Folding of actin by CCT/TriC |
10 |
3.94e-05 |
3.25e-04 |
0.88100 |
-7.91e-01 |
3.89e-01 |
1.49e-05 |
3.34e-02 |
Establishment of Sister Chromatid Cohesion |
11 |
6.11e-05 |
4.68e-04 |
0.83800 |
-4.88e-01 |
6.81e-01 |
5.03e-03 |
9.08e-05 |
Cohesin Loading onto Chromatin |
10 |
1.73e-04 |
1.13e-03 |
0.83200 |
-5.00e-01 |
6.65e-01 |
6.14e-03 |
2.70e-04 |
tRNA processing in the mitochondrion |
18 |
1.74e-07 |
3.29e-06 |
0.71800 |
1.16e-01 |
7.09e-01 |
3.95e-01 |
1.91e-07 |
ATF6 (ATF6-alpha) activates chaperone genes |
10 |
3.04e-03 |
1.41e-02 |
0.67700 |
-5.66e-01 |
3.72e-01 |
1.95e-03 |
4.16e-02 |
Attenuation phase |
22 |
2.93e-06 |
3.39e-05 |
0.67300 |
-5.80e-01 |
3.41e-01 |
2.45e-06 |
5.65e-03 |
MyD88 deficiency (TLR2/4) |
10 |
3.85e-03 |
1.69e-02 |
0.66900 |
-4.32e-01 |
5.11e-01 |
1.79e-02 |
5.18e-03 |
Classical antibody-mediated complement activation |
22 |
3.07e-06 |
3.53e-05 |
0.64400 |
-1.77e-01 |
6.19e-01 |
1.50e-01 |
5.07e-07 |
Formation of tubulin folding intermediates by CCT/TriC |
20 |
3.45e-05 |
2.91e-04 |
0.64200 |
-5.09e-01 |
3.90e-01 |
8.09e-05 |
2.50e-03 |
Prefoldin mediated transfer of substrate to CCT/TriC |
25 |
3.93e-06 |
4.34e-05 |
0.63400 |
-4.67e-01 |
4.30e-01 |
5.37e-05 |
2.00e-04 |
IRAK4 deficiency (TLR2/4) |
11 |
4.39e-03 |
1.87e-02 |
0.62800 |
-3.71e-01 |
5.06e-01 |
3.30e-02 |
3.65e-03 |
Cytosolic iron-sulfur cluster assembly |
13 |
1.97e-03 |
9.67e-03 |
0.61700 |
5.07e-01 |
-3.53e-01 |
1.56e-03 |
2.77e-02 |
Glucuronidation |
16 |
6.47e-04 |
3.53e-03 |
0.60900 |
4.48e-01 |
-4.13e-01 |
1.93e-03 |
4.27e-03 |
Regulation of TLR by endogenous ligand |
15 |
1.37e-04 |
9.55e-04 |
0.60500 |
4.64e-02 |
6.03e-01 |
7.56e-01 |
5.23e-05 |
CD28 dependent Vav1 pathway |
12 |
4.16e-03 |
1.78e-02 |
0.60200 |
-3.38e-01 |
4.98e-01 |
4.27e-02 |
2.80e-03 |
Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding |
27 |
5.89e-06 |
6.25e-05 |
0.60100 |
-4.38e-01 |
4.10e-01 |
8.05e-05 |
2.23e-04 |
Role of LAT2/NTAL/LAB on calcium mobilization |
29 |
1.70e-06 |
2.11e-05 |
0.58900 |
-2.44e-01 |
5.37e-01 |
2.30e-02 |
5.67e-07 |
Signaling by Hippo |
20 |
1.41e-04 |
9.72e-04 |
0.58400 |
-2.66e-01 |
5.20e-01 |
3.92e-02 |
5.71e-05 |
ATF6 (ATF6-alpha) activates chaperones |
12 |
5.54e-03 |
2.20e-02 |
0.58300 |
-4.97e-01 |
3.04e-01 |
2.85e-03 |
6.79e-02 |
Scavenging of heme from plasma |
29 |
6.98e-07 |
1.03e-05 |
0.57400 |
-7.35e-02 |
5.69e-01 |
4.94e-01 |
1.12e-07 |
CD22 mediated BCR regulation |
20 |
1.18e-04 |
8.34e-04 |
0.57000 |
-1.57e-01 |
5.48e-01 |
2.25e-01 |
2.22e-05 |
Pyrimidine salvage |
10 |
1.25e-02 |
4.29e-02 |
0.57000 |
5.33e-01 |
-2.00e-01 |
3.49e-03 |
2.74e-01 |
FCGR activation |
28 |
1.93e-05 |
1.74e-04 |
0.55400 |
-3.01e-01 |
4.65e-01 |
5.85e-03 |
2.08e-05 |
Elastic fibre formation |
37 |
1.43e-09 |
6.91e-08 |
0.54900 |
2.34e-01 |
4.97e-01 |
1.37e-02 |
1.70e-07 |
HSF1 activation |
24 |
1.54e-04 |
1.05e-03 |
0.54200 |
-4.21e-01 |
3.42e-01 |
3.56e-04 |
3.74e-03 |
Creation of C4 and C2 activators |
26 |
1.72e-05 |
1.62e-04 |
0.54200 |
-1.12e-01 |
5.31e-01 |
3.24e-01 |
2.82e-06 |
eNOS activation |
11 |
1.27e-02 |
4.32e-02 |
0.54000 |
-1.76e-01 |
5.10e-01 |
3.13e-01 |
3.39e-03 |
Activation of BAD and translocation to mitochondria |
15 |
3.35e-03 |
1.52e-02 |
0.53600 |
-2.18e-01 |
4.90e-01 |
1.44e-01 |
1.03e-03 |
RHO GTPases activate IQGAPs |
11 |
8.83e-03 |
3.18e-02 |
0.53500 |
-5.58e-02 |
5.32e-01 |
7.49e-01 |
2.23e-03 |
Apoptosis induced DNA fragmentation |
13 |
8.97e-04 |
4.74e-03 |
0.53400 |
4.14e-01 |
3.37e-01 |
9.81e-03 |
3.54e-02 |
Cellular hexose transport |
16 |
2.77e-03 |
1.30e-02 |
0.53300 |
4.72e-01 |
-2.47e-01 |
1.08e-03 |
8.73e-02 |
Metabolism of nitric oxide: NOS3 activation and regulation |
15 |
3.51e-03 |
1.57e-02 |
0.53000 |
-1.97e-01 |
4.92e-01 |
1.87e-01 |
9.60e-04 |
Synthesis of active ubiquitin: roles of E1 and E2 enzymes |
30 |
2.72e-05 |
2.40e-04 |
0.52900 |
-3.13e-01 |
4.26e-01 |
2.96e-03 |
5.29e-05 |
Mismatch repair (MMR) directed by MSH2:MSH3 (MutSbeta) |
12 |
7.93e-03 |
2.98e-02 |
0.52800 |
5.18e-01 |
-9.83e-02 |
1.87e-03 |
5.56e-01 |
Cell-extracellular matrix interactions |
16 |
8.00e-04 |
4.28e-03 |
0.52600 |
3.13e-02 |
5.25e-01 |
8.29e-01 |
2.74e-04 |
HSP90 chaperone cycle for steroid hormone receptors (SHR) |
37 |
3.12e-06 |
3.56e-05 |
0.52200 |
-2.96e-01 |
4.30e-01 |
1.84e-03 |
6.00e-06 |
EPHB-mediated forward signaling |
34 |
4.22e-06 |
4.59e-05 |
0.52000 |
-1.83e-01 |
4.86e-01 |
6.46e-02 |
9.30e-07 |
Josephin domain DUBs |
11 |
1.66e-02 |
5.35e-02 |
0.51900 |
-4.96e-01 |
1.52e-01 |
4.38e-03 |
3.84e-01 |
Mitotic Telophase/Cytokinesis |
13 |
1.25e-02 |
4.29e-02 |
0.51700 |
-2.93e-01 |
4.27e-01 |
6.76e-02 |
7.75e-03 |
Sema3A PAK dependent Axon repulsion |
16 |
5.00e-03 |
2.04e-02 |
0.51100 |
-2.76e-01 |
4.30e-01 |
5.60e-02 |
2.88e-03 |
CTLA4 inhibitory signaling |
20 |
5.00e-04 |
2.84e-03 |
0.51100 |
-8.70e-02 |
5.03e-01 |
5.01e-01 |
9.78e-05 |
Defective CFTR causes cystic fibrosis |
60 |
2.63e-09 |
1.05e-07 |
0.51000 |
-4.29e-01 |
2.76e-01 |
8.76e-09 |
2.21e-04 |
Formation of the ternary complex, and subsequently, the 43S complex |
36 |
4.74e-08 |
1.17e-06 |
0.51000 |
1.96e-01 |
4.70e-01 |
4.20e-02 |
1.04e-06 |
Hh mutants that don't undergo autocatalytic processing are degraded by ERAD |
55 |
1.92e-08 |
5.61e-07 |
0.50600 |
-4.24e-01 |
2.75e-01 |
5.17e-08 |
4.26e-04 |
Response of EIF2AK1 (HRI) to heme deficiency |
15 |
7.13e-03 |
2.71e-02 |
0.50300 |
-2.28e-01 |
4.49e-01 |
1.26e-01 |
2.62e-03 |
Molecules associated with elastic fibres |
27 |
6.32e-06 |
6.67e-05 |
0.50200 |
1.53e-01 |
4.78e-01 |
1.69e-01 |
1.73e-05 |
CDC6 association with the ORC:origin complex |
11 |
8.79e-03 |
3.18e-02 |
0.50100 |
1.09e-01 |
4.89e-01 |
5.30e-01 |
4.94e-03 |
Acetylcholine binding and downstream events |
11 |
7.08e-03 |
2.70e-02 |
0.49900 |
-1.96e-01 |
-4.59e-01 |
2.62e-01 |
8.43e-03 |
Postsynaptic nicotinic acetylcholine receptors |
11 |
7.08e-03 |
2.70e-02 |
0.49900 |
-1.96e-01 |
-4.59e-01 |
2.62e-01 |
8.43e-03 |
AUF1 (hnRNP D0) binds and destabilizes mRNA |
54 |
7.27e-08 |
1.59e-06 |
0.49500 |
-3.83e-01 |
3.14e-01 |
1.12e-06 |
6.62e-05 |
Cross-presentation of soluble exogenous antigens (endosomes) |
48 |
4.51e-07 |
6.95e-06 |
0.49400 |
-3.91e-01 |
3.03e-01 |
2.82e-06 |
2.83e-04 |
Negative regulation of NOTCH4 signaling |
52 |
1.64e-07 |
3.15e-06 |
0.49300 |
-3.49e-01 |
3.48e-01 |
1.31e-05 |
1.40e-05 |
Gluconeogenesis |
30 |
4.13e-06 |
4.53e-05 |
0.49300 |
4.82e-01 |
1.01e-01 |
4.87e-06 |
3.37e-01 |
Translesion synthesis by POLK |
17 |
4.04e-04 |
2.38e-03 |
0.49200 |
3.16e-01 |
3.77e-01 |
2.39e-02 |
7.12e-03 |
Translesion synthesis by REV1 |
16 |
6.41e-04 |
3.51e-03 |
0.49200 |
3.40e-01 |
3.55e-01 |
1.86e-02 |
1.39e-02 |
Glutamate and glutamine metabolism |
13 |
3.99e-03 |
1.74e-02 |
0.48800 |
4.60e-01 |
1.65e-01 |
4.10e-03 |
3.03e-01 |
Binding and Uptake of Ligands by Scavenger Receptors |
54 |
4.40e-09 |
1.58e-07 |
0.48600 |
-4.27e-02 |
4.84e-01 |
5.88e-01 |
7.54e-10 |
MET activates RAP1 and RAC1 |
11 |
4.07e-02 |
1.07e-01 |
0.48300 |
-3.00e-01 |
3.79e-01 |
8.53e-02 |
2.94e-02 |
Activation of RAC1 |
12 |
2.92e-02 |
8.37e-02 |
0.47900 |
-2.39e-01 |
4.15e-01 |
1.51e-01 |
1.28e-02 |
Olfactory Signaling Pathway |
209 |
2.09e-38 |
2.93e-35 |
0.47700 |
-2.16e-01 |
-4.25e-01 |
7.91e-08 |
3.03e-26 |
Antigen activates B Cell Receptor (BCR) leading to generation of second messengers |
44 |
1.52e-06 |
1.94e-05 |
0.47700 |
-1.75e-01 |
4.43e-01 |
4.50e-02 |
3.60e-07 |
N-glycan trimming in the ER and Calnexin/Calreticulin cycle |
35 |
2.06e-05 |
1.85e-04 |
0.47600 |
-4.49e-01 |
1.59e-01 |
4.28e-06 |
1.04e-01 |
Cargo concentration in the ER |
29 |
2.32e-04 |
1.47e-03 |
0.47400 |
-4.12e-01 |
2.34e-01 |
1.21e-04 |
2.89e-02 |
Bicarbonate transporters |
10 |
5.12e-02 |
1.26e-01 |
0.47100 |
4.37e-01 |
-1.77e-01 |
1.67e-02 |
3.34e-01 |
Miscellaneous substrates |
10 |
3.11e-02 |
8.63e-02 |
0.47000 |
4.70e-01 |
-1.28e-05 |
1.00e-02 |
1.00e+00 |
GPVI-mediated activation cascade |
32 |
1.70e-04 |
1.13e-03 |
0.46800 |
-3.17e-01 |
3.44e-01 |
1.89e-03 |
7.51e-04 |
CD28 co-stimulation |
33 |
1.38e-04 |
9.60e-04 |
0.46600 |
-3.02e-01 |
3.55e-01 |
2.67e-03 |
4.20e-04 |
Citric acid cycle (TCA cycle) |
22 |
1.63e-04 |
1.10e-03 |
0.46600 |
2.01e-01 |
4.20e-01 |
1.03e-01 |
6.42e-04 |
Regulation of activated PAK-2p34 by proteasome mediated degradation |
49 |
1.79e-06 |
2.20e-05 |
0.46500 |
-3.72e-01 |
2.80e-01 |
6.78e-06 |
7.01e-04 |
Regulation of Apoptosis |
52 |
8.17e-07 |
1.18e-05 |
0.46400 |
-3.78e-01 |
2.69e-01 |
2.41e-06 |
8.05e-04 |
Frs2-mediated activation |
12 |
3.51e-02 |
9.42e-02 |
0.46400 |
-2.13e-01 |
4.12e-01 |
2.02e-01 |
1.35e-02 |
Mismatch repair (MMR) directed by MSH2:MSH6 (MutSalpha) |
12 |
2.44e-02 |
7.21e-02 |
0.46200 |
4.54e-01 |
-8.54e-02 |
6.45e-03 |
6.09e-01 |
AMER1 mutants destabilize the destruction complex |
14 |
4.72e-03 |
1.95e-02 |
0.46200 |
1.68e-01 |
4.30e-01 |
2.78e-01 |
5.32e-03 |
APC truncation mutants have impaired AXIN binding |
14 |
4.72e-03 |
1.95e-02 |
0.46200 |
1.68e-01 |
4.30e-01 |
2.78e-01 |
5.32e-03 |
AXIN missense mutants destabilize the destruction complex |
14 |
4.72e-03 |
1.95e-02 |
0.46200 |
1.68e-01 |
4.30e-01 |
2.78e-01 |
5.32e-03 |
AXIN mutants destabilize the destruction complex, activating WNT signaling |
14 |
4.72e-03 |
1.95e-02 |
0.46200 |
1.68e-01 |
4.30e-01 |
2.78e-01 |
5.32e-03 |
Truncations of AMER1 destabilize the destruction complex |
14 |
4.72e-03 |
1.95e-02 |
0.46200 |
1.68e-01 |
4.30e-01 |
2.78e-01 |
5.32e-03 |
truncated APC mutants destabilize the destruction complex |
14 |
4.72e-03 |
1.95e-02 |
0.46200 |
1.68e-01 |
4.30e-01 |
2.78e-01 |
5.32e-03 |
Calnexin/calreticulin cycle |
26 |
6.05e-04 |
3.35e-03 |
0.45900 |
-4.30e-01 |
1.61e-01 |
1.46e-04 |
1.57e-01 |
Regulation of KIT signaling |
16 |
1.57e-02 |
5.14e-02 |
0.45800 |
-3.20e-01 |
3.28e-01 |
2.65e-02 |
2.32e-02 |
Regulation of RUNX3 expression and activity |
53 |
1.05e-06 |
1.43e-05 |
0.45800 |
-3.45e-01 |
3.02e-01 |
1.41e-05 |
1.46e-04 |
FCERI mediated Ca+2 mobilization |
44 |
3.15e-06 |
3.56e-05 |
0.45700 |
-1.35e-01 |
4.36e-01 |
1.23e-01 |
5.46e-07 |
Vif-mediated degradation of APOBEC3G |
52 |
1.47e-06 |
1.92e-05 |
0.45700 |
-3.48e-01 |
2.96e-01 |
1.45e-05 |
2.21e-04 |
rRNA processing in the mitochondrion |
22 |
4.47e-04 |
2.58e-03 |
0.45600 |
8.29e-02 |
4.48e-01 |
5.01e-01 |
2.74e-04 |
Amino acid transport across the plasma membrane |
31 |
3.89e-04 |
2.32e-03 |
0.45300 |
3.10e-01 |
-3.30e-01 |
2.86e-03 |
1.46e-03 |
Gene and protein expression by JAK-STAT signaling after Interleukin-12 stimulation |
31 |
1.71e-04 |
1.13e-03 |
0.45200 |
-1.40e-01 |
4.29e-01 |
1.77e-01 |
3.51e-05 |
FBXL7 down-regulates AURKA during mitotic entry and in early mitosis |
54 |
1.21e-06 |
1.62e-05 |
0.45000 |
-3.54e-01 |
2.79e-01 |
7.03e-06 |
3.88e-04 |
Hedgehog ligand biogenesis |
64 |
6.79e-08 |
1.53e-06 |
0.45000 |
-3.88e-01 |
2.28e-01 |
8.27e-08 |
1.61e-03 |
FCERI mediated MAPK activation |
45 |
2.48e-06 |
2.92e-05 |
0.44900 |
-1.01e-01 |
4.38e-01 |
2.39e-01 |
3.78e-07 |
Prolonged ERK activation events |
14 |
2.97e-02 |
8.38e-02 |
0.44900 |
-2.75e-01 |
3.55e-01 |
7.53e-02 |
2.15e-02 |
Hh mutants abrogate ligand secretion |
58 |
4.04e-07 |
6.36e-06 |
0.44800 |
-3.77e-01 |
2.43e-01 |
7.04e-07 |
1.37e-03 |
Syndecan interactions |
19 |
9.74e-04 |
5.11e-03 |
0.44700 |
1.89e-01 |
4.05e-01 |
1.54e-01 |
2.22e-03 |
Ribosomal scanning and start codon recognition |
43 |
3.35e-07 |
5.68e-06 |
0.44700 |
1.17e-01 |
4.31e-01 |
1.85e-01 |
9.86e-07 |
Translation initiation complex formation |
43 |
3.40e-07 |
5.68e-06 |
0.44600 |
1.19e-01 |
4.30e-01 |
1.77e-01 |
1.06e-06 |
Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S |
44 |
2.16e-07 |
3.94e-06 |
0.44600 |
1.30e-01 |
4.27e-01 |
1.37e-01 |
9.62e-07 |
Protein ubiquitination |
65 |
9.55e-08 |
2.03e-06 |
0.44600 |
-2.60e-01 |
3.62e-01 |
2.88e-04 |
4.47e-07 |
Vpu mediated degradation of CD4 |
51 |
3.49e-06 |
3.89e-05 |
0.44400 |
-3.55e-01 |
2.67e-01 |
1.15e-05 |
9.65e-04 |
Mismatch Repair |
13 |
2.88e-02 |
8.28e-02 |
0.44200 |
4.26e-01 |
-1.17e-01 |
7.84e-03 |
4.67e-01 |
Na+/Cl- dependent neurotransmitter transporters |
15 |
1.16e-02 |
4.03e-02 |
0.44000 |
2.23e-02 |
-4.39e-01 |
8.81e-01 |
3.23e-03 |
Synthesis, secretion, and inactivation of Glucagon-like Peptide-1 (GLP-1) |
11 |
5.53e-02 |
1.32e-01 |
0.44000 |
-4.15e-01 |
1.45e-01 |
1.72e-02 |
4.06e-01 |
Translesion synthesis by POLI |
17 |
2.01e-03 |
9.80e-03 |
0.43900 |
3.37e-01 |
2.81e-01 |
1.62e-02 |
4.47e-02 |
Suppression of phagosomal maturation |
13 |
4.46e-02 |
1.14e-01 |
0.43800 |
-2.73e-01 |
3.43e-01 |
8.79e-02 |
3.24e-02 |
Interleukin-6 signaling |
10 |
8.98e-02 |
1.92e-01 |
0.43700 |
-2.43e-01 |
3.63e-01 |
1.84e-01 |
4.66e-02 |
Regulation of signaling by CBL |
18 |
1.35e-02 |
4.53e-02 |
0.43600 |
-2.52e-01 |
3.57e-01 |
6.46e-02 |
8.81e-03 |
Incretin synthesis, secretion, and inactivation |
12 |
4.25e-02 |
1.10e-01 |
0.43600 |
-4.17e-01 |
1.28e-01 |
1.24e-02 |
4.42e-01 |
HSF1-dependent transactivation |
31 |
5.15e-04 |
2.91e-03 |
0.43500 |
-3.84e-01 |
2.05e-01 |
2.19e-04 |
4.86e-02 |
Regulation of actin dynamics for phagocytic cup formation |
76 |
1.57e-09 |
7.15e-08 |
0.43400 |
-9.74e-02 |
4.22e-01 |
1.43e-01 |
1.93e-10 |
Formation of ATP by chemiosmotic coupling |
16 |
3.96e-03 |
1.74e-02 |
0.43200 |
3.79e-01 |
2.08e-01 |
8.71e-03 |
1.49e-01 |
Smooth Muscle Contraction |
29 |
3.83e-04 |
2.30e-03 |
0.43100 |
-7.26e-02 |
4.25e-01 |
4.99e-01 |
7.40e-05 |
NIK-->noncanonical NF-kB signaling |
58 |
1.68e-06 |
2.11e-05 |
0.42900 |
-3.37e-01 |
2.66e-01 |
8.99e-06 |
4.61e-04 |
Degradation of GLI1 by the proteasome |
58 |
1.52e-06 |
1.94e-05 |
0.42900 |
-3.52e-01 |
2.45e-01 |
3.48e-06 |
1.27e-03 |
Nephrin family interactions |
21 |
2.25e-03 |
1.09e-02 |
0.42800 |
8.36e-03 |
4.28e-01 |
9.47e-01 |
6.80e-04 |
Diseases associated with N-glycosylation of proteins |
16 |
4.00e-03 |
1.74e-02 |
0.42800 |
-3.51e-01 |
-2.46e-01 |
1.52e-02 |
8.89e-02 |
MET activates RAS signaling |
11 |
5.93e-02 |
1.39e-01 |
0.42800 |
-1.11e-01 |
4.13e-01 |
5.24e-01 |
1.76e-02 |
Misspliced GSK3beta mutants stabilize beta-catenin |
15 |
8.87e-03 |
3.18e-02 |
0.42800 |
1.01e-01 |
4.16e-01 |
4.98e-01 |
5.33e-03 |
S33 mutants of beta-catenin aren't phosphorylated |
15 |
8.87e-03 |
3.18e-02 |
0.42800 |
1.01e-01 |
4.16e-01 |
4.98e-01 |
5.33e-03 |
S37 mutants of beta-catenin aren't phosphorylated |
15 |
8.87e-03 |
3.18e-02 |
0.42800 |
1.01e-01 |
4.16e-01 |
4.98e-01 |
5.33e-03 |
S45 mutants of beta-catenin aren't phosphorylated |
15 |
8.87e-03 |
3.18e-02 |
0.42800 |
1.01e-01 |
4.16e-01 |
4.98e-01 |
5.33e-03 |
T41 mutants of beta-catenin aren't phosphorylated |
15 |
8.87e-03 |
3.18e-02 |
0.42800 |
1.01e-01 |
4.16e-01 |
4.98e-01 |
5.33e-03 |
phosphorylation site mutants of CTNNB1 are not targeted to the proteasome by the destruction complex |
15 |
8.87e-03 |
3.18e-02 |
0.42800 |
1.01e-01 |
4.16e-01 |
4.98e-01 |
5.33e-03 |
Degradation of GLI2 by the proteasome |
58 |
1.94e-06 |
2.35e-05 |
0.42600 |
-3.46e-01 |
2.49e-01 |
5.35e-06 |
1.05e-03 |
Caspase-mediated cleavage of cytoskeletal proteins |
12 |
1.92e-02 |
5.98e-02 |
0.42500 |
1.77e-01 |
3.87e-01 |
2.89e-01 |
2.04e-02 |
Processing and activation of SUMO |
10 |
9.43e-02 |
1.98e-01 |
0.42500 |
-1.87e-01 |
3.82e-01 |
3.07e-01 |
3.65e-02 |
Common Pathway of Fibrin Clot Formation |
16 |
7.47e-03 |
2.83e-02 |
0.42400 |
8.61e-02 |
4.15e-01 |
5.51e-01 |
4.03e-03 |
CLEC7A (Dectin-1) induces NFAT activation |
11 |
3.55e-02 |
9.47e-02 |
0.42400 |
7.91e-02 |
4.16e-01 |
6.50e-01 |
1.69e-02 |
Formation of the cornified envelope |
26 |
2.57e-03 |
1.22e-02 |
0.42200 |
3.70e-01 |
-2.03e-01 |
1.10e-03 |
7.28e-02 |
E3 ubiquitin ligases ubiquitinate target proteins |
45 |
4.23e-05 |
3.45e-04 |
0.42200 |
-2.39e-01 |
3.48e-01 |
5.51e-03 |
5.46e-05 |
Regulation of IFNG signaling |
13 |
4.71e-02 |
1.18e-01 |
0.42200 |
-1.72e-01 |
3.85e-01 |
2.82e-01 |
1.62e-02 |
GLI3 is processed to GLI3R by the proteasome |
58 |
2.66e-06 |
3.11e-05 |
0.42200 |
-3.35e-01 |
2.55e-01 |
1.01e-05 |
7.70e-04 |
Formation of a pool of free 40S subunits |
67 |
1.80e-10 |
1.10e-08 |
0.42100 |
2.61e-01 |
3.30e-01 |
2.19e-04 |
2.97e-06 |
Regulation of PTEN stability and activity |
68 |
3.60e-07 |
5.95e-06 |
0.42100 |
-2.90e-01 |
3.04e-01 |
3.48e-05 |
1.45e-05 |
Ubiquitin Mediated Degradation of Phosphorylated Cdc25A |
51 |
1.28e-05 |
1.23e-04 |
0.42000 |
-3.41e-01 |
2.45e-01 |
2.47e-05 |
2.50e-03 |
p53-Independent DNA Damage Response |
51 |
1.28e-05 |
1.23e-04 |
0.42000 |
-3.41e-01 |
2.45e-01 |
2.47e-05 |
2.50e-03 |
p53-Independent G1/S DNA damage checkpoint |
51 |
1.28e-05 |
1.23e-04 |
0.42000 |
-3.41e-01 |
2.45e-01 |
2.47e-05 |
2.50e-03 |
Ubiquitin-dependent degradation of Cyclin D |
51 |
1.40e-05 |
1.34e-04 |
0.42000 |
-3.32e-01 |
2.56e-01 |
4.04e-05 |
1.57e-03 |
CD28 dependent PI3K/Akt signaling |
22 |
8.60e-03 |
3.15e-02 |
0.41800 |
-2.98e-01 |
2.94e-01 |
1.56e-02 |
1.71e-02 |
Regulation of ornithine decarboxylase (ODC) |
50 |
1.73e-05 |
1.62e-04 |
0.41800 |
-3.45e-01 |
2.35e-01 |
2.45e-05 |
4.01e-03 |
Acetylcholine Neurotransmitter Release Cycle |
11 |
8.60e-02 |
1.87e-01 |
0.41700 |
2.10e-01 |
-3.61e-01 |
2.27e-01 |
3.84e-02 |
Unwinding of DNA |
12 |
1.90e-02 |
5.93e-02 |
0.41700 |
2.66e-01 |
3.21e-01 |
1.10e-01 |
5.39e-02 |
RORA activates gene expression |
18 |
2.14e-02 |
6.46e-02 |
0.41600 |
-2.99e-01 |
2.89e-01 |
2.81e-02 |
3.40e-02 |
Degradation of AXIN |
54 |
9.93e-06 |
1.00e-04 |
0.41500 |
-3.17e-01 |
2.68e-01 |
5.61e-05 |
6.66e-04 |
Elevation of cytosolic Ca2+ levels |
15 |
9.91e-03 |
3.51e-02 |
0.41400 |
3.87e-01 |
1.49e-01 |
9.51e-03 |
3.19e-01 |
Activation of NF-kappaB in B cells |
66 |
8.09e-07 |
1.18e-05 |
0.41400 |
-3.19e-01 |
2.65e-01 |
7.64e-06 |
2.02e-04 |
FCERI mediated NF-kB activation |
91 |
4.57e-09 |
1.60e-07 |
0.41300 |
-2.58e-01 |
3.22e-01 |
2.16e-05 |
1.10e-07 |
Regulation of localization of FOXO transcription factors |
12 |
4.56e-02 |
1.16e-01 |
0.41100 |
-2.69e-02 |
4.10e-01 |
8.72e-01 |
1.40e-02 |
Peptide chain elongation |
55 |
2.51e-08 |
6.75e-07 |
0.41000 |
3.17e-01 |
2.60e-01 |
4.79e-05 |
8.52e-04 |
Autodegradation of the E3 ubiquitin ligase COP1 |
50 |
2.89e-05 |
2.53e-04 |
0.40900 |
-3.32e-01 |
2.39e-01 |
4.99e-05 |
3.49e-03 |
Dectin-1 mediated noncanonical NF-kB signaling |
61 |
3.24e-06 |
3.64e-05 |
0.40900 |
-3.19e-01 |
2.56e-01 |
1.68e-05 |
5.56e-04 |
Platelet sensitization by LDL |
17 |
6.21e-03 |
2.42e-02 |
0.40800 |
1.46e-01 |
3.81e-01 |
2.97e-01 |
6.47e-03 |
Lysosphingolipid and LPA receptors |
13 |
4.81e-02 |
1.20e-01 |
0.40700 |
3.94e-01 |
-1.03e-01 |
1.39e-02 |
5.19e-01 |
Viral mRNA Translation |
56 |
2.25e-08 |
6.45e-07 |
0.40700 |
3.11e-01 |
2.63e-01 |
5.77e-05 |
6.53e-04 |
Signaling by the B Cell Receptor (BCR) |
123 |
8.95e-12 |
7.37e-10 |
0.40600 |
-2.27e-01 |
3.37e-01 |
1.34e-05 |
1.17e-10 |
Activation of PPARGC1A (PGC-1alpha) by phosphorylation |
10 |
9.13e-02 |
1.94e-01 |
0.40600 |
3.99e-01 |
-7.38e-02 |
2.87e-02 |
6.86e-01 |
Eicosanoids |
10 |
8.37e-02 |
1.83e-01 |
0.40600 |
4.04e-01 |
-3.81e-02 |
2.70e-02 |
8.35e-01 |
PECAM1 interactions |
12 |
4.87e-02 |
1.22e-01 |
0.40500 |
-2.03e-02 |
4.04e-01 |
9.03e-01 |
1.53e-02 |
Advanced glycosylation endproduct receptor signaling |
11 |
8.06e-02 |
1.78e-01 |
0.40400 |
-1.07e-01 |
3.90e-01 |
5.38e-01 |
2.51e-02 |
Other semaphorin interactions |
19 |
1.97e-02 |
6.08e-02 |
0.40400 |
-2.19e-01 |
3.40e-01 |
9.88e-02 |
1.03e-02 |
Pentose phosphate pathway |
14 |
1.37e-02 |
4.59e-02 |
0.40400 |
2.27e-01 |
3.34e-01 |
1.42e-01 |
3.04e-02 |
Regulation of RAS by GAPs |
67 |
1.54e-06 |
1.94e-05 |
0.40200 |
-2.85e-01 |
2.85e-01 |
5.67e-05 |
5.63e-05 |
SCF-beta-TrCP mediated degradation of Emi1 |
54 |
1.79e-05 |
1.66e-04 |
0.40200 |
-3.26e-01 |
2.37e-01 |
3.52e-05 |
2.65e-03 |
Tie2 Signaling |
18 |
2.21e-02 |
6.63e-02 |
0.40100 |
-1.68e-01 |
3.64e-01 |
2.18e-01 |
7.46e-03 |
Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane |
11 |
8.52e-02 |
1.86e-01 |
0.40100 |
3.85e-01 |
-1.10e-01 |
2.69e-02 |
5.28e-01 |
ER-Phagosome pathway |
78 |
1.58e-07 |
3.07e-06 |
0.40000 |
-3.32e-01 |
2.23e-01 |
4.14e-07 |
6.64e-04 |
Signaling by NOTCH4 |
79 |
1.44e-07 |
2.93e-06 |
0.39900 |
-2.26e-01 |
3.28e-01 |
5.17e-04 |
4.53e-07 |
Trafficking and processing of endosomal TLR |
11 |
1.12e-01 |
2.25e-01 |
0.39900 |
-2.33e-01 |
3.23e-01 |
1.81e-01 |
6.32e-02 |
FCGR3A-mediated phagocytosis |
74 |
5.10e-08 |
1.19e-06 |
0.39800 |
-8.08e-02 |
3.90e-01 |
2.30e-01 |
6.83e-09 |
Leishmania phagocytosis |
74 |
5.10e-08 |
1.19e-06 |
0.39800 |
-8.08e-02 |
3.90e-01 |
2.30e-01 |
6.83e-09 |
Parasite infection |
74 |
5.10e-08 |
1.19e-06 |
0.39800 |
-8.08e-02 |
3.90e-01 |
2.30e-01 |
6.83e-09 |
VEGFR2 mediated vascular permeability |
27 |
3.19e-03 |
1.47e-02 |
0.39700 |
-1.38e-01 |
3.72e-01 |
2.16e-01 |
8.16e-04 |
Interleukin-12 signaling |
37 |
4.36e-04 |
2.54e-03 |
0.39600 |
-1.53e-01 |
3.66e-01 |
1.06e-01 |
1.19e-04 |
Potential therapeutics for SARS |
78 |
1.54e-07 |
3.04e-06 |
0.39600 |
-1.94e-01 |
3.46e-01 |
3.12e-03 |
1.32e-07 |
Erythropoietin activates Phosphoinositide-3-kinase (PI3K) |
12 |
9.60e-02 |
2.00e-01 |
0.39500 |
-3.15e-01 |
2.39e-01 |
5.88e-02 |
1.52e-01 |
Antigen processing-Cross presentation |
91 |
2.30e-08 |
6.45e-07 |
0.39400 |
-3.16e-01 |
2.36e-01 |
1.96e-07 |
1.03e-04 |
HuR (ELAVL1) binds and stabilizes mRNA |
10 |
1.40e-01 |
2.64e-01 |
0.39300 |
-2.06e-01 |
3.34e-01 |
2.58e-01 |
