Classical antibody-mediated complement activation |
10 |
6.32e-09 |
4.74e-08 |
1.5000 |
0.256000 |
6.84e-01 |
0.896000 |
9.48e-01 |
1.61e-01 |
1.78e-04 |
9.16e-07 |
2.05e-07 |
Unwinding of DNA |
12 |
1.21e-13 |
1.89e-12 |
1.3400 |
0.705000 |
7.05e-01 |
0.864000 |
-2.31e-01 |
2.32e-05 |
2.32e-05 |
2.19e-07 |
1.66e-01 |
Creation of C4 and C2 activators |
11 |
7.68e-08 |
4.50e-07 |
1.3200 |
0.265000 |
7.10e-01 |
0.742000 |
7.94e-01 |
1.28e-01 |
4.55e-05 |
2.02e-05 |
5.13e-06 |
Initial triggering of complement |
18 |
3.07e-11 |
3.35e-10 |
1.2700 |
0.349000 |
6.92e-01 |
0.673000 |
7.47e-01 |
1.03e-02 |
3.71e-07 |
7.58e-07 |
4.01e-08 |
Peptide chain elongation |
55 |
3.62e-26 |
2.07e-24 |
1.1400 |
0.604000 |
5.73e-01 |
0.549000 |
5.57e-01 |
9.17e-15 |
1.92e-13 |
1.95e-12 |
9.38e-13 |
Viral mRNA Translation |
55 |
1.21e-25 |
6.60e-24 |
1.1200 |
0.613000 |
5.45e-01 |
0.523000 |
5.62e-01 |
3.61e-15 |
2.61e-12 |
1.90e-11 |
5.45e-13 |
DNA strand elongation |
32 |
5.30e-28 |
3.31e-26 |
1.1200 |
0.542000 |
5.38e-01 |
0.791000 |
-2.11e-01 |
1.09e-07 |
1.41e-07 |
9.12e-15 |
3.94e-02 |
Selenocysteine synthesis |
58 |
5.52e-25 |
2.90e-23 |
1.0900 |
0.571000 |
5.55e-01 |
0.508000 |
5.43e-01 |
5.14e-14 |
2.72e-13 |
2.23e-11 |
8.89e-13 |
Eukaryotic Translation Termination |
58 |
5.66e-24 |
2.32e-22 |
1.0600 |
0.561000 |
5.06e-01 |
0.524000 |
5.26e-01 |
1.44e-13 |
2.60e-11 |
4.96e-12 |
4.11e-12 |
Eukaryotic Translation Elongation |
59 |
9.44e-24 |
3.75e-22 |
1.0500 |
0.544000 |
5.17e-01 |
0.525000 |
5.15e-01 |
4.99e-13 |
6.59e-12 |
3.07e-12 |
7.85e-12 |
FCGR activation |
16 |
8.32e-07 |
4.21e-06 |
1.0500 |
0.253000 |
5.05e-01 |
0.544000 |
6.97e-01 |
8.00e-02 |
4.65e-04 |
1.65e-04 |
1.36e-06 |
Processive synthesis on the lagging strand |
15 |
4.64e-11 |
4.84e-10 |
1.0300 |
0.493000 |
5.09e-01 |
0.716000 |
-2.23e-01 |
9.38e-04 |
6.50e-04 |
1.57e-06 |
1.34e-01 |
Activation of the pre-replicative complex |
31 |
1.53e-23 |
5.27e-22 |
1.0300 |
0.586000 |
4.81e-01 |
0.613000 |
-3.25e-01 |
1.66e-08 |
3.60e-06 |
3.44e-09 |
1.76e-03 |
SRP-dependent cotranslational protein targeting to membrane |
76 |
5.08e-30 |
3.92e-28 |
1.0300 |
0.481000 |
4.45e-01 |
0.521000 |
5.94e-01 |
4.44e-13 |
2.10e-11 |
4.03e-15 |
3.22e-19 |
Response of EIF2AK4 (GCN2) to amino acid deficiency |
65 |
4.87e-24 |
2.06e-22 |
1.0100 |
0.590000 |
5.53e-01 |
0.440000 |
4.18e-01 |
1.97e-16 |
1.31e-14 |
8.34e-10 |
5.69e-09 |
Formation of a pool of free 40S subunits |
65 |
2.18e-24 |
9.85e-23 |
1.0100 |
0.503000 |
4.68e-01 |
0.544000 |
4.97e-01 |
2.24e-12 |
6.76e-11 |
3.34e-14 |
4.18e-12 |
Removal of the Flap Intermediate |
14 |
6.56e-10 |
5.90e-09 |
1.0100 |
0.472000 |
4.81e-01 |
0.714000 |
-2.16e-01 |
2.23e-03 |
1.84e-03 |
3.71e-06 |
1.62e-01 |
Lagging Strand Synthesis |
20 |
2.91e-14 |
4.84e-13 |
0.9910 |
0.444000 |
4.36e-01 |
0.746000 |
-1.98e-01 |
5.95e-04 |
7.37e-04 |
7.54e-09 |
1.26e-01 |
Leading Strand Synthesis |
14 |
7.29e-10 |
6.42e-09 |
0.9840 |
0.407000 |
3.96e-01 |
0.787000 |
-1.63e-01 |
8.34e-03 |
1.03e-02 |
3.40e-07 |
2.90e-01 |
Polymerase switching |
14 |
7.29e-10 |
6.42e-09 |
0.9840 |
0.407000 |
3.96e-01 |
0.787000 |
-1.63e-01 |
8.34e-03 |
1.03e-02 |
3.40e-07 |
2.90e-01 |
Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC) |
60 |
9.57e-21 |
2.85e-19 |
0.9690 |
0.511000 |
4.58e-01 |
0.504000 |
4.62e-01 |
7.36e-12 |
8.92e-10 |
1.50e-11 |
5.90e-10 |
Condensation of Prometaphase Chromosomes |
11 |
1.54e-06 |
7.54e-06 |
0.9530 |
0.531000 |
5.40e-01 |
0.475000 |
-3.30e-01 |
2.29e-03 |
1.92e-03 |
6.34e-03 |
5.83e-02 |
Mucopolysaccharidoses |
11 |
2.12e-04 |
8.01e-04 |
0.9520 |
-0.232000 |
-4.46e-02 |
0.647000 |
6.56e-01 |
1.83e-01 |
7.98e-01 |
2.01e-04 |
1.64e-04 |
G1/S-Specific Transcription |
26 |
4.52e-18 |
1.10e-16 |
0.9500 |
0.454000 |
4.42e-01 |
0.637000 |
-3.09e-01 |
6.18e-05 |
9.49e-05 |
1.85e-08 |
6.43e-03 |
Cholesterol biosynthesis |
23 |
1.53e-07 |
8.41e-07 |
0.9490 |
-0.333000 |
-5.08e-01 |
-0.487000 |
-5.44e-01 |
5.77e-03 |
2.46e-05 |
5.34e-05 |
6.35e-06 |
Mismatch repair (MMR) directed by MSH2:MSH6 (MutSalpha) |
14 |
1.18e-07 |
6.68e-07 |
0.9340 |
0.443000 |
4.35e-01 |
0.693000 |
-8.05e-02 |
4.11e-03 |
4.82e-03 |
7.08e-06 |
6.02e-01 |
L13a-mediated translational silencing of Ceruloplasmin expression |
73 |
1.21e-23 |
4.69e-22 |
0.9330 |
0.480000 |
4.29e-01 |
0.508000 |
4.44e-01 |
1.32e-12 |
2.46e-10 |
5.94e-14 |
5.31e-11 |
Interferon alpha/beta signaling |
45 |
2.21e-14 |
3.73e-13 |
0.9270 |
0.416000 |
6.19e-01 |
0.345000 |
4.30e-01 |
1.39e-06 |
6.72e-13 |
6.27e-05 |
6.11e-07 |
Polo-like kinase mediated events |
15 |
3.64e-09 |
2.83e-08 |
0.9160 |
0.518000 |
3.92e-01 |
0.578000 |
-2.90e-01 |
5.17e-04 |
8.61e-03 |
1.06e-04 |
5.20e-02 |
Condensation of Prophase Chromosomes |
13 |
9.05e-08 |
5.19e-07 |
0.9120 |
0.535000 |
4.26e-01 |
0.470000 |
-3.78e-01 |
8.37e-04 |
7.79e-03 |
3.37e-03 |
1.82e-02 |
GTP hydrolysis and joining of the 60S ribosomal subunit |
75 |
5.04e-23 |
1.69e-21 |
0.9110 |
0.473000 |
4.30e-01 |
0.489000 |
4.27e-01 |
1.38e-12 |
1.27e-10 |
2.51e-13 |
1.66e-10 |
Establishment of Sister Chromatid Cohesion |
10 |
7.19e-05 |
2.86e-04 |
0.9050 |
0.719000 |
3.46e-01 |
0.049000 |
-4.24e-01 |
8.17e-05 |
5.83e-02 |
7.88e-01 |
2.01e-02 |
PCNA-Dependent Long Patch Base Excision Repair |
21 |
1.86e-11 |
2.14e-10 |
0.9040 |
0.442000 |
4.06e-01 |
0.663000 |
-1.31e-01 |
4.51e-04 |
1.30e-03 |
1.46e-07 |
2.98e-01 |
Mitotic Telophase/Cytokinesis |
12 |
3.06e-06 |
1.46e-05 |
0.9020 |
0.676000 |
3.47e-01 |
0.142000 |
-4.65e-01 |
5.05e-05 |
3.73e-02 |
3.93e-01 |
5.31e-03 |
Selenoamino acid metabolism |
70 |
1.38e-20 |
4.03e-19 |
0.9020 |
0.468000 |
4.53e-01 |
0.446000 |
4.35e-01 |
1.25e-11 |
5.82e-11 |
1.07e-10 |
3.02e-10 |
Formation of the ternary complex, and subsequently, the 43S complex |
39 |
1.83e-11 |
2.13e-10 |
0.8930 |
0.439000 |
4.03e-01 |
0.519000 |
4.16e-01 |
2.13e-06 |
1.33e-05 |
2.05e-08 |
6.84e-06 |
G0 and Early G1 |
25 |
1.09e-14 |
1.91e-13 |
0.8830 |
0.465000 |
4.33e-01 |
0.496000 |
-3.60e-01 |
5.73e-05 |
1.80e-04 |
1.77e-05 |
1.82e-03 |
Cap-dependent Translation Initiation |
81 |
1.33e-23 |
4.73e-22 |
0.8820 |
0.444000 |
4.06e-01 |
0.504000 |
4.03e-01 |
5.18e-12 |
2.81e-10 |
4.52e-15 |
3.59e-10 |
Eukaryotic Translation Initiation |
81 |
1.33e-23 |
4.73e-22 |
0.8820 |
0.444000 |
4.06e-01 |
0.504000 |
4.03e-01 |
5.18e-12 |
2.81e-10 |
4.52e-15 |
3.59e-10 |
HDMs demethylate histones |
21 |
1.97e-06 |
9.56e-06 |
0.8760 |
-0.174000 |
-4.10e-01 |
-0.446000 |
-6.08e-01 |
1.68e-01 |
1.14e-03 |
3.98e-04 |
1.40e-06 |
Transcription of E2F targets under negative control by p107 (RBL1) and p130 (RBL2) in complex with HDAC1 |
15 |
6.72e-08 |
3.95e-07 |
0.8710 |
0.479000 |
4.02e-01 |
0.558000 |
-2.38e-01 |
1.31e-03 |
7.07e-03 |
1.84e-04 |
1.11e-01 |
LGI-ADAM interactions |
11 |
1.67e-03 |
5.38e-03 |
0.8640 |
-0.470000 |
-6.07e-01 |
-0.391000 |
-6.78e-02 |
6.97e-03 |
4.92e-04 |
2.49e-02 |
6.97e-01 |
Mismatch repair (MMR) directed by MSH2:MSH3 (MutSbeta) |
14 |
4.10e-06 |
1.91e-05 |
0.8550 |
0.393000 |
4.26e-01 |
0.627000 |
-4.42e-02 |
1.09e-02 |
5.76e-03 |
4.85e-05 |
7.75e-01 |
Trafficking and processing of endosomal TLR |
11 |
1.89e-03 |
5.97e-03 |
0.8530 |
0.216000 |
1.16e-01 |
0.492000 |
6.53e-01 |
2.15e-01 |
5.07e-01 |
4.72e-03 |
1.78e-04 |
Activation of ATR in response to replication stress |
35 |
4.75e-17 |
9.74e-16 |
0.8440 |
0.488000 |
4.09e-01 |
0.499000 |
-2.39e-01 |
5.85e-07 |
2.89e-05 |
3.21e-07 |
1.44e-02 |
Transcription of E2F targets under negative control by DREAM complex |
18 |
4.75e-09 |
3.64e-08 |
0.8250 |
0.410000 |
4.04e-01 |
0.521000 |
-2.80e-01 |
2.62e-03 |
2.98e-03 |
1.32e-04 |
3.95e-02 |
Termination of translesion DNA synthesis |
29 |
2.03e-13 |
3.00e-12 |
0.8220 |
0.409000 |
4.04e-01 |
0.560000 |
-1.76e-01 |
1.37e-04 |
1.64e-04 |
1.81e-07 |
1.01e-01 |
Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S |
46 |
2.71e-11 |
2.98e-10 |
0.8060 |
0.414000 |
3.62e-01 |
0.482000 |
3.39e-01 |
1.20e-06 |
2.23e-05 |
1.52e-08 |
7.00e-05 |
Presynaptic depolarization and calcium channel opening |
11 |
9.75e-03 |
2.45e-02 |
0.8000 |
-0.224000 |
-2.79e-01 |
-0.565000 |
-4.39e-01 |
1.98e-01 |
1.09e-01 |
1.17e-03 |
1.17e-02 |
Regulation of IFNA signaling |
12 |
4.92e-03 |
1.38e-02 |
0.7980 |
0.287000 |
4.82e-01 |
0.279000 |
4.94e-01 |
8.52e-02 |
3.83e-03 |
9.42e-02 |
3.02e-03 |
Mismatch Repair |
15 |
2.83e-06 |
1.36e-05 |
0.7980 |
0.358000 |
3.81e-01 |
0.594000 |
-1.06e-01 |
1.65e-02 |
1.07e-02 |
6.89e-05 |
4.77e-01 |
Translation initiation complex formation |
45 |
9.41e-11 |
9.73e-10 |
0.7970 |
0.402000 |
3.48e-01 |
0.478000 |
3.52e-01 |
3.02e-06 |
5.52e-05 |
2.96e-08 |
4.47e-05 |
Gap-filling DNA repair synthesis and ligation in GG-NER |
23 |
2.78e-10 |
2.70e-09 |
0.7960 |
0.380000 |
3.53e-01 |
0.582000 |
-1.62e-01 |
1.63e-03 |
3.38e-03 |
1.38e-06 |
1.79e-01 |
Phosphorylation of CD3 and TCR zeta chains |
11 |
1.39e-03 |
4.54e-03 |
0.7900 |
0.374000 |
6.30e-01 |
-0.295000 |
-1.66e-02 |
3.17e-02 |
2.95e-04 |
8.99e-02 |
9.24e-01 |
Ribosomal scanning and start codon recognition |
46 |
1.11e-10 |
1.13e-09 |
0.7850 |
0.413000 |
3.55e-01 |
0.461000 |
3.29e-01 |
1.28e-06 |
3.20e-05 |
6.55e-08 |
1.13e-04 |
Resolution of AP sites via the multiple-nucleotide patch replacement pathway |
24 |
2.46e-10 |
2.41e-09 |
0.7830 |
0.379000 |
3.19e-01 |
0.592000 |
-1.34e-01 |
1.32e-03 |
6.86e-03 |
5.19e-07 |
2.58e-01 |
DNA Replication Pre-Initiation |
77 |
6.37e-29 |
4.64e-27 |
0.7810 |
0.366000 |
3.53e-01 |
0.592000 |
-1.68e-02 |
2.79e-08 |
8.81e-08 |
2.55e-19 |
7.99e-01 |
Recognition of DNA damage by PCNA-containing replication complex |
28 |
2.13e-12 |
2.72e-11 |
0.7750 |
0.459000 |
2.74e-01 |
0.528000 |
-1.91e-01 |
2.67e-05 |
1.22e-02 |
1.33e-06 |
8.08e-02 |
E2F mediated regulation of DNA replication |
20 |
1.21e-09 |
1.02e-08 |
0.7730 |
0.408000 |
2.11e-01 |
0.587000 |
-2.03e-01 |
1.60e-03 |
1.03e-01 |
5.41e-06 |
1.17e-01 |
Phase 2 - plateau phase |
16 |
5.28e-04 |
1.84e-03 |
0.7720 |
-0.247000 |
-2.85e-01 |
-0.597000 |
-3.13e-01 |
8.73e-02 |
4.83e-02 |
3.59e-05 |
3.03e-02 |
Inhibition of replication initiation of damaged DNA by RB1/E2F1 |
12 |
1.51e-06 |
7.47e-06 |
0.7700 |
0.286000 |
1.11e-01 |
0.663000 |
-2.42e-01 |
8.67e-02 |
5.04e-01 |
7.00e-05 |
1.46e-01 |
Orc1 removal from chromatin |
63 |
9.26e-20 |
2.59e-18 |
0.7660 |
0.358000 |
3.59e-01 |
0.570000 |
7.18e-02 |
9.23e-07 |
8.48e-07 |
5.25e-15 |
3.25e-01 |
Striated Muscle Contraction |
28 |
7.73e-09 |
5.66e-08 |
0.7600 |
-0.039100 |
1.88e-01 |
-0.615000 |
-4.03e-01 |
7.21e-01 |
8.54e-02 |
1.78e-08 |
2.23e-04 |
Assembly of the pre-replicative complex |
61 |
1.62e-19 |
4.42e-18 |
0.7580 |
0.318000 |
3.31e-01 |
0.598000 |
7.61e-02 |
1.75e-05 |
7.94e-06 |
6.18e-16 |
3.05e-01 |
G1/S Transition |
119 |
4.04e-44 |
7.58e-42 |
0.7580 |
0.378000 |
3.56e-01 |
0.547000 |
-7.12e-02 |
1.10e-12 |
2.01e-11 |
6.53e-25 |
1.81e-01 |
Cyclin A/B1/B2 associated events during G2/M transition |
22 |
1.84e-08 |
1.23e-07 |
0.7550 |
0.514000 |
2.89e-01 |
0.434000 |
-1.81e-01 |
2.97e-05 |
1.88e-02 |
4.23e-04 |
1.42e-01 |
Cross-presentation of soluble exogenous antigens (endosomes) |
45 |
3.39e-11 |
3.67e-10 |
0.7530 |
0.256000 |
3.02e-01 |
0.584000 |
2.65e-01 |
2.98e-03 |
4.64e-04 |
1.24e-11 |
2.13e-03 |
Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC) |
80 |
1.30e-16 |
2.50e-15 |
0.7520 |
0.444000 |
3.88e-01 |
0.364000 |
2.94e-01 |
7.02e-12 |
1.97e-09 |
1.94e-08 |
5.78e-06 |
Nonsense-Mediated Decay (NMD) |
80 |
1.30e-16 |
2.50e-15 |
0.7520 |
0.444000 |
3.88e-01 |
0.364000 |
2.94e-01 |
7.02e-12 |
1.97e-09 |
1.94e-08 |
5.78e-06 |
EGR2 and SOX10-mediated initiation of Schwann cell myelination |
21 |
3.61e-04 |
1.30e-03 |
0.7470 |
-0.312000 |
-3.43e-01 |
-0.424000 |
-4.05e-01 |
1.33e-02 |
6.57e-03 |
7.73e-04 |
1.31e-03 |
Regulation of expression of SLITs and ROBOs |
120 |
7.26e-25 |
3.67e-23 |
0.7430 |
0.362000 |
3.53e-01 |
0.438000 |
3.23e-01 |
7.89e-12 |
2.48e-11 |
1.18e-16 |
1.03e-09 |
Telomere C-strand (Lagging Strand) Synthesis |
33 |
1.27e-14 |
2.19e-13 |
0.7430 |
0.293000 |
3.52e-01 |
0.534000 |
-2.38e-01 |
3.59e-03 |
4.71e-04 |
1.12e-07 |
1.79e-02 |
Activation of gene expression by SREBF (SREBP) |
41 |
1.86e-08 |
1.24e-07 |
0.7350 |
-0.174000 |
-3.31e-01 |
-0.404000 |
-4.87e-01 |
5.34e-02 |
2.43e-04 |
7.70e-06 |
6.95e-08 |
HSF1-dependent transactivation |
31 |
3.91e-06 |
1.84e-05 |
0.7340 |
-0.495000 |
-4.62e-01 |
-0.103000 |
-2.64e-01 |
1.88e-06 |
8.63e-06 |
3.19e-01 |
1.11e-02 |
Synthesis of DNA |
112 |
3.21e-38 |
3.83e-36 |
0.7260 |
0.352000 |
3.02e-01 |
0.557000 |
-3.64e-02 |
1.31e-10 |
3.35e-08 |
2.13e-24 |
5.07e-01 |
DNA Replication |
119 |
1.41e-41 |
2.31e-39 |
0.7240 |
0.353000 |
2.99e-01 |
0.554000 |
-5.73e-02 |
3.21e-11 |
1.82e-08 |
1.62e-25 |
2.82e-01 |
tRNA processing in the mitochondrion |
16 |
8.47e-04 |
2.87e-03 |
0.7210 |
0.105000 |
1.47e-01 |
-0.527000 |
-4.57e-01 |
4.67e-01 |
3.08e-01 |
2.61e-04 |
1.57e-03 |
Polymerase switching on the C-strand of the telomere |
25 |
1.14e-09 |
9.70e-09 |
0.7180 |
0.290000 |
3.55e-01 |
0.521000 |
-1.86e-01 |
1.20e-02 |
2.14e-03 |
6.62e-06 |
1.08e-01 |
Mitotic G1 phase and G1/S transition |
135 |
1.37e-44 |
3.37e-42 |
0.7160 |
0.381000 |
3.45e-01 |
0.490000 |
-9.15e-02 |
2.39e-14 |
4.50e-12 |
9.21e-23 |
6.72e-02 |
Ubiquitin Mediated Degradation of Phosphorylated Cdc25A |
46 |
2.59e-11 |
2.88e-10 |
0.7070 |
0.199000 |
2.86e-01 |
0.584000 |
1.96e-01 |
1.99e-02 |
7.86e-04 |
7.44e-12 |
2.16e-02 |
p53-Independent DNA Damage Response |
46 |
2.59e-11 |
2.88e-10 |
0.7070 |
0.199000 |
2.86e-01 |
0.584000 |
1.96e-01 |
1.99e-02 |
7.86e-04 |
7.44e-12 |
2.16e-02 |
p53-Independent G1/S DNA damage checkpoint |
46 |
2.59e-11 |
2.88e-10 |
0.7070 |
0.199000 |
2.86e-01 |
0.584000 |
1.96e-01 |
1.99e-02 |
7.86e-04 |
7.44e-12 |
2.16e-02 |
CDC6 association with the ORC:origin complex |
10 |
1.34e-03 |
4.39e-03 |
0.7070 |
0.450000 |
2.48e-01 |
0.449000 |
-1.83e-01 |
1.37e-02 |
1.74e-01 |
1.39e-02 |
3.16e-01 |
Metabolism of polyamines |
52 |
7.76e-12 |
9.42e-11 |
0.7040 |
0.248000 |
2.97e-01 |
0.550000 |
2.08e-01 |
1.95e-03 |
2.14e-04 |
6.88e-12 |
9.41e-03 |
Deposition of new CENPA-containing nucleosomes at the centromere |
22 |
1.27e-08 |
8.93e-08 |
0.7040 |
0.337000 |
2.24e-01 |
0.547000 |
-1.80e-01 |
6.30e-03 |
6.91e-02 |
8.84e-06 |
1.44e-01 |
Nucleosome assembly |
22 |
1.27e-08 |
8.93e-08 |
0.7040 |
0.337000 |
2.24e-01 |
0.547000 |
-1.80e-01 |
6.30e-03 |
6.91e-02 |
8.84e-06 |
1.44e-01 |
CDT1 association with the CDC6:ORC:origin complex |
52 |
4.35e-13 |
6.20e-12 |
0.7020 |
0.269000 |
2.70e-01 |
0.571000 |
1.49e-01 |
8.09e-04 |
7.73e-04 |
1.04e-12 |
6.37e-02 |
SCF(Skp2)-mediated degradation of p27/p21 |
52 |
4.45e-13 |
6.28e-12 |
0.7010 |
0.257000 |
3.32e-01 |
0.547000 |
1.23e-01 |
1.35e-03 |
3.45e-05 |
8.54e-12 |
1.25e-01 |
Processive synthesis on the C-strand of the telomere |
19 |
4.70e-07 |
2.46e-06 |
0.6980 |
0.283000 |
4.17e-01 |
0.402000 |
-2.68e-01 |
3.30e-02 |
1.64e-03 |
2.42e-03 |
4.33e-02 |
Ubiquitin-dependent degradation of Cyclin D |
46 |
4.82e-10 |
4.46e-09 |
0.6980 |
0.212000 |
2.69e-01 |
0.557000 |
2.44e-01 |
1.29e-02 |
1.59e-03 |
6.54e-11 |
4.26e-03 |
Regulation of activated PAK-2p34 by proteasome mediated degradation |
44 |
1.03e-09 |
8.83e-09 |
0.6890 |
0.223000 |
2.71e-01 |
0.555000 |
2.11e-01 |
1.06e-02 |
1.88e-03 |
1.96e-10 |
1.54e-02 |
Glycogen storage diseases |
11 |
2.71e-02 |
5.65e-02 |
0.6870 |
-0.431000 |
-5.13e-01 |
0.043500 |
1.41e-01 |
1.32e-02 |
3.20e-03 |
8.03e-01 |
4.18e-01 |
Regulation of Complement cascade |
31 |
1.06e-05 |
4.75e-05 |
0.6860 |
0.239000 |
3.64e-01 |
0.254000 |
4.65e-01 |
2.12e-02 |
4.57e-04 |
1.45e-02 |
7.49e-06 |
Regulation of ornithine decarboxylase (ODC) |
46 |
1.65e-10 |
1.64e-09 |
0.6800 |
0.222000 |
2.34e-01 |
0.569000 |
1.87e-01 |
9.23e-03 |
6.05e-03 |
2.47e-11 |
2.87e-02 |
Removal of the Flap Intermediate from the C-strand |
17 |
1.23e-05 |
5.47e-05 |
0.6780 |
0.283000 |
4.36e-01 |
0.363000 |
-2.41e-01 |
4.37e-02 |
1.88e-03 |
9.65e-03 |
8.49e-02 |
Vif-mediated degradation of APOBEC3G |
45 |
1.50e-09 |
1.23e-08 |
0.6780 |
0.221000 |
2.56e-01 |
0.547000 |
2.14e-01 |
1.02e-02 |
3.01e-03 |
2.21e-10 |
1.31e-02 |
Translesion synthesis by POLI |
15 |
4.53e-05 |
1.88e-04 |
0.6760 |
0.321000 |
2.50e-01 |
0.520000 |
-1.46e-01 |
3.12e-02 |
9.38e-02 |
4.91e-04 |
3.28e-01 |
Negative regulation of NOTCH4 signaling |
48 |
1.36e-09 |
1.13e-08 |
0.6760 |
0.257000 |
2.87e-01 |
0.511000 |
2.16e-01 |
2.07e-03 |
5.76e-04 |
9.01e-10 |
9.76e-03 |
Translesion synthesis by Y family DNA polymerases bypasses lesions on DNA template |
35 |
1.23e-11 |
1.47e-10 |
0.6730 |
0.327000 |
3.01e-01 |
0.474000 |
-1.76e-01 |
8.22e-04 |
2.07e-03 |
1.21e-06 |
7.15e-02 |
Chk1/Chk2(Cds1) mediated inactivation of Cyclin B:Cdk1 complex |
12 |
9.80e-03 |
2.46e-02 |
0.6720 |
0.401000 |
4.51e-01 |
0.283000 |
-9.10e-02 |
1.62e-02 |
6.85e-03 |
9.00e-02 |
5.85e-01 |
Laminin interactions |
22 |
1.74e-05 |
7.60e-05 |
0.6720 |
-0.222000 |
-2.85e-02 |
-0.582000 |
-2.51e-01 |
7.14e-02 |
8.17e-01 |
2.27e-06 |
4.16e-02 |
S Phase |
152 |
1.54e-44 |
3.37e-42 |
0.6720 |
0.366000 |
2.96e-01 |
0.474000 |
-7.21e-02 |
6.93e-15 |
3.16e-10 |
6.87e-24 |
1.26e-01 |
Generation of second messenger molecules |
22 |
5.74e-06 |
2.65e-05 |
0.6720 |
0.238000 |
4.64e-01 |
-0.417000 |
-7.16e-02 |
5.37e-02 |
1.63e-04 |
7.12e-04 |
5.61e-01 |
Translesion synthesis by REV1 |
14 |
6.15e-05 |
2.47e-04 |
0.6710 |
0.329000 |
2.42e-01 |
0.490000 |
-2.05e-01 |
3.29e-02 |
1.17e-01 |
1.49e-03 |
1.84e-01 |
Hyaluronan uptake and degradation |
11 |
4.06e-02 |
7.77e-02 |
0.6650 |
0.242000 |
2.03e-01 |
0.502000 |
3.02e-01 |
1.65e-01 |
2.44e-01 |
3.93e-03 |
8.31e-02 |
PI-3K cascade:FGFR2 |
12 |
7.19e-04 |
2.46e-03 |
0.6640 |
-0.012500 |
-5.60e-01 |
-0.269000 |
-2.35e-01 |
9.40e-01 |
7.91e-04 |
1.06e-01 |
1.58e-01 |
SCF-beta-TrCP mediated degradation of Emi1 |
49 |
3.53e-11 |
3.77e-10 |
0.6640 |
0.212000 |
2.45e-01 |
0.560000 |
1.51e-01 |
1.03e-02 |
3.02e-03 |
1.22e-11 |
6.78e-02 |
Extension of Telomeres |
48 |
2.15e-17 |
4.56e-16 |
0.6620 |
0.262000 |
3.13e-01 |
0.462000 |
-2.40e-01 |
1.71e-03 |
1.75e-04 |
3.01e-08 |
4.02e-03 |
Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell |
48 |
2.85e-08 |
1.81e-07 |
0.6610 |
0.285000 |
3.89e-01 |
0.183000 |
4.13e-01 |
6.46e-04 |
3.12e-06 |
2.86e-02 |
7.41e-07 |
DNA Damage Bypass |
44 |
3.35e-14 |
5.49e-13 |
0.6600 |
0.375000 |
2.63e-01 |
0.436000 |
-1.91e-01 |
1.66e-05 |
2.57e-03 |
5.76e-07 |
2.87e-02 |
Translesion synthesis by POLK |
15 |
8.51e-05 |
3.34e-04 |
0.6550 |
0.333000 |
2.69e-01 |
0.456000 |
-1.93e-01 |
2.54e-02 |
7.17e-02 |
2.25e-03 |
1.95e-01 |
ATF6 (ATF6-alpha) activates chaperone genes |
10 |
9.19e-05 |
3.58e-04 |
0.6540 |
0.364000 |
-1.99e-01 |
0.502000 |
-6.00e-02 |
4.63e-02 |
2.77e-01 |
5.96e-03 |
7.43e-01 |
Heme biosynthesis |
13 |
3.93e-05 |
1.65e-04 |
0.6520 |
-0.209000 |
-2.27e-01 |
0.472000 |
-3.28e-01 |
1.92e-01 |
1.56e-01 |
3.24e-03 |
4.09e-02 |
Common Pathway of Fibrin Clot Formation |
10 |
1.58e-03 |
5.10e-03 |
0.6520 |
0.305000 |
2.34e-01 |
-0.274000 |
4.49e-01 |
9.47e-02 |
2.00e-01 |
1.33e-01 |
1.40e-02 |
Autodegradation of the E3 ubiquitin ligase COP1 |
46 |
1.97e-09 |
1.59e-08 |
0.6510 |
0.186000 |
2.39e-01 |
0.543000 |
1.92e-01 |
2.94e-02 |
5.06e-03 |
1.84e-10 |
2.40e-02 |
rRNA processing in the mitochondrion |
17 |
3.25e-03 |
9.71e-03 |
0.6510 |
0.116000 |
6.34e-02 |
-0.407000 |
-4.90e-01 |
4.09e-01 |
6.51e-01 |
3.68e-03 |
4.64e-04 |
Defective CFTR causes cystic fibrosis |
52 |
2.26e-09 |
1.78e-08 |
0.6500 |
0.197000 |
2.47e-01 |
0.506000 |
2.58e-01 |
1.38e-02 |
2.04e-03 |
2.80e-10 |
1.28e-03 |
Signaling by FGFR4 in disease |
10 |
2.86e-02 |
5.88e-02 |
0.6480 |
0.147000 |
-1.65e-01 |
-0.351000 |
-4.98e-01 |
4.23e-01 |
3.66e-01 |
5.44e-02 |
6.36e-03 |
Attenuation phase |
21 |
7.92e-04 |
2.70e-03 |
0.6460 |
-0.427000 |
-3.81e-01 |
0.008280 |
-2.99e-01 |
7.09e-04 |
2.52e-03 |
9.48e-01 |
1.76e-02 |
Influenza Viral RNA Transcription and Replication |
96 |
1.91e-17 |
4.17e-16 |
0.6450 |
0.319000 |
2.44e-01 |
0.456000 |
2.16e-01 |
7.05e-08 |
3.71e-05 |
1.13e-14 |
2.57e-04 |
Vpu mediated degradation of CD4 |
46 |
4.91e-09 |
3.74e-08 |
0.6430 |
0.216000 |
2.52e-01 |
0.520000 |
1.79e-01 |
1.12e-02 |
3.18e-03 |
1.02e-09 |
3.55e-02 |
FBXL7 down-regulates AURKA during mitotic entry and in early mitosis |
49 |
2.13e-09 |
1.70e-08 |
0.6400 |
0.211000 |
2.47e-01 |
0.517000 |
1.92e-01 |
1.08e-02 |
2.75e-03 |
3.75e-10 |
2.04e-02 |
cGMP effects |
12 |
1.88e-04 |
7.17e-04 |
0.6390 |
-0.145000 |
9.65e-02 |
-0.610000 |
7.49e-02 |
3.83e-01 |
5.63e-01 |
2.51e-04 |
6.53e-01 |
Diseases of carbohydrate metabolism |
27 |
5.72e-05 |
2.30e-04 |
0.6390 |
-0.269000 |
-2.18e-01 |
0.385000 |
3.74e-01 |
1.54e-02 |
5.05e-02 |
5.43e-04 |
7.72e-04 |
WNT5A-dependent internalization of FZD2, FZD5 and ROR2 |
13 |
9.49e-03 |
2.40e-02 |
0.6380 |
-0.256000 |
-1.82e-01 |
0.505000 |
2.30e-01 |
1.10e-01 |
2.55e-01 |
1.60e-03 |
1.50e-01 |
Signaling by FGFR3 fusions in cancer |
10 |
1.15e-02 |
2.80e-02 |
0.6380 |
0.334000 |
-7.98e-02 |
-0.293000 |
-4.51e-01 |
6.72e-02 |
6.62e-01 |
1.09e-01 |
1.36e-02 |
P2Y receptors |
10 |
4.32e-02 |
8.18e-02 |
0.6370 |
0.416000 |
3.84e-01 |
-0.109000 |
2.71e-01 |
2.29e-02 |
3.54e-02 |
5.50e-01 |
1.37e-01 |
PD-1 signaling |
10 |
2.15e-02 |
4.68e-02 |
0.6370 |
0.232000 |
4.61e-01 |
-0.351000 |
-1.26e-01 |
2.04e-01 |
1.16e-02 |
5.44e-02 |
4.90e-01 |
Cyclin E associated events during G1/S transition |
75 |
2.27e-16 |
4.26e-15 |
0.6360 |
0.269000 |
3.02e-01 |
0.486000 |
6.39e-02 |
5.62e-05 |
6.10e-06 |
3.32e-13 |
3.39e-01 |
The role of GTSE1 in G2/M progression after G2 checkpoint |
54 |
1.62e-11 |
1.90e-10 |
0.6360 |
0.196000 |
2.41e-01 |
0.538000 |
1.34e-01 |
1.28e-02 |
2.19e-03 |
7.85e-12 |
8.83e-02 |
Hh mutants that don't undergo autocatalytic processing are degraded by ERAD |
48 |
7.66e-09 |
5.65e-08 |
0.6340 |
0.164000 |
2.20e-01 |
0.524000 |
2.28e-01 |
4.96e-02 |
8.55e-03 |
3.35e-10 |
6.20e-03 |
G2/M Checkpoints |
124 |
4.64e-31 |
3.81e-29 |
0.6320 |
0.314000 |
3.03e-01 |
0.455000 |
-4.95e-02 |
1.58e-09 |
6.09e-09 |
2.35e-18 |
3.42e-01 |
Complement cascade |
34 |
3.42e-05 |
1.44e-04 |
0.6320 |
0.228000 |
3.54e-01 |
0.239000 |
4.05e-01 |
2.13e-02 |
3.53e-04 |
1.60e-02 |
4.33e-05 |
Cyclin A:Cdk2-associated events at S phase entry |
77 |
2.70e-17 |
5.63e-16 |
0.6320 |
0.263000 |
3.01e-01 |
0.487000 |
4.20e-02 |
6.57e-05 |
5.18e-06 |
1.47e-13 |
5.25e-01 |
Switching of origins to a post-replicative state |
83 |
2.08e-19 |
5.57e-18 |
0.6310 |
0.294000 |
2.48e-01 |
0.499000 |
3.38e-02 |
3.76e-06 |
9.49e-05 |
4.16e-15 |
5.95e-01 |
G beta:gamma signalling through BTK |
13 |
7.16e-03 |
1.91e-02 |
0.6210 |
0.021800 |
1.57e-01 |
0.159000 |
5.79e-01 |
8.92e-01 |
3.29e-01 |
3.22e-01 |
3.02e-04 |
HDR through Homologous Recombination (HRR) |
61 |
3.54e-19 |
9.10e-18 |
0.6180 |
0.288000 |
2.30e-01 |
0.454000 |
-2.02e-01 |
1.03e-04 |
1.94e-03 |
8.93e-10 |
6.30e-03 |
AUF1 (hnRNP D0) binds and destabilizes mRNA |
48 |
1.43e-09 |
1.18e-08 |
0.6170 |
0.154000 |
1.96e-01 |
0.542000 |
1.59e-01 |
6.60e-02 |
1.89e-02 |
8.40e-11 |
5.64e-02 |
Hh mutants abrogate ligand secretion |
50 |
8.15e-09 |
5.91e-08 |
0.6160 |
0.156000 |
2.11e-01 |
0.514000 |
2.17e-01 |
5.62e-02 |
1.01e-02 |
3.29e-10 |
7.98e-03 |
Downregulation of SMAD2/3:SMAD4 transcriptional activity |
20 |
4.00e-04 |
1.41e-03 |
0.6150 |
0.026800 |
-3.42e-01 |
-0.312000 |
-4.04e-01 |
8.36e-01 |
8.15e-03 |
1.58e-02 |
1.75e-03 |
Effects of PIP2 hydrolysis |
22 |
1.42e-04 |
5.49e-04 |
0.6130 |
-0.347000 |
-5.45e-02 |
-0.388000 |
-3.19e-01 |
4.83e-03 |
6.58e-01 |
1.65e-03 |
9.63e-03 |
Regulation of Apoptosis |
47 |
2.98e-08 |
1.87e-07 |
0.6120 |
0.184000 |
2.03e-01 |
0.509000 |
2.01e-01 |
2.94e-02 |
1.63e-02 |
1.58e-09 |
1.71e-02 |
Prostacyclin signalling through prostacyclin receptor |
14 |
8.53e-03 |
2.19e-02 |
0.6100 |
0.031400 |
1.79e-01 |
0.188000 |
5.51e-01 |
8.39e-01 |
2.47e-01 |
2.24e-01 |
3.55e-04 |
Chromosome Maintenance |
82 |
2.48e-24 |
1.09e-22 |
0.6090 |
0.252000 |
2.55e-01 |
0.464000 |
-1.66e-01 |
7.95e-05 |
6.53e-05 |
3.95e-13 |
9.54e-03 |
ER-Phagosome pathway |
69 |
7.24e-10 |
6.42e-09 |
0.6080 |
0.200000 |
2.65e-01 |
0.423000 |
2.84e-01 |
4.19e-03 |
1.43e-04 |
1.22e-09 |
4.68e-05 |
Constitutive Signaling by NOTCH1 HD Domain Mutants |
12 |
2.32e-04 |
8.69e-04 |
0.6060 |
-0.452000 |
1.24e-01 |
-0.323000 |
-2.07e-01 |
6.74e-03 |
4.57e-01 |
5.24e-02 |
2.15e-01 |
Signaling by NOTCH1 HD Domain Mutants in Cancer |
12 |
2.32e-04 |
8.69e-04 |
0.6060 |
-0.452000 |
1.24e-01 |
-0.323000 |
-2.07e-01 |
6.74e-03 |
4.57e-01 |
5.24e-02 |
2.15e-01 |
Activation of APC/C and APC/C:Cdc20 mediated degradation of mitotic proteins |
70 |
1.96e-14 |
3.34e-13 |
0.6040 |
0.249000 |
2.02e-01 |
0.505000 |
8.61e-02 |
3.27e-04 |
3.54e-03 |
2.69e-13 |
2.13e-01 |
Translesion Synthesis by POLH |
16 |
1.36e-05 |
6.05e-05 |
0.6040 |
0.144000 |
6.89e-02 |
0.547000 |
-2.02e-01 |
3.20e-01 |
6.33e-01 |
1.52e-04 |
1.63e-01 |
Antigen processing-Cross presentation |
83 |
4.46e-11 |
4.69e-10 |
0.6040 |
0.223000 |
2.83e-01 |
0.374000 |
3.07e-01 |
4.39e-04 |
8.53e-06 |
3.94e-09 |
1.34e-06 |
Signaling by Leptin |
10 |
1.46e-01 |
2.19e-01 |
0.6010 |
-0.296000 |
-4.11e-01 |
-0.279000 |
-1.64e-01 |
1.05e-01 |
2.43e-02 |
1.27e-01 |
3.69e-01 |
Resolution of D-loop Structures through Synthesis-Dependent Strand Annealing (SDSA) |
24 |
1.43e-08 |
9.91e-08 |
0.6010 |
0.185000 |
1.21e-01 |
0.486000 |
-2.76e-01 |
1.17e-01 |
3.07e-01 |
3.79e-05 |
1.92e-02 |
APC:Cdc20 mediated degradation of cell cycle proteins prior to satisfation of the cell cycle checkpoint |
67 |
3.01e-13 |
4.39e-12 |
0.6000 |
0.237000 |
1.97e-01 |
0.504000 |
1.05e-01 |
8.08e-04 |
5.42e-03 |
9.35e-13 |
1.39e-01 |
Collagen chain trimerization |
32 |
3.87e-10 |
3.65e-09 |
0.6000 |
-0.455000 |
-7.76e-02 |
-0.348000 |
1.63e-01 |
8.50e-06 |
4.48e-01 |
6.71e-04 |
1.12e-01 |
Diseases associated with N-glycosylation of proteins |
16 |
6.80e-03 |
1.83e-02 |
0.6000 |
-0.228000 |
-3.38e-01 |
0.358000 |
2.55e-01 |
1.15e-01 |
1.93e-02 |
1.32e-02 |
7.70e-02 |
FRS-mediated FGFR2 signaling |
14 |
4.67e-03 |
1.33e-02 |
0.5980 |
-0.072000 |
-4.80e-01 |
-0.267000 |
-2.26e-01 |
6.41e-01 |
1.88e-03 |
8.32e-02 |
1.43e-01 |
APC/C:Cdc20 mediated degradation of mitotic proteins |
69 |
9.73e-14 |
1.56e-12 |
0.5980 |
0.242000 |
1.97e-01 |
0.501000 |
9.39e-02 |
5.08e-04 |
4.70e-03 |
6.35e-13 |
1.78e-01 |
Formation of Fibrin Clot (Clotting Cascade) |
17 |
3.31e-04 |
1.20e-03 |
0.5970 |
0.312000 |
2.07e-01 |
-0.090200 |
4.56e-01 |
2.60e-02 |
1.39e-01 |
5.20e-01 |
1.13e-03 |
FRS-mediated FGFR4 signaling |
11 |
1.36e-02 |
3.22e-02 |
0.5960 |
-0.026400 |
-4.66e-01 |
-0.202000 |
-3.11e-01 |
8.80e-01 |
7.46e-03 |
2.46e-01 |
7.42e-02 |
Cdc20:Phospho-APC/C mediated degradation of Cyclin A |
66 |
1.01e-12 |
1.34e-11 |
0.5950 |
0.228000 |
1.88e-01 |
0.504000 |
1.14e-01 |
1.40e-03 |
8.46e-03 |
1.44e-12 |
1.11e-01 |
Regulation of cholesterol biosynthesis by SREBP (SREBF) |
54 |
8.84e-08 |
5.09e-07 |
0.5940 |
-0.108000 |
-3.09e-01 |
-0.320000 |
-3.78e-01 |
1.69e-01 |
8.53e-05 |
4.70e-05 |
1.61e-06 |
Resolution of Sister Chromatid Cohesion |
95 |
1.18e-32 |
1.03e-30 |
0.5920 |
0.308000 |
1.18e-01 |
0.375000 |
-3.18e-01 |
2.28e-07 |
4.76e-02 |
2.77e-10 |
8.77e-08 |
PI-3K cascade:FGFR3 |
10 |
4.22e-03 |
1.22e-02 |
0.5920 |
0.151000 |
-4.19e-01 |
