Establishment of Sister Chromatid Cohesion |
10 |
4.25e-04 |
6.30e-03 |
0.7240 |
7.14e-01 |
0.120000 |
9.25e-05 |
5.11e-01 |
Mitotic Telophase/Cytokinesis |
10 |
5.54e-04 |
7.61e-03 |
0.7150 |
6.85e-01 |
0.204000 |
1.76e-04 |
2.64e-01 |
Glucuronidation |
11 |
4.90e-04 |
7.09e-03 |
0.6930 |
5.60e-01 |
0.408000 |
1.29e-03 |
1.90e-02 |
Viral mRNA Translation |
37 |
2.92e-11 |
9.17e-09 |
0.6540 |
6.27e-01 |
-0.183000 |
3.97e-11 |
5.42e-02 |
Peptide chain elongation |
37 |
1.12e-10 |
2.02e-08 |
0.6360 |
6.14e-01 |
-0.164000 |
1.00e-10 |
8.51e-02 |
Constitutive Signaling by NOTCH1 HD Domain Mutants |
10 |
2.48e-03 |
2.48e-02 |
0.6190 |
-4.60e-01 |
0.414000 |
1.17e-02 |
2.34e-02 |
Signaling by NOTCH1 HD Domain Mutants in Cancer |
10 |
2.48e-03 |
2.48e-02 |
0.6190 |
-4.60e-01 |
0.414000 |
1.17e-02 |
2.34e-02 |
Selenocysteine synthesis |
40 |
1.80e-10 |
2.84e-08 |
0.6030 |
5.67e-01 |
-0.206000 |
5.45e-10 |
2.42e-02 |
Dissolution of Fibrin Clot |
10 |
6.20e-03 |
5.31e-02 |
0.5920 |
5.20e-01 |
0.284000 |
4.41e-03 |
1.20e-01 |
Activation of the pre-replicative complex |
26 |
1.25e-06 |
4.91e-05 |
0.5910 |
5.91e-01 |
0.013600 |
1.86e-07 |
9.04e-01 |
Response of EIF2AK4 (GCN2) to amino acid deficiency |
44 |
2.07e-10 |
2.89e-08 |
0.5800 |
5.78e-01 |
-0.043000 |
3.28e-11 |
6.22e-01 |
Eukaryotic Translation Termination |
40 |
2.36e-09 |
2.12e-07 |
0.5700 |
5.52e-01 |
-0.140000 |
1.50e-09 |
1.27e-01 |
Cyclin A/B1/B2 associated events during G2/M transition |
19 |
1.17e-04 |
2.20e-03 |
0.5580 |
5.44e-01 |
-0.124000 |
4.00e-05 |
3.50e-01 |
DNA strand elongation |
26 |
9.02e-06 |
2.59e-04 |
0.5440 |
5.43e-01 |
-0.036400 |
1.66e-06 |
7.48e-01 |
Eukaryotic Translation Elongation |
40 |
1.78e-08 |
1.12e-06 |
0.5400 |
5.25e-01 |
-0.126000 |
8.96e-09 |
1.68e-01 |
Heme degradation |
10 |
1.07e-02 |
7.80e-02 |
0.5400 |
2.90e-01 |
-0.455000 |
1.12e-01 |
1.28e-02 |
Recognition of DNA damage by PCNA-containing replication complex |
21 |
8.30e-05 |
1.68e-03 |
0.5400 |
5.15e-01 |
-0.160000 |
4.37e-05 |
2.04e-01 |
Mitophagy |
19 |
3.22e-04 |
5.13e-03 |
0.5320 |
-2.05e-02 |
-0.531000 |
8.77e-01 |
6.07e-05 |
Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC) |
41 |
3.76e-08 |
1.97e-06 |
0.5230 |
5.12e-01 |
-0.105000 |
1.37e-08 |
2.47e-01 |
Formation of a pool of free 40S subunits |
46 |
4.55e-09 |
3.57e-07 |
0.5220 |
4.97e-01 |
-0.157000 |
5.36e-09 |
6.62e-02 |
HSF1-dependent transactivation |
26 |
2.72e-05 |
6.58e-04 |
0.5180 |
-5.18e-01 |
0.015100 |
4.80e-06 |
8.94e-01 |
Condensation of Prophase Chromosomes |
10 |
2.00e-02 |
1.22e-01 |
0.5180 |
4.86e-01 |
0.179000 |
7.85e-03 |
3.26e-01 |
Processive synthesis on the lagging strand |
12 |
8.26e-03 |
6.45e-02 |
0.5160 |
5.16e-01 |
-0.007710 |
1.99e-03 |
9.63e-01 |
PINK1-PRKN Mediated Mitophagy |
13 |
5.56e-03 |
4.82e-02 |
0.5150 |
1.01e-02 |
-0.515000 |
9.50e-01 |
1.30e-03 |
PCNA-Dependent Long Patch Base Excision Repair |
17 |
1.13e-03 |
1.36e-02 |
0.5110 |
4.97e-01 |
-0.116000 |
3.85e-04 |
4.07e-01 |
Negative regulation of TCF-dependent signaling by WNT ligand antagonists |
10 |
2.31e-02 |
1.34e-01 |
0.5050 |
-4.95e-01 |
-0.101000 |
6.72e-03 |
5.79e-01 |
Termination of translesion DNA synthesis |
23 |
1.68e-04 |
3.05e-03 |
0.4970 |
4.85e-01 |
-0.109000 |
5.63e-05 |
3.65e-01 |
Transcription of E2F targets under negative control by p107 (RBL1) and p130 (RBL2) in complex with HDAC1 |
14 |
6.48e-03 |
5.51e-02 |
0.4970 |
4.59e-01 |
0.192000 |
2.98e-03 |
2.13e-01 |
Removal of the Flap Intermediate |
11 |
1.64e-02 |
1.07e-01 |
0.4960 |
4.91e-01 |
-0.068300 |
4.80e-03 |
6.95e-01 |
Selenoamino acid metabolism |
53 |
1.85e-09 |
1.79e-07 |
0.4950 |
4.50e-01 |
-0.206000 |
1.45e-08 |
9.40e-03 |
Nucleotide-like (purinergic) receptors |
11 |
2.05e-02 |
1.24e-01 |
0.4940 |
2.54e-01 |
0.424000 |
1.44e-01 |
1.49e-02 |
L13a-mediated translational silencing of Ceruloplasmin expression |
50 |
8.78e-09 |
6.14e-07 |
0.4930 |
4.77e-01 |
-0.123000 |
5.41e-09 |
1.34e-01 |
Polo-like kinase mediated events |
13 |
9.45e-03 |
7.12e-02 |
0.4910 |
4.88e-01 |
0.059300 |
2.33e-03 |
7.12e-01 |
G1/S-Specific Transcription |
24 |
2.38e-04 |
4.10e-03 |
0.4900 |
4.25e-01 |
0.245000 |
3.18e-04 |
3.75e-02 |
Chk1/Chk2(Cds1) mediated inactivation of Cyclin B:Cdk1 complex |
11 |
1.75e-02 |
1.09e-01 |
0.4890 |
4.70e-01 |
-0.137000 |
7.02e-03 |
4.30e-01 |
Translesion synthesis by REV1 |
11 |
1.86e-02 |
1.15e-01 |
0.4850 |
4.62e-01 |
-0.148000 |
7.94e-03 |
3.97e-01 |
Translesion synthesis by POLK |
12 |
1.34e-02 |
9.22e-02 |
0.4830 |
4.57e-01 |
-0.157000 |
6.16e-03 |
3.46e-01 |
Synthesis of PIPs at the late endosome membrane |
10 |
3.08e-02 |
1.59e-01 |
0.4820 |
7.10e-03 |
0.482000 |
9.69e-01 |
8.34e-03 |
Attenuation phase |
17 |
2.58e-03 |
2.53e-02 |
0.4810 |
-4.78e-01 |
0.054600 |
6.47e-04 |
6.97e-01 |
GTP hydrolysis and joining of the 60S ribosomal subunit |
52 |
1.23e-08 |
8.12e-07 |
0.4790 |
4.67e-01 |
-0.106000 |
5.59e-09 |
1.87e-01 |
G0 and Early G1 |
24 |
3.44e-04 |
5.41e-03 |
0.4770 |
4.53e-01 |
0.148000 |
1.23e-04 |
2.09e-01 |
Defective B3GALTL causes Peters-plus syndrome (PpS) |
29 |
3.74e-05 |
8.70e-04 |
0.4760 |
-2.00e-01 |
0.432000 |
6.23e-02 |
5.59e-05 |
Gap-filling DNA repair synthesis and ligation in GG-NER |
19 |
1.45e-03 |
1.65e-02 |
0.4740 |
4.61e-01 |
-0.110000 |
4.99e-04 |
4.07e-01 |
SRP-dependent cotranslational protein targeting to membrane |
55 |
6.93e-09 |
5.13e-07 |
0.4730 |
4.56e-01 |
-0.122000 |
4.82e-09 |
1.17e-01 |
LGI-ADAM interactions |
11 |
2.69e-02 |
1.47e-01 |
0.4720 |
-4.60e-01 |
-0.107000 |
8.26e-03 |
5.38e-01 |
Cholesterol biosynthesis |
20 |
1.51e-03 |
1.68e-02 |
0.4720 |
-4.39e-01 |
-0.173000 |
6.74e-04 |
1.80e-01 |
Activation of ATR in response to replication stress |
28 |
8.03e-05 |
1.68e-03 |
0.4720 |
4.70e-01 |
-0.041600 |
1.66e-05 |
7.03e-01 |
Mismatch repair (MMR) directed by MSH2:MSH6 (MutSalpha) |
12 |
2.03e-02 |
1.24e-01 |
0.4690 |
4.60e-01 |
0.088200 |
5.77e-03 |
5.97e-01 |
Lagging Strand Synthesis |
17 |
3.45e-03 |
3.32e-02 |
0.4670 |
4.52e-01 |
-0.115000 |
1.25e-03 |
4.10e-01 |
Resolution of AP sites via the multiple-nucleotide patch replacement pathway |
19 |
1.98e-03 |
2.10e-02 |
0.4660 |
4.66e-01 |
-0.021500 |
4.41e-04 |
8.71e-01 |
Organic cation/anion/zwitterion transport |
10 |
4.41e-02 |
1.99e-01 |
0.4640 |
2.17e-01 |
0.410000 |
2.35e-01 |
2.47e-02 |
CLEC7A (Dectin-1) induces NFAT activation |
10 |
4.35e-02 |
1.98e-01 |
0.4630 |
1.38e-01 |
0.442000 |
4.51e-01 |
1.56e-02 |
O-glycosylation of TSR domain-containing proteins |
30 |
4.89e-05 |
1.10e-03 |
0.4620 |
-2.06e-01 |
0.413000 |
5.10e-02 |
8.91e-05 |
Gene and protein expression by JAK-STAT signaling after Interleukin-12 stimulation |
26 |
3.14e-04 |
5.07e-03 |
0.4510 |
4.41e-01 |
-0.095400 |
1.01e-04 |
4.00e-01 |
Translesion synthesis by POLI |
12 |
2.43e-02 |
1.38e-01 |
0.4510 |
4.42e-01 |
-0.088200 |
8.03e-03 |
5.97e-01 |
Transport of vitamins, nucleosides, and related molecules |
26 |
4.51e-04 |
6.59e-03 |
0.4460 |
-3.95e-02 |
-0.444000 |
7.27e-01 |
8.81e-05 |
Collagen chain trimerization |
32 |
6.08e-05 |
1.32e-03 |
0.4420 |
-3.89e-01 |
0.209000 |
1.39e-04 |
4.05e-02 |
Cap-dependent Translation Initiation |
58 |
3.34e-08 |
1.91e-06 |
0.4410 |
4.28e-01 |
-0.107000 |
1.80e-08 |
1.58e-01 |
Eukaryotic Translation Initiation |
58 |
3.34e-08 |
1.91e-06 |
0.4410 |
4.28e-01 |
-0.107000 |
1.80e-08 |
1.58e-01 |
Glucagon-type ligand receptors |
13 |
2.82e-02 |
1.51e-01 |
0.4370 |
-3.02e-01 |
-0.316000 |
5.93e-02 |
4.88e-02 |
Interferon alpha/beta signaling |
41 |
9.38e-06 |
2.62e-04 |
0.4350 |
4.34e-01 |
0.029100 |
1.51e-06 |
7.47e-01 |
Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC) |
58 |
1.02e-07 |
4.60e-06 |
0.4290 |
4.29e-01 |
-0.025500 |
1.66e-08 |
7.37e-01 |
Nonsense-Mediated Decay (NMD) |
58 |
1.02e-07 |
4.60e-06 |
0.4290 |
4.29e-01 |
-0.025500 |
1.66e-08 |
7.37e-01 |
Interleukin-12 signaling |
30 |
2.47e-04 |
4.20e-03 |
0.4280 |
4.26e-01 |
-0.042500 |
5.46e-05 |
6.87e-01 |
E2F mediated regulation of DNA replication |
18 |
8.09e-03 |
6.44e-02 |
0.4280 |
4.07e-01 |
0.130000 |
2.78e-03 |
3.39e-01 |
Phosphorylation of CD3 and TCR zeta chains |
10 |
7.17e-02 |
2.73e-01 |
0.4250 |
4.01e-01 |
0.139000 |
2.81e-02 |
4.47e-01 |
CRMPs in Sema3A signaling |
14 |
2.31e-02 |
1.34e-01 |
0.4210 |
-5.39e-02 |
0.418000 |
7.27e-01 |
6.80e-03 |
Lysine catabolism |
10 |
6.33e-02 |
2.48e-01 |
0.4210 |
3.68e-01 |
-0.205000 |
4.40e-02 |
2.62e-01 |
Formation of the ternary complex, and subsequently, the 43S complex |
26 |
9.41e-04 |
1.18e-02 |
0.4210 |
4.18e-01 |
-0.050700 |
2.30e-04 |
6.55e-01 |
Removal of the Flap Intermediate from the C-strand |
12 |
3.80e-02 |
1.83e-01 |
0.4200 |
3.96e-01 |
-0.141000 |
1.76e-02 |
3.97e-01 |
Leading Strand Synthesis |
13 |
3.07e-02 |
1.59e-01 |
0.4190 |
4.10e-01 |
-0.088400 |
1.06e-02 |
5.81e-01 |
Polymerase switching |
13 |
3.07e-02 |
1.59e-01 |
0.4190 |
4.10e-01 |
-0.088400 |
1.06e-02 |
5.81e-01 |
DNA Damage Bypass |
34 |
1.47e-04 |
2.71e-03 |
0.4140 |
4.12e-01 |
-0.043900 |
3.24e-05 |
6.58e-01 |
Surfactant metabolism |
12 |
5.18e-02 |
2.16e-01 |
0.4120 |
-1.53e-01 |
-0.382000 |
3.58e-01 |
2.20e-02 |
Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S |
30 |
5.02e-04 |
7.11e-03 |
0.4090 |
4.06e-01 |
-0.050200 |
1.20e-04 |
6.35e-01 |
KSRP (KHSRP) binds and destabilizes mRNA |
14 |
2.63e-02 |
1.46e-01 |
0.4080 |
2.64e-01 |
-0.311000 |
8.78e-02 |
4.40e-02 |
Transcription of E2F targets under negative control by DREAM complex |
17 |
1.63e-02 |
1.07e-01 |
0.4070 |
3.90e-01 |
0.115000 |
5.39e-03 |
4.13e-01 |
Ribosomal scanning and start codon recognition |
30 |
5.57e-04 |
7.61e-03 |
0.4060 |
4.04e-01 |
-0.042700 |
1.28e-04 |
6.86e-01 |
Synthesis of PC |
21 |
5.70e-03 |
4.91e-02 |
0.4060 |
-4.05e-01 |
-0.030000 |
1.31e-03 |
8.12e-01 |
Retrograde neurotrophin signalling |
14 |
2.72e-02 |
1.48e-01 |
0.4060 |
-2.65e-01 |
0.307000 |
8.64e-02 |
4.65e-02 |
Mismatch repair (MMR) directed by MSH2:MSH3 (MutSbeta) |
12 |
5.44e-02 |
2.24e-01 |
0.4040 |
4.01e-01 |
0.050600 |
1.62e-02 |
7.62e-01 |
Interleukin-12 family signaling |
36 |
1.70e-04 |
3.05e-03 |
0.3990 |
3.94e-01 |
-0.059800 |
4.30e-05 |
5.35e-01 |
Orc1 removal from chromatin |
54 |
2.32e-06 |
8.36e-05 |
0.3960 |
3.76e-01 |
-0.124000 |
1.83e-06 |
1.15e-01 |
Signaling by BMP |
20 |
9.27e-03 |
7.07e-02 |
0.3930 |
-3.72e-02 |
0.392000 |
7.74e-01 |
2.43e-03 |
Translesion synthesis by Y family DNA polymerases bypasses lesions on DNA template |
28 |
1.47e-03 |
1.65e-02 |
0.3930 |
3.92e-01 |
-0.025100 |
3.28e-04 |
8.18e-01 |
ERBB2 Activates PTK6 Signaling |
10 |
9.19e-02 |
3.21e-01 |
0.3910 |
-3.18e-01 |
0.227000 |
8.12e-02 |
2.14e-01 |
Translation initiation complex formation |
29 |
1.25e-03 |
1.49e-02 |
0.3900 |
3.88e-01 |
-0.042000 |
3.01e-04 |
6.95e-01 |
Early Phase of HIV Life Cycle |
10 |
1.13e-01 |
3.57e-01 |
0.3880 |
3.37e-01 |
0.194000 |
6.54e-02 |
2.89e-01 |
Incretin synthesis, secretion, and inactivation |
10 |
9.67e-02 |
3.32e-01 |
0.3880 |
-1.90e-01 |
0.338000 |
2.99e-01 |
6.43e-02 |
Signaling by FGFR3 fusions in cancer |
10 |
9.83e-02 |
3.36e-01 |
0.3860 |
3.41e-01 |
-0.182000 |
6.20e-02 |
3.20e-01 |
Processive synthesis on the C-strand of the telomere |
14 |
4.27e-02 |
1.96e-01 |
0.3850 |
3.80e-01 |
-0.058300 |
1.37e-02 |
7.06e-01 |
Pre-NOTCH Processing in Golgi |
14 |
4.09e-02 |
1.91e-01 |
0.3850 |
-3.59e-01 |
0.137000 |
2.00e-02 |
3.74e-01 |
Mitotic G1 phase and G1/S transition |
120 |
2.79e-12 |
1.17e-09 |
0.3840 |
3.83e-01 |
-0.034000 |
4.75e-13 |
5.21e-01 |
G1/S Transition |
106 |
5.42e-11 |
1.36e-08 |
0.3840 |
3.80e-01 |
-0.058500 |
1.51e-11 |
2.99e-01 |
DNA Replication Pre-Initiation |
66 |
3.85e-07 |
1.62e-05 |
0.3840 |
3.76e-01 |
-0.076300 |
1.31e-07 |
2.84e-01 |
ERBB2 Regulates Cell Motility |
12 |
6.39e-02 |
2.48e-01 |
0.3830 |
-2.96e-01 |
0.243000 |
7.62e-02 |
1.45e-01 |
Transport of bile salts and organic acids, metal ions and amine compounds |
45 |
8.19e-05 |
1.68e-03 |
0.3810 |
3.13e-01 |
0.218000 |
2.84e-04 |
1.15e-02 |
CREB1 phosphorylation through the activation of Adenylate Cyclase |
10 |
1.09e-01 |
3.53e-01 |
0.3800 |
-1.01e-01 |
0.367000 |
5.82e-01 |
4.47e-02 |
Carnitine metabolism |
11 |
1.01e-01 |
3.37e-01 |
0.3790 |
-3.36e-01 |
-0.177000 |
5.40e-02 |
3.10e-01 |
CD28 dependent Vav1 pathway |
12 |
8.22e-02 |
2.95e-01 |
0.3760 |
3.67e-01 |
0.082400 |
2.79e-02 |
6.21e-01 |
Activation of AMPK downstream of NMDARs |
10 |
1.18e-01 |
3.66e-01 |
0.3750 |
-3.72e-01 |
0.045500 |
4.15e-02 |
8.03e-01 |
Mismatch Repair |
13 |
6.97e-02 |
2.67e-01 |
0.3730 |
3.61e-01 |
0.094900 |
2.42e-02 |
5.53e-01 |
Glycogen synthesis |
10 |
1.26e-01 |
3.82e-01 |
0.3730 |
-3.72e-01 |
-0.026900 |
4.18e-02 |
8.83e-01 |
Polymerase switching on the C-strand of the telomere |
21 |
1.18e-02 |
8.34e-02 |
0.3730 |
3.65e-01 |
-0.072400 |
3.76e-03 |
5.66e-01 |
S Phase |
135 |
7.62e-13 |
4.79e-10 |
0.3700 |
3.64e-01 |
-0.067900 |
3.31e-13 |
1.74e-01 |
NCAM1 interactions |
27 |
3.87e-03 |
3.66e-02 |
0.3700 |
-3.69e-01 |
0.019100 |
9.06e-04 |
8.63e-01 |
Initial triggering of complement |
18 |
2.27e-02 |
1.34e-01 |
0.3670 |
2.67e-01 |
-0.252000 |
5.03e-02 |
6.45e-02 |
Receptor-type tyrosine-protein phosphatases |
13 |
7.36e-02 |
2.74e-01 |
0.3640 |
-3.29e-02 |
0.363000 |
8.37e-01 |
2.36e-02 |
Synthesis of DNA |
97 |
3.25e-09 |
2.73e-07 |
0.3640 |
3.53e-01 |
-0.089500 |
2.05e-09 |
1.28e-01 |
DNA Replication |
104 |
1.08e-09 |
1.13e-07 |
0.3620 |
3.53e-01 |
-0.076800 |
5.01e-10 |
1.77e-01 |
Post-chaperonin tubulin folding pathway |
17 |
4.13e-02 |
1.92e-01 |
0.3600 |
-1.72e-01 |
-0.316000 |
2.21e-01 |
2.39e-02 |
Assembly of collagen fibrils and other multimeric structures |
43 |
2.70e-04 |
4.42e-03 |
0.3570 |
-3.56e-01 |
0.013600 |
5.34e-05 |
8.77e-01 |
Adherens junctions interactions |
13 |
7.77e-02 |
2.84e-01 |
0.3560 |
-1.53e-01 |
0.321000 |
3.39e-01 |
4.48e-02 |
Synthesis of pyrophosphates in the cytosol |
10 |
1.57e-01 |
4.31e-01 |
0.3520 |
-3.37e-02 |
-0.351000 |
8.54e-01 |
5.48e-02 |
Metal ion SLC transporters |
17 |
4.56e-02 |
2.03e-01 |
0.3500 |
3.47e-01 |
0.043100 |
1.33e-02 |
7.58e-01 |
Nicotinamide salvaging |
13 |
8.33e-02 |
2.97e-01 |
0.3500 |
2.19e-01 |
-0.273000 |
1.71e-01 |
8.89e-02 |
NOTCH2 Activation and Transmission of Signal to the Nucleus |
13 |
8.37e-02 |
2.97e-01 |
0.3500 |
-2.86e-01 |
0.202000 |
7.47e-02 |
2.08e-01 |
Telomere C-strand (Lagging Strand) Synthesis |
27 |
6.95e-03 |
5.83e-02 |
0.3480 |
3.45e-01 |
-0.048500 |
1.93e-03 |
6.63e-01 |
Regulation of IFNG signaling |
12 |
1.26e-01 |
3.82e-01 |
0.3450 |
1.69e-01 |
0.301000 |
3.11e-01 |
7.08e-02 |
Influenza Viral RNA Transcription and Replication |
69 |
3.57e-06 |
1.21e-04 |
0.3450 |
3.35e-01 |
-0.083400 |
1.52e-06 |
2.31e-01 |
Translesion Synthesis by POLH |
11 |
1.30e-01 |
3.90e-01 |
0.3450 |
2.86e-01 |
-0.193000 |
1.01e-01 |
2.67e-01 |
Collagen biosynthesis and modifying enzymes |
50 |
1.00e-04 |
1.94e-03 |
0.3450 |
-3.07e-01 |
0.158000 |
1.79e-04 |
5.37e-02 |
Diseases of carbohydrate metabolism |
22 |
2.26e-02 |
1.34e-01 |
0.3450 |
-3.08e-01 |
-0.154000 |
1.23e-02 |
2.11e-01 |
Effects of PIP2 hydrolysis |
22 |
2.15e-02 |
1.28e-01 |
0.3440 |
-3.36e-01 |
-0.073200 |
6.34e-03 |
5.52e-01 |
Regulation of expression of SLITs and ROBOs |
95 |
4.02e-08 |
2.02e-06 |
0.3440 |
3.38e-01 |
-0.061600 |
1.24e-08 |
3.01e-01 |
Phase II - Conjugation of compounds |
66 |
9.05e-06 |
2.59e-04 |
0.3440 |
3.43e-01 |
0.019500 |
1.44e-06 |
7.84e-01 |
Zinc transporters |
10 |
1.75e-01 |
4.63e-01 |
0.3430 |
3.38e-01 |
0.055500 |
6.40e-02 |
7.61e-01 |
Cyclin D associated events in G1 |
37 |
1.59e-03 |
1.74e-02 |
0.3420 |
3.41e-01 |
0.032600 |
3.38e-04 |
7.31e-01 |
G1 Phase |
37 |
1.59e-03 |
1.74e-02 |
0.3420 |
3.41e-01 |
0.032600 |
3.38e-04 |
7.31e-01 |
Elevation of cytosolic Ca2+ levels |
10 |
1.76e-01 |
4.63e-01 |
0.3420 |
-3.39e-01 |
-0.048900 |
6.37e-02 |
7.89e-01 |
Assembly of the pre-replicative complex |
52 |
9.63e-05 |
1.89e-03 |
0.3410 |
3.30e-01 |
-0.086200 |
3.88e-05 |
2.83e-01 |
Regulation of FZD by ubiquitination |
10 |
1.88e-01 |
4.77e-01 |
0.3410 |
-2.69e-01 |
-0.209000 |
1.41e-01 |
2.52e-01 |
DCC mediated attractive signaling |
13 |
1.13e-01 |
3.57e-01 |
0.3400 |
1.44e-01 |
0.308000 |
3.69e-01 |
5.44e-02 |
Caspase-mediated cleavage of cytoskeletal proteins |
11 |
1.39e-01 |
4.04e-01 |
0.3390 |
-1.98e-01 |
0.275000 |
2.56e-01 |
1.14e-01 |
Regulation of pyruvate dehydrogenase (PDH) complex |
12 |
1.30e-01 |
3.90e-01 |
0.3390 |
-4.43e-02 |
-0.336000 |
7.91e-01 |
4.41e-02 |
Cleavage of the damaged pyrimidine |
13 |
1.01e-01 |
3.37e-01 |
0.3380 |
1.38e-01 |
-0.308000 |
3.88e-01 |
5.46e-02 |
Depyrimidination |
13 |
1.01e-01 |
3.37e-01 |
0.3380 |
1.38e-01 |
-0.308000 |
3.88e-01 |
5.46e-02 |
Recognition and association of DNA glycosylase with site containing an affected pyrimidine |
13 |
1.01e-01 |
3.37e-01 |
0.3380 |
1.38e-01 |
-0.308000 |
3.88e-01 |
5.46e-02 |
Creation of C4 and C2 activators |
11 |
1.50e-01 |
4.25e-01 |
0.3340 |
1.30e-01 |
-0.307000 |
4.55e-01 |
7.78e-02 |
Formation of Fibrin Clot (Clotting Cascade) |
15 |
8.49e-02 |
3.00e-01 |
0.3340 |
3.28e-01 |
0.063700 |
2.81e-02 |
6.69e-01 |
SCF(Skp2)-mediated degradation of p27/p21 |
46 |
3.67e-04 |
5.70e-03 |
0.3320 |
2.78e-01 |
-0.182000 |
1.11e-03 |
3.27e-02 |
Activation of Matrix Metalloproteinases |
17 |
6.09e-02 |
2.43e-01 |
0.3320 |
-3.31e-01 |
-0.022400 |
1.80e-02 |
8.73e-01 |
Signaling by Activin |
10 |
1.90e-01 |
4.80e-01 |
0.3310 |
-3.29e-01 |
0.038700 |
7.21e-02 |
8.32e-01 |
Glutathione synthesis and recycling |
11 |
1.53e-01 |
4.28e-01 |
0.3310 |
1.77e-01 |
-0.279000 |
3.08e-01 |
1.09e-01 |
Heme biosynthesis |
11 |
1.81e-01 |
4.67e-01 |
0.3280 |
-2.75e-01 |
-0.178000 |
1.14e-01 |
3.06e-01 |
Regulation of IFNA signaling |
12 |
1.55e-01 |
4.28e-01 |
0.3270 |
2.90e-01 |
0.152000 |
8.20e-02 |
3.63e-01 |
Influenza Infection |
82 |
1.69e-06 |
6.44e-05 |
0.3260 |
3.18e-01 |
-0.074100 |
6.69e-07 |
2.47e-01 |
ATF6 (ATF6-alpha) activates chaperones |
10 |
2.13e-01 |
5.07e-01 |
0.3260 |
3.03e-01 |
0.118000 |
9.66e-02 |
5.17e-01 |
G2/M Checkpoints |
107 |
3.66e-08 |
1.97e-06 |
0.3250 |
3.18e-01 |
-0.067000 |
1.41e-08 |
2.32e-01 |
Negative regulation of NOTCH4 signaling |
42 |
1.05e-03 |
1.31e-02 |
0.3240 |
2.80e-01 |
-0.163000 |
1.71e-03 |
6.70e-02 |
Inhibition of replication initiation of damaged DNA by RB1/E2F1 |
12 |
1.62e-01 |
4.40e-01 |
0.3230 |
2.89e-01 |
0.145000 |
8.31e-02 |
3.83e-01 |
Regulation of localization of FOXO transcription factors |
12 |
1.49e-01 |
4.25e-01 |
0.3230 |
4.44e-02 |
-0.320000 |
7.90e-01 |
5.49e-02 |
Meiotic synapsis |
24 |
2.18e-02 |
1.29e-01 |
0.3210 |
2.99e-01 |
-0.118000 |
1.13e-02 |
3.17e-01 |
Erythropoietin activates Phosphoinositide-3-kinase (PI3K) |
10 |
2.22e-01 |
5.21e-01 |
0.3210 |
3.02e-01 |
0.110000 |
9.87e-02 |
5.47e-01 |
HDR through Homologous Recombination (HRR) or Single Strand Annealing (SSA) |
77 |
6.33e-06 |
1.94e-04 |
0.3210 |
3.17e-01 |
-0.048000 |
1.56e-06 |
4.67e-01 |
Interleukin-35 Signalling |
10 |
2.14e-01 |
5.09e-01 |
0.3200 |
3.20e-01 |
-0.005490 |
7.96e-02 |
9.76e-01 |
mRNA decay by 3' to 5' exoribonuclease |
11 |
1.73e-01 |
4.61e-01 |