6.72e-02 |
Glutathione synthesis and recycling |
12 |
5.49e-02 |
1.32e-01 |
0.39200 |
-3.92e-01 |
-4.66e-03 |
1.89e-02 |
9.78e-01 |
Activation of the AP-1 family of transcription factors |
10 |
1.26e-01 |
2.45e-01 |
0.39000 |
-1.33e-01 |
3.67e-01 |
4.68e-01 |
4.43e-02 |
Cap-dependent Translation Initiation |
85 |
5.33e-11 |
3.40e-09 |
0.39000 |
1.73e-01 |
3.50e-01 |
5.89e-03 |
2.50e-08 |
Eukaryotic Translation Initiation |
85 |
5.33e-11 |
3.40e-09 |
0.39000 |
1.73e-01 |
3.50e-01 |
5.89e-03 |
2.50e-08 |
GTP hydrolysis and joining of the 60S ribosomal subunit |
78 |
3.66e-10 |
1.97e-08 |
0.39000 |
1.75e-01 |
3.49e-01 |
7.75e-03 |
1.00e-07 |
Serotonin Neurotransmitter Release Cycle |
15 |
4.41e-02 |
1.13e-01 |
0.38900 |
1.20e-01 |
-3.70e-01 |
4.20e-01 |
1.31e-02 |
Killing mechanisms |
11 |
1.22e-01 |
2.39e-01 |
0.38900 |
2.14e-01 |
-3.25e-01 |
2.18e-01 |
6.23e-02 |
WNT5:FZD7-mediated leishmania damping |
11 |
1.22e-01 |
2.39e-01 |
0.38900 |
2.14e-01 |
-3.25e-01 |
2.18e-01 |
6.23e-02 |
Receptor-type tyrosine-protein phosphatases |
17 |
3.98e-02 |
1.05e-01 |
0.38900 |
3.16e-01 |
-2.26e-01 |
2.40e-02 |
1.06e-01 |
RHO GTPases Activate WASPs and WAVEs |
36 |
2.84e-04 |
1.77e-03 |
0.38700 |
-3.19e-02 |
3.86e-01 |
7.41e-01 |
6.16e-05 |
Scavenging by Class A Receptors |
16 |
1.95e-02 |
6.04e-02 |
0.38600 |
4.68e-02 |
3.84e-01 |
7.46e-01 |
7.91e-03 |
L13a-mediated translational silencing of Ceruloplasmin expression |
77 |
7.06e-10 |
3.66e-08 |
0.38600 |
1.82e-01 |
3.40e-01 |
5.86e-03 |
2.50e-07 |
Downstream signaling events of B Cell Receptor (BCR) |
80 |
4.41e-07 |
6.87e-06 |
0.38500 |
-2.60e-01 |
2.84e-01 |
5.79e-05 |
1.14e-05 |
Interleukin-10 signaling |
31 |
3.40e-03 |
1.53e-02 |
0.38500 |
-2.48e-01 |
2.94e-01 |
1.67e-02 |
4.68e-03 |
DCC mediated attractive signaling |
13 |
9.10e-02 |
1.94e-01 |
0.38400 |
-3.05e-01 |
2.34e-01 |
5.68e-02 |
1.45e-01 |
FOXO-mediated transcription of cell cycle genes |
15 |
1.90e-02 |
5.93e-02 |
0.38400 |
3.58e-01 |
1.39e-01 |
1.65e-02 |
3.51e-01 |
Regulation of mRNA stability by proteins that bind AU-rich elements |
87 |
1.41e-07 |
2.91e-06 |
0.38400 |
-2.73e-01 |
2.70e-01 |
1.11e-05 |
1.37e-05 |
Apoptotic execution phase |
49 |
2.16e-06 |
2.56e-05 |
0.38200 |
1.66e-01 |
3.44e-01 |
4.51e-02 |
3.10e-05 |
Synaptic adhesion-like molecules |
21 |
2.28e-02 |
6.80e-02 |
0.38100 |
2.92e-01 |
-2.44e-01 |
2.04e-02 |
5.29e-02 |
Norepinephrine Neurotransmitter Release Cycle |
15 |
5.58e-02 |
1.33e-01 |
0.38000 |
1.49e-01 |
-3.50e-01 |
3.18e-01 |
1.89e-02 |
Downregulation of SMAD2/3:SMAD4 transcriptional activity |
23 |
1.60e-02 |
5.22e-02 |
0.38000 |
-2.97e-01 |
2.38e-01 |
1.38e-02 |
4.82e-02 |
Keratinization |
39 |
5.80e-04 |
3.25e-03 |
0.38000 |
3.48e-01 |
-1.53e-01 |
1.71e-04 |
9.74e-02 |
PCNA-Dependent Long Patch Base Excision Repair |
20 |
4.26e-03 |
1.82e-02 |
0.37900 |
2.93e-01 |
2.42e-01 |
2.35e-02 |
6.15e-02 |
RHO GTPases Activate ROCKs |
19 |
1.13e-02 |
3.94e-02 |
0.37900 |
4.52e-02 |
3.76e-01 |
7.33e-01 |
4.57e-03 |
Eukaryotic Translation Elongation |
58 |
1.52e-07 |
3.04e-06 |
0.37800 |
2.82e-01 |
2.52e-01 |
2.08e-04 |
9.11e-04 |
Fc epsilon receptor (FCERI) signaling |
143 |
6.39e-12 |
5.60e-10 |
0.37800 |
-1.98e-01 |
3.22e-01 |
4.42e-05 |
3.24e-11 |
Cristae formation |
29 |
4.15e-04 |
2.42e-03 |
0.37600 |
2.56e-01 |
2.75e-01 |
1.71e-02 |
1.03e-02 |
Infection with Mycobacterium tuberculosis |
26 |
8.34e-03 |
3.09e-02 |
0.37500 |
-1.65e-01 |
3.37e-01 |
1.46e-01 |
2.91e-03 |
Platelet calcium homeostasis |
26 |
1.09e-03 |
5.63e-03 |
0.37300 |
3.03e-01 |
2.18e-01 |
7.54e-03 |
5.43e-02 |
CDT1 association with the CDC6:ORC:origin complex |
58 |
4.79e-05 |
3.82e-04 |
0.37300 |
-2.49e-01 |
2.78e-01 |
1.07e-03 |
2.58e-04 |
MET receptor recycling |
10 |
1.28e-01 |
2.46e-01 |
0.37200 |
-3.69e-01 |
4.85e-02 |
4.33e-02 |
7.91e-01 |
Response of Mtb to phagocytosis |
22 |
2.13e-02 |
6.45e-02 |
0.37200 |
-2.02e-01 |
3.12e-01 |
1.02e-01 |
1.12e-02 |
RHO GTPases activate PAKs |
21 |
1.65e-02 |
5.35e-02 |
0.37100 |
-8.60e-02 |
3.61e-01 |
4.95e-01 |
4.18e-03 |
Metalloprotease DUBs |
20 |
3.04e-02 |
8.50e-02 |
0.36900 |
-1.82e-01 |
3.21e-01 |
1.60e-01 |
1.30e-02 |
Endogenous sterols |
19 |
9.64e-03 |
3.43e-02 |
0.36900 |
1.36e-01 |
3.43e-01 |
3.05e-01 |
9.70e-03 |
Interleukin-12 family signaling |
46 |
2.55e-04 |
1.61e-03 |
0.36800 |
-1.46e-01 |
3.38e-01 |
8.70e-02 |
7.21e-05 |
Eukaryotic Translation Termination |
60 |
2.07e-07 |
3.82e-06 |
0.36800 |
2.69e-01 |
2.51e-01 |
3.20e-04 |
7.76e-04 |
InlB-mediated entry of Listeria monocytogenes into host cell |
14 |
9.23e-02 |
1.95e-01 |
0.36700 |
-3.05e-01 |
2.05e-01 |
4.81e-02 |
1.85e-01 |
ABC transporters in lipid homeostasis |
15 |
5.45e-02 |
1.31e-01 |
0.36700 |
3.60e-01 |
-7.27e-02 |
1.59e-02 |
6.26e-01 |
IRF3-mediated induction of type I IFN |
13 |
1.04e-01 |
2.13e-01 |
0.36700 |
-3.23e-01 |
1.73e-01 |
4.35e-02 |
2.79e-01 |
Oxygen-dependent proline hydroxylation of Hypoxia-inducible Factor Alpha |
64 |
2.44e-05 |
2.17e-04 |
0.36700 |
-2.57e-01 |
2.62e-01 |
3.76e-04 |
2.98e-04 |
Selenocysteine synthesis |
60 |
2.60e-07 |
4.62e-06 |
0.36600 |
2.92e-01 |
2.20e-01 |
9.03e-05 |
3.16e-03 |
YAP1- and WWTR1 (TAZ)-stimulated gene expression |
12 |
1.36e-01 |
2.59e-01 |
0.36600 |
-2.42e-01 |
2.75e-01 |
1.47e-01 |
9.90e-02 |
COPI-independent Golgi-to-ER retrograde traffic |
33 |
2.69e-03 |
1.28e-02 |
0.36600 |
-1.34e-01 |
3.40e-01 |
1.84e-01 |
7.18e-04 |
RUNX3 regulates NOTCH signaling |
14 |
3.70e-02 |
9.83e-02 |
0.36500 |
1.12e-01 |
3.48e-01 |
4.70e-01 |
2.42e-02 |
Response of EIF2AK4 (GCN2) to amino acid deficiency |
68 |
3.40e-08 |
8.67e-07 |
0.36500 |
2.38e-01 |
2.77e-01 |
6.94e-04 |
7.69e-05 |
Downstream TCR signaling |
88 |
4.66e-07 |
7.10e-06 |
0.36500 |
-2.92e-01 |
2.19e-01 |
2.21e-06 |
3.98e-04 |
Reduction of cytosolic Ca++ levels |
11 |
6.57e-02 |
1.52e-01 |
0.36400 |
1.88e-01 |
3.12e-01 |
2.81e-01 |
7.28e-02 |
BBSome-mediated cargo-targeting to cilium |
21 |
2.18e-02 |
6.55e-02 |
0.36400 |
-3.46e-01 |
1.13e-01 |
5.99e-03 |
3.71e-01 |
Chaperone Mediated Autophagy |
16 |
7.25e-02 |
1.65e-01 |
0.36400 |
-2.44e-01 |
2.70e-01 |
9.16e-02 |
6.12e-02 |
Stabilization of p53 |
54 |
1.41e-04 |
9.71e-04 |
0.36400 |
-2.82e-01 |
2.30e-01 |
3.42e-04 |
3.44e-03 |
Constitutive Signaling by Overexpressed ERBB2 |
11 |
1.28e-01 |
2.46e-01 |
0.36400 |
-8.72e-02 |
3.53e-01 |
6.17e-01 |
4.25e-02 |
Signaling by SCF-KIT |
42 |
1.01e-03 |
5.24e-03 |
0.36400 |
-2.27e-01 |
2.84e-01 |
1.10e-02 |
1.44e-03 |
Signal regulatory protein family interactions |
12 |
7.02e-02 |
1.61e-01 |
0.36400 |
-3.59e-01 |
-5.83e-02 |
3.14e-02 |
7.26e-01 |
Chk1/Chk2(Cds1) mediated inactivation of Cyclin B:Cdk1 complex |
13 |
5.77e-02 |
1.36e-01 |
0.36400 |
5.00e-02 |
3.60e-01 |
7.55e-01 |
2.46e-02 |
The role of GTSE1 in G2/M progression after G2 checkpoint |
59 |
6.68e-05 |
5.00e-04 |
0.36300 |
-2.72e-01 |
2.40e-01 |
2.96e-04 |
1.44e-03 |
Regulation of pyruvate dehydrogenase (PDH) complex |
15 |
5.75e-02 |
1.36e-01 |
0.36200 |
-6.57e-02 |
3.56e-01 |
6.60e-01 |
1.69e-02 |
Constitutive Signaling by EGFRvIII |
15 |
8.70e-02 |
1.88e-01 |
0.36100 |
-2.90e-01 |
2.15e-01 |
5.21e-02 |
1.49e-01 |
Signaling by EGFRvIII in Cancer |
15 |
8.70e-02 |
1.88e-01 |
0.36100 |
-2.90e-01 |
2.15e-01 |
5.21e-02 |
1.49e-01 |
Fatty acids |
11 |
1.47e-01 |
2.73e-01 |
0.36000 |
3.35e-01 |
-1.31e-01 |
5.42e-02 |
4.52e-01 |
Translesion Synthesis by POLH |
18 |
1.91e-02 |
5.95e-02 |
0.36000 |
7.20e-02 |
3.52e-01 |
5.97e-01 |
9.64e-03 |
NOTCH4 Activation and Transmission of Signal to the Nucleus |
10 |
2.02e-01 |
3.41e-01 |
0.35900 |
-2.43e-01 |
2.64e-01 |
1.83e-01 |
1.48e-01 |
Beta-catenin phosphorylation cascade |
17 |
1.90e-02 |
5.93e-02 |
0.35900 |
1.42e-01 |
3.29e-01 |
3.10e-01 |
1.87e-02 |
Synthesis of very long-chain fatty acyl-CoAs |
19 |
2.05e-02 |
6.29e-02 |
0.35800 |
1.32e-02 |
3.58e-01 |
9.20e-01 |
6.88e-03 |
Resolution of AP sites via the multiple-nucleotide patch replacement pathway |
24 |
2.96e-03 |
1.38e-02 |
0.35800 |
2.80e-01 |
2.23e-01 |
1.75e-02 |
5.87e-02 |
TCR signaling |
109 |
2.92e-08 |
7.58e-07 |
0.35800 |
-2.85e-01 |
2.16e-01 |
2.73e-07 |
9.70e-05 |
Formation of Senescence-Associated Heterochromatin Foci (SAHF) |
16 |
3.69e-02 |
9.80e-02 |
0.35700 |
3.56e-01 |
2.65e-02 |
1.37e-02 |
8.54e-01 |
Erythropoietin activates RAS |
14 |
8.33e-02 |
1.82e-01 |
0.35600 |
-9.51e-02 |
3.43e-01 |
5.38e-01 |
2.61e-02 |
NOTCH4 Intracellular Domain Regulates Transcription |
18 |
1.77e-02 |
5.62e-02 |
0.35600 |
1.11e-01 |
3.38e-01 |
4.15e-01 |
1.29e-02 |
G-protein beta:gamma signalling |
30 |
6.44e-03 |
2.49e-02 |
0.35600 |
-1.40e-01 |
3.27e-01 |
1.85e-01 |
1.92e-03 |
Negative regulation of MET activity |
20 |
4.43e-02 |
1.14e-01 |
0.35500 |
-2.42e-01 |
2.59e-01 |
6.06e-02 |
4.48e-02 |
Recognition of DNA damage by PCNA-containing replication complex |
29 |
1.32e-03 |
6.70e-03 |
0.35400 |
1.48e-01 |
3.22e-01 |
1.68e-01 |
2.68e-03 |
Activation of IRF3/IRF7 mediated by TBK1/IKK epsilon |
16 |
7.63e-02 |
1.71e-01 |
0.35300 |
-3.10e-01 |
1.68e-01 |
3.16e-02 |
2.45e-01 |
Constitutive Signaling by Ligand-Responsive EGFR Cancer Variants |
19 |
5.23e-02 |
1.28e-01 |
0.35300 |
-2.80e-01 |
2.15e-01 |
3.47e-02 |
1.05e-01 |
Signaling by Ligand-Responsive EGFR Variants in Cancer |
19 |
5.23e-02 |
1.28e-01 |
0.35300 |
-2.80e-01 |
2.15e-01 |
3.47e-02 |
1.05e-01 |
SLBP Dependent Processing of Replication-Dependent Histone Pre-mRNAs |
10 |
9.42e-02 |
1.98e-01 |
0.35200 |
-2.55e-01 |
-2.43e-01 |
1.63e-01 |
1.83e-01 |
Organic cation/anion/zwitterion transport |
13 |
5.08e-02 |
1.26e-01 |
0.35200 |
-1.68e-01 |
-3.10e-01 |
2.95e-01 |
5.33e-02 |
Interleukin-35 Signalling |
11 |
1.85e-01 |
3.21e-01 |
0.35200 |
-2.62e-01 |
2.35e-01 |
1.32e-01 |
1.78e-01 |
DARPP-32 events |
23 |
5.26e-03 |
2.12e-02 |
0.35100 |
1.71e-01 |
3.06e-01 |
1.55e-01 |
1.10e-02 |
Signaling by Leptin |
10 |
1.25e-01 |
2.45e-01 |
0.35000 |
3.44e-01 |
6.60e-02 |
5.96e-02 |
7.18e-01 |
Interleukin-3, Interleukin-5 and GM-CSF signaling |
39 |
2.63e-03 |
1.25e-02 |
0.34900 |
-2.82e-01 |
2.05e-01 |
2.28e-03 |
2.68e-02 |
Assembly of the pre-replicative complex |
67 |
3.78e-05 |
3.14e-04 |
0.34800 |
-2.01e-01 |
2.84e-01 |
4.37e-03 |
5.74e-05 |
Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC) |
62 |
6.74e-07 |
1.00e-05 |
0.34800 |
2.15e-01 |
2.74e-01 |
3.36e-03 |
1.94e-04 |
Fcgamma receptor (FCGR) dependent phagocytosis |
100 |
8.78e-08 |
1.89e-06 |
0.34800 |
-1.24e-01 |
3.25e-01 |
3.17e-02 |
1.96e-08 |
Signaling by PDGFR in disease |
19 |
5.29e-02 |
1.29e-01 |
0.34800 |
-1.76e-01 |
3.00e-01 |
1.85e-01 |
2.35e-02 |
RAF activation |
33 |
2.79e-03 |
1.31e-02 |
0.34700 |
-4.74e-02 |
3.44e-01 |
6.37e-01 |
6.26e-04 |
Base-Excision Repair, AP Site Formation |
24 |
2.73e-02 |
7.93e-02 |
0.34700 |
2.73e-01 |
-2.14e-01 |
2.05e-02 |
6.94e-02 |
TP53 Regulates Transcription of Genes Involved in G1 Cell Cycle Arrest |
13 |
1.26e-01 |
2.45e-01 |
0.34700 |
3.17e-01 |
-1.39e-01 |
4.76e-02 |
3.85e-01 |
STING mediated induction of host immune responses |
16 |
7.58e-02 |
1.71e-01 |
0.34500 |
-3.24e-01 |
1.19e-01 |
2.48e-02 |
4.12e-01 |
ER Quality Control Compartment (ERQC) |
21 |
3.56e-02 |
9.50e-02 |
0.34400 |
-3.20e-01 |
1.25e-01 |
1.11e-02 |
3.21e-01 |
Apoptotic cleavage of cellular proteins |
35 |
5.92e-04 |
3.30e-03 |
0.34300 |
1.33e-01 |
3.16e-01 |
1.74e-01 |
1.21e-03 |
Metabolism of polyamines |
58 |
1.99e-04 |
1.29e-03 |
0.34200 |
-2.82e-01 |
1.94e-01 |
2.05e-04 |
1.08e-02 |
Keratan sulfate degradation |
10 |
1.47e-01 |
2.73e-01 |
0.34200 |
3.77e-02 |
3.40e-01 |
8.36e-01 |
6.30e-02 |
p75NTR recruits signalling complexes |
13 |
1.49e-01 |
2.75e-01 |
0.34100 |
-2.81e-01 |
1.94e-01 |
7.97e-02 |
2.26e-01 |
Aspartate and asparagine metabolism |
11 |
9.62e-02 |
2.00e-01 |
0.34100 |
1.49e-01 |
3.07e-01 |
3.93e-01 |
7.81e-02 |
CLEC7A (Dectin-1) signaling |
97 |
9.51e-07 |
1.34e-05 |
0.34000 |
-2.23e-01 |
2.57e-01 |
1.54e-04 |
1.19e-05 |
Cytosolic tRNA aminoacylation |
24 |
3.00e-02 |
8.41e-02 |
0.34000 |
-1.82e-01 |
2.87e-01 |
1.23e-01 |
1.50e-02 |
Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell |
103 |
3.99e-07 |
6.35e-06 |
0.34000 |
-2.69e-01 |
2.08e-01 |
2.51e-06 |
2.73e-04 |
Orc1 removal from chromatin |
69 |
4.77e-05 |
3.82e-04 |
0.33900 |
-1.96e-01 |
2.77e-01 |
4.91e-03 |
6.91e-05 |
FCGR3A-mediated IL10 synthesis |
52 |
3.70e-04 |
2.23e-03 |
0.33900 |
-1.33e-01 |
3.11e-01 |
9.77e-02 |
1.03e-04 |
Synthesis of PIPs at the early endosome membrane |
16 |
1.04e-01 |
2.13e-01 |
0.33800 |
-2.19e-01 |
2.58e-01 |
1.30e-01 |
7.42e-02 |
Signalling to ERKs |
32 |
9.69e-03 |
3.44e-02 |
0.33800 |
-1.78e-01 |
2.87e-01 |
8.13e-02 |
4.96e-03 |
Autodegradation of Cdh1 by Cdh1:APC/C |
62 |
1.64e-04 |
1.10e-03 |
0.33700 |
-2.47e-01 |
2.30e-01 |
7.69e-04 |
1.75e-03 |
Translocation of SLC2A4 (GLUT4) to the plasma membrane |
51 |
1.82e-04 |
1.18e-03 |
0.33700 |
-4.17e-02 |
3.35e-01 |
6.07e-01 |
3.56e-05 |
Glycogen breakdown (glycogenolysis) |
14 |
5.93e-02 |
1.39e-01 |
0.33700 |
1.12e-01 |
3.18e-01 |
4.70e-01 |
3.95e-02 |
Free fatty acids regulate insulin secretion |
10 |
2.48e-01 |
3.94e-01 |
0.33600 |
-2.40e-01 |
2.34e-01 |
1.88e-01 |
2.00e-01 |
Digestion and absorption |
13 |
7.67e-02 |
1.72e-01 |
0.33600 |
3.21e-01 |
9.75e-02 |
4.50e-02 |
5.43e-01 |
Receptor Mediated Mitophagy |
11 |
2.08e-01 |
3.47e-01 |
0.33500 |
-1.80e-01 |
2.83e-01 |
3.02e-01 |
1.04e-01 |
G beta:gamma signalling through PI3Kgamma |
23 |
2.92e-02 |
8.37e-02 |
0.33500 |
-1.07e-01 |
3.18e-01 |
3.75e-01 |
8.36e-03 |
Listeria monocytogenes entry into host cells |
19 |
7.00e-02 |
1.61e-01 |
0.33500 |
-2.65e-01 |
2.05e-01 |
4.53e-02 |
1.23e-01 |
Activation of BH3-only proteins |
29 |
8.37e-03 |
3.09e-02 |
0.33500 |
-4.95e-02 |
3.31e-01 |
6.44e-01 |
2.02e-03 |
Signaling by PDGFRA extracellular domain mutants |
12 |
1.21e-01 |
2.38e-01 |
0.33500 |
2.31e-03 |
3.35e-01 |
9.89e-01 |
4.48e-02 |
Signaling by PDGFRA transmembrane, juxtamembrane and kinase domain mutants |
12 |
1.21e-01 |
2.38e-01 |
0.33500 |
2.31e-03 |
3.35e-01 |
9.89e-01 |
4.48e-02 |
SCF(Skp2)-mediated degradation of p27/p21 |
58 |
3.38e-04 |
2.05e-03 |
0.33400 |
-2.30e-01 |
2.42e-01 |
2.45e-03 |
1.42e-03 |
Cytochrome c-mediated apoptotic response |
11 |
1.28e-01 |
2.46e-01 |
0.33300 |
5.83e-02 |
3.28e-01 |
7.38e-01 |
5.96e-02 |
Regulation of RUNX2 expression and activity |
70 |
6.64e-05 |
5.00e-04 |
0.33300 |
-2.59e-01 |
2.10e-01 |
1.84e-04 |
2.43e-03 |
Phosphorylation of CD3 and TCR zeta chains |
16 |
6.68e-02 |
1.54e-01 |
0.33300 |
-3.32e-01 |
2.15e-02 |
2.14e-02 |
8.81e-01 |
Activated PKN1 stimulates transcription of AR (androgen receptor) regulated genes KLK2 and KLK3 |
16 |
3.49e-02 |
9.38e-02 |
0.33200 |
2.45e-01 |
2.25e-01 |
9.04e-02 |
1.20e-01 |
Aberrant regulation of mitotic G1/S transition in cancer due to RB1 defects |
17 |
2.97e-02 |
8.38e-02 |
0.33100 |
2.70e-01 |
1.92e-01 |
5.38e-02 |
1.70e-01 |
Defective binding of RB1 mutants to E2F1,(E2F2, E2F3) |
17 |
2.97e-02 |
8.38e-02 |
0.33100 |
2.70e-01 |
1.92e-01 |
5.38e-02 |
1.70e-01 |
Integrin cell surface interactions |
58 |
3.79e-05 |
3.14e-04 |
0.33100 |
1.71e-02 |
3.31e-01 |
8.22e-01 |
1.32e-05 |
LGI-ADAM interactions |
12 |
1.92e-01 |
3.29e-01 |
0.33100 |
1.92e-01 |
-2.70e-01 |
2.51e-01 |
1.05e-01 |
Gastrin-CREB signalling pathway via PKC and MAPK |
17 |
7.70e-02 |
1.72e-01 |
0.33100 |
-9.92e-02 |
3.16e-01 |
4.79e-01 |
2.43e-02 |
Role of phospholipids in phagocytosis |
40 |
4.49e-03 |
1.91e-02 |
0.33000 |
-2.14e-01 |
2.52e-01 |
1.92e-02 |
5.92e-03 |
Regulation of innate immune responses to cytosolic DNA |
15 |
9.32e-02 |
1.96e-01 |
0.33000 |
-3.25e-01 |
5.68e-02 |
2.95e-02 |
7.04e-01 |
Costimulation by the CD28 family |
61 |
2.93e-04 |
1.79e-03 |
0.32800 |
-2.12e-01 |
2.51e-01 |
4.28e-03 |
7.03e-04 |
SRP-dependent cotranslational protein targeting to membrane |
79 |
9.05e-07 |
1.29e-05 |
0.32800 |
3.60e-02 |
3.26e-01 |
5.81e-01 |
5.45e-07 |
Diseases associated with the TLR signaling cascade |
22 |
5.35e-02 |
1.30e-01 |
0.32800 |
-2.11e-01 |
2.50e-01 |
8.62e-02 |
4.22e-02 |
Diseases of Immune System |
22 |
5.35e-02 |
1.30e-01 |
0.32800 |
-2.11e-01 |
2.50e-01 |
8.62e-02 |
4.22e-02 |
TP53 Regulates Transcription of Genes Involved in G2 Cell Cycle Arrest |
18 |
5.78e-02 |
1.37e-01 |
0.32700 |
3.24e-01 |
-4.24e-02 |
1.73e-02 |
7.55e-01 |
Cellular response to hypoxia |
73 |
6.17e-05 |
4.70e-04 |
0.32700 |
-2.59e-01 |
1.99e-01 |
1.28e-04 |
3.34e-03 |
Downregulation of TGF-beta receptor signaling |
26 |
2.45e-02 |
7.22e-02 |
0.32600 |
-1.17e-01 |
3.04e-01 |
3.01e-01 |
7.33e-03 |
Presynaptic depolarization and calcium channel opening |
11 |
2.08e-01 |
3.46e-01 |
0.32500 |
1.12e-01 |
-3.05e-01 |
5.20e-01 |
8.00e-02 |
Purine salvage |
12 |
1.79e-01 |
3.12e-01 |
0.32500 |
-3.07e-01 |
1.07e-01 |
6.60e-02 |
5.23e-01 |
TICAM1-dependent activation of IRF3/IRF7 |
12 |
1.75e-01 |
3.08e-01 |
0.32400 |
-3.10e-01 |
9.42e-02 |
6.30e-02 |
5.72e-01 |
CREB1 phosphorylation through the activation of Adenylate Cyclase |
11 |
1.68e-01 |
3.02e-01 |
0.32200 |
-3.61e-03 |
3.22e-01 |
9.83e-01 |
6.43e-02 |
RHO GTPases activate PKNs |
43 |
7.37e-04 |
3.97e-03 |
0.32200 |
2.62e-02 |
3.21e-01 |
7.66e-01 |
2.75e-04 |
Spry regulation of FGF signaling |
16 |
1.05e-01 |
2.14e-01 |
0.32200 |
-1.06e-01 |
3.04e-01 |
4.62e-01 |
3.55e-02 |
Uptake and function of anthrax toxins |
10 |
1.78e-01 |
3.12e-01 |
0.32100 |
3.17e-01 |
5.11e-02 |
8.26e-02 |
7.80e-01 |
PTK6 Regulates RHO GTPases, RAS GTPase and MAP kinases |
14 |
1.45e-01 |
2.69e-01 |
0.32100 |
-1.18e-01 |
2.98e-01 |
4.45e-01 |
5.32e-02 |
Assembly of active LPL and LIPC lipase complexes |
16 |
1.25e-01 |
2.45e-01 |
0.32000 |
2.70e-01 |
-1.72e-01 |
6.16e-02 |
2.35e-01 |
Signaling by KIT in disease |
20 |
5.71e-02 |
1.36e-01 |
0.32000 |
-8.29e-02 |
3.09e-01 |
5.21e-01 |
1.69e-02 |
Signaling by phosphorylated juxtamembrane, extracellular and kinase domain KIT mutants |
20 |
5.71e-02 |
1.36e-01 |
0.32000 |
-8.29e-02 |
3.09e-01 |
5.21e-01 |
1.69e-02 |
Class C/3 (Metabotropic glutamate/pheromone receptors) |
12 |
1.96e-01 |
3.33e-01 |
0.32000 |
1.26e-01 |
-2.94e-01 |
4.51e-01 |
7.81e-02 |
Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC) |
81 |
3.38e-07 |
5.68e-06 |
0.31900 |
1.31e-01 |
2.91e-01 |
4.24e-02 |
6.16e-06 |
Nonsense-Mediated Decay (NMD) |
81 |
3.38e-07 |
5.68e-06 |
0.31900 |
1.31e-01 |
2.91e-01 |
4.24e-02 |
6.16e-06 |
IKK complex recruitment mediated by RIP1 |
20 |
6.79e-02 |
1.56e-01 |
0.31900 |
-1.27e-01 |
2.92e-01 |
3.25e-01 |
2.38e-02 |
Formation of Fibrin Clot (Clotting Cascade) |
28 |
6.34e-03 |
2.46e-02 |
0.31700 |
1.21e-01 |
2.93e-01 |
2.69e-01 |
7.35e-03 |
Cell surface interactions at the vascular wall |
132 |
3.12e-09 |
1.22e-07 |
0.31500 |
-3.27e-02 |
3.14e-01 |
5.17e-01 |
4.94e-10 |
Transport of inorganic cations/anions and amino acids/oligopeptides |
97 |
6.76e-06 |
6.97e-05 |
0.31500 |
2.00e-01 |
-2.43e-01 |
6.68e-04 |
3.49e-05 |
BMAL1:CLOCK,NPAS2 activates circadian gene expression |
26 |
3.52e-02 |
9.42e-02 |
0.31400 |
-1.38e-01 |
2.82e-01 |
2.23e-01 |
1.28e-02 |
Signaling by FGFR3 fusions in cancer |
10 |
2.76e-01 |
4.23e-01 |
0.31400 |
-1.39e-01 |
2.82e-01 |
4.47e-01 |
1.23e-01 |
APC/C:Cdc20 mediated degradation of Securin |
66 |
3.29e-04 |
2.01e-03 |
0.31400 |
-2.27e-01 |
2.17e-01 |
1.42e-03 |
2.35e-03 |
mitochondrial fatty acid beta-oxidation of saturated fatty acids |
10 |
2.94e-01 |
4.43e-01 |
0.31400 |
-2.47e-01 |
1.94e-01 |
1.77e-01 |
2.89e-01 |
Degradation of DVL |
56 |
1.09e-03 |
5.63e-03 |
0.31300 |
-2.50e-01 |
1.88e-01 |
1.24e-03 |
1.48e-02 |
ABC transporter disorders |
73 |
8.44e-05 |
6.13e-04 |
0.31300 |
-2.85e-01 |
1.29e-01 |
2.61e-05 |
5.68e-02 |
PD-1 signaling |
16 |
7.99e-02 |
1.77e-01 |
0.31200 |
-3.11e-01 |
-2.66e-02 |
3.15e-02 |
8.54e-01 |
TICAM1, RIP1-mediated IKK complex recruitment |
17 |
1.10e-01 |
2.22e-01 |
0.31000 |
-1.09e-01 |
2.90e-01 |
4.35e-01 |
3.82e-02 |
G alpha (s) signalling events |
298 |
1.03e-23 |
4.83e-21 |
0.31000 |
-1.68e-01 |
-2.61e-01 |
6.21e-07 |
1.09e-14 |
MAPK6/MAPK4 signaling |
85 |
4.15e-05 |
3.40e-04 |
0.31000 |
-2.02e-01 |
2.35e-01 |
1.33e-03 |
1.76e-04 |
Influenza Viral RNA Transcription and Replication |
103 |
8.50e-09 |
2.84e-07 |
0.31000 |
2.48e-01 |
1.85e-01 |
1.35e-05 |
1.17e-03 |
Phase 0 - rapid depolarisation |
24 |
4.70e-02 |
1.18e-01 |
0.31000 |
2.85e-01 |
-1.22e-01 |
1.58e-02 |
3.01e-01 |
Transcriptional regulation by RUNX3 |
93 |
1.28e-05 |
1.23e-04 |
0.30900 |
-1.59e-01 |
2.65e-01 |
8.24e-03 |
1.02e-05 |
RUNX1 regulates transcription of genes involved in differentiation of HSCs |
77 |
1.25e-04 |
8.77e-04 |
0.30800 |
-2.13e-01 |
2.22e-01 |
1.21e-03 |
7.73e-04 |
GAB1 signalosome |
14 |
1.36e-01 |
2.59e-01 |
0.30700 |
-3.06e-01 |
2.80e-02 |
4.75e-02 |
8.56e-01 |
Pausing and recovery of Tat-mediated HIV elongation |
30 |
4.67e-03 |
1.95e-02 |
0.30700 |
2.00e-01 |
2.33e-01 |
5.81e-02 |
2.72e-02 |
Tat-mediated HIV elongation arrest and recovery |
30 |
4.67e-03 |
1.95e-02 |
0.30700 |
2.00e-01 |
2.33e-01 |
5.81e-02 |
2.72e-02 |
SARS-CoV Infections |
139 |
7.13e-08 |
1.59e-06 |
0.30700 |
-1.66e-01 |
2.58e-01 |
7.62e-04 |
1.50e-07 |
Intrinsic Pathway for Apoptosis |
48 |
7.29e-04 |
3.94e-03 |
0.30700 |
1.60e-02 |
3.06e-01 |
8.48e-01 |
2.43e-04 |
Endosomal Sorting Complex Required For Transport (ESCRT) |
30 |
1.46e-02 |
4.84e-02 |
0.30500 |
-2.70e-02 |
3.04e-01 |
7.98e-01 |
3.93e-03 |
Regulation of glycolysis by fructose 2,6-bisphosphate metabolism |