-0.207000 |
-3.30e-01 |
4.08e-01 |
2.19e-02 |
2.57e-01 |
7.04e-02 |
TP53 Regulates Transcription of Death Receptors and Ligands |
11 |
4.30e-02 |
8.15e-02 |
0.5900 |
-0.207000 |
-6.35e-02 |
-0.499000 |
-2.28e-01 |
2.35e-01 |
7.15e-01 |
4.15e-03 |
1.90e-01 |
Interferon gamma signaling |
63 |
8.53e-10 |
7.41e-09 |
0.5890 |
0.247000 |
3.41e-01 |
0.098400 |
4.01e-01 |
7.10e-04 |
2.95e-06 |
1.77e-01 |
3.87e-08 |
Competing endogenous RNAs (ceRNAs) regulate PTEN translation |
10 |
1.58e-01 |
2.32e-01 |
0.5880 |
-0.233000 |
-3.01e-01 |
-0.385000 |
-2.31e-01 |
2.01e-01 |
9.96e-02 |
3.53e-02 |
2.06e-01 |
Retrograde neurotrophin signalling |
13 |
2.10e-02 |
4.58e-02 |
0.5880 |
-0.278000 |
-1.66e-01 |
0.450000 |
1.94e-01 |
8.26e-02 |
2.99e-01 |
4.94e-03 |
2.25e-01 |
Signaling by FGFR3 in disease |
14 |
5.54e-03 |
1.54e-02 |
0.5870 |
0.166000 |
-2.19e-01 |
-0.304000 |
-4.21e-01 |
2.83e-01 |
1.56e-01 |
4.89e-02 |
6.43e-03 |
Signaling by FGFR3 point mutants in cancer |
14 |
5.54e-03 |
1.54e-02 |
0.5870 |
0.166000 |
-2.19e-01 |
-0.304000 |
-4.21e-01 |
2.83e-01 |
1.56e-01 |
4.89e-02 |
6.43e-03 |
Purine catabolism |
16 |
7.58e-03 |
2.01e-02 |
0.5860 |
0.114000 |
2.32e-01 |
0.499000 |
1.65e-01 |
4.30e-01 |
1.09e-01 |
5.48e-04 |
2.54e-01 |
Homologous DNA Pairing and Strand Exchange |
40 |
4.61e-12 |
5.65e-11 |
0.5850 |
0.250000 |
1.75e-01 |
0.450000 |
-2.16e-01 |
6.22e-03 |
5.60e-02 |
8.62e-07 |
1.79e-02 |
Regulation of pyruvate dehydrogenase (PDH) complex |
15 |
1.11e-02 |
2.72e-02 |
0.5850 |
-0.021600 |
-3.48e-01 |
-0.302000 |
-3.60e-01 |
8.85e-01 |
1.96e-02 |
4.30e-02 |
1.59e-02 |
Presynaptic phase of homologous DNA pairing and strand exchange |
37 |
2.43e-10 |
2.40e-09 |
0.5840 |
0.273000 |
2.04e-01 |
0.432000 |
-1.94e-01 |
4.02e-03 |
3.21e-02 |
5.40e-06 |
4.15e-02 |
Regulation of APC/C activators between G1/S and early anaphase |
74 |
3.26e-15 |
5.93e-14 |
0.5840 |
0.243000 |
1.92e-01 |
0.492000 |
4.80e-02 |
3.06e-04 |
4.27e-03 |
2.50e-13 |
4.76e-01 |
Stabilization of p53 |
50 |
2.50e-08 |
1.61e-07 |
0.5830 |
0.204000 |
2.35e-01 |
0.473000 |
1.40e-01 |
1.25e-02 |
4.03e-03 |
7.51e-09 |
8.69e-02 |
APC/C-mediated degradation of cell cycle proteins |
81 |
9.79e-18 |
2.22e-16 |
0.5830 |
0.245000 |
1.94e-01 |
0.492000 |
1.08e-02 |
1.40e-04 |
2.59e-03 |
2.00e-14 |
8.66e-01 |
Regulation of mitotic cell cycle |
81 |
9.79e-18 |
2.22e-16 |
0.5830 |
0.245000 |
1.94e-01 |
0.492000 |
1.08e-02 |
1.40e-04 |
2.59e-03 |
2.00e-14 |
8.66e-01 |
Telomere Maintenance |
62 |
1.05e-16 |
2.12e-15 |
0.5830 |
0.222000 |
2.63e-01 |
0.443000 |
-1.58e-01 |
2.49e-03 |
3.42e-04 |
1.70e-09 |
3.16e-02 |
Formation of Senescence-Associated Heterochromatin Foci (SAHF) |
10 |
3.34e-03 |
9.94e-03 |
0.5810 |
-0.201000 |
-1.88e-01 |
0.356000 |
-3.66e-01 |
2.72e-01 |
3.03e-01 |
5.10e-02 |
4.48e-02 |
Influenza Infection |
112 |
3.44e-18 |
8.53e-17 |
0.5800 |
0.310000 |
2.04e-01 |
0.421000 |
1.49e-01 |
1.52e-08 |
2.03e-04 |
1.56e-14 |
6.55e-03 |
Translation |
230 |
3.88e-33 |
3.63e-31 |
0.5780 |
0.139000 |
1.07e-01 |
0.453000 |
3.13e-01 |
3.08e-04 |
5.48e-03 |
2.95e-32 |
3.29e-16 |
Autodegradation of Cdh1 by Cdh1:APC/C |
58 |
4.99e-10 |
4.58e-09 |
0.5740 |
0.164000 |
1.61e-01 |
0.505000 |
1.50e-01 |
3.14e-02 |
3.42e-02 |
3.00e-11 |
4.83e-02 |
HDR through Homologous Recombination (HRR) or Single Strand Annealing (SSA) |
89 |
1.26e-22 |
4.15e-21 |
0.5740 |
0.307000 |
2.29e-01 |
0.388000 |
-1.78e-01 |
5.64e-07 |
1.87e-04 |
2.49e-10 |
3.68e-03 |
APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins in late mitosis/early G1 |
68 |
8.86e-13 |
1.19e-11 |
0.5710 |
0.201000 |
1.60e-01 |
0.501000 |
9.54e-02 |
4.26e-03 |
2.24e-02 |
8.97e-13 |
1.74e-01 |
Resolution of D-Loop Structures |
30 |
6.70e-09 |
4.97e-08 |
0.5690 |
0.225000 |
1.60e-01 |
0.436000 |
-2.40e-01 |
3.32e-02 |
1.29e-01 |
3.58e-05 |
2.31e-02 |
Amplification of signal from unattached kinetochores via a MAD2 inhibitory signal |
83 |
3.78e-28 |
2.48e-26 |
0.5680 |
0.243000 |
7.13e-02 |
0.397000 |
-3.18e-01 |
1.36e-04 |
2.62e-01 |
4.01e-10 |
5.82e-07 |
Amplification of signal from the kinetochores |
83 |
3.78e-28 |
2.48e-26 |
0.5680 |
0.243000 |
7.13e-02 |
0.397000 |
-3.18e-01 |
1.36e-04 |
2.62e-01 |
4.01e-10 |
5.82e-07 |
FOXO-mediated transcription of oxidative stress, metabolic and neuronal genes |
20 |
9.04e-03 |
2.30e-02 |
0.5670 |
-0.012100 |
-1.35e-01 |
-0.323000 |
-4.46e-01 |
9.25e-01 |
2.95e-01 |
1.25e-02 |
5.48e-04 |
TP53 Regulates Transcription of Genes Involved in G2 Cell Cycle Arrest |
17 |
1.85e-05 |
8.02e-05 |
0.5660 |
0.082300 |
1.72e-01 |
0.472000 |
-2.47e-01 |
5.57e-01 |
2.20e-01 |
7.47e-04 |
7.77e-02 |
ABC transporter disorders |
60 |
1.35e-08 |
9.40e-08 |
0.5660 |
0.148000 |
1.89e-01 |
0.464000 |
2.17e-01 |
4.73e-02 |
1.15e-02 |
5.09e-10 |
3.70e-03 |
CDK-mediated phosphorylation and removal of Cdc6 |
66 |
9.42e-12 |
1.13e-10 |
0.5650 |
0.208000 |
1.79e-01 |
0.484000 |
9.59e-02 |
3.49e-03 |
1.18e-02 |
1.03e-11 |
1.78e-01 |
Mitochondrial translation elongation |
85 |
1.42e-13 |
2.17e-12 |
0.5650 |
-0.042900 |
-4.00e-02 |
0.499000 |
2.57e-01 |
4.94e-01 |
5.25e-01 |
1.74e-15 |
4.31e-05 |
Degradation of DVL |
50 |
3.68e-08 |
2.26e-07 |
0.5640 |
0.170000 |
2.03e-01 |
0.480000 |
1.34e-01 |
3.82e-02 |
1.31e-02 |
4.47e-09 |
1.02e-01 |
Resolution of D-loop Structures through Holliday Junction Intermediates |
29 |
2.49e-08 |
1.61e-07 |
0.5610 |
0.233000 |
1.42e-01 |
0.435000 |
-2.25e-01 |
2.97e-02 |
1.85e-01 |
4.95e-05 |
3.57e-02 |
Transport of Ribonucleoproteins into the Host Nucleus |
27 |
4.12e-09 |
3.18e-08 |
0.5610 |
0.007080 |
-1.72e-01 |
0.313000 |
-4.33e-01 |
9.49e-01 |
1.23e-01 |
4.85e-03 |
9.99e-05 |
Mitochondrial translation termination |
85 |
2.03e-13 |
3.00e-12 |
0.5610 |
-0.030300 |
-4.98e-02 |
0.494000 |
2.59e-01 |
6.29e-01 |
4.28e-01 |
3.50e-15 |
3.66e-05 |
Resolution of Abasic Sites (AP sites) |
37 |
1.96e-07 |
1.06e-06 |
0.5610 |
0.183000 |
2.85e-01 |
0.447000 |
-1.46e-02 |
5.40e-02 |
2.76e-03 |
2.58e-06 |
8.78e-01 |
Nuclear import of Rev protein |
28 |
8.15e-10 |
7.13e-09 |
0.5610 |
0.028300 |
-1.28e-01 |
0.378000 |
-3.92e-01 |
7.96e-01 |
2.42e-01 |
5.32e-04 |
3.27e-04 |
APC/C:Cdc20 mediated degradation of Securin |
62 |
4.60e-10 |
4.31e-09 |
0.5600 |
0.196000 |
1.51e-01 |
0.480000 |
1.49e-01 |
7.81e-03 |
3.94e-02 |
6.33e-11 |
4.29e-02 |
ATF6 (ATF6-alpha) activates chaperones |
12 |
3.26e-04 |
1.19e-03 |
0.5600 |
0.333000 |
-1.75e-01 |
0.414000 |
-2.03e-02 |
4.56e-02 |
2.93e-01 |
1.31e-02 |
9.03e-01 |
ADP signalling through P2Y purinoceptor 12 |
16 |
1.04e-02 |
2.57e-02 |
0.5590 |
0.147000 |
1.62e-01 |
0.129000 |
4.98e-01 |
3.09e-01 |
2.63e-01 |
3.70e-01 |
5.68e-04 |
Signaling by WNT in cancer |
28 |
2.60e-03 |
7.96e-03 |
0.5580 |
-0.262000 |
-3.70e-01 |
-0.150000 |
-2.90e-01 |
1.66e-02 |
7.10e-04 |
1.70e-01 |
7.90e-03 |
Hedgehog ligand biogenesis |
53 |
1.58e-07 |
8.67e-07 |
0.5570 |
0.115000 |
1.51e-01 |
0.474000 |
2.25e-01 |
1.49e-01 |
5.72e-02 |
2.48e-09 |
4.68e-03 |
Defective TPR may confer susceptibility towards thyroid papillary carcinoma (TPC) |
25 |
2.34e-08 |
1.53e-07 |
0.5560 |
-0.009120 |
-1.50e-01 |
0.342000 |
-4.12e-01 |
9.37e-01 |
1.95e-01 |
3.10e-03 |
3.59e-04 |
Regulation of Glucokinase by Glucokinase Regulatory Protein |
25 |
2.34e-08 |
1.53e-07 |
0.5560 |
-0.009120 |
-1.50e-01 |
0.342000 |
-4.12e-01 |
9.37e-01 |
1.95e-01 |
3.10e-03 |
3.59e-04 |
Synthesis, secretion, and deacylation of Ghrelin |
10 |
1.37e-01 |
2.07e-01 |
0.5560 |
0.178000 |
1.44e-01 |
0.217000 |
4.58e-01 |
3.30e-01 |
4.31e-01 |
2.36e-01 |
1.21e-02 |
Mitochondrial translation initiation |
85 |
1.32e-12 |
1.71e-11 |
0.5550 |
-0.045300 |
-4.45e-02 |
0.476000 |
2.76e-01 |
4.71e-01 |
4.79e-01 |
3.17e-14 |
1.08e-05 |
MASTL Facilitates Mitotic Progression |
10 |
1.56e-02 |
3.62e-02 |
0.5550 |
0.369000 |
1.20e-01 |
0.373000 |
-1.35e-01 |
4.35e-02 |
5.12e-01 |
4.12e-02 |
4.61e-01 |
Degradation of cysteine and homocysteine |
11 |
5.72e-03 |
1.58e-02 |
0.5540 |
-0.061700 |
-2.10e-01 |
0.501000 |
-9.07e-02 |
7.23e-01 |
2.29e-01 |
4.01e-03 |
6.02e-01 |
Degradation of GLI1 by the proteasome |
53 |
4.78e-08 |
2.89e-07 |
0.5530 |
0.175000 |
1.67e-01 |
0.471000 |
1.58e-01 |
2.80e-02 |
3.61e-02 |
2.95e-09 |
4.69e-02 |
Interactions of Rev with host cellular proteins |
31 |
1.14e-10 |
1.14e-09 |
0.5510 |
0.071200 |
-6.90e-02 |
0.389000 |
-3.78e-01 |
4.93e-01 |
5.06e-01 |
1.81e-04 |
2.72e-04 |
RUNX1 regulates transcription of genes involved in differentiation of HSCs |
62 |
1.36e-08 |
9.41e-08 |
0.5510 |
0.165000 |
2.29e-01 |
0.439000 |
1.77e-01 |
2.52e-02 |
1.85e-03 |
2.26e-09 |
1.58e-02 |
Homology Directed Repair |
95 |
1.33e-23 |
4.73e-22 |
0.5500 |
0.270000 |
1.98e-01 |
0.395000 |
-1.84e-01 |
5.40e-06 |
8.61e-04 |
3.03e-11 |
2.01e-03 |
Activated NTRK2 signals through FRS2 and FRS3 |
10 |
1.08e-01 |
1.70e-01 |
0.5490 |
-0.143000 |
-4.44e-01 |
-0.212000 |
-1.96e-01 |
4.32e-01 |
1.51e-02 |
2.46e-01 |
2.83e-01 |
CD28 dependent Vav1 pathway |
12 |
9.51e-02 |
1.53e-01 |
0.5480 |
0.363000 |
3.63e-01 |
-0.086600 |
1.72e-01 |
2.96e-02 |
2.96e-02 |
6.03e-01 |
3.02e-01 |
Miscellaneous transport and binding events |
18 |
7.14e-03 |
1.91e-02 |
0.5480 |
-0.201000 |
-4.31e-01 |
0.000852 |
-2.72e-01 |
1.41e-01 |
1.53e-03 |
9.95e-01 |
4.60e-02 |
NCAM1 interactions |
26 |
1.92e-04 |
7.28e-04 |
0.5470 |
-0.432000 |
-2.32e-01 |
-0.229000 |
8.33e-02 |
1.36e-04 |
4.11e-02 |
4.36e-02 |
4.63e-01 |
Gene and protein expression by JAK-STAT signaling after Interleukin-12 stimulation |
30 |
1.89e-03 |
5.97e-03 |
0.5470 |
0.425000 |
3.36e-01 |
0.054500 |
4.58e-02 |
5.67e-05 |
1.43e-03 |
6.05e-01 |
6.64e-01 |
PI-3K cascade:FGFR1 |
11 |
7.65e-03 |
2.02e-02 |
0.5460 |
0.068400 |
-4.44e-01 |
-0.151000 |
-2.72e-01 |
6.95e-01 |
1.08e-02 |
3.86e-01 |
1.19e-01 |
Diseases associated with glycosylation precursor biosynthesis |
18 |
6.19e-03 |
1.68e-02 |
0.5460 |
-0.214000 |
-7.67e-02 |
0.197000 |
4.55e-01 |
1.16e-01 |
5.73e-01 |
1.49e-01 |
8.27e-04 |
Signal regulatory protein family interactions |
13 |
4.94e-02 |
9.09e-02 |
0.5450 |
0.019900 |
5.58e-03 |
0.246000 |
4.87e-01 |
9.01e-01 |
9.72e-01 |
1.25e-01 |
2.39e-03 |
Rev-mediated nuclear export of HIV RNA |
30 |
4.67e-10 |
4.34e-09 |
0.5450 |
0.053200 |
-6.93e-02 |
0.391000 |
-3.69e-01 |
6.14e-01 |
5.11e-01 |
2.09e-04 |
4.66e-04 |
NEP/NS2 Interacts with the Cellular Export Machinery |
27 |
6.41e-09 |
4.78e-08 |
0.5450 |
0.044600 |
-1.35e-01 |
0.345000 |
-3.97e-01 |
6.89e-01 |
2.25e-01 |
1.93e-03 |
3.57e-04 |
Glutamate binding, activation of AMPA receptors and synaptic plasticity |
24 |
1.14e-02 |
2.77e-02 |
0.5450 |
-0.293000 |
-2.48e-01 |
-0.303000 |
-2.39e-01 |
1.29e-02 |
3.54e-02 |
1.02e-02 |
4.30e-02 |
Trafficking of AMPA receptors |
24 |
1.14e-02 |
2.77e-02 |
0.5450 |
-0.293000 |
-2.48e-01 |
-0.303000 |
-2.39e-01 |
1.29e-02 |
3.54e-02 |
1.02e-02 |
4.30e-02 |
Degradation of GLI2 by the proteasome |
52 |
8.20e-08 |
4.76e-07 |
0.5440 |
0.154000 |
1.65e-01 |
0.472000 |
1.51e-01 |
5.57e-02 |
4.03e-02 |
3.87e-09 |
6.05e-02 |
GLI3 is processed to GLI3R by the proteasome |
52 |
1.67e-07 |
9.04e-07 |
0.5420 |
0.168000 |
1.67e-01 |
0.461000 |
1.60e-01 |
3.66e-02 |
3.70e-02 |
8.99e-09 |
4.63e-02 |
Pentose phosphate pathway |
13 |
4.64e-02 |
8.68e-02 |
0.5420 |
0.125000 |
1.63e-01 |
0.477000 |
1.56e-01 |
4.37e-01 |
3.10e-01 |
2.91e-03 |
3.31e-01 |
Antimicrobial peptides |
13 |
1.50e-02 |
3.49e-02 |
0.5400 |
0.138000 |
4.29e-01 |
-0.063200 |
2.90e-01 |
3.90e-01 |
7.35e-03 |
6.93e-01 |
7.00e-02 |
Export of Viral Ribonucleoproteins from Nucleus |
28 |
1.02e-08 |
7.31e-08 |
0.5390 |
0.009770 |
-1.64e-01 |
0.298000 |
-4.18e-01 |
9.29e-01 |
1.32e-01 |
6.37e-03 |
1.29e-04 |
SUMOylation of DNA replication proteins |
40 |
3.55e-12 |
4.43e-11 |
0.5360 |
0.186000 |
6.43e-02 |
0.383000 |
-3.20e-01 |
4.24e-02 |
4.82e-01 |
2.73e-05 |
4.70e-04 |
Regulation of necroptotic cell death |
12 |
8.27e-03 |
2.17e-02 |
0.5360 |
0.088400 |
3.11e-01 |
-0.426000 |
4.07e-02 |
5.96e-01 |
6.20e-02 |
1.06e-02 |
8.07e-01 |
Cell Cycle Checkpoints |
235 |
2.75e-55 |
1.20e-52 |
0.5360 |
0.275000 |
1.79e-01 |
0.394000 |
-1.56e-01 |
4.74e-13 |
2.37e-06 |
2.88e-25 |
3.92e-05 |
VLDLR internalisation and degradation |
11 |
4.08e-02 |
7.80e-02 |
0.5360 |
0.008790 |
1.70e-01 |
0.499000 |
9.71e-02 |
9.60e-01 |
3.30e-01 |
4.20e-03 |
5.77e-01 |
NIK-->noncanonical NF-kB signaling |
52 |
2.01e-07 |
1.08e-06 |
0.5320 |
0.164000 |
1.72e-01 |
0.455000 |
1.41e-01 |
4.05e-02 |
3.18e-02 |
1.40e-08 |
7.89e-02 |
Activation of Matrix Metalloproteinases |
17 |
8.46e-03 |
2.19e-02 |
0.5310 |
-0.344000 |
-2.27e-01 |
0.023300 |
3.34e-01 |
1.42e-02 |
1.05e-01 |
8.68e-01 |
1.72e-02 |
Postmitotic nuclear pore complex (NPC) reformation |
25 |
7.87e-08 |
4.59e-07 |
0.5290 |
0.061700 |
-1.21e-01 |
0.407000 |
-3.10e-01 |
5.94e-01 |
2.96e-01 |
4.30e-04 |
7.25e-03 |
Apoptotic factor-mediated response |
13 |
2.69e-02 |
5.63e-02 |
0.5290 |
-0.125000 |
1.19e-01 |
0.464000 |
1.86e-01 |
4.37e-01 |
4.57e-01 |
3.77e-03 |
2.45e-01 |
Regulation of RUNX3 expression and activity |
48 |
1.76e-06 |
8.59e-06 |
0.5240 |
0.163000 |
2.13e-01 |
0.430000 |
1.30e-01 |
5.06e-02 |
1.06e-02 |
2.49e-07 |
1.20e-01 |
Mitochondrial translation |
91 |
1.12e-12 |
1.47e-11 |
0.5230 |
-0.053800 |
-7.07e-02 |
0.460000 |
2.34e-01 |
3.76e-01 |
2.44e-01 |
3.61e-14 |
1.19e-04 |
Pyruvate metabolism |
26 |
1.51e-04 |
5.82e-04 |
0.5230 |
0.005260 |
-3.20e-01 |
-0.122000 |
-3.96e-01 |
9.63e-01 |
4.76e-03 |
2.83e-01 |
4.82e-04 |
Regulation of FZD by ubiquitination |
13 |
1.84e-01 |
2.59e-01 |
0.5230 |
-0.305000 |
-3.15e-01 |
-0.227000 |
-1.71e-01 |
5.66e-02 |
4.93e-02 |
1.56e-01 |
2.85e-01 |
Vpr-mediated nuclear import of PICs |
29 |
1.58e-08 |
1.09e-07 |
0.5220 |
-0.012600 |
-1.68e-01 |
0.346000 |
-3.54e-01 |
9.07e-01 |
1.18e-01 |
1.28e-03 |
9.72e-04 |
Interleukin-12 signaling |
35 |
5.99e-04 |
2.07e-03 |
0.5220 |
0.428000 |
2.81e-01 |
0.052300 |
9.11e-02 |
1.21e-05 |
3.99e-03 |
5.92e-01 |
3.51e-01 |
Transport of the SLBP Dependant Mature mRNA |
31 |
5.32e-09 |
4.01e-08 |
0.5220 |
-0.037500 |
-1.35e-01 |
0.310000 |
-3.96e-01 |
7.18e-01 |
1.93e-01 |
2.78e-03 |
1.36e-04 |
Synthesis of PE |
11 |
1.68e-02 |
3.85e-02 |
0.5210 |
-0.433000 |
-9.82e-03 |
-0.250000 |
-1.45e-01 |
1.28e-02 |
9.55e-01 |
1.52e-01 |
4.06e-01 |
Dectin-1 mediated noncanonical NF-kB signaling |
53 |
1.65e-07 |
9.00e-07 |
0.5200 |
0.148000 |
1.61e-01 |
0.455000 |
1.27e-01 |
6.29e-02 |
4.25e-02 |
1.04e-08 |
1.10e-01 |
Sulfur amino acid metabolism |
20 |
2.15e-05 |
9.29e-05 |
0.5200 |
0.022900 |
-2.74e-01 |
0.424000 |
-1.23e-01 |
8.59e-01 |
3.42e-02 |
1.02e-03 |
3.40e-01 |
G1/S DNA Damage Checkpoints |
60 |
5.10e-09 |
3.87e-08 |
0.5200 |
0.189000 |
2.38e-01 |
0.418000 |
5.23e-02 |
1.14e-02 |
1.45e-03 |
2.10e-08 |
4.84e-01 |
EML4 and NUDC in mitotic spindle formation |
87 |
7.85e-25 |
3.81e-23 |
0.5180 |
0.223000 |
4.75e-02 |
0.366000 |
-2.88e-01 |
3.36e-04 |
4.45e-01 |
3.80e-09 |
3.43e-06 |
Formation of the beta-catenin:TCF transactivating complex |
29 |
1.70e-03 |
5.44e-03 |
0.5170 |
-0.261000 |
-1.70e-01 |
-0.173000 |
-3.75e-01 |
1.51e-02 |
1.14e-01 |
1.06e-01 |
4.70e-04 |
Misspliced GSK3beta mutants stabilize beta-catenin |
14 |
1.90e-02 |
4.21e-02 |
0.5170 |
-0.046500 |
-3.08e-01 |
-0.059100 |
-4.08e-01 |
7.63e-01 |
4.58e-02 |
7.02e-01 |
8.16e-03 |
S33 mutants of beta-catenin aren't phosphorylated |
14 |
1.90e-02 |
4.21e-02 |
0.5170 |
-0.046500 |
-3.08e-01 |
-0.059100 |
-4.08e-01 |
7.63e-01 |
4.58e-02 |
7.02e-01 |
8.16e-03 |
S37 mutants of beta-catenin aren't phosphorylated |
14 |
1.90e-02 |
4.21e-02 |
0.5170 |
-0.046500 |
-3.08e-01 |
-0.059100 |
-4.08e-01 |
7.63e-01 |
4.58e-02 |
7.02e-01 |
8.16e-03 |
S45 mutants of beta-catenin aren't phosphorylated |
14 |
1.90e-02 |
4.21e-02 |
0.5170 |
-0.046500 |
-3.08e-01 |
-0.059100 |
-4.08e-01 |
7.63e-01 |
4.58e-02 |
7.02e-01 |
8.16e-03 |
T41 mutants of beta-catenin aren't phosphorylated |
14 |
1.90e-02 |
4.21e-02 |
0.5170 |
-0.046500 |
-3.08e-01 |
-0.059100 |
-4.08e-01 |
7.63e-01 |
4.58e-02 |
7.02e-01 |
8.16e-03 |
phosphorylation site mutants of CTNNB1 are not targeted to the proteasome by the destruction complex |
14 |
1.90e-02 |
4.21e-02 |
0.5170 |
-0.046500 |
-3.08e-01 |
-0.059100 |
-4.08e-01 |
7.63e-01 |
4.58e-02 |
7.02e-01 |
8.16e-03 |
Transport of the SLBP independent Mature mRNA |
30 |
2.92e-08 |
1.84e-07 |
0.5170 |
-0.059700 |
-1.62e-01 |
0.297000 |
-3.87e-01 |
5.72e-01 |
1.24e-01 |
4.93e-03 |
2.48e-04 |
Degradation of AXIN |
49 |
1.53e-06 |
7.51e-06 |
0.5160 |
0.206000 |
1.78e-01 |
0.422000 |
1.18e-01 |
1.27e-02 |
3.09e-02 |
3.22e-07 |
1.52e-01 |
Prolactin receptor signaling |
11 |
1.51e-01 |
2.23e-01 |
0.5160 |
-0.126000 |
-3.72e-01 |
-0.249000 |
-2.22e-01 |
4.70e-01 |
3.25e-02 |
1.53e-01 |
2.02e-01 |
Separation of Sister Chromatids |
154 |
4.19e-35 |
4.23e-33 |
0.5150 |
0.253000 |
1.20e-01 |
0.412000 |
-1.32e-01 |
6.53e-08 |
1.01e-02 |
1.16e-18 |
4.81e-03 |
Oxygen-dependent proline hydroxylation of Hypoxia-inducible Factor Alpha |
57 |
6.93e-07 |
3.54e-06 |
0.5150 |
0.198000 |
1.89e-01 |
0.407000 |
1.58e-01 |
9.84e-03 |
1.36e-02 |
1.10e-07 |
3.96e-02 |
Regulation of PTEN mRNA translation |
11 |
2.09e-01 |
2.87e-01 |
0.5150 |
-0.145000 |
-2.03e-01 |
-0.387000 |
-2.30e-01 |
4.05e-01 |
2.44e-01 |
2.62e-02 |
1.87e-01 |
G beta:gamma signalling through PLC beta |
15 |
1.65e-02 |
3.79e-02 |
0.5140 |
-0.083700 |
4.49e-02 |
0.122000 |
4.90e-01 |
5.75e-01 |
7.63e-01 |
4.12e-01 |
1.01e-03 |
Assembly of collagen fibrils and other multimeric structures |
45 |
1.13e-10 |
1.14e-09 |
0.5140 |
-0.392000 |
-2.40e-02 |
-0.326000 |
5.67e-02 |
5.41e-06 |
7.80e-01 |
1.52e-04 |
5.11e-01 |
G beta:gamma signalling through CDC42 |
15 |
1.35e-02 |
3.21e-02 |
0.5140 |
0.006070 |
1.09e-01 |
0.077900 |
4.96e-01 |
9.68e-01 |
4.65e-01 |
6.02e-01 |
8.82e-04 |
FRS-mediated FGFR3 signaling |
12 |
2.85e-02 |
5.87e-02 |
0.5130 |
0.054500 |
-3.49e-01 |
-0.215000 |
-3.04e-01 |
7.44e-01 |
3.62e-02 |
1.96e-01 |
6.86e-02 |
p53-Dependent G1 DNA Damage Response |
58 |
3.23e-08 |
2.01e-07 |
0.5130 |
0.191000 |
2.27e-01 |
0.413000 |
6.70e-02 |
1.21e-02 |
2.82e-03 |
5.22e-08 |
3.78e-01 |
p53-Dependent G1/S DNA damage checkpoint |
58 |
3.23e-08 |
2.01e-07 |
0.5130 |
0.191000 |
2.27e-01 |
0.413000 |
6.70e-02 |
1.21e-02 |
2.82e-03 |
5.22e-08 |
3.78e-01 |
NS1 Mediated Effects on Host Pathways |
33 |
1.20e-09 |
1.01e-08 |
0.5130 |
0.065700 |
-8.44e-02 |
0.297000 |
-4.04e-01 |
5.14e-01 |
4.02e-01 |
3.16e-03 |
5.88e-05 |
Base Excision Repair |
45 |
4.41e-08 |
2.69e-07 |
0.5120 |
0.172000 |
2.99e-01 |
0.373000 |
-6.58e-02 |
4.64e-02 |
5.23e-04 |
1.50e-05 |
4.45e-01 |
TP53 regulates transcription of additional cell cycle genes whose exact role in the p53 pathway remain uncertain |
19 |
7.68e-03 |
2.02e-02 |
0.5100 |
0.008000 |
-1.16e-02 |
-0.159000 |
-4.85e-01 |
9.52e-01 |
9.30e-01 |
2.29e-01 |
2.55e-04 |
STING mediated induction of host immune responses |
12 |
9.63e-02 |
1.55e-01 |
0.5100 |
0.239000 |
4.36e-01 |
-0.101000 |
-5.19e-02 |
1.53e-01 |
8.87e-03 |
5.44e-01 |
7.56e-01 |
Purine salvage |
12 |
1.60e-01 |
2.33e-01 |
0.5080 |
0.325000 |
2.36e-01 |
0.291000 |
1.09e-01 |
5.11e-02 |
1.56e-01 |
8.07e-02 |
5.14e-01 |
Initiation of Nuclear Envelope (NE) Reformation |
19 |
2.13e-04 |
8.02e-04 |
0.5070 |
0.185000 |
2.34e-02 |
0.460000 |
-1.04e-01 |
1.62e-01 |
8.60e-01 |
5.19e-04 |
4.32e-01 |
Mitotic Spindle Checkpoint |
100 |
1.92e-27 |
1.15e-25 |
0.5070 |
0.225000 |
3.37e-02 |
0.367000 |
-2.66e-01 |
1.05e-04 |
5.61e-01 |
2.35e-10 |
4.32e-06 |
Ion homeostasis |
41 |
2.88e-04 |
1.05e-03 |
0.5060 |
-0.214000 |
-3.07e-01 |
-0.310000 |
-1.44e-01 |
1.80e-02 |
6.71e-04 |
6.08e-04 |
1.12e-01 |
Processing of DNA double-strand break ends |
58 |
3.53e-11 |
3.77e-10 |
0.5050 |
0.280000 |
2.07e-01 |
0.322000 |
-1.73e-01 |
2.23e-04 |
6.56e-03 |
2.26e-05 |
2.25e-02 |
Cytosolic sulfonation of small molecules |
15 |
8.22e-02 |
1.37e-01 |
0.5050 |
0.138000 |
3.18e-01 |
0.166000 |
3.27e-01 |
3.53e-01 |
3.28e-02 |
2.66e-01 |
2.84e-02 |
Thromboxane signalling through TP receptor |
19 |
9.88e-03 |
2.47e-02 |
0.5040 |
-0.125000 |
5.45e-02 |
0.190000 |
4.47e-01 |
3.45e-01 |
6.81e-01 |
1.53e-01 |
7.47e-04 |
Downstream signaling of activated FGFR4 |
16 |
2.26e-02 |
4.88e-02 |
0.5040 |
0.021400 |
-2.80e-01 |
-0.213000 |
-3.60e-01 |
8.82e-01 |
5.23e-02 |
1.40e-01 |
1.26e-02 |
Downstream signaling of activated FGFR2 |
19 |
1.25e-02 |
3.01e-02 |
0.5040 |
-0.019700 |
-3.20e-01 |
-0.259000 |
-2.90e-01 |
8.82e-01 |
1.58e-02 |
5.04e-02 |
2.88e-02 |
TP53 Regulates Transcription of Genes Involved in G1 Cell Cycle Arrest |
13 |
8.01e-03 |
2.10e-02 |
0.5030 |
0.171000 |
3.06e-01 |
0.217000 |
-2.88e-01 |
2.86e-01 |
5.60e-02 |
1.75e-01 |
7.20e-02 |
Transport of Mature mRNAs Derived from Intronless Transcripts |
38 |
3.80e-10 |
3.61e-09 |
0.5030 |
-0.006950 |
-1.26e-01 |
0.257000 |
-4.13e-01 |
9.41e-01 |
1.81e-01 |
6.14e-03 |
1.04e-05 |
Meiotic recombination |
22 |
4.40e-05 |
1.83e-04 |
0.5010 |
0.149000 |
1.29e-01 |
0.424000 |
-1.81e-01 |
2.26e-01 |
2.97e-01 |
5.81e-04 |
1.41e-01 |
ADP signalling through P2Y purinoceptor 1 |
20 |
5.14e-03 |
1.44e-02 |
0.5000 |
-0.030800 |
-5.09e-03 |
0.134000 |
4.81e-01 |
8.11e-01 |
9.69e-01 |
2.99e-01 |
1.98e-04 |
Elevation of cytosolic Ca2+ levels |
12 |
3.34e-02 |
6.66e-02 |
0.5000 |
-0.387000 |
-7.88e-02 |
-0.302000 |
-5.06e-02 |
2.04e-02 |
6.36e-01 |
7.02e-02 |
7.61e-01 |
RORA activates gene expression |
17 |
6.02e-02 |
1.07e-01 |
0.4980 |
-0.037200 |
-1.96e-01 |
-0.258000 |
-3.77e-01 |
7.91e-01 |
1.63e-01 |
6.60e-02 |
7.12e-03 |
Transport of Mature mRNA Derived from an Intronless Transcript |
37 |
2.06e-09 |
1.66e-08 |
0.4970 |
-0.024100 |
-1.47e-01 |
0.244000 |
-4.06e-01 |
8.00e-01 |
1.21e-01 |
1.01e-02 |
1.91e-05 |
Detoxification of Reactive Oxygen Species |
29 |
6.88e-03 |
1.85e-02 |
0.4960 |
0.103000 |
1.82e-01 |
0.369000 |
2.58e-01 |
3.35e-01 |
8.97e-02 |
5.90e-04 |
1.62e-02 |
Telomere C-strand synthesis initiation |
12 |
2.02e-02 |
4.44e-02 |
0.4960 |
0.151000 |
3.59e-01 |
0.246000 |
-1.84e-01 |
3.65e-01 |
3.13e-02 |
1.40e-01 |
2.70e-01 |
HDR through Single Strand Annealing (SSA) |
36 |
8.47e-08 |
4.89e-07 |
0.4950 |
0.215000 |
1.54e-01 |
0.366000 |
-2.05e-01 |
2.59e-02 |
1.10e-01 |
1.48e-04 |
3.34e-02 |
Interactions of Vpr with host cellular proteins |
31 |
3.38e-08 |
2.09e-07 |
0.4950 |
-0.009950 |
-1.52e-01 |
0.324000 |
-3.42e-01 |
9.24e-01 |
1.43e-01 |
1.80e-03 |
9.86e-04 |
FOXO-mediated transcription of cell cycle genes |
15 |
1.13e-01 |
1.76e-01 |
0.4950 |
-0.073700 |
-1.09e-01 |
-0.273000 |
-3.91e-01 |
6.21e-01 |
4.64e-01 |
6.70e-02 |
8.75e-03 |
Pyruvate metabolism and Citric Acid (TCA) cycle |
50 |
6.50e-10 |
5.88e-09 |
0.4930 |
0.115000 |
-2.41e-01 |
-0.058600 |
-4.10e-01 |
1.61e-01 |
3.24e-03 |
4.74e-01 |
5.38e-07 |
Antigen Presentation: Folding, assembly and peptide loading of class I MHC |
17 |
2.04e-03 |
6.41e-03 |
0.4910 |
0.257000 |
-1.13e-01 |
0.232000 |
3.30e-01 |
6.71e-02 |
4.19e-01 |
9.77e-02 |
1.86e-02 |
Citric acid cycle (TCA cycle) |
22 |
7.74e-05 |
3.07e-04 |
0.4900 |
0.207000 |
-1.32e-01 |
0.017000 |
-4.24e-01 |
9.34e-02 |
2.85e-01 |
8.90e-01 |
5.75e-04 |
CLEC7A (Dectin-1) induces NFAT activation |
10 |
2.23e-01 |
3.02e-01 |
0.4880 |
0.130000 |
-8.80e-03 |
-0.393000 |
-2.57e-01 |
4.77e-01 |
9.62e-01 |
3.13e-02 |
1.59e-01 |
Glycogen synthesis |
12 |
1.87e-01 |
2.62e-01 |
0.4870 |
-0.378000 |
-2.88e-01 |
-0.056000 |
8.60e-02 |
2.32e-02 |
8.36e-02 |
7.37e-01 |
6.06e-01 |
MET activates PTK2 signaling |
17 |
1.30e-02 |
3.11e-02 |
0.4850 |
-0.207000 |
-4.55e-02 |
-0.426000 |
-9.34e-02 |
1.40e-01 |
7.45e-01 |
2.35e-03 |
5.05e-01 |
FRS-mediated FGFR1 signaling |
13 |
3.88e-02 |
7.48e-02 |
0.4850 |
-0.008090 |
-3.76e-01 |
-0.167000 |
-2.56e-01 |
9.60e-01 |
1.89e-02 |
2.97e-01 |
1.10e-01 |
IRAK2 mediated activation of TAK1 complex upon TLR7/8 or 9 stimulation |
13 |
1.64e-01 |
2.37e-01 |
0.4840 |
-0.317000 |
-3.38e-01 |
0.090800 |
-1.07e-01 |
4.80e-02 |
3.49e-02 |
5.71e-01 |
5.04e-01 |
TRAF6-mediated induction of TAK1 complex within TLR4 complex |
13 |
1.64e-01 |
2.37e-01 |
0.4840 |
-0.317000 |
-3.38e-01 |
0.090800 |
-1.07e-01 |
4.80e-02 |
3.49e-02 |
5.71e-01 |
5.04e-01 |
Nitric oxide stimulates guanylate cyclase |
18 |
9.74e-04 |
3.25e-03 |
0.4810 |
-0.248000 |
-6.50e-04 |
-0.406000 |
6.40e-02 |
6.81e-02 |
9.96e-01 |
2.83e-03 |
6.38e-01 |
ATF4 activates genes in response to endoplasmic reticulum stress |
24 |
4.77e-03 |
1.35e-02 |
0.4800 |
0.321000 |
2.82e-01 |
0.170000 |
-1.39e-01 |
6.46e-03 |
1.70e-02 |
1.49e-01 |
2.38e-01 |
PECAM1 interactions |
11 |
4.71e-02 |
8.78e-02 |
0.4800 |
0.129000 |
3.26e-01 |
-0.313000 |
9.88e-02 |
4.58e-01 |
6.15e-02 |
7.26e-02 |
5.70e-01 |
Metabolism of porphyrins |
21 |
2.78e-04 |
1.02e-03 |
0.4790 |
-0.080400 |
-7.19e-02 |
0.456000 |
-9.80e-02 |
5.24e-01 |
5.69e-01 |
2.99e-04 |
4.37e-01 |
G2/M DNA damage checkpoint |
58 |
1.75e-09 |
1.43e-08 |
0.4790 |
0.265000 |
2.21e-01 |
0.293000 |
-1.55e-01 |
4.81e-04 |
3.65e-03 |
1.15e-04 |
4.15e-02 |
Mitochondrial iron-sulfur cluster biogenesis |
12 |
1.43e-02 |
3.35e-02 |
0.4780 |
-0.210000 |
-1.86e-02 |
0.418000 |
-9.45e-02 |
2.08e-01 |
9.11e-01 |
1.22e-02 |
5.71e-01 |
InlB-mediated entry of Listeria monocytogenes into host cell |
13 |
1.76e-01 |
2.50e-01 |
0.4770 |
-0.127000 |
-3.21e-01 |
-0.186000 |
-2.71e-01 |
4.26e-01 |
4.51e-02 |
2.45e-01 |
9.11e-02 |
Regulation of beta-cell development |
20 |
7.56e-02 |
1.27e-01 |
0.4760 |
-0.120000 |
-1.68e-01 |
-0.325000 |
-2.80e-01 |
3.51e-01 |
1.93e-01 |
1.20e-02 |
3.00e-02 |
Activation of SMO |
14 |
1.24e-01 |
1.90e-01 |
0.4760 |
-0.159000 |
-3.21e-02 |
0.305000 |
3.28e-01 |
3.04e-01 |
8.35e-01 |
4.79e-02 |
3.38e-02 |
Interleukin-12 family signaling |
41 |
3.91e-04 |
1.39e-03 |
0.4760 |
0.399000 |
2.33e-01 |
0.039000 |
1.09e-01 |
1.01e-05 |
1.00e-02 |
6.66e-01 |
2.26e-01 |
AMER1 mutants destabilize the destruction complex |
13 |
3.76e-02 |
7.29e-02 |
0.4740 |
0.009570 |
-2.79e-01 |
-0.056500 |
-3.80e-01 |
9.52e-01 |
8.19e-02 |
7.24e-01 |
1.78e-02 |
APC truncation mutants have impaired AXIN binding |
13 |
3.76e-02 |
7.29e-02 |
0.4740 |
0.009570 |
-2.79e-01 |
-0.056500 |
-3.80e-01 |
9.52e-01 |
8.19e-02 |
7.24e-01 |
1.78e-02 |
AXIN missense mutants destabilize the destruction complex |
13 |
3.76e-02 |
7.29e-02 |
0.4740 |
0.009570 |
-2.79e-01 |
-0.056500 |
-3.80e-01 |
9.52e-01 |
8.19e-02 |
7.24e-01 |
1.78e-02 |
AXIN mutants destabilize the destruction complex, activating WNT signaling |
13 |
3.76e-02 |
7.29e-02 |
0.4740 |
0.009570 |
-2.79e-01 |
-0.056500 |
-3.80e-01 |
9.52e-01 |
8.19e-02 |
7.24e-01 |
1.78e-02 |
Truncations of AMER1 destabilize the destruction complex |
13 |
3.76e-02 |
7.29e-02 |
0.4740 |
0.009570 |
-2.79e-01 |
-0.056500 |
-3.80e-01 |
9.52e-01 |
8.19e-02 |
7.24e-01 |
1.78e-02 |
truncated APC mutants destabilize the destruction complex |
13 |
3.76e-02 |
7.29e-02 |
0.4740 |
0.009570 |
-2.79e-01 |
-0.056500 |
-3.80e-01 |
9.52e-01 |
8.19e-02 |
7.24e-01 |
1.78e-02 |
Nucleotide salvage |
20 |
4.92e-02 |
9.09e-02 |
0.4740 |
0.211000 |
2.60e-01 |
0.316000 |
1.14e-01 |
1.03e-01 |
4.38e-02 |
1.46e-02 |
3.77e-01 |
Deadenylation of mRNA |
24 |
3.51e-03 |
1.03e-02 |
0.4740 |
0.185000 |
8.72e-02 |
-0.122000 |
-4.10e-01 |
1.17e-01 |
4.60e-01 |
2.99e-01 |
5.14e-04 |
Collagen biosynthesis and modifying enzymes |
50 |
1.04e-10 |
1.07e-09 |
0.4740 |
-0.359000 |
-2.69e-02 |
-0.155000 |
2.67e-01 |
1.15e-05 |
7.42e-01 |
