.444 |
p.FSHD | 0.084 |
p.hu_model | 0.241 |
p.Watt_m | 0.000703 |
p.Jones_m | 0.00111 |
Gene | Watt_m | Jones_m |
---|---|---|
PTPN6 | 4751 | 5055 |
RAC2 | 4898 | 4759 |
PDPN | 4537 | 4445 |
RHOG | 4878 | 3843 |
LYN | 3940 | 4433 |
RHOA | 4149 | 3875 |
FYN | 3642 | 4010 |
RHOB | 5078 | 2440 |
CDC42 | 746 | 2621 |
PIK3R3 | 569 | 3244 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
CDC42 | 1017 | 3281 | 746 | 2621 |
FYN | 4466 | -2813 | 3642 | 4010 |
LYN | 3429 | 775 | 3940 | 4433 |
PDPK1 | -3714 | 3416 | 2198 | -1065 |
PDPN | -52 | -3260 | 4537 | 4445 |
PIK3CA | -2357 | 362 | 2782 | -3797 |
PIK3CB | -3283 | 2736 | 4946 | -128 |
PIK3R1 | -5317 | 2872 | -3114 | 468 |
PIK3R3 | 3206 | 3161 | 569 | 3244 |
PTPN11 | -1703 | -1554 | -660 | -1108 |
PTPN6 | 3645 | -920 | 4751 | 5055 |
RAC1 | -458 | 2502 | 1441 | -618 |
RAC2 | 2914 | 39 | 4898 | 4759 |
RHOA | 2232 | 532 | 4149 | 3875 |
RHOB | 3771 | 4568 | 5078 | 2440 |
RHOG | 3718 | -1192 | 4878 | 3843 |
VAV2 | 4713 | -4898 | -893 | 3870 |
VAV3 | 2792 | 184 | -1056 | 5070 |
Activation of PPARGC1A (PGC-1alpha) by phosphorylation
metric | value |
---|---|
setSize | 10 |
pMANOVA | 0.0497 |
p.adjustMANOVA | 0.0906 |
s.dist | 0.7 |
s.FSHD | -0.198 |
s.hu_model | -0.379 |
s.Watt_m | -0.426 |
s.Jones_m | -0.356 |
p.FSHD | 0.278 |
p.hu_model | 0.0382 |
p.Watt_m | 0.0198 |
p.Jones_m | 0.0512 |
Gene | Watt_m | hu_model |
---|---|---|
PRKAG3 | -5227 | -5473 |
PPARGC1A | -4951 | -4158 |
PRKAA2 | -5106 | -3176 |
PRKAG2 | -3494 | -3194 |
PRKAB2 | -2793 | -2300 |
MAPK14 | -1619 | -1541 |
MAPK11 | -331 | -3339 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
MAPK11 | 4482 | -3339 | -331 | 383 |
MAPK12 | -2405 | -5202 | 636 | -4819 |
MAPK14 | -3218 | -1541 | -1619 | -4979 |
PPARGC1A | -2174 | -4158 | -4951 | 1255 |
PRKAA2 | -3931 | -3176 | -5106 | -4407 |
PRKAB1 | 2454 | 3409 | 1794 | 2829 |
PRKAB2 | -2523 | -2300 | -2793 | -5257 |
PRKAG1 | -3078 | 2084 | -1788 | -2783 |
PRKAG2 | -382 | -3194 | -3494 | 2548 |
PRKAG3 | -1474 | -5473 | -5227 | -3870 |
Heparan sulfate/heparin (HS-GAG) metabolism
metric | value |
---|---|
setSize | 34 |
pMANOVA | 3.73e-07 |
p.adjustMANOVA | 3.32e-06 |
s.dist | 0.695 |
s.FSHD | 0.537 |
s.hu_model | -0.272 |
s.Watt_m | 0.173 |
s.Jones_m | 0.3 |
p.FSHD | 5.94e-08 |
p.hu_model | 0.00601 |
p.Watt_m | 0.0804 |
p.Jones_m | 0.00248 |
Gene | FSHD | Jones_m |
---|---|---|
SDC2 | 4456 | 5008 |
BGN | 4348 | 5088 |
VCAN | 4971 | 4285 |
GUSB | 4047 | 5097 |
EXT1 | 4706 | 3717 |
SDC3 | 3721 | 4191 |