0.3200 |
1.78e-01 |
-0.266000 |
3.08e-01 |
1.27e-01 |
Metabolism of Angiotensinogen to Angiotensins |
12 |
1.54e-01 |
4.28e-01 |
0.3180 |
-2.97e-01 |
0.112000 |
7.47e-02 |
5.00e-01 |
Purine salvage |
10 |
2.16e-01 |
5.10e-01 |
0.3160 |
3.04e-01 |
-0.088000 |
9.64e-02 |
6.30e-01 |
Defective EXT1 causes exostoses 1, TRPS2 and CHDS |
12 |
1.54e-01 |
4.28e-01 |
0.3160 |
-2.50e-01 |
0.193000 |
1.33e-01 |
2.48e-01 |
Defective EXT2 causes exostoses 2 |
12 |
1.54e-01 |
4.28e-01 |
0.3160 |
-2.50e-01 |
0.193000 |
1.33e-01 |
2.48e-01 |
Antigen Presentation: Folding, assembly and peptide loading of class I MHC |
15 |
1.15e-01 |
3.60e-01 |
0.3160 |
2.78e-01 |
0.150000 |
6.26e-02 |
3.15e-01 |
Selective autophagy |
46 |
1.39e-03 |
1.63e-02 |
0.3160 |
-1.85e-01 |
-0.256000 |
3.05e-02 |
2.69e-03 |
ATF4 activates genes in response to endoplasmic reticulum stress |
21 |
4.73e-02 |
2.03e-01 |
0.3150 |
3.00e-01 |
0.097000 |
1.74e-02 |
4.42e-01 |
Activated NOTCH1 Transmits Signal to the Nucleus |
22 |
3.48e-02 |
1.71e-01 |
0.3140 |
-2.92e-01 |
0.116000 |
1.77e-02 |
3.46e-01 |
RHO GTPases activate IQGAPs |
10 |
2.42e-01 |
5.47e-01 |
0.3140 |
2.24e-01 |
0.221000 |
2.21e-01 |
2.27e-01 |
Switching of origins to a post-replicative state |
72 |
2.12e-05 |
5.45e-04 |
0.3120 |
2.96e-01 |
-0.100000 |
1.46e-05 |
1.43e-01 |
G beta:gamma signalling through BTK |
10 |
2.41e-01 |
5.45e-01 |
0.3120 |
-9.90e-02 |
-0.296000 |
5.88e-01 |
1.05e-01 |
Peptide hormone metabolism |
50 |
5.22e-04 |
7.30e-03 |
0.3110 |
-1.91e-01 |
0.246000 |
1.97e-02 |
2.62e-03 |
IRAK2 mediated activation of TAK1 complex upon TLR7/8 or 9 stimulation |
11 |
1.96e-01 |
4.88e-01 |
0.3110 |
-3.00e-01 |
0.081800 |
8.54e-02 |
6.39e-01 |
TRAF6-mediated induction of TAK1 complex within TLR4 complex |
11 |
1.96e-01 |
4.88e-01 |
0.3110 |
-3.00e-01 |
0.081800 |
8.54e-02 |
6.39e-01 |
CDT1 association with the CDC6:ORC:origin complex |
44 |
1.45e-03 |
1.65e-02 |
0.3100 |
2.85e-01 |
-0.122000 |
1.07e-03 |
1.61e-01 |
IRE1alpha activates chaperones |
44 |
2.37e-03 |
2.42e-02 |
0.3090 |
-2.08e-01 |
-0.229000 |
1.71e-02 |
8.57e-03 |
Insulin receptor recycling |
17 |
9.57e-02 |
3.30e-01 |
0.3070 |
-8.79e-02 |
-0.294000 |
5.31e-01 |
3.59e-02 |
Transcriptional Regulation by E2F6 |
30 |
1.45e-02 |
9.63e-02 |
0.3060 |
3.06e-01 |
-0.017100 |
3.77e-03 |
8.71e-01 |
Processing of DNA double-strand break ends |
50 |
7.93e-04 |
1.07e-02 |
0.3060 |
2.96e-01 |
-0.076300 |
2.96e-04 |
3.51e-01 |
EGR2 and SOX10-mediated initiation of Schwann cell myelination |
21 |
5.47e-02 |
2.24e-01 |
0.3050 |
-3.03e-01 |
-0.034100 |
1.62e-02 |
7.87e-01 |
G beta:gamma signalling through PI3Kgamma |
16 |
1.10e-01 |
3.53e-01 |
0.3050 |
-3.14e-02 |
-0.303000 |
8.28e-01 |
3.59e-02 |
Cyclin E associated events during G1/S transition |
67 |
7.49e-05 |
1.60e-03 |
0.3030 |
2.73e-01 |
-0.131000 |
1.13e-04 |
6.34e-02 |
Telomere C-strand synthesis initiation |
10 |
2.56e-01 |
5.67e-01 |
0.3030 |
3.01e-01 |
0.034700 |
9.99e-02 |
8.49e-01 |
HDR through Homologous Recombination (HRR) |
50 |
1.13e-03 |
1.36e-02 |
0.3020 |
3.01e-01 |
0.017300 |
2.30e-04 |
8.32e-01 |
Growth hormone receptor signaling |
17 |
9.77e-02 |
3.35e-01 |
0.3000 |
-4.41e-02 |
0.297000 |
7.53e-01 |
3.41e-02 |
Collagen formation |
68 |
8.58e-05 |
1.71e-03 |
0.2990 |
-2.80e-01 |
0.105000 |
6.50e-05 |
1.35e-01 |
Synthesis of Leukotrienes (LT) and Eoxins (EX) |
15 |
1.44e-01 |
4.18e-01 |
0.2990 |
2.67e-01 |
0.133000 |
7.32e-02 |
3.72e-01 |
Pyruvate metabolism |
23 |
4.62e-02 |
2.03e-01 |
0.2990 |
6.47e-04 |
-0.299000 |
9.96e-01 |
1.32e-02 |
Extension of Telomeres |
40 |
4.66e-03 |
4.28e-02 |
0.2980 |
2.97e-01 |
-0.024800 |
1.15e-03 |
7.87e-01 |
Insulin processing |
19 |
7.22e-02 |
2.74e-01 |
0.2980 |
-1.53e-01 |
0.256000 |
2.49e-01 |
5.35e-02 |
Regulation of activated PAK-2p34 by proteasome mediated degradation |
38 |
5.19e-03 |
4.57e-02 |
0.2980 |
2.43e-01 |
-0.173000 |
9.56e-03 |
6.59e-02 |
G beta:gamma signalling through PLC beta |
12 |
2.18e-01 |
5.14e-01 |
0.2970 |
-2.08e-01 |
-0.213000 |
2.13e-01 |
2.03e-01 |
Synthesis of IP3 and IP4 in the cytosol |
20 |
6.96e-02 |
2.67e-01 |
0.2970 |
-2.95e-01 |
0.031000 |
2.24e-02 |
8.10e-01 |
Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell |
48 |
1.66e-03 |
1.80e-02 |
0.2960 |
2.90e-01 |
-0.061500 |
5.26e-04 |
4.61e-01 |
Apoptotic factor-mediated response |
12 |
2.22e-01 |
5.21e-01 |
0.2950 |
-1.66e-01 |
-0.244000 |
3.20e-01 |
1.44e-01 |
PERK regulates gene expression |
24 |
4.92e-02 |
2.10e-01 |
0.2940 |
2.65e-01 |
0.129000 |
2.49e-02 |
2.75e-01 |
Cytosolic sulfonation of small molecules |
13 |
1.98e-01 |
4.89e-01 |
0.2940 |
2.34e-01 |
0.179000 |
1.45e-01 |
2.65e-01 |
Vif-mediated degradation of APOBEC3G |
39 |
5.31e-03 |
4.64e-02 |
0.2940 |
2.41e-01 |
-0.167000 |
9.17e-03 |
7.06e-02 |
DARPP-32 events |
21 |
7.39e-02 |
2.74e-01 |
0.2940 |
1.78e-01 |
0.234000 |
1.59e-01 |
6.39e-02 |
GRB2 events in EGFR signaling |
10 |
2.90e-01 |
6.03e-01 |
0.2940 |
-1.91e-01 |
-0.223000 |
2.96e-01 |
2.22e-01 |
Dual Incision in GG-NER |
33 |
1.19e-02 |
8.34e-02 |
0.2930 |
2.30e-01 |
-0.183000 |
2.24e-02 |
6.98e-02 |
RUNX3 regulates NOTCH signaling |
13 |
1.78e-01 |
4.63e-01 |
0.2930 |
-1.01e-01 |
0.275000 |
5.29e-01 |
8.58e-02 |
Cyclin A:Cdk2-associated events at S phase entry |
69 |
1.06e-04 |
2.02e-03 |
0.2930 |
2.66e-01 |
-0.123000 |
1.33e-04 |
7.83e-02 |
Diseases associated with O-glycosylation of proteins |
41 |
4.21e-03 |
3.92e-02 |
0.2930 |
-1.59e-01 |
0.246000 |
7.90e-02 |
6.41e-03 |
RNA Polymerase III Chain Elongation |
13 |
1.86e-01 |
4.74e-01 |
0.2920 |
4.49e-02 |
-0.288000 |
7.79e-01 |
7.19e-02 |
NOTCH3 Activation and Transmission of Signal to the Nucleus |
18 |
9.32e-02 |
3.24e-01 |
0.2910 |
-2.37e-01 |
0.169000 |
8.22e-02 |
2.15e-01 |
Signal transduction by L1 |
19 |
8.45e-02 |
3.00e-01 |
0.2900 |
1.15e-01 |
-0.266000 |
3.86e-01 |
4.47e-02 |
Cross-presentation of soluble exogenous antigens (endosomes) |
41 |
4.81e-03 |
4.36e-02 |
0.2890 |
2.50e-01 |
-0.146000 |
5.62e-03 |
1.07e-01 |
Telomere Maintenance |
49 |
2.13e-03 |
2.21e-02 |
0.2890 |
2.88e-01 |
-0.024300 |
5.02e-04 |
7.69e-01 |
p75NTR signals via NF-kB |
10 |
2.72e-01 |
5.89e-01 |
0.2880 |
-2.29e-01 |
0.175000 |
2.10e-01 |
3.37e-01 |
Metabolism of porphyrins |
20 |
8.75e-02 |
3.07e-01 |
0.2870 |
-4.93e-02 |
-0.283000 |
7.03e-01 |
2.86e-02 |
Chromosome Maintenance |
63 |
4.18e-04 |
6.30e-03 |
0.2870 |
2.86e-01 |
-0.013600 |
8.54e-05 |
8.52e-01 |
Resolution of Sister Chromatid Cohesion |
83 |
4.26e-05 |
9.75e-04 |
0.2860 |
2.85e-01 |
0.023600 |
7.37e-06 |
7.11e-01 |
Transferrin endocytosis and recycling |
22 |
7.62e-02 |
2.80e-01 |
0.2850 |
-2.07e-01 |
-0.197000 |
9.30e-02 |
1.11e-01 |
EPHB-mediated forward signaling |
30 |
2.96e-02 |
1.55e-01 |
0.2850 |
2.46e-01 |
0.145000 |
1.99e-02 |
1.71e-01 |
Degradation of AXIN |
42 |
4.93e-03 |
4.42e-02 |
0.2850 |
2.33e-01 |
-0.164000 |
9.12e-03 |
6.54e-02 |
XBP1(S) activates chaperone genes |
42 |
7.61e-03 |
6.25e-02 |
0.2850 |
-2.04e-01 |
-0.199000 |
2.25e-02 |
2.59e-02 |
Homology Directed Repair |
81 |
5.68e-05 |
1.25e-03 |
0.2830 |
2.82e-01 |
-0.026700 |
1.18e-05 |
6.78e-01 |
Interleukin-7 signaling |
16 |
1.36e-01 |
3.98e-01 |
0.2830 |
-1.50e-01 |
0.240000 |
2.98e-01 |
9.68e-02 |
Collagen degradation |
24 |
5.06e-02 |
2.14e-01 |
0.2820 |
-2.36e-01 |
0.155000 |
4.55e-02 |
1.88e-01 |
Deposition of new CENPA-containing nucleosomes at the centromere |
16 |
1.50e-01 |
4.25e-01 |
0.2820 |
2.81e-01 |
0.028400 |
5.20e-02 |
8.44e-01 |
Nucleosome assembly |
16 |
1.50e-01 |
4.25e-01 |
0.2820 |
2.81e-01 |
0.028400 |
5.20e-02 |
8.44e-01 |
Degradation of cysteine and homocysteine |
10 |
2.98e-01 |
6.12e-01 |
0.2820 |
4.73e-02 |
-0.278000 |
7.96e-01 |
1.28e-01 |
Triglyceride catabolism |
14 |
1.86e-01 |
4.74e-01 |
0.2820 |
-2.47e-02 |
0.281000 |
8.73e-01 |
6.89e-02 |
Diseases associated with N-glycosylation of proteins |
16 |
1.37e-01 |
4.01e-01 |
0.2820 |
-2.16e-01 |
0.181000 |
1.34e-01 |
2.11e-01 |
WNT5A-dependent internalization of FZD2, FZD5 and ROR2 |
13 |
2.26e-01 |
5.26e-01 |
0.2810 |
-2.44e-01 |
-0.140000 |
1.28e-01 |
3.83e-01 |
Metabolism of polyamines |
49 |
2.47e-03 |
2.48e-02 |
0.2810 |
2.44e-01 |
-0.139000 |
3.11e-03 |
9.32e-02 |
Inhibition of DNA recombination at telomere |
13 |
2.06e-01 |
4.99e-01 |
0.2810 |
2.62e-01 |
-0.101000 |
1.02e-01 |
5.28e-01 |
IL-6-type cytokine receptor ligand interactions |
11 |
2.89e-01 |
6.03e-01 |
0.2800 |
2.29e-01 |
0.161000 |
1.88e-01 |
3.57e-01 |
FCGR activation |
15 |
1.59e-01 |
4.35e-01 |
0.2800 |
2.17e-01 |
-0.176000 |
1.45e-01 |
2.37e-01 |
Free fatty acids regulate insulin secretion |
10 |
3.07e-01 |
6.23e-01 |
0.2790 |
-2.77e-01 |
0.035900 |
1.30e-01 |
8.44e-01 |
NRAGE signals death through JNK |
54 |
1.47e-03 |
1.65e-02 |
0.2790 |
-2.38e-01 |
0.145000 |
2.48e-03 |
6.56e-02 |
Sema4D induced cell migration and growth-cone collapse |
19 |
1.16e-01 |
3.60e-01 |
0.2780 |
-2.71e-01 |
-0.062600 |
4.13e-02 |
6.37e-01 |
Signaling by Retinoic Acid |
31 |
2.59e-02 |
1.45e-01 |
0.2750 |
1.40e-01 |
-0.237000 |
1.78e-01 |
2.24e-02 |
Metalloprotease DUBs |
16 |
1.81e-01 |
4.66e-01 |
0.2730 |
2.11e-01 |
0.173000 |
1.45e-01 |
2.30e-01 |
Regulation of Complement cascade |
31 |
2.75e-02 |
1.49e-01 |
0.2730 |
2.22e-01 |
-0.158000 |
3.25e-02 |
1.27e-01 |
APC/C:Cdc20 mediated degradation of mitotic proteins |
61 |
9.24e-04 |
1.18e-02 |
0.2730 |
2.50e-01 |
-0.108000 |
7.32e-04 |
1.45e-01 |
Activation of APC/C and APC/C:Cdc20 mediated degradation of mitotic proteins |
61 |
9.24e-04 |
1.18e-02 |
0.2730 |
2.50e-01 |
-0.108000 |
7.32e-04 |
1.45e-01 |
Glycogen metabolism |
21 |
9.56e-02 |
3.30e-01 |
0.2720 |
-2.72e-01 |
0.018100 |
3.12e-02 |
8.86e-01 |
Postmitotic nuclear pore complex (NPC) reformation |
20 |
9.94e-02 |
3.37e-01 |
0.2720 |
1.51e-01 |
-0.227000 |
2.44e-01 |
7.93e-02 |
FBXL7 down-regulates AURKA during mitotic entry and in early mitosis |
43 |
7.06e-03 |
5.88e-02 |
0.2720 |
2.27e-01 |
-0.150000 |
9.96e-03 |
9.00e-02 |
G2/M DNA damage checkpoint |
51 |
3.28e-03 |
3.17e-02 |
0.2710 |
2.66e-01 |
-0.055100 |
1.03e-03 |
4.96e-01 |
HSF1 activation |
19 |
1.26e-01 |
3.82e-01 |
0.2700 |
-2.70e-01 |
-0.020700 |
4.20e-02 |
8.76e-01 |
Synthesis of PIPs at the early endosome membrane |
15 |
1.90e-01 |
4.80e-01 |
0.2700 |
-3.37e-02 |
0.268000 |
8.21e-01 |
7.23e-02 |
Gap-filling DNA repair synthesis and ligation in TC-NER |
49 |
4.38e-03 |
4.05e-02 |
0.2680 |
2.43e-01 |
-0.113000 |
3.28e-03 |
1.73e-01 |
Vpu mediated degradation of CD4 |
40 |
1.19e-02 |
8.34e-02 |
0.2670 |
2.35e-01 |
-0.128000 |
1.03e-02 |
1.61e-01 |
Base Excision Repair |
37 |
1.69e-02 |
1.07e-01 |
0.2670 |
2.45e-01 |
-0.106000 |
9.82e-03 |
2.67e-01 |
Other semaphorin interactions |
18 |
1.48e-01 |
4.25e-01 |
0.2670 |
1.97e-02 |
0.266000 |
8.85e-01 |
5.06e-02 |
Binding and Uptake of Ligands by Scavenger Receptors |
28 |
5.18e-02 |
2.16e-01 |
0.2670 |
-2.65e-01 |
-0.030900 |
1.52e-02 |
7.77e-01 |
Diseases associated with glycosylation precursor biosynthesis |
16 |
1.74e-01 |
4.61e-01 |
0.2670 |
-2.55e-01 |
0.079700 |
7.80e-02 |
5.81e-01 |
Formation of Incision Complex in GG-NER |
32 |
2.88e-02 |
1.53e-01 |
0.2670 |
1.55e-01 |
-0.217000 |
1.29e-01 |
3.40e-02 |
ROS and RNS production in phagocytes |
26 |
6.13e-02 |
2.43e-01 |
0.2670 |
2.46e-02 |
-0.265000 |
8.28e-01 |
1.92e-02 |
rRNA processing in the nucleus and cytosol |
117 |
2.66e-06 |
9.28e-05 |
0.2660 |
2.27e-01 |
-0.140000 |
2.40e-05 |
8.90e-03 |
Processing of Intronless Pre-mRNAs |
12 |
2.81e-01 |
5.95e-01 |
0.2660 |
2.65e-01 |
0.022800 |
1.12e-01 |
8.91e-01 |
HDMs demethylate histones |
19 |
1.24e-01 |
3.78e-01 |
0.2650 |
-1.94e-01 |
0.181000 |
1.44e-01 |
1.72e-01 |
Presynaptic phase of homologous DNA pairing and strand exchange |
32 |
3.31e-02 |
1.67e-01 |
0.2650 |
2.63e-01 |
-0.035900 |
1.02e-02 |
7.26e-01 |
Cell Cycle Checkpoints |
204 |
5.42e-10 |
6.82e-08 |
0.2640 |
2.60e-01 |
-0.044100 |
1.66e-10 |
2.79e-01 |
Activation of RAC1 |
12 |
2.98e-01 |
6.12e-01 |
0.2640 |
2.31e-01 |
0.127000 |
1.65e-01 |
4.47e-01 |
Assembly of active LPL and LIPC lipase complexes |
11 |
3.15e-01 |
6.32e-01 |
0.2640 |
-2.64e-01 |
0.015100 |
1.30e-01 |
9.31e-01 |
Formation of the Early Elongation Complex |
25 |
8.08e-02 |
2.91e-01 |
0.2640 |
-1.16e-01 |
-0.237000 |
3.17e-01 |
4.05e-02 |
Formation of the HIV-1 Early Elongation Complex |
25 |
8.08e-02 |
2.91e-01 |
0.2640 |
-1.16e-01 |
-0.237000 |
3.17e-01 |
4.05e-02 |
Signaling by PDGFRA extracellular domain mutants |
12 |
2.73e-01 |
5.89e-01 |
0.2630 |
2.11e-01 |
-0.157000 |
2.05e-01 |
3.46e-01 |
Signaling by PDGFRA transmembrane, juxtamembrane and kinase domain mutants |
12 |
2.73e-01 |
5.89e-01 |
0.2630 |
2.11e-01 |
-0.157000 |
2.05e-01 |
3.46e-01 |
Interferon gamma signaling |
61 |
1.74e-03 |
1.86e-02 |
0.2630 |
2.62e-01 |
-0.018900 |
3.97e-04 |
7.99e-01 |
Signaling by FGFR4 in disease |
10 |
3.39e-01 |
6.61e-01 |
0.2630 |
1.54e-01 |
-0.213000 |
3.98e-01 |
2.43e-01 |
The role of GTSE1 in G2/M progression after G2 checkpoint |
46 |
7.22e-03 |
5.98e-02 |
0.2620 |
2.02e-01 |
-0.167000 |
1.80e-02 |
4.96e-02 |
Thrombin signalling through proteinase activated receptors (PARs) |
22 |
1.14e-01 |
3.58e-01 |
0.2620 |
-1.77e-01 |
-0.194000 |
1.52e-01 |
1.16e-01 |
Gastrin-CREB signalling pathway via PKC and MAPK |
16 |
2.07e-01 |
5.00e-01 |
0.2620 |
-1.91e-01 |
-0.179000 |
1.87e-01 |
2.14e-01 |
RNA Polymerase III Transcription Initiation |
28 |
5.52e-02 |
2.25e-01 |
0.2620 |
2.09e-02 |
-0.261000 |
8.48e-01 |
1.69e-02 |
Stabilization of p53 |
43 |
1.05e-02 |
7.74e-02 |
0.2620 |
2.33e-01 |
-0.118000 |
8.20e-03 |
1.79e-01 |
Purine ribonucleoside monophosphate biosynthesis |
11 |
3.29e-01 |
6.50e-01 |
0.2620 |
-4.71e-02 |
-0.257000 |
7.87e-01 |
1.40e-01 |
Regulation of APC/C activators between G1/S and early anaphase |
65 |
1.12e-03 |
1.36e-02 |
0.2610 |
2.44e-01 |
-0.093100 |
6.94e-04 |
1.95e-01 |
RA biosynthesis pathway |
13 |
2.58e-01 |
5.68e-01 |
0.2600 |
2.50e-01 |
-0.072500 |
1.19e-01 |
6.51e-01 |
Ub-specific processing proteases |
150 |
1.61e-07 |
6.97e-06 |
0.2600 |
2.18e-01 |
-0.141000 |
4.13e-06 |
2.93e-03 |
Ubiquitin Mediated Degradation of Phosphorylated Cdc25A |
39 |
1.70e-02 |
1.07e-01 |
0.2600 |
2.30e-01 |
-0.121000 |
1.31e-02 |
1.91e-01 |
p53-Independent DNA Damage Response |
39 |
1.70e-02 |
1.07e-01 |
0.2600 |
2.30e-01 |
-0.121000 |
1.31e-02 |
1.91e-01 |
p53-Independent G1/S DNA damage checkpoint |
39 |
1.70e-02 |
1.07e-01 |
0.2600 |
2.30e-01 |
-0.121000 |
1.31e-02 |
1.91e-01 |
Ubiquitin-dependent degradation of Cyclin D |
40 |
1.53e-02 |
1.01e-01 |
0.2600 |
2.30e-01 |
-0.120000 |
1.18e-02 |
1.90e-01 |
RET signaling |
33 |
3.77e-02 |
1.83e-01 |
0.2600 |
-2.55e-01 |
-0.051000 |
1.14e-02 |
6.12e-01 |
APC:Cdc20 mediated degradation of cell cycle proteins prior to satisfation of the cell cycle checkpoint |
59 |
2.30e-03 |
2.37e-02 |
0.2590 |
2.44e-01 |
-0.086100 |
1.19e-03 |
2.53e-01 |
Biological oxidations |
129 |
2.28e-06 |
8.36e-05 |
0.2590 |
2.57e-01 |
-0.032800 |
5.03e-07 |
5.21e-01 |
Major pathway of rRNA processing in the nucleolus and cytosol |
110 |
1.18e-05 |
3.22e-04 |
0.2590 |
2.25e-01 |
-0.127000 |
4.59e-05 |
2.20e-02 |
TP53 Regulates Transcription of Death Receptors and Ligands |
11 |
3.48e-01 |
6.69e-01 |
0.2580 |
-1.94e-01 |
-0.170000 |
2.64e-01 |
3.29e-01 |
RNA Polymerase III Transcription Initiation From Type 2 Promoter |
19 |
1.46e-01 |
4.23e-01 |
0.2570 |
6.92e-02 |
-0.247000 |
6.02e-01 |
6.19e-02 |
Regulation of ornithine decarboxylase (ODC) |
42 |
1.36e-02 |
9.26e-02 |
0.2560 |
2.14e-01 |
-0.142000 |
1.67e-02 |
1.12e-01 |
Antigen activates B Cell Receptor (BCR) leading to generation of second messengers |
30 |
4.97e-02 |
2.11e-01 |
0.2560 |
2.51e-01 |
-0.050900 |
1.73e-02 |
6.30e-01 |
rRNA processing |
124 |
3.74e-06 |
1.24e-04 |
0.2560 |
2.22e-01 |
-0.127000 |
2.12e-05 |
1.45e-02 |
Glyoxylate metabolism and glycine degradation |
21 |
1.28e-01 |
3.87e-01 |
0.2550 |
6.34e-03 |
-0.255000 |
9.60e-01 |
4.31e-02 |
Cell-cell junction organization |
26 |
7.87e-02 |
2.86e-01 |
0.2550 |
-1.38e-02 |
0.254000 |
9.03e-01 |
2.48e-02 |
FOXO-mediated transcription of cell death genes |
13 |
2.85e-01 |
5.98e-01 |
0.2540 |
9.49e-03 |
0.254000 |
9.53e-01 |
1.13e-01 |
APC/C-mediated degradation of cell cycle proteins |
72 |
8.96e-04 |
1.17e-02 |
0.2530 |
2.46e-01 |
-0.058100 |
3.07e-04 |
3.95e-01 |
Regulation of mitotic cell cycle |
72 |
8.96e-04 |
1.17e-02 |
0.2530 |
2.46e-01 |
-0.058100 |
3.07e-04 |
3.95e-01 |
Cellular hexose transport |
12 |
3.31e-01 |
6.53e-01 |
0.2530 |
-1.97e-01 |
-0.159000 |
2.38e-01 |
3.40e-01 |
Cdc20:Phospho-APC/C mediated degradation of Cyclin A |
58 |
3.49e-03 |
3.32e-02 |
0.2520 |
2.34e-01 |
-0.093100 |
2.08e-03 |
2.20e-01 |
Laminin interactions |
22 |
1.35e-01 |
3.98e-01 |
0.2510 |
-2.10e-01 |
-0.138000 |
8.78e-02 |
2.64e-01 |
Oxygen-dependent proline hydroxylation of Hypoxia-inducible Factor Alpha |
49 |
8.21e-03 |
6.45e-02 |
0.2510 |
2.00e-01 |
-0.151000 |
1.54e-02 |
6.76e-02 |
RNA Polymerase III Transcription Initiation From Type 3 Promoter |
23 |
1.13e-01 |
3.57e-01 |
0.2510 |
9.95e-03 |
-0.251000 |
9.34e-01 |
3.76e-02 |
Antigen processing-Cross presentation |
75 |
8.46e-04 |
1.13e-02 |
0.2510 |
2.50e-01 |
-0.013600 |
1.81e-04 |
8.39e-01 |
CD209 (DC-SIGN) signaling |
19 |
1.67e-01 |
4.49e-01 |
0.2500 |
-2.40e-02 |
0.249000 |
8.57e-01 |
6.08e-02 |
Dual incision in TC-NER |
50 |
8.11e-03 |
6.44e-02 |
0.2490 |
2.21e-01 |
-0.116000 |
6.95e-03 |
1.57e-01 |
Base-Excision Repair, AP Site Formation |
15 |
2.39e-01 |
5.45e-01 |
0.2490 |
6.89e-02 |
-0.239000 |
6.44e-01 |
1.08e-01 |
RNA Polymerase III Transcription Initiation From Type 1 Promoter |
20 |
1.46e-01 |
4.23e-01 |
0.2490 |
1.07e-01 |
-0.225000 |
4.09e-01 |
8.14e-02 |
SEMA3A-Plexin repulsion signaling by inhibiting Integrin adhesion |
13 |
2.85e-01 |
5.98e-01 |
0.2480 |
-1.63e-01 |
0.188000 |
3.09e-01 |
2.42e-01 |
Interferon Signaling |
128 |
7.37e-06 |
2.21e-04 |
0.2480 |
2.48e-01 |
-0.018900 |
1.38e-06 |
7.12e-01 |
Activation of gene expression by SREBF (SREBP) |
39 |
3.18e-02 |
1.63e-01 |
0.2480 |
-2.04e-01 |
-0.141000 |
2.79e-02 |
1.27e-01 |
Resolution of D-loop Structures through Holliday Junction Intermediates |
26 |
1.00e-01 |
3.37e-01 |
0.2480 |
2.10e-01 |
0.131000 |
6.35e-02 |
2.48e-01 |
RHO GTPases Activate NADPH Oxidases |
18 |
1.78e-01 |
4.63e-01 |
0.2480 |
1.93e-01 |
-0.155000 |
1.56e-01 |
2.55e-01 |
HS-GAG biosynthesis |
21 |
1.35e-01 |
3.98e-01 |
0.2480 |
-1.26e-01 |
0.213000 |
3.17e-01 |
9.12e-02 |
Regulation of mRNA stability by proteins that bind AU-rich elements |
69 |
1.43e-03 |
1.65e-02 |
0.2470 |
1.37e-01 |
-0.206000 |
4.87e-02 |
3.18e-03 |
SCF-beta-TrCP mediated degradation of Emi1 |
43 |
1.73e-02 |
1.09e-01 |
0.2470 |
2.28e-01 |
-0.094800 |
9.62e-03 |
2.82e-01 |
Complement cascade |
35 |
3.59e-02 |
1.75e-01 |
0.2470 |
1.87e-01 |
-0.161000 |
5.61e-02 |
9.88e-02 |
Disassembly of the destruction complex and recruitment of AXIN to the membrane |
26 |
9.33e-02 |
3.24e-01 |
0.2470 |
-2.47e-01 |
0.000267 |
2.95e-02 |
9.98e-01 |
Resolution of D-Loop Structures |
27 |
9.40e-02 |
3.26e-01 |
0.2470 |
