Leading Strand Synthesis |
12 |
1.02e-05 |
9.80e-05 |
0.79900 |
7.95e-01 |
8.11e-02 |
1.87e-06 |
0.627000 |
Polymerase switching |
12 |
1.02e-05 |
9.80e-05 |
0.79900 |
7.95e-01 |
8.11e-02 |
1.87e-06 |
0.627000 |
DNA strand elongation |
23 |
3.42e-10 |
1.52e-08 |
0.79500 |
7.92e-01 |
-6.91e-02 |
4.70e-11 |
0.566000 |
Lagging Strand Synthesis |
16 |
6.65e-07 |
8.44e-06 |
0.77000 |
7.66e-01 |
7.61e-02 |
1.13e-07 |
0.598000 |
Inhibition of replication initiation of damaged DNA by RB1/E2F1 |
12 |
3.25e-05 |
2.77e-04 |
0.75700 |
6.70e-01 |
3.51e-01 |
5.81e-05 |
0.035400 |
Mismatch repair (MMR) directed by MSH2:MSH6 (MutSalpha) |
12 |
4.04e-05 |
3.29e-04 |
0.74900 |
7.28e-01 |
1.77e-01 |
1.26e-05 |
0.288000 |
Processive synthesis on the lagging strand |
12 |
4.89e-05 |
3.76e-04 |
0.74200 |
7.40e-01 |
6.10e-02 |
9.04e-06 |
0.715000 |
Removal of the Flap Intermediate |
11 |
1.21e-04 |
8.51e-04 |
0.74000 |
7.39e-01 |
-1.61e-02 |
2.17e-05 |
0.926000 |
GP1b-IX-V activation signalling |
10 |
4.99e-04 |
2.86e-03 |
0.71200 |
-7.10e-01 |
6.38e-02 |
1.02e-04 |
0.727000 |
E2F mediated regulation of DNA replication |
18 |
1.50e-06 |
1.76e-05 |
0.70300 |
5.50e-01 |
4.38e-01 |
5.32e-05 |
0.001290 |
PCNA-Dependent Long Patch Base Excision Repair |
15 |
2.47e-05 |
2.24e-04 |
0.68600 |
6.60e-01 |
1.87e-01 |
9.52e-06 |
0.211000 |
Translesion Synthesis by POLH |
10 |
8.83e-04 |
4.64e-03 |
0.68400 |
6.34e-01 |
2.55e-01 |
5.14e-04 |
0.162000 |
Mismatch repair (MMR) directed by MSH2:MSH3 (MutSbeta) |
12 |
2.91e-04 |
1.84e-03 |
0.67200 |
6.51e-01 |
1.68e-01 |
9.53e-05 |
0.313000 |
Heme biosynthesis |
11 |
6.77e-04 |
3.68e-03 |
0.66400 |
6.15e-01 |
2.52e-01 |
4.16e-04 |
0.148000 |
WNT5A-dependent internalization of FZD2, FZD5 and ROR2 |
12 |
3.69e-04 |
2.24e-03 |
0.66100 |
5.22e-01 |
4.06e-01 |
1.73e-03 |
0.015000 |
Mismatch Repair |
13 |
3.06e-04 |
1.91e-03 |
0.64400 |
6.12e-01 |
2.00e-01 |
1.34e-04 |
0.213000 |
Condensation of Prophase Chromosomes |
10 |
2.07e-03 |
1.01e-02 |
0.64100 |
4.14e-01 |
4.89e-01 |
2.34e-02 |
0.007440 |
G1/S-Specific Transcription |
23 |
7.67e-07 |
9.65e-06 |
0.63900 |
6.19e-01 |
1.55e-01 |
2.72e-07 |
0.197000 |
Initiation of Nuclear Envelope (NE) Reformation |
14 |
1.91e-04 |
1.29e-03 |
0.63800 |
5.79e-01 |
2.68e-01 |
1.77e-04 |
0.083200 |
Gap-filling DNA repair synthesis and ligation in GG-NER |
17 |
4.62e-05 |
3.64e-04 |
0.62500 |
6.10e-01 |
1.39e-01 |
1.34e-05 |
0.323000 |
Formation of the ternary complex, and subsequently, the 43S complex |
17 |
4.66e-05 |
3.65e-04 |
0.62500 |
6.10e-01 |
1.36e-01 |
1.33e-05 |
0.332000 |
cGMP effects |
13 |
5.26e-04 |
2.98e-03 |
0.62200 |
-6.15e-01 |
-9.58e-02 |
1.25e-04 |
0.550000 |
Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S |
21 |
5.22e-06 |
5.51e-05 |
0.62100 |
5.79e-01 |
2.25e-01 |
4.44e-06 |
0.074500 |
Ubiquitin Mediated Degradation of Phosphorylated Cdc25A |
33 |
6.76e-09 |
1.56e-07 |
0.61700 |
6.17e-01 |
5.82e-03 |
8.60e-10 |
0.954000 |
p53-Independent DNA Damage Response |
33 |
6.76e-09 |
1.56e-07 |
0.61700 |
6.17e-01 |
5.82e-03 |
8.60e-10 |
0.954000 |
p53-Independent G1/S DNA damage checkpoint |
33 |
6.76e-09 |
1.56e-07 |
0.61700 |
6.17e-01 |
5.82e-03 |
8.60e-10 |
0.954000 |
Ribosomal scanning and start codon recognition |
20 |
1.32e-05 |
1.23e-04 |
0.61100 |
5.73e-01 |
2.14e-01 |
9.23e-06 |
0.097700 |
Translation initiation complex formation |
20 |
1.32e-05 |
1.23e-04 |
0.61100 |
5.73e-01 |
2.14e-01 |
9.23e-06 |
0.097700 |
Cross-presentation of soluble exogenous antigens (endosomes) |
36 |
2.09e-09 |
6.50e-08 |
0.60900 |
6.02e-01 |
-9.22e-02 |
4.01e-10 |
0.339000 |
Recognition of DNA damage by PCNA-containing replication complex |
18 |
4.75e-05 |
3.68e-04 |
0.60700 |
5.96e-01 |
1.14e-01 |
1.19e-05 |
0.404000 |
Cyclin A/B1/B2 associated events during G2/M transition |
12 |
1.36e-03 |
6.81e-03 |
0.60500 |
5.24e-01 |
3.01e-01 |
1.67e-03 |
0.070900 |
Assembly of the pre-replicative complex |
46 |
1.49e-11 |
9.77e-10 |
0.60200 |
6.01e-01 |
3.04e-02 |
1.78e-12 |
0.722000 |
Resolution of AP sites via the multiple-nucleotide patch replacement pathway |
17 |
9.68e-05 |
7.01e-04 |
0.60200 |
5.73e-01 |
1.83e-01 |
4.29e-05 |
0.193000 |
DNA Replication Pre-Initiation |
58 |
3.00e-14 |
2.66e-12 |
0.59900 |
5.97e-01 |
4.69e-02 |
3.70e-15 |
0.537000 |
Formation of a pool of free 40S subunits |
34 |
1.41e-08 |
2.83e-07 |
0.59500 |
5.75e-01 |
1.55e-01 |
6.72e-09 |
0.117000 |
SCF-beta-TrCP mediated degradation of Emi1 |
37 |
3.85e-09 |
9.60e-08 |
0.59100 |
5.91e-01 |
1.27e-02 |
4.88e-10 |
0.893000 |
Ubiquitin-dependent degradation of Cyclin D |
35 |
1.64e-08 |
3.25e-07 |
0.58500 |
5.84e-01 |
2.55e-02 |
2.22e-09 |
0.794000 |
L13a-mediated translational silencing of Ceruloplasmin expression |
38 |
3.58e-09 |
9.10e-08 |
0.58400 |
5.52e-01 |
1.90e-01 |
3.93e-09 |
0.042400 |
Regulation of activated PAK-2p34 by proteasome mediated degradation |
33 |
5.07e-08 |
7.99e-07 |
0.58300 |
5.83e-01 |
2.04e-02 |
6.97e-09 |
0.840000 |
Transcription of E2F targets under negative control by p107 (RBL1) and p130 (RBL2) in complex with HDAC1 |
13 |
1.39e-03 |
6.90e-03 |
0.58000 |
5.52e-01 |
1.79e-01 |
5.71e-04 |
0.263000 |
Hh mutants that don't undergo autocatalytic processing are degraded by ERAD |
35 |
2.31e-08 |
4.28e-07 |
0.57900 |
5.79e-01 |
-3.40e-03 |
3.03e-09 |
0.972000 |
CDT1 association with the CDC6:ORC:origin complex |
39 |
3.13e-09 |
8.22e-08 |
0.57900 |
5.78e-01 |
2.62e-02 |
4.08e-10 |
0.777000 |
Regulation of ornithine decarboxylase (ODC) |
35 |
2.34e-08 |
4.28e-07 |
0.57900 |
5.79e-01 |
-5.84e-04 |
3.07e-09 |
0.995000 |
Activation of the pre-replicative complex |
23 |
9.82e-06 |
9.76e-05 |
0.57800 |
5.75e-01 |
5.74e-02 |
1.78e-06 |
0.634000 |
Telomere C-strand (Lagging Strand) Synthesis |
25 |
3.65e-06 |
3.88e-05 |
0.57800 |
5.78e-01 |
2.42e-02 |
5.77e-07 |
0.834000 |
Metabolism of polyamines |
40 |
2.19e-09 |
6.64e-08 |
0.57700 |
5.77e-01 |
-1.15e-02 |
2.71e-10 |
0.900000 |
Phase 2 - plateau phase |
17 |
2.13e-04 |
1.38e-03 |
0.57500 |
-5.35e-01 |
-2.13e-01 |
1.36e-04 |
0.129000 |
Digestion |
11 |
4.37e-03 |
2.01e-02 |
0.57400 |
-5.72e-01 |
5.46e-02 |
1.03e-03 |
0.754000 |
Cap-dependent Translation Initiation |
45 |
2.26e-10 |
1.08e-08 |
0.57400 |
5.57e-01 |
1.39e-01 |
1.05e-10 |
0.108000 |
Eukaryotic Translation Initiation |
45 |
2.26e-10 |
1.08e-08 |
0.57400 |
5.57e-01 |
1.39e-01 |
1.05e-10 |
0.108000 |
Vif-mediated degradation of APOBEC3G |
34 |
5.60e-08 |
8.71e-07 |
0.57300 |
5.72e-01 |
2.35e-02 |
7.78e-09 |
0.813000 |
Orc1 removal from chromatin |
47 |
1.01e-10 |
5.59e-09 |
0.57200 |
5.71e-01 |
3.28e-02 |
1.28e-11 |
0.698000 |
Autodegradation of the E3 ubiquitin ligase COP1 |
35 |
4.42e-08 |
7.19e-07 |
0.56900 |
5.67e-01 |
-4.07e-02 |
6.37e-09 |
0.677000 |
Deposition of new CENPA-containing nucleosomes at the centromere |
16 |
4.41e-04 |
2.58e-03 |
0.56800 |
5.68e-01 |
-1.44e-02 |
8.49e-05 |
0.920000 |
Nucleosome assembly |
16 |
4.41e-04 |
2.58e-03 |
0.56800 |
5.68e-01 |
-1.44e-02 |
8.49e-05 |
0.920000 |
AUF1 (hnRNP D0) binds and destabilizes mRNA |
36 |
3.30e-08 |
5.78e-07 |
0.56500 |
5.65e-01 |
-2.07e-02 |
4.44e-09 |
0.830000 |
GTP hydrolysis and joining of the 60S ribosomal subunit |
39 |
8.03e-09 |
1.79e-07 |
0.56400 |
5.35e-01 |
1.80e-01 |
7.45e-09 |
0.052600 |
Defective CFTR causes cystic fibrosis |
38 |
1.36e-08 |
2.78e-07 |
0.56400 |
5.64e-01 |
2.09e-02 |
1.81e-09 |
0.823000 |
Hh mutants abrogate ligand secretion |
37 |
2.37e-08 |
4.28e-07 |
0.56300 |
5.63e-01 |
-4.31e-03 |
3.11e-09 |
0.964000 |
Metabolism of porphyrins |
21 |
4.76e-05 |
3.68e-04 |
0.56100 |
4.73e-01 |
3.02e-01 |
1.75e-04 |
0.016600 |
Termination of translesion DNA synthesis |
21 |
4.95e-05 |
3.78e-04 |
0.56100 |
5.57e-01 |
6.50e-02 |
9.84e-06 |
0.606000 |
Translesion synthesis by POLI |
11 |
5.60e-03 |
2.45e-02 |
0.56100 |
5.60e-01 |
2.72e-02 |
1.30e-03 |
0.876000 |
Peptide chain elongation |
28 |
1.86e-06 |
2.15e-05 |
0.56000 |
5.21e-01 |
2.05e-01 |
1.82e-06 |
0.060400 |
Polymerase switching on the C-strand of the telomere |
21 |
5.51e-05 |
4.15e-04 |
0.55800 |
5.58e-01 |
1.72e-02 |
9.59e-06 |
0.892000 |
G1/S Transition |
92 |
2.74e-19 |
4.26e-17 |
0.55700 |
5.47e-01 |
1.09e-01 |
1.33e-19 |
0.070800 |
Heme degradation |
11 |
6.04e-03 |
2.59e-02 |
0.55600 |
3.75e-01 |
4.10e-01 |
3.12e-02 |
0.018700 |
Cholesterol biosynthesis |
16 |
6.33e-04 |
3.50e-03 |
0.55400 |
-5.41e-01 |
-1.18e-01 |
1.80e-04 |
0.413000 |
FBXL7 down-regulates AURKA during mitotic entry and in early mitosis |
37 |
4.66e-08 |
7.43e-07 |
0.55200 |
5.52e-01 |
2.08e-02 |
6.41e-09 |
0.827000 |
Synthesis of DNA |
86 |
1.34e-17 |
1.52e-15 |
0.55000 |
5.50e-01 |
-6.87e-03 |
1.20e-18 |
0.913000 |
Striated Muscle Contraction |
30 |
1.23e-06 |
1.46e-05 |
0.55000 |
-5.12e-01 |
-2.00e-01 |
1.21e-06 |
0.058700 |
SCF(Skp2)-mediated degradation of p27/p21 |
39 |
2.31e-08 |
4.28e-07 |
0.54900 |
5.48e-01 |
3.01e-02 |
3.23e-09 |
0.745000 |
Regulation of Apoptosis |
35 |
1.49e-07 |
2.18e-06 |
0.54800 |
5.48e-01 |
-8.87e-04 |
2.05e-08 |
0.993000 |
DNA Replication |
93 |
8.70e-19 |
1.08e-16 |
0.54700 |
5.47e-01 |
1.13e-02 |
7.71e-20 |
0.851000 |
The role of GTSE1 in G2/M progression after G2 checkpoint |
40 |
1.86e-08 |
3.56e-07 |
0.54500 |
5.38e-01 |
8.96e-02 |
4.07e-09 |
0.327000 |
Transcription of E2F targets under negative control by DREAM complex |
16 |
8.38e-04 |
4.46e-03 |
0.54300 |
5.15e-01 |
1.72e-01 |
3.62e-04 |
0.234000 |
Vpu mediated degradation of CD4 |
34 |
3.49e-07 |
4.94e-06 |
0.54100 |
5.40e-01 |
-1.20e-02 |
4.97e-08 |
0.904000 |
Autodegradation of Cdh1 by Cdh1:APC/C |
45 |
7.19e-09 |
1.63e-07 |
0.52800 |
5.23e-01 |
-6.98e-02 |
1.25e-09 |
0.418000 |
Extension of Telomeres |
35 |
4.49e-07 |
6.01e-06 |
0.52800 |
5.20e-01 |
8.97e-02 |
1.01e-07 |
0.359000 |
VLDLR internalisation and degradation |
10 |
1.53e-02 |
5.61e-02 |
0.52800 |
5.13e-01 |
1.23e-01 |
4.95e-03 |
0.502000 |
Negative regulation of NOTCH4 signaling |
37 |
2.25e-07 |
3.26e-06 |
0.52600 |
5.26e-01 |
1.11e-02 |
3.18e-08 |
0.907000 |
Translesion synthesis by REV1 |
10 |
1.62e-02 |
5.87e-02 |
0.52400 |
5.23e-01 |
3.52e-02 |
4.19e-03 |
0.847000 |
Mitotic G1 phase and G1/S transition |
104 |
3.32e-19 |
4.59e-17 |
0.52300 |
5.15e-01 |
9.33e-02 |
1.19e-19 |
0.101000 |
Resolution of D-loop Structures through Synthesis-Dependent Strand Annealing (SDSA) |
19 |
4.39e-04 |
2.58e-03 |
0.52200 |
4.85e-01 |
-1.93e-01 |
2.54e-04 |
0.145000 |
Eukaryotic Translation Elongation |
31 |
3.12e-06 |
3.43e-05 |
0.52200 |
4.82e-01 |
2.01e-01 |
3.47e-06 |
0.053400 |
RUNX1 regulates transcription of genes involved in differentiation of HSCs |
49 |
2.59e-09 |
7.33e-08 |
0.52000 |
5.14e-01 |
-7.59e-02 |
4.82e-10 |
0.359000 |
Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC) |
30 |
5.28e-06 |
5.52e-05 |
0.51900 |
4.73e-01 |
2.14e-01 |
7.30e-06 |
0.042800 |
G0 and Early G1 |
21 |
2.07e-04 |
1.36e-03 |
0.51900 |
5.06e-01 |
1.16e-01 |
6.08e-05 |
0.356000 |
APC:Cdc20 mediated degradation of cell cycle proteins prior to satisfation of the cell cycle checkpoint |
53 |
6.65e-10 |
2.43e-08 |
0.51600 |
5.16e-01 |
-6.92e-03 |
7.98e-11 |
0.931000 |
Cdc20:Phospho-APC/C mediated degradation of Cyclin A |
52 |
1.03e-09 |
3.48e-08 |
0.51600 |
5.16e-01 |
6.67e-03 |
1.26e-10 |
0.934000 |
Platelet Adhesion to exposed collagen |
11 |
1.27e-02 |
4.75e-02 |
0.51500 |
-4.75e-01 |
2.01e-01 |
6.40e-03 |
0.249000 |
Laminin interactions |
22 |
1.68e-04 |
1.15e-03 |
0.51300 |
-5.04e-01 |
-9.45e-02 |
4.23e-05 |
0.443000 |
Hedgehog ligand biogenesis |
41 |
1.02e-07 |
1.55e-06 |
0.51200 |
5.11e-01 |
-3.70e-02 |
1.50e-08 |
0.682000 |
APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins in late mitosis/early G1 |
54 |
6.37e-10 |
2.40e-08 |
0.51200 |
5.12e-01 |
-1.95e-02 |
7.82e-11 |
0.805000 |
APC/C:Cdc20 mediated degradation of mitotic proteins |
55 |
4.33e-10 |
1.75e-08 |
0.51200 |
5.12e-01 |
9.91e-03 |
5.20e-11 |
0.899000 |
Activation of APC/C and APC/C:Cdc20 mediated degradation of mitotic proteins |
55 |
4.33e-10 |
1.75e-08 |
0.51200 |
5.12e-01 |
9.91e-03 |
5.20e-11 |
0.899000 |
Homologous DNA Pairing and Strand Exchange |
28 |
1.77e-05 |
1.63e-04 |
0.51200 |
4.79e-01 |
-1.80e-01 |
1.17e-05 |
0.098800 |
Degradation of DVL |
38 |
3.86e-07 |
5.27e-06 |
0.51000 |
5.09e-01 |
2.56e-02 |
5.74e-08 |
0.785000 |
Generation of second messenger molecules |
22 |
2.03e-04 |
1.35e-03 |
0.50900 |
-4.88e-01 |
1.45e-01 |
7.57e-05 |
0.239000 |
CDK-mediated phosphorylation and removal of Cdc6 |
51 |
3.14e-09 |
8.22e-08 |
0.50700 |
5.02e-01 |
-6.73e-02 |
5.45e-10 |
0.406000 |
Eukaryotic Translation Termination |
30 |
9.98e-06 |
9.78e-05 |
0.50600 |
4.90e-01 |
1.27e-01 |
3.47e-06 |
0.230000 |
Cyclin A:Cdk2-associated events at S phase entry |
58 |
2.51e-10 |
1.16e-08 |
0.50500 |
5.03e-01 |
4.18e-02 |
3.50e-11 |
0.582000 |
Cyclin E associated events during G1/S transition |
56 |
5.43e-10 |
2.11e-08 |
0.50500 |
5.02e-01 |
5.17e-02 |
8.31e-11 |
0.504000 |
APC/C-mediated degradation of cell cycle proteins |
64 |
2.69e-11 |
1.59e-09 |
0.50400 |
5.01e-01 |
5.33e-02 |
4.07e-12 |
0.462000 |
Regulation of mitotic cell cycle |
64 |
2.69e-11 |
1.59e-09 |
0.50400 |
5.01e-01 |
5.33e-02 |
4.07e-12 |
0.462000 |
Regulation of APC/C activators between G1/S and early anaphase |
57 |
4.36e-10 |
1.75e-08 |
0.50300 |
5.02e-01 |
3.30e-02 |
5.78e-11 |
0.667000 |
Defects of contact activation system (CAS) and kallikrein/kinin system (KKS) |
12 |
1.07e-02 |
4.15e-02 |
0.50300 |
-4.91e-01 |
1.08e-01 |
3.24e-03 |
0.518000 |
Diseases of hemostasis |
12 |
1.07e-02 |
4.15e-02 |
0.50300 |
-4.91e-01 |
1.08e-01 |
3.24e-03 |
0.518000 |
SRP-dependent cotranslational protein targeting to membrane |
43 |
8.82e-08 |
1.36e-06 |
0.50200 |
4.80e-01 |
1.46e-01 |
5.11e-08 |
0.098700 |
TNF receptor superfamily (TNFSF) members mediating non-canonical NF-kB pathway |
12 |
1.14e-02 |
4.34e-02 |
0.50000 |
-4.22e-01 |
2.68e-01 |
1.14e-02 |
0.108000 |
Presynaptic phase of homologous DNA pairing and strand exchange |
25 |
9.17e-05 |
6.67e-04 |
0.49900 |
4.55e-01 |
-2.04e-01 |
8.14e-05 |
0.077000 |
Viral mRNA Translation |
28 |
2.95e-05 |
2.59e-04 |
0.49800 |
4.72e-01 |
1.59e-01 |
1.54e-05 |
0.146000 |
Degradation of GLI1 by the proteasome |
39 |
6.06e-07 |
7.94e-06 |
0.49500 |
4.95e-01 |
-2.48e-03 |
8.74e-08 |
0.979000 |
APC/C:Cdc20 mediated degradation of Securin |
49 |
1.75e-08 |
3.41e-07 |
0.49400 |
4.92e-01 |
-4.42e-02 |
2.60e-09 |
0.593000 |
TP53 Regulates Transcription of Genes Involved in G2 Cell Cycle Arrest |
16 |
3.05e-03 |
1.44e-02 |
0.49100 |
4.85e-01 |
7.64e-02 |
7.79e-04 |
0.597000 |
Postmitotic nuclear pore complex (NPC) reformation |
20 |
7.19e-04 |
3.86e-03 |
0.49100 |
4.72e-01 |
1.37e-01 |
2.62e-04 |
0.290000 |
Switching of origins to a post-replicative state |
64 |
1.03e-10 |
5.59e-09 |
0.49000 |
4.90e-01 |
-1.83e-02 |
1.22e-11 |
0.801000 |
Activation of ATR in response to replication stress |
23 |
2.75e-04 |
1.75e-03 |
0.48800 |
4.86e-01 |
3.81e-02 |
5.45e-05 |
0.752000 |
Mitochondrial translation elongation |
56 |
2.51e-09 |
7.33e-08 |
0.48600 |
4.86e-01 |
2.44e-02 |
3.29e-10 |
0.752000 |
Chromosome Maintenance |
56 |
2.89e-09 |
8.00e-08 |
0.48500 |
4.84e-01 |
1.86e-02 |
3.73e-10 |
0.810000 |
GLI3 is processed to GLI3R by the proteasome |
39 |
1.12e-06 |
1.35e-05 |
0.48500 |
4.84e-01 |
2.05e-02 |
1.70e-07 |
0.824000 |
HDR through Homologous Recombination (HRR) |
42 |
4.09e-07 |
5.53e-06 |
0.48400 |
4.78e-01 |
-7.72e-02 |
8.40e-08 |
0.387000 |
Resolution of D-loop Structures through Holliday Junction Intermediates |
22 |
4.63e-04 |
2.67e-03 |
0.48300 |
4.46e-01 |
-1.86e-01 |
2.92e-04 |
0.131000 |
NIK-->noncanonical NF-kB signaling |
38 |
1.95e-06 |
2.23e-05 |
0.48100 |
4.74e-01 |
-8.02e-02 |
4.20e-07 |
0.393000 |
Purine catabolism |
14 |
7.81e-03 |
3.16e-02 |
0.48100 |
4.79e-01 |
3.57e-02 |
1.90e-03 |
0.817000 |
TP53 Regulates Transcription of Death Receptors and Ligands |
10 |
3.20e-02 |
1.05e-01 |
0.48000 |
-3.74e-01 |
3.01e-01 |
4.05e-02 |
0.099300 |
Translesion synthesis by Y family DNA polymerases bypasses lesions on DNA template |
26 |
1.24e-04 |
8.64e-04 |
0.48000 |
4.67e-01 |
1.12e-01 |
3.80e-05 |
0.322000 |
Translocation of ZAP-70 to Immunological synapse |
11 |
2.26e-02 |
7.78e-02 |
0.48000 |
-4.73e-01 |
8.15e-02 |
6.61e-03 |
0.640000 |
ABC transporter disorders |
46 |
1.34e-07 |
1.99e-06 |
0.48000 |
4.79e-01 |
-1.33e-02 |
1.87e-08 |
0.876000 |
Translesion synthesis by POLK |
11 |
2.25e-02 |
7.78e-02 |
0.48000 |
4.75e-01 |
6.38e-02 |
6.35e-03 |
0.714000 |
Degradation of GLI2 by the proteasome |
40 |
1.11e-06 |
1.35e-05 |
0.47900 |
4.78e-01 |
2.15e-02 |
1.70e-07 |
0.814000 |
Resolution of D-Loop Structures |
23 |
3.90e-04 |
2.35e-03 |
0.47800 |
4.47e-01 |
-1.69e-01 |
2.05e-04 |
0.161000 |
Presynaptic depolarization and calcium channel opening |
11 |
2.30e-02 |
7.92e-02 |
0.47800 |
-4.75e-01 |
-5.46e-02 |
6.40e-03 |
0.754000 |
Mitochondrial translation termination |
56 |
5.15e-09 |
1.26e-07 |
0.47700 |
4.77e-01 |
1.37e-02 |
6.62e-10 |
0.860000 |
Selenocysteine synthesis |
30 |
3.81e-05 |
3.14e-04 |
0.47500 |
4.32e-01 |
1.97e-01 |
4.17e-05 |
0.061900 |
FCGR activation |
15 |
6.33e-03 |
2.66e-02 |
0.47500 |
4.63e-01 |
-1.08e-01 |
1.93e-03 |
0.468000 |
Digestion and absorption |
12 |
1.77e-02 |
6.35e-02 |
0.47400 |
-4.61e-01 |
1.10e-01 |
5.69e-03 |
0.510000 |
Degradation of AXIN |
36 |
6.03e-06 |
6.26e-05 |
0.47200 |
4.71e-01 |
-3.39e-02 |
1.00e-06 |
0.725000 |
Dectin-1 mediated noncanonical NF-kB signaling |
40 |
1.63e-06 |
1.89e-05 |
0.47200 |
4.65e-01 |
-8.32e-02 |
3.65e-07 |
0.363000 |
Stabilization of p53 |
38 |
3.22e-06 |
3.47e-05 |
0.47200 |
4.70e-01 |
-3.58e-02 |
5.26e-07 |
0.702000 |
Oxygen-dependent proline hydroxylation of Hypoxia-inducible Factor Alpha |
43 |
6.44e-07 |
8.27e-06 |
0.47000 |
4.65e-01 |
7.29e-02 |
1.35e-07 |
0.409000 |
Retrograde neurotrophin signalling |
12 |
1.88e-02 |
6.66e-02 |
0.47000 |
4.63e-01 |
7.90e-02 |
5.48e-03 |
0.636000 |
Telomere Maintenance |
42 |
9.67e-07 |
1.19e-05 |
0.46900 |
4.65e-01 |
6.33e-02 |
1.87e-07 |
0.478000 |
Apoptotic factor-mediated response |
11 |
2.73e-02 |
9.17e-02 |
0.46700 |
4.66e-01 |
2.86e-02 |
7.42e-03 |
0.870000 |
Aberrant regulation of mitotic G1/S transition in cancer due to RB1 defects |
13 |
1.49e-02 |
5.48e-02 |
0.46400 |
3.51e-01 |
3.03e-01 |
2.86e-02 |
0.058300 |
Defective binding of RB1 mutants to E2F1,(E2F2, E2F3) |
13 |
1.49e-02 |
5.48e-02 |
0.46400 |
3.51e-01 |
3.03e-01 |
2.86e-02 |
0.058300 |
S Phase |
118 |
3.98e-17 |
4.13e-15 |
0.46300 |
4.61e-01 |
4.35e-02 |
5.22e-18 |
0.416000 |
DNA Damage Bypass |
31 |
5.00e-05 |
3.79e-04 |
0.46100 |
4.43e-01 |
1.29e-01 |
1.98e-05 |
0.213000 |
SUMOylation of DNA replication proteins |
32 |
3.84e-05 |
3.15e-04 |
0.46000 |
4.36e-01 |
1.48e-01 |
2.00e-05 |
0.149000 |
G2/M Checkpoints |
90 |
6.08e-13 |
5.05e-11 |
0.45800 |
4.56e-01 |
4.04e-02 |
8.13e-14 |
0.509000 |
Common Pathway of Fibrin Clot Formation |
12 |
2.31e-02 |
7.92e-02 |
0.45700 |
-4.01e-01 |
-2.18e-01 |
1.61e-02 |
0.190000 |
Phosphorylation of CD3 and TCR zeta chains |