5.88e-02 |
1.11e-03 |
Listeria monocytogenes entry into host cells |
17 |
8.30e-02 |
1.38e-01 |
0.4740 |
-0.144000 |
-3.41e-01 |
-0.165000 |
-2.46e-01 |
3.05e-01 |
1.50e-02 |
2.40e-01 |
7.91e-02 |
RIPK1-mediated regulated necrosis |
14 |
1.42e-02 |
3.34e-02 |
0.4730 |
0.109000 |
3.23e-01 |
-0.309000 |
1.10e-01 |
4.82e-01 |
3.66e-02 |
4.56e-02 |
4.75e-01 |
Regulated Necrosis |
14 |
1.42e-02 |
3.34e-02 |
0.4730 |
0.109000 |
3.23e-01 |
-0.309000 |
1.10e-01 |
4.82e-01 |
3.66e-02 |
4.56e-02 |
4.75e-01 |
Synthesis of bile acids and bile salts via 7alpha-hydroxycholesterol |
12 |
1.16e-01 |
1.81e-01 |
0.4720 |
0.142000 |
-4.12e-02 |
0.265000 |
3.61e-01 |
3.95e-01 |
8.05e-01 |
1.12e-01 |
3.04e-02 |
Downstream signaling of activated FGFR3 |
17 |
2.86e-02 |
5.88e-02 |
0.4720 |
0.075800 |
-2.09e-01 |
-0.222000 |
-3.52e-01 |
5.89e-01 |
1.36e-01 |
1.14e-01 |
1.20e-02 |
Signaling by ROBO receptors |
162 |
7.97e-13 |
1.08e-11 |
0.4710 |
0.230000 |
2.38e-01 |
0.258000 |
2.15e-01 |
4.79e-07 |
1.88e-07 |
1.67e-08 |
2.37e-06 |
IRAK4 deficiency (TLR2/4) |
11 |
1.17e-01 |
1.83e-01 |
0.4710 |
-0.052800 |
1.06e-01 |
0.115000 |
4.41e-01 |
7.62e-01 |
5.43e-01 |
5.10e-01 |
1.13e-02 |
Mitotic Metaphase and Anaphase |
206 |
3.47e-41 |
5.06e-39 |
0.4710 |
0.202000 |
7.95e-02 |
0.400000 |
-1.20e-01 |
6.58e-07 |
4.99e-02 |
4.90e-23 |
3.00e-03 |
Processing of Intronless Pre-mRNAs |
17 |
7.41e-03 |
1.97e-02 |
0.4700 |
0.158000 |
-4.53e-02 |
-0.037700 |
-4.38e-01 |
2.61e-01 |
7.46e-01 |
7.88e-01 |
1.75e-03 |
Glycogen metabolism |
23 |
2.28e-02 |
4.92e-02 |
0.4690 |
-0.289000 |
-2.49e-01 |
-0.270000 |
-4.19e-02 |
1.65e-02 |
3.89e-02 |
2.52e-02 |
7.28e-01 |
Cell Cycle, Mitotic |
457 |
2.46e-89 |
1.61e-86 |
0.4690 |
0.216000 |
1.40e-01 |
0.352000 |
-1.72e-01 |
3.46e-15 |
3.64e-07 |
9.41e-38 |
4.08e-10 |
Glucagon-type ligand receptors |
16 |
1.71e-02 |
3.90e-02 |
0.4680 |
-0.169000 |
7.40e-02 |
0.100000 |
4.18e-01 |
2.43e-01 |
6.09e-01 |
4.88e-01 |
3.77e-03 |
CASP8 activity is inhibited |
10 |
6.06e-02 |
1.07e-01 |
0.4670 |
0.063300 |
3.00e-01 |
-0.349000 |
4.56e-02 |
7.29e-01 |
1.00e-01 |
5.58e-02 |
8.03e-01 |
Dimerization of procaspase-8 |
10 |
6.06e-02 |
1.07e-01 |
0.4670 |
0.063300 |
3.00e-01 |
-0.349000 |
4.56e-02 |
7.29e-01 |
1.00e-01 |
5.58e-02 |
8.03e-01 |
Regulation by c-FLIP |
10 |
6.06e-02 |
1.07e-01 |
0.4670 |
0.063300 |
3.00e-01 |
-0.349000 |
4.56e-02 |
7.29e-01 |
1.00e-01 |
5.58e-02 |
8.03e-01 |
Mitotic Anaphase |
205 |
2.24e-40 |
2.94e-38 |
0.4670 |
0.199000 |
7.51e-02 |
0.398000 |
-1.18e-01 |
1.00e-06 |
6.46e-02 |
1.03e-22 |
3.60e-03 |
MyD88 deficiency (TLR2/4) |
10 |
1.72e-01 |
2.46e-01 |
0.4650 |
-0.034400 |
1.11e-01 |
0.116000 |
4.35e-01 |
8.51e-01 |
5.42e-01 |
5.24e-01 |
1.73e-02 |
SUMOylation of SUMOylation proteins |
29 |
8.56e-07 |
4.32e-06 |
0.4650 |
0.019900 |
-1.34e-01 |
0.276000 |
-3.49e-01 |
8.53e-01 |
2.12e-01 |
1.02e-02 |
1.16e-03 |
IRF3-mediated induction of type I IFN |
10 |
2.10e-01 |
2.87e-01 |
0.4650 |
0.197000 |
4.14e-01 |
-0.032400 |
-6.46e-02 |
2.80e-01 |
2.33e-02 |
8.59e-01 |
7.24e-01 |
RUNX1 regulates genes involved in megakaryocyte differentiation and platelet function |
33 |
8.72e-03 |
2.23e-02 |
0.4640 |
-0.168000 |
-1.32e-01 |
-0.302000 |
-2.80e-01 |
9.43e-02 |
1.89e-01 |
2.66e-03 |
5.45e-03 |
Nuclear Pore Complex (NPC) Disassembly |
31 |
1.65e-07 |
9.00e-07 |
0.4630 |
0.071100 |
-9.67e-02 |
0.327000 |
-3.05e-01 |
4.93e-01 |
3.52e-01 |
1.65e-03 |
3.25e-03 |
FOXO-mediated transcription of cell death genes |
14 |
4.66e-03 |
1.33e-02 |
0.4630 |
0.074200 |
-9.18e-02 |
0.161000 |
-4.18e-01 |
6.31e-01 |
5.52e-01 |
2.96e-01 |
6.83e-03 |
MECP2 regulates neuronal receptors and channels |
12 |
1.63e-01 |
2.36e-01 |
0.4630 |
0.209000 |
2.82e-01 |
-0.283000 |
-1.05e-01 |
2.10e-01 |
9.05e-02 |
9.00e-02 |
5.28e-01 |
Transferrin endocytosis and recycling |
24 |
2.06e-02 |
4.52e-02 |
0.4630 |
-0.218000 |
-2.00e-01 |
0.273000 |
2.28e-01 |
6.42e-02 |
8.99e-02 |
2.05e-02 |
5.34e-02 |
Regulation of MECP2 expression and activity |
28 |
1.04e-02 |
2.57e-02 |
0.4630 |
-0.062100 |
-2.45e-01 |
-0.216000 |
-3.23e-01 |
5.70e-01 |
2.50e-02 |
4.85e-02 |
3.14e-03 |
Regulation of RAS by GAPs |
60 |
3.25e-06 |
1.54e-05 |
0.4620 |
0.187000 |
2.31e-01 |
0.345000 |
7.96e-02 |
1.22e-02 |
2.01e-03 |
3.92e-06 |
2.87e-01 |
Metabolism of Angiotensinogen to Angiotensins |
11 |
1.81e-01 |
2.56e-01 |
0.4620 |
-0.255000 |
-2.28e-01 |
0.071700 |
3.02e-01 |
1.43e-01 |
1.91e-01 |
6.81e-01 |
8.32e-02 |
Synthesis of Leukotrienes (LT) and Eoxins (EX) |
14 |
1.27e-01 |
1.94e-01 |
0.4600 |
0.210000 |
2.65e-01 |
0.024800 |
3.12e-01 |
1.75e-01 |
8.65e-02 |
8.72e-01 |
4.34e-02 |
Acetylcholine regulates insulin secretion |
10 |
2.58e-01 |
3.39e-01 |
0.4600 |
-0.388000 |
-2.19e-01 |
-0.075300 |
8.48e-02 |
3.36e-02 |
2.30e-01 |
6.80e-01 |
6.42e-01 |
Constitutive Signaling by EGFRvIII |
15 |
1.64e-01 |
2.37e-01 |
0.4600 |
-0.128000 |
-1.81e-01 |
-0.188000 |
-3.57e-01 |
3.92e-01 |
2.26e-01 |
2.08e-01 |
1.68e-02 |
Signaling by EGFRvIII in Cancer |
15 |
1.64e-01 |
2.37e-01 |
0.4600 |
-0.128000 |
-1.81e-01 |
-0.188000 |
-3.57e-01 |
3.92e-01 |
2.26e-01 |
2.08e-01 |
1.68e-02 |
Presynaptic function of Kainate receptors |
16 |
2.74e-02 |
5.69e-02 |
0.4590 |
-0.033800 |
5.63e-02 |
0.074900 |
4.48e-01 |
8.15e-01 |
6.97e-01 |
6.04e-01 |
1.90e-03 |
SHC-mediated cascade:FGFR2 |
12 |
8.63e-02 |
1.42e-01 |
0.4590 |
0.022900 |
-3.20e-01 |
-0.231000 |
-2.33e-01 |
8.91e-01 |
5.50e-02 |
1.67e-01 |
1.62e-01 |
Transcriptional Regulation by E2F6 |
33 |
1.04e-04 |
4.03e-04 |
0.4590 |
0.328000 |
1.69e-01 |
0.243000 |
-1.23e-01 |
1.11e-03 |
9.28e-02 |
1.58e-02 |
2.21e-01 |
Asymmetric localization of PCP proteins |
58 |
4.53e-06 |
2.11e-05 |
0.4580 |
-0.000948 |
7.43e-02 |
0.413000 |
1.83e-01 |
9.90e-01 |
3.28e-01 |
5.47e-08 |
1.57e-02 |
Protein methylation |
11 |
2.28e-01 |
3.09e-01 |
0.4560 |
0.267000 |
1.40e-01 |
0.120000 |
3.20e-01 |
1.25e-01 |
4.20e-01 |
4.91e-01 |
6.60e-02 |
Disassembly of the destruction complex and recruitment of AXIN to the membrane |
26 |
1.42e-02 |
3.34e-02 |
0.4560 |
-0.257000 |
-2.94e-01 |
0.025000 |
-2.34e-01 |
2.33e-02 |
9.55e-03 |
8.25e-01 |
3.87e-02 |
Viral Messenger RNA Synthesis |
38 |
3.84e-08 |
2.35e-07 |
0.4560 |
-0.041400 |
-1.20e-01 |
0.380000 |
-2.17e-01 |
6.59e-01 |
1.99e-01 |
5.07e-05 |
2.09e-02 |
Aberrant regulation of mitotic G1/S transition in cancer due to RB1 defects |
17 |
5.89e-03 |
1.62e-02 |
0.4550 |
0.193000 |
2.28e-01 |
0.217000 |
-2.65e-01 |
1.68e-01 |
1.03e-01 |
1.21e-01 |
5.86e-02 |
Defective binding of RB1 mutants to E2F1,(E2F2, E2F3) |
17 |
5.89e-03 |
1.62e-02 |
0.4550 |
0.193000 |
2.28e-01 |
0.217000 |
-2.65e-01 |
1.68e-01 |
1.03e-01 |
1.21e-01 |
5.86e-02 |
Metabolism of folate and pterines |
15 |
3.98e-02 |
7.65e-02 |
0.4540 |
-0.234000 |
-1.61e-01 |
0.355000 |
-3.55e-03 |
1.17e-01 |
2.79e-01 |
1.74e-02 |
9.81e-01 |
EGFR downregulation |
26 |
2.56e-02 |
5.41e-02 |
0.4540 |
-0.201000 |
-3.64e-01 |
-0.133000 |
-1.26e-01 |
7.65e-02 |
1.34e-03 |
2.39e-01 |
2.68e-01 |
VEGFR2 mediated cell proliferation |
19 |
5.67e-02 |
1.02e-01 |
0.4530 |
-0.033600 |
4.93e-02 |
-0.353000 |
-2.78e-01 |
8.00e-01 |
7.10e-01 |
7.79e-03 |
3.59e-02 |
Long-term potentiation |
16 |
1.26e-02 |
3.04e-02 |
0.4530 |
-0.147000 |
-8.33e-02 |
-0.417000 |
4.66e-02 |
3.09e-01 |
5.64e-01 |
3.84e-03 |
7.47e-01 |
EPHB-mediated forward signaling |
32 |
2.12e-03 |
6.60e-03 |
0.4510 |
0.260000 |
2.15e-01 |
0.002650 |
3.01e-01 |
1.11e-02 |
3.57e-02 |
9.79e-01 |
3.26e-03 |
Gluconeogenesis |
25 |
3.11e-02 |
6.30e-02 |
0.4510 |
-0.216000 |
-2.24e-01 |
-0.106000 |
-3.09e-01 |
6.20e-02 |
5.29e-02 |
3.58e-01 |
7.45e-03 |
DAG and IP3 signaling |
38 |
7.00e-03 |
1.88e-02 |
0.4500 |
-0.175000 |
-2.44e-01 |
-0.271000 |
-1.96e-01 |
6.19e-02 |
9.21e-03 |
3.88e-03 |
3.65e-02 |
Ras activation upon Ca2+ influx through NMDA receptor |
15 |
6.93e-02 |
1.20e-01 |
0.4480 |
-0.138000 |
-3.92e-02 |
-0.407000 |
-1.22e-01 |
3.53e-01 |
7.93e-01 |
6.40e-03 |
4.14e-01 |
PKA activation in glucagon signalling |
15 |
1.21e-01 |
1.86e-01 |
0.4480 |
-0.222000 |
-3.75e-01 |
0.102000 |
1.95e-02 |
1.37e-01 |
1.19e-02 |
4.92e-01 |
8.96e-01 |
Nucleotide-like (purinergic) receptors |
13 |
8.78e-02 |
1.44e-01 |
0.4480 |
0.256000 |
2.49e-01 |
-0.171000 |
2.09e-01 |
1.10e-01 |
1.20e-01 |
2.85e-01 |
1.93e-01 |
Signaling by FGFR2 IIIa TM |
18 |
2.75e-02 |
5.71e-02 |
0.4470 |
-0.125000 |
-2.64e-01 |
0.326000 |
8.83e-02 |
3.59e-01 |
5.27e-02 |
1.66e-02 |
5.17e-01 |
Mitotic Prometaphase |
175 |
2.71e-36 |
2.97e-34 |
0.4460 |
0.183000 |
7.35e-02 |
0.305000 |
-2.59e-01 |
3.27e-05 |
9.42e-02 |
3.62e-12 |
3.59e-09 |
TP53 Regulates Transcription of Cell Cycle Genes |
46 |
1.02e-08 |
7.31e-08 |
0.4460 |
0.126000 |
1.57e-01 |
0.169000 |
-3.61e-01 |
1.41e-01 |
6.58e-02 |
4.73e-02 |
2.35e-05 |
G-protein activation |
17 |
1.59e-02 |
3.67e-02 |
0.4460 |
0.013400 |
5.44e-02 |
0.017700 |
4.42e-01 |
9.24e-01 |
6.98e-01 |
8.99e-01 |
1.60e-03 |
Cell Cycle |
570 |
1.80e-98 |
2.36e-95 |
0.4460 |
0.204000 |
1.43e-01 |
0.332000 |
-1.61e-01 |
1.34e-16 |
7.05e-09 |
2.24e-41 |
7.69e-11 |
Major pathway of rRNA processing in the nucleolus and cytosol |
140 |
1.00e-09 |
8.64e-09 |
0.4460 |
0.265000 |
2.59e-01 |
0.189000 |
1.59e-01 |
6.22e-08 |
1.29e-07 |
1.19e-04 |
1.18e-03 |
activated TAK1 mediates p38 MAPK activation |
18 |
4.35e-02 |
8.22e-02 |
0.4450 |
-0.130000 |
-3.71e-01 |
-0.032500 |
-2.06e-01 |
3.40e-01 |
6.38e-03 |
8.11e-01 |
1.31e-01 |
Cyclin D associated events in G1 |
41 |
2.21e-05 |
9.43e-05 |
0.4450 |
0.305000 |
1.88e-01 |
0.222000 |
-1.42e-01 |
7.19e-04 |
3.72e-02 |
1.40e-02 |
1.17e-01 |
G1 Phase |
41 |
2.21e-05 |
9.43e-05 |
0.4450 |
0.305000 |
1.88e-01 |
0.222000 |
-1.42e-01 |
7.19e-04 |
3.72e-02 |
1.40e-02 |
1.17e-01 |
DNA Double-Strand Break Repair |
122 |
4.73e-21 |
1.44e-19 |
0.4450 |
0.209000 |
1.46e-01 |
0.318000 |
-1.78e-01 |
6.72e-05 |
5.41e-03 |
1.46e-09 |
6.93e-04 |
Cytosolic iron-sulfur cluster assembly |
11 |
2.09e-02 |
4.58e-02 |
0.4440 |
-0.239000 |
4.94e-03 |
0.171000 |
-3.33e-01 |
1.70e-01 |
9.77e-01 |
3.25e-01 |
5.60e-02 |
DNA Damage/Telomere Stress Induced Senescence |
26 |
2.16e-05 |
9.29e-05 |
0.4430 |
0.062600 |
1.16e-01 |
0.216000 |
-3.64e-01 |
5.81e-01 |
3.08e-01 |
5.65e-02 |
1.32e-03 |
Plasma lipoprotein clearance |
24 |
2.77e-02 |
5.73e-02 |
0.4430 |
-0.048200 |
1.22e-01 |
0.331000 |
2.64e-01 |
6.83e-01 |
3.03e-01 |
5.02e-03 |
2.51e-02 |
Receptor-type tyrosine-protein phosphatases |
12 |
3.10e-02 |
6.28e-02 |
0.4430 |
-0.142000 |
-2.02e-01 |
-0.176000 |
3.23e-01 |
3.96e-01 |
2.25e-01 |
2.91e-01 |
5.26e-02 |
Unblocking of NMDA receptors, glutamate binding and activation |
14 |
2.40e-02 |
5.13e-02 |
0.4420 |
-0.138000 |
-1.26e-01 |
-0.389000 |
9.73e-02 |
3.70e-01 |
4.13e-01 |
1.18e-02 |
5.29e-01 |
Norepinephrine Neurotransmitter Release Cycle |
10 |
2.59e-01 |
3.39e-01 |
0.4420 |
-0.047600 |
-1.94e-02 |
-0.414000 |
-1.48e-01 |
7.95e-01 |
9.16e-01 |
2.35e-02 |
4.16e-01 |
Signaling by BMP |
20 |
2.49e-03 |
7.68e-03 |
0.4420 |
0.016100 |
-3.19e-01 |
-0.305000 |
-2.88e-02 |
9.01e-01 |
1.37e-02 |
1.82e-02 |
8.24e-01 |
Collagen degradation |
24 |
2.86e-03 |
8.66e-03 |
0.4400 |
-0.273000 |
-1.68e-01 |
-0.075000 |
2.92e-01 |
2.05e-02 |
1.54e-01 |
5.25e-01 |
1.32e-02 |
Nephrin family interactions |
18 |
1.50e-02 |
3.49e-02 |
0.4400 |
0.067600 |
3.34e-01 |
-0.233000 |
-1.53e-01 |
6.20e-01 |
1.42e-02 |
8.76e-02 |
2.62e-01 |
Dual Incision in GG-NER |
39 |
7.51e-06 |
3.43e-05 |
0.4400 |
0.179000 |
1.51e-01 |
0.359000 |
-9.69e-02 |
5.32e-02 |
1.03e-01 |
1.03e-04 |
2.95e-01 |
Serotonin Neurotransmitter Release Cycle |
10 |
2.76e-01 |
3.58e-01 |
0.4400 |
-0.050200 |
-7.29e-02 |
-0.408000 |
-1.39e-01 |
7.83e-01 |
6.90e-01 |
2.56e-02 |
4.47e-01 |
Cardiac conduction |
87 |
1.21e-07 |
6.81e-07 |
0.4390 |
-0.126000 |
-2.30e-01 |
-0.326000 |
-1.34e-01 |
4.19e-02 |
2.14e-04 |
1.52e-07 |
3.06e-02 |
Synthesis of PC |
24 |
9.31e-03 |
2.36e-02 |
0.4390 |
-0.343000 |
-1.46e-01 |
-0.018100 |
-2.33e-01 |
3.67e-03 |
2.17e-01 |
8.78e-01 |
4.86e-02 |
CS/DS degradation |
10 |
2.51e-01 |
3.31e-01 |
0.4390 |
-0.241000 |
-2.00e-02 |
0.209000 |
3.01e-01 |
1.86e-01 |
9.13e-01 |
2.53e-01 |
9.93e-02 |
Insulin processing |
20 |
8.62e-02 |
1.42e-01 |
0.4390 |
-0.118000 |
-1.69e-01 |
-0.344000 |
-1.78e-01 |
3.62e-01 |
1.91e-01 |
7.74e-03 |
1.69e-01 |
Uptake and actions of bacterial toxins |
24 |
8.93e-02 |
1.47e-01 |
0.4370 |
-0.218000 |
-2.44e-01 |
-0.230000 |
-1.76e-01 |
6.44e-02 |
3.86e-02 |
5.15e-02 |
1.35e-01 |
SUMOylation of ubiquitinylation proteins |
33 |
9.24e-07 |
4.64e-06 |
0.4360 |
0.007930 |
-9.77e-02 |
0.248000 |
-3.45e-01 |
9.37e-01 |
3.32e-01 |
1.38e-02 |
6.02e-04 |
rRNA processing in the nucleus and cytosol |
149 |
6.44e-10 |
5.87e-09 |
0.4360 |
0.260000 |
2.71e-01 |
0.174000 |
1.38e-01 |
4.85e-08 |
1.15e-08 |
2.58e-04 |
3.77e-03 |
Blood group systems biosynthesis |
12 |
8.30e-02 |
1.38e-01 |
0.4360 |
-0.112000 |
-3.33e-01 |
0.256000 |
-3.30e-02 |
5.01e-01 |
4.60e-02 |
1.24e-01 |
8.43e-01 |
Transcriptional regulation by small RNAs |
42 |
1.69e-08 |
1.15e-07 |
0.4360 |
-0.022800 |
-1.41e-01 |
0.311000 |
-2.70e-01 |
7.99e-01 |
1.14e-01 |
4.95e-04 |
2.50e-03 |
TNF receptor superfamily (TNFSF) members mediating non-canonical NF-kB pathway |
11 |
8.36e-03 |
2.17e-02 |
0.4350 |
-0.165000 |
3.21e-01 |
-0.177000 |
1.67e-01 |
3.45e-01 |
6.54e-02 |
3.10e-01 |
3.38e-01 |
Phase 0 - rapid depolarisation |
28 |
4.09e-03 |
1.18e-02 |
0.4350 |
-0.143000 |
-1.87e-01 |
-0.364000 |
-3.68e-02 |
1.92e-01 |
8.76e-02 |
8.59e-04 |
7.36e-01 |
SHC-mediated cascade:FGFR3 |
10 |
1.47e-01 |
2.19e-01 |
0.4340 |
0.194000 |
-1.31e-01 |
-0.161000 |
-3.28e-01 |
2.89e-01 |
4.73e-01 |
3.78e-01 |
7.26e-02 |
Biosynthesis of specialized proresolving mediators (SPMs) |
13 |
1.16e-01 |
1.81e-01 |
0.4320 |
0.133000 |
3.09e-01 |
-0.045200 |
2.67e-01 |
4.07e-01 |
5.34e-02 |
7.78e-01 |
9.54e-02 |
Early Phase of HIV Life Cycle |
13 |
1.77e-01 |
2.51e-01 |
0.4300 |
0.335000 |
2.18e-01 |
0.080700 |
-1.38e-01 |
3.66e-02 |
1.74e-01 |
6.15e-01 |
3.89e-01 |
Zinc transporters |
13 |
2.99e-01 |
3.82e-01 |
0.4300 |
0.303000 |
2.83e-01 |
-0.104000 |
-4.79e-02 |
5.85e-02 |
7.70e-02 |
5.18e-01 |
7.65e-01 |
Telomere Extension By Telomerase |
21 |
2.49e-03 |
7.68e-03 |
0.4300 |
0.140000 |
2.63e-01 |
0.178000 |
-2.54e-01 |
2.66e-01 |
3.72e-02 |
1.58e-01 |
4.39e-02 |
TNFR2 non-canonical NF-kB pathway |
74 |
5.27e-06 |
2.44e-05 |
0.4290 |
0.088900 |
1.86e-01 |
0.335000 |
1.72e-01 |
1.86e-01 |
5.66e-03 |
6.45e-07 |
1.08e-02 |
Cytochrome c-mediated apoptotic response |
10 |
2.38e-01 |
3.19e-01 |
0.4280 |
-0.172000 |
6.95e-04 |
0.368000 |
1.34e-01 |
3.48e-01 |
9.97e-01 |
4.38e-02 |
4.64e-01 |
Post-chaperonin tubulin folding pathway |
17 |
4.61e-02 |
8.63e-02 |
0.4270 |
-0.179000 |
-9.24e-02 |
0.371000 |
6.54e-02 |
2.01e-01 |
5.10e-01 |
8.06e-03 |
6.41e-01 |
Abortive elongation of HIV-1 transcript in the absence of Tat |
22 |
3.65e-03 |
1.07e-02 |
0.4270 |
-0.160000 |
-1.35e-01 |
0.366000 |
-6.59e-02 |
1.93e-01 |
2.72e-01 |
2.93e-03 |
5.93e-01 |
Cargo concentration in the ER |
22 |
1.99e-02 |
4.40e-02 |
0.4270 |
-0.009110 |
-1.74e-01 |
0.251000 |
2.98e-01 |
9.41e-01 |
1.59e-01 |
4.15e-02 |
1.55e-02 |
Nucleobase catabolism |
30 |
3.65e-02 |
7.14e-02 |
0.4260 |
0.121000 |
1.45e-01 |
0.297000 |
2.40e-01 |
2.50e-01 |
1.69e-01 |
4.88e-03 |
2.29e-02 |
Constitutive Signaling by Ligand-Responsive EGFR Cancer Variants |
17 |
1.60e-01 |
2.33e-01 |
0.4260 |
-0.155000 |
-1.86e-01 |
-0.132000 |
-3.25e-01 |
2.70e-01 |
1.84e-01 |
3.48e-01 |
2.04e-02 |
Signaling by Ligand-Responsive EGFR Variants in Cancer |
17 |
1.60e-01 |
2.33e-01 |
0.4260 |
-0.155000 |
-1.86e-01 |
-0.132000 |
-3.25e-01 |
2.70e-01 |
1.84e-01 |
3.48e-01 |
2.04e-02 |
Voltage gated Potassium channels |
20 |
6.02e-02 |
1.07e-01 |
0.4250 |
-0.296000 |
-1.61e-01 |
-0.253000 |
-6.04e-02 |
2.22e-02 |
2.12e-01 |
5.05e-02 |
6.40e-01 |
Glutamate and glutamine metabolism |
11 |
2.80e-01 |
3.62e-01 |
0.4240 |
-0.072200 |
6.17e-02 |
0.368000 |
1.88e-01 |
6.79e-01 |
7.23e-01 |
3.45e-02 |
2.81e-01 |
Synthesis of IP2, IP, and Ins in the cytosol |
13 |
1.19e-01 |
1.85e-01 |
0.4240 |
-0.165000 |
-3.50e-01 |
-0.145000 |
9.47e-02 |
3.02e-01 |
2.89e-02 |
3.66e-01 |
5.54e-01 |
Budding and maturation of HIV virion |
23 |
3.15e-02 |
6.36e-02 |
0.4240 |
-0.008770 |
-1.19e-01 |
0.271000 |
3.03e-01 |
9.42e-01 |
3.23e-01 |
2.43e-02 |
1.20e-02 |
Regulation of PTEN stability and activity |
62 |
3.88e-06 |
1.83e-05 |
0.4230 |
0.135000 |
1.21e-01 |
0.374000 |
8.17e-02 |
6.64e-02 |
9.92e-02 |
3.70e-07 |
2.66e-01 |
Metal ion SLC transporters |
21 |
1.07e-01 |
1.68e-01 |
0.4230 |
0.338000 |
2.20e-01 |
0.078900 |
1.01e-01 |
7.42e-03 |
8.10e-02 |
5.31e-01 |
4.21e-01 |
Glycogen breakdown (glycogenolysis) |
14 |
2.21e-01 |
3.01e-01 |
0.4220 |
-0.134000 |
-1.23e-01 |
-0.350000 |
-1.50e-01 |
3.87e-01 |
4.25e-01 |
2.34e-02 |
3.32e-01 |
Late endosomal microautophagy |
25 |
2.58e-02 |
5.44e-02 |
0.4220 |
-0.071600 |
-1.36e-01 |
0.329000 |
2.14e-01 |
5.36e-01 |
2.38e-01 |
4.42e-03 |
6.41e-02 |
PERK regulates gene expression |
28 |
9.50e-03 |
2.40e-02 |
0.4220 |
0.303000 |
2.21e-01 |
0.169000 |
-9.35e-02 |
5.59e-03 |
4.29e-02 |
1.23e-01 |
3.92e-01 |
Regulation of glycolysis by fructose 2,6-bisphosphate metabolism |
11 |
1.95e-01 |
2.71e-01 |
0.4210 |
-0.025000 |
-2.41e-01 |
-0.065400 |
-3.38e-01 |
8.86e-01 |
1.67e-01 |
7.07e-01 |
5.22e-02 |
Energy dependent regulation of mTOR by LKB1-AMPK |
28 |
1.63e-02 |
3.74e-02 |
0.4200 |
-0.169000 |
-3.38e-01 |
-0.003120 |
-1.83e-01 |
1.23e-01 |
1.99e-03 |
9.77e-01 |
9.33e-02 |
JNK (c-Jun kinases) phosphorylation and activation mediated by activated human TAK1 |
17 |
3.81e-02 |
7.37e-02 |
0.4190 |
-0.056600 |
-3.78e-01 |
-0.115000 |
-1.27e-01 |
6.87e-01 |
6.96e-03 |
4.11e-01 |
3.65e-01 |
RUNX1 interacts with co-factors whose precise effect on RUNX1 targets is not known |
36 |
8.75e-04 |
2.96e-03 |
0.4190 |
-0.105000 |
-2.64e-01 |
-0.002590 |
-3.07e-01 |
2.76e-01 |
6.12e-03 |
9.79e-01 |
1.44e-03 |
Defects in vitamin and cofactor metabolism |
19 |
1.75e-01 |
2.50e-01 |
0.4180 |
-0.177000 |
-2.96e-01 |
-0.138000 |
-1.93e-01 |
1.82e-01 |
2.57e-02 |
2.98e-01 |
1.45e-01 |
MicroRNA (miRNA) biogenesis |
23 |
1.61e-02 |
3.72e-02 |
0.4180 |
-0.207000 |
-1.78e-01 |
0.316000 |
1.42e-02 |
8.54e-02 |
1.40e-01 |
8.70e-03 |
9.06e-01 |
Collagen formation |
70 |
3.99e-12 |
4.94e-11 |
0.4180 |
-0.322000 |
-1.54e-02 |
-0.191000 |
1.84e-01 |
3.14e-06 |
8.24e-01 |
5.74e-03 |
7.79e-03 |
Defects in cobalamin (B12) metabolism |
11 |
2.93e-01 |
3.76e-01 |
0.4170 |
-0.149000 |
-3.69e-01 |
-0.046300 |
-1.18e-01 |
3.93e-01 |
3.42e-02 |
7.90e-01 |
4.99e-01 |
RET signaling |
32 |
4.76e-02 |
8.87e-02 |
0.4160 |
-0.235000 |
-2.26e-01 |
-0.185000 |
-1.82e-01 |
2.14e-02 |
2.71e-02 |
7.09e-02 |
7.52e-02 |
Metabolism of amino acids and derivatives |
242 |
1.57e-17 |
3.48e-16 |
0.4160 |
0.206000 |
1.64e-01 |
0.286000 |
1.47e-01 |
3.53e-08 |
1.16e-05 |
1.96e-14 |
8.36e-05 |
TRAF6 mediated IRF7 activation |
15 |
1.53e-01 |
2.26e-01 |
0.4130 |
0.188000 |
3.16e-01 |
-0.090000 |
-1.65e-01 |
2.08e-01 |
3.39e-02 |
5.46e-01 |
2.68e-01 |
Regulation of RUNX2 expression and activity |
63 |
4.61e-05 |
1.90e-04 |
0.4130 |
0.175000 |
1.15e-01 |
0.329000 |
1.37e-01 |
1.64e-02 |
1.16e-01 |
6.39e-06 |
5.98e-02 |
PKMTs methylate histone lysines |
37 |
1.39e-03 |
4.52e-03 |
0.4130 |
0.018700 |
-6.10e-02 |
-0.119000 |
-3.90e-01 |
8.44e-01 |
5.21e-01 |
2.12e-01 |
3.99e-05 |
Plasma lipoprotein assembly |
10 |
4.13e-01 |
4.96e-01 |
0.4130 |
0.004120 |
-5.62e-02 |
0.272000 |
3.06e-01 |
9.82e-01 |
7.58e-01 |
1.37e-01 |
9.41e-02 |
Interferon Signaling |
145 |
1.68e-08 |
1.15e-07 |
0.4120 |
0.216000 |
2.35e-01 |
0.188000 |
1.80e-01 |
7.13e-06 |
1.09e-06 |
9.74e-05 |
1.82e-04 |
Host Interactions of HIV factors |
112 |
7.54e-14 |
1.22e-12 |
0.4120 |
0.131000 |
1.36e-01 |
0.365000 |
-3.17e-02 |
1.65e-02 |
1.33e-02 |
2.64e-11 |
5.63e-01 |
CaMK IV-mediated phosphorylation of CREB |
10 |
3.53e-01 |
4.38e-01 |
0.4110 |
0.032800 |
-5.80e-02 |
-0.374000 |
-1.56e-01 |
8.58e-01 |
7.51e-01 |
4.04e-02 |
3.92e-01 |
UCH proteinases |
78 |
6.40e-08 |
3.78e-07 |
0.4110 |
0.145000 |
1.77e-01 |
0.341000 |
1.75e-02 |
2.67e-02 |
6.87e-03 |
1.99e-07 |
7.90e-01 |
Activation of RAC1 |
12 |
1.57e-01 |
2.30e-01 |
0.4110 |
0.226000 |
-1.55e-02 |
-0.313000 |
-1.41e-01 |
1.76e-01 |
9.26e-01 |
6.06e-02 |
3.99e-01 |
Signaling by NTRK3 (TRKC) |
17 |
1.76e-01 |
2.50e-01 |
0.4110 |
-0.049800 |
-7.71e-02 |
-0.348000 |
-1.97e-01 |
7.22e-01 |
5.82e-01 |
1.29e-02 |
1.59e-01 |
Thrombin signalling through proteinase activated receptors (PARs) |
25 |
2.11e-02 |
4.61e-02 |
0.4100 |
-0.112000 |
2.69e-02 |
0.155000 |
3.62e-01 |
3.33e-01 |
8.16e-01 |
1.80e-01 |
1.72e-03 |
Negative regulation of FGFR2 signaling |
21 |
1.51e-02 |
3.52e-02 |
0.4090 |
-0.084800 |
-3.94e-01 |
-0.033300 |
-6.46e-02 |
5.01e-01 |
1.78e-03 |
7.92e-01 |
6.09e-01 |
CREB1 phosphorylation through NMDA receptor-mediated activation of RAS signaling |
23 |
6.41e-02 |
1.12e-01 |
0.4090 |
-0.063000 |
-8.52e-02 |
-0.356000 |
-1.73e-01 |
6.01e-01 |
4.80e-01 |
3.16e-03 |
1.52e-01 |
Glucose metabolism |
74 |
8.83e-09 |
6.37e-08 |
0.4090 |
-0.137000 |
-2.29e-01 |
0.099400 |
-2.94e-01 |
4.24e-02 |
6.77e-04 |
1.40e-01 |
1.23e-05 |
HSF1 activation |
23 |
1.73e-02 |
3.95e-02 |
0.4090 |
-0.211000 |
-2.10e-01 |
0.089600 |
-2.66e-01 |
8.06e-02 |
8.12e-02 |
4.57e-01 |
2.71e-02 |
Non-integrin membrane-ECM interactions |
39 |
4.81e-05 |
1.97e-04 |
0.4090 |
-0.195000 |
-2.56e-02 |
-0.358000 |
3.90e-04 |
3.48e-02 |
7.83e-01 |
1.10e-04 |
9.97e-01 |
CaM pathway |
32 |
2.97e-02 |
6.08e-02 |
0.4080 |
-0.149000 |
-2.70e-01 |
-0.226000 |
-1.42e-01 |
1.45e-01 |
8.15e-03 |
2.73e-02 |
1.64e-01 |
Calmodulin induced events |
32 |
2.97e-02 |
6.08e-02 |
0.4080 |
-0.149000 |
-2.70e-01 |
-0.226000 |
-1.42e-01 |
1.45e-01 |
8.15e-03 |
2.73e-02 |
1.64e-01 |
Meiotic synapsis |
27 |
3.40e-03 |
1.01e-02 |
0.4080 |
0.193000 |
2.48e-01 |
0.116000 |
-2.32e-01 |
8.29e-02 |
2.55e-02 |
2.99e-01 |
3.71e-02 |
Signaling by NOTCH4 |
74 |
3.98e-05 |
1.66e-04 |
0.4060 |
0.137000 |
1.90e-01 |
0.299000 |
1.42e-01 |
4.23e-02 |
4.67e-03 |
8.56e-06 |
3.43e-02 |
Platelet calcium homeostasis |
22 |
3.08e-02 |
6.26e-02 |
0.4050 |
-0.265000 |
-1.13e-01 |
-0.282000 |
-3.67e-02 |
3.14e-02 |
3.59e-01 |
2.21e-02 |
7.66e-01 |
Cellular response to heat stress |
86 |
1.83e-08 |
1.23e-07 |
0.4040 |
-0.164000 |
-2.34e-01 |
0.050300 |
-2.82e-01 |
8.72e-03 |
1.81e-04 |
4.21e-01 |
6.37e-06 |
DAP12 signaling |
25 |
5.89e-02 |
1.05e-01 |
0.4040 |
0.220000 |
3.33e-01 |
-0.055800 |
-2.31e-02 |
5.68e-02 |
3.96e-03 |
6.29e-01 |
8.42e-01 |
Endosomal Sorting Complex Required For Transport (ESCRT) |
26 |
2.61e-02 |
5.49e-02 |
0.4030 |
0.011500 |
-1.04e-01 |
0.251000 |
2.97e-01 |
9.19e-01 |
3.59e-01 |
2.69e-02 |
8.77e-03 |
Regulation of TP53 Activity through Methylation |
14 |
1.72e-01 |
2.46e-01 |
0.4030 |
-0.167000 |
-8.06e-02 |
-0.093400 |
-3.45e-01 |
2.81e-01 |
6.02e-01 |
5.45e-01 |
2.54e-02 |
M Phase |
322 |
5.85e-50 |
1.92e-47 |
0.4010 |
0.158000 |
7.02e-02 |
0.330000 |
-1.49e-01 |
1.30e-06 |
3.13e-02 |
3.29e-24 |
4.92e-06 |
Cellular response to hypoxia |
64 |
5.07e-05 |
2.07e-04 |
0.4010 |
0.123000 |
1.30e-01 |
0.340000 |
1.15e-01 |
9.01e-02 |
7.31e-02 |
2.61e-06 |
1.12e-01 |
Synthesis of PIPs at the early endosome membrane |
16 |
1.88e-01 |
2.63e-01 |
0.4000 |
0.021100 |
3.88e-02 |
-0.345000 |
-1.97e-01 |
8.84e-01 |
7.88e-01 |
1.67e-02 |
1.73e-01 |
RHO GTPases Activate Formins |
109 |
5.89e-18 |
1.41e-16 |
0.4000 |
0.155000 |
6.86e-02 |
0.273000 |
-2.38e-01 |
5.13e-03 |
2.17e-01 |
9.09e-07 |
1.85e-05 |
ERBB2 Regulates Cell Motility |
12 |
3.04e-01 |
3.86e-01 |
0.3990 |
-0.329000 |
-1.88e-01 |
-0.020000 |
1.23e-01 |
4.85e-02 |
2.59e-01 |
9.04e-01 |
4.62e-01 |
Assembly and cell surface presentation of NMDA receptors |
15 |
3.87e-02 |
7.48e-02 |
0.3990 |
-0.092200 |
-2.13e-01 |
-0.303000 |
1.17e-01 |
5.37e-01 |
1.54e-01 |
4.24e-02 |
4.32e-01 |
SEMA3A-Plexin repulsion signaling by inhibiting Integrin adhesion |
14 |
9.23e-02 |
1.51e-01 |
0.3980 |
-0.223000 |
8.02e-04 |
0.060900 |
3.24e-01 |
1.48e-01 |
9.96e-01 |
6.93e-01 |
3.59e-02 |
Metabolism of non-coding RNA |
48 |
2.86e-08 |
1.81e-07 |
0.3980 |
0.071100 |
-7.70e-02 |
0.338000 |
-1.81e-01 |
3.94e-01 |
3.57e-01 |
5.09e-05 |
3.00e-02 |
snRNP Assembly |
48 |
2.86e-08 |
1.81e-07 |
0.3980 |
0.071100 |
-7.70e-02 |
0.338000 |
-1.81e-01 |
3.94e-01 |
3.57e-01 |
5.09e-05 |
3.00e-02 |
Cobalamin (Cbl, vitamin B12) transport and metabolism |
12 |
3.77e-01 |
4.63e-01 |
0.3970 |
-0.149000 |
-3.23e-01 |
-0.112000 |
-1.36e-01 |
3.71e-01 |
5.26e-02 |
5.00e-01 |
4.15e-01 |
Signal amplification |
27 |
1.28e-02 |
3.07e-02 |
0.3960 |
0.042200 |
3.20e-02 |
0.092400 |
3.82e-01 |
7.05e-01 |
7.73e-01 |
4.06e-01 |
5.97e-04 |
Nuclear Envelope (NE) Reassembly |
64 |
3.43e-10 |
3.31e-09 |
0.3960 |
0.033500 |
-8.59e-02 |
0.364000 |
-1.27e-01 |
6.43e-01 |
2.35e-01 |
4.89e-07 |
7.93e-02 |
Beta-catenin phosphorylation cascade |
16 |
9.42e-02 |
1.53e-01 |
0.3960 |
-0.079700 |
-2.36e-01 |
0.002350 |
-3.07e-01 |
5.81e-01 |
1.02e-01 |
9.87e-01 |
3.35e-02 |
ABC-family proteins mediated transport |
84 |
2.65e-06 |
1.28e-05 |
0.3960 |
0.092100 |
8.16e-02 |
0.345000 |
1.48e-01 |
1.45e-01 |
1.97e-01 |
4.53e-08 |
1.90e-02 |
Interleukin-10 signaling |
24 |
4.95e-02 |
9.09e-02 |
0.3960 |
0.165000 |
8.94e-02 |
0.122000 |
3.26e-01 |
1.61e-01 |
4.48e-01 |
2.99e-01 |
5.73e-03 |
Signaling by ERBB2 ECD mutants |
15 |
2.58e-01 |
3.38e-01 |
0.3950 |
-0.157000 |
-1.25e-01 |
-0.130000 |
-3.14e-01 |
2.91e-01 |
4.02e-01 |
3.83e-01 |
3.54e-02 |
Negative regulation of NMDA receptor-mediated neuronal transmission |
16 |
6.57e-02 |
1.15e-01 |
0.3940 |
-0.206000 |
-1.72e-01 |
-0.269000 |
1.06e-01 |
1.54e-01 |
2.34e-01 |
6.27e-02 |
4.65e-01 |
p130Cas linkage to MAPK signaling for integrins |
12 |
4.93e-02 |
9.09e-02 |
0.3920 |
0.082800 |
8.31e-02 |
-0.293000 |
2.32e-01 |
6.20e-01 |
6.18e-01 |
7.88e-02 |
1.63e-01 |
Synaptic adhesion-like molecules |
15 |
7.13e-02 |
1.22e-01 |
0.3910 |
-0.116000 |
-2.02e-01 |
-0.013500 |
3.14e-01 |
4.36e-01 |
1.76e-01 |
9.28e-01 |
3.51e-02 |
Circadian Clock |
63 |
1.76e-05 |
7.64e-05 |
0.3910 |
0.090500 |
-1.45e-01 |
-0.211000 |
-2.82e-01 |
2.14e-01 |
4.65e-02 |
3.81e-03 |
1.11e-04 |
Gap-filling DNA repair synthesis and ligation in TC-NER |
61 |
5.59e-07 |
2.89e-06 |
0.3910 |
0.156000 |
1.40e-01 |
0.323000 |
-6.91e-02 |
3.49e-02 |
5.90e-02 |
1.30e-05 |
3.51e-01 |
Meiosis |
47 |
3.98e-06 |
1.86e-05 |
0.3900 |
0.152000 |
1.86e-01 |
0.235000 |
-1.97e-01 |
7.16e-02 |
2.72e-02 |
5.32e-03 |
1.93e-02 |
Nuclear Envelope Breakdown |
48 |
4.47e-08 |
2.71e-07 |
0.3900 |
0.023500 |
-3.97e-02 |
0.309000 |
-2.34e-01 |
7.79e-01 |
6.35e-01 |
2.18e-04 |
5.15e-03 |
GRB2:SOS provides linkage to MAPK signaling for Integrins |
12 |
4.38e-02 |
8.26e-02 |
0.3900 |
0.067200 |
8.36e-03 |
-0.324000 |
2.05e-01 |
6.87e-01 |
9.60e-01 |
5.17e-02 |
2.19e-01 |
FCERI mediated Ca+2 mobilization |
27 |
2.87e-02 |
5.89e-02 |
0.3890 |
0.138000 |
1.45e-01 |
-0.312000 |
-1.17e-01 |
2.14e-01 |
1.94e-01 |
4.97e-03 |
2.92e-01 |
Negative regulation of FGFR4 signaling |
18 |
3.05e-02 |
6.21e-02 |
0.3890 |
-0.059000 |
-3.71e-01 |
0.045600 |
-8.96e-02 |
6.65e-01 |
6.45e-03 |
7.38e-01 |
5.11e-01 |
Cleavage of the damaged purine |
11 |
9.38e-02 |
1.52e-01 |
0.3890 |
0.043500 |