GLB1L | 4309 | 3448 |
GLB1 | 3757 | 3737 |
NAGLU | 3005 | 4335 |
SGSH | 3076 | 3931 |
B3GALT6 | 3823 | 3103 |
HS6ST2 | 2263 | 5065 |
SLC35D2 | 4063 | 2705 |
SDC1 | 3944 | 2683 |
IDS | 1662 | 4417 |
HSPG2 | 2035 | 2942 |
GPC6 | 4618 | 804 |
AGRN | 3889 | 760 |
XYLT2 | 2228 | 1093 |
GLCE | 611 | 2011 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
AGRN | 3889 | -4843 | -2922 | 760 |
B3GALT6 | 3823 | -1236 | 4092 | 3103 |
B3GAT3 | 4055 | -4180 | 1326 | -1191 |
B4GALT7 | 746 | -4099 | -1523 | 513 |
BGN | 4348 | -1456 | 3875 | 5088 |
CSPG4 | 3730 | -5557 | 531 | -99 |
DCN | 4452 | -1036 | -890 | -1620 |
EXT1 | 4706 | 3854 | 4979 | 3717 |
EXT2 | 2935 | 2055 | 910 | -1968 |
GLB1 | 3757 | -2214 | 915 | 3737 |
GLB1L | 4309 | -1803 | -412 | 3448 |
GLCE | 611 | 3934 | 3950 | 2011 |
GPC1 | -1704 | -5207 | -2934 | -1700 |
GPC4 | -587 | -5108 | -3461 | -1575 |
GPC6 | 4618 | -2353 | 156 | 804 |
GUSB | 4047 | 1905 | 4109 | 5097 |
HS2ST1 | 1636 | 1665 | 2475 | -1244 |
HS3ST5 | -3043 | -1621 | -1199 | -5303 |
HS6ST1 | -1736 | -2492 | 5088 | 2340 |
HS6ST2 | 2263 | -4491 | 273 | 5065 |
HSPG2 | 2035 | -5289 | -401 | 2942 |
IDS | 1662 | -2441 | -3581 | 4417 |
IDUA | 4027 | -3817 | -4684 | 75 |
NAGLU | 3005 | -3661 | -707 | 4335 |
NDST1 | 936 | -3038 | -3033 | -2695 |
SDC1 | 3944 | -2017 | 209 | 2683 |
SDC2 | 4456 | 1739 | 4436 | 5008 |
SDC3 | 3721 | -4560 | 2780 | 4191 |
SDC4 | 1095 | -2361 | 5103 | 946 |
SGSH | 3076 | 701 | -507 | 3931 |
SLC35D2 | 4063 | -2826 | 1777 | 2705 |
VCAN | 4971 | 1662 | 4386 | 4285 |
XYLT1 | 3695 | 2589 | 2917 | -2537 |
XYLT2 | 2228 | -1124 | 1315 | 1093 |
Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs)
metric | value |
---|---|
setSize | 65 |
pMANOVA | 2.15e-13 |
p.adjustMANOVA | 5.63e-12 |
s.dist | 0.694 |
s.FSHD | 0.557 |
s.hu_model | -0.0937 |
s.Watt_m | 0.169 |
s.Jones_m | 0.367 |
p.FSHD | 8.07e-15 |
p.hu_model | 0.192 |
p.Watt_m | 0.0188 |
p.Jones_m | 3.29e-07 |
Gene | FSHD | Jones_m |
---|---|---|
SPP1 | 4998 | 5215 |
TIMP1 | 4933 | 4988 |
FAM20A | 4935 | 4942 |
SDC2 | 4456 | 5008 |
SHISA5 | 4734 | 4670 |
VCAN | 4971 | 4285 |
CKAP4 | 4586 | 4360 |
IGFBP4 | 4241 | 4649 |
APP | 3990 | 4891 |
C3 | 4737 | 4049 |
FN1 | 4783 | 4002 |
FSTL1 | 4592 | 4104 |
APOE | 3947 | 4717 |
LGALS1 | 3933 | 4634 |
CSF1 | 4653 | 3814 |
IGF2 | 3751 | 4708 |
TNC | 5019 | 3460 |
LAMC1 | 4113 | 4089 |
FUCA2 | 3762 | 4218 |
HSP90B1 | 3464 | 4544 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
ADAM10 | 2507 | -1489 | -1018.0 | 3455.0 |