13 |
1.76e-02 |
6.32e-02 |
0.45500 |
-4.46e-01 |
-8.96e-02 |
5.37e-03 |
0.576000 |
Translation |
150 |
1.06e-20 |
3.31e-18 |
0.45400 |
4.53e-01 |
3.52e-02 |
1.19e-21 |
0.458000 |
Mitochondrial translation initiation |
56 |
3.46e-08 |
5.90e-07 |
0.45300 |
4.51e-01 |
4.16e-02 |
5.39e-09 |
0.590000 |
Processive synthesis on the C-strand of the telomere |
13 |
1.83e-02 |
6.52e-02 |
0.45300 |
4.48e-01 |
6.30e-02 |
5.13e-03 |
0.694000 |
HDMs demethylate histones |
15 |
1.03e-02 |
4.02e-02 |
0.45200 |
-3.95e-01 |
2.19e-01 |
8.04e-03 |
0.142000 |
GABA synthesis, release, reuptake and degradation |
11 |
3.45e-02 |
1.12e-01 |
0.45200 |
-4.51e-01 |
-3.31e-02 |
9.67e-03 |
0.849000 |
Rev-mediated nuclear export of HIV RNA |
24 |
6.66e-04 |
3.63e-03 |
0.45100 |
4.34e-01 |
1.21e-01 |
2.32e-04 |
0.306000 |
Surfactant metabolism |
13 |
1.91e-02 |
6.75e-02 |
0.45100 |
-7.42e-02 |
-4.44e-01 |
6.43e-01 |
0.005540 |
Nuclear import of Rev protein |
23 |
9.35e-04 |
4.89e-03 |
0.45000 |
4.44e-01 |
7.21e-02 |
2.30e-04 |
0.550000 |
Metabolism of folate and pterines |
14 |
1.56e-02 |
5.73e-02 |
0.44500 |
4.41e-01 |
-6.27e-02 |
4.28e-03 |
0.685000 |
HDR through Single Strand Annealing (SSA) |
26 |
4.57e-04 |
2.64e-03 |
0.44500 |
3.83e-01 |
-2.27e-01 |
7.28e-04 |
0.044900 |
Amplification of signal from unattached kinetochores via a MAD2 inhibitory signal |
68 |
1.75e-09 |
5.58e-08 |
0.44500 |
4.37e-01 |
8.57e-02 |
4.77e-10 |
0.222000 |
Amplification of signal from the kinetochores |
68 |
1.75e-09 |
5.58e-08 |
0.44500 |
4.37e-01 |
8.57e-02 |
4.77e-10 |
0.222000 |
Defective EXT1 causes exostoses 1, TRPS2 and CHDS |
10 |
5.22e-02 |
1.50e-01 |
0.44400 |
-8.79e-03 |
-4.44e-01 |
9.62e-01 |
0.015100 |
Defective EXT2 causes exostoses 2 |
10 |
5.22e-02 |
1.50e-01 |
0.44400 |
-8.79e-03 |
-4.44e-01 |
9.62e-01 |
0.015100 |
Interactions of Rev with host cellular proteins |
25 |
6.25e-04 |
3.48e-03 |
0.44300 |
4.30e-01 |
1.08e-01 |
1.99e-04 |
0.348000 |
Nitric oxide stimulates guanylate cyclase |
18 |
5.11e-03 |
2.30e-02 |
0.44200 |
-4.31e-01 |
-9.65e-02 |
1.54e-03 |
0.479000 |
Separation of Sister Chromatids |
124 |
2.19e-16 |
2.10e-14 |
0.44200 |
4.40e-01 |
4.40e-02 |
3.02e-17 |
0.398000 |
Golgi Cisternae Pericentriolar Stack Reorganization |
11 |
4.06e-02 |
1.27e-01 |
0.44000 |
2.72e-01 |
3.46e-01 |
1.19e-01 |
0.047000 |
Fanconi Anemia Pathway |
22 |
1.72e-03 |
8.42e-03 |
0.44000 |
4.39e-01 |
-2.17e-02 |
3.64e-04 |
0.860000 |
Constitutive Signaling by NOTCH1 HD Domain Mutants |
10 |
5.54e-02 |
1.58e-01 |
0.43900 |
-4.25e-01 |
-1.09e-01 |
1.99e-02 |
0.550000 |
Signaling by NOTCH1 HD Domain Mutants in Cancer |
10 |
5.54e-02 |
1.58e-01 |
0.43900 |
-4.25e-01 |
-1.09e-01 |
1.99e-02 |
0.550000 |
Insulin processing |
16 |
1.00e-02 |
3.93e-02 |
0.43900 |
-4.02e-01 |
1.75e-01 |
5.34e-03 |
0.225000 |
Assembly of collagen fibrils and other multimeric structures |
37 |
2.65e-05 |
2.36e-04 |
0.43500 |
-3.65e-01 |
-2.38e-01 |
1.23e-04 |
0.012500 |
Hyaluronan metabolism |
11 |
4.52e-02 |
1.36e-01 |
0.43400 |
3.57e-01 |
-2.47e-01 |
4.03e-02 |
0.156000 |
Regulation of RUNX3 expression and activity |
37 |
3.13e-05 |
2.69e-04 |
0.43300 |
4.22e-01 |
-1.00e-01 |
9.22e-06 |
0.291000 |
Mitochondrial translation |
62 |
3.55e-08 |
5.98e-07 |
0.43000 |
4.30e-01 |
4.37e-03 |
4.73e-09 |
0.953000 |
Incretin synthesis, secretion, and inactivation |
10 |
6.38e-02 |
1.75e-01 |
0.42800 |
-4.03e-01 |
-1.43e-01 |
2.73e-02 |
0.433000 |
alpha-linolenic (omega3) and linoleic (omega6) acid metabolism |
10 |
6.44e-02 |
1.75e-01 |
0.42800 |
2.67e-02 |
4.27e-01 |
8.84e-01 |
0.019400 |
alpha-linolenic acid (ALA) metabolism |
10 |
6.44e-02 |
1.75e-01 |
0.42800 |
2.67e-02 |
4.27e-01 |
8.84e-01 |
0.019400 |
Mitotic Metaphase and Anaphase |
166 |
2.74e-20 |
6.81e-18 |
0.42700 |
4.18e-01 |
8.91e-02 |
1.79e-20 |
0.048500 |
Resolution of Sister Chromatid Cohesion |
77 |
7.37e-10 |
2.62e-08 |
0.42700 |
4.12e-01 |
1.15e-01 |
4.45e-10 |
0.080900 |
Nuclear Envelope (NE) Reassembly |
51 |
8.66e-07 |
1.08e-05 |
0.42700 |
3.69e-01 |
2.16e-01 |
5.31e-06 |
0.007810 |
Elevation of cytosolic Ca2+ levels |
10 |
6.50e-02 |
1.76e-01 |
0.42600 |
-3.32e-01 |
-2.68e-01 |
6.95e-02 |
0.143000 |
NEP/NS2 Interacts with the Cellular Export Machinery |
22 |
2.58e-03 |
1.25e-02 |
0.42500 |
4.06e-01 |
1.24e-01 |
9.76e-04 |
0.313000 |
Mitotic Anaphase |
165 |
6.76e-20 |
1.40e-17 |
0.42400 |
4.16e-01 |
8.59e-02 |
3.84e-20 |
0.057800 |
Removal of the Flap Intermediate from the C-strand |
12 |
3.97e-02 |
1.25e-01 |
0.42400 |
4.24e-01 |
-7.48e-03 |
1.11e-02 |
0.964000 |
Initial triggering of complement |
19 |
6.27e-03 |
2.65e-02 |
0.42300 |
4.11e-01 |
-9.65e-02 |
1.91e-03 |
0.467000 |
ER-Phagosome pathway |
54 |
5.68e-07 |
7.52e-06 |
0.42200 |
4.17e-01 |
-6.96e-02 |
1.20e-07 |
0.377000 |
HDR through Homologous Recombination (HRR) or Single Strand Annealing (SSA) |
66 |
2.61e-08 |
4.65e-07 |
0.42100 |
4.19e-01 |
4.23e-02 |
4.18e-09 |
0.553000 |
Influenza Viral RNA Transcription and Replication |
56 |
3.64e-07 |
5.09e-06 |
0.42100 |
4.12e-01 |
8.29e-02 |
9.60e-08 |
0.284000 |
Homology Directed Repair |
70 |
1.00e-08 |
2.15e-07 |
0.42000 |
4.18e-01 |
4.04e-02 |
1.55e-09 |
0.560000 |
Diseases of DNA repair |
10 |
7.10e-02 |
1.85e-01 |
0.41900 |
3.08e-01 |
2.84e-01 |
9.18e-02 |
0.120000 |
Regulation of expression of SLITs and ROBOs |
80 |
7.68e-10 |
2.66e-08 |
0.41900 |
4.04e-01 |
1.11e-01 |
4.44e-10 |
0.085300 |
EML4 and NUDC in mitotic spindle formation |
71 |
8.75e-09 |
1.91e-07 |
0.41800 |
4.13e-01 |
6.63e-02 |
1.85e-09 |
0.335000 |
Resolution of Abasic Sites (AP sites) |
30 |
3.89e-04 |
2.35e-03 |
0.41800 |
4.10e-01 |
7.83e-02 |
1.00e-04 |
0.458000 |
Defective TPR may confer susceptibility towards thyroid papillary carcinoma (TPC) |
20 |
5.36e-03 |
2.38e-02 |
0.41700 |
4.07e-01 |
9.19e-02 |
1.63e-03 |
0.477000 |
Regulation of Glucokinase by Glucokinase Regulatory Protein |
20 |
5.36e-03 |
2.38e-02 |
0.41700 |
4.07e-01 |
9.19e-02 |
1.63e-03 |
0.477000 |
Vpr-mediated nuclear import of PICs |
23 |
2.59e-03 |
1.25e-02 |
0.41500 |
3.98e-01 |
1.19e-01 |
9.59e-04 |
0.322000 |
SUMOylation of SUMOylation proteins |
22 |
3.40e-03 |
1.59e-02 |
0.41500 |
3.96e-01 |
1.23e-01 |
1.30e-03 |
0.318000 |
MET activates PTK2 signaling |
16 |
1.62e-02 |
5.87e-02 |
0.41400 |
-3.95e-01 |
-1.25e-01 |
6.25e-03 |
0.386000 |
Regulation of PTEN stability and activity |
46 |
8.07e-06 |
8.24e-05 |
0.41300 |
4.13e-01 |
-1.99e-05 |
1.28e-06 |
1.000000 |
Receptor-type tyrosine-protein phosphatases |
10 |
7.94e-02 |
1.99e-01 |
0.41100 |
-8.07e-02 |
-4.03e-01 |
6.59e-01 |
0.027400 |
Glutamate and glutamine metabolism |
11 |
6.27e-02 |
1.73e-01 |
0.41000 |
3.82e-01 |
-1.51e-01 |
2.84e-02 |
0.387000 |
Regulation of necroptotic cell death |
12 |
4.97e-02 |
1.45e-01 |
0.40900 |
-3.81e-01 |
1.48e-01 |
2.22e-02 |
0.375000 |
Mitochondrial protein import |
44 |
1.78e-05 |
1.63e-04 |
0.40800 |
3.70e-01 |
-1.73e-01 |
2.19e-05 |
0.047500 |
Selenoamino acid metabolism |
39 |
5.78e-05 |
4.31e-04 |
0.40800 |
3.82e-01 |
1.45e-01 |
3.72e-05 |
0.118000 |
Defective B4GALT7 causes EDS, progeroid type |
14 |
3.06e-02 |
1.01e-01 |
0.40700 |
-1.22e-01 |
-3.88e-01 |
4.30e-01 |
0.011900 |
Antimicrobial peptides |
21 |
5.62e-03 |
2.46e-02 |
0.40500 |
-3.14e-01 |
-2.56e-01 |
1.27e-02 |
0.042600 |
Budding and maturation of HIV virion |
15 |
2.54e-02 |
8.58e-02 |
0.40500 |
3.62e-01 |
-1.82e-01 |
1.53e-02 |
0.223000 |
Asymmetric localization of PCP proteins |
47 |
1.01e-05 |
9.78e-05 |
0.40500 |
4.05e-01 |
-1.35e-04 |
1.61e-06 |
0.999000 |
Activation of gene expression by SREBF (SREBP) |
35 |
1.97e-04 |
1.32e-03 |
0.40400 |
-3.73e-01 |
1.56e-01 |
1.36e-04 |
0.110000 |
G1/S DNA Damage Checkpoints |
45 |
1.75e-05 |
1.62e-04 |
0.40400 |
4.04e-01 |
-3.29e-03 |
2.86e-06 |
0.970000 |
Syndecan interactions |
16 |
2.01e-02 |
7.04e-02 |
0.40300 |
-3.26e-01 |
-2.37e-01 |
2.40e-02 |
0.101000 |
FOXO-mediated transcription of cell death genes |
13 |
4.19e-02 |
1.30e-01 |
0.40300 |
2.37e-01 |
3.26e-01 |
1.39e-01 |
0.042200 |
p53-Dependent G1 DNA Damage Response |
44 |
2.52e-05 |
2.25e-04 |
0.40100 |
4.01e-01 |
-1.45e-02 |
4.22e-06 |
0.868000 |
p53-Dependent G1/S DNA damage checkpoint |
44 |
2.52e-05 |
2.25e-04 |
0.40100 |
4.01e-01 |
-1.45e-02 |
4.22e-06 |
0.868000 |
Cell Cycle Checkpoints |
183 |
1.15e-19 |
2.05e-17 |
0.40100 |
3.99e-01 |
4.30e-02 |
1.68e-20 |
0.318000 |
HCMV Late Events |
37 |
1.41e-04 |
9.73e-04 |
0.40000 |
3.96e-01 |
5.63e-02 |
3.08e-05 |
0.554000 |
Intrinsic Pathway of Fibrin Clot Formation |
14 |
3.51e-02 |
1.13e-01 |
0.40000 |
-3.99e-01 |
1.72e-02 |
9.69e-03 |
0.911000 |
Mitotic Spindle Checkpoint |
83 |
2.55e-09 |
7.33e-08 |
0.40000 |
3.97e-01 |
4.60e-02 |
4.22e-10 |
0.470000 |
Nucleobase biosynthesis |
13 |
4.46e-02 |
1.35e-01 |
0.40000 |
3.99e-01 |
1.32e-02 |
1.27e-02 |
0.935000 |
Activation of NF-kappaB in B cells |
44 |
3.30e-05 |
2.78e-04 |
0.39600 |
3.92e-01 |
-5.56e-02 |
6.78e-06 |
0.524000 |
Platelet Aggregation (Plug Formation) |
28 |
1.49e-03 |
7.37e-03 |
0.39500 |
-3.70e-01 |
1.37e-01 |
7.02e-04 |
0.211000 |
Response of EIF2AK4 (GCN2) to amino acid deficiency |
33 |
4.51e-04 |
2.62e-03 |
0.39400 |
3.67e-01 |
1.44e-01 |
2.65e-04 |
0.152000 |
Metabolism of non-coding RNA |
34 |
4.21e-04 |
2.49e-03 |
0.39000 |
3.66e-01 |
1.35e-01 |
2.21e-04 |
0.173000 |
snRNP Assembly |
34 |
4.21e-04 |
2.49e-03 |
0.39000 |
3.66e-01 |
1.35e-01 |
2.21e-04 |
0.173000 |
Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC) |
44 |
4.34e-05 |
3.46e-04 |
0.39000 |
3.16e-01 |
2.28e-01 |
2.84e-04 |
0.008970 |
Nonsense-Mediated Decay (NMD) |
44 |
4.34e-05 |
3.46e-04 |
0.39000 |
3.16e-01 |
2.28e-01 |
2.84e-04 |
0.008970 |
Cellular response to hypoxia |
51 |
9.87e-06 |
9.76e-05 |
0.38900 |
3.84e-01 |
6.14e-02 |
2.16e-06 |
0.449000 |
Na+/Cl- dependent neurotransmitter transporters |
10 |
1.05e-01 |
2.44e-01 |
0.38800 |
-7.29e-02 |
3.81e-01 |
6.90e-01 |
0.036800 |
Nucleobase catabolism |
24 |
4.44e-03 |
2.03e-02 |
0.38800 |
3.87e-01 |
3.23e-02 |
1.04e-03 |
0.784000 |
Regulation of pyruvate dehydrogenase (PDH) complex |
11 |
8.36e-02 |
2.06e-01 |
0.38700 |
-3.04e-01 |
-2.40e-01 |
8.11e-02 |
0.168000 |
Degradation of cysteine and homocysteine |
10 |
1.06e-01 |
2.45e-01 |
0.38700 |
3.87e-01 |
7.59e-04 |
3.41e-02 |
0.997000 |
Sulfur amino acid metabolism |
17 |
2.23e-02 |
7.75e-02 |
0.38700 |
3.79e-01 |
-7.53e-02 |
6.79e-03 |
0.591000 |
CLEC7A (Dectin-1) induces NFAT activation |
10 |
1.07e-01 |
2.47e-01 |
0.38700 |
-3.71e-01 |
1.08e-01 |
4.21e-02 |
0.554000 |
PD-1 signaling |
12 |
6.98e-02 |
1.83e-01 |
0.38400 |
-3.74e-01 |
-8.75e-02 |
2.48e-02 |
0.600000 |
MAP3K8 (TPL2)-dependent MAPK1/3 activation |
10 |
1.11e-01 |
2.53e-01 |
0.38300 |
-3.78e-01 |
6.22e-02 |
3.83e-02 |
0.734000 |
Transport of Ribonucleoproteins into the Host Nucleus |
22 |
7.82e-03 |
3.16e-02 |
0.38300 |
3.68e-01 |
1.07e-01 |
2.81e-03 |
0.386000 |
Dopamine Neurotransmitter Release Cycle |
11 |
8.83e-02 |
2.15e-01 |
0.38300 |
-3.64e-01 |
-1.21e-01 |
3.68e-02 |
0.488000 |
RAS processing |
12 |
7.06e-02 |
1.84e-01 |
0.38300 |
2.74e-01 |
2.68e-01 |
1.00e-01 |
0.109000 |
Mitotic G2-G2/M phases |
129 |
6.63e-13 |
5.16e-11 |
0.38200 |
3.67e-01 |
1.05e-01 |
6.53e-13 |
0.039200 |
tRNA Aminoacylation |
17 |
2.47e-02 |
8.37e-02 |
0.38200 |
3.42e-01 |
-1.70e-01 |
1.47e-02 |
0.225000 |
Transport of the SLBP Dependant Mature mRNA |
24 |
5.27e-03 |
2.37e-02 |
0.38200 |
3.73e-01 |
8.25e-02 |
1.58e-03 |
0.484000 |
Influenza Infection |
68 |
3.72e-07 |
5.15e-06 |
0.38200 |
3.72e-01 |
8.46e-02 |
1.15e-07 |
0.228000 |
Base Excision Repair |
37 |
3.13e-04 |
1.95e-03 |
0.38100 |
3.61e-01 |
1.23e-01 |
1.48e-04 |
0.194000 |
HS-GAG biosynthesis |
18 |
2.03e-02 |
7.09e-02 |
0.38100 |
1.32e-01 |
-3.57e-01 |
3.34e-01 |
0.008720 |
Depolymerisation of the Nuclear Lamina |
12 |
7.34e-02 |
1.89e-01 |
0.38000 |
2.99e-01 |
2.35e-01 |
7.32e-02 |
0.158000 |
Cell Cycle, Mitotic |
356 |
1.84e-33 |
2.28e-30 |
0.38000 |
3.69e-01 |
9.22e-02 |
1.22e-32 |
0.003030 |
Synthesis of active ubiquitin: roles of E1 and E2 enzymes |
18 |
1.99e-02 |
7.01e-02 |
0.38000 |
2.85e-01 |
2.52e-01 |
3.66e-02 |
0.064300 |
Antigen processing-Cross presentation |
67 |
6.18e-07 |
8.01e-06 |
0.37900 |
3.56e-01 |
-1.30e-01 |
4.96e-07 |
0.065600 |
Cyclin D associated events in G1 |
31 |
1.26e-03 |
6.43e-03 |
0.37900 |
3.19e-01 |
2.04e-01 |
2.12e-03 |
0.049900 |
G1 Phase |
31 |
1.26e-03 |
6.43e-03 |
0.37900 |
3.19e-01 |
2.04e-01 |
2.12e-03 |
0.049900 |
Non-integrin membrane-ECM interactions |
35 |
5.42e-04 |
3.05e-03 |
0.37800 |
-3.43e-01 |
-1.59e-01 |
4.43e-04 |
0.104000 |
LGI-ADAM interactions |
13 |
6.12e-02 |
1.70e-01 |
0.37800 |
-3.69e-01 |
-8.32e-02 |
2.12e-02 |
0.604000 |
Interferon alpha/beta signaling |
37 |
3.61e-04 |
2.20e-03 |
0.37800 |
3.66e-01 |
9.31e-02 |
1.16e-04 |
0.327000 |
G2/M Transition |
127 |
1.85e-12 |
1.28e-10 |
0.37800 |
3.65e-01 |
9.82e-02 |
1.34e-12 |
0.056700 |
Cytosolic sulfonation of small molecules |
14 |
5.14e-02 |
1.49e-01 |
0.37600 |
3.76e-01 |
1.43e-02 |
1.49e-02 |
0.926000 |
Viral Messenger RNA Synthesis |
25 |
5.29e-03 |
2.37e-02 |
0.37400 |
3.73e-01 |
2.93e-02 |
1.25e-03 |
0.800000 |
Mitotic Prophase |
61 |
2.83e-06 |
3.21e-05 |
0.37400 |
3.24e-01 |
1.87e-01 |
1.27e-05 |
0.011500 |
Long-term potentiation |
17 |
2.84e-02 |
9.47e-02 |
0.37400 |
-3.67e-01 |
-6.98e-02 |
8.80e-03 |
0.618000 |
tRNA processing in the nucleus |
41 |
1.90e-04 |
1.29e-03 |
0.37400 |
3.71e-01 |
4.36e-02 |
3.97e-05 |
0.629000 |
Nuclear Pore Complex (NPC) Disassembly |
25 |
5.35e-03 |
2.38e-02 |
0.37300 |
3.64e-01 |
8.54e-02 |
1.66e-03 |
0.460000 |
p130Cas linkage to MAPK signaling for integrins |
10 |
1.24e-01 |
2.78e-01 |
0.37300 |
-3.53e-01 |
1.22e-01 |
5.33e-02 |
0.505000 |
Formation of Fibrin Clot (Clotting Cascade) |
23 |
8.24e-03 |
3.32e-02 |
0.37300 |
-3.65e-01 |
-7.70e-02 |
2.46e-03 |
0.523000 |
PCP/CE pathway |
66 |
1.14e-06 |
1.37e-05 |
0.37200 |
3.61e-01 |
8.94e-02 |
3.92e-07 |
0.210000 |
Diseases of carbohydrate metabolism |
22 |
1.03e-02 |
4.02e-02 |
0.37200 |
3.55e-01 |
1.11e-01 |
3.91e-03 |
0.370000 |
Interactions of Vpr with host cellular proteins |
25 |
5.59e-03 |
2.45e-02 |
0.37200 |
3.68e-01 |
5.73e-02 |
1.47e-03 |
0.620000 |
Processing of DNA double-strand break ends |
41 |
2.19e-04 |
1.42e-03 |
0.37000 |
3.61e-01 |
8.10e-02 |
6.29e-05 |
0.370000 |
NS1 Mediated Effects on Host Pathways |
25 |
6.07e-03 |
2.60e-02 |
0.36900 |
3.65e-01 |
5.20e-02 |
1.57e-03 |
0.653000 |
Transport of the SLBP independent Mature mRNA |
23 |
9.45e-03 |
3.72e-02 |
0.36800 |
3.57e-01 |
8.66e-02 |
3.03e-03 |
0.473000 |
Host Interactions of HIV factors |
91 |
1.08e-08 |
2.29e-07 |
0.36700 |
3.60e-01 |
7.60e-02 |
3.21e-09 |
0.211000 |
M Phase |
256 |
8.20e-23 |
3.40e-20 |
0.36700 |
3.57e-01 |
8.58e-02 |
1.18e-22 |
0.018800 |
Collagen chain trimerization |
33 |
1.35e-03 |
6.76e-03 |
0.36500 |
-3.38e-01 |
-1.38e-01 |
7.80e-04 |
0.169000 |
Tristetraprolin (TTP, ZFP36) binds and destabilizes mRNA |
11 |
1.14e-01 |
2.60e-01 |
0.36300 |
-1.48e-01 |
3.32e-01 |
3.94e-01 |
0.056900 |
Activation of RAC1 |
10 |
1.41e-01 |
3.05e-01 |
0.36200 |
-2.98e-01 |
2.06e-01 |
1.03e-01 |
0.260000 |
Defective B3GALT6 causes EDSP2 and SEMDJL1 |
13 |
7.78e-02 |
1.96e-01 |
0.36200 |
-1.05e-01 |
-3.46e-01 |
5.11e-01 |
0.030800 |
Nuclear Envelope Breakdown |
37 |
7.11e-04 |
3.83e-03 |
0.36200 |
3.50e-01 |
8.99e-02 |
2.29e-04 |
0.345000 |
Export of Viral Ribonucleoproteins from Nucleus |
23 |
1.10e-02 |
4.22e-02 |
0.36100 |
3.47e-01 |
1.02e-01 |
4.01e-03 |
0.397000 |
Mitotic Prometaphase |
140 |
1.55e-12 |
1.14e-10 |
0.36100 |
3.50e-01 |
8.81e-02 |
9.07e-13 |
0.072700 |
FCERI mediated Ca+2 mobilization |
24 |
9.57e-03 |
3.76e-02 |
0.36000 |
-3.15e-01 |
1.76e-01 |
7.64e-03 |
0.137000 |
PECAM1 interactions |
10 |
1.45e-01 |
3.08e-01 |
0.36000 |
-3.32e-01 |
1.39e-01 |
6.93e-02 |
0.446000 |
Downregulation of SMAD2/3:SMAD4 transcriptional activity |
14 |
6.64e-02 |
1.78e-01 |
0.36000 |
-3.60e-01 |
1.57e-03 |
1.99e-02 |
0.992000 |
Transferrin endocytosis and recycling |
17 |
3.69e-02 |
1.18e-01 |
0.35900 |
3.21e-01 |
1.61e-01 |
2.19e-02 |
0.251000 |
Transport of Mature mRNAs Derived from Intronless Transcripts |
29 |
3.66e-03 |
1.69e-02 |
0.35900 |
3.41e-01 |
1.13e-01 |
1.49e-03 |
0.294000 |
Post-chaperonin tubulin folding pathway |
16 |
4.50e-02 |
1.35e-01 |
0.35900 |
2.44e-01 |
2.63e-01 |
9.05e-02 |
0.068900 |
Purine ribonucleoside monophosphate biosynthesis |
11 |
1.25e-01 |
2.80e-01 |
0.35500 |
3.44e-01 |
8.68e-02 |
4.83e-02 |
0.618000 |
Ras activation upon Ca2+ influx through NMDA receptor |
16 |
4.94e-02 |
1.45e-01 |
0.35400 |
-3.54e-01 |
-1.38e-02 |
1.43e-02 |
0.924000 |
Hedgehog 'on' state |
54 |
4.25e-05 |
3.44e-04 |
0.35400 |
3.45e-01 |
-7.83e-02 |
1.19e-05 |
0.320000 |
Dual Incision in GG-NER |
31 |
3.02e-03 |
1.43e-02 |
0.35400 |
3.49e-01 |
5.36e-02 |
7.64e-04 |
0.606000 |
Carnitine metabolism |
11 |
1.27e-01 |
2.83e-01 |
0.35300 |
-3.00e-01 |
-1.86e-01 |
8.49e-02 |
0.286000 |
Plasma lipoprotein clearance |
25 |
9.45e-03 |
3.72e-02 |
0.35300 |
3.39e-01 |
9.72e-02 |
3.37e-03 |
0.400000 |
Diseases of programmed cell death |
18 |
3.61e-02 |
1.16e-01 |
0.35000 |
2.98e-01 |
1.84e-01 |
2.87e-02 |
0.176000 |
AURKA Activation by TPX2 |
57 |
3.10e-05 |
2.68e-04 |
0.34900 |
3.34e-01 |
1.00e-01 |
1.30e-05 |
0.192000 |
Glutathione synthesis and recycling |
10 |
1.63e-01 |
3.37e-01 |
0.34800 |
3.30e-02 |
-3.47e-01 |
8.57e-01 |
0.057700 |
Transport of Mature mRNA Derived from an Intronless Transcript |
28 |
6.28e-03 |
2.65e-02 |
0.34700 |
3.27e-01 |
1.17e-01 |
2.75e-03 |
0.284000 |
Diseases associated with N-glycosylation of proteins |
14 |
8.05e-02 |
2.01e-01 |
0.34700 |
3.43e-01 |
-5.11e-02 |
2.63e-02 |
0.741000 |
SUMOylation of ubiquitinylation proteins |
26 |
9.33e-03 |
3.70e-02 |
0.34600 |
3.32e-01 |
9.95e-02 |
3.44e-03 |
0.380000 |
DNA Double-Strand Break Repair |
90 |
1.12e-07 |
1.68e-06 |
0.34600 |
3.46e-01 |
3.48e-04 |
1.53e-08 |
0.995000 |
XBP1(S) activates chaperone genes |
38 |
1.16e-03 |
5.99e-03 |
0.34600 |
3.18e-01 |
-1.35e-01 |
6.97e-04 |
0.150000 |
Telomere C-strand synthesis initiation |
11 |
1.40e-01 |
3.02e-01 |
0.34500 |
3.41e-01 |
5.25e-02 |
5.01e-02 |
0.763000 |
ABC-family proteins mediated transport |
65 |
9.60e-06 |
9.71e-05 |
0.34500 |
3.45e-01 |
8.77e-03 |
1.55e-06 |
0.903000 |
Creation of C4 and C2 activators |
13 |
9.82e-02 |
2.31e-01 |
0.34500 |
3.44e-01 |
2.52e-02 |
3.17e-02 |
0.875000 |
Diseases associated with the TLR signaling cascade |
18 |
4.25e-02 |
1.31e-01 |
0.34200 |
-5.74e-02 |
-3.37e-01 |
6.73e-01 |
0.013300 |
Diseases of Immune System |
18 |
4.25e-02 |
1.31e-01 |
0.34200 |
-5.74e-02 |
-3.37e-01 |
6.73e-01 |
0.013300 |
Gap-filling DNA repair synthesis and ligation in TC-NER |
42 |
6.40e-04 |
3.51e-03 |
0.34200 |
3.19e-01 |
1.24e-01 |
3.58e-04 |
0.165000 |
Detoxification of Reactive Oxygen Species |
20 |
3.03e-02 |
1.00e-01 |
0.34200 |
3.41e-01 |
2.11e-02 |
8.32e-03 |
0.870000 |
UCH proteinases |
60 |
3.05e-05 |
2.66e-04 |
0.34000 |
3.38e-01 |
4.49e-02 |
6.26e-06 |
0.548000 |
