| IRAK4 deficiency (TLR2/4) |
10 |
1.45e-06 |
9.18e-06 |
1.19000 |
0.813000 |
0.875000 |
8.51e-06 |
1.65e-06 |
| MyD88 deficiency (TLR2/4) |
10 |
1.45e-06 |
9.18e-06 |
1.19000 |
0.813000 |
0.875000 |
8.51e-06 |
1.65e-06 |
| Regulation of TLR by endogenous ligand |
11 |
4.26e-06 |
2.48e-05 |
1.09000 |
0.798000 |
0.746000 |
4.59e-06 |
1.81e-05 |
| alpha-linolenic (omega3) and linoleic (omega6) acid metabolism |
12 |
2.22e-06 |
1.37e-05 |
1.07000 |
0.713000 |
0.798000 |
1.90e-05 |
1.69e-06 |
| alpha-linolenic acid (ALA) metabolism |
12 |
2.22e-06 |
1.37e-05 |
1.07000 |
0.713000 |
0.798000 |
1.90e-05 |
1.69e-06 |
| Translocation of ZAP-70 to Immunological synapse |
24 |
2.61e-11 |
4.87e-10 |
0.98700 |
-0.550000 |
-0.819000 |
3.10e-06 |
3.60e-12 |
| Erythrocytes take up carbon dioxide and release oxygen |
11 |
1.14e-04 |
4.96e-04 |
0.93800 |
0.670000 |
0.656000 |
1.19e-04 |
1.64e-04 |
| O2/CO2 exchange in erythrocytes |
11 |
1.14e-04 |
4.96e-04 |
0.93800 |
0.670000 |
0.656000 |
1.19e-04 |
1.64e-04 |
| Hyaluronan uptake and degradation |
12 |
6.18e-05 |
2.86e-04 |
0.90000 |
0.537000 |
0.722000 |
1.29e-03 |
1.48e-05 |
| Uptake and function of anthrax toxins |
10 |
5.79e-04 |
2.15e-03 |
0.86500 |
0.518000 |
0.693000 |
4.59e-03 |
1.47e-04 |
| WNT5A-dependent internalization of FZD2, FZD5 and ROR2 |
11 |
1.17e-04 |
5.01e-04 |
0.84200 |
0.403000 |
0.739000 |
2.06e-02 |
2.17e-05 |
| Advanced glycosylation endproduct receptor signaling |
12 |
2.06e-04 |
8.37e-04 |
0.84100 |
0.501000 |
0.676000 |
2.65e-03 |
5.01e-05 |
| p130Cas linkage to MAPK signaling for integrins |
11 |
8.77e-04 |
3.11e-03 |
0.82400 |
0.560000 |
0.605000 |
1.31e-03 |
5.14e-04 |
| Detoxification of Reactive Oxygen Species |
31 |
4.79e-09 |
4.60e-08 |
0.80700 |
0.605000 |
0.533000 |
5.35e-09 |
2.73e-07 |
| ROS and RNS production in phagocytes |
31 |
4.57e-09 |
4.45e-08 |
0.80600 |
0.610000 |
0.528000 |
4.14e-09 |
3.65e-07 |
| Unwinding of DNA |
12 |
4.92e-04 |
1.85e-03 |
0.80400 |
-0.492000 |
-0.635000 |
3.17e-03 |
1.38e-04 |
| Insulin receptor recycling |
21 |
3.68e-06 |
2.16e-05 |
0.79700 |
0.568000 |
0.559000 |
6.62e-06 |
9.21e-06 |
| PD-1 signaling |
28 |
2.29e-09 |
2.38e-08 |
0.78100 |
-0.372000 |
-0.687000 |
6.63e-04 |
3.12e-10 |
| Neutrophil degranulation |
456 |
5.75e-107 |
7.84e-104 |
0.76000 |
0.536000 |
0.539000 |
3.01e-86 |
2.42e-87 |
| Phosphorylation of CD3 and TCR zeta chains |
27 |
2.34e-07 |
1.73e-06 |
0.75800 |
-0.463000 |
-0.600000 |
3.13e-05 |
6.63e-08 |
| Dissolution of Fibrin Clot |
12 |
1.32e-03 |
4.50e-03 |
0.75600 |
0.479000 |
0.585000 |
4.08e-03 |
4.47e-04 |
| GRB2:SOS provides linkage to MAPK signaling for Integrins |
12 |
1.70e-03 |
5.57e-03 |
0.75200 |
0.540000 |
0.524000 |
1.20e-03 |
1.67e-03 |
| Golgi Cisternae Pericentriolar Stack Reorganization |
14 |
6.29e-04 |
2.32e-03 |
0.74900 |
0.519000 |
0.540000 |
7.78e-04 |
4.69e-04 |
| NOTCH4 Activation and Transmission of Signal to the Nucleus |
10 |
4.88e-03 |
1.44e-02 |
0.74300 |
0.471000 |
0.574000 |
9.91e-03 |
1.67e-03 |
| HuR (ELAVL1) binds and stabilizes mRNA |
10 |
5.50e-03 |
1.60e-02 |
0.73000 |
0.573000 |
0.452000 |
1.70e-03 |
1.32e-02 |
| Signaling by Leptin |
10 |
6.91e-03 |
1.94e-02 |
0.72800 |
0.523000 |
0.507000 |
4.21e-03 |
5.54e-03 |
| COPI-independent Golgi-to-ER retrograde traffic |
33 |
1.39e-08 |
1.23e-07 |
0.72600 |
0.406000 |
0.602000 |
5.34e-05 |
2.14e-09 |
| RHO GTPases Activate WASPs and WAVEs |
35 |
1.28e-08 |
1.14e-07 |
0.72000 |
0.425000 |
0.580000 |
1.32e-05 |
2.78e-09 |
| RHO GTPases Activate NADPH Oxidases |
21 |
4.40e-05 |
2.13e-04 |
0.70600 |
0.453000 |
0.541000 |
3.24e-04 |
1.78e-05 |
| PTK6 Regulates RHO GTPases, RAS GTPase and MAP kinases |
13 |
5.42e-04 |
2.04e-03 |
0.70200 |
0.331000 |
0.619000 |
3.86e-02 |
1.10e-04 |
| Transferrin endocytosis and recycling |
26 |
6.00e-06 |
3.41e-05 |
0.70100 |
0.481000 |
0.510000 |
2.15e-05 |
6.73e-06 |
| Cargo concentration in the ER |
30 |
5.35e-07 |
3.74e-06 |
0.69900 |
0.425000 |
0.555000 |
5.63e-05 |
1.44e-07 |
| Budding and maturation of HIV virion |
26 |
7.33e-06 |
4.06e-05 |
0.69600 |
0.480000 |
0.503000 |
2.23e-05 |
8.90e-06 |
| Endosomal Sorting Complex Required For Transport (ESCRT) |
29 |
2.53e-06 |
1.56e-05 |
0.68800 |
0.489000 |
0.484000 |
5.07e-06 |
6.42e-06 |
| Cross-presentation of soluble exogenous antigens (endosomes) |
47 |
1.46e-10 |
2.23e-09 |
0.68800 |
0.562000 |
0.397000 |
2.57e-11 |
2.46e-06 |
| The NLRP3 inflammasome |
15 |
7.59e-04 |
2.74e-03 |
0.68700 |
0.560000 |
0.398000 |
1.75e-04 |
7.62e-03 |
| Regulation of ornithine decarboxylase (ODC) |
49 |
6.29e-11 |
1.09e-09 |
0.68300 |
0.562000 |
0.387000 |
9.77e-12 |
2.70e-06 |
| Formation of ATP by chemiosmotic coupling |
18 |
3.96e-04 |
1.52e-03 |
0.68000 |
0.466000 |
0.495000 |
6.13e-04 |
2.76e-04 |
| EPHB-mediated forward signaling |
32 |
1.00e-06 |
6.70e-06 |
0.67800 |
0.493000 |
0.465000 |
1.40e-06 |
5.27e-06 |
| Diseases associated with the TLR signaling cascade |
23 |
6.14e-05 |
2.85e-04 |
0.67000 |
0.484000 |
0.464000 |
5.95e-05 |
1.18e-04 |
| Diseases of Immune System |
23 |
6.14e-05 |
2.85e-04 |
0.67000 |
0.484000 |
0.464000 |
5.95e-05 |
1.18e-04 |
| MET activates RAP1 and RAC1 |
10 |
6.88e-03 |
1.94e-02 |
0.66800 |
0.338000 |
0.576000 |
6.44e-02 |
1.60e-03 |
| Hh mutants that don’t undergo autocatalytic processing are degraded by ERAD |
53 |
3.67e-11 |
6.67e-10 |
0.66800 |
0.545000 |
0.386000 |
6.52e-12 |
1.17e-06 |
| Regulation of activated PAK-2p34 by proteasome mediated degradation |
48 |
2.60e-10 |
3.62e-09 |
0.66300 |
0.552000 |
0.367000 |
3.56e-11 |
1.11e-05 |
| Platelet sensitization by LDL |
16 |
3.03e-04 |
1.19e-03 |
0.66200 |
0.319000 |
0.580000 |
2.69e-02 |
5.85e-05 |
| IRAK1 recruits IKK complex |
10 |
8.50e-03 |
2.34e-02 |
0.65900 |
0.340000 |
0.564000 |
6.25e-02 |
2.02e-03 |
| IRAK1 recruits IKK complex upon TLR7/8 or 9 stimulation |
10 |
8.50e-03 |
2.34e-02 |
0.65900 |
0.340000 |
0.564000 |
6.25e-02 |
2.02e-03 |
| Pentose phosphate pathway |
13 |
5.13e-03 |
1.50e-02 |
0.65500 |
0.438000 |
0.487000 |
6.22e-03 |
2.38e-03 |
| Regulation of Apoptosis |
51 |
9.12e-11 |
1.50e-09 |
0.65300 |
0.549000 |
0.353000 |
1.13e-11 |
1.26e-05 |
| AUF1 (hnRNP D0) binds and destabilizes mRNA |
53 |
1.33e-10 |
2.07e-09 |
0.64100 |
0.533000 |
0.356000 |
1.85e-11 |
7.13e-06 |
| Hh mutants abrogate ligand secretion |
54 |
1.81e-10 |
2.65e-09 |
0.63700 |
0.523000 |
0.363000 |
2.95e-11 |
3.84e-06 |
| Inflammasomes |
20 |
1.23e-04 |
5.29e-04 |
0.63500 |
0.548000 |
0.322000 |
2.21e-05 |
1.27e-02 |
| Butyrophilin (BTN) family interactions |
10 |
1.31e-02 |
3.41e-02 |
0.63500 |