ANO8 | -2885 | -2337 | -5040.0 | -3537.0 |
APLP2 | 3574 | 1301 | -569.0 | -816.0 |
APOE | 3947 | -1411 | -88.0 | 4717.0 |
APOL1 | 5079 | 1818 | -2495.5 | -690.5 |
APP | 3990 | -2756 | 574.0 | 4891.0 |
BMP4 | 2116 | 329 | 908.0 | 307.0 |
C3 | 4737 | 4276 | 1818.0 | 4049.0 |
CALU | -927 | 3219 | 4824.0 | 4008.0 |
CDH2 | 2915 | 599 | -268.0 | 4575.0 |
CKAP4 | 4586 | -3769 | 4592.0 | 4360.0 |
CSF1 | 4653 | -4188 | 4312.0 | 3814.0 |
CYR61 | 2129 | 1076 | 4962.0 | 3481.0 |
DNAJC3 | 2002 | 1932 | 1321.0 | 729.0 |
EVA1A | 1031 | 654 | 2986.0 | -1047.0 |
FAM20A | 4935 | -1723 | 1537.0 | 4942.0 |
FAM20C | 2832 | -5416 | 1698.0 | 2083.0 |
FBN1 | 4504 | 636 | 3601.0 | 2988.0 |
FN1 | 4783 | 33 | 3978.0 | 4002.0 |
FSTL1 | 4592 | 1443 | 3660.0 | 4104.0 |
FUCA2 | 3762 | -2131 | -4136.0 | 4218.0 |
GAS6 | 1347 | -4951 | -3118.0 | 4035.0 |
GOLM1 | 3066 | 1461 | -1602.0 | -3332.0 |
HRC | -1857 | -4700 | -4971.0 | -4363.0 |
HSP90B1 | 3464 | 456 | 4896.0 | 4544.0 |
IGF2 | 3751 | -4694 | -2998.0 | 4708.0 |
IGFBP3 | 2320 | 2898 | -4792.0 | -2376.0 |
IGFBP4 | 4241 | -308 | 2374.0 | 4649.0 |
IGFBP5 | 759 | -5367 | -5313.0 | 1564.0 |
IGFBP6 | 4675 | -1958 | 1566.0 | -1497.0 |
IGFBP7 | 3664 | 500 | 1346.0 | 3683.0 |
KTN1 | -4560 | 1411 | -1533.0 | 2648.0 |
LAMB1 | 2539 | -455 | -385.0 | 3101.0 |
LAMB2 | 3450 | -4834 | -3037.0 | -2486.0 |
LAMC1 | 4113 | -3181 | 2501.0 | 4089.0 |
LGALS1 | 3933 | -4021 | 1865.0 | 4634.0 |
LTBP1 | 555 | -67 | -1267.0 | 4963.0 |
MBTPS1 | 1045 | -3785 | -2964.0 | 358.0 |
MEN1 | 3596 | 1333 | 2467.0 | 1939.0 |
MFGE8 | 2123 | -2870 | 4847.0 | -1422.0 |
MGAT4A | 2876 | 265 | 3278.0 | 943.0 |
MIA3 | -3311 | 2906 | -3524.0 | -2382.0 |
MMP2 | 4410 | -689 | -1983.0 | 2240.0 |
MXRA8 | 4710 | -3829 | -1251.0 | 801.0 |
NUCB1 | 1327 | -4026 | 1564.0 | 4017.0 |
P4HB | -184 | -2493 | 4004.0 | 3152.0 |
PDIA6 | 1211 | -110 | 5042.0 | 4192.0 |
PENK | 4673 | 625 | -2141.0 | -1988.0 |
PNPLA2 | 1605 | -4949 | -4831.0 | -2696.0 |
PRKCSH | 3145 | -267 | 532.0 | 4720.0 |
PRSS23 | 2962 | 3908 | 864.0 | -4834.0 |
QSOX1 | 678 | 2026 | 2964.0 | 4617.0 |
RCN1 | 3972 | 1882 | 3387.0 | 3797.0 |
SDC2 | 4456 | 1739 | 4436.0 | 5008.0 |
SHISA5 | 4734 | -1707 | 4521.0 | 4670.0 |
SPARCL1 | 2798 | -800 | -4717.0 | -3494.0 |
SPP1 | 4998 | 1150 | 3009.0 | 5215.0 |
STC2 | 2900 | -4655 | 3143.0 | -4693.0 |
TGOLN2 | 1572 | 2925 | 1277.0 | 2519.0 |
TIMP1 | 4933 | -1301 | 5188.0 | 4988.0 |
TMEM132A | -971 | 1292 | 593.0 | 4220.0 |
TNC | 5019 | 793 | 4283.0 | 3460.0 |