Cell Cycle |
443 |
4.25e-33 |
2.64e-30 |
0.34000 |
3.33e-01 |
7.28e-02 |
9.97e-33 |
0.009290 |
Regulation of RUNX2 expression and activity |
49 |
2.07e-04 |
1.36e-03 |
0.34000 |
3.40e-01 |
-4.69e-03 |
3.81e-05 |
0.955000 |
SARS-CoV-1 Infection |
29 |
6.74e-03 |
2.80e-02 |
0.33900 |
3.04e-01 |
1.50e-01 |
4.63e-03 |
0.163000 |
Formation of the cornified envelope |
21 |
2.74e-02 |
9.18e-02 |
0.33700 |
-2.35e-01 |
-2.43e-01 |
6.28e-02 |
0.054500 |
Transcriptional regulation by small RNAs |
29 |
7.23e-03 |
2.99e-02 |
0.33700 |
3.24e-01 |
9.01e-02 |
2.51e-03 |
0.401000 |
Phase 0 - rapid depolarisation |
29 |
7.52e-03 |
3.09e-02 |
0.33600 |
-3.33e-01 |
-3.91e-02 |
1.91e-03 |
0.716000 |
ECM proteoglycans |
42 |
8.71e-04 |
4.59e-03 |
0.33400 |
-2.81e-01 |
-1.81e-01 |
1.62e-03 |
0.043100 |
Late endosomal microautophagy |
18 |
5.03e-02 |
1.46e-01 |
0.33400 |
2.88e-01 |
-1.69e-01 |
3.45e-02 |
0.216000 |
VEGFR2 mediated cell proliferation |
19 |
4.22e-02 |
1.30e-01 |
0.33400 |
-3.33e-01 |
2.59e-02 |
1.21e-02 |
0.845000 |
IRE1alpha activates chaperones |
40 |
1.31e-03 |
6.65e-03 |
0.33400 |
3.17e-01 |
-1.03e-01 |
5.19e-04 |
0.262000 |
Glutamate Neurotransmitter Release Cycle |
15 |
8.18e-02 |
2.03e-01 |
0.33300 |
-3.20e-01 |
-9.48e-02 |
3.21e-02 |
0.525000 |
Loss of Nlp from mitotic centrosomes |
55 |
1.10e-04 |
7.86e-04 |
0.33300 |
3.22e-01 |
8.53e-02 |
3.76e-05 |
0.274000 |
Loss of proteins required for interphase microtubule organization from the centrosome |
55 |
1.10e-04 |
7.86e-04 |
0.33300 |
3.22e-01 |
8.53e-02 |
3.76e-05 |
0.274000 |
Effects of PIP2 hydrolysis |
19 |
4.26e-02 |
1.31e-01 |
0.33200 |
-2.91e-01 |
-1.60e-01 |
2.80e-02 |
0.226000 |
Telomere Extension By Telomerase |
15 |
8.26e-02 |
2.05e-01 |
0.33200 |
2.46e-01 |
2.24e-01 |
9.93e-02 |
0.134000 |
TICAM1, RIP1-mediated IKK complex recruitment |
12 |
1.42e-01 |
3.06e-01 |
0.33000 |
-3.17e-01 |
9.20e-02 |
5.77e-02 |
0.581000 |
Regulation of PLK1 Activity at G2/M Transition |
62 |
4.41e-05 |
3.50e-04 |
0.32900 |
2.99e-01 |
1.35e-01 |
4.63e-05 |
0.065400 |
Glycogen breakdown (glycogenolysis) |
12 |
1.44e-01 |
3.08e-01 |
0.32800 |
-3.24e-01 |
5.68e-02 |
5.24e-02 |
0.733000 |
Transcription-Coupled Nucleotide Excision Repair (TC-NER) |
53 |
1.97e-04 |
1.32e-03 |
0.32800 |
3.25e-01 |
4.61e-02 |
4.37e-05 |
0.562000 |
EGR2 and SOX10-mediated initiation of Schwann cell myelination |
22 |
2.98e-02 |
9.90e-02 |
0.32700 |
-3.23e-01 |
5.02e-02 |
8.77e-03 |
0.684000 |
Nef-mediates down modulation of cell surface receptors by recruiting them to clathrin adapters |
16 |
7.69e-02 |
1.94e-01 |
0.32700 |
1.10e-01 |
3.08e-01 |
4.47e-01 |
0.033200 |
Cleavage of the damaged purine |
10 |
2.01e-01 |
3.85e-01 |
0.32700 |
1.93e-01 |
2.64e-01 |
2.92e-01 |
0.149000 |
Depurination |
10 |
2.01e-01 |
3.85e-01 |
0.32700 |
1.93e-01 |
2.64e-01 |
2.92e-01 |
0.149000 |
Recognition and association of DNA glycosylase with site containing an affected purine |
10 |
2.01e-01 |
3.85e-01 |
0.32700 |
1.93e-01 |
2.64e-01 |
2.92e-01 |
0.149000 |
Citric acid cycle (TCA cycle) |
15 |
9.14e-02 |
2.18e-01 |
0.32700 |
-5.88e-02 |
3.21e-01 |
6.93e-01 |
0.031300 |
Regulation of beta-cell development |
20 |
4.17e-02 |
1.30e-01 |
0.32600 |
-2.69e-01 |
1.84e-01 |
3.70e-02 |
0.154000 |
APC-Cdc20 mediated degradation of Nek2A |
19 |
4.86e-02 |
1.43e-01 |
0.32600 |
3.20e-01 |
-6.43e-02 |
1.58e-02 |
0.628000 |
Assembly and cell surface presentation of NMDA receptors |
16 |
7.75e-02 |
1.95e-01 |
0.32600 |
-3.07e-01 |
-1.10e-01 |
3.35e-02 |
0.447000 |
Ion homeostasis |
37 |
2.86e-03 |
1.37e-02 |
0.32600 |
-3.01e-01 |
1.24e-01 |
1.53e-03 |
0.191000 |
Ca2+ pathway |
48 |
5.12e-04 |
2.91e-03 |
0.32600 |
-3.01e-01 |
1.23e-01 |
3.08e-04 |
0.140000 |
Global Genome Nucleotide Excision Repair (GG-NER) |
60 |
7.56e-05 |
5.61e-04 |
0.32500 |
3.22e-01 |
4.73e-02 |
1.65e-05 |
0.527000 |
Rap1 signalling |
14 |
1.10e-01 |
2.52e-01 |
0.32500 |
-3.14e-01 |
8.41e-02 |
4.20e-02 |
0.586000 |
CREB1 phosphorylation through NMDA receptor-mediated activation of RAS signaling |
24 |
2.39e-02 |
8.18e-02 |
0.32300 |
-3.16e-01 |
6.39e-02 |
7.35e-03 |
0.588000 |
PI-3K cascade:FGFR4 |
11 |
1.79e-01 |
3.61e-01 |
0.32200 |
-2.26e-01 |
-2.30e-01 |
1.95e-01 |
0.187000 |
Degradation of beta-catenin by the destruction complex |
61 |
9.00e-05 |
6.59e-04 |
0.32000 |
3.18e-01 |
3.14e-02 |
1.76e-05 |
0.671000 |
Endosomal Sorting Complex Required For Transport (ESCRT) |
18 |
6.42e-02 |
1.75e-01 |
0.31900 |
3.19e-01 |
-9.46e-03 |
1.92e-02 |
0.945000 |
Regulation of RAS by GAPs |
49 |
5.78e-04 |
3.23e-03 |
0.31900 |
3.10e-01 |
7.26e-02 |
1.72e-04 |
0.380000 |
TRAF6 mediated IRF7 activation |
15 |
1.04e-01 |
2.41e-01 |
0.31800 |
-7.17e-02 |
3.10e-01 |
6.31e-01 |
0.037800 |
LDL clearance |
13 |
1.39e-01 |
3.01e-01 |
0.31800 |
2.95e-01 |
1.19e-01 |
6.60e-02 |
0.456000 |
CASP8 activity is inhibited |
10 |
2.21e-01 |
4.05e-01 |
0.31800 |
-3.00e-01 |
1.04e-01 |
1.00e-01 |
0.568000 |
Dimerization of procaspase-8 |
10 |
2.21e-01 |
4.05e-01 |
0.31800 |
-3.00e-01 |
1.04e-01 |
1.00e-01 |
0.568000 |
Regulation by c-FLIP |
10 |
2.21e-01 |
4.05e-01 |
0.31800 |
-3.00e-01 |
1.04e-01 |
1.00e-01 |
0.568000 |
Uptake and actions of bacterial toxins |
26 |
1.96e-02 |
6.93e-02 |
0.31700 |
-2.94e-01 |
-1.20e-01 |
9.55e-03 |
0.290000 |
FCERI mediated NF-kB activation |
54 |
2.99e-04 |
1.88e-03 |
0.31700 |
3.17e-01 |
1.27e-03 |
5.62e-05 |
0.987000 |
Iron uptake and transport |
36 |
4.62e-03 |
2.10e-02 |
0.31500 |
2.74e-01 |
1.57e-01 |
4.54e-03 |
0.103000 |
Recruitment of NuMA to mitotic centrosomes |
64 |
8.36e-05 |
6.16e-04 |
0.31300 |
3.06e-01 |
6.67e-02 |
2.34e-05 |
0.357000 |
Hedgehog 'off' state |
71 |
3.29e-05 |
2.78e-04 |
0.31200 |
3.09e-01 |
4.37e-02 |
6.92e-06 |
0.525000 |
Defective B3GALTL causes Peters-plus syndrome (PpS) |
30 |
1.25e-02 |
4.70e-02 |
0.31200 |
-1.99e-01 |
-2.40e-01 |
5.88e-02 |
0.023300 |
RHO GTPases Activate Formins |
88 |
2.96e-06 |
3.33e-05 |
0.31100 |
3.04e-01 |
6.88e-02 |
8.83e-07 |
0.266000 |
HCMV Infection |
59 |
2.04e-04 |
1.35e-03 |
0.31100 |
3.10e-01 |
2.18e-02 |
3.93e-05 |
0.772000 |
O-glycosylation of TSR domain-containing proteins |
31 |
1.13e-02 |
4.32e-02 |
0.31000 |
-1.84e-01 |
-2.50e-01 |
7.71e-02 |
0.016000 |
Inactivation of APC/C via direct inhibition of the APC/C complex |
18 |
7.67e-02 |
1.94e-01 |
0.30900 |
3.07e-01 |
-2.83e-02 |
2.40e-02 |
0.835000 |
Inhibition of the proteolytic activity of APC/C required for the onset of anaphase by mitotic spindle checkpoint components |
18 |
7.67e-02 |
1.94e-01 |
0.30900 |
3.07e-01 |
-2.83e-02 |
2.40e-02 |
0.835000 |
Nucleotide-like (purinergic) receptors |
10 |
2.39e-01 |
4.25e-01 |
0.30900 |
-2.59e-02 |
-3.08e-01 |
8.87e-01 |
0.092100 |
HS-GAG degradation |
15 |
1.18e-01 |
2.66e-01 |
0.30800 |
-1.08e-02 |
-3.08e-01 |
9.42e-01 |
0.038800 |
Translation of structural proteins |
18 |
7.67e-02 |
1.94e-01 |
0.30800 |
2.55e-01 |
1.72e-01 |
6.08e-02 |
0.206000 |
Deregulated CDK5 triggers multiple neurodegenerative pathways in Alzheimer's disease models |
17 |
8.88e-02 |
2.15e-01 |
0.30800 |
2.62e-01 |
1.61e-01 |
6.11e-02 |
0.251000 |
Neurodegenerative Diseases |
17 |
8.88e-02 |
2.15e-01 |
0.30800 |
2.62e-01 |
1.61e-01 |
6.11e-02 |
0.251000 |
Aberrant regulation of mitotic cell cycle due to RB1 defects |
30 |
1.44e-02 |
5.35e-02 |
0.30700 |
2.99e-01 |
7.14e-02 |
4.68e-03 |
0.499000 |
Diseases of mitotic cell cycle |
30 |
1.44e-02 |
5.35e-02 |
0.30700 |
2.99e-01 |
7.14e-02 |
4.68e-03 |
0.499000 |
G2/M DNA damage checkpoint |
43 |
2.41e-03 |
1.17e-02 |
0.30600 |
3.03e-01 |
4.36e-02 |
5.94e-04 |
0.621000 |
Voltage gated Potassium channels |
21 |
5.27e-02 |
1.51e-01 |
0.30600 |
-3.06e-01 |
8.23e-03 |
1.53e-02 |
0.948000 |
ERCC6 (CSB) and EHMT2 (G9a) positively regulate rRNA expression |
13 |
1.63e-01 |
3.37e-01 |
0.30600 |
1.80e-01 |
-2.47e-01 |
2.61e-01 |
0.123000 |
Mitochondrial tRNA aminoacylation |
12 |
1.90e-01 |
3.74e-01 |
0.30500 |
2.37e-01 |
-1.91e-01 |
1.55e-01 |
0.252000 |
Collagen formation |
61 |
2.08e-04 |
1.36e-03 |
0.30400 |
-2.38e-01 |
-1.90e-01 |
1.34e-03 |
0.010200 |
Neurexins and neuroligins |
37 |
5.81e-03 |
2.51e-02 |
0.30400 |
-2.00e-01 |
-2.29e-01 |
3.51e-02 |
0.015900 |
FOXO-mediated transcription of oxidative stress, metabolic and neuronal genes |
19 |
7.22e-02 |
1.87e-01 |
0.30400 |
-3.00e-01 |
5.26e-02 |
2.38e-02 |
0.692000 |
Cardiac conduction |
83 |
1.19e-05 |
1.13e-04 |
0.30300 |
-3.00e-01 |
4.41e-02 |
2.42e-06 |
0.488000 |
RIPK1-mediated regulated necrosis |
14 |
1.48e-01 |
3.14e-01 |
0.30300 |
-2.69e-01 |
1.39e-01 |
8.20e-02 |
0.367000 |
Regulated Necrosis |
14 |
1.48e-01 |
3.14e-01 |
0.30300 |
-2.69e-01 |
1.39e-01 |
8.20e-02 |
0.367000 |
Integrin cell surface interactions |
52 |
8.56e-04 |
4.53e-03 |
0.30100 |
-2.73e-01 |
-1.28e-01 |
6.83e-04 |
0.111000 |
Unblocking of NMDA receptors, glutamate binding and activation |
14 |
1.50e-01 |
3.18e-01 |
0.30100 |
-3.00e-01 |
-2.40e-02 |
5.24e-02 |
0.877000 |
Glutamate binding, activation of AMPA receptors and synaptic plasticity |
23 |
4.45e-02 |
1.35e-01 |
0.30000 |
-2.94e-01 |
-6.19e-02 |
1.47e-02 |
0.607000 |
Trafficking of AMPA receptors |
23 |
4.45e-02 |
1.35e-01 |
0.30000 |
-2.94e-01 |
-6.19e-02 |
1.47e-02 |
0.607000 |
APC/C:Cdc20 mediated degradation of Cyclin B |
18 |
8.80e-02 |
2.15e-01 |
0.30000 |
2.98e-01 |
-3.80e-02 |
2.87e-02 |
0.780000 |
Platelet calcium homeostasis |
20 |
6.76e-02 |
1.80e-01 |
0.30000 |
-2.87e-01 |
-8.55e-02 |
2.63e-02 |
0.508000 |
Regulation of IFNA signaling |
10 |
2.60e-01 |
4.48e-01 |
0.29900 |
2.95e-01 |
5.19e-02 |
1.06e-01 |
0.777000 |
Regulation of cholesterol biosynthesis by SREBP (SREBF) |
45 |
2.61e-03 |
1.25e-02 |
0.29800 |
-2.93e-01 |
5.16e-02 |
6.75e-04 |
0.550000 |
Fatty acyl-CoA biosynthesis |
22 |
5.51e-02 |
1.58e-01 |
0.29700 |
-1.93e-01 |
2.26e-01 |
1.17e-01 |
0.066300 |
Glycogen metabolism |
19 |
8.13e-02 |
2.02e-01 |
0.29700 |
-2.94e-01 |
3.99e-02 |
2.63e-02 |
0.763000 |
Anchoring of the basal body to the plasma membrane |
75 |
5.57e-05 |
4.18e-04 |
0.29600 |
2.90e-01 |
6.03e-02 |
1.49e-05 |
0.368000 |
Dual incision in TC-NER |
43 |
3.64e-03 |
1.69e-02 |
0.29500 |
2.89e-01 |
5.86e-02 |
1.03e-03 |
0.507000 |
Blood group systems biosynthesis |
12 |
2.11e-01 |
3.99e-01 |
0.29500 |
2.69e-01 |
-1.20e-01 |
1.07e-01 |
0.471000 |
HIV Infection |
152 |
3.17e-09 |
8.22e-08 |
0.29500 |
2.94e-01 |
1.78e-02 |
4.29e-10 |
0.706000 |
SUMOylation of DNA damage response and repair proteins |
50 |
1.50e-03 |
7.37e-03 |
0.29500 |
2.64e-01 |
1.30e-01 |
1.25e-03 |
0.111000 |
Muscle contraction |
134 |
3.35e-08 |
5.79e-07 |
0.29400 |
-2.93e-01 |
2.72e-02 |
5.08e-09 |
0.588000 |
Activated NOTCH1 Transmits Signal to the Nucleus |
20 |
7.39e-02 |
1.90e-01 |
0.29400 |
-1.96e-01 |
-2.20e-01 |
1.30e-01 |
0.089100 |
eNOS activation |
10 |
2.76e-01 |
4.65e-01 |
0.29300 |
-6.95e-02 |
-2.84e-01 |
7.04e-01 |
0.120000 |
Antiviral mechanism by IFN-stimulated genes |
53 |
1.14e-03 |
5.92e-03 |
0.29200 |
2.53e-01 |
1.46e-01 |
1.44e-03 |
0.067100 |
Metabolism of nucleotides |
72 |
1.08e-04 |
7.79e-04 |
0.29100 |
2.85e-01 |
6.07e-02 |
2.97e-05 |
0.374000 |
Aberrant regulation of mitotic exit in cancer due to RB1 defects |
18 |
1.02e-01 |
2.39e-01 |
0.29100 |
2.85e-01 |
-5.97e-02 |
3.64e-02 |
0.661000 |
The role of Nef in HIV-1 replication and disease pathogenesis |
23 |
5.39e-02 |
1.55e-01 |
0.29100 |
7.23e-02 |
2.82e-01 |
5.49e-01 |
0.019400 |
Deactivation of the beta-catenin transactivating complex |
27 |
3.35e-02 |
1.10e-01 |
0.28900 |
-2.33e-01 |
-1.71e-01 |
3.60e-02 |
0.124000 |
Meiotic synapsis |
24 |
4.89e-02 |
1.44e-01 |
0.28900 |
1.80e-01 |
2.26e-01 |
1.26e-01 |
0.055300 |
mTORC1-mediated signalling |
17 |
1.18e-01 |
2.66e-01 |
0.28900 |
1.30e-01 |
2.58e-01 |
3.54e-01 |
0.065500 |
Synthesis of PIPs at the early endosome membrane |
14 |
1.75e-01 |
3.56e-01 |
0.28800 |
-2.78e-01 |
7.73e-02 |
7.20e-02 |
0.617000 |
Spry regulation of FGF signaling |
10 |
2.87e-01 |
4.76e-01 |
0.28800 |
1.68e-01 |
2.34e-01 |
3.57e-01 |
0.201000 |
Protein-protein interactions at synapses |
53 |
1.39e-03 |
6.90e-03 |
0.28800 |
-1.76e-01 |
-2.28e-01 |
2.69e-02 |
0.004200 |
Synthesis of PC |
19 |
9.48e-02 |
2.24e-01 |
0.28800 |
4.60e-02 |
2.84e-01 |
7.28e-01 |
0.032200 |
ISG15 antiviral mechanism |
47 |
2.96e-03 |
1.41e-02 |
0.28700 |
2.46e-01 |
1.49e-01 |
3.55e-03 |
0.078300 |
Centrosome maturation |
65 |
3.30e-04 |
2.03e-03 |
0.28700 |
2.79e-01 |
6.68e-02 |
1.00e-04 |
0.352000 |
Recruitment of mitotic centrosome proteins and complexes |
65 |
3.30e-04 |
2.03e-03 |
0.28700 |
2.79e-01 |
6.68e-02 |
1.00e-04 |
0.352000 |
Regulation of KIT signaling |
11 |
2.59e-01 |
4.47e-01 |
0.28700 |
-2.47e-01 |
1.46e-01 |
1.57e-01 |
0.402000 |
MAPK6/MAPK4 signaling |
61 |
5.76e-04 |
3.23e-03 |
0.28600 |
2.77e-01 |
6.95e-02 |
1.82e-04 |
0.349000 |
PI3K Cascade |
29 |
2.85e-02 |
9.47e-02 |
0.28600 |
-1.45e-01 |
-2.46e-01 |
1.76e-01 |
0.021900 |
Signaling by NOTCH4 |
61 |
6.38e-04 |
3.51e-03 |
0.28400 |
2.83e-01 |
2.49e-02 |
1.34e-04 |
0.737000 |
Platelet sensitization by LDL |
14 |
1.85e-01 |
3.67e-01 |
0.28400 |
2.59e-01 |
-1.16e-01 |
9.30e-02 |
0.453000 |
Deadenylation of mRNA |
17 |
1.31e-01 |
2.89e-01 |
0.28300 |
-1.24e-01 |
2.55e-01 |
3.78e-01 |
0.069200 |
FOXO-mediated transcription of cell cycle genes |
13 |
2.12e-01 |
3.99e-01 |
0.28200 |
-2.82e-01 |
3.21e-03 |
7.82e-02 |
0.984000 |
Regulation of FZD by ubiquitination |
11 |
2.73e-01 |
4.61e-01 |
0.28100 |
-2.67e-01 |
8.75e-02 |
1.25e-01 |
0.616000 |
NCAM1 interactions |
26 |
4.58e-02 |
1.37e-01 |
0.28100 |
-1.77e-01 |
-2.18e-01 |
1.19e-01 |
0.054100 |
HIV elongation arrest and recovery |
15 |
1.72e-01 |
3.50e-01 |
0.28100 |
2.10e-01 |
-1.85e-01 |
1.58e-01 |
0.214000 |
Pausing and recovery of HIV elongation |
15 |
1.72e-01 |
3.50e-01 |
0.28100 |
2.10e-01 |
-1.85e-01 |
1.58e-01 |
0.214000 |
Pausing and recovery of Tat-mediated HIV elongation |
15 |
1.72e-01 |
3.50e-01 |
0.28100 |
2.10e-01 |
-1.85e-01 |
1.58e-01 |
0.214000 |
Tat-mediated HIV elongation arrest and recovery |
15 |
1.72e-01 |
3.50e-01 |
0.28100 |
2.10e-01 |
-1.85e-01 |
1.58e-01 |
0.214000 |
Formation of tubulin folding intermediates by CCT/TriC |
15 |
1.71e-01 |
3.50e-01 |
0.28000 |
5.96e-02 |
2.74e-01 |
6.90e-01 |
0.066600 |
Regulation of TNFR1 signaling |
24 |
6.15e-02 |
1.70e-01 |
0.27800 |
-2.74e-01 |
-5.14e-02 |
2.04e-02 |
0.663000 |
DNA Repair |
197 |
1.64e-10 |
8.50e-09 |
0.27800 |
2.76e-01 |
3.32e-02 |
2.71e-11 |
0.424000 |
ER Quality Control Compartment (ERQC) |
11 |
2.83e-01 |
4.73e-01 |
0.27700 |
1.22e-01 |
-2.49e-01 |
4.85e-01 |
0.152000 |
Signal regulatory protein family interactions |
11 |
2.84e-01 |
4.74e-01 |
0.27600 |
2.76e-01 |
1.06e-02 |
1.13e-01 |
0.951000 |
NOD1/2 Signaling Pathway |
24 |
6.47e-02 |
1.75e-01 |
0.27600 |
-2.76e-01 |
9.53e-03 |
1.93e-02 |
0.936000 |
NOTCH2 Activation and Transmission of Signal to the Nucleus |
13 |
2.25e-01 |
4.08e-01 |
0.27600 |
-1.91e-01 |
-1.99e-01 |
2.33e-01 |
0.214000 |
Gap junction trafficking |
13 |
2.26e-01 |
4.08e-01 |
0.27600 |
2.29e-01 |
1.54e-01 |
1.53e-01 |
0.336000 |
Signaling by FGFR4 in disease |
10 |
3.22e-01 |
5.06e-01 |
0.27500 |
-2.69e-01 |
5.83e-02 |
1.41e-01 |
0.750000 |
FCERI mediated MAPK activation |
25 |
6.02e-02 |
1.68e-01 |
0.27500 |
-1.55e-01 |
2.27e-01 |
1.80e-01 |
0.049800 |
Signaling by RAF1 mutants |
27 |
4.91e-02 |
1.44e-01 |
0.27400 |
-2.33e-01 |
1.44e-01 |
3.66e-02 |
0.195000 |
TRAF3-dependent IRF activation pathway |
13 |
2.34e-01 |
4.17e-01 |
0.27300 |
-3.85e-02 |
2.71e-01 |
8.10e-01 |
0.091200 |
MicroRNA (miRNA) biogenesis |
13 |
2.36e-01 |
4.19e-01 |
0.27300 |
1.98e-01 |
-1.88e-01 |
2.16e-01 |
0.242000 |
A tetrasaccharide linker sequence is required for GAG synthesis |
17 |
1.49e-01 |
3.17e-01 |
0.27300 |
-1.41e-01 |
-2.34e-01 |
3.15e-01 |
0.095500 |
Nonhomologous End-Joining (NHEJ) |
24 |
6.96e-02 |
1.83e-01 |
0.27200 |
2.61e-01 |
7.59e-02 |
2.68e-02 |
0.520000 |
Regulation of mRNA stability by proteins that bind AU-rich elements |
60 |
1.32e-03 |
6.66e-03 |
0.27200 |
2.70e-01 |
3.10e-02 |
2.99e-04 |
0.679000 |
Mitochondrial calcium ion transport |
16 |
1.69e-01 |
3.47e-01 |
0.27200 |
1.65e-01 |
2.16e-01 |
2.52e-01 |
0.135000 |
CRMPs in Sema3A signaling |
13 |
2.40e-01 |
4.25e-01 |
0.27100 |
-2.70e-01 |
2.03e-02 |
9.21e-02 |
0.899000 |
Defective B3GAT3 causes JDSSDHD |
14 |
2.15e-01 |
4.02e-01 |
0.27000 |
-6.06e-02 |
-2.63e-01 |
6.95e-01 |
0.087900 |
Gluconeogenesis |
22 |
8.95e-02 |
2.16e-01 |
0.27000 |
-2.17e-01 |
-1.61e-01 |
7.87e-02 |
0.191000 |
Metalloprotease DUBs |
15 |
1.94e-01 |
3.80e-01 |
0.27000 |
8.68e-02 |
2.56e-01 |
5.61e-01 |
0.086600 |
Termination of O-glycan biosynthesis |
12 |
2.71e-01 |
4.60e-01 |
0.27000 |
2.24e-01 |
-1.50e-01 |
1.79e-01 |
0.367000 |
Late Phase of HIV Life Cycle |
84 |
1.13e-04 |
8.00e-04 |
0.27000 |
2.65e-01 |
-5.20e-02 |
2.83e-05 |
0.411000 |
Insulin receptor recycling |
12 |
2.71e-01 |
4.60e-01 |
0.27000 |
2.20e-02 |
2.69e-01 |
8.95e-01 |
0.107000 |
Signaling by NTRK3 (TRKC) |
15 |
1.96e-01 |
3.81e-01 |
0.26900 |
-2.69e-01 |
-4.33e-04 |
7.09e-02 |
0.998000 |
Signaling by NODAL |
16 |
1.78e-01 |
3.59e-01 |
0.26900 |
1.64e-01 |
-2.13e-01 |
2.55e-01 |
0.140000 |
Phosphorylation of the APC/C |
17 |
1.60e-01 |
3.33e-01 |
0.26800 |
2.66e-01 |
-3.48e-02 |
5.75e-02 |
0.804000 |
HCMV Early Events |
44 |
8.88e-03 |
3.53e-02 |
0.26800 |
2.68e-01 |
-9.71e-03 |
2.12e-03 |
0.911000 |
Nucleotide Excision Repair |
75 |
3.21e-04 |
1.99e-03 |
0.26800 |
2.59e-01 |
6.72e-02 |
1.05e-04 |
0.315000 |
MECP2 regulates neuronal receptors and channels |
11 |
3.07e-01 |
4.94e-01 |
0.26700 |
-2.33e-01 |
-1.31e-01 |
1.82e-01 |
0.451000 |
Signaling by cytosolic FGFR1 fusion mutants |
16 |
1.82e-01 |
3.65e-01 |
0.26700 |
-2.28e-01 |
1.40e-01 |
1.15e-01 |
0.333000 |
Interleukin-7 signaling |
14 |
2.24e-01 |
4.06e-01 |
0.26700 |
-2.26e-01 |
-1.42e-01 |
1.44e-01 |
0.357000 |
Gene and protein expression by JAK-STAT signaling after Interleukin-12 stimulation |
25 |
6.98e-02 |
1.83e-01 |
0.26700 |
4.10e-02 |
2.63e-01 |
7.23e-01 |
0.022700 |
Regulation of Complement cascade |
31 |
3.78e-02 |
1.20e-01 |
0.26600 |
1.96e-01 |
-1.80e-01 |
5.92e-02 |
0.082200 |
Diseases associated with O-glycosylation of proteins |
46 |
7.71e-03 |
3.14e-02 |
0.26600 |
-1.42e-01 |
-2.24e-01 |
9.64e-02 |
0.008490 |
Signaling by Leptin |
10 |
3.54e-01 |
5.37e-01 |
0.26400 |
-2.61e-01 |
3.47e-02 |
1.53e-01 |
0.849000 |
mRNA decay by 3' to 5' exoribonuclease |
10 |
3.52e-01 |
5.37e-01 |
0.26300 |
2.26e-01 |
1.35e-01 |
2.16e-01 |
0.458000 |
Activation of Matrix Metalloproteinases |
18 |
1.54e-01 |
3.24e-01 |
0.26300 |
-1.30e-01 |
-2.29e-01 |
3.41e-01 |
0.093200 |
Molecules associated with elastic fibres |
26 |
6.78e-02 |
1.80e-01 |
0.26300 |
-2.58e-01 |
-5.02e-02 |
2.29e-02 |
0.658000 |
PI-3K cascade:FGFR2 |
12 |
2.91e-01 |
4.79e-01 |
0.26200 |
-2.47e-01 |
-8.59e-02 |
1.38e-01 |
0.607000 |
Reduction of cytosolic Ca++ levels |
10 |
3.62e-01 |
5.46e-01 |
0.26100 |
-2.42e-01 |
9.69e-02 |
1.85e-01 |
0.596000 |
Tight junction interactions |
12 |
2.93e-01 |