-0.339000 |
-0.537000 |
6.38e-02 |
3.27e-03 |
| Generation of second messenger molecules |
38 |
4.49e-08 |
3.69e-07 |
0.63400 |
-0.324000 |
-0.545000 |
5.52e-04 |
5.99e-09 |
| Ubiquitin Mediated Degradation of Phosphorylated Cdc25A |
50 |
6.52e-10 |
7.87e-09 |
0.63100 |
0.531000 |
0.341000 |
8.37e-11 |
3.01e-05 |
| p53-Independent DNA Damage Response |
50 |
6.52e-10 |
7.87e-09 |
0.63100 |
0.531000 |
0.341000 |
8.37e-11 |
3.01e-05 |
| p53-Independent G1/S DNA damage checkpoint |
50 |
6.52e-10 |
7.87e-09 |
0.63100 |
0.531000 |
0.341000 |
8.37e-11 |
3.01e-05 |
| Smooth Muscle Contraction |
30 |
1.08e-05 |
5.75e-05 |
0.63100 |
0.406000 |
0.483000 |
1.18e-04 |
4.74e-06 |
| Vif-mediated degradation of APOBEC3G |
52 |
4.96e-10 |
6.32e-09 |
0.63000 |
0.522000 |
0.353000 |
7.29e-11 |
1.05e-05 |
| Defective CFTR causes cystic fibrosis |
58 |
9.45e-11 |
1.53e-09 |
0.63000 |
0.509000 |
0.372000 |
2.04e-11 |
9.73e-07 |
| ATF6 (ATF6-alpha) activates chaperone genes |
10 |
1.12e-02 |
2.98e-02 |
0.62600 |
0.546000 |
0.306000 |
2.76e-03 |
9.36e-02 |
| FBXL7 down-regulates AURKA during mitotic entry and in early mitosis |
52 |
4.62e-10 |
6.00e-09 |
0.62500 |
0.524000 |
0.339000 |
5.98e-11 |
2.29e-05 |
| Interleukin-1 signaling |
97 |
4.68e-16 |
2.13e-14 |
0.61900 |
0.467000 |
0.406000 |
1.77e-15 |
4.61e-12 |
| Vpu mediated degradation of CD4 |
50 |
1.44e-09 |
1.60e-08 |
0.61800 |
0.521000 |
0.334000 |
1.87e-10 |
4.41e-05 |
| RNA Polymerase I Promoter Opening |
19 |
1.59e-04 |
6.63e-04 |
0.61800 |
0.280000 |
0.551000 |
3.43e-02 |
3.22e-05 |
| Degradation of GLI2 by the proteasome |
56 |
2.30e-10 |
3.26e-09 |
0.61800 |
0.512000 |
0.346000 |
3.32e-11 |
7.62e-06 |
| GLI3 is processed to GLI3R by the proteasome |
56 |
2.30e-10 |
3.26e-09 |
0.61800 |
0.512000 |
0.346000 |
3.32e-11 |
7.62e-06 |
| MAP2K and MAPK activation |
34 |
2.70e-06 |
1.63e-05 |
0.61600 |
0.370000 |
0.493000 |
1.86e-04 |
6.56e-07 |
| Negative regulation of NOTCH4 signaling |
54 |
5.24e-10 |
6.61e-09 |
0.61300 |
0.513000 |
0.335000 |
6.95e-11 |
2.03e-05 |
| Hedgehog ligand biogenesis |
58 |
2.71e-10 |
3.71e-09 |
0.61300 |
0.498000 |
0.356000 |
5.09e-11 |
2.70e-06 |
| Negative regulation of MET activity |
18 |
1.23e-03 |
4.19e-03 |
0.61200 |
0.368000 |
0.489000 |
6.88e-03 |
3.24e-04 |
| Translation of Replicase and Assembly of the Replication Transcription Complex |
12 |
1.49e-02 |
3.81e-02 |
0.60900 |
0.450000 |
0.410000 |
6.95e-03 |
1.38e-02 |
| NIK–>noncanonical NF-kB signaling |
57 |
1.30e-10 |
2.04e-09 |
0.60800 |
0.516000 |
0.321000 |
1.54e-11 |
2.68e-05 |
| Antimicrobial peptides |
33 |
1.16e-06 |
7.65e-06 |
0.60600 |
0.525000 |
0.302000 |
1.73e-07 |
2.70e-03 |
| Ubiquitin-dependent degradation of Cyclin D |
50 |
4.17e-09 |
4.12e-08 |
0.60400 |
0.507000 |
0.328000 |
5.64e-10 |
5.93e-05 |
| Folding of actin by CCT/TriC |
10 |
4.78e-03 |
1.42e-02 |
0.60300 |
0.570000 |
0.197000 |
1.81e-03 |
2.80e-01 |
| InlB-mediated entry of Listeria monocytogenes into host cell |
12 |
1.65e-02 |
4.16e-02 |
0.60200 |
0.409000 |
0.442000 |
1.42e-02 |
7.99e-03 |
| Metabolism of polyamines |
57 |
1.84e-10 |
2.67e-09 |
0.60000 |
0.512000 |
0.312000 |
2.16e-11 |
4.49e-05 |
| Cytochrome c-mediated apoptotic response |
13 |
1.06e-02 |
2.86e-02 |
0.60000 |
0.467000 |
0.376000 |
3.52e-03 |
1.89e-02 |
| Formation of apoptosome |
11 |
2.41e-02 |
5.48e-02 |
0.60000 |
0.438000 |
0.410000 |
1.19e-02 |
1.86e-02 |
| Regulation of the apoptosome activity |
11 |
2.41e-02 |
5.48e-02 |
0.60000 |
0.438000 |
0.410000 |
1.19e-02 |
1.86e-02 |
| Degradation of GLI1 by the proteasome |
57 |
6.15e-10 |
7.63e-09 |
0.59900 |
0.496000 |
0.336000 |
9.16e-11 |
1.11e-05 |
| RHO GTPases activate IQGAPs |
11 |
1.03e-02 |
2.77e-02 |
0.59800 |
0.285000 |
0.526000 |
1.02e-01 |
2.54e-03 |
| mTORC1-mediated signalling |
24 |
3.24e-04 |
1.27e-03 |
0.59700 |
0.430000 |
0.414000 |
2.67e-04 |
4.40e-04 |
| Hyaluronan metabolism |
15 |
2.73e-03 |
8.58e-03 |
0.59700 |
0.306000 |
0.512000 |
4.02e-02 |
5.91e-04 |
| Deregulated CDK5 triggers multiple neurodegenerative pathways in Alzheimer’s disease models |
20 |
8.61e-04 |
3.06e-03 |
0.59400 |
0.353000 |
0.478000 |
6.33e-03 |
2.15e-04 |
| Neurodegenerative Diseases |
20 |
8.61e-04 |
3.06e-03 |
0.59400 |
0.353000 |
0.478000 |
6.33e-03 |
2.15e-04 |
| GRB2 events in EGFR signaling |
10 |
2.82e-02 |
6.20e-02 |
0.59400 |
0.346000 |
0.483000 |
5.84e-02 |
8.22e-03 |
| SHC1 events in EGFR signaling |
11 |
1.95e-02 |
4.62e-02 |
0.59300 |
0.343000 |
0.484000 |
4.85e-02 |
5.45e-03 |
| Dectin-1 mediated noncanonical NF-kB signaling |
58 |
2.75e-10 |
3.71e-09 |
0.59300 |
0.503000 |
0.314000 |
3.31e-11 |
3.56e-05 |
| Retrograde neurotrophin signalling |
12 |
5.63e-03 |
1.63e-02 |
0.59200 |
0.260000 |
0.532000 |
1.19e-01 |
1.43e-03 |
| Degradation of DVL |
54 |
5.38e-09 |
5.09e-08 |
0.58900 |
0.481000 |
0.340000 |
9.71e-10 |
1.53e-05 |
| Signaling by high-kinase activity BRAF mutants |
31 |
2.36e-05 |
1.18e-04 |
0.58700 |
0.349000 |
0.471000 |
7.60e-04 |
5.52e-06 |
| The role of GTSE1 in G2/M progression after G2 checkpoint |
58 |
3.09e-10 |
4.13e-09 |
0.58500 |
0.502000 |
0.301000 |
3.64e-11 |
7.50e-05 |
| activated TAK1 mediates p38 MAPK activation |
19 |
1.40e-03 |
4.72e-03 |
0.58400 |
0.338000 |
0.476000 |
1.07e-02 |
3.31e-04 |
| Autodegradation of the E3 ubiquitin ligase COP1 |
49 |
1.44e-08 |
1.27e-07 |
0.58300 |
0.496000 |
0.307000 |
1.89e-09 |
2.00e-04 |
| Antigen processing-Cross presentation |
97 |
1.34e-14 |
5.09e-13 |
0.58100 |
0.457000 |
0.360000 |
7.43e-15 |
9.10e-10 |
| Regulation of IFNG signaling |
14 |
1.23e-02 |
3.22e-02 |
0.57800 |
0.401000 |
0.417000 |
9.41e-03 |
6.92e-03 |
| SCF-beta-TrCP mediated degradation of Emi1 |
53 |
2.78e-09 |
2.85e-08 |
0.57700 |
0.498000 |
0.292000 |
3.46e-10 |
2.35e-04 |
| Trafficking of GluR2-containing AMPA receptors |
12 |
4.26e-04 |
1.62e-03 |
0.57700 |
0.081700 |
0.571000 |
6.24e-01 |
6.10e-04 |
| Oxygen-dependent proline hydroxylation of Hypoxia-inducible Factor Alpha |
64 |
1.37e-09 |
1.53e-08 |
0.57600 |
0.444000 |
0.367000 |
8.09e-10 |
3.83e-07 |
| Activation of the AP-1 family of transcription factors |
10 |
4.28e-02 |
8.67e-02 |
0.57500 |
0.435000 |
0.377000 |
1.73e-02 |
3.92e-02 |
| Platelet degranulation |
104 |
5.72e-15 |
2.36e-13 |
0.57200 |
0.363000 |
0.442000 |
1.51e-10 |
6.13e-15 |
| ATF6 (ATF6-alpha) activates chaperones |
12 |
2.09e-02 |
4.88e-02 |
0.56900 |
0.456000 |
0.341000 |
6.24e-03 |
4.10e-02 |
| Response to elevated platelet cytosolic Ca2+ |
108 |
1.77e-15 |
7.55e-14 |
0.56900 |
0.353000 |
0.446000 |
2.17e-10 |
1.17e-15 |
| Apoptotic factor-mediated response |