VCAN | 4971 | 1662 | 4386.0 | 4285.0 |
VWA1 | 4411 | -3948 | 775.0 | -2565.0 |
WFS1 | 2862 | -2541 | 2538.0 | -1791.0 |
EGR2 and SOX10-mediated initiation of Schwann cell myelination
metric | value |
---|---|
setSize | 20 |
pMANOVA | 6.74e-05 |
p.adjustMANOVA | 0.000322 |
s.dist | 0.689 |
s.FSHD | 0.179 |
s.hu_model | -0.422 |
s.Watt_m | 0.311 |
s.Jones_m | 0.409 |
p.FSHD | 0.167 |
p.hu_model | 0.00108 |
p.Watt_m | 0.0162 |
p.Jones_m | 0.00155 |
Gene | hu_model | Jones_m |
---|---|---|
DAG1 | -5174 | 4271 |
NAB2 | -5261 | 2780 |
NAB1 | -3059 | 4493 |
LAMC1 | -3181 | 4089 |
DRP2 | -3953 | 3025 |
WWTR1 | -2471 | 4765 |
EGR2 | -3698 | 3020 |
SMARCA4 | -3825 | 2758 |
TEAD1 | -4238 | 2380 |
LAMA2 | -3750 | 2040 |
SREBF2 | -4643 | 1416 |
MBP | -2383 | 1599 |
CYP51A1 | -1693 | 1505 |
UTRN | -3592 | 700 |
PMP22 | -1275 | 1539 |
PRX | -2535 | 663 |
LAMB1 | -455 | 3101 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
CYP51A1 | 1436 | -1693 | 4999 | 1505 |
DAG1 | -4941 | -5174 | 2661 | 4271 |
DRP2 | 885 | -3953 | 504 | 3025 |
EGR2 | 5000 | -3698 | 5027 | 3020 |
HDAC2 | -2232 | 4350 | -1093 | -2901 |
HMGCR | -1171 | 960 | 4584 | 3959 |
LAMA2 | 3038 | -3750 | -756 | 2040 |
LAMB1 | 2539 | -455 | -385 | 3101 |
LAMC1 | 4113 | -3181 | 2501 | 4089 |
MBP | -4293 | -2383 | 1140 | 1599 |
NAB1 | 3443 | -3059 | 2596 | 4493 |
NAB2 | 4732 | -5261 | 4372 | 2780 |
PMP22 | 2803 | -1275 | 1627 | 1539 |
PRX | -860 | -2535 | 1467 | 663 |
SMARCA4 | 634 | -3825 | -1390 | 2758 |
SREBF2 | -496 | -4643 | 4470 | 1416 |
TEAD1 | -4942 | -4238 | -1861 | 2380 |
UTRN | 1484 | -3592 | -3351 | 700 |
WWTR1 | 3398 | -2471 | 801 | 4765 |
YAP1 | 602 | -474 | 3820 | -2892 |
Assembly of collagen fibrils and other multimeric structures
metric | value |
---|---|
setSize | 42 |
pMANOVA | 4.73e-10 |
p.adjustMANOVA | 6.68e-09 |
s.dist | 0.688 |
s.FSHD | 0.506 |
s.hu_model | -0.284 |
s.Watt_m | 0.00267 |
s.Jones_m | 0.37 |
p.FSHD | 1.42e-08 |
p.hu_model | 0.00146 |
p.Watt_m | 0.976 |
p.Jones_m | 3.32e-05 |
Gene | FSHD | Jones_m |
---|---|---|
LOXL3 | 4563 | 4925 |
COL8A1 | 4315 | 5058 |
LAMC2 | 4587 | 4436 |
CTSS | 3773 | 5148 |
LOXL1 | 4187 | 4524 |
COL5A2 | 4413 | 4122 |
CD151 | 4172 | 4305 |
LOXL2 | 5054 | 3520 |
LOX | 4606 | 3765 |
PCOLCE | 4784 | 3588 |
COL3A1 | 4565 | 3575 |
COL6A3 | 4171 | 3393 |
BMP1 | 3427 | 4072 |
COL6A2 | 4692 | 2927 |
COL6A1 | 4823 | 2788 |
COL18A1 | 4351 | 3090 |
CTSB | 2843 | 4639 |
LOXL4 | 3456 | 3757 |
COL5A1 | 4323 | 2999 |
COL4A2 | 3851 | 3295 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