4.81e-01 |
0.26100 |
-1.70e-01 |
-1.97e-01 |
3.07e-01 |
0.236000 |
FRS-mediated FGFR4 signaling |
11 |
3.26e-01 |
5.10e-01 |
0.26000 |
-2.14e-01 |
-1.48e-01 |
2.19e-01 |
0.395000 |
Transcriptional Regulation by E2F6 |
27 |
6.57e-02 |
1.77e-01 |
0.25900 |
2.31e-01 |
1.18e-01 |
3.83e-02 |
0.287000 |
IKK complex recruitment mediated by RIP1 |
15 |
2.23e-01 |
4.06e-01 |
0.25800 |
-2.58e-01 |
-2.13e-02 |
8.43e-02 |
0.886000 |
Sealing of the nuclear envelope (NE) by ESCRT-III |
19 |
1.50e-01 |
3.18e-01 |
0.25800 |
1.05e-01 |
2.35e-01 |
4.26e-01 |
0.076000 |
Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane |
10 |
3.71e-01 |
5.56e-01 |
0.25700 |
8.31e-02 |
2.43e-01 |
6.49e-01 |
0.183000 |
Role of phospholipids in phagocytosis |
25 |
8.67e-02 |
2.13e-01 |
0.25600 |
1.23e-01 |
-2.24e-01 |
2.85e-01 |
0.052200 |
ERKs are inactivated |
11 |
3.38e-01 |
5.25e-01 |
0.25600 |
2.25e-01 |
1.22e-01 |
1.96e-01 |
0.484000 |
p38MAPK events |
12 |
3.10e-01 |
4.96e-01 |
0.25600 |
-2.11e-01 |
1.45e-01 |
2.06e-01 |
0.385000 |
Synthesis of bile acids and bile salts via 7alpha-hydroxycholesterol |
11 |
3.41e-01 |
5.28e-01 |
0.25600 |
2.56e-01 |
-6.91e-03 |
1.42e-01 |
0.968000 |
Conversion from APC/C:Cdc20 to APC/C:Cdh1 in late anaphase |
18 |
1.74e-01 |
3.54e-01 |
0.25500 |
2.43e-01 |
-7.72e-02 |
7.45e-02 |
0.571000 |
Netrin-1 signaling |
40 |
2.07e-02 |
7.19e-02 |
0.25500 |
-2.54e-01 |
-1.29e-02 |
5.42e-03 |
0.888000 |
Antigen Presentation: Folding, assembly and peptide loading of class I MHC |
13 |
2.83e-01 |
4.73e-01 |
0.25400 |
2.52e-01 |
3.52e-02 |
1.16e-01 |
0.826000 |
EPHA-mediated growth cone collapse |
11 |
3.47e-01 |
5.33e-01 |
0.25400 |
-1.74e-01 |
1.85e-01 |
3.17e-01 |
0.288000 |
Processing of SMDT1 |
11 |
3.46e-01 |
5.32e-01 |
0.25400 |
2.36e-01 |
9.16e-02 |
1.75e-01 |
0.599000 |
TGF-beta receptor signaling in EMT (epithelial to mesenchymal transition) |
10 |
3.80e-01 |
5.65e-01 |
0.25400 |
-1.64e-01 |
-1.93e-01 |
3.68e-01 |
0.291000 |
DAG and IP3 signaling |
33 |
4.21e-02 |
1.30e-01 |
0.25300 |
-2.52e-01 |
2.65e-02 |
1.23e-02 |
0.792000 |
Apoptotic cleavage of cellular proteins |
30 |
5.74e-02 |
1.62e-01 |
0.25300 |
-1.63e-01 |
1.93e-01 |
1.22e-01 |
0.067100 |
Antigen activates B Cell Receptor (BCR) leading to generation of second messengers |
25 |
9.47e-02 |
2.24e-01 |
0.25200 |
-2.05e-01 |
1.46e-01 |
7.65e-02 |
0.207000 |
Insertion of tail-anchored proteins into the endoplasmic reticulum membrane |
12 |
3.24e-01 |
5.07e-01 |
0.25000 |
2.45e-01 |
4.95e-02 |
1.41e-01 |
0.767000 |
SARS-CoV Infections |
55 |
5.72e-03 |
2.48e-02 |
0.25000 |
2.23e-01 |
1.14e-01 |
4.29e-03 |
0.144000 |
Collagen biosynthesis and modifying enzymes |
47 |
1.25e-02 |
4.70e-02 |
0.24900 |
-1.88e-01 |
-1.63e-01 |
2.57e-02 |
0.052800 |
Signaling by FGFR3 in disease |
13 |
3.01e-01 |
4.88e-01 |
0.24900 |
-2.46e-01 |
3.72e-02 |
1.25e-01 |
0.816000 |
Signaling by FGFR3 point mutants in cancer |
13 |
3.01e-01 |
4.88e-01 |
0.24900 |
-2.46e-01 |
3.72e-02 |
1.25e-01 |
0.816000 |
RNA Polymerase I Transcription Termination |
16 |
2.29e-01 |
4.12e-01 |
0.24900 |
1.25e-01 |
-2.15e-01 |
3.86e-01 |
0.137000 |
PTK6 Regulates RHO GTPases, RAS GTPase and MAP kinases |
12 |
3.32e-01 |
5.17e-01 |
0.24800 |
-9.61e-02 |
2.29e-01 |
5.65e-01 |
0.170000 |
Downstream signaling of activated FGFR4 |
16 |
2.29e-01 |
4.12e-01 |
0.24800 |
-2.16e-01 |
-1.21e-01 |
1.34e-01 |
0.403000 |
Downstream signaling events of B Cell Receptor (BCR) |
56 |
6.12e-03 |
2.60e-02 |
0.24700 |
2.44e-01 |
-3.66e-02 |
1.58e-03 |
0.636000 |
Class I peroxisomal membrane protein import |
10 |
4.03e-01 |
5.86e-01 |
0.24700 |
1.53e-01 |
-1.94e-01 |
4.02e-01 |
0.289000 |
Chondroitin sulfate biosynthesis |
16 |
2.31e-01 |
4.14e-01 |
0.24700 |
9.41e-02 |
2.28e-01 |
5.15e-01 |
0.114000 |
Gene Silencing by RNA |
43 |
2.00e-02 |
7.02e-02 |
0.24700 |
2.45e-01 |
2.64e-02 |
5.44e-03 |
0.765000 |
RHO GTPases activate PKNs |
27 |
8.68e-02 |
2.13e-01 |
0.24600 |
-1.57e-01 |
1.90e-01 |
1.57e-01 |
0.088100 |
Integrin signaling |
20 |
1.64e-01 |
3.38e-01 |
0.24600 |
-2.45e-01 |
2.62e-02 |
5.84e-02 |
0.839000 |
HIV Life Cycle |
92 |
2.56e-04 |
1.64e-03 |
0.24600 |
2.45e-01 |
-2.29e-02 |
5.09e-05 |
0.705000 |
Acyl chain remodelling of PS |
14 |
2.83e-01 |
4.73e-01 |
0.24600 |
2.30e-02 |
-2.44e-01 |
8.82e-01 |
0.113000 |
Smooth Muscle Contraction |
26 |
9.65e-02 |
2.27e-01 |
0.24500 |
-2.03e-02 |
2.44e-01 |
8.58e-01 |
0.031100 |
Apoptotic execution phase |
37 |
3.68e-02 |
1.18e-01 |
0.24500 |
-1.33e-01 |
2.06e-01 |
1.62e-01 |
0.030600 |
IRS-mediated signalling |
32 |
5.63e-02 |
1.60e-01 |
0.24500 |
-1.50e-01 |
-1.93e-01 |
1.42e-01 |
0.058500 |
DNA Damage Recognition in GG-NER |
25 |
1.07e-01 |
2.47e-01 |
0.24400 |
2.44e-01 |
-1.43e-02 |
3.48e-02 |
0.901000 |
Interferon Signaling |
116 |
3.38e-05 |
2.81e-04 |
0.24400 |
2.33e-01 |
7.33e-02 |
1.54e-05 |
0.174000 |
DNA Damage/Telomere Stress Induced Senescence |
20 |
1.68e-01 |
3.47e-01 |
0.24400 |
2.29e-01 |
8.24e-02 |
7.59e-02 |
0.524000 |
Complex I biogenesis |
35 |
4.48e-02 |
1.35e-01 |
0.24400 |
2.43e-01 |
1.53e-02 |
1.29e-02 |
0.876000 |
Meiotic recombination |
19 |
1.86e-01 |
3.68e-01 |
0.24300 |
2.34e-01 |
6.49e-02 |
7.74e-02 |
0.624000 |
Myogenesis |
22 |
1.42e-01 |
3.06e-01 |
0.24300 |
-1.58e-01 |
-1.84e-01 |
1.99e-01 |
0.135000 |
Amine ligand-binding receptors |
14 |
2.92e-01 |
4.79e-01 |
0.24200 |
-2.02e-01 |
-1.33e-01 |
1.90e-01 |
0.391000 |
Dissolution of Fibrin Clot |
11 |
3.82e-01 |
5.66e-01 |
0.24200 |
-5.53e-02 |
2.35e-01 |
7.51e-01 |
0.176000 |
Metabolism of amino acids and derivatives |
197 |
4.45e-08 |
7.19e-07 |
0.24200 |
2.38e-01 |
-3.97e-02 |
9.28e-09 |
0.338000 |
DCC mediated attractive signaling |
12 |
3.51e-01 |
5.36e-01 |
0.24100 |
-2.40e-01 |
2.32e-02 |
1.50e-01 |
0.889000 |
PERK regulates gene expression |
19 |
1.90e-01 |
3.74e-01 |
0.24100 |
1.47e-01 |
1.91e-01 |
2.66e-01 |
0.150000 |
Negative epigenetic regulation of rRNA expression |
28 |
8.84e-02 |
2.15e-01 |
0.24100 |
1.83e-01 |
-1.57e-01 |
9.44e-02 |
0.150000 |
Glyoxylate metabolism and glycine degradation |
23 |
1.35e-01 |
2.94e-01 |
0.24100 |
-1.19e-01 |
-2.09e-01 |
3.23e-01 |
0.082400 |
Elastic fibre formation |
31 |
6.80e-02 |
1.81e-01 |
0.24100 |
-2.40e-01 |
-1.67e-02 |
2.08e-02 |
0.872000 |
Formation of the Early Elongation Complex |
19 |
1.93e-01 |
3.79e-01 |
0.24100 |
2.40e-01 |
9.74e-03 |
6.99e-02 |
0.941000 |
Formation of the HIV-1 Early Elongation Complex |
19 |
1.93e-01 |
3.79e-01 |
0.24100 |
2.40e-01 |
9.74e-03 |
6.99e-02 |
0.941000 |
Transport of Mature Transcript to Cytoplasm |
59 |
6.02e-03 |
2.59e-02 |
0.24100 |
2.02e-01 |
1.30e-01 |
7.28e-03 |
0.084300 |
Neurotransmitter release cycle |
25 |
1.16e-01 |
2.62e-01 |
0.24000 |
-2.26e-01 |
-7.83e-02 |
5.01e-02 |
0.498000 |
MHC class II antigen presentation |
84 |
7.92e-04 |
4.23e-03 |
0.23900 |
2.01e-01 |
-1.30e-01 |
1.47e-03 |
0.039900 |
TNFR1-induced NFkappaB signaling pathway |
22 |
1.52e-01 |
3.19e-01 |
0.23900 |
-2.20e-01 |
-9.38e-02 |
7.45e-02 |
0.446000 |
RHO GTPases activate IQGAPs |
10 |
4.26e-01 |
6.03e-01 |
0.23800 |
2.31e-01 |
5.71e-02 |
2.05e-01 |
0.755000 |
Butyrate Response Factor 1 (BRF1) binds and destabilizes mRNA |
11 |
3.94e-01 |
5.79e-01 |
0.23800 |
-4.25e-02 |
2.34e-01 |
8.07e-01 |
0.179000 |
Glycosphingolipid metabolism |
26 |
1.11e-01 |
2.53e-01 |
0.23800 |
2.38e-01 |
4.58e-03 |
3.59e-02 |
0.968000 |
Extracellular matrix organization |
204 |
3.83e-08 |
6.36e-07 |
0.23800 |
-1.79e-01 |
-1.57e-01 |
1.15e-05 |
0.000124 |
Circadian Clock |
53 |
1.18e-02 |
4.48e-02 |
0.23700 |
-2.06e-01 |
1.18e-01 |
9.67e-03 |
0.137000 |
Signaling by Type 1 Insulin-like Growth Factor 1 Receptor (IGF1R) |
37 |
4.44e-02 |
1.35e-01 |
0.23700 |
-1.21e-01 |
-2.03e-01 |
2.02e-01 |
0.032500 |
FRS-mediated FGFR2 signaling |
12 |
3.66e-01 |
5.51e-01 |
0.23700 |
-2.36e-01 |
-1.08e-02 |
1.57e-01 |
0.948000 |
NOTCH4 Intracellular Domain Regulates Transcription |
18 |
2.24e-01 |
4.06e-01 |
0.23600 |
-1.48e-01 |
1.84e-01 |
2.77e-01 |
0.177000 |
Heparan sulfate/heparin (HS-GAG) metabolism |
34 |
5.93e-02 |
1.66e-01 |
0.23600 |
8.22e-02 |
-2.21e-01 |
4.07e-01 |
0.025600 |
Biosynthesis of specialized proresolving mediators (SPMs) |
12 |
3.67e-01 |
5.52e-01 |
0.23600 |
2.36e-01 |
6.84e-03 |
1.57e-01 |
0.967000 |
RORA activates gene expression |
16 |
2.65e-01 |
4.52e-01 |
0.23600 |
-2.00e-01 |
1.25e-01 |
1.65e-01 |
0.389000 |
TNF signaling |
31 |
7.56e-02 |
1.93e-01 |
0.23600 |
-2.35e-01 |
-2.32e-02 |
2.38e-02 |
0.823000 |
Transcriptional regulation by RUNX2 |
81 |
1.22e-03 |
6.27e-03 |
0.23600 |
2.35e-01 |
2.19e-02 |
2.66e-04 |
0.733000 |
Respiratory electron transport |
59 |
7.57e-03 |
3.10e-02 |
0.23600 |
2.32e-01 |
-4.19e-02 |
2.08e-03 |
0.578000 |
RNA Polymerase I Transcription Initiation |
29 |
9.10e-02 |
2.18e-01 |
0.23600 |
1.49e-01 |
-1.82e-01 |
1.64e-01 |
0.089700 |
Sialic acid metabolism |
23 |
1.51e-01 |
3.18e-01 |
0.23500 |
1.92e-01 |
-1.35e-01 |
1.11e-01 |
0.262000 |
Synthesis of Prostaglandins (PG) and Thromboxanes (TX) |
10 |
4.37e-01 |
6.09e-01 |
0.23500 |
4.32e-02 |
2.31e-01 |
8.13e-01 |
0.206000 |
Disorders of transmembrane transporters |
110 |
1.23e-04 |
8.59e-04 |
0.23500 |
2.34e-01 |
1.63e-02 |
2.31e-05 |
0.769000 |
Abortive elongation of HIV-1 transcript in the absence of Tat |
12 |
3.72e-01 |
5.56e-01 |
0.23500 |
2.33e-01 |
-2.25e-02 |
1.62e-01 |
0.893000 |
Regulation of insulin secretion |
55 |
1.09e-02 |
4.20e-02 |
0.23400 |
-2.23e-01 |
-7.25e-02 |
4.31e-03 |
0.353000 |
GPVI-mediated activation cascade |
25 |
1.29e-01 |
2.86e-01 |
0.23400 |
-2.34e-01 |
1.47e-02 |
4.33e-02 |
0.899000 |
RNA Polymerase I Promoter Escape |
16 |
2.71e-01 |
4.60e-01 |
0.23400 |
2.01e-01 |
-1.19e-01 |
1.63e-01 |
0.410000 |
Downstream signaling of activated FGFR2 |
17 |
2.50e-01 |
4.35e-01 |
0.23300 |
-2.32e-01 |
-2.55e-02 |
9.79e-02 |
0.856000 |
Regulation of TP53 Activity through Phosphorylation |
63 |
6.13e-03 |
2.60e-02 |
0.23300 |
1.93e-01 |
-1.32e-01 |
8.27e-03 |
0.071200 |
Triglyceride catabolism |
13 |
3.45e-01 |
5.32e-01 |
0.23300 |
-1.51e-01 |
-1.77e-01 |
3.45e-01 |
0.268000 |
NoRC negatively regulates rRNA expression |
25 |
1.32e-01 |
2.89e-01 |
0.23300 |
1.83e-01 |
-1.45e-01 |
1.14e-01 |
0.210000 |
Cell junction organization |
51 |
1.59e-02 |
5.80e-02 |
0.23300 |
-2.08e-01 |
-1.05e-01 |
1.04e-02 |
0.193000 |
DNA Double Strand Break Response |
32 |
7.53e-02 |
1.93e-01 |
0.23200 |
2.27e-01 |
5.10e-02 |
2.66e-02 |
0.618000 |
RNA Polymerase I Promoter Clearance |
32 |
7.70e-02 |
1.94e-01 |
0.23200 |
1.99e-01 |
-1.20e-01 |
5.18e-02 |
0.242000 |
Signaling by Activin |
10 |
4.47e-01 |
6.17e-01 |
0.23200 |
-2.27e-01 |
4.50e-02 |
2.13e-01 |
0.805000 |
CTLA4 inhibitory signaling |
19 |
2.18e-01 |
4.05e-01 |
0.23200 |
2.08e-01 |
-1.02e-01 |
1.16e-01 |
0.444000 |
Regulation of gene expression in late stage (branching morphogenesis) pancreatic bud precursor cells |
11 |
4.16e-01 |
5.98e-01 |
0.23100 |
-1.76e-01 |
1.49e-01 |
3.11e-01 |
0.391000 |
RUNX1 regulates genes involved in megakaryocyte differentiation and platelet function |
32 |
7.69e-02 |
1.94e-01 |
0.23100 |
-2.10e-01 |
-9.73e-02 |
4.02e-02 |
0.341000 |
ATF4 activates genes in response to endoplasmic reticulum stress |
16 |
2.77e-01 |
4.66e-01 |
0.23100 |
1.42e-01 |
1.82e-01 |
3.27e-01 |
0.207000 |
CS/DS degradation |
11 |
4.18e-01 |
5.98e-01 |
0.23000 |
2.06e-01 |
-1.03e-01 |
2.37e-01 |
0.554000 |
Prefoldin mediated transfer of substrate to CCT/TriC |
19 |
2.20e-01 |
4.05e-01 |
0.23000 |
1.19e-01 |
1.97e-01 |
3.70e-01 |
0.137000 |
Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding |
20 |
2.06e-01 |
3.95e-01 |
0.22900 |
6.33e-02 |
2.20e-01 |
6.24e-01 |
0.088100 |
Signaling by EGFR |
35 |
6.42e-02 |
1.75e-01 |
0.22900 |
-2.26e-01 |
-3.88e-02 |
2.10e-02 |
0.692000 |
Transport of Mature mRNA derived from an Intron-Containing Transcript |
53 |
1.60e-02 |
5.84e-02 |
0.22800 |
1.94e-01 |
1.21e-01 |
1.49e-02 |
0.129000 |
Signaling by BMP |
21 |
1.95e-01 |
3.80e-01 |
0.22800 |
-1.76e-01 |
-1.45e-01 |
1.63e-01 |
0.251000 |
Prolonged ERK activation events |
12 |
3.98e-01 |
5.84e-01 |
0.22700 |
-1.09e-01 |
1.99e-01 |
5.14e-01 |
0.233000 |
Gap junction trafficking and regulation |
15 |
3.18e-01 |
5.03e-01 |
0.22500 |
1.96e-01 |
1.12e-01 |
1.90e-01 |
0.455000 |
SUMOylation of RNA binding proteins |
35 |
7.03e-02 |
1.84e-01 |
0.22500 |
2.07e-01 |
8.84e-02 |
3.44e-02 |
0.366000 |
Unfolded Protein Response (UPR) |
64 |
8.35e-03 |
3.35e-02 |
0.22400 |
2.21e-01 |
-3.75e-02 |
2.27e-03 |
0.604000 |
Lewis blood group biosynthesis |
10 |
4.74e-01 |
6.42e-01 |
0.22400 |
1.73e-01 |
-1.42e-01 |
3.44e-01 |
0.437000 |
Kinesins |
29 |
1.15e-01 |
2.61e-01 |
0.22400 |
6.19e-02 |
-2.15e-01 |
5.64e-01 |
0.045400 |
Meiosis |
41 |
4.65e-02 |
1.39e-01 |
0.22300 |
1.80e-01 |
1.33e-01 |
4.67e-02 |
0.142000 |
TGF-beta receptor signaling activates SMADs |
18 |
2.61e-01 |
4.48e-01 |
0.22300 |
-1.94e-01 |
-1.09e-01 |
1.54e-01 |
0.423000 |
Formation of TC-NER Pre-Incision Complex |
32 |
9.28e-02 |
2.21e-01 |
0.22300 |
2.20e-01 |
3.62e-02 |
3.16e-02 |
0.723000 |
Gamma carboxylation, hypusine formation and arylsulfatase activation |
21 |
2.13e-01 |
3.99e-01 |
0.22200 |
1.62e-01 |
-1.52e-01 |
1.98e-01 |
0.228000 |
IGF1R signaling cascade |
36 |
6.93e-02 |
1.83e-01 |
0.22200 |
-9.78e-02 |
-2.00e-01 |
3.10e-01 |
0.038300 |
Other semaphorin interactions |
18 |
2.67e-01 |
4.55e-01 |
0.22200 |
-2.01e-01 |
9.32e-02 |
1.39e-01 |
0.494000 |
Formation of HIV elongation complex in the absence of HIV Tat |
23 |
1.85e-01 |
3.67e-01 |
0.22200 |
2.04e-01 |
-8.57e-02 |
8.99e-02 |
0.477000 |
Formation of HIV-1 elongation complex containing HIV-1 Tat |
23 |
1.85e-01 |
3.67e-01 |
0.22200 |
2.04e-01 |
-8.57e-02 |
8.99e-02 |
0.477000 |
HIV Transcription Elongation |
23 |
1.85e-01 |
3.67e-01 |
0.22200 |
2.04e-01 |
-8.57e-02 |
8.99e-02 |
0.477000 |
Tat-mediated elongation of the HIV-1 transcript |
23 |
1.85e-01 |
3.67e-01 |
0.22200 |
2.04e-01 |
-8.57e-02 |
8.99e-02 |
0.477000 |
PI-3K cascade:FGFR3 |
10 |
4.79e-01 |
6.47e-01 |
0.22100 |
-1.85e-01 |
-1.21e-01 |
3.11e-01 |
0.506000 |
Protein localization |
108 |
4.03e-04 |
2.41e-03 |
0.22100 |
2.08e-01 |
-7.40e-02 |
1.91e-04 |
0.185000 |
Signaling by Hedgehog |
93 |
1.20e-03 |
6.20e-03 |
0.22100 |
2.18e-01 |
-3.11e-02 |
2.80e-04 |
0.605000 |
Plasma lipoprotein assembly, remodeling, and clearance |
45 |
3.84e-02 |
1.21e-01 |
0.22000 |
2.16e-01 |
-4.46e-02 |
1.23e-02 |
0.605000 |
Glucuronidation |
10 |
4.85e-01 |
6.52e-01 |
0.22000 |
-1.76e-01 |
1.32e-01 |
3.34e-01 |
0.471000 |
Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks |
31 |
1.05e-01 |
2.44e-01 |
0.22000 |
2.03e-01 |
8.50e-02 |
5.06e-02 |
0.413000 |
Signaling by ROBO receptors |
114 |
2.75e-04 |
1.75e-03 |
0.22000 |
2.02e-01 |
8.59e-02 |
1.99e-04 |
0.114000 |
Protein ubiquitination |
37 |
6.86e-02 |
1.82e-01 |
0.22000 |
1.45e-01 |
1.65e-01 |
1.28e-01 |
0.082400 |
IRS-related events triggered by IGF1R |
35 |
7.93e-02 |
1.99e-01 |
0.22000 |
-1.16e-01 |
-1.86e-01 |
2.35e-01 |
0.056500 |
Degradation of the extracellular matrix |
70 |
6.38e-03 |
2.68e-02 |
0.22000 |
-1.42e-01 |
-1.68e-01 |
4.09e-02 |
0.015300 |
WNT5A-dependent internalization of FZD4 |
12 |
4.19e-01 |
5.98e-01 |
0.21900 |
1.97e-01 |
9.64e-02 |
2.37e-01 |
0.563000 |
N-glycan trimming in the ER and Calnexin/Calreticulin cycle |
21 |
2.22e-01 |
4.05e-01 |
0.21900 |
2.19e-01 |
5.67e-03 |
8.27e-02 |
0.964000 |
NOTCH2 intracellular domain regulates transcription |
10 |
4.91e-01 |
6.58e-01 |
0.21800 |
-1.63e-01 |
1.45e-01 |
3.72e-01 |
0.427000 |
TNFR2 non-canonical NF-kB pathway |
67 |
8.76e-03 |
3.51e-02 |
0.21800 |
2.16e-01 |
2.26e-02 |
2.21e-03 |
0.749000 |
Negative regulation of NMDA receptor-mediated neuronal transmission |
15 |
3.44e-01 |
5.32e-01 |
0.21800 |
-2.04e-01 |
-7.58e-02 |
1.72e-01 |
0.611000 |
TP53 Regulates Transcription of Genes Involved in G1 Cell Cycle Arrest |
11 |
4.59e-01 |
6.27e-01 |
0.21700 |
2.10e-01 |
5.60e-02 |
2.29e-01 |
0.748000 |
Respiratory electron transport, ATP synthesis by chemiosmotic coupling, and heat production by uncoupling proteins. |
64 |
1.14e-02 |
4.34e-02 |
0.21700 |
2.13e-01 |
-3.90e-02 |
3.24e-03 |
0.590000 |
Adrenaline,noradrenaline inhibits insulin secretion |
19 |
2.65e-01 |
4.52e-01 |
0.21600 |
-2.15e-01 |
-2.31e-02 |
1.05e-01 |
0.862000 |
TP53 Regulates Transcription of Cell Cycle Genes |
39 |
6.58e-02 |
1.77e-01 |
0.21600 |
2.10e-01 |
4.85e-02 |
2.31e-02 |
0.601000 |
Interleukin-1 signaling |
71 |
7.25e-03 |
2.99e-02 |
0.21600 |
2.10e-01 |
5.04e-02 |
2.30e-03 |
0.463000 |
tRNA processing |
75 |
5.72e-03 |
2.48e-02 |
0.21500 |
2.12e-01 |
3.27e-02 |
1.50e-03 |
0.625000 |
G-protein activation |
14 |
3.79e-01 |
5.63e-01 |
0.21500 |
-1.76e-01 |
-1.24e-01 |
2.55e-01 |
0.424000 |
Transmission across Chemical Synapses |
151 |
3.35e-05 |
2.80e-04 |
0.21400 |
-2.00e-01 |
-7.70e-02 |
2.33e-05 |
0.104000 |
Nephrin family interactions |
17 |
3.11e-01 |
4.97e-01 |
0.21400 |
-2.08e-01 |
5.05e-02 |
1.37e-01 |
0.719000 |
Processing of Capped Intronless Pre-mRNA |
17 |
3.11e-01 |
4.97e-01 |
0.21400 |
1.26e-01 |
1.73e-01 |
3.70e-01 |
0.217000 |
Neuronal System |
225 |
2.66e-07 |
3.80e-06 |
0.21400 |
-2.02e-01 |
-7.08e-02 |
2.17e-07 |
0.068500 |
Retrograde transport at the Trans-Golgi-Network |
36 |
8.60e-02 |
2.12e-01 |
0.21300 |
-2.11e-01 |
-3.32e-02 |
2.88e-02 |
0.730000 |
Paradoxical activation of RAF signaling by kinase inactive BRAF |
30 |
1.32e-01 |
2.89e-01 |
0.21300 |
-2.02e-01 |
6.80e-02 |
5.60e-02 |
0.519000 |
Signaling by RAS mutants |
30 |
1.32e-01 |
2.89e-01 |
0.21300 |
-2.02e-01 |
6.80e-02 |
5.60e-02 |
0.519000 |
Signaling by moderate kinase activity BRAF mutants |
30 |
1.32e-01 |
2.89e-01 |
0.21300 |
-2.02e-01 |
6.80e-02 |
5.60e-02 |
0.519000 |
Signaling downstream of RAS mutants |
30 |
1.32e-01 |
2.89e-01 |
0.21300 |
-2.02e-01 |
6.80e-02 |
5.60e-02 |
0.519000 |
Pyruvate metabolism |
21 |
2.40e-01 |
4.25e-01 |
0.21300 |
-1.16e-01 |
-1.78e-01 |
3.57e-01 |
0.158000 |
Signaling by PDGF |
45 |
4.78e-02 |
1.42e-01 |
0.21200 |
-2.07e-01 |
-4.75e-02 |
1.63e-02 |
0.582000 |
Ion transport by P-type ATPases |
34 |
1.02e-01 |
2.39e-01 |
0.21200 |
-2.12e-01 |
9.72e-03 |
3.28e-02 |
0.922000 |
Formation of Incision Complex in GG-NER |
28 |
1.52e-01 |
3.20e-01 |
0.21200 |
1.95e-01 |
8.16e-02 |
7.38e-02 |
0.455000 |
Interleukin-35 Signalling |
11 |
4.81e-01 |
6.48e-01 |
0.21100 |
-4.13e-02 |
2.07e-01 |
8.13e-01 |
0.235000 |
Nucleotide salvage |
16 |
3.45e-01 |
5.32e-01 |
0.21000 |
2.05e-01 |
4.89e-02 |
1.56e-01 |
0.735000 |
TRP channels |
16 |
3.45e-01 |
5.32e-01 |
0.21000 |
-1.57e-01 |
-1.40e-01 |
2.77e-01 |
0.333000 |
G-protein beta:gamma signalling |
21 |
2.49e-01 |
4.35e-01 |
0.21000 |
-2.03e-01 |
-5.32e-02 |
1.07e-01 |
0.673000 |
Trafficking of GluR2-containing AMPA receptors |
10 |
5.16e-01 |
6.84e-01 |
0.21000 |
8.19e-02 |
1.93e-01 |
6.54e-01 |
0.290000 |
Metabolic disorders of biological oxidation enzymes |
19 |
2.86e-01 |
4.75e-01 |
0.21000 |
-2.01e-01 |
-5.87e-02 |
1.29e-01 |
0.658000 |
RUNX3 regulates NOTCH signaling |
