| 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 |