BMP1 | 3427 | -4914 | 43 | 4072 |
CD151 | 4172 | -5328 | -921 | 4305 |
COL11A1 | 4414 | 2113 | -2198 | -116 |
COL11A2 | -2800 | -2814 | -4013 | -1603 |
COL15A1 | 2478 | -169 | 1436 | 1179 |
COL18A1 | 4351 | -2864 | 2677 | 3090 |
COL1A1 | 4847 | -1617 | 7 | 676 |
COL1A2 | 4681 | -1689 | -375 | 1250 |
COL24A1 | -3035 | -5069 | -4749 | 5120 |
COL27A1 | 1066 | -5022 | 3972 | 2845 |
COL3A1 | 4565 | 2950 | 2503 | 3575 |
COL4A1 | 3805 | -4695 | 688 | 3236 |
COL4A2 | 3851 | -4973 | 861 | 3295 |
COL4A3 | -2253 | -3782 | -4833 | -1934 |
COL4A4 | -2804 | -2983 | -3940 | -28 |
COL4A5 | -4216 | -4266 | -3428 | -289 |
COL5A1 | 4323 | -1537 | 2338 | 2999 |
COL5A2 | 4413 | -2991 | 3064 | 4122 |
COL5A3 | 3094 | -1534 | 3807 | 1554 |
COL6A1 | 4823 | -1919 | 2015 | 2788 |
COL6A2 | 4692 | -1812 | 2344 | 2927 |
COL6A3 | 4171 | -119 | 2648 | 3393 |
COL6A6 | 1139 | -2109 | -3933 | 45 |
COL7A1 | -425 | -3189 | -3985 | -2664 |
COL8A1 | 4315 | 881 | 4752 | 5058 |
COL8A2 | 4912 | -457 | -2292 | -563 |
CTSB | 2843 | -1183 | -789 | 4639 |
CTSS | 3773 | -338 | 5035 | 5148 |
CTSV | -84 | 2189 | 34 | 331 |
DST | -3834 | -1727 | -4289 | -4863 |
ITGA6 | 1799 | -990 | -5243 | -114 |
LAMA3 | 3451 | -999 | -4332 | -2201 |
LAMB3 | 2231 | -4929 | -4569 | 386 |
LAMC2 | 4587 | 1336 | 5102 | 4436 |
LOX | 4606 | 4062 | 3160 | 3765 |
LOXL1 | 4187 | -1569 | 3956 | 4524 |
LOXL2 | 5054 | -3017 | 2997 | 3520 |
LOXL3 | 4563 | -1100 | 1944 | 4925 |
LOXL4 | 3456 | 552 | 27 | 3757 |
PCOLCE | 4784 | -618 | 2120 | 3588 |
PLEC | -3017 | -5409 | -1604 | -3459 |
PXDN | 3490 | -1421 | -3444 | 3436 |
Synthesis of bile acids and bile salts
metric | value |
---|---|
setSize | 18 |
pMANOVA | 0.007 |
p.adjustMANOVA | 0.0176 |
s.dist | 0.687 |
s.FSHD | -0.392 |
s.hu_model | -0.0986 |
s.Watt_m | -0.395 |
s.Jones_m | -0.391 |
p.FSHD | 0.004 |
p.hu_model | 0.469 |
p.Watt_m | 0.0037 |
p.Jones_m | 0.00413 |
Gene | Watt_m | FSHD |
---|---|---|
CYP27A1 | -5277 | -5269 |
SCP2 | -4882 | -5322 |
OSBPL1A | -4753 | -4645 |
RXRA | -4147 | -4228 |
OSBPL9 | -4648 | -3420 |
AMACR | -4008 | -3399 |
HSD17B4 | -3004 | -4299 |
NCOA2 | -4995 | -2521 |
OSBPL6 | -5101 | -1996 |
OSBP | -1243 | -4893 |
NCOA1 | -1158 | -2128 |
CYP39A1 | -1247 | -1308 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
ACOT8 | -2551 | -946 | 417 | 820 |
AMACR | -3399 | 4127 | -4008 | 40 |
CYP27A1 | -5269 | -4450 | -5277 | -5087 |
CYP39A1 | -1308 | 1651 | -1247 | -2478 |
HSD17B4 | -4299 | 680 | -3004 | -3754 |