11 |
1.46e-01 |
2.72e-01 |
0.30500 |
2.56e-01 |
1.66e-01 |
1.42e-01 |
3.39e-01 |
Degradation of beta-catenin by the destruction complex |
84 |
6.09e-05 |
4.68e-04 |
0.30500 |
-1.83e-01 |
2.43e-01 |
3.70e-03 |
1.16e-04 |
Signal transduction by L1 |
21 |
5.14e-02 |
1.26e-01 |
0.30500 |
-2.07e-02 |
3.04e-01 |
8.69e-01 |
1.59e-02 |
Cleavage of the damaged pyrimidine |
22 |
7.87e-02 |
1.75e-01 |
0.30300 |
2.48e-01 |
-1.75e-01 |
4.40e-02 |
1.56e-01 |
Depyrimidination |
22 |
7.87e-02 |
1.75e-01 |
0.30300 |
2.48e-01 |
-1.75e-01 |
4.40e-02 |
1.56e-01 |
Recognition and association of DNA glycosylase with site containing an affected pyrimidine |
22 |
7.87e-02 |
1.75e-01 |
0.30300 |
2.48e-01 |
-1.75e-01 |
4.40e-02 |
1.56e-01 |
Cyclin E associated events during G1/S transition |
81 |
8.14e-05 |
5.94e-04 |
0.30300 |
-1.60e-01 |
2.57e-01 |
1.27e-02 |
6.33e-05 |
MECP2 regulates neuronal receptors and channels |
15 |
1.07e-01 |
2.17e-01 |
0.30300 |
2.68e-02 |
3.01e-01 |
8.57e-01 |
4.33e-02 |
Glucose metabolism |
85 |
1.09e-06 |
1.47e-05 |
0.30300 |
2.87e-01 |
9.66e-02 |
4.92e-06 |
1.24e-01 |
Resolution of Abasic Sites (AP sites) |
37 |
5.09e-03 |
2.07e-02 |
0.30200 |
3.02e-01 |
3.33e-04 |
1.50e-03 |
9.97e-01 |
Formation of Incision Complex in GG-NER |
42 |
3.29e-03 |
1.50e-02 |
0.30200 |
-3.24e-02 |
3.00e-01 |
7.17e-01 |
7.74e-04 |
GRB2:SOS provides linkage to MAPK signaling for Integrins |
15 |
8.83e-02 |
1.90e-01 |
0.30100 |
1.03e-01 |
2.83e-01 |
4.89e-01 |
5.78e-02 |
Interaction between L1 and Ankyrins |
25 |
3.09e-02 |
8.61e-02 |
0.29900 |
2.99e-01 |
-4.88e-03 |
9.73e-03 |
9.66e-01 |
DAP12 signaling |
29 |
4.02e-02 |
1.06e-01 |
0.29900 |
-1.90e-01 |
2.31e-01 |
7.69e-02 |
3.15e-02 |
Early Phase of HIV Life Cycle |
14 |
1.65e-01 |
2.99e-01 |
0.29900 |
-5.86e-02 |
2.93e-01 |
7.04e-01 |
5.78e-02 |
DNA strand elongation |
31 |
6.32e-03 |
2.45e-02 |
0.29800 |
2.66e-01 |
1.35e-01 |
1.04e-02 |
1.92e-01 |
C-type lectin receptors (CLRs) |
127 |
9.77e-07 |
1.36e-05 |
0.29800 |
-2.08e-01 |
2.13e-01 |
5.08e-05 |
3.52e-05 |
Disassembly of the destruction complex and recruitment of AXIN to the membrane |
28 |
9.98e-03 |
3.52e-02 |
0.29800 |
2.56e-01 |
1.51e-01 |
1.89e-02 |
1.66e-01 |
Cooperation of PDCL (PhLP1) and TRiC/CCT in G-protein beta folding |
39 |
1.33e-02 |
4.48e-02 |
0.29700 |
-1.69e-01 |
2.44e-01 |
6.77e-02 |
8.36e-03 |
rRNA processing |
176 |
9.46e-12 |
7.37e-10 |
0.29600 |
4.33e-02 |
2.92e-01 |
3.22e-01 |
2.31e-11 |
GRB2 events in EGFR signaling |
10 |
3.13e-01 |
4.59e-01 |
0.29300 |
-1.03e-01 |
2.74e-01 |
5.71e-01 |
1.33e-01 |
Chemokine receptors bind chemokines |
39 |
1.48e-02 |
4.88e-02 |
0.29300 |
-2.42e-01 |
1.66e-01 |
8.97e-03 |
7.35e-02 |
Recycling pathway of L1 |
27 |
3.74e-02 |
9.91e-02 |
0.29200 |
-6.44e-02 |
2.85e-01 |
5.62e-01 |
1.04e-02 |
Apoptosis |
164 |
4.27e-09 |
1.57e-07 |
0.29200 |
-8.27e-02 |
2.80e-01 |
6.80e-02 |
6.17e-10 |
MAPK targets/ Nuclear events mediated by MAP kinases |
30 |
2.98e-02 |
8.38e-02 |
0.29200 |
-8.77e-02 |
2.78e-01 |
4.06e-01 |
8.38e-03 |
Processive synthesis on the C-strand of the telomere |
18 |
8.13e-02 |
1.79e-01 |
0.29200 |
2.90e-01 |
3.15e-02 |
3.33e-02 |
8.17e-01 |
Semaphorin interactions |
64 |
6.38e-04 |
3.51e-03 |
0.29100 |
-9.58e-02 |
2.75e-01 |
1.85e-01 |
1.45e-04 |
Initial triggering of complement |
33 |
2.10e-02 |
6.38e-02 |
0.29100 |
-8.30e-02 |
2.79e-01 |
4.09e-01 |
5.63e-03 |
HIV elongation arrest and recovery |
32 |
6.11e-03 |
2.39e-02 |
0.29000 |
1.81e-01 |
2.27e-01 |
7.71e-02 |
2.62e-02 |
Pausing and recovery of HIV elongation |
32 |
6.11e-03 |
2.39e-02 |
0.29000 |
1.81e-01 |
2.27e-01 |
7.71e-02 |
2.62e-02 |
Apoptotic factor-mediated response |
14 |
1.07e-01 |
2.16e-01 |
0.29000 |
1.93e-01 |
2.16e-01 |
2.10e-01 |
1.61e-01 |
Hedgehog 'on' state |
83 |
1.69e-04 |
1.13e-03 |
0.29000 |
-2.33e-01 |
1.72e-01 |
2.44e-04 |
6.69e-03 |
DNA Replication Pre-Initiation |
83 |
1.50e-04 |
1.02e-03 |
0.28900 |
-1.52e-01 |
2.46e-01 |
1.64e-02 |
1.07e-04 |
TGF-beta receptor signaling activates SMADs |
32 |
2.98e-02 |
8.38e-02 |
0.28900 |
-1.21e-01 |
2.62e-01 |
2.36e-01 |
1.02e-02 |
Signaling by EGFR in Cancer |
22 |
1.04e-01 |
2.13e-01 |
0.28800 |
-2.15e-01 |
1.92e-01 |
8.10e-02 |
1.18e-01 |
Major pathway of rRNA processing in the nucleolus and cytosol |
145 |
2.19e-09 |
9.05e-08 |
0.28700 |
5.02e-02 |
2.82e-01 |
2.98e-01 |
4.49e-09 |
Interleukin receptor SHC signaling |
22 |
9.22e-02 |
1.95e-01 |
0.28600 |
-2.62e-01 |
1.16e-01 |
3.36e-02 |
3.45e-01 |
E2F mediated regulation of DNA replication |
22 |
3.32e-02 |
8.97e-02 |
0.28600 |
1.74e-01 |
2.27e-01 |
1.58e-01 |
6.51e-02 |
Cdc20:Phospho-APC/C mediated degradation of Cyclin A |
70 |
8.69e-04 |
4.61e-03 |
0.28600 |
-2.03e-01 |
2.02e-01 |
3.37e-03 |
3.57e-03 |
Transcriptional regulation of pluripotent stem cells |
16 |
8.62e-02 |
1.87e-01 |
0.28500 |
2.35e-01 |
1.62e-01 |
1.04e-01 |
2.61e-01 |
EPHA-mediated growth cone collapse |
15 |
1.46e-01 |
2.71e-01 |
0.28500 |
3.05e-03 |
2.85e-01 |
9.84e-01 |
5.57e-02 |
WNT5A-dependent internalization of FZD2, FZD5 and ROR2 |
13 |
1.94e-01 |
3.31e-01 |
0.28500 |
-6.03e-03 |
2.85e-01 |
9.70e-01 |
7.53e-02 |
G beta:gamma signalling through CDC42 |
18 |
9.68e-02 |
2.01e-01 |
0.28500 |
1.29e-02 |
2.85e-01 |
9.24e-01 |
3.66e-02 |
Asymmetric localization of PCP proteins |
63 |
1.83e-03 |
8.99e-03 |
0.28500 |
-2.15e-01 |
1.87e-01 |
3.20e-03 |
1.05e-02 |
Blood group systems biosynthesis |
12 |
3.00e-01 |
4.49e-01 |
0.28400 |
-1.78e-01 |
2.21e-01 |
2.86e-01 |
1.84e-01 |
Lewis blood group biosynthesis |
12 |
3.00e-01 |
4.49e-01 |
0.28400 |
-1.78e-01 |
2.21e-01 |
2.86e-01 |
1.84e-01 |
p130Cas linkage to MAPK signaling for integrins |
15 |
1.05e-01 |
2.14e-01 |
0.28400 |
1.49e-01 |
2.42e-01 |
3.18e-01 |
1.05e-01 |
Dual Incision in GG-NER |
40 |
2.25e-03 |
1.09e-02 |
0.28400 |
1.78e-01 |
2.21e-01 |
5.13e-02 |
1.56e-02 |
Regulation of expression of SLITs and ROBOs |
134 |
1.34e-07 |
2.81e-06 |
0.28200 |
-3.36e-02 |
2.80e-01 |
5.03e-01 |
2.14e-08 |
Golgi Associated Vesicle Biogenesis |
54 |
4.82e-03 |
1.98e-02 |
0.28200 |
-1.73e-01 |
2.22e-01 |
2.79e-02 |
4.71e-03 |
RNA Polymerase I Promoter Opening |
12 |
1.70e-01 |
3.04e-01 |
0.28200 |
1.45e-01 |
2.42e-01 |
3.85e-01 |
1.47e-01 |
Influenza Infection |
119 |
2.42e-08 |
6.64e-07 |
0.28200 |
1.51e-01 |
2.38e-01 |
4.50e-03 |
7.67e-06 |
Leading Strand Synthesis |
13 |
1.90e-01 |
3.27e-01 |
0.28100 |
2.81e-01 |
1.82e-02 |
7.95e-02 |
9.09e-01 |
Polymerase switching |
13 |
1.90e-01 |
3.27e-01 |
0.28100 |
2.81e-01 |
1.82e-02 |
7.95e-02 |
9.09e-01 |
Signaling by ROBO receptors |
177 |
1.58e-09 |
7.15e-08 |
0.28100 |
-4.72e-02 |
2.77e-01 |
2.80e-01 |
2.01e-10 |
Post-chaperonin tubulin folding pathway |
17 |
1.30e-01 |
2.49e-01 |
0.28100 |
-2.22e-02 |
2.81e-01 |
8.74e-01 |
4.53e-02 |
Rap1 signalling |
15 |
2.18e-01 |
3.56e-01 |
0.28100 |
-1.39e-01 |
2.44e-01 |
3.51e-01 |
1.01e-01 |
Deregulated CDK5 triggers multiple neurodegenerative pathways in Alzheimer's disease models |
20 |
5.23e-02 |
1.28e-01 |
0.28100 |
2.39e-01 |
1.48e-01 |
6.40e-02 |
2.53e-01 |
Neurodegenerative Diseases |
20 |
5.23e-02 |
1.28e-01 |
0.28100 |
2.39e-01 |
1.48e-01 |
6.40e-02 |
2.53e-01 |
IRAK2 mediated activation of TAK1 complex upon TLR7/8 or 9 stimulation |
14 |
2.31e-01 |
3.73e-01 |
0.28100 |
-1.10e-01 |
2.58e-01 |
4.74e-01 |
9.46e-02 |
Laminin interactions |
23 |
3.31e-02 |
8.95e-02 |
0.28100 |
2.29e-01 |
1.62e-01 |
5.75e-02 |
1.78e-01 |
CD209 (DC-SIGN) signaling |
19 |
1.53e-01 |
2.80e-01 |
0.28000 |
-1.60e-01 |
2.30e-01 |
2.26e-01 |
8.27e-02 |
UCH proteinases |
87 |
2.13e-04 |
1.37e-03 |
0.28000 |
-2.20e-01 |
1.73e-01 |
4.01e-04 |
5.19e-03 |
Signaling by ERBB2 |
48 |
9.64e-03 |
3.43e-02 |
0.28000 |
-2.04e-01 |
1.91e-01 |
1.43e-02 |
2.20e-02 |
Deadenylation of mRNA |
22 |
1.14e-01 |
2.28e-01 |
0.28000 |
-2.33e-01 |
1.54e-01 |
5.83e-02 |
2.10e-01 |
Golgi Cisternae Pericentriolar Stack Reorganization |
13 |
2.45e-01 |
3.91e-01 |
0.28000 |
-8.23e-02 |
2.67e-01 |
6.08e-01 |
9.53e-02 |
VEGFA-VEGFR2 Pathway |
93 |
6.73e-05 |
5.00e-04 |
0.27900 |
-1.10e-01 |
2.57e-01 |
6.78e-02 |
1.86e-05 |
Regulation of HSF1-mediated heat shock response |
77 |
4.07e-04 |
2.39e-03 |
0.27900 |
-1.20e-01 |
2.52e-01 |
6.92e-02 |
1.37e-04 |
RNA Polymerase II Pre-transcription Events |
79 |
2.19e-04 |
1.40e-03 |
0.27900 |
-8.30e-02 |
2.66e-01 |
2.02e-01 |
4.44e-05 |
Platelet homeostasis |
79 |
1.03e-05 |
1.03e-04 |
0.27800 |
1.60e-01 |
2.28e-01 |
1.40e-02 |
4.65e-04 |
Signaling by VEGF |
101 |
3.08e-05 |
2.63e-04 |
0.27800 |
-1.06e-01 |
2.57e-01 |
6.65e-02 |
7.95e-06 |
Mitochondrial tRNA aminoacylation |
21 |
4.58e-02 |
1.16e-01 |
0.27800 |
-1.84e-01 |
-2.09e-01 |
1.45e-01 |
9.79e-02 |
Miscellaneous transport and binding events |
23 |
1.03e-01 |
2.13e-01 |
0.27800 |
-2.40e-01 |
1.41e-01 |
4.67e-02 |
2.43e-01 |
Signaling by FGFR4 in disease |
11 |
3.50e-01 |
4.94e-01 |
0.27800 |
-1.83e-01 |
2.09e-01 |
2.93e-01 |
2.31e-01 |
CDK-mediated phosphorylation and removal of Cdc6 |
70 |
1.30e-03 |
6.63e-03 |
0.27800 |
-2.00e-01 |
1.92e-01 |
3.79e-03 |
5.45e-03 |
Activation of ATR in response to replication stress |
37 |
4.64e-03 |
1.95e-02 |
0.27800 |
2.22e-01 |
1.66e-01 |
1.93e-02 |
8.08e-02 |
Synthesis of Leukotrienes (LT) and Eoxins (EX) |
18 |
8.88e-02 |
1.90e-01 |
0.27700 |
2.65e-01 |
8.07e-02 |
5.17e-02 |
5.54e-01 |
Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs) |
103 |
5.36e-07 |
8.07e-06 |
0.27700 |
1.27e-01 |
2.46e-01 |
2.62e-02 |
1.64e-05 |
Fertilization |
15 |
1.95e-01 |
3.32e-01 |
0.27700 |
6.13e-02 |
-2.70e-01 |
6.81e-01 |
7.05e-02 |
TP53 regulates transcription of additional cell cycle genes whose exact role in the p53 pathway remain uncertain |
19 |
8.90e-02 |
1.90e-01 |
0.27600 |
4.09e-02 |
2.73e-01 |
7.58e-01 |
3.91e-02 |
SHC1 events in EGFR signaling |
11 |
3.19e-01 |
4.62e-01 |
0.27600 |
-9.27e-02 |
2.60e-01 |
5.95e-01 |
1.35e-01 |
Interleukin-1 signaling |
96 |
9.53e-05 |
6.82e-04 |
0.27500 |
-1.39e-01 |
2.37e-01 |
1.84e-02 |
5.88e-05 |
APC:Cdc20 mediated degradation of cell cycle proteins prior to satisfation of the cell cycle checkpoint |
71 |
1.37e-03 |
6.90e-03 |
0.27500 |
-1.96e-01 |
1.92e-01 |
4.37e-03 |
5.06e-03 |
Signaling by RAF1 mutants |
38 |
1.65e-02 |
5.35e-02 |
0.27500 |
-5.65e-02 |
2.69e-01 |
5.47e-01 |
4.17e-03 |
Respiratory electron transport, ATP synthesis by chemiosmotic coupling, and heat production by uncoupling proteins. |
120 |
5.69e-08 |
1.31e-06 |
0.27400 |
2.38e-01 |
1.37e-01 |
6.91e-06 |
9.66e-03 |
Cyclin A:Cdk2-associated events at S phase entry |
83 |
3.58e-04 |
2.16e-03 |
0.27400 |
-1.41e-01 |
2.35e-01 |
2.68e-02 |
2.11e-04 |
Glycogen synthesis |
15 |
1.49e-01 |
2.75e-01 |
0.27400 |
5.05e-02 |
2.69e-01 |
7.35e-01 |
7.10e-02 |
Sealing of the nuclear envelope (NE) by ESCRT-III |
23 |
8.65e-02 |
1.87e-01 |
0.27400 |
-6.23e-02 |
2.66e-01 |
6.05e-01 |
2.70e-02 |
TICAM1,TRAF6-dependent induction of TAK1 complex |
11 |
3.03e-01 |
4.53e-01 |
0.27200 |
-4.33e-02 |
2.69e-01 |
8.04e-01 |
1.23e-01 |
Programmed Cell Death |
175 |
1.23e-08 |
3.74e-07 |
0.27200 |
-6.16e-02 |
2.65e-01 |
1.61e-01 |
1.59e-09 |
Post-translational protein phosphorylation |
90 |
5.27e-06 |
5.64e-05 |
0.27200 |
1.22e-01 |
2.43e-01 |
4.51e-02 |
7.00e-05 |
rRNA processing in the nucleus and cytosol |
154 |
7.37e-09 |
2.52e-07 |
0.27200 |
3.75e-02 |
2.69e-01 |
4.23e-01 |
8.49e-09 |
Cellular response to heat stress |
93 |
1.61e-04 |
1.09e-03 |
0.27100 |
-1.35e-01 |
2.35e-01 |
2.45e-02 |
8.91e-05 |
TNFR2 non-canonical NF-kB pathway |
90 |
2.85e-04 |
1.77e-03 |
0.27100 |
-2.08e-01 |
1.74e-01 |
6.57e-04 |
4.45e-03 |
Plasma lipoprotein remodeling |
27 |
5.63e-02 |
1.34e-01 |
0.27100 |
2.67e-01 |
-4.67e-02 |
1.65e-02 |
6.75e-01 |
Membrane binding and targetting of GAG proteins |
14 |
2.18e-01 |
3.56e-01 |
0.27100 |
-3.30e-02 |
2.69e-01 |
8.31e-01 |
8.19e-02 |
Synthesis And Processing Of GAG, GAGPOL Polyproteins |
14 |
2.18e-01 |
3.56e-01 |
0.27100 |
-3.30e-02 |
2.69e-01 |
8.31e-01 |
8.19e-02 |
Constitutive Signaling by NOTCH1 HD Domain Mutants |
15 |
2.52e-01 |
3.97e-01 |
0.27000 |
-2.24e-01 |
1.52e-01 |
1.34e-01 |
3.10e-01 |
Signaling by NOTCH1 HD Domain Mutants in Cancer |
15 |
2.52e-01 |
3.97e-01 |
0.27000 |
-2.24e-01 |
1.52e-01 |
1.34e-01 |
3.10e-01 |
Interleukin-27 signaling |
10 |
4.01e-01 |
5.42e-01 |
0.27000 |
-1.57e-01 |
2.20e-01 |
3.91e-01 |
2.29e-01 |
Extra-nuclear estrogen signaling |
67 |
9.35e-04 |
4.93e-03 |
0.27000 |
-5.52e-02 |
2.64e-01 |
4.35e-01 |
1.88e-04 |
Regulation of Complement cascade |
52 |
5.48e-03 |
2.19e-02 |
0.26900 |
-7.84e-02 |
2.58e-01 |
3.28e-01 |
1.31e-03 |
SEMA3A-Plexin repulsion signaling by inhibiting Integrin adhesion |
14 |
2.64e-01 |
4.09e-01 |
0.26800 |
-1.10e-01 |
2.45e-01 |
4.76e-01 |
1.13e-01 |
EPH-Ephrin signaling |
89 |
4.54e-05 |
3.66e-04 |
0.26800 |
5.55e-04 |
2.68e-01 |
9.93e-01 |
1.25e-05 |
Cleavage of the damaged purine |
17 |
2.19e-01 |
3.56e-01 |
0.26800 |
2.13e-01 |
-1.62e-01 |
1.28e-01 |
2.48e-01 |
Depurination |
17 |
2.19e-01 |
3.56e-01 |
0.26800 |
2.13e-01 |
-1.62e-01 |
1.28e-01 |
2.48e-01 |
Recognition and association of DNA glycosylase with site containing an affected purine |
17 |
2.19e-01 |
3.56e-01 |
0.26800 |
2.13e-01 |
-1.62e-01 |
1.28e-01 |
2.48e-01 |
ADP signalling through P2Y purinoceptor 12 |
19 |
1.21e-01 |
2.38e-01 |
0.26700 |
-3.23e-03 |
2.67e-01 |
9.81e-01 |
4.40e-02 |
Methylation |
12 |
2.94e-01 |
4.44e-01 |
0.26700 |
-2.61e-01 |
5.44e-02 |
1.18e-01 |
7.44e-01 |
Non-integrin membrane-ECM interactions |
41 |
4.09e-03 |
1.76e-02 |
0.26700 |
1.63e-01 |
2.11e-01 |
7.03e-02 |
1.97e-02 |
Respiratory electron transport |
99 |
2.09e-06 |
2.50e-05 |
0.26600 |
2.21e-01 |
1.48e-01 |
1.44e-04 |
1.12e-02 |
Lagging Strand Synthesis |
19 |
1.15e-01 |
2.30e-01 |
0.26600 |
2.65e-01 |
1.76e-02 |
4.56e-02 |
8.95e-01 |
Pyruvate metabolism |
28 |
7.57e-02 |
1.71e-01 |
0.26500 |
-1.15e-01 |
2.39e-01 |
2.91e-01 |
2.85e-02 |
IRAK2 mediated activation of TAK1 complex |
10 |
3.60e-01 |
5.04e-01 |
0.26500 |
-4.84e-02 |
2.61e-01 |
7.91e-01 |
1.53e-01 |
p38MAPK events |
13 |
2.60e-01 |
4.07e-01 |
0.26500 |
-3.64e-02 |
2.62e-01 |
8.20e-01 |
1.02e-01 |
Pyruvate metabolism and Citric Acid (TCA) cycle |
52 |
3.41e-03 |
1.53e-02 |
0.26400 |
1.41e-03 |
2.64e-01 |
9.86e-01 |
1.00e-03 |
Branched-chain amino acid catabolism |
21 |
1.51e-01 |
2.78e-01 |
0.26300 |
-2.34e-01 |
1.20e-01 |
6.29e-02 |
3.40e-01 |
Translation |
256 |
4.93e-11 |
3.40e-09 |
0.26300 |
-8.73e-02 |
2.48e-01 |
1.65e-02 |
9.09e-12 |
DNA Damage/Telomere Stress Induced Senescence |
39 |
1.27e-02 |
4.33e-02 |
0.26300 |
2.62e-01 |
2.22e-02 |
4.71e-03 |
8.10e-01 |
Gap-filling DNA repair synthesis and ligation in GG-NER |
24 |
4.36e-02 |
1.13e-01 |
0.26200 |
1.73e-01 |
1.97e-01 |
1.41e-01 |
9.54e-02 |
Dissolution of Fibrin Clot |
12 |
2.60e-01 |
4.07e-01 |
0.26200 |
2.52e-02 |
2.61e-01 |
8.80e-01 |
1.18e-01 |
Activated NOTCH1 Transmits Signal to the Nucleus |
29 |
7.30e-02 |
1.66e-01 |
0.26200 |
-2.38e-01 |
1.09e-01 |
2.66e-02 |
3.08e-01 |
Glucagon-type ligand receptors |
23 |
7.97e-02 |
1.77e-01 |
0.26200 |
1.42e-02 |
2.61e-01 |
9.06e-01 |
3.00e-02 |
Signaling by Activin |
12 |
2.80e-01 |
4.27e-01 |
0.26200 |
2.62e-01 |
-7.84e-03 |
1.17e-01 |
9.62e-01 |
Switching of origins to a post-replicative state |
88 |
4.52e-04 |
2.59e-03 |
0.26100 |
-1.28e-01 |
2.28e-01 |
3.87e-02 |
2.17e-04 |
Glycolysis |
66 |
2.92e-04 |
1.79e-03 |
0.26000 |
2.34e-01 |
1.14e-01 |
1.02e-03 |
1.11e-01 |
Transcription of E2F targets under negative control by DREAM complex |
19 |
1.41e-01 |
2.65e-01 |
0.26000 |
-1.58e-02 |
2.59e-01 |
9.05e-01 |
5.06e-02 |
The role of Nef in HIV-1 replication and disease pathogenesis |
27 |
1.02e-01 |
2.10e-01 |
0.25900 |
-1.44e-01 |
2.16e-01 |
1.97e-01 |
5.24e-02 |
Degradation of cysteine and homocysteine |
13 |
3.38e-01 |
4.82e-01 |
0.25900 |
1.99e-01 |
-1.65e-01 |
2.13e-01 |
3.02e-01 |
Transcription of the HIV genome |
68 |
1.34e-03 |
6.79e-03 |
0.25900 |
-4.48e-02 |
2.55e-01 |
5.23e-01 |
2.78e-04 |
Phase 2 - plateau phase |
12 |
3.70e-01 |
5.13e-01 |
0.25800 |
2.04e-01 |
-1.57e-01 |
2.21e-01 |
3.45e-01 |
ECM proteoglycans |
47 |
3.01e-03 |
1.40e-02 |
0.25700 |
2.14e-01 |
1.42e-01 |
1.11e-02 |
9.30e-02 |
APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins in late mitosis/early G1 |
72 |
2.89e-03 |
1.35e-02 |
0.25700 |
-1.71e-01 |
1.91e-01 |
1.19e-02 |
5.13e-03 |
trans-Golgi Network Vesicle Budding |
70 |
3.42e-03 |
1.53e-02 |
0.25600 |
-1.74e-01 |
1.88e-01 |
1.19e-02 |
6.44e-03 |
Polymerase switching on the C-strand of the telomere |
25 |
1.28e-01 |
2.46e-01 |
0.25600 |
2.08e-01 |
-1.50e-01 |
7.19e-02 |
1.94e-01 |
NOTCH2 intracellular domain regulates transcription |
11 |
2.54e-01 |
3.99e-01 |
0.25600 |
1.94e-01 |
1.67e-01 |
2.64e-01 |
3.38e-01 |
Platelet degranulation |
118 |
5.21e-06 |
5.61e-05 |
0.25600 |
4.45e-03 |
2.56e-01 |
9.34e-01 |
1.57e-06 |
Activation of the pre-replicative complex |
32 |
1.88e-02 |
5.92e-02 |
0.25600 |
1.62e-01 |
1.98e-01 |
1.12e-01 |
5.26e-02 |
JNK (c-Jun kinases) phosphorylation and activation mediated by activated human TAK1 |
16 |
1.65e-01 |
2.99e-01 |
0.25600 |
6.22e-02 |
2.48e-01 |
6.67e-01 |
8.61e-02 |
Zinc transporters |
16 |
2.03e-01 |
3.41e-01 |
0.25600 |
-2.55e-01 |
1.58e-02 |
7.73e-02 |
9.13e-01 |
Base Excision Repair |
51 |
6.55e-03 |
2.52e-02 |
0.25500 |
2.55e-01 |
-2.10e-02 |
1.67e-03 |
7.96e-01 |
Synthesis of PE |
13 |
3.33e-01 |
4.77e-01 |
0.25500 |
2.27e-01 |
-1.17e-01 |
1.57e-01 |
4.65e-01 |
Anti-inflammatory response favouring Leishmania parasite infection |
125 |
1.81e-05 |
1.66e-04 |
0.25500 |
-8.98e-02 |
2.39e-01 |
8.33e-02 |
4.05e-06 |
Leishmania parasite growth and survival |
125 |
1.81e-05 |
1.66e-04 |
0.25500 |
-8.98e-02 |
2.39e-01 |
8.33e-02 |
4.05e-06 |
EGR2 and SOX10-mediated initiation of Schwann cell myelination |
25 |
7.58e-02 |
1.71e-01 |
0.25500 |
8.64e-03 |
2.55e-01 |
9.40e-01 |
2.76e-02 |
Signaling by high-kinase activity BRAF mutants |
33 |
4.67e-02 |
1.18e-01 |
0.25500 |
-5.30e-02 |
2.49e-01 |
5.98e-01 |
1.33e-02 |
Budding and maturation of HIV virion |
26 |
7.50e-02 |
1.70e-01 |
0.25500 |
-1.15e-02 |
2.54e-01 |
9.19e-01 |
2.49e-02 |
Prostacyclin signalling through prostacyclin receptor |
17 |
1.99e-01 |
3.36e-01 |
0.25400 |
-3.93e-02 |
2.51e-01 |
7.79e-01 |
7.27e-02 |
SIRT1 negatively regulates rRNA expression |
17 |
1.28e-01 |
2.46e-01 |
0.25400 |
2.15e-01 |
1.37e-01 |
1.26e-01 |
3.29e-01 |
Fatty acyl-CoA biosynthesis |
29 |
8.05e-02 |
1.78e-01 |
0.25400 |
-9.18e-02 |
2.37e-01 |
3.92e-01 |
2.71e-02 |
Vitamin D (calciferol) metabolism |
11 |
3.42e-01 |
4.86e-01 |
0.25400 |
2.53e-01 |
-1.97e-02 |
1.47e-01 |
9.10e-01 |
Paradoxical activation of RAF signaling by kinase inactive BRAF |
41 |
2.54e-02 |
7.41e-02 |
0.25400 |
-6.84e-02 |
2.44e-01 |
4.49e-01 |
6.86e-03 |
Signaling by RAS mutants |
41 |
2.54e-02 |
7.41e-02 |
0.25400 |
-6.84e-02 |
2.44e-01 |
4.49e-01 |
6.86e-03 |
Signaling by moderate kinase activity BRAF mutants |
41 |
2.54e-02 |
7.41e-02 |
0.25400 |
-6.84e-02 |
2.44e-01 |
4.49e-01 |
6.86e-03 |
Signaling downstream of RAS mutants |
41 |
2.54e-02 |
7.41e-02 |
0.25400 |
-6.84e-02 |
2.44e-01 |
4.49e-01 |
6.86e-03 |
Voltage gated Potassium channels |
35 |
3.12e-02 |
8.64e-02 |
0.25300 |
9.22e-03 |
-2.53e-01 |
9.25e-01 |
9.56e-03 |
APC/C:Cdc20 mediated degradation of mitotic proteins |
73 |
3.10e-03 |
1.43e-02 |
0.25300 |
-1.70e-01 |
1.88e-01 |
1.21e-02 |
5.56e-03 |
Signaling by EGFR |
46 |
2.27e-02 |
6.79e-02 |
0.25300 |
-2.21e-01 |
1.24e-01 |
9.56e-03 |
1.46e-01 |
Condensation of Prometaphase Chromosomes |
11 |
2.64e-01 |
4.09e-01 |
0.25300 |
1.63e-01 |
1.93e-01 |
3.49e-01 |
2.68e-01 |
HIV Infection |
222 |
1.07e-08 |
3.42e-07 |
0.25200 |
-1.06e-01 |
2.29e-01 |
6.37e-03 |
4.51e-09 |
p53-Dependent G1 DNA Damage Response |
62 |
7.81e-03 |
2.94e-02 |
0.25200 |
-1.74e-01 |
1.82e-01 |
1.78e-02 |
1.32e-02 |
p53-Dependent G1/S DNA damage checkpoint |
62 |
7.81e-03 |
2.94e-02 |
0.25200 |
-1.74e-01 |
1.82e-01 |
1.78e-02 |
1.32e-02 |
Regulation of gene expression in late stage (branching morphogenesis) pancreatic bud precursor cells |
14 |
1.86e-01 |
3.21e-01 |
0.25200 |
1.63e-01 |
1.92e-01 |
2.90e-01 |
2.15e-01 |
Signaling by BMP |
23 |
8.97e-02 |
1.92e-01 |
0.25100 |
3.42e-02 |
2.49e-01 |
7.77e-01 |
3.86e-02 |
Ketone body metabolism |
10 |
4.51e-01 |
5.87e-01 |
0.25100 |
-2.08e-01 |
1.41e-01 |
2.55e-01 |
4.40e-01 |
TRAF6-mediated induction of TAK1 complex within TLR4 complex |
15 |
2.79e-01 |
4.27e-01 |
0.25100 |
-8.86e-02 |
2.35e-01 |
5.53e-01 |
1.15e-01 |
O-glycosylation of TSR domain-containing proteins |
37 |
1.20e-02 |
4.13e-02 |
0.25100 |
1.73e-01 |
1.82e-01 |
6.87e-02 |
5.58e-02 |
Selenoamino acid metabolism |
83 |
5.28e-05 |
4.16e-04 |
0.25100 |
1.55e-01 |
1.97e-01 |
1.44e-02 |
1.94e-03 |
Complex I biogenesis |
55 |
1.48e-03 |
7.42e-03 |
0.25100 |
1.99e-01 |
1.53e-01 |
1.08e-02 |
5.04e-02 |
Pregnenolone biosynthesis |
11 |
2.96e-01 |
4.46e-01 |
0.25000 |
-7.74e-02 |
-2.38e-01 |
6.57e-01 |
1.71e-01 |
Transcriptional Regulation by E2F6 |
34 |
5.38e-02 |
1.30e-01 |
0.25000 |
-7.56e-02 |
2.38e-01 |
4.46e-01 |
1.62e-02 |
Retrograde neurotrophin signalling |
14 |
3.00e-01 |
4.50e-01 |
0.25000 |
-7.51e-02 |
2.38e-01 |
6.27e-01 |
1.23e-01 |
Interleukin-2 signaling |
11 |
2.84e-01 |
4.32e-01 |
0.25000 |
-2.23e-01 |
-1.13e-01 |
2.01e-01 |
5.18e-01 |
Interleukin-2 family signaling |
36 |
3.42e-02 |
9.21e-02 |
0.24900 |
-2.48e-01 |