18 |
2.13e-03 |
6.85e-03 |
0.56900 |
0.476000 |
0.310000 |
4.66e-04 |
2.27e-02 |
| Late endosomal microautophagy |
29 |
1.52e-04 |
6.38e-04 |
0.56800 |
0.413000 |
0.390000 |
1.18e-04 |
2.81e-04 |
| Response of EIF2AK1 (HRI) to heme deficiency |
14 |
3.56e-03 |
1.09e-02 |
0.56700 |
0.512000 |
0.243000 |
9.04e-04 |
1.16e-01 |
| Signal transduction by L1 |
20 |
3.61e-04 |
1.40e-03 |
0.56500 |
0.246000 |
0.509000 |
5.72e-02 |
8.12e-05 |
| Cellular response to hypoxia |
71 |
5.74e-10 |
7.17e-09 |
0.56500 |
0.412000 |
0.386000 |
1.84e-09 |
1.87e-08 |
| Signal regulatory protein family interactions |
12 |
2.83e-02 |
6.21e-02 |
0.56200 |
0.390000 |
0.405000 |
1.93e-02 |
1.51e-02 |
| Synthesis of active ubiquitin: roles of E1 and E2 enzymes |
30 |
1.35e-04 |
5.70e-04 |
0.56100 |
0.416000 |
0.375000 |
7.86e-05 |
3.74e-04 |
| ER-Phagosome pathway |
82 |
6.25e-12 |
1.44e-10 |
0.55900 |
0.453000 |
0.328000 |
1.28e-12 |
2.87e-07 |
| Lysosome Vesicle Biogenesis |
32 |
5.17e-05 |
2.45e-04 |
0.55900 |
0.338000 |
0.445000 |
9.37e-04 |
1.33e-05 |
| Interleukin-6 signaling |
10 |
5.19e-02 |
1.01e-01 |
0.55800 |
0.420000 |
0.368000 |
2.16e-02 |
4.41e-02 |
| Mitochondrial iron-sulfur cluster biogenesis |
13 |
3.51e-03 |
1.07e-02 |
0.55600 |
0.520000 |
0.197000 |
1.18e-03 |
2.19e-01 |
| COPI-mediated anterograde transport |
78 |
5.18e-11 |
9.29e-10 |
0.55500 |
0.338000 |
0.441000 |
2.53e-07 |
1.62e-11 |
| Metabolism of Angiotensinogen to Angiotensins |
11 |
9.60e-03 |
2.60e-02 |
0.55500 |
0.515000 |
0.205000 |
3.09e-03 |
2.38e-01 |
| RHO GTPases Activate ROCKs |
18 |
2.84e-03 |
8.87e-03 |
0.55200 |
0.297000 |
0.466000 |
2.93e-02 |
6.26e-04 |
| Cristae formation |
31 |
1.07e-04 |
4.74e-04 |
0.55000 |
0.431000 |
0.342000 |
3.24e-05 |
9.91e-04 |
| IRAK2 mediated activation of TAK1 complex upon TLR7/8 or 9 stimulation |
15 |
1.44e-02 |
3.69e-02 |
0.54900 |
0.397000 |
0.379000 |
7.83e-03 |
1.10e-02 |
| Autodegradation of Cdh1 by Cdh1:APC/C |
64 |
8.68e-10 |
1.00e-08 |
0.54700 |
0.467000 |
0.286000 |
1.06e-10 |
7.53e-05 |
| MyD88:MAL(TIRAP) cascade initiated on plasma membrane |
92 |
3.97e-12 |
9.49e-11 |
0.54700 |
0.353000 |
0.417000 |
4.95e-09 |
4.38e-12 |
| Toll Like Receptor 2 (TLR2) Cascade |
92 |
3.97e-12 |
9.49e-11 |
0.54700 |
0.353000 |
0.417000 |
4.95e-09 |
4.38e-12 |
| Toll Like Receptor TLR1:TLR2 Cascade |
92 |
3.97e-12 |
9.49e-11 |
0.54700 |
0.353000 |
0.417000 |
4.95e-09 |
4.38e-12 |
| Toll Like Receptor TLR6:TLR2 Cascade |
92 |
3.97e-12 |
9.49e-11 |
0.54700 |
0.353000 |
0.417000 |
4.95e-09 |
4.38e-12 |
| APC/C:Cdc20 mediated degradation of Securin |
66 |
9.94e-10 |
1.13e-08 |
0.54200 |
0.458000 |
0.290000 |
1.26e-10 |
4.54e-05 |
| Degradation of AXIN |
53 |
7.74e-08 |
6.10e-07 |
0.54100 |
0.453000 |
0.294000 |
1.12e-08 |
2.09e-04 |
| COPII-mediated vesicle transport |
65 |
2.83e-09 |
2.88e-08 |
0.54000 |
0.302000 |
0.448000 |
2.50e-05 |
4.23e-10 |
| WNT5A-dependent internalization of FZD4 |
13 |
1.81e-03 |
5.91e-03 |
0.54000 |
0.133000 |
0.523000 |
4.05e-01 |
1.09e-03 |
| Stabilization of p53 |
54 |
5.25e-08 |
4.28e-07 |
0.53900 |
0.455000 |
0.290000 |
7.34e-09 |
2.26e-04 |
| CD22 mediated BCR regulation |
58 |
2.23e-20 |
1.90e-18 |
0.53900 |
0.069000 |
-0.534000 |
3.63e-01 |
1.87e-12 |
| Response of Mtb to phagocytosis |
22 |
2.58e-03 |
8.15e-03 |
0.53700 |
0.378000 |
0.382000 |
2.12e-03 |
1.94e-03 |
| RHO GTPases activate KTN1 |
11 |
5.06e-02 |
9.85e-02 |
0.53700 |
0.368000 |
0.391000 |
3.48e-02 |
2.46e-02 |
| DNA strand elongation |
32 |
3.43e-06 |
2.03e-05 |
0.53700 |
-0.201000 |
-0.498000 |
4.96e-02 |
1.09e-06 |
| Pyrimidine salvage |
10 |
6.60e-02 |
1.22e-01 |
0.53600 |
0.397000 |
0.360000 |
2.96e-02 |
4.85e-02 |
| Spry regulation of FGF signaling |
16 |
8.44e-03 |
2.34e-02 |
0.53500 |
0.297000 |
0.444000 |
3.96e-02 |
2.08e-03 |
| ABC transporter disorders |
69 |
3.39e-09 |
3.37e-08 |
0.53400 |
0.427000 |
0.321000 |
8.59e-10 |
4.05e-06 |
| Josephin domain DUBs |
10 |
6.87e-02 |
1.27e-01 |
0.53400 |
0.369000 |
0.386000 |
4.33e-02 |
3.47e-02 |
| Infection with Mycobacterium tuberculosis |
26 |
9.89e-04 |
3.42e-03 |
0.53200 |
0.385000 |
0.367000 |
6.72e-04 |
1.19e-03 |
| VLDLR internalisation and degradation |
11 |
9.92e-03 |
2.68e-02 |
0.53200 |
0.171000 |
0.503000 |
3.26e-01 |
3.83e-03 |
| Cell recruitment (pro-inflammatory response) |
22 |
9.65e-04 |
3.35e-03 |
0.53100 |
0.459000 |
0.267000 |
1.95e-04 |
3.02e-02 |
| Purinergic signaling in leishmaniasis infection |
22 |
9.65e-04 |
3.35e-03 |
0.53100 |
0.459000 |
0.267000 |
1.95e-04 |
3.02e-02 |
| Signaling by RAF1 mutants |
34 |
1.04e-04 |
4.67e-04 |
0.53000 |
0.339000 |
0.407000 |
6.23e-04 |
3.97e-05 |
| Regulation of PTEN stability and activity |
66 |
2.68e-08 |
2.24e-07 |
0.52800 |
0.395000 |
0.351000 |
2.84e-08 |
8.12e-07 |
| Regulation of mRNA stability by proteins that bind AU-rich elements |
87 |
8.27e-12 |
1.85e-10 |
0.52800 |
0.442000 |
0.289000 |
1.03e-12 |
3.15e-06 |
| CDT1 association with the CDC6:ORC:origin complex |
57 |
1.64e-08 |
1.43e-07 |
0.52700 |
0.458000 |
0.261000 |
2.18e-09 |
6.58e-04 |
| MET activates RAS signaling |
10 |
7.02e-02 |
1.29e-01 |
0.52300 |
0.407000 |
0.328000 |
2.57e-02 |
7.23e-02 |
| Regulation of RUNX3 expression and activity |
55 |
2.11e-07 |
1.59e-06 |
0.52300 |
0.429000 |
0.299000 |
3.75e-08 |
1.26e-04 |
| ER to Golgi Anterograde Transport |
129 |
4.01e-16 |
1.88e-14 |
0.52200 |
0.304000 |
0.424000 |
2.52e-09 |
8.03e-17 |
| Activation of NF-kappaB in B cells |
65 |
1.90e-08 |
1.62e-07 |
0.52100 |
0.423000 |
0.304000 |
3.71e-09 |
2.28e-05 |
| Assembly Of The HIV Virion |
15 |
2.27e-02 |
5.23e-02 |
0.51900 |
0.365000 |
0.368000 |
1.43e-02 |
1.36e-02 |
| Iron uptake and transport |
52 |
1.86e-06 |
1.17e-05 |
0.51900 |
0.384000 |
0.348000 |
1.62e-06 |
1.41e-05 |
| Gap junction trafficking |
13 |
1.78e-02 |
4.42e-02 |
0.51800 |
0.250000 |
0.454000 |
1.18e-01 |
4.61e-03 |
| APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins in late mitosis/early G1 |
72 |
1.71e-09 |
1.86e-08 |
0.51700 |
0.432000 |
0.285000 |
2.38e-10 |
2.83e-05 |
| Classical antibody-mediated complement activation |
68 |
3.04e-23 |
4.60e-21 |
0.51700 |
0.098600 |
-0.507000 |
1.60e-01 |
4.48e-13 |
| Energy dependent regulation of mTOR by LKB1-AMPK |
27 |
1.04e-03 |
3.58e-03 |
0.51300 |
0.326000 |
0.397000 |
3.41e-03 |
3.54e-04 |
| Scavenging of heme from plasma |
70 |
3.83e-27 |
7.46e-25 |
0.51300 |
0.192000 |
-0.476000 |
5.38e-03 |
5.82e-12 |
| Alpha-protein kinase 1 signaling pathway |
11 |
5.94e-02 |
1.14e-01 |
0.51300 |
0.402000 |
0.318000 |
2.08e-02 |
6.81e-02 |
| trans-Golgi Network Vesicle Budding |