2.02e-01 |
0.141000 |
6.90e-02 |
2.05e-01 |
STING mediated induction of host immune responses |
12 |
3.32e-01 |
6.53e-01 |
0.2460 |
2.43e-01 |
-0.036400 |
1.45e-01 |
8.27e-01 |
TRAF6 mediated IRF7 activation |
15 |
2.71e-01 |
5.89e-01 |
0.2460 |
1.95e-01 |
0.150000 |
1.92e-01 |
3.15e-01 |
WNT5A-dependent internalization of FZD4 |
14 |
2.96e-01 |
6.10e-01 |
0.2460 |
-2.03e-01 |
-0.139000 |
1.90e-01 |
3.67e-01 |
Plasma lipoprotein remodeling |
14 |
2.95e-01 |
6.09e-01 |
0.2460 |
-2.13e-01 |
-0.122000 |
1.67e-01 |
4.29e-01 |
Metabolism of amino acids and derivatives |
225 |
8.87e-10 |
1.01e-07 |
0.2460 |
1.96e-01 |
-0.148000 |
4.50e-07 |
1.41e-04 |
Synthesis of bile acids and bile salts via 7alpha-hydroxycholesterol |
14 |
2.93e-01 |
6.07e-01 |
0.2450 |
2.27e-01 |
0.094100 |
1.42e-01 |
5.42e-01 |
Sulfur amino acid metabolism |
19 |
1.69e-01 |
4.53e-01 |
0.2450 |
1.29e-01 |
-0.208000 |
3.30e-01 |
1.16e-01 |
Homologous DNA Pairing and Strand Exchange |
35 |
4.19e-02 |
1.94e-01 |
0.2440 |
2.38e-01 |
-0.052300 |
1.48e-02 |
5.93e-01 |
CDK-mediated phosphorylation and removal of Cdc6 |
58 |
4.78e-03 |
4.35e-02 |
0.2440 |
2.12e-01 |
-0.120000 |
5.25e-03 |
1.14e-01 |
NGF-stimulated transcription |
33 |
4.70e-02 |
2.03e-01 |
0.2440 |
-1.69e-01 |
0.175000 |
9.27e-02 |
8.17e-02 |
MET activates PTK2 signaling |
17 |
2.34e-01 |
5.41e-01 |
0.2440 |
-1.95e-01 |
-0.146000 |
1.65e-01 |
2.97e-01 |
Separation of Sister Chromatids |
134 |
6.14e-06 |
1.93e-04 |
0.2430 |
2.38e-01 |
-0.049700 |
2.02e-06 |
3.22e-01 |
YAP1- and WWTR1 (TAZ)-stimulated gene expression |
14 |
2.75e-01 |
5.91e-01 |
0.2430 |
-1.51e-01 |
0.190000 |
3.27e-01 |
2.18e-01 |
Sealing of the nuclear envelope (NE) by ESCRT-III |
22 |
1.55e-01 |
4.28e-01 |
0.2430 |
-1.85e-01 |
-0.157000 |
1.33e-01 |
2.03e-01 |
Regulation of Apoptosis |
40 |
2.61e-02 |
1.45e-01 |
0.2420 |
2.08e-01 |
-0.124000 |
2.30e-02 |
1.75e-01 |
p53-Dependent G1 DNA Damage Response |
51 |
9.88e-03 |
7.35e-02 |
0.2420 |
2.14e-01 |
-0.113000 |
8.30e-03 |
1.64e-01 |
p53-Dependent G1/S DNA damage checkpoint |
51 |
9.88e-03 |
7.35e-02 |
0.2420 |
2.14e-01 |
-0.113000 |
8.30e-03 |
1.64e-01 |
Glutathione conjugation |
28 |
7.83e-02 |
2.85e-01 |
0.2410 |
1.90e-01 |
-0.149000 |
8.15e-02 |
1.74e-01 |
Initiation of Nuclear Envelope (NE) Reformation |
17 |
2.17e-01 |
5.12e-01 |
0.2410 |
2.27e-01 |
-0.083300 |
1.06e-01 |
5.52e-01 |
TAK1 activates NFkB by phosphorylation and activation of IKKs complex |
22 |
1.49e-01 |
4.25e-01 |
0.2410 |
-2.40e-01 |
-0.023900 |
5.14e-02 |
8.46e-01 |
CD28 co-stimulation |
31 |
7.36e-02 |
2.74e-01 |
0.2410 |
2.22e-01 |
0.093400 |
3.27e-02 |
3.68e-01 |
Non-integrin membrane-ECM interactions |
37 |
4.68e-02 |
2.03e-01 |
0.2400 |
-1.61e-01 |
-0.178000 |
8.95e-02 |
6.13e-02 |
Signaling by WNT in cancer |
25 |
1.16e-01 |
3.60e-01 |
0.2400 |
-2.40e-01 |
0.003800 |
3.81e-02 |
9.74e-01 |
APC/C:Cdc20 mediated degradation of Securin |
54 |
8.02e-03 |
6.44e-02 |
0.2400 |
1.98e-01 |
-0.135000 |
1.19e-02 |
8.67e-02 |
Nucleobase biosynthesis |
13 |
3.38e-01 |
6.59e-01 |
0.2390 |
-7.38e-02 |
-0.227000 |
6.45e-01 |
1.56e-01 |
SUMOylation of DNA replication proteins |
34 |
5.59e-02 |
2.27e-01 |
0.2390 |
2.38e-01 |
0.022600 |
1.65e-02 |
8.20e-01 |
Golgi Cisternae Pericentriolar Stack Reorganization |
12 |
3.48e-01 |
6.69e-01 |
0.2390 |
2.24e-01 |
-0.082400 |
1.79e-01 |
6.21e-01 |
GRB2:SOS provides linkage to MAPK signaling for Integrins |
12 |
3.50e-01 |
6.70e-01 |
0.2380 |
7.82e-02 |
-0.225000 |
6.39e-01 |
1.77e-01 |
Degradation of DVL |
44 |
2.10e-02 |
1.26e-01 |
0.2370 |
1.81e-01 |
-0.153000 |
3.79e-02 |
7.87e-02 |
RHO GTPases Activate WASPs and WAVEs |
34 |
6.38e-02 |
2.48e-01 |
0.2370 |
2.09e-01 |
0.111000 |
3.51e-02 |
2.62e-01 |
Hh mutants that don't undergo autocatalytic processing are degraded by ERAD |
41 |
2.89e-02 |
1.53e-01 |
0.2360 |
1.92e-01 |
-0.136000 |
3.36e-02 |
1.31e-01 |
Hh mutants abrogate ligand secretion |
43 |
2.43e-02 |
1.38e-01 |
0.2360 |
1.82e-01 |
-0.149000 |
3.87e-02 |
9.12e-02 |
Olfactory Signaling Pathway |
13 |
3.52e-01 |
6.72e-01 |
0.2360 |
-2.06e-01 |
-0.113000 |
1.97e-01 |
4.80e-01 |
Activation of BAD and translocation to mitochondria |
14 |
3.05e-01 |
6.21e-01 |
0.2350 |
2.27e-01 |
-0.063400 |
1.42e-01 |
6.81e-01 |
Resolution of Abasic Sites (AP sites) |
31 |
7.55e-02 |
2.79e-01 |
0.2330 |
2.25e-01 |
-0.062800 |
3.05e-02 |
5.45e-01 |
Autodegradation of the E3 ubiquitin ligase COP1 |
40 |
3.41e-02 |
1.70e-01 |
0.2330 |
2.00e-01 |
-0.119000 |
2.85e-02 |
1.91e-01 |
Class B/2 (Secretin family receptors) |
40 |
4.43e-02 |
1.99e-01 |
0.2330 |
-1.95e-01 |
-0.127000 |
3.33e-02 |
1.63e-01 |
Glutamate binding, activation of AMPA receptors and synaptic plasticity |
25 |
1.32e-01 |
3.92e-01 |
0.2320 |
-2.32e-01 |
0.010500 |
4.50e-02 |
9.28e-01 |
Trafficking of AMPA receptors |
25 |
1.32e-01 |
3.92e-01 |
0.2320 |
-2.32e-01 |
0.010500 |
4.50e-02 |
9.28e-01 |
NF-kB activation through FADD/RIP-1 pathway mediated by caspase-8 and -10 |
11 |
4.27e-01 |
7.31e-01 |
0.2310 |
1.07e-01 |
0.205000 |
5.38e-01 |
2.40e-01 |
Meiosis |
43 |
2.89e-02 |
1.53e-01 |
0.2310 |
2.09e-01 |
-0.098800 |
1.80e-02 |
2.63e-01 |
Negative regulation of NMDA receptor-mediated neuronal transmission |
15 |
3.10e-01 |
6.27e-01 |
0.2310 |
-2.23e-01 |
-0.060900 |
1.36e-01 |
6.83e-01 |
G1/S DNA Damage Checkpoints |
53 |
1.30e-02 |
8.97e-02 |
0.2310 |
2.11e-01 |
-0.091900 |
7.81e-03 |
2.48e-01 |
Generation of second messenger molecules |
20 |
1.95e-01 |
4.86e-01 |
0.2300 |
2.17e-01 |
-0.078000 |
9.32e-02 |
5.46e-01 |
Scavenging by Class A Receptors |
13 |
3.41e-01 |
6.61e-01 |
0.2300 |
-1.87e-01 |
0.134000 |
2.42e-01 |
4.04e-01 |
Diseases of glycosylation |
105 |
1.81e-04 |
3.20e-03 |
0.2300 |
-1.63e-01 |
0.162000 |
4.06e-03 |
4.09e-03 |
Platelet calcium homeostasis |
20 |
2.00e-01 |
4.92e-01 |
0.2290 |
-2.23e-01 |
0.055000 |
8.48e-02 |
6.70e-01 |
Prolactin receptor signaling |
11 |
4.06e-01 |
7.16e-01 |
0.2290 |
-1.21e-01 |
0.195000 |
4.87e-01 |
2.63e-01 |
Defective CFTR causes cystic fibrosis |
43 |
3.09e-02 |
1.59e-01 |
0.2290 |
2.14e-01 |
-0.083000 |
1.55e-02 |
3.47e-01 |
ER-Phagosome pathway |
61 |
8.52e-03 |
6.62e-02 |
0.2290 |
2.29e-01 |
0.004710 |
2.03e-03 |
9.49e-01 |
Signaling by PDGF |
46 |
2.35e-02 |
1.36e-01 |
0.2290 |
-1.68e-01 |
0.156000 |
4.95e-02 |
6.83e-02 |
SMAD2/SMAD3:SMAD4 heterotrimer regulates transcription |
24 |
1.65e-01 |
4.46e-01 |
0.2280 |
1.24e-01 |
0.191000 |
2.92e-01 |
1.05e-01 |
Butyrate Response Factor 1 (BRF1) binds and destabilizes mRNA |
13 |
3.51e-01 |
6.70e-01 |
0.2280 |
1.11e-01 |
-0.199000 |
4.88e-01 |
2.15e-01 |
Telomere Extension By Telomerase |
17 |
2.61e-01 |
5.73e-01 |
0.2270 |
2.23e-01 |
-0.047000 |
1.12e-01 |
7.37e-01 |
Signaling by ERBB2 TMD/JMD mutants |
19 |
2.24e-01 |
5.23e-01 |
0.2270 |
-2.24e-01 |
0.041500 |
9.17e-02 |
7.54e-01 |
Transcriptional regulation by the AP-2 (TFAP2) family of transcription factors |
25 |
1.36e-01 |
3.98e-01 |
0.2270 |
-1.00e-01 |
0.204000 |
3.85e-01 |
7.80e-02 |
Transcriptional regulation of pluripotent stem cells |
14 |
3.46e-01 |
6.68e-01 |
0.2260 |
3.68e-02 |
0.223000 |
8.12e-01 |
1.48e-01 |
Activation of SMO |
13 |
3.56e-01 |
6.77e-01 |
0.2260 |
-1.94e-01 |
0.116000 |
2.26e-01 |
4.68e-01 |
Transcription-Coupled Nucleotide Excision Repair (TC-NER) |
61 |
8.13e-03 |
6.44e-02 |
0.2260 |
1.97e-01 |
-0.111000 |
7.97e-03 |
1.35e-01 |
Autodegradation of Cdh1 by Cdh1:APC/C |
50 |
1.90e-02 |
1.16e-01 |
0.2250 |
1.61e-01 |
-0.158000 |
4.90e-02 |
5.39e-02 |
Cell death signalling via NRAGE, NRIF and NADE |
62 |
7.72e-03 |
6.31e-02 |
0.2250 |
-1.94e-01 |
0.113000 |
8.23e-03 |
1.23e-01 |
APC/C:Cdc20 mediated degradation of Cyclin B |
18 |
2.50e-01 |
5.58e-01 |
0.2250 |
2.19e-01 |
-0.049100 |
1.08e-01 |
7.18e-01 |
Aquaporin-mediated transport |
33 |
8.73e-02 |
3.07e-01 |
0.2240 |
-2.17e-01 |
-0.056600 |
3.10e-02 |
5.74e-01 |
Caspase activation via extrinsic apoptotic signalling pathway |
22 |
1.78e-01 |
4.63e-01 |
0.2240 |
-1.78e-01 |
0.136000 |
1.49e-01 |
2.69e-01 |
Degradation of GLI1 by the proteasome |
47 |
2.58e-02 |
1.45e-01 |
0.2240 |
1.86e-01 |
-0.124000 |
2.73e-02 |
1.42e-01 |
Reproduction |
52 |
1.75e-02 |
1.09e-01 |
0.2240 |
1.85e-01 |
-0.126000 |
2.13e-02 |
1.17e-01 |
Formation of the beta-catenin:TCF transactivating complex |
29 |
1.05e-01 |
3.46e-01 |
0.2240 |
-1.93e-01 |
0.113000 |
7.20e-02 |
2.95e-01 |
DAP12 signaling |
24 |
1.57e-01 |
4.31e-01 |
0.2230 |
2.00e-01 |
-0.098100 |
8.95e-02 |
4.06e-01 |
Competing endogenous RNAs (ceRNAs) regulate PTEN translation |
10 |
4.78e-01 |
7.66e-01 |
0.2230 |
-2.21e-01 |
-0.026100 |
2.26e-01 |
8.86e-01 |
Netrin-1 signaling |
42 |
4.34e-02 |
1.98e-01 |
0.2230 |
-1.62e-02 |
0.222000 |
8.56e-01 |
1.28e-02 |
Peroxisomal lipid metabolism |
24 |
1.57e-01 |
4.31e-01 |
0.2230 |
1.84e-01 |
-0.126000 |
1.19e-01 |
2.87e-01 |
Trafficking and processing of endosomal TLR |
11 |
4.37e-01 |
7.37e-01 |
0.2230 |
2.20e-01 |
-0.032000 |
2.06e-01 |
8.54e-01 |
Adrenaline,noradrenaline inhibits insulin secretion |
18 |
2.72e-01 |
5.89e-01 |
0.2230 |
-7.63e-02 |
-0.209000 |
5.75e-01 |
1.25e-01 |
MECP2 regulates neuronal receptors and channels |
11 |
4.59e-01 |
7.52e-01 |
0.2220 |
1.51e-01 |
0.162000 |
3.85e-01 |
3.52e-01 |
Ion homeostasis |
41 |
4.50e-02 |
2.01e-01 |
0.2210 |
-1.98e-01 |
0.099000 |
2.87e-02 |
2.73e-01 |
Voltage gated Potassium channels |
24 |
1.61e-01 |
4.38e-01 |
0.2210 |
-1.69e-01 |
0.142000 |
1.52e-01 |
2.29e-01 |
Sema4D in semaphorin signaling |
22 |
2.10e-01 |
5.03e-01 |
0.2210 |
-2.05e-01 |
-0.082300 |
9.65e-02 |
5.04e-01 |
BMAL1:CLOCK,NPAS2 activates circadian gene expression |
22 |
1.88e-01 |
4.76e-01 |
0.2210 |
1.49e-01 |
-0.163000 |
2.28e-01 |
1.86e-01 |
Signaling by NOTCH2 |
21 |
2.05e-01 |
4.99e-01 |
0.2200 |
-1.13e-01 |
0.189000 |
3.71e-01 |
1.33e-01 |
AUF1 (hnRNP D0) binds and destabilizes mRNA |
42 |
4.26e-02 |
1.96e-01 |
0.2190 |
1.63e-01 |
-0.147000 |
6.84e-02 |
9.88e-02 |
Deadenylation of mRNA |
20 |
2.50e-01 |
5.58e-01 |
0.2190 |
1.83e-01 |
0.121000 |
1.57e-01 |
3.50e-01 |
NIK-->noncanonical NF-kB signaling |
45 |
3.48e-02 |
1.71e-01 |
0.2190 |
1.82e-01 |
-0.122000 |
3.53e-02 |
1.56e-01 |
Signaling by NOTCH3 |
39 |
5.51e-02 |
2.25e-01 |
0.2180 |
-1.43e-01 |
0.165000 |
1.22e-01 |
7.53e-02 |
Processing of Capped Intronless Pre-mRNA |
19 |
2.75e-01 |
5.91e-01 |
0.2170 |
1.71e-01 |
0.134000 |
1.97e-01 |
3.12e-01 |
AKT phosphorylates targets in the cytosol |
13 |
3.93e-01 |
7.09e-01 |
0.2170 |
4.52e-02 |
-0.212000 |
7.78e-01 |
1.85e-01 |
Thromboxane signalling through TP receptor |
15 |
3.60e-01 |
6.79e-01 |
0.2160 |
-2.01e-01 |
-0.079700 |
1.78e-01 |
5.93e-01 |
SHC1 events in EGFR signaling |
11 |
4.78e-01 |
7.66e-01 |
0.2160 |
-1.34e-01 |
-0.170000 |
4.43e-01 |
3.30e-01 |
Uptake and actions of bacterial toxins |
24 |
1.80e-01 |
4.66e-01 |
0.2160 |
-2.08e-01 |
0.058800 |
7.84e-02 |
6.18e-01 |
APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins in late mitosis/early G1 |
59 |
1.45e-02 |
9.63e-02 |
0.2160 |
1.96e-01 |
-0.090400 |
9.36e-03 |
2.30e-01 |
Nitric oxide stimulates guanylate cyclase |
19 |
2.58e-01 |
5.68e-01 |
0.2160 |
-2.08e-01 |
0.056500 |
1.17e-01 |
6.70e-01 |
Nicotinate metabolism |
22 |
2.04e-01 |
4.99e-01 |
0.2150 |
1.14e-01 |
-0.183000 |
3.53e-01 |
1.38e-01 |
FRS-mediated FGFR4 signaling |
12 |
4.37e-01 |
7.37e-01 |
0.2150 |
-1.53e-02 |
-0.215000 |
9.27e-01 |
1.98e-01 |
Presynaptic depolarization and calcium channel opening |
11 |
4.64e-01 |
7.54e-01 |
0.2150 |
-2.13e-01 |
0.026200 |
2.21e-01 |
8.81e-01 |
Purine catabolism |
16 |
3.21e-01 |
6.41e-01 |
0.2140 |
9.63e-02 |
-0.191000 |
5.05e-01 |
1.86e-01 |
Pyruvate metabolism and Citric Acid (TCA) cycle |
42 |
5.15e-02 |
2.16e-01 |
0.2140 |
9.48e-02 |
-0.191000 |
2.88e-01 |
3.19e-02 |
Response of EIF2AK1 (HRI) to heme deficiency |
11 |
4.61e-01 |
7.52e-01 |
0.2130 |
-7.46e-02 |
0.200000 |
6.68e-01 |
2.51e-01 |
Phosphorylation of the APC/C |
17 |
3.04e-01 |
6.19e-01 |
0.2130 |
1.91e-01 |
-0.092700 |
1.72e-01 |
5.08e-01 |
Glycogen breakdown (glycogenolysis) |
14 |
3.75e-01 |
6.90e-01 |
0.2120 |
-1.24e-01 |
0.172000 |
4.22e-01 |
2.66e-01 |
rRNA modification in the nucleus and cytosol |
46 |
4.19e-02 |
1.94e-01 |
0.2120 |
7.97e-02 |
-0.196000 |
3.50e-01 |
2.16e-02 |
DNA Double-Strand Break Repair |
105 |
9.27e-04 |
1.18e-02 |
0.2110 |
2.11e-01 |
0.002030 |
1.88e-04 |
9.71e-01 |
activated TAK1 mediates p38 MAPK activation |
17 |
3.38e-01 |
6.59e-01 |
0.2110 |
-1.62e-01 |
-0.135000 |
2.47e-01 |
3.37e-01 |
Antimicrobial peptides |
12 |
4.57e-01 |
7.52e-01 |
0.2090 |
2.08e-01 |
0.022600 |
2.12e-01 |
8.92e-01 |
Keratan sulfate/keratin metabolism |
24 |
1.94e-01 |
4.86e-01 |
0.2090 |
-1.70e-01 |
0.122000 |
1.49e-01 |
3.03e-01 |
Synthesis of PA |
23 |
2.23e-01 |
5.21e-01 |
0.2090 |
-2.09e-01 |
-0.004730 |
8.30e-02 |
9.69e-01 |
GLI3 is processed to GLI3R by the proteasome |
46 |
4.51e-02 |
2.01e-01 |
0.2080 |
1.79e-01 |
-0.107000 |
3.62e-02 |
2.10e-01 |
Regulation of RUNX3 expression and activity |
42 |
6.02e-02 |
2.41e-01 |
0.2070 |
1.75e-01 |
-0.112000 |
5.01e-02 |
2.11e-01 |
G alpha (12/13) signalling events |
65 |
1.43e-02 |
9.60e-02 |
0.2070 |
-2.02e-01 |
0.044500 |
4.80e-03 |
5.35e-01 |
Resolution of D-loop Structures through Synthesis-Dependent Strand Annealing (SDSA) |
23 |
2.38e-01 |
5.45e-01 |
0.2070 |
1.92e-01 |
0.077700 |
1.11e-01 |
5.19e-01 |
Degradation of GLI2 by the proteasome |
46 |
4.66e-02 |
2.03e-01 |
0.2070 |
1.63e-01 |
-0.127000 |
5.61e-02 |
1.36e-01 |
Mitochondrial tRNA aminoacylation |
15 |
3.98e-01 |
7.14e-01 |
0.2070 |
-1.29e-01 |
-0.161000 |
3.88e-01 |
2.79e-01 |
Cell-extracellular matrix interactions |
14 |
4.05e-01 |
7.15e-01 |
0.2060 |
-2.05e-01 |
0.026100 |
1.85e-01 |
8.66e-01 |
Amplification of signal from unattached kinetochores via a MAD2 inhibitory signal |
71 |
1.10e-02 |
7.94e-02 |
0.2060 |
2.06e-01 |
0.003710 |
2.69e-03 |
9.57e-01 |
Amplification of signal from the kinetochores |
71 |
1.10e-02 |
7.94e-02 |
0.2060 |
2.06e-01 |
0.003710 |
2.69e-03 |
9.57e-01 |
Costimulation by the CD28 family |
52 |
3.77e-02 |
1.83e-01 |
0.2060 |
2.05e-01 |
0.022900 |
1.06e-02 |
7.75e-01 |
IRF3-mediated induction of type I IFN |
10 |
5.23e-01 |
7.87e-01 |
0.2060 |
2.03e-01 |
-0.038600 |
2.67e-01 |
8.33e-01 |
IKK complex recruitment mediated by RIP1 |
15 |
3.74e-01 |
6.89e-01 |
0.2060 |
-7.42e-02 |
0.192000 |
6.19e-01 |
1.97e-01 |
Defective B3GALT6 causes EDSP2 and SEMDJL1 |
15 |
3.71e-01 |
6.89e-01 |
0.2060 |
-1.23e-01 |
0.165000 |
4.10e-01 |
2.69e-01 |
PKA activation in glucagon signalling |
16 |
3.58e-01 |
6.78e-01 |
0.2050 |
-2.02e-01 |
0.036100 |
1.62e-01 |
8.02e-01 |
O-linked glycosylation |
65 |
1.41e-02 |
9.55e-02 |
0.2050 |
-1.20e-01 |
0.167000 |
9.57e-02 |
2.01e-02 |
RUNX1 regulates transcription of genes involved in differentiation of HSCs |
56 |
2.56e-02 |
1.45e-01 |
0.2050 |
1.75e-01 |
-0.108000 |
2.39e-02 |
1.63e-01 |
VxPx cargo-targeting to cilium |
17 |
3.40e-01 |
6.61e-01 |
0.2050 |
-2.08e-02 |
0.204000 |
8.82e-01 |
1.46e-01 |
Regulation of glycolysis by fructose 2,6-bisphosphate metabolism |
11 |
5.04e-01 |
7.82e-01 |
0.2050 |
-1.91e-02 |
-0.204000 |
9.13e-01 |
2.42e-01 |
Regulation of RAS by GAPs |
54 |
3.22e-02 |
1.64e-01 |
0.2050 |
2.00e-01 |
-0.042900 |
1.11e-02 |
5.86e-01 |
Glycosphingolipid metabolism |
31 |
1.55e-01 |
4.28e-01 |
0.2040 |
-1.77e-01 |
-0.103000 |
8.90e-02 |
3.23e-01 |
Regulation of TP53 Activity through Methylation |
11 |
4.90e-01 |
7.71e-01 |
0.2040 |
-1.04e-01 |
0.175000 |
5.49e-01 |
3.14e-01 |
Uptake and function of anthrax toxins |
11 |
4.89e-01 |
7.71e-01 |
0.2040 |
-1.56e-01 |
0.131000 |
3.70e-01 |
4.52e-01 |
PRC2 methylates histones and DNA |
12 |
4.61e-01 |
7.52e-01 |
0.2040 |
1.84e-01 |
-0.088600 |
2.71e-01 |
5.95e-01 |
Abortive elongation of HIV-1 transcript in the absence of Tat |
16 |
3.83e-01 |
7.00e-01 |
0.2040 |
-1.04e-01 |
-0.175000 |
4.71e-01 |
2.26e-01 |
Citric acid cycle (TCA cycle) |
18 |
3.21e-01 |
6.41e-01 |
0.2040 |
1.99e-01 |
-0.042100 |
1.44e-01 |
7.57e-01 |
p75 NTR receptor-mediated signalling |
75 |
8.69e-03 |
6.67e-02 |
0.2020 |
-1.53e-01 |
0.131000 |
2.19e-02 |
5.01e-02 |
Downstream TCR signaling |
69 |
1.36e-02 |
9.26e-02 |
0.2010 |
1.88e-01 |
-0.073000 |
7.13e-03 |
2.95e-01 |
Inflammasomes |
18 |
3.21e-01 |
6.41e-01 |
0.2010 |
-1.13e-01 |
0.167000 |
4.08e-01 |
2.21e-01 |
GAB1 signalosome |
14 |
4.23e-01 |
7.31e-01 |
0.2010 |
-1.99e-01 |
0.026400 |
1.97e-01 |
8.64e-01 |
Acyl chain remodelling of PG |
10 |
5.39e-01 |
8.02e-01 |
0.2010 |
-1.94e-01 |
0.052100 |
2.89e-01 |
7.76e-01 |
PI3K events in ERBB2 signaling |
14 |
4.15e-01 |
7.24e-01 |
0.2010 |
-1.52e-01 |
0.130000 |
3.24e-01 |
3.98e-01 |
Cell Cycle, Mitotic |
402 |
6.79e-11 |
1.42e-08 |
0.2000 |
2.00e-01 |
-0.007260 |
8.98e-12 |
8.04e-01 |
Mitotic Metaphase and Anaphase |
182 |
1.58e-05 |
4.23e-04 |
0.2000 |
1.87e-01 |
-0.071000 |
1.49e-05 |
9.98e-02 |
Metabolism of folate and pterines |
14 |
4.35e-01 |
7.37e-01 |
0.2000 |
-1.99e-01 |
-0.014000 |
1.97e-01 |
9.28e-01 |
Regulation of TP53 Degradation |
29 |
1.75e-01 |
4.63e-01 |
0.2000 |
1.99e-01 |
-0.013100 |
6.36e-02 |
9.03e-01 |
Signaling by ROBO receptors |
133 |
3.82e-04 |
5.85e-03 |
0.1990 |
1.99e-01 |
-0.002410 |
7.44e-05 |
9.62e-01 |
TP53 Regulates Transcription of Genes Involved in G2 Cell Cycle Arrest |
16 |
4.03e-01 |
7.15e-01 |
0.1990 |
1.51e-01 |
0.129000 |
2.95e-01 |
3.72e-01 |
Peroxisomal protein import |
48 |
5.18e-02 |
2.16e-01 |
0.1990 |
1.40e-01 |
-0.141000 |
9.33e-02 |
9.13e-02 |
Chemokine receptors bind chemokines |
27 |
2.09e-01 |
5.03e-01 |
0.1990 |
1.92e-01 |
0.051000 |
8.41e-02 |
6.47e-01 |
Meiotic recombination |
21 |
2.74e-01 |
5.90e-01 |
0.1990 |
1.49e-01 |
-0.131000 |
2.36e-01 |
2.99e-01 |
Ca2+ pathway |
49 |
5.87e-02 |
2.38e-01 |
0.1990 |
-1.93e-01 |
-0.047800 |
1.97e-02 |
5.63e-01 |
Mitotic Anaphase |
181 |
1.91e-05 |
5.01e-04 |
0.1980 |
1.83e-01 |
-0.075500 |
2.20e-05 |
8.07e-02 |
NCAM signaling for neurite out-growth |
47 |
6.47e-02 |
2.51e-01 |
0.1980 |
-1.97e-01 |
-0.027200 |
1.99e-02 |
7.47e-01 |
Cell Cycle |
496 |
5.99e-13 |
4.79e-10 |
0.1980 |
1.98e-01 |
-0.000211 |
6.61e-14 |
9.94e-01 |
DAP12 interactions |
27 |
1.92e-01 |
4.82e-01 |
0.1980 |
1.66e-01 |
-0.108000 |
1.36e-01 |
3.30e-01 |
CS/DS degradation |
11 |
5.13e-01 |
7.84e-01 |
0.1980 |
-1.83e-01 |
0.076600 |
2.94e-01 |
6.60e-01 |
HDR through Single Strand Annealing (SSA) |
31 |
1.57e-01 |
4.31e-01 |
0.1980 |
1.94e-01 |
-0.038900 |
6.16e-02 |
7.08e-01 |
TCR signaling |
89 |
5.05e-03 |
4.47e-02 |
0.1980 |
1.93e-01 |
-0.042500 |
1.66e-03 |
4.89e-01 |
RAS processing |
17 |
3.56e-01 |
6.77e-01 |
0.1970 |
1.40e-01 |
-0.138000 |
3.17e-01 |
3.23e-01 |
Synthesis of very long-chain fatty acyl-CoAs |
14 |
4.43e-01 |
7.40e-01 |
0.1970 |
4.89e-04 |
0.197000 |
9.97e-01 |
2.02e-01 |
Dectin-1 mediated noncanonical NF-kB signaling |
46 |
6.24e-02 |
2.46e-01 |
0.1970 |
1.62e-01 |
-0.111000 |
5.69e-02 |
1.92e-01 |
Global Genome Nucleotide Excision Repair (GG-NER) |
68 |
1.69e-02 |
1.07e-01 |
0.1970 |
1.71e-01 |
-0.097300 |
1.48e-02 |
1.66e-01 |
Negative regulators of DDX58/IFIH1 signaling |
24 |
2.36e-01 |