3.32e-01 |
0.099300 |
-1.70e-01 |
8.03e-01 |
5.65e-02 |
5.69e-01 |
3.28e-01 |
Depurination |
11 |
9.38e-02 |
1.52e-01 |
0.3890 |
0.043500 |
3.32e-01 |
0.099300 |
-1.70e-01 |
8.03e-01 |
5.65e-02 |
5.69e-01 |
3.28e-01 |
Recognition and association of DNA glycosylase with site containing an affected purine |
11 |
9.38e-02 |
1.52e-01 |
0.3890 |
0.043500 |
3.32e-01 |
0.099300 |
-1.70e-01 |
8.03e-01 |
5.65e-02 |
5.69e-01 |
3.28e-01 |
Transcriptional activation of mitochondrial biogenesis |
50 |
3.25e-03 |
9.71e-03 |
0.3880 |
-0.009440 |
-1.33e-01 |
-0.232000 |
-2.80e-01 |
9.08e-01 |
1.03e-01 |
4.53e-03 |
6.09e-04 |
Pre-NOTCH Processing in Golgi |
16 |
1.52e-01 |
2.24e-01 |
0.3880 |
-0.333000 |
-1.44e-01 |
0.135000 |
2.16e-02 |
2.12e-02 |
3.20e-01 |
3.49e-01 |
8.81e-01 |
PKA activation |
16 |
1.19e-01 |
1.85e-01 |
0.3880 |
-0.136000 |
-3.53e-01 |
0.058200 |
5.98e-02 |
3.47e-01 |
1.45e-02 |
6.87e-01 |
6.79e-01 |
Hyaluronan metabolism |
14 |
3.69e-01 |
4.55e-01 |
0.3870 |
0.061700 |
8.87e-02 |
0.306000 |
2.10e-01 |
6.90e-01 |
5.66e-01 |
4.74e-02 |
1.74e-01 |
Free fatty acids regulate insulin secretion |
10 |
5.76e-01 |
6.36e-01 |
0.3850 |
-0.290000 |
-2.51e-01 |
-0.029400 |
2.21e-02 |
1.12e-01 |
1.69e-01 |
8.72e-01 |
9.04e-01 |
Uptake and function of anthrax toxins |
11 |
3.92e-01 |
4.77e-01 |
0.3840 |
-0.168000 |
-3.45e-01 |
-0.014100 |
-1.24e-02 |
3.35e-01 |
4.74e-02 |
9.36e-01 |
9.43e-01 |
Phosphorylation of the APC/C |
20 |
5.94e-03 |
1.62e-02 |
0.3840 |
0.241000 |
-2.30e-02 |
0.290000 |
-7.16e-02 |
6.24e-02 |
8.58e-01 |
2.50e-02 |
5.79e-01 |
Glycolysis |
58 |
4.77e-07 |
2.49e-06 |
0.3840 |
-0.086300 |
-1.97e-01 |
0.128000 |
-2.91e-01 |
2.56e-01 |
9.50e-03 |
9.25e-02 |
1.26e-04 |
Translation of Replicase and Assembly of the Replication Transcription Complex |
11 |
2.91e-01 |
3.74e-01 |
0.3830 |
0.049500 |
-1.17e-01 |
0.309000 |
1.88e-01 |
7.76e-01 |
5.02e-01 |
7.62e-02 |
2.79e-01 |
Inactivation of APC/C via direct inhibition of the APC/C complex |
21 |
4.54e-03 |
1.30e-02 |
0.3820 |
0.187000 |
-4.03e-02 |
0.323000 |
-7.13e-02 |
1.38e-01 |
7.49e-01 |
1.04e-02 |
5.72e-01 |
Inhibition of the proteolytic activity of APC/C required for the onset of anaphase by mitotic spindle checkpoint components |
21 |
4.54e-03 |
1.30e-02 |
0.3820 |
0.187000 |
-4.03e-02 |
0.323000 |
-7.13e-02 |
1.38e-01 |
7.49e-01 |
1.04e-02 |
5.72e-01 |
Activation of G protein gated Potassium channels |
18 |
2.34e-02 |
5.03e-02 |
0.3820 |
0.059400 |
1.07e-01 |
-0.094000 |
3.50e-01 |
6.63e-01 |
4.32e-01 |
4.90e-01 |
1.03e-02 |
G protein gated Potassium channels |
18 |
2.34e-02 |
5.03e-02 |
0.3820 |
0.059400 |
1.07e-01 |
-0.094000 |
3.50e-01 |
6.63e-01 |
4.32e-01 |
4.90e-01 |
1.03e-02 |
Inhibition of voltage gated Ca2+ channels via Gbeta/gamma subunits |
18 |
2.34e-02 |
5.03e-02 |
0.3820 |
0.059400 |
1.07e-01 |
-0.094000 |
3.50e-01 |
6.63e-01 |
4.32e-01 |
4.90e-01 |
1.03e-02 |
Activation of NF-kappaB in B cells |
61 |
2.80e-05 |
1.19e-04 |
0.3820 |
0.130000 |
1.47e-01 |
0.326000 |
2.89e-02 |
8.05e-02 |
4.74e-02 |
1.05e-05 |
6.97e-01 |
APC-Cdc20 mediated degradation of Nek2A |
24 |
2.01e-03 |
6.33e-03 |
0.3810 |
0.170000 |
-2.14e-02 |
0.329000 |
-8.98e-02 |
1.51e-01 |
8.56e-01 |
5.29e-03 |
4.47e-01 |
Nucleobase biosynthesis |
15 |
7.22e-02 |
1.23e-01 |
0.3810 |
0.006170 |
4.36e-02 |
0.378000 |
-1.73e-02 |
9.67e-01 |
7.70e-01 |
1.12e-02 |
9.08e-01 |
Carnitine metabolism |
12 |
2.55e-01 |
3.36e-01 |
0.3810 |
-0.237000 |
-1.87e-02 |
-0.223000 |
-1.97e-01 |
1.55e-01 |
9.11e-01 |
1.82e-01 |
2.37e-01 |
Disorders of developmental biology |
11 |
1.50e-01 |
2.23e-01 |
0.3800 |
0.128000 |
-1.95e-01 |
-0.079600 |
-2.90e-01 |
4.63e-01 |
2.62e-01 |
6.48e-01 |
9.63e-02 |
Loss of function of MECP2 in Rett syndrome |
11 |
1.50e-01 |
2.23e-01 |
0.3800 |
0.128000 |
-1.95e-01 |
-0.079600 |
-2.90e-01 |
4.63e-01 |
2.62e-01 |
6.48e-01 |
9.63e-02 |
Pervasive developmental disorders |
11 |
1.50e-01 |
2.23e-01 |
0.3800 |
0.128000 |
-1.95e-01 |
-0.079600 |
-2.90e-01 |
4.63e-01 |
2.62e-01 |
6.48e-01 |
9.63e-02 |
LDL clearance |
15 |
2.73e-01 |
3.55e-01 |
0.3790 |
-0.061200 |
2.79e-02 |
0.322000 |
1.89e-01 |
6.82e-01 |
8.52e-01 |
3.08e-02 |
2.06e-01 |
Role of phospholipids in phagocytosis |
27 |
2.50e-02 |
5.31e-02 |
0.3790 |
0.007680 |
2.54e-01 |
0.216000 |
1.80e-01 |
9.45e-01 |
2.22e-02 |
5.23e-02 |
1.06e-01 |
Activation of the AP-1 family of transcription factors |
10 |
2.39e-01 |
3.19e-01 |
0.3790 |
0.034600 |
-2.90e-01 |
-0.108000 |
-2.16e-01 |
8.50e-01 |
1.12e-01 |
5.55e-01 |
2.37e-01 |
FGFR2 mutant receptor activation |
21 |
6.87e-02 |
1.19e-01 |
0.3780 |
-0.146000 |
-3.00e-01 |
0.176000 |
2.54e-02 |
2.47e-01 |
1.73e-02 |
1.62e-01 |
8.40e-01 |
Hedgehog 'on' state |
75 |
8.77e-05 |
3.43e-04 |
0.3780 |
0.092600 |
9.50e-02 |
0.317000 |
1.59e-01 |
1.66e-01 |
1.55e-01 |
2.15e-06 |
1.74e-02 |
TNFs bind their physiological receptors |
11 |
4.02e-01 |
4.85e-01 |
0.3780 |
-0.039700 |
1.31e-01 |
0.172000 |
3.07e-01 |
8.20e-01 |
4.51e-01 |
3.24e-01 |
7.76e-02 |
Mitotic G2-G2/M phases |
175 |
1.47e-21 |
4.71e-20 |
0.3780 |
0.129000 |
9.22e-02 |
0.330000 |
-9.13e-02 |
3.31e-03 |
3.60e-02 |
5.27e-14 |
3.78e-02 |
G2/M Transition |
173 |
4.56e-21 |
1.42e-19 |
0.3770 |
0.131000 |
9.37e-02 |
0.328000 |
-8.99e-02 |
3.02e-03 |
3.41e-02 |
1.02e-13 |
4.20e-02 |
Translation of structural proteins |
26 |
5.83e-02 |
1.05e-01 |
0.3760 |
-0.171000 |
-1.82e-01 |
0.259000 |
1.10e-01 |
1.30e-01 |
1.09e-01 |
2.25e-02 |
3.33e-01 |
rRNA processing |
166 |
2.39e-08 |
1.55e-07 |
0.3760 |
0.245000 |
2.51e-01 |
0.114000 |
7.31e-02 |
5.35e-08 |
2.75e-08 |
1.14e-02 |
1.05e-01 |
Prolonged ERK activation events |
13 |
1.91e-01 |
2.67e-01 |
0.3750 |
0.006430 |
-2.81e-01 |
-0.137000 |
-2.08e-01 |
9.68e-01 |
7.95e-02 |
3.94e-01 |
1.95e-01 |
Transcription-Coupled Nucleotide Excision Repair (TC-NER) |
75 |
3.01e-07 |
1.59e-06 |
0.3750 |
0.140000 |
8.79e-02 |
0.336000 |
2.22e-05 |
3.62e-02 |
1.89e-01 |
4.89e-07 |
1.00e+00 |
Post NMDA receptor activation events |
51 |
1.10e-02 |
2.71e-02 |
0.3750 |
-0.151000 |
-2.11e-01 |
-0.218000 |
-1.59e-01 |
6.20e-02 |
9.05e-03 |
7.17e-03 |
4.97e-02 |
Signaling by cytosolic FGFR1 fusion mutants |
18 |
2.42e-01 |
3.21e-01 |
0.3740 |
-0.034000 |
-1.80e-01 |
-0.248000 |
-2.13e-01 |
8.03e-01 |
1.87e-01 |
6.86e-02 |
1.18e-01 |
Surfactant metabolism |
14 |
2.33e-01 |
3.13e-01 |
0.3740 |
-0.064100 |
-7.60e-02 |
0.123000 |
3.39e-01 |
6.78e-01 |
6.23e-01 |
4.24e-01 |
2.81e-02 |
FCGR3A-mediated phagocytosis |
61 |
4.60e-04 |
1.61e-03 |
0.3740 |
0.159000 |
2.57e-01 |
0.016400 |
2.20e-01 |
3.23e-02 |
5.17e-04 |
8.25e-01 |
3.00e-03 |
Leishmania phagocytosis |
61 |
4.60e-04 |
1.61e-03 |
0.3740 |
0.159000 |
2.57e-01 |
0.016400 |
2.20e-01 |
3.23e-02 |
5.17e-04 |
8.25e-01 |
3.00e-03 |
Parasite infection |
61 |
4.60e-04 |
1.61e-03 |
0.3740 |
0.159000 |
2.57e-01 |
0.016400 |
2.20e-01 |
3.23e-02 |
5.17e-04 |
8.25e-01 |
3.00e-03 |
Phase II - Conjugation of compounds |
66 |
4.92e-04 |
1.72e-03 |
0.3740 |
0.276000 |
1.47e-01 |
0.142000 |
1.48e-01 |
1.06e-04 |
3.88e-02 |
4.68e-02 |
3.82e-02 |
PI3K events in ERBB2 signaling |
13 |
3.78e-01 |
4.63e-01 |
0.3740 |
-0.248000 |
-2.41e-01 |
-0.131000 |
5.33e-02 |
1.21e-01 |
1.33e-01 |
4.14e-01 |
7.39e-01 |
Inwardly rectifying K+ channels |
20 |
2.61e-02 |
5.49e-02 |
0.3730 |
0.088600 |
1.03e-01 |
-0.061700 |
3.42e-01 |
4.93e-01 |
4.25e-01 |
6.33e-01 |
8.10e-03 |
TRAF3-dependent IRF activation pathway |
13 |
2.06e-01 |
2.82e-01 |
0.3730 |
0.117000 |
3.20e-01 |
-0.055700 |
-1.42e-01 |
4.63e-01 |
4.61e-02 |
7.28e-01 |
3.76e-01 |
Signaling by ERBB2 TMD/JMD mutants |
18 |
2.30e-01 |
3.10e-01 |
0.3730 |
-0.300000 |
-1.62e-01 |
-0.128000 |
-8.13e-02 |
2.78e-02 |
2.34e-01 |
3.49e-01 |
5.51e-01 |
Signaling by NODAL |
13 |
1.18e-01 |
1.84e-01 |
0.3730 |
-0.039800 |
-3.16e-01 |
0.179000 |
7.16e-02 |
8.04e-01 |
4.83e-02 |
2.63e-01 |
6.55e-01 |
Golgi Cisternae Pericentriolar Stack Reorganization |
14 |
1.03e-01 |
1.63e-01 |
0.3730 |
0.177000 |
-1.17e-02 |
0.327000 |
2.36e-02 |
2.51e-01 |
9.40e-01 |
3.43e-02 |
8.78e-01 |
Constitutive Signaling by AKT1 E17K in Cancer |
25 |
2.40e-02 |
5.13e-02 |
0.3720 |
-0.039600 |
-2.00e-01 |
-0.021500 |
-3.11e-01 |
7.32e-01 |
8.42e-02 |
8.53e-01 |
7.10e-03 |
Processing of SMDT1 |
15 |
2.12e-01 |
2.91e-01 |
0.3720 |
0.103000 |
-2.37e-02 |
0.318000 |
1.62e-01 |
4.89e-01 |
8.74e-01 |
3.32e-02 |
2.78e-01 |
Transcriptional activity of SMAD2/SMAD3:SMAD4 heterotrimer |
39 |
3.02e-03 |
9.06e-03 |
0.3720 |
0.090200 |
-8.48e-02 |
-0.126000 |
-3.27e-01 |
3.30e-01 |
3.60e-01 |
1.73e-01 |
4.11e-04 |
Nicotinamide salvaging |
13 |
4.20e-01 |
5.02e-01 |
0.3710 |
0.174000 |
2.79e-01 |
0.021200 |
1.69e-01 |
2.76e-01 |
8.12e-02 |
8.95e-01 |
2.92e-01 |
Triglyceride catabolism |
15 |
1.93e-01 |
2.69e-01 |
0.3700 |
0.029300 |
2.33e-02 |
-0.104000 |
-3.54e-01 |
8.44e-01 |
8.76e-01 |
4.85e-01 |
1.78e-02 |
YAP1- and WWTR1 (TAZ)-stimulated gene expression |
13 |
5.22e-01 |
5.92e-01 |
0.3700 |
-0.221000 |
-2.72e-01 |
-0.092100 |
-7.60e-02 |
1.68e-01 |
8.96e-02 |
5.65e-01 |
6.35e-01 |
Integrin cell surface interactions |
51 |
1.35e-07 |
7.53e-07 |
0.3700 |
-0.074000 |
1.40e-01 |
-0.312000 |
1.22e-01 |
3.61e-01 |
8.47e-02 |
1.19e-04 |
1.33e-01 |
Notch-HLH transcription pathway |
25 |
1.59e-01 |
2.33e-01 |
0.3700 |
-0.087700 |
-1.19e-01 |
-0.270000 |
-2.05e-01 |
4.48e-01 |
3.02e-01 |
1.95e-02 |
7.63e-02 |
BMAL1:CLOCK,NPAS2 activates circadian gene expression |
24 |
2.76e-02 |
5.71e-02 |
0.3700 |
0.131000 |
-1.23e-01 |
-0.276000 |
-1.68e-01 |
2.68e-01 |
2.97e-01 |
1.92e-02 |
1.55e-01 |
CRMPs in Sema3A signaling |
15 |
2.55e-02 |
5.41e-02 |
0.3690 |
-0.118000 |
8.43e-02 |
-0.312000 |
1.33e-01 |
4.28e-01 |
5.72e-01 |
3.63e-02 |
3.73e-01 |
Ca-dependent events |
34 |
3.16e-02 |
6.36e-02 |
0.3690 |
-0.113000 |
-2.65e-01 |
-0.203000 |
-1.11e-01 |
2.57e-01 |
7.57e-03 |
4.10e-02 |
2.63e-01 |
Regulation of HSF1-mediated heat shock response |
69 |
1.02e-07 |
5.79e-07 |
0.3680 |
-0.098400 |
-1.91e-01 |
0.141000 |
-2.64e-01 |
1.58e-01 |
6.25e-03 |
4.24e-02 |
1.51e-04 |
Regulation of TLR by endogenous ligand |
10 |
9.90e-02 |
1.58e-01 |
0.3680 |
-0.156000 |
1.09e-01 |
-0.168000 |
2.67e-01 |
3.92e-01 |
5.51e-01 |
3.58e-01 |
1.44e-01 |
GRB2 events in ERBB2 signaling |
13 |
4.28e-01 |
5.09e-01 |
0.3680 |
-0.247000 |
-2.07e-01 |
-0.177000 |
-1.69e-02 |
1.23e-01 |
1.96e-01 |
2.70e-01 |
9.16e-01 |
HCMV Late Events |
47 |
1.20e-05 |
5.37e-05 |
0.3680 |
0.002430 |
-1.18e-01 |
0.345000 |
-4.70e-02 |
9.77e-01 |
1.60e-01 |
4.28e-05 |
5.77e-01 |
Scavenging by Class A Receptors |
13 |
1.71e-01 |
2.45e-01 |
0.3680 |
-0.139000 |
2.08e-02 |
0.038000 |
3.38e-01 |
3.84e-01 |
8.97e-01 |
8.13e-01 |
3.50e-02 |
IRE1alpha activates chaperones |
49 |
1.27e-03 |
4.21e-03 |
0.3680 |
-0.137000 |
-2.17e-01 |
0.248000 |
9.03e-02 |
9.80e-02 |
8.79e-03 |
2.66e-03 |
2.74e-01 |
Gene Silencing by RNA |
59 |
1.04e-07 |
5.93e-07 |
0.3680 |
-0.086500 |
-1.39e-01 |
0.252000 |
-2.12e-01 |
2.51e-01 |
6.56e-02 |
8.18e-04 |
4.93e-03 |
tRNA Aminoacylation |
24 |
6.72e-02 |
1.17e-01 |
0.3680 |
-0.148000 |
-1.66e-01 |
0.280000 |
8.35e-02 |
2.08e-01 |
1.59e-01 |
1.75e-02 |
4.79e-01 |
Glyoxylate metabolism and glycine degradation |
24 |
8.44e-02 |
1.39e-01 |
0.3670 |
-0.051000 |
-1.77e-01 |
-0.102000 |
-3.01e-01 |
6.66e-01 |
1.33e-01 |
3.87e-01 |
1.07e-02 |
Metabolism of nucleotides |
85 |
2.76e-05 |
1.18e-04 |
0.3670 |
0.101000 |
1.06e-01 |
0.309000 |
1.33e-01 |
1.08e-01 |
9.29e-02 |
8.33e-07 |
3.40e-02 |
Interleukin-35 Signalling |
10 |
2.00e-01 |
2.76e-01 |
0.3660 |
0.315000 |
3.97e-02 |
-0.157000 |
9.25e-02 |
8.45e-02 |
8.28e-01 |
3.91e-01 |
6.13e-01 |
ROS and RNS production in phagocytes |
28 |
6.69e-02 |
1.16e-01 |
0.3660 |
-0.000192 |
1.62e-01 |
0.191000 |
2.67e-01 |
9.99e-01 |
1.38e-01 |
7.98e-02 |
1.47e-02 |
Regulation of TP53 Degradation |
32 |
5.73e-04 |
1.98e-03 |
0.3660 |
0.143000 |
-5.86e-02 |
0.051500 |
-3.28e-01 |
1.63e-01 |
5.67e-01 |
6.14e-01 |
1.34e-03 |
Assembly Of The HIV Virion |
13 |
3.44e-01 |
4.29e-01 |
0.3660 |
-0.157000 |
-1.95e-01 |
0.250000 |
9.16e-02 |
3.27e-01 |
2.23e-01 |
1.18e-01 |
5.67e-01 |
Lewis blood group biosynthesis |
10 |
1.46e-01 |
2.18e-01 |
0.3660 |
0.025500 |
-3.22e-01 |
0.158000 |
6.53e-02 |
8.89e-01 |
7.77e-02 |
3.86e-01 |
7.21e-01 |
Muscle contraction |
143 |
3.48e-10 |
3.34e-09 |
0.3660 |
-0.133000 |
-6.20e-02 |
-0.316000 |
-1.11e-01 |
6.28e-03 |
2.02e-01 |
7.30e-11 |
2.22e-02 |
Metabolism of steroid hormones |
18 |
5.46e-02 |
9.89e-02 |
0.3650 |
0.081200 |
3.69e-02 |
-0.010400 |
3.54e-01 |
5.51e-01 |
7.86e-01 |
9.39e-01 |
9.28e-03 |
Syndecan interactions |
19 |
9.70e-03 |
2.45e-02 |
0.3650 |
-0.079800 |
-8.09e-03 |
-0.305000 |
1.84e-01 |
5.47e-01 |
9.51e-01 |
2.14e-02 |
1.66e-01 |
CREB1 phosphorylation through the activation of Adenylate Cyclase |
10 |
2.84e-01 |
3.66e-01 |
0.3640 |
-0.070000 |
-3.31e-01 |
0.121000 |
6.13e-02 |
7.02e-01 |
7.01e-02 |
5.07e-01 |
7.37e-01 |
G beta:gamma signalling through PI3Kgamma |
20 |
9.35e-02 |
1.52e-01 |
0.3630 |
0.071300 |
1.49e-01 |
0.031500 |
3.22e-01 |
5.81e-01 |
2.50e-01 |
8.07e-01 |
1.26e-02 |
Mitotic Prophase |
77 |
4.24e-11 |
4.49e-10 |
0.3630 |
0.078100 |
-2.45e-02 |
0.302000 |
-1.85e-01 |
2.37e-01 |
7.11e-01 |
4.83e-06 |
5.13e-03 |
Transcriptional regulation of pluripotent stem cells |
14 |
3.07e-02 |
6.24e-02 |
0.3620 |
0.038100 |
-3.22e-01 |
-0.121000 |
1.05e-01 |
8.05e-01 |
3.69e-02 |
4.31e-01 |
4.98e-01 |
Degradation of beta-catenin by the destruction complex |
75 |
3.30e-06 |
1.56e-05 |
0.3610 |
0.111000 |
1.03e-01 |
0.327000 |
2.52e-02 |
9.60e-02 |
1.25e-01 |
9.84e-07 |
7.07e-01 |
TAK1 activates NFkB by phosphorylation and activation of IKKs complex |
24 |
2.22e-01 |
3.02e-01 |
0.3610 |
-0.234000 |
-2.27e-01 |
-0.057000 |
-1.44e-01 |
4.76e-02 |
5.42e-02 |
6.29e-01 |
2.22e-01 |
Pausing and recovery of Tat-mediated HIV elongation |
26 |
3.00e-03 |
8.99e-03 |
0.3610 |
-0.073900 |
-7.75e-03 |
0.339000 |
-9.75e-02 |
5.14e-01 |
9.45e-01 |
2.76e-03 |
3.90e-01 |
Tat-mediated HIV elongation arrest and recovery |
26 |
3.00e-03 |
8.99e-03 |
0.3610 |
-0.073900 |
-7.75e-03 |
0.339000 |
-9.75e-02 |
5.14e-01 |
9.45e-01 |
2.76e-03 |
3.90e-01 |
GPVI-mediated activation cascade |
30 |
7.64e-03 |
2.02e-02 |
0.3600 |
0.092600 |
3.19e-01 |
-0.125000 |
6.11e-02 |
3.80e-01 |
2.49e-03 |
2.37e-01 |
5.63e-01 |
PCP/CE pathway |
85 |
3.20e-06 |
1.53e-05 |
0.3600 |
-0.043200 |
6.25e-02 |
0.331000 |
1.19e-01 |
4.92e-01 |
3.20e-01 |
1.35e-07 |
5.92e-02 |
Regulation of TNFR1 signaling |
27 |
3.33e-02 |
6.65e-02 |
0.3600 |
0.075500 |
2.27e-01 |
-0.224000 |
-1.48e-01 |
4.97e-01 |
4.10e-02 |
4.45e-02 |
1.82e-01 |
Interleukin-2 signaling |
11 |
4.58e-01 |
5.33e-01 |
0.3600 |
0.025100 |
6.18e-02 |
-0.315000 |
-1.60e-01 |
8.86e-01 |
7.23e-01 |
7.06e-02 |
3.57e-01 |
Methylation |
11 |
1.22e-01 |
1.88e-01 |
0.3600 |
0.263000 |
-1.73e-02 |
0.223000 |
-9.97e-02 |
1.31e-01 |
9.21e-01 |
2.00e-01 |
5.67e-01 |
SHC-mediated cascade:FGFR1 |
11 |
2.43e-01 |
3.22e-01 |
0.3590 |
0.107000 |
-1.83e-01 |
-0.109000 |
-2.69e-01 |
5.39e-01 |
2.94e-01 |
5.32e-01 |
1.22e-01 |
EPHA-mediated growth cone collapse |
14 |
7.22e-02 |
1.23e-01 |
0.3590 |
0.011800 |
3.00e-01 |
-0.139000 |
1.39e-01 |
9.39e-01 |
5.20e-02 |
3.66e-01 |
3.68e-01 |
Diseases of programmed cell death |
20 |
7.58e-03 |
2.01e-02 |
0.3590 |
-0.019300 |
1.13e-01 |
0.301000 |
-1.59e-01 |
8.81e-01 |
3.81e-01 |
2.00e-02 |
2.17e-01 |
TICAM1, RIP1-mediated IKK complex recruitment |
16 |
3.41e-01 |
4.25e-01 |
0.3580 |
0.023700 |
-5.57e-02 |
-0.289000 |
-2.03e-01 |
8.70e-01 |
7.00e-01 |
4.55e-02 |
1.59e-01 |
Interleukin-7 signaling |
20 |
1.63e-01 |
2.36e-01 |
0.3580 |
-0.104000 |
1.73e-02 |
-0.258000 |
-2.25e-01 |
4.19e-01 |
8.94e-01 |
4.58e-02 |
8.15e-02 |
PLC beta mediated events |
47 |
8.53e-03 |
2.19e-02 |
0.3580 |
-0.117000 |
-2.34e-01 |
-0.225000 |
-9.47e-02 |
1.64e-01 |
5.49e-03 |
7.58e-03 |
2.62e-01 |
NF-kB activation through FADD/RIP-1 pathway mediated by caspase-8 and -10 |
11 |
3.09e-01 |
3.91e-01 |
0.3570 |
0.098400 |
3.34e-01 |
-0.073500 |
-3.51e-02 |
5.72e-01 |
5.54e-02 |
6.73e-01 |
8.40e-01 |
Calnexin/calreticulin cycle |
23 |
2.65e-02 |
5.55e-02 |
0.3570 |
-0.049000 |
-2.85e-01 |
0.186000 |
9.66e-02 |
6.84e-01 |
1.82e-02 |
1.22e-01 |
4.23e-01 |
Activation of kainate receptors upon glutamate binding |
23 |
4.02e-02 |
7.71e-02 |
0.3570 |
0.001540 |
4.22e-02 |
0.035100 |
3.53e-01 |
9.90e-01 |
7.26e-01 |
7.71e-01 |
3.42e-03 |
Dual incision in TC-NER |
62 |
8.67e-06 |
3.94e-05 |
0.3570 |
0.140000 |
1.19e-01 |
0.302000 |
-4.91e-02 |
5.75e-02 |
1.07e-01 |
3.90e-05 |
5.04e-01 |
HCMV Early Events |
53 |
1.44e-07 |
7.99e-07 |
0.3570 |
0.056100 |
-8.64e-02 |
0.221000 |
-2.61e-01 |
4.81e-01 |
2.77e-01 |
5.43e-03 |
1.04e-03 |
Rap1 signalling |
15 |
3.03e-01 |
3.86e-01 |
0.3570 |
-0.097600 |
-1.49e-03 |
-0.297000 |
-1.72e-01 |
5.13e-01 |
9.92e-01 |
4.68e-02 |
2.48e-01 |
Membrane binding and targetting of GAG proteins |
11 |
5.12e-01 |
5.82e-01 |
0.3560 |
-0.187000 |
-2.27e-01 |
0.183000 |
8.10e-02 |
2.82e-01 |
1.92e-01 |
2.94e-01 |
6.42e-01 |
Synthesis And Processing Of GAG, GAGPOL Polyproteins |
11 |
5.12e-01 |
5.82e-01 |
0.3560 |
-0.187000 |
-2.27e-01 |
0.183000 |
8.10e-02 |
2.82e-01 |
1.92e-01 |
2.94e-01 |
6.42e-01 |
Regulation of gene expression in late stage (branching morphogenesis) pancreatic bud precursor cells |
13 |
4.89e-01 |
5.62e-01 |
0.3550 |
-0.034000 |
-8.20e-02 |
-0.285000 |
-1.92e-01 |
8.32e-01 |
6.09e-01 |
7.49e-02 |
2.31e-01 |
Mitochondrial tRNA aminoacylation |
18 |
2.13e-01 |
2.91e-01 |
0.3550 |
-0.141000 |
-2.15e-01 |
0.221000 |
1.05e-01 |
3.01e-01 |
1.15e-01 |
1.05e-01 |
4.39e-01 |
N-glycan trimming in the ER and Calnexin/Calreticulin cycle |
31 |
1.08e-02 |
2.67e-02 |
0.3540 |
-0.044900 |
-2.36e-01 |
0.220000 |
1.39e-01 |
6.66e-01 |
2.33e-02 |
3.40e-02 |
1.79e-01 |
Triglyceride metabolism |
23 |
6.29e-02 |
1.11e-01 |
0.3540 |
-0.053300 |
6.87e-02 |
-0.143000 |
-3.12e-01 |
6.58e-01 |
5.69e-01 |
2.34e-01 |
9.70e-03 |
Response of EIF2AK1 (HRI) to heme deficiency |
14 |
8.72e-02 |
1.43e-01 |
0.3540 |
0.107000 |
1.66e-01 |
0.212000 |
-2.03e-01 |
4.89e-01 |
2.82e-01 |
1.70e-01 |
1.89e-01 |
Cell recruitment (pro-inflammatory response) |
19 |
9.90e-02 |
1.58e-01 |
0.3540 |
-0.055200 |
1.81e-01 |
0.113000 |
2.76e-01 |
6.77e-01 |
1.71e-01 |
3.94e-01 |
3.72e-02 |
Purinergic signaling in leishmaniasis infection |
19 |
9.90e-02 |
1.58e-01 |
0.3540 |
-0.055200 |
1.81e-01 |
0.113000 |
2.76e-01 |
6.77e-01 |
1.71e-01 |
3.94e-01 |
3.72e-02 |
Signaling by EGFR |
45 |
4.37e-02 |
8.25e-02 |
0.3530 |
-0.151000 |
-1.74e-01 |
-0.178000 |
-2.00e-01 |
7.94e-02 |
4.39e-02 |
3.86e-02 |
2.04e-02 |
DAP12 interactions |
28 |
9.88e-02 |
1.58e-01 |
0.3530 |
0.184000 |
2.90e-01 |
-0.034200 |
7.25e-02 |
9.21e-02 |
7.86e-03 |
7.54e-01 |
5.07e-01 |
APC/C:Cdc20 mediated degradation of Cyclin B |
22 |
9.84e-03 |
2.46e-02 |
0.3530 |
0.187000 |
-2.93e-02 |
0.291000 |
-6.25e-02 |
1.29e-01 |
8.12e-01 |
1.81e-02 |
6.12e-01 |
Mitochondrial protein import |
59 |
5.12e-05 |
2.08e-04 |
0.3530 |
0.026400 |
6.02e-02 |
0.345000 |
3.14e-02 |
7.26e-01 |
4.24e-01 |
4.56e-06 |
6.77e-01 |
IRS-mediated signalling |
33 |
3.40e-02 |
6.73e-02 |
0.3520 |
-0.011400 |
-1.93e-01 |
-0.149000 |
-2.53e-01 |
9.10e-01 |
5.48e-02 |
1.38e-01 |
1.19e-02 |
Transport of bile salts and organic acids, metal ions and amine compounds |
49 |
1.04e-02 |
2.57e-02 |
0.3520 |
0.295000 |
1.86e-01 |
-0.014700 |
4.49e-02 |
3.57e-04 |
2.45e-02 |
8.59e-01 |
5.87e-01 |
Synthesis of very long-chain fatty acyl-CoAs |
13 |
3.80e-01 |
4.65e-01 |
0.3520 |
-0.081500 |
-1.29e-01 |
-0.075800 |
-3.08e-01 |
6.11e-01 |
4.19e-01 |
6.36e-01 |
5.49e-02 |
Biosynthesis of the N-glycan precursor (dolichol lipid-linked oligosaccharide, LLO) and transfer to a nascent protein |
68 |
2.34e-04 |
8.72e-04 |
0.3510 |
-0.108000 |
-1.96e-01 |
0.176000 |
2.05e-01 |
1.22e-01 |
5.31e-03 |
1.20e-02 |
3.42e-03 |
Chondroitin sulfate biosynthesis |
15 |
8.29e-02 |
1.38e-01 |
0.3510 |
-0.146000 |
1.61e-01 |
0.061000 |
2.69e-01 |
3.29e-01 |
2.80e-01 |
6.83e-01 |
7.16e-02 |
Arachidonic acid metabolism |
36 |
1.77e-02 |
3.99e-02 |
0.3500 |
0.142000 |
2.47e-01 |
-0.031600 |
2.01e-01 |
1.41e-01 |
1.02e-02 |
7.43e-01 |
3.70e-02 |
TNFR1-induced NFkappaB signaling pathway |
24 |
5.34e-02 |
9.73e-02 |
0.3500 |
0.014200 |
1.78e-01 |
-0.193000 |
-2.31e-01 |
9.04e-01 |
1.31e-01 |
1.01e-01 |
5.05e-02 |
RHO GTPases Activate NADPH Oxidases |
19 |
2.49e-01 |
3.29e-01 |
0.3500 |
0.186000 |
2.85e-01 |
-0.071700 |
4.36e-02 |
1.61e-01 |
3.18e-02 |
5.88e-01 |
7.42e-01 |
Antigen activates B Cell Receptor (BCR) leading to generation of second messengers |
32 |
6.38e-02 |
1.12e-01 |
0.3500 |
0.240000 |
2.07e-01 |
-0.148000 |
-2.15e-02 |
1.91e-02 |
4.32e-02 |
1.48e-01 |
8.33e-01 |
Regulation of TP53 Activity through Phosphorylation |
86 |
2.45e-11 |
2.79e-10 |
0.3500 |
0.108000 |
2.93e-02 |
0.216000 |
-2.52e-01 |
8.50e-02 |
6.39e-01 |
5.44e-04 |
5.64e-05 |
Stimuli-sensing channels |
51 |
1.59e-02 |
3.67e-02 |
0.3490 |
-0.248000 |
-1.82e-01 |
-0.147000 |
-7.12e-02 |
2.20e-03 |
2.46e-02 |
6.89e-02 |
3.79e-01 |
Synthesis of PA |
24 |
2.57e-01 |
3.38e-01 |
0.3480 |
-0.184000 |
-1.83e-01 |
-0.117000 |
-2.01e-01 |
1.19e-01 |
1.22e-01 |
3.21e-01 |
8.84e-02 |
Signaling by PDGF |
47 |
3.94e-03 |
1.14e-02 |
0.3480 |
-0.191000 |
-1.05e-01 |
-0.266000 |
-5.60e-02 |
2.36e-02 |
2.12e-01 |
1.64e-03 |
5.07e-01 |
Regulation of mRNA stability by proteins that bind AU-rich elements |
80 |
9.95e-06 |
4.49e-05 |
0.3480 |
0.105000 |
1.30e-01 |
0.303000 |
3.43e-02 |
1.04e-01 |
4.53e-02 |
2.82e-06 |
5.96e-01 |
Sialic acid metabolism |
25 |
8.39e-02 |
1.39e-01 |
0.3480 |
-0.117000 |
-2.07e-01 |
0.232000 |
1.03e-01 |
3.12e-01 |
7.38e-02 |
4.46e-02 |
3.75e-01 |
Incretin synthesis, secretion, and inactivation |
10 |
2.14e-01 |
2.92e-01 |
0.3470 |
-0.000790 |
1.55e-01 |
-0.130000 |
2.82e-01 |
9.97e-01 |
3.97e-01 |
4.76e-01 |
1.23e-01 |
RHO GTPases activate KTN1 |
10 |
2.33e-01 |
3.13e-01 |
0.3460 |
-0.126000 |
5.88e-03 |
-0.082400 |
3.12e-01 |
4.92e-01 |
9.74e-01 |
6.52e-01 |
8.75e-02 |
Regulation of FOXO transcriptional activity by acetylation |
10 |
2.29e-01 |
3.09e-01 |
0.3460 |
0.043200 |
-1.12e-03 |
0.089700 |
-3.31e-01 |
8.13e-01 |
9.95e-01 |
6.23e-01 |
6.97e-02 |
Formation of the cornified envelope |
15 |
3.90e-01 |
4.76e-01 |
0.3460 |
-0.117000 |
-2.37e-01 |
-0.207000 |
-8.40e-02 |
4.33e-01 |
1.12e-01 |
1.66e-01 |
5.73e-01 |
AURKA Activation by TPX2 |
71 |
2.34e-09 |
1.84e-08 |
0.3460 |
0.044900 |
1.83e-02 |
0.270000 |
-2.10e-01 |
5.14e-01 |
7.90e-01 |
8.61e-05 |
2.19e-03 |
Plasma lipoprotein assembly, remodeling, and clearance |
47 |
1.36e-02 |
3.22e-02 |
0.3450 |
-0.074400 |
3.12e-02 |
0.246000 |
2.29e-01 |
3.78e-01 |
7.12e-01 |
3.55e-03 |
6.76e-03 |
NF-kB is activated and signals survival |
11 |
5.01e-01 |
5.75e-01 |
0.3450 |
-0.292000 |
-1.58e-01 |
0.052800 |
-7.64e-02 |
9.33e-02 |
3.64e-01 |
7.62e-01 |
6.61e-01 |
Transcriptional regulation of granulopoiesis |
26 |
3.52e-02 |
6.93e-02 |
0.3450 |
0.086400 |
2.49e-01 |
0.222000 |
-1.32e-02 |
4.46e-01 |
2.81e-02 |
4.97e-02 |
9.08e-01 |
Signaling by Erythropoietin |
24 |
1.82e-01 |
2.57e-01 |
0.3450 |
-0.005220 |
-1.86e-02 |
-0.194000 |
-2.85e-01 |
9.65e-01 |
8.75e-01 |
1.01e-01 |
1.58e-02 |
Deregulated CDK5 triggers multiple neurodegenerative pathways in Alzheimer's disease models |
19 |
1.30e-02 |
3.11e-02 |
0.3440 |
-0.019400 |
9.59e-02 |
0.269000 |
-1.92e-01 |
8.84e-01 |
4.70e-01 |
4.26e-02 |
1.48e-01 |
Neurodegenerative Diseases |
19 |
1.30e-02 |
3.11e-02 |
0.3440 |
-0.019400 |
9.59e-02 |
0.269000 |
-1.92e-01 |
8.84e-01 |
4.70e-01 |
4.26e-02 |
1.48e-01 |
XBP1(S) activates chaperone genes |
47 |
4.30e-03 |
1.24e-02 |
0.3440 |
-0.129000 |
-1.87e-01 |
0.247000 |
7.75e-02 |
1.26e-01 |
2.66e-02 |
3.46e-03 |
3.58e-01 |
Smooth Muscle Contraction |
34 |
8.37e-05 |
3.30e-04 |
0.3430 |
-0.122000 |
2.45e-01 |
-0.057800 |
1.99e-01 |
2.19e-01 |
1.34e-02 |
5.60e-01 |
4.48e-02 |
Class B/2 (Secretin family receptors) |
42 |
8.65e-03 |
2.22e-02 |
0.3430 |
-0.160000 |
-6.66e-02 |
0.105000 |
2.76e-01 |
7.23e-02 |
4.56e-01 |
2.40e-01 |
1.98e-03 |
NOTCH4 Activation and Transmission of Signal to the Nucleus |
11 |
2.42e-01 |
3.21e-01 |
0.3420 |
0.000467 |
3.07e-01 |
0.017500 |
1.50e-01 |
9.98e-01 |
7.76e-02 |
9.20e-01 |
3.89e-01 |
COPII-mediated vesicle transport |
58 |
2.51e-03 |
7.70e-03 |
0.3420 |
-0.156000 |
-2.23e-01 |
0.177000 |
1.07e-01 |
3.98e-02 |
3.41e-03 |
1.97e-02 |
1.58e-01 |
Depolymerisation of the Nuclear Lamina |
15 |
4.79e-02 |
8.91e-02 |
0.3410 |
0.019600 |
1.56e-01 |
0.205000 |
-2.23e-01 |
8.96e-01 |
2.97e-01 |
1.69e-01 |
1.34e-01 |
SUMOylation of transcription cofactors |
39 |
2.73e-02 |
5.69e-02 |
0.3410 |
0.021100 |
-8.50e-02 |
-0.153000 |
-2.92e-01 |
8.20e-01 |
3.58e-01 |
9.75e-02 |
1.63e-03 |
Negative regulation of MET activity |
19 |
3.12e-01 |
3.93e-01 |
0.3410 |
-0.106000 |
-2.53e-01 |
-0.138000 |
-1.48e-01 |
4.22e-01 |
5.68e-02 |
2.99e-01 |
2.64e-01 |
ECM proteoglycans |
40 |
1.36e-03 |
4.46e-03 |
0.3400 |
-0.092300 |
-1.36e-02 |
-0.327000 |
3.81e-03 |
3.13e-01 |
8.82e-01 |
3.49e-04 |
9.67e-01 |
Transport of inorganic cations/anions and amino acids/oligopeptides |
65 |
5.15e-03 |
1.44e-02 |
0.3400 |
-0.099300 |
-1.78e-01 |
-0.227000 |
-1.49e-01 |
1.67e-01 |
1.32e-02 |
1.53e-03 |
3.76e-02 |
tRNA processing in the nucleus |
51 |
1.03e-05 |
4.61e-05 |
0.3390 |
-0.055100 |
-5.01e-02 |
0.309000 |
-1.19e-01 |
4.96e-01 |
5.36e-01 |
1.38e-04 |
1.40e-01 |
Synthesis of active ubiquitin: roles of E1 and E2 enzymes |
25 |
1.72e-03 |
5.50e-03 |
0.3390 |
0.114000 |
-1.47e-01 |
0.196000 |
-2.06e-01 |
3.26e-01 |
2.03e-01 |
9.07e-02 |
7.51e-02 |
Aberrant regulation of mitotic exit in cancer due to RB1 defects |
20 |
1.33e-02 |
3.16e-02 |
0.3390 |
0.081500 |
-1.48e-01 |
0.279000 |
-9.30e-02 |
5.28e-01 |
2.51e-01 |
3.09e-02 |
4.72e-01 |
TP53 regulates transcription of several additional cell death genes whose specific roles in p53-dependent apoptosis remain uncertain |
11 |
6.39e-01 |
6.90e-01 |
0.3390 |
-0.054000 |
-5.20e-02 |
-0.249000 |
-2.17e-01 |
7.57e-01 |
7.65e-01 |
1.53e-01 |
2.12e-01 |
Regulation of innate immune responses to cytosolic DNA |
11 |
5.19e-01 |
5.89e-01 |
0.3390 |
0.113000 |
2.97e-01 |
0.072100 |
9.34e-02 |
5.15e-01 |
8.84e-02 |
6.79e-01 |
5.92e-01 |
Synthesis of IP3 and IP4 in the cytosol |
21 |
5.43e-02 |
9.86e-02 |
0.3390 |
-0.331000 |
-5.68e-02 |
-0.032700 |
3.38e-02 |
8.74e-03 |
6.52e-01 |
7.96e-01 |
7.89e-01 |
Cristae formation |
11 |
2.99e-01 |
3.82e-01 |
0.3380 |
0.187000 |
3.29e-02 |
0.279000 |
-1.12e-02 |
2.82e-01 |
8.50e-01 |
1.09e-01 |
9.49e-01 |
SUMOylation of RNA binding proteins |
41 |
8.28e-05 |
3.27e-04 |
0.3380 |
0.002790 |
-1.44e-01 |
0.169000 |
-2.55e-01 |
9.75e-01 |
1.10e-01 |
6.18e-02 |
4.82e-03 |
Integration of energy metabolism |
85 |
2.03e-03 |
6.38e-03 |
0.3380 |
-0.178000 |
-2.24e-01 |
-0.109000 |
-1.43e-01 |
4.68e-03 |
3.61e-04 |
8.20e-02 |
2.31e-02 |
PI3K Cascade |
29 |
7.08e-02 |
1.22e-01 |
0.3380 |
-0.039500 |
-2.27e-01 |
-0.120000 |
-2.15e-01 |
7.13e-01 |
3.43e-02 |
2.63e-01 |
4.47e-02 |
Signaling by FGFR1 in disease |
31 |
4.88e-02 |
9.04e-02 |
0.3370 |
0.036700 |
-1.64e-01 |
-0.203000 |
-2.10e-01 |
7.24e-01 |
1.13e-01 |
5.09e-02 |
4.27e-02 |
FOXO-mediated transcription |
52 |
5.24e-03 |
1.46e-02 |
0.3370 |
0.027800 |
-4.20e-02 |
-0.138000 |
-3.03e-01 |
7.29e-01 |
6.01e-01 |