69 |
4.62e-09 |
4.46e-08 |
0.50800 |
0.269000 |
0.431000 |
1.13e-04 |
5.92e-10 |
| Regulation of glycolysis by fructose 2,6-bisphosphate metabolism |
11 |
4.03e-02 |
8.29e-02 |
0.50800 |
0.251000 |
0.441000 |
1.49e-01 |
1.13e-02 |
| Erythropoietin activates RAS |
13 |
4.31e-02 |
8.72e-02 |
0.50700 |
0.346000 |
0.371000 |
3.10e-02 |
2.07e-02 |
| RUNX1 regulates transcription of genes involved in differentiation of HSCs |
82 |
2.77e-09 |
2.85e-08 |
0.50700 |
0.361000 |
0.356000 |
1.63e-08 |
2.51e-08 |
| Integrin signaling |
22 |
1.65e-03 |
5.43e-03 |
0.50600 |
0.249000 |
0.440000 |
4.34e-02 |
3.48e-04 |
| GAB1 signalosome |
14 |
2.64e-03 |
8.34e-03 |
0.50500 |
0.126000 |
0.489000 |
4.15e-01 |
1.52e-03 |
| Cdc20:Phospho-APC/C mediated degradation of Cyclin A |
71 |
8.51e-10 |
9.91e-09 |
0.50400 |
0.442000 |
0.240000 |
1.13e-10 |
4.58e-04 |
| Effects of PIP2 hydrolysis |
24 |
4.50e-04 |
1.71e-03 |
0.50300 |
-0.457000 |
-0.212000 |
1.08e-04 |
7.23e-02 |
| Respiratory electron transport |
101 |
1.86e-11 |
3.76e-10 |
0.50300 |
0.391000 |
0.317000 |
1.08e-11 |
3.80e-08 |
| SCF(Skp2)-mediated degradation of p27/p21 |
60 |
2.96e-08 |
2.46e-07 |
0.50300 |
0.439000 |
0.246000 |
4.06e-09 |
9.92e-04 |
| Collagen degradation |
28 |
3.93e-04 |
1.51e-03 |
0.50300 |
0.256000 |
0.432000 |
1.88e-02 |
7.48e-05 |
| Prolonged ERK activation events |
13 |
2.21e-02 |
5.10e-02 |
0.50300 |
0.241000 |
0.441000 |
1.33e-01 |
5.85e-03 |
| Paradoxical activation of RAF signaling by kinase inactive BRAF |
38 |
1.15e-04 |
4.96e-04 |
0.50300 |
0.337000 |
0.373000 |
3.30e-04 |
6.79e-05 |
| Signaling by RAS mutants |
38 |
1.15e-04 |
4.96e-04 |
0.50300 |
0.337000 |
0.373000 |
3.30e-04 |
6.79e-05 |
| Signaling by moderate kinase activity BRAF mutants |
38 |
1.15e-04 |
4.96e-04 |
0.50300 |
0.337000 |
0.373000 |
3.30e-04 |
6.79e-05 |
| Signaling downstream of RAS mutants |
38 |
1.15e-04 |
4.96e-04 |
0.50300 |
0.337000 |
0.373000 |
3.30e-04 |
6.79e-05 |
| Platelet Adhesion to exposed collagen |
13 |
4.11e-02 |
8.42e-02 |
0.50200 |
0.313000 |
0.392000 |
5.04e-02 |
1.43e-02 |
| Golgi Associated Vesicle Biogenesis |
55 |
4.29e-07 |
3.07e-06 |
0.50100 |
0.272000 |
0.421000 |
4.82e-04 |
6.46e-08 |
| Gene and protein expression by JAK-STAT signaling after Interleukin-12 stimulation |
36 |
8.04e-05 |
3.65e-04 |
0.50100 |
0.416000 |
0.279000 |
1.53e-05 |
3.75e-03 |
| HDR through MMEJ (alt-NHEJ) |
10 |
8.62e-02 |
1.49e-01 |
0.50000 |
-0.307000 |
-0.394000 |
9.22e-02 |
3.08e-02 |
| Biotin transport and metabolism |
11 |
6.81e-02 |
1.26e-01 |
0.50000 |
-0.393000 |
-0.308000 |
2.39e-02 |
7.70e-02 |
| Creation of C4 and C2 activators |
70 |
8.44e-23 |
9.58e-21 |
0.49700 |
0.112000 |
-0.484000 |
1.06e-01 |
2.41e-12 |
| TRAF6 mediated induction of NFkB and MAP kinases upon TLR7/8 or 9 activation |
87 |
1.61e-09 |
1.77e-08 |
0.49600 |
0.327000 |
0.373000 |
1.35e-07 |
1.88e-09 |
| Signaling by NOTCH4 |
78 |
6.11e-09 |
5.67e-08 |
0.49500 |
0.395000 |
0.299000 |
1.63e-09 |
4.90e-06 |
| APC:Cdc20 mediated degradation of cell cycle proteins prior to satisfation of the cell cycle checkpoint |
72 |
1.07e-09 |
1.21e-08 |
0.49500 |
0.437000 |
0.234000 |
1.48e-10 |
5.99e-04 |
| MTOR signalling |
39 |
1.10e-04 |
4.83e-04 |
0.49500 |
0.320000 |
0.377000 |
5.37e-04 |
4.62e-05 |
| Membrane binding and targetting of GAG proteins |
13 |
5.03e-02 |
9.80e-02 |
0.49500 |
0.359000 |
0.340000 |
2.49e-02 |
3.39e-02 |
| Synthesis And Processing Of GAG, GAGPOL Polyproteins |
13 |
5.03e-02 |
9.80e-02 |
0.49500 |
0.359000 |
0.340000 |
2.49e-02 |
3.39e-02 |
| CDK-mediated phosphorylation and removal of Cdc6 |
71 |
5.59e-09 |
5.26e-08 |
0.49400 |
0.423000 |
0.256000 |
7.07e-10 |
1.93e-04 |
| FCGR activation |
75 |
8.30e-23 |
9.58e-21 |
0.49400 |
0.079900 |
-0.488000 |
2.31e-01 |
2.73e-13 |
| Toll Like Receptor 4 (TLR4) Cascade |
121 |
7.69e-13 |
2.05e-11 |
0.49400 |
0.326000 |
0.371000 |
5.97e-10 |
1.80e-12 |
| Regulated proteolysis of p75NTR |
11 |
7.63e-02 |
1.36e-01 |
0.49400 |
0.317000 |
0.378000 |
6.89e-02 |
2.97e-02 |
| LDL clearance |
17 |
1.87e-02 |
4.51e-02 |
0.49300 |
0.316000 |
0.379000 |
2.40e-02 |
6.82e-03 |
| MASTL Facilitates Mitotic Progression |
10 |
2.74e-02 |
6.04e-02 |
0.49300 |
0.467000 |
0.160000 |
1.06e-02 |
3.81e-01 |
| Interleukin-1 family signaling |
124 |
5.86e-13 |
1.60e-11 |
0.49200 |
0.359000 |
0.336000 |
4.74e-12 |
9.59e-11 |
| Respiratory electron transport, ATP synthesis by chemiosmotic coupling, and heat production by uncoupling proteins. |
124 |
3.60e-13 |
1.02e-11 |
0.49100 |
0.378000 |
0.314000 |
3.72e-13 |
1.50e-09 |
| Suppression of phagosomal maturation |
12 |
6.39e-02 |
1.20e-01 |
0.49100 |
0.321000 |
0.371000 |
5.40e-02 |
2.62e-02 |
| Activation of APC/C and APC/C:Cdc20 mediated degradation of mitotic proteins |
75 |
8.14e-10 |
9.56e-09 |
0.49000 |
0.431000 |
0.234000 |
1.08e-10 |
4.61e-04 |
| APC/C:Cdc20 mediated degradation of mitotic proteins |
74 |
9.19e-10 |
1.05e-08 |
0.49000 |
0.432000 |
0.231000 |
1.27e-10 |
5.93e-04 |
| IKK complex recruitment mediated by RIP1 |
23 |
5.00e-03 |
1.47e-02 |
0.49000 |
0.376000 |
0.314000 |
1.81e-03 |
9.07e-03 |
| Toll Like Receptor 7/8 (TLR7/8) Cascade |
89 |
1.82e-09 |
1.96e-08 |
0.48900 |
0.324000 |
0.366000 |
1.30e-07 |
2.29e-09 |
| Signal amplification |
28 |
1.87e-03 |
6.05e-03 |
0.48800 |
0.334000 |
0.356000 |
2.22e-03 |
1.10e-03 |
| Glycogen synthesis |
13 |
5.44e-02 |
1.05e-01 |
0.48800 |
0.340000 |
0.351000 |
3.39e-02 |
2.85e-02 |
| Growth hormone receptor signaling |
20 |
1.10e-02 |
2.94e-02 |
0.48700 |
0.366000 |
0.322000 |
4.61e-03 |
1.27e-02 |
| DARPP-32 events |
22 |
3.41e-03 |
1.04e-02 |
0.48600 |
0.253000 |
0.415000 |
3.97e-02 |
7.50e-04 |
| CLEC7A (Dectin-1) signaling |
96 |
2.50e-10 |
3.51e-09 |
0.48500 |
0.383000 |
0.298000 |
8.76e-11 |
4.45e-07 |
| EPH-Ephrin signaling |
78 |
3.12e-08 |
2.58e-07 |
0.48500 |
0.327000 |
0.359000 |
6.11e-07 |
4.35e-08 |
| Prefoldin mediated transfer of substrate to CCT/TriC |
26 |
1.82e-03 |
5.91e-03 |
0.48300 |
0.401000 |
0.270000 |
4.05e-04 |
1.71e-02 |
| Platelet Aggregation (Plug Formation) |
28 |
3.46e-04 |
1.35e-03 |
0.48300 |
0.215000 |
0.432000 |
4.85e-02 |
7.44e-05 |
| RHO GTPases activate PKNs |
47 |
7.63e-07 |
5.17e-06 |
0.48300 |
0.198000 |
0.440000 |
1.87e-02 |
1.78e-07 |
| CD28 dependent PI3K/Akt signaling |
22 |
5.42e-03 |
1.58e-02 |
0.48100 |
-0.395000 |
-0.275000 |
1.34e-03 |
2.55e-02 |
| Packaging Of Telomere Ends |
20 |
8.89e-04 |
3.15e-03 |
0.48100 |
0.148000 |
0.458000 |
2.53e-01 |
3.92e-04 |
| Scavenging by Class A Receptors |
11 |
3.11e-02 |
6.71e-02 |
0.47900 |