5.44e-01 |
0.1960 |
1.33e-01 |
-0.144000 |
2.59e-01 |
2.22e-01 |
RUNX2 regulates bone development |
27 |
2.02e-01 |
4.96e-01 |
0.1960 |
-7.89e-02 |
0.179000 |
4.78e-01 |
1.07e-01 |
APC-Cdc20 mediated degradation of Nek2A |
20 |
3.15e-01 |
6.32e-01 |
0.1960 |
1.95e-01 |
-0.013000 |
1.31e-01 |
9.20e-01 |
Antiviral mechanism by IFN-stimulated genes |
56 |
3.90e-02 |
1.85e-01 |
0.1950 |
1.92e-01 |
-0.037000 |
1.31e-02 |
6.32e-01 |
SHC-mediated cascade:FGFR1 |
12 |
4.97e-01 |
7.76e-01 |
0.1950 |
1.89e-01 |
-0.048600 |
2.57e-01 |
7.71e-01 |
Glucagon-like Peptide-1 (GLP1) regulates insulin secretion |
29 |
1.94e-01 |
4.86e-01 |
0.1950 |
-1.94e-01 |
-0.009220 |
7.02e-02 |
9.32e-01 |
p38MAPK events |
12 |
4.94e-01 |
7.74e-01 |
0.1940 |
1.66e-01 |
-0.101000 |
3.20e-01 |
5.45e-01 |
Signaling by the B Cell Receptor (BCR) |
96 |
4.17e-03 |
3.91e-02 |
0.1940 |
1.88e-01 |
-0.046400 |
1.47e-03 |
4.33e-01 |
Prostacyclin signalling through prostacyclin receptor |
11 |
5.49e-01 |
8.13e-01 |
0.1930 |
-7.56e-02 |
-0.178000 |
6.64e-01 |
3.07e-01 |
mRNA 3'-end processing |
42 |
1.03e-01 |
3.44e-01 |
0.1930 |
1.70e-01 |
0.091500 |
5.63e-02 |
3.05e-01 |
RNA Polymerase II Transcription Termination |
49 |
7.25e-02 |
2.74e-01 |
0.1930 |
1.47e-01 |
0.125000 |
7.46e-02 |
1.30e-01 |
COPII-mediated vesicle transport |
51 |
5.25e-02 |
2.18e-01 |
0.1930 |
-1.63e-01 |
0.103000 |
4.45e-02 |
2.02e-01 |
TGF-beta receptor signaling in EMT (epithelial to mesenchymal transition) |
10 |
5.60e-01 |
8.17e-01 |
0.1930 |
-1.55e-01 |
0.115000 |
3.97e-01 |
5.30e-01 |
Nephrin family interactions |
19 |
3.59e-01 |
6.79e-01 |
0.1930 |
7.67e-02 |
0.177000 |
5.63e-01 |
1.83e-01 |
ABC transporter disorders |
53 |
4.71e-02 |
2.03e-01 |
0.1930 |
1.63e-01 |
-0.103000 |
4.06e-02 |
1.95e-01 |
Synthesis of Prostaglandins (PG) and Thromboxanes (TX) |
10 |
5.88e-01 |
8.27e-01 |
0.1920 |
-1.32e-01 |
-0.140000 |
4.71e-01 |
4.44e-01 |
Semaphorin interactions |
59 |
3.49e-02 |
1.71e-01 |
0.1920 |
-8.26e-02 |
0.173000 |
2.73e-01 |
2.15e-02 |
HSP90 chaperone cycle for steroid hormone receptors (SHR) |
31 |
1.69e-01 |
4.54e-01 |
0.1920 |
-1.02e-01 |
0.162000 |
3.24e-01 |
1.18e-01 |
Deubiquitination |
215 |
5.71e-06 |
1.84e-04 |
0.1920 |
1.71e-01 |
-0.087700 |
1.77e-05 |
2.73e-02 |
Biosynthesis of specialized proresolving mediators (SPMs) |
13 |
4.77e-01 |
7.66e-01 |
0.1920 |
1.73e-01 |
-0.082500 |
2.80e-01 |
6.07e-01 |
Other interleukin signaling |
17 |
4.07e-01 |
7.16e-01 |
0.1910 |
8.54e-02 |
0.171000 |
5.42e-01 |
2.23e-01 |
Reduction of cytosolic Ca++ levels |
10 |
5.66e-01 |
8.21e-01 |
0.1910 |
-1.06e-01 |
0.159000 |
5.61e-01 |
3.85e-01 |
Adenylate cyclase activating pathway |
10 |
5.92e-01 |
8.29e-01 |
0.1910 |
-1.43e-01 |
-0.127000 |
4.35e-01 |
4.87e-01 |
Complex I biogenesis |
39 |
1.11e-01 |
3.53e-01 |
0.1910 |
8.32e-02 |
-0.172000 |
3.69e-01 |
6.35e-02 |
Tight junction interactions |
11 |
5.58e-01 |
8.16e-01 |
0.1900 |
5.94e-02 |
0.181000 |
7.33e-01 |
2.99e-01 |
A tetrasaccharide linker sequence is required for GAG synthesis |
19 |
3.60e-01 |
6.79e-01 |
0.1900 |
-1.89e-01 |
-0.019700 |
1.54e-01 |
8.82e-01 |
Nonhomologous End-Joining (NHEJ) |
29 |
2.10e-01 |
5.03e-01 |
0.1900 |
1.89e-01 |
0.016900 |
7.78e-02 |
8.75e-01 |
Signaling by FGFR |
58 |
4.68e-02 |
2.03e-01 |
0.1900 |
4.95e-02 |
0.183000 |
5.15e-01 |
1.58e-02 |
Nucleotide salvage |
18 |
3.72e-01 |
6.89e-01 |
0.1890 |
1.82e-01 |
-0.051200 |
1.81e-01 |
7.07e-01 |
Regulation of PTEN stability and activity |
53 |
5.30e-02 |
2.19e-01 |
0.1890 |
1.51e-01 |
-0.114000 |
5.83e-02 |
1.52e-01 |
Aberrant regulation of mitotic G1/S transition in cancer due to RB1 defects |
16 |
4.39e-01 |
7.38e-01 |
0.1880 |
1.71e-01 |
0.078800 |
2.37e-01 |
5.86e-01 |
Defective binding of RB1 mutants to E2F1,(E2F2, E2F3) |
16 |
4.39e-01 |
7.38e-01 |
0.1880 |
1.71e-01 |
0.078800 |
2.37e-01 |
5.86e-01 |
Mitotic Spindle Checkpoint |
86 |
1.03e-02 |
7.63e-02 |
0.1880 |
1.87e-01 |
-0.016800 |
2.71e-03 |
7.88e-01 |
Infection with Mycobacterium tuberculosis |
21 |
3.21e-01 |
6.41e-01 |
0.1880 |
1.82e-01 |
-0.046800 |
1.49e-01 |
7.11e-01 |
Arachidonic acid metabolism |
36 |
1.48e-01 |
4.25e-01 |
0.1880 |
1.87e-01 |
-0.013000 |
5.19e-02 |
8.92e-01 |
Energy dependent regulation of mTOR by LKB1-AMPK |
25 |
2.67e-01 |
5.82e-01 |
0.1880 |
-1.88e-01 |
0.000924 |
1.04e-01 |
9.94e-01 |
ADP signalling through P2Y purinoceptor 1 |
17 |
4.24e-01 |
7.31e-01 |
0.1870 |
-1.07e-01 |
-0.154000 |
4.45e-01 |
2.73e-01 |
Hyaluronan uptake and degradation |
10 |
5.97e-01 |
8.29e-01 |
0.1870 |
1.82e-01 |
0.043700 |
3.19e-01 |
8.11e-01 |
Translation of structural proteins |
21 |
3.42e-01 |
6.61e-01 |
0.1870 |
-1.78e-01 |
-0.055900 |
1.57e-01 |
6.58e-01 |
Cell junction organization |
47 |
7.73e-02 |
2.83e-01 |
0.1870 |
-1.30e-01 |
0.134000 |
1.22e-01 |
1.13e-01 |
HS-GAG degradation |
17 |
4.05e-01 |
7.15e-01 |
0.1870 |
-1.83e-01 |
0.038500 |
1.92e-01 |
7.83e-01 |
The citric acid (TCA) cycle and respiratory electron transport |
111 |
2.56e-03 |
2.53e-02 |
0.1860 |
1.09e-01 |
-0.151000 |
4.83e-02 |
6.00e-03 |
BBSome-mediated cargo-targeting to cilium |
17 |
4.00e-01 |
7.14e-01 |
0.1860 |
1.57e-01 |
-0.100000 |
2.63e-01 |
4.75e-01 |
Pre-NOTCH Expression and Processing |
43 |
9.90e-02 |
3.37e-01 |
0.1860 |
-1.53e-01 |
0.106000 |
8.28e-02 |
2.32e-01 |
EML4 and NUDC in mitotic spindle formation |
75 |
2.12e-02 |
1.27e-01 |
0.1860 |
1.86e-01 |
0.005130 |
5.49e-03 |
9.39e-01 |
TP53 Regulates Transcription of Genes Involved in G1 Cell Cycle Arrest |
13 |
5.21e-01 |
7.87e-01 |
0.1850 |
1.73e-01 |
0.065400 |
2.79e-01 |
6.83e-01 |
Signaling by KIT in disease |
20 |
3.73e-01 |
6.89e-01 |
0.1850 |
1.17e-01 |
0.143000 |
3.64e-01 |
2.67e-01 |
Signaling by phosphorylated juxtamembrane, extracellular and kinase domain KIT mutants |
20 |
3.73e-01 |
6.89e-01 |
0.1850 |
1.17e-01 |
0.143000 |
3.64e-01 |
2.67e-01 |
Presynaptic function of Kainate receptors |
13 |
5.29e-01 |
7.93e-01 |
0.1850 |
-1.37e-01 |
-0.124000 |
3.92e-01 |
4.40e-01 |
Defective B4GALT7 causes EDS, progeroid type |
16 |
4.29e-01 |
7.32e-01 |
0.1840 |
-1.54e-01 |
0.101000 |
2.85e-01 |
4.86e-01 |
SHC-mediated cascade:FGFR4 |
11 |
5.64e-01 |
8.21e-01 |
0.1840 |
5.57e-02 |
-0.175000 |
7.49e-01 |
3.14e-01 |
RAF activation |
32 |
1.98e-01 |
4.89e-01 |
0.1840 |
8.78e-04 |
-0.184000 |
9.93e-01 |
7.22e-02 |
ABC transporters in lipid homeostasis |
12 |
5.47e-01 |
8.12e-01 |
0.1830 |
1.22e-02 |
0.183000 |
9.42e-01 |
2.72e-01 |
Interleukin-6 signaling |
10 |
5.96e-01 |
8.29e-01 |
0.1830 |
1.64e-01 |
-0.079500 |
3.68e-01 |
6.63e-01 |
FGFR2 alternative splicing |
18 |
4.01e-01 |
7.15e-01 |
0.1820 |
-3.78e-02 |
0.178000 |
7.82e-01 |
1.90e-01 |
Nucleotide Excision Repair |
86 |
1.24e-02 |
8.63e-02 |
0.1820 |
1.68e-01 |
-0.070900 |
7.23e-03 |
2.56e-01 |
Extracellular matrix organization |
211 |
3.00e-05 |
7.12e-04 |
0.1820 |
-1.81e-01 |
0.017900 |
6.22e-06 |
6.55e-01 |
Response of Mtb to phagocytosis |
18 |
3.94e-01 |
7.10e-01 |
0.1820 |
1.39e-01 |
-0.117000 |
3.06e-01 |
3.90e-01 |
Metabolism of nitric oxide: NOS3 activation and regulation |
14 |
5.15e-01 |
7.85e-01 |
0.1820 |
1.21e-01 |
0.136000 |
4.34e-01 |
3.80e-01 |
Interconversion of nucleotide di- and triphosphates |
22 |
3.28e-01 |
6.50e-01 |
0.1810 |
5.85e-02 |
-0.172000 |
6.35e-01 |
1.63e-01 |
Miscellaneous transport and binding events |
18 |
3.99e-01 |
7.14e-01 |
0.1810 |
-1.55e-01 |
0.094200 |
2.56e-01 |
4.89e-01 |
RUNX1 regulates genes involved in megakaryocyte differentiation and platelet function |
33 |
1.86e-01 |
4.74e-01 |
0.1810 |
-1.57e-01 |
0.090900 |
1.20e-01 |
3.66e-01 |
TRP channels |
12 |
5.48e-01 |
8.12e-01 |
0.1810 |
4.31e-02 |
-0.176000 |
7.96e-01 |
2.92e-01 |
Pentose phosphate pathway |
13 |
5.14e-01 |
7.85e-01 |
0.1810 |
1.33e-01 |
-0.123000 |
4.07e-01 |
4.44e-01 |
Formation of HIV-1 elongation complex containing HIV-1 Tat |
30 |
2.41e-01 |
5.45e-01 |
0.1810 |
-6.42e-02 |
-0.169000 |
5.43e-01 |
1.10e-01 |
HIV Transcription Elongation |
30 |
2.41e-01 |
5.45e-01 |
0.1810 |
-6.42e-02 |
-0.169000 |
5.43e-01 |
1.10e-01 |
Tat-mediated elongation of the HIV-1 transcript |
30 |
2.41e-01 |
5.45e-01 |
0.1810 |
-6.42e-02 |
-0.169000 |
5.43e-01 |
1.10e-01 |
Blood group systems biosynthesis |
11 |
5.84e-01 |
8.24e-01 |
0.1800 |
-9.73e-03 |
0.180000 |
9.55e-01 |
3.02e-01 |
Triglyceride metabolism |
22 |
3.30e-01 |
6.53e-01 |
0.1800 |
-8.84e-02 |
0.157000 |
4.73e-01 |
2.03e-01 |
Glycerophospholipid biosynthesis |
87 |
1.69e-02 |
1.07e-01 |
0.1800 |
-1.69e-01 |
-0.060600 |
6.44e-03 |
3.29e-01 |
Phase I - Functionalization of compounds |
59 |
5.30e-02 |
2.19e-01 |
0.1800 |
1.65e-01 |
-0.070800 |
2.83e-02 |
3.48e-01 |
Transcriptional Regulation by MECP2 |
42 |
1.21e-01 |
3.74e-01 |
0.1800 |
-1.04e-01 |
0.146000 |
2.42e-01 |
1.02e-01 |
Integrin signaling |
24 |
3.12e-01 |
6.30e-01 |
0.1800 |
1.14e-02 |
-0.179000 |
9.23e-01 |
1.29e-01 |
Phase 2 - plateau phase |
17 |
4.38e-01 |
7.38e-01 |
0.1790 |
-1.79e-01 |
0.007730 |
2.01e-01 |
9.56e-01 |
Post-translational protein phosphorylation |
67 |
3.47e-02 |
1.71e-01 |
0.1790 |
-1.33e-01 |
0.121000 |
6.01e-02 |
8.84e-02 |
CD28 dependent PI3K/Akt signaling |
20 |
3.97e-01 |
7.14e-01 |
0.1790 |
1.27e-01 |
0.126000 |
3.25e-01 |
3.29e-01 |
Platelet Aggregation (Plug Formation) |
25 |
2.94e-01 |
6.08e-01 |
0.1790 |
4.31e-02 |
-0.174000 |
7.10e-01 |
1.33e-01 |
EGFR downregulation |
24 |
3.13e-01 |
6.31e-01 |
0.1790 |
-1.77e-01 |
0.026100 |
1.34e-01 |
8.25e-01 |
Sphingolipid metabolism |
62 |
5.93e-02 |
2.38e-01 |
0.1780 |
-1.30e-01 |
-0.122000 |
7.74e-02 |
9.62e-02 |
Role of phospholipids in phagocytosis |
26 |
2.92e-01 |
6.07e-01 |
0.1780 |
-1.68e-02 |
-0.178000 |
8.82e-01 |
1.17e-01 |
Formation of tubulin folding intermediates by CCT/TriC |
16 |
4.72e-01 |
7.60e-01 |
0.1780 |
-3.31e-02 |
-0.175000 |
8.19e-01 |
2.25e-01 |
NR1H3 & NR1H2 regulate gene expression linked to cholesterol transport and efflux |
28 |
2.80e-01 |
5.94e-01 |
0.1780 |
-1.30e-01 |
-0.122000 |
2.34e-01 |
2.66e-01 |
Transcriptional activity of SMAD2/SMAD3:SMAD4 heterotrimer |
35 |
2.05e-01 |
4.99e-01 |
0.1770 |
9.95e-02 |
0.147000 |
3.08e-01 |
1.33e-01 |
NR1H2 and NR1H3-mediated signaling |
35 |
2.05e-01 |
4.99e-01 |
0.1770 |
-1.57e-01 |
-0.082700 |
1.09e-01 |
3.98e-01 |
Glucagon signaling in metabolic regulation |
24 |
3.38e-01 |
6.59e-01 |
0.1770 |
-1.58e-01 |
-0.079900 |
1.81e-01 |
4.99e-01 |
Host Interactions of HIV factors |
100 |
8.66e-03 |
6.67e-02 |
0.1760 |
1.63e-01 |
-0.067300 |
5.06e-03 |
2.46e-01 |
RAB geranylgeranylation |
45 |
1.17e-01 |
3.63e-01 |
0.1760 |
1.63e-01 |
-0.066500 |
5.90e-02 |
4.41e-01 |
Pre-NOTCH Transcription and Translation |
30 |
2.37e-01 |
5.44e-01 |
0.1760 |
-9.37e-02 |
0.149000 |
3.75e-01 |
1.59e-01 |
Regulation of RUNX2 expression and activity |
57 |
7.37e-02 |
2.74e-01 |
0.1760 |
1.75e-01 |
0.013700 |
2.25e-02 |
8.58e-01 |
Degradation of the extracellular matrix |
70 |
4.31e-02 |
1.97e-01 |
0.1750 |
-1.70e-01 |
-0.042600 |
1.41e-02 |
5.38e-01 |
Interleukin-6 family signaling |
17 |
4.65e-01 |
7.54e-01 |
0.1750 |
1.70e-01 |
0.041800 |
2.25e-01 |
7.65e-01 |
TP53 Regulates Transcription of DNA Repair Genes |
48 |
1.04e-01 |
3.46e-01 |
0.1750 |
6.04e-02 |
-0.164000 |
4.69e-01 |
4.92e-02 |
Branched-chain amino acid catabolism |
20 |
3.87e-01 |
7.03e-01 |
0.1740 |
1.42e-01 |
-0.101000 |
2.71e-01 |
4.35e-01 |
Diseases of metabolism |
163 |
5.03e-04 |
7.11e-03 |
0.1740 |
-1.53e-01 |
0.082600 |
7.53e-04 |
6.98e-02 |
Respiratory electron transport |
66 |
4.43e-02 |
1.99e-01 |
0.1740 |
1.26e-01 |
-0.120000 |
7.68e-02 |
9.20e-02 |
Regulation of KIT signaling |
16 |
4.98e-01 |
7.76e-01 |
0.1740 |
1.28e-01 |
0.118000 |
3.75e-01 |
4.14e-01 |
Formation of HIV elongation complex in the absence of HIV Tat |
31 |
2.53e-01 |
5.62e-01 |
0.1740 |
-4.38e-02 |
-0.168000 |
6.73e-01 |
1.05e-01 |
Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs) |
73 |
3.39e-02 |
1.70e-01 |
0.1730 |
-1.19e-01 |
0.125000 |
7.92e-02 |
6.51e-02 |
Heparan sulfate/heparin (HS-GAG) metabolism |
37 |
1.86e-01 |
4.74e-01 |
0.1720 |
-1.67e-01 |
0.042600 |
7.88e-02 |
6.54e-01 |
Nuclear Pore Complex (NPC) Disassembly |
27 |
3.13e-01 |
6.31e-01 |
0.1720 |
1.56e-01 |
0.074200 |
1.62e-01 |
5.05e-01 |
Ion transport by P-type ATPases |
34 |
2.08e-01 |
5.01e-01 |
0.1720 |
-1.29e-01 |
0.114000 |
1.94e-01 |
2.50e-01 |
TP53 Regulates Transcription of Cell Cycle Genes |
44 |
1.53e-01 |
4.28e-01 |
0.1720 |
1.51e-01 |
0.082700 |
8.42e-02 |
3.43e-01 |
Regulation of gene expression in late stage (branching morphogenesis) pancreatic bud precursor cells |
12 |
5.81e-01 |
8.24e-01 |
0.1720 |
-4.26e-02 |
0.166000 |
7.98e-01 |
3.18e-01 |
RIPK1-mediated regulated necrosis |
14 |
5.55e-01 |
8.16e-01 |
0.1710 |
1.16e-01 |
0.126000 |
4.54e-01 |
4.14e-01 |
Regulated Necrosis |
14 |
5.55e-01 |
8.16e-01 |
0.1710 |
1.16e-01 |
0.126000 |
4.54e-01 |
4.14e-01 |
Loss of Nlp from mitotic centrosomes |
59 |
7.31e-02 |
2.74e-01 |
0.1710 |
-3.11e-02 |
0.168000 |
6.80e-01 |
2.57e-02 |
Loss of proteins required for interphase microtubule organization from the centrosome |
59 |
7.31e-02 |
2.74e-01 |
0.1710 |
-3.11e-02 |
0.168000 |
6.80e-01 |
2.57e-02 |
tRNA Aminoacylation |
20 |
4.32e-01 |
7.34e-01 |
0.1710 |
-1.46e-01 |
-0.088300 |
2.59e-01 |
4.94e-01 |
Activation of NF-kappaB in B cells |
55 |
8.35e-02 |
2.97e-01 |
0.1700 |
1.36e-01 |
-0.102000 |
8.10e-02 |
1.90e-01 |
ER Quality Control Compartment (ERQC) |
12 |
5.81e-01 |
8.24e-01 |
0.1700 |
-1.17e-01 |
0.124000 |
4.85e-01 |
4.57e-01 |
Sema3A PAK dependent Axon repulsion |
15 |
5.12e-01 |
7.84e-01 |
0.1700 |
-7.03e-02 |
0.154000 |
6.37e-01 |
3.01e-01 |
E3 ubiquitin ligases ubiquitinate target proteins |
26 |
3.33e-01 |
6.54e-01 |
0.1690 |
1.66e-01 |
0.031300 |
1.42e-01 |
7.83e-01 |
SHC-mediated cascade:FGFR3 |
12 |
5.85e-01 |
8.24e-01 |
0.1690 |
1.29e-01 |
-0.109000 |
4.39e-01 |
5.13e-01 |
Keratan sulfate biosynthesis |
20 |
4.10e-01 |
7.19e-01 |
0.1690 |
-1.29e-01 |
0.109000 |
3.17e-01 |
4.01e-01 |
MicroRNA (miRNA) biogenesis |
15 |
5.22e-01 |
7.87e-01 |
0.1690 |
-1.67e-01 |
0.022900 |
2.62e-01 |
8.78e-01 |
Downregulation of ERBB2 signaling |
20 |
4.32e-01 |
7.34e-01 |
0.1690 |
-1.65e-01 |
-0.035500 |
2.02e-01 |
7.83e-01 |
Hedgehog ligand biogenesis |
46 |
1.30e-01 |
3.90e-01 |
0.1690 |
1.33e-01 |
-0.104000 |
1.18e-01 |
2.24e-01 |
Integration of energy metabolism |
85 |
2.83e-02 |
1.51e-01 |
0.1690 |
-1.67e-01 |
-0.023200 |
7.85e-03 |
7.12e-01 |
FCERI mediated NF-kB activation |
64 |
5.91e-02 |
2.38e-01 |
0.1690 |
1.37e-01 |
-0.098200 |
5.82e-02 |
1.75e-01 |
Regulation of TP53 Expression and Degradation |
30 |
2.81e-01 |
5.95e-01 |
0.1680 |
1.68e-01 |
-0.001690 |
1.12e-01 |
9.87e-01 |
RNA Polymerase I Transcription Termination |
21 |
4.33e-01 |
7.36e-01 |
0.1660 |
-1.02e-01 |
-0.132000 |
4.21e-01 |
2.96e-01 |
Respiratory electron transport, ATP synthesis by chemiosmotic coupling, and heat production by uncoupling proteins. |
71 |
4.74e-02 |
2.03e-01 |
0.1660 |
1.29e-01 |
-0.104000 |
6.01e-02 |
1.29e-01 |
Synthesis of active ubiquitin: roles of E1 and E2 enzymes |
19 |
4.46e-01 |
7.43e-01 |
0.1660 |
5.89e-02 |
-0.155000 |
6.57e-01 |
2.42e-01 |
DAG and IP3 signaling |
36 |
2.26e-01 |
5.26e-01 |
0.1660 |
-1.66e-01 |
0.003470 |
8.52e-02 |
9.71e-01 |
Post NMDA receptor activation events |
53 |
1.05e-01 |
3.46e-01 |
0.1660 |
-1.52e-01 |
0.065500 |
5.52e-02 |
4.10e-01 |
PECAM1 interactions |
11 |
6.47e-01 |
8.46e-01 |
0.1660 |
1.33e-01 |
0.098900 |
4.45e-01 |
5.70e-01 |
Signaling by NOTCH4 |
65 |
6.21e-02 |
2.46e-01 |
0.1660 |
1.27e-01 |
-0.107000 |
7.78e-02 |
1.37e-01 |
Iron uptake and transport |
41 |
1.86e-01 |
4.74e-01 |
0.1650 |
-9.70e-04 |
-0.165000 |
9.91e-01 |
6.70e-02 |
G alpha (z) signalling events |
34 |
2.64e-01 |
5.77e-01 |
0.1650 |
-1.13e-01 |
-0.121000 |
2.55e-01 |
2.23e-01 |
PI-3K cascade:FGFR1 |
12 |
6.21e-01 |
8.30e-01 |
0.1650 |
1.52e-01 |
0.065100 |
3.62e-01 |
6.96e-01 |
Transport of Mature mRNA derived from an Intron-Containing Transcript |
55 |
1.17e-01 |
3.63e-01 |
0.1650 |
1.27e-01 |
0.105000 |
1.02e-01 |
1.80e-01 |
The NLRP3 inflammasome |
13 |
5.76e-01 |
8.24e-01 |
0.1650 |
-1.21e-01 |
0.112000 |
4.51e-01 |
4.84e-01 |
Trafficking of GluR2-containing AMPA receptors |
14 |
5.61e-01 |
8.18e-01 |
0.1650 |
-1.62e-01 |
0.031300 |
2.95e-01 |
8.40e-01 |
Interaction between L1 and Ankyrins |
23 |
3.80e-01 |
6.96e-01 |
0.1650 |
-8.09e-02 |
0.143000 |
5.02e-01 |
2.34e-01 |
Downstream signaling events of B Cell Receptor (BCR) |
67 |
6.39e-02 |
2.48e-01 |
0.1650 |
1.62e-01 |
-0.029700 |
2.21e-02 |
6.75e-01 |
Inactivation of APC/C via direct inhibition of the APC/C complex |
19 |
4.58e-01 |
7.52e-01 |
0.1640 |
1.61e-01 |
-0.030700 |
2.23e-01 |
8.17e-01 |
Inhibition of the proteolytic activity of APC/C required for the onset of anaphase by mitotic spindle checkpoint components |
19 |
4.58e-01 |
7.52e-01 |
0.1640 |
1.61e-01 |
-0.030700 |
2.23e-01 |
8.17e-01 |
Regulation of necroptotic cell death |
12 |
6.28e-01 |
8.35e-01 |
0.1640 |
9.55e-02 |
0.133000 |
5.67e-01 |
4.24e-01 |
Signaling by TGFB family members |
76 |
4.73e-02 |
2.03e-01 |
0.1640 |
1.62e-03 |
0.164000 |
9.81e-01 |
1.35e-02 |
Interleukin receptor SHC signaling |
20 |
4.37e-01 |
7.37e-01 |
0.1640 |
5.66e-02 |
-0.154000 |
6.61e-01 |
2.34e-01 |
Formation of the cornified envelope |
17 |
5.08e-01 |
7.83e-01 |
0.1640 |
-1.85e-02 |
-0.163000 |
8.95e-01 |
2.46e-01 |
Signaling by FGFR1 |
35 |
2.57e-01 |
5.68e-01 |
0.1640 |
7.00e-02 |
0.148000 |
4.74e-01 |
1.30e-01 |
Sphingolipid de novo biosynthesis |
31 |
3.02e-01 |
6.17e-01 |
0.1640 |
-8.25e-02 |
-0.141000 |
4.27e-01 |
1.74e-01 |
RHO GTPases activate CIT |
18 |
4.86e-01 |
7.71e-01 |
0.1630 |
6.78e-03 |
-0.163000 |
9.60e-01 |
2.31e-01 |
Stimuli-sensing channels |
52 |
1.23e-01 |
3.77e-01 |
0.1630 |
-1.60e-01 |
0.028900 |
4.56e-02 |
7.19e-01 |
Intra-Golgi traffic |
34 |
2.49e-01 |
5.56e-01 |
0.1630 |
-1.48e-01 |
0.067800 |
1.36e-01 |
4.94e-01 |
p130Cas linkage to MAPK signaling for integrins |
12 |
6.10e-01 |
8.29e-01 |
0.1620 |
9.07e-02 |
-0.135000 |
5.87e-01 |
4.19e-01 |
Signaling by NOTCH1 |
61 |
8.22e-02 |
2.95e-01 |
0.1620 |
-1.31e-01 |
0.095300 |
7.63e-02 |
1.98e-01 |
Retrograde transport at the Trans-Golgi-Network |
40 |
1.94e-01 |
4.86e-01 |
0.1620 |
-9.62e-02 |
0.130000 |
2.93e-01 |
1.54e-01 |
Carboxyterminal post-translational modifications of tubulin |
25 |
3.88e-01 |
7.03e-01 |
0.1620 |
-7.27e-02 |
-0.145000 |
5.29e-01 |
2.11e-01 |
Mitotic Prometaphase |
152 |
3.19e-03 |
3.11e-02 |
0.1620 |
1.54e-01 |
0.047800 |
1.06e-03 |
3.11e-01 |
Vasopressin regulates renal water homeostasis via Aquaporins |
30 |
3.22e-01 |
6.42e-01 |
0.1610 |
-1.46e-01 |
-0.067800 |
1.65e-01 |
5.21e-01 |
FCGR3A-mediated phagocytosis |
58 |
1.11e-01 |
3.53e-01 |
0.1610 |
1.53e-01 |
0.052700 |
4.47e-02 |
4.88e-01 |
Leishmania phagocytosis |
58 |
1.11e-01 |
3.53e-01 |
0.1610 |
1.53e-01 |
0.052700 |
4.47e-02 |
4.88e-01 |
Parasite infection |
58 |
1.11e-01 |
3.53e-01 |
0.1610 |
1.53e-01 |
0.052700 |
4.47e-02 |
4.88e-01 |
FRS-mediated FGFR3 signaling |
13 |
5.94e-01 |
8.29e-01 |
0.1610 |
5.80e-02 |
-0.150000 |
7.18e-01 |
3.48e-01 |