13 |
4.26e-01 |
6.03e-01 |
0.20900 |
-2.09e-01 |
1.53e-02 |
1.92e-01 |
0.924000 |
Downregulation of TGF-beta receptor signaling |
16 |
3.51e-01 |
5.36e-01 |
0.20900 |
-2.03e-01 |
-5.01e-02 |
1.61e-01 |
0.729000 |
TNFs bind their physiological receptors |
19 |
2.91e-01 |
4.79e-01 |
0.20800 |
-4.25e-02 |
2.04e-01 |
7.49e-01 |
0.124000 |
CD28 dependent PI3K/Akt signaling |
20 |
2.72e-01 |
4.61e-01 |
0.20800 |
-5.41e-02 |
-2.01e-01 |
6.75e-01 |
0.120000 |
Interleukin-12 family signaling |
40 |
7.51e-02 |
1.93e-01 |
0.20800 |
7.07e-02 |
1.95e-01 |
4.39e-01 |
0.032600 |
Purine salvage |
11 |
4.91e-01 |
6.58e-01 |
0.20700 |
1.70e-01 |
1.18e-01 |
3.28e-01 |
0.499000 |
Transcriptional activation of mitochondrial biogenesis |
45 |
5.70e-02 |
1.61e-01 |
0.20700 |
-1.85e-01 |
9.28e-02 |
3.21e-02 |
0.282000 |
EGFR downregulation |
19 |
3.00e-01 |
4.88e-01 |
0.20600 |
-2.06e-01 |
4.10e-03 |
1.21e-01 |
0.975000 |
Cell recruitment (pro-inflammatory response) |
19 |
3.04e-01 |
4.91e-01 |
0.20500 |
1.18e-01 |
-1.68e-01 |
3.73e-01 |
0.206000 |
Purinergic signaling in leishmaniasis infection |
19 |
3.04e-01 |
4.91e-01 |
0.20500 |
1.18e-01 |
-1.68e-01 |
3.73e-01 |
0.206000 |
Cilium Assembly |
141 |
1.58e-04 |
1.09e-03 |
0.20500 |
2.05e-01 |
1.08e-03 |
2.87e-05 |
0.982000 |
Activation of BAD and translocation to mitochondria |
14 |
4.18e-01 |
5.98e-01 |
0.20400 |
5.49e-02 |
1.96e-01 |
7.22e-01 |
0.204000 |
PLC beta mediated events |
42 |
7.53e-02 |
1.93e-01 |
0.20300 |
-2.02e-01 |
-2.37e-02 |
2.40e-02 |
0.791000 |
TP53 Regulates Transcription of Cell Death Genes |
30 |
1.60e-01 |
3.33e-01 |
0.20200 |
-2.02e-01 |
5.65e-03 |
5.55e-02 |
0.957000 |
Signaling by MET |
53 |
3.94e-02 |
1.24e-01 |
0.20200 |
-1.97e-01 |
-4.65e-02 |
1.34e-02 |
0.558000 |
Biosynthesis of DHA-derived SPMs |
10 |
5.43e-01 |
7.08e-01 |
0.20200 |
1.99e-01 |
3.42e-02 |
2.77e-01 |
0.851000 |
RNA Polymerase I Transcription |
33 |
1.38e-01 |
3.00e-01 |
0.20100 |
1.73e-01 |
-1.01e-01 |
8.54e-02 |
0.314000 |
Nucleotide-binding domain, leucine rich repeat containing receptor (NLR) signaling pathways |
40 |
9.07e-02 |
2.18e-01 |
0.20100 |
-1.96e-01 |
4.14e-02 |
3.19e-02 |
0.651000 |
CaM pathway |
27 |
2.00e-01 |
3.85e-01 |
0.20000 |
-1.99e-01 |
-1.44e-02 |
7.35e-02 |
0.897000 |
Calmodulin induced events |
27 |
2.00e-01 |
3.85e-01 |
0.20000 |
-1.99e-01 |
-1.44e-02 |
7.35e-02 |
0.897000 |
VxPx cargo-targeting to cilium |
13 |
4.61e-01 |
6.28e-01 |
0.19900 |
1.78e-01 |
8.88e-02 |
2.66e-01 |
0.580000 |
MET promotes cell motility |
26 |
2.15e-01 |
4.02e-01 |
0.19900 |
-1.97e-01 |
2.71e-02 |
8.22e-02 |
0.811000 |
G alpha (12/13) signalling events |
61 |
2.71e-02 |
9.11e-02 |
0.19900 |
-1.16e-01 |
-1.61e-01 |
1.17e-01 |
0.029600 |
Calnexin/calreticulin cycle |
14 |
4.43e-01 |
6.13e-01 |
0.19700 |
1.86e-01 |
-6.64e-02 |
2.29e-01 |
0.667000 |
Synthesis of PIPs at the plasma membrane |
47 |
6.61e-02 |
1.77e-01 |
0.19700 |
-1.55e-01 |
1.21e-01 |
6.57e-02 |
0.150000 |
Ovarian tumor domain proteases |
26 |
2.22e-01 |
4.05e-01 |
0.19700 |
-1.56e-01 |
1.21e-01 |
1.70e-01 |
0.287000 |
RHO GTPases Activate WASPs and WAVEs |
30 |
1.77e-01 |
3.58e-01 |
0.19700 |
-7.59e-02 |
1.82e-01 |
4.72e-01 |
0.085500 |
Senescence-Associated Secretory Phenotype (SASP) |
37 |
1.18e-01 |
2.66e-01 |
0.19700 |
1.91e-01 |
-4.59e-02 |
4.42e-02 |
0.629000 |
Keratinization |
27 |
2.11e-01 |
3.99e-01 |
0.19600 |
-1.68e-01 |
-1.00e-01 |
1.30e-01 |
0.369000 |
Bile acid and bile salt metabolism |
20 |
3.17e-01 |
5.03e-01 |
0.19600 |
1.87e-01 |
5.71e-02 |
1.48e-01 |
0.659000 |
Intrinsic Pathway for Apoptosis |
42 |
9.03e-02 |
2.18e-01 |
0.19500 |
1.77e-01 |
8.23e-02 |
4.71e-02 |
0.357000 |
COPI-dependent Golgi-to-ER retrograde traffic |
57 |
4.00e-02 |
1.25e-01 |
0.19500 |
1.21e-01 |
-1.53e-01 |
1.15e-01 |
0.046100 |
MAP2K and MAPK activation |
25 |
2.43e-01 |
4.29e-01 |
0.19500 |
-1.46e-01 |
1.30e-01 |
2.08e-01 |
0.262000 |
SHC-mediated cascade:FGFR4 |
10 |
5.66e-01 |
7.25e-01 |
0.19500 |
-1.25e-01 |
-1.49e-01 |
4.93e-01 |
0.415000 |
Biosynthesis of the N-glycan precursor (dolichol lipid-linked oligosaccharide, LLO) and transfer to a nascent protein |
60 |
3.42e-02 |
1.12e-01 |
0.19400 |
1.92e-01 |
-3.06e-02 |
1.02e-02 |
0.682000 |
Negative regulation of MET activity |
13 |
4.80e-01 |
6.48e-01 |
0.19400 |
-1.89e-01 |
4.63e-02 |
2.39e-01 |
0.773000 |
NGF-stimulated transcription |
27 |
2.20e-01 |
4.05e-01 |
0.19400 |
-1.67e-01 |
9.85e-02 |
1.33e-01 |
0.376000 |
Binding and Uptake of Ligands by Scavenger Receptors |
27 |
2.21e-01 |
4.05e-01 |
0.19400 |
9.59e-02 |
-1.68e-01 |
3.89e-01 |
0.131000 |
Interconversion of nucleotide di- and triphosphates |
22 |
2.92e-01 |
4.79e-01 |
0.19300 |
1.80e-01 |
7.04e-02 |
1.45e-01 |
0.568000 |
Downstream signaling of activated FGFR3 |
15 |
4.33e-01 |
6.09e-01 |
0.19300 |
-1.88e-01 |
-4.10e-02 |
2.07e-01 |
0.783000 |
Formation of the beta-catenin:TCF transactivating complex |
29 |
1.99e-01 |
3.85e-01 |
0.19200 |
-1.78e-01 |
-7.21e-02 |
9.64e-02 |
0.502000 |
BMAL1:CLOCK,NPAS2 activates circadian gene expression |
19 |
3.49e-01 |
5.36e-01 |
0.19200 |
-1.79e-01 |
-7.05e-02 |
1.78e-01 |
0.595000 |
Post NMDA receptor activation events |
49 |
6.94e-02 |
1.83e-01 |
0.19100 |
-1.90e-01 |
-1.88e-02 |
2.16e-02 |
0.820000 |
Transport of inorganic cations/anions and amino acids/oligopeptides |
68 |
2.47e-02 |
8.37e-02 |
0.19100 |
-1.80e-01 |
-6.22e-02 |
1.02e-02 |
0.376000 |
Synthesis of very long-chain fatty acyl-CoAs |
15 |
4.42e-01 |
6.13e-01 |
0.19100 |
-5.46e-02 |
1.83e-01 |
7.14e-01 |
0.220000 |
Interleukin-37 signaling |
15 |
4.42e-01 |
6.13e-01 |
0.19100 |
-1.89e-01 |
2.74e-02 |
2.06e-01 |
0.854000 |
Lysosome Vesicle Biogenesis |
25 |
2.58e-01 |
4.45e-01 |
0.19000 |
1.87e-01 |
3.42e-02 |
1.06e-01 |
0.767000 |
Class B/2 (Secretin family receptors) |
49 |
7.04e-02 |
1.84e-01 |
0.19000 |
1.33e-01 |
1.36e-01 |
1.09e-01 |
0.099700 |
DARPP-32 events |
19 |
3.60e-01 |
5.44e-01 |
0.18900 |
7.02e-02 |
1.76e-01 |
5.96e-01 |
0.185000 |
Erythropoietin activates Phosphoinositide-3-kinase (PI3K) |
10 |
5.87e-01 |
7.41e-01 |
0.18900 |
-6.05e-02 |
1.79e-01 |
7.41e-01 |
0.328000 |
G alpha (z) signalling events |
31 |
1.94e-01 |
3.80e-01 |
0.18800 |
-1.82e-01 |
4.64e-02 |
7.89e-02 |
0.655000 |
RET signaling |
32 |
1.82e-01 |
3.65e-01 |
0.18800 |
-1.29e-01 |
-1.37e-01 |
2.06e-01 |
0.181000 |
Transport of vitamins, nucleosides, and related molecules |
28 |
2.30e-01 |
4.13e-01 |
0.18700 |
-2.68e-02 |
1.86e-01 |
8.07e-01 |
0.089500 |
Synthesis of IP2, IP, and Ins in the cytosol |
12 |
5.33e-01 |
6.98e-01 |
0.18700 |
-1.61e-01 |
9.62e-02 |
3.35e-01 |
0.564000 |
CD209 (DC-SIGN) signaling |
18 |
3.92e-01 |
5.77e-01 |
0.18700 |
-1.34e-01 |
1.31e-01 |
3.26e-01 |
0.338000 |
Metabolism of nitric oxide: NOS3 activation and regulation |
14 |
4.81e-01 |
6.48e-01 |
0.18700 |
9.88e-03 |
-1.87e-01 |
9.49e-01 |
0.227000 |
IL-6-type cytokine receptor ligand interactions |
12 |
5.33e-01 |
6.98e-01 |
0.18700 |
-7.04e-02 |
-1.73e-01 |
6.73e-01 |
0.300000 |
G beta:gamma signalling through CDC42 |
11 |
5.63e-01 |
7.24e-01 |
0.18600 |
-1.70e-01 |
-7.69e-02 |
3.30e-01 |
0.659000 |
Activation of NMDA receptors and postsynaptic events |
54 |
6.09e-02 |
1.69e-01 |
0.18600 |
-1.80e-01 |
-4.71e-02 |
2.22e-02 |
0.550000 |
RMTs methylate histone arginines |
25 |
2.74e-01 |
4.63e-01 |
0.18600 |
1.85e-01 |
1.89e-02 |
1.10e-01 |
0.870000 |
Signaling by NOTCH2 |
23 |
3.04e-01 |
4.91e-01 |
0.18600 |
-1.79e-01 |
-4.95e-02 |
1.37e-01 |
0.681000 |
Base-Excision Repair, AP Site Formation |
17 |
4.15e-01 |
5.98e-01 |
0.18600 |
1.70e-01 |
7.36e-02 |
2.24e-01 |
0.599000 |
G-protein mediated events |
43 |
1.10e-01 |
2.53e-01 |
0.18500 |
-1.81e-01 |
-3.97e-02 |
4.05e-02 |
0.653000 |
TP53 Regulates Transcription of DNA Repair Genes |
38 |
1.43e-01 |
3.07e-01 |
0.18500 |
1.85e-01 |
3.51e-03 |
4.88e-02 |
0.970000 |
mRNA Splicing - Minor Pathway |
30 |
2.19e-01 |
4.05e-01 |
0.18400 |
1.65e-01 |
-8.12e-02 |
1.17e-01 |
0.442000 |
Peptide hormone metabolism |
44 |
1.08e-01 |
2.48e-01 |
0.18400 |
-1.77e-01 |
5.16e-02 |
4.24e-02 |
0.554000 |
Neurotransmitter receptors and postsynaptic signal transmission |
114 |
3.32e-03 |
1.56e-02 |
0.18300 |
-1.63e-01 |
-8.41e-02 |
2.73e-03 |
0.122000 |
HSF1-dependent transactivation |
24 |
3.01e-01 |
4.88e-01 |
0.18300 |
-1.82e-01 |
1.71e-02 |
1.23e-01 |
0.885000 |
Golgi-to-ER retrograde transport |
83 |
1.63e-02 |
5.89e-02 |
0.18300 |
1.29e-01 |
-1.30e-01 |
4.31e-02 |
0.041100 |
Endogenous sterols |
17 |
4.27e-01 |
6.04e-01 |
0.18200 |
-1.52e-01 |
-1.00e-01 |
2.77e-01 |
0.475000 |
PTEN Regulation |
101 |
6.78e-03 |
2.81e-02 |
0.18200 |
1.74e-01 |
5.43e-02 |
2.59e-03 |
0.347000 |
O-linked glycosylation |
68 |
3.50e-02 |
1.13e-01 |
0.18200 |
-5.85e-02 |
-1.72e-01 |
4.05e-01 |
0.014400 |
Arachidonic acid metabolism |
36 |
1.70e-01 |
3.48e-01 |
0.18100 |
9.47e-02 |
1.54e-01 |
3.26e-01 |
0.109000 |
G alpha (q) signalling events |
118 |
3.35e-03 |
1.57e-02 |
0.18000 |
-1.75e-01 |
-4.09e-02 |
1.02e-03 |
0.444000 |
Insulin receptor signalling cascade |
38 |
1.62e-01 |
3.35e-01 |
0.17900 |
-1.35e-01 |
-1.17e-01 |
1.49e-01 |
0.213000 |
Notch-HLH transcription pathway |
22 |
3.49e-01 |
5.36e-01 |
0.17900 |
-1.64e-01 |
-6.98e-02 |
1.82e-01 |
0.571000 |
Stimuli-sensing channels |
55 |
7.29e-02 |
1.89e-01 |
0.17800 |
-1.62e-01 |
-7.42e-02 |
3.77e-02 |
0.342000 |
Ca-dependent events |
29 |
2.54e-01 |
4.40e-01 |
0.17800 |
-1.73e-01 |
4.36e-02 |
1.08e-01 |
0.685000 |
TNFR1-induced proapoptotic signaling |
12 |
5.67e-01 |
7.25e-01 |
0.17800 |
-1.74e-01 |
3.73e-02 |
2.97e-01 |
0.823000 |
Signaling by Erythropoietin |
20 |
3.93e-01 |
5.78e-01 |
0.17700 |
-1.43e-01 |
1.05e-01 |
2.70e-01 |
0.417000 |
RNA Polymerase II Transcription Termination |
46 |
1.16e-01 |
2.62e-01 |
0.17700 |
7.82e-02 |
1.59e-01 |
3.60e-01 |
0.063100 |
Oncogene Induced Senescence |
24 |
3.28e-01 |
5.11e-01 |
0.17600 |
1.69e-03 |
1.76e-01 |
9.89e-01 |
0.135000 |
Regulation of TP53 Activity |
116 |
4.87e-03 |
2.20e-02 |
0.17600 |
1.50e-01 |
-9.18e-02 |
5.26e-03 |
0.088400 |
Constitutive Signaling by EGFRvIII |
13 |
5.48e-01 |
7.09e-01 |
0.17600 |
-7.47e-02 |
1.60e-01 |
6.41e-01 |
0.319000 |
Constitutive Signaling by Ligand-Responsive EGFR Cancer Variants |
13 |
5.48e-01 |
7.09e-01 |
0.17600 |
-7.47e-02 |
1.60e-01 |
6.41e-01 |
0.319000 |
Signaling by EGFRvIII in Cancer |
13 |
5.48e-01 |
7.09e-01 |
0.17600 |
-7.47e-02 |
1.60e-01 |
6.41e-01 |
0.319000 |
Signaling by Ligand-Responsive EGFR Variants in Cancer |
13 |
5.48e-01 |
7.09e-01 |
0.17600 |
-7.47e-02 |
1.60e-01 |
6.41e-01 |
0.319000 |
Complement cascade |
37 |
1.82e-01 |
3.65e-01 |
0.17600 |
9.67e-02 |
-1.47e-01 |
3.09e-01 |
0.122000 |
Gastrin-CREB signalling pathway via PKC and MAPK |
14 |
5.24e-01 |
6.91e-01 |
0.17600 |
-6.34e-02 |
1.64e-01 |
6.82e-01 |
0.288000 |
Metal ion SLC transporters |
18 |
4.36e-01 |
6.09e-01 |
0.17600 |
1.74e-01 |
-2.59e-02 |
2.02e-01 |
0.849000 |
Interleukin-12 signaling |
32 |
2.28e-01 |
4.12e-01 |
0.17500 |
5.82e-02 |
1.66e-01 |
5.69e-01 |
0.105000 |
VEGFR2 mediated vascular permeability |
25 |
3.16e-01 |
5.03e-01 |
0.17500 |
1.54e-02 |
-1.75e-01 |
8.94e-01 |
0.131000 |
SEMA3A-Plexin repulsion signaling by inhibiting Integrin adhesion |
12 |
5.74e-01 |
7.30e-01 |
0.17500 |
1.64e-01 |
6.20e-02 |
3.25e-01 |
0.710000 |
Signaling by KIT in disease |
17 |
4.60e-01 |
6.27e-01 |
0.17500 |
-1.59e-01 |
7.43e-02 |
2.58e-01 |
0.596000 |
Signaling by phosphorylated juxtamembrane, extracellular and kinase domain KIT mutants |
17 |
4.60e-01 |
6.27e-01 |
0.17500 |
-1.59e-01 |
7.43e-02 |
2.58e-01 |
0.596000 |
Regulation of MECP2 expression and activity |
23 |
3.50e-01 |
5.36e-01 |
0.17500 |
-1.46e-01 |
9.59e-02 |
2.25e-01 |
0.426000 |
FRS-mediated FGFR3 signaling |
10 |
6.33e-01 |
7.79e-01 |
0.17500 |
-1.72e-01 |
-3.12e-02 |
3.47e-01 |
0.864000 |
SUMOylation of chromatin organization proteins |
40 |
1.61e-01 |
3.35e-01 |
0.17400 |
1.55e-01 |
8.08e-02 |
9.08e-02 |
0.377000 |
Response of Mtb to phagocytosis |
17 |
4.62e-01 |
6.29e-01 |
0.17400 |
3.63e-02 |
1.70e-01 |
7.96e-01 |
0.225000 |
HIV Transcription Initiation |
31 |
2.47e-01 |
4.32e-01 |
0.17400 |
1.58e-01 |
-7.34e-02 |
1.29e-01 |
0.480000 |
RNA Polymerase II HIV Promoter Escape |
31 |
2.47e-01 |
4.32e-01 |
0.17400 |
1.58e-01 |
-7.34e-02 |
1.29e-01 |
0.480000 |
RNA Polymerase II Promoter Escape |
31 |
2.47e-01 |
4.32e-01 |
0.17400 |
1.58e-01 |
-7.34e-02 |
1.29e-01 |
0.480000 |
RNA Polymerase II Transcription Initiation |
31 |
2.47e-01 |
4.32e-01 |
0.17400 |
1.58e-01 |
-7.34e-02 |
1.29e-01 |
0.480000 |
RNA Polymerase II Transcription Initiation And Promoter Clearance |
31 |
2.47e-01 |
4.32e-01 |
0.17400 |
1.58e-01 |
-7.34e-02 |
1.29e-01 |
0.480000 |
RNA Polymerase II Transcription Pre-Initiation And Promoter Opening |
31 |
2.47e-01 |
4.32e-01 |
0.17400 |
1.58e-01 |
-7.34e-02 |
1.29e-01 |
0.480000 |
Synthesis of IP3 and IP4 in the cytosol |
20 |
4.05e-01 |
5.87e-01 |
0.17400 |
-3.58e-02 |
1.70e-01 |
7.82e-01 |
0.188000 |
Platelet homeostasis |
63 |
5.79e-02 |
1.63e-01 |
0.17400 |
-1.53e-01 |
-8.29e-02 |
3.63e-02 |
0.256000 |
G beta:gamma signalling through PI3Kgamma |
16 |
4.87e-01 |
6.55e-01 |
0.17300 |
-1.72e-01 |
2.37e-02 |
2.35e-01 |
0.870000 |
Downstream TCR signaling |
64 |
5.75e-02 |
1.62e-01 |
0.17300 |
1.72e-01 |
1.54e-02 |
1.73e-02 |
0.831000 |
CD28 dependent Vav1 pathway |
11 |
6.15e-01 |
7.66e-01 |
0.17200 |
-9.94e-02 |
1.40e-01 |
5.68e-01 |
0.420000 |
Signaling by FGFR1 in disease |
27 |
3.04e-01 |
4.91e-01 |
0.17200 |
-1.43e-01 |
9.51e-02 |
1.98e-01 |
0.393000 |
WNT ligand biogenesis and trafficking |
16 |
4.93e-01 |
6.58e-01 |
0.17200 |
1.69e-01 |
3.23e-02 |
2.43e-01 |
0.823000 |
Cargo concentration in the ER |
19 |
4.35e-01 |
6.09e-01 |
0.17100 |
1.34e-01 |
-1.07e-01 |
3.12e-01 |
0.421000 |
Signaling by SCF-KIT |
36 |
2.07e-01 |
3.95e-01 |
0.17100 |
-1.61e-01 |
5.90e-02 |
9.50e-02 |
0.540000 |
Cleavage of the damaged pyrimidine |
15 |
5.19e-01 |
6.85e-01 |
0.17100 |
1.68e-01 |
2.87e-02 |
2.59e-01 |
0.847000 |
Depyrimidination |
15 |
5.19e-01 |
6.85e-01 |
0.17100 |
1.68e-01 |
2.87e-02 |
2.59e-01 |
0.847000 |
Recognition and association of DNA glycosylase with site containing an affected pyrimidine |
15 |
5.19e-01 |
6.85e-01 |
0.17100 |
1.68e-01 |
2.87e-02 |
2.59e-01 |
0.847000 |
Downstream signal transduction |
26 |
3.24e-01 |
5.07e-01 |
0.17100 |
-1.40e-01 |
9.81e-02 |
2.18e-01 |
0.387000 |
Signalling to ERKs |
28 |
2.98e-01 |
4.88e-01 |
0.17000 |
-9.25e-02 |
1.43e-01 |
3.97e-01 |
0.190000 |
STING mediated induction of host immune responses |
10 |
6.47e-01 |
7.88e-01 |
0.17000 |
-5.76e-04 |
1.70e-01 |
9.97e-01 |
0.351000 |
Chaperone Mediated Autophagy |
13 |
5.70e-01 |
7.27e-01 |
0.17000 |
9.97e-02 |
-1.38e-01 |
5.34e-01 |
0.389000 |
Phase I - Functionalization of compounds |
57 |
8.66e-02 |
2.13e-01 |
0.16900 |
3.00e-02 |
1.67e-01 |
6.96e-01 |
0.029600 |
Signal transduction by L1 |
15 |
5.26e-01 |
6.92e-01 |
0.16900 |
2.22e-02 |
1.68e-01 |
8.82e-01 |
0.261000 |
Transcriptional regulation of granulopoiesis |
29 |
2.88e-01 |
4.76e-01 |
0.16900 |
1.33e-01 |
1.04e-01 |
2.15e-01 |
0.332000 |
Interferon gamma signaling |
55 |
9.71e-02 |
2.29e-01 |
0.16900 |
1.68e-01 |
-6.68e-03 |
3.09e-02 |
0.932000 |
Glutathione conjugation |
27 |
3.19e-01 |
5.03e-01 |
0.16900 |
1.42e-01 |
-9.04e-02 |
2.01e-01 |
0.416000 |
O-linked glycosylation of mucins |
33 |
2.47e-01 |
4.32e-01 |
0.16800 |
3.69e-02 |
-1.64e-01 |
7.14e-01 |
0.102000 |
Potassium Channels |
51 |
1.16e-01 |
2.62e-01 |
0.16800 |
-1.65e-01 |
3.07e-02 |
4.11e-02 |
0.705000 |
Apoptosis |
130 |
4.32e-03 |
1.99e-02 |
0.16800 |
1.56e-01 |
6.16e-02 |
2.18e-03 |
0.227000 |
NOTCH1 Intracellular Domain Regulates Transcription |
37 |
2.16e-01 |
4.03e-01 |
0.16700 |
-1.41e-01 |
8.85e-02 |
1.37e-01 |
0.352000 |
RHO GTPases activate PAKs |
18 |
4.75e-01 |
6.42e-01 |
0.16700 |
-1.47e-01 |
7.85e-02 |
2.81e-01 |
0.564000 |
Retinoid metabolism and transport |
25 |
3.54e-01 |
5.37e-01 |
0.16700 |
7.05e-03 |
-1.66e-01 |
9.51e-01 |
0.150000 |
Synaptic adhesion-like molecules |
14 |
5.64e-01 |
7.24e-01 |
0.16500 |
2.74e-02 |
-1.63e-01 |
8.59e-01 |
0.291000 |
Programmed Cell Death |
133 |
4.50e-03 |
2.05e-02 |
0.16500 |
1.54e-01 |
6.14e-02 |
2.30e-03 |
0.223000 |
Interleukin-17 signaling |
52 |
1.22e-01 |
2.74e-01 |
0.16500 |
-1.56e-01 |
5.32e-02 |
5.19e-02 |
0.507000 |
Caspase activation via Death Receptors in the presence of ligand |
14 |
5.66e-01 |
7.25e-01 |
0.16500 |
-1.63e-01 |
-2.45e-02 |
2.91e-01 |
0.874000 |
Cargo trafficking to the periciliary membrane |
33 |
2.63e-01 |
4.50e-01 |
0.16500 |
1.62e-01 |
-3.07e-02 |
1.08e-01 |
0.761000 |
COPI-independent Golgi-to-ER retrograde traffic |
26 |
3.51e-01 |
5.36e-01 |
0.16400 |
1.44e-01 |
-7.83e-02 |
2.03e-01 |
0.490000 |
Regulation of TP53 Activity through Acetylation |
23 |
3.97e-01 |
5.83e-01 |
0.16400 |
9.22e-02 |
-1.36e-01 |
4.44e-01 |
0.260000 |
Toll Like Receptor 3 (TLR3) Cascade |
71 |
5.88e-02 |
1.65e-01 |
0.16400 |
-1.16e-01 |
1.16e-01 |
9.29e-02 |
0.090400 |
Cellular responses to external stimuli |
323 |
3.14e-06 |
3.43e-05 |
0.16400 |
1.59e-01 |
3.89e-02 |
1.03e-06 |
0.232000 |
Estrogen-dependent nuclear events downstream of ESR-membrane signaling |
18 |
4.88e-01 |
6.55e-01 |
0.16300 |
-6.75e-02 |
1.49e-01 |
6.20e-01 |
0.275000 |
CLEC7A (Dectin-1) signaling |
69 |
6.47e-02 |
1.75e-01 |
0.16300 |
1.61e-01 |
-2.93e-02 |
2.12e-02 |
0.675000 |
Signaling by WNT in cancer |
26 |
3.53e-01 |
5.37e-01 |
0.16300 |
-1.20e-01 |
-1.10e-01 |
2.89e-01 |
0.330000 |
Signaling by high-kinase activity BRAF mutants |
23 |
4.03e-01 |
5.86e-01 |
0.16300 |
-1.31e-01 |
9.69e-02 |
2.77e-01 |
0.421000 |
Interleukin-2 family signaling |
29 |
3.19e-01 |
5.03e-01 |
0.16200 |
-1.62e-01 |
9.69e-03 |
1.31e-01 |
0.928000 |
ROS and RNS production in phagocytes |
22 |
4.20e-01 |
5.98e-01 |
0.16200 |
1.58e-01 |
3.72e-02 |
2.00e-01 |
0.763000 |
VEGFA-VEGFR2 Pathway |
85 |
3.63e-02 |
1.17e-01 |
0.16200 |
-1.52e-01 |
-5.38e-02 |
1.53e-02 |
0.392000 |
Transcription of the HIV genome |
44 |
1.82e-01 |
3.65e-01 |
0.16100 |
1.31e-01 |
-9.41e-02 |
1.33e-01 |
0.281000 |
Signalling to RAS |
16 |
5.37e-01 |
7.01e-01 |
0.16100 |
-9.56e-02 |
1.30e-01 |
5.08e-01 |
0.368000 |
Signaling by FGFR2 in disease |
21 |
4.47e-01 |
6.17e-01 |
0.16000 |
-1.60e-01 |
-3.74e-03 |
2.05e-01 |
0.976000 |
Attenuation phase |
15 |
5.68e-01 |
7.25e-01 |
0.15900 |
-1.40e-01 |
7.55e-02 |
3.48e-01 |
0.613000 |
Positive epigenetic regulation of rRNA expression |
32 |
3.00e-01 |
4.88e-01 |
0.15900 |
6.17e-02 |
-1.46e-01 |
5.46e-01 |
0.152000 |
Cellular responses to stress |
319 |
7.95e-06 |
8.18e-05 |
0.15900 |
1.54e-01 |
3.92e-02 |
2.72e-06 |
0.232000 |
Selective autophagy |
43 |
2.00e-01 |
3.85e-01 |
0.15900 |
4.03e-02 |
-1.53e-01 |
6.48e-01 |
0.082300 |
Metabolism of steroid hormones |
21 |
4.54e-01 |
6.21e-01 |
0.15800 |
-5.31e-02 |
-1.49e-01 |
6.74e-01 |
0.237000 |
SHC-mediated cascade:FGFR2 |
11 |
6.63e-01 |
8.03e-01 |
0.15800 |
-1.58e-01 |
1.02e-03 |
3.65e-01 |
0.995000 |