0.177000 |
0.445000 |
3.09e-01 |
1.06e-02 |
| Toll-like Receptor Cascades |
143 |
3.96e-14 |
1.32e-12 |
0.47900 |
0.322000 |
0.354000 |
2.73e-11 |
2.48e-13 |
| MyD88 dependent cascade initiated on endosome |
88 |
5.14e-09 |
4.90e-08 |
0.47900 |
0.316000 |
0.359000 |
2.96e-07 |
5.59e-09 |
| SHC1 events in ERBB4 signaling |
10 |
8.75e-02 |
1.51e-01 |
0.47700 |
0.403000 |
0.257000 |
2.75e-02 |
1.60e-01 |
| HSP90 chaperone cycle for steroid hormone receptors (SHR) |
36 |
2.43e-04 |
9.64e-04 |
0.47700 |
0.276000 |
0.389000 |
4.18e-03 |
5.31e-05 |
| Activation of the pre-replicative complex |
32 |
4.51e-05 |
2.17e-04 |
0.47600 |
-0.174000 |
-0.443000 |
8.85e-02 |
1.46e-05 |
| MyD88 cascade initiated on plasma membrane |
82 |
1.81e-08 |
1.55e-07 |
0.47500 |
0.301000 |
0.367000 |
2.40e-06 |
8.68e-09 |
| Toll Like Receptor 10 (TLR10) Cascade |
82 |
1.81e-08 |
1.55e-07 |
0.47500 |
0.301000 |
0.367000 |
2.40e-06 |
8.68e-09 |
| Toll Like Receptor 5 (TLR5) Cascade |
82 |
1.81e-08 |
1.55e-07 |
0.47500 |
0.301000 |
0.367000 |
2.40e-06 |
8.68e-09 |
| Mucopolysaccharidoses |
11 |
7.09e-02 |
1.30e-01 |
0.47500 |
0.256000 |
0.400000 |
1.41e-01 |
2.16e-02 |
| EGFR downregulation |
26 |
1.48e-04 |
6.24e-04 |
0.47500 |
0.148000 |
0.451000 |
1.90e-01 |
6.85e-05 |
| Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding |
29 |
1.42e-03 |
4.79e-03 |
0.47400 |
0.384000 |
0.277000 |
3.46e-04 |
9.72e-03 |
| Amyloid fiber formation |
51 |
1.04e-05 |
5.58e-05 |
0.47300 |
0.277000 |
0.383000 |
6.15e-04 |
2.22e-06 |
| Activated PKN1 stimulates transcription of AR (androgen receptor) regulated genes KLK2 and KLK3 |
22 |
5.74e-05 |
2.71e-04 |
0.47200 |
0.058000 |
0.468000 |
6.38e-01 |
1.42e-04 |
| Complex I biogenesis |
55 |
1.04e-05 |
5.58e-05 |
0.47200 |
0.341000 |
0.325000 |
1.19e-05 |
2.98e-05 |
| Apoptosis induced DNA fragmentation |
10 |
7.34e-02 |
1.32e-01 |
0.47100 |
0.221000 |
0.416000 |
2.27e-01 |
2.27e-02 |
| Initial triggering of complement |
77 |
1.26e-22 |
1.32e-20 |
0.47100 |
0.109000 |
-0.458000 |
9.93e-02 |
3.62e-12 |
| Innate Immune System |
963 |
8.82e-86 |
6.01e-83 |
0.47000 |
0.357000 |
0.306000 |
4.15e-79 |
2.68e-58 |
| Recycling pathway of L1 |
26 |
4.84e-04 |
1.83e-03 |
0.46600 |
0.178000 |
0.431000 |
1.17e-01 |
1.41e-04 |
| SUMOylation of immune response proteins |
11 |
8.26e-02 |
1.45e-01 |
0.46600 |
0.260000 |
0.387000 |
1.36e-01 |
2.62e-02 |
| Toll Like Receptor 9 (TLR9) Cascade |
92 |
5.87e-09 |
5.48e-08 |
0.46600 |
0.305000 |
0.352000 |
4.10e-07 |
5.42e-09 |
| Defects of contact activation system (CAS) and kallikrein/kinin system (KKS) |
12 |
3.95e-02 |
8.15e-02 |
0.46500 |
0.202000 |
0.419000 |
2.26e-01 |
1.19e-02 |
| Diseases of hemostasis |
12 |
3.95e-02 |
8.15e-02 |
0.46500 |
0.202000 |
0.419000 |
2.26e-01 |
1.19e-02 |
| Calnexin/calreticulin cycle |
26 |
3.70e-03 |
1.12e-02 |
0.46400 |
0.276000 |
0.373000 |
1.49e-02 |
9.82e-04 |
| Chk1/Chk2(Cds1) mediated inactivation of Cyclin B:Cdk1 complex |
12 |
4.89e-02 |
9.63e-02 |
0.46200 |
0.408000 |
0.217000 |
1.43e-02 |
1.93e-01 |
| Common Pathway of Fibrin Clot Formation |
14 |
3.78e-02 |
7.87e-02 |
0.46200 |
0.239000 |
0.395000 |
1.21e-01 |
1.05e-02 |
| Signalling to ERKs |
31 |
2.07e-03 |
6.66e-03 |
0.46100 |
0.322000 |
0.330000 |
1.92e-03 |
1.47e-03 |
| Activation of IRF3/IRF7 mediated by TBK1/IKK epsilon |
17 |
1.91e-02 |
4.56e-02 |
0.46000 |
0.394000 |
0.237000 |
4.90e-03 |
9.05e-02 |
| Nucleotide salvage |
21 |
1.29e-02 |
3.36e-02 |
0.45800 |
0.365000 |
0.277000 |
3.81e-03 |
2.82e-02 |
| Post-translational protein phosphorylation |
68 |
1.23e-06 |
8.01e-06 |
0.45700 |
0.292000 |
0.351000 |
3.15e-05 |
5.45e-07 |
| The citric acid (TCA) cycle and respiratory electron transport |
172 |
1.46e-15 |
6.41e-14 |
0.45600 |
0.351000 |
0.290000 |
1.93e-15 |
4.96e-11 |
| Regulation of APC/C activators between G1/S and early anaphase |
79 |
2.22e-09 |
2.35e-08 |
0.45500 |
0.408000 |
0.203000 |
3.72e-10 |
1.79e-03 |
| Signaling by PDGFRA extracellular domain mutants |
12 |
8.43e-02 |
1.47e-01 |
0.45300 |
0.366000 |
0.268000 |
2.83e-02 |
1.08e-01 |
| Signaling by PDGFRA transmembrane, juxtamembrane and kinase domain mutants |
12 |
8.43e-02 |
1.47e-01 |
0.45300 |
0.366000 |
0.268000 |
2.83e-02 |
1.08e-01 |
| ERK/MAPK targets |
22 |
1.17e-02 |
3.09e-02 |
0.45300 |
0.277000 |
0.359000 |
2.46e-02 |
3.55e-03 |
| ADP signalling through P2Y purinoceptor 1 |
21 |
1.75e-02 |
4.38e-02 |
0.45300 |
0.329000 |
0.311000 |
9.04e-03 |
1.37e-02 |
| Citric acid cycle (TCA cycle) |
22 |
1.46e-02 |
3.73e-02 |
0.45200 |
0.314000 |
0.326000 |
1.08e-02 |
8.14e-03 |
| Signaling by BRAF and RAF fusions |
57 |
1.35e-05 |
7.15e-05 |
0.45200 |
0.287000 |
0.349000 |
1.81e-04 |
5.08e-06 |
| Receptor Mediated Mitophagy |
11 |
1.17e-01 |
1.91e-01 |
0.45100 |
0.293000 |
0.344000 |
9.29e-02 |
4.83e-02 |
| Gastrin-CREB signalling pathway via PKC and MAPK |
14 |
3.89e-02 |
8.07e-02 |
0.45000 |
0.220000 |
0.393000 |
1.54e-01 |
1.09e-02 |
| Hedgehog ‘on’ state |
74 |
2.24e-07 |
1.67e-06 |
0.45000 |
0.369000 |
0.256000 |
3.94e-08 |
1.36e-04 |
| FRS-mediated FGFR3 signaling |
11 |
7.16e-02 |
1.30e-01 |
0.44900 |
0.398000 |
0.208000 |
2.22e-02 |
2.31e-01 |
| G1/S DNA Damage Checkpoints |
65 |
5.79e-07 |
4.02e-06 |
0.44900 |
0.384000 |
0.232000 |
8.35e-08 |
1.19e-03 |
| Diseases associated with glycosylation precursor biosynthesis |
18 |
2.19e-02 |
5.07e-02 |
0.44900 |
0.375000 |
0.246000 |
5.82e-03 |
7.04e-02 |
| p53-Dependent G1 DNA Damage Response |
63 |
1.16e-06 |
7.65e-06 |
0.44900 |
0.381000 |
0.238000 |
1.74e-07 |
1.07e-03 |
| p53-Dependent G1/S DNA damage checkpoint |
63 |
1.16e-06 |
7.65e-06 |
0.44900 |
0.381000 |
0.238000 |
1.74e-07 |
1.07e-03 |
| Regulation of RUNX2 expression and activity |
66 |
3.52e-07 |
2.55e-06 |
0.44800 |
0.388000 |
0.225000 |
5.02e-08 |
1.55e-03 |
| RHO GTPases activate PAKs |
20 |
5.94e-03 |
1.70e-02 |
0.44800 |
0.187000 |
0.407000 |
1.49e-01 |
1.61e-03 |
| DNA methylation |
20 |
2.76e-03 |
8.64e-03 |
0.44700 |
0.146000 |
0.423000 |
2.58e-01 |
1.06e-03 |
| MAP kinase activation |
63 |
5.52e-06 |
3.16e-05 |
0.44600 |
0.282000 |
0.346000 |
1.09e-04 |
2.03e-06 |
| Asymmetric localization of PCP proteins |
60 |
7.60e-06 |
4.16e-05 |
0.44400 |
0.356000 |
0.265000 |
1.78e-06 |
3.83e-04 |
| Golgi-to-ER retrograde transport |
111 |
7.08e-10 |
8.39e-09 |
0.44300 |
0.279000 |
0.345000 |
3.89e-07 |
3.43e-10 |
| Gluconeogenesis |
28 |
5.97e-03 |
1.71e-02 |
0.44200 |
0.315000 |
0.310000 |
3.93e-03 |
4.57e-03 |
| Incretin synthesis, secretion, and inactivation |
10 |
2.71e-02 |
6.00e-02 |
0.44100 |
0.435000 |
0.077200 |
1.73e-02 |
6.73e-01 |