Keratinization |
22 |
4.12e-01 |
7.21e-01 |
0.1610 |
1.09e-01 |
-0.118000 |
3.75e-01 |
3.40e-01 |
Biosynthesis of DHA-derived SPMs |
11 |
6.43e-01 |
8.44e-01 |
0.1600 |
1.19e-01 |
-0.107000 |
4.95e-01 |
5.37e-01 |
TP53 regulates transcription of several additional cell death genes whose specific roles in p53-dependent apoptosis remain uncertain |
11 |
6.49e-01 |
8.46e-01 |
0.1600 |
-4.78e-02 |
0.153000 |
7.84e-01 |
3.81e-01 |
Amine ligand-binding receptors |
11 |
6.56e-01 |
8.51e-01 |
0.1600 |
1.60e-01 |
0.004030 |
3.59e-01 |
9.82e-01 |
PCP/CE pathway |
75 |
6.09e-02 |
2.43e-01 |
0.1600 |
-4.06e-02 |
-0.154000 |
5.44e-01 |
2.09e-02 |
Cellular response to heat stress |
72 |
6.29e-02 |
2.47e-01 |
0.1600 |
-1.59e-01 |
0.016800 |
2.00e-02 |
8.06e-01 |
SUMO E3 ligases SUMOylate target proteins |
131 |
8.14e-03 |
6.44e-02 |
0.1600 |
1.47e-01 |
0.062600 |
3.79e-03 |
2.17e-01 |
Potential therapeutics for SARS |
32 |
3.09e-01 |
6.27e-01 |
0.1600 |
1.34e-01 |
0.086300 |
1.89e-01 |
3.98e-01 |
TNFR2 non-canonical NF-kB pathway |
62 |
8.75e-02 |
3.07e-01 |
0.1590 |
1.27e-01 |
-0.095100 |
8.33e-02 |
1.96e-01 |
Gluconeogenesis |
24 |
4.03e-01 |
7.15e-01 |
0.1590 |
-1.59e-01 |
0.002880 |
1.78e-01 |
9.81e-01 |
Mitochondrial calcium ion transport |
16 |
5.56e-01 |
8.16e-01 |
0.1590 |
-5.26e-02 |
-0.150000 |
7.16e-01 |
3.00e-01 |
GRB2 events in ERBB2 signaling |
14 |
5.98e-01 |
8.29e-01 |
0.1580 |
-1.52e-01 |
-0.046200 |
3.26e-01 |
7.65e-01 |
Transport of Mature Transcript to Cytoplasm |
62 |
1.05e-01 |
3.46e-01 |
0.1580 |
1.44e-01 |
0.065700 |
4.99e-02 |
3.72e-01 |
DNA Repair |
222 |
2.63e-04 |
4.35e-03 |
0.1580 |
1.58e-01 |
-0.006540 |
5.20e-05 |
8.67e-01 |
Oncogene Induced Senescence |
27 |
3.61e-01 |
6.79e-01 |
0.1580 |
-1.76e-02 |
0.157000 |
8.75e-01 |
1.58e-01 |
Nuclear Envelope (NE) Reassembly |
57 |
1.13e-01 |
3.57e-01 |
0.1580 |
5.10e-02 |
-0.149000 |
5.06e-01 |
5.13e-02 |
RNA Polymerase III Abortive And Retractive Initiation |
33 |
2.83e-01 |
5.96e-01 |
0.1570 |
5.74e-02 |
-0.147000 |
5.68e-01 |
1.45e-01 |
RNA Polymerase III Transcription |
33 |
2.83e-01 |
5.96e-01 |
0.1570 |
5.74e-02 |
-0.147000 |
5.68e-01 |
1.45e-01 |
Formation of RNA Pol II elongation complex |
42 |
2.15e-01 |
5.10e-01 |
0.1570 |
-2.71e-02 |
-0.155000 |
7.62e-01 |
8.23e-02 |
RNA Polymerase II Transcription Elongation |
42 |
2.15e-01 |
5.10e-01 |
0.1570 |
-2.71e-02 |
-0.155000 |
7.62e-01 |
8.23e-02 |
Signaling by EGFR in Cancer |
18 |
5.23e-01 |
7.87e-01 |
0.1570 |
-1.47e-01 |
-0.055200 |
2.80e-01 |
6.85e-01 |
Formation of TC-NER Pre-Incision Complex |
38 |
2.33e-01 |
5.39e-01 |
0.1570 |
1.11e-01 |
-0.111000 |
2.38e-01 |
2.37e-01 |
Interleukin-2 family signaling |
33 |
2.83e-01 |
5.96e-01 |
0.1570 |
1.30e-01 |
-0.087600 |
1.97e-01 |
3.84e-01 |
Mitochondrial protein import |
49 |
1.64e-01 |
4.45e-01 |
0.1560 |
1.38e-02 |
-0.156000 |
8.67e-01 |
5.95e-02 |
AURKA Activation by TPX2 |
61 |
1.08e-01 |
3.52e-01 |
0.1560 |
-5.31e-03 |
0.156000 |
9.43e-01 |
3.54e-02 |
Late endosomal microautophagy |
22 |
4.65e-01 |
7.54e-01 |
0.1550 |
-8.69e-02 |
-0.129000 |
4.81e-01 |
2.96e-01 |
Cellular response to hypoxia |
56 |
1.23e-01 |
3.77e-01 |
0.1550 |
1.16e-01 |
-0.103000 |
1.35e-01 |
1.82e-01 |
G-protein activation |
15 |
5.96e-01 |
8.29e-01 |
0.1550 |
-1.21e-01 |
-0.096200 |
4.16e-01 |
5.19e-01 |
Ion channel transport |
100 |
2.92e-02 |
1.54e-01 |
0.1540 |
-1.54e-01 |
-0.005050 |
7.86e-03 |
9.31e-01 |
Defective B3GAT3 causes JDSSDHD |
16 |
5.53e-01 |
8.16e-01 |
0.1540 |
-1.22e-01 |
0.093600 |
3.97e-01 |
5.17e-01 |
WNT ligand biogenesis and trafficking |
12 |
6.65e-01 |
8.57e-01 |
0.1540 |
-1.08e-01 |
-0.109000 |
5.18e-01 |
5.11e-01 |
Signaling by high-kinase activity BRAF mutants |
30 |
3.46e-01 |
6.68e-01 |
0.1530 |
6.30e-03 |
-0.153000 |
9.52e-01 |
1.46e-01 |
Constitutive Signaling by NOTCH1 HD+PEST Domain Mutants |
47 |
1.78e-01 |
4.63e-01 |
0.1530 |
-1.09e-01 |
0.108000 |
1.98e-01 |
1.99e-01 |
Constitutive Signaling by NOTCH1 PEST Domain Mutants |
47 |
1.78e-01 |
4.63e-01 |
0.1530 |
-1.09e-01 |
0.108000 |
1.98e-01 |
1.99e-01 |
Signaling by NOTCH1 HD+PEST Domain Mutants in Cancer |
47 |
1.78e-01 |
4.63e-01 |
0.1530 |
-1.09e-01 |
0.108000 |
1.98e-01 |
1.99e-01 |
Signaling by NOTCH1 PEST Domain Mutants in Cancer |
47 |
1.78e-01 |
4.63e-01 |
0.1530 |
-1.09e-01 |
0.108000 |
1.98e-01 |
1.99e-01 |
Signaling by NOTCH1 in Cancer |
47 |
1.78e-01 |
4.63e-01 |
0.1530 |
-1.09e-01 |
0.108000 |
1.98e-01 |
1.99e-01 |
SUMOylation of DNA damage response and repair proteins |
56 |
1.48e-01 |
4.25e-01 |
0.1530 |
1.40e-01 |
0.062100 |
6.97e-02 |
4.22e-01 |
NOTCH3 Intracellular Domain Regulates Transcription |
22 |
4.48e-01 |
7.44e-01 |
0.1530 |
-6.88e-02 |
0.137000 |
5.77e-01 |
2.66e-01 |
SUMOylation |
137 |
9.34e-03 |
7.08e-02 |
0.1530 |
1.48e-01 |
0.041000 |
2.92e-03 |
4.08e-01 |
Caspase activation via Death Receptors in the presence of ligand |
15 |
5.80e-01 |
8.24e-01 |
0.1530 |
-7.75e-02 |
0.132000 |
6.04e-01 |
3.78e-01 |
Translation |
178 |
1.74e-03 |
1.86e-02 |
0.1520 |
1.32e-01 |
-0.075900 |
2.41e-03 |
8.19e-02 |
Assembly Of The HIV Virion |
10 |
7.17e-01 |
8.83e-01 |
0.1520 |
-1.07e-01 |
-0.108000 |
5.59e-01 |
5.53e-01 |
Activation of PPARGC1A (PGC-1alpha) by phosphorylation |
10 |
7.18e-01 |
8.83e-01 |
0.1510 |
-1.32e-01 |
-0.074900 |
4.71e-01 |
6.82e-01 |
Paradoxical activation of RAF signaling by kinase inactive BRAF |
38 |
2.80e-01 |
5.94e-01 |
0.1510 |
-4.45e-02 |
-0.145000 |
6.35e-01 |
1.23e-01 |
Signaling by RAS mutants |
38 |
2.80e-01 |
5.94e-01 |
0.1510 |
-4.45e-02 |
-0.145000 |
6.35e-01 |
1.23e-01 |
Signaling by moderate kinase activity BRAF mutants |
38 |
2.80e-01 |
5.94e-01 |
0.1510 |
-4.45e-02 |
-0.145000 |
6.35e-01 |
1.23e-01 |
Signaling downstream of RAS mutants |
38 |
2.80e-01 |
5.94e-01 |
0.1510 |
-4.45e-02 |
-0.145000 |
6.35e-01 |
1.23e-01 |
Signaling by ERBB2 KD Mutants |
22 |
4.60e-01 |
7.52e-01 |
0.1510 |
-1.41e-01 |
0.056000 |
2.54e-01 |
6.49e-01 |
Deadenylation-dependent mRNA decay |
44 |
2.27e-01 |
5.26e-01 |
0.1510 |
1.50e-01 |
0.020900 |
8.63e-02 |
8.10e-01 |
SUMOylation of intracellular receptors |
25 |
4.17e-01 |
7.24e-01 |
0.1510 |
1.44e-01 |
-0.043800 |
2.11e-01 |
7.05e-01 |
Downstream signaling of activated FGFR1 |
21 |
5.04e-01 |
7.82e-01 |
0.1500 |
1.24e-01 |
0.084600 |
3.24e-01 |
5.02e-01 |
RNA Pol II CTD phosphorylation and interaction with CE |
20 |
5.20e-01 |
7.87e-01 |
0.1500 |
-7.83e-02 |
-0.128000 |
5.44e-01 |
3.20e-01 |
RNA Pol II CTD phosphorylation and interaction with CE during HIV infection |
20 |
5.20e-01 |
7.87e-01 |
0.1500 |
-7.83e-02 |
-0.128000 |
5.44e-01 |
3.20e-01 |
Nucleobase catabolism |
27 |
4.06e-01 |
7.16e-01 |
0.1500 |
1.48e-01 |
0.028600 |
1.85e-01 |
7.97e-01 |
ISG15 antiviral mechanism |
50 |
1.85e-01 |
4.74e-01 |
0.1500 |
1.50e-01 |
0.000842 |
6.64e-02 |
9.92e-01 |
Metabolism of RNA |
492 |
7.54e-08 |
3.65e-06 |
0.1500 |
1.41e-01 |
-0.051900 |
1.19e-07 |
5.09e-02 |
Autophagy |
101 |
3.87e-02 |
1.85e-01 |
0.1500 |
-8.26e-02 |
-0.125000 |
1.52e-01 |
3.01e-02 |
DNA Double Strand Break Response |
35 |
2.99e-01 |
6.12e-01 |
0.1500 |
1.41e-01 |
-0.049400 |
1.48e-01 |
6.13e-01 |
Vpr-mediated nuclear import of PICs |
24 |
4.63e-01 |
7.53e-01 |
0.1490 |
8.35e-02 |
0.124000 |
4.79e-01 |
2.94e-01 |
Sialic acid metabolism |
23 |
4.59e-01 |
7.52e-01 |
0.1490 |
-1.47e-01 |
0.027400 |
2.24e-01 |
8.20e-01 |
ER to Golgi Anterograde Transport |
108 |
2.60e-02 |
1.45e-01 |
0.1490 |
-1.44e-01 |
0.038400 |
9.86e-03 |
4.91e-01 |
G-protein beta:gamma signalling |
23 |
4.73e-01 |
7.61e-01 |
0.1490 |
-3.92e-02 |
-0.144000 |
7.45e-01 |
2.33e-01 |
tRNA modification in the nucleus and cytosol |
32 |
3.38e-01 |
6.60e-01 |
0.1490 |
4.04e-02 |
-0.143000 |
6.93e-01 |
1.61e-01 |
Signaling by ERBB2 ECD mutants |
15 |
6.11e-01 |
8.29e-01 |
0.1490 |
-1.48e-01 |
-0.018400 |
3.23e-01 |
9.02e-01 |
Diseases associated with the TLR signaling cascade |
20 |
5.08e-01 |
7.83e-01 |
0.1490 |
-1.43e-01 |
0.041400 |
2.69e-01 |
7.48e-01 |
Diseases of Immune System |
20 |
5.08e-01 |
7.83e-01 |
0.1490 |
-1.43e-01 |
0.041400 |
2.69e-01 |
7.48e-01 |
Signaling by FGFR3 in disease |
16 |
5.77e-01 |
8.24e-01 |
0.1480 |
1.22e-01 |
-0.084400 |
3.98e-01 |
5.59e-01 |
Signaling by FGFR3 point mutants in cancer |
16 |
5.77e-01 |
8.24e-01 |
0.1480 |
1.22e-01 |
-0.084400 |
3.98e-01 |
5.59e-01 |
Apoptotic cleavage of cellular proteins |
31 |
3.47e-01 |
6.69e-01 |
0.1480 |
-6.87e-02 |
0.131000 |
5.08e-01 |
2.06e-01 |
Regulation of cholesterol biosynthesis by SREBP (SREBF) |
50 |
2.08e-01 |
5.01e-01 |
0.1480 |
-1.16e-01 |
-0.091700 |
1.55e-01 |
2.63e-01 |
Pausing and recovery of Tat-mediated HIV elongation |
20 |
5.23e-01 |
7.87e-01 |
0.1480 |
-2.71e-02 |
-0.146000 |
8.34e-01 |
2.60e-01 |
Tat-mediated HIV elongation arrest and recovery |
20 |
5.23e-01 |
7.87e-01 |
0.1480 |
-2.71e-02 |
-0.146000 |
8.34e-01 |
2.60e-01 |
Regulation of insulin secretion |
58 |
1.49e-01 |
4.25e-01 |
0.1480 |
-1.48e-01 |
0.001620 |
5.15e-02 |
9.83e-01 |
Activation of G protein gated Potassium channels |
16 |
5.82e-01 |
8.24e-01 |
0.1480 |
5.31e-02 |
-0.138000 |
7.13e-01 |
3.39e-01 |
G protein gated Potassium channels |
16 |
5.82e-01 |
8.24e-01 |
0.1480 |
5.31e-02 |
-0.138000 |
7.13e-01 |
3.39e-01 |
Inhibition of voltage gated Ca2+ channels via Gbeta/gamma subunits |
16 |
5.82e-01 |
8.24e-01 |
0.1480 |
5.31e-02 |
-0.138000 |
7.13e-01 |
3.39e-01 |
RIP-mediated NFkB activation via ZBP1 |
15 |
6.14e-01 |
8.29e-01 |
0.1480 |
-1.47e-01 |
-0.013900 |
3.24e-01 |
9.26e-01 |
FRS-mediated FGFR1 signaling |
13 |
6.43e-01 |
8.44e-01 |
0.1470 |
1.13e-01 |
-0.094600 |
4.80e-01 |
5.55e-01 |
Downregulation of SMAD2/3:SMAD4 transcriptional activity |
17 |
5.84e-01 |
8.24e-01 |
0.1470 |
4.32e-02 |
0.141000 |
7.58e-01 |
3.16e-01 |
Regulation of actin dynamics for phagocytic cup formation |
60 |
1.54e-01 |
4.28e-01 |
0.1470 |
1.31e-01 |
0.066400 |
7.97e-02 |
3.74e-01 |
G beta:gamma signalling through CDC42 |
12 |
6.90e-01 |
8.69e-01 |
0.1470 |
-9.71e-02 |
-0.110000 |
5.60e-01 |
5.11e-01 |
TRAF3-dependent IRF activation pathway |
13 |
6.69e-01 |
8.57e-01 |
0.1460 |
1.24e-01 |
0.077900 |
4.39e-01 |
6.27e-01 |
Rho GTPase cycle |
122 |
1.86e-02 |
1.15e-01 |
0.1460 |
-1.38e-01 |
0.048300 |
8.61e-03 |
3.58e-01 |
JNK (c-Jun kinases) phosphorylation and activation mediated by activated human TAK1 |
16 |
5.89e-01 |
8.27e-01 |
0.1460 |
-8.47e-02 |
0.119000 |
5.58e-01 |
4.12e-01 |
SHC1 events in ERBB2 signaling |
20 |
5.37e-01 |
8.00e-01 |
0.1460 |
-1.39e-01 |
-0.042100 |
2.81e-01 |
7.45e-01 |
HIV elongation arrest and recovery |
21 |
5.13e-01 |
7.84e-01 |
0.1460 |
1.17e-03 |
-0.146000 |
9.93e-01 |
2.48e-01 |
Pausing and recovery of HIV elongation |
21 |
5.13e-01 |
7.84e-01 |
0.1460 |
1.17e-03 |
-0.146000 |
9.93e-01 |
2.48e-01 |
ADP signalling through P2Y purinoceptor 12 |
14 |
6.39e-01 |
8.42e-01 |
0.1450 |
1.96e-02 |
-0.144000 |
8.99e-01 |
3.51e-01 |
VEGFR2 mediated vascular permeability |
26 |
4.35e-01 |
7.37e-01 |
0.1450 |
-2.06e-02 |
0.144000 |
8.56e-01 |
2.05e-01 |
PIWI-interacting RNA (piRNA) biogenesis |
11 |
7.15e-01 |
8.83e-01 |
0.1450 |
1.28e-01 |
0.068000 |
4.61e-01 |
6.96e-01 |
Notch-HLH transcription pathway |
24 |
4.55e-01 |
7.50e-01 |
0.1450 |
-8.98e-02 |
0.114000 |
4.47e-01 |
3.34e-01 |
ZBP1(DAI) mediated induction of type I IFNs |
18 |
5.78e-01 |
8.24e-01 |
0.1450 |
-1.29e-01 |
-0.066200 |
3.44e-01 |
6.27e-01 |
N-glycan antennae elongation in the medial/trans-Golgi |
19 |
5.58e-01 |
8.16e-01 |
0.1440 |
1.86e-02 |
0.143000 |
8.88e-01 |
2.82e-01 |
Macroautophagy |
90 |
7.02e-02 |
2.68e-01 |
0.1440 |
-9.74e-02 |
-0.106000 |
1.11e-01 |
8.35e-02 |
Interactions of Rev with host cellular proteins |
26 |
4.48e-01 |
7.44e-01 |
0.1430 |
1.43e-01 |
-0.009400 |
2.08e-01 |
9.34e-01 |
TRAF6 mediated NF-kB activation |
20 |
5.32e-01 |
7.94e-01 |
0.1430 |
-1.32e-01 |
0.053900 |
3.05e-01 |
6.76e-01 |
Erythropoietin activates RAS |
12 |
6.84e-01 |
8.65e-01 |
0.1430 |
1.27e-01 |
-0.064600 |
4.45e-01 |
6.98e-01 |
Biosynthesis of the N-glycan precursor (dolichol lipid-linked oligosaccharide, LLO) and transfer to a nascent protein |
60 |
1.52e-01 |
4.28e-01 |
0.1430 |
-1.32e-01 |
0.054300 |
7.69e-02 |
4.68e-01 |
Regulation of PTEN mRNA translation |
11 |
7.08e-01 |
8.81e-01 |
0.1430 |
-1.35e-01 |
0.046900 |
4.39e-01 |
7.88e-01 |
Interleukin-10 signaling |
24 |
4.82e-01 |
7.69e-01 |
0.1430 |
1.43e-01 |
0.005470 |
2.27e-01 |
9.63e-01 |
Recruitment of NuMA to mitotic centrosomes |
68 |
1.23e-01 |
3.77e-01 |
0.1420 |
-3.57e-02 |
0.138000 |
6.11e-01 |
5.01e-02 |
NEP/NS2 Interacts with the Cellular Export Machinery |
23 |
5.05e-01 |
7.82e-01 |
0.1420 |
1.39e-01 |
0.030400 |
2.50e-01 |
8.01e-01 |
Signaling by EGFR |
42 |
2.70e-01 |
5.88e-01 |
0.1420 |
-1.22e-01 |
0.071700 |
1.71e-01 |
4.22e-01 |
Assembly and cell surface presentation of NMDA receptors |
17 |
6.10e-01 |
8.29e-01 |
0.1420 |
-6.05e-02 |
-0.128000 |
6.66e-01 |
3.61e-01 |
Platelet homeostasis |
65 |
1.49e-01 |
4.25e-01 |
0.1420 |
-1.37e-01 |
-0.036000 |
5.66e-02 |
6.16e-01 |
PLC beta mediated events |
46 |
2.40e-01 |
5.45e-01 |
0.1410 |
-1.21e-01 |
0.073100 |
1.56e-01 |
3.91e-01 |
Visual phototransduction |
50 |
2.41e-01 |
5.45e-01 |
0.1410 |
-1.20e-01 |
-0.073100 |
1.42e-01 |
3.71e-01 |
Inactivation, recovery and regulation of the phototransduction cascade |
17 |
6.09e-01 |
8.29e-01 |
0.1400 |
-1.39e-01 |
-0.022100 |
3.23e-01 |
8.75e-01 |
The phototransduction cascade |
17 |
6.09e-01 |
8.29e-01 |
0.1400 |
-1.39e-01 |
-0.022100 |
3.23e-01 |
8.75e-01 |
UCH proteinases |
68 |
1.32e-01 |
3.92e-01 |
0.1400 |
1.38e-01 |
-0.026200 |
4.99e-02 |
7.09e-01 |
Kinesins |
36 |
3.64e-01 |
6.83e-01 |
0.1400 |
1.10e-01 |
0.085800 |
2.52e-01 |
3.73e-01 |
Mitochondrial Fatty Acid Beta-Oxidation |
27 |
4.43e-01 |
7.40e-01 |
0.1390 |
1.22e-01 |
-0.066900 |
2.72e-01 |
5.48e-01 |
Amino acid transport across the plasma membrane |
23 |
5.08e-01 |
7.83e-01 |
0.1390 |
1.38e-01 |
-0.018200 |
2.52e-01 |
8.80e-01 |
Gamma carboxylation, hypusine formation and arylsulfatase activation |
26 |
4.66e-01 |
7.54e-01 |
0.1390 |
-1.38e-01 |
0.020700 |
2.25e-01 |
8.55e-01 |
MET activates RAP1 and RAC1 |
11 |
7.36e-01 |
8.94e-01 |
0.1390 |
1.25e-01 |
0.060900 |
4.75e-01 |
7.27e-01 |
G-protein mediated events |
47 |
2.45e-01 |
5.52e-01 |
0.1390 |
-1.12e-01 |
0.081200 |
1.83e-01 |
3.36e-01 |
Metabolism of non-coding RNA |
39 |
3.27e-01 |
6.48e-01 |
0.1380 |
1.38e-01 |
-0.002160 |
1.35e-01 |
9.81e-01 |
snRNP Assembly |
39 |
3.27e-01 |
6.48e-01 |
0.1380 |
1.38e-01 |
-0.002160 |
1.35e-01 |
9.81e-01 |
Cell-Cell communication |
78 |
1.01e-01 |
3.37e-01 |
0.1380 |
-5.78e-02 |
0.125000 |
3.78e-01 |
5.58e-02 |
Protein localization |
123 |
2.67e-02 |
1.47e-01 |
0.1380 |
7.97e-02 |
-0.113000 |
1.28e-01 |
3.14e-02 |
CaM pathway |
30 |
4.26e-01 |
7.31e-01 |
0.1380 |
-1.38e-01 |
-0.004460 |
1.92e-01 |
9.66e-01 |
Calmodulin induced events |
30 |
4.26e-01 |
7.31e-01 |
0.1380 |
-1.38e-01 |
-0.004460 |
1.92e-01 |
9.66e-01 |
EPH-ephrin mediated repulsion of cells |
41 |
2.98e-01 |
6.12e-01 |
0.1380 |
-1.15e-01 |
0.075400 |
2.02e-01 |
4.04e-01 |
Transcriptional Regulation by VENTX |
34 |
3.74e-01 |
6.89e-01 |
0.1380 |
-1.33e-01 |
0.034500 |
1.79e-01 |
7.28e-01 |
Unblocking of NMDA receptors, glutamate binding and activation |
15 |
6.61e-01 |
8.55e-01 |
0.1370 |
-1.30e-01 |
-0.043400 |
3.82e-01 |
7.71e-01 |
Degradation of beta-catenin by the destruction complex |
70 |
1.33e-01 |
3.93e-01 |
0.1370 |
1.24e-01 |
-0.056900 |
7.23e-02 |
4.11e-01 |
M Phase |
282 |
4.20e-04 |
6.30e-03 |
0.1370 |
1.37e-01 |
-0.006900 |
8.63e-05 |
8.43e-01 |
Signaling by NTRK3 (TRKC) |
17 |
6.28e-01 |
8.35e-01 |
0.1370 |
-4.08e-02 |
-0.131000 |
7.71e-01 |
3.52e-01 |
Physiological factors |
11 |
7.28e-01 |
8.89e-01 |
0.1370 |
-1.25e-01 |
0.054100 |
4.72e-01 |
7.56e-01 |
Metabolism of nucleotides |
77 |
1.08e-01 |
3.52e-01 |
0.1360 |
8.49e-02 |
-0.107000 |
1.98e-01 |
1.06e-01 |
Myogenesis |
21 |
5.57e-01 |
8.16e-01 |
0.1360 |
-1.23e-02 |
0.135000 |
9.22e-01 |
2.83e-01 |
MAP2K and MAPK activation |
32 |
4.17e-01 |
7.24e-01 |
0.1350 |
-7.16e-03 |
-0.135000 |
9.44e-01 |
1.86e-01 |
Cell recruitment (pro-inflammatory response) |
18 |
6.09e-01 |
8.29e-01 |
0.1350 |
-1.75e-02 |
0.134000 |
8.98e-01 |
3.26e-01 |
Purinergic signaling in leishmaniasis infection |
18 |
6.09e-01 |
8.29e-01 |
0.1350 |
-1.75e-02 |
0.134000 |
8.98e-01 |
3.26e-01 |
Adaptive Immune System |
542 |
1.09e-06 |
4.42e-05 |
0.1350 |
1.27e-01 |
0.045300 |
5.79e-07 |
7.46e-02 |
Synthesis of glycosylphosphatidylinositol (GPI) |
14 |
6.75e-01 |
8.60e-01 |
0.1340 |
-1.19e-01 |
0.061800 |
4.40e-01 |
6.89e-01 |
FGFR2 mutant receptor activation |
17 |
6.19e-01 |
8.30e-01 |
0.1340 |
-9.90e-02 |
0.090900 |
4.80e-01 |
5.17e-01 |
Transport to the Golgi and subsequent modification |
131 |
2.65e-02 |
1.46e-01 |
0.1340 |
-1.19e-01 |
0.062300 |
1.91e-02 |
2.19e-01 |
RUNX2 regulates osteoblast differentiation |
22 |
5.50e-01 |
8.13e-01 |
0.1330 |
-4.45e-02 |
0.125000 |
7.18e-01 |
3.09e-01 |
TBC/RABGAPs |
35 |
4.14e-01 |
7.24e-01 |
0.1320 |
-9.77e-02 |
-0.089400 |
3.17e-01 |
3.60e-01 |
mRNA decay by 5' to 3' exoribonuclease |
13 |
7.20e-01 |
8.84e-01 |
0.1320 |
7.32e-02 |
0.110000 |
6.48e-01 |
4.91e-01 |
NOTCH4 Intracellular Domain Regulates Transcription |
17 |
6.35e-01 |
8.40e-01 |
0.1320 |
-1.29e-01 |
0.027900 |
3.56e-01 |
8.42e-01 |
Synaptic adhesion-like molecules |
17 |
6.52e-01 |
8.49e-01 |
0.1320 |
-1.07e-01 |
-0.077200 |
4.44e-01 |
5.82e-01 |
Transcriptional activation of mitochondrial biogenesis |
49 |
2.79e-01 |
5.94e-01 |
0.1320 |
-5.58e-03 |
-0.132000 |
9.46e-01 |
1.10e-01 |
Chaperone Mediated Autophagy |
13 |
7.17e-01 |
8.83e-01 |
0.1320 |
-2.91e-02 |
-0.129000 |
8.56e-01 |
4.22e-01 |
Ras activation upon Ca2+ influx through NMDA receptor |
15 |
6.81e-01 |
8.63e-01 |
0.1320 |
-1.29e-01 |
-0.028500 |
3.88e-01 |
8.49e-01 |
Processing of Capped Intron-Containing Pre-mRNA |
180 |
1.10e-02 |
7.94e-02 |
0.1310 |
1.29e-01 |
0.024200 |
2.96e-03 |
5.77e-01 |
mRNA Splicing - Major Pathway |
133 |
3.50e-02 |
1.71e-01 |
0.1310 |
1.30e-01 |
0.016600 |
9.89e-03 |
7.42e-01 |
Deactivation of the beta-catenin transactivating complex |
31 |
4.46e-01 |
7.42e-01 |
0.1300 |
-1.25e-01 |
0.037900 |
2.30e-01 |
7.15e-01 |
Activation of IRF3/IRF7 mediated by TBK1/IKK epsilon |
12 |
7.33e-01 |
8.93e-01 |
0.1290 |
-1.14e-01 |
0.061200 |
4.96e-01 |
7.14e-01 |
Class I MHC mediated antigen processing & presentation |
289 |
1.12e-03 |
1.36e-02 |
0.1290 |
1.17e-01 |
0.053500 |
6.63e-04 |
1.20e-01 |
TICAM1, RIP1-mediated IKK complex recruitment |
12 |
7.45e-01 |
8.98e-01 |
0.1290 |
2.10e-02 |
0.127000 |
9.00e-01 |
4.47e-01 |
PKMTs methylate histone lysines |
35 |
4.17e-01 |
7.24e-01 |
0.1290 |
-1.28e-02 |
0.128000 |
8.96e-01 |
1.91e-01 |
RNA Polymerase I Promoter Escape |
21 |
6.08e-01 |
8.29e-01 |
0.1290 |
-8.37e-02 |
-0.097500 |
5.07e-01 |
4.39e-01 |
Tristetraprolin (TTP, ZFP36) binds and destabilizes mRNA |
14 |
7.02e-01 |
8.79e-01 |
0.1280 |
4.08e-02 |
-0.121000 |
7.92e-01 |
4.32e-01 |
Vitamin B5 (pantothenate) metabolism |
12 |
7.54e-01 |
9.04e-01 |
0.1280 |
7.93e-02 |
0.100000 |
6.34e-01 |