HSD3B7 | 4131 | -4317 | 1041 | 2290 |
NCOA1 | -2128 | 2605 | -1158 | -3029 |
NCOA2 | -2521 | 143 | -4995 | -4281 |
OSBP | -4893 | 2376 | -1243 | -4260 |
OSBPL1A | -4645 | -2922 | -4753 | -3878 |
OSBPL2 | 1819 | -4677 | -3391 | -1830 |
OSBPL3 | -4049 | -3458 | 4659 | 5209 |
OSBPL6 | -1996 | 4551 | -5101 | -4902 |
OSBPL7 | 269 | -5523 | 2530 | -583 |
OSBPL9 | -3420 | 3692 | -4648 | -4997 |
PTGIS | 3434 | -1895 | 927 | 1214 |
RXRA | -4228 | -5455 | -4147 | -5038 |
SCP2 | -5322 | -854 | -4882 | -3079 |
Heme biosynthesis
metric | value |
---|---|
setSize | 12 |
pMANOVA | 0.0148 |
p.adjustMANOVA | 0.0323 |
s.dist | 0.686 |
s.FSHD | -0.132 |
s.hu_model | -0.127 |
s.Watt_m | -0.58 |
s.Jones_m | -0.317 |
p.FSHD | 0.429 |
p.hu_model | 0.445 |
p.Watt_m | 0.000499 |
p.Jones_m | 0.0577 |
Gene | Watt_m | Jones_m |
---|---|---|
ALAS1 | -4662 | -3557 |
UROS | -4368 | -3793 |
CPOX | -3532 | -3818 |
UROD | -3208 | -3454 |
ALAD | -3590 | -2479 |
FLVCR1 | -4625 | -1867 |
COX15 | -5153 | -1164 |
FECH | -4097 | -1024 |
HMBS | -1585 | -2365 |
COX10 | -3678 | -199 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
ABCG2 | 4473 | -2433 | 4905 | 2385 |
ALAD | 58 | -3806 | -3590 | -2479 |
ALAS1 | -3427 | 3203 | -4662 | -3557 |
COX10 | -3212 | 2711 | -3678 | -199 |
COX15 | -2709 | 562 | -5153 | -1164 |
CPOX | -3627 | -857 | -3532 | -3818 |
FECH | -3784 | -3719 | -4097 | -1024 |
FLVCR1 | 4000 | 1415 | -4625 | -1867 |
HMBS | -3597 | -3907 | -1585 | -2365 |
PPOX | 2819 | -3736 | -3635 | 915 |
UROD | -94 | 785 | -3208 | -3454 |
UROS | -1409 | -1824 | -4368 | -3793 |
Post-translational protein phosphorylation
metric | value |
---|---|
setSize | 62 |
pMANOVA | 4.3e-12 |
p.adjustMANOVA | 9.12e-11 |
s.dist | 0.686 |
s.FSHD | 0.543 |
s.hu_model | -0.0784 |
s.Watt_m | 0.187 |
s.Jones_m | 0.367 |
p.FSHD | 1.48e-13 |
p.hu_model | 0.287 |
p.Watt_m | 0.011 |
p.Jones_m | 5.9e-07 |
Gene | FSHD | Jones_m |
---|---|---|
SPP1 | 4998 | 5215 |
TIMP1 | 4933 | 4988 |
FAM20A | 4935 | 4942 |
SDC2 | 4456 | 5008 |
SHISA5 | 4734 | 4670 |
VCAN | 4971 | 4285 |
CKAP4 | 4586 | 4360 |
IGFBP4 | 4241 | 4649 |
APP | 3990 | 4891 |
C3 | 4737 | 4049 |
FN1 | 4783 | 4002 |
FSTL1 | 4592 | 4104 |
APOE | 3947 | 4717 |
LGALS1 | 3933 | 4634 |
CSF1 | 4653 | 3814 |
TNC | 5019 | 3460 |
LAMC1 | 4113 | 4089 |
FUCA2 | 3762 | 4218 |
HSP90B1 | 3464 | 4544 |
RCN1 | 3972 | 3797 |
FSHD | hu_model | Watt_m | Jones_m | |
---|---|---|---|---|
ADAM10 | 2507 | -1489 | -1018.0 | 3455.0 |
ANO8 | -2885 | -2337 | -5040.0 | -3537.0 |