COPI-mediated anterograde transport |
65 |
9.05e-02 |
2.18e-01 |
0.15800 |
1.09e-01 |
-1.14e-01 |
1.30e-01 |
0.112000 |
Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs) |
68 |
8.01e-02 |
2.00e-01 |
0.15800 |
-6.87e-02 |
-1.42e-01 |
3.28e-01 |
0.043500 |
MAPK targets/ Nuclear events mediated by MAP kinases |
26 |
3.83e-01 |
5.66e-01 |
0.15700 |
-7.88e-02 |
1.36e-01 |
4.87e-01 |
0.229000 |
COPII-mediated vesicle transport |
48 |
1.69e-01 |
3.47e-01 |
0.15700 |
1.52e-01 |
3.97e-02 |
6.82e-02 |
0.634000 |
Signaling by Retinoic Acid |
31 |
3.18e-01 |
5.03e-01 |
0.15700 |
-1.34e-01 |
-8.21e-02 |
1.98e-01 |
0.429000 |
Synthesis of bile acids and bile salts |
18 |
5.15e-01 |
6.83e-01 |
0.15700 |
1.53e-01 |
3.40e-02 |
2.61e-01 |
0.803000 |
mRNA decay by 5' to 3' exoribonuclease |
12 |
6.44e-01 |
7.84e-01 |
0.15600 |
-5.45e-02 |
-1.47e-01 |
7.44e-01 |
0.380000 |
Branched-chain amino acid catabolism |
19 |
5.01e-01 |
6.67e-01 |
0.15600 |
-1.53e-01 |
3.17e-02 |
2.49e-01 |
0.811000 |
PI-3K cascade:FGFR1 |
11 |
6.69e-01 |
8.07e-01 |
0.15600 |
-1.31e-01 |
-8.43e-02 |
4.51e-01 |
0.628000 |
Interaction between L1 and Ankyrins |
22 |
4.53e-01 |
6.21e-01 |
0.15500 |
-9.29e-02 |
1.25e-01 |
4.51e-01 |
0.312000 |
FCGR3A-mediated IL10 synthesis |
36 |
2.71e-01 |
4.60e-01 |
0.15500 |
1.48e-01 |
4.90e-02 |
1.26e-01 |
0.611000 |
Asparagine N-linked glycosylation |
205 |
6.93e-04 |
3.75e-03 |
0.15500 |
1.52e-01 |
-3.37e-02 |
1.94e-04 |
0.408000 |
Cell-Cell communication |
78 |
6.00e-02 |
1.68e-01 |
0.15500 |
-1.41e-01 |
-6.54e-02 |
3.17e-02 |
0.319000 |
Triglyceride metabolism |
19 |
5.03e-01 |
6.69e-01 |
0.15500 |
-1.47e-01 |
-4.85e-02 |
2.66e-01 |
0.715000 |
Nuclear signaling by ERBB4 |
23 |
4.37e-01 |
6.09e-01 |
0.15500 |
5.06e-02 |
-1.47e-01 |
6.74e-01 |
0.224000 |
MAP kinase activation |
48 |
1.79e-01 |
3.61e-01 |
0.15500 |
-1.41e-01 |
6.47e-02 |
9.13e-02 |
0.438000 |
Acyl chain remodelling of PG |
13 |
6.29e-01 |
7.78e-01 |
0.15400 |
-8.44e-02 |
-1.29e-01 |
5.99e-01 |
0.421000 |
Major pathway of rRNA processing in the nucleolus and cytosol |
91 |
4.00e-02 |
1.25e-01 |
0.15400 |
1.42e-01 |
5.97e-02 |
1.96e-02 |
0.326000 |
Sema4D in semaphorin signaling |
19 |
5.12e-01 |
6.80e-01 |
0.15400 |
4.08e-02 |
-1.48e-01 |
7.58e-01 |
0.264000 |
Signaling by NOTCH1 |
56 |
1.39e-01 |
3.01e-01 |
0.15400 |
-1.53e-01 |
-1.20e-02 |
4.77e-02 |
0.877000 |
SUMOylation of transcription factors |
13 |
6.33e-01 |
7.79e-01 |
0.15300 |
-1.51e-01 |
2.50e-02 |
3.45e-01 |
0.876000 |
Basigin interactions |
21 |
4.80e-01 |
6.48e-01 |
0.15300 |
3.01e-02 |
-1.50e-01 |
8.11e-01 |
0.235000 |
Diseases associated with glycosaminoglycan metabolism |
30 |
3.50e-01 |
5.36e-01 |
0.15300 |
-6.48e-02 |
-1.38e-01 |
5.40e-01 |
0.190000 |
JNK (c-Jun kinases) phosphorylation and activation mediated by activated human TAK1 |
14 |
6.14e-01 |
7.66e-01 |
0.15300 |
-1.44e-01 |
5.06e-02 |
3.51e-01 |
0.743000 |
Repression of WNT target genes |
11 |
6.82e-01 |
8.15e-01 |
0.15200 |
-1.49e-01 |
3.28e-02 |
3.93e-01 |
0.851000 |
Carboxyterminal post-translational modifications of tubulin |
24 |
4.35e-01 |
6.09e-01 |
0.15200 |
-9.55e-03 |
1.52e-01 |
9.35e-01 |
0.198000 |
Synthesis of PA |
25 |
4.19e-01 |
5.98e-01 |
0.15200 |
-4.54e-02 |
-1.45e-01 |
6.94e-01 |
0.209000 |
mRNA 3'-end processing |
40 |
2.50e-01 |
4.35e-01 |
0.15200 |
3.99e-02 |
1.47e-01 |
6.63e-01 |
0.109000 |
Inactivation, recovery and regulation of the phototransduction cascade |
18 |
5.36e-01 |
7.01e-01 |
0.15200 |
-1.51e-01 |
2.16e-02 |
2.69e-01 |
0.874000 |
The phototransduction cascade |
18 |
5.36e-01 |
7.01e-01 |
0.15200 |
-1.51e-01 |
2.16e-02 |
2.69e-01 |
0.874000 |
Constitutive Signaling by NOTCH1 HD+PEST Domain Mutants |
45 |
2.12e-01 |
3.99e-01 |
0.15200 |
-1.43e-01 |
5.24e-02 |
9.78e-02 |
0.544000 |
Constitutive Signaling by NOTCH1 PEST Domain Mutants |
45 |
2.12e-01 |
3.99e-01 |
0.15200 |
-1.43e-01 |
5.24e-02 |
9.78e-02 |
0.544000 |
Signaling by NOTCH1 HD+PEST Domain Mutants in Cancer |
45 |
2.12e-01 |
3.99e-01 |
0.15200 |
-1.43e-01 |
5.24e-02 |
9.78e-02 |
0.544000 |
Signaling by NOTCH1 PEST Domain Mutants in Cancer |
45 |
2.12e-01 |
3.99e-01 |
0.15200 |
-1.43e-01 |
5.24e-02 |
9.78e-02 |
0.544000 |
Signaling by NOTCH1 in Cancer |
45 |
2.12e-01 |
3.99e-01 |
0.15200 |
-1.43e-01 |
5.24e-02 |
9.78e-02 |
0.544000 |
Caspase-mediated cleavage of cytoskeletal proteins |
10 |
7.09e-01 |
8.39e-01 |
0.15200 |
-9.31e-02 |
1.20e-01 |
6.10e-01 |
0.511000 |
Glucagon-like Peptide-1 (GLP1) regulates insulin secretion |
26 |
4.06e-01 |
5.88e-01 |
0.15200 |
-1.17e-01 |
-9.69e-02 |
3.02e-01 |
0.393000 |
Signaling by VEGF |
91 |
4.46e-02 |
1.35e-01 |
0.15100 |
-1.41e-01 |
-5.51e-02 |
2.04e-02 |
0.364000 |
Signaling by FGFR1 |
30 |
3.58e-01 |
5.42e-01 |
0.15100 |
-1.69e-02 |
1.50e-01 |
8.72e-01 |
0.154000 |
Role of LAT2/NTAL/LAB on calcium mobilization |
13 |
6.41e-01 |
7.82e-01 |
0.15100 |
6.79e-02 |
1.35e-01 |
6.72e-01 |
0.401000 |
Potential therapeutics for SARS |
26 |
4.13e-01 |
5.97e-01 |
0.15000 |
1.31e-01 |
7.34e-02 |
2.47e-01 |
0.517000 |
Mitophagy |
17 |
5.63e-01 |
7.24e-01 |
0.15000 |
1.20e-01 |
9.04e-02 |
3.94e-01 |
0.519000 |
FOXO-mediated transcription |
49 |
1.96e-01 |
3.81e-01 |
0.15000 |
-1.36e-01 |
6.22e-02 |
9.99e-02 |
0.452000 |
Post-translational modification: synthesis of GPI-anchored proteins |
51 |
1.84e-01 |
3.67e-01 |
0.14900 |
-4.48e-02 |
1.42e-01 |
5.80e-01 |
0.078800 |
RNA Polymerase III Transcription Termination |
15 |
6.08e-01 |
7.61e-01 |
0.14900 |
1.01e-01 |
-1.09e-01 |
4.97e-01 |
0.463000 |
ERBB2 Activates PTK6 Signaling |
10 |
7.18e-01 |
8.45e-01 |
0.14800 |
-1.27e-01 |
-7.59e-02 |
4.86e-01 |
0.678000 |
Synthesis of substrates in N-glycan biosythesis |
48 |
2.08e-01 |
3.97e-01 |
0.14800 |
1.48e-01 |
-5.41e-03 |
7.64e-02 |
0.948000 |
Ub-specific processing proteases |
123 |
1.82e-02 |
6.49e-02 |
0.14800 |
1.05e-01 |
1.04e-01 |
4.42e-02 |
0.047400 |
Prolactin receptor signaling |
12 |
6.74e-01 |
8.12e-01 |
0.14800 |
4.65e-02 |
1.40e-01 |
7.81e-01 |
0.400000 |
Transcriptional regulation by RUNX1 |
132 |
1.44e-02 |
5.35e-02 |
0.14700 |
1.40e-01 |
-4.53e-02 |
5.52e-03 |
0.371000 |
Signaling by ERBB2 ECD mutants |
14 |
6.37e-01 |
7.79e-01 |
0.14700 |
-6.27e-02 |
1.33e-01 |
6.85e-01 |
0.390000 |
Ion channel transport |
97 |
4.47e-02 |
1.35e-01 |
0.14700 |
-1.46e-01 |
-1.16e-02 |
1.30e-02 |
0.843000 |
RNA Polymerase III Transcription Initiation From Type 1 Promoter |
17 |
5.79e-01 |
7.34e-01 |
0.14600 |
1.19e-01 |
8.52e-02 |
3.96e-01 |
0.543000 |
Collagen degradation |
28 |
4.08e-01 |
5.90e-01 |
0.14600 |
-9.83e-02 |
-1.08e-01 |
3.68e-01 |
0.323000 |
Frs2-mediated activation |
10 |
7.30e-01 |
8.49e-01 |
0.14500 |
7.75e-03 |
1.45e-01 |
9.66e-01 |
0.429000 |
N-glycan antennae elongation in the medial/trans-Golgi |
16 |
6.04e-01 |
7.59e-01 |
0.14500 |
-1.06e-01 |
-9.81e-02 |
4.62e-01 |
0.497000 |
Cell-cell junction organization |
29 |
4.04e-01 |
5.87e-01 |
0.14400 |
-1.04e-01 |
-1.00e-01 |
3.35e-01 |
0.350000 |
Transcriptional Regulation by MECP2 |
41 |
2.82e-01 |
4.73e-01 |
0.14400 |
-1.44e-01 |
-8.50e-04 |
1.12e-01 |
0.992000 |
Regulation of RUNX1 Expression and Activity |
14 |
6.50e-01 |
7.90e-01 |
0.14400 |
-8.84e-02 |
1.13e-01 |
5.67e-01 |
0.463000 |
Sema3A PAK dependent Axon repulsion |
12 |
6.93e-01 |
8.25e-01 |
0.14300 |
-5.95e-02 |
1.30e-01 |
7.21e-01 |
0.435000 |
Metabolism of RNA |
429 |
3.08e-06 |
3.42e-05 |
0.14300 |
1.34e-01 |
5.11e-02 |
2.63e-06 |
0.072300 |
GPCR downstream signalling |
389 |
9.72e-06 |
9.76e-05 |
0.14300 |
-1.25e-01 |
-6.91e-02 |
2.71e-05 |
0.020400 |
RNA Pol II CTD phosphorylation and interaction with CE |
15 |
6.34e-01 |
7.79e-01 |
0.14300 |
1.12e-01 |
-8.77e-02 |
4.51e-01 |
0.557000 |
RNA Pol II CTD phosphorylation and interaction with CE during HIV infection |
15 |
6.34e-01 |
7.79e-01 |
0.14300 |
1.12e-01 |
-8.77e-02 |
4.51e-01 |
0.557000 |
Glycosaminoglycan metabolism |
81 |
8.70e-02 |
2.13e-01 |
0.14300 |
1.34e-01 |
-4.78e-02 |
3.71e-02 |
0.458000 |
Processing of Capped Intron-Containing Pre-mRNA |
162 |
7.68e-03 |
3.13e-02 |
0.14200 |
1.37e-01 |
3.79e-02 |
2.66e-03 |
0.407000 |
trans-Golgi Network Vesicle Budding |
50 |
2.20e-01 |
4.05e-01 |
0.14200 |
1.37e-01 |
3.84e-02 |
9.40e-02 |
0.639000 |
Inositol phosphate metabolism |
36 |
3.38e-01 |
5.25e-01 |
0.14200 |
-1.01e-01 |
9.99e-02 |
2.93e-01 |
0.300000 |
KSRP (KHSRP) binds and destabilizes mRNA |
13 |
6.75e-01 |
8.12e-01 |
0.14200 |
-4.63e-02 |
1.35e-01 |
7.73e-01 |
0.401000 |
Regulation of signaling by CBL |
15 |
6.36e-01 |
7.79e-01 |
0.14200 |
-6.32e-02 |
1.27e-01 |
6.72e-01 |
0.393000 |
Listeria monocytogenes entry into host cells |
13 |
6.76e-01 |
8.12e-01 |
0.14200 |
-1.21e-01 |
7.40e-02 |
4.49e-01 |
0.644000 |
Integration of energy metabolism |
84 |
8.05e-02 |
2.01e-01 |
0.14200 |
-1.42e-01 |
9.48e-03 |
2.51e-02 |
0.881000 |
Aggrephagy |
15 |
6.37e-01 |
7.79e-01 |
0.14200 |
7.45e-02 |
-1.21e-01 |
6.18e-01 |
0.418000 |
Formation of RNA Pol II elongation complex |
33 |
3.71e-01 |
5.56e-01 |
0.14200 |
1.39e-01 |
2.48e-02 |
1.66e-01 |
0.805000 |
RNA Polymerase II Transcription Elongation |
33 |
3.71e-01 |
5.56e-01 |
0.14200 |
1.39e-01 |
2.48e-02 |
1.66e-01 |
0.805000 |
PI Metabolism |
68 |
1.33e-01 |
2.90e-01 |
0.14100 |
-1.33e-01 |
4.76e-02 |
5.81e-02 |
0.498000 |
ER to Golgi Anterograde Transport |
102 |
4.99e-02 |
1.45e-01 |
0.14100 |
1.17e-01 |
-7.88e-02 |
4.20e-02 |
0.170000 |
TBC/RABGAPs |
33 |
3.76e-01 |
5.60e-01 |
0.14100 |
1.37e-01 |
3.11e-02 |
1.73e-01 |
0.757000 |
The NLRP3 inflammasome |
11 |
7.24e-01 |
8.45e-01 |
0.14000 |
6.48e-02 |
-1.24e-01 |
7.10e-01 |
0.475000 |
Diseases of glycosylation |
104 |
4.76e-02 |
1.42e-01 |
0.14000 |
-2.21e-02 |
-1.39e-01 |
6.97e-01 |
0.014900 |
Growth hormone receptor signaling |
19 |
5.72e-01 |
7.29e-01 |
0.14000 |
8.23e-02 |
1.13e-01 |
5.35e-01 |
0.394000 |
SHC1 events in ERBB4 signaling |
10 |
7.46e-01 |
8.56e-01 |
0.14000 |
-1.10e-01 |
-8.57e-02 |
5.47e-01 |
0.639000 |
Processing of Intronless Pre-mRNAs |
11 |
7.26e-01 |
8.46e-01 |
0.13900 |
1.31e-02 |
1.39e-01 |
9.40e-01 |
0.425000 |
Synthesis of glycosylphosphatidylinositol (GPI) |
12 |
7.05e-01 |
8.37e-01 |
0.13900 |
8.21e-02 |
1.12e-01 |
6.23e-01 |
0.500000 |
Inwardly rectifying K+ channels |
19 |
5.76e-01 |
7.32e-01 |
0.13900 |
-4.90e-02 |
-1.30e-01 |
7.11e-01 |
0.326000 |
Reproduction |
50 |
2.36e-01 |
4.19e-01 |
0.13900 |
1.09e-01 |
8.58e-02 |
1.82e-01 |
0.294000 |
Free fatty acids regulate insulin secretion |
11 |
7.28e-01 |
8.47e-01 |
0.13900 |
-6.21e-02 |
-1.24e-01 |
7.21e-01 |
0.477000 |
Amyloid fiber formation |
30 |
4.22e-01 |
6.00e-01 |
0.13900 |
1.11e-02 |
1.38e-01 |
9.16e-01 |
0.191000 |
Beta-catenin independent WNT signaling |
107 |
4.72e-02 |
1.40e-01 |
0.13800 |
1.01e-01 |
9.42e-02 |
7.09e-02 |
0.093100 |
MyD88-independent TLR4 cascade |
74 |
1.26e-01 |
2.80e-01 |
0.13700 |
-1.14e-01 |
7.61e-02 |
8.92e-02 |
0.258000 |
TRIF(TICAM1)-mediated TLR4 signaling |
74 |
1.26e-01 |
2.80e-01 |
0.13700 |
-1.14e-01 |
7.61e-02 |
8.92e-02 |
0.258000 |
CD28 co-stimulation |
29 |
4.39e-01 |
6.11e-01 |
0.13700 |
-1.16e-01 |
-7.41e-02 |
2.81e-01 |
0.490000 |
Sema4D induced cell migration and growth-cone collapse |
16 |
6.36e-01 |
7.79e-01 |
0.13700 |
-6.99e-02 |
-1.18e-01 |
6.29e-01 |
0.414000 |
Sphingolipid de novo biosynthesis |
27 |
4.70e-01 |
6.38e-01 |
0.13700 |
-5.20e-02 |
1.27e-01 |
6.40e-01 |
0.255000 |
Regulation of HSF1-mediated heat shock response |
51 |
2.44e-01 |
4.30e-01 |
0.13600 |
1.27e-01 |
4.86e-02 |
1.17e-01 |
0.549000 |
FGFR1 mutant receptor activation |
21 |
5.65e-01 |
7.25e-01 |
0.13500 |
-1.24e-01 |
5.32e-02 |
3.25e-01 |
0.673000 |
Transport of bile salts and organic acids, metal ions and amine compounds |
51 |
2.51e-01 |
4.36e-01 |
0.13500 |
5.47e-03 |
1.35e-01 |
9.46e-01 |
0.096900 |
Extra-nuclear estrogen signaling |
57 |
2.14e-01 |
4.01e-01 |
0.13400 |
-1.22e-01 |
-5.74e-02 |
1.13e-01 |
0.454000 |
Recycling pathway of L1 |
24 |
5.22e-01 |
6.88e-01 |
0.13400 |
5.90e-02 |
1.21e-01 |
6.17e-01 |
0.306000 |
NRAGE signals death through JNK |
51 |
2.52e-01 |
4.37e-01 |
0.13400 |
-1.29e-01 |
-3.71e-02 |
1.11e-01 |
0.647000 |
Translocation of SLC2A4 (GLUT4) to the plasma membrane |
44 |
3.11e-01 |
4.97e-01 |
0.13400 |
-1.19e-01 |
6.12e-02 |
1.73e-01 |
0.483000 |
Phase II - Conjugation of compounds |
63 |
1.87e-01 |
3.69e-01 |
0.13400 |
1.33e-01 |
1.64e-02 |
6.93e-02 |
0.823000 |
PKA-mediated phosphorylation of CREB |
15 |
6.70e-01 |
8.09e-01 |
0.13300 |
1.35e-02 |
1.33e-01 |
9.28e-01 |
0.374000 |
Interleukin-3, Interleukin-5 and GM-CSF signaling |
32 |
4.31e-01 |
6.09e-01 |
0.13300 |
-1.20e-01 |
5.65e-02 |
2.40e-01 |
0.580000 |
Signaling by NTRK2 (TRKB) |
19 |
6.07e-01 |
7.61e-01 |
0.13300 |
-8.93e-02 |
9.82e-02 |
5.01e-01 |
0.459000 |
Cooperation of PDCL (PhLP1) and TRiC/CCT in G-protein beta folding |
23 |
5.48e-01 |
7.09e-01 |
0.13200 |
-1.32e-01 |
5.45e-03 |
2.73e-01 |
0.964000 |
FGFR2 mutant receptor activation |
12 |
7.31e-01 |
8.49e-01 |
0.13200 |
-6.76e-02 |
-1.13e-01 |
6.85e-01 |
0.498000 |
Diseases associated with glycosylation precursor biosynthesis |
15 |
6.78e-01 |
8.13e-01 |
0.13100 |
1.05e-01 |
7.88e-02 |
4.81e-01 |
0.598000 |
Synthesis, secretion, and deacylation of Ghrelin |
10 |
7.73e-01 |
8.70e-01 |
0.13100 |
5.54e-02 |
-1.19e-01 |
7.62e-01 |
0.515000 |
Signaling by PDGFRA extracellular domain mutants |
11 |
7.53e-01 |
8.57e-01 |
0.13100 |
7.22e-02 |
1.09e-01 |
6.79e-01 |
0.530000 |
Signaling by PDGFRA transmembrane, juxtamembrane and kinase domain mutants |
11 |
7.53e-01 |
8.57e-01 |
0.13100 |
7.22e-02 |
1.09e-01 |
6.79e-01 |
0.530000 |
Death Receptor Signalling |
108 |
6.43e-02 |
1.75e-01 |
0.13100 |
-1.27e-01 |
-3.07e-02 |
2.29e-02 |
0.582000 |
Metabolism of fat-soluble vitamins |
26 |
5.15e-01 |
6.83e-01 |
0.13100 |
2.33e-02 |
-1.29e-01 |
8.37e-01 |
0.257000 |
Nuclear Events (kinase and transcription factor activation) |
46 |
3.14e-01 |
5.01e-01 |
0.13000 |
-8.59e-02 |
9.77e-02 |
3.14e-01 |
0.252000 |
SHC1 events in ERBB2 signaling |
18 |
6.34e-01 |
7.79e-01 |
0.13000 |
-1.29e-01 |
1.37e-02 |
3.42e-01 |
0.920000 |
Golgi Associated Vesicle Biogenesis |
39 |
3.72e-01 |
5.56e-01 |
0.13000 |
8.53e-02 |
9.80e-02 |
3.57e-01 |
0.290000 |
Signaling by ERBB2 in Cancer |
21 |
5.90e-01 |
7.43e-01 |
0.13000 |
-1.08e-01 |
7.15e-02 |
3.90e-01 |
0.571000 |
Acyl chain remodelling of PC |
19 |
6.21e-01 |
7.69e-01 |
0.13000 |
1.12e-01 |
-6.52e-02 |
3.98e-01 |
0.623000 |
Class A/1 (Rhodopsin-like receptors) |
135 |
3.43e-02 |
1.12e-01 |
0.13000 |
-9.35e-02 |
-8.97e-02 |
6.15e-02 |
0.072700 |
Metabolism of steroids |
96 |
9.14e-02 |
2.18e-01 |
0.12900 |
-1.29e-01 |
-3.54e-03 |
2.88e-02 |
0.952000 |
Signaling by FGFR in disease |
38 |
3.87e-01 |
5.73e-01 |
0.12900 |
-1.28e-01 |
2.01e-02 |
1.73e-01 |
0.830000 |
Dectin-2 family |
10 |
7.79e-01 |
8.73e-01 |
0.12900 |
1.71e-02 |
1.28e-01 |
9.26e-01 |
0.484000 |
MyD88 cascade initiated on plasma membrane |
61 |
2.22e-01 |
4.05e-01 |
0.12900 |
-8.59e-02 |
9.62e-02 |
2.47e-01 |
0.194000 |
Toll Like Receptor 10 (TLR10) Cascade |
61 |
2.22e-01 |
4.05e-01 |
0.12900 |
-8.59e-02 |
9.62e-02 |
2.47e-01 |
0.194000 |
Toll Like Receptor 5 (TLR5) Cascade |
61 |
2.22e-01 |
4.05e-01 |
0.12900 |
-8.59e-02 |
9.62e-02 |
2.47e-01 |
0.194000 |
SUMOylation of transcription cofactors |
33 |
4.41e-01 |
6.12e-01 |
0.12900 |
-1.23e-01 |
-3.83e-02 |
2.22e-01 |
0.704000 |
Platelet activation, signaling and aggregation |
186 |
1.08e-02 |
4.17e-02 |
0.12800 |
-1.28e-01 |
5.64e-03 |
2.65e-03 |
0.895000 |
GRB2 events in ERBB2 signaling |
12 |
7.45e-01 |
8.56e-01 |
0.12800 |
-1.20e-01 |
4.53e-02 |
4.72e-01 |
0.786000 |
Biological oxidations |
124 |
4.84e-02 |
1.43e-01 |
0.12800 |
8.99e-02 |
9.11e-02 |
8.46e-02 |
0.080600 |
Deubiquitination |
182 |
1.24e-02 |
4.66e-02 |
0.12800 |
6.80e-02 |
1.08e-01 |
1.15e-01 |
0.012300 |
EPH-ephrin mediated repulsion of cells |
36 |
4.17e-01 |
5.98e-01 |
0.12800 |
1.21e-01 |
-4.00e-02 |
2.08e-01 |
0.678000 |
rRNA processing in the nucleus and cytosol |
97 |
9.63e-02 |
2.27e-01 |
0.12700 |
1.20e-01 |
4.33e-02 |
4.22e-02 |
0.462000 |
RNA Polymerase II Pre-transcription Events |
52 |
2.86e-01 |
4.75e-01 |
0.12700 |
1.26e-01 |
-1.56e-02 |
1.16e-01 |
0.846000 |
Oncogenic MAPK signaling |
56 |
2.61e-01 |
4.48e-01 |
0.12700 |
-1.19e-01 |
4.45e-02 |
1.24e-01 |
0.565000 |
Intraflagellar transport |
34 |
4.44e-01 |
6.14e-01 |
0.12700 |
9.46e-02 |
-8.42e-02 |
3.40e-01 |
0.396000 |
Opioid Signalling |
65 |
2.12e-01 |
3.99e-01 |
0.12700 |
-1.25e-01 |
1.74e-02 |
8.09e-02 |
0.809000 |
G alpha (s) signalling events |
77 |
1.59e-01 |
3.33e-01 |
0.12600 |
-1.18e-01 |
-4.58e-02 |
7.45e-02 |
0.488000 |
PKA activation in glucagon signalling |
14 |
7.15e-01 |
8.43e-01 |
0.12600 |
7.40e-02 |
1.02e-01 |
6.32e-01 |
0.508000 |
Association of TriC/CCT with target proteins during biosynthesis |
29 |
5.00e-01 |
6.67e-01 |
0.12600 |
8.73e-02 |
9.11e-02 |
4.16e-01 |
0.396000 |
Acyl chain remodelling of PE |
17 |
6.68e-01 |
8.07e-01 |
0.12600 |
9.93e-02 |
-7.77e-02 |
4.79e-01 |
0.579000 |
Infectious disease |
459 |
2.81e-05 |
2.48e-04 |
0.12600 |
1.25e-01 |
1.52e-02 |
5.57e-06 |
0.582000 |
Costimulation by the CD28 family |
50 |
3.05e-01 |
4.92e-01 |
0.12600 |
-7.38e-02 |
-1.02e-01 |
3.67e-01 |
0.213000 |
PI3K events in ERBB2 signaling |
13 |
7.38e-01 |
8.53e-01 |
0.12500 |
-1.25e-01 |
-7.74e-03 |
4.36e-01 |
0.961000 |
Cell-extracellular matrix interactions |
14 |
7.21e-01 |
8.45e-01 |
0.12500 |
-1.24e-01 |
-1.18e-02 |
4.21e-01 |
0.939000 |
Caspase activation via extrinsic apoptotic signalling pathway |
21 |
6.12e-01 |
7.65e-01 |
0.12500 |
-1.01e-01 |
-7.36e-02 |
4.25e-01 |
0.559000 |
rRNA processing |
104 |
9.12e-02 |
2.18e-01 |
0.12400 |
1.13e-01 |
5.22e-02 |
4.75e-02 |
0.358000 |
Presynaptic function of Kainate receptors |
13 |
7.41e-01 |
8.55e-01 |
0.12400 |
-1.21e-01 |
-2.75e-02 |
4.51e-01 |
0.864000 |
Ephrin signaling |
17 |
6.79e-01 |
8.13e-01 |
0.12300 |
-1.22e-01 |
1.82e-02 |
3.84e-01 |
0.897000 |
PINK1-PRKN Mediated Mitophagy |
13 |
7.47e-01 |
8.56e-01 |
0.12200 |
1.21e-01 |
1.86e-02 |
4.51e-01 |
0.908000 |
TP53 regulates transcription of several additional cell death genes whose specific roles in p53-dependent apoptosis remain uncertain |
10 |
7.99e-01 |
8.86e-01 |
0.12200 |
-1.19e-01 |
-2.63e-02 |
5.13e-01 |
0.885000 |
Vitamin B5 (pantothenate) metabolism |
12 |
7.64e-01 |
8.64e-01 |
0.12200 |
-1.20e-01 |
-2.31e-02 |
4.72e-01 |
0.890000 |
Glycolysis |
51 |
3.20e-01 |
5.04e-01 |
0.12200 |
1.12e-01 |
4.84e-02 |
1.66e-01 |
0.550000 |
Pre-NOTCH Processing in Golgi |
14 |
7.34e-01 |
8.51e-01 |
0.12200 |
9.97e-02 |
-6.96e-02 |
5.18e-01 |
0.652000 |
Signaling by ERBB2 |
36 |
4.51e-01 |
6.20e-01 |
0.12100 |
-1.12e-01 |
-4.68e-02 |
2.45e-01 |
0.627000 |
Scavenging by Class A Receptors |
11 |
7.85e-01 |
8.76e-01 |
0.12100 |
-2.30e-03 |
1.21e-01 |
9.89e-01 |
0.487000 |
TP53 regulates transcription of additional cell cycle genes whose exact role in the p53 pathway remain uncertain |
15 |
7.20e-01 |
8.45e-01 |
0.12100 |
-1.16e-01 |
3.40e-02 |
4.37e-01 |
0.819000 |