| Synthesis, secretion, and inactivation of Glucagon-like Peptide-1 (GLP-1) |
10 |
2.71e-02 |
6.00e-02 |
0.44100 |
0.435000 |
0.077200 |
1.73e-02 |
6.73e-01 |
| MAP3K8 (TPL2)-dependent MAPK1/3 activation |
16 |
4.67e-02 |
9.31e-02 |
0.44100 |
0.268000 |
0.350000 |
6.30e-02 |
1.55e-02 |
| RAB geranylgeranylation |
61 |
1.06e-05 |
5.66e-05 |
0.43900 |
0.273000 |
0.344000 |
2.25e-04 |
3.32e-06 |
| Pyruvate metabolism |
28 |
5.65e-03 |
1.63e-02 |
0.43900 |
0.337000 |
0.282000 |
2.05e-03 |
9.85e-03 |
| G beta:gamma signalling through CDC42 |
17 |
4.03e-02 |
8.29e-02 |
0.43800 |
0.347000 |
0.268000 |
1.33e-02 |
5.55e-02 |
| Processive synthesis on the lagging strand |
15 |
8.16e-04 |
2.92e-03 |
0.43800 |
0.021300 |
-0.438000 |
8.86e-01 |
3.33e-03 |
| Activation of Matrix Metalloproteinases |
23 |
1.56e-02 |
3.95e-02 |
0.43800 |
0.298000 |
0.321000 |
1.34e-02 |
7.61e-03 |
| Autophagy |
123 |
2.74e-10 |
3.71e-09 |
0.43800 |
0.306000 |
0.313000 |
4.39e-09 |
2.09e-09 |
| Phase 0 - rapid depolarisation |
22 |
1.55e-02 |
3.94e-02 |
0.43800 |
-0.348000 |
-0.265000 |
4.66e-03 |
3.16e-02 |
| TAK1 activates NFkB by phosphorylation and activation of IKKs complex |
27 |
7.05e-03 |
1.97e-02 |
0.43700 |
0.280000 |
0.335000 |
1.17e-02 |
2.55e-03 |
| Translocation of SLC2A4 (GLUT4) to the plasma membrane |
48 |
1.03e-04 |
4.65e-04 |
0.43700 |
0.258000 |
0.352000 |
1.99e-03 |
2.38e-05 |
| MAPK6/MAPK4 signaling |
82 |
1.56e-07 |
1.19e-06 |
0.43500 |
0.354000 |
0.254000 |
3.07e-08 |
7.06e-05 |
| Activation of ATR in response to replication stress |
36 |
9.21e-05 |
4.16e-04 |
0.43500 |
-0.162000 |
-0.403000 |
9.21e-02 |
2.81e-05 |
| Sealing of the nuclear envelope (NE) by ESCRT-III |
25 |
6.91e-03 |
1.94e-02 |
0.43400 |
0.237000 |
0.364000 |
4.04e-02 |
1.65e-03 |
| Downstream signaling events of B Cell Receptor (BCR) |
79 |
3.33e-07 |
2.43e-06 |
0.43200 |
0.351000 |
0.252000 |
6.58e-08 |
1.07e-04 |
| APC/C-mediated degradation of cell cycle proteins |
86 |
2.88e-09 |
2.88e-08 |
0.43200 |
0.388000 |
0.190000 |
5.07e-10 |
2.27e-03 |
| Regulation of mitotic cell cycle |
86 |
2.88e-09 |
2.88e-08 |
0.43200 |
0.388000 |
0.190000 |
5.07e-10 |
2.27e-03 |
| TRAF6-mediated induction of TAK1 complex within TLR4 complex |
16 |
6.04e-02 |
1.15e-01 |
0.43200 |
0.316000 |
0.294000 |
2.87e-02 |
4.16e-02 |
| ADP signalling through P2Y purinoceptor 12 |
18 |
4.24e-02 |
8.61e-02 |
0.43100 |
0.318000 |
0.292000 |
1.96e-02 |
3.20e-02 |
| PCP/CE pathway |
86 |
3.06e-07 |
2.24e-06 |
0.43100 |
0.292000 |
0.317000 |
2.94e-06 |
3.74e-07 |
| MyD88-independent TLR4 cascade |
96 |
5.83e-08 |
4.70e-07 |
0.43000 |
0.292000 |
0.315000 |
7.40e-07 |
9.40e-08 |
| TRIF(TICAM1)-mediated TLR4 signaling |
96 |
5.83e-08 |
4.70e-07 |
0.43000 |
0.292000 |
0.315000 |
7.40e-07 |
9.40e-08 |
| Tryptophan catabolism |
12 |
1.18e-01 |
1.92e-01 |
0.42900 |
0.334000 |
0.269000 |
4.54e-02 |
1.06e-01 |
| Transcriptional regulation of granulopoiesis |
46 |
2.13e-04 |
8.57e-04 |
0.42800 |
0.253000 |
0.345000 |
2.96e-03 |
5.02e-05 |
| Interleukin-17 signaling |
68 |
5.99e-06 |
3.41e-05 |
0.42700 |
0.268000 |
0.333000 |
1.29e-04 |
2.09e-06 |
| Role of LAT2/NTAL/LAB on calcium mobilization |
73 |
1.98e-19 |
1.30e-17 |
0.42600 |
0.150000 |
-0.399000 |
2.71e-02 |
3.62e-09 |
| Constitutive Signaling by EGFRvIII |
14 |
8.58e-02 |
1.49e-01 |
0.42500 |
0.332000 |
0.265000 |
3.15e-02 |
8.63e-02 |
| Signaling by EGFRvIII in Cancer |
14 |
8.58e-02 |
1.49e-01 |
0.42500 |
0.332000 |
0.265000 |
3.15e-02 |
8.63e-02 |
| Transport to the Golgi and subsequent modification |
155 |
7.81e-14 |
2.53e-12 |
0.42400 |
0.223000 |
0.361000 |
1.74e-06 |
8.01e-15 |
| Nucleotide-binding domain, leucine rich repeat containing receptor (NLR) signaling pathways |
51 |
8.74e-05 |
3.96e-04 |
0.42400 |
0.347000 |
0.244000 |
1.81e-05 |
2.59e-03 |
| RAF activation |
32 |
4.58e-03 |
1.36e-02 |
0.42300 |
0.291000 |
0.307000 |
4.36e-03 |
2.63e-03 |
| Glycogen breakdown (glycogenolysis) |
13 |
7.11e-02 |
1.30e-01 |
0.42300 |
0.208000 |
0.368000 |
1.94e-01 |
2.16e-02 |
| ER Quality Control Compartment (ERQC) |
21 |
2.50e-02 |
5.67e-02 |
0.42200 |
0.257000 |
0.335000 |
4.18e-02 |
7.87e-03 |
| Pre-NOTCH Processing in Golgi |
18 |
2.11e-04 |
8.52e-04 |
0.42000 |
-0.050600 |
0.417000 |
7.10e-01 |
2.20e-03 |
| Insertion of tail-anchored proteins into the endoplasmic reticulum membrane |
22 |
2.58e-02 |
5.75e-02 |
0.41900 |
0.279000 |
0.313000 |
2.34e-02 |
1.12e-02 |
| Signaling by MET |
60 |
1.78e-05 |
9.24e-05 |
0.41800 |
0.233000 |
0.348000 |
1.84e-03 |
3.18e-06 |
| Amino acids regulate mTORC1 |
50 |
2.33e-04 |
9.30e-04 |
0.41600 |
0.263000 |
0.323000 |
1.31e-03 |
7.82e-05 |
| TNFR1-induced proapoptotic signaling |
12 |
5.05e-02 |
9.83e-02 |
0.41600 |
-0.142000 |
-0.391000 |
3.94e-01 |
1.90e-02 |
| C-type lectin receptors (CLRs) |
128 |
4.07e-10 |
5.34e-09 |
0.41600 |
0.328000 |
0.255000 |
1.41e-10 |
5.98e-07 |
| AKT phosphorylates targets in the cytosol |
14 |
2.84e-02 |
6.22e-02 |
0.41500 |
0.135000 |
0.393000 |
3.81e-01 |
1.09e-02 |
| ERKs are inactivated |
13 |
7.24e-02 |
1.31e-01 |
0.41500 |
0.197000 |
0.366000 |
2.20e-01 |
2.23e-02 |
| Lagging Strand Synthesis |
20 |
5.76e-04 |
2.14e-03 |
0.41500 |
-0.025400 |
-0.415000 |
8.44e-01 |
1.33e-03 |
| Glycogen storage diseases |
13 |
1.21e-01 |
1.95e-01 |
0.41500 |
0.307000 |
0.279000 |
5.50e-02 |
8.18e-02 |
| Regulation of TP53 Activity through Acetylation |
29 |
6.70e-04 |
2.46e-03 |
0.41500 |
-0.392000 |
-0.137000 |
2.61e-04 |
2.02e-01 |
| RAB GEFs exchange GTP for GDP on RABs |
87 |
1.19e-08 |
1.08e-07 |
0.41400 |
0.184000 |
0.371000 |
3.08e-03 |
2.09e-09 |
| Interleukin-12 signaling |
44 |
2.54e-04 |
1.01e-03 |
0.41300 |
0.354000 |
0.213000 |
4.72e-05 |
1.47e-02 |
| Degradation of beta-catenin by the destruction complex |
83 |
7.78e-07 |
5.25e-06 |
0.41200 |
0.332000 |
0.245000 |
1.76e-07 |
1.12e-04 |
| Thromboxane signalling through TP receptor |
20 |
3.83e-02 |
7.96e-02 |
0.41200 |
0.317000 |
0.263000 |
1.42e-02 |
4.17e-02 |
| Triglyceride catabolism |
16 |
6.49e-02 |
1.21e-01 |
0.41100 |
0.238000 |
0.334000 |
9.86e-02 |
2.06e-02 |
| PINK1-PRKN Mediated Mitophagy |
21 |
6.01e-03 |
1.71e-02 |
0.41000 |
0.386000 |
0.138000 |
2.19e-03 |
2.73e-01 |
| Inhibition of DNA recombination at telomere |
35 |
9.07e-04 |
3.20e-03 |
0.41000 |
0.189000 |
0.364000 |
5.29e-02 |
1.95e-04 |
| Removal of the Flap Intermediate |
14 |
1.54e-03 |
5.14e-03 |
0.41000 |
0.062400 |
-0.405000 |
6.86e-01 |
8.67e-03 |
| Regulation of RAS by GAPs |
66 |
2.31e-05 |
1.16e-04 |
0.40900 |
0.318000 |
0.258000 |
8.12e-06 |
2.83e-04 |
| Chaperone Mediated Autophagy |