APLP2 | 3574 | 1301 | -569.0 | -816.0 |
APOE | 3947 | -1411 | -88.0 | 4717.0 |
APOL1 | 5079 | 1818 | -2495.5 | -690.5 |
APP | 3990 | -2756 | 574.0 | 4891.0 |
BMP4 | 2116 | 329 | 908.0 | 307.0 |
C3 | 4737 | 4276 | 1818.0 | 4049.0 |
CALU | -927 | 3219 | 4824.0 | 4008.0 |
CDH2 | 2915 | 599 | -268.0 | 4575.0 |
CKAP4 | 4586 | -3769 | 4592.0 | 4360.0 |
CSF1 | 4653 | -4188 | 4312.0 | 3814.0 |
CYR61 | 2129 | 1076 | 4962.0 | 3481.0 |
DNAJC3 | 2002 | 1932 | 1321.0 | 729.0 |
EVA1A | 1031 | 654 | 2986.0 | -1047.0 |
FAM20A | 4935 | -1723 | 1537.0 | 4942.0 |
FAM20C | 2832 | -5416 | 1698.0 | 2083.0 |
FBN1 | 4504 | 636 | 3601.0 | 2988.0 |
FN1 | 4783 | 33 | 3978.0 | 4002.0 |
FSTL1 | 4592 | 1443 | 3660.0 | 4104.0 |
FUCA2 | 3762 | -2131 | -4136.0 | 4218.0 |
GAS6 | 1347 | -4951 | -3118.0 | 4035.0 |
GOLM1 | 3066 | 1461 | -1602.0 | -3332.0 |
HRC | -1857 | -4700 | -4971.0 | -4363.0 |
HSP90B1 | 3464 | 456 | 4896.0 | 4544.0 |
IGFBP3 | 2320 | 2898 | -4792.0 | -2376.0 |
IGFBP4 | 4241 | -308 | 2374.0 | 4649.0 |
IGFBP5 | 759 | -5367 | -5313.0 | 1564.0 |
IGFBP7 | 3664 | 500 | 1346.0 | 3683.0 |
KTN1 | -4560 | 1411 | -1533.0 | 2648.0 |
LAMB1 | 2539 | -455 | -385.0 | 3101.0 |
LAMB2 | 3450 | -4834 | -3037.0 | -2486.0 |
LAMC1 | 4113 | -3181 | 2501.0 | 4089.0 |
LGALS1 | 3933 | -4021 | 1865.0 | 4634.0 |
LTBP1 | 555 | -67 | -1267.0 | 4963.0 |
MBTPS1 | 1045 | -3785 | -2964.0 | 358.0 |
MEN1 | 3596 | 1333 | 2467.0 | 1939.0 |
MFGE8 | 2123 | -2870 | 4847.0 | -1422.0 |
MGAT4A | 2876 | 265 | 3278.0 | 943.0 |
MIA3 | -3311 | 2906 | -3524.0 | -2382.0 |
MXRA8 | 4710 | -3829 | -1251.0 | 801.0 |
NUCB1 | 1327 | -4026 | 1564.0 | 4017.0 |
P4HB | -184 | -2493 | 4004.0 | 3152.0 |
PDIA6 | 1211 | -110 | 5042.0 | 4192.0 |
PENK | 4673 | 625 | -2141.0 | -1988.0 |
PNPLA2 | 1605 | -4949 | -4831.0 | -2696.0 |
PRKCSH | 3145 | -267 | 532.0 | 4720.0 |
PRSS23 | 2962 | 3908 | 864.0 | -4834.0 |
QSOX1 | 678 | 2026 | 2964.0 | 4617.0 |
RCN1 | 3972 | 1882 | 3387.0 | 3797.0 |
SDC2 | 4456 | 1739 | 4436.0 | 5008.0 |
SHISA5 | 4734 | -1707 | 4521.0 | 4670.0 |
SPARCL1 | 2798 | -800 | -4717.0 | -3494.0 |
SPP1 | 4998 | 1150 | 3009.0 | 5215.0 |
STC2 | 2900 | -4655 | 3143.0 | -4693.0 |
TGOLN2 | 1572 | 2925 | 1277.0 | 2519.0 |
TIMP1 | 4933 | -1301 | 5188.0 | 4988.0 |
TMEM132A | -971 | 1292 | 593.0 | 4220.0 |
TNC | 5019 | 793 | 4283.0 | 3460.0 |
VCAN | 4971 | 1662 | 4386.0 | 4285.0 |
VWA1 | 4411 | -3948 | 775.0 | -2565.0 |
WFS1 | 2862 | -2541 | 2538.0 | -1791.0 |
Here is the session info with all the versions of packages used.