8.47e-02 |
1.58e-04 |
Negative regulation of FGFR1 signaling |
20 |
5.64e-02 |
1.02e-01 |
0.3370 |
-0.043900 |
-3.22e-01 |
0.043600 |
-7.60e-02 |
7.34e-01 |
1.27e-02 |
7.36e-01 |
5.56e-01 |
Aquaporin-mediated transport |
34 |
4.51e-02 |
8.47e-02 |
0.3370 |
-0.148000 |
-2.16e-01 |
0.108000 |
1.81e-01 |
1.34e-01 |
2.92e-02 |
2.75e-01 |
6.78e-02 |
PIWI-interacting RNA (piRNA) biogenesis |
16 |
2.82e-01 |
3.64e-01 |
0.3360 |
-0.003440 |
6.46e-03 |
0.320000 |
1.04e-01 |
9.81e-01 |
9.64e-01 |
2.67e-02 |
4.73e-01 |
Regulation of TP53 Activity through Association with Co-factors |
12 |
5.14e-01 |
5.84e-01 |
0.3360 |
-0.113000 |
-2.73e-01 |
-0.138000 |
-8.23e-02 |
4.99e-01 |
1.02e-01 |
4.07e-01 |
6.22e-01 |
Netrin-1 signaling |
41 |
2.18e-02 |
4.74e-02 |
0.3360 |
-0.013900 |
-1.19e-01 |
-0.284000 |
-1.33e-01 |
8.78e-01 |
1.87e-01 |
1.65e-03 |
1.41e-01 |
Regulation of IFNG signaling |
13 |
2.30e-01 |
3.09e-01 |
0.3360 |
0.190000 |
9.50e-02 |
-0.077100 |
2.48e-01 |
2.36e-01 |
5.53e-01 |
6.31e-01 |
1.21e-01 |
Asparagine N-linked glycosylation |
247 |
7.65e-15 |
1.36e-13 |
0.3350 |
-0.113000 |
-2.14e-01 |
0.166000 |
1.62e-01 |
2.27e-03 |
7.63e-09 |
7.68e-06 |
1.27e-05 |
Fanconi Anemia Pathway |
31 |
2.05e-03 |
6.42e-03 |
0.3350 |
0.034900 |
5.92e-02 |
0.307000 |
-1.16e-01 |
7.37e-01 |
5.68e-01 |
3.10e-03 |
2.66e-01 |
DNA Repair |
266 |
1.70e-24 |
7.98e-23 |
0.3350 |
0.140000 |
1.25e-01 |
0.259000 |
-1.01e-01 |
9.35e-05 |
4.89e-04 |
4.55e-13 |
4.81e-03 |
Inflammasomes |
19 |
4.70e-03 |
1.33e-02 |
0.3350 |
-0.150000 |
2.82e-01 |
-0.056300 |
8.26e-02 |
2.59e-01 |
3.33e-02 |
6.71e-01 |
5.33e-01 |
Assembly of active LPL and LIPC lipase complexes |
11 |
6.07e-01 |
6.62e-01 |
0.3350 |
-0.272000 |
-1.82e-01 |
0.018200 |
6.92e-02 |
1.19e-01 |
2.97e-01 |
9.17e-01 |
6.91e-01 |
Erythropoietin activates Phosphoinositide-3-kinase (PI3K) |
11 |
5.75e-01 |
6.36e-01 |
0.3340 |
0.217000 |
1.25e-01 |
-0.135000 |
-1.76e-01 |
2.14e-01 |
4.71e-01 |
4.39e-01 |
3.13e-01 |
Gap junction trafficking |
13 |
5.27e-01 |
5.95e-01 |
0.3340 |
-0.061400 |
-5.04e-02 |
0.241000 |
2.17e-01 |
7.02e-01 |
7.53e-01 |
1.32e-01 |
1.76e-01 |
HS-GAG degradation |
19 |
7.95e-02 |
1.33e-01 |
0.3340 |
-0.200000 |
5.97e-03 |
0.019500 |
2.67e-01 |
1.32e-01 |
9.64e-01 |
8.83e-01 |
4.43e-02 |
Cleavage of the damaged pyrimidine |
16 |
9.52e-02 |
1.53e-01 |
0.3340 |
0.016400 |
3.18e-01 |
0.100000 |
6.63e-03 |
9.09e-01 |
2.78e-02 |
4.87e-01 |
9.63e-01 |
Depyrimidination |
16 |
9.52e-02 |
1.53e-01 |
0.3340 |
0.016400 |
3.18e-01 |
0.100000 |
6.63e-03 |
9.09e-01 |
2.78e-02 |
4.87e-01 |
9.63e-01 |
Recognition and association of DNA glycosylase with site containing an affected pyrimidine |
16 |
9.52e-02 |
1.53e-01 |
0.3340 |
0.016400 |
3.18e-01 |
0.100000 |
6.63e-03 |
9.09e-01 |
2.78e-02 |
4.87e-01 |
9.63e-01 |
RUNX3 regulates NOTCH signaling |
14 |
4.82e-01 |
5.56e-01 |
0.3330 |
-0.089800 |
-7.81e-02 |
-0.278000 |
-1.41e-01 |
5.61e-01 |
6.13e-01 |
7.20e-02 |
3.61e-01 |
Ca2+ pathway |
51 |
3.54e-03 |
1.04e-02 |
0.3330 |
-0.197000 |
-1.26e-01 |
-0.237000 |
-1.66e-02 |
1.52e-02 |
1.19e-01 |
3.43e-03 |
8.38e-01 |
Formation of tubulin folding intermediates by CCT/TriC |
19 |
2.44e-02 |
5.20e-02 |
0.3320 |
0.024900 |
-1.29e-01 |
0.180000 |
-2.46e-01 |
8.51e-01 |
3.30e-01 |
1.75e-01 |
6.33e-02 |
Purine ribonucleoside monophosphate biosynthesis |
12 |
2.89e-01 |
3.71e-01 |
0.3320 |
0.030000 |
1.31e-01 |
0.303000 |
-9.69e-03 |
8.57e-01 |
4.33e-01 |
6.88e-02 |
9.54e-01 |
Signaling by EGFR in Cancer |
20 |
3.92e-01 |
4.77e-01 |
0.3310 |
-0.177000 |
-1.95e-01 |
-0.080300 |
-1.84e-01 |
1.70e-01 |
1.31e-01 |
5.34e-01 |
1.55e-01 |
Selective autophagy |
52 |
1.53e-02 |
3.55e-02 |
0.3310 |
-0.195000 |
-2.47e-01 |
0.042300 |
-9.41e-02 |
1.53e-02 |
2.06e-03 |
5.98e-01 |
2.41e-01 |
Formation of the Early Elongation Complex |
32 |
2.24e-02 |
4.86e-02 |
0.3310 |
-0.147000 |
-1.11e-01 |
0.275000 |
1.12e-02 |
1.51e-01 |
2.78e-01 |
7.08e-03 |
9.13e-01 |
Formation of the HIV-1 Early Elongation Complex |
32 |
2.24e-02 |
4.86e-02 |
0.3310 |
-0.147000 |
-1.11e-01 |
0.275000 |
1.12e-02 |
1.51e-01 |
2.78e-01 |
7.08e-03 |
9.13e-01 |
MAP3K8 (TPL2)-dependent MAPK1/3 activation |
14 |
4.33e-01 |
5.13e-01 |
0.3310 |
-0.002700 |
-1.48e-01 |
-0.253000 |
-1.53e-01 |
9.86e-01 |
3.38e-01 |
1.01e-01 |
3.21e-01 |
TRP channels |
12 |
1.97e-01 |
2.73e-01 |
0.3310 |
0.034000 |
2.30e-01 |
-0.159000 |
1.73e-01 |
8.38e-01 |
1.67e-01 |
3.40e-01 |
2.99e-01 |
Glycosphingolipid metabolism |
33 |
2.63e-02 |
5.51e-02 |
0.3300 |
-0.141000 |
5.52e-02 |
0.142000 |
2.57e-01 |
1.62e-01 |
5.84e-01 |
1.59e-01 |
1.07e-02 |
Diseases of DNA repair |
10 |
4.24e-01 |
5.05e-01 |
0.3300 |
-0.105000 |
7.60e-02 |
0.293000 |
7.82e-02 |
5.64e-01 |
6.77e-01 |
1.09e-01 |
6.69e-01 |
KSRP (KHSRP) binds and destabilizes mRNA |
16 |
4.47e-01 |
5.24e-01 |
0.3290 |
0.259000 |
1.94e-01 |
0.034200 |
-5.02e-02 |
7.33e-02 |
1.79e-01 |
8.13e-01 |
7.28e-01 |
Global Genome Nucleotide Excision Repair (GG-NER) |
80 |
8.17e-06 |
3.72e-05 |
0.3290 |
0.159000 |
8.90e-02 |
0.274000 |
-8.15e-03 |
1.39e-02 |
1.69e-01 |
2.35e-05 |
9.00e-01 |
Hedgehog 'off' state |
90 |
4.05e-05 |
1.69e-04 |
0.3290 |
0.042400 |
3.91e-03 |
0.301000 |
1.25e-01 |
4.88e-01 |
9.49e-01 |
8.10e-07 |
4.00e-02 |
Dopamine Neurotransmitter Release Cycle |
13 |
2.00e-01 |
2.76e-01 |
0.3290 |
0.064600 |
-5.50e-02 |
-0.317000 |
2.06e-02 |
6.87e-01 |
7.31e-01 |
4.78e-02 |
8.98e-01 |
Deactivation of the beta-catenin transactivating complex |
34 |
1.33e-01 |
2.02e-01 |
0.3290 |
-0.149000 |
-1.36e-01 |
-0.132000 |
-2.23e-01 |
1.33e-01 |
1.70e-01 |
1.82e-01 |
2.45e-02 |
Plasma lipoprotein remodeling |
15 |
3.18e-01 |
3.99e-01 |
0.3280 |
-0.143000 |
5.41e-02 |
0.190000 |
2.20e-01 |
3.38e-01 |
7.17e-01 |
2.03e-01 |
1.40e-01 |
NRAGE signals death through JNK |
54 |
5.85e-03 |
1.61e-02 |
0.3280 |
-0.248000 |
-1.41e-01 |
-0.162000 |
-1.57e-02 |
1.66e-03 |
7.29e-02 |
3.91e-02 |
8.42e-01 |
Neutrophil degranulation |
353 |
2.25e-15 |
4.16e-14 |
0.3280 |
0.073500 |
1.34e-01 |
0.149000 |
2.49e-01 |
1.84e-02 |
1.79e-05 |
1.70e-06 |
1.22e-15 |
SUMO E3 ligases SUMOylate target proteins |
143 |
3.36e-13 |
4.85e-12 |
0.3280 |
0.143000 |
3.77e-02 |
0.053200 |
-2.88e-01 |
3.25e-03 |
4.37e-01 |
2.73e-01 |
3.02e-09 |
HIV elongation arrest and recovery |
28 |
3.47e-03 |
1.02e-02 |
0.3280 |
-0.036200 |
1.48e-02 |
0.293000 |
-1.41e-01 |
7.40e-01 |
8.92e-01 |
7.27e-03 |
1.98e-01 |
Pausing and recovery of HIV elongation |
28 |
3.47e-03 |
1.02e-02 |
0.3280 |
-0.036200 |
1.48e-02 |
0.293000 |
-1.41e-01 |
7.40e-01 |
8.92e-01 |
7.27e-03 |
1.98e-01 |
Defective EXT1 causes exostoses 1, TRPS2 and CHDS |
13 |
4.37e-01 |
5.15e-01 |
0.3270 |
-0.292000 |
-1.31e-01 |
-0.011000 |
6.79e-02 |
6.84e-02 |
4.12e-01 |
9.45e-01 |
6.72e-01 |
Defective EXT2 causes exostoses 2 |
13 |
4.37e-01 |
5.15e-01 |
0.3270 |
-0.292000 |
-1.31e-01 |
-0.011000 |
6.79e-02 |
6.84e-02 |
4.12e-01 |
9.45e-01 |
6.72e-01 |
NOTCH1 Intracellular Domain Regulates Transcription |
43 |
6.60e-02 |
1.15e-01 |
0.3270 |
-0.075700 |
-1.57e-01 |
-0.208000 |
-1.83e-01 |
3.91e-01 |
7.54e-02 |
1.81e-02 |
3.85e-02 |
Recruitment of NuMA to mitotic centrosomes |
79 |
2.17e-09 |
1.73e-08 |
0.3260 |
0.011900 |
-1.94e-02 |
0.250000 |
-2.09e-01 |
8.55e-01 |
7.66e-01 |
1.27e-04 |
1.35e-03 |
Loss of Nlp from mitotic centrosomes |
68 |
5.14e-08 |
3.08e-07 |
0.3260 |
0.011100 |
-1.46e-02 |
0.253000 |
-2.04e-01 |
8.74e-01 |
8.35e-01 |
3.17e-04 |
3.58e-03 |
Loss of proteins required for interphase microtubule organization from the centrosome |
68 |
5.14e-08 |
3.08e-07 |
0.3260 |
0.011100 |
-1.46e-02 |
0.253000 |
-2.04e-01 |
8.74e-01 |
8.35e-01 |
3.17e-04 |
3.58e-03 |
Vasopressin regulates renal water homeostasis via Aquaporins |
32 |
5.29e-02 |
9.65e-02 |
0.3260 |
-0.100000 |
-1.84e-01 |
0.123000 |
2.17e-01 |
3.26e-01 |
7.17e-02 |
2.28e-01 |
3.41e-02 |
Regulation of TP53 Expression and Degradation |
33 |
2.83e-03 |
8.57e-03 |
0.3260 |
0.116000 |
-7.20e-02 |
0.042300 |
-2.93e-01 |
2.51e-01 |
4.74e-01 |
6.74e-01 |
3.63e-03 |
Regulation of KIT signaling |
16 |
2.27e-01 |
3.07e-01 |
0.3250 |
0.120000 |
1.68e-01 |
-0.251000 |
1.39e-02 |
4.05e-01 |
2.46e-01 |
8.21e-02 |
9.23e-01 |
G-protein mediated events |
48 |
2.00e-02 |
4.43e-02 |
0.3250 |
-0.109000 |
-2.13e-01 |
-0.206000 |
-7.74e-02 |
1.91e-01 |
1.09e-02 |
1.35e-02 |
3.54e-01 |
Erythropoietin activates RAS |
13 |
4.20e-01 |
5.02e-01 |
0.3250 |
0.065400 |
-3.15e-02 |
-0.105000 |
-2.99e-01 |
6.83e-01 |
8.44e-01 |
5.14e-01 |
6.20e-02 |
Activation of BAD and translocation to mitochondria |
14 |
6.18e-01 |
6.72e-01 |
0.3250 |
0.224000 |
2.26e-01 |
0.035800 |
5.54e-02 |
1.47e-01 |
1.43e-01 |
8.16e-01 |
7.20e-01 |
FCERI mediated NF-kB activation |
72 |
1.78e-04 |
6.82e-04 |
0.3240 |
0.143000 |
1.12e-01 |
0.268000 |
2.02e-02 |
3.56e-02 |
1.02e-01 |
8.59e-05 |
7.68e-01 |
mRNA decay by 3' to 5' exoribonuclease |
15 |
5.65e-01 |
6.28e-01 |
0.3240 |
0.127000 |
1.52e-01 |
0.215000 |
1.40e-01 |
3.95e-01 |
3.07e-01 |
1.50e-01 |
3.48e-01 |
Killing mechanisms |
10 |
6.57e-01 |
7.05e-01 |
0.3240 |
-0.237000 |
-1.47e-01 |
0.098200 |
1.32e-01 |
1.94e-01 |
4.22e-01 |
5.91e-01 |
4.70e-01 |
WNT5:FZD7-mediated leishmania damping |
10 |
6.57e-01 |
7.05e-01 |
0.3240 |
-0.237000 |
-1.47e-01 |
0.098200 |
1.32e-01 |
1.94e-01 |
4.22e-01 |
5.91e-01 |
4.70e-01 |
Regulation of localization of FOXO transcription factors |
11 |
3.38e-01 |
4.22e-01 |
0.3240 |
0.126000 |
1.82e-02 |
0.011200 |
-2.98e-01 |
4.69e-01 |
9.17e-01 |
9.49e-01 |
8.73e-02 |
Downstream signaling of activated FGFR1 |
21 |
1.22e-01 |
1.88e-01 |
0.3240 |
0.045900 |
-1.96e-01 |
-0.138000 |
-2.12e-01 |
7.16e-01 |
1.19e-01 |
2.74e-01 |
9.24e-02 |
IL-6-type cytokine receptor ligand interactions |
12 |
2.70e-01 |
3.51e-01 |
0.3230 |
0.245000 |
7.09e-02 |
-0.112000 |
1.64e-01 |
1.41e-01 |
6.71e-01 |
5.01e-01 |
3.27e-01 |
Mitochondrial biogenesis |
69 |
1.31e-03 |
4.33e-03 |
0.3230 |
0.010700 |
-1.31e-01 |
-0.144000 |
-2.58e-01 |
8.78e-01 |
6.10e-02 |
3.82e-02 |
2.14e-04 |
Reduction of cytosolic Ca++ levels |
10 |
5.63e-01 |
6.27e-01 |
0.3230 |
-0.119000 |
-1.54e-01 |
-0.258000 |
-1.98e-02 |
5.15e-01 |
3.99e-01 |
1.58e-01 |
9.13e-01 |
SUMOylation |
149 |
1.28e-13 |
1.98e-12 |
0.3230 |
0.143000 |
3.51e-02 |
0.060300 |
-2.81e-01 |
2.58e-03 |
4.61e-01 |
2.05e-01 |
3.36e-09 |
RHO GTPases Activate WASPs and WAVEs |
35 |
4.19e-02 |
7.97e-02 |
0.3230 |
0.208000 |
1.83e-01 |
-0.086500 |
1.42e-01 |
3.33e-02 |
6.09e-02 |
3.76e-01 |
1.46e-01 |
Ovarian tumor domain proteases |
34 |
7.26e-02 |
1.23e-01 |
0.3230 |
0.051800 |
4.72e-02 |
-0.159000 |
-2.72e-01 |
6.01e-01 |
6.34e-01 |
1.08e-01 |
6.07e-03 |
Aberrant regulation of mitotic cell cycle due to RB1 defects |
36 |
9.47e-04 |
3.18e-03 |
0.3220 |
0.143000 |
3.56e-02 |
0.237000 |
-1.61e-01 |
1.38e-01 |
7.12e-01 |
1.38e-02 |
9.55e-02 |
Diseases of mitotic cell cycle |
36 |
9.47e-04 |
3.18e-03 |
0.3220 |
0.143000 |
3.56e-02 |
0.237000 |
-1.61e-01 |
1.38e-01 |
7.12e-01 |
1.38e-02 |
9.55e-02 |
Signaling by ERBB2 KD Mutants |
21 |
4.01e-01 |
4.85e-01 |
0.3220 |
-0.203000 |
-1.52e-01 |
-0.146000 |
-1.35e-01 |
1.07e-01 |
2.28e-01 |
2.48e-01 |
2.84e-01 |
Gastrin-CREB signalling pathway via PKC and MAPK |
16 |
4.81e-01 |
5.56e-01 |
0.3210 |
-0.199000 |
-1.08e-01 |
-0.166000 |
-1.56e-01 |
1.67e-01 |
4.56e-01 |
2.49e-01 |
2.81e-01 |
Adherens junctions interactions |
14 |
5.62e-01 |
6.27e-01 |
0.3210 |
-0.154000 |
-2.00e-01 |
-0.187000 |
-6.61e-02 |
3.19e-01 |
1.95e-01 |
2.26e-01 |
6.68e-01 |
Olfactory Signaling Pathway |
12 |
3.68e-01 |
4.54e-01 |
0.3210 |
-0.101000 |
-2.46e-02 |
0.302000 |
3.25e-02 |
5.46e-01 |
8.83e-01 |
7.01e-02 |
8.46e-01 |
Binding and Uptake of Ligands by Scavenger Receptors |
30 |
6.02e-02 |
1.07e-01 |
0.3200 |
-0.171000 |
4.22e-04 |
0.135000 |
2.35e-01 |
1.06e-01 |
9.97e-01 |
2.02e-01 |
2.58e-02 |
SUMOylation of DNA damage response and repair proteins |
66 |
3.07e-07 |
1.62e-06 |
0.3200 |
0.120000 |
1.71e-03 |
0.178000 |
-2.38e-01 |
9.35e-02 |
9.81e-01 |
1.24e-02 |
8.49e-04 |
ERCC6 (CSB) and EHMT2 (G9a) positively regulate rRNA expression |
15 |
9.75e-02 |
1.56e-01 |
0.3200 |
0.062400 |
1.13e-01 |
0.161000 |
-2.44e-01 |
6.76e-01 |
4.49e-01 |
2.80e-01 |
1.02e-01 |
Branched-chain amino acid catabolism |
21 |
6.98e-02 |
1.20e-01 |
0.3190 |
0.085900 |
-2.02e-01 |
-0.184000 |
-1.41e-01 |
4.96e-01 |
1.10e-01 |
1.45e-01 |
2.62e-01 |
Negative regulation of FGFR3 signaling |
19 |
6.76e-02 |
1.17e-01 |
0.3180 |
-0.006180 |
-3.02e-01 |
0.024200 |
-9.67e-02 |
9.63e-01 |
2.26e-02 |
8.55e-01 |
4.66e-01 |
Downstream TCR signaling |
78 |
2.03e-04 |
7.69e-04 |
0.3180 |
0.183000 |
1.61e-01 |
0.202000 |
-2.72e-02 |
5.15e-03 |
1.41e-02 |
2.07e-03 |
6.78e-01 |
Glutamate Neurotransmitter Release Cycle |
16 |
4.32e-01 |
5.13e-01 |
0.3180 |
-0.024400 |
1.01e-02 |
-0.271000 |
-1.64e-01 |
8.66e-01 |
9.44e-01 |
6.11e-02 |
2.55e-01 |
Maturation of nucleoprotein |
10 |
5.35e-01 |
6.01e-01 |
0.3170 |
0.095800 |
2.16e-01 |
-0.038000 |
2.07e-01 |
6.00e-01 |
2.36e-01 |
8.35e-01 |
2.56e-01 |
Ub-specific processing proteases |
165 |
1.20e-09 |
1.01e-08 |
0.3170 |
0.215000 |
1.46e-01 |
0.016500 |
-1.81e-01 |
2.06e-06 |
1.25e-03 |
7.15e-01 |
6.42e-05 |
SARS-CoV-1 Infection |
41 |
1.31e-02 |
3.13e-02 |
0.3170 |
-0.043800 |
-1.34e-01 |
0.269000 |
9.00e-02 |
6.28e-01 |
1.38e-01 |
2.89e-03 |
3.19e-01 |
TCR signaling |
99 |
2.82e-04 |
1.03e-03 |
0.3160 |
0.195000 |
2.33e-01 |
0.081900 |
-3.01e-02 |
8.14e-04 |
6.24e-05 |
1.60e-01 |
6.06e-01 |
WNT5A-dependent internalization of FZD4 |
15 |
2.42e-01 |
3.21e-01 |
0.3160 |
-0.264000 |
-8.46e-02 |
0.132000 |
-7.44e-02 |
7.67e-02 |
5.71e-01 |
3.75e-01 |
6.18e-01 |
Constitutive Signaling by Overexpressed ERBB2 |
10 |
5.55e-01 |
6.21e-01 |
0.3160 |
-0.023800 |
-7.60e-02 |
-0.054500 |
-3.00e-01 |
8.96e-01 |
6.77e-01 |
7.65e-01 |
1.00e-01 |
Biosynthesis of DHA-derived SPMs |
11 |
3.60e-01 |
4.47e-01 |
0.3150 |
0.071500 |
2.22e-01 |
-0.128000 |
1.69e-01 |
6.82e-01 |
2.02e-01 |
4.64e-01 |
3.32e-01 |
Regulation of PLK1 Activity at G2/M Transition |
84 |
2.51e-09 |
1.96e-08 |
0.3150 |
0.026200 |
-3.64e-02 |
0.230000 |
-2.10e-01 |
6.78e-01 |
5.65e-01 |
2.65e-04 |
9.02e-04 |
Processing of Capped Intronless Pre-mRNA |
26 |
1.74e-02 |
3.95e-02 |
0.3140 |
0.136000 |
3.78e-02 |
0.107000 |
-2.59e-01 |
2.31e-01 |
7.39e-01 |
3.44e-01 |
2.23e-02 |
Glutathione conjugation |
28 |
3.89e-02 |
7.49e-02 |
0.3140 |
0.181000 |
-2.77e-02 |
0.226000 |
1.18e-01 |
9.79e-02 |
8.00e-01 |
3.86e-02 |
2.81e-01 |
PKA-mediated phosphorylation of CREB |
18 |
1.34e-01 |
2.04e-01 |
0.3130 |
-0.052500 |
-3.09e-01 |
-0.007790 |
1.04e-02 |
7.00e-01 |
2.34e-02 |
9.54e-01 |
9.39e-01 |
HSP90 chaperone cycle for steroid hormone receptors (SHR) |
33 |
7.48e-02 |
1.26e-01 |
0.3130 |
-0.123000 |
-1.94e-01 |
-0.000264 |
-2.13e-01 |
2.23e-01 |
5.37e-02 |
9.98e-01 |
3.42e-02 |
Synthesis of substrates in N-glycan biosythesis |
54 |
9.88e-03 |
2.47e-02 |
0.3120 |
-0.086300 |
-1.46e-01 |
0.161000 |
2.07e-01 |
2.73e-01 |
6.34e-02 |
4.13e-02 |
8.58e-03 |
Iron uptake and transport |
48 |
1.78e-02 |
4.01e-02 |
0.3110 |
0.010300 |
-7.74e-02 |
0.227000 |
1.98e-01 |
9.02e-01 |
3.54e-01 |
6.51e-03 |
1.78e-02 |
SUMOylation of chromatin organization proteins |
49 |
8.70e-05 |
3.41e-04 |
0.3110 |
0.021700 |
-1.45e-01 |
0.123000 |
-2.44e-01 |
7.93e-01 |
7.87e-02 |
1.36e-01 |
3.11e-03 |
Base-Excision Repair, AP Site Formation |
18 |
6.99e-02 |
1.20e-01 |
0.3100 |
-0.029600 |
2.88e-01 |
0.107000 |
3.16e-02 |
8.28e-01 |
3.47e-02 |
4.30e-01 |
8.17e-01 |
SMAD2/SMAD3:SMAD4 heterotrimer regulates transcription |
27 |
7.44e-02 |
1.25e-01 |
0.3100 |
0.092000 |
1.05e-01 |
-0.041400 |
-2.73e-01 |
4.08e-01 |
3.44e-01 |
7.10e-01 |
1.40e-02 |
MAPK6/MAPK4 signaling |
77 |
1.48e-04 |
5.72e-04 |
0.3100 |
0.041900 |
9.85e-02 |
0.287000 |
4.54e-02 |
5.26e-01 |
1.35e-01 |
1.36e-05 |
4.92e-01 |
ER to Golgi Anterograde Transport |
120 |
1.76e-05 |
7.64e-05 |
0.3090 |
-0.146000 |
-2.05e-01 |
0.148000 |
1.03e-01 |
5.88e-03 |
1.09e-04 |
5.20e-03 |
5.18e-02 |
Amine ligand-binding receptors |
12 |
3.64e-01 |
4.49e-01 |
0.3090 |
0.113000 |
-1.50e-01 |
-0.155000 |
-1.91e-01 |
4.99e-01 |
3.70e-01 |
3.54e-01 |
2.52e-01 |
Signaling by FGFR4 |
28 |
5.87e-02 |
1.05e-01 |
0.3090 |
-0.005530 |
-2.26e-01 |
-0.058400 |
-2.02e-01 |
9.60e-01 |
3.88e-02 |
5.93e-01 |
6.39e-02 |
Signaling by Hippo |
19 |
1.85e-01 |
2.60e-01 |
0.3090 |
-0.052000 |
-2.71e-01 |
-0.133000 |
-3.80e-02 |
6.95e-01 |
4.08e-02 |
3.16e-01 |
7.74e-01 |
Glucagon signaling in metabolic regulation |
25 |
1.45e-01 |
2.18e-01 |
0.3080 |
-0.071100 |
-1.37e-01 |
0.111000 |
2.43e-01 |
5.39e-01 |
2.35e-01 |
3.36e-01 |
3.58e-02 |
NOTCH2 Activation and Transmission of Signal to the Nucleus |
18 |
1.12e-02 |
2.76e-02 |
0.3080 |
-0.203000 |
2.12e-01 |
-0.086700 |
3.32e-02 |
1.36e-01 |
1.19e-01 |
5.24e-01 |
8.07e-01 |
Ion transport by P-type ATPases |
36 |
4.22e-02 |
8.02e-02 |
0.3070 |
-0.152000 |
-1.63e-01 |
-0.209000 |
2.65e-02 |
1.14e-01 |
9.09e-02 |
2.97e-02 |
7.83e-01 |
DCC mediated attractive signaling |
13 |
3.92e-01 |
4.77e-01 |
0.3070 |
0.136000 |
1.64e-01 |
-0.216000 |
4.65e-02 |
3.95e-01 |
3.07e-01 |
1.77e-01 |
7.72e-01 |
Tie2 Signaling |
16 |
4.05e-01 |
4.88e-01 |
0.3070 |
0.045000 |
-1.29e-01 |
-0.173000 |
-2.13e-01 |
7.55e-01 |
3.72e-01 |
2.32e-01 |
1.40e-01 |
Downstream signaling events of B Cell Receptor (BCR) |
73 |
3.80e-04 |
1.36e-03 |
0.3070 |
0.153000 |
1.45e-01 |
0.221000 |
-2.49e-02 |
2.36e-02 |
3.22e-02 |
1.12e-03 |
7.13e-01 |
Centrosome maturation |
80 |
2.07e-08 |
1.36e-07 |
0.3060 |
0.005620 |
-5.50e-03 |
0.228000 |
-2.04e-01 |
9.31e-01 |
9.32e-01 |
4.21e-04 |
1.61e-03 |
Recruitment of mitotic centrosome proteins and complexes |
80 |
2.07e-08 |
1.36e-07 |
0.3060 |
0.005620 |
-5.50e-03 |
0.228000 |
-2.04e-01 |
9.31e-01 |
9.32e-01 |
4.21e-04 |
1.61e-03 |
NCAM signaling for neurite out-growth |
46 |
3.36e-02 |
6.66e-02 |
0.3060 |
-0.233000 |
-1.47e-01 |
-0.134000 |
4.59e-03 |
6.40e-03 |
8.52e-02 |
1.16e-01 |
9.57e-01 |
NGF-stimulated transcription |
34 |
1.40e-01 |
2.10e-01 |
0.3060 |
-0.160000 |
-2.49e-01 |
-0.075600 |
-7.26e-03 |
1.07e-01 |
1.19e-02 |
4.46e-01 |
9.42e-01 |
GRB2 events in EGFR signaling |
10 |
7.64e-01 |
8.04e-01 |
0.3060 |
-0.201000 |
-2.19e-01 |
-0.070300 |
6.26e-03 |
2.71e-01 |
2.30e-01 |
7.00e-01 |
9.73e-01 |
Other interleukin signaling |
19 |
2.70e-01 |
3.51e-01 |
0.3060 |
0.060800 |
2.15e-01 |
0.028900 |
2.06e-01 |
6.46e-01 |
1.05e-01 |
8.27e-01 |
1.19e-01 |
Trafficking of GluR2-containing AMPA receptors |
13 |
4.76e-01 |
5.52e-01 |
0.3050 |
-0.261000 |
-1.01e-01 |
-0.016100 |
-1.21e-01 |
1.04e-01 |
5.30e-01 |
9.20e-01 |
4.49e-01 |
SHC1 events in ERBB2 signaling |
19 |
4.03e-01 |
4.86e-01 |
0.3050 |
-0.207000 |
-1.23e-01 |
-0.175000 |
-6.45e-02 |
1.18e-01 |
3.52e-01 |
1.87e-01 |
6.26e-01 |
Spry regulation of FGF signaling |
14 |
4.22e-01 |
5.03e-01 |
0.3050 |
-0.114000 |
-2.58e-01 |
0.115000 |
-8.49e-03 |
4.62e-01 |
9.51e-02 |
4.55e-01 |
9.56e-01 |
Antiviral mechanism by IFN-stimulated genes |
70 |
1.54e-05 |
6.74e-05 |
0.3040 |
0.158000 |
7.93e-02 |
0.220000 |
-1.13e-01 |
2.22e-02 |
2.52e-01 |
1.45e-03 |
1.03e-01 |
CD28 co-stimulation |
32 |
1.51e-01 |
2.23e-01 |
0.3040 |
0.230000 |
1.46e-01 |
-0.111000 |
-7.74e-02 |
2.45e-02 |
1.53e-01 |
2.76e-01 |
4.49e-01 |
Reproduction |
55 |
7.57e-04 |
2.59e-03 |
0.3040 |
0.131000 |
1.83e-01 |
0.147000 |
-1.42e-01 |
9.19e-02 |
1.91e-02 |
5.92e-02 |
6.97e-02 |
MTOR signalling |
39 |
8.75e-03 |
2.23e-02 |
0.3040 |
-0.066900 |
-2.42e-01 |
0.094900 |
-1.42e-01 |
4.70e-01 |
9.07e-03 |
3.05e-01 |
1.24e-01 |
Transport of Mature Transcript to Cytoplasm |
74 |
7.98e-07 |
4.06e-06 |
0.3030 |
0.086400 |
7.91e-02 |
0.151000 |
-2.36e-01 |
1.99e-01 |
2.40e-01 |
2.52e-02 |
4.56e-04 |
Chemokine receptors bind chemokines |
26 |
5.86e-02 |
1.05e-01 |
0.3030 |
0.120000 |
1.47e-01 |
-0.113000 |
2.08e-01 |
2.89e-01 |
1.96e-01 |
3.19e-01 |
6.65e-02 |
Cell junction organization |
50 |
4.81e-03 |
1.36e-02 |
0.3030 |
-0.161000 |
-5.23e-02 |
-0.250000 |
-2.92e-02 |
4.91e-02 |
5.23e-01 |
2.28e-03 |
7.21e-01 |
Activation of NMDA receptors and postsynaptic events |
58 |
1.90e-02 |
4.21e-02 |
0.3020 |
-0.098800 |
-1.86e-01 |
-0.200000 |
-8.47e-02 |
1.94e-01 |
1.45e-02 |
8.44e-03 |
2.65e-01 |
Extracellular matrix organization |
218 |
2.13e-19 |
5.59e-18 |
0.3020 |
-0.200000 |
-2.60e-02 |
-0.184000 |
1.30e-01 |
4.15e-07 |
5.09e-01 |
3.02e-06 |
1.01e-03 |
Sealing of the nuclear envelope (NE) by ESCRT-III |
22 |
2.57e-01 |
3.38e-01 |
0.3010 |
-0.138000 |
-1.18e-01 |
0.230000 |
7.17e-02 |
2.62e-01 |
3.40e-01 |
6.23e-02 |
5.60e-01 |
Downstream signal transduction |
28 |
2.84e-01 |
3.66e-01 |
0.3010 |
-0.033900 |
-4.89e-02 |
-0.217000 |
-2.00e-01 |
7.56e-01 |
6.54e-01 |
4.73e-02 |
6.67e-02 |
The NLRP3 inflammasome |
14 |
1.20e-01 |
1.86e-01 |
0.3000 |
-0.165000 |
1.88e-01 |
0.069200 |
1.50e-01 |
2.85e-01 |
2.24e-01 |
6.54e-01 |
3.30e-01 |
Regulation of actin dynamics for phagocytic cup formation |
63 |
1.68e-02 |
3.84e-02 |
0.3000 |
0.138000 |
2.06e-01 |
0.033800 |
1.66e-01 |
5.93e-02 |
4.76e-03 |
6.43e-01 |
2.32e-02 |
Chondroitin sulfate/dermatan sulfate metabolism |
41 |
6.35e-03 |
1.72e-02 |
0.3000 |
-0.131000 |
9.36e-02 |
0.073800 |
2.42e-01 |
1.46e-01 |
3.00e-01 |
4.14e-01 |
7.47e-03 |
Signaling by FGFR2 in disease |
31 |
4.88e-02 |
9.04e-02 |
0.2990 |
-0.051700 |
-2.57e-01 |
0.006100 |
-1.44e-01 |
6.18e-01 |
1.34e-02 |
9.53e-01 |
1.66e-01 |
TNF signaling |
37 |
5.60e-02 |
1.01e-01 |
0.2990 |
0.038100 |
1.36e-01 |
-0.218000 |
-1.48e-01 |
6.88e-01 |
1.54e-01 |
2.17e-02 |
1.20e-01 |
Signaling by KIT in disease |
20 |
3.91e-01 |
4.76e-01 |
0.2980 |
0.109000 |
5.35e-02 |
-0.221000 |
-1.60e-01 |
3.97e-01 |
6.79e-01 |
8.76e-02 |
2.17e-01 |
Signaling by phosphorylated juxtamembrane, extracellular and kinase domain KIT mutants |
20 |
3.91e-01 |
4.76e-01 |
0.2980 |
0.109000 |
5.35e-02 |
-0.221000 |
-1.60e-01 |
3.97e-01 |
6.79e-01 |
8.76e-02 |
2.17e-01 |
FCGR3A-mediated IL10 synthesis |
39 |
1.25e-01 |
1.92e-01 |
0.2980 |
0.013100 |
8.09e-02 |
0.167000 |
2.33e-01 |
8.87e-01 |
3.82e-01 |
7.14e-02 |
1.19e-02 |
Gap junction trafficking and regulation |
15 |
5.28e-01 |
5.95e-01 |
0.2970 |
-0.038700 |
-8.70e-02 |
0.203000 |
1.95e-01 |
7.95e-01 |
5.60e-01 |
1.73e-01 |
1.91e-01 |
Peptide ligand-binding receptors |
62 |
3.99e-04 |
1.41e-03 |
0.2970 |
0.021700 |
1.40e-01 |
-0.023200 |
2.60e-01 |
7.68e-01 |
5.61e-02 |
7.53e-01 |
4.05e-04 |
Regulated proteolysis of p75NTR |
11 |
6.77e-01 |
7.23e-01 |
0.2970 |
-0.131000 |
-1.73e-01 |
0.126000 |
1.58e-01 |
4.51e-01 |
3.21e-01 |
4.70e-01 |
3.63e-01 |
Regulation of TP53 Activity through Acetylation |
29 |
1.29e-02 |
3.10e-02 |
0.2970 |
-0.033400 |
1.20e-02 |
0.091000 |
-2.80e-01 |
7.56e-01 |
9.11e-01 |
3.96e-01 |
9.07e-03 |
Molecules associated with elastic fibres |
27 |
5.37e-02 |
9.77e-02 |
0.2970 |
-0.002580 |
-3.40e-02 |
-0.294000 |
1.16e-02 |
9.82e-01 |
7.60e-01 |
8.13e-03 |
9.17e-01 |
Elastic fibre formation |
37 |
1.24e-02 |
3.01e-02 |
0.2960 |
-0.112000 |
-8.42e-02 |
-0.254000 |
5.77e-02 |
2.37e-01 |
3.76e-01 |
7.43e-03 |
5.44e-01 |
HIV Infection |
204 |
1.18e-13 |
1.87e-12 |
0.2950 |
0.067600 |
3.55e-02 |
0.285000 |
-1.02e-02 |
9.72e-02 |
3.84e-01 |
2.64e-12 |
8.03e-01 |
RNA Polymerase III Chain Elongation |
18 |
5.36e-01 |
6.03e-01 |
0.2950 |
0.010600 |
6.16e-02 |
0.201000 |
2.07e-01 |
9.38e-01 |
6.51e-01 |
1.41e-01 |
1.29e-01 |
Nucleotide Excision Repair |
105 |
1.19e-06 |
5.91e-06 |
0.2950 |
0.125000 |
8.19e-02 |
0.252000 |
-3.26e-02 |
2.69e-02 |
1.48e-01 |
8.52e-06 |
5.65e-01 |
Deubiquitination |
238 |
7.27e-13 |
9.93e-12 |
0.2950 |
0.184000 |
1.15e-01 |
0.002960 |
-1.99e-01 |
1.11e-06 |
2.24e-03 |
9.37e-01 |
1.36e-07 |
Interconversion of nucleotide di- and triphosphates |
24 |
1.89e-01 |
2.65e-01 |
0.2950 |
0.073700 |
2.90e-02 |
0.275000 |
6.92e-02 |
5.32e-01 |
8.06e-01 |
1.97e-02 |
5.57e-01 |
Signaling by ERBB2 in Cancer |
22 |
4.86e-01 |
5.60e-01 |
0.2940 |
-0.167000 |
-1.36e-01 |
-0.150000 |
-1.31e-01 |
1.74e-01 |
2.69e-01 |
2.23e-01 |
2.86e-01 |
HCMV Infection |
73 |
2.18e-06 |
1.06e-05 |
0.2940 |
0.045400 |
-8.78e-02 |
0.265000 |
-7.83e-02 |
5.02e-01 |
1.95e-01 |
8.97e-05 |
2.48e-01 |
Costimulation by the CD28 family |
55 |
4.00e-02 |
7.68e-02 |
0.2940 |
0.214000 |
1.68e-01 |
-0.080900 |
-7.42e-02 |
5.98e-03 |
3.11e-02 |
3.00e-01 |
3.42e-01 |
Conversion from APC/C:Cdc20 to APC/C:Cdh1 in late anaphase |
20 |
5.06e-02 |
9.28e-02 |
0.2930 |
0.079400 |
-1.29e-01 |
0.240000 |
-7.17e-02 |
5.39e-01 |
3.19e-01 |
6.28e-02 |
5.79e-01 |
Insulin receptor recycling |
19 |
4.38e-01 |
5.15e-01 |
0.2920 |
-0.112000 |
-6.36e-02 |
0.154000 |
2.12e-01 |
3.98e-01 |
6.31e-01 |
2.44e-01 |
1.09e-01 |
Insertion of tail-anchored proteins into the endoplasmic reticulum membrane |
18 |
4.22e-01 |
5.03e-01 |
0.2920 |
0.093800 |
1.05e-01 |
0.247000 |
6.95e-02 |
4.91e-01 |
4.43e-01 |
6.99e-02 |
6.10e-01 |
Ion channel transport |
103 |
8.87e-04 |
2.99e-03 |
0.2920 |
-0.208000 |
-1.72e-01 |
-0.110000 |
4.21e-03 |
2.63e-04 |
2.62e-03 |
5.35e-02 |
9.41e-01 |
PRC2 methylates histones and DNA |
14 |
3.38e-01 |
4.22e-01 |
0.2920 |
0.257000 |
4.37e-02 |
0.002720 |
-1.30e-01 |
9.54e-02 |
7.77e-01 |
9.86e-01 |
4.00e-01 |
Regulation of insulin secretion |
58 |
5.28e-02 |
9.65e-02 |
0.2910 |
-0.160000 |
-1.74e-01 |
-0.156000 |
-7.05e-02 |
3.56e-02 |
2.20e-02 |
4.07e-02 |
3.54e-01 |
Insulin receptor signalling cascade |
38 |
7.42e-02 |
1.25e-01 |
0.2910 |
-0.003040 |
-1.57e-01 |
-0.116000 |
-2.16e-01 |
9.74e-01 |
9.33e-02 |
2.18e-01 |
2.11e-02 |
SLBP Dependent Processing of Replication-Dependent Histone Pre-mRNAs |
11 |
4.17e-01 |
5.00e-01 |
0.2900 |
-0.005910 |
2.00e-02 |
0.287000 |
-3.62e-02 |
9.73e-01 |
9.09e-01 |
9.98e-02 |
8.35e-01 |
Frs2-mediated activation |
11 |
4.19e-01 |
5.01e-01 |
0.2890 |
0.005880 |
-2.58e-01 |
-0.031700 |
-1.27e-01 |
9.73e-01 |
1.38e-01 |
8.56e-01 |
4.67e-01 |
MET activates RAP1 and RAC1 |
11 |
3.07e-01 |
3.89e-01 |
0.2890 |
0.116000 |
-1.28e-01 |
0.056800 |
2.24e-01 |
5.07e-01 |
4.63e-01 |
7.45e-01 |
1.98e-01 |
Interleukin-17 signaling |
63 |
9.75e-03 |
2.45e-02 |
0.2890 |
-0.049000 |
-2.12e-01 |
-0.111000 |
-1.54e-01 |
5.02e-01 |
3.67e-03 |
1.29e-01 |
3.46e-02 |
RHO GTPases activate PAKs |
21 |
1.00e-01 |
1.60e-01 |
0.2880 |
0.027000 |
2.32e-01 |
-0.160000 |
5.27e-02 |
8.31e-01 |
6.60e-02 |
2.04e-01 |
6.76e-01 |
Protein-protein interactions at synapses |
55 |
9.96e-04 |
3.31e-03 |
0.2880 |
-0.123000 |
-1.35e-01 |
-0.183000 |
1.26e-01 |
1.14e-01 |
8.45e-02 |
1.89e-02 |
1.06e-01 |
G-protein beta:gamma signalling |
27 |
7.53e-02 |
1.27e-01 |
0.2870 |
0.035400 |
1.03e-01 |
-0.031300 |
2.64e-01 |
7.50e-01 |
3.53e-01 |
7.78e-01 |
1.78e-02 |
Oncogene Induced Senescence |
29 |
3.34e-02 |
6.66e-02 |
0.2860 |
-0.047300 |
4.63e-02 |
0.009180 |
-2.79e-01 |
6.60e-01 |
6.66e-01 |
9.32e-01 |
9.46e-03 |
Inactivation, recovery and regulation of the phototransduction cascade |
19 |
5.72e-01 |
6.33e-01 |
0.2860 |
-0.180000 |
-1.62e-01 |
-0.136000 |
-6.72e-02 |
1.74e-01 |
2.22e-01 |
3.04e-01 |
6.12e-01 |
The phototransduction cascade |
19 |
5.72e-01 |
6.33e-01 |
0.2860 |
-0.180000 |
-1.62e-01 |
-0.136000 |
-6.72e-02 |
1.74e-01 |
2.22e-01 |
3.04e-01 |
6.12e-01 |
Transcriptional regulation by RUNX2 |
106 |
6.61e-04 |
2.27e-03 |
0.2860 |
0.110000 |
5.89e-02 |
0.224000 |
1.26e-01 |
5.17e-02 |
2.95e-01 |
6.92e-05 |
2.48e-02 |