2.24e-02 |
9.93e-03 |
8.16e-01 |
Host Interactions of HIV factors |
126 |
6.12e-05 |
4.68e-04 |
0.24900 |
-1.52e-01 |
1.97e-01 |
3.21e-03 |
1.31e-04 |
Sialic acid metabolism |
28 |
7.57e-02 |
1.71e-01 |
0.24900 |
-3.14e-02 |
2.47e-01 |
7.73e-01 |
2.36e-02 |
Response to elevated platelet cytosolic Ca2+ |
123 |
8.33e-06 |
8.53e-05 |
0.24900 |
-1.02e-02 |
2.49e-01 |
8.45e-01 |
1.90e-06 |
Activation of the phototransduction cascade |
10 |
4.02e-01 |
5.42e-01 |
0.24900 |
3.82e-02 |
-2.46e-01 |
8.34e-01 |
1.78e-01 |
Translation of structural proteins |
28 |
1.11e-01 |
2.24e-01 |
0.24900 |
-2.10e-01 |
1.34e-01 |
5.46e-02 |
2.20e-01 |
S Phase |
158 |
9.88e-07 |
1.36e-05 |
0.24900 |
-5.55e-02 |
2.43e-01 |
2.30e-01 |
1.46e-07 |
PCP/CE pathway |
89 |
1.13e-03 |
5.83e-03 |
0.24800 |
-1.90e-01 |
1.60e-01 |
1.94e-03 |
9.29e-03 |
Defective B3GALTL causes Peters-plus syndrome (PpS) |
36 |
1.49e-02 |
4.90e-02 |
0.24800 |
1.69e-01 |
1.81e-01 |
7.87e-02 |
5.98e-02 |
Signaling by TGF-beta Receptor Complex |
73 |
3.25e-03 |
1.48e-02 |
0.24800 |
-1.21e-01 |
2.16e-01 |
7.44e-02 |
1.42e-03 |
Intrinsic Pathway of Fibrin Clot Formation |
16 |
1.56e-01 |
2.85e-01 |
0.24700 |
1.70e-01 |
1.80e-01 |
2.39e-01 |
2.14e-01 |
Activation of APC/C and APC/C:Cdc20 mediated degradation of mitotic proteins |
74 |
4.03e-03 |
1.74e-02 |
0.24600 |
-1.67e-01 |
1.81e-01 |
1.31e-02 |
7.28e-03 |
p75NTR signals via NF-kB |
16 |
3.02e-01 |
4.51e-01 |
0.24600 |
-1.62e-01 |
1.85e-01 |
2.62e-01 |
2.00e-01 |
Formation of RNA Pol II elongation complex |
57 |
6.12e-03 |
2.39e-02 |
0.24600 |
-3.17e-02 |
2.44e-01 |
6.79e-01 |
1.47e-03 |
RNA Polymerase II Transcription Elongation |
57 |
6.12e-03 |
2.39e-02 |
0.24600 |
-3.17e-02 |
2.44e-01 |
6.79e-01 |
1.47e-03 |
Defects in vitamin and cofactor metabolism |
21 |
1.21e-01 |
2.38e-01 |
0.24500 |
-2.42e-01 |
-3.96e-02 |
5.52e-02 |
7.54e-01 |
Signalling to RAS |
19 |
2.12e-01 |
3.51e-01 |
0.24500 |
-8.11e-02 |
2.31e-01 |
5.41e-01 |
8.14e-02 |
Alpha-protein kinase 1 signaling pathway |
11 |
3.27e-01 |
4.69e-01 |
0.24500 |
4.76e-02 |
2.40e-01 |
7.85e-01 |
1.68e-01 |
ER to Golgi Anterograde Transport |
126 |
7.20e-05 |
5.31e-04 |
0.24500 |
-1.27e-01 |
2.09e-01 |
1.38e-02 |
5.18e-05 |
Processing of Intronless Pre-mRNAs |
17 |
2.11e-01 |
3.49e-01 |
0.24500 |
-2.44e-01 |
1.40e-02 |
8.13e-02 |
9.20e-01 |
Triglyceride catabolism |
18 |
1.31e-01 |
2.51e-01 |
0.24400 |
1.53e-01 |
1.90e-01 |
2.61e-01 |
1.62e-01 |
Triglyceride biosynthesis |
12 |
4.14e-01 |
5.54e-01 |
0.24400 |
1.82e-01 |
-1.62e-01 |
2.76e-01 |
3.30e-01 |
Carnitine metabolism |
12 |
3.18e-01 |
4.62e-01 |
0.24300 |
2.43e-01 |
1.56e-02 |
1.45e-01 |
9.26e-01 |
Keratan sulfate biosynthesis |
24 |
7.59e-02 |
1.71e-01 |
0.24300 |
1.03e-01 |
2.20e-01 |
3.83e-01 |
6.24e-02 |
Ion transport by P-type ATPases |
46 |
1.55e-02 |
5.08e-02 |
0.24300 |
-9.99e-03 |
2.42e-01 |
9.07e-01 |
4.45e-03 |
COPII-mediated vesicle transport |
63 |
1.05e-02 |
3.68e-02 |
0.24200 |
-1.65e-01 |
1.77e-01 |
2.35e-02 |
1.51e-02 |
Translocation of ZAP-70 to Immunological synapse |
13 |
2.62e-01 |
4.08e-01 |
0.24200 |
-2.31e-01 |
-7.21e-02 |
1.49e-01 |
6.53e-01 |
VEGFR2 mediated cell proliferation |
19 |
2.54e-01 |
3.99e-01 |
0.24200 |
-1.67e-01 |
1.74e-01 |
2.07e-01 |
1.88e-01 |
DAP12 interactions |
34 |
8.62e-02 |
1.87e-01 |
0.24100 |
-1.79e-01 |
1.63e-01 |
7.16e-02 |
1.01e-01 |
RUNX2 regulates osteoblast differentiation |
22 |
1.18e-01 |
2.36e-01 |
0.24100 |
3.60e-02 |
2.39e-01 |
7.70e-01 |
5.28e-02 |
Pyrimidine catabolism |
12 |
2.70e-01 |
4.16e-01 |
0.24100 |
2.01e-01 |
1.34e-01 |
2.29e-01 |
4.23e-01 |
Regulation of APC/C activators between G1/S and early anaphase |
78 |
3.78e-03 |
1.67e-02 |
0.24100 |
-1.73e-01 |
1.68e-01 |
8.43e-03 |
1.03e-02 |
Caspase activation via Death Receptors in the presence of ligand |
13 |
3.93e-01 |
5.36e-01 |
0.24100 |
-1.81e-01 |
1.59e-01 |
2.58e-01 |
3.22e-01 |
Signaling by ERBB2 ECD mutants |
16 |
3.18e-01 |
4.62e-01 |
0.24100 |
-1.72e-01 |
1.68e-01 |
2.33e-01 |
2.44e-01 |
The citric acid (TCA) cycle and respiratory electron transport |
168 |
1.10e-08 |
3.43e-07 |
0.24100 |
1.62e-01 |
1.78e-01 |
2.88e-04 |
7.32e-05 |
Processive synthesis on the lagging strand |
14 |
3.40e-01 |
4.84e-01 |
0.24100 |
2.22e-01 |
-9.29e-02 |
1.50e-01 |
5.47e-01 |
Signaling by Erythropoietin |
25 |
1.64e-01 |
2.98e-01 |
0.24100 |
-1.44e-01 |
1.93e-01 |
2.12e-01 |
9.58e-02 |
RHO GTPases Activate NADPH Oxidases |
21 |
1.77e-01 |
3.11e-01 |
0.24000 |
-2.35e-01 |
5.19e-02 |
6.25e-02 |
6.81e-01 |
G1/S Transition |
128 |
2.93e-05 |
2.55e-04 |
0.24000 |
-5.43e-02 |
2.34e-01 |
2.89e-01 |
4.92e-06 |
Telomere C-strand (Lagging Strand) Synthesis |
33 |
7.21e-02 |
1.65e-01 |
0.24000 |
2.30e-01 |
-6.98e-02 |
2.24e-02 |
4.88e-01 |
Toll-like Receptor Cascades |
138 |
1.08e-05 |
1.06e-04 |
0.24000 |
-4.42e-02 |
2.36e-01 |
3.71e-01 |
1.74e-06 |
G1/S DNA Damage Checkpoints |
64 |
1.07e-02 |
3.75e-02 |
0.24000 |
-1.70e-01 |
1.69e-01 |
1.84e-02 |
1.96e-02 |
Removal of the Flap Intermediate from the C-strand |
16 |
2.38e-01 |
3.81e-01 |
0.23900 |
2.39e-01 |
-4.04e-04 |
9.74e-02 |
9.98e-01 |
Glycogen metabolism |
26 |
8.26e-02 |
1.81e-01 |
0.23900 |
3.86e-02 |
2.36e-01 |
7.33e-01 |
3.71e-02 |
Sema4D induced cell migration and growth-cone collapse |
20 |
1.19e-01 |
2.36e-01 |
0.23900 |
2.05e-01 |
1.24e-01 |
1.13e-01 |
3.38e-01 |
Infectious disease |
693 |
4.47e-24 |
3.13e-21 |
0.23900 |
-5.48e-02 |
2.32e-01 |
1.46e-02 |
3.51e-25 |
Signaling by PDGF |
50 |
1.81e-02 |
5.72e-02 |
0.23800 |
-5.72e-02 |
2.31e-01 |
4.84e-01 |
4.65e-03 |
G beta:gamma signalling through BTK |
16 |
2.50e-01 |
3.96e-01 |
0.23800 |
-1.59e-02 |
2.38e-01 |
9.12e-01 |
9.96e-02 |
Mitochondrial Fatty Acid Beta-Oxidation |
34 |
6.68e-02 |
1.54e-01 |
0.23800 |
-6.09e-02 |
2.30e-01 |
5.39e-01 |
2.02e-02 |
Sema4D in semaphorin signaling |
24 |
7.89e-02 |
1.75e-01 |
0.23700 |
1.35e-01 |
1.95e-01 |
2.53e-01 |
9.77e-02 |
Circadian Clock |
67 |
4.88e-03 |
2.00e-02 |
0.23700 |
-5.48e-02 |
2.31e-01 |
4.38e-01 |
1.11e-03 |
Signaling by Hedgehog |
133 |
7.99e-05 |
5.87e-04 |
0.23500 |
-2.07e-01 |
1.12e-01 |
3.83e-05 |
2.61e-02 |
Cholesterol biosynthesis |
24 |
1.92e-01 |
3.29e-01 |
0.23400 |
1.92e-01 |
-1.33e-01 |
1.03e-01 |
2.59e-01 |
PTEN Regulation |
139 |
8.95e-05 |
6.47e-04 |
0.23400 |
-1.61e-01 |
1.70e-01 |
1.08e-03 |
5.59e-04 |
Downregulation of ERBB2:ERBB3 signaling |
13 |
4.02e-01 |
5.42e-01 |
0.23400 |
-1.16e-01 |
2.03e-01 |
4.69e-01 |
2.05e-01 |
FGFR2 ligand binding and activation |
10 |
5.05e-01 |
6.22e-01 |
0.23200 |
1.94e-01 |
-1.28e-01 |
2.88e-01 |
4.83e-01 |
SHC1 events in ERBB4 signaling |
12 |
3.87e-01 |
5.31e-01 |
0.23200 |
-3.70e-02 |
2.29e-01 |
8.24e-01 |
1.69e-01 |
Insulin processing |
25 |
1.74e-01 |
3.08e-01 |
0.23200 |
-1.06e-01 |
2.07e-01 |
3.58e-01 |
7.38e-02 |
Ion homeostasis |
43 |
1.79e-02 |
5.65e-02 |
0.23100 |
7.00e-02 |
2.20e-01 |
4.27e-01 |
1.26e-02 |
Activated NTRK2 signals through FRS2 and FRS3 |
11 |
4.68e-01 |
5.95e-01 |
0.23000 |
-1.04e-01 |
2.06e-01 |
5.51e-01 |
2.38e-01 |
Disorders of Developmental Biology |
13 |
3.94e-01 |
5.36e-01 |
0.23000 |
-7.95e-02 |
2.16e-01 |
6.20e-01 |
1.78e-01 |
Disorders of Nervous System Development |
13 |
3.94e-01 |
5.36e-01 |
0.23000 |
-7.95e-02 |
2.16e-01 |
6.20e-01 |
1.78e-01 |
Loss of function of MECP2 in Rett syndrome |
13 |
3.94e-01 |
5.36e-01 |
0.23000 |
-7.95e-02 |
2.16e-01 |
6.20e-01 |
1.78e-01 |
Pervasive developmental disorders |
13 |
3.94e-01 |
5.36e-01 |
0.23000 |
-7.95e-02 |
2.16e-01 |
6.20e-01 |
1.78e-01 |
rRNA modification in the nucleus and cytosol |
55 |
1.99e-02 |
6.15e-02 |
0.23000 |
-8.10e-02 |
2.15e-01 |
2.99e-01 |
5.78e-03 |
Aggrephagy |
20 |
2.70e-01 |
4.16e-01 |
0.23000 |
-1.54e-01 |
1.70e-01 |
2.32e-01 |
1.88e-01 |
COPI-mediated anterograde transport |
77 |
4.84e-03 |
1.98e-02 |
0.23000 |
-9.55e-02 |
2.09e-01 |
1.48e-01 |
1.54e-03 |
NRIF signals cell death from the nucleus |
16 |
3.51e-01 |
4.94e-01 |
0.23000 |
-1.45e-01 |
1.78e-01 |
3.16e-01 |
2.18e-01 |
DNA Damage Bypass |
46 |
1.31e-02 |
4.42e-02 |
0.22900 |
8.26e-02 |
2.14e-01 |
3.33e-01 |
1.20e-02 |
Signaling by NODAL |
16 |
2.84e-01 |
4.32e-01 |
0.22900 |
2.28e-01 |
-2.34e-02 |
1.15e-01 |
8.71e-01 |
Hedgehog 'off' state |
98 |
1.50e-03 |
7.48e-03 |
0.22900 |
-1.96e-01 |
1.18e-01 |
8.11e-04 |
4.37e-02 |
HIV Transcription Initiation |
46 |
3.19e-02 |
8.70e-02 |
0.22900 |
-4.61e-02 |
2.24e-01 |
5.89e-01 |
8.65e-03 |
RNA Polymerase II HIV Promoter Escape |
46 |
3.19e-02 |
8.70e-02 |
0.22900 |
-4.61e-02 |
2.24e-01 |
5.89e-01 |
8.65e-03 |
RNA Polymerase II Promoter Escape |
46 |
3.19e-02 |
8.70e-02 |
0.22900 |
-4.61e-02 |
2.24e-01 |
5.89e-01 |
8.65e-03 |
RNA Polymerase II Transcription Initiation |
46 |
3.19e-02 |
8.70e-02 |
0.22900 |
-4.61e-02 |
2.24e-01 |
5.89e-01 |
8.65e-03 |
RNA Polymerase II Transcription Initiation And Promoter Clearance |
46 |
3.19e-02 |
8.70e-02 |
0.22900 |
-4.61e-02 |
2.24e-01 |
5.89e-01 |
8.65e-03 |
RNA Polymerase II Transcription Pre-Initiation And Promoter Opening |
46 |
3.19e-02 |
8.70e-02 |
0.22900 |
-4.61e-02 |
2.24e-01 |
5.89e-01 |
8.65e-03 |
Asparagine N-linked glycosylation |
265 |
4.38e-08 |
1.10e-06 |
0.22800 |
-1.80e-01 |
1.40e-01 |
4.83e-07 |
8.72e-05 |
Transcriptional activity of SMAD2/SMAD3:SMAD4 heterotrimer |
44 |
5.64e-02 |
1.35e-01 |
0.22800 |
-1.30e-01 |
1.88e-01 |
1.37e-01 |
3.13e-02 |
SLC-mediated transmembrane transport |
217 |
9.57e-07 |
1.34e-05 |
0.22800 |
1.44e-01 |
-1.77e-01 |
2.56e-04 |
7.60e-06 |
NF-kB is activated and signals survival |
13 |
4.33e-01 |
5.70e-01 |
0.22800 |
-1.73e-01 |
1.48e-01 |
2.80e-01 |
3.55e-01 |
PERK regulates gene expression |
30 |
1.37e-01 |
2.60e-01 |
0.22800 |
-1.18e-01 |
1.95e-01 |
2.64e-01 |
6.45e-02 |
Regulation of TP53 Expression and Degradation |
34 |
5.83e-02 |
1.37e-01 |
0.22700 |
1.82e-02 |
2.26e-01 |
8.55e-01 |
2.23e-02 |
Estrogen-dependent nuclear events downstream of ESR-membrane signaling |
21 |
2.16e-01 |
3.55e-01 |
0.22700 |
-5.38e-02 |
2.20e-01 |
6.70e-01 |
8.03e-02 |
CRMPs in Sema3A signaling |
16 |
3.61e-01 |
5.05e-01 |
0.22700 |
-1.48e-01 |
1.71e-01 |
3.05e-01 |
2.36e-01 |
RAF-independent MAPK1/3 activation |
22 |
1.81e-01 |
3.16e-01 |
0.22600 |
-1.62e-02 |
2.25e-01 |
8.95e-01 |
6.73e-02 |
Interleukin-4 and Interleukin-13 signaling |
95 |
4.98e-04 |
2.84e-03 |
0.22600 |
4.07e-03 |
2.26e-01 |
9.45e-01 |
1.47e-04 |
Signaling by WNT in cancer |
33 |
4.14e-02 |
1.08e-01 |
0.22600 |
1.68e-01 |
1.50e-01 |
9.47e-02 |
1.35e-01 |
Extracellular matrix organization |
252 |
2.09e-10 |
1.22e-08 |
0.22500 |
6.98e-02 |
2.14e-01 |
5.70e-02 |
4.94e-09 |
Mitochondrial translation |
94 |
2.05e-03 |
9.97e-03 |
0.22500 |
-1.01e-01 |
2.02e-01 |
9.15e-02 |
7.38e-04 |
Signaling by FGFR2 IIIa TM |
19 |
1.69e-01 |
3.04e-01 |
0.22500 |
1.04e-01 |
2.00e-01 |
4.35e-01 |
1.31e-01 |
AKT phosphorylates targets in the cytosol |
14 |
3.08e-01 |
4.55e-01 |
0.22500 |
3.34e-02 |
2.22e-01 |
8.29e-01 |
1.50e-01 |
VLDLR internalisation and degradation |
12 |
4.61e-01 |
5.93e-01 |
0.22500 |
-1.94e-01 |
1.12e-01 |
2.44e-01 |
5.00e-01 |
Signaling by TGFB family members |
96 |
1.01e-03 |
5.25e-03 |
0.22400 |
-4.65e-02 |
2.19e-01 |
4.31e-01 |
2.04e-04 |
Synthesis of PIPs at the plasma membrane |
52 |
2.31e-02 |
6.85e-02 |
0.22400 |
-4.33e-02 |
2.20e-01 |
5.90e-01 |
6.05e-03 |
Leishmania infection |
204 |
3.73e-07 |
6.08e-06 |
0.22400 |
-3.74e-02 |
2.21e-01 |
3.59e-01 |
5.45e-08 |
TP53 Regulates Transcription of Cell Cycle Genes |
46 |
1.43e-02 |
4.73e-02 |
0.22400 |
1.99e-01 |
1.04e-01 |
1.98e-02 |
2.23e-01 |
Tetrahydrobiopterin (BH4) synthesis, recycling, salvage and regulation |
10 |
5.11e-01 |
6.26e-01 |
0.22400 |
-2.08e-01 |
8.36e-02 |
2.55e-01 |
6.47e-01 |
Mitotic G1 phase and G1/S transition |
145 |
3.02e-05 |
2.60e-04 |
0.22400 |
-4.32e-02 |
2.20e-01 |
3.70e-01 |
5.07e-06 |
G-protein activation |
24 |
1.39e-01 |
2.62e-01 |
0.22400 |
2.49e-02 |
2.22e-01 |
8.33e-01 |
5.93e-02 |
Mitochondrial translation initiation |
88 |
2.33e-03 |
1.12e-02 |
0.22300 |
-6.38e-02 |
2.14e-01 |
3.02e-01 |
5.24e-04 |
TP53 Regulates Transcription of Caspase Activators and Caspases |
11 |
3.67e-01 |
5.10e-01 |
0.22300 |
-2.00e-01 |
-9.94e-02 |
2.52e-01 |
5.68e-01 |
Processing of Capped Intronless Pre-mRNA |
25 |
1.01e-01 |
2.09e-01 |
0.22300 |
-1.96e-01 |
-1.07e-01 |
9.07e-02 |
3.56e-01 |
Cyclin A/B1/B2 associated events during G2/M transition |
24 |
1.34e-01 |
2.56e-01 |
0.22300 |
2.19e-01 |
4.17e-02 |
6.37e-02 |
7.24e-01 |
Opioid Signalling |
84 |
5.73e-04 |
3.22e-03 |
0.22300 |
8.36e-02 |
2.06e-01 |
1.86e-01 |
1.09e-03 |
Intra-Golgi traffic |
41 |
4.41e-02 |
1.13e-01 |
0.22300 |
-1.00e-02 |
2.22e-01 |
9.12e-01 |
1.38e-02 |
Polo-like kinase mediated events |
16 |
3.57e-01 |
5.01e-01 |
0.22300 |
1.98e-01 |
-1.01e-01 |
1.70e-01 |
4.84e-01 |
Transport to the Golgi and subsequent modification |
153 |
6.74e-05 |
5.00e-04 |
0.22200 |
-1.06e-01 |
1.95e-01 |
2.38e-02 |
3.35e-05 |
Mitochondrial translation termination |
88 |
2.76e-03 |
1.30e-02 |
0.22100 |
-6.83e-02 |
2.10e-01 |
2.69e-01 |
6.48e-04 |
Separation of Sister Chromatids |
166 |
2.96e-05 |
2.56e-04 |
0.22100 |
-1.03e-01 |
1.96e-01 |
2.21e-02 |
1.38e-05 |
MAP2K and MAPK activation |
37 |
7.48e-02 |
1.70e-01 |
0.22100 |
-4.50e-02 |
2.16e-01 |
6.36e-01 |
2.28e-02 |
Regulation of TP53 Degradation |
33 |
6.46e-02 |
1.50e-01 |
0.22100 |
4.71e-02 |
2.16e-01 |
6.40e-01 |
3.22e-02 |
Zinc influx into cells by the SLC39 gene family |
10 |
4.10e-01 |
5.50e-01 |
0.22000 |
-1.96e-01 |
-1.00e-01 |
2.83e-01 |
5.83e-01 |
RAB geranylgeranylation |
59 |
1.05e-02 |
3.68e-02 |
0.22000 |
1.22e-02 |
2.19e-01 |
8.71e-01 |
3.59e-03 |
TP53 regulates transcription of several additional cell death genes whose specific roles in p53-dependent apoptosis remain uncertain |
13 |
4.40e-01 |
5.78e-01 |
0.22000 |
-1.98e-01 |
9.57e-02 |
2.17e-01 |
5.50e-01 |
Adaptive Immune System |
663 |
3.43e-17 |
6.01e-15 |
0.21900 |
-1.41e-01 |
1.67e-01 |
6.49e-10 |
2.84e-13 |
Removal of the Flap Intermediate |
13 |
4.44e-01 |
5.82e-01 |
0.21900 |
1.95e-01 |
-9.87e-02 |
2.22e-01 |
5.38e-01 |
Formation of HIV-1 elongation complex containing HIV-1 Tat |
42 |
2.95e-02 |
8.38e-02 |
0.21800 |
6.94e-02 |
2.07e-01 |
4.37e-01 |
2.06e-02 |
HIV Transcription Elongation |
42 |
2.95e-02 |
8.38e-02 |
0.21800 |
6.94e-02 |
2.07e-01 |
4.37e-01 |
2.06e-02 |
Tat-mediated elongation of the HIV-1 transcript |
42 |
2.95e-02 |
8.38e-02 |
0.21800 |
6.94e-02 |
2.07e-01 |
4.37e-01 |
2.06e-02 |
TRP channels |
20 |
3.11e-01 |
4.59e-01 |
0.21700 |
1.59e-01 |
-1.48e-01 |
2.18e-01 |
2.52e-01 |
Clathrin-mediated endocytosis |
133 |
1.24e-04 |
8.72e-04 |
0.21700 |
-4.15e-02 |
2.13e-01 |
4.09e-01 |
2.22e-05 |
Diseases of programmed cell death |
26 |
1.05e-01 |
2.14e-01 |
0.21700 |
1.92e-01 |
1.01e-01 |
9.02e-02 |
3.72e-01 |
Global Genome Nucleotide Excision Repair (GG-NER) |
82 |
1.62e-03 |
8.07e-03 |
0.21700 |
3.40e-02 |
2.14e-01 |
5.95e-01 |
8.05e-04 |
Iron uptake and transport |
56 |
3.09e-02 |
8.61e-02 |
0.21700 |
-8.73e-02 |
1.99e-01 |
2.59e-01 |
1.02e-02 |
Glucagon-like Peptide-1 (GLP1) regulates insulin secretion |
38 |
3.38e-02 |
9.11e-02 |
0.21700 |
1.59e-01 |
1.47e-01 |
9.01e-02 |
1.16e-01 |
Downstream signal transduction |
29 |
1.77e-01 |
3.11e-01 |
0.21700 |
-1.11e-01 |
1.86e-01 |
3.02e-01 |
8.30e-02 |
PI-3K cascade:FGFR4 |
12 |
4.29e-01 |
5.67e-01 |
0.21600 |
-2.15e-01 |
1.93e-02 |
1.97e-01 |
9.08e-01 |
Synthesis of glycosylphosphatidylinositol (GPI) |
17 |
2.91e-01 |
4.41e-01 |
0.21600 |
3.86e-03 |
-2.16e-01 |
9.78e-01 |
1.23e-01 |
Aberrant regulation of mitotic cell cycle due to RB1 defects |
35 |
5.10e-02 |
1.26e-01 |
0.21600 |
1.94e-01 |
9.49e-02 |
4.76e-02 |
3.31e-01 |
Diseases of mitotic cell cycle |
35 |
5.10e-02 |
1.26e-01 |
0.21600 |
1.94e-01 |
9.49e-02 |
4.76e-02 |
3.31e-01 |
Mitochondrial translation elongation |
88 |
3.58e-03 |
1.59e-02 |
0.21500 |
-6.11e-02 |
2.06e-01 |
3.22e-01 |
8.26e-04 |
PLC beta mediated events |
50 |
1.72e-02 |
5.51e-02 |
0.21500 |
6.49e-02 |
2.05e-01 |
4.28e-01 |
1.22e-02 |
Late endosomal microautophagy |
29 |
1.17e-01 |
2.33e-01 |
0.21500 |
1.07e-02 |
2.15e-01 |
9.21e-01 |
4.54e-02 |
HCMV Late Events |
63 |
4.56e-03 |
1.93e-02 |
0.21500 |
1.86e-01 |
1.08e-01 |
1.08e-02 |
1.38e-01 |
Vesicle-mediated transport |
622 |
2.63e-17 |
5.27e-15 |
0.21500 |
-6.29e-02 |
2.05e-01 |
7.76e-03 |
3.39e-18 |
G-protein mediated events |
51 |
1.67e-02 |
5.35e-02 |
0.21500 |
6.03e-02 |
2.06e-01 |
4.57e-01 |
1.10e-02 |
Antigen Presentation: Folding, assembly and peptide loading of class I MHC |
19 |
3.37e-01 |
4.81e-01 |
0.21400 |
-1.72e-01 |
1.28e-01 |
1.95e-01 |
3.35e-01 |
Synthesis of Prostaglandins (PG) and Thromboxanes (TX) |
13 |
3.76e-01 |
5.18e-01 |
0.21400 |
2.53e-02 |
2.12e-01 |
8.74e-01 |
1.85e-01 |
Transport of vitamins, nucleosides, and related molecules |
34 |
1.45e-01 |
2.69e-01 |
0.21400 |
1.68e-01 |
-1.32e-01 |
8.95e-02 |
1.84e-01 |
Mitophagy |
27 |
2.18e-01 |
3.56e-01 |
0.21400 |
-1.43e-01 |
1.59e-01 |
1.99e-01 |
1.54e-01 |
Phase 4 - resting membrane potential |
11 |
4.28e-01 |
5.67e-01 |
0.21300 |
-2.10e-01 |
-4.07e-02 |
2.29e-01 |
8.15e-01 |
EPH-ephrin mediated repulsion of cells |
47 |
2.86e-02 |
8.24e-02 |
0.21300 |
3.11e-02 |
2.11e-01 |
7.12e-01 |
1.23e-02 |
Dopamine Neurotransmitter Release Cycle |
20 |
3.12e-01 |
4.59e-01 |
0.21300 |
1.07e-01 |
-1.85e-01 |
4.09e-01 |
1.53e-01 |
Nef-mediates down modulation of cell surface receptors by recruiting them to clathrin adapters |
20 |
2.68e-01 |
4.13e-01 |
0.21300 |
-3.79e-02 |
2.10e-01 |
7.70e-01 |
1.05e-01 |
Platelet activation, signaling and aggregation |
242 |
3.93e-07 |
6.34e-06 |
0.21200 |
-6.71e-02 |
2.02e-01 |
7.26e-02 |
7.04e-08 |
Formation of HIV elongation complex in the absence of HIV Tat |
44 |
3.10e-02 |
8.61e-02 |
0.21200 |
6.12e-02 |
2.03e-01 |
4.83e-01 |
1.96e-02 |
Signal amplification |
29 |
1.63e-01 |
2.97e-01 |
0.21200 |
-6.03e-02 |
2.04e-01 |
5.74e-01 |
5.78e-02 |
Oncogenic MAPK signaling |
77 |
6.97e-03 |
2.67e-02 |
0.21200 |
-4.28e-02 |
2.08e-01 |
5.17e-01 |
1.62e-03 |
EGFR downregulation |
27 |
2.13e-01 |
3.52e-01 |
0.21200 |
-1.82e-01 |
1.09e-01 |
1.02e-01 |
3.27e-01 |
Basigin interactions |
24 |
1.52e-01 |
2.79e-01 |
0.21200 |
2.02e-01 |
6.25e-02 |
8.65e-02 |
5.96e-01 |
Synthesis, secretion, and deacylation of Ghrelin |
13 |
4.87e-01 |
6.09e-01 |
0.21100 |
-1.60e-01 |
1.39e-01 |
3.19e-01 |
3.87e-01 |
tRNA Aminoacylation |
42 |
6.27e-02 |
1.46e-01 |
0.21100 |
-2.09e-01 |
2.89e-02 |
1.89e-02 |
7.46e-01 |
Inwardly rectifying K+ channels |
28 |
1.98e-01 |
3.35e-01 |
0.21100 |
-9.53e-02 |
1.88e-01 |
3.83e-01 |
8.47e-02 |
HIV Life Cycle |
145 |
6.69e-05 |
5.00e-04 |
0.21100 |
-2.10e-02 |
2.10e-01 |
6.63e-01 |
1.32e-05 |
Downregulation of ERBB2 signaling |
27 |
2.27e-01 |
3.66e-01 |
0.21100 |
-1.58e-01 |
1.40e-01 |
1.57e-01 |
2.08e-01 |
Platelet Adhesion to exposed collagen |
12 |
4.99e-01 |
6.18e-01 |
0.21100 |
-1.89e-01 |
9.31e-02 |
2.57e-01 |
5.76e-01 |
Downstream signaling of activated FGFR1 |
23 |
2.64e-01 |
4.09e-01 |
0.21100 |
-1.89e-01 |
9.32e-02 |
1.17e-01 |
4.39e-01 |
Toll Like Receptor 4 (TLR4) Cascade |
117 |
5.94e-04 |
3.30e-03 |
0.21100 |
-4.11e-02 |
2.06e-01 |
4.43e-01 |
1.16e-04 |
Negative regulation of MAPK pathway |
42 |
5.02e-02 |
1.25e-01 |
0.21100 |
1.29e-02 |
2.10e-01 |
8.85e-01 |
1.85e-02 |
Cargo recognition for clathrin-mediated endocytosis |
95 |
3.84e-03 |
1.69e-02 |
0.21000 |
-8.25e-02 |
1.94e-01 |
1.65e-01 |
1.12e-03 |
Complement cascade |
59 |
2.43e-02 |
7.19e-02 |
0.21000 |
-4.46e-02 |
2.05e-01 |
5.53e-01 |
6.40e-03 |
Biotin transport and metabolism |
11 |
4.01e-01 |
5.42e-01 |
0.21000 |
-1.73e-01 |
-1.20e-01 |
3.22e-01 |
4.91e-01 |
Biosynthesis of DHA-derived SPMs |
13 |
3.62e-01 |
5.05e-01 |
0.21000 |
6.86e-02 |
1.98e-01 |
6.69e-01 |
2.15e-01 |
SHC1 events in ERBB2 signaling |
20 |
3.36e-01 |
4.80e-01 |
0.21000 |
-1.41e-01 |
1.55e-01 |
2.74e-01 |
2.29e-01 |
Vasopressin regulates renal water homeostasis via Aquaporins |
39 |
3.87e-02 |
1.02e-01 |
0.21000 |
1.31e-01 |
1.64e-01 |
1.56e-01 |
7.68e-02 |
Synthesis of DNA |
116 |
7.91e-04 |
4.25e-03 |
0.20900 |
-5.10e-02 |
2.03e-01 |
3.44e-01 |
1.59e-04 |
G2/M Checkpoints |
133 |
4.50e-04 |
2.59e-03 |
0.20900 |
-8.08e-02 |
1.93e-01 |
1.08e-01 |
1.23e-04 |
HDR through MMEJ (alt-NHEJ) |
10 |
5.50e-01 |
6.61e-01 |
0.20900 |
-6.67e-02 |
1.98e-01 |
7.15e-01 |
2.78e-01 |
Biosynthesis of specialized proresolving mediators (SPMs) |
15 |
3.21e-01 |
4.63e-01 |
0.20800 |
6.02e-02 |
1.99e-01 |
6.87e-01 |
1.82e-01 |
Dual incision in TC-NER |
64 |
5.98e-03 |
2.36e-02 |
0.20800 |
1.04e-01 |
1.80e-01 |
1.49e-01 |
1.30e-02 |
ESR-mediated signaling |
160 |
4.48e-05 |
3.63e-04 |
0.20800 |
-3.34e-02 |
2.05e-01 |
4.67e-01 |
7.84e-06 |
Insertion of tail-anchored proteins into the endoplasmic reticulum membrane |
21 |
3.07e-01 |
4.55e-01 |
0.20700 |
-1.87e-01 |
9.06e-02 |
1.39e-01 |
4.72e-01 |
MET promotes cell motility |
29 |
1.73e-01 |
3.08e-01 |
0.20700 |
-5.08e-02 |
2.01e-01 |
6.36e-01 |
6.12e-02 |
Cargo trafficking to the periciliary membrane |
47 |
5.01e-02 |
1.25e-01 |
0.20700 |
-2.06e-01 |
2.54e-02 |
1.48e-02 |
7.64e-01 |
Extension of Telomeres |
49 |
5.71e-02 |
1.36e-01 |
0.20700 |
1.96e-01 |
-6.67e-02 |
1.77e-02 |
4.20e-01 |
TAK1 activates NFkB by phosphorylation and activation of IKKs complex |
24 |
1.52e-01 |
2.79e-01 |
0.20700 |
9.60e-02 |
1.83e-01 |
4.16e-01 |
1.21e-01 |
Senescence-Associated Secretory Phenotype (SASP) |