sessionInfo()
## R version 4.0.3 (2020-10-10)
## Platform: x86_64-pc-linux-gnu (64-bit)
## Running under: Ubuntu 18.04.5 LTS
##
## Matrix products: default
## BLAS: /usr/lib/x86_64-linux-gnu/blas/libblas.so.3.7.1
## LAPACK: /usr/lib/x86_64-linux-gnu/lapack/liblapack.so.3.7.1
##
## locale:
## [1] LC_CTYPE=en_US.UTF-8 LC_NUMERIC=C
## [3] LC_TIME=en_US.UTF-8 LC_COLLATE=en_US.UTF-8
## [5] LC_MONETARY=en_US.UTF-8 LC_MESSAGES=en_US.UTF-8
## [7] LC_PAPER=en_US.UTF-8 LC_NAME=C
## [9] LC_ADDRESS=C LC_TELEPHONE=C
## [11] LC_MEASUREMENT=en_US.UTF-8 LC_IDENTIFICATION=C
##
## attached base packages:
## [1] parallel stats4 stats graphics grDevices utils datasets
## [8] methods base
##
## other attached packages:
## [1] pkgload_1.1.0 GGally_2.0.0
## [3] ggplot2_3.3.2 reshape2_1.4.4
## [5] beeswarm_0.2.3 gtools_3.8.2
## [7] tibble_3.0.4 dplyr_1.0.2
## [9] echarts4r_0.3.3 gplots_3.1.0
## [11] UpSetR_1.4.0 eulerr_6.1.0
## [13] getDEE2_1.0.0 edgeR_3.32.0
## [15] limma_3.46.0 DESeq2_1.30.0
## [17] SummarizedExperiment_1.20.0 Biobase_2.50.0
## [19] MatrixGenerics_1.2.0 matrixStats_0.57.0
## [21] GenomicRanges_1.42.0 GenomeInfoDb_1.26.0
## [23] IRanges_2.24.0 S4Vectors_0.28.0
## [25] BiocGenerics_0.36.0 mitch_1.2.2
##
## loaded via a namespace (and not attached):
## [1] bitops_1.0-6 bit64_4.0.5 progress_1.2.2
## [4] RColorBrewer_1.1-2 httr_1.4.2 rprojroot_1.3-2
## [7] backports_1.2.0 tools_4.0.3 R6_2.5.0
## [10] KernSmooth_2.23-18 DBI_1.1.0 colorspace_2.0-0
## [13] withr_2.3.0 htm2txt_2.1.1 prettyunits_1.1.1
## [16] tidyselect_1.1.0 gridExtra_2.3 bit_4.0.4
## [19] compiler_4.0.3 desc_1.2.0 DelayedArray_0.16.0
## [22] labeling_0.4.2 caTools_1.18.0 scales_1.1.1
## [25] genefilter_1.72.0 stringr_1.4.0 digest_0.6.27
## [28] rmarkdown_2.5 XVector_0.30.0 pkgconfig_2.0.3
## [31] htmltools_0.5.0 highr_0.8 fastmap_1.0.1
## [34] htmlwidgets_1.5.2 rlang_0.4.8 RSQLite_2.2.1
## [37] shiny_1.5.0 generics_0.1.0 farver_2.0.3
## [40] jsonlite_1.7.1 BiocParallel_1.24.1 RCurl_1.98-1.2
## [43] magrittr_1.5 GenomeInfoDbData_1.2.4 Matrix_1.2-18
## [46] Rcpp_1.0.5 munsell_0.5.0 lifecycle_0.2.0
## [49] yaml_2.2.1 stringi_1.5.3 MASS_7.3-53
## [52] zlibbioc_1.36.0 plyr_1.8.6 grid_4.0.3
## [55] blob_1.2.1 promises_1.1.1 crayon_1.3.4
## [58] lattice_0.20-41 splines_4.0.3 annotate_1.68.0
## [61] hms_0.5.3 polylabelr_0.2.0 locfit_1.5-9.4
## [64] knitr_1.30 pillar_1.4.6 geneplotter_1.68.0
## [67] XML_3.99-0.5 glue_1.4.2 evaluate_0.14
## [70] vctrs_0.3.4 httpuv_1.5.4 testthat_3.0.0
## [73] gtable_0.3.0 purrr_0.3.4 polyclip_1.10-0
## [76] assertthat_0.2.1 reshape_0.8.8 xfun_0.19
## [79] mime_0.9 xtable_1.8-4 later_1.1.0.1
## [82] survival_3.2-7 AnnotationDbi_1.52.0 memoise_1.1.0
## [85] ellipsis_0.3.1
END of report