5.47e-01 |
PI3K Cascade |
29 |
4.88e-01 |
7.71e-01 |
0.1280 |
-1.42e-02 |
0.127000 |
8.95e-01 |
2.37e-01 |
Synthesis of bile acids and bile salts |
22 |
5.92e-01 |
8.29e-01 |
0.1280 |
4.09e-02 |
0.121000 |
7.40e-01 |
3.26e-01 |
B-WICH complex positively regulates rRNA expression |
24 |
5.66e-01 |
8.21e-01 |
0.1280 |
1.18e-01 |
0.047800 |
3.16e-01 |
6.85e-01 |
Signaling by ERBB2 in Cancer |
23 |
5.59e-01 |
8.17e-01 |
0.1270 |
-1.09e-01 |
0.065700 |
3.65e-01 |
5.86e-01 |
Ephrin signaling |
19 |
6.22e-01 |
8.30e-01 |
0.1270 |
-1.17e-01 |
0.050000 |
3.77e-01 |
7.06e-01 |
Constitutive Signaling by Overexpressed ERBB2 |
10 |
7.86e-01 |
9.23e-01 |
0.1270 |
-1.35e-02 |
-0.126000 |
9.41e-01 |
4.89e-01 |
Class I peroxisomal membrane protein import |
15 |
7.05e-01 |
8.79e-01 |
0.1270 |
6.93e-02 |
0.107000 |
6.42e-01 |
4.75e-01 |
RNA Polymerase III Transcription Termination |
18 |
6.36e-01 |
8.40e-01 |
0.1270 |
1.05e-01 |
-0.071200 |
4.40e-01 |
6.01e-01 |
Beta-catenin phosphorylation cascade |
16 |
6.70e-01 |
8.57e-01 |
0.1270 |
-6.91e-02 |
0.106000 |
6.32e-01 |
4.62e-01 |
Signaling by SCF-KIT |
42 |
3.71e-01 |
6.89e-01 |
0.1270 |
2.48e-02 |
0.124000 |
7.82e-01 |
1.64e-01 |
Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks |
34 |
4.32e-01 |
7.34e-01 |
0.1270 |
1.16e-01 |
-0.049500 |
2.40e-01 |
6.17e-01 |
CASP8 activity is inhibited |
10 |
7.94e-01 |
9.26e-01 |
0.1260 |
7.11e-02 |
0.104000 |
6.97e-01 |
5.67e-01 |
Dimerization of procaspase-8 |
10 |
7.94e-01 |
9.26e-01 |
0.1260 |
7.11e-02 |
0.104000 |
6.97e-01 |
5.67e-01 |
Regulation by c-FLIP |
10 |
7.94e-01 |
9.26e-01 |
0.1260 |
7.11e-02 |
0.104000 |
6.97e-01 |
5.67e-01 |
FOXO-mediated transcription of cell cycle genes |
15 |
6.90e-01 |
8.69e-01 |
0.1260 |
-5.64e-02 |
0.113000 |
7.05e-01 |
4.49e-01 |
Constitutive Signaling by EGFRvIII |
15 |
7.06e-01 |
8.79e-01 |
0.1260 |
-1.17e-01 |
-0.046600 |
4.31e-01 |
7.55e-01 |
Constitutive Signaling by Ligand-Responsive EGFR Cancer Variants |
15 |
7.06e-01 |
8.79e-01 |
0.1260 |
-1.17e-01 |
-0.046600 |
4.31e-01 |
7.55e-01 |
Signaling by EGFRvIII in Cancer |
15 |
7.06e-01 |
8.79e-01 |
0.1260 |
-1.17e-01 |
-0.046600 |
4.31e-01 |
7.55e-01 |
Signaling by Ligand-Responsive EGFR Variants in Cancer |
15 |
7.06e-01 |
8.79e-01 |
0.1260 |
-1.17e-01 |
-0.046600 |
4.31e-01 |
7.55e-01 |
Asymmetric localization of PCP proteins |
52 |
2.91e-01 |
6.05e-01 |
0.1260 |
-8.21e-03 |
-0.126000 |
9.19e-01 |
1.16e-01 |
Rev-mediated nuclear export of HIV RNA |
25 |
5.56e-01 |
8.16e-01 |
0.1260 |
1.24e-01 |
0.022200 |
2.83e-01 |
8.48e-01 |
RHO GTPases activate PKNs |
31 |
4.88e-01 |
7.71e-01 |
0.1260 |
-3.66e-02 |
-0.120000 |
7.24e-01 |
2.47e-01 |
PKA activation |
17 |
6.68e-01 |
8.57e-01 |
0.1250 |
-1.23e-01 |
0.022300 |
3.80e-01 |
8.74e-01 |
mRNA Splicing |
141 |
3.98e-02 |
1.88e-01 |
0.1240 |
1.24e-01 |
0.006160 |
1.11e-02 |
9.00e-01 |
Inositol phosphate metabolism |
41 |
4.03e-01 |
7.15e-01 |
0.1240 |
-7.81e-02 |
-0.096700 |
3.87e-01 |
2.85e-01 |
Regulation of beta-cell development |
21 |
6.08e-01 |
8.29e-01 |
0.1240 |
-1.18e-01 |
0.037400 |
3.48e-01 |
7.67e-01 |
Regulation of signaling by CBL |
18 |
6.65e-01 |
8.57e-01 |
0.1240 |
1.22e-01 |
0.020200 |
3.70e-01 |
8.82e-01 |
Negative regulation of FGFR2 signaling |
21 |
6.06e-01 |
8.29e-01 |
0.1240 |
-6.35e-02 |
0.106000 |
6.14e-01 |
3.99e-01 |
Listeria monocytogenes entry into host cells |
15 |
7.00e-01 |
8.78e-01 |
0.1240 |
-1.03e-01 |
0.068700 |
4.91e-01 |
6.45e-01 |
Nuclear Events (kinase and transcription factor activation) |
55 |
2.70e-01 |
5.88e-01 |
0.1240 |
-9.26e-02 |
0.081800 |
2.35e-01 |
2.95e-01 |
EPHA-mediated growth cone collapse |
13 |
7.39e-01 |
8.94e-01 |
0.1230 |
-3.05e-02 |
0.119000 |
8.49e-01 |
4.56e-01 |
Regulation of PLK1 Activity at G2/M Transition |
71 |
2.03e-01 |
4.99e-01 |
0.1230 |
1.54e-02 |
0.122000 |
8.23e-01 |
7.53e-02 |
Signalling to ERKs |
32 |
4.71e-01 |
7.60e-01 |
0.1230 |
6.41e-02 |
-0.105000 |
5.31e-01 |
3.04e-01 |
Negative epigenetic regulation of rRNA expression |
36 |
4.28e-01 |
7.32e-01 |
0.1230 |
9.83e-02 |
-0.073900 |
3.08e-01 |
4.43e-01 |
Asparagine N-linked glycosylation |
217 |
6.73e-03 |
5.68e-02 |
0.1230 |
-1.09e-01 |
0.057100 |
5.96e-03 |
1.49e-01 |
Nuclear signaling by ERBB4 |
24 |
5.73e-01 |
8.24e-01 |
0.1230 |
-1.16e-01 |
0.039600 |
3.24e-01 |
7.37e-01 |
Protein ubiquitination |
42 |
3.83e-01 |
7.00e-01 |
0.1230 |
1.20e-01 |
-0.025000 |
1.79e-01 |
7.79e-01 |
Post-translational modification: synthesis of GPI-anchored proteins |
55 |
2.78e-01 |
5.94e-01 |
0.1220 |
-7.02e-02 |
0.100000 |
3.68e-01 |
1.99e-01 |
Regulation of TNFR1 signaling |
25 |
5.79e-01 |
8.24e-01 |
0.1220 |
1.19e-01 |
0.025800 |
3.03e-01 |
8.23e-01 |
Glycosaminoglycan metabolism |
89 |
1.31e-01 |
3.92e-01 |
0.1220 |
-1.09e-01 |
0.053400 |
7.50e-02 |
3.85e-01 |
Centrosome maturation |
69 |
2.11e-01 |
5.03e-01 |
0.1210 |
-4.21e-02 |
0.114000 |
5.46e-01 |
1.03e-01 |
Recruitment of mitotic centrosome proteins and complexes |
69 |
2.11e-01 |
5.03e-01 |
0.1210 |
-4.21e-02 |
0.114000 |
5.46e-01 |
1.03e-01 |
NS1 Mediated Effects on Host Pathways |
27 |
5.64e-01 |
8.21e-01 |
0.1210 |
1.11e-01 |
0.046900 |
3.17e-01 |
6.73e-01 |
Lysosome Vesicle Biogenesis |
27 |
5.57e-01 |
8.16e-01 |
0.1210 |
-1.20e-01 |
-0.012100 |
2.80e-01 |
9.14e-01 |
Insertion of tail-anchored proteins into the endoplasmic reticulum membrane |
15 |
7.18e-01 |
8.83e-01 |
0.1210 |
1.20e-01 |
-0.015200 |
4.23e-01 |
9.19e-01 |
Tetrahydrobiopterin (BH4) synthesis, recycling, salvage and regulation |
10 |
8.06e-01 |
9.36e-01 |
0.1200 |
1.19e-01 |
-0.008850 |
5.14e-01 |
9.61e-01 |
FCERI mediated Ca+2 mobilization |
25 |
5.99e-01 |
8.29e-01 |
0.1200 |
8.71e-02 |
0.081800 |
4.51e-01 |
4.79e-01 |
DNA Damage/Telomere Stress Induced Senescence |
23 |
6.03e-01 |
8.29e-01 |
0.1190 |
1.10e-01 |
-0.046800 |
3.63e-01 |
6.98e-01 |
Hedgehog 'on' state |
68 |
2.23e-01 |
5.21e-01 |
0.1190 |
9.12e-02 |
-0.076600 |
1.94e-01 |
2.75e-01 |
Signaling by Receptor Tyrosine Kinases |
394 |
2.17e-04 |
3.79e-03 |
0.1190 |
-7.13e-02 |
0.095300 |
1.59e-02 |
1.28e-03 |
CTLA4 inhibitory signaling |
21 |
6.41e-01 |
8.43e-01 |
0.1190 |
1.19e-01 |
-0.001920 |
3.46e-01 |
9.88e-01 |
MAP3K8 (TPL2)-dependent MAPK1/3 activation |
12 |
7.86e-01 |
9.23e-01 |
0.1180 |
6.44e-02 |
0.099000 |
6.99e-01 |
5.53e-01 |
Dopamine Neurotransmitter Release Cycle |
14 |
7.55e-01 |
9.05e-01 |
0.1180 |
9.42e-02 |
0.071100 |
5.42e-01 |
6.45e-01 |
RNA Polymerase I Transcription |
39 |
4.54e-01 |
7.50e-01 |
0.1180 |
-4.41e-02 |
-0.109000 |
6.34e-01 |
2.37e-01 |
Nucleotide-binding domain, leucine rich repeat containing receptor (NLR) signaling pathways |
44 |
3.84e-01 |
7.01e-01 |
0.1180 |
-8.65e-02 |
0.080300 |
3.21e-01 |
3.57e-01 |
G2/M Transition |
149 |
4.57e-02 |
2.03e-01 |
0.1180 |
1.18e-01 |
-0.007730 |
1.35e-02 |
8.71e-01 |
Diseases associated with glycosaminoglycan metabolism |
33 |
4.90e-01 |
7.71e-01 |
0.1180 |
-9.25e-02 |
0.072900 |
3.58e-01 |
4.69e-01 |
Export of Viral Ribonucleoproteins from Nucleus |
24 |
6.20e-01 |
8.30e-01 |
0.1180 |
9.44e-02 |
0.070100 |
4.23e-01 |
5.52e-01 |
Negative regulation of MAPK pathway |
38 |
4.61e-01 |
7.52e-01 |
0.1180 |
-2.16e-02 |
-0.116000 |
8.18e-01 |
2.18e-01 |
Constitutive Signaling by AKT1 E17K in Cancer |
24 |
6.10e-01 |
8.29e-01 |
0.1170 |
-7.74e-03 |
-0.117000 |
9.48e-01 |
3.21e-01 |
RUNX1 interacts with co-factors whose precise effect on RUNX1 targets is not known |
35 |
4.71e-01 |
7.60e-01 |
0.1170 |
-9.57e-02 |
0.068100 |
3.28e-01 |
4.86e-01 |
RHO GTPases Activate ROCKs |
18 |
6.81e-01 |
8.63e-01 |
0.1170 |
-9.71e-02 |
0.065200 |
4.76e-01 |
6.32e-01 |
RHO GTPases Activate Formins |
94 |
1.54e-01 |
4.28e-01 |
0.1170 |
1.13e-01 |
0.031000 |
5.97e-02 |
6.04e-01 |
Chondroitin sulfate/dermatan sulfate metabolism |
40 |
4.40e-01 |
7.38e-01 |
0.1170 |
-1.17e-01 |
0.006520 |
2.02e-01 |
9.43e-01 |
Nuclear import of Rev protein |
24 |
6.12e-01 |
8.29e-01 |
0.1170 |
1.17e-01 |
-0.004190 |
3.23e-01 |
9.72e-01 |
Neddylation |
180 |
2.40e-02 |
1.38e-01 |
0.1170 |
1.08e-01 |
-0.044300 |
1.29e-02 |
3.07e-01 |
Signaling by RAF1 mutants |
35 |
4.93e-01 |
7.73e-01 |
0.1160 |
-6.55e-03 |
-0.116000 |
9.47e-01 |
2.34e-01 |
Regulation of TP53 Activity through Phosphorylation |
76 |
2.05e-01 |
4.99e-01 |
0.1160 |
1.06e-01 |
-0.047300 |
1.10e-01 |
4.76e-01 |
Synthesis of substrates in N-glycan biosythesis |
48 |
3.69e-01 |
6.89e-01 |
0.1160 |
-1.06e-01 |
0.048000 |
2.06e-01 |
5.66e-01 |
Regulation of RUNX1 Expression and Activity |
16 |
7.15e-01 |
8.83e-01 |
0.1160 |
-9.23e-02 |
0.070100 |
5.23e-01 |
6.27e-01 |
Acyl chain remodelling of PE |
15 |
7.40e-01 |
8.94e-01 |
0.1160 |
1.16e-01 |
0.004470 |
4.37e-01 |
9.76e-01 |
Signaling by TGF-beta Receptor Complex |
57 |
3.34e-01 |
6.56e-01 |
0.1160 |
6.98e-02 |
0.092400 |
3.62e-01 |
2.28e-01 |
Mitotic G2-G2/M phases |
151 |
5.03e-02 |
2.13e-01 |
0.1150 |
1.15e-01 |
-0.002900 |
1.47e-02 |
9.51e-01 |
Negative regulation of FGFR1 signaling |
19 |
6.94e-01 |
8.72e-01 |
0.1150 |
5.25e-02 |
0.103000 |
6.92e-01 |
4.39e-01 |
NOTCH1 Intracellular Domain Regulates Transcription |
40 |
4.40e-01 |
7.38e-01 |
0.1150 |
-6.04e-02 |
0.097800 |
5.09e-01 |
2.85e-01 |
Fc epsilon receptor (FCERI) signaling |
111 |
1.07e-01 |
3.51e-01 |
0.1150 |
1.10e-01 |
-0.034400 |
4.64e-02 |
5.32e-01 |
Role of LAT2/NTAL/LAB on calcium mobilization |
13 |
7.74e-01 |
9.19e-01 |
0.1150 |
1.15e-01 |
0.005280 |
4.74e-01 |
9.74e-01 |
SARS-CoV-1 Infection |
36 |
4.86e-01 |
7.71e-01 |
0.1150 |
-1.10e-01 |
0.030300 |
2.52e-01 |
7.53e-01 |
Intraflagellar transport |
35 |
4.90e-01 |
7.71e-01 |
0.1150 |
5.92e-02 |
-0.098000 |
5.45e-01 |
3.16e-01 |
Beta-catenin independent WNT signaling |
117 |
1.12e-01 |
3.57e-01 |
0.1140 |
-6.18e-02 |
-0.096200 |
2.49e-01 |
7.30e-02 |
Aberrant regulation of mitotic cell cycle due to RB1 defects |
33 |
5.23e-01 |
7.87e-01 |
0.1140 |
1.14e-01 |
-0.009870 |
2.59e-01 |
9.22e-01 |
Diseases of mitotic cell cycle |
33 |
5.23e-01 |
7.87e-01 |
0.1140 |
1.14e-01 |
-0.009870 |
2.59e-01 |
9.22e-01 |
MAPK6/MAPK4 signaling |
71 |
2.44e-01 |
5.50e-01 |
0.1130 |
6.08e-02 |
-0.095500 |
3.76e-01 |
1.65e-01 |
Chondroitin sulfate biosynthesis |
16 |
7.38e-01 |
8.94e-01 |
0.1130 |
-1.13e-01 |
-0.008620 |
4.36e-01 |
9.52e-01 |
Signaling by NTRKs |
119 |
9.87e-02 |
3.37e-01 |
0.1130 |
-1.06e-01 |
0.039000 |
4.66e-02 |
4.63e-01 |
GABA receptor activation |
33 |
5.28e-01 |
7.92e-01 |
0.1120 |
2.99e-02 |
-0.108000 |
7.67e-01 |
2.81e-01 |
Smooth Muscle Contraction |
34 |
5.29e-01 |
7.93e-01 |
0.1120 |
-1.12e-01 |
-0.012800 |
2.61e-01 |
8.98e-01 |
mRNA Capping |
21 |
6.85e-01 |
8.65e-01 |
0.1120 |
-8.22e-02 |
-0.076200 |
5.14e-01 |
5.46e-01 |
Regulation of MECP2 expression and activity |
25 |
6.25e-01 |
8.33e-01 |
0.1120 |
-1.12e-01 |
0.003990 |
3.34e-01 |
9.72e-01 |
ECM proteoglycans |
40 |
4.88e-01 |
7.71e-01 |
0.1120 |
-9.08e-02 |
-0.065100 |
3.21e-01 |
4.76e-01 |
Regulation of TP53 Activity through Association with Co-factors |
12 |
7.96e-01 |
9.28e-01 |
0.1110 |
-1.04e-01 |
0.039500 |
5.34e-01 |
8.13e-01 |
Transport of Mature mRNAs Derived from Intronless Transcripts |
31 |
5.67e-01 |
8.22e-01 |
0.1110 |
1.11e-01 |
0.007170 |
2.87e-01 |
9.45e-01 |
Transport of the SLBP Dependant Mature mRNA |
25 |
6.44e-01 |
8.44e-01 |
0.1110 |
8.53e-02 |
0.070400 |
4.60e-01 |
5.42e-01 |
Striated Muscle Contraction |
29 |
5.92e-01 |
8.29e-01 |
0.1100 |
-1.71e-02 |
-0.109000 |
8.73e-01 |
3.09e-01 |
Inwardly rectifying K+ channels |
21 |
6.78e-01 |
8.61e-01 |
0.1100 |
1.63e-02 |
-0.109000 |
8.97e-01 |
3.87e-01 |
Signaling by FGFR2 |
49 |
4.08e-01 |
7.16e-01 |
0.1100 |
-1.15e-02 |
0.110000 |
8.90e-01 |
1.85e-01 |
Activation of GABAB receptors |
30 |
5.79e-01 |
8.24e-01 |
0.1100 |
8.22e-03 |
-0.110000 |
9.38e-01 |
2.99e-01 |
GABA B receptor activation |
30 |
5.79e-01 |
8.24e-01 |
0.1100 |
8.22e-03 |
-0.110000 |
9.38e-01 |
2.99e-01 |
Factors involved in megakaryocyte development and platelet production |
98 |
1.74e-01 |
4.61e-01 |
0.1100 |
6.41e-03 |
0.110000 |
9.13e-01 |
6.14e-02 |
Transcriptional regulation by RUNX2 |
98 |
1.79e-01 |
4.63e-01 |
0.1090 |
1.08e-01 |
0.018700 |
6.58e-02 |
7.49e-01 |
Synthesis of PIPs at the Golgi membrane |
14 |
7.70e-01 |
9.17e-01 |
0.1090 |
-8.73e-02 |
0.065600 |
5.72e-01 |
6.71e-01 |
Recycling pathway of L1 |
27 |
6.13e-01 |
8.29e-01 |
0.1090 |
-2.59e-02 |
0.106000 |
8.16e-01 |
3.42e-01 |
Detoxification of Reactive Oxygen Species |
26 |
6.33e-01 |
8.40e-01 |
0.1090 |
1.08e-01 |
0.012700 |
3.41e-01 |
9.11e-01 |
N-Glycan antennae elongation |
12 |
8.14e-01 |
9.37e-01 |
0.1080 |
3.05e-02 |
0.104000 |
8.55e-01 |
5.33e-01 |
TP53 regulates transcription of additional cell cycle genes whose exact role in the p53 pathway remain uncertain |
18 |
7.30e-01 |
8.91e-01 |
0.1080 |
-1.20e-03 |
0.108000 |
9.93e-01 |
4.28e-01 |
Cardiac conduction |
97 |
1.73e-01 |
4.61e-01 |
0.1080 |
-7.96e-02 |
0.072800 |
1.76e-01 |
2.16e-01 |
Regulation of PTEN gene transcription |
54 |
3.81e-01 |
6.98e-01 |
0.1080 |
-3.93e-02 |
0.100000 |
6.18e-01 |
2.03e-01 |
Signaling by ERBB2 |
38 |
5.30e-01 |
7.93e-01 |
0.1080 |
-9.40e-02 |
-0.052200 |
3.16e-01 |
5.78e-01 |
Disorders of transmembrane transporters |
116 |
1.31e-01 |
3.91e-01 |
0.1070 |
1.03e-01 |
-0.030200 |
5.58e-02 |
5.76e-01 |
Defects in vitamin and cofactor metabolism |
14 |
7.92e-01 |
9.26e-01 |
0.1070 |
-9.62e-02 |
-0.047100 |
5.33e-01 |
7.60e-01 |
COPI-independent Golgi-to-ER retrograde traffic |
29 |
5.96e-01 |
8.29e-01 |
0.1070 |
-8.78e-02 |
0.061200 |
4.13e-01 |
5.69e-01 |
MET promotes cell motility |
28 |
6.18e-01 |
8.30e-01 |
0.1070 |
3.41e-03 |
-0.107000 |
9.75e-01 |
3.28e-01 |
Glucose metabolism |
70 |
3.02e-01 |
6.17e-01 |
0.1060 |
-1.05e-01 |
0.017900 |
1.30e-01 |
7.96e-01 |
Association of TriC/CCT with target proteins during biosynthesis |
30 |
6.16e-01 |
8.30e-01 |
0.1060 |
7.52e-02 |
0.075000 |
4.76e-01 |
4.78e-01 |
Transport of Ribonucleoproteins into the Host Nucleus |
23 |
6.88e-01 |
8.67e-01 |
0.1060 |
9.55e-02 |
0.045900 |
4.28e-01 |
7.03e-01 |
Circadian Clock |
58 |
3.69e-01 |
6.89e-01 |
0.1060 |
1.01e-01 |
-0.031800 |
1.84e-01 |
6.76e-01 |
Anchoring of the basal body to the plasma membrane |
80 |
2.52e-01 |
5.60e-01 |
0.1060 |
-4.29e-02 |
0.096700 |
5.07e-01 |
1.35e-01 |
Signaling by Hippo |
19 |
7.23e-01 |
8.85e-01 |
0.1060 |
-2.42e-02 |
0.103000 |
8.55e-01 |
4.38e-01 |
Elastic fibre formation |
34 |
5.71e-01 |
8.24e-01 |
0.1060 |
-1.04e-01 |
-0.019300 |
2.95e-01 |
8.45e-01 |
Signaling by Type 1 Insulin-like Growth Factor 1 Receptor (IGF1R) |
38 |
5.35e-01 |
7.97e-01 |
0.1060 |
1.63e-02 |
0.104000 |
8.62e-01 |
2.66e-01 |
Potassium Channels |
57 |
3.75e-01 |
6.89e-01 |
0.1060 |
-9.42e-02 |
0.047500 |
2.19e-01 |
5.35e-01 |
Plasma lipoprotein assembly, remodeling, and clearance |
44 |
4.99e-01 |
7.78e-01 |
0.1050 |
-9.02e-02 |
-0.053100 |
3.01e-01 |
5.43e-01 |
Interactions of Vpr with host cellular proteins |
26 |
6.68e-01 |
8.57e-01 |
0.1040 |
8.04e-02 |
0.066000 |
4.78e-01 |
5.60e-01 |
Nuclear Receptor transcription pathway |
44 |
4.81e-01 |
7.68e-01 |
0.1040 |
4.17e-02 |
-0.095100 |
6.33e-01 |
2.75e-01 |
Metabolism of carbohydrates |
217 |
3.17e-02 |
1.63e-01 |
0.1030 |
-1.02e-01 |
0.014100 |
9.71e-03 |
7.22e-01 |
cGMP effects |
13 |
8.09e-01 |
9.36e-01 |
0.1030 |
-9.94e-02 |
0.027700 |
5.35e-01 |
8.63e-01 |
SUMOylation of DNA methylation proteins |
15 |
7.82e-01 |
9.23e-01 |
0.1030 |
-9.03e-02 |
0.048800 |
5.45e-01 |
7.43e-01 |
Mitochondrial biogenesis |
67 |
3.53e-01 |
6.74e-01 |
0.1030 |
-1.60e-02 |
-0.101000 |
8.21e-01 |
1.52e-01 |
Constitutive Signaling by Aberrant PI3K in Cancer |
56 |
4.26e-01 |
7.31e-01 |
0.1020 |
2.56e-02 |
0.098800 |
7.41e-01 |
2.02e-01 |
Downregulation of TGF-beta receptor signaling |
19 |
7.44e-01 |
8.97e-01 |
0.1020 |
1.02e-01 |
-0.001730 |
4.43e-01 |
9.90e-01 |
RHO GTPase Effectors |
202 |
4.64e-02 |
2.03e-01 |
0.1020 |
1.02e-01 |
0.004400 |
1.32e-02 |
9.15e-01 |
SHC1 events in ERBB4 signaling |
12 |
8.25e-01 |
9.40e-01 |
0.1020 |
5.23e-02 |
-0.087100 |
7.54e-01 |
6.01e-01 |
Death Receptor Signalling |
112 |
1.67e-01 |
4.49e-01 |
0.1020 |
-6.52e-02 |
0.077900 |
2.34e-01 |
1.55e-01 |
Transport of the SLBP independent Mature mRNA |
24 |
7.02e-01 |
8.79e-01 |
0.1010 |
6.29e-02 |
0.079400 |
5.94e-01 |
5.01e-01 |
Regulation of HSF1-mediated heat shock response |
56 |
4.22e-01 |
7.30e-01 |
0.1000 |
-9.32e-02 |
0.036300 |
2.28e-01 |
6.38e-01 |
Ca-dependent events |
32 |
6.17e-01 |
8.30e-01 |
0.1000 |
-9.98e-02 |
0.007310 |
3.29e-01 |
9.43e-01 |
Activation of NMDA receptors and postsynaptic events |
62 |
3.86e-01 |
7.03e-01 |
0.1000 |
-9.39e-02 |
0.034400 |
2.02e-01 |
6.40e-01 |
Cytochrome P450 - arranged by substrate type |
31 |
6.42e-01 |
8.43e-01 |
0.0997 |
8.34e-02 |
0.054700 |
4.22e-01 |
5.99e-01 |
mTORC1-mediated signalling |
20 |
7.39e-01 |
8.94e-01 |
0.0992 |
9.56e-02 |
-0.026700 |
4.60e-01 |
8.36e-01 |
HIV Infection |
176 |
7.09e-02 |
2.70e-01 |
0.0990 |
8.50e-02 |
-0.050700 |
5.26e-02 |
2.48e-01 |
Interleukin-37 signaling |
18 |
7.74e-01 |
9.19e-01 |
0.0988 |
-9.34e-02 |
-0.032000 |
4.93e-01 |
8.14e-01 |
tRNA processing in the nucleus |
47 |
5.10e-01 |
7.84e-01 |
0.0983 |
1.09e-02 |
0.097700 |
8.98e-01 |
2.47e-01 |
Mitochondrial translation initiation |
64 |
3.99e-01 |
7.14e-01 |
0.0981 |
-3.24e-03 |
-0.098100 |
9.64e-01 |
1.75e-01 |
Mitotic Prophase |
66 |
4.00e-01 |
7.15e-01 |
0.0981 |
8.59e-02 |
0.047400 |
2.28e-01 |
5.06e-01 |
G alpha (s) signalling events |
80 |
3.26e-01 |
6.48e-01 |
0.0978 |
-9.55e-02 |
-0.021100 |
1.40e-01 |
7.45e-01 |
Muscle contraction |
154 |
1.10e-01 |
3.53e-01 |
0.0976 |
-9.59e-02 |
0.018600 |
4.07e-02 |
6.92e-01 |
Cell surface interactions at the vascular wall |
93 |
2.54e-01 |
5.63e-01 |
0.0976 |
5.07e-02 |
-0.083400 |
3.99e-01 |
1.65e-01 |
Glutamate and glutamine metabolism |
12 |
8.49e-01 |
9.41e-01 |
0.0972 |
-5.62e-02 |
-0.079300 |
7.36e-01 |
6.35e-01 |
Antigen processing: Ubiquitination & Proteasome degradation |
242 |
3.85e-02 |
1.84e-01 |
0.0971 |
8.95e-02 |
0.037600 |
1.69e-02 |
3.16e-01 |
Oncogenic MAPK signaling |
68 |
3.89e-01 |
7.04e-01 |
0.0967 |
-9.64e-02 |
-0.008240 |
1.70e-01 |
9.07e-01 |
Signaling by BRAF and RAF fusions |
54 |
4.80e-01 |
7.68e-01 |
0.0964 |
-9.31e-02 |
-0.025100 |
2.37e-01 |
7.50e-01 |
InlB-mediated entry of Listeria monocytogenes into host cell |
11 |
8.64e-01 |
9.46e-01 |
0.0961 |
-7.30e-02 |
-0.062600 |
6.75e-01 |
7.19e-01 |
Neuronal System |
244 |
3.29e-02 |
1.67e-01 |
0.0960 |
-8.76e-02 |
0.039400 |
1.91e-02 |
2.91e-01 |
Nef-mediates down modulation of cell surface receptors by recruiting them to clathrin adapters |
18 |
7.74e-01 |
9.19e-01 |
0.0960 |
3.82e-02 |
-0.088000 |
7.79e-01 |
5.18e-01 |
Cargo trafficking to the periciliary membrane |
38 |
6.06e-01 |
8.29e-01 |
0.0956 |
8.25e-02 |
0.048400 |
3.79e-01 |
6.06e-01 |
Transcriptional regulation of white adipocyte differentiation |
70 |
3.86e-01 |
7.03e-01 |
0.0956 |
4.57e-03 |
0.095400 |
9.47e-01 |
1.68e-01 |
Cargo recognition for clathrin-mediated endocytosis |
72 |
3.71e-01 |
6.89e-01 |
0.0955 |
-9.48e-02 |
0.011300 |
1.65e-01 |
8.68e-01 |
Acyl chain remodelling of PC |