55 |
1.67e-02 |
5.35e-02 |
0.20600 |
1.97e-01 |
5.98e-02 |
1.14e-02 |
4.43e-01 |
Purine ribonucleoside monophosphate biosynthesis |
10 |
4.55e-01 |
5.88e-01 |
0.20600 |
9.95e-02 |
1.81e-01 |
5.86e-01 |
3.23e-01 |
Metal ion SLC transporters |
24 |
2.80e-01 |
4.27e-01 |
0.20500 |
-1.68e-01 |
1.18e-01 |
1.54e-01 |
3.16e-01 |
APC/C-mediated degradation of cell cycle proteins |
85 |
1.16e-02 |
4.03e-02 |
0.20500 |
-1.22e-01 |
1.65e-01 |
5.12e-02 |
8.72e-03 |
Regulation of mitotic cell cycle |
85 |
1.16e-02 |
4.03e-02 |
0.20500 |
-1.22e-01 |
1.65e-01 |
5.12e-02 |
8.72e-03 |
Signaling by Interleukins |
381 |
7.80e-10 |
3.90e-08 |
0.20500 |
-7.69e-02 |
1.90e-01 |
1.03e-02 |
2.09e-10 |
Mucopolysaccharidoses |
11 |
4.91e-01 |
6.12e-01 |
0.20500 |
-2.05e-01 |
8.86e-03 |
2.40e-01 |
9.59e-01 |
Generation of second messenger molecules |
27 |
2.07e-01 |
3.46e-01 |
0.20400 |
-1.97e-01 |
5.35e-02 |
7.63e-02 |
6.31e-01 |
Transcriptional regulation by RUNX2 |
114 |
2.20e-03 |
1.07e-02 |
0.20400 |
-9.11e-02 |
1.82e-01 |
9.31e-02 |
7.91e-04 |
MyD88-independent TLR4 cascade |
91 |
4.03e-03 |
1.74e-02 |
0.20400 |
-3.11e-02 |
2.01e-01 |
6.08e-01 |
9.15e-04 |
TRIF(TICAM1)-mediated TLR4 signaling |
91 |
4.03e-03 |
1.74e-02 |
0.20400 |
-3.11e-02 |
2.01e-01 |
6.08e-01 |
9.15e-04 |
Signaling by FGFR4 |
33 |
1.82e-01 |
3.17e-01 |
0.20300 |
-1.20e-01 |
1.64e-01 |
2.32e-01 |
1.04e-01 |
DNA Replication |
123 |
6.83e-04 |
3.71e-03 |
0.20300 |
-3.73e-02 |
1.99e-01 |
4.75e-01 |
1.35e-04 |
Telomere Maintenance |
71 |
1.16e-02 |
4.03e-02 |
0.20300 |
2.03e-01 |
-1.21e-02 |
3.19e-03 |
8.60e-01 |
MAP kinase activation |
60 |
2.14e-02 |
6.46e-02 |
0.20300 |
-1.69e-03 |
2.03e-01 |
9.82e-01 |
6.65e-03 |
SUMOylation of transcription cofactors |
42 |
9.90e-02 |
2.05e-01 |
0.20200 |
-1.89e-01 |
7.14e-02 |
3.40e-02 |
4.23e-01 |
Dermatan sulfate biosynthesis |
11 |
4.30e-01 |
5.68e-01 |
0.20200 |
1.67e-01 |
1.14e-01 |
3.38e-01 |
5.13e-01 |
Telomere C-strand synthesis initiation |
13 |
4.84e-01 |
6.06e-01 |
0.20200 |
6.47e-02 |
-1.91e-01 |
6.86e-01 |
2.32e-01 |
Metabolism of steroid hormones |
23 |
1.70e-01 |
3.05e-01 |
0.20200 |
-1.61e-01 |
-1.22e-01 |
1.82e-01 |
3.10e-01 |
FOXO-mediated transcription of oxidative stress, metabolic and neuronal genes |
28 |
1.15e-01 |
2.30e-01 |
0.20200 |
1.52e-01 |
1.33e-01 |
1.64e-01 |
2.25e-01 |
Interleukin-1 family signaling |
126 |
1.44e-03 |
7.24e-03 |
0.20200 |
-9.93e-02 |
1.76e-01 |
5.46e-02 |
6.68e-04 |
IRE1alpha activates chaperones |
50 |
5.86e-02 |
1.38e-01 |
0.20200 |
-1.94e-01 |
5.30e-02 |
1.74e-02 |
5.17e-01 |
Heme degradation |
12 |
4.02e-01 |
5.42e-01 |
0.20100 |
1.09e-01 |
1.70e-01 |
5.14e-01 |
3.09e-01 |
Activation of G protein gated Potassium channels |
24 |
2.64e-01 |
4.09e-01 |
0.20100 |
-6.38e-02 |
1.91e-01 |
5.89e-01 |
1.06e-01 |
G protein gated Potassium channels |
24 |
2.64e-01 |
4.09e-01 |
0.20100 |
-6.38e-02 |
1.91e-01 |
5.89e-01 |
1.06e-01 |
Inhibition of voltage gated Ca2+ channels via Gbeta/gamma subunits |
24 |
2.64e-01 |
4.09e-01 |
0.20100 |
-6.38e-02 |
1.91e-01 |
5.89e-01 |
1.06e-01 |
Diseases of signal transduction by growth factor receptors and second messengers |
362 |
9.24e-09 |
3.01e-07 |
0.20100 |
-9.65e-02 |
1.77e-01 |
1.67e-03 |
8.66e-09 |
Nervous system development |
494 |
2.15e-13 |
2.52e-11 |
0.20100 |
-1.98e-02 |
2.00e-01 |
4.53e-01 |
3.27e-14 |
Thromboxane signalling through TP receptor |
21 |
3.07e-01 |
4.55e-01 |
0.20100 |
-5.59e-02 |
1.93e-01 |
6.58e-01 |
1.26e-01 |
XBP1(S) activates chaperone genes |
48 |
6.79e-02 |
1.56e-01 |
0.20100 |
-1.93e-01 |
5.43e-02 |
2.07e-02 |
5.15e-01 |
Metabolism of RNA |
629 |
2.03e-14 |
2.85e-12 |
0.20100 |
-9.31e-02 |
1.78e-01 |
7.40e-05 |
3.92e-14 |
Hyaluronan metabolism |
16 |
4.52e-01 |
5.87e-01 |
0.20000 |
1.36e-01 |
-1.47e-01 |
3.47e-01 |
3.08e-01 |
Myogenesis |
23 |
2.52e-01 |
3.98e-01 |
0.20000 |
-2.19e-02 |
1.99e-01 |
8.56e-01 |
9.88e-02 |
Mitochondrial calcium ion transport |
22 |
2.48e-01 |
3.94e-01 |
0.20000 |
4.74e-03 |
2.00e-01 |
9.69e-01 |
1.05e-01 |
Viral Messenger RNA Synthesis |
44 |
4.38e-02 |
1.13e-01 |
0.20000 |
1.87e-01 |
6.97e-02 |
3.19e-02 |
4.24e-01 |
Negative regulation of the PI3K/AKT network |
94 |
5.20e-03 |
2.11e-02 |
0.20000 |
-4.89e-02 |
1.94e-01 |
4.13e-01 |
1.19e-03 |
Metabolism of Angiotensinogen to Angiotensins |
13 |
4.69e-01 |
5.95e-01 |
0.20000 |
1.97e-01 |
-3.22e-02 |
2.19e-01 |
8.41e-01 |
Initiation of Nuclear Envelope (NE) Reformation |
19 |
2.65e-01 |
4.09e-01 |
0.20000 |
1.91e-01 |
5.89e-02 |
1.50e-01 |
6.57e-01 |
PI-3K cascade:FGFR1 |
13 |
4.81e-01 |
6.05e-01 |
0.19900 |
-1.94e-01 |
4.46e-02 |
2.26e-01 |
7.81e-01 |
MET activates PTK2 signaling |
18 |
2.91e-01 |
4.41e-01 |
0.19900 |
5.01e-02 |
1.93e-01 |
7.13e-01 |
1.57e-01 |
Negative regulators of DDX58/IFIH1 signaling |
32 |
2.09e-01 |
3.47e-01 |
0.19900 |
-1.26e-01 |
1.53e-01 |
2.17e-01 |
1.33e-01 |
Signaling by FGFR3 |
34 |
1.79e-01 |
3.12e-01 |
0.19900 |
-9.67e-02 |
1.74e-01 |
3.29e-01 |
8.01e-02 |
ERK/MAPK targets |
21 |
2.61e-01 |
4.08e-01 |
0.19800 |
1.72e-02 |
1.98e-01 |
8.92e-01 |
1.17e-01 |
Pre-NOTCH Processing in Golgi |
17 |
3.85e-01 |
5.29e-01 |
0.19800 |
-4.21e-02 |
1.94e-01 |
7.64e-01 |
1.67e-01 |
Late Phase of HIV Life Cycle |
132 |
3.94e-04 |
2.33e-03 |
0.19800 |
-1.25e-02 |
1.97e-01 |
8.04e-01 |
9.07e-05 |
Diseases associated with O-glycosylation of proteins |
58 |
1.64e-02 |
5.35e-02 |
0.19700 |
1.80e-01 |
8.22e-02 |
1.81e-02 |
2.79e-01 |
Unfolded Protein Response (UPR) |
89 |
1.26e-02 |
4.32e-02 |
0.19700 |
-1.66e-01 |
1.06e-01 |
6.73e-03 |
8.34e-02 |
Axon guidance |
472 |
1.93e-12 |
2.08e-10 |
0.19700 |
-1.71e-02 |
1.96e-01 |
5.25e-01 |
3.19e-13 |
Ub-specific processing proteases |
164 |
3.94e-04 |
2.33e-03 |
0.19700 |
-1.28e-01 |
1.50e-01 |
4.73e-03 |
9.32e-04 |
Mitotic Metaphase and Anaphase |
221 |
9.70e-06 |
9.85e-05 |
0.19700 |
-6.54e-02 |
1.86e-01 |
9.48e-02 |
1.97e-06 |
PIWI-interacting RNA (piRNA) biogenesis |
22 |
2.47e-01 |
3.93e-01 |
0.19700 |
1.96e-01 |
2.02e-02 |
1.12e-01 |
8.70e-01 |
Mitotic Anaphase |
220 |
1.05e-05 |
1.04e-04 |
0.19700 |
-6.45e-02 |
1.86e-01 |
1.00e-01 |
2.09e-06 |
FOXO-mediated transcription |
61 |
1.62e-02 |
5.27e-02 |
0.19700 |
5.65e-02 |
1.88e-01 |
4.46e-01 |
1.09e-02 |
Negative regulation of FGFR1 signaling |
24 |
3.04e-01 |
4.54e-01 |
0.19700 |
-9.73e-02 |
1.71e-01 |
4.10e-01 |
1.47e-01 |
ERKs are inactivated |
12 |
4.97e-01 |
6.17e-01 |
0.19700 |
-1.75e-02 |
1.96e-01 |
9.16e-01 |
2.40e-01 |
RHO GTPase Effectors |
246 |
3.36e-07 |
5.68e-06 |
0.19700 |
6.60e-03 |
1.96e-01 |
8.59e-01 |
1.19e-07 |
Assembly of collagen fibrils and other multimeric structures |
44 |
6.43e-02 |
1.49e-01 |
0.19600 |
1.56e-02 |
1.96e-01 |
8.58e-01 |
2.48e-02 |
Synthesis of bile acids and bile salts |
27 |
1.48e-01 |
2.74e-01 |
0.19600 |
9.17e-02 |
1.73e-01 |
4.10e-01 |
1.20e-01 |
HDACs deacetylate histones |
40 |
1.10e-01 |
2.22e-01 |
0.19600 |
-3.70e-02 |
1.92e-01 |
6.85e-01 |
3.57e-02 |
mRNA 3'-end processing |
54 |
6.09e-02 |
1.42e-01 |
0.19600 |
-1.84e-01 |
6.57e-02 |
1.93e-02 |
4.04e-01 |
RUNX1 interacts with co-factors whose precise effect on RUNX1 targets is not known |
36 |
1.68e-01 |
3.02e-01 |
0.19500 |
-1.75e-01 |
8.72e-02 |
6.97e-02 |
3.65e-01 |
Signaling by BRAF and RAF fusions |
60 |
4.04e-02 |
1.06e-01 |
0.19500 |
-4.92e-02 |
1.89e-01 |
5.10e-01 |
1.14e-02 |
VxPx cargo-targeting to cilium |
18 |
3.53e-01 |
4.97e-01 |
0.19500 |
-1.95e-01 |
1.54e-02 |
1.53e-01 |
9.10e-01 |
Processing of SMDT1 |
15 |
4.28e-01 |
5.67e-01 |
0.19500 |
-2.35e-02 |
1.94e-01 |
8.75e-01 |
1.94e-01 |
Intra-Golgi and retrograde Golgi-to-ER traffic |
175 |
2.22e-04 |
1.42e-03 |
0.19500 |
-9.93e-02 |
1.68e-01 |
2.37e-02 |
1.32e-04 |
Signaling by ERBB2 in Cancer |
24 |
3.26e-01 |
4.69e-01 |
0.19400 |
-1.29e-01 |
1.46e-01 |
2.76e-01 |
2.17e-01 |
Negative regulation of FGFR4 signaling |
23 |
3.36e-01 |
4.80e-01 |
0.19400 |
-1.04e-01 |
1.63e-01 |
3.87e-01 |
1.76e-01 |
Abortive elongation of HIV-1 transcript in the absence of Tat |
23 |
1.95e-01 |
3.32e-01 |
0.19300 |
1.35e-01 |
1.38e-01 |
2.61e-01 |
2.52e-01 |
AKT phosphorylates targets in the nucleus |
10 |
5.04e-01 |
6.22e-01 |
0.19300 |
8.58e-02 |
1.73e-01 |
6.38e-01 |
3.43e-01 |
Signaling by NOTCH |
179 |
2.91e-04 |
1.79e-03 |
0.19300 |
-1.32e-01 |
1.40e-01 |
2.36e-03 |
1.21e-03 |
ADP signalling through P2Y purinoceptor 1 |
22 |
2.97e-01 |
4.47e-01 |
0.19300 |
-2.34e-02 |
1.91e-01 |
8.50e-01 |
1.21e-01 |
RAB GEFs exchange GTP for GDP on RABs |
86 |
1.36e-02 |
4.55e-02 |
0.19200 |
-6.61e-02 |
1.81e-01 |
2.90e-01 |
3.78e-03 |
RNA Pol II CTD phosphorylation and interaction with CE |
27 |
1.61e-01 |
2.94e-01 |
0.19200 |
8.24e-02 |
1.74e-01 |
4.59e-01 |
1.18e-01 |
RNA Pol II CTD phosphorylation and interaction with CE during HIV infection |
27 |
1.61e-01 |
2.94e-01 |
0.19200 |
8.24e-02 |
1.74e-01 |
4.59e-01 |
1.18e-01 |
Chylomicron assembly |
10 |
4.95e-01 |
6.15e-01 |
0.19200 |
1.44e-01 |
1.28e-01 |
4.31e-01 |
4.84e-01 |
Translation of Replicase and Assembly of the Replication Transcription Complex |
11 |
4.61e-01 |
5.93e-01 |
0.19200 |
1.37e-01 |
1.35e-01 |
4.32e-01 |
4.38e-01 |
Adherens junctions interactions |
25 |
3.13e-01 |
4.59e-01 |
0.19200 |
-1.06e-01 |
1.60e-01 |
3.58e-01 |
1.67e-01 |
Transcription-Coupled Nucleotide Excision Repair (TC-NER) |
77 |
5.90e-03 |
2.34e-02 |
0.19200 |
7.93e-02 |
1.75e-01 |
2.29e-01 |
8.12e-03 |
Beta-catenin independent WNT signaling |
141 |
1.72e-03 |
8.48e-03 |
0.19100 |
-1.19e-01 |
1.50e-01 |
1.52e-02 |
2.14e-03 |
ERCC6 (CSB) and EHMT2 (G9a) positively regulate rRNA expression |
25 |
3.12e-01 |
4.59e-01 |
0.19100 |
-9.56e-02 |
1.65e-01 |
4.08e-01 |
1.53e-01 |
Synthesis of PIPs at the late endosome membrane |
11 |
5.86e-01 |
6.88e-01 |
0.19100 |
-1.76e-01 |
7.34e-02 |
3.12e-01 |
6.73e-01 |
mRNA Splicing - Major Pathway |
172 |
4.41e-04 |
2.55e-03 |
0.19100 |
-1.16e-01 |
1.51e-01 |
8.81e-03 |
6.26e-04 |
Ethanol oxidation |
11 |
6.01e-01 |
7.00e-01 |
0.19000 |
-9.50e-02 |
1.65e-01 |
5.85e-01 |
3.44e-01 |
Thrombin signalling through proteinase activated receptors (PARs) |
29 |
2.45e-01 |
3.91e-01 |
0.19000 |
-6.96e-02 |
1.77e-01 |
5.17e-01 |
9.90e-02 |
Toll Like Receptor 3 (TLR3) Cascade |
88 |
8.35e-03 |
3.09e-02 |
0.19000 |
-1.55e-02 |
1.89e-01 |
8.02e-01 |
2.17e-03 |
TP53 Regulates Transcription of Cell Death Genes |
36 |
1.85e-01 |
3.21e-01 |
0.19000 |
-1.69e-01 |
8.58e-02 |
7.87e-02 |
3.73e-01 |
Mitochondrial iron-sulfur cluster biogenesis |
11 |
5.14e-01 |
6.28e-01 |
0.19000 |
1.87e-01 |
3.25e-02 |
2.83e-01 |
8.52e-01 |
Hemostasis |
547 |
1.75e-13 |
2.22e-11 |
0.19000 |
-7.04e-03 |
1.89e-01 |
7.79e-01 |
4.52e-14 |
Signaling by ERBB4 |
52 |
9.28e-02 |
1.96e-01 |
0.19000 |
-9.73e-02 |
1.63e-01 |
2.25e-01 |
4.26e-02 |
TNF receptor superfamily (TNFSF) members mediating non-canonical NF-kB pathway |
14 |
5.32e-01 |
6.46e-01 |
0.18900 |
-1.58e-01 |
1.03e-01 |
3.05e-01 |
5.05e-01 |
Neutrophil degranulation |
416 |
2.06e-09 |
8.77e-08 |
0.18900 |
-5.58e-02 |
1.80e-01 |
5.19e-02 |
3.10e-10 |
Innate Immune System |
893 |
2.85e-18 |
6.66e-16 |
0.18900 |
-6.99e-02 |
1.75e-01 |
4.43e-04 |
1.05e-18 |
Assembly Of The HIV Virion |
16 |
3.83e-01 |
5.27e-01 |
0.18900 |
3.24e-02 |
1.86e-01 |
8.23e-01 |
1.98e-01 |
tRNA modification in the nucleus and cytosol |
43 |
9.12e-02 |
1.94e-01 |
0.18900 |
-7.46e-06 |
-1.89e-01 |
1.00e+00 |
3.24e-02 |
PI5P, PP2A and IER3 Regulate PI3K/AKT Signaling |
87 |
1.19e-02 |
4.10e-02 |
0.18800 |
-3.57e-02 |
1.85e-01 |
5.65e-01 |
2.91e-03 |
PIP3 activates AKT signaling |
248 |
1.84e-05 |
1.67e-04 |
0.18800 |
-1.04e-01 |
1.57e-01 |
5.07e-03 |
2.19e-05 |
Detoxification of Reactive Oxygen Species |
33 |
2.37e-01 |
3.81e-01 |
0.18800 |
-1.28e-01 |
1.38e-01 |
2.03e-01 |
1.72e-01 |
Nucleotide Excision Repair |
108 |
1.27e-03 |
6.51e-03 |
0.18800 |
5.64e-02 |
1.79e-01 |
3.12e-01 |
1.31e-03 |
Inhibition of DNA recombination at telomere |
28 |
1.71e-01 |
3.05e-01 |
0.18700 |
1.74e-01 |
6.98e-02 |
1.11e-01 |
5.23e-01 |
Insulin receptor recycling |
24 |
2.54e-01 |
4.00e-01 |
0.18700 |
1.68e-02 |
1.86e-01 |
8.87e-01 |
1.14e-01 |
Signaling by MET |
66 |
4.60e-02 |
1.16e-01 |
0.18700 |
-7.02e-02 |
1.73e-01 |
3.24e-01 |
1.49e-02 |
MyD88:MAL(TIRAP) cascade initiated on plasma membrane |
89 |
8.21e-03 |
3.05e-02 |
0.18700 |
-4.18e-03 |
1.87e-01 |
9.46e-01 |
2.35e-03 |
Toll Like Receptor 2 (TLR2) Cascade |
89 |
8.21e-03 |
3.05e-02 |
0.18700 |
-4.18e-03 |
1.87e-01 |
9.46e-01 |
2.35e-03 |
Toll Like Receptor TLR1:TLR2 Cascade |
89 |
8.21e-03 |
3.05e-02 |
0.18700 |
-4.18e-03 |
1.87e-01 |
9.46e-01 |
2.35e-03 |
Toll Like Receptor TLR6:TLR2 Cascade |
89 |
8.21e-03 |
3.05e-02 |
0.18700 |
-4.18e-03 |
1.87e-01 |
9.46e-01 |
2.35e-03 |
Membrane Trafficking |
570 |
5.56e-12 |
5.20e-10 |
0.18600 |
-6.42e-02 |
1.75e-01 |
9.14e-03 |
1.15e-12 |
Aflatoxin activation and detoxification |
14 |
4.37e-01 |
5.75e-01 |
0.18600 |
-4.11e-02 |
-1.81e-01 |
7.90e-01 |
2.40e-01 |
Ephrin signaling |
18 |
3.19e-01 |
4.62e-01 |
0.18500 |
8.75e-02 |
1.63e-01 |
5.21e-01 |
2.30e-01 |
Integrin signaling |
27 |
2.07e-01 |
3.46e-01 |
0.18500 |
3.77e-02 |
1.81e-01 |
7.34e-01 |
1.03e-01 |
G0 and Early G1 |
26 |
1.91e-01 |
3.29e-01 |
0.18500 |
9.09e-02 |
1.61e-01 |
4.23e-01 |
1.54e-01 |
NOD1/2 Signaling Pathway |
29 |
2.24e-01 |
3.63e-01 |
0.18500 |
-1.84e-02 |
1.84e-01 |
8.64e-01 |
8.59e-02 |
Deubiquitination |
236 |
5.21e-05 |
4.13e-04 |
0.18500 |
-1.15e-01 |
1.44e-01 |
2.33e-03 |
1.42e-04 |
Signaling by FGFR1 |
41 |
1.79e-01 |
3.12e-01 |
0.18400 |
-1.30e-01 |
1.30e-01 |
1.49e-01 |
1.49e-01 |
Nucleobase biosynthesis |
13 |
4.77e-01 |
6.02e-01 |
0.18400 |
1.81e-01 |
3.18e-02 |
2.58e-01 |
8.43e-01 |
NOTCH3 Intracellular Domain Regulates Transcription |
24 |
2.43e-01 |
3.89e-01 |
0.18400 |
5.03e-02 |
1.77e-01 |
6.70e-01 |
1.34e-01 |
TGF-beta receptor signaling in EMT (epithelial to mesenchymal transition) |
16 |
5.13e-01 |
6.27e-01 |
0.18400 |
-1.30e-01 |
1.30e-01 |
3.68e-01 |
3.69e-01 |
WNT5A-dependent internalization of FZD4 |
15 |
4.84e-01 |
6.06e-01 |
0.18300 |
-3.68e-02 |
1.80e-01 |
8.05e-01 |
2.28e-01 |
Adrenaline,noradrenaline inhibits insulin secretion |
26 |
2.20e-01 |
3.58e-01 |
0.18300 |
1.77e-01 |
4.75e-02 |
1.19e-01 |
6.75e-01 |
G beta:gamma signalling through PLC beta |
18 |
4.01e-01 |
5.42e-01 |
0.18300 |
-1.54e-02 |
1.82e-01 |
9.10e-01 |
1.80e-01 |
Nuclear Pore Complex (NPC) Disassembly |
36 |
1.27e-01 |
2.46e-01 |
0.18300 |
1.78e-01 |
4.06e-02 |
6.40e-02 |
6.74e-01 |
Ovarian tumor domain proteases |
37 |
1.51e-01 |
2.78e-01 |
0.18300 |
-1.04e-02 |
1.83e-01 |
9.13e-01 |
5.48e-02 |
Signaling by cytosolic FGFR1 fusion mutants |
18 |
4.28e-01 |
5.67e-01 |
0.18300 |
-4.44e-02 |
1.77e-01 |
7.45e-01 |
1.93e-01 |
RNA Polymerase III Transcription Termination |
21 |
3.58e-01 |
5.02e-01 |
0.18300 |
1.80e-01 |
-2.89e-02 |
1.53e-01 |
8.19e-01 |
RNA Polymerase III Chain Elongation |
16 |
4.73e-01 |
5.97e-01 |
0.18200 |
1.77e-01 |
-4.25e-02 |
2.21e-01 |
7.68e-01 |
Gap-filling DNA repair synthesis and ligation in TC-NER |
63 |
2.10e-02 |
6.38e-02 |
0.18200 |
9.25e-02 |
1.56e-01 |
2.04e-01 |
3.18e-02 |
Competing endogenous RNAs (ceRNAs) regulate PTEN translation |
10 |
6.26e-01 |
7.19e-01 |
0.18200 |
4.23e-02 |
-1.77e-01 |
8.17e-01 |
3.33e-01 |
Condensation of Prophase Chromosomes |
22 |
2.66e-01 |
4.11e-01 |
0.18100 |
1.63e-01 |
7.90e-02 |
1.85e-01 |
5.21e-01 |
PKA-mediated phosphorylation of CREB |
19 |
3.16e-01 |
4.62e-01 |
0.18100 |
8.34e-02 |
1.61e-01 |
5.29e-01 |
2.24e-01 |
Antiviral mechanism by IFN-stimulated genes |
76 |
4.46e-02 |
1.14e-01 |
0.18100 |
-1.10e-01 |
1.44e-01 |
9.84e-02 |
2.95e-02 |
Nitric oxide stimulates guanylate cyclase |
19 |
3.06e-01 |
4.55e-01 |
0.18100 |
1.35e-01 |
1.21e-01 |
3.09e-01 |
3.62e-01 |
Toll Like Receptor 7/8 (TLR7/8) Cascade |
85 |
1.28e-02 |
4.34e-02 |
0.18100 |
3.52e-04 |
1.81e-01 |
9.96e-01 |
3.94e-03 |
Beta-oxidation of very long chain fatty acids |
11 |
6.40e-01 |
7.29e-01 |
0.18100 |
1.22e-01 |
-1.34e-01 |
4.84e-01 |
4.43e-01 |
RHO GTPases activate CIT |
19 |
3.24e-01 |
4.66e-01 |
0.18000 |
7.72e-02 |
1.63e-01 |
5.60e-01 |
2.19e-01 |
FOXO-mediated transcription of cell death genes |
15 |
4.87e-01 |
6.09e-01 |
0.18000 |
2.45e-02 |
-1.78e-01 |
8.69e-01 |
2.32e-01 |
NOTCH2 Activation and Transmission of Signal to the Nucleus |
22 |
3.09e-01 |
4.57e-01 |
0.18000 |
-1.79e-01 |
-2.19e-02 |
1.47e-01 |
8.59e-01 |
Signaling by NTRK1 (TRKA) |
106 |
5.44e-03 |
2.18e-02 |
0.18000 |
-9.88e-03 |
1.79e-01 |
8.61e-01 |
1.43e-03 |
Protein-protein interactions at synapses |
80 |
4.15e-02 |
1.08e-01 |
0.18000 |
1.20e-01 |
-1.34e-01 |
6.37e-02 |
3.89e-02 |
Ca-dependent events |
35 |
1.24e-01 |
2.43e-01 |
0.18000 |
8.70e-02 |
1.57e-01 |
3.73e-01 |
1.08e-01 |
Termination of O-glycan biosynthesis |
16 |
4.22e-01 |
5.62e-01 |
0.17900 |
1.77e-01 |
2.91e-02 |
2.20e-01 |
8.40e-01 |
NGF-stimulated transcription |
33 |
1.38e-01 |
2.61e-01 |
0.17900 |
1.53e-01 |
9.45e-02 |
1.30e-01 |
3.48e-01 |
Interactions of Vpr with host cellular proteins |
36 |
1.20e-01 |
2.38e-01 |
0.17900 |
1.60e-01 |
7.97e-02 |
9.57e-02 |
4.08e-01 |
SUMOylation of immune response proteins |
11 |
6.30e-01 |
7.21e-01 |
0.17900 |
1.61e-01 |
-7.79e-02 |
3.54e-01 |
6.55e-01 |
TNFs bind their physiological receptors |
20 |
4.31e-01 |
5.69e-01 |
0.17900 |
1.62e-01 |
-7.70e-02 |
2.11e-01 |
5.51e-01 |
PINK1-PRKN Mediated Mitophagy |
20 |
4.52e-01 |
5.87e-01 |
0.17900 |
-1.14e-01 |
1.38e-01 |
3.77e-01 |
2.86e-01 |
ERBB2 Activates PTK6 Signaling |
11 |
5.13e-01 |
6.27e-01 |
0.17900 |
-1.15e-01 |
-1.37e-01 |
5.09e-01 |
4.31e-01 |
mRNA Capping |
29 |
2.23e-01 |
3.62e-01 |
0.17900 |
1.40e-02 |
1.78e-01 |
8.96e-01 |
9.70e-02 |
Retrograde transport at the Trans-Golgi-Network |
45 |
1.21e-01 |
2.38e-01 |
0.17800 |
-2.56e-02 |
1.77e-01 |
7.67e-01 |
4.04e-02 |
TRAF6 mediated NF-kB activation |
21 |
3.45e-01 |
4.89e-01 |
0.17800 |
1.78e-01 |
8.33e-03 |
1.58e-01 |
9.47e-01 |
Toll Like Receptor 9 (TLR9) Cascade |
88 |
1.43e-02 |
4.73e-02 |
0.17800 |
-9.50e-03 |
1.78e-01 |
8.78e-01 |
4.01e-03 |
Amyloid fiber formation |
50 |
4.99e-02 |
1.24e-01 |
0.17800 |
1.29e-01 |
1.22e-01 |
1.15e-01 |
1.35e-01 |
Depolymerisation of the Nuclear Lamina |
15 |
4.55e-01 |
5.88e-01 |
0.17700 |
1.75e-01 |
2.82e-02 |
2.41e-01 |
8.50e-01 |
Transcriptional regulation of granulopoiesis |
38 |
1.13e-01 |
2.28e-01 |
0.17700 |
8.06e-02 |
1.57e-01 |
3.90e-01 |
9.38e-02 |
Positive epigenetic regulation of rRNA expression |
52 |
1.27e-01 |
2.46e-01 |
0.17600 |
-8.92e-02 |
1.52e-01 |
2.66e-01 |
5.76e-02 |
activated TAK1 mediates p38 MAPK activation |
17 |
3.69e-01 |
5.12e-01 |
0.17600 |
1.17e-01 |
1.31e-01 |
4.03e-01 |
3.50e-01 |
Gap junction trafficking and regulation |
23 |
3.07e-01 |
4.55e-01 |
0.17600 |
2.56e-02 |
1.74e-01 |
8.32e-01 |
1.49e-01 |
TRAF6 mediated induction of NFkB and MAP kinases upon TLR7/8 or 9 activation |
83 |
1.73e-02 |
5.54e-02 |
0.17500 |
8.35e-03 |
1.75e-01 |
8.95e-01 |
5.92e-03 |
Erythrocytes take up carbon dioxide and release oxygen |
10 |
5.67e-01 |
6.74e-01 |
0.17500 |
1.53e-01 |
8.57e-02 |
4.04e-01 |
6.39e-01 |
O2/CO2 exchange in erythrocytes |
10 |
5.67e-01 |
6.74e-01 |
0.17500 |
1.53e-01 |
8.57e-02 |
4.04e-01 |
6.39e-01 |
MyD88 dependent cascade initiated on endosome |
84 |
1.84e-02 |
5.79e-02 |
0.17400 |
6.27e-04 |
1.74e-01 |
9.92e-01 |
5.77e-03 |
Transcriptional regulation by small RNAs |
56 |
6.26e-02 |
1.46e-01 |
0.17400 |
1.73e-01 |
1.85e-02 |
2.52e-02 |
8.11e-01 |
TRAF3-dependent IRF activation pathway |
12 |
5.51e-01 |
6.62e-01 |
0.17300 |
-1.72e-01 |
-2.23e-02 |
3.03e-01 |
8.94e-01 |
RNA Polymerase II Transcription Termination |
62 |
5.97e-02 |
1.40e-01 |
0.17300 |
-1.72e-01 |
1.03e-02 |
1.90e-02 |
8.89e-01 |
Regulation of IFNA signaling |
24 |
3.16e-01 |
4.61e-01 |
0.17300 |
-1.19e-02 |
-1.72e-01 |
9.20e-01 |
1.44e-01 |
Cytochrome P450 - arranged by substrate type |
46 |
7.98e-02 |
1.77e-01 |
0.17200 |
1.50e-01 |
8.49e-02 |
7.86e-02 |
3.19e-01 |
Golgi-to-ER retrograde transport |
112 |
1.67e-02 |
5.35e-02 |
0.17200 |
-1.13e-01 |
1.30e-01 |
3.90e-02 |
1.76e-02 |
ABC-family proteins mediated transport |
97 |
2.84e-02 |
8.21e-02 |
0.17200 |
-1.34e-01 |
1.08e-01 |
2.23e-02 |
6.70e-02 |
Translesion synthesis by Y family DNA polymerases bypasses lesions on DNA template |
37 |
1.26e-01 |
2.45e-01 |
0.17200 |
1.07e-01 |
1.35e-01 |
2.62e-01 |
1.55e-01 |
ZBP1(DAI) mediated induction of type I IFNs |
21 |
4.64e-01 |
5.95e-01 |
0.17200 |
-1.20e-01 |
1.23e-01 |
3.39e-01 |
3.30e-01 |
Triglyceride metabolism |
30 |
2.12e-01 |
3.51e-01 |
0.17200 |
1.65e-01 |
4.93e-02 |
1.19e-01 |
6.40e-01 |
MyD88 cascade initiated on plasma membrane |
77 |
2.08e-02 |
6.36e-02 |
0.17200 |
3.72e-02 |
1.68e-01 |
5.73e-01 |
1.10e-02 |
Toll Like Receptor 10 (TLR10) Cascade |
77 |
2.08e-02 |
6.36e-02 |
0.17200 |
3.72e-02 |
1.68e-01 |
5.73e-01 |
1.10e-02 |
Toll Like Receptor 5 (TLR5) Cascade |
77 |
2.08e-02 |
6.36e-02 |
0.17200 |
3.72e-02 |
1.68e-01 |
5.73e-01 |
1.10e-02 |
Regulation of TP53 Activity through Acetylation |
29 |
3.13e-01 |
4.59e-01 |
0.17200 |
-5.69e-02 |
1.62e-01 |
5.96e-01 |
1.31e-01 |
Nuclear Events (kinase and transcription factor activation) |
54 |
5.24e-02 |
1.28e-01 |
0.17200 |
8.64e-02 |
1.48e-01 |
2.72e-01 |
5.95e-02 |
Chaperonin-mediated protein folding |
87 |
3.26e-02 |
8.85e-02 |
0.17100 |
-6.16e-02 |
1.60e-01 |
3.21e-01 |
1.00e-02 |
Signaling by FGFR1 in disease |
31 |
2.71e-01 |
4.16e-01 |
0.17100 |
-3.46e-02 |
1.68e-01 |