19 |
1.65e-02 |
4.16e-02 |
0.40700 |
0.372000 |
0.163000 |
4.96e-03 |
2.17e-01 |
| Signaling by NTRKs |
114 |
1.11e-08 |
1.01e-07 |
0.40600 |
0.252000 |
0.319000 |
3.49e-06 |
3.89e-09 |
| Notch-HLH transcription pathway |
28 |
1.08e-03 |
3.71e-03 |
0.40600 |
0.132000 |
0.384000 |
2.28e-01 |
4.30e-04 |
| Frs2-mediated activation |
11 |
9.96e-02 |
1.68e-01 |
0.40600 |
0.171000 |
0.369000 |
3.27e-01 |
3.42e-02 |
| Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs) |
78 |
4.80e-06 |
2.77e-05 |
0.40500 |
0.262000 |
0.310000 |
6.46e-05 |
2.25e-06 |
| Programmed Cell Death |
179 |
4.51e-13 |
1.25e-11 |
0.40500 |
0.317000 |
0.252000 |
2.46e-13 |
5.87e-09 |
| Platelet activation, signaling and aggregation |
219 |
1.75e-18 |
1.03e-16 |
0.40500 |
0.196000 |
0.354000 |
5.63e-07 |
1.72e-19 |
| Constitutive Signaling by Overexpressed ERBB2 |
11 |
1.74e-01 |
2.61e-01 |
0.40300 |
0.318000 |
0.248000 |
6.82e-02 |
1.54e-01 |
| Signaling by NTRK1 (TRKA) |
100 |
1.61e-07 |
1.22e-06 |
0.40100 |
0.249000 |
0.314000 |
1.62e-05 |
5.52e-08 |
| Role of phospholipids in phagocytosis |
87 |
3.75e-17 |
1.89e-15 |
0.40100 |
0.054400 |
-0.397000 |
3.81e-01 |
1.45e-10 |
| Nucleobase catabolism |
28 |
5.68e-03 |
1.63e-02 |
0.40100 |
0.351000 |
0.195000 |
1.32e-03 |
7.44e-02 |
| MAPK targets/ Nuclear events mediated by MAP kinases |
31 |
8.38e-03 |
2.33e-02 |
0.40100 |
0.257000 |
0.308000 |
1.34e-02 |
3.01e-03 |
| Signaling by Insulin receptor |
59 |
1.38e-04 |
5.83e-04 |
0.40000 |
0.271000 |
0.294000 |
3.14e-04 |
9.30e-05 |
| Processing of SMDT1 |
15 |
9.49e-03 |
2.58e-02 |
0.40000 |
0.396000 |
0.056800 |
7.92e-03 |
7.03e-01 |
| Negative regulation of FGFR3 signaling |
20 |
4.60e-02 |
9.18e-02 |
0.40000 |
0.255000 |
0.308000 |
4.83e-02 |
1.71e-02 |
| Fanconi Anemia Pathway |
36 |
2.72e-03 |
8.55e-03 |
0.40000 |
-0.228000 |
-0.329000 |
1.80e-02 |
6.41e-04 |
| Assembly of the pre-replicative complex |
66 |
5.29e-06 |
3.04e-05 |
0.40000 |
0.350000 |
0.193000 |
8.60e-07 |
6.64e-03 |
| Syndecan interactions |
19 |
4.85e-02 |
9.61e-02 |
0.40000 |
0.321000 |
0.238000 |
1.55e-02 |
7.22e-02 |
| Resolution of AP sites via the multiple-nucleotide patch replacement pathway |
24 |
9.59e-04 |
3.35e-03 |
0.39900 |
-0.075300 |
-0.392000 |
5.23e-01 |
8.80e-04 |
| Signaling by cytosolic FGFR1 fusion mutants |
17 |
7.77e-02 |
1.38e-01 |
0.39900 |
0.294000 |
0.270000 |
3.60e-02 |
5.37e-02 |
| AKT phosphorylates targets in the nucleus |
10 |
6.38e-02 |
1.20e-01 |
0.39900 |
-0.389000 |
-0.088100 |
3.32e-02 |
6.29e-01 |
| Biosynthesis of specialized proresolving mediators (SPMs) |
16 |
7.39e-02 |
1.33e-01 |
0.39700 |
0.328000 |
0.225000 |
2.33e-02 |
1.20e-01 |
| Formation of tubulin folding intermediates by CCT/TriC |
22 |
2.62e-02 |
5.82e-02 |
0.39700 |
0.332000 |
0.218000 |
7.10e-03 |
7.67e-02 |
| Activation of G protein gated Potassium channels |
20 |
1.88e-02 |
4.51e-02 |
0.39700 |
0.359000 |
0.168000 |
5.40e-03 |
1.94e-01 |
| G protein gated Potassium channels |
20 |
1.88e-02 |
4.51e-02 |
0.39700 |
0.359000 |
0.168000 |
5.40e-03 |
1.94e-01 |
| Inhibition of voltage gated Ca2+ channels via Gbeta/gamma subunits |
20 |
1.88e-02 |
4.51e-02 |
0.39700 |
0.359000 |
0.168000 |
5.40e-03 |
1.94e-01 |
| ABC-family proteins mediated transport |
92 |
4.57e-07 |
3.23e-06 |
0.39600 |
0.322000 |
0.230000 |
8.95e-08 |
1.33e-04 |
| N-glycan trimming in the ER and Calnexin/Calreticulin cycle |
35 |
3.59e-03 |
1.09e-02 |
0.39500 |
0.223000 |
0.326000 |
2.24e-02 |
8.51e-04 |
| Interleukin-12 family signaling |
53 |
1.30e-04 |
5.51e-04 |
0.39300 |
0.336000 |
0.205000 |
2.34e-05 |
9.85e-03 |
| Apoptosis |
167 |
1.27e-11 |
2.75e-10 |
0.39300 |
0.309000 |
0.243000 |
5.41e-12 |
5.84e-08 |
| Interferon alpha/beta signaling |
57 |
5.28e-05 |
2.50e-04 |
0.39300 |
-0.198000 |
-0.340000 |
9.69e-03 |
9.10e-06 |
| Clathrin-mediated endocytosis |
125 |
1.01e-10 |
1.61e-09 |
0.39200 |
0.179000 |
0.349000 |
5.66e-04 |
1.52e-11 |
| Signaling by EGFR in Cancer |
22 |
4.04e-02 |
8.29e-02 |
0.39100 |
0.256000 |
0.296000 |
3.77e-02 |
1.62e-02 |
| Macroautophagy |
109 |
1.67e-07 |
1.27e-06 |
0.39100 |
0.268000 |
0.285000 |
1.36e-06 |
2.80e-07 |
| O-glycosylation of TSR domain-containing proteins |
25 |
2.79e-02 |
6.14e-02 |
0.39000 |
-0.267000 |
-0.285000 |
2.10e-02 |
1.37e-02 |
| FRS-mediated FGFR4 signaling |
12 |
9.35e-02 |
1.60e-01 |
0.38900 |
0.356000 |
0.156000 |
3.27e-02 |
3.49e-01 |
| PCNA-Dependent Long Patch Base Excision Repair |
21 |
5.45e-04 |
2.04e-03 |
0.38800 |
0.006030 |
-0.388000 |
9.62e-01 |
2.08e-03 |
| Asparagine N-linked glycosylation |
269 |
1.43e-17 |
7.80e-16 |
0.38700 |
0.243000 |
0.302000 |
7.07e-12 |
1.48e-17 |
| Membrane Trafficking |
555 |
5.19e-40 |
1.77e-37 |
0.38700 |
0.197000 |
0.333000 |
2.01e-15 |
3.07e-41 |
| Diseases of carbohydrate metabolism |
29 |
1.70e-02 |
4.25e-02 |
0.38600 |
0.260000 |
0.286000 |
1.55e-02 |
7.78e-03 |
| VxPx cargo-targeting to cilium |
19 |
1.86e-02 |
4.51e-02 |
0.38500 |
0.135000 |
0.361000 |
3.07e-01 |
6.50e-03 |
| Constitutive Signaling by Ligand-Responsive EGFR Cancer Variants |
18 |
6.18e-02 |
1.16e-01 |
0.38500 |
0.320000 |
0.214000 |
1.88e-02 |
1.15e-01 |
| Signaling by Ligand-Responsive EGFR Variants in Cancer |
18 |
6.18e-02 |
1.16e-01 |
0.38500 |
0.320000 |
0.214000 |
1.88e-02 |
1.15e-01 |
| Pyruvate metabolism and Citric Acid (TCA) cycle |
52 |
6.38e-04 |
2.34e-03 |
0.38500 |
0.294000 |
0.248000 |
2.46e-04 |
1.96e-03 |
| Glycogen metabolism |
23 |
3.50e-02 |
7.36e-02 |
0.38500 |
0.234000 |
0.305000 |
5.21e-02 |
1.13e-02 |
| Interleukin-4 and Interleukin-13 signaling |
92 |
4.35e-07 |
3.11e-06 |
0.38400 |
0.326000 |
0.203000 |
6.31e-08 |
7.44e-04 |
| Acyl chain remodelling of PI |
10 |
1.56e-01 |
2.39e-01 |
0.38400 |
0.164000 |
0.348000 |
3.70e-01 |
5.69e-02 |
| Protein ubiquitination |
72 |
3.73e-05 |
1.82e-04 |
0.38400 |
0.244000 |
0.296000 |
3.44e-04 |
1.38e-05 |
| Mitotic Telophase/Cytokinesis |
13 |
1.17e-01 |
1.91e-01 |
0.38300 |
0.191000 |
0.331000 |
2.33e-01 |
3.85e-02 |
| Oncogenic MAPK signaling |
73 |
2.88e-05 |
1.43e-04 |
0.38100 |
0.230000 |
0.304000 |
6.84e-04 |
7.29e-06 |
| Cleavage of the damaged purine |
24 |
4.05e-03 |
1.21e-02 |
0.38100 |
0.106000 |
0.366000 |
3.68e-01 |
1.93e-03 |
| Depurination |
24 |
4.05e-03 |
1.21e-02 |
0.38100 |
0.106000 |
0.366000 |
3.68e-01 |
1.93e-03 |
| Recognition and association of DNA glycosylase with site containing an affected purine |
24 |
4.05e-03 |
1.21e-02 |
0.38100 |
0.106000 |
0.366000 |
3.68e-01 |
1.93e-03 |
| SHC1 events in ERBB2 signaling |
17 |
9.93e-02 |
1.67e-01 |
0.38000 |
0.275000 |
0.262000 |