17 |
7.85e-01 |
9.23e-01 |
0.0954 |
6.73e-02 |
-0.067600 |
6.31e-01 |
6.30e-01 |
Spry regulation of FGF signaling |
12 |
8.44e-01 |
9.41e-01 |
0.0951 |
-6.20e-02 |
0.072200 |
7.10e-01 |
6.65e-01 |
IGF1R signaling cascade |
37 |
6.14e-01 |
8.29e-01 |
0.0951 |
3.30e-02 |
0.089200 |
7.28e-01 |
3.48e-01 |
COPI-mediated anterograde transport |
70 |
3.94e-01 |
7.10e-01 |
0.0951 |
-9.37e-02 |
-0.016200 |
1.76e-01 |
8.15e-01 |
RNA Polymerase I Transcription Initiation |
35 |
6.36e-01 |
8.40e-01 |
0.0950 |
-6.18e-02 |
-0.072200 |
5.28e-01 |
4.60e-01 |
RNA Polymerase I Promoter Clearance |
38 |
6.09e-01 |
8.29e-01 |
0.0948 |
-3.58e-02 |
-0.087800 |
7.02e-01 |
3.49e-01 |
Fcgamma receptor (FCGR) dependent phagocytosis |
83 |
3.40e-01 |
6.61e-01 |
0.0947 |
8.82e-02 |
0.034600 |
1.66e-01 |
5.87e-01 |
C-type lectin receptors (CLRs) |
101 |
2.58e-01 |
5.68e-01 |
0.0944 |
9.34e-02 |
-0.013300 |
1.05e-01 |
8.17e-01 |
Transport of Mature mRNA Derived from an Intronless Transcript |
30 |
6.73e-01 |
8.59e-01 |
0.0943 |
9.35e-02 |
0.012300 |
3.76e-01 |
9.08e-01 |
SUMOylation of chromatin organization proteins |
44 |
5.77e-01 |
8.24e-01 |
0.0933 |
6.20e-02 |
0.069700 |
4.77e-01 |
4.24e-01 |
Signaling by NTRK1 (TRKA) |
104 |
2.47e-01 |
5.55e-01 |
0.0932 |
-7.81e-02 |
0.051000 |
1.70e-01 |
3.70e-01 |
Neurexins and neuroligins |
37 |
6.18e-01 |
8.30e-01 |
0.0932 |
-9.32e-02 |
-0.002040 |
3.27e-01 |
9.83e-01 |
Rap1 signalling |
15 |
8.25e-01 |
9.40e-01 |
0.0931 |
-9.14e-02 |
-0.017600 |
5.40e-01 |
9.06e-01 |
RORA activates gene expression |
17 |
8.07e-01 |
9.36e-01 |
0.0928 |
-2.77e-02 |
-0.088600 |
8.43e-01 |
5.27e-01 |
PI-3K cascade:FGFR3 |
12 |
8.58e-01 |
9.42e-01 |
0.0922 |
9.21e-02 |
0.004590 |
5.81e-01 |
9.78e-01 |
Oxidative Stress Induced Senescence |
55 |
4.84e-01 |
7.71e-01 |
0.0920 |
-7.30e-02 |
0.056000 |
3.49e-01 |
4.73e-01 |
TP53 Regulates Transcription of Genes Involved in Cytochrome C Release |
14 |
8.36e-01 |
9.41e-01 |
0.0919 |
-9.12e-02 |
0.011700 |
5.55e-01 |
9.40e-01 |
CLEC7A (Dectin-1) signaling |
80 |
3.57e-01 |
6.77e-01 |
0.0919 |
8.82e-02 |
-0.025800 |
1.73e-01 |
6.91e-01 |
Downstream signaling of activated FGFR3 |
18 |
7.89e-01 |
9.25e-01 |
0.0919 |
7.90e-02 |
-0.046900 |
5.62e-01 |
7.30e-01 |
Activation of kainate receptors upon glutamate binding |
20 |
7.85e-01 |
9.23e-01 |
0.0917 |
-5.65e-02 |
-0.072200 |
6.62e-01 |
5.77e-01 |
Calnexin/calreticulin cycle |
15 |
8.29e-01 |
9.40e-01 |
0.0913 |
-2.51e-04 |
0.091300 |
9.99e-01 |
5.41e-01 |
EPH-Ephrin signaling |
79 |
3.65e-01 |
6.85e-01 |
0.0910 |
-3.80e-02 |
0.082700 |
5.60e-01 |
2.05e-01 |
NoRC negatively regulates rRNA expression |
33 |
6.54e-01 |
8.50e-01 |
0.0909 |
4.93e-02 |
-0.076400 |
6.24e-01 |
4.48e-01 |
MTOR signalling |
35 |
6.60e-01 |
8.55e-01 |
0.0909 |
-5.77e-02 |
-0.070200 |
5.55e-01 |
4.73e-01 |
Downstream signaling of activated FGFR4 |
17 |
8.06e-01 |
9.36e-01 |
0.0907 |
2.85e-02 |
-0.086100 |
8.39e-01 |
5.39e-01 |
ERKs are inactivated |
13 |
8.47e-01 |
9.41e-01 |
0.0907 |
4.04e-02 |
-0.081100 |
8.01e-01 |
6.13e-01 |
Transcriptional regulation of granulopoiesis |
28 |
7.09e-01 |
8.81e-01 |
0.0904 |
9.03e-02 |
-0.003120 |
4.08e-01 |
9.77e-01 |
Metabolism of steroid hormones |
18 |
8.06e-01 |
9.36e-01 |
0.0900 |
8.82e-02 |
0.018000 |
5.17e-01 |
8.95e-01 |
MAPK targets/ Nuclear events mediated by MAP kinases |
30 |
7.00e-01 |
8.78e-01 |
0.0897 |
8.83e-02 |
0.015900 |
4.03e-01 |
8.81e-01 |
The role of Nef in HIV-1 replication and disease pathogenesis |
25 |
7.42e-01 |
8.96e-01 |
0.0882 |
8.53e-02 |
-0.022500 |
4.60e-01 |
8.45e-01 |
Adenylate cyclase inhibitory pathway |
14 |
8.55e-01 |
9.42e-01 |
0.0880 |
-4.31e-02 |
-0.076800 |
7.80e-01 |
6.19e-01 |
Unfolded Protein Response (UPR) |
74 |
4.44e-01 |
7.40e-01 |
0.0875 |
-4.61e-02 |
-0.074300 |
4.93e-01 |
2.70e-01 |
trans-Golgi Network Vesicle Budding |
58 |
5.23e-01 |
7.87e-01 |
0.0875 |
-8.36e-02 |
-0.025800 |
2.72e-01 |
7.34e-01 |
Misspliced GSK3beta mutants stabilize beta-catenin |
14 |
8.48e-01 |
9.41e-01 |
0.0871 |
-3.63e-02 |
0.079200 |
8.14e-01 |
6.08e-01 |
S33 mutants of beta-catenin aren't phosphorylated |
14 |
8.48e-01 |
9.41e-01 |
0.0871 |
-3.63e-02 |
0.079200 |
8.14e-01 |
6.08e-01 |
S37 mutants of beta-catenin aren't phosphorylated |
14 |
8.48e-01 |
9.41e-01 |
0.0871 |
-3.63e-02 |
0.079200 |
8.14e-01 |
6.08e-01 |
S45 mutants of beta-catenin aren't phosphorylated |
14 |
8.48e-01 |
9.41e-01 |
0.0871 |
-3.63e-02 |
0.079200 |
8.14e-01 |
6.08e-01 |
T41 mutants of beta-catenin aren't phosphorylated |
14 |
8.48e-01 |
9.41e-01 |
0.0871 |
-3.63e-02 |
0.079200 |
8.14e-01 |
6.08e-01 |
phosphorylation site mutants of CTNNB1 are not targeted to the proteasome by the destruction complex |
14 |
8.48e-01 |
9.41e-01 |
0.0871 |
-3.63e-02 |
0.079200 |
8.14e-01 |
6.08e-01 |
TCF dependent signaling in response to WNT |
134 |
2.36e-01 |
5.44e-01 |
0.0871 |
-6.07e-02 |
-0.062400 |
2.26e-01 |
2.14e-01 |
Signaling by WNT |
206 |
1.11e-01 |
3.53e-01 |
0.0868 |
-7.28e-02 |
-0.047300 |
7.29e-02 |
2.44e-01 |
ABC-family proteins mediated transport |
74 |
4.27e-01 |
7.31e-01 |
0.0864 |
7.94e-02 |
-0.034200 |
2.38e-01 |
6.12e-01 |
Neutrophil degranulation |
334 |
2.32e-02 |
1.34e-01 |
0.0864 |
7.68e-02 |
-0.039600 |
1.66e-02 |
2.17e-01 |
HCMV Early Events |
46 |
6.10e-01 |
8.29e-01 |
0.0863 |
7.58e-02 |
0.041300 |
3.74e-01 |
6.28e-01 |
Interleukin-1 signaling |
79 |
4.04e-01 |
7.15e-01 |
0.0861 |
4.26e-02 |
-0.074800 |
5.13e-01 |
2.51e-01 |
Integrin cell surface interactions |
50 |
5.88e-01 |
8.27e-01 |
0.0860 |
-5.02e-02 |
-0.069800 |
5.40e-01 |
3.94e-01 |
Infectious disease |
501 |
4.95e-03 |
4.42e-02 |
0.0859 |
8.59e-02 |
0.002840 |
1.12e-03 |
9.14e-01 |
Bile acid and bile salt metabolism |
24 |
7.76e-01 |
9.20e-01 |
0.0857 |
5.39e-02 |
0.066700 |
6.48e-01 |
5.72e-01 |
FOXO-mediated transcription of oxidative stress, metabolic and neuronal genes |
21 |
7.87e-01 |
9.23e-01 |
0.0855 |
-6.44e-02 |
0.056300 |
6.10e-01 |
6.55e-01 |
Activation of BH3-only proteins |
27 |
7.52e-01 |
9.02e-01 |
0.0852 |
7.95e-02 |
0.030800 |
4.75e-01 |
7.82e-01 |
FRS-mediated FGFR2 signaling |
15 |
8.55e-01 |
9.42e-01 |
0.0852 |
-5.72e-02 |
-0.063100 |
7.01e-01 |
6.72e-01 |
Protein-protein interactions at synapses |
60 |
5.12e-01 |
7.84e-01 |
0.0848 |
-7.18e-02 |
0.045300 |
3.37e-01 |
5.45e-01 |
Negative regulation of MET activity |
17 |
8.26e-01 |
9.40e-01 |
0.0847 |
-6.45e-02 |
0.054900 |
6.45e-01 |
6.95e-01 |
Fanconi Anemia Pathway |
22 |
7.89e-01 |
9.25e-01 |
0.0846 |
8.45e-02 |
-0.003950 |
4.93e-01 |
9.74e-01 |
IRS-related events triggered by IGF1R |
36 |
6.87e-01 |
8.66e-01 |
0.0844 |
2.17e-02 |
0.081500 |
8.22e-01 |
3.98e-01 |
PI-3K cascade:FGFR2 |
14 |
8.57e-01 |
9.42e-01 |
0.0842 |
-3.62e-02 |
0.076000 |
8.15e-01 |
6.22e-01 |
Interleukin-15 signaling |
13 |
8.70e-01 |
9.48e-01 |
0.0842 |
8.38e-02 |
-0.007970 |
6.01e-01 |
9.60e-01 |
Signaling by GPCR |
407 |
1.49e-02 |
9.88e-02 |
0.0838 |
-8.28e-02 |
0.013200 |
4.47e-03 |
6.51e-01 |
Platelet sensitization by LDL |
15 |
8.58e-01 |
9.42e-01 |
0.0834 |
-2.30e-02 |
-0.080200 |
8.78e-01 |
5.91e-01 |
MHC class II antigen presentation |
88 |
4.17e-01 |
7.24e-01 |
0.0833 |
4.75e-02 |
0.068500 |
4.42e-01 |
2.68e-01 |
Signaling by Interleukins |
323 |
3.35e-02 |
1.68e-01 |
0.0831 |
6.43e-02 |
-0.052700 |
4.86e-02 |
1.06e-01 |
Translation of Replicase and Assembly of the Replication Transcription Complex |
11 |
8.88e-01 |
9.58e-01 |
0.0830 |
-4.88e-02 |
0.067200 |
7.79e-01 |
7.00e-01 |
Regulation of TP53 Activity through Acetylation |
27 |
7.64e-01 |
9.11e-01 |
0.0827 |
-3.14e-02 |
-0.076500 |
7.78e-01 |
4.92e-01 |
eNOS activation |
10 |
9.07e-01 |
9.66e-01 |
0.0821 |
6.97e-02 |
0.043400 |
7.03e-01 |
8.12e-01 |
Phospholipid metabolism |
162 |
1.97e-01 |
4.89e-01 |
0.0821 |
-8.20e-02 |
0.003200 |
7.25e-02 |
9.44e-01 |
Signaling by NODAL |
12 |
8.88e-01 |
9.58e-01 |
0.0818 |
-1.20e-02 |
-0.080900 |
9.43e-01 |
6.28e-01 |
Fatty acid metabolism |
122 |
2.86e-01 |
5.99e-01 |
0.0814 |
6.11e-02 |
-0.053700 |
2.45e-01 |
3.07e-01 |
Mitochondrial translation elongation |
64 |
5.32e-01 |
7.95e-01 |
0.0812 |
-1.68e-04 |
-0.081200 |
9.98e-01 |
2.62e-01 |
Nuclear Envelope Breakdown |
41 |
6.79e-01 |
8.61e-01 |
0.0812 |
5.17e-02 |
0.062600 |
5.67e-01 |
4.88e-01 |
Positive epigenetic regulation of rRNA expression |
36 |
7.10e-01 |
8.81e-01 |
0.0809 |
7.60e-02 |
0.027600 |
4.30e-01 |
7.74e-01 |
TP53 Regulates Metabolic Genes |
70 |
5.03e-01 |
7.82e-01 |
0.0806 |
-7.98e-02 |
0.011600 |
2.49e-01 |
8.67e-01 |
Glycolysis |
54 |
5.97e-01 |
8.29e-01 |
0.0801 |
-7.99e-02 |
-0.006180 |
3.10e-01 |
9.37e-01 |
NOD1/2 Signaling Pathway |
27 |
7.63e-01 |
9.11e-01 |
0.0801 |
-6.13e-02 |
0.051600 |
5.82e-01 |
6.43e-01 |
PI Metabolism |
75 |
4.98e-01 |
7.76e-01 |
0.0798 |
2.03e-02 |
0.077100 |
7.62e-01 |
2.49e-01 |
Signaling by VEGF |
94 |
4.21e-01 |
7.28e-01 |
0.0796 |
2.31e-02 |
0.076100 |
7.00e-01 |
2.03e-01 |
Negative regulation of the PI3K/AKT network |
86 |
4.53e-01 |
7.50e-01 |
0.0795 |
2.21e-02 |
0.076300 |
7.24e-01 |
2.22e-01 |
VEGFA-VEGFR2 Pathway |
88 |
4.53e-01 |
7.50e-01 |
0.0791 |
3.89e-02 |
0.068900 |
5.29e-01 |
2.65e-01 |
PKA-mediated phosphorylation of CREB |
18 |
8.39e-01 |
9.41e-01 |
0.0790 |
-6.50e-02 |
0.045000 |
6.33e-01 |
7.41e-01 |
Long-term potentiation |
18 |
8.44e-01 |
9.41e-01 |
0.0788 |
-7.82e-02 |
0.009220 |
5.66e-01 |
9.46e-01 |
Innate Immune System |
698 |
2.08e-03 |
2.18e-02 |
0.0784 |
7.64e-02 |
-0.017700 |
7.01e-04 |
4.32e-01 |
Interleukin-20 family signaling |
15 |
8.66e-01 |
9.46e-01 |
0.0783 |
-4.45e-02 |
0.064400 |
7.66e-01 |
6.66e-01 |
N-glycan trimming in the ER and Calnexin/Calreticulin cycle |
23 |
8.09e-01 |
9.36e-01 |
0.0780 |
-8.17e-03 |
0.077600 |
9.46e-01 |
5.20e-01 |
Defective TPR may confer susceptibility towards thyroid papillary carcinoma (TPC) |
22 |
8.25e-01 |
9.40e-01 |
0.0778 |
3.51e-02 |
0.069400 |
7.76e-01 |
5.73e-01 |
Regulation of Glucokinase by Glucokinase Regulatory Protein |
22 |
8.25e-01 |
9.40e-01 |
0.0778 |
3.51e-02 |
0.069400 |
7.76e-01 |
5.73e-01 |
G alpha (q) signalling events |
117 |
3.50e-01 |
6.70e-01 |
0.0773 |
-7.69e-02 |
0.008380 |
1.52e-01 |
8.76e-01 |
Fatty acyl-CoA biosynthesis |
22 |
8.19e-01 |
9.40e-01 |
0.0770 |
-7.43e-02 |
0.020100 |
5.46e-01 |
8.70e-01 |
Synthesis of PIPs at the plasma membrane |
51 |
6.47e-01 |
8.46e-01 |
0.0768 |
6.90e-02 |
0.033700 |
3.95e-01 |
6.77e-01 |
Transmission across Chemical Synapses |
158 |
2.53e-01 |
5.62e-01 |
0.0764 |
-7.61e-02 |
0.005750 |
9.97e-02 |
9.01e-01 |
Synthesis of IP2, IP, and Ins in the cytosol |
14 |
8.85e-01 |
9.58e-01 |
0.0762 |
-7.61e-02 |
0.003710 |
6.22e-01 |
9.81e-01 |
GPCR downstream signalling |
376 |
4.07e-02 |
1.91e-01 |
0.0756 |
-7.22e-02 |
0.022600 |
1.71e-02 |
4.56e-01 |
Signaling by cytosolic FGFR1 fusion mutants |
18 |
8.54e-01 |
9.42e-01 |
0.0754 |
-2.57e-02 |
0.070900 |
8.51e-01 |
6.03e-01 |
Hyaluronan metabolism |
13 |
8.95e-01 |
9.59e-01 |
0.0750 |
4.88e-03 |
-0.074900 |
9.76e-01 |
6.40e-01 |
SUMOylation of SUMOylation proteins |
23 |
8.29e-01 |
9.40e-01 |
0.0749 |
6.78e-02 |
0.032000 |
5.74e-01 |
7.91e-01 |
Metabolism |
1447 |
2.28e-05 |
5.67e-04 |
0.0737 |
2.98e-02 |
-0.067400 |
6.63e-02 |
3.17e-05 |
ADORA2B mediated anti-inflammatory cytokines production |
56 |
6.24e-01 |
8.32e-01 |
0.0737 |
-6.25e-02 |
0.039100 |
4.19e-01 |
6.13e-01 |
Toll Like Receptor 4 (TLR4) Cascade |
107 |
4.10e-01 |
7.19e-01 |
0.0734 |
-3.95e-02 |
0.061900 |
4.81e-01 |
2.70e-01 |
ERCC6 (CSB) and EHMT2 (G9a) positively regulate rRNA expression |
14 |
8.93e-01 |
9.59e-01 |
0.0725 |
2.22e-02 |
-0.069000 |
8.86e-01 |
6.55e-01 |
CREB1 phosphorylation through NMDA receptor-mediated activation of RAS signaling |
23 |
8.28e-01 |
9.40e-01 |
0.0724 |
-5.53e-02 |
0.046800 |
6.46e-01 |
6.98e-01 |
SUMOylation of RNA binding proteins |
36 |
7.66e-01 |
9.12e-01 |
0.0719 |
4.83e-02 |
0.053300 |
6.16e-01 |
5.81e-01 |
SUMOylation of ubiquitinylation proteins |
28 |
8.13e-01 |
9.37e-01 |
0.0715 |
6.44e-02 |
0.031100 |
5.55e-01 |
7.76e-01 |
Signalling to RAS |
19 |
8.61e-01 |
9.44e-01 |
0.0714 |
6.50e-02 |
-0.029400 |
6.24e-01 |
8.24e-01 |
MET activates RAS signaling |
10 |
9.26e-01 |
9.70e-01 |
0.0714 |
-6.84e-04 |
-0.071400 |
9.97e-01 |
6.96e-01 |
Transcriptional Regulation by TP53 |
295 |
1.05e-01 |
3.46e-01 |
0.0709 |
5.94e-02 |
-0.038800 |
8.11e-02 |
2.55e-01 |
Endosomal Sorting Complex Required For Transport (ESCRT) |
22 |
8.51e-01 |
9.41e-01 |
0.0708 |
-2.26e-02 |
-0.067100 |
8.54e-01 |
5.86e-01 |
Signaling by MET |
58 |
6.38e-01 |
8.42e-01 |
0.0707 |
3.55e-02 |
-0.061100 |
6.41e-01 |
4.21e-01 |
Interleukin-1 family signaling |
104 |
4.60e-01 |
7.52e-01 |
0.0703 |
1.27e-02 |
-0.069200 |
8.23e-01 |
2.24e-01 |
Signal Transduction |
1625 |
2.30e-05 |
5.67e-04 |
0.0699 |
-5.92e-02 |
0.037200 |
1.26e-04 |
1.58e-02 |
Apoptotic execution phase |
38 |
7.59e-01 |
9.08e-01 |
0.0694 |
-5.73e-03 |
0.069200 |
9.51e-01 |
4.61e-01 |
Molecules associated with elastic fibres |
26 |
8.26e-01 |
9.40e-01 |
0.0693 |
-1.66e-02 |
0.067300 |
8.84e-01 |
5.53e-01 |
Hedgehog 'off' state |
84 |
5.40e-01 |
8.02e-01 |
0.0689 |
3.43e-02 |
-0.059800 |
5.87e-01 |
3.45e-01 |
Conversion from APC/C:Cdc20 to APC/C:Cdh1 in late anaphase |
18 |
8.75e-01 |
9.51e-01 |
0.0689 |
4.13e-02 |
-0.055100 |
7.62e-01 |
6.86e-01 |
Signaling by FGFR3 |
28 |
8.27e-01 |
9.40e-01 |
0.0684 |
6.26e-02 |
0.027400 |
5.66e-01 |
8.02e-01 |
RNA Polymerase II Pre-transcription Events |
62 |
6.49e-01 |
8.46e-01 |
0.0683 |
-4.11e-04 |
-0.068300 |
9.96e-01 |
3.53e-01 |
Golgi Associated Vesicle Biogenesis |
46 |
7.31e-01 |
8.91e-01 |
0.0683 |
-6.50e-02 |
-0.021100 |
4.46e-01 |
8.05e-01 |
Estrogen-dependent gene expression |
76 |
5.80e-01 |
8.24e-01 |
0.0681 |
-3.18e-02 |
0.060200 |
6.33e-01 |
3.65e-01 |
HDACs deacetylate histones |
26 |
8.33e-01 |
9.41e-01 |
0.0675 |
6.22e-02 |
-0.026400 |
5.83e-01 |
8.16e-01 |
TNF signaling |
33 |
8.07e-01 |
9.36e-01 |
0.0673 |
4.45e-02 |
0.050500 |
6.58e-01 |
6.16e-01 |
Axon guidance |
396 |
7.62e-02 |
2.80e-01 |
0.0667 |
-4.81e-03 |
0.066500 |
8.71e-01 |
2.42e-02 |
Immune System |
1413 |
2.53e-04 |
4.25e-03 |
0.0667 |
6.66e-02 |
0.003050 |
4.71e-05 |
8.52e-01 |
Nervous system development |
414 |
6.63e-02 |
2.56e-01 |
0.0665 |
-1.71e-02 |
0.064300 |
5.53e-01 |
2.60e-02 |
mRNA Splicing - Minor Pathway |
37 |
7.83e-01 |
9.23e-01 |
0.0663 |
4.26e-03 |
-0.066100 |
9.64e-01 |
4.87e-01 |
Class A/1 (Rhodopsin-like receptors) |
112 |
4.95e-01 |
7.75e-01 |
0.0662 |
5.57e-02 |
0.035800 |
3.10e-01 |
5.13e-01 |
Vesicle-mediated transport |
514 |
3.82e-02 |
1.83e-01 |
0.0661 |
-6.54e-02 |
0.009680 |
1.21e-02 |
7.10e-01 |
Mitochondrial translation termination |
64 |
6.53e-01 |
8.49e-01 |
0.0661 |
1.63e-02 |
-0.064100 |
8.22e-01 |
3.76e-01 |
Negative regulation of FGFR3 signaling |
19 |
8.85e-01 |
9.58e-01 |
0.0659 |
1.47e-02 |
0.064300 |
9.12e-01 |
6.28e-01 |
MyD88-independent TLR4 cascade |
83 |
5.72e-01 |
8.24e-01 |
0.0659 |
-5.34e-02 |
0.038600 |
4.01e-01 |
5.44e-01 |
TRIF(TICAM1)-mediated TLR4 signaling |
83 |
5.72e-01 |
8.24e-01 |
0.0659 |
-5.34e-02 |
0.038600 |
4.01e-01 |
5.44e-01 |
COPI-dependent Golgi-to-ER retrograde traffic |
69 |
6.30e-01 |
8.36e-01 |
0.0656 |
5.47e-02 |
-0.036400 |
4.33e-01 |
6.02e-01 |
GPVI-mediated activation cascade |
27 |
8.46e-01 |
9.41e-01 |
0.0656 |
5.59e-02 |
0.034300 |
6.15e-01 |
7.58e-01 |
Phase 0 - rapid depolarisation |
31 |
8.15e-01 |
9.37e-01 |
0.0654 |
-2.74e-02 |
0.059400 |
7.92e-01 |
5.67e-01 |
Metabolism of water-soluble vitamins and cofactors |
90 |
5.76e-01 |
8.24e-01 |
0.0654 |
-3.60e-02 |
-0.054600 |
5.55e-01 |
3.72e-01 |
Epigenetic regulation of gene expression |
70 |
6.29e-01 |
8.35e-01 |
0.0653 |
4.16e-02 |
-0.050400 |
5.48e-01 |
4.67e-01 |
IRS-mediated signalling |
33 |
8.13e-01 |
9.37e-01 |
0.0652 |
1.20e-02 |
0.064100 |
9.05e-01 |
5.24e-01 |
Transcriptional regulation by small RNAs |
33 |
8.10e-01 |
9.36e-01 |
0.0648 |
6.36e-02 |
-0.012400 |
5.27e-01 |
9.02e-01 |
Activation of HOX genes during differentiation |
42 |
7.63e-01 |
9.11e-01 |
0.0643 |
3.27e-02 |
-0.055400 |
7.14e-01 |
5.35e-01 |
Activation of anterior HOX genes in hindbrain development during early embryogenesis |
42 |
7.63e-01 |
9.11e-01 |
0.0643 |
3.27e-02 |
-0.055400 |
7.14e-01 |
5.35e-01 |
Repression of WNT target genes |
12 |
9.33e-01 |
9.70e-01 |
0.0633 |
-4.73e-02 |
-0.042100 |
7.77e-01 |
8.01e-01 |
FGFR1 mutant receptor activation |
23 |
8.75e-01 |
9.51e-01 |
0.0631 |
2.64e-02 |
0.057300 |
8.27e-01 |
6.34e-01 |
Toll-like Receptor Cascades |
122 |
4.87e-01 |
7.71e-01 |
0.0626 |
-9.09e-03 |
0.062000 |
8.63e-01 |
2.38e-01 |
DNA Damage Recognition in GG-NER |
27 |
8.51e-01 |
9.41e-01 |
0.0624 |
6.03e-02 |
-0.016100 |
5.88e-01 |
8.85e-01 |
MyD88:MAL(TIRAP) cascade initiated on plasma membrane |
81 |
6.13e-01 |
8.29e-01 |
0.0623 |
-3.95e-02 |
0.048200 |
5.39e-01 |
4.54e-01 |
Toll Like Receptor 2 (TLR2) Cascade |
81 |
6.13e-01 |
8.29e-01 |
0.0623 |
-3.95e-02 |
0.048200 |
5.39e-01 |
4.54e-01 |
Toll Like Receptor TLR1:TLR2 Cascade |
81 |
6.13e-01 |
8.29e-01 |
0.0623 |
-3.95e-02 |
0.048200 |
5.39e-01 |
4.54e-01 |
Toll Like Receptor TLR6:TLR2 Cascade |
81 |
6.13e-01 |
8.29e-01 |
0.0623 |
-3.95e-02 |
0.048200 |
5.39e-01 |
4.54e-01 |
Prefoldin mediated transfer of substrate to CCT/TriC |
19 |
8.96e-01 |
9.59e-01 |
0.0622 |
4.33e-03 |
0.062100 |
9.74e-01 |
6.40e-01 |
Mitochondrial translation |
70 |
6.75e-01 |
8.60e-01 |
0.0620 |
-1.68e-02 |
-0.059700 |
8.08e-01 |
3.89e-01 |
MyD88 cascade initiated on plasma membrane |
70 |
6.71e-01 |
8.57e-01 |
0.0618 |
-6.18e-02 |
-0.001210 |
3.72e-01 |
9.86e-01 |
Toll Like Receptor 10 (TLR10) Cascade |
70 |
6.71e-01 |
8.57e-01 |
0.0618 |
-6.18e-02 |
-0.001210 |
3.72e-01 |
9.86e-01 |
Toll Like Receptor 5 (TLR5) Cascade |
70 |
6.71e-01 |
8.57e-01 |
0.0618 |
-6.18e-02 |
-0.001210 |
3.72e-01 |
9.86e-01 |
Toll Like Receptor 9 (TLR9) Cascade |
81 |
6.20e-01 |
8.30e-01 |
0.0616 |
-4.02e-02 |
0.046700 |
5.33e-01 |
4.68e-01 |
Chromatin modifying enzymes |
168 |
3.74e-01 |
6.89e-01 |
0.0616 |
-3.99e-02 |
0.047000 |
3.74e-01 |
2.95e-01 |
Chromatin organization |
168 |
3.74e-01 |
6.89e-01 |
0.0616 |
-3.99e-02 |
0.047000 |
3.74e-01 |
2.95e-01 |
LDL clearance |
15 |
9.21e-01 |
9.69e-01 |
0.0616 |
-5.28e-02 |
-0.031700 |
7.24e-01 |
8.32e-01 |
Cooperation of PDCL (PhLP1) and TRiC/CCT in G-protein beta folding |
26 |
8.63e-01 |
9.45e-01 |
0.0615 |
5.00e-04 |
-0.061500 |
9.96e-01 |
5.87e-01 |
RNA Polymerase II Transcription |
892 |
1.19e-02 |
8.34e-02 |
0.0611 |
4.93e-02 |
0.036000 |
1.42e-02 |
7.34e-02 |
Regulation of TP53 Activity |
135 |
4.66e-01 |
7.54e-01 |
0.0609 |
5.69e-02 |
-0.021700 |
2.55e-01 |
6.64e-01 |
SLC transporter disorders |
63 |
7.16e-01 |
8.83e-01 |
0.0607 |
5.19e-02 |
0.031500 |
4.77e-01 |
6.66e-01 |
RMTs methylate histone arginines |
29 |
8.58e-01 |
9.42e-01 |
0.0605 |
-4.91e-02 |
-0.035500 |
6.48e-01 |
7.41e-01 |
Metabolism of steroids |
103 |
5.84e-01 |
8.24e-01 |
0.0605 |
-4.57e-02 |
-0.039700 |
4.24e-01 |
4.87e-01 |
Cytokine Signaling in Immune system |
599 |
3.94e-02 |
1.87e-01 |
0.0605 |
5.42e-02 |
-0.026900 |
2.52e-02 |
2.67e-01 |