7.39e-01 |
1.06e-01 |
Keratan sulfate/keratin metabolism |
29 |
2.17e-01 |
3.55e-01 |
0.17100 |
6.45e-02 |
1.59e-01 |
5.48e-01 |
1.39e-01 |
Activation of GABAB receptors |
37 |
2.14e-01 |
3.53e-01 |
0.17100 |
-3.81e-02 |
1.67e-01 |
6.88e-01 |
7.92e-02 |
GABA B receptor activation |
37 |
2.14e-01 |
3.53e-01 |
0.17100 |
-3.81e-02 |
1.67e-01 |
6.88e-01 |
7.92e-02 |
Butyrate Response Factor 1 (BRF1) binds and destabilizes mRNA |
16 |
4.62e-01 |
5.93e-01 |
0.17100 |
2.18e-02 |
1.69e-01 |
8.80e-01 |
2.41e-01 |
Resolution of Sister Chromatid Cohesion |
103 |
8.60e-03 |
3.15e-02 |
0.17100 |
5.94e-03 |
1.71e-01 |
9.17e-01 |
2.79e-03 |
Aberrant regulation of mitotic exit in cancer due to RB1 defects |
19 |
3.84e-01 |
5.27e-01 |
0.17100 |
1.65e-01 |
4.31e-02 |
2.13e-01 |
7.45e-01 |
Defective EXT1 causes exostoses 1, TRPS2 and CHDS |
14 |
5.32e-01 |
6.46e-01 |
0.17100 |
-4.76e-03 |
1.70e-01 |
9.75e-01 |
2.69e-01 |
Defective EXT2 causes exostoses 2 |
14 |
5.32e-01 |
6.46e-01 |
0.17100 |
-4.76e-03 |
1.70e-01 |
9.75e-01 |
2.69e-01 |
DNA methylation |
13 |
5.35e-01 |
6.48e-01 |
0.17000 |
1.69e-01 |
2.21e-02 |
2.91e-01 |
8.90e-01 |
Ca2+ pathway |
59 |
5.16e-02 |
1.27e-01 |
0.17000 |
4.61e-02 |
1.64e-01 |
5.40e-01 |
2.98e-02 |
Cytosolic sulfonation of small molecules |
21 |
3.95e-01 |
5.37e-01 |
0.17000 |
9.25e-03 |
-1.70e-01 |
9.42e-01 |
1.78e-01 |
Arachidonic acid metabolism |
45 |
8.51e-02 |
1.86e-01 |
0.17000 |
1.17e-01 |
1.23e-01 |
1.74e-01 |
1.54e-01 |
Diseases associated with visual transduction |
10 |
5.81e-01 |
6.84e-01 |
0.17000 |
-1.37e-01 |
-1.00e-01 |
4.53e-01 |
5.84e-01 |
Diseases of the neuronal system |
10 |
5.81e-01 |
6.84e-01 |
0.17000 |
-1.37e-01 |
-1.00e-01 |
4.53e-01 |
5.84e-01 |
Retinoid cycle disease events |
10 |
5.81e-01 |
6.84e-01 |
0.17000 |
-1.37e-01 |
-1.00e-01 |
4.53e-01 |
5.84e-01 |
Meiotic recombination |
34 |
1.78e-01 |
3.12e-01 |
0.16900 |
1.60e-01 |
5.57e-02 |
1.07e-01 |
5.75e-01 |
Nuclear Envelope (NE) Reassembly |
67 |
4.20e-02 |
1.09e-01 |
0.16900 |
2.35e-02 |
1.67e-01 |
7.40e-01 |
1.78e-02 |
HS-GAG degradation |
21 |
3.55e-01 |
4.99e-01 |
0.16900 |
-1.64e-01 |
-4.12e-02 |
1.93e-01 |
7.44e-01 |
RUNX2 regulates bone development |
29 |
2.08e-01 |
3.46e-01 |
0.16900 |
1.15e-01 |
1.24e-01 |
2.85e-01 |
2.48e-01 |
Bile acid and bile salt metabolism |
33 |
1.74e-01 |
3.08e-01 |
0.16900 |
8.76e-02 |
1.44e-01 |
3.84e-01 |
1.52e-01 |
Centrosome maturation |
81 |
1.28e-02 |
4.33e-02 |
0.16900 |
1.15e-01 |
1.24e-01 |
7.43e-02 |
5.48e-02 |
Recruitment of mitotic centrosome proteins and complexes |
81 |
1.28e-02 |
4.33e-02 |
0.16900 |
1.15e-01 |
1.24e-01 |
7.43e-02 |
5.48e-02 |
Glutamate Neurotransmitter Release Cycle |
19 |
5.03e-01 |
6.21e-01 |
0.16800 |
8.45e-02 |
-1.45e-01 |
5.24e-01 |
2.73e-01 |
HCMV Infection |
90 |
8.78e-03 |
3.18e-02 |
0.16800 |
9.06e-02 |
1.42e-01 |
1.38e-01 |
2.04e-02 |
Intracellular signaling by second messengers |
286 |
3.22e-05 |
2.74e-04 |
0.16800 |
-7.54e-02 |
1.50e-01 |
2.87e-02 |
1.30e-05 |
DNA Damage Recognition in GG-NER |
38 |
1.85e-01 |
3.21e-01 |
0.16800 |
3.44e-03 |
1.68e-01 |
9.71e-01 |
7.38e-02 |
TRAF6 mediated IRF7 activation |
26 |
3.01e-01 |
4.51e-01 |
0.16700 |
-1.94e-02 |
-1.66e-01 |
8.64e-01 |
1.42e-01 |
Caspase activation via extrinsic apoptotic signalling pathway |
22 |
4.66e-01 |
5.95e-01 |
0.16700 |
-1.23e-01 |
1.14e-01 |
3.19e-01 |
3.56e-01 |
Cellular responses to external stimuli |
470 |
1.78e-09 |
7.78e-08 |
0.16700 |
2.38e-03 |
1.67e-01 |
9.30e-01 |
6.23e-10 |
Cyclin D associated events in G1 |
46 |
9.54e-02 |
1.99e-01 |
0.16700 |
7.38e-02 |
1.50e-01 |
3.87e-01 |
7.86e-02 |
G1 Phase |
46 |
9.54e-02 |
1.99e-01 |
0.16700 |
7.38e-02 |
1.50e-01 |
3.87e-01 |
7.86e-02 |
Lysosome Vesicle Biogenesis |
34 |
2.61e-01 |
4.08e-01 |
0.16700 |
-1.62e-01 |
3.93e-02 |
1.02e-01 |
6.92e-01 |
FGFR2 mutant receptor activation |
24 |
3.12e-01 |
4.59e-01 |
0.16700 |
1.60e-01 |
4.65e-02 |
1.75e-01 |
6.93e-01 |
MAPK1/MAPK3 signaling |
255 |
1.73e-04 |
1.13e-03 |
0.16700 |
-1.06e-01 |
1.29e-01 |
3.66e-03 |
4.18e-04 |
Cellular responses to stress |
465 |
3.24e-09 |
1.23e-07 |
0.16700 |
-2.36e-03 |
1.66e-01 |
9.31e-01 |
8.88e-10 |
Signaling by Nuclear Receptors |
228 |
9.20e-05 |
6.61e-04 |
0.16600 |
-1.97e-02 |
1.65e-01 |
6.08e-01 |
1.77e-05 |
Interferon gamma signaling |
69 |
4.48e-02 |
1.14e-01 |
0.16600 |
-1.66e-01 |
-1.54e-02 |
1.74e-02 |
8.25e-01 |
Nuclear Envelope Breakdown |
53 |
8.76e-02 |
1.89e-01 |
0.16600 |
1.64e-01 |
2.65e-02 |
3.93e-02 |
7.39e-01 |
SARS-CoV-2 Infection |
63 |
1.16e-01 |
2.32e-01 |
0.16600 |
-1.02e-01 |
1.31e-01 |
1.62e-01 |
7.28e-02 |
mRNA Splicing |
180 |
2.28e-03 |
1.10e-02 |
0.16600 |
-1.03e-01 |
1.30e-01 |
1.73e-02 |
2.74e-03 |
TP53 Regulates Transcription of DNA Repair Genes |
60 |
4.45e-02 |
1.14e-01 |
0.16500 |
1.22e-01 |
1.11e-01 |
1.02e-01 |
1.36e-01 |
Dectin-2 family |
18 |
4.53e-01 |
5.87e-01 |
0.16500 |
-1.65e-01 |
-1.02e-02 |
2.26e-01 |
9.40e-01 |
MAPK family signaling cascades |
291 |
5.33e-05 |
4.17e-04 |
0.16500 |
-9.31e-02 |
1.37e-01 |
6.45e-03 |
6.36e-05 |
AURKA Activation by TPX2 |
72 |
2.47e-02 |
7.27e-02 |
0.16500 |
1.03e-01 |
1.29e-01 |
1.31e-01 |
5.86e-02 |
Aquaporin-mediated transport |
44 |
1.04e-01 |
2.13e-01 |
0.16500 |
1.19e-01 |
1.14e-01 |
1.73e-01 |
1.90e-01 |
Signaling by NTRK3 (TRKC) |
17 |
4.61e-01 |
5.93e-01 |
0.16500 |
1.62e-01 |
2.81e-02 |
2.47e-01 |
8.41e-01 |
ISG15 antiviral mechanism |
68 |
9.16e-02 |
1.94e-01 |
0.16400 |
-7.21e-02 |
1.48e-01 |
3.04e-01 |
3.54e-02 |
Negative regulation of FGFR2 signaling |
25 |
3.64e-01 |
5.08e-01 |
0.16400 |
-1.72e-02 |
1.63e-01 |
8.82e-01 |
1.58e-01 |
Class I MHC mediated antigen processing & presentation |
341 |
1.52e-05 |
1.44e-04 |
0.16400 |
-1.20e-01 |
1.11e-01 |
1.39e-04 |
4.44e-04 |
Unblocking of NMDA receptors, glutamate binding and activation |
20 |
5.09e-01 |
6.25e-01 |
0.16400 |
1.35e-01 |
-9.20e-02 |
2.95e-01 |
4.76e-01 |
RAF/MAP kinase cascade |
250 |
2.77e-04 |
1.73e-03 |
0.16400 |
-1.05e-01 |
1.26e-01 |
4.47e-03 |
6.30e-04 |
Notch-HLH transcription pathway |
27 |
2.60e-01 |
4.07e-01 |
0.16300 |
1.38e-01 |
8.79e-02 |
2.16e-01 |
4.29e-01 |
SARS-CoV-1 Infection |
46 |
1.82e-01 |
3.17e-01 |
0.16300 |
-4.52e-02 |
1.57e-01 |
5.96e-01 |
6.58e-02 |
Interleukin-20 family signaling |
16 |
5.84e-01 |
6.87e-01 |
0.16300 |
8.93e-02 |
-1.37e-01 |
5.36e-01 |
3.44e-01 |
Formation of TC-NER Pre-Incision Complex |
53 |
1.15e-01 |
2.30e-01 |
0.16300 |
-8.04e-03 |
1.63e-01 |
9.19e-01 |
4.03e-02 |
Gap junction trafficking |
21 |
3.94e-01 |
5.36e-01 |
0.16300 |
2.53e-02 |
1.61e-01 |
8.41e-01 |
2.02e-01 |
SUMOylation of ubiquitinylation proteins |
38 |
1.79e-01 |
3.12e-01 |
0.16300 |
1.58e-01 |
3.66e-02 |
9.10e-02 |
6.96e-01 |
PKA activation |
17 |
4.29e-01 |
5.67e-01 |
0.16300 |
1.32e-01 |
9.45e-02 |
3.45e-01 |
5.00e-01 |
Loss of Nlp from mitotic centrosomes |
69 |
3.27e-02 |
8.85e-02 |
0.16200 |
9.70e-02 |
1.30e-01 |
1.64e-01 |
6.17e-02 |
Loss of proteins required for interphase microtubule organization from the centrosome |
69 |
3.27e-02 |
8.85e-02 |
0.16200 |
9.70e-02 |
1.30e-01 |
1.64e-01 |
6.17e-02 |
Activation of SMO |
17 |
4.28e-01 |
5.67e-01 |
0.16200 |
-1.25e-01 |
-1.04e-01 |
3.73e-01 |
4.59e-01 |
FRS-mediated FGFR1 signaling |
15 |
6.14e-01 |
7.10e-01 |
0.16200 |
-1.14e-01 |
1.15e-01 |
4.45e-01 |
4.39e-01 |
Termination of translesion DNA synthesis |
31 |
2.24e-01 |
3.63e-01 |
0.16200 |
1.44e-01 |
7.34e-02 |
1.64e-01 |
4.80e-01 |
ADORA2B mediated anti-inflammatory cytokines production |
78 |
5.40e-02 |
1.30e-01 |
0.16100 |
-3.17e-02 |
1.58e-01 |
6.29e-01 |
1.57e-02 |
HDR through Single Strand Annealing (SSA) |
37 |
1.75e-01 |
3.08e-01 |
0.16100 |
1.48e-01 |
6.42e-02 |
1.19e-01 |
4.99e-01 |
Cell Cycle Checkpoints |
249 |
5.47e-05 |
4.26e-04 |
0.16100 |
-7.59e-03 |
1.61e-01 |
8.37e-01 |
1.25e-05 |
Recruitment of NuMA to mitotic centrosomes |
80 |
2.01e-02 |
6.20e-02 |
0.16100 |
1.26e-01 |
1.00e-01 |
5.17e-02 |
1.22e-01 |
mRNA decay by 5' to 3' exoribonuclease |
15 |
5.07e-01 |
6.22e-01 |
0.16100 |
4.77e-02 |
1.53e-01 |
7.49e-01 |
3.04e-01 |
FRS-mediated FGFR4 signaling |
14 |
6.38e-01 |
7.27e-01 |
0.16100 |
-1.27e-01 |
9.88e-02 |
4.12e-01 |
5.22e-01 |
NOTCH1 Intracellular Domain Regulates Transcription |
47 |
1.41e-01 |
2.65e-01 |
0.16100 |
1.27e-02 |
1.60e-01 |
8.80e-01 |
5.78e-02 |
Signaling by ERBB2 KD Mutants |
23 |
4.82e-01 |
6.06e-01 |
0.16000 |
-1.16e-01 |
1.11e-01 |
3.35e-01 |
3.59e-01 |
Metabolism of folate and pterines |
17 |
5.52e-01 |
6.62e-01 |
0.16000 |
1.51e-01 |
-5.26e-02 |
2.80e-01 |
7.07e-01 |
Chromosome Maintenance |
95 |
2.28e-02 |
6.80e-02 |
0.16000 |
1.60e-01 |
-2.78e-03 |
7.01e-03 |
9.63e-01 |
FLT3 Signaling |
264 |
2.62e-04 |
1.64e-03 |
0.16000 |
-1.07e-01 |
1.19e-01 |
2.82e-03 |
8.91e-04 |
Assembly and cell surface presentation of NMDA receptors |
24 |
4.68e-01 |
5.95e-01 |
0.16000 |
1.20e-01 |
-1.05e-01 |
3.09e-01 |
3.71e-01 |
ROS and RNS production in phagocytes |
35 |
2.76e-01 |
4.23e-01 |
0.16000 |
-3.02e-02 |
1.57e-01 |
7.58e-01 |
1.08e-01 |
Interconversion of nucleotide di- and triphosphates |
27 |
3.23e-01 |
4.65e-01 |
0.16000 |
1.59e-01 |
1.79e-02 |
1.54e-01 |
8.72e-01 |
Cytosolic sensors of pathogen-associated DNA |
61 |
1.43e-01 |
2.67e-01 |
0.16000 |
-1.31e-01 |
9.14e-02 |
7.76e-02 |
2.17e-01 |
Regulation of RUNX1 Expression and Activity |
17 |
4.71e-01 |
5.96e-01 |
0.15900 |
-4.37e-02 |
-1.53e-01 |
7.55e-01 |
2.74e-01 |
RA biosynthesis pathway |
19 |
4.71e-01 |
5.96e-01 |
0.15800 |
-1.58e-01 |
-2.11e-03 |
2.32e-01 |
9.87e-01 |
G alpha (z) signalling events |
44 |
2.06e-01 |
3.46e-01 |
0.15800 |
-3.31e-02 |
1.55e-01 |
7.04e-01 |
7.56e-02 |
Homologous DNA Pairing and Strand Exchange |
42 |
1.63e-01 |
2.97e-01 |
0.15800 |
1.54e-01 |
3.86e-02 |
8.52e-02 |
6.65e-01 |
SUMOylation of SUMOylation proteins |
35 |
1.95e-01 |
3.32e-01 |
0.15800 |
1.34e-01 |
8.41e-02 |
1.71e-01 |
3.89e-01 |
RIP-mediated NFkB activation via ZBP1 |
17 |
5.79e-01 |
6.83e-01 |
0.15800 |
-7.65e-02 |
1.38e-01 |
5.85e-01 |
3.24e-01 |
Signaling by WNT |
264 |
1.79e-04 |
1.17e-03 |
0.15700 |
-5.64e-02 |
1.47e-01 |
1.15e-01 |
4.30e-05 |
Regulation of FZD by ubiquitination |
18 |
4.67e-01 |
5.95e-01 |
0.15700 |
1.52e-01 |
3.73e-02 |
2.64e-01 |
7.84e-01 |
Presynaptic phase of homologous DNA pairing and strand exchange |
39 |
1.67e-01 |
3.02e-01 |
0.15700 |
1.32e-01 |
8.49e-02 |
1.55e-01 |
3.59e-01 |
RNA polymerase II transcribes snRNA genes |
71 |
7.15e-02 |
1.64e-01 |
0.15600 |
-1.10e-02 |
1.56e-01 |
8.73e-01 |
2.30e-02 |
Glyoxylate metabolism and glycine degradation |
28 |
3.60e-01 |
5.04e-01 |
0.15600 |
1.55e-01 |
-1.82e-02 |
1.55e-01 |
8.68e-01 |
The NLRP3 inflammasome |
15 |
6.26e-01 |
7.19e-01 |
0.15600 |
-8.06e-02 |
1.34e-01 |
5.89e-01 |
3.69e-01 |
Negative regulation of FGFR3 signaling |
23 |
4.49e-01 |
5.87e-01 |
0.15600 |
-3.45e-02 |
1.52e-01 |
7.74e-01 |
2.06e-01 |
Oncogene Induced Senescence |
32 |
2.80e-01 |
4.27e-01 |
0.15600 |
1.56e-01 |
1.46e-02 |
1.28e-01 |
8.86e-01 |
Amine ligand-binding receptors |
16 |
5.40e-01 |
6.51e-01 |
0.15600 |
-4.18e-03 |
-1.56e-01 |
9.77e-01 |
2.81e-01 |
Glutathione conjugation |
30 |
2.52e-01 |
3.97e-01 |
0.15600 |
1.20e-01 |
9.89e-02 |
2.54e-01 |
3.49e-01 |
Signaling by NOTCH1 |
71 |
1.14e-01 |
2.28e-01 |
0.15600 |
-8.49e-02 |
1.31e-01 |
2.16e-01 |
5.70e-02 |
RAS processing |
19 |
5.37e-01 |
6.49e-01 |
0.15500 |
-5.30e-02 |
1.46e-01 |
6.89e-01 |
2.70e-01 |
Class I peroxisomal membrane protein import |
20 |
4.17e-01 |
5.57e-01 |
0.15500 |
1.42e-01 |
6.26e-02 |
2.71e-01 |
6.28e-01 |
TP53 Regulates Metabolic Genes |
84 |
2.88e-02 |
8.28e-02 |
0.15500 |
4.70e-02 |
1.48e-01 |
4.57e-01 |
1.92e-02 |
SHC-mediated cascade:FGFR2 |
14 |
5.28e-01 |
6.43e-01 |
0.15500 |
1.18e-01 |
1.00e-01 |
4.43e-01 |
5.16e-01 |
Sphingolipid de novo biosynthesis |
44 |
2.46e-01 |
3.92e-01 |
0.15400 |
-1.43e-01 |
5.67e-02 |
9.99e-02 |
5.15e-01 |
Signaling by Rho GTPases |
370 |
1.31e-06 |
1.73e-05 |
0.15400 |
1.49e-03 |
1.54e-01 |
9.61e-01 |
3.86e-07 |
Cell-Cell communication |
108 |
1.77e-02 |
5.62e-02 |
0.15400 |
2.95e-03 |
1.54e-01 |
9.58e-01 |
5.72e-03 |
EML4 and NUDC in mitotic spindle formation |
94 |
2.35e-02 |
6.98e-02 |
0.15400 |
3.01e-02 |
1.51e-01 |
6.14e-01 |
1.16e-02 |
Plasma lipoprotein assembly |
17 |
5.87e-01 |
6.88e-01 |
0.15300 |
1.42e-01 |
-5.90e-02 |
3.12e-01 |
6.74e-01 |
Activation of AMPK downstream of NMDARs |
10 |
7.04e-01 |
7.85e-01 |
0.15300 |
1.52e-01 |
-1.63e-02 |
4.05e-01 |
9.29e-01 |
Ras activation upon Ca2+ influx through NMDA receptor |
19 |
4.67e-01 |
5.95e-01 |
0.15300 |
1.49e-01 |
3.35e-02 |
2.60e-01 |
8.00e-01 |
Metabolism of proteins |
1749 |
2.08e-21 |
7.29e-19 |
0.15300 |
-6.58e-02 |
1.38e-01 |
7.12e-06 |
4.61e-21 |
Synthesis of PIPs at the Golgi membrane |
18 |
5.73e-01 |
6.77e-01 |
0.15300 |
-1.40e-01 |
5.98e-02 |
3.02e-01 |
6.61e-01 |
TCF dependent signaling in response to WNT |
172 |
5.38e-03 |
2.16e-02 |
0.15300 |
-6.34e-02 |
1.39e-01 |
1.52e-01 |
1.71e-03 |
Regulation of PLK1 Activity at G2/M Transition |
87 |
2.79e-02 |
8.09e-02 |
0.15300 |
5.02e-02 |
1.44e-01 |
4.19e-01 |
2.03e-02 |
Protein folding |
93 |
4.56e-02 |
1.16e-01 |
0.15200 |
-3.09e-02 |
1.49e-01 |
6.07e-01 |
1.30e-02 |
CaM pathway |
33 |
2.39e-01 |
3.82e-01 |
0.15200 |
8.37e-02 |
1.27e-01 |
4.05e-01 |
2.06e-01 |
Calmodulin induced events |
33 |
2.39e-01 |
3.82e-01 |
0.15200 |
8.37e-02 |
1.27e-01 |
4.05e-01 |
2.06e-01 |
Cobalamin (Cbl, vitamin B12) transport and metabolism |
16 |
4.97e-01 |
6.17e-01 |
0.15200 |
-8.95e-02 |
-1.23e-01 |
5.35e-01 |
3.94e-01 |
Inflammasomes |
20 |
5.05e-01 |
6.22e-01 |
0.15200 |
-1.51e-01 |
2.14e-02 |
2.44e-01 |
8.68e-01 |
cGMP effects |
15 |
5.20e-01 |
6.34e-01 |
0.15200 |
1.22e-01 |
9.02e-02 |
4.12e-01 |
5.45e-01 |
Transferrin endocytosis and recycling |
30 |
2.95e-01 |
4.45e-01 |
0.15100 |
5.05e-02 |
1.43e-01 |
6.32e-01 |
1.76e-01 |
Processing of Capped Intron-Containing Pre-mRNA |
231 |
1.67e-03 |
8.27e-03 |
0.15000 |
-9.55e-02 |
1.16e-01 |
1.26e-02 |
2.42e-03 |
NS1 Mediated Effects on Host Pathways |
38 |
2.09e-01 |
3.47e-01 |
0.15000 |
6.61e-02 |
1.35e-01 |
4.81e-01 |
1.51e-01 |
Sodium/Calcium exchangers |
10 |
7.49e-01 |
8.23e-01 |
0.15000 |
1.32e-01 |
-7.05e-02 |
4.70e-01 |
7.00e-01 |
M Phase |
348 |
6.40e-06 |
6.69e-05 |
0.14900 |
1.48e-03 |
1.49e-01 |
9.62e-01 |
1.85e-06 |
Diseases associated with glycosaminoglycan metabolism |
38 |
2.16e-01 |
3.55e-01 |
0.14900 |
6.20e-02 |
1.35e-01 |
5.09e-01 |
1.49e-01 |
Constitutive Signaling by NOTCH1 HD+PEST Domain Mutants |
57 |
1.74e-01 |
3.08e-01 |
0.14900 |
-4.20e-02 |
1.43e-01 |
5.84e-01 |
6.25e-02 |
Constitutive Signaling by NOTCH1 PEST Domain Mutants |
57 |
1.74e-01 |
3.08e-01 |
0.14900 |
-4.20e-02 |
1.43e-01 |
5.84e-01 |
6.25e-02 |
Signaling by NOTCH1 HD+PEST Domain Mutants in Cancer |
57 |
1.74e-01 |
3.08e-01 |
0.14900 |
-4.20e-02 |
1.43e-01 |
5.84e-01 |
6.25e-02 |
Signaling by NOTCH1 PEST Domain Mutants in Cancer |
57 |
1.74e-01 |
3.08e-01 |
0.14900 |
-4.20e-02 |
1.43e-01 |
5.84e-01 |
6.25e-02 |
Signaling by NOTCH1 in Cancer |
57 |
1.74e-01 |
3.08e-01 |
0.14900 |
-4.20e-02 |
1.43e-01 |
5.84e-01 |
6.25e-02 |
Defective TPR may confer susceptibility towards thyroid papillary carcinoma (TPC) |
30 |
3.19e-01 |
4.62e-01 |
0.14900 |
1.45e-01 |
3.51e-02 |
1.71e-01 |
7.39e-01 |
Regulation of Glucokinase by Glucokinase Regulatory Protein |
30 |
3.19e-01 |
4.62e-01 |
0.14900 |
1.45e-01 |
3.51e-02 |
1.71e-01 |
7.39e-01 |
Signaling by Receptor Tyrosine Kinases |
451 |
1.49e-06 |
1.94e-05 |
0.14900 |
-4.34e-02 |
1.42e-01 |
1.16e-01 |
2.51e-07 |
CREB1 phosphorylation through NMDA receptor-mediated activation of RAS signaling |
27 |
3.41e-01 |
4.85e-01 |
0.14800 |
6.02e-02 |
1.35e-01 |
5.88e-01 |
2.24e-01 |
Energy dependent regulation of mTOR by LKB1-AMPK |
29 |
4.53e-01 |
5.87e-01 |
0.14800 |
1.18e-01 |
-9.01e-02 |
2.73e-01 |
4.01e-01 |
Mitotic G2-G2/M phases |
183 |
3.32e-03 |
1.51e-02 |
0.14800 |
-2.84e-02 |
1.45e-01 |
5.08e-01 |
7.30e-04 |
Pre-NOTCH Transcription and Translation |
41 |
1.95e-01 |
3.32e-01 |
0.14800 |
1.33e-01 |
6.51e-02 |
1.42e-01 |
4.71e-01 |
G2/M Transition |
181 |
3.65e-03 |
1.62e-02 |
0.14800 |
-2.93e-02 |
1.45e-01 |
4.97e-01 |
8.06e-04 |
Constitutive Signaling by Aberrant PI3K in Cancer |
60 |
1.92e-01 |
3.29e-01 |
0.14700 |
-1.25e-01 |
7.82e-02 |
9.46e-02 |
2.95e-01 |
GABA receptor activation |
48 |
2.21e-01 |
3.58e-01 |
0.14700 |
-2.59e-02 |
1.45e-01 |
7.56e-01 |
8.23e-02 |
Sphingolipid metabolism |
81 |
8.14e-02 |
1.79e-01 |
0.14700 |
-1.44e-01 |
3.04e-02 |
2.51e-02 |
6.36e-01 |
Cellular Senescence |
136 |
6.70e-03 |
2.57e-02 |
0.14700 |
1.43e-01 |
3.28e-02 |
3.92e-03 |
5.10e-01 |
Downstream signaling of activated FGFR4 |
19 |
5.88e-01 |
6.88e-01 |
0.14700 |
-1.30e-01 |
6.87e-02 |
3.27e-01 |
6.04e-01 |
MAP3K8 (TPL2)-dependent MAPK1/3 activation |
16 |
5.93e-01 |
6.93e-01 |
0.14700 |
-1.21e-02 |
1.46e-01 |
9.33e-01 |
3.11e-01 |
Cell Cycle, Mitotic |
488 |
2.55e-08 |
6.75e-07 |
0.14700 |
3.31e-02 |
1.43e-01 |
2.13e-01 |
7.29e-08 |
Immune System |
1784 |
4.99e-20 |
1.40e-17 |
0.14600 |
-6.31e-02 |
1.32e-01 |
1.37e-05 |
9.46e-20 |
LDL clearance |
19 |
5.68e-01 |
6.74e-01 |
0.14600 |
-4.03e-02 |
1.41e-01 |
7.61e-01 |
2.89e-01 |
SMAD2/SMAD3:SMAD4 heterotrimer regulates transcription |
32 |
3.63e-01 |
5.06e-01 |
0.14600 |
-1.87e-02 |
1.45e-01 |
8.55e-01 |
1.56e-01 |
Developmental Biology |
770 |
5.30e-12 |
5.20e-10 |
0.14600 |
1.98e-02 |
1.45e-01 |
3.52e-01 |
1.16e-11 |
FGFR1 mutant receptor activation |
24 |
4.70e-01 |
5.96e-01 |
0.14500 |
-1.71e-02 |
1.44e-01 |
8.85e-01 |
2.21e-01 |
Interleukin-17 signaling |
66 |
9.49e-02 |
1.99e-01 |
0.14500 |
2.79e-02 |
1.43e-01 |
6.96e-01 |
4.52e-02 |
RHO GTPases Activate Formins |
117 |
2.20e-02 |
6.61e-02 |
0.14500 |
-2.90e-03 |
1.45e-01 |
9.57e-01 |
6.71e-03 |
Mitotic Prophase |
89 |
2.95e-02 |
8.38e-02 |
0.14500 |
8.73e-02 |
1.16e-01 |
1.55e-01 |
5.90e-02 |
Acyl chain remodelling of PE |
20 |
5.48e-01 |
6.59e-01 |
0.14500 |
1.42e-01 |
-3.04e-02 |
2.73e-01 |
8.14e-01 |
Neddylation |
224 |
3.22e-03 |
1.48e-02 |
0.14500 |
-1.08e-01 |
9.62e-02 |
5.36e-03 |
1.33e-02 |
Regulation of TP53 Activity through Association with Co-factors |
13 |
6.02e-01 |
7.00e-01 |
0.14500 |
1.24e-01 |
7.41e-02 |
4.38e-01 |
6.44e-01 |
PI3K events in ERBB2 signaling |
14 |
6.03e-01 |
7.00e-01 |
0.14500 |
-1.40e-01 |
-3.60e-02 |
3.64e-01 |
8.15e-01 |
PI Metabolism |
82 |
9.13e-02 |
1.94e-01 |
0.14500 |
-3.75e-02 |
1.40e-01 |
5.58e-01 |
2.89e-02 |
Formation of the Early Elongation Complex |
33 |
2.90e-01 |
4.40e-01 |
0.14400 |
5.60e-02 |
1.33e-01 |
5.78e-01 |
1.87e-01 |
Formation of the HIV-1 Early Elongation Complex |
33 |
2.90e-01 |
4.40e-01 |
0.14400 |
5.60e-02 |
1.33e-01 |
5.78e-01 |
1.87e-01 |
Glycosphingolipid metabolism |
37 |
2.99e-01 |
4.49e-01 |
0.14400 |
-1.44e-01 |
-9.74e-04 |
1.30e-01 |
9.92e-01 |
Mitotic Prometaphase |
184 |
9.93e-04 |
5.20e-03 |
0.14400 |
6.29e-02 |
1.30e-01 |
1.42e-01 |
2.47e-03 |
Defects in cobalamin (B12) metabolism |
13 |
6.09e-01 |
7.04e-01 |
0.14400 |
-1.28e-01 |
-6.66e-02 |
4.26e-01 |
6.78e-01 |
Disease |
1333 |
8.84e-17 |
1.38e-14 |
0.14300 |
-2.17e-02 |
1.42e-01 |
1.89e-01 |
9.26e-18 |
Amplification of signal from unattached kinetochores via a MAD2 inhibitory signal |
90 |
4.24e-02 |
1.10e-01 |
0.14300 |
3.28e-02 |
1.40e-01 |
5.91e-01 |
2.23e-02 |
Amplification of signal from the kinetochores |
90 |
4.24e-02 |
1.10e-01 |
0.14300 |
3.28e-02 |
1.40e-01 |
5.91e-01 |
2.23e-02 |
Activation of Matrix Metalloproteinases |
22 |
5.58e-01 |
6.67e-01 |
0.14300 |
-1.27e-01 |
6.54e-02 |
3.02e-01 |
5.95e-01 |
Signaling by FGFR2 in disease |
34 |
2.77e-01 |
4.23e-01 |
0.14300 |
7.36e-02 |
1.22e-01 |
4.58e-01 |
2.18e-01 |
Estrogen-dependent gene expression |
97 |
4.88e-02 |
1.22e-01 |
0.14200 |
-5.73e-03 |
1.42e-01 |
9.22e-01 |
1.55e-02 |
Regulation of insulin secretion |
69 |
7.16e-02 |
1.64e-01 |
0.14200 |
1.05e-01 |
9.52e-02 |
1.30e-01 |
1.72e-01 |
GRB2 events in ERBB2 signaling |
14 |
7.03e-01 |
7.85e-01 |
0.14200 |
-8.43e-02 |
1.14e-01 |
5.85e-01 |
4.60e-01 |
Cell recruitment (pro-inflammatory response) |
22 |
4.51e-01 |
5.87e-01 |
0.14100 |
5.51e-02 |
1.30e-01 |
6.55e-01 |
2.90e-01 |
Purinergic signaling in leishmaniasis infection |
22 |
4.51e-01 |
5.87e-01 |
0.14100 |
5.51e-02 |
1.30e-01 |
6.55e-01 |
2.90e-01 |
Tristetraprolin (TTP, ZFP36) binds and destabilizes mRNA |
16 |
6.08e-01 |
7.04e-01 |
0.14100 |
-1.32e-03 |
1.41e-01 |
9.93e-01 |
3.29e-01 |
Metabolism of cofactors |
19 |
6.02e-01 |
7.00e-01 |
0.14100 |
-1.32e-01 |
4.86e-02 |
3.20e-01 |
7.14e-01 |
L1CAM interactions |
92 |
3.80e-02 |
1.00e-01 |
0.14000 |
5.67e-02 |
1.28e-01 |
3.48e-01 |
3.35e-02 |
Muscle contraction |
144 |
5.60e-03 |
2.22e-02 |
0.14000 |
6.60e-02 |
1.24e-01 |
1.72e-01 |
1.04e-02 |
DAG and IP3 signaling |
39 |
2.36e-01 |
3.81e-01 |
0.14000 |
8.19e-02 |
1.14e-01 |
3.76e-01 |
2.19e-01 |
Mitochondrial protein import |
61 |
1.09e-01 |
2.22e-01 |
0.14000 |
1.23e-01 |
6.78e-02 |
9.76e-02 |
3.60e-01 |
Cytokine Signaling in Immune system |
736 |
1.47e-08 |
4.37e-07 |
0.14000 |
-6.04e-02 |
1.26e-01 |
5.56e-03 |
6.86e-09 |
Glycerophospholipid biosynthesis |
114 |
5.46e-02 |
1.31e-01 |
0.14000 |
1.27e-01 |
-5.97e-02 |
1.98e-02 |
2.72e-01 |
Fatty acid metabolism |
150 |
9.37e-03 |
3.35e-02 |
0.13900 |
1.07e-02 |
1.39e-01 |
8.21e-01 |
3.38e-03 |
Gamma carboxylation, hypusine formation and arylsulfatase activation |
34 |
3.20e-01 |
4.63e-01 |
0.13900 |