Signaling by Type 1 Insulin-like Growth Factor 1 Receptor (IGF1R) |
38 |
1.06e-01 |
1.67e-01 |
0.2860 |
-0.004990 |
-1.35e-01 |
-0.124000 |
-2.19e-01 |
9.58e-01 |
1.50e-01 |
1.87e-01 |
1.96e-02 |
Transcriptional Regulation by MECP2 |
46 |
1.31e-01 |
2.00e-01 |
0.2850 |
-0.069600 |
-1.44e-01 |
-0.162000 |
-1.72e-01 |
4.15e-01 |
9.13e-02 |
5.77e-02 |
4.38e-02 |
Signaling by FGFR3 |
29 |
7.81e-02 |
1.31e-01 |
0.2850 |
0.027300 |
-1.86e-01 |
-0.068900 |
-2.03e-01 |
7.99e-01 |
8.37e-02 |
5.21e-01 |
5.84e-02 |
Transport to the Golgi and subsequent modification |
145 |
6.08e-06 |
2.79e-05 |
0.2850 |
-0.117000 |
-1.94e-01 |
0.126000 |
1.18e-01 |
1.54e-02 |
5.67e-05 |
9.07e-03 |
1.42e-02 |
Regulation of TP53 Activity |
147 |
6.80e-13 |
9.39e-12 |
0.2850 |
0.057300 |
-2.05e-02 |
0.142000 |
-2.39e-01 |
2.31e-01 |
6.69e-01 |
3.13e-03 |
5.69e-07 |
ISG15 antiviral mechanism |
62 |
3.00e-05 |
1.27e-04 |
0.2840 |
0.112000 |
1.37e-02 |
0.210000 |
-1.56e-01 |
1.29e-01 |
8.52e-01 |
4.28e-03 |
3.44e-02 |
IRS-related events triggered by IGF1R |
36 |
9.35e-02 |
1.52e-01 |
0.2840 |
-0.000180 |
-1.68e-01 |
-0.118000 |
-1.97e-01 |
9.99e-01 |
8.20e-02 |
2.21e-01 |
4.14e-02 |
Inhibition of DNA recombination at telomere |
20 |
2.57e-01 |
3.38e-01 |
0.2840 |
0.063000 |
1.69e-01 |
0.219000 |
2.70e-03 |
6.26e-01 |
1.91e-01 |
8.95e-02 |
9.83e-01 |
The role of Nef in HIV-1 replication and disease pathogenesis |
25 |
2.02e-01 |
2.78e-01 |
0.2830 |
0.079700 |
2.51e-01 |
0.101000 |
2.88e-02 |
4.91e-01 |
3.01e-02 |
3.83e-01 |
8.03e-01 |
EPH-ephrin mediated repulsion of cells |
41 |
6.70e-02 |
1.16e-01 |
0.2820 |
-0.085200 |
4.88e-02 |
0.138000 |
2.26e-01 |
3.46e-01 |
5.89e-01 |
1.27e-01 |
1.22e-02 |
Negative regulation of MAPK pathway |
40 |
5.22e-02 |
9.55e-02 |
0.2820 |
-0.047900 |
-1.54e-01 |
-0.028600 |
-2.30e-01 |
6.01e-01 |
9.28e-02 |
7.55e-01 |
1.18e-02 |
Nonhomologous End-Joining (NHEJ) |
33 |
6.11e-02 |
1.08e-01 |
0.2810 |
0.213000 |
9.42e-02 |
0.132000 |
-8.38e-02 |
3.41e-02 |
3.49e-01 |
1.90e-01 |
4.05e-01 |
RNA Polymerase III Transcription Termination |
23 |
4.97e-01 |
5.70e-01 |
0.2810 |
0.063900 |
1.06e-01 |
0.170000 |
1.86e-01 |
5.96e-01 |
3.81e-01 |
1.59e-01 |
1.22e-01 |
NOD1/2 Signaling Pathway |
29 |
2.83e-01 |
3.66e-01 |
0.2810 |
-0.065600 |
-3.53e-02 |
-0.229000 |
-1.44e-01 |
5.41e-01 |
7.42e-01 |
3.31e-02 |
1.78e-01 |
Transport of Mature mRNA derived from an Intron-Containing Transcript |
65 |
5.13e-05 |
2.08e-04 |
0.2800 |
0.082800 |
9.60e-02 |
0.153000 |
-1.98e-01 |
2.49e-01 |
1.81e-01 |
3.34e-02 |
5.83e-03 |
mRNA 3'-end processing |
52 |
2.01e-02 |
4.44e-02 |
0.2800 |
0.150000 |
1.70e-01 |
0.002940 |
-1.64e-01 |
6.19e-02 |
3.39e-02 |
9.71e-01 |
4.05e-02 |
Tight junction interactions |
10 |
4.77e-01 |
5.52e-01 |
0.2800 |
-0.038900 |
-1.27e-01 |
-0.234000 |
7.71e-02 |
8.31e-01 |
4.88e-01 |
2.00e-01 |
6.73e-01 |
SUMOylation of transcription factors |
15 |
6.02e-01 |
6.59e-01 |
0.2800 |
0.079200 |
-1.77e-02 |
-0.199000 |
-1.79e-01 |
5.96e-01 |
9.06e-01 |
1.83e-01 |
2.29e-01 |
RAF activation |
34 |
1.32e-01 |
2.02e-01 |
0.2790 |
-0.006150 |
-1.57e-01 |
-0.105000 |
-2.05e-01 |
9.51e-01 |
1.14e-01 |
2.89e-01 |
3.86e-02 |
Metabolism of nitric oxide: NOS3 activation and regulation |
15 |
5.48e-01 |
6.14e-01 |
0.2780 |
0.149000 |
1.55e-01 |
-0.023500 |
1.75e-01 |
3.19e-01 |
2.99e-01 |
8.75e-01 |
2.41e-01 |
Formation of HIV-1 elongation complex containing HIV-1 Tat |
38 |
1.75e-02 |
3.95e-02 |
0.2770 |
-0.105000 |
-6.07e-02 |
0.245000 |
-4.88e-02 |
2.62e-01 |
5.18e-01 |
9.10e-03 |
6.03e-01 |
HIV Transcription Elongation |
38 |
1.75e-02 |
3.95e-02 |
0.2770 |
-0.105000 |
-6.07e-02 |
0.245000 |
-4.88e-02 |
2.62e-01 |
5.18e-01 |
9.10e-03 |
6.03e-01 |
Tat-mediated elongation of the HIV-1 transcript |
38 |
1.75e-02 |
3.95e-02 |
0.2770 |
-0.105000 |
-6.07e-02 |
0.245000 |
-4.88e-02 |
2.62e-01 |
5.18e-01 |
9.10e-03 |
6.03e-01 |
Signaling by PDGFRA extracellular domain mutants |
12 |
4.55e-01 |
5.31e-01 |
0.2770 |
0.202000 |
8.09e-03 |
-0.015700 |
-1.89e-01 |
2.27e-01 |
9.61e-01 |
9.25e-01 |
2.58e-01 |
Signaling by PDGFRA transmembrane, juxtamembrane and kinase domain mutants |
12 |
4.55e-01 |
5.31e-01 |
0.2770 |
0.202000 |
8.09e-03 |
-0.015700 |
-1.89e-01 |
2.27e-01 |
9.61e-01 |
9.25e-01 |
2.58e-01 |
Amino acid transport across the plasma membrane |
21 |
1.90e-01 |
2.66e-01 |
0.2760 |
0.057000 |
-1.67e-01 |
-0.076300 |
-1.99e-01 |
6.52e-01 |
1.85e-01 |
5.45e-01 |
1.15e-01 |
Late Phase of HIV Life Cycle |
120 |
1.24e-08 |
8.79e-08 |
0.2760 |
-0.018000 |
-9.65e-02 |
0.247000 |
-7.57e-02 |
7.34e-01 |
6.85e-02 |
3.10e-06 |
1.53e-01 |
Fcgamma receptor (FCGR) dependent phagocytosis |
86 |
3.47e-03 |
1.02e-02 |
0.2760 |
0.091800 |
2.08e-01 |
0.040700 |
1.51e-01 |
1.42e-01 |
8.48e-04 |
5.15e-01 |
1.58e-02 |
Receptor Mediated Mitophagy |
11 |
6.78e-01 |
7.23e-01 |
0.2750 |
-0.105000 |
-2.33e-01 |
0.035800 |
-9.62e-02 |
5.46e-01 |
1.81e-01 |
8.37e-01 |
5.81e-01 |
Biotin transport and metabolism |
11 |
8.28e-01 |
8.58e-01 |
0.2750 |
-0.112000 |
-1.42e-01 |
-0.119000 |
-1.69e-01 |
5.20e-01 |
4.15e-01 |
4.93e-01 |
3.33e-01 |
Formation of TC-NER Pre-Incision Complex |
50 |
2.53e-02 |
5.35e-02 |
0.2740 |
0.041700 |
-2.96e-02 |
0.253000 |
9.25e-02 |
6.10e-01 |
7.18e-01 |
1.97e-03 |
2.58e-01 |
TGF-beta receptor signaling activates SMADs |
29 |
2.04e-02 |
4.47e-02 |
0.2740 |
0.063800 |
-2.36e-01 |
-0.024500 |
-1.22e-01 |
5.52e-01 |
2.82e-02 |
8.19e-01 |
2.55e-01 |
Downregulation of TGF-beta receptor signaling |
24 |
3.54e-02 |
6.96e-02 |
0.2740 |
0.085800 |
-2.27e-01 |
-0.017100 |
-1.25e-01 |
4.67e-01 |
5.39e-02 |
8.85e-01 |
2.89e-01 |
Activated NOTCH1 Transmits Signal to the Nucleus |
26 |
3.47e-02 |
6.84e-02 |
0.2730 |
-0.232000 |
4.90e-02 |
-0.129000 |
-4.68e-02 |
4.09e-02 |
6.66e-01 |
2.57e-01 |
6.80e-01 |
Defective B3GALTL causes Peters-plus syndrome (PpS) |
29 |
2.76e-02 |
5.71e-02 |
0.2730 |
-0.143000 |
3.74e-02 |
-0.224000 |
4.96e-02 |
1.82e-01 |
7.28e-01 |
3.70e-02 |
6.44e-01 |
ER Quality Control Compartment (ERQC) |
18 |
4.35e-01 |
5.14e-01 |
0.2730 |
-0.098600 |
-2.12e-01 |
0.096900 |
1.03e-01 |
4.69e-01 |
1.20e-01 |
4.77e-01 |
4.51e-01 |
Negative regulators of DDX58/IFIH1 signaling |
30 |
1.63e-01 |
2.36e-01 |
0.2730 |
0.126000 |
1.33e-01 |
-0.033500 |
-1.99e-01 |
2.31e-01 |
2.09e-01 |
7.51e-01 |
5.92e-02 |
Synthesis of Prostaglandins (PG) and Thromboxanes (TX) |
11 |
3.00e-01 |
3.83e-01 |
0.2720 |
-0.088000 |
2.13e-01 |
-0.038500 |
1.41e-01 |
6.13e-01 |
2.22e-01 |
8.25e-01 |
4.20e-01 |
COPI-mediated anterograde transport |
77 |
8.29e-03 |
2.17e-02 |
0.2720 |
-0.118000 |
-1.63e-01 |
0.154000 |
9.87e-02 |
7.41e-02 |
1.36e-02 |
1.99e-02 |
1.35e-01 |
Disorders of transmembrane transporters |
124 |
1.53e-06 |
7.51e-06 |
0.2710 |
0.062500 |
3.86e-02 |
0.261000 |
5.34e-03 |
2.31e-01 |
4.59e-01 |
5.29e-07 |
9.18e-01 |
MET receptor recycling |
10 |
7.85e-01 |
8.22e-01 |
0.2710 |
-0.049800 |
-1.42e-01 |
-0.084100 |
-2.08e-01 |
7.85e-01 |
4.35e-01 |
6.45e-01 |
2.54e-01 |
Respiratory electron transport |
97 |
2.69e-03 |
8.20e-03 |
0.2710 |
0.128000 |
1.85e-01 |
0.149000 |
2.29e-02 |
3.02e-02 |
1.71e-03 |
1.11e-02 |
6.97e-01 |
Lysosome Vesicle Biogenesis |
30 |
2.34e-01 |
3.13e-01 |
0.2690 |
0.007810 |
8.27e-02 |
0.236000 |
9.89e-02 |
9.41e-01 |
4.33e-01 |
2.50e-02 |
3.49e-01 |
Mitochondrial calcium ion transport |
20 |
2.53e-01 |
3.34e-01 |
0.2690 |
0.038100 |
-1.01e-01 |
0.235000 |
7.58e-02 |
7.68e-01 |
4.35e-01 |
6.94e-02 |
5.58e-01 |
Caspase activation via Death Receptors in the presence of ligand |
15 |
1.59e-01 |
2.33e-01 |
0.2690 |
-0.085900 |
1.35e-01 |
-0.167000 |
1.37e-01 |
5.65e-01 |
3.65e-01 |
2.63e-01 |
3.59e-01 |
p38MAPK events |
12 |
6.58e-01 |
7.05e-01 |
0.2690 |
0.162000 |
3.26e-02 |
-0.179000 |
-1.14e-01 |
3.31e-01 |
8.45e-01 |
2.82e-01 |
4.96e-01 |
Metabolism of steroids |
109 |
9.76e-04 |
3.25e-03 |
0.2690 |
-0.046300 |
-1.75e-01 |
-0.160000 |
-1.18e-01 |
4.05e-01 |
1.62e-03 |
3.93e-03 |
3.39e-02 |
SUMOylation of intracellular receptors |
25 |
2.95e-01 |
3.77e-01 |
0.2690 |
0.133000 |
-3.44e-03 |
-0.147000 |
-1.81e-01 |
2.49e-01 |
9.76e-01 |
2.05e-01 |
1.17e-01 |
WNT ligand biogenesis and trafficking |
13 |
6.26e-01 |
6.79e-01 |
0.2670 |
-0.005590 |
-5.94e-02 |
0.113000 |
2.34e-01 |
9.72e-01 |
7.11e-01 |
4.80e-01 |
1.44e-01 |
TP53 Regulates Transcription of DNA Repair Genes |
57 |
2.33e-04 |
8.72e-04 |
0.2670 |
0.016600 |
7.43e-02 |
0.212000 |
-1.42e-01 |
8.29e-01 |
3.32e-01 |
5.57e-03 |
6.35e-02 |
Beta-oxidation of very long chain fatty acids |
10 |
6.37e-01 |
6.89e-01 |
0.2670 |
-0.076400 |
1.36e-01 |
0.119000 |
1.81e-01 |
6.76e-01 |
4.55e-01 |
5.15e-01 |
3.23e-01 |
COPI-independent Golgi-to-ER retrograde traffic |
30 |
1.26e-01 |
1.92e-01 |
0.2670 |
-0.070000 |
-2.27e-01 |
0.115000 |
3.95e-02 |
5.07e-01 |
3.16e-02 |
2.77e-01 |
7.08e-01 |
MHC class II antigen presentation |
90 |
8.43e-03 |
2.19e-02 |
0.2660 |
0.052000 |
4.14e-02 |
0.218000 |
1.38e-01 |
3.95e-01 |
4.98e-01 |
3.58e-04 |
2.37e-02 |
Defective B4GALT7 causes EDS, progeroid type |
16 |
1.64e-01 |
2.37e-01 |
0.2660 |
-0.223000 |
5.44e-02 |
-0.134000 |
1.72e-02 |
1.23e-01 |
7.07e-01 |
3.52e-01 |
9.05e-01 |
TP53 Regulates Transcription of Cell Death Genes |
36 |
1.51e-01 |
2.23e-01 |
0.2660 |
0.038300 |
9.47e-02 |
-0.214000 |
-1.20e-01 |
6.91e-01 |
3.26e-01 |
2.65e-02 |
2.13e-01 |
Signaling by MET |
61 |
4.43e-02 |
8.34e-02 |
0.2650 |
0.026700 |
-6.90e-02 |
-0.200000 |
-1.57e-01 |
7.19e-01 |
3.52e-01 |
6.82e-03 |
3.37e-02 |
MAP kinase activation |
60 |
1.15e-02 |
2.81e-02 |
0.2650 |
-0.020900 |
-2.07e-01 |
-0.085800 |
-1.41e-01 |
7.80e-01 |
5.62e-03 |
2.51e-01 |
5.95e-02 |
RNA Polymerase II Transcription Termination |
61 |
1.10e-02 |
2.70e-02 |
0.2650 |
0.142000 |
1.74e-01 |
0.058900 |
-1.28e-01 |
5.58e-02 |
1.89e-02 |
4.27e-01 |
8.34e-02 |
Biological oxidations |
130 |
2.62e-04 |
9.66e-04 |
0.2650 |
0.206000 |
9.58e-02 |
0.103000 |
8.84e-02 |
4.95e-05 |
6.00e-02 |
4.27e-02 |
8.26e-02 |
Other semaphorin interactions |
19 |
1.43e-01 |
2.15e-01 |
0.2650 |
0.005150 |
1.06e-01 |
-0.210000 |
1.22e-01 |
9.69e-01 |
4.22e-01 |
1.13e-01 |
3.59e-01 |
Signaling by NOTCH1 |
66 |
4.94e-02 |
9.09e-02 |
0.2650 |
-0.117000 |
-7.49e-02 |
-0.186000 |
-1.27e-01 |
1.01e-01 |
2.93e-01 |
8.91e-03 |
7.41e-02 |
ERKs are inactivated |
13 |
7.10e-01 |
7.52e-01 |
0.2650 |
0.034000 |
6.11e-02 |
0.232000 |
1.07e-01 |
8.32e-01 |
7.03e-01 |
1.48e-01 |
5.03e-01 |
Signaling by the B Cell Receptor (BCR) |
104 |
1.81e-03 |
5.76e-03 |
0.2650 |
0.178000 |
1.61e-01 |
0.106000 |
-3.23e-02 |
1.70e-03 |
4.58e-03 |
6.26e-02 |
5.70e-01 |
Downregulation of ERBB2 signaling |
23 |
4.46e-01 |
5.23e-01 |
0.2650 |
-0.204000 |
-1.51e-01 |
-0.034100 |
6.53e-02 |
9.03e-02 |
2.09e-01 |
7.77e-01 |
5.88e-01 |
Interleukin receptor SHC signaling |
21 |
3.13e-01 |
3.93e-01 |
0.2650 |
0.066400 |
1.42e-01 |
-0.210000 |
-3.39e-02 |
5.98e-01 |
2.60e-01 |
9.52e-02 |
7.88e-01 |
NOTCH4 Intracellular Domain Regulates Transcription |
18 |
4.65e-01 |
5.41e-01 |
0.2650 |
-0.120000 |
-4.84e-02 |
-0.223000 |
-5.97e-02 |
3.78e-01 |
7.22e-01 |
1.02e-01 |
6.61e-01 |
Oxidative Stress Induced Senescence |
60 |
3.40e-02 |
6.73e-02 |
0.2640 |
-0.076200 |
-1.39e-01 |
-0.045700 |
-2.06e-01 |
3.08e-01 |
6.19e-02 |
5.41e-01 |
5.75e-03 |
O-glycosylation of TSR domain-containing proteins |
30 |
3.12e-02 |
6.31e-02 |
0.2640 |
-0.152000 |
2.92e-02 |
-0.207000 |
5.45e-02 |
1.51e-01 |
7.82e-01 |
4.96e-02 |
6.06e-01 |
DARPP-32 events |
21 |
3.27e-02 |
6.56e-02 |
0.2640 |
0.171000 |
-1.57e-01 |
0.118000 |
-4.02e-02 |
1.75e-01 |
2.12e-01 |
3.49e-01 |
7.50e-01 |
IGF1R signaling cascade |
37 |
1.23e-01 |
1.90e-01 |
0.2630 |
0.011600 |
-1.40e-01 |
-0.101000 |
-1.99e-01 |
9.03e-01 |
1.40e-01 |
2.90e-01 |
3.66e-02 |
Interleukin-6 family signaling |
18 |
2.61e-01 |
3.42e-01 |
0.2630 |
0.182000 |
5.69e-02 |
-0.090000 |
1.58e-01 |
1.81e-01 |
6.76e-01 |
5.09e-01 |
2.47e-01 |
Cell-extracellular matrix interactions |
16 |
1.75e-01 |
2.49e-01 |
0.2630 |
-0.171000 |
5.44e-02 |
-0.103000 |
1.63e-01 |
2.38e-01 |
7.06e-01 |
4.77e-01 |
2.58e-01 |
FGFR1 mutant receptor activation |
24 |
2.44e-01 |
3.23e-01 |
0.2630 |
0.035900 |
-1.56e-01 |
-0.172000 |
-1.20e-01 |
7.61e-01 |
1.87e-01 |
1.46e-01 |
3.11e-01 |
IKK complex recruitment mediated by RIP1 |
19 |
5.28e-01 |
5.95e-01 |
0.2630 |
-0.052700 |
-5.49e-02 |
-0.233000 |
-9.63e-02 |
6.91e-01 |
6.79e-01 |
7.94e-02 |
4.67e-01 |
Signaling by NOTCH2 |
27 |
9.52e-02 |
1.53e-01 |
0.2630 |
-0.080900 |
1.16e-01 |
-0.193000 |
-1.09e-01 |
4.67e-01 |
2.97e-01 |
8.32e-02 |
3.26e-01 |
Platelet degranulation |
100 |
5.45e-05 |
2.21e-04 |
0.2620 |
-0.001070 |
8.84e-02 |
0.001700 |
2.46e-01 |
9.85e-01 |
1.27e-01 |
9.77e-01 |
2.16e-05 |
Post-translational protein phosphorylation |
70 |
1.57e-03 |
5.08e-03 |
0.2610 |
-0.160000 |
-9.60e-02 |
-0.066200 |
1.70e-01 |
2.07e-02 |
1.65e-01 |
3.39e-01 |
1.39e-02 |
DNA Damage Recognition in GG-NER |
35 |
7.88e-02 |
1.32e-01 |
0.2610 |
0.044000 |
-2.03e-02 |
0.254000 |
3.55e-02 |
6.53e-01 |
8.36e-01 |
9.32e-03 |
7.16e-01 |
Heparan sulfate/heparin (HS-GAG) metabolism |
39 |
9.51e-02 |
1.53e-01 |
0.2610 |
-0.167000 |
-3.07e-02 |
0.086500 |
1.77e-01 |
7.06e-02 |
7.40e-01 |
3.50e-01 |
5.54e-02 |
DNA Double Strand Break Response |
38 |
8.35e-03 |
2.17e-02 |
0.2600 |
0.107000 |
-6.95e-03 |
0.195000 |
-1.35e-01 |
2.55e-01 |
9.41e-01 |
3.80e-02 |
1.50e-01 |
Fatty acyl-CoA biosynthesis |
23 |
3.68e-01 |
4.54e-01 |
0.2600 |
-0.128000 |
-7.02e-03 |
-0.161000 |
-1.59e-01 |
2.90e-01 |
9.54e-01 |
1.82e-01 |
1.86e-01 |
Anchoring of the basal body to the plasma membrane |
92 |
1.13e-06 |
5.64e-06 |
0.2600 |
-0.006650 |
-2.19e-02 |
0.219000 |
-1.37e-01 |
9.12e-01 |
7.17e-01 |
2.81e-04 |
2.29e-02 |
Respiratory electron transport, ATP synthesis by chemiosmotic coupling, and heat production by uncoupling proteins. |
103 |
3.48e-03 |
1.02e-02 |
0.2600 |
0.131000 |
1.82e-01 |
0.130000 |
1.36e-02 |
2.18e-02 |
1.43e-03 |
2.26e-02 |
8.12e-01 |
Signaling by RAF1 mutants |
34 |
5.11e-02 |
9.36e-02 |
0.2600 |
0.011700 |
3.51e-02 |
-0.256000 |
2.19e-02 |
9.06e-01 |
7.23e-01 |
9.80e-03 |
8.26e-01 |
Chaperone Mediated Autophagy |
15 |
4.81e-01 |
5.56e-01 |
0.2590 |
-0.076300 |
-1.06e-01 |
0.224000 |
2.14e-03 |
6.09e-01 |
4.79e-01 |
1.34e-01 |
9.89e-01 |
mRNA Splicing - Major Pathway |
167 |
8.15e-09 |
5.91e-08 |
0.2590 |
0.120000 |
1.31e-01 |
0.137000 |
-1.28e-01 |
7.66e-03 |
3.46e-03 |
2.25e-03 |
4.30e-03 |
SLBP independent Processing of Histone Pre-mRNAs |
10 |
6.92e-01 |
7.35e-01 |
0.2580 |
-0.069200 |
-4.57e-02 |
0.243000 |
2.77e-02 |
7.05e-01 |
8.02e-01 |
1.83e-01 |
8.79e-01 |
Response of Mtb to phagocytosis |
20 |
2.31e-01 |
3.11e-01 |
0.2580 |
0.084600 |
5.14e-02 |
0.042200 |
-2.35e-01 |
5.12e-01 |
6.91e-01 |
7.44e-01 |
6.95e-02 |
Deadenylation-dependent mRNA decay |
54 |
1.77e-02 |
3.99e-02 |
0.2580 |
0.140000 |
6.88e-02 |
-0.008040 |
-2.05e-01 |
7.64e-02 |
3.82e-01 |
9.19e-01 |
9.19e-03 |
Kinesins |
35 |
8.00e-02 |
1.33e-01 |
0.2570 |
0.124000 |
1.22e-01 |
0.046000 |
-1.84e-01 |
2.06e-01 |
2.13e-01 |
6.38e-01 |
5.96e-02 |
Interleukin-2 family signaling |
34 |
1.28e-01 |
1.96e-01 |
0.2570 |
0.133000 |
4.80e-02 |
-0.211000 |
-3.73e-02 |
1.79e-01 |
6.28e-01 |
3.33e-02 |
7.07e-01 |
p75NTR signals via NF-kB |
14 |
6.48e-01 |
6.98e-01 |
0.2560 |
-0.229000 |
-1.00e-01 |
0.005220 |
-5.29e-02 |
1.37e-01 |
5.17e-01 |
9.73e-01 |
7.32e-01 |
Processing of Capped Intron-Containing Pre-mRNA |
220 |
6.31e-13 |
8.80e-12 |
0.2550 |
0.105000 |
9.84e-02 |
0.145000 |
-1.53e-01 |
7.27e-03 |
1.22e-02 |
2.29e-04 |
1.00e-04 |
GAB1 signalosome |
14 |
6.45e-01 |
6.96e-01 |
0.2550 |
-0.208000 |
-1.15e-01 |
-0.057700 |
7.06e-02 |
1.78e-01 |
4.56e-01 |
7.08e-01 |
6.47e-01 |
RHO GTPases activate IQGAPs |
10 |
6.00e-01 |
6.56e-01 |
0.2540 |
0.222000 |
3.02e-02 |
0.105000 |
-5.84e-02 |
2.24e-01 |
8.69e-01 |
5.67e-01 |
7.49e-01 |
Chromatin modifying enzymes |
185 |
2.59e-07 |
1.38e-06 |
0.2530 |
-0.019500 |
-8.04e-02 |
-0.035000 |
-2.37e-01 |
6.48e-01 |
5.99e-02 |
4.13e-01 |
3.04e-08 |
Chromatin organization |
185 |
2.59e-07 |
1.38e-06 |
0.2530 |
-0.019500 |
-8.04e-02 |
-0.035000 |
-2.37e-01 |
6.48e-01 |
5.99e-02 |
4.13e-01 |
3.04e-08 |
HIV Life Cycle |
132 |
1.72e-08 |
1.16e-07 |
0.2530 |
0.009970 |
-7.34e-02 |
0.227000 |
-8.40e-02 |
8.44e-01 |
1.46e-01 |
7.02e-06 |
9.64e-02 |
The canonical retinoid cycle in rods (twilight vision) |
10 |
8.58e-01 |
8.84e-01 |
0.2530 |
-0.128000 |
-7.76e-02 |
-0.117000 |
-1.67e-01 |
4.84e-01 |
6.71e-01 |
5.21e-01 |
3.61e-01 |
Bile acid and bile salt metabolism |
25 |
1.95e-01 |
2.72e-01 |
0.2520 |
0.039900 |
-9.88e-02 |
0.091300 |
2.10e-01 |
7.30e-01 |
3.93e-01 |
4.30e-01 |
6.94e-02 |
TBC/RABGAPs |
40 |
6.23e-02 |
1.10e-01 |
0.2520 |
-0.065700 |
-1.61e-01 |
0.052100 |
-1.75e-01 |
4.73e-01 |
7.79e-02 |
5.69e-01 |
5.54e-02 |
Nuclear signaling by ERBB4 |
25 |
3.11e-01 |
3.92e-01 |
0.2520 |
-0.074800 |
-5.15e-02 |
0.059500 |
2.28e-01 |
5.17e-01 |
6.56e-01 |
6.07e-01 |
4.88e-02 |
CD28 dependent PI3K/Akt signaling |
21 |
4.17e-01 |
5.00e-01 |
0.2520 |
0.146000 |
4.21e-02 |
-0.068000 |
-1.89e-01 |
2.46e-01 |
7.38e-01 |
5.90e-01 |
1.34e-01 |
HIV Transcription Initiation |
45 |
7.24e-02 |
1.23e-01 |
0.2500 |
-0.028700 |
-9.83e-02 |
0.215000 |
7.37e-02 |
7.39e-01 |
2.54e-01 |
1.25e-02 |
3.93e-01 |
RNA Polymerase II HIV Promoter Escape |
45 |
7.24e-02 |
1.23e-01 |
0.2500 |
-0.028700 |
-9.83e-02 |
0.215000 |
7.37e-02 |
7.39e-01 |
2.54e-01 |
1.25e-02 |
3.93e-01 |
RNA Polymerase II Promoter Escape |
45 |
7.24e-02 |
1.23e-01 |
0.2500 |
-0.028700 |
-9.83e-02 |
0.215000 |
7.37e-02 |
7.39e-01 |
2.54e-01 |
1.25e-02 |
3.93e-01 |
RNA Polymerase II Transcription Initiation |
45 |
7.24e-02 |
1.23e-01 |
0.2500 |
-0.028700 |
-9.83e-02 |
0.215000 |
7.37e-02 |
7.39e-01 |
2.54e-01 |
1.25e-02 |
3.93e-01 |
RNA Polymerase II Transcription Initiation And Promoter Clearance |
45 |
7.24e-02 |
1.23e-01 |
0.2500 |
-0.028700 |
-9.83e-02 |
0.215000 |
7.37e-02 |
7.39e-01 |
2.54e-01 |
1.25e-02 |
3.93e-01 |
RNA Polymerase II Transcription Pre-Initiation And Promoter Opening |
45 |
7.24e-02 |
1.23e-01 |
0.2500 |
-0.028700 |
-9.83e-02 |
0.215000 |
7.37e-02 |
7.39e-01 |
2.54e-01 |
1.25e-02 |
3.93e-01 |
Complex I biogenesis |
54 |
9.32e-02 |
1.52e-01 |
0.2490 |
0.061600 |
1.65e-01 |
0.158000 |
7.80e-02 |
4.34e-01 |
3.64e-02 |
4.46e-02 |
3.22e-01 |
TNFR1-induced proapoptotic signaling |
13 |
3.79e-01 |
4.64e-01 |
0.2490 |
-0.043500 |
1.92e-01 |
-0.140000 |
-5.88e-02 |
7.86e-01 |
2.30e-01 |
3.82e-01 |
7.14e-01 |
Neuronal System |
230 |
5.65e-07 |
2.91e-06 |
0.2480 |
-0.102000 |
-1.19e-01 |
-0.188000 |
-3.87e-02 |
7.94e-03 |
1.88e-03 |
9.28e-07 |
3.14e-01 |
Neurexins and neuroligins |
35 |
1.22e-01 |
1.88e-01 |
0.2480 |
-0.137000 |
-8.34e-02 |
-0.187000 |
2.88e-02 |
1.60e-01 |
3.94e-01 |
5.57e-02 |
7.68e-01 |
Inositol phosphate metabolism |
40 |
3.33e-01 |
4.17e-01 |
0.2480 |
-0.174000 |
-1.51e-01 |
-0.084100 |
-3.88e-02 |
5.67e-02 |
9.97e-02 |
3.58e-01 |
6.71e-01 |
Formation of HIV elongation complex in the absence of HIV Tat |
40 |
2.20e-02 |
4.78e-02 |
0.2480 |
-0.077300 |
-4.22e-02 |
0.217000 |
-8.15e-02 |
3.98e-01 |
6.44e-01 |
1.76e-02 |
3.73e-01 |
Regulation of RUNX1 Expression and Activity |
17 |
5.86e-01 |
6.45e-01 |
0.2480 |
-0.061900 |
1.82e-02 |
-0.208000 |
-1.18e-01 |
6.59e-01 |
8.96e-01 |
1.37e-01 |
4.01e-01 |
Transmission across Chemical Synapses |
158 |
3.43e-04 |
1.24e-03 |
0.2480 |
-0.081500 |
-1.21e-01 |
-0.184000 |
-7.90e-02 |
7.80e-02 |
8.65e-03 |
6.96e-05 |
8.75e-02 |
mRNA Capping |
28 |
3.11e-01 |
3.92e-01 |
0.2470 |
-0.124000 |
-1.12e-01 |
0.179000 |
2.67e-02 |
2.55e-01 |
3.03e-01 |
1.00e-01 |
8.07e-01 |
MyD88 cascade initiated on plasma membrane |
77 |
3.36e-02 |
6.66e-02 |
0.2470 |
-0.096000 |
-2.03e-01 |
-0.057000 |
-8.34e-02 |
1.46e-01 |
2.05e-03 |
3.88e-01 |
2.07e-01 |
Toll Like Receptor 10 (TLR10) Cascade |
77 |
3.36e-02 |
6.66e-02 |
0.2470 |
-0.096000 |
-2.03e-01 |
-0.057000 |
-8.34e-02 |
1.46e-01 |
2.05e-03 |
3.88e-01 |
2.07e-01 |
Toll Like Receptor 5 (TLR5) Cascade |
77 |
3.36e-02 |
6.66e-02 |
0.2470 |
-0.096000 |
-2.03e-01 |
-0.057000 |
-8.34e-02 |
1.46e-01 |
2.05e-03 |
3.88e-01 |
2.07e-01 |
AKT phosphorylates targets in the cytosol |
14 |
5.56e-01 |
6.21e-01 |
0.2460 |
-0.031000 |
-1.64e-01 |
0.014400 |
-1.80e-01 |
8.41e-01 |
2.88e-01 |
9.26e-01 |
2.43e-01 |
Cell-cell junction organization |
26 |
2.76e-01 |
3.58e-01 |
0.2460 |
-0.060400 |
-1.28e-01 |
-0.201000 |
-1.91e-03 |
5.94e-01 |
2.60e-01 |
7.56e-02 |
9.87e-01 |
Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs) |
76 |
1.49e-03 |
4.84e-03 |
0.2460 |
-0.145000 |
-8.42e-02 |
-0.070800 |
1.65e-01 |
2.87e-02 |
2.05e-01 |
2.86e-01 |
1.31e-02 |
RNA Pol II CTD phosphorylation and interaction with CE |
26 |
3.75e-01 |
4.61e-01 |
0.2450 |
-0.098700 |
-6.21e-02 |
0.204000 |
7.20e-02 |
3.84e-01 |
5.84e-01 |
7.24e-02 |
5.25e-01 |
RNA Pol II CTD phosphorylation and interaction with CE during HIV infection |
26 |
3.75e-01 |
4.61e-01 |
0.2450 |
-0.098700 |
-6.21e-02 |
0.204000 |
7.20e-02 |
3.84e-01 |
5.84e-01 |
7.24e-02 |
5.25e-01 |
Sema4D induced cell migration and growth-cone collapse |
20 |
1.60e-01 |
2.33e-01 |
0.2450 |
-0.233000 |
2.66e-02 |
-0.056800 |
4.56e-02 |
7.15e-02 |
8.37e-01 |
6.60e-01 |
7.24e-01 |
Formation of RNA Pol II elongation complex |
53 |
8.49e-03 |
2.19e-02 |
0.2450 |
-0.081500 |
-1.09e-01 |
0.172000 |
-1.08e-01 |
3.05e-01 |
1.68e-01 |
3.02e-02 |
1.72e-01 |
RNA Polymerase II Transcription Elongation |
53 |
8.49e-03 |
2.19e-02 |
0.2450 |
-0.081500 |
-1.09e-01 |
0.172000 |
-1.08e-01 |
3.05e-01 |
1.68e-01 |
3.02e-02 |
1.72e-01 |
Macroautophagy |
102 |
1.61e-03 |
5.18e-03 |
0.2440 |
-0.109000 |
-1.88e-01 |
0.094100 |
-5.74e-02 |
5.66e-02 |
1.02e-03 |
1.01e-01 |
3.18e-01 |
Interleukin-6 signaling |
10 |
4.56e-01 |
5.31e-01 |
0.2430 |
0.158000 |
-4.60e-02 |
-0.132000 |
1.22e-01 |
3.88e-01 |
8.01e-01 |
4.70e-01 |
5.05e-01 |
mRNA decay by 5' to 3' exoribonuclease |
15 |
5.46e-01 |
6.13e-01 |
0.2430 |
0.078100 |
-4.47e-02 |
-0.047800 |
-2.21e-01 |
6.00e-01 |
7.64e-01 |
7.49e-01 |
1.39e-01 |
Autophagy |
114 |
3.88e-04 |
1.39e-03 |
0.2430 |
-0.096400 |
-1.87e-01 |
0.117000 |
-3.35e-02 |
7.58e-02 |
5.80e-04 |
3.10e-02 |
5.38e-01 |
MET activates RAS signaling |
10 |
8.06e-01 |
8.39e-01 |
0.2430 |
-0.010600 |
4.38e-03 |
-0.087100 |
-2.27e-01 |
9.54e-01 |
9.81e-01 |
6.33e-01 |
2.15e-01 |
RIP-mediated NFkB activation via ZBP1 |
17 |
5.68e-01 |
6.30e-01 |
0.2430 |
-0.228000 |
-8.28e-02 |
0.011900 |
-1.19e-02 |
1.04e-01 |
5.55e-01 |
9.32e-01 |
9.32e-01 |
Interleukin-1 signaling |
89 |
8.35e-03 |
2.17e-02 |
0.2420 |
0.029000 |
4.41e-02 |
0.224000 |
7.48e-02 |
6.37e-01 |
4.73e-01 |
2.69e-04 |
2.23e-01 |
Signaling by Hedgehog |
119 |
1.72e-03 |
5.50e-03 |
0.2420 |
-0.006930 |
-4.19e-02 |
0.206000 |
1.20e-01 |
8.96e-01 |
4.30e-01 |
1.09e-04 |
2.46e-02 |
Acyl chain remodelling of PC |
18 |
6.66e-01 |
7.13e-01 |
0.2420 |
0.106000 |
1.08e-01 |
0.180000 |
5.73e-02 |
4.38e-01 |
4.28e-01 |
1.87e-01 |
6.74e-01 |
Endogenous sterols |
17 |
2.69e-01 |
3.51e-01 |
0.2410 |
-0.065300 |
-3.93e-02 |
-0.143000 |
1.79e-01 |
6.41e-01 |
7.79e-01 |
3.06e-01 |
2.02e-01 |
mRNA Splicing - Minor Pathway |
48 |
2.61e-02 |
5.49e-02 |
0.2410 |
-0.021100 |
-1.82e-02 |
0.239000 |
-1.02e-02 |
8.01e-01 |
8.27e-01 |
4.12e-03 |
9.03e-01 |
Oncogenic MAPK signaling |
71 |
7.54e-02 |
1.27e-01 |
0.2410 |
-0.095800 |
-1.31e-01 |
-0.163000 |
-7.30e-02 |
1.63e-01 |
5.72e-02 |
1.76e-02 |
2.88e-01 |
Anti-inflammatory response favouring Leishmania parasite infection |
88 |
3.87e-03 |
1.12e-02 |
0.2410 |
-0.001120 |
9.65e-02 |
0.047700 |
2.15e-01 |
9.86e-01 |
1.18e-01 |
4.40e-01 |
4.89e-04 |
Leishmania parasite growth and survival |
88 |
3.87e-03 |
1.12e-02 |
0.2410 |
-0.001120 |
9.65e-02 |
0.047700 |
2.15e-01 |
9.86e-01 |
1.18e-01 |
4.40e-01 |
4.89e-04 |
Signaling by Retinoic Acid |
32 |
3.10e-01 |
3.92e-01 |
0.2410 |
0.090600 |
-2.09e-02 |
-0.139000 |
-1.73e-01 |
3.76e-01 |
8.38e-01 |
1.74e-01 |
9.02e-02 |
Repression of WNT target genes |
11 |
5.83e-01 |
6.43e-01 |
0.2400 |
-0.120000 |
2.57e-02 |
-0.014300 |
-2.06e-01 |
4.92e-01 |
8.83e-01 |
9.35e-01 |
2.37e-01 |
Synthesis of PIPs at the late endosome membrane |
11 |
7.82e-01 |
8.21e-01 |
0.2390 |
0.088200 |
5.91e-02 |
-0.204000 |
-6.60e-02 |
6.13e-01 |
7.34e-01 |
2.41e-01 |
7.05e-01 |
Class I peroxisomal membrane protein import |
19 |
5.26e-01 |
5.95e-01 |
0.2390 |
0.047500 |
6.80e-03 |
0.071100 |
2.23e-01 |
7.20e-01 |
9.59e-01 |
5.92e-01 |
9.19e-02 |
BBSome-mediated cargo-targeting to cilium |
20 |
9.15e-02 |
1.50e-01 |
0.2390 |
0.218000 |
-8.93e-02 |
-0.000621 |
4.03e-02 |
9.15e-02 |
4.89e-01 |
9.96e-01 |
7.55e-01 |
G alpha (12/13) signalling events |
70 |
1.06e-02 |
2.62e-02 |
0.2390 |
-0.181000 |
-9.24e-02 |
-0.088900 |
8.90e-02 |
8.95e-03 |
1.82e-01 |
1.99e-01 |
1.99e-01 |
Innate Immune System |
746 |
2.00e-17 |
4.31e-16 |
0.2380 |
0.065100 |
1.34e-01 |
0.081900 |
1.66e-01 |
2.81e-03 |
6.57e-10 |
1.70e-04 |
2.26e-14 |
Diseases of metabolism |
174 |
5.57e-05 |
2.25e-04 |
0.2380 |
-0.167000 |
-1.03e-01 |
0.038300 |
1.29e-01 |
1.51e-04 |
1.98e-02 |
3.84e-01 |
3.48e-03 |
Integrin signaling |
24 |
2.85e-01 |
3.67e-01 |
0.2380 |
0.002660 |
1.42e-02 |
-0.237000 |
-8.95e-03 |
9.82e-01 |
9.04e-01 |
4.45e-02 |
9.40e-01 |
Constitutive Signaling by NOTCH1 HD+PEST Domain Mutants |
52 |
2.00e-01 |
2.76e-01 |
0.2370 |
-0.090300 |
-5.89e-02 |
-0.172000 |
-1.24e-01 |
2.60e-01 |
4.63e-01 |
3.24e-02 |
1.23e-01 |
Constitutive Signaling by NOTCH1 PEST Domain Mutants |
52 |
2.00e-01 |
2.76e-01 |
0.2370 |
-0.090300 |
-5.89e-02 |
-0.172000 |
-1.24e-01 |
2.60e-01 |
4.63e-01 |
3.24e-02 |
1.23e-01 |
Signaling by NOTCH1 HD+PEST Domain Mutants in Cancer |
52 |
2.00e-01 |
2.76e-01 |
0.2370 |
-0.090300 |
-5.89e-02 |
-0.172000 |
-1.24e-01 |
2.60e-01 |
4.63e-01 |
3.24e-02 |
1.23e-01 |
Signaling by NOTCH1 PEST Domain Mutants in Cancer |
52 |
2.00e-01 |
2.76e-01 |
0.2370 |
-0.090300 |
-5.89e-02 |
-0.172000 |
-1.24e-01 |
2.60e-01 |
4.63e-01 |
3.24e-02 |
1.23e-01 |
Signaling by NOTCH1 in Cancer |
52 |
2.00e-01 |
2.76e-01 |
0.2370 |
-0.090300 |
-5.89e-02 |
-0.172000 |
-1.24e-01 |
2.60e-01 |
4.63e-01 |
3.24e-02 |
1.23e-01 |
Class A/1 (Rhodopsin-like receptors) |
112 |
1.51e-05 |
6.65e-05 |
0.2370 |
0.065900 |
1.05e-01 |
-0.116000 |
1.66e-01 |
2.29e-01 |
5.60e-02 |
3.41e-02 |
2.49e-03 |
A tetrasaccharide linker sequence is required for GAG synthesis |
20 |
1.68e-01 |
2.42e-01 |
0.2370 |
-0.207000 |
4.99e-02 |
-0.104000 |
-1.20e-02 |
1.09e-01 |
6.99e-01 |
4.23e-01 |
9.26e-01 |
Signalling to ERKs |
30 |
1.60e-01 |
2.33e-01 |
0.2370 |
0.080500 |
-1.29e-01 |
-0.119000 |
-1.37e-01 |
4.46e-01 |
2.23e-01 |
2.59e-01 |
1.94e-01 |
MET promotes cell motility |
28 |
1.63e-01 |
2.36e-01 |
0.2370 |
-0.006180 |
-4.38e-02 |
-0.231000 |
2.67e-02 |
9.55e-01 |
6.88e-01 |
3.45e-02 |
8.07e-01 |
Activation of GABAB receptors |
30 |
1.02e-01 |
1.62e-01 |
0.2370 |
0.041400 |
2.21e-02 |
-0.060000 |
2.24e-01 |
6.95e-01 |
8.34e-01 |
5.70e-01 |
3.38e-02 |
GABA B receptor activation |
30 |
1.02e-01 |
1.62e-01 |
0.2370 |
0.041400 |
2.21e-02 |
-0.060000 |
2.24e-01 |
6.95e-01 |
8.34e-01 |
5.70e-01 |
3.38e-02 |
NOTCH3 Activation and Transmission of Signal to the Nucleus |
22 |
7.13e-02 |
1.22e-01 |
0.2360 |
-0.173000 |
1.34e-01 |
0.087800 |
1.65e-02 |
1.60e-01 |
2.77e-01 |
4.76e-01 |
8.94e-01 |
Glycosaminoglycan metabolism |
93 |
5.98e-03 |
1.63e-02 |
0.2360 |
-0.107000 |
3.18e-03 |