TRAF6 mediated induction of NFkB and MAP kinases upon TLR7/8 or 9 activation |
77 |
6.55e-01 |
8.50e-01 |
0.0600 |
-5.73e-02 |
0.017700 |
3.85e-01 |
7.89e-01 |
Neurotransmitter receptors and postsynaptic signal transmission |
120 |
5.22e-01 |
7.87e-01 |
0.0599 |
-5.87e-02 |
0.011900 |
2.68e-01 |
8.22e-01 |
Gene Silencing by RNA |
47 |
7.78e-01 |
9.21e-01 |
0.0594 |
-6.27e-03 |
0.059100 |
9.41e-01 |
4.84e-01 |
TGF-beta receptor signaling activates SMADs |
22 |
8.90e-01 |
9.59e-01 |
0.0594 |
5.91e-02 |
-0.005060 |
6.31e-01 |
9.67e-01 |
Deregulated CDK5 triggers multiple neurodegenerative pathways in Alzheimer's disease models |
17 |
9.12e-01 |
9.67e-01 |
0.0588 |
3.51e-02 |
-0.047200 |
8.02e-01 |
7.36e-01 |
Neurodegenerative Diseases |
17 |
9.12e-01 |
9.67e-01 |
0.0588 |
3.51e-02 |
-0.047200 |
8.02e-01 |
7.36e-01 |
PI5P, PP2A and IER3 Regulate PI3K/AKT Signaling |
81 |
6.66e-01 |
8.57e-01 |
0.0587 |
1.68e-02 |
0.056300 |
7.95e-01 |
3.82e-01 |
Gap junction trafficking and regulation |
16 |
9.22e-01 |
9.69e-01 |
0.0586 |
5.51e-03 |
0.058300 |
9.70e-01 |
6.86e-01 |
Aberrant regulation of mitotic exit in cancer due to RB1 defects |
18 |
9.09e-01 |
9.66e-01 |
0.0584 |
4.44e-02 |
-0.037900 |
7.44e-01 |
7.81e-01 |
SUMOylation of transcription factors |
14 |
9.33e-01 |
9.70e-01 |
0.0582 |
5.61e-02 |
0.015400 |
7.16e-01 |
9.20e-01 |
Estrogen-dependent nuclear events downstream of ESR-membrane signaling |
21 |
8.96e-01 |
9.59e-01 |
0.0580 |
4.37e-02 |
-0.038100 |
7.29e-01 |
7.63e-01 |
Gene expression (Transcription) |
990 |
1.24e-02 |
8.63e-02 |
0.0579 |
4.80e-02 |
0.032400 |
1.23e-02 |
9.07e-02 |
Generic Transcription Pathway |
796 |
2.80e-02 |
1.51e-01 |
0.0577 |
4.91e-02 |
0.030400 |
2.05e-02 |
1.52e-01 |
Depolymerisation of the Nuclear Lamina |
14 |
9.35e-01 |
9.70e-01 |
0.0576 |
-2.85e-02 |
-0.050100 |
8.54e-01 |
7.46e-01 |
VEGFR2 mediated cell proliferation |
19 |
9.13e-01 |
9.67e-01 |
0.0576 |
-2.62e-02 |
-0.051300 |
8.44e-01 |
6.99e-01 |
TNFR1-induced proapoptotic signaling |
13 |
9.36e-01 |
9.70e-01 |
0.0572 |
-3.32e-02 |
0.046600 |
8.36e-01 |
7.71e-01 |
Transcriptional regulation by RUNX3 |
81 |
6.78e-01 |
8.61e-01 |
0.0572 |
5.62e-02 |
0.010700 |
3.83e-01 |
8.68e-01 |
Clathrin-mediated endocytosis |
106 |
6.02e-01 |
8.29e-01 |
0.0568 |
-5.68e-02 |
-0.001570 |
3.13e-01 |
9.78e-01 |
HIV Transcription Initiation |
37 |
8.39e-01 |
9.41e-01 |
0.0568 |
-1.16e-02 |
-0.055600 |
9.03e-01 |
5.59e-01 |
RNA Polymerase II HIV Promoter Escape |
37 |
8.39e-01 |
9.41e-01 |
0.0568 |
-1.16e-02 |
-0.055600 |
9.03e-01 |
5.59e-01 |
RNA Polymerase II Promoter Escape |
37 |
8.39e-01 |
9.41e-01 |
0.0568 |
-1.16e-02 |
-0.055600 |
9.03e-01 |
5.59e-01 |
RNA Polymerase II Transcription Initiation |
37 |
8.39e-01 |
9.41e-01 |
0.0568 |
-1.16e-02 |
-0.055600 |
9.03e-01 |
5.59e-01 |
RNA Polymerase II Transcription Initiation And Promoter Clearance |
37 |
8.39e-01 |
9.41e-01 |
0.0568 |
-1.16e-02 |
-0.055600 |
9.03e-01 |
5.59e-01 |
RNA Polymerase II Transcription Pre-Initiation And Promoter Opening |
37 |
8.39e-01 |
9.41e-01 |
0.0568 |
-1.16e-02 |
-0.055600 |
9.03e-01 |
5.59e-01 |
PTK6 Regulates RHO GTPases, RAS GTPase and MAP kinases |
11 |
9.50e-01 |
9.78e-01 |
0.0567 |
3.66e-02 |
0.043300 |
8.33e-01 |
8.04e-01 |
Ovarian tumor domain proteases |
28 |
8.75e-01 |
9.51e-01 |
0.0564 |
-2.24e-03 |
0.056300 |
9.84e-01 |
6.06e-01 |
Transcriptional regulation by RUNX1 |
146 |
5.12e-01 |
7.84e-01 |
0.0559 |
5.54e-02 |
0.007580 |
2.49e-01 |
8.75e-01 |
Retinoid metabolism and transport |
25 |
8.92e-01 |
9.59e-01 |
0.0559 |
-5.42e-02 |
-0.013400 |
6.39e-01 |
9.08e-01 |
Leishmania infection |
158 |
4.85e-01 |
7.71e-01 |
0.0557 |
3.63e-03 |
0.055600 |
9.37e-01 |
2.29e-01 |
Downstream signal transduction |
28 |
8.74e-01 |
9.51e-01 |
0.0557 |
-2.61e-02 |
0.049200 |
8.11e-01 |
6.53e-01 |
HCMV Infection |
64 |
7.39e-01 |
8.94e-01 |
0.0557 |
5.40e-02 |
-0.013400 |
4.55e-01 |
8.53e-01 |
Neurotransmitter release cycle |
28 |
8.80e-01 |
9.54e-01 |
0.0553 |
-5.94e-03 |
-0.055000 |
9.57e-01 |
6.14e-01 |
Anti-inflammatory response favouring Leishmania parasite infection |
89 |
6.65e-01 |
8.57e-01 |
0.0553 |
-5.53e-02 |
0.002360 |
3.68e-01 |
9.69e-01 |
Leishmania parasite growth and survival |
89 |
6.65e-01 |
8.57e-01 |
0.0553 |
-5.53e-02 |
0.002360 |
3.68e-01 |
9.69e-01 |
Budding and maturation of HIV virion |
19 |
9.17e-01 |
9.69e-01 |
0.0553 |
-5.49e-02 |
-0.006570 |
6.79e-01 |
9.61e-01 |
SLC-mediated transmembrane transport |
155 |
4.91e-01 |
7.71e-01 |
0.0552 |
5.41e-02 |
-0.010600 |
2.46e-01 |
8.20e-01 |
ERK/MAPK targets |
22 |
9.03e-01 |
9.62e-01 |
0.0546 |
4.84e-02 |
-0.025300 |
6.95e-01 |
8.37e-01 |
Cellular responses to external stimuli |
368 |
1.98e-01 |
4.89e-01 |
0.0545 |
5.33e-02 |
-0.011800 |
8.16e-02 |
7.01e-01 |
HCMV Late Events |
41 |
8.29e-01 |
9.40e-01 |
0.0542 |
4.23e-02 |
-0.034000 |
6.40e-01 |
7.07e-01 |
Glutamate Neurotransmitter Release Cycle |
16 |
9.34e-01 |
9.70e-01 |
0.0542 |
-2.76e-02 |
-0.046600 |
8.48e-01 |
7.47e-01 |
PI-3K cascade:FGFR4 |
11 |
9.53e-01 |
9.79e-01 |
0.0535 |
1.54e-02 |
-0.051300 |
9.30e-01 |
7.68e-01 |
Cellular Senescence |
108 |
6.20e-01 |
8.30e-01 |
0.0535 |
-4.01e-02 |
0.035400 |
4.73e-01 |
5.26e-01 |
Metabolism of vitamins and cofactors |
135 |
5.82e-01 |
8.24e-01 |
0.0531 |
-3.31e-02 |
-0.041500 |
5.07e-01 |
4.06e-01 |
Developmental Biology |
619 |
8.03e-02 |
2.91e-01 |
0.0530 |
-1.25e-02 |
0.051500 |
6.01e-01 |
3.08e-02 |
Opioid Signalling |
70 |
7.39e-01 |
8.94e-01 |
0.0527 |
-2.98e-02 |
0.043500 |
6.67e-01 |
5.30e-01 |
Membrane Trafficking |
487 |
1.38e-01 |
4.04e-01 |
0.0527 |
-5.17e-02 |
0.010300 |
5.32e-02 |
6.99e-01 |
Signaling by PDGFR in disease |
19 |
9.27e-01 |
9.70e-01 |
0.0526 |
3.11e-02 |
0.042400 |
8.14e-01 |
7.49e-01 |
Syndecan interactions |
17 |
9.32e-01 |
9.70e-01 |
0.0526 |
-5.01e-03 |
-0.052300 |
9.71e-01 |
7.09e-01 |
Metabolism of fat-soluble vitamins |
27 |
8.96e-01 |
9.59e-01 |
0.0526 |
-5.08e-02 |
-0.013500 |
6.48e-01 |
9.03e-01 |
MyD88 dependent cascade initiated on endosome |
78 |
7.18e-01 |
8.83e-01 |
0.0524 |
-4.60e-02 |
0.025100 |
4.83e-01 |
7.02e-01 |
Toll Like Receptor 7/8 (TLR7/8) Cascade |
78 |
7.18e-01 |
8.83e-01 |
0.0524 |
-4.60e-02 |
0.025100 |
4.83e-01 |
7.02e-01 |
Interleukin-3, Interleukin-5 and GM-CSF signaling |
37 |
8.64e-01 |
9.46e-01 |
0.0523 |
-2.78e-02 |
-0.044300 |
7.70e-01 |
6.41e-01 |
Signaling by NTRK2 (TRKB) |
21 |
9.17e-01 |
9.69e-01 |
0.0523 |
8.16e-03 |
-0.051600 |
9.48e-01 |
6.82e-01 |
Diseases of programmed cell death |
18 |
9.26e-01 |
9.70e-01 |
0.0521 |
3.31e-02 |
-0.040200 |
8.08e-01 |
7.68e-01 |
FCERI mediated MAPK activation |
27 |
8.96e-01 |
9.59e-01 |
0.0513 |
4.68e-02 |
-0.021000 |
6.74e-01 |
8.50e-01 |
Cellular responses to stress |
363 |
2.48e-01 |
5.55e-01 |
0.0511 |
5.07e-02 |
-0.006580 |
9.96e-02 |
8.31e-01 |
MAPK family signaling cascades |
251 |
3.96e-01 |
7.13e-01 |
0.0511 |
-2.90e-02 |
-0.042100 |
4.31e-01 |
2.54e-01 |
SARS-CoV Infections |
67 |
7.77e-01 |
9.21e-01 |
0.0509 |
1.79e-02 |
0.047600 |
8.01e-01 |
5.01e-01 |
RAF-independent MAPK1/3 activation |
21 |
9.19e-01 |
9.69e-01 |
0.0508 |
2.36e-02 |
-0.045000 |
8.52e-01 |
7.21e-01 |
Viral Messenger RNA Synthesis |
29 |
8.96e-01 |
9.59e-01 |
0.0507 |
4.98e-02 |
0.009560 |
6.42e-01 |
9.29e-01 |
DDX58/IFIH1-mediated induction of interferon-alpha/beta |
48 |
8.29e-01 |
9.40e-01 |
0.0502 |
-2.60e-02 |
0.043000 |
7.55e-01 |
6.07e-01 |
PI3K/AKT Signaling in Cancer |
81 |
7.50e-01 |
9.02e-01 |
0.0497 |
2.45e-02 |
0.043200 |
7.03e-01 |
5.02e-01 |
Prolonged ERK activation events |
14 |
9.50e-01 |
9.78e-01 |
0.0496 |
-3.05e-03 |
-0.049500 |
9.84e-01 |
7.49e-01 |
Negative regulation of FGFR4 signaling |
18 |
9.33e-01 |
9.70e-01 |
0.0495 |
-3.66e-02 |
0.033400 |
7.88e-01 |
8.06e-01 |
Amino acids regulate mTORC1 |
42 |
8.66e-01 |
9.46e-01 |
0.0489 |
-3.65e-02 |
-0.032500 |
6.82e-01 |
7.16e-01 |
Signaling by Insulin receptor |
54 |
8.30e-01 |
9.40e-01 |
0.0488 |
-2.03e-02 |
-0.044400 |
7.96e-01 |
5.73e-01 |
Protein folding |
73 |
7.79e-01 |
9.21e-01 |
0.0486 |
-1.82e-02 |
-0.045000 |
7.88e-01 |
5.07e-01 |
Cargo concentration in the ER |
20 |
9.34e-01 |
9.70e-01 |
0.0485 |
-1.63e-02 |
-0.045700 |
9.00e-01 |
7.23e-01 |
RHO GTPases activate PAKs |
21 |
9.32e-01 |
9.70e-01 |
0.0485 |
3.66e-02 |
0.031800 |
7.72e-01 |
8.01e-01 |
Insulin receptor signalling cascade |
38 |
8.80e-01 |
9.54e-01 |
0.0481 |
1.86e-02 |
0.044400 |
8.43e-01 |
6.36e-01 |
RNA polymerase II transcribes snRNA genes |
58 |
8.22e-01 |
9.40e-01 |
0.0481 |
-4.63e-02 |
-0.013000 |
5.43e-01 |
8.64e-01 |
PPARA activates gene expression |
100 |
7.22e-01 |
8.84e-01 |
0.0477 |
2.38e-02 |
0.041300 |
6.82e-01 |
4.76e-01 |
Transport of small molecules |
463 |
2.41e-01 |
5.45e-01 |
0.0472 |
-3.35e-02 |
-0.033200 |
2.21e-01 |
2.25e-01 |
Metabolic disorders of biological oxidation enzymes |
18 |
9.45e-01 |
9.76e-01 |
0.0460 |
4.52e-02 |
0.008790 |
7.40e-01 |
9.49e-01 |
Acyl chain remodelling of PS |
13 |
9.60e-01 |
9.83e-01 |
0.0450 |
-3.93e-02 |
0.021900 |
8.06e-01 |
8.91e-01 |
TNFR1-induced NFkappaB signaling pathway |
24 |
9.34e-01 |
9.70e-01 |
0.0446 |
2.40e-02 |
0.037600 |
8.38e-01 |
7.50e-01 |
Regulation of lipid metabolism by PPARalpha |
102 |
7.50e-01 |
9.02e-01 |
0.0444 |
2.25e-02 |
0.038300 |
6.96e-01 |
5.05e-01 |
Tie2 Signaling |
15 |
9.56e-01 |
9.81e-01 |
0.0442 |
1.67e-02 |
-0.041000 |
9.11e-01 |
7.84e-01 |
Endogenous sterols |
18 |
9.49e-01 |
9.77e-01 |
0.0433 |
-3.29e-02 |
0.028200 |
8.09e-01 |
8.36e-01 |
Signaling by Erythropoietin |
23 |
9.41e-01 |
9.72e-01 |
0.0430 |
2.79e-02 |
0.032800 |
8.17e-01 |
7.86e-01 |
Diseases of signal transduction by growth factor receptors and second messengers |
308 |
4.21e-01 |
7.28e-01 |
0.0430 |
-3.40e-02 |
0.026200 |
3.08e-01 |
4.31e-01 |
Signal amplification |
24 |
9.38e-01 |
9.71e-01 |
0.0427 |
-1.16e-02 |
-0.041100 |
9.22e-01 |
7.28e-01 |
Plasma lipoprotein clearance |
24 |
9.39e-01 |
9.71e-01 |
0.0425 |
-3.89e-02 |
-0.017100 |
7.41e-01 |
8.85e-01 |
Intra-Golgi and retrograde Golgi-to-ER traffic |
153 |
6.69e-01 |
8.57e-01 |
0.0417 |
-1.08e-02 |
0.040200 |
8.19e-01 |
3.92e-01 |
Signaling by ERBB4 |
39 |
9.11e-01 |
9.67e-01 |
0.0407 |
-3.52e-02 |
-0.020500 |
7.04e-01 |
8.25e-01 |
Rab regulation of trafficking |
104 |
7.82e-01 |
9.23e-01 |
0.0403 |
-1.26e-02 |
-0.038300 |
8.24e-01 |
5.01e-01 |
Signaling by FGFR2 IIIa TM |
12 |
9.71e-01 |
9.87e-01 |
0.0400 |
-3.57e-02 |
0.017900 |
8.30e-01 |
9.15e-01 |
Translocation of SLC2A4 (GLUT4) to the plasma membrane |
50 |
8.88e-01 |
9.58e-01 |
0.0400 |
3.54e-03 |
0.039800 |
9.65e-01 |
6.27e-01 |
Signaling by Non-Receptor Tyrosine Kinases |
43 |
8.99e-01 |
9.60e-01 |
0.0399 |
-2.05e-02 |
0.034200 |
8.17e-01 |
6.98e-01 |
Signaling by PTK6 |
43 |
8.99e-01 |
9.60e-01 |
0.0399 |
-2.05e-02 |
0.034200 |
8.17e-01 |
6.98e-01 |
Signaling by FGFR in disease |
45 |
9.00e-01 |
9.60e-01 |
0.0397 |
5.42e-03 |
0.039300 |
9.50e-01 |
6.48e-01 |
MAPK1/MAPK3 signaling |
218 |
6.12e-01 |
8.29e-01 |
0.0395 |
-9.07e-03 |
-0.038400 |
8.18e-01 |
3.30e-01 |
Apoptosis |
137 |
7.26e-01 |
8.88e-01 |
0.0394 |
3.87e-02 |
-0.007160 |
4.36e-01 |
8.85e-01 |
RAB GEFs exchange GTP for GDP on RABs |
78 |
8.35e-01 |
9.41e-01 |
0.0393 |
3.93e-02 |
-0.001150 |
5.50e-01 |
9.86e-01 |
Programmed Cell Death |
140 |
7.22e-01 |
8.84e-01 |
0.0392 |
3.82e-02 |
-0.008800 |
4.36e-01 |
8.58e-01 |
Platelet activation, signaling and aggregation |
197 |
6.48e-01 |
8.46e-01 |
0.0392 |
-1.30e-02 |
-0.036900 |
7.54e-01 |
3.73e-01 |
Signaling by NOTCH |
147 |
7.13e-01 |
8.83e-01 |
0.0391 |
-3.84e-02 |
0.007350 |
4.23e-01 |
8.78e-01 |
RAF/MAP kinase cascade |
213 |
6.36e-01 |
8.40e-01 |
0.0385 |
-1.37e-02 |
-0.036000 |
7.31e-01 |
3.67e-01 |
Cilium Assembly |
152 |
7.17e-01 |
8.83e-01 |
0.0383 |
-2.66e-03 |
0.038200 |
9.55e-01 |
4.18e-01 |
Intrinsic Pathway for Apoptosis |
42 |
9.10e-01 |
9.67e-01 |
0.0379 |
2.99e-02 |
-0.023200 |
7.37e-01 |
7.95e-01 |
FOXO-mediated transcription |
51 |
9.00e-01 |
9.60e-01 |
0.0374 |
5.39e-03 |
0.037000 |
9.47e-01 |
6.48e-01 |
Metabolism of lipids |
527 |
3.64e-01 |
6.83e-01 |
0.0371 |
-3.44e-02 |
-0.014000 |
1.81e-01 |
5.88e-01 |
Metabolism of cofactors |
19 |
9.61e-01 |
9.83e-01 |
0.0371 |
3.70e-02 |
-0.003090 |
7.80e-01 |
9.81e-01 |
Platelet degranulation |
96 |
8.27e-01 |
9.40e-01 |
0.0370 |
3.43e-02 |
0.013700 |
5.62e-01 |
8.16e-01 |
Post-translational protein modification |
1002 |
1.71e-01 |
4.58e-01 |
0.0363 |
3.45e-02 |
0.011000 |
7.02e-02 |
5.63e-01 |
tRNA processing |
85 |
8.55e-01 |
9.42e-01 |
0.0353 |
3.51e-02 |
0.004020 |
5.76e-01 |
9.49e-01 |
Response to elevated platelet cytosolic Ca2+ |
100 |
8.32e-01 |
9.41e-01 |
0.0350 |
3.49e-02 |
-0.002770 |
5.47e-01 |
9.62e-01 |
Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding |
21 |
9.62e-01 |
9.83e-01 |
0.0350 |
1.30e-03 |
-0.035000 |
9.92e-01 |
7.81e-01 |
Metabolism of proteins |
1374 |
1.08e-01 |
3.53e-01 |
0.0350 |
3.49e-02 |
0.000920 |
3.51e-02 |
9.56e-01 |
FLT3 Signaling |
226 |
6.85e-01 |
8.66e-01 |
0.0344 |
-2.73e-02 |
-0.020900 |
4.81e-01 |
5.90e-01 |
Transport of inorganic cations/anions and amino acids/oligopeptides |
74 |
8.77e-01 |
9.52e-01 |
0.0341 |
-8.96e-03 |
0.032900 |
8.94e-01 |
6.25e-01 |
Toll Like Receptor 3 (TLR3) Cascade |
79 |
8.68e-01 |
9.47e-01 |
0.0340 |
-2.63e-02 |
0.021400 |
6.86e-01 |
7.42e-01 |
PTEN Regulation |
118 |
8.10e-01 |
9.36e-01 |
0.0339 |
2.60e-02 |
-0.021800 |
6.27e-01 |
6.83e-01 |
Amyloid fiber formation |
32 |
9.47e-01 |
9.77e-01 |
0.0339 |
-6.08e-03 |
-0.033400 |
9.53e-01 |
7.44e-01 |
HIV Life Cycle |
108 |
8.38e-01 |
9.41e-01 |
0.0332 |
3.32e-02 |
0.001970 |
5.52e-01 |
9.72e-01 |
Cytosolic sensors of pathogen-associated DNA |
48 |
9.22e-01 |
9.69e-01 |
0.0330 |
2.03e-02 |
-0.026100 |
8.08e-01 |
7.55e-01 |
Basigin interactions |
20 |
9.67e-01 |
9.86e-01 |
0.0327 |
-1.52e-02 |
0.028900 |
9.06e-01 |
8.23e-01 |
Interleukin-2 signaling |
10 |
9.84e-01 |
9.90e-01 |
0.0325 |
-8.87e-03 |
0.031300 |
9.61e-01 |
8.64e-01 |
Senescence-Associated Secretory Phenotype (SASP) |
39 |
9.38e-01 |
9.71e-01 |
0.0325 |
1.29e-02 |
-0.029800 |
8.89e-01 |
7.48e-01 |
Gap junction trafficking |
14 |
9.78e-01 |
9.89e-01 |
0.0324 |
-1.11e-02 |
0.030400 |
9.42e-01 |
8.44e-01 |
G alpha (i) signalling events |
188 |
7.46e-01 |
8.99e-01 |
0.0321 |
-3.06e-02 |
0.009450 |
4.70e-01 |
8.24e-01 |
Signaling by Hedgehog |
111 |
8.49e-01 |
9.41e-01 |
0.0320 |
-1.29e-02 |
-0.029300 |
8.15e-01 |
5.95e-01 |
Signaling by FGFR1 in disease |
30 |
9.55e-01 |
9.81e-01 |
0.0318 |
3.12e-02 |
-0.005860 |
7.68e-01 |
9.56e-01 |
Transcription of the HIV genome |
53 |
9.25e-01 |
9.70e-01 |
0.0313 |
4.43e-03 |
-0.031000 |
9.56e-01 |
6.97e-01 |
Signal regulatory protein family interactions |
13 |
9.81e-01 |
9.89e-01 |
0.0311 |
3.00e-02 |
-0.007990 |
8.51e-01 |
9.60e-01 |
ESR-mediated signaling |
133 |
8.22e-01 |
9.40e-01 |
0.0309 |
-1.86e-02 |
0.024700 |
7.12e-01 |
6.24e-01 |
AMER1 mutants destabilize the destruction complex |
13 |
9.82e-01 |
9.89e-01 |
0.0309 |
1.98e-02 |
0.023700 |
9.02e-01 |
8.82e-01 |
APC truncation mutants have impaired AXIN binding |
13 |
9.82e-01 |
9.89e-01 |
0.0309 |
1.98e-02 |
0.023700 |
9.02e-01 |
8.82e-01 |
AXIN missense mutants destabilize the destruction complex |
13 |
9.82e-01 |
9.89e-01 |
0.0309 |
1.98e-02 |
0.023700 |
9.02e-01 |
8.82e-01 |
AXIN mutants destabilize the destruction complex, activating WNT signaling |
13 |
9.82e-01 |
9.89e-01 |
0.0309 |
1.98e-02 |
0.023700 |
9.02e-01 |
8.82e-01 |
Truncations of AMER1 destabilize the destruction complex |
13 |
9.82e-01 |
9.89e-01 |
0.0309 |
1.98e-02 |
0.023700 |
9.02e-01 |
8.82e-01 |
truncated APC mutants destabilize the destruction complex |
13 |
9.82e-01 |
9.89e-01 |
0.0309 |
1.98e-02 |
0.023700 |
9.02e-01 |
8.82e-01 |
Signaling by FGFR4 |
27 |
9.63e-01 |
9.83e-01 |
0.0307 |
3.02e-02 |
0.005440 |
7.86e-01 |
9.61e-01 |
Disease |
1017 |
2.89e-01 |
6.03e-01 |
0.0298 |
-4.16e-05 |
0.029800 |
9.98e-01 |
1.16e-01 |
Interleukin-17 signaling |
59 |
9.23e-01 |
9.69e-01 |
0.0298 |
-2.75e-02 |
0.011400 |
7.15e-01 |
8.80e-01 |
Extra-nuclear estrogen signaling |
61 |
9.21e-01 |
9.69e-01 |
0.0298 |
4.96e-03 |
-0.029300 |
9.47e-01 |
6.92e-01 |
VLDLR internalisation and degradation |
11 |
9.86e-01 |
9.91e-01 |
0.0297 |
1.75e-02 |
0.024000 |
9.20e-01 |
8.90e-01 |
L1CAM interactions |
86 |
8.92e-01 |
9.59e-01 |
0.0296 |
-2.89e-02 |
0.006200 |
6.43e-01 |
9.21e-01 |
O-linked glycosylation of mucins |
31 |
9.62e-01 |
9.83e-01 |
0.0293 |
-2.51e-02 |
-0.015200 |
8.09e-01 |
8.83e-01 |
Signaling by Nuclear Receptors |
185 |
7.95e-01 |
9.26e-01 |
0.0288 |
5.09e-03 |
-0.028300 |
9.05e-01 |
5.08e-01 |
GPCR ligand binding |
155 |
8.43e-01 |
9.41e-01 |
0.0276 |
-2.68e-02 |
-0.006430 |
5.66e-01 |
8.91e-01 |
HATs acetylate histones |
64 |
9.34e-01 |
9.70e-01 |
0.0269 |
-2.68e-02 |
-0.002100 |
7.11e-01 |
9.77e-01 |
Peptide ligand-binding receptors |
65 |
9.33e-01 |
9.70e-01 |
0.0264 |
-8.80e-03 |
0.024900 |
9.02e-01 |
7.29e-01 |
Signaling by Rho GTPases |
315 |
7.38e-01 |
8.94e-01 |
0.0263 |
1.76e-02 |
0.019500 |
5.93e-01 |
5.55e-01 |
SUMOylation of transcription cofactors |
36 |
9.70e-01 |
9.87e-01 |
0.0240 |
-2.27e-02 |
-0.007860 |
8.14e-01 |
9.35e-01 |
Processing of SMDT1 |
11 |
9.91e-01 |
9.94e-01 |
0.0230 |
-7.07e-03 |
-0.021900 |
9.68e-01 |
9.00e-01 |
PIP3 activates AKT signaling |
217 |
8.51e-01 |
9.41e-01 |
0.0229 |
1.94e-02 |
0.012200 |
6.24e-01 |
7.57e-01 |
Signaling by FGFR2 in disease |
27 |
9.80e-01 |
9.89e-01 |
0.0224 |
-5.14e-03 |
-0.021800 |
9.63e-01 |
8.45e-01 |
SHC-mediated cascade:FGFR2 |
14 |
9.90e-01 |
9.94e-01 |
0.0219 |
-4.46e-03 |
-0.021400 |
9.77e-01 |
8.90e-01 |
Chaperonin-mediated protein folding |
67 |
9.62e-01 |
9.83e-01 |
0.0197 |
-2.56e-03 |
-0.019500 |
9.71e-01 |
7.83e-01 |
TP53 Regulates Transcription of Cell Death Genes |
34 |
9.80e-01 |
9.89e-01 |
0.0195 |
1.91e-02 |
-0.004010 |
8.47e-01 |
9.68e-01 |
FCGR3A-mediated IL10 synthesis |
38 |
9.85e-01 |
9.90e-01 |
0.0169 |
-1.18e-02 |
-0.012100 |
9.00e-01 |
8.97e-01 |
Late Phase of HIV Life Cycle |
99 |
9.66e-01 |
9.86e-01 |
0.0149 |
1.10e-02 |
-0.010000 |
8.50e-01 |
8.63e-01 |
Intracellular signaling by second messengers |
252 |
9.22e-01 |
9.69e-01 |
0.0145 |
-1.11e-02 |
0.009320 |
7.62e-01 |
8.00e-01 |
Golgi-to-ER retrograde transport |
98 |
9.69e-01 |
9.87e-01 |
0.0145 |
1.24e-02 |
-0.007450 |
8.32e-01 |
8.99e-01 |
Interleukin-4 and Interleukin-13 signaling |
82 |
9.77e-01 |
9.89e-01 |
0.0141 |
-4.97e-03 |
-0.013200 |
9.38e-01 |
8.37e-01 |
Frs2-mediated activation |
12 |
9.96e-01 |
9.97e-01 |
0.0139 |
-4.79e-03 |
0.013000 |
9.77e-01 |
9.38e-01 |
Downstream signaling of activated FGFR2 |
20 |
9.95e-01 |
9.97e-01 |
0.0126 |
-9.54e-03 |
0.008260 |
9.41e-01 |
9.49e-01 |
Hemostasis |
426 |
9.17e-01 |
9.69e-01 |
0.0121 |
-1.07e-02 |
-0.005640 |
7.08e-01 |
8.43e-01 |
MAP kinase activation |
56 |
9.91e-01 |
9.94e-01 |
0.0103 |
2.98e-03 |
0.009910 |
9.69e-01 |
8.98e-01 |
Organelle biogenesis and maintenance |
219 |
9.79e-01 |
9.89e-01 |
0.0083 |
-6.81e-03 |
-0.004750 |
8.63e-01 |
9.04e-01 |
Aggrephagy |
14 |
9.99e-01 |
9.99e-01 |
0.0070 |
3.16e-03 |
-0.006240 |
9.84e-01 |
9.68e-01 |