-3.66e-02 |
-1.34e-01 |
7.12e-01 |
1.77e-01 |
Mitochondrial biogenesis |
89 |
4.18e-02 |
1.09e-01 |
0.13900 |
7.35e-02 |
1.17e-01 |
2.31e-01 |
5.57e-02 |
Regulation of beta-cell development |
29 |
3.50e-01 |
4.94e-01 |
0.13800 |
1.10e-01 |
8.38e-02 |
3.04e-01 |
4.35e-01 |
Mitotic Spindle Checkpoint |
106 |
3.00e-02 |
8.41e-02 |
0.13800 |
3.78e-02 |
1.33e-01 |
5.02e-01 |
1.83e-02 |
Nucleotide-binding domain, leucine rich repeat containing receptor (NLR) signaling pathways |
48 |
3.11e-01 |
4.59e-01 |
0.13800 |
-7.00e-02 |
1.19e-01 |
4.02e-01 |
1.54e-01 |
PKA activation in glucagon signalling |
16 |
5.69e-01 |
6.74e-01 |
0.13800 |
1.20e-01 |
6.82e-02 |
4.07e-01 |
6.37e-01 |
SLC transporter disorders |
90 |
1.21e-01 |
2.38e-01 |
0.13800 |
8.80e-02 |
-1.06e-01 |
1.49e-01 |
8.25e-02 |
Transcriptional Regulation by VENTX |
35 |
4.41e-01 |
5.78e-01 |
0.13800 |
9.95e-02 |
-9.52e-02 |
3.09e-01 |
3.30e-01 |
Presynaptic function of Kainate receptors |
19 |
5.84e-01 |
6.87e-01 |
0.13700 |
-1.29e-02 |
1.36e-01 |
9.22e-01 |
3.03e-01 |
Transcriptional Regulation by TP53 |
340 |
2.37e-05 |
2.12e-04 |
0.13700 |
2.81e-02 |
1.34e-01 |
3.75e-01 |
2.26e-05 |
Negative regulation of NMDA receptor-mediated neuronal transmission |
20 |
6.21e-01 |
7.15e-01 |
0.13700 |
7.29e-02 |
-1.16e-01 |
5.73e-01 |
3.69e-01 |
MicroRNA (miRNA) biogenesis |
24 |
5.58e-01 |
6.67e-01 |
0.13600 |
1.23e-01 |
-5.99e-02 |
2.98e-01 |
6.12e-01 |
MHC class II antigen presentation |
95 |
9.87e-02 |
2.04e-01 |
0.13600 |
-5.69e-02 |
1.24e-01 |
3.38e-01 |
3.69e-02 |
RIPK1-mediated regulated necrosis |
26 |
5.02e-01 |
6.21e-01 |
0.13600 |
-2.98e-02 |
1.33e-01 |
7.92e-01 |
2.40e-01 |
Regulated Necrosis |
26 |
5.02e-01 |
6.21e-01 |
0.13600 |
-2.98e-02 |
1.33e-01 |
7.92e-01 |
2.40e-01 |
Regulation of necroptotic cell death |
26 |
5.02e-01 |
6.21e-01 |
0.13600 |
-2.98e-02 |
1.33e-01 |
7.92e-01 |
2.40e-01 |
PI3K/AKT Signaling in Cancer |
87 |
1.37e-01 |
2.60e-01 |
0.13600 |
-1.02e-01 |
9.07e-02 |
1.02e-01 |
1.44e-01 |
Vpr-mediated nuclear import of PICs |
34 |
3.11e-01 |
4.59e-01 |
0.13600 |
1.17e-01 |
6.86e-02 |
2.36e-01 |
4.89e-01 |
RNA Polymerase III Transcription Initiation From Type 3 Promoter |
26 |
4.68e-01 |
5.95e-01 |
0.13600 |
1.36e-01 |
2.83e-03 |
2.31e-01 |
9.80e-01 |
SUMOylation of DNA replication proteins |
46 |
2.05e-01 |
3.44e-01 |
0.13600 |
7.52e-02 |
1.13e-01 |
3.78e-01 |
1.85e-01 |
RUNX1 regulates genes involved in megakaryocyte differentiation and platelet function |
43 |
3.51e-01 |
4.94e-01 |
0.13600 |
1.25e-01 |
-5.35e-02 |
1.57e-01 |
5.44e-01 |
Sulfur amino acid metabolism |
26 |
5.50e-01 |
6.61e-01 |
0.13500 |
7.64e-02 |
-1.12e-01 |
5.00e-01 |
3.25e-01 |
Heme biosynthesis |
13 |
7.17e-01 |
7.97e-01 |
0.13500 |
-1.30e-01 |
3.48e-02 |
4.16e-01 |
8.28e-01 |
Biosynthesis of the N-glycan precursor (dolichol lipid-linked oligosaccharide, LLO) and transfer to a nascent protein |
72 |
1.31e-01 |
2.51e-01 |
0.13500 |
-1.35e-01 |
2.97e-03 |
4.79e-02 |
9.65e-01 |
Transcriptional regulation by RUNX1 |
174 |
2.09e-02 |
6.38e-02 |
0.13500 |
-9.35e-02 |
9.70e-02 |
3.36e-02 |
2.76e-02 |
RNA Polymerase I Transcription Initiation |
44 |
3.49e-01 |
4.94e-01 |
0.13500 |
-1.23e-01 |
5.47e-02 |
1.58e-01 |
5.30e-01 |
RNA Polymerase III Abortive And Retractive Initiation |
39 |
3.68e-01 |
5.11e-01 |
0.13400 |
1.31e-01 |
-3.11e-02 |
1.58e-01 |
7.37e-01 |
RNA Polymerase III Transcription |
39 |
3.68e-01 |
5.11e-01 |
0.13400 |
1.31e-01 |
-3.11e-02 |
1.58e-01 |
7.37e-01 |
Synthesis of IP3 and IP4 in the cytosol |
25 |
5.07e-01 |
6.22e-01 |
0.13400 |
-1.30e-02 |
1.34e-01 |
9.11e-01 |
2.47e-01 |
Synthesis of PA |
32 |
4.91e-01 |
6.12e-01 |
0.13400 |
9.78e-02 |
-9.19e-02 |
3.39e-01 |
3.69e-01 |
Phosphorylation of the APC/C |
19 |
5.37e-01 |
6.49e-01 |
0.13400 |
1.21e-01 |
5.70e-02 |
3.61e-01 |
6.67e-01 |
Signaling by NTRKs |
125 |
2.79e-02 |
8.09e-02 |
0.13400 |
8.54e-03 |
1.33e-01 |
8.69e-01 |
1.00e-02 |
Deadenylation-dependent mRNA decay |
52 |
3.14e-01 |
4.59e-01 |
0.13300 |
-7.86e-02 |
1.08e-01 |
3.27e-01 |
1.79e-01 |
Maturation of nucleoprotein |
10 |
7.92e-01 |
8.56e-01 |
0.13300 |
-5.78e-02 |
1.20e-01 |
7.52e-01 |
5.11e-01 |
Collagen formation |
75 |
1.35e-01 |
2.58e-01 |
0.13300 |
-1.07e-02 |
1.33e-01 |
8.73e-01 |
4.73e-02 |
Regulation of gene expression in beta cells |
13 |
6.73e-01 |
7.59e-01 |
0.13300 |
1.28e-01 |
3.38e-02 |
4.24e-01 |
8.33e-01 |
Signaling by NTRK2 (TRKB) |
25 |
5.69e-01 |
6.74e-01 |
0.13200 |
-6.37e-02 |
1.16e-01 |
5.81e-01 |
3.15e-01 |
Postmitotic nuclear pore complex (NPC) reformation |
27 |
4.90e-01 |
6.12e-01 |
0.13200 |
-1.18e-02 |
1.32e-01 |
9.15e-01 |
2.36e-01 |
Transport of Ribonucleoproteins into the Host Nucleus |
32 |
3.47e-01 |
4.92e-01 |
0.13200 |
1.03e-01 |
8.33e-02 |
3.15e-01 |
4.15e-01 |
Collagen chain trimerization |
34 |
4.81e-01 |
6.05e-01 |
0.13200 |
-9.96e-02 |
8.64e-02 |
3.15e-01 |
3.83e-01 |
Post-translational protein modification |
1238 |
1.16e-11 |
8.56e-10 |
0.13200 |
-6.85e-02 |
1.12e-01 |
6.11e-05 |
4.99e-11 |
Gene Silencing by RNA |
79 |
1.40e-01 |
2.64e-01 |
0.13100 |
1.29e-01 |
-2.36e-02 |
4.75e-02 |
7.17e-01 |
Synthesis of PC |
27 |
4.92e-01 |
6.12e-01 |
0.13100 |
-5.33e-03 |
1.30e-01 |
9.62e-01 |
2.41e-01 |
Signaling by NOTCH3 |
47 |
3.35e-01 |
4.79e-01 |
0.13000 |
-3.95e-02 |
1.24e-01 |
6.40e-01 |
1.41e-01 |
Cell junction organization |
76 |
9.71e-02 |
2.02e-01 |
0.13000 |
5.43e-02 |
1.18e-01 |
4.14e-01 |
7.51e-02 |
Netrin-1 signaling |
46 |
3.20e-01 |
4.63e-01 |
0.13000 |
-1.97e-02 |
1.28e-01 |
8.17e-01 |
1.32e-01 |
Intraflagellar transport |
40 |
3.13e-01 |
4.59e-01 |
0.13000 |
-1.25e-01 |
-3.26e-02 |
1.70e-01 |
7.21e-01 |
SUMOylation of DNA damage response and repair proteins |
75 |
9.84e-02 |
2.04e-01 |
0.12900 |
6.65e-02 |
1.11e-01 |
3.19e-01 |
9.80e-02 |
Tight junction interactions |
24 |
6.04e-01 |
7.00e-01 |
0.12900 |
6.97e-02 |
-1.09e-01 |
5.55e-01 |
3.58e-01 |
Fanconi Anemia Pathway |
35 |
4.46e-01 |
5.83e-01 |
0.12900 |
1.24e-01 |
-3.52e-02 |
2.05e-01 |
7.19e-01 |
Inactivation of APC/C via direct inhibition of the APC/C complex |
20 |
5.53e-01 |
6.62e-01 |
0.12800 |
1.18e-01 |
4.89e-02 |
3.59e-01 |
7.05e-01 |
Inhibition of the proteolytic activity of APC/C required for the onset of anaphase by mitotic spindle checkpoint components |
20 |
5.53e-01 |
6.62e-01 |
0.12800 |
1.18e-01 |
4.89e-02 |
3.59e-01 |
7.05e-01 |
Growth hormone receptor signaling |
20 |
5.63e-01 |
6.72e-01 |
0.12800 |
1.23e-01 |
3.67e-02 |
3.43e-01 |
7.76e-01 |
SHC-mediated cascade:FGFR3 |
12 |
6.92e-01 |
7.76e-01 |
0.12800 |
1.08e-01 |
6.90e-02 |
5.18e-01 |
6.79e-01 |
RNA Polymerase III Transcription Initiation |
34 |
4.67e-01 |
5.95e-01 |
0.12800 |
1.22e-01 |
-3.78e-02 |
2.19e-01 |
7.03e-01 |
Regulation of TP53 Activity through Methylation |
17 |
7.02e-01 |
7.84e-01 |
0.12800 |
6.36e-02 |
-1.11e-01 |
6.50e-01 |
4.30e-01 |
G2/M DNA damage checkpoint |
61 |
1.89e-01 |
3.27e-01 |
0.12700 |
2.23e-02 |
1.26e-01 |
7.63e-01 |
9.02e-02 |
Kinesins |
40 |
4.50e-01 |
5.87e-01 |
0.12700 |
8.56e-02 |
-9.40e-02 |
3.49e-01 |
3.04e-01 |
RNA Polymerase III Transcription Initiation From Type 2 Promoter |
25 |
5.87e-01 |
6.88e-01 |
0.12700 |
1.16e-01 |
-5.09e-02 |
3.15e-01 |
6.60e-01 |
Interleukin-6 family signaling |
21 |
5.67e-01 |
6.74e-01 |
0.12700 |
2.20e-02 |
1.25e-01 |
8.61e-01 |
3.23e-01 |
HCMV Early Events |
67 |
1.32e-01 |
2.52e-01 |
0.12600 |
9.04e-02 |
8.84e-02 |
2.01e-01 |
2.11e-01 |
SUMOylation of DNA methylation proteins |
16 |
6.27e-01 |
7.19e-01 |
0.12600 |
-5.63e-02 |
-1.13e-01 |
6.97e-01 |
4.35e-01 |
Antimicrobial peptides |
23 |
6.38e-01 |
7.27e-01 |
0.12600 |
-9.05e-02 |
8.74e-02 |
4.53e-01 |
4.68e-01 |
Meiosis |
60 |
1.70e-01 |
3.05e-01 |
0.12600 |
1.05e-01 |
6.95e-02 |
1.61e-01 |
3.52e-01 |
RNA Polymerase III Transcription Initiation From Type 1 Promoter |
26 |
5.86e-01 |
6.88e-01 |
0.12500 |
1.13e-01 |
-5.31e-02 |
3.18e-01 |
6.39e-01 |
Metabolism of carbohydrates |
264 |
6.33e-04 |
3.50e-03 |
0.12500 |
1.14e-01 |
5.02e-02 |
1.40e-03 |
1.61e-01 |
Regulation of TP53 Activity |
152 |
1.76e-02 |
5.61e-02 |
0.12500 |
2.83e-02 |
1.22e-01 |
5.47e-01 |
9.68e-03 |
Glucagon signaling in metabolic regulation |
28 |
4.42e-01 |
5.79e-01 |
0.12500 |
6.70e-02 |
1.05e-01 |
5.40e-01 |
3.34e-01 |
Transport of bile salts and organic acids, metal ions and amine compounds |
76 |
1.58e-01 |
2.89e-01 |
0.12400 |
-2.99e-03 |
-1.24e-01 |
9.64e-01 |
6.19e-02 |
Phase I - Functionalization of compounds |
85 |
8.68e-02 |
1.88e-01 |
0.12400 |
7.07e-02 |
1.02e-01 |
2.60e-01 |
1.05e-01 |
SUMOylation of transcription factors |
17 |
6.18e-01 |
7.13e-01 |
0.12300 |
6.09e-02 |
1.07e-01 |
6.64e-01 |
4.43e-01 |
NOTCH3 Activation and Transmission of Signal to the Nucleus |
24 |
6.32e-01 |
7.23e-01 |
0.12300 |
-1.02e-01 |
6.90e-02 |
3.87e-01 |
5.59e-01 |
Heparan sulfate/heparin (HS-GAG) metabolism |
51 |
2.38e-01 |
3.81e-01 |
0.12300 |
-6.50e-02 |
-1.04e-01 |
4.22e-01 |
1.97e-01 |
Resolution of D-loop Structures through Synthesis-Dependent Strand Annealing (SDSA) |
26 |
5.58e-01 |
6.67e-01 |
0.12300 |
1.22e-01 |
-1.46e-02 |
2.82e-01 |
8.97e-01 |
ERBB2 Regulates Cell Motility |
13 |
7.82e-01 |
8.49e-01 |
0.12300 |
-1.01e-01 |
6.99e-02 |
5.29e-01 |
6.63e-01 |
Antigen processing: Ubiquitination & Proteasome degradation |
288 |
5.23e-03 |
2.11e-02 |
0.12300 |
-8.45e-02 |
8.87e-02 |
1.38e-02 |
9.79e-03 |
Abacavir transport and metabolism |
10 |
7.61e-01 |
8.33e-01 |
0.12200 |
5.19e-02 |
1.11e-01 |
7.76e-01 |
5.44e-01 |
Adenylate cyclase inhibitory pathway |
13 |
7.30e-01 |
8.07e-01 |
0.12200 |
9.21e-03 |
1.22e-01 |
9.54e-01 |
4.47e-01 |
RET signaling |
40 |
4.05e-01 |
5.45e-01 |
0.12200 |
-1.21e-01 |
6.82e-03 |
1.84e-01 |
9.41e-01 |
Nonhomologous End-Joining (NHEJ) |
35 |
4.84e-01 |
6.06e-01 |
0.12100 |
-1.18e-01 |
2.79e-02 |
2.28e-01 |
7.75e-01 |
Cardiac conduction |
95 |
7.35e-02 |
1.67e-01 |
0.12100 |
9.69e-02 |
7.24e-02 |
1.03e-01 |
2.23e-01 |
Cell Cycle |
607 |
2.46e-07 |
4.42e-06 |
0.12100 |
4.11e-02 |
1.14e-01 |
8.59e-02 |
1.95e-06 |
Interleukin-7 signaling |
22 |
6.14e-01 |
7.10e-01 |
0.12000 |
1.20e-01 |
-7.40e-03 |
3.29e-01 |
9.52e-01 |
Synthesis of bile acids and bile salts via 7alpha-hydroxycholesterol |
17 |
6.46e-01 |
7.33e-01 |
0.12000 |
4.18e-02 |
1.13e-01 |
7.65e-01 |
4.22e-01 |
Conversion from APC/C:Cdc20 to APC/C:Cdh1 in late anaphase |
19 |
6.25e-01 |
7.18e-01 |
0.11900 |
1.14e-01 |
3.38e-02 |
3.90e-01 |
7.99e-01 |
Post NMDA receptor activation events |
60 |
2.07e-01 |
3.46e-01 |
0.11900 |
1.02e-01 |
6.15e-02 |
1.73e-01 |
4.10e-01 |
Adenylate cyclase activating pathway |
10 |
8.40e-01 |
8.92e-01 |
0.11900 |
7.50e-02 |
-9.19e-02 |
6.82e-01 |
6.15e-01 |
Signaling by Insulin receptor |
65 |
2.92e-01 |
4.41e-01 |
0.11800 |
-4.02e-02 |
1.11e-01 |
5.76e-01 |
1.21e-01 |
G alpha (12/13) signalling events |
76 |
2.09e-01 |
3.47e-01 |
0.11800 |
-1.42e-02 |
1.17e-01 |
8.31e-01 |
7.81e-02 |
B-WICH complex positively regulates rRNA expression |
37 |
4.53e-01 |
5.87e-01 |
0.11800 |
-4.38e-03 |
1.18e-01 |
9.63e-01 |
2.15e-01 |
RNA Polymerase I Promoter Clearance |
56 |
3.72e-01 |
5.14e-01 |
0.11800 |
-5.97e-02 |
1.01e-01 |
4.40e-01 |
1.89e-01 |
RNA Polymerase I Transcription |
56 |
3.72e-01 |
5.14e-01 |
0.11800 |
-5.97e-02 |
1.01e-01 |
4.40e-01 |
1.89e-01 |
APC/C:Cdc20 mediated degradation of Cyclin B |
23 |
5.48e-01 |
6.59e-01 |
0.11700 |
8.90e-02 |
7.66e-02 |
4.60e-01 |
5.25e-01 |
G1/S-Specific Transcription |
28 |
5.31e-01 |
6.46e-01 |
0.11700 |
1.54e-02 |
1.16e-01 |
8.88e-01 |
2.89e-01 |
The canonical retinoid cycle in rods (twilight vision) |
17 |
6.45e-01 |
7.33e-01 |
0.11700 |
-6.88e-02 |
-9.45e-02 |
6.23e-01 |
5.00e-01 |
Defects of contact activation system (CAS) and kallikrein/kinin system (KKS) |
12 |
7.63e-01 |
8.33e-01 |
0.11700 |
1.16e-01 |
1.56e-02 |
4.88e-01 |
9.25e-01 |
Diseases of hemostasis |
12 |
7.63e-01 |
8.33e-01 |
0.11700 |
1.16e-01 |
1.56e-02 |
4.88e-01 |
9.25e-01 |
Pre-NOTCH Expression and Processing |
57 |
2.38e-01 |
3.81e-01 |
0.11700 |
5.84e-02 |
1.01e-01 |
4.46e-01 |
1.87e-01 |
G alpha (q) signalling events |
159 |
4.50e-02 |
1.14e-01 |
0.11600 |
-1.95e-02 |
1.15e-01 |
6.72e-01 |
1.28e-02 |
Telomere Extension By Telomerase |
22 |
6.88e-01 |
7.71e-01 |
0.11600 |
9.68e-02 |
-6.41e-02 |
4.32e-01 |
6.03e-01 |
Regulation of TP53 Activity through Phosphorylation |
90 |
1.06e-01 |
2.15e-01 |
0.11600 |
6.25e-02 |
9.75e-02 |
3.06e-01 |
1.10e-01 |
Transcription of E2F targets under negative control by p107 (RBL1) and p130 (RBL2) in complex with HDAC1 |
16 |
6.75e-01 |
7.60e-01 |
0.11600 |
5.13e-02 |
1.04e-01 |
7.22e-01 |
4.72e-01 |
Nicotinamide salvaging |
18 |
6.33e-01 |
7.24e-01 |
0.11600 |
7.66e-02 |
8.66e-02 |
5.74e-01 |
5.25e-01 |
Deactivation of the beta-catenin transactivating complex |
39 |
4.80e-01 |
6.05e-01 |
0.11500 |
-1.12e-01 |
2.48e-02 |
2.26e-01 |
7.89e-01 |
Transcriptional Regulation by MECP2 |
52 |
4.26e-01 |
5.66e-01 |
0.11500 |
-6.62e-02 |
9.34e-02 |
4.09e-01 |
2.44e-01 |
Acyl chain remodelling of PS |
16 |
7.08e-01 |
7.88e-01 |
0.11400 |
1.13e-01 |
1.44e-02 |
4.32e-01 |
9.21e-01 |
Packaging Of Telomere Ends |
13 |
7.84e-01 |
8.50e-01 |
0.11400 |
1.12e-01 |
-2.34e-02 |
4.85e-01 |
8.84e-01 |
Peroxisomal protein import |
61 |
3.76e-01 |
5.19e-01 |
0.11400 |
-8.67e-02 |
7.37e-02 |
2.42e-01 |
3.20e-01 |
HDR through Homologous Recombination (HRR) |
65 |
2.15e-01 |
3.54e-01 |
0.11300 |
1.00e-01 |
5.34e-02 |
1.63e-01 |
4.56e-01 |
Peptide ligand-binding receptors |
110 |
1.42e-01 |
2.67e-01 |
0.11300 |
-3.10e-02 |
1.09e-01 |
5.75e-01 |
4.90e-02 |
Inhibition of replication initiation of damaged DNA by RB1/E2F1 |
13 |
7.30e-01 |
8.07e-01 |
0.11300 |
8.26e-02 |
7.70e-02 |
6.06e-01 |
6.31e-01 |
Collagen degradation |
30 |
6.24e-01 |
7.18e-01 |
0.11300 |
-7.29e-02 |
8.58e-02 |
4.89e-01 |
4.16e-01 |
Regulation of cholesterol biosynthesis by SREBP (SREBF) |
55 |
4.19e-01 |
5.59e-01 |
0.11200 |
-9.18e-02 |
6.48e-02 |
2.39e-01 |
4.06e-01 |
Nucleotide-like (purinergic) receptors |
15 |
7.20e-01 |
7.99e-01 |
0.11200 |
-3.11e-02 |
-1.08e-01 |
8.35e-01 |
4.70e-01 |
COPI-dependent Golgi-to-ER retrograde traffic |
79 |
2.68e-01 |
4.13e-01 |
0.11200 |
-1.04e-01 |
4.13e-02 |
1.11e-01 |
5.26e-01 |
Regulation of PTEN gene transcription |
60 |
3.92e-01 |
5.36e-01 |
0.11200 |
-6.41e-02 |
9.15e-02 |
3.91e-01 |
2.21e-01 |
Epigenetic regulation of gene expression |
93 |
2.05e-01 |
3.45e-01 |
0.11200 |
-3.41e-02 |
1.06e-01 |
5.71e-01 |
7.69e-02 |
SHC-mediated cascade:FGFR1 |
13 |
7.92e-01 |
8.56e-01 |
0.11100 |
-1.89e-02 |
1.09e-01 |
9.06e-01 |
4.95e-01 |
Vitamin B5 (pantothenate) metabolism |
16 |
7.43e-01 |
8.17e-01 |
0.11100 |
-1.10e-01 |
8.58e-03 |
4.45e-01 |
9.53e-01 |
Acyl chain remodelling of PG |
12 |
8.28e-01 |
8.84e-01 |
0.11000 |
-9.73e-02 |
5.23e-02 |
5.60e-01 |
7.54e-01 |
Metabolism of fat-soluble vitamins |
43 |
4.39e-01 |
5.77e-01 |
0.11000 |
5.47e-04 |
1.10e-01 |
9.95e-01 |
2.11e-01 |
Signaling by ERBB2 TMD/JMD mutants |
20 |
7.29e-01 |
8.07e-01 |
0.11000 |
-4.92e-02 |
9.85e-02 |
7.03e-01 |
4.46e-01 |
GPCR downstream signalling |
710 |
1.85e-07 |
3.45e-06 |
0.11000 |
-7.53e-02 |
-7.96e-02 |
6.84e-04 |
3.30e-04 |
Glutamate binding, activation of AMPA receptors and synaptic plasticity |
28 |
6.07e-01 |
7.03e-01 |
0.10900 |
1.09e-01 |
-1.15e-02 |
3.20e-01 |
9.16e-01 |
Trafficking of AMPA receptors |
28 |
6.07e-01 |
7.03e-01 |
0.10900 |
1.09e-01 |
-1.15e-02 |
3.20e-01 |
9.16e-01 |
Gap junction assembly |
13 |
7.99e-01 |
8.60e-01 |
0.10900 |
1.07e-01 |
-1.98e-02 |
5.03e-01 |
9.02e-01 |
Diseases associated with glycosylation precursor biosynthesis |
18 |
6.82e-01 |
7.66e-01 |
0.10900 |
-4.14e-02 |
-1.00e-01 |
7.61e-01 |
4.61e-01 |
Metabolism of nucleotides |
93 |
1.96e-01 |
3.33e-01 |
0.10800 |
1.08e-01 |
-1.16e-02 |
7.28e-02 |
8.46e-01 |
mTORC1-mediated signalling |
24 |
6.69e-01 |
7.55e-01 |
0.10800 |
-1.06e-01 |
2.36e-02 |
3.70e-01 |
8.41e-01 |
FRS-mediated FGFR2 signaling |
16 |
7.37e-01 |
8.12e-01 |
0.10800 |
1.22e-02 |
1.07e-01 |
9.33e-01 |
4.59e-01 |
Retinoid metabolism and transport |
39 |
4.39e-01 |
5.77e-01 |
0.10700 |
4.70e-02 |
9.66e-02 |
6.12e-01 |
2.97e-01 |
Defective B3GALT6 causes EDSP2 and SEMDJL1 |
20 |
6.65e-01 |
7.52e-01 |
0.10700 |
3.48e-02 |
1.02e-01 |
7.88e-01 |
4.32e-01 |
Acyl chain remodelling of PI |
11 |
8.38e-01 |
8.91e-01 |
0.10700 |
1.04e-01 |
-2.71e-02 |
5.52e-01 |
8.76e-01 |
NEP/NS2 Interacts with the Cellular Export Machinery |
32 |
5.04e-01 |
6.22e-01 |
0.10700 |
8.81e-02 |
6.03e-02 |
3.88e-01 |
5.55e-01 |
alpha-linolenic (omega3) and linoleic (omega6) acid metabolism |
12 |
8.45e-01 |
8.96e-01 |
0.10600 |
6.83e-02 |
-8.14e-02 |
6.82e-01 |
6.25e-01 |
alpha-linolenic acid (ALA) metabolism |
12 |
8.45e-01 |
8.96e-01 |
0.10600 |
6.83e-02 |
-8.14e-02 |
6.82e-01 |
6.25e-01 |
Death Receptor Signalling |
135 |
1.19e-01 |
2.36e-01 |
0.10600 |
-2.62e-02 |
1.03e-01 |
5.99e-01 |
3.93e-02 |
Signaling by FGFR in disease |
54 |
3.17e-01 |
4.62e-01 |
0.10600 |
6.75e-02 |
8.17e-02 |
3.91e-01 |
2.99e-01 |
p75 NTR receptor-mediated signalling |
95 |
2.41e-01 |
3.85e-01 |
0.10600 |
-3.66e-02 |
9.90e-02 |
5.38e-01 |
9.57e-02 |
Rab regulation of trafficking |
117 |
1.66e-01 |
3.00e-01 |
0.10500 |
-2.60e-02 |
1.01e-01 |
6.28e-01 |
5.82e-02 |
Collagen biosynthesis and modifying enzymes |
56 |
4.65e-01 |
5.95e-01 |
0.10500 |
-6.21e-02 |
8.43e-02 |
4.22e-01 |
2.75e-01 |
Signaling by FGFR2 |
63 |
3.55e-01 |
4.99e-01 |
0.10500 |
-9.48e-03 |
1.04e-01 |
8.96e-01 |
1.53e-01 |
Integration of energy metabolism |
98 |
1.36e-01 |
2.59e-01 |
0.10400 |
8.53e-02 |
5.99e-02 |
1.45e-01 |
3.06e-01 |
Metabolism of porphyrins |
23 |
6.96e-01 |
7.79e-01 |
0.10400 |
-1.84e-02 |
1.02e-01 |
8.79e-01 |
3.95e-01 |
Synthesis of substrates in N-glycan biosythesis |
58 |
4.12e-01 |
5.52e-01 |
0.10300 |
-1.01e-01 |
2.19e-02 |
1.83e-01 |
7.73e-01 |
TBC/RABGAPs |
43 |
4.30e-01 |
5.68e-01 |
0.10300 |
8.96e-02 |
5.07e-02 |
3.09e-01 |
5.65e-01 |
Signaling by Retinoic Acid |
38 |
5.67e-01 |
6.74e-01 |
0.10300 |
-2.40e-02 |
9.99e-02 |
7.98e-01 |
2.87e-01 |
Interferon alpha/beta signaling |
59 |
3.27e-01 |
4.69e-01 |
0.10300 |
-3.99e-02 |
-9.45e-02 |
5.96e-01 |
2.10e-01 |
RHO GTPases activate KTN1 |
11 |
8.67e-01 |
9.09e-01 |
0.10200 |
-7.32e-02 |
7.17e-02 |
6.74e-01 |
6.81e-01 |
Stimuli-sensing channels |
82 |
3.44e-01 |
4.88e-01 |
0.10200 |
8.33e-02 |
-5.90e-02 |
1.92e-01 |
3.56e-01 |
Regulation of MECP2 expression and activity |
29 |
6.56e-01 |
7.44e-01 |
0.10200 |
-9.82e-02 |
2.72e-02 |
3.60e-01 |
8.00e-01 |
Signaling by Non-Receptor Tyrosine Kinases |
52 |
3.97e-01 |
5.38e-01 |
0.10100 |
2.54e-02 |
9.83e-02 |
7.51e-01 |
2.21e-01 |
Signaling by PTK6 |
52 |
3.97e-01 |
5.38e-01 |
0.10100 |
2.54e-02 |
9.83e-02 |
7.51e-01 |
2.21e-01 |
Degradation of the extracellular matrix |
86 |
1.99e-01 |
3.36e-01 |
0.10100 |
4.66e-02 |
8.98e-02 |
4.55e-01 |
1.50e-01 |
Neurexins and neuroligins |
52 |
4.76e-01 |
6.02e-01 |
0.10100 |
2.41e-02 |
-9.76e-02 |
7.64e-01 |
2.24e-01 |
Export of Viral Ribonucleoproteins from Nucleus |
33 |
5.41e-01 |
6.53e-01 |
0.09960 |
5.54e-02 |
8.28e-02 |
5.82e-01 |
4.11e-01 |
Activation of kainate receptors upon glutamate binding |
27 |
6.03e-01 |
7.00e-01 |
0.09930 |
6.61e-02 |
7.42e-02 |
5.53e-01 |
5.05e-01 |
WNT ligand biogenesis and trafficking |
19 |
7.78e-01 |
8.45e-01 |
0.09910 |
-3.54e-02 |
9.26e-02 |
7.90e-01 |
4.85e-01 |
Meiotic synapsis |
34 |
5.38e-01 |
6.50e-01 |
0.09870 |
5.28e-02 |
8.34e-02 |
5.94e-01 |
4.00e-01 |
Transcriptional activation of mitochondrial biogenesis |
52 |
5.35e-01 |
6.48e-01 |
0.09870 |
-7.31e-02 |
6.63e-02 |
3.62e-01 |
4.09e-01 |
Signaling by GPCR |
758 |
1.82e-06 |
2.22e-05 |
0.09810 |
-6.56e-02 |
-7.30e-02 |
2.27e-03 |
6.87e-04 |
Class B/2 (Secretin family receptors) |
61 |
4.06e-01 |
5.46e-01 |
0.09810 |
-4.46e-03 |
9.80e-02 |
9.52e-01 |
1.86e-01 |
Nuclear signaling by ERBB4 |
28 |
6.61e-01 |
7.49e-01 |
0.09810 |
-4.60e-03 |
9.80e-02 |
9.66e-01 |
3.70e-01 |
Trafficking of GluR2-containing AMPA receptors |
17 |
7.96e-01 |
8.58e-01 |
0.09770 |
9.47e-02 |
-2.42e-02 |
4.99e-01 |
8.63e-01 |
Interferon Signaling |
168 |
1.44e-01 |
2.69e-01 |
0.09700 |
-6.95e-02 |
6.77e-02 |
1.21e-01 |
1.31e-01 |
Nucleobase catabolism |
36 |
6.20e-01 |
7.14e-01 |
0.09700 |
9.42e-02 |
-2.31e-02 |
3.28e-01 |
8.11e-01 |
Regulation of TNFR1 signaling |
35 |
6.66e-01 |
7.53e-01 |
0.09640 |
-7.74e-02 |
5.75e-02 |
4.29e-01 |
5.56e-01 |
Reproduction |
75 |
3.36e-01 |
4.80e-01 |
0.09610 |
9.61e-02 |
1.49e-03 |
1.50e-01 |
9.82e-01 |
SUMOylation |
165 |
1.43e-01 |
2.67e-01 |
0.09600 |
-4.58e-02 |
8.44e-02 |
3.11e-01 |
6.17e-02 |
Rho GTPase cycle |
134 |
1.74e-01 |
3.08e-01 |
0.09560 |
-1.95e-02 |
9.36e-02 |
6.97e-01 |
6.17e-02 |
Transcriptional regulation of white adipocyte differentiation |
80 |
3.92e-01 |
5.36e-01 |
0.09520 |
-4.41e-02 |
8.44e-02 |
4.96e-01 |
1.92e-01 |
Nuclear Receptor transcription pathway |
50 |
4.59e-01 |
5.92e-01 |
0.09500 |
-9.21e-02 |
-2.33e-02 |
2.60e-01 |
7.76e-01 |
Nuclear import of Rev protein |
33 |
5.95e-01 |
6.94e-01 |
0.09490 |
9.09e-02 |
2.73e-02 |
3.66e-01 |
7.86e-01 |
Cell death signalling via NRAGE, NRIF and NADE |
74 |
4.03e-01 |
5.42e-01 |
0.09480 |
-2.97e-02 |
9.01e-02 |
6.59e-01 |
1.81e-01 |
Effects of PIP2 hydrolysis |
25 |
6.75e-01 |
7.60e-01 |
0.09480 |
-2.67e-02 |
-9.10e-02 |
8.17e-01 |
4.31e-01 |
N-Glycan antennae elongation |
14 |
8.48e-01 |
8.99e-01 |
0.09420 |
8.65e-02 |
-3.74e-02 |
5.75e-01 |
8.08e-01 |