0.102000 |
1.84e-01 |
7.38e-02 |
9.58e-01 |
8.93e-02 |
2.19e-03 |
mRNA Splicing |
175 |
1.98e-07 |
1.07e-06 |
0.2360 |
0.116000 |
1.19e-01 |
0.128000 |
-1.09e-01 |
8.56e-03 |
6.62e-03 |
3.52e-03 |
1.35e-02 |
Response to elevated platelet cytosolic Ca2+ |
105 |
6.38e-05 |
2.55e-04 |
0.2350 |
-0.008600 |
9.23e-02 |
-0.035000 |
2.14e-01 |
8.79e-01 |
1.03e-01 |
5.37e-01 |
1.59e-04 |
Signaling by FGFR1 |
36 |
1.03e-01 |
1.63e-01 |
0.2350 |
0.021200 |
-1.71e-01 |
-0.042900 |
-1.54e-01 |
8.26e-01 |
7.63e-02 |
6.56e-01 |
1.10e-01 |
Metabolism of RNA |
598 |
5.00e-19 |
1.26e-17 |
0.2350 |
0.135000 |
1.32e-01 |
0.132000 |
-4.54e-02 |
2.24e-08 |
5.27e-08 |
4.69e-08 |
6.03e-02 |
Retrograde transport at the Trans-Golgi-Network |
44 |
2.92e-01 |
3.75e-01 |
0.2350 |
-0.080400 |
-6.85e-02 |
-0.178000 |
-1.10e-01 |
3.57e-01 |
4.32e-01 |
4.06e-02 |
2.08e-01 |
eNOS activation |
11 |
6.05e-01 |
6.61e-01 |
0.2340 |
0.114000 |
5.42e-02 |
-0.101000 |
1.69e-01 |
5.14e-01 |
7.56e-01 |
5.62e-01 |
3.31e-01 |
Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks |
37 |
2.40e-02 |
5.13e-02 |
0.2340 |
0.082800 |
-3.11e-02 |
0.174000 |
-1.28e-01 |
3.84e-01 |
7.44e-01 |
6.73e-02 |
1.77e-01 |
Infection with Mycobacterium tuberculosis |
23 |
3.30e-01 |
4.14e-01 |
0.2340 |
0.130000 |
1.05e-01 |
0.133000 |
-9.32e-02 |
2.79e-01 |
3.83e-01 |
2.69e-01 |
4.39e-01 |
Suppression of phagosomal maturation |
11 |
8.16e-01 |
8.47e-01 |
0.2330 |
-0.077100 |
-9.46e-02 |
-0.035700 |
-1.95e-01 |
6.58e-01 |
5.87e-01 |
8.38e-01 |
2.63e-01 |
Signaling by TGF-beta Receptor Complex |
67 |
2.14e-03 |
6.67e-03 |
0.2330 |
0.088800 |
-1.20e-01 |
-0.028800 |
-1.76e-01 |
2.09e-01 |
9.04e-02 |
6.84e-01 |
1.28e-02 |
Synthesis of bile acids and bile salts |
22 |
1.74e-01 |
2.48e-01 |
0.2320 |
0.040600 |
-1.73e-01 |
0.052900 |
1.40e-01 |
7.42e-01 |
1.60e-01 |
6.68e-01 |
2.56e-01 |
Keratan sulfate/keratin metabolism |
25 |
5.26e-01 |
5.95e-01 |
0.2320 |
-0.162000 |
-1.37e-01 |
0.001880 |
9.38e-02 |
1.62e-01 |
2.34e-01 |
9.87e-01 |
4.17e-01 |
Protein ubiquitination |
56 |
1.77e-03 |
5.65e-03 |
0.2320 |
0.081900 |
-1.01e-01 |
0.086900 |
-1.71e-01 |
2.90e-01 |
1.90e-01 |
2.61e-01 |
2.67e-02 |
Mitochondrial Fatty Acid Beta-Oxidation |
31 |
3.05e-01 |
3.87e-01 |
0.2320 |
0.093200 |
2.07e-01 |
0.021600 |
-4.23e-02 |
3.70e-01 |
4.61e-02 |
8.35e-01 |
6.84e-01 |
Apoptotic cleavage of cellular proteins |
32 |
4.83e-01 |
5.56e-01 |
0.2310 |
-0.057200 |
-8.48e-02 |
-0.104000 |
-1.80e-01 |
5.75e-01 |
4.07e-01 |
3.11e-01 |
7.85e-02 |
HS-GAG biosynthesis |
22 |
6.17e-01 |
6.72e-01 |
0.2310 |
-0.150000 |
-1.02e-01 |
0.091700 |
1.09e-01 |
2.24e-01 |
4.06e-01 |
4.57e-01 |
3.76e-01 |
Transport of vitamins, nucleosides, and related molecules |
29 |
9.80e-02 |
1.57e-01 |
0.2300 |
-0.032000 |
1.94e-01 |
-0.021900 |
1.19e-01 |
7.66e-01 |
7.13e-02 |
8.38e-01 |
2.68e-01 |
Degradation of the extracellular matrix |
70 |
4.26e-03 |
1.23e-02 |
0.2300 |
-0.174000 |
-4.83e-02 |
-0.107000 |
9.43e-02 |
1.20e-02 |
4.86e-01 |
1.21e-01 |
1.73e-01 |
SLC transporter disorders |
64 |
4.92e-03 |
1.38e-02 |
0.2300 |
-0.018500 |
-1.03e-01 |
0.068500 |
-1.93e-01 |
7.98e-01 |
1.56e-01 |
3.44e-01 |
7.62e-03 |
Paradoxical activation of RAF signaling by kinase inactive BRAF |
38 |
1.38e-01 |
2.08e-01 |
0.2300 |
-0.050400 |
1.05e-02 |
-0.221000 |
-3.30e-02 |
5.91e-01 |
9.11e-01 |
1.82e-02 |
7.25e-01 |
Signaling by RAS mutants |
38 |
1.38e-01 |
2.08e-01 |
0.2300 |
-0.050400 |
1.05e-02 |
-0.221000 |
-3.30e-02 |
5.91e-01 |
9.11e-01 |
1.82e-02 |
7.25e-01 |
Signaling by moderate kinase activity BRAF mutants |
38 |
1.38e-01 |
2.08e-01 |
0.2300 |
-0.050400 |
1.05e-02 |
-0.221000 |
-3.30e-02 |
5.91e-01 |
9.11e-01 |
1.82e-02 |
7.25e-01 |
Signaling downstream of RAS mutants |
38 |
1.38e-01 |
2.08e-01 |
0.2300 |
-0.050400 |
1.05e-02 |
-0.221000 |
-3.30e-02 |
5.91e-01 |
9.11e-01 |
1.82e-02 |
7.25e-01 |
Synthesis of glycosylphosphatidylinositol (GPI) |
18 |
5.88e-01 |
6.46e-01 |
0.2280 |
0.009320 |
-3.41e-02 |
0.076000 |
2.12e-01 |
9.45e-01 |
8.02e-01 |
5.77e-01 |
1.19e-01 |
Acyl chain remodelling of PE |
16 |
7.41e-01 |
7.82e-01 |
0.2270 |
0.157000 |
6.89e-02 |
0.084400 |
1.22e-01 |
2.76e-01 |
6.33e-01 |
5.59e-01 |
3.97e-01 |
Infectious disease |
563 |
2.76e-12 |
3.48e-11 |
0.2270 |
0.105000 |
8.87e-02 |
0.166000 |
7.09e-02 |
2.49e-05 |
3.63e-04 |
2.35e-11 |
4.42e-03 |
Glycerophospholipid biosynthesis |
95 |
3.10e-02 |
6.28e-02 |
0.2260 |
-0.157000 |
-8.68e-02 |
-0.067400 |
-1.20e-01 |
8.48e-03 |
1.44e-01 |
2.57e-01 |
4.38e-02 |
NRIF signals cell death from the nucleus |
14 |
7.77e-01 |
8.16e-01 |
0.2260 |
0.045700 |
-1.55e-02 |
0.135000 |
1.74e-01 |
7.67e-01 |
9.20e-01 |
3.82e-01 |
2.59e-01 |
Platelet Aggregation (Plug Formation) |
25 |
2.95e-01 |
3.77e-01 |
0.2260 |
0.035000 |
5.10e-02 |
-0.217000 |
8.33e-03 |
7.62e-01 |
6.59e-01 |
6.06e-02 |
9.43e-01 |
Interleukin-3, Interleukin-5 and GM-CSF signaling |
38 |
2.85e-01 |
3.67e-01 |
0.2250 |
-0.023800 |
-9.38e-03 |
-0.208000 |
-8.34e-02 |
8.00e-01 |
9.20e-01 |
2.68e-02 |
3.74e-01 |
Diseases associated with the TLR signaling cascade |
22 |
5.11e-01 |
5.82e-01 |
0.2250 |
-0.178000 |
-8.68e-02 |
-0.015500 |
1.05e-01 |
1.49e-01 |
4.81e-01 |
9.00e-01 |
3.92e-01 |
Diseases of Immune System |
22 |
5.11e-01 |
5.82e-01 |
0.2250 |
-0.178000 |
-8.68e-02 |
-0.015500 |
1.05e-01 |
1.49e-01 |
4.81e-01 |
9.00e-01 |
3.92e-01 |
Platelet sensitization by LDL |
15 |
5.18e-01 |
5.88e-01 |
0.2240 |
-0.031900 |
-1.26e-01 |
0.178000 |
-4.35e-02 |
8.31e-01 |
3.99e-01 |
2.33e-01 |
7.71e-01 |
RHO GTPases activate CIT |
19 |
4.55e-01 |
5.31e-01 |
0.2240 |
0.035400 |
1.79e-01 |
-0.057600 |
-1.17e-01 |
7.89e-01 |
1.77e-01 |
6.64e-01 |
3.76e-01 |
Prefoldin mediated transfer of substrate to CCT/TriC |
24 |
1.82e-01 |
2.57e-01 |
0.2230 |
0.108000 |
2.35e-03 |
0.160000 |
-1.12e-01 |
3.59e-01 |
9.84e-01 |
1.75e-01 |
3.42e-01 |
RAB geranylgeranylation |
46 |
4.73e-02 |
8.81e-02 |
0.2230 |
0.151000 |
2.65e-02 |
-0.025200 |
1.61e-01 |
7.69e-02 |
7.56e-01 |
7.68e-01 |
5.97e-02 |
RUNX2 regulates osteoblast differentiation |
22 |
3.98e-01 |
4.82e-01 |
0.2230 |
-0.054400 |
-2.51e-02 |
0.005680 |
2.15e-01 |
6.59e-01 |
8.39e-01 |
9.63e-01 |
8.16e-02 |
Nucleotide-binding domain, leucine rich repeat containing receptor (NLR) signaling pathways |
47 |
3.29e-02 |
6.59e-02 |
0.2230 |
-0.103000 |
7.67e-02 |
-0.165000 |
-7.65e-02 |
2.20e-01 |
3.63e-01 |
5.11e-02 |
3.64e-01 |
Apoptotic execution phase |
40 |
3.49e-01 |
4.35e-01 |
0.2220 |
-0.010800 |
-5.88e-02 |
-0.102000 |
-1.88e-01 |
9.06e-01 |
5.20e-01 |
2.67e-01 |
3.96e-02 |
RNA Polymerase II Pre-transcription Events |
75 |
2.37e-03 |
7.33e-03 |
0.2220 |
-0.041500 |
-1.18e-01 |
0.163000 |
-8.45e-02 |
5.35e-01 |
7.78e-02 |
1.49e-02 |
2.06e-01 |
RHO GTPase Effectors |
219 |
1.39e-07 |
7.70e-07 |
0.2220 |
0.125000 |
1.09e-01 |
0.070000 |
-1.30e-01 |
1.55e-03 |
5.48e-03 |
7.53e-02 |
9.75e-04 |
Platelet homeostasis |
69 |
2.60e-03 |
7.96e-03 |
0.2220 |
-0.140000 |
-2.05e-02 |
-0.113000 |
1.28e-01 |
4.43e-02 |
7.69e-01 |
1.05e-01 |
6.68e-02 |
Intraflagellar transport |
36 |
2.68e-01 |
3.50e-01 |
0.2220 |
0.064700 |
-3.40e-02 |
0.129000 |
1.65e-01 |
5.02e-01 |
7.24e-01 |
1.82e-01 |
8.70e-02 |
Glucagon-like Peptide-1 (GLP1) regulates insulin secretion |
31 |
4.17e-01 |
5.00e-01 |
0.2210 |
-0.169000 |
-1.17e-01 |
-0.050000 |
6.58e-02 |
1.04e-01 |
2.61e-01 |
6.30e-01 |
5.26e-01 |
Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding |
26 |
1.36e-01 |
2.06e-01 |
0.2210 |
0.098200 |
-1.94e-02 |
0.144000 |
-1.34e-01 |
3.86e-01 |
8.64e-01 |
2.03e-01 |
2.38e-01 |
RMTs methylate histone arginines |
29 |
1.71e-01 |
2.45e-01 |
0.2210 |
-0.058800 |
-9.22e-02 |
0.164000 |
-1.00e-01 |
5.84e-01 |
3.90e-01 |
1.28e-01 |
3.51e-01 |
SHC1 events in ERBB4 signaling |
11 |
8.51e-01 |
8.78e-01 |
0.2200 |
-0.039900 |
-1.15e-01 |
-0.172000 |
-6.22e-02 |
8.19e-01 |
5.09e-01 |
3.23e-01 |
7.21e-01 |
Interleukin-15 signaling |
14 |
4.01e-01 |
4.85e-01 |
0.2200 |
0.103000 |
-1.61e-01 |
-0.091500 |
-6.06e-02 |
5.06e-01 |
2.98e-01 |
5.54e-01 |
6.95e-01 |
Cell surface interactions at the vascular wall |
95 |
1.16e-03 |
3.84e-03 |
0.2190 |
0.051200 |
1.59e-01 |
-0.099300 |
1.02e-01 |
3.90e-01 |
7.44e-03 |
9.49e-02 |
8.74e-02 |
Transcriptional Regulation by TP53 |
332 |
1.12e-16 |
2.23e-15 |
0.2190 |
0.046500 |
3.09e-02 |
0.108000 |
-1.82e-01 |
1.47e-01 |
3.35e-01 |
8.12e-04 |
1.30e-08 |
Toll Like Receptor 3 (TLR3) Cascade |
86 |
5.60e-02 |
1.01e-01 |
0.2190 |
-0.039300 |
-1.40e-01 |
-0.111000 |
-1.20e-01 |
5.30e-01 |
2.46e-02 |
7.48e-02 |
5.54e-02 |
Leishmania infection |
162 |
4.73e-05 |
1.95e-04 |
0.2190 |
0.024100 |
1.17e-01 |
0.009910 |
1.84e-01 |
5.97e-01 |
1.07e-02 |
8.28e-01 |
5.76e-05 |
Peroxisomal lipid metabolism |
25 |
6.49e-01 |
6.99e-01 |
0.2190 |
0.169000 |
1.25e-01 |
-0.002610 |
6.01e-02 |
1.43e-01 |
2.80e-01 |
9.82e-01 |
6.03e-01 |
RNA Polymerase I Promoter Escape |
30 |
4.95e-01 |
5.68e-01 |
0.2190 |
-0.044100 |
-7.12e-02 |
0.151000 |
1.34e-01 |
6.76e-01 |
5.00e-01 |
1.52e-01 |
2.05e-01 |
Signaling by NTRKs |
121 |
9.31e-03 |
2.36e-02 |
0.2180 |
-0.106000 |
-1.90e-01 |
-0.015900 |
2.95e-04 |
4.37e-02 |
3.11e-04 |
7.63e-01 |
9.96e-01 |
VxPx cargo-targeting to cilium |
18 |
4.55e-01 |
5.31e-01 |
0.2180 |
-0.018500 |
-1.69e-01 |
0.137000 |
1.10e-03 |
8.92e-01 |
2.16e-01 |
3.13e-01 |
9.94e-01 |
Diseases associated with O-glycosylation of proteins |
41 |
2.82e-02 |
5.81e-02 |
0.2180 |
-0.109000 |
5.43e-02 |
-0.171000 |
5.78e-02 |
2.26e-01 |
5.48e-01 |
5.78e-02 |
5.22e-01 |
Diseases of glycosylation |
107 |
1.33e-03 |
4.37e-03 |
0.2170 |
-0.150000 |
-4.02e-02 |
0.002160 |
1.52e-01 |
7.43e-03 |
4.73e-01 |
9.69e-01 |
6.62e-03 |
MyD88-independent TLR4 cascade |
90 |
7.29e-02 |
1.23e-01 |
0.2160 |
-0.063800 |
-1.45e-01 |
-0.106000 |
-1.01e-01 |
2.96e-01 |
1.74e-02 |
8.17e-02 |
9.88e-02 |
TRIF(TICAM1)-mediated TLR4 signaling |
90 |
7.29e-02 |
1.23e-01 |
0.2160 |
-0.063800 |
-1.45e-01 |
-0.106000 |
-1.01e-01 |
2.96e-01 |
1.74e-02 |
8.17e-02 |
9.88e-02 |
rRNA modification in the nucleus and cytosol |
53 |
1.72e-01 |
2.46e-01 |
0.2160 |
0.088900 |
1.24e-01 |
-0.069600 |
-1.36e-01 |
2.63e-01 |
1.19e-01 |
3.81e-01 |
8.72e-02 |
Pre-NOTCH Expression and Processing |
47 |
2.43e-01 |
3.22e-01 |
0.2160 |
-0.167000 |
-9.49e-02 |
-0.002380 |
-9.87e-02 |
4.83e-02 |
2.60e-01 |
9.77e-01 |
2.42e-01 |
RAF-independent MAPK1/3 activation |
21 |
4.18e-01 |
5.00e-01 |
0.2150 |
0.016300 |
-1.79e-01 |
-0.084600 |
-8.31e-02 |
8.97e-01 |
1.56e-01 |
5.02e-01 |
5.10e-01 |
Neurotransmitter receptors and postsynaptic signal transmission |
118 |
7.27e-03 |
1.94e-02 |
0.2150 |
-0.064300 |
-1.14e-01 |
-0.166000 |
-3.75e-02 |
2.29e-01 |
3.23e-02 |
1.87e-03 |
4.82e-01 |
Myogenesis |
23 |
4.33e-01 |
5.13e-01 |
0.2150 |
-0.011200 |
-1.78e-01 |
-0.109000 |
-5.07e-02 |
9.26e-01 |
1.41e-01 |
3.65e-01 |
6.74e-01 |
Keratan sulfate biosynthesis |
20 |
8.01e-01 |
8.35e-01 |
0.2150 |
-0.133000 |
-1.46e-01 |
-0.071000 |
-4.39e-02 |
3.02e-01 |
2.59e-01 |
5.83e-01 |
7.34e-01 |
Regulation of signaling by CBL |
18 |
7.44e-01 |
7.84e-01 |
0.2150 |
0.113000 |
5.05e-02 |
-0.119000 |
-1.29e-01 |
4.08e-01 |
7.11e-01 |
3.81e-01 |
3.45e-01 |
Caspase activation via extrinsic apoptotic signalling pathway |
24 |
1.32e-01 |
2.02e-01 |
0.2140 |
-0.170000 |
7.07e-02 |
-0.070500 |
8.33e-02 |
1.49e-01 |
5.49e-01 |
5.50e-01 |
4.80e-01 |
Signaling by FGFR2 |
55 |
9.36e-02 |
1.52e-01 |
0.2140 |
-0.052700 |
-1.76e-01 |
0.011100 |
-1.09e-01 |
5.00e-01 |
2.39e-02 |
8.87e-01 |
1.63e-01 |
Signaling by NTRK2 (TRKB) |
22 |
5.67e-01 |
6.29e-01 |
0.2130 |
-0.022800 |
-1.29e-01 |
-0.160000 |
-5.08e-02 |
8.54e-01 |
2.94e-01 |
1.94e-01 |
6.80e-01 |
Intra-Golgi traffic |
40 |
3.63e-01 |
4.49e-01 |
0.2130 |
-0.145000 |
-1.24e-01 |
0.009340 |
9.32e-02 |
1.13e-01 |
1.74e-01 |
9.19e-01 |
3.08e-01 |
Senescence-Associated Secretory Phenotype (SASP) |
44 |
4.17e-02 |
7.96e-02 |
0.2130 |
-0.008640 |
-4.62e-03 |
0.198000 |
-7.74e-02 |
9.21e-01 |
9.58e-01 |
2.33e-02 |
3.75e-01 |
Nuclear Receptor transcription pathway |
41 |
3.87e-01 |
4.73e-01 |
0.2120 |
-0.007720 |
-8.07e-02 |
-0.162000 |
-1.11e-01 |
9.32e-01 |
3.71e-01 |
7.24e-02 |
2.21e-01 |
Interleukin-20 family signaling |
15 |
5.86e-01 |
6.45e-01 |
0.2120 |
-0.049500 |
-6.98e-03 |
-0.023100 |
2.05e-01 |
7.40e-01 |
9.63e-01 |
8.77e-01 |
1.69e-01 |
Sphingolipid metabolism |
65 |
4.92e-02 |
9.09e-02 |
0.2120 |
-0.099500 |
-2.07e-02 |
0.035800 |
1.83e-01 |
1.66e-01 |
7.73e-01 |
6.18e-01 |
1.09e-02 |
Unfolded Protein Response (UPR) |
84 |
6.65e-03 |
1.80e-02 |
0.2120 |
0.013500 |
-8.21e-02 |
0.192000 |
3.73e-02 |
8.31e-01 |
1.94e-01 |
2.43e-03 |
5.55e-01 |
Protein localization |
144 |
2.29e-03 |
7.10e-03 |
0.2110 |
0.073600 |
7.63e-02 |
0.178000 |
4.16e-02 |
1.28e-01 |
1.15e-01 |
2.31e-04 |
3.89e-01 |
Nicotinate metabolism |
24 |
3.76e-01 |
4.61e-01 |
0.2110 |
0.051400 |
1.49e-01 |
-0.127000 |
6.05e-02 |
6.63e-01 |
2.08e-01 |
2.82e-01 |
6.08e-01 |
GPCR ligand binding |
157 |
1.05e-06 |
5.24e-06 |
0.2110 |
-0.012500 |
5.31e-02 |
-0.067900 |
1.92e-01 |
7.87e-01 |
2.52e-01 |
1.43e-01 |
3.43e-05 |
TRAF6 mediated NF-kB activation |
21 |
4.04e-01 |
4.87e-01 |
0.2110 |
-0.166000 |
1.11e-02 |
-0.068200 |
-1.10e-01 |
1.88e-01 |
9.30e-01 |
5.89e-01 |
3.84e-01 |
Potassium Channels |
49 |
2.50e-02 |
5.31e-02 |
0.2110 |
-0.083300 |
-1.02e-02 |
-0.164000 |
1.02e-01 |
3.14e-01 |
9.02e-01 |
4.72e-02 |
2.16e-01 |
MAP2K and MAPK activation |
33 |
1.40e-01 |
2.10e-01 |
0.2110 |
-0.003330 |
1.38e-01 |
-0.157000 |
2.30e-02 |
9.74e-01 |
1.70e-01 |
1.18e-01 |
8.20e-01 |
Defective B3GAT3 causes JDSSDHD |
16 |
3.99e-01 |
4.83e-01 |
0.2110 |
-0.191000 |
3.86e-02 |
-0.080400 |
-2.92e-03 |
1.87e-01 |
7.89e-01 |
5.78e-01 |
9.84e-01 |
N-glycan antennae elongation in the medial/trans-Golgi |
20 |
4.35e-01 |
5.14e-01 |
0.2100 |
0.035900 |
-8.03e-02 |
0.039500 |
1.87e-01 |
7.81e-01 |
5.34e-01 |
7.60e-01 |
1.48e-01 |
Cellular Senescence |
118 |
2.45e-04 |
9.08e-04 |
0.2100 |
-0.043100 |
-7.11e-02 |
0.053400 |
-1.85e-01 |
4.20e-01 |
1.83e-01 |
3.17e-01 |
5.16e-04 |
ZBP1(DAI) mediated induction of type I IFNs |
20 |
5.64e-01 |
6.27e-01 |
0.2100 |
-0.200000 |
-5.05e-02 |
-0.034900 |
-2.17e-02 |
1.23e-01 |
6.96e-01 |
7.87e-01 |
8.67e-01 |
Signaling by BRAF and RAF fusions |
55 |
1.09e-01 |
1.71e-01 |
0.2090 |
-0.094600 |
-8.97e-02 |
-0.163000 |
1.28e-02 |
2.25e-01 |
2.50e-01 |
3.62e-02 |
8.70e-01 |
G alpha (q) signalling events |
120 |
6.88e-05 |
2.74e-04 |
0.2090 |
-0.057400 |
3.33e-02 |
-0.196000 |
2.99e-02 |
2.79e-01 |
5.30e-01 |
2.10e-04 |
5.72e-01 |
Peptide hormone metabolism |
48 |
1.09e-01 |
1.71e-01 |
0.2090 |
-0.113000 |
-9.23e-02 |
-0.134000 |
6.75e-02 |
1.74e-01 |
2.69e-01 |
1.10e-01 |
4.19e-01 |
Nuclear Events (kinase and transcription factor activation) |
56 |
1.90e-01 |
2.66e-01 |
0.2090 |
-0.090300 |
-1.87e-01 |
-0.024800 |
-8.09e-03 |
2.43e-01 |
1.57e-02 |
7.49e-01 |
9.17e-01 |
GABA receptor activation |
35 |
8.04e-02 |
1.34e-01 |
0.2090 |
0.044700 |
-3.88e-02 |
-0.072400 |
1.87e-01 |
6.48e-01 |
6.92e-01 |
4.59e-01 |
5.62e-02 |
EPH-Ephrin signaling |
81 |
1.25e-02 |
3.01e-02 |
0.2080 |
-0.011500 |
1.23e-01 |
0.020500 |
1.66e-01 |
8.59e-01 |
5.59e-02 |
7.50e-01 |
9.84e-03 |
FGFR2 alternative splicing |
23 |
4.34e-01 |
5.14e-01 |
0.2080 |
-0.086100 |
-9.16e-02 |
0.157000 |
-5.34e-02 |
4.75e-01 |
4.47e-01 |
1.93e-01 |
6.58e-01 |
RHO GTPases activate PKNs |
32 |
3.14e-01 |
3.95e-01 |
0.2080 |
-0.021600 |
9.05e-02 |
-0.160000 |
-9.36e-02 |
8.33e-01 |
3.76e-01 |
1.16e-01 |
3.59e-01 |
Role of LAT2/NTAL/LAB on calcium mobilization |
14 |
8.41e-01 |
8.68e-01 |
0.2060 |
0.160000 |
1.09e-01 |
0.001100 |
-7.03e-02 |
2.99e-01 |
4.79e-01 |
9.94e-01 |
6.49e-01 |
Cargo trafficking to the periciliary membrane |
45 |
3.24e-02 |
6.51e-02 |
0.2060 |
0.112000 |
-9.49e-02 |
0.131000 |
6.06e-02 |
1.92e-01 |
2.71e-01 |
1.28e-01 |
4.82e-01 |
Negative epigenetic regulation of rRNA expression |
48 |
3.04e-01 |
3.87e-01 |
0.2060 |
0.093000 |
6.73e-02 |
0.161000 |
5.61e-02 |
2.65e-01 |
4.20e-01 |
5.33e-02 |
5.02e-01 |
Signaling by high-kinase activity BRAF mutants |
29 |
2.91e-01 |
3.74e-01 |
0.2060 |
0.029400 |
1.23e-01 |
-0.162000 |
1.61e-02 |
7.84e-01 |
2.52e-01 |
1.32e-01 |
8.81e-01 |
Signaling by FGFR in disease |
50 |
1.59e-01 |
2.33e-01 |
0.2040 |
-0.018000 |
-1.63e-01 |
-0.051200 |
-1.11e-01 |
8.26e-01 |
4.69e-02 |
5.31e-01 |
1.76e-01 |
Transcription of the HIV genome |
64 |
1.22e-02 |
2.95e-02 |
0.2040 |
-0.022200 |
-7.84e-02 |
0.169000 |
-7.94e-02 |
7.59e-01 |
2.78e-01 |
1.94e-02 |
2.73e-01 |
Transcriptional regulation by the AP-2 (TFAP2) family of transcription factors |
26 |
1.87e-01 |
2.63e-01 |
0.2030 |
-0.053300 |
1.12e-01 |
0.006700 |
-1.61e-01 |
6.38e-01 |
3.21e-01 |
9.53e-01 |
1.56e-01 |
Sema4D in semaphorin signaling |
24 |
2.33e-01 |
3.13e-01 |
0.2030 |
-0.148000 |
7.83e-02 |
0.025100 |
1.13e-01 |
2.10e-01 |
5.07e-01 |
8.32e-01 |
3.40e-01 |
TRAF6 mediated induction of NFkB and MAP kinases upon TLR7/8 or 9 activation |
84 |
9.97e-02 |
1.59e-01 |
0.2030 |
-0.089300 |
-1.72e-01 |
-0.020500 |
-5.52e-02 |
1.58e-01 |
6.41e-03 |
7.45e-01 |
3.82e-01 |
RNA polymerase II transcribes snRNA genes |
70 |
1.53e-02 |
3.55e-02 |
0.2020 |
-0.054200 |
-9.49e-02 |
0.090400 |
-1.44e-01 |
4.33e-01 |
1.70e-01 |
1.92e-01 |
3.69e-02 |
Nef-mediates down modulation of cell surface receptors by recruiting them to clathrin adapters |
18 |
5.89e-01 |
6.47e-01 |
0.2020 |
0.031900 |
1.29e-01 |
0.151000 |
-1.78e-02 |
8.15e-01 |
3.43e-01 |
2.66e-01 |
8.96e-01 |
Cellular responses to external stimuli |
426 |
1.56e-12 |
2.01e-11 |
0.2020 |
0.070200 |
4.78e-02 |
0.183000 |
-1.17e-02 |
1.36e-02 |
9.32e-02 |
1.17e-10 |
6.81e-01 |
Signaling by TGFB family members |
84 |
2.88e-03 |
8.67e-03 |
0.2020 |
0.038400 |
-1.66e-01 |
-0.043000 |
-9.93e-02 |
5.43e-01 |
8.50e-03 |
4.96e-01 |
1.16e-01 |
RNA Polymerase I Transcription Termination |
30 |
5.89e-01 |
6.47e-01 |
0.2020 |
-0.056900 |
-3.56e-02 |
0.110000 |
1.55e-01 |
5.90e-01 |
7.36e-01 |
2.98e-01 |
1.41e-01 |
Potential therapeutics for SARS |
34 |
5.10e-01 |
5.82e-01 |
0.2020 |
0.135000 |
1.32e-01 |
0.025200 |
-6.57e-02 |
1.73e-01 |
1.82e-01 |
7.99e-01 |
5.07e-01 |
PTK6 Regulates RHO GTPases, RAS GTPase and MAP kinases |
13 |
8.87e-01 |
9.05e-01 |
0.2000 |
0.119000 |
1.44e-01 |
-0.039100 |
-6.11e-02 |
4.59e-01 |
3.69e-01 |
8.07e-01 |
7.03e-01 |
Rho GTPase cycle |
128 |
3.33e-04 |
1.21e-03 |
0.2000 |
-0.135000 |
7.82e-03 |
-0.144000 |
-3.04e-02 |
8.45e-03 |
8.79e-01 |
4.97e-03 |
5.54e-01 |
Neurotransmitter release cycle |
27 |
4.36e-01 |
5.14e-01 |
0.2000 |
-0.019700 |
-1.03e-01 |
-0.170000 |
-9.57e-03 |
8.59e-01 |
3.53e-01 |
1.27e-01 |
9.31e-01 |
Synthesis of PIPs at the Golgi membrane |
15 |
8.38e-01 |
8.67e-01 |
0.1980 |
-0.026600 |
-2.35e-02 |
-0.080400 |
-1.77e-01 |
8.58e-01 |
8.75e-01 |
5.90e-01 |
2.35e-01 |
SUMOylation of DNA methylation proteins |
16 |
7.77e-01 |
8.16e-01 |
0.1970 |
-0.062900 |
-1.51e-01 |
-0.110000 |
-9.25e-03 |
6.63e-01 |
2.97e-01 |
4.45e-01 |
9.49e-01 |
HDACs deacetylate histones |
30 |
2.16e-01 |
2.94e-01 |
0.1970 |
0.105000 |
5.61e-03 |
0.080000 |
-1.46e-01 |
3.19e-01 |
9.58e-01 |
4.49e-01 |
1.66e-01 |
Cellular responses to stress |
422 |
1.24e-11 |
1.47e-10 |
0.1970 |
0.067200 |
4.38e-02 |
0.179000 |
-7.97e-03 |
1.86e-02 |
1.25e-01 |
3.36e-10 |
7.80e-01 |
RA biosynthesis pathway |
13 |
7.08e-01 |
7.50e-01 |
0.1960 |
0.191000 |
1.67e-02 |
0.016100 |
-3.44e-02 |
2.32e-01 |
9.17e-01 |
9.20e-01 |
8.30e-01 |
Semaphorin interactions |
63 |
4.56e-03 |
1.30e-02 |
0.1950 |
-0.083400 |
9.26e-02 |
-0.111000 |
1.02e-01 |
2.53e-01 |
2.04e-01 |
1.29e-01 |
1.62e-01 |
Interaction between L1 and Ankyrins |
21 |
6.90e-01 |
7.34e-01 |
0.1950 |
-0.167000 |
-7.97e-02 |
-0.051800 |
3.39e-02 |
1.84e-01 |
5.27e-01 |
6.81e-01 |
7.88e-01 |
MAPK targets/ Nuclear events mediated by MAP kinases |
31 |
1.76e-01 |
2.50e-01 |
0.1950 |
0.052300 |
-1.63e-01 |
-0.025900 |
-8.91e-02 |
6.14e-01 |
1.16e-01 |
8.03e-01 |
3.91e-01 |
Transcriptional Regulation by VENTX |
35 |
4.97e-01 |
5.70e-01 |
0.1950 |
-0.129000 |
-1.15e-01 |
0.084400 |
-2.88e-02 |
1.87e-01 |
2.38e-01 |
3.88e-01 |
7.68e-01 |
Metabolism of fat-soluble vitamins |
30 |
5.90e-01 |
6.47e-01 |
0.1940 |
-0.056500 |
3.07e-02 |
0.123000 |
1.36e-01 |
5.93e-01 |
7.71e-01 |
2.45e-01 |
1.97e-01 |
Glutathione synthesis and recycling |
10 |
8.25e-01 |
8.56e-01 |
0.1940 |
0.091600 |
-3.86e-02 |
0.157000 |
5.63e-02 |
6.16e-01 |
8.33e-01 |
3.90e-01 |
7.58e-01 |
NoRC negatively regulates rRNA expression |
45 |
4.30e-01 |
5.11e-01 |
0.1940 |
0.056700 |
3.84e-02 |
0.161000 |
8.43e-02 |
5.11e-01 |
6.56e-01 |
6.20e-02 |
3.28e-01 |
Mitophagy |
25 |
5.33e-01 |
6.00e-01 |
0.1940 |
-0.072200 |
-1.42e-01 |
0.100000 |
-4.86e-02 |
5.32e-01 |
2.20e-01 |
3.87e-01 |
6.74e-01 |
Cell death signalling via NRAGE, NRIF and NADE |
68 |
1.20e-01 |
1.86e-01 |
0.1940 |
-0.156000 |
-7.50e-02 |
-0.086000 |
1.71e-02 |
2.63e-02 |
2.86e-01 |
2.21e-01 |
8.07e-01 |
Signaling by PDGFR in disease |
20 |
6.30e-01 |
6.82e-01 |
0.1920 |
0.039800 |
-1.02e-01 |
-0.063700 |
-1.45e-01 |
7.58e-01 |
4.32e-01 |
6.22e-01 |
2.61e-01 |
Cell-Cell communication |
80 |
6.26e-03 |
1.70e-02 |
0.1920 |
-0.085000 |
3.61e-02 |
-0.167000 |
2.02e-02 |
1.89e-01 |
5.77e-01 |
9.92e-03 |
7.55e-01 |
Visual phototransduction |
54 |
2.69e-01 |
3.51e-01 |
0.1920 |
-0.162000 |
-8.71e-02 |
-0.037400 |
3.88e-02 |
3.95e-02 |
2.68e-01 |
6.35e-01 |
6.23e-01 |
Signalling to RAS |
17 |
7.89e-01 |
8.26e-01 |
0.1920 |
0.100000 |
1.95e-03 |
-0.120000 |
-1.11e-01 |
4.75e-01 |
9.89e-01 |
3.91e-01 |
4.30e-01 |
CLEC7A (Dectin-1) signaling |
89 |
4.09e-02 |
7.81e-02 |
0.1920 |
0.074800 |
5.86e-02 |
0.166000 |
1.21e-02 |
2.23e-01 |
3.40e-01 |
6.89e-03 |
8.44e-01 |
NOTCH3 Intracellular Domain Regulates Transcription |
22 |
7.16e-01 |
7.57e-01 |
0.1910 |
-0.111000 |
-6.25e-02 |
-0.139000 |
-2.97e-02 |
3.68e-01 |
6.12e-01 |
2.61e-01 |
8.09e-01 |
SHC1 events in EGFR signaling |
11 |
9.46e-01 |
9.57e-01 |
0.1900 |
-0.143000 |
-1.23e-01 |
-0.016200 |
-1.90e-02 |
4.10e-01 |
4.81e-01 |
9.26e-01 |
9.13e-01 |
ABC transporters in lipid homeostasis |
14 |
5.05e-01 |
5.78e-01 |
0.1900 |
0.064100 |
-1.71e-01 |
0.021700 |
-4.73e-02 |
6.78e-01 |
2.67e-01 |
8.88e-01 |
7.59e-01 |
Translocation of SLC2A4 (GLUT4) to the plasma membrane |
50 |
2.13e-01 |
2.91e-01 |
0.1890 |
0.018900 |
-1.22e-01 |
-0.107000 |
-9.50e-02 |
8.17e-01 |
1.34e-01 |
1.91e-01 |
2.45e-01 |
Estrogen-dependent gene expression |
81 |
6.78e-02 |
1.17e-01 |
0.1890 |
-0.057300 |
-7.97e-02 |
-0.002770 |
-1.61e-01 |
3.74e-01 |
2.16e-01 |
9.66e-01 |
1.23e-02 |
Signaling by NTRK1 (TRKA) |
105 |
5.86e-02 |
1.05e-01 |
0.1880 |
-0.074000 |
-1.65e-01 |
-0.019300 |
-4.91e-02 |
1.91e-01 |
3.52e-03 |
7.33e-01 |
3.86e-01 |
Synthesis of PIPs at the plasma membrane |
51 |
2.20e-01 |
3.00e-01 |
0.1880 |
0.062000 |
-2.77e-02 |
-0.166000 |
-5.86e-02 |
4.44e-01 |
7.33e-01 |
4.09e-02 |
4.70e-01 |
CTLA4 inhibitory signaling |
21 |
5.99e-01 |
6.56e-01 |
0.1880 |
0.112000 |
-8.79e-03 |
0.142000 |
5.16e-02 |
3.75e-01 |
9.44e-01 |
2.60e-01 |
6.83e-01 |
The citric acid (TCA) cycle and respiratory electron transport |
149 |
2.55e-04 |
9.43e-04 |
0.1870 |
0.114000 |
4.71e-02 |
0.062200 |
-1.26e-01 |
1.61e-02 |
3.23e-01 |
1.91e-01 |
8.09e-03 |
N-Glycan antennae elongation |
13 |
7.59e-01 |
8.00e-01 |
0.1870 |
0.060100 |
-5.81e-02 |
0.061300 |
1.56e-01 |
7.07e-01 |
7.17e-01 |
7.02e-01 |
3.31e-01 |
Signaling by SCF-KIT |
42 |
2.79e-01 |
3.61e-01 |
0.1870 |
0.016600 |
3.31e-02 |
-0.182000 |
-2.04e-02 |
8.52e-01 |
7.11e-01 |
4.12e-02 |
8.19e-01 |
Metabolism of carbohydrates |
227 |
5.12e-04 |
1.79e-03 |
0.1860 |
-0.124000 |
-9.40e-02 |
0.101000 |
4.43e-03 |
1.30e-03 |
1.50e-02 |
8.78e-03 |
9.09e-01 |
Pre-NOTCH Transcription and Translation |
32 |
5.41e-01 |
6.07e-01 |
0.1860 |
-0.119000 |
-3.33e-02 |
-0.063800 |
-1.24e-01 |
2.46e-01 |
7.44e-01 |
5.33e-01 |
2.26e-01 |
Growth hormone receptor signaling |
19 |
8.12e-01 |
8.45e-01 |
0.1860 |
-0.068100 |
-1.52e-01 |
-0.074100 |
-3.48e-02 |
6.08e-01 |
2.51e-01 |
5.76e-01 |
7.93e-01 |
Regulation of lipid metabolism by PPARalpha |
109 |
5.91e-03 |
1.62e-02 |
0.1860 |
0.011600 |
-1.14e-02 |
0.003720 |
-1.85e-01 |
8.35e-01 |
8.37e-01 |
9.47e-01 |
8.71e-04 |
Sema3A PAK dependent Axon repulsion |
16 |
6.26e-01 |
6.79e-01 |
0.1860 |
-0.129000 |
-1.26e-02 |
-0.067900 |
1.14e-01 |
3.73e-01 |
9.31e-01 |
6.38e-01 |
4.28e-01 |
TGF-beta receptor signaling in EMT (epithelial to mesenchymal transition) |
13 |
8.95e-01 |
9.13e-01 |
0.1840 |
-0.129000 |
-1.12e-01 |
-0.042900 |
5.39e-02 |
4.20e-01 |
4.85e-01 |
7.89e-01 |
7.36e-01 |
DDX58/IFIH1-mediated induction of interferon-alpha/beta |
55 |
2.28e-01 |
3.09e-01 |
0.1840 |
-0.028200 |
4.45e-02 |
-0.091400 |
-1.51e-01 |
7.17e-01 |
5.69e-01 |
2.42e-01 |
5.32e-02 |
TCF dependent signaling in response to WNT |
143 |
3.94e-04 |
1.40e-03 |
0.1840 |
-0.064900 |
-8.15e-02 |
0.118000 |
-9.41e-02 |
1.81e-01 |
9.34e-02 |
1.49e-02 |
5.27e-02 |
Retinoid metabolism and transport |
27 |
5.05e-01 |
5.78e-01 |
0.1830 |
-0.110000 |
2.74e-02 |
0.063100 |
1.30e-01 |
3.25e-01 |
8.05e-01 |
5.71e-01 |
2.42e-01 |
Signaling by ERBB2 |
42 |
6.46e-01 |
6.96e-01 |
0.1830 |
-0.107000 |
-1.01e-01 |
-0.088200 |
-6.42e-02 |
2.32e-01 |
2.56e-01 |
3.23e-01 |
4.72e-01 |
CD209 (DC-SIGN) signaling |
19 |
7.99e-01 |
8.34e-01 |
0.1830 |
-0.033300 |
2.67e-02 |
-0.133000 |
-1.18e-01 |
8.02e-01 |
8.40e-01 |
3.15e-01 |
3.73e-01 |
RNA Polymerase III Transcription Initiation From Type 1 Promoter |
28 |
6.87e-01 |
7.31e-01 |
0.1830 |
0.044000 |
1.26e-02 |
0.156000 |
8.37e-02 |
6.87e-01 |
9.08e-01 |
1.53e-01 |
4.44e-01 |
MyD88 dependent cascade initiated on endosome |
85 |
1.53e-01 |
2.26e-01 |
0.1820 |
-0.078500 |
-1.59e-01 |
-0.008710 |
-4.29e-02 |
2.12e-01 |
1.16e-02 |
8.90e-01 |
4.95e-01 |
Toll Like Receptor 7/8 (TLR7/8) Cascade |
85 |
1.53e-01 |
2.26e-01 |
0.1820 |
-0.078500 |
-1.59e-01 |
-0.008710 |
-4.29e-02 |
2.12e-01 |
1.16e-02 |
8.90e-01 |
4.95e-01 |
G alpha (z) signalling events |
36 |
1.85e-01 |
2.61e-01 |
0.1820 |
-0.079400 |
-7.62e-03 |
-0.099100 |
1.30e-01 |
4.10e-01 |
9.37e-01 |
3.04e-01 |
1.77e-01 |
Beta-catenin independent WNT signaling |
128 |
1.82e-02 |
4.10e-02 |
0.1820 |
-0.061600 |
2.90e-02 |
0.146000 |
8.50e-02 |
2.30e-01 |
5.72e-01 |
4.51e-03 |
9.74e-02 |
Platelet activation, signaling and aggregation |
208 |
5.97e-07 |
3.06e-06 |
0.1810 |
-0.022800 |
8.87e-02 |
-0.064700 |
1.42e-01 |
5.73e-01 |
2.79e-02 |
1.09e-01 |
4.15e-04 |
Ephrin signaling |
19 |
4.85e-01 |
5.58e-01 |
0.1810 |
-0.125000 |
3.46e-02 |
-0.121000 |
3.54e-02 |
3.46e-01 |
7.94e-01 |
3.61e-01 |
7.89e-01 |
Cilium Assembly |
171 |
3.62e-05 |
1.52e-04 |
0.1800 |
0.026200 |
-4.91e-02 |
0.169000 |
-2.72e-02 |
5.56e-01 |
2.69e-01 |
1.41e-04 |
5.40e-01 |
Golgi-to-ER retrograde transport |
103 |
1.43e-02 |
3.35e-02 |
0.1800 |
0.008290 |
-8.73e-02 |
0.151000 |
4.50e-02 |
8.85e-01 |
1.26e-01 |
8.40e-03 |
4.31e-01 |
PPARA activates gene expression |
107 |
7.75e-03 |
2.04e-02 |
0.1800 |
0.012800 |
-2.04e-02 |
0.012400 |
-1.78e-01 |
8.19e-01 |
7.16e-01 |
8.24e-01 |
1.52e-03 |
Metalloprotease DUBs |
18 |
8.82e-01 |
9.03e-01 |
0.1790 |
0.142000 |
9.86e-02 |
0.045300 |
1.56e-02 |
2.97e-01 |
4.69e-01 |
7.40e-01 |
9.09e-01 |
Programmed Cell Death |
151 |
6.36e-03 |
1.72e-02 |
0.1790 |
0.023600 |
7.22e-02 |
0.159000 |
3.06e-02 |
6.18e-01 |
1.27e-01 |
7.60e-04 |
5.17e-01 |
Apoptosis |