ERBB2 Regulates Cell Motility |
11 |
7.85e-01 |
8.76e-01 |
0.12100 |
-8.16e-02 |
-8.93e-02 |
6.40e-01 |
0.608000 |
Signaling by NOTCH |
135 |
5.67e-02 |
1.61e-01 |
0.12000 |
1.19e-01 |
1.11e-02 |
1.71e-02 |
0.825000 |
Semaphorin interactions |
53 |
3.22e-01 |
5.06e-01 |
0.12000 |
-1.12e-01 |
-4.12e-02 |
1.58e-01 |
0.604000 |
Activation of kainate receptors upon glutamate binding |
21 |
6.38e-01 |
7.79e-01 |
0.11900 |
-1.02e-01 |
-6.26e-02 |
4.20e-01 |
0.620000 |
FRS-mediated FGFR1 signaling |
11 |
7.91e-01 |
8.81e-01 |
0.11900 |
-1.19e-01 |
-2.39e-03 |
4.94e-01 |
0.989000 |
Protein folding |
68 |
2.36e-01 |
4.19e-01 |
0.11900 |
5.16e-02 |
1.07e-01 |
4.62e-01 |
0.126000 |
Metabolism of carbohydrates |
198 |
1.64e-02 |
5.90e-02 |
0.11900 |
1.11e-01 |
-4.36e-02 |
7.55e-03 |
0.292000 |
FGFR2 alternative splicing |
13 |
7.62e-01 |
8.62e-01 |
0.11800 |
-6.56e-03 |
1.18e-01 |
9.67e-01 |
0.461000 |
Signaling by Non-Receptor Tyrosine Kinases |
40 |
4.36e-01 |
6.09e-01 |
0.11800 |
-8.00e-03 |
1.18e-01 |
9.30e-01 |
0.198000 |
Signaling by PTK6 |
40 |
4.36e-01 |
6.09e-01 |
0.11800 |
-8.00e-03 |
1.18e-01 |
9.30e-01 |
0.198000 |
Thromboxane signalling through TP receptor |
14 |
7.50e-01 |
8.56e-01 |
0.11700 |
9.24e-02 |
-7.25e-02 |
5.50e-01 |
0.639000 |
Rho GTPase cycle |
112 |
1.01e-01 |
2.36e-01 |
0.11700 |
-1.17e-01 |
-1.38e-03 |
3.22e-02 |
0.980000 |
Regulation of glycolysis by fructose 2,6-bisphosphate metabolism |
11 |
7.97e-01 |
8.86e-01 |
0.11700 |
-4.70e-02 |
1.08e-01 |
7.87e-01 |
0.537000 |
Inflammasomes |
16 |
7.21e-01 |
8.45e-01 |
0.11700 |
-7.59e-02 |
8.90e-02 |
5.99e-01 |
0.538000 |
RAB geranylgeranylation |
37 |
4.71e-01 |
6.39e-01 |
0.11700 |
-1.17e-01 |
-5.75e-03 |
2.20e-01 |
0.952000 |
mRNA Splicing - Major Pathway |
117 |
9.43e-02 |
2.24e-01 |
0.11700 |
1.14e-01 |
2.57e-02 |
3.42e-02 |
0.632000 |
Mitochondrial biogenesis |
60 |
2.99e-01 |
4.88e-01 |
0.11600 |
-1.11e-01 |
3.54e-02 |
1.38e-01 |
0.636000 |
Chaperonin-mediated protein folding |
62 |
2.87e-01 |
4.76e-01 |
0.11600 |
3.13e-03 |
1.16e-01 |
9.66e-01 |
0.114000 |
Neddylation |
164 |
3.84e-02 |
1.21e-01 |
0.11600 |
1.13e-01 |
-2.49e-02 |
1.26e-02 |
0.584000 |
NCAM signaling for neurite out-growth |
44 |
4.14e-01 |
5.97e-01 |
0.11600 |
-9.01e-02 |
-7.25e-02 |
3.02e-01 |
0.406000 |
Post-translational protein phosphorylation |
59 |
3.08e-01 |
4.94e-01 |
0.11600 |
-3.98e-02 |
-1.09e-01 |
5.98e-01 |
0.150000 |
Amino acid transport across the plasma membrane |
26 |
5.95e-01 |
7.48e-01 |
0.11500 |
-1.07e-01 |
-4.40e-02 |
3.47e-01 |
0.698000 |
GAB1 signalosome |
12 |
7.88e-01 |
8.78e-01 |
0.11500 |
-4.33e-02 |
-1.07e-01 |
7.95e-01 |
0.523000 |
Lysine catabolism |
10 |
8.19e-01 |
9.03e-01 |
0.11500 |
7.66e-02 |
8.58e-02 |
6.75e-01 |
0.638000 |
Toll Like Receptor 4 (TLR4) Cascade |
95 |
1.56e-01 |
3.27e-01 |
0.11500 |
-1.09e-01 |
3.72e-02 |
6.78e-02 |
0.531000 |
Interleukin receptor SHC signaling |
18 |
7.01e-01 |
8.33e-01 |
0.11500 |
-8.90e-02 |
-7.24e-02 |
5.14e-01 |
0.595000 |
RHO GTPases activate CIT |
16 |
7.31e-01 |
8.49e-01 |
0.11500 |
-5.35e-02 |
1.01e-01 |
7.11e-01 |
0.483000 |
Interleukin-1 family signaling |
95 |
1.57e-01 |
3.29e-01 |
0.11400 |
1.01e-01 |
5.25e-02 |
8.83e-02 |
0.378000 |
ADP signalling through P2Y purinoceptor 12 |
13 |
7.75e-01 |
8.71e-01 |
0.11400 |
-5.29e-02 |
-1.01e-01 |
7.41e-01 |
0.528000 |
Interleukin-10 signaling |
28 |
5.80e-01 |
7.35e-01 |
0.11400 |
1.06e-01 |
-4.17e-02 |
3.31e-01 |
0.703000 |
Regulation of localization of FOXO transcription factors |
10 |
8.22e-01 |
9.04e-01 |
0.11400 |
9.03e-02 |
6.96e-02 |
6.21e-01 |
0.703000 |
RAF-independent MAPK1/3 activation |
18 |
7.06e-01 |
8.37e-01 |
0.11400 |
-5.06e-02 |
1.02e-01 |
7.10e-01 |
0.454000 |
Cargo recognition for clathrin-mediated endocytosis |
65 |
2.85e-01 |
4.75e-01 |
0.11400 |
1.10e-01 |
2.85e-02 |
1.25e-01 |
0.691000 |
The canonical retinoid cycle in rods (twilight vision) |
13 |
7.77e-01 |
8.73e-01 |
0.11400 |
-2.47e-02 |
-1.11e-01 |
8.78e-01 |
0.489000 |
Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell |
63 |
2.99e-01 |
4.88e-01 |
0.11400 |
1.11e-01 |
-2.52e-02 |
1.29e-01 |
0.730000 |
Transcriptional Regulation by TP53 |
252 |
8.82e-03 |
3.52e-02 |
0.11300 |
1.06e-01 |
-3.99e-02 |
3.94e-03 |
0.278000 |
Mitochondrial Fatty Acid Beta-Oxidation |
25 |
6.21e-01 |
7.69e-01 |
0.11300 |
7.46e-02 |
-8.51e-02 |
5.19e-01 |
0.462000 |
Negative regulation of FGFR1 signaling |
16 |
7.36e-01 |
8.52e-01 |
0.11300 |
6.57e-02 |
9.17e-02 |
6.49e-01 |
0.526000 |
RHO GTPases Activate NADPH Oxidases |
18 |
7.10e-01 |
8.39e-01 |
0.11300 |
-1.11e-01 |
-1.64e-02 |
4.13e-01 |
0.904000 |
Tie2 Signaling |
15 |
7.51e-01 |
8.57e-01 |
0.11300 |
-7.12e-02 |
-8.72e-02 |
6.33e-01 |
0.559000 |
Sphingolipid metabolism |
53 |
3.66e-01 |
5.51e-01 |
0.11200 |
9.04e-02 |
6.70e-02 |
2.56e-01 |
0.400000 |
Acyl chain remodelling of PI |
12 |
7.99e-01 |
8.86e-01 |
0.11200 |
5.48e-02 |
-9.78e-02 |
7.43e-01 |
0.558000 |
Signaling by TGF-beta Receptor Complex |
48 |
4.05e-01 |
5.87e-01 |
0.11200 |
-5.82e-02 |
-9.58e-02 |
4.86e-01 |
0.252000 |
Organelle biogenesis and maintenance |
201 |
2.52e-02 |
8.53e-02 |
0.11100 |
1.11e-01 |
1.15e-02 |
6.99e-03 |
0.780000 |
RHO GTPase Effectors |
186 |
3.29e-02 |
1.08e-01 |
0.11100 |
7.05e-02 |
8.62e-02 |
9.88e-02 |
0.043600 |
Signaling by GPCR |
423 |
5.09e-04 |
2.90e-03 |
0.11100 |
-9.25e-02 |
-6.17e-02 |
1.23e-03 |
0.031000 |
mRNA Splicing |
124 |
1.03e-01 |
2.40e-01 |
0.11100 |
1.10e-01 |
1.24e-02 |
3.42e-02 |
0.811000 |
NR1H3 & NR1H2 regulate gene expression linked to cholesterol transport and efflux |
27 |
6.08e-01 |
7.61e-01 |
0.11100 |
1.11e-01 |
7.09e-03 |
3.19e-01 |
0.949000 |
Plasma lipoprotein remodeling |
16 |
7.49e-01 |
8.56e-01 |
0.11000 |
7.01e-02 |
-8.48e-02 |
6.27e-01 |
0.557000 |
Transcriptional regulation of white adipocyte differentiation |
66 |
3.05e-01 |
4.92e-01 |
0.11000 |
4.23e-02 |
1.01e-01 |
5.53e-01 |
0.156000 |
Infection with Mycobacterium tuberculosis |
21 |
6.85e-01 |
8.17e-01 |
0.11000 |
8.91e-02 |
6.36e-02 |
4.80e-01 |
0.614000 |
mRNA Capping |
16 |
7.51e-01 |
8.57e-01 |
0.10900 |
9.16e-02 |
-5.98e-02 |
5.26e-01 |
0.679000 |
Defects in vitamin and cofactor metabolism |
15 |
7.65e-01 |
8.64e-01 |
0.10900 |
-1.06e-01 |
2.81e-02 |
4.78e-01 |
0.850000 |
RHO GTPases Activate ROCKs |
13 |
7.94e-01 |
8.83e-01 |
0.10900 |
-1.08e-01 |
1.03e-02 |
4.98e-01 |
0.949000 |
Signaling by BRAF and RAF fusions |
44 |
4.59e-01 |
6.27e-01 |
0.10900 |
-1.04e-01 |
3.26e-02 |
2.33e-01 |
0.708000 |
PPARA activates gene expression |
91 |
2.00e-01 |
3.85e-01 |
0.10900 |
4.47e-02 |
9.94e-02 |
4.62e-01 |
0.102000 |
Inhibition of DNA recombination at telomere |
12 |
8.10e-01 |
8.95e-01 |
0.10800 |
1.04e-01 |
2.88e-02 |
5.32e-01 |
0.863000 |
Signaling by ERBB2 KD Mutants |
20 |
7.06e-01 |
8.37e-01 |
0.10800 |
-1.03e-01 |
3.18e-02 |
4.25e-01 |
0.806000 |
Nuclear Receptor transcription pathway |
41 |
4.98e-01 |
6.65e-01 |
0.10700 |
-1.07e-01 |
2.09e-03 |
2.38e-01 |
0.982000 |
Neutrophil degranulation |
316 |
5.39e-03 |
2.38e-02 |
0.10700 |
1.02e-01 |
-2.95e-02 |
1.87e-03 |
0.370000 |
Activation of G protein gated Potassium channels |
16 |
7.61e-01 |
8.62e-01 |
0.10600 |
-7.78e-02 |
-7.27e-02 |
5.90e-01 |
0.615000 |
G protein gated Potassium channels |
16 |
7.61e-01 |
8.62e-01 |
0.10600 |
-7.78e-02 |
-7.27e-02 |
5.90e-01 |
0.615000 |
Inhibition of voltage gated Ca2+ channels via Gbeta/gamma subunits |
16 |
7.61e-01 |
8.62e-01 |
0.10600 |
-7.78e-02 |
-7.27e-02 |
5.90e-01 |
0.615000 |
Cell surface interactions at the vascular wall |
93 |
2.09e-01 |
3.98e-01 |
0.10600 |
-8.19e-02 |
-6.77e-02 |
1.73e-01 |
0.260000 |
TCF dependent signaling in response to WNT |
121 |
1.33e-01 |
2.91e-01 |
0.10600 |
1.03e-01 |
-2.43e-02 |
5.05e-02 |
0.645000 |
Metabolism of proteins |
1234 |
1.11e-08 |
2.30e-07 |
0.10600 |
1.05e-01 |
7.27e-03 |
1.57e-09 |
0.677000 |
SUMOylation of DNA methylation proteins |
15 |
7.80e-01 |
8.73e-01 |
0.10500 |
-7.10e-02 |
7.79e-02 |
6.34e-01 |
0.602000 |
G alpha (i) signalling events |
200 |
3.81e-02 |
1.21e-01 |
0.10500 |
-8.88e-02 |
-5.62e-02 |
3.12e-02 |
0.172000 |
Toll Like Receptor 9 (TLR9) Cascade |
69 |
3.27e-01 |
5.11e-01 |
0.10400 |
-4.16e-02 |
9.58e-02 |
5.50e-01 |
0.170000 |
Constitutive Signaling by Aberrant PI3K in Cancer |
53 |
4.21e-01 |
5.99e-01 |
0.10400 |
-1.01e-01 |
-2.52e-02 |
2.02e-01 |
0.752000 |
Regulation of gene expression by Hypoxia-inducible Factor |
10 |
8.50e-01 |
9.19e-01 |
0.10400 |
1.30e-02 |
1.03e-01 |
9.43e-01 |
0.572000 |
Signaling by FGFR2 |
39 |
5.33e-01 |
6.98e-01 |
0.10400 |
-5.31e-02 |
8.95e-02 |
5.67e-01 |
0.334000 |
Signaling by the B Cell Receptor (BCR) |
80 |
2.77e-01 |
4.66e-01 |
0.10400 |
1.02e-01 |
1.83e-02 |
1.15e-01 |
0.778000 |
Transport to the Golgi and subsequent modification |
122 |
1.45e-01 |
3.08e-01 |
0.10400 |
8.61e-02 |
-5.77e-02 |
1.02e-01 |
0.273000 |
Disassembly of the destruction complex and recruitment of AXIN to the membrane |
24 |
6.81e-01 |
8.15e-01 |
0.10400 |
8.33e-02 |
-6.15e-02 |
4.80e-01 |
0.602000 |
Cell death signalling via NRAGE, NRIF and NADE |
59 |
3.89e-01 |
5.74e-01 |
0.10300 |
-1.00e-01 |
-2.50e-02 |
1.83e-01 |
0.740000 |
Activation of BH3-only proteins |
27 |
6.52e-01 |
7.91e-01 |
0.10300 |
6.51e-02 |
7.93e-02 |
5.58e-01 |
0.476000 |
HATs acetylate histones |
58 |
4.03e-01 |
5.86e-01 |
0.10200 |
7.62e-02 |
6.82e-02 |
3.16e-01 |
0.370000 |
The citric acid (TCA) cycle and respiratory electron transport |
99 |
2.17e-01 |
4.03e-01 |
0.10200 |
9.84e-02 |
-2.72e-02 |
9.15e-02 |
0.641000 |
PRC2 methylates histones and DNA |
11 |
8.43e-01 |
9.16e-01 |
0.10200 |
2.85e-03 |
1.02e-01 |
9.87e-01 |
0.560000 |
Deadenylation-dependent mRNA decay |
39 |
5.48e-01 |
7.09e-01 |
0.10200 |
-1.27e-02 |
1.01e-01 |
8.91e-01 |
0.276000 |
Chemokine receptors bind chemokines |
31 |
6.20e-01 |
7.69e-01 |
0.10100 |
-8.93e-02 |
-4.81e-02 |
3.90e-01 |
0.643000 |
PKA activation |
14 |
8.05e-01 |
8.91e-01 |
0.10100 |
4.12e-02 |
9.26e-02 |
7.89e-01 |
0.549000 |
Other interleukin signaling |
16 |
7.81e-01 |
8.74e-01 |
0.10100 |
-6.14e-02 |
-8.06e-02 |
6.71e-01 |
0.577000 |
Downstream signaling of activated FGFR1 |
19 |
7.49e-01 |
8.56e-01 |
0.10100 |
-1.01e-01 |
2.30e-03 |
4.47e-01 |
0.986000 |
ERK/MAPK targets |
19 |
7.49e-01 |
8.56e-01 |
0.10100 |
3.00e-02 |
9.62e-02 |
8.21e-01 |
0.468000 |
Autophagy |
91 |
2.58e-01 |
4.45e-01 |
0.10000 |
9.95e-02 |
9.67e-03 |
1.01e-01 |
0.874000 |
Hemostasis |
400 |
3.20e-03 |
1.51e-02 |
0.09960 |
-9.84e-02 |
-1.56e-02 |
8.21e-04 |
0.596000 |
Thrombin signalling through proteinase activated receptors (PARs) |
22 |
7.22e-01 |
8.45e-01 |
0.09950 |
3.44e-02 |
-9.34e-02 |
7.80e-01 |
0.449000 |
Signal amplification |
22 |
7.22e-01 |
8.45e-01 |
0.09940 |
1.62e-02 |
-9.81e-02 |
8.96e-01 |
0.426000 |
Amino acids regulate mTORC1 |
33 |
6.14e-01 |
7.66e-01 |
0.09940 |
-6.28e-03 |
9.92e-02 |
9.50e-01 |
0.324000 |
Transcriptional activity of SMAD2/SMAD3:SMAD4 heterotrimer |
30 |
6.42e-01 |
7.83e-01 |
0.09920 |
-9.48e-02 |
-2.91e-02 |
3.69e-01 |
0.783000 |
Class I MHC mediated antigen processing & presentation |
261 |
2.43e-02 |
8.28e-02 |
0.09870 |
9.77e-02 |
-1.41e-02 |
6.92e-03 |
0.697000 |
activated TAK1 mediates p38 MAPK activation |
14 |
8.15e-01 |
8.99e-01 |
0.09860 |
-6.62e-02 |
-7.30e-02 |
6.68e-01 |
0.636000 |
Transcriptional regulation by RUNX3 |
75 |
3.38e-01 |
5.25e-01 |
0.09850 |
9.85e-02 |
4.33e-04 |
1.41e-01 |
0.995000 |
DDX58/IFIH1-mediated induction of interferon-alpha/beta |
44 |
5.31e-01 |
6.98e-01 |
0.09840 |
-6.44e-02 |
7.44e-02 |
4.60e-01 |
0.394000 |
Pre-NOTCH Transcription and Translation |
29 |
6.58e-01 |
7.98e-01 |
0.09830 |
-3.16e-02 |
9.31e-02 |
7.69e-01 |
0.386000 |
Signaling by Receptor Tyrosine Kinases |
358 |
6.67e-03 |
2.79e-02 |
0.09820 |
-9.74e-02 |
-1.18e-02 |
1.68e-03 |
0.705000 |
E3 ubiquitin ligases ubiquitinate target proteins |
22 |
7.34e-01 |
8.51e-01 |
0.09690 |
2.29e-02 |
9.41e-02 |
8.53e-01 |
0.445000 |
Signaling by PDGFR in disease |
18 |
7.79e-01 |
8.73e-01 |
0.09610 |
3.74e-03 |
9.61e-02 |
9.78e-01 |
0.481000 |
Antigen processing: Ubiquitination & Proteasome degradation |
219 |
5.21e-02 |
1.50e-01 |
0.09570 |
9.11e-02 |
2.92e-02 |
2.08e-02 |
0.459000 |
SUMO E3 ligases SUMOylate target proteins |
119 |
1.99e-01 |
3.85e-01 |
0.09540 |
8.52e-02 |
4.29e-02 |
1.09e-01 |
0.421000 |
RNA Polymerase III Transcription Initiation From Type 2 Promoter |
16 |
8.04e-01 |
8.90e-01 |
0.09530 |
8.18e-02 |
4.89e-02 |
5.71e-01 |
0.735000 |
Cellular hexose transport |
12 |
8.50e-01 |
9.19e-01 |
0.09520 |
-9.35e-02 |
1.79e-02 |
5.75e-01 |
0.915000 |
YAP1- and WWTR1 (TAZ)-stimulated gene expression |
11 |
8.62e-01 |
9.25e-01 |
0.09510 |
-9.14e-02 |
2.61e-02 |
6.00e-01 |
0.881000 |
HDACs deacetylate histones |
22 |
7.42e-01 |
8.56e-01 |
0.09500 |
9.16e-02 |
2.51e-02 |
4.57e-01 |
0.839000 |
ADORA2B mediated anti-inflammatory cytokines production |
62 |
4.35e-01 |
6.09e-01 |
0.09500 |
-9.45e-02 |
9.66e-03 |
1.99e-01 |
0.896000 |
SLC-mediated transmembrane transport |
155 |
1.30e-01 |
2.88e-01 |
0.09450 |
-8.68e-02 |
3.74e-02 |
6.31e-02 |
0.423000 |
MyD88 dependent cascade initiated on endosome |
66 |
4.18e-01 |
5.98e-01 |
0.09440 |
-4.60e-02 |
8.24e-02 |
5.19e-01 |
0.248000 |
Toll Like Receptor 7/8 (TLR7/8) Cascade |
66 |
4.18e-01 |
5.98e-01 |
0.09440 |
-4.60e-02 |
8.24e-02 |
5.19e-01 |
0.248000 |
Activation of HOX genes during differentiation |
40 |
5.86e-01 |
7.40e-01 |
0.09430 |
6.28e-02 |
7.03e-02 |
4.92e-01 |
0.442000 |
Activation of anterior HOX genes in hindbrain development during early embryogenesis |
40 |
5.86e-01 |
7.40e-01 |
0.09430 |
6.28e-02 |
7.03e-02 |
4.92e-01 |
0.442000 |
MyD88:MAL(TIRAP) cascade initiated on plasma membrane |
69 |
4.03e-01 |
5.86e-01 |
0.09420 |
-7.91e-02 |
5.12e-02 |
2.56e-01 |
0.463000 |
Toll Like Receptor 2 (TLR2) Cascade |
69 |
4.03e-01 |
5.86e-01 |
0.09420 |
-7.91e-02 |
5.12e-02 |
2.56e-01 |
0.463000 |
Toll Like Receptor TLR1:TLR2 Cascade |
69 |
4.03e-01 |
5.86e-01 |
0.09420 |
-7.91e-02 |
5.12e-02 |
2.56e-01 |
0.463000 |
Toll Like Receptor TLR6:TLR2 Cascade |
69 |
4.03e-01 |
5.86e-01 |
0.09420 |
-7.91e-02 |
5.12e-02 |
2.56e-01 |
0.463000 |
Glucagon signaling in metabolic regulation |
21 |
7.56e-01 |
8.59e-01 |
0.09420 |
3.98e-02 |
8.54e-02 |
7.52e-01 |
0.498000 |
RAB GEFs exchange GTP for GDP on RABs |
66 |
4.24e-01 |
6.03e-01 |
0.09350 |
-4.08e-02 |
8.41e-02 |
5.67e-01 |
0.238000 |
SUMOylation |
124 |
2.00e-01 |
3.85e-01 |
0.09340 |
8.70e-02 |
3.40e-02 |
9.51e-02 |
0.515000 |
ABC transporters in lipid homeostasis |
12 |
8.56e-01 |
9.23e-01 |
0.09330 |
-8.40e-02 |
4.05e-02 |
6.14e-01 |
0.808000 |
C-type lectin receptors (CLRs) |
91 |
3.09e-01 |
4.95e-01 |
0.09320 |
9.28e-02 |
8.43e-03 |
1.27e-01 |
0.890000 |
TRAF6 mediated induction of NFkB and MAP kinases upon TLR7/8 or 9 activation |
65 |
4.34e-01 |
6.09e-01 |
0.09300 |
-6.18e-02 |
6.95e-02 |
3.90e-01 |
0.333000 |
Fc epsilon receptor (FCERI) signaling |
97 |
2.91e-01 |
4.79e-01 |
0.09240 |
6.88e-02 |
6.16e-02 |
2.43e-01 |
0.296000 |
RA biosynthesis pathway |
13 |
8.48e-01 |
9.19e-01 |
0.09200 |
1.98e-03 |
9.19e-02 |
9.90e-01 |
0.566000 |
SUMOylation of intracellular receptors |
23 |
7.49e-01 |
8.56e-01 |
0.09180 |
-4.66e-02 |
7.91e-02 |
6.99e-01 |
0.511000 |
Erythropoietin activates RAS |
10 |
8.82e-01 |
9.39e-01 |
0.09160 |
5.44e-02 |
7.36e-02 |
7.66e-01 |
0.687000 |
Estrogen-dependent gene expression |
65 |
4.47e-01 |
6.17e-01 |
0.09140 |
-6.01e-02 |
6.88e-02 |
4.03e-01 |
0.338000 |
Pyruvate metabolism and Citric Acid (TCA) cycle |
37 |
6.32e-01 |
7.79e-01 |
0.09120 |
-9.05e-02 |
1.12e-02 |
3.41e-01 |
0.906000 |
RNA polymerase II transcribes snRNA genes |
46 |
5.67e-01 |
7.25e-01 |
0.09110 |
8.11e-02 |
-4.14e-02 |
3.42e-01 |
0.627000 |
Pre-NOTCH Expression and Processing |
42 |
5.95e-01 |
7.48e-01 |
0.09100 |
5.62e-03 |
9.08e-02 |
9.50e-01 |
0.309000 |
Signaling by TGFB family members |
68 |
4.32e-01 |
6.09e-01 |
0.09080 |
-5.25e-02 |
-7.40e-02 |
4.55e-01 |
0.292000 |
Clathrin-mediated endocytosis |
96 |
3.15e-01 |
5.01e-01 |
0.08990 |
8.77e-02 |
1.99e-02 |
1.38e-01 |
0.736000 |
Negative regulation of FGFR3 signaling |
15 |
8.34e-01 |
9.09e-01 |
0.08960 |
4.28e-02 |
7.87e-02 |
7.74e-01 |
0.598000 |
RUNX2 regulates osteoblast differentiation |
17 |
8.22e-01 |
9.04e-01 |
0.08760 |
2.66e-02 |
8.34e-02 |
8.50e-01 |
0.552000 |
RIP-mediated NFkB activation via ZBP1 |
15 |
8.43e-01 |
9.16e-01 |
0.08720 |
2.72e-02 |
-8.28e-02 |
8.55e-01 |
0.579000 |
ESR-mediated signaling |
118 |
2.67e-01 |
4.55e-01 |
0.08690 |
-8.54e-02 |
1.60e-02 |
1.10e-01 |
0.765000 |
Response to elevated platelet cytosolic Ca2+ |
93 |
3.54e-01 |
5.37e-01 |
0.08680 |
-7.51e-02 |
4.36e-02 |
2.12e-01 |
0.469000 |
Signaling by ERBB2 TMD/JMD mutants |
17 |
8.27e-01 |
9.04e-01 |
0.08660 |
-7.95e-02 |
3.45e-02 |
5.71e-01 |
0.806000 |
N-Glycan antennae elongation |
10 |
8.94e-01 |
9.50e-01 |
0.08650 |
2.51e-02 |
-8.28e-02 |
8.91e-01 |
0.650000 |
Peroxisomal lipid metabolism |
22 |
7.82e-01 |
8.74e-01 |
0.08650 |
6.71e-02 |
-5.46e-02 |
5.86e-01 |
0.658000 |
Regulation of lipid metabolism by PPARalpha |
93 |
3.54e-01 |
5.37e-01 |
0.08650 |
3.43e-02 |
7.94e-02 |
5.69e-01 |
0.187000 |
G beta:gamma signalling through PLC beta |
12 |
8.75e-01 |
9.33e-01 |
0.08620 |
-7.96e-02 |
-3.30e-02 |
6.33e-01 |
0.843000 |
p75 NTR receptor-mediated signalling |
73 |
4.49e-01 |
6.18e-01 |
0.08570 |
-6.07e-02 |
-6.05e-02 |
3.71e-01 |
0.372000 |
Signaling by NTRK1 (TRKA) |
92 |
3.72e-01 |
5.56e-01 |
0.08520 |
-4.63e-02 |
7.15e-02 |
4.44e-01 |
0.237000 |
Negative regulation of FGFR2 signaling |
17 |
8.33e-01 |
9.08e-01 |
0.08490 |
-2.79e-02 |
8.02e-02 |
8.42e-01 |
0.567000 |
NOTCH3 Activation and Transmission of Signal to the Nucleus |
18 |
8.24e-01 |
9.04e-01 |
0.08490 |
2.42e-02 |
-8.13e-02 |
8.59e-01 |
0.550000 |
Metabolism |
1332 |
3.24e-06 |
3.47e-05 |
0.08480 |
8.46e-02 |
6.35e-03 |
5.38e-07 |
0.707000 |
Nicotinate metabolism |
19 |
8.15e-01 |
8.99e-01 |
0.08470 |
-7.12e-02 |
-4.58e-02 |
5.91e-01 |
0.730000 |
Synthesis of Leukotrienes (LT) and Eoxins (EX) |
14 |
8.62e-01 |
9.25e-01 |
0.08390 |
4.19e-02 |
7.27e-02 |
7.86e-01 |
0.638000 |
Phospholipid metabolism |
151 |
2.16e-01 |
4.03e-01 |
0.08290 |
-7.60e-02 |
3.32e-02 |
1.08e-01 |
0.483000 |
Chondroitin sulfate/dermatan sulfate metabolism |
37 |
6.83e-01 |
8.15e-01 |
0.08290 |
7.28e-02 |
3.97e-02 |
4.44e-01 |
0.677000 |
MTOR signalling |
30 |
7.39e-01 |
8.54e-01 |
0.08190 |
7.08e-02 |
4.12e-02 |
5.02e-01 |
0.696000 |
Signaling by Insulin receptor |
48 |
6.17e-01 |
7.67e-01 |
0.08190 |
-6.63e-02 |
-4.80e-02 |
4.27e-01 |
0.565000 |
Interleukin-6 family signaling |
17 |
8.47e-01 |
9.18e-01 |
0.08080 |
-1.36e-02 |
-7.97e-02 |
9.23e-01 |
0.570000 |
Visual phototransduction |
56 |
5.85e-01 |
7.40e-01 |
0.08000 |
-5.37e-02 |
-5.93e-02 |
4.88e-01 |
0.443000 |
Rab regulation of trafficking |
93 |
4.16e-01 |
5.98e-01 |
0.07960 |
-4.75e-03 |
7.95e-02 |
9.37e-01 |
0.186000 |
Glucose metabolism |
64 |
5.47e-01 |
7.09e-01 |
0.07950 |
7.71e-02 |
-1.94e-02 |
2.87e-01 |