SUMO E3 ligases SUMOylate target proteins |
159 |
1.68e-01 |
3.02e-01 |
0.09370 |
-4.44e-02 |
8.24e-02 |
3.34e-01 |
7.32e-02 |
Activation of NMDA receptors and postsynaptic events |
73 |
3.18e-01 |
4.62e-01 |
0.09340 |
8.61e-02 |
3.63e-02 |
2.04e-01 |
5.92e-01 |
IRS-related events triggered by IGF1R |
40 |
6.42e-01 |
7.31e-01 |
0.09320 |
-8.00e-02 |
4.77e-02 |
3.81e-01 |
6.02e-01 |
SHC-mediated cascade:FGFR4 |
12 |
8.65e-01 |
9.09e-01 |
0.09310 |
-2.57e-02 |
8.95e-02 |
8.77e-01 |
5.92e-01 |
Neuronal System |
328 |
3.20e-02 |
8.73e-02 |
0.09290 |
5.96e-02 |
-7.12e-02 |
6.42e-02 |
2.71e-02 |
Phase II - Conjugation of compounds |
85 |
4.10e-01 |
5.50e-01 |
0.09220 |
5.98e-02 |
-7.02e-02 |
3.41e-01 |
2.64e-01 |
IGF1R signaling cascade |
41 |
6.44e-01 |
7.32e-01 |
0.09220 |
-7.78e-02 |
4.95e-02 |
3.89e-01 |
5.84e-01 |
Defective B4GALT7 causes EDS, progeroid type |
20 |
7.24e-01 |
8.04e-01 |
0.09210 |
6.93e-02 |
6.08e-02 |
5.92e-01 |
6.38e-01 |
Pexophagy |
11 |
8.51e-01 |
8.99e-01 |
0.09210 |
8.89e-02 |
2.38e-02 |
6.10e-01 |
8.91e-01 |
Negative epigenetic regulation of rRNA expression |
55 |
4.69e-01 |
5.95e-01 |
0.09190 |
9.16e-03 |
9.14e-02 |
9.07e-01 |
2.41e-01 |
Uptake and actions of bacterial toxins |
25 |
7.75e-01 |
8.43e-01 |
0.09000 |
5.10e-02 |
-7.42e-02 |
6.59e-01 |
5.21e-01 |
RNA Polymerase II Transcription |
1047 |
3.78e-05 |
3.14e-04 |
0.08960 |
-4.11e-02 |
7.96e-02 |
2.59e-02 |
1.65e-05 |
ATF4 activates genes in response to endoplasmic reticulum stress |
25 |
7.35e-01 |
8.11e-01 |
0.08930 |
-3.35e-03 |
8.92e-02 |
9.77e-01 |
4.40e-01 |
SUMOylation of chromatin organization proteins |
56 |
5.07e-01 |
6.22e-01 |
0.08920 |
-5.40e-03 |
8.91e-02 |
9.44e-01 |
2.49e-01 |
Transport of Mature Transcript to Cytoplasm |
80 |
4.54e-01 |
5.87e-01 |
0.08900 |
-7.20e-02 |
5.23e-02 |
2.66e-01 |
4.19e-01 |
Insulin receptor signalling cascade |
42 |
6.65e-01 |
7.52e-01 |
0.08870 |
-6.26e-02 |
6.28e-02 |
4.83e-01 |
4.81e-01 |
Constitutive Signaling by AKT1 E17K in Cancer |
26 |
7.50e-01 |
8.23e-01 |
0.08840 |
-2.06e-02 |
8.60e-02 |
8.56e-01 |
4.48e-01 |
CS/DS degradation |
14 |
8.15e-01 |
8.75e-01 |
0.08800 |
5.21e-02 |
7.10e-02 |
7.36e-01 |
6.46e-01 |
Potassium Channels |
83 |
3.80e-01 |
5.23e-01 |
0.08790 |
7.15e-03 |
-8.76e-02 |
9.10e-01 |
1.68e-01 |
Metabolism of amino acids and derivatives |
308 |
1.42e-02 |
4.73e-02 |
0.08780 |
3.75e-02 |
7.94e-02 |
2.59e-01 |
1.69e-02 |
SUMOylation of RNA binding proteins |
47 |
5.15e-01 |
6.29e-01 |
0.08780 |
3.99e-02 |
7.82e-02 |
6.36e-01 |
3.54e-01 |
NCAM signaling for neurite out-growth |
53 |
4.70e-01 |
5.96e-01 |
0.08770 |
4.38e-02 |
7.60e-02 |
5.82e-01 |
3.39e-01 |
APC-Cdc20 mediated degradation of Nek2A |
25 |
6.95e-01 |
7.78e-01 |
0.08770 |
6.76e-02 |
5.58e-02 |
5.58e-01 |
6.29e-01 |
Signaling by Type 1 Insulin-like Growth Factor 1 Receptor (IGF1R) |
42 |
6.74e-01 |
7.59e-01 |
0.08700 |
-6.77e-02 |
5.47e-02 |
4.48e-01 |
5.40e-01 |
Signaling by FGFR |
74 |
4.92e-01 |
6.12e-01 |
0.08700 |
-4.58e-02 |
7.39e-02 |
4.96e-01 |
2.72e-01 |
Phenylalanine and tyrosine metabolism |
10 |
8.96e-01 |
9.26e-01 |
0.08620 |
-1.27e-02 |
8.53e-02 |
9.44e-01 |
6.41e-01 |
Selective autophagy |
57 |
5.35e-01 |
6.48e-01 |
0.08590 |
-1.04e-02 |
8.53e-02 |
8.92e-01 |
2.66e-01 |
Peptide hormone metabolism |
64 |
5.61e-01 |
6.70e-01 |
0.08420 |
-4.27e-02 |
7.25e-02 |
5.55e-01 |
3.16e-01 |
Metabolism |
1871 |
2.52e-10 |
1.41e-08 |
0.08410 |
6.64e-02 |
5.16e-02 |
2.99e-06 |
2.85e-04 |
Striated Muscle Contraction |
24 |
7.37e-01 |
8.12e-01 |
0.08350 |
3.60e-02 |
7.53e-02 |
7.60e-01 |
5.23e-01 |
Long-term potentiation |
22 |
8.25e-01 |
8.82e-01 |
0.08340 |
4.72e-02 |
-6.88e-02 |
7.02e-01 |
5.77e-01 |
Reversible hydration of carbon dioxide |
10 |
9.11e-01 |
9.35e-01 |
0.08290 |
2.73e-02 |
-7.83e-02 |
8.81e-01 |
6.68e-01 |
Regulation of PTEN mRNA translation |
11 |
8.73e-01 |
9.13e-01 |
0.08250 |
-3.35e-02 |
-7.53e-02 |
8.47e-01 |
6.65e-01 |
FRS-mediated FGFR3 signaling |
14 |
8.70e-01 |
9.10e-01 |
0.08220 |
-1.21e-02 |
8.13e-02 |
9.37e-01 |
5.99e-01 |
Negative regulation of TCF-dependent signaling by WNT ligand antagonists |
14 |
8.89e-01 |
9.22e-01 |
0.08190 |
4.99e-02 |
-6.50e-02 |
7.47e-01 |
6.74e-01 |
PI-3K cascade:FGFR3 |
12 |
8.81e-01 |
9.18e-01 |
0.08190 |
-8.19e-02 |
-1.12e-03 |
6.23e-01 |
9.95e-01 |
PRC2 methylates histones and DNA |
22 |
7.66e-01 |
8.35e-01 |
0.08180 |
3.26e-02 |
7.50e-02 |
7.92e-01 |
5.42e-01 |
Downstream signaling of activated FGFR2 |
21 |
8.25e-01 |
8.82e-01 |
0.08140 |
-2.39e-02 |
7.79e-02 |
8.50e-01 |
5.37e-01 |
Diseases of carbohydrate metabolism |
32 |
7.05e-01 |
7.86e-01 |
0.08060 |
-7.94e-02 |
-1.39e-02 |
4.37e-01 |
8.92e-01 |
Acyl chain remodelling of PC |
21 |
7.72e-01 |
8.41e-01 |
0.08060 |
-6.23e-02 |
-5.12e-02 |
6.21e-01 |
6.85e-01 |
Synthesis of IP2, IP, and Ins in the cytosol |
14 |
8.93e-01 |
9.24e-01 |
0.08030 |
4.67e-02 |
-6.54e-02 |
7.62e-01 |
6.72e-01 |
Platelet Aggregation (Plug Formation) |
36 |
6.50e-01 |
7.38e-01 |
0.08030 |
4.01e-02 |
6.96e-02 |
6.77e-01 |
4.70e-01 |
Xenobiotics |
13 |
8.73e-01 |
9.13e-01 |
0.08020 |
8.00e-02 |
5.76e-03 |
6.17e-01 |
9.71e-01 |
Gene expression (Transcription) |
1171 |
1.05e-04 |
7.50e-04 |
0.08010 |
-3.35e-02 |
7.27e-02 |
5.62e-02 |
3.36e-05 |
Disorders of transmembrane transporters |
163 |
2.01e-01 |
3.39e-01 |
0.07950 |
-7.95e-02 |
-6.95e-04 |
8.04e-02 |
9.88e-01 |
Lysine catabolism |
12 |
8.82e-01 |
9.18e-01 |
0.07940 |
-7.86e-02 |
-1.16e-02 |
6.37e-01 |
9.45e-01 |
P2Y receptors |
11 |
9.04e-01 |
9.30e-01 |
0.07920 |
1.37e-02 |
-7.80e-02 |
9.37e-01 |
6.54e-01 |
Metabolic disorders of biological oxidation enzymes |
29 |
7.98e-01 |
8.60e-01 |
0.07910 |
6.11e-02 |
-5.02e-02 |
5.69e-01 |
6.40e-01 |
A tetrasaccharide linker sequence is required for GAG synthesis |
26 |
7.74e-01 |
8.43e-01 |
0.07900 |
-1.16e-03 |
-7.90e-02 |
9.92e-01 |
4.86e-01 |
tRNA processing in the nucleus |
59 |
5.28e-01 |
6.43e-01 |
0.07800 |
2.65e-02 |
7.34e-02 |
7.25e-01 |
3.30e-01 |
Ion channel transport |
149 |
1.92e-01 |
3.29e-01 |
0.07710 |
4.40e-02 |
6.33e-02 |
3.55e-01 |
1.83e-01 |
Post-translational modification: synthesis of GPI-anchored proteins |
76 |
5.70e-01 |
6.74e-01 |
0.07670 |
4.26e-02 |
-6.38e-02 |
5.21e-01 |
3.37e-01 |
Generic Transcription Pathway |
932 |
8.57e-04 |
4.57e-03 |
0.07650 |
-2.36e-02 |
7.28e-02 |
2.27e-01 |
1.89e-04 |
IL-6-type cytokine receptor ligand interactions |
15 |
8.61e-01 |
9.08e-01 |
0.07590 |
7.35e-02 |
1.91e-02 |
6.22e-01 |
8.98e-01 |
Transport of Mature mRNA derived from an Intron-Containing Transcript |
72 |
5.98e-01 |
6.97e-01 |
0.07580 |
-5.97e-02 |
4.67e-02 |
3.81e-01 |
4.93e-01 |
TNF signaling |
44 |
7.33e-01 |
8.09e-01 |
0.07530 |
-4.61e-02 |
5.95e-02 |
5.97e-01 |
4.95e-01 |
NoRC negatively regulates rRNA expression |
52 |
6.30e-01 |
7.21e-01 |
0.07510 |
1.15e-03 |
7.51e-02 |
9.89e-01 |
3.49e-01 |
Prolactin receptor signaling |
11 |
9.27e-01 |
9.47e-01 |
0.07450 |
-5.10e-02 |
5.43e-02 |
7.70e-01 |
7.55e-01 |
Recycling of bile acids and salts |
12 |
9.04e-01 |
9.30e-01 |
0.07430 |
-5.58e-03 |
7.40e-02 |
9.73e-01 |
6.57e-01 |
Anchoring of the basal body to the plasma membrane |
96 |
3.71e-01 |
5.14e-01 |
0.07410 |
5.89e-02 |
4.50e-02 |
3.19e-01 |
4.47e-01 |
Neurotransmitter release cycle |
40 |
7.38e-01 |
8.12e-01 |
0.07360 |
1.84e-02 |
-7.13e-02 |
8.40e-01 |
4.36e-01 |
HDR through Homologous Recombination (HRR) or Single Strand Annealing (SSA) |
94 |
4.14e-01 |
5.54e-01 |
0.07270 |
6.83e-02 |
2.49e-02 |
2.53e-01 |
6.77e-01 |
N-glycan antennae elongation in the medial/trans-Golgi |
22 |
8.58e-01 |
9.05e-01 |
0.07250 |
-2.91e-02 |
6.64e-02 |
8.13e-01 |
5.90e-01 |
Protein localization |
157 |
2.62e-01 |
4.08e-01 |
0.07210 |
9.33e-03 |
7.15e-02 |
8.40e-01 |
1.23e-01 |
Downstream signaling of activated FGFR3 |
19 |
8.85e-01 |
9.19e-01 |
0.07210 |
-4.56e-02 |
5.58e-02 |
7.31e-01 |
6.74e-01 |
PPARA activates gene expression |
114 |
4.87e-01 |
6.09e-01 |
0.07150 |
-4.65e-02 |
5.44e-02 |
3.92e-01 |
3.17e-01 |
DNA Repair |
280 |
8.88e-02 |
1.90e-01 |
0.07140 |
6.92e-02 |
1.74e-02 |
4.68e-02 |
6.16e-01 |
Hyaluronan uptake and degradation |
12 |
9.18e-01 |
9.42e-01 |
0.07140 |
6.91e-02 |
-1.78e-02 |
6.79e-01 |
9.15e-01 |
O-linked glycosylation |
97 |
4.57e-01 |
5.89e-01 |
0.07120 |
7.11e-02 |
3.35e-03 |
2.26e-01 |
9.55e-01 |
Formation of the beta-catenin:TCF transactivating complex |
40 |
7.10e-01 |
7.90e-01 |
0.07120 |
-7.00e-02 |
-1.31e-02 |
4.44e-01 |
8.86e-01 |
Signal Transduction |
2201 |
6.59e-06 |
6.84e-05 |
0.07110 |
-4.34e-02 |
5.63e-02 |
1.07e-03 |
2.25e-05 |
TNFR1-induced proapoptotic signaling |
13 |
9.24e-01 |
9.47e-01 |
0.07000 |
-4.43e-02 |
5.41e-02 |
7.82e-01 |
7.35e-01 |
Signaling by NOTCH2 |
32 |
8.24e-01 |
8.82e-01 |
0.06990 |
-4.48e-02 |
5.37e-02 |
6.61e-01 |
5.99e-01 |
Defective B3GAT3 causes JDSSDHD |
20 |
8.34e-01 |
8.88e-01 |
0.06990 |
3.56e-02 |
6.02e-02 |
7.83e-01 |
6.41e-01 |
Processing of DNA double-strand break ends |
62 |
5.70e-01 |
6.74e-01 |
0.06930 |
4.32e-02 |
5.42e-02 |
5.56e-01 |
4.61e-01 |
Signaling by FGFR3 in disease |
16 |
8.86e-01 |
9.20e-01 |
0.06850 |
4.24e-03 |
6.84e-02 |
9.77e-01 |
6.36e-01 |
Signaling by FGFR3 point mutants in cancer |
16 |
8.86e-01 |
9.20e-01 |
0.06850 |
4.24e-03 |
6.84e-02 |
9.77e-01 |
6.36e-01 |
Interactions of Rev with host cellular proteins |
36 |
7.31e-01 |
8.08e-01 |
0.06770 |
4.48e-02 |
5.08e-02 |
6.42e-01 |
5.98e-01 |
RNA Polymerase I Promoter Escape |
37 |
7.26e-01 |
8.05e-01 |
0.06750 |
4.57e-02 |
4.97e-02 |
6.31e-01 |
6.01e-01 |
Regulated proteolysis of p75NTR |
11 |
9.25e-01 |
9.47e-01 |
0.06720 |
8.96e-04 |
6.72e-02 |
9.96e-01 |
7.00e-01 |
Chromatin modifying enzymes |
211 |
3.07e-01 |
4.55e-01 |
0.06690 |
-5.62e-02 |
3.64e-02 |
1.60e-01 |
3.63e-01 |
Chromatin organization |
211 |
3.07e-01 |
4.55e-01 |
0.06690 |
-5.62e-02 |
3.64e-02 |
1.60e-01 |
3.63e-01 |
DNA Double Strand Break Response |
43 |
7.85e-01 |
8.52e-01 |
0.06680 |
-3.73e-02 |
5.55e-02 |
6.73e-01 |
5.29e-01 |
Inositol phosphate metabolism |
46 |
6.95e-01 |
7.78e-01 |
0.06680 |
2.21e-02 |
6.30e-02 |
7.96e-01 |
4.60e-01 |
DDX58/IFIH1-mediated induction of interferon-alpha/beta |
71 |
6.76e-01 |
7.60e-01 |
0.06660 |
-4.03e-02 |
5.30e-02 |
5.57e-01 |
4.40e-01 |
PI3K Cascade |
33 |
7.62e-01 |
8.33e-01 |
0.06590 |
-5.03e-02 |
-4.25e-02 |
6.17e-01 |
6.72e-01 |
Deposition of new CENPA-containing nucleosomes at the centromere |
32 |
7.88e-01 |
8.53e-01 |
0.06570 |
6.37e-02 |
1.61e-02 |
5.33e-01 |
8.75e-01 |
Nucleosome assembly |
32 |
7.88e-01 |
8.53e-01 |
0.06570 |
6.37e-02 |
1.61e-02 |
5.33e-01 |
8.75e-01 |
IRS-mediated signalling |
37 |
8.14e-01 |
8.75e-01 |
0.06560 |
-5.81e-02 |
3.05e-02 |
5.41e-01 |
7.48e-01 |
Homology Directed Repair |
100 |
4.67e-01 |
5.95e-01 |
0.06550 |
6.14e-02 |
2.29e-02 |
2.89e-01 |
6.93e-01 |
SUMOylation of intracellular receptors |
29 |
8.32e-01 |
8.87e-01 |
0.06520 |
-6.48e-02 |
7.42e-03 |
5.46e-01 |
9.45e-01 |
Purine catabolism |
18 |
9.01e-01 |
9.30e-01 |
0.06470 |
-1.94e-02 |
6.17e-02 |
8.87e-01 |
6.50e-01 |
Rev-mediated nuclear export of HIV RNA |
35 |
7.65e-01 |
8.35e-01 |
0.06410 |
5.39e-02 |
3.47e-02 |
5.81e-01 |
7.23e-01 |
Peroxisomal lipid metabolism |
28 |
8.69e-01 |
9.10e-01 |
0.06370 |
-4.59e-02 |
4.42e-02 |
6.74e-01 |
6.86e-01 |
tRNA processing |
121 |
4.10e-01 |
5.50e-01 |
0.06370 |
2.82e-02 |
5.71e-02 |
5.93e-01 |
2.79e-01 |
TNFR1-induced NFkappaB signaling pathway |
26 |
8.30e-01 |
8.85e-01 |
0.06330 |
2.26e-02 |
5.91e-02 |
8.42e-01 |
6.02e-01 |
Surfactant metabolism |
20 |
8.78e-01 |
9.16e-01 |
0.06320 |
-6.30e-02 |
-5.36e-03 |
6.26e-01 |
9.67e-01 |
Phospholipid metabolism |
195 |
2.57e-01 |
4.04e-01 |
0.06320 |
6.00e-02 |
1.97e-02 |
1.49e-01 |
6.35e-01 |
Activation of gene expression by SREBF (SREBP) |
42 |
8.03e-01 |
8.64e-01 |
0.06290 |
-5.74e-02 |
2.56e-02 |
5.20e-01 |
7.74e-01 |
Diseases of glycosylation |
129 |
3.86e-01 |
5.29e-01 |
0.06280 |
5.06e-02 |
3.71e-02 |
3.21e-01 |
4.67e-01 |
Regulation of lipid metabolism by PPARalpha |
116 |
5.64e-01 |
6.72e-01 |
0.06260 |
-3.39e-02 |
5.26e-02 |
5.29e-01 |
3.28e-01 |
The phototransduction cascade |
30 |
8.24e-01 |
8.82e-01 |
0.06260 |
-7.73e-03 |
-6.21e-02 |
9.42e-01 |
5.56e-01 |
Defective C1GALT1C1 causes Tn polyagglutination syndrome (TNPS) |
10 |
9.51e-01 |
9.62e-01 |
0.06260 |
5.31e-02 |
-3.30e-02 |
7.71e-01 |
8.56e-01 |
Transcriptional regulation by the AP-2 (TFAP2) family of transcription factors |
26 |
8.39e-01 |
8.92e-01 |
0.06220 |
1.73e-02 |
5.97e-02 |
8.79e-01 |
5.98e-01 |
Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks |
42 |
8.22e-01 |
8.82e-01 |
0.06140 |
-4.35e-02 |
4.33e-02 |
6.25e-01 |
6.27e-01 |
Plasma lipoprotein clearance |
32 |
8.67e-01 |
9.09e-01 |
0.05990 |
-4.62e-02 |
3.80e-02 |
6.51e-01 |
7.10e-01 |
PI-3K cascade:FGFR2 |
14 |
9.40e-01 |
9.55e-01 |
0.05960 |
-4.41e-02 |
4.00e-02 |
7.75e-01 |
7.95e-01 |
GABA synthesis, release, reuptake and degradation |
13 |
9.43e-01 |
9.57e-01 |
0.05930 |
3.00e-02 |
-5.12e-02 |
8.51e-01 |
7.49e-01 |
Tryptophan catabolism |
14 |
9.41e-01 |
9.55e-01 |
0.05930 |
-3.85e-02 |
4.51e-02 |
8.03e-01 |
7.70e-01 |
Metabolism of non-coding RNA |
52 |
7.54e-01 |
8.26e-01 |
0.05920 |
-1.31e-03 |
5.92e-02 |
9.87e-01 |
4.60e-01 |
snRNP Assembly |
52 |
7.54e-01 |
8.26e-01 |
0.05920 |
-1.31e-03 |
5.92e-02 |
9.87e-01 |
4.60e-01 |
Biological oxidations |
175 |
3.65e-01 |
5.08e-01 |
0.05910 |
5.85e-02 |
8.51e-03 |
1.83e-01 |
8.46e-01 |
Nucleotide salvage |
21 |
8.91e-01 |
9.23e-01 |
0.05890 |
5.89e-02 |
8.91e-04 |
6.40e-01 |
9.94e-01 |
NCAM1 interactions |
33 |
8.49e-01 |
8.99e-01 |
0.05770 |
6.63e-03 |
-5.73e-02 |
9.47e-01 |
5.69e-01 |
Transmission across Chemical Synapses |
212 |
4.24e-01 |
5.64e-01 |
0.05640 |
4.96e-02 |
-2.69e-02 |
2.14e-01 |
5.01e-01 |
G alpha (i) signalling events |
281 |
1.90e-01 |
3.27e-01 |
0.05630 |
3.80e-02 |
4.15e-02 |
2.75e-01 |
2.32e-01 |
DNA Double-Strand Break Repair |
128 |
4.82e-01 |
6.06e-01 |
0.05590 |
4.97e-02 |
2.55e-02 |
3.32e-01 |
6.19e-01 |
FGFR2 alternative splicing |
26 |
8.63e-01 |
9.08e-01 |
0.05520 |
4.74e-02 |
2.83e-02 |
6.76e-01 |
8.03e-01 |
Chondroitin sulfate/dermatan sulfate metabolism |
50 |
8.17e-01 |
8.77e-01 |
0.05500 |
-5.11e-02 |
2.03e-02 |
5.32e-01 |
8.04e-01 |
O-linked glycosylation of mucins |
50 |
7.66e-01 |
8.35e-01 |
0.05470 |
-1.87e-02 |
-5.15e-02 |
8.19e-01 |
5.29e-01 |
Other interleukin signaling |
19 |
9.03e-01 |
9.30e-01 |
0.05390 |
2.62e-02 |
4.72e-02 |
8.43e-01 |
7.22e-01 |
Nicotinate metabolism |
30 |
8.51e-01 |
8.99e-01 |
0.05330 |
3.61e-02 |
3.92e-02 |
7.32e-01 |
7.10e-01 |
Interleukin-15 signaling |
14 |
9.48e-01 |
9.60e-01 |
0.05290 |
-5.02e-02 |
1.67e-02 |
7.45e-01 |
9.14e-01 |
RNA Polymerase I Transcription Termination |
27 |
8.67e-01 |
9.09e-01 |
0.05290 |
-3.44e-02 |
-4.01e-02 |
7.57e-01 |
7.18e-01 |
Resolution of D-Loop Structures |
33 |
8.95e-01 |
9.25e-01 |
0.05220 |
3.75e-02 |
-3.63e-02 |
7.09e-01 |
7.18e-01 |
Oxidative Stress Induced Senescence |
71 |
7.08e-01 |
7.88e-01 |
0.05210 |
4.83e-02 |
1.96e-02 |
4.82e-01 |
7.76e-01 |
Interleukin-37 signaling |
19 |
9.44e-01 |
9.57e-01 |
0.04940 |
-3.54e-02 |
3.45e-02 |
7.89e-01 |
7.95e-01 |
Transport of the SLBP Dependant Mature mRNA |
36 |
8.54e-01 |
9.02e-01 |
0.04890 |
2.18e-02 |
4.38e-02 |
8.21e-01 |
6.50e-01 |
Factors involved in megakaryocyte development and platelet production |
126 |
5.89e-01 |
6.88e-01 |
0.04820 |
2.05e-02 |
4.36e-02 |
6.91e-01 |
3.99e-01 |
Transport of the SLBP independent Mature mRNA |
35 |
8.62e-01 |
9.08e-01 |
0.04810 |
2.18e-02 |
4.29e-02 |
8.23e-01 |
6.61e-01 |
Autophagy |
119 |
6.87e-01 |
7.71e-01 |
0.04630 |
-6.32e-03 |
4.59e-02 |
9.05e-01 |
3.88e-01 |
Carboxyterminal post-translational modifications of tubulin |
28 |
9.28e-01 |
9.47e-01 |
0.04600 |
-3.92e-02 |
2.39e-02 |
7.19e-01 |
8.27e-01 |
Plasma lipoprotein assembly, remodeling, and clearance |
64 |
8.33e-01 |
8.87e-01 |
0.04560 |
4.36e-02 |
-1.34e-02 |
5.47e-01 |
8.53e-01 |
NR1H2 and NR1H3-mediated signaling |
44 |
8.82e-01 |
9.19e-01 |
0.04530 |
1.31e-02 |
-4.34e-02 |
8.80e-01 |
6.19e-01 |
HATs acetylate histones |
87 |
7.89e-01 |
8.53e-01 |
0.04530 |
-1.74e-02 |
4.19e-02 |
7.80e-01 |
5.00e-01 |
Protein methylation |
14 |
9.49e-01 |
9.61e-01 |
0.04500 |
1.96e-02 |
4.05e-02 |
8.99e-01 |
7.93e-01 |
KSRP (KHSRP) binds and destabilizes mRNA |
16 |
9.41e-01 |
9.55e-01 |
0.04480 |
2.96e-02 |
3.36e-02 |
8.38e-01 |
8.16e-01 |
Chondroitin sulfate biosynthesis |
20 |
9.51e-01 |
9.62e-01 |
0.04470 |
-3.48e-02 |
2.81e-02 |
7.88e-01 |
8.28e-01 |
Association of TriC/CCT with target proteins during biosynthesis |
39 |
8.70e-01 |
9.10e-01 |
0.04430 |
-4.01e-02 |
-1.88e-02 |
6.65e-01 |
8.39e-01 |
Organelle biogenesis and maintenance |
271 |
4.51e-01 |
5.87e-01 |
0.04430 |
-3.14e-03 |
4.42e-02 |
9.29e-01 |
2.12e-01 |
MTOR signalling |
41 |
8.75e-01 |
9.13e-01 |
0.04410 |
4.34e-02 |
7.75e-03 |
6.31e-01 |
9.32e-01 |
NR1H3 & NR1H2 regulate gene expression linked to cholesterol transport and efflux |
35 |
9.09e-01 |
9.35e-01 |
0.04390 |
1.08e-02 |
-4.25e-02 |
9.12e-01 |
6.63e-01 |
Metabolism of lipids |
660 |
1.36e-01 |
2.59e-01 |
0.04390 |
4.39e-03 |
4.37e-02 |
8.48e-01 |
5.72e-02 |
NRAGE signals death through JNK |
57 |
8.65e-01 |
9.09e-01 |
0.04330 |
-1.43e-02 |
4.09e-02 |
8.52e-01 |
5.93e-01 |
Transport of small molecules |
634 |
1.85e-01 |
3.21e-01 |
0.04180 |
4.18e-02 |
1.05e-03 |
7.43e-02 |
9.64e-01 |
Neurotransmitter receptors and postsynaptic signal transmission |
160 |
6.17e-01 |
7.12e-01 |
0.04160 |
3.97e-02 |
1.25e-02 |
3.87e-01 |
7.85e-01 |
Cilium Assembly |
182 |
6.38e-01 |
7.27e-01 |
0.04150 |
-4.08e-02 |
7.66e-03 |
3.43e-01 |
8.59e-01 |
HS-GAG biosynthesis |
28 |
9.36e-01 |
9.54e-01 |
0.04010 |
-5.94e-03 |
3.96e-02 |
9.57e-01 |
7.17e-01 |
RMTs methylate histone arginines |
36 |
9.01e-01 |
9.30e-01 |
0.03990 |
3.62e-02 |
1.68e-02 |
7.07e-01 |
8.62e-01 |
Regulation of gene expression by Hypoxia-inducible Factor |
11 |
9.79e-01 |
9.86e-01 |
0.03900 |
-2.90e-02 |
2.62e-02 |
8.68e-01 |
8.80e-01 |
Inactivation, recovery and regulation of the phototransduction cascade |
29 |
9.25e-01 |
9.47e-01 |
0.03860 |
-1.58e-02 |
-3.52e-02 |
8.83e-01 |
7.43e-01 |
Amino acids regulate mTORC1 |
51 |
8.84e-01 |
9.19e-01 |
0.03830 |
3.81e-02 |
4.59e-03 |
6.38e-01 |
9.55e-01 |
PKMTs methylate histone lysines |
44 |
9.25e-01 |
9.47e-01 |
0.03750 |
-3.04e-02 |
2.20e-02 |
7.27e-01 |
8.01e-01 |
TP53 Regulates Transcription of Genes Involved in Cytochrome C Release |
18 |
9.69e-01 |
9.78e-01 |
0.03650 |
-1.61e-02 |
3.28e-02 |
9.06e-01 |
8.10e-01 |
Cell-cell junction organization |
51 |
8.90e-01 |
9.23e-01 |
0.03500 |
1.84e-02 |
2.97e-02 |
8.20e-01 |
7.14e-01 |
mRNA Splicing - Minor Pathway |
50 |
9.32e-01 |
9.51e-01 |
0.03370 |
2.19e-02 |
-2.57e-02 |
7.89e-01 |
7.54e-01 |
Metabolism of water-soluble vitamins and cofactors |
114 |
8.23e-01 |
8.82e-01 |
0.03290 |
-1.08e-03 |
-3.29e-02 |
9.84e-01 |
5.45e-01 |
Transport of Mature mRNAs Derived from Intronless Transcripts |
42 |
9.34e-01 |
9.52e-01 |
0.03250 |
-1.24e-03 |
3.25e-02 |
9.89e-01 |
7.16e-01 |
Transport of Mature mRNA Derived from an Intronless Transcript |
41 |
9.40e-01 |
9.55e-01 |
0.03150 |
-1.78e-03 |
3.15e-02 |
9.84e-01 |
7.28e-01 |
Class A/1 (Rhodopsin-like receptors) |
191 |
8.55e-01 |
9.03e-01 |
0.02580 |
-1.56e-02 |
2.05e-02 |
7.10e-01 |
6.26e-01 |
GPCR ligand binding |
264 |
7.95e-01 |
8.58e-01 |
0.02510 |
-6.59e-03 |
2.43e-02 |
8.54e-01 |
4.98e-01 |
Eicosanoid ligand-binding receptors |
11 |
9.88e-01 |
9.92e-01 |
0.02450 |
-1.23e-02 |
-2.11e-02 |
9.44e-01 |
9.03e-01 |
Resolution of D-loop Structures through Holliday Junction Intermediates |
32 |
9.78e-01 |
9.85e-01 |
0.02380 |
1.83e-02 |
-1.51e-02 |
8.58e-01 |
8.82e-01 |
mRNA decay by 3' to 5' exoribonuclease |
15 |
9.89e-01 |
9.92e-01 |
0.02340 |
2.24e-02 |
-6.54e-03 |
8.80e-01 |
9.65e-01 |
Visual phototransduction |
83 |
9.27e-01 |
9.47e-01 |
0.02260 |
-8.41e-03 |
-2.09e-02 |
8.95e-01 |
7.42e-01 |
Metabolism of steroids |
128 |
9.02e-01 |
9.30e-01 |
0.02090 |
1.01e-02 |
1.83e-02 |
8.43e-01 |
7.21e-01 |
Activation of HOX genes during differentiation |
69 |
9.64e-01 |
9.73e-01 |
0.02060 |
-1.08e-02 |
1.76e-02 |
8.77e-01 |
8.01e-01 |
Activation of anterior HOX genes in hindbrain development during early embryogenesis |
69 |
9.64e-01 |
9.73e-01 |
0.02060 |
-1.08e-02 |
1.76e-02 |
8.77e-01 |
8.01e-01 |
Macroautophagy |
108 |
9.37e-01 |
9.54e-01 |
0.01850 |
6.19e-03 |
1.74e-02 |
9.12e-01 |
7.55e-01 |
Regulation of FOXO transcriptional activity by acetylation |
10 |
9.95e-01 |
9.97e-01 |
0.01630 |
-6.64e-03 |
-1.49e-02 |
9.71e-01 |
9.35e-01 |
HDMs demethylate histones |
23 |
9.94e-01 |
9.97e-01 |
0.01430 |
-6.97e-03 |
1.25e-02 |
9.54e-01 |
9.18e-01 |
Metabolism of vitamins and cofactors |
175 |
9.70e-01 |
9.78e-01 |
0.01180 |
-9.57e-03 |
6.86e-03 |
8.27e-01 |
8.76e-01 |
Glycosaminoglycan metabolism |
114 |
9.82e-01 |
9.88e-01 |
0.01110 |
9.52e-03 |
-5.73e-03 |
8.61e-01 |
9.16e-01 |
Repression of WNT target genes |
14 |
9.98e-01 |
9.99e-01 |
0.00971 |
4.01e-03 |
8.84e-03 |
9.79e-01 |
9.54e-01 |
Glycogen storage diseases |
15 |
9.99e-01 |
9.99e-01 |
0.00706 |
-6.92e-03 |
1.39e-03 |
9.63e-01 |
9.93e-01 |
NF-kB activation through FADD/RIP-1 pathway mediated by caspase-8 and -10 |
10 |
9.99e-01 |
9.99e-01 |
0.00697 |
-6.96e-03 |
3.71e-04 |
9.70e-01 |
9.98e-01 |
Diseases of metabolism |
217 |
9.86e-01 |
9.91e-01 |
0.00596 |
2.54e-03 |
5.40e-03 |
9.49e-01 |
8.91e-01 |