148 |
5.35e-03 |
1.49e-02 |
0.1790 |
0.023900 |
6.84e-02 |
0.162000 |
2.24e-02 |
6.17e-01 |
1.52e-01 |
6.97e-04 |
6.39e-01 |
COPI-dependent Golgi-to-ER retrograde traffic |
73 |
9.73e-02 |
1.56e-01 |
0.1780 |
0.040500 |
-2.94e-02 |
0.165000 |
4.70e-02 |
5.50e-01 |
6.65e-01 |
1.52e-02 |
4.88e-01 |
Interleukin-4 and Interleukin-13 signaling |
85 |
1.18e-02 |
2.87e-02 |
0.1780 |
-0.009210 |
2.89e-02 |
-0.056700 |
1.66e-01 |
8.83e-01 |
6.46e-01 |
3.67e-01 |
8.32e-03 |
Adrenaline,noradrenaline inhibits insulin secretion |
21 |
5.79e-01 |
6.39e-01 |
0.1770 |
-0.007520 |
2.91e-02 |
-0.030500 |
1.72e-01 |
9.52e-01 |
8.18e-01 |
8.09e-01 |
1.72e-01 |
VEGFA-VEGFR2 Pathway |
90 |
1.22e-01 |
1.88e-01 |
0.1770 |
0.047000 |
6.34e-02 |
-0.143000 |
-6.83e-02 |
4.42e-01 |
2.99e-01 |
1.91e-02 |
2.63e-01 |
TP53 Regulates Transcription of Genes Involved in Cytochrome C Release |
16 |
8.85e-01 |
9.04e-01 |
0.1760 |
-0.025200 |
1.00e-02 |
-0.113000 |
-1.32e-01 |
8.62e-01 |
9.45e-01 |
4.35e-01 |
3.60e-01 |
Interleukin-37 signaling |
18 |
5.50e-01 |
6.16e-01 |
0.1750 |
-0.101000 |
2.45e-02 |
-0.125000 |
6.54e-02 |
4.60e-01 |
8.57e-01 |
3.57e-01 |
6.31e-01 |
Positive epigenetic regulation of rRNA expression |
45 |
1.49e-01 |
2.22e-01 |
0.1750 |
0.082600 |
2.61e-02 |
0.092800 |
-1.21e-01 |
3.38e-01 |
7.62e-01 |
2.82e-01 |
1.61e-01 |
Keratinization |
20 |
6.96e-01 |
7.39e-01 |
0.1750 |
-0.023500 |
-1.09e-01 |
-0.134000 |
5.18e-04 |
8.56e-01 |
3.98e-01 |
2.98e-01 |
9.97e-01 |
C-type lectin receptors (CLRs) |
109 |
6.45e-02 |
1.13e-01 |
0.1750 |
0.081500 |
8.63e-02 |
0.128000 |
7.46e-03 |
1.42e-01 |
1.20e-01 |
2.12e-02 |
8.93e-01 |
Aggrephagy |
17 |
8.39e-01 |
8.67e-01 |
0.1740 |
-0.101000 |
-1.10e-01 |
0.081600 |
-3.86e-02 |
4.72e-01 |
4.33e-01 |
5.60e-01 |
7.83e-01 |
Cargo recognition for clathrin-mediated endocytosis |
85 |
6.38e-02 |
1.12e-01 |
0.1740 |
-0.048200 |
-1.48e-01 |
0.077500 |
-1.10e-02 |
4.44e-01 |
1.86e-02 |
2.18e-01 |
8.61e-01 |
Toll Like Receptor 9 (TLR9) Cascade |
88 |
1.68e-01 |
2.42e-01 |
0.1730 |
-0.072300 |
-1.52e-01 |
-0.007390 |
-3.96e-02 |
2.42e-01 |
1.36e-02 |
9.05e-01 |
5.22e-01 |
ADORA2B mediated anti-inflammatory cytokines production |
54 |
1.37e-01 |
2.08e-01 |
0.1730 |
0.013100 |
3.39e-03 |
-0.022400 |
1.71e-01 |
8.68e-01 |
9.66e-01 |
7.76e-01 |
2.95e-02 |
Sphingolipid de novo biosynthesis |
32 |
3.98e-01 |
4.82e-01 |
0.1720 |
-0.056400 |
-9.89e-02 |
-0.073500 |
1.06e-01 |
5.81e-01 |
3.33e-01 |
4.72e-01 |
3.01e-01 |
Transcriptional regulation by RUNX3 |
88 |
8.35e-02 |
1.38e-01 |
0.1710 |
0.041200 |
1.14e-01 |
0.121000 |
2.20e-03 |
5.04e-01 |
6.60e-02 |
5.02e-02 |
9.72e-01 |
Defective B3GALT6 causes EDSP2 and SEMDJL1 |
16 |
6.12e-01 |
6.67e-01 |
0.1700 |
-0.146000 |
2.98e-02 |
-0.060100 |
5.69e-02 |
3.13e-01 |
8.36e-01 |
6.78e-01 |
6.94e-01 |
RUNX2 regulates bone development |
28 |
5.58e-01 |
6.24e-01 |
0.1690 |
-0.069900 |
-9.32e-02 |
-0.034300 |
1.18e-01 |
5.23e-01 |
3.94e-01 |
7.54e-01 |
2.80e-01 |
FCERI mediated MAPK activation |
30 |
6.58e-01 |
7.05e-01 |
0.1690 |
0.063200 |
3.12e-02 |
-0.147000 |
-4.66e-02 |
5.50e-01 |
7.68e-01 |
1.65e-01 |
6.59e-01 |
p75NTR recruits signalling complexes |
11 |
8.69e-01 |
8.93e-01 |
0.1690 |
-0.159000 |
-1.92e-02 |
-0.052300 |
-1.49e-02 |
3.62e-01 |
9.12e-01 |
7.64e-01 |
9.32e-01 |
trans-Golgi Network Vesicle Budding |
65 |
3.80e-01 |
4.65e-01 |
0.1690 |
-0.030200 |
-4.01e-02 |
0.120000 |
1.08e-01 |
6.74e-01 |
5.77e-01 |
9.46e-02 |
1.34e-01 |
PTEN Regulation |
131 |
2.80e-03 |
8.52e-03 |
0.1690 |
0.017500 |
-2.89e-03 |
0.166000 |
-2.66e-02 |
7.30e-01 |
9.55e-01 |
1.08e-03 |
5.99e-01 |
Intrinsic Pathway for Apoptosis |
44 |
4.24e-01 |
5.05e-01 |
0.1680 |
0.013000 |
8.02e-02 |
0.144000 |
2.95e-02 |
8.82e-01 |
3.58e-01 |
9.86e-02 |
7.35e-01 |
MyD88:MAL(TIRAP) cascade initiated on plasma membrane |
88 |
2.39e-01 |
3.19e-01 |
0.1670 |
-0.072100 |
-1.40e-01 |
-0.045900 |
-3.06e-02 |
2.43e-01 |
2.30e-02 |
4.58e-01 |
6.20e-01 |
Toll Like Receptor 2 (TLR2) Cascade |
88 |
2.39e-01 |
3.19e-01 |
0.1670 |
-0.072100 |
-1.40e-01 |
-0.045900 |
-3.06e-02 |
2.43e-01 |
2.30e-02 |
4.58e-01 |
6.20e-01 |
Toll Like Receptor TLR1:TLR2 Cascade |
88 |
2.39e-01 |
3.19e-01 |
0.1670 |
-0.072100 |
-1.40e-01 |
-0.045900 |
-3.06e-02 |
2.43e-01 |
2.30e-02 |
4.58e-01 |
6.20e-01 |
Toll Like Receptor TLR6:TLR2 Cascade |
88 |
2.39e-01 |
3.19e-01 |
0.1670 |
-0.072100 |
-1.40e-01 |
-0.045900 |
-3.06e-02 |
2.43e-01 |
2.30e-02 |
4.58e-01 |
6.20e-01 |
Fc epsilon receptor (FCERI) signaling |
121 |
5.63e-02 |
1.02e-01 |
0.1670 |
0.110000 |
9.11e-02 |
0.079100 |
-3.43e-02 |
3.71e-02 |
8.40e-02 |
1.34e-01 |
5.15e-01 |
Adaptive Immune System |
577 |
5.91e-06 |
2.72e-05 |
0.1660 |
0.129000 |
9.00e-02 |
0.038900 |
3.53e-02 |
1.59e-07 |
2.55e-04 |
1.14e-01 |
1.51e-01 |
SARS-CoV Infections |
75 |
1.17e-01 |
1.82e-01 |
0.1650 |
0.037400 |
-1.32e-02 |
0.159000 |
1.94e-02 |
5.76e-01 |
8.44e-01 |
1.74e-02 |
7.71e-01 |
RNA Polymerase I Promoter Clearance |
48 |
3.40e-01 |
4.25e-01 |
0.1630 |
-0.006470 |
-2.26e-02 |
0.160000 |
1.40e-02 |
9.38e-01 |
7.87e-01 |
5.48e-02 |
8.67e-01 |
Gamma carboxylation, hypusine formation and arylsulfatase activation |
30 |
6.78e-01 |
7.23e-01 |
0.1620 |
-0.101000 |
-1.10e-02 |
0.104000 |
7.17e-02 |
3.38e-01 |
9.17e-01 |
3.26e-01 |
4.97e-01 |
Opioid Signalling |
74 |
7.30e-02 |
1.23e-01 |
0.1620 |
-0.011200 |
-1.29e-01 |
-0.093700 |
2.22e-02 |
8.68e-01 |
5.47e-02 |
1.64e-01 |
7.41e-01 |
Golgi Associated Vesicle Biogenesis |
51 |
4.75e-01 |
5.51e-01 |
0.1590 |
-0.054900 |
-1.12e-01 |
0.070700 |
6.96e-02 |
4.98e-01 |
1.69e-01 |
3.83e-01 |
3.90e-01 |
Signaling by VEGF |
98 |
1.21e-01 |
1.86e-01 |
0.1590 |
0.014800 |
6.06e-02 |
-0.135000 |
-5.60e-02 |
8.00e-01 |
3.01e-01 |
2.12e-02 |
3.39e-01 |
Phospholipid metabolism |
173 |
6.42e-02 |
1.12e-01 |
0.1590 |
-0.070900 |
-3.84e-02 |
-0.097000 |
-9.65e-02 |
1.09e-01 |
3.85e-01 |
2.81e-02 |
2.90e-02 |
E3 ubiquitin ligases ubiquitinate target proteins |
39 |
2.63e-01 |
3.45e-01 |
0.1590 |
0.080900 |
-7.33e-02 |
0.002320 |
-1.15e-01 |
3.82e-01 |
4.28e-01 |
9.80e-01 |
2.14e-01 |
Transcriptional regulation of white adipocyte differentiation |
75 |
5.83e-02 |
1.05e-01 |
0.1580 |
0.028100 |
-1.39e-02 |
0.049400 |
-1.47e-01 |
6.74e-01 |
8.36e-01 |
4.60e-01 |
2.78e-02 |
Immune System |
1518 |
7.59e-15 |
1.36e-13 |
0.1580 |
0.060600 |
9.05e-02 |
0.035100 |
1.09e-01 |
1.26e-04 |
9.91e-09 |
2.61e-02 |
4.60e-12 |
Carboxyterminal post-translational modifications of tubulin |
26 |
6.82e-01 |
7.27e-01 |
0.1570 |
-0.085900 |
2.13e-05 |
0.128000 |
2.92e-02 |
4.48e-01 |
1.00e+00 |
2.57e-01 |
7.96e-01 |
Interleukin-1 family signaling |
114 |
1.92e-01 |
2.67e-01 |
0.1570 |
0.002900 |
2.91e-02 |
0.130000 |
8.31e-02 |
9.57e-01 |
5.92e-01 |
1.65e-02 |
1.26e-01 |
Signaling by Insulin receptor |
56 |
4.44e-01 |
5.21e-01 |
0.1560 |
-0.045500 |
-1.30e-01 |
-0.012700 |
-7.29e-02 |
5.57e-01 |
9.32e-02 |
8.70e-01 |
3.46e-01 |
Caspase-mediated cleavage of cytoskeletal proteins |
12 |
8.87e-01 |
9.05e-01 |
0.1550 |
-0.146000 |
-2.48e-02 |
0.007460 |
-4.65e-02 |
3.81e-01 |
8.82e-01 |
9.64e-01 |
7.80e-01 |
Estrogen-dependent nuclear events downstream of ESR-membrane signaling |
21 |
6.69e-01 |
7.15e-01 |
0.1550 |
0.038400 |
-1.17e-01 |
-0.079400 |
-5.08e-02 |
7.61e-01 |
3.52e-01 |
5.29e-01 |
6.87e-01 |
Signaling by FGFR |
63 |
1.77e-01 |
2.51e-01 |
0.1550 |
-0.008010 |
-1.29e-01 |
0.018900 |
-8.29e-02 |
9.13e-01 |
7.59e-02 |
7.95e-01 |
2.56e-01 |
Basigin interactions |
20 |
5.81e-01 |
6.41e-01 |
0.1550 |
-0.022400 |
1.50e-01 |
0.014000 |
-2.98e-02 |
8.62e-01 |
2.47e-01 |
9.14e-01 |
8.18e-01 |
Activation of IRF3/IRF7 mediated by TBK1/IKK epsilon |
14 |
8.59e-01 |
8.85e-01 |
0.1550 |
-0.152000 |
-2.39e-02 |
-0.011100 |
-7.91e-03 |
3.24e-01 |
8.77e-01 |
9.43e-01 |
9.59e-01 |
Signaling by NOTCH3 |
43 |
2.03e-01 |
2.79e-01 |
0.1540 |
-0.140000 |
3.29e-02 |
-0.047900 |
-2.75e-02 |
1.11e-01 |
7.09e-01 |
5.87e-01 |
7.55e-01 |
GPCR downstream signalling |
381 |
1.23e-07 |
6.89e-07 |
0.1540 |
-0.064100 |
-1.34e-02 |
-0.137000 |
2.68e-02 |
3.29e-02 |
6.57e-01 |
4.93e-06 |
3.73e-01 |
RNA Polymerase III Transcription Initiation From Type 2 Promoter |
27 |
7.89e-01 |
8.26e-01 |
0.1530 |
0.015100 |
-1.95e-02 |
0.136000 |
6.62e-02 |
8.92e-01 |
8.61e-01 |
2.22e-01 |
5.52e-01 |
alpha-linolenic (omega3) and linoleic (omega6) acid metabolism |
10 |
8.98e-01 |
9.14e-01 |
0.1530 |
-0.087600 |
-9.48e-05 |
0.015500 |
-1.24e-01 |
6.32e-01 |
1.00e+00 |
9.32e-01 |
4.97e-01 |
alpha-linolenic acid (ALA) metabolism |
10 |
8.98e-01 |
9.14e-01 |
0.1530 |
-0.087600 |
-9.48e-05 |
0.015500 |
-1.24e-01 |
6.32e-01 |
1.00e+00 |
9.32e-01 |
4.97e-01 |
PI Metabolism |
79 |
3.63e-01 |
4.49e-01 |
0.1510 |
0.043200 |
2.83e-02 |
-0.124000 |
-6.89e-02 |
5.08e-01 |
6.64e-01 |
5.71e-02 |
2.91e-01 |
TICAM1-dependent activation of IRF3/IRF7 |
10 |
9.34e-01 |
9.46e-01 |
0.1500 |
0.021900 |
6.44e-02 |
-0.016200 |
-1.32e-01 |
9.04e-01 |
7.24e-01 |
9.29e-01 |
4.69e-01 |
Factors involved in megakaryocyte development and platelet production |
101 |
4.26e-02 |
8.08e-02 |
0.1490 |
0.011700 |
3.96e-02 |
0.016600 |
-1.43e-01 |
8.39e-01 |
4.93e-01 |
7.74e-01 |
1.34e-02 |
Gene expression (Transcription) |
1084 |
8.65e-20 |
2.47e-18 |
0.1490 |
0.044100 |
1.16e-03 |
0.021100 |
-1.41e-01 |
1.62e-02 |
9.50e-01 |
2.51e-01 |
1.44e-14 |
Peroxisomal protein import |
54 |
6.26e-01 |
6.79e-01 |
0.1490 |
0.125000 |
7.85e-02 |
-0.012600 |
1.86e-03 |
1.11e-01 |
3.19e-01 |
8.72e-01 |
9.81e-01 |
Signaling by GPCR |
411 |
3.17e-07 |
1.67e-06 |
0.1480 |
-0.080600 |
-3.50e-02 |
-0.112000 |
4.08e-02 |
5.36e-03 |
2.27e-01 |
1.08e-04 |
1.59e-01 |
Phase I - Functionalization of compounds |
60 |
3.75e-01 |
4.61e-01 |
0.1480 |
0.133000 |
3.65e-02 |
0.050600 |
1.62e-02 |
7.44e-02 |
6.25e-01 |
4.99e-01 |
8.28e-01 |
Death Receptor Signalling |
122 |
3.56e-02 |
6.97e-02 |
0.1480 |
-0.043500 |
3.18e-02 |
-0.135000 |
-2.54e-02 |
4.08e-01 |
5.46e-01 |
1.02e-02 |
6.29e-01 |
B-WICH complex positively regulates rRNA expression |
32 |
5.27e-01 |
5.95e-01 |
0.1470 |
0.099300 |
1.58e-02 |
0.052900 |
-9.40e-02 |
3.31e-01 |
8.77e-01 |
6.05e-01 |
3.57e-01 |
RNA Polymerase II Transcription |
968 |
1.32e-16 |
2.51e-15 |
0.1470 |
0.050100 |
6.56e-03 |
0.015800 |
-1.37e-01 |
9.52e-03 |
7.34e-01 |
4.13e-01 |
1.34e-12 |
Neddylation |
205 |
5.55e-04 |
1.93e-03 |
0.1460 |
0.112000 |
-7.26e-03 |
0.092100 |
4.22e-03 |
5.71e-03 |
8.58e-01 |
2.34e-02 |
9.17e-01 |
HATs acetylate histones |
74 |
1.11e-01 |
1.74e-01 |
0.1450 |
-0.004540 |
-1.75e-02 |
0.047900 |
-1.36e-01 |
9.46e-01 |
7.94e-01 |
4.76e-01 |
4.35e-02 |
NR1H3 & NR1H2 regulate gene expression linked to cholesterol transport and efflux |
30 |
8.37e-01 |
8.67e-01 |
0.1450 |
-0.092800 |
-9.34e-02 |
0.060900 |
5.49e-03 |
3.79e-01 |
3.76e-01 |
5.64e-01 |
9.58e-01 |
Organelle biogenesis and maintenance |
240 |
1.46e-05 |
6.46e-05 |
0.1450 |
0.021900 |
-7.33e-02 |
0.079100 |
-9.47e-02 |
5.61e-01 |
5.15e-02 |
3.56e-02 |
1.18e-02 |
Signal transduction by L1 |
21 |
7.32e-01 |
7.73e-01 |
0.1450 |
0.051000 |
1.36e-02 |
-0.035600 |
1.30e-01 |
6.86e-01 |
9.14e-01 |
7.78e-01 |
3.02e-01 |
RNA Polymerase I Transcription |
49 |
4.48e-01 |
5.25e-01 |
0.1450 |
-0.014000 |
-8.92e-03 |
0.143000 |
8.16e-03 |
8.66e-01 |
9.14e-01 |
8.27e-02 |
9.21e-01 |
Activation of HOX genes during differentiation |
54 |
2.29e-01 |
3.09e-01 |
0.1440 |
0.000317 |
-6.03e-02 |
0.121000 |
-5.00e-02 |
9.97e-01 |
4.44e-01 |
1.23e-01 |
5.25e-01 |
Activation of anterior HOX genes in hindbrain development during early embryogenesis |
54 |
2.29e-01 |
3.09e-01 |
0.1440 |
0.000317 |
-6.03e-02 |
0.121000 |
-5.00e-02 |
9.97e-01 |
4.44e-01 |
1.23e-01 |
5.25e-01 |
Protein folding |
84 |
4.13e-01 |
4.96e-01 |
0.1440 |
0.019900 |
-6.31e-03 |
0.106000 |
9.58e-02 |
7.53e-01 |
9.21e-01 |
9.46e-02 |
1.30e-01 |
G alpha (s) signalling events |
76 |
1.08e-01 |
1.70e-01 |
0.1440 |
-0.030700 |
-1.18e-02 |
-0.045800 |
1.33e-01 |
6.44e-01 |
8.59e-01 |
4.91e-01 |
4.59e-02 |
p75 NTR receptor-mediated signalling |
84 |
1.46e-01 |
2.18e-01 |
0.1440 |
-0.115000 |
-2.89e-02 |
-0.073600 |
3.57e-02 |
6.94e-02 |
6.48e-01 |
2.44e-01 |
5.73e-01 |
Fatty acid metabolism |
129 |
5.42e-02 |
9.84e-02 |
0.1440 |
0.036700 |
1.30e-01 |
-0.049400 |
3.44e-03 |
4.72e-01 |
1.12e-02 |
3.33e-01 |
9.46e-01 |
Regulation of PTEN gene transcription |
58 |
4.74e-01 |
5.50e-01 |
0.1430 |
-0.053900 |
-8.38e-02 |
0.013500 |
-1.02e-01 |
4.78e-01 |
2.70e-01 |
8.59e-01 |
1.79e-01 |
mTORC1-mediated signalling |
23 |
7.98e-01 |
8.34e-01 |
0.1430 |
0.026500 |
-3.37e-02 |
0.132000 |
3.62e-02 |
8.26e-01 |
7.79e-01 |
2.74e-01 |
7.64e-01 |
Diseases associated with glycosaminoglycan metabolism |
33 |
5.50e-01 |
6.16e-01 |
0.1430 |
-0.125000 |
-1.11e-02 |
-0.055500 |
4.12e-02 |
2.15e-01 |
9.12e-01 |
5.81e-01 |
6.82e-01 |
RHO GTPases Activate ROCKs |
19 |
6.55e-01 |
7.05e-01 |
0.1430 |
-0.064600 |
6.51e-02 |
-0.077900 |
7.72e-02 |
6.26e-01 |
6.23e-01 |
5.57e-01 |
5.60e-01 |
Class I MHC mediated antigen processing & presentation |
318 |
1.76e-04 |
6.74e-04 |
0.1430 |
0.119000 |
1.91e-02 |
0.069000 |
3.11e-02 |
2.72e-04 |
5.61e-01 |
3.53e-02 |
3.42e-01 |
RAS processing |
19 |
7.19e-01 |
7.60e-01 |
0.1420 |
0.089000 |
-1.67e-02 |
0.096800 |
-5.15e-02 |
5.02e-01 |
9.00e-01 |
4.65e-01 |
6.98e-01 |
Generic Transcription Pathway |
854 |
1.98e-13 |
2.99e-12 |
0.1410 |
0.050600 |
7.17e-03 |
0.012300 |
-1.31e-01 |
1.34e-02 |
7.26e-01 |
5.48e-01 |
1.34e-10 |
TP53 Regulates Metabolic Genes |
82 |
3.33e-01 |
4.17e-01 |
0.1390 |
-0.071200 |
-7.41e-02 |
0.021200 |
-9.10e-02 |
2.66e-01 |
2.47e-01 |
7.41e-01 |
1.55e-01 |
PINK1-PRKN Mediated Mitophagy |
18 |
8.78e-01 |
8.99e-01 |
0.1390 |
-0.061800 |
-7.74e-02 |
0.090900 |
-3.47e-02 |
6.50e-01 |
5.70e-01 |
5.05e-01 |
7.99e-01 |
Formation of Incision Complex in GG-NER |
40 |
4.42e-01 |
5.19e-01 |
0.1380 |
0.109000 |
-9.39e-03 |
0.083900 |
-7.94e-03 |
2.32e-01 |
9.18e-01 |
3.59e-01 |
9.31e-01 |
SUMOylation of immune response proteins |
11 |
9.80e-01 |
9.84e-01 |
0.1380 |
-0.020300 |
-1.68e-02 |
-0.085500 |
-1.05e-01 |
9.07e-01 |
9.23e-01 |
6.24e-01 |
5.47e-01 |
Butyrate Response Factor 1 (BRF1) binds and destabilizes mRNA |
16 |
8.66e-01 |
8.90e-01 |
0.1380 |
0.066800 |
-3.39e-02 |
0.053800 |
1.02e-01 |
6.44e-01 |
8.14e-01 |
7.10e-01 |
4.79e-01 |
Amyloid fiber formation |
35 |
8.71e-01 |
8.94e-01 |
0.1370 |
0.029800 |
5.69e-02 |
0.089700 |
8.15e-02 |
7.60e-01 |
5.60e-01 |
3.58e-01 |
4.04e-01 |
RNA Polymerase I Transcription Initiation |
45 |
6.34e-01 |
6.86e-01 |
0.1360 |
-0.024400 |
-3.22e-02 |
0.126000 |
2.79e-02 |
7.77e-01 |
7.08e-01 |
1.43e-01 |
7.46e-01 |
Vitamin B5 (pantothenate) metabolism |
15 |
9.13e-01 |
9.28e-01 |
0.1360 |
0.097500 |
5.84e-03 |
-0.087400 |
-3.45e-02 |
5.13e-01 |
9.69e-01 |
5.58e-01 |
8.17e-01 |
Acyl chain remodelling of PG |
11 |
8.85e-01 |
9.04e-01 |
0.1340 |
-0.106000 |
3.80e-02 |
-0.071900 |
-9.26e-03 |
5.42e-01 |
8.27e-01 |
6.80e-01 |
9.58e-01 |
O-linked glycosylation |
66 |
3.61e-01 |
4.48e-01 |
0.1330 |
-0.095500 |
-4.36e-02 |
-0.052100 |
6.38e-02 |
1.80e-01 |
5.40e-01 |
4.65e-01 |
3.70e-01 |
Signaling by Receptor Tyrosine Kinases |
412 |
9.58e-04 |
3.20e-03 |
0.1320 |
-0.080600 |
-7.22e-02 |
-0.075300 |
1.24e-02 |
5.29e-03 |
1.25e-02 |
9.21e-03 |
6.68e-01 |
Metabolism of proteins |
1541 |
9.03e-18 |
2.11e-16 |
0.1320 |
0.051400 |
-1.91e-02 |
0.114000 |
3.57e-02 |
1.05e-03 |
2.23e-01 |
2.83e-13 |
2.30e-02 |
NR1H2 and NR1H3-mediated signaling |
37 |
6.85e-01 |
7.29e-01 |
0.1320 |
-0.125000 |
-2.81e-02 |
-0.028600 |
-1.31e-03 |
1.87e-01 |
7.68e-01 |
7.64e-01 |
9.89e-01 |
G alpha (i) signalling events |
196 |
2.76e-03 |
8.40e-03 |
0.1300 |
-0.038900 |
-2.26e-02 |
-0.107000 |
5.98e-02 |
3.50e-01 |
5.86e-01 |
1.02e-02 |
1.50e-01 |
Amino acids regulate mTORC1 |
48 |
7.36e-01 |
7.77e-01 |
0.1290 |
-0.067100 |
-7.73e-02 |
0.029600 |
7.35e-02 |
4.22e-01 |
3.55e-01 |
7.23e-01 |
3.79e-01 |
Signaling by Rho GTPases |
337 |
8.17e-04 |
2.78e-03 |
0.1290 |
0.033500 |
6.77e-02 |
-0.015500 |
-1.04e-01 |
2.93e-01 |
3.37e-02 |
6.26e-01 |
1.16e-03 |
Toll Like Receptor 4 (TLR4) Cascade |
116 |
3.01e-01 |
3.83e-01 |
0.1290 |
-0.056300 |
-7.46e-02 |
-0.088200 |
-8.44e-03 |
2.96e-01 |
1.66e-01 |
1.01e-01 |
8.75e-01 |
Transcriptional regulation by RUNX1 |
154 |
4.46e-02 |
8.39e-02 |
0.1280 |
0.052700 |
5.07e-02 |
0.099600 |
-3.47e-02 |
2.60e-01 |
2.79e-01 |
3.33e-02 |
4.59e-01 |
O-linked glycosylation of mucins |
31 |
8.62e-01 |
8.87e-01 |
0.1250 |
-0.043000 |
-6.11e-02 |
0.044700 |
9.01e-02 |
6.79e-01 |
5.56e-01 |
6.67e-01 |
3.86e-01 |
Association of TriC/CCT with target proteins during biosynthesis |
36 |
5.99e-01 |
6.56e-01 |
0.1250 |
0.072900 |
-2.13e-02 |
0.099500 |
-3.18e-03 |
4.50e-01 |
8.25e-01 |
3.02e-01 |
9.74e-01 |
Post-translational modification: synthesis of GPI-anchored proteins |
54 |
5.62e-01 |
6.27e-01 |
0.1250 |
-0.040500 |
-3.86e-02 |
0.004400 |
1.12e-01 |
6.07e-01 |
6.24e-01 |
9.55e-01 |
1.57e-01 |
SLC-mediated transmembrane transport |
150 |
1.56e-01 |
2.30e-01 |
0.1240 |
0.017700 |
2.37e-02 |
-0.115000 |
-3.48e-02 |
7.09e-01 |
6.17e-01 |
1.51e-02 |
4.63e-01 |
tRNA processing |
106 |
6.04e-02 |
1.07e-01 |
0.1240 |
-0.002160 |
3.49e-03 |
0.088500 |
-8.66e-02 |
9.69e-01 |
9.51e-01 |
1.16e-01 |
1.24e-01 |
Activation of BH3-only proteins |
27 |
9.06e-01 |
9.21e-01 |
0.1240 |
0.073900 |
7.77e-02 |
-0.009540 |
-6.10e-02 |
5.06e-01 |
4.85e-01 |
9.32e-01 |
5.84e-01 |
Signaling by Interleukins |
347 |
1.47e-02 |
3.44e-02 |
0.1230 |
0.059400 |
6.15e-02 |
0.010300 |
8.74e-02 |
5.87e-02 |
5.04e-02 |
7.42e-01 |
5.43e-03 |
Acyl chain remodelling of PS |
14 |
8.72e-01 |
8.94e-01 |
0.1220 |
0.018300 |
-3.14e-02 |
-0.077000 |
8.78e-02 |
9.06e-01 |
8.39e-01 |
6.18e-01 |
5.69e-01 |
Cooperation of PDCL (PhLP1) and TRiC/CCT in G-protein beta folding |
32 |
6.30e-01 |
6.82e-01 |
0.1210 |
0.071600 |
-1.31e-02 |
-0.032200 |
9.10e-02 |
4.84e-01 |
8.98e-01 |
7.53e-01 |
3.73e-01 |
Metabolism of water-soluble vitamins and cofactors |
101 |
5.28e-01 |
5.95e-01 |
0.1210 |
-0.081100 |
-7.96e-02 |
0.040000 |
-2.49e-03 |
1.60e-01 |
1.67e-01 |
4.88e-01 |
9.66e-01 |
Hemostasis |
444 |
5.08e-07 |
2.64e-06 |
0.1200 |
-0.017600 |
7.06e-02 |
-0.065000 |
7.07e-02 |
5.28e-01 |
1.14e-02 |
1.98e-02 |
1.13e-02 |
Vesicle-mediated transport |
557 |
3.60e-04 |
1.30e-03 |
0.1190 |
-0.047800 |
-9.89e-02 |
0.036600 |
2.60e-02 |
5.61e-02 |
7.67e-05 |
1.44e-01 |
2.99e-01 |
Antigen processing: Ubiquitination & Proteasome degradation |
268 |
6.55e-04 |
2.26e-03 |
0.1180 |
0.098500 |
-9.58e-03 |
0.054100 |
-3.40e-02 |
5.74e-03 |
7.88e-01 |
1.29e-01 |
3.41e-01 |
Membrane Trafficking |
528 |
2.38e-04 |
8.85e-04 |
0.1170 |
-0.039000 |
-1.05e-01 |
0.032400 |
1.37e-02 |
1.29e-01 |
4.49e-05 |
2.07e-01 |
5.93e-01 |
Rab regulation of trafficking |
113 |
3.08e-01 |
3.90e-01 |
0.1170 |
-0.020100 |
-9.18e-02 |
-0.008320 |
-6.85e-02 |
7.13e-01 |
9.23e-02 |
8.79e-01 |
2.09e-01 |
Signaling by WNT |
221 |
6.54e-02 |
1.14e-01 |
0.1150 |
-0.066700 |
-6.51e-02 |
0.056900 |
-3.63e-02 |
8.86e-02 |
9.65e-02 |
1.46e-01 |
3.54e-01 |
Axon guidance |
426 |
5.62e-03 |
1.56e-02 |
0.1130 |
0.016200 |
7.33e-02 |
0.024400 |
8.12e-02 |
5.68e-01 |
1.00e-02 |
3.92e-01 |
4.32e-03 |
Cytochrome P450 - arranged by substrate type |
30 |
8.07e-01 |
8.39e-01 |
0.1130 |
0.038300 |
2.86e-02 |
-0.029900 |
9.78e-02 |
7.16e-01 |
7.87e-01 |
7.77e-01 |
3.54e-01 |
Recycling pathway of L1 |
27 |
8.46e-01 |
8.73e-01 |
0.1130 |
-0.035000 |
-3.45e-02 |
0.027900 |
-9.74e-02 |
7.53e-01 |
7.56e-01 |
8.02e-01 |
3.81e-01 |
Adenylate cyclase inhibitory pathway |
12 |
9.25e-01 |
9.39e-01 |
0.1120 |
0.014300 |
-1.05e-01 |
-0.008840 |
3.52e-02 |
9.32e-01 |
5.28e-01 |
9.58e-01 |
8.33e-01 |
ESR-mediated signaling |
140 |
4.08e-01 |
4.92e-01 |
0.1120 |
-0.021100 |
-3.83e-02 |
-0.040600 |
-9.49e-02 |
6.67e-01 |
4.35e-01 |
4.08e-01 |
5.32e-02 |
Extra-nuclear estrogen signaling |
63 |
6.58e-01 |
7.05e-01 |
0.1110 |
0.032000 |
3.12e-02 |
-0.100000 |
-1.69e-02 |
6.60e-01 |
6.69e-01 |
1.69e-01 |
8.16e-01 |
Epigenetic regulation of gene expression |
84 |
3.34e-01 |
4.18e-01 |
0.1090 |
0.060100 |
1.20e-02 |
0.034900 |
-8.34e-02 |
3.42e-01 |
8.50e-01 |
5.81e-01 |
1.87e-01 |
Metabolism of vitamins and cofactors |
148 |
4.37e-01 |
5.15e-01 |
0.1090 |
-0.069800 |
-6.06e-02 |
0.047800 |
3.15e-02 |
1.43e-01 |
2.04e-01 |
3.17e-01 |
5.09e-01 |
Signaling by NOTCH |
159 |
4.60e-02 |
8.62e-02 |
0.1080 |
-0.042700 |
3.82e-02 |
0.091300 |
-1.21e-02 |
3.54e-01 |
4.07e-01 |
4.76e-02 |
7.93e-01 |
ERK/MAPK targets |
22 |
7.95e-01 |
8.31e-01 |
0.1070 |
0.042900 |
-8.17e-02 |
0.035500 |
-4.06e-02 |
7.28e-01 |
5.07e-01 |
7.73e-01 |
7.42e-01 |
Constitutive Signaling by Aberrant PI3K in Cancer |
53 |
5.09e-01 |
5.82e-01 |
0.1070 |
-0.019200 |
7.65e-03 |
-0.085000 |
6.13e-02 |
8.09e-01 |
9.23e-01 |
2.85e-01 |
4.41e-01 |
Chaperonin-mediated protein folding |
78 |
6.30e-01 |
6.82e-01 |
0.1050 |
0.037400 |
-1.46e-02 |
0.071700 |
6.59e-02 |
5.68e-01 |
8.24e-01 |
2.74e-01 |
3.15e-01 |
PI3K/AKT Signaling in Cancer |
79 |
7.81e-01 |
8.20e-01 |
0.1050 |
-0.016100 |
-4.84e-02 |
-0.069200 |
-6.04e-02 |
8.05e-01 |
4.57e-01 |
2.88e-01 |
3.54e-01 |
Cytokine Signaling in Immune system |
647 |
3.82e-03 |
1.11e-02 |
0.1050 |
0.048100 |
6.46e-02 |
0.008360 |
6.67e-02 |
3.92e-02 |
5.58e-03 |
7.20e-01 |
4.22e-03 |
Intra-Golgi and retrograde Golgi-to-ER traffic |
165 |
1.81e-01 |
2.56e-01 |
0.1040 |
-0.011900 |
-7.44e-02 |
0.058100 |
4.18e-02 |
7.93e-01 |
1.00e-01 |
1.99e-01 |
3.55e-01 |
Downregulation of ERBB2:ERBB3 signaling |
11 |
9.95e-01 |
9.96e-01 |
0.1030 |
-0.060200 |
-7.63e-02 |
-0.024100 |
-2.24e-02 |
7.30e-01 |
6.62e-01 |
8.90e-01 |
8.98e-01 |
Transport of small molecules |
477 |
2.29e-02 |
4.93e-02 |
0.1020 |
-0.042300 |
-5.41e-02 |
0.053400 |
5.41e-02 |
1.17e-01 |
4.47e-02 |
4.76e-02 |
4.48e-02 |
Diseases of signal transduction by growth factor receptors and second messengers |
330 |
1.45e-01 |
2.18e-01 |
0.1020 |
-0.047200 |
-7.26e-02 |
-0.017400 |
-5.19e-02 |
1.43e-01 |
2.43e-02 |
5.90e-01 |
1.07e-01 |
Signaling by ERBB4 |
43 |
8.06e-01 |
8.39e-01 |
0.1020 |
-0.034300 |
-7.82e-02 |
-0.047600 |
2.96e-02 |
6.98e-01 |
3.75e-01 |
5.89e-01 |
7.37e-01 |
Intracellular signaling by second messengers |
269 |
3.52e-02 |
6.93e-02 |
0.1010 |
-0.029100 |
-5.88e-02 |
0.034500 |
-6.88e-02 |
4.14e-01 |
9.83e-02 |
3.33e-01 |
5.32e-02 |
PIP3 activates AKT signaling |
232 |
1.85e-02 |
4.16e-02 |
0.0995 |
-0.000397 |
-2.54e-02 |
0.083200 |
-4.83e-02 |
9.92e-01 |
5.07e-01 |
2.97e-02 |
2.07e-01 |
Metabolic disorders of biological oxidation enzymes |
19 |
9.69e-01 |
9.77e-01 |
0.0995 |
-0.027100 |
-9.01e-02 |
-0.013500 |
-2.91e-02 |
8.38e-01 |
4.97e-01 |
9.19e-01 |
8.26e-01 |
Signal Transduction |
1705 |
9.55e-06 |
4.32e-05 |
0.0960 |
-0.053500 |
-3.53e-02 |
-0.062500 |
-3.48e-02 |
3.73e-04 |
1.90e-02 |
3.19e-05 |
2.08e-02 |
L1CAM interactions |
84 |
6.10e-01 |
6.65e-01 |
0.0957 |
-0.065400 |
-2.13e-02 |
-0.066400 |
5.58e-03 |
3.01e-01 |
7.36e-01 |
2.94e-01 |
9.30e-01 |
Metabolism of cofactors |
18 |
9.30e-01 |
9.43e-01 |
0.0940 |
0.007290 |
-8.38e-02 |
0.010400 |
4.06e-02 |
9.57e-01 |
5.38e-01 |
9.39e-01 |
7.65e-01 |
Metabolism of lipids |
566 |
3.55e-02 |
6.97e-02 |
0.0937 |
-0.028900 |
-1.09e-02 |
-0.067700 |
-5.69e-02 |
2.44e-01 |
6.59e-01 |
6.39e-03 |
2.19e-02 |
Toll-like Receptor Cascades |
132 |
3.23e-01 |
4.06e-01 |
0.0925 |
-0.031600 |
-5.67e-02 |
-0.043000 |
5.00e-02 |
5.32e-01 |
2.61e-01 |
3.94e-01 |
3.23e-01 |
Cytosolic sensors of pathogen-associated DNA |
57 |
5.65e-01 |
6.28e-01 |
0.0924 |
-0.034000 |
7.72e-02 |
0.033500 |
1.70e-02 |
6.57e-01 |
3.14e-01 |
6.62e-01 |
8.24e-01 |
Metabolism |
1569 |
5.59e-08 |
3.32e-07 |
0.0902 |
0.024400 |
1.89e-02 |
0.084700 |
3.50e-04 |
1.17e-01 |
2.25e-01 |
5.18e-08 |
9.82e-01 |
Signaling by Nuclear Receptors |
195 |
4.67e-01 |
5.43e-01 |
0.0884 |
0.000120 |
-9.06e-03 |
-0.039600 |
-7.85e-02 |
9.98e-01 |
8.28e-01 |
3.42e-01 |
5.97e-02 |
tRNA modification in the nucleus and cytosol |
38 |
9.34e-01 |
9.46e-01 |
0.0877 |
0.015700 |
4.03e-02 |
0.012200 |
7.54e-02 |
8.67e-01 |
6.67e-01 |
8.97e-01 |
4.22e-01 |
Clathrin-mediated endocytosis |
122 |
4.82e-01 |
5.56e-01 |
0.0869 |
-0.014100 |
-7.00e-02 |
0.048600 |
1.02e-02 |
7.89e-01 |
1.83e-01 |
3.55e-01 |
8.46e-01 |
VEGFR2 mediated vascular permeability |
27 |
9.27e-01 |
9.41e-01 |
0.0862 |
-0.001510 |
-7.88e-02 |
0.004130 |
-3.48e-02 |
9.89e-01 |
4.79e-01 |
9.70e-01 |
7.55e-01 |
Nervous system development |
444 |
3.22e-02 |
6.49e-02 |
0.0846 |
0.003590 |
5.68e-02 |
0.008110 |
6.21e-02 |
8.98e-01 |
4.16e-02 |
7.71e-01 |
2.61e-02 |
Disease |
1107 |
2.10e-03 |
6.56e-03 |
0.0802 |
0.007730 |
-7.40e-04 |
0.073000 |
3.23e-02 |
6.71e-01 |
9.68e-01 |
5.88e-05 |
7.53e-02 |
RNA Polymerase III Abortive And Retractive Initiation |
41 |
9.75e-01 |
9.81e-01 |
0.0783 |
0.021300 |
3.49e-02 |
0.054200 |
3.91e-02 |
8.14e-01 |
6.99e-01 |
5.48e-01 |
6.65e-01 |
RNA Polymerase III Transcription |
41 |
9.75e-01 |
9.81e-01 |
0.0783 |
0.021300 |
3.49e-02 |
0.054200 |
3.91e-02 |
8.14e-01 |
6.99e-01 |
5.48e-01 |
6.65e-01 |
Post-translational protein modification |
1100 |
5.24e-08 |
3.13e-07 |
0.0768 |
0.038200 |
-4.36e-02 |
0.041600 |
-2.84e-02 |
3.61e-02 |
1.67e-02 |
2.23e-02 |
1.19e-01 |
Tristetraprolin (TTP, ZFP36) binds and destabilizes mRNA |
16 |
9.63e-01 |
9.73e-01 |
0.0768 |
0.061500 |
-2.10e-02 |
-0.007720 |
4.02e-02 |
6.70e-01 |
8.85e-01 |
9.57e-01 |
7.81e-01 |
RAB GEFs exchange GTP for GDP on RABs |
83 |
7.05e-01 |
7.48e-01 |
0.0751 |
0.016400 |
-5.97e-02 |
-0.021000 |
-3.69e-02 |
7.97e-01 |
3.48e-01 |
7.41e-01 |
5.62e-01 |
RNA Polymerase III Transcription Initiation From Type 3 Promoter |
28 |
9.82e-01 |
9.86e-01 |
0.0741 |
-0.009120 |
2.60e-02 |
0.032300 |
6.08e-02 |
9.33e-01 |
8.12e-01 |
7.68e-01 |
5.78e-01 |
Signaling by Non-Receptor Tyrosine Kinases |
48 |
9.69e-01 |
9.77e-01 |
0.0623 |
-0.045400 |
-3.00e-02 |
-0.013900 |
2.69e-02 |
5.86e-01 |
7.19e-01 |
8.68e-01 |
7.47e-01 |
Signaling by PTK6 |
48 |
9.69e-01 |
9.77e-01 |
0.0623 |
-0.045400 |
-3.00e-02 |
-0.013900 |
2.69e-02 |
5.86e-01 |
7.19e-01 |
8.68e-01 |
7.47e-01 |
RNA Polymerase III Transcription Initiation |
36 |
9.87e-01 |
9.90e-01 |
0.0620 |
-0.011400 |
3.12e-03 |
0.053500 |
2.89e-02 |
9.06e-01 |
9.74e-01 |
5.79e-01 |
7.64e-01 |
PI5P, PP2A and IER3 Regulate PI3K/AKT Signaling |
80 |
9.56e-01 |
9.67e-01 |
0.0561 |
-0.027700 |
-4.38e-02 |
0.002630 |
2.12e-02 |
6.68e-01 |
4.99e-01 |
9.68e-01 |
7.43e-01 |
MAPK family signaling cascades |
261 |
8.77e-01 |
8.98e-01 |
0.0444 |
-0.035500 |
-1.64e-02 |
-0.013900 |
-1.60e-02 |
3.26e-01 |
6.51e-01 |
7.00e-01 |
6.58e-01 |
Negative regulation of the PI3K/AKT network |
87 |
9.92e-01 |
9.94e-01 |
0.0326 |
-0.009560 |
-2.97e-02 |
-0.007010 |
-6.62e-03 |
8.78e-01 |
6.33e-01 |
9.10e-01 |
9.15e-01 |
FLT3 Signaling |
237 |
9.78e-01 |
9.84e-01 |
0.0309 |
-0.024800 |
-1.77e-02 |
-0.000691 |
-4.97e-03 |
5.12e-01 |
6.41e-01 |
9.85e-01 |
8.96e-01 |
Developmental Biology |
665 |
8.15e-01 |
8.46e-01 |
0.0293 |
-0.003530 |
1.45e-02 |
0.012900 |
2.16e-02 |
8.78e-01 |
5.27e-01 |
5.74e-01 |
3.48e-01 |
RAF/MAP kinase cascade |
223 |
9.93e-01 |
9.95e-01 |
0.0166 |
-0.014400 |
-8.62e-04 |
0.001380 |
8.14e-03 |
7.13e-01 |
9.82e-01 |
9.72e-01 |
8.35e-01 |
MAPK1/MAPK3 signaling |
228 |
9.96e-01 |
9.96e-01 |
0.0131 |
-0.009940 |
2.14e-03 |
0.000839 |
8.28e-03 |
7.97e-01 |
9.56e-01 |
9.83e-01 |
8.30e-01 |