0.789000 |
Activation of GABAB receptors |
28 |
7.68e-01 |
8.66e-01 |
0.07920 |
-4.07e-02 |
-6.79e-02 |
7.09e-01 |
0.534000 |
GABA B receptor activation |
28 |
7.68e-01 |
8.66e-01 |
0.07920 |
-4.07e-02 |
-6.79e-02 |
7.09e-01 |
0.534000 |
Beta-catenin phosphorylation cascade |
15 |
8.69e-01 |
9.30e-01 |
0.07890 |
6.74e-02 |
4.10e-02 |
6.51e-01 |
0.784000 |
NOTCH3 Intracellular Domain Regulates Transcription |
21 |
8.26e-01 |
9.04e-01 |
0.07810 |
-1.02e-02 |
7.74e-02 |
9.35e-01 |
0.539000 |
Toll-like Receptor Cascades |
107 |
3.81e-01 |
5.65e-01 |
0.07810 |
-7.25e-02 |
2.89e-02 |
1.96e-01 |
0.606000 |
Diseases of metabolism |
163 |
2.31e-01 |
4.14e-01 |
0.07800 |
-1.67e-03 |
-7.80e-02 |
9.71e-01 |
0.087000 |
NF-kB activation through FADD/RIP-1 pathway mediated by caspase-8 and -10 |
11 |
9.05e-01 |
9.56e-01 |
0.07780 |
-5.75e-02 |
5.23e-02 |
7.41e-01 |
0.764000 |
Transcriptional Regulation by VENTX |
32 |
7.49e-01 |
8.56e-01 |
0.07770 |
7.71e-02 |
-1.00e-02 |
4.51e-01 |
0.922000 |
Platelet degranulation |
89 |
4.52e-01 |
6.20e-01 |
0.07760 |
-4.12e-02 |
6.58e-02 |
5.03e-01 |
0.284000 |
Cytosolic sensors of pathogen-associated DNA |
44 |
6.75e-01 |
8.12e-01 |
0.07740 |
2.24e-03 |
7.73e-02 |
9.80e-01 |
0.375000 |
Macroautophagy |
80 |
4.92e-01 |
6.58e-01 |
0.07720 |
7.72e-02 |
-1.67e-03 |
2.34e-01 |
0.979000 |
Cellular response to heat stress |
67 |
5.54e-01 |
7.15e-01 |
0.07680 |
3.46e-02 |
6.86e-02 |
6.25e-01 |
0.333000 |
Activation of IRF3/IRF7 mediated by TBK1/IKK epsilon |
12 |
9.00e-01 |
9.52e-01 |
0.07630 |
-6.87e-02 |
-3.31e-02 |
6.80e-01 |
0.843000 |
Downregulation of ERBB2 signaling |
18 |
8.56e-01 |
9.23e-01 |
0.07590 |
-6.69e-02 |
-3.59e-02 |
6.23e-01 |
0.792000 |
Energy dependent regulation of mTOR by LKB1-AMPK |
20 |
8.42e-01 |
9.16e-01 |
0.07580 |
-7.33e-02 |
-1.91e-02 |
5.70e-01 |
0.882000 |
Regulation of PTEN gene transcription |
46 |
6.79e-01 |
8.13e-01 |
0.07510 |
-5.48e-04 |
7.51e-02 |
9.95e-01 |
0.379000 |
PI3K/AKT Signaling in Cancer |
76 |
5.31e-01 |
6.98e-01 |
0.07470 |
-7.43e-02 |
-7.42e-03 |
2.63e-01 |
0.911000 |
PKMTs methylate histone lysines |
32 |
7.71e-01 |
8.67e-01 |
0.07390 |
-7.33e-02 |
8.82e-03 |
4.73e-01 |
0.931000 |
Signaling by NTRKs |
105 |
4.34e-01 |
6.09e-01 |
0.07330 |
-2.93e-02 |
6.72e-02 |
6.05e-01 |
0.235000 |
RNA Polymerase III Chain Elongation |
11 |
9.15e-01 |
9.58e-01 |
0.07320 |
7.32e-02 |
9.14e-05 |
6.74e-01 |
1.000000 |
Signaling by FGFR4 |
24 |
8.26e-01 |
9.04e-01 |
0.07310 |
-6.99e-02 |
2.13e-02 |
5.54e-01 |
0.857000 |
L1CAM interactions |
76 |
5.56e-01 |
7.16e-01 |
0.07220 |
-4.56e-02 |
5.60e-02 |
4.93e-01 |
0.399000 |
PIP3 activates AKT signaling |
194 |
2.27e-01 |
4.11e-01 |
0.07190 |
6.64e-02 |
2.76e-02 |
1.12e-01 |
0.510000 |
Signaling by Nuclear Receptors |
171 |
2.87e-01 |
4.76e-01 |
0.07020 |
-6.86e-02 |
-1.48e-02 |
1.23e-01 |
0.739000 |
Glucagon-type ligand receptors |
15 |
8.95e-01 |
9.50e-01 |
0.07010 |
-1.89e-04 |
7.01e-02 |
9.99e-01 |
0.638000 |
Assembly of active LPL and LIPC lipase complexes |
13 |
9.09e-01 |
9.56e-01 |
0.06970 |
-4.41e-02 |
-5.40e-02 |
7.83e-01 |
0.736000 |
Adherens junctions interactions |
15 |
8.96e-01 |
9.51e-01 |
0.06960 |
-4.90e-02 |
-4.95e-02 |
7.43e-01 |
0.740000 |
tRNA modification in the nucleus and cytosol |
28 |
8.21e-01 |
9.04e-01 |
0.06860 |
5.42e-03 |
6.84e-02 |
9.60e-01 |
0.531000 |
Misspliced GSK3beta mutants stabilize beta-catenin |
13 |
9.13e-01 |
9.56e-01 |
0.06830 |
9.18e-03 |
-6.77e-02 |
9.54e-01 |
0.673000 |
S33 mutants of beta-catenin aren't phosphorylated |
13 |
9.13e-01 |
9.56e-01 |
0.06830 |
9.18e-03 |
-6.77e-02 |
9.54e-01 |
0.673000 |
S37 mutants of beta-catenin aren't phosphorylated |
13 |
9.13e-01 |
9.56e-01 |
0.06830 |
9.18e-03 |
-6.77e-02 |
9.54e-01 |
0.673000 |
S45 mutants of beta-catenin aren't phosphorylated |
13 |
9.13e-01 |
9.56e-01 |
0.06830 |
9.18e-03 |
-6.77e-02 |
9.54e-01 |
0.673000 |
T41 mutants of beta-catenin aren't phosphorylated |
13 |
9.13e-01 |
9.56e-01 |
0.06830 |
9.18e-03 |
-6.77e-02 |
9.54e-01 |
0.673000 |
phosphorylation site mutants of CTNNB1 are not targeted to the proteasome by the destruction complex |
13 |
9.13e-01 |
9.56e-01 |
0.06830 |
9.18e-03 |
-6.77e-02 |
9.54e-01 |
0.673000 |
Metabolism of water-soluble vitamins and cofactors |
86 |
5.55e-01 |
7.15e-01 |
0.06800 |
6.47e-02 |
-2.09e-02 |
3.01e-01 |
0.739000 |
Signaling by FGFR |
50 |
7.13e-01 |
8.41e-01 |
0.06750 |
-3.51e-02 |
5.76e-02 |
6.68e-01 |
0.481000 |
Oxidative Stress Induced Senescence |
51 |
7.10e-01 |
8.39e-01 |
0.06710 |
-6.63e-02 |
-1.04e-02 |
4.14e-01 |
0.898000 |
SLC transporter disorders |
64 |
6.51e-01 |
7.91e-01 |
0.06690 |
5.55e-02 |
3.74e-02 |
4.43e-01 |
0.605000 |
TP53 Regulates Metabolic Genes |
61 |
6.66e-01 |
8.06e-01 |
0.06690 |
2.11e-02 |
-6.35e-02 |
7.76e-01 |
0.392000 |
Signaling by EGFR in Cancer |
15 |
9.06e-01 |
9.56e-01 |
0.06640 |
-5.69e-03 |
6.61e-02 |
9.70e-01 |
0.658000 |
DAP12 signaling |
22 |
8.68e-01 |
9.30e-01 |
0.06550 |
-2.66e-04 |
6.55e-02 |
9.98e-01 |
0.595000 |
HSP90 chaperone cycle for steroid hormone receptors (SHR) |
28 |
8.43e-01 |
9.16e-01 |
0.06400 |
5.24e-02 |
-3.68e-02 |
6.32e-01 |
0.736000 |
RUNX2 regulates bone development |
22 |
8.75e-01 |
9.33e-01 |
0.06390 |
-4.13e-02 |
4.88e-02 |
7.37e-01 |
0.692000 |
Regulation of TP53 Activity through Association with Co-factors |
11 |
9.35e-01 |
9.74e-01 |
0.06370 |
2.74e-02 |
5.75e-02 |
8.75e-01 |
0.742000 |
Intra-Golgi and retrograde Golgi-to-ER traffic |
134 |
4.49e-01 |
6.18e-01 |
0.06360 |
3.25e-02 |
-5.47e-02 |
5.18e-01 |
0.276000 |
FCGR3A-mediated phagocytosis |
54 |
7.24e-01 |
8.45e-01 |
0.06330 |
7.60e-03 |
6.28e-02 |
9.23e-01 |
0.425000 |
Leishmania phagocytosis |
54 |
7.24e-01 |
8.45e-01 |
0.06330 |
7.60e-03 |
6.28e-02 |
9.23e-01 |
0.425000 |
Parasite infection |
54 |
7.24e-01 |
8.45e-01 |
0.06330 |
7.60e-03 |
6.28e-02 |
9.23e-01 |
0.425000 |
RNA Polymerase III Transcription Initiation |
23 |
8.71e-01 |
9.32e-01 |
0.06320 |
1.23e-02 |
6.20e-02 |
9.19e-01 |
0.607000 |
Regulation of IFNG signaling |
10 |
9.42e-01 |
9.79e-01 |
0.06320 |
2.32e-02 |
-5.88e-02 |
8.99e-01 |
0.747000 |
Signaling by Hippo |
17 |
9.04e-01 |
9.56e-01 |
0.06290 |
-6.20e-02 |
1.07e-02 |
6.58e-01 |
0.939000 |
Adenylate cyclase inhibitory pathway |
12 |
9.33e-01 |
9.73e-01 |
0.06190 |
8.79e-03 |
-6.13e-02 |
9.58e-01 |
0.713000 |
Adaptive Immune System |
513 |
6.29e-02 |
1.73e-01 |
0.06150 |
5.95e-02 |
-1.56e-02 |
2.28e-02 |
0.549000 |
TCR signaling |
81 |
6.34e-01 |
7.79e-01 |
0.06140 |
5.13e-02 |
3.37e-02 |
4.25e-01 |
0.601000 |
RNA Polymerase III Transcription Initiation From Type 3 Promoter |
19 |
8.98e-01 |
9.51e-01 |
0.06140 |
-6.10e-02 |
-6.25e-03 |
6.45e-01 |
0.962000 |
DAP12 interactions |
26 |
8.66e-01 |
9.29e-01 |
0.06070 |
5.15e-02 |
3.22e-02 |
6.50e-01 |
0.777000 |
Signaling by FGFR3 |
24 |
8.79e-01 |
9.37e-01 |
0.06000 |
-1.84e-02 |
5.71e-02 |
8.76e-01 |
0.628000 |
Peptide ligand-binding receptors |
73 |
6.86e-01 |
8.17e-01 |
0.05880 |
-2.18e-02 |
-5.46e-02 |
7.47e-01 |
0.421000 |
Signal Transduction |
1528 |
1.23e-03 |
6.31e-03 |
0.05820 |
-5.77e-02 |
-7.71e-03 |
2.87e-04 |
0.628000 |
Epigenetic regulation of gene expression |
59 |
7.47e-01 |
8.56e-01 |
0.05770 |
3.20e-02 |
-4.81e-02 |
6.72e-01 |
0.524000 |
GPCR ligand binding |
191 |
3.92e-01 |
5.77e-01 |
0.05760 |
-5.08e-02 |
-2.71e-02 |
2.28e-01 |
0.520000 |
Interleukin-20 family signaling |
12 |
9.42e-01 |
9.79e-01 |
0.05740 |
5.53e-02 |
1.56e-02 |
7.40e-01 |
0.925000 |
HSF1 activation |
18 |
9.16e-01 |
9.58e-01 |
0.05700 |
1.61e-02 |
5.47e-02 |
9.06e-01 |
0.688000 |
RAF activation |
28 |
8.75e-01 |
9.33e-01 |
0.05670 |
-4.28e-02 |
3.71e-02 |
6.95e-01 |
0.734000 |
BBSome-mediated cargo-targeting to cilium |
16 |
9.27e-01 |
9.68e-01 |
0.05650 |
5.41e-02 |
-1.60e-02 |
7.08e-01 |
0.912000 |
Fatty acid metabolism |
118 |
5.73e-01 |
7.30e-01 |
0.05640 |
-1.59e-03 |
5.64e-02 |
9.76e-01 |
0.292000 |
Signaling by Rho GTPases |
290 |
2.60e-01 |
4.48e-01 |
0.05640 |
-2.71e-03 |
5.63e-02 |
9.37e-01 |
0.101000 |
GABA receptor activation |
32 |
8.60e-01 |
9.25e-01 |
0.05600 |
-4.55e-02 |
-3.26e-02 |
6.56e-01 |
0.750000 |
Metabolism of vitamins and cofactors |
128 |
5.89e-01 |
7.43e-01 |
0.05290 |
4.14e-02 |
-3.30e-02 |
4.20e-01 |
0.521000 |
Keratan sulfate biosynthesis |
17 |
9.33e-01 |
9.73e-01 |
0.05240 |
-3.50e-02 |
3.91e-02 |
8.03e-01 |
0.780000 |
RUNX1 interacts with co-factors whose precise effect on RUNX1 targets is not known |
30 |
8.89e-01 |
9.46e-01 |
0.05140 |
-3.09e-02 |
4.11e-02 |
7.70e-01 |
0.697000 |
Post-translational protein modification |
907 |
3.68e-02 |
1.18e-01 |
0.05140 |
5.12e-02 |
4.96e-03 |
1.06e-02 |
0.804000 |
Cobalamin (Cbl, vitamin B12) transport and metabolism |
10 |
9.64e-01 |
9.87e-01 |
0.04980 |
-4.95e-02 |
5.70e-03 |
7.87e-01 |
0.975000 |
AMER1 mutants destabilize the destruction complex |
12 |
9.58e-01 |
9.84e-01 |
0.04910 |
1.54e-02 |
-4.67e-02 |
9.26e-01 |
0.780000 |
APC truncation mutants have impaired AXIN binding |
12 |
9.58e-01 |
9.84e-01 |
0.04910 |
1.54e-02 |
-4.67e-02 |
9.26e-01 |
0.780000 |
AXIN missense mutants destabilize the destruction complex |
12 |
9.58e-01 |
9.84e-01 |
0.04910 |
1.54e-02 |
-4.67e-02 |
9.26e-01 |
0.780000 |
AXIN mutants destabilize the destruction complex, activating WNT signaling |
12 |
9.58e-01 |
9.84e-01 |
0.04910 |
1.54e-02 |
-4.67e-02 |
9.26e-01 |
0.780000 |
Truncations of AMER1 destabilize the destruction complex |
12 |
9.58e-01 |
9.84e-01 |
0.04910 |
1.54e-02 |
-4.67e-02 |
9.26e-01 |
0.780000 |
truncated APC mutants destabilize the destruction complex |
12 |
9.58e-01 |
9.84e-01 |
0.04910 |
1.54e-02 |
-4.67e-02 |
9.26e-01 |
0.780000 |
Metabolism of cofactors |
17 |
9.43e-01 |
9.79e-01 |
0.04780 |
-1.08e-05 |
4.78e-02 |
1.00e+00 |
0.733000 |
Interleukin-4 and Interleukin-13 signaling |
78 |
7.69e-01 |
8.66e-01 |
0.04760 |
2.74e-03 |
-4.75e-02 |
9.67e-01 |
0.469000 |
Signaling by Interleukins |
298 |
3.77e-01 |
5.61e-01 |
0.04730 |
1.56e-02 |
4.47e-02 |
6.45e-01 |
0.188000 |
Chromatin modifying enzymes |
150 |
6.17e-01 |
7.67e-01 |
0.04670 |
-2.72e-05 |
4.67e-02 |
1.00e+00 |
0.325000 |
Chromatin organization |
150 |
6.17e-01 |
7.67e-01 |
0.04670 |
-2.72e-05 |
4.67e-02 |
1.00e+00 |
0.325000 |
Reversible hydration of carbon dioxide |
10 |
9.69e-01 |
9.89e-01 |
0.04630 |
3.12e-02 |
-3.41e-02 |
8.64e-01 |
0.852000 |
Aflatoxin activation and detoxification |
10 |
9.69e-01 |
9.89e-01 |
0.04610 |
-2.19e-02 |
-4.06e-02 |
9.05e-01 |
0.824000 |
Innate Immune System |
652 |
1.42e-01 |
3.06e-01 |
0.04600 |
4.60e-02 |
-1.47e-03 |
4.84e-02 |
0.950000 |
Disease |
963 |
6.70e-02 |
1.79e-01 |
0.04530 |
4.50e-02 |
5.15e-03 |
2.09e-02 |
0.792000 |
ZBP1(DAI) mediated induction of type I IFNs |
18 |
9.49e-01 |
9.82e-01 |
0.04390 |
-2.32e-02 |
-3.73e-02 |
8.65e-01 |
0.784000 |
Factors involved in megakaryocyte development and platelet production |
80 |
7.97e-01 |
8.86e-01 |
0.04380 |
2.15e-02 |
-3.81e-02 |
7.40e-01 |
0.556000 |
Interleukin-15 signaling |
11 |
9.69e-01 |
9.89e-01 |
0.04370 |
-1.70e-02 |
4.02e-02 |
9.22e-01 |
0.817000 |
rRNA modification in the nucleus and cytosol |
42 |
8.90e-01 |
9.47e-01 |
0.04300 |
-1.76e-02 |
-3.92e-02 |
8.44e-01 |
0.660000 |
Gene expression (Transcription) |
866 |
1.12e-01 |
2.55e-01 |
0.04270 |
3.85e-02 |
1.86e-02 |
5.99e-02 |
0.363000 |
Cytokine Signaling in Immune system |
559 |
2.33e-01 |
4.16e-01 |
0.04270 |
1.91e-02 |
3.82e-02 |
4.46e-01 |
0.127000 |
TRAF6-mediated induction of TAK1 complex within TLR4 complex |
10 |
9.74e-01 |
9.93e-01 |
0.04240 |
3.03e-02 |
-2.97e-02 |
8.68e-01 |
0.871000 |
AKT phosphorylates targets in the cytosol |
13 |
9.66e-01 |
9.88e-01 |
0.04230 |
-1.45e-03 |
-4.23e-02 |
9.93e-01 |
0.792000 |
Transport of small molecules |
447 |
3.19e-01 |
5.03e-01 |
0.04210 |
3.57e-02 |
2.22e-02 |
2.00e-01 |
0.426000 |
Negative regulation of the PI3K/AKT network |
82 |
8.08e-01 |
8.94e-01 |
0.04170 |
-4.01e-02 |
-1.13e-02 |
5.31e-01 |
0.860000 |
Signaling by WNT |
192 |
6.20e-01 |
7.69e-01 |
0.04100 |
3.71e-02 |
1.76e-02 |
3.78e-01 |
0.676000 |
B-WICH complex positively regulates rRNA expression |
21 |
9.49e-01 |
9.82e-01 |
0.04080 |
-1.90e-02 |
-3.61e-02 |
8.80e-01 |
0.774000 |
Metabolism of lipids |
488 |
3.22e-01 |
5.06e-01 |
0.04030 |
-3.39e-02 |
2.18e-02 |
2.05e-01 |
0.414000 |
Negative regulators of DDX58/IFIH1 signaling |
21 |
9.55e-01 |
9.84e-01 |
0.03830 |
-3.07e-02 |
-2.29e-02 |
8.08e-01 |
0.856000 |
EPH-Ephrin signaling |
69 |
8.62e-01 |
9.25e-01 |
0.03810 |
8.68e-03 |
-3.71e-02 |
9.01e-01 |
0.595000 |
RNA Polymerase III Abortive And Retractive Initiation |
27 |
9.44e-01 |
9.79e-01 |
0.03780 |
3.70e-02 |
-8.05e-03 |
7.40e-01 |
0.942000 |
RNA Polymerase III Transcription |
27 |
9.44e-01 |
9.79e-01 |
0.03780 |
3.70e-02 |
-8.05e-03 |
7.40e-01 |
0.942000 |
PI5P, PP2A and IER3 Regulate PI3K/AKT Signaling |
77 |
8.51e-01 |
9.20e-01 |
0.03750 |
-3.03e-02 |
-2.21e-02 |
6.47e-01 |
0.738000 |
Metabolism of Angiotensinogen to Angiotensins |
11 |
9.77e-01 |
9.94e-01 |
0.03730 |
8.35e-03 |
3.64e-02 |
9.62e-01 |
0.835000 |
Peroxisomal protein import |
45 |
9.12e-01 |
9.56e-01 |
0.03690 |
3.17e-02 |
1.88e-02 |
7.13e-01 |
0.827000 |
RNA Polymerase II Transcription |
779 |
2.32e-01 |
4.15e-01 |
0.03660 |
3.18e-02 |
1.81e-02 |
1.38e-01 |
0.399000 |
Anti-inflammatory response favouring Leishmania parasite infection |
94 |
8.29e-01 |
9.05e-01 |
0.03650 |
-3.37e-02 |
-1.42e-02 |
5.73e-01 |
0.813000 |
Leishmania parasite growth and survival |
94 |
8.29e-01 |
9.05e-01 |
0.03650 |
-3.37e-02 |
-1.42e-02 |
5.73e-01 |
0.813000 |
Cellular Senescence |
100 |
8.26e-01 |
9.04e-01 |
0.03590 |
3.53e-02 |
-6.61e-03 |
5.43e-01 |
0.909000 |
Vesicle-mediated transport |
464 |
4.28e-01 |
6.04e-01 |
0.03580 |
3.28e-02 |
-1.42e-02 |
2.31e-01 |
0.604000 |
Glycerophospholipid biosynthesis |
83 |
8.59e-01 |
9.25e-01 |
0.03510 |
-2.82e-02 |
2.09e-02 |
6.57e-01 |
0.742000 |
RAF/MAP kinase cascade |
183 |
7.36e-01 |
8.52e-01 |
0.03380 |
3.06e-02 |
-1.42e-02 |
4.77e-01 |
0.741000 |
FLT3 Signaling |
196 |
7.21e-01 |
8.45e-01 |
0.03370 |
2.77e-02 |
-1.92e-02 |
5.06e-01 |
0.644000 |
Immune System |
1345 |
1.36e-01 |
2.96e-01 |
0.03350 |
3.19e-02 |
1.04e-02 |
5.79e-02 |
0.537000 |
Regulation of actin dynamics for phagocytic cup formation |
55 |
9.12e-01 |
9.56e-01 |
0.03340 |
1.60e-02 |
2.93e-02 |
8.38e-01 |
0.707000 |
Signaling by NOTCH3 |
38 |
9.40e-01 |
9.78e-01 |
0.03310 |
-1.89e-02 |
2.72e-02 |
8.40e-01 |
0.772000 |
Transcriptional regulation by the AP-2 (TFAP2) family of transcription factors |
23 |
9.63e-01 |
9.87e-01 |
0.03300 |
3.05e-02 |
1.25e-02 |
8.00e-01 |
0.918000 |
Miscellaneous transport and binding events |
15 |
9.76e-01 |
9.94e-01 |
0.03270 |
2.80e-02 |
-1.69e-02 |
8.51e-01 |
0.910000 |
Intracellular signaling by second messengers |
226 |
7.02e-01 |
8.34e-01 |
0.03250 |
2.14e-02 |
2.45e-02 |
5.82e-01 |
0.527000 |
MAPK1/MAPK3 signaling |
188 |
7.61e-01 |
8.62e-01 |
0.03150 |
2.97e-02 |
-1.04e-02 |
4.85e-01 |
0.807000 |
Membrane Trafficking |
438 |
5.48e-01 |
7.09e-01 |
0.03090 |
3.08e-02 |
-2.74e-03 |
2.74e-01 |
0.922000 |
Cytochrome P450 - arranged by substrate type |
29 |
9.60e-01 |
9.85e-01 |
0.03080 |
-2.05e-02 |
2.29e-02 |
8.48e-01 |
0.831000 |
Negative regulation of MAPK pathway |
33 |
9.58e-01 |
9.84e-01 |
0.02950 |
-1.56e-02 |
2.51e-02 |
8.77e-01 |
0.803000 |
TP53 Regulates Transcription of Genes Involved in Cytochrome C Release |
13 |
9.84e-01 |
9.98e-01 |
0.02890 |
-2.67e-02 |
1.13e-02 |
8.68e-01 |
0.944000 |
Leishmania infection |
159 |
8.29e-01 |
9.05e-01 |
0.02820 |
-2.79e-02 |
-4.38e-03 |
5.46e-01 |
0.924000 |
Generic Transcription Pathway |
694 |
4.67e-01 |
6.35e-01 |
0.02790 |
2.71e-02 |
6.69e-03 |
2.31e-01 |
0.768000 |
Nervous system development |
380 |
6.81e-01 |
8.15e-01 |
0.02640 |
-2.63e-02 |
-2.28e-03 |
3.83e-01 |
0.940000 |
Developmental Biology |
594 |
5.78e-01 |
7.34e-01 |
0.02550 |
-2.52e-02 |
4.34e-03 |
3.02e-01 |
0.859000 |
TRAF6 mediated NF-kB activation |
19 |
9.82e-01 |
9.97e-01 |
0.02510 |
1.61e-02 |
1.93e-02 |
9.03e-01 |
0.884000 |
SHC-mediated cascade:FGFR1 |
10 |
9.91e-01 |
9.99e-01 |
0.02410 |
-2.12e-02 |
1.14e-02 |
9.08e-01 |
0.950000 |
Regulation of TP53 Degradation |
28 |
9.78e-01 |
9.94e-01 |
0.02290 |
2.24e-02 |
4.44e-03 |
8.37e-01 |
0.968000 |
Aquaporin-mediated transport |
31 |
9.76e-01 |
9.94e-01 |
0.02280 |
-1.28e-02 |
1.89e-02 |
9.02e-01 |
0.856000 |
Diseases of signal transduction by growth factor receptors and second messengers |
276 |
8.61e-01 |
9.25e-01 |
0.01930 |
-1.02e-02 |
1.64e-02 |
7.71e-01 |
0.642000 |
Fcgamma receptor (FCGR) dependent phagocytosis |
75 |
9.61e-01 |
9.86e-01 |
0.01890 |
1.63e-02 |
-9.51e-03 |
8.07e-01 |
0.887000 |
TAK1 activates NFkB by phosphorylation and activation of IKKs complex |
19 |
9.90e-01 |
9.99e-01 |
0.01880 |
2.06e-03 |
-1.87e-02 |
9.88e-01 |
0.888000 |
SMAD2/SMAD3:SMAD4 heterotrimer regulates transcription |
21 |
9.89e-01 |
9.99e-01 |
0.01870 |
-2.16e-03 |
-1.86e-02 |
9.86e-01 |
0.883000 |
Zinc transporters |
11 |
9.95e-01 |
9.99e-01 |
0.01760 |
1.68e-02 |
-5.31e-03 |
9.23e-01 |
0.976000 |
NR1H2 and NR1H3-mediated signaling |
35 |
9.84e-01 |
9.98e-01 |
0.01740 |
-1.57e-03 |
1.73e-02 |
9.87e-01 |
0.859000 |
Vasopressin regulates renal water homeostasis via Aquaporins |
28 |
9.88e-01 |
9.99e-01 |
0.01720 |
-1.58e-02 |
7.00e-03 |
8.85e-01 |
0.949000 |
Prostacyclin signalling through prostacyclin receptor |
11 |
9.96e-01 |
9.99e-01 |
0.01640 |
-1.61e-02 |
3.53e-03 |
9.27e-01 |
0.984000 |
Intra-Golgi traffic |
33 |
9.90e-01 |
9.99e-01 |
0.01470 |
-6.96e-03 |
1.29e-02 |
9.45e-01 |
0.898000 |
Axon guidance |
361 |
8.98e-01 |
9.51e-01 |
0.01430 |
-1.39e-02 |
-3.61e-03 |
6.54e-01 |
0.907000 |
Regulation of TP53 Expression and Degradation |
29 |
9.91e-01 |
9.99e-01 |
0.01410 |
1.39e-02 |
-2.61e-03 |
8.97e-01 |
0.981000 |
Synthesis of PIPs at the Golgi membrane |
11 |
9.97e-01 |
9.99e-01 |
0.01290 |
-1.16e-02 |
-5.69e-03 |
9.47e-01 |
0.974000 |
Keratan sulfate/keratin metabolism |
21 |
9.95e-01 |
9.99e-01 |
0.01240 |
1.18e-02 |
-3.55e-03 |
9.25e-01 |
0.978000 |
MAPK family signaling cascades |
216 |
9.55e-01 |
9.84e-01 |
0.01210 |
8.32e-03 |
8.74e-03 |
8.34e-01 |
0.826000 |
Constitutive Signaling by AKT1 E17K in Cancer |
22 |
9.96e-01 |
9.99e-01 |
0.01150 |
5.65e-03 |
-1.00e-02 |
9.63e-01 |
0.935000 |
Signaling by ERBB4 |
37 |
9.95e-01 |
9.99e-01 |
0.00958 |
-8.73e-03 |
-3.96e-03 |
9.27e-01 |
0.967000 |
Negative regulation of FGFR4 signaling |
16 |
9.98e-01 |
9.99e-01 |
0.00853 |
5.03e-04 |
-8.52e-03 |
9.97e-01 |
0.953000 |
Transcriptional regulation of pluripotent stem cells |
17 |
9.99e-01 |
9.99e-01 |
0.00666 |
-4.54e-03 |
4.88e-03 |
9.74e-01 |
0.972000 |
Uptake and function of anthrax toxins |
11 |
9.99e-01 |
9.99e-01 |
0.00609 |
5.94e-03 |
1.35e-03 |
9.73e-01 |
0.994000 |
ADP signalling through P2Y purinoceptor 1 |
17 |
9.99e-01 |
9.99e-01 |
0.00455 |
6.94e-04 |
4.49e-03 |
9.96e-01 |
0.974000 |
EPHB-mediated forward signaling |
24 |
9.99e-01 |
9.99e-01 |
0.00430 |
4.30e-03 |
-3.81e-05 |
9.71e-01 |
1.000000 |