4.95e-02 |
6.10e-02 |
| Heme degradation |
10 |
2.29e-01 |
3.22e-01 |
0.38000 |
0.218000 |
0.311000 |
2.33e-01 |
8.85e-02 |
| Formation of Fibrin Clot (Clotting Cascade) |
26 |
2.86e-02 |
6.24e-02 |
0.37700 |
0.240000 |
0.290000 |
3.38e-02 |
1.04e-02 |
| Processing and activation of SUMO |
10 |
2.50e-01 |
3.44e-01 |
0.37700 |
0.295000 |
0.234000 |
1.06e-01 |
2.00e-01 |
| Trafficking and processing of endosomal TLR |
13 |
1.53e-01 |
2.35e-01 |
0.37600 |
0.307000 |
0.217000 |
5.49e-02 |
1.76e-01 |
| Gap junction trafficking and regulation |
15 |
9.39e-02 |
1.60e-01 |
0.37600 |
0.190000 |
0.324000 |
2.03e-01 |
2.96e-02 |
| Endogenous sterols |
16 |
1.22e-01 |
1.97e-01 |
0.37400 |
0.269000 |
0.260000 |
6.25e-02 |
7.18e-02 |
| HDACs deacetylate histones |
47 |
4.33e-06 |
2.51e-05 |
0.37300 |
0.059700 |
0.368000 |
4.79e-01 |
1.26e-05 |
| Orc1 removal from chromatin |
69 |
3.05e-06 |
1.82e-05 |
0.37200 |
0.343000 |
0.144000 |
8.55e-07 |
3.80e-02 |
| Caspase activation via extrinsic apoptotic signalling pathway |
25 |
3.13e-02 |
6.75e-02 |
0.37100 |
0.300000 |
0.218000 |
9.36e-03 |
5.93e-02 |
| Interleukin-15 signaling |
14 |
1.22e-01 |
1.97e-01 |
0.37100 |
0.317000 |
0.193000 |
4.01e-02 |
2.12e-01 |
| mitochondrial fatty acid beta-oxidation of saturated fatty acids |
11 |
2.37e-01 |
3.31e-01 |
0.37100 |
0.244000 |
0.279000 |
1.61e-01 |
1.09e-01 |
| Toll Like Receptor 3 (TLR3) Cascade |
92 |
6.90e-06 |
3.89e-05 |
0.37100 |
0.251000 |
0.273000 |
3.11e-05 |
6.18e-06 |
| Cargo recognition for clathrin-mediated endocytosis |
88 |
9.06e-07 |
6.09e-06 |
0.36900 |
0.175000 |
0.324000 |
4.43e-03 |
1.42e-07 |
| Interleukin-10 signaling |
35 |
1.62e-03 |
5.35e-03 |
0.36900 |
0.341000 |
0.140000 |
4.81e-04 |
1.52e-01 |
| Regulation of Complement cascade |
93 |
1.30e-19 |
9.59e-18 |
0.36600 |
0.174000 |
-0.322000 |
3.80e-03 |
7.80e-08 |
| TNFR2 non-canonical NF-kB pathway |
95 |
6.89e-10 |
8.24e-09 |
0.36500 |
0.354000 |
0.089200 |
2.46e-09 |
1.33e-01 |
| Synthesis of PIPs at the late endosome membrane |
11 |
1.25e-01 |
2.00e-01 |
0.36500 |
0.127000 |
0.342000 |
4.65e-01 |
4.95e-02 |
| Beta-catenin phosphorylation cascade |
17 |
4.81e-02 |
9.55e-02 |
0.36400 |
0.139000 |
0.336000 |
3.21e-01 |
1.64e-02 |
| Cyclin E associated events during G1/S transition |
83 |
7.39e-06 |
4.08e-05 |
0.36300 |
0.308000 |
0.192000 |
1.18e-06 |
2.54e-03 |
| Negative regulation of FGFR1 signaling |
24 |
3.93e-02 |
8.14e-02 |
0.36300 |
0.207000 |
0.298000 |
7.93e-02 |
1.16e-02 |
| Cell-extracellular matrix interactions |
14 |
1.45e-01 |
2.27e-01 |
0.36300 |
0.200000 |
0.302000 |
1.94e-01 |
5.04e-02 |
| Negative regulation of FGFR4 signaling |
21 |
7.25e-02 |
1.31e-01 |
0.36200 |
0.238000 |
0.273000 |
5.92e-02 |
3.01e-02 |
| GRB2 events in ERBB2 signaling |
11 |
1.87e-01 |
2.75e-01 |
0.36200 |
0.318000 |
0.173000 |
6.77e-02 |
3.19e-01 |
| Activation of BAD and translocation to mitochondria |
15 |
1.51e-01 |
2.33e-01 |
0.36200 |
0.278000 |
0.232000 |
6.23e-02 |
1.20e-01 |
| Erythropoietin activates Phosphoinositide-3-kinase (PI3K) |
11 |
1.15e-01 |
1.89e-01 |
0.36200 |
0.113000 |
0.343000 |
5.16e-01 |
4.86e-02 |
| Signaling by Interleukins |
385 |
3.30e-21 |
3.00e-19 |
0.36100 |
0.274000 |
0.235000 |
2.66e-20 |
2.17e-15 |
| Defective B3GALTL causes Peters-plus syndrome (PpS) |
24 |
5.28e-02 |
1.02e-01 |
0.36100 |
-0.248000 |
-0.263000 |
3.56e-02 |
2.60e-02 |
| Synthesis of PC |
23 |
5.41e-02 |
1.05e-01 |
0.36100 |
0.282000 |
0.225000 |
1.91e-02 |
6.18e-02 |
| G beta:gamma signalling through BTK |
15 |
1.56e-01 |
2.38e-01 |
0.36000 |
0.274000 |
0.234000 |
6.63e-02 |
1.17e-01 |
| Intra-Golgi and retrograde Golgi-to-ER traffic |
179 |
1.84e-11 |
3.76e-10 |
0.36000 |
0.192000 |
0.304000 |
8.89e-06 |
2.15e-12 |
| FCERI mediated Ca+2 mobilization |
88 |
1.90e-14 |
6.96e-13 |
0.36000 |
0.058600 |
-0.355000 |
3.42e-01 |
8.57e-09 |
| Binding and Uptake of Ligands by Scavenger Receptors |
91 |
2.01e-19 |
1.30e-17 |
0.36000 |
0.214000 |
-0.289000 |
4.13e-04 |
1.92e-06 |
| Aggrephagy |
21 |
8.01e-02 |
1.41e-01 |
0.35800 |
0.258000 |
0.248000 |
4.09e-02 |
4.90e-02 |
| FGFR1 mutant receptor activation |
23 |
6.22e-02 |
1.17e-01 |
0.35800 |
0.264000 |
0.241000 |
2.84e-02 |
4.50e-02 |
| Selective autophagy |
57 |
1.04e-03 |
3.58e-03 |
0.35800 |
0.264000 |
0.241000 |
5.67e-04 |
1.63e-03 |
| Cooperation of PDCL (PhLP1) and TRiC/CCT in G-protein beta folding |
36 |
1.22e-02 |
3.20e-02 |
0.35800 |
0.274000 |
0.230000 |
4.51e-03 |
1.68e-02 |
| TP53 Regulates Metabolic Genes |
85 |
3.89e-05 |
1.89e-04 |
0.35700 |
0.255000 |
0.250000 |
4.67e-05 |
6.84e-05 |
| JNK (c-Jun kinases) phosphorylation and activation mediated by activated human TAK1 |
18 |
9.12e-02 |
1.57e-01 |
0.35600 |
0.197000 |
0.297000 |
1.48e-01 |
2.92e-02 |
| Intrinsic Pathway of Fibrin Clot Formation |
16 |
1.49e-01 |
2.31e-01 |
0.35600 |
0.260000 |
0.243000 |
7.22e-02 |
9.19e-02 |
| Complement cascade |
97 |
2.43e-19 |
1.51e-17 |
0.35600 |
0.169000 |
-0.313000 |
3.96e-03 |
1.00e-07 |
| Caspase activation via Death Receptors in the presence of ligand |
16 |
4.15e-02 |
8.49e-02 |
0.35500 |
0.341000 |
0.101000 |
1.83e-02 |
4.86e-01 |
| E3 ubiquitin ligases ubiquitinate target proteins |
52 |
1.57e-03 |
5.21e-03 |
0.35500 |
0.216000 |
0.282000 |
7.15e-03 |
4.36e-04 |
| Purine ribonucleoside monophosphate biosynthesis |
10 |
9.57e-03 |
2.60e-02 |
0.35400 |
0.270000 |
-0.229000 |
1.39e-01 |
2.11e-01 |
| Signaling by NOTCH |
182 |
1.21e-10 |
1.92e-09 |
0.35300 |
0.205000 |
0.287000 |
1.83e-06 |
2.25e-11 |
| Signaling by SCF-KIT |
40 |
8.51e-03 |
2.34e-02 |
0.35300 |
0.270000 |
0.227000 |
3.11e-03 |
1.31e-02 |
| Signaling by EGFR |
45 |
9.88e-04 |
3.42e-03 |
0.35200 |
0.153000 |
0.317000 |
7.52e-02 |
2.31e-04 |
| G-protein activation |
23 |
6.81e-02 |
1.26e-01 |
0.35200 |
0.258000 |
0.239000 |
3.19e-02 |
4.71e-02 |
| Metabolism of porphyrins |
22 |
6.05e-02 |
1.15e-01 |
0.35000 |
0.196000 |
0.290000 |
1.11e-01 |
1.84e-02 |
| HDMs demethylate histones |
22 |
4.72e-05 |
2.26e-04 |
0.34900 |
-0.228000 |
0.265000 |
6.42e-02 |
3.16e-02 |
| Nucleobase biosynthesis |
13 |
3.62e-03 |
1.10e-02 |
0.34900 |
0.176000 |
-0.302000 |
2.73e-01 |
5.94e-02 |
| Signaling by Erythropoietin |
24 |
3.53e-02 |
7.42e-02 |
0.34900 |
0.170000 |
0.305000 |
1.50e-01 |
9.79e-03 |
| G-protein beta:gamma signalling |
29 |
1.95e-02 |
4.62e-02 |
0.34800 |
0.175000 |
0.301000 |
1.03e-01 |
5.01e-03 |
| Pexophagy |
11 |
2.81e-01 |
3.79e-01 |
0.34800 |
0.227000 |
0.264000 |
1.92e-01 |
1.30e-01 |
| Glutathione conjugation |
26 |
3.03e-02 |
6.59e-02 |
0.34800 |
0.300000 |
0.177000 |
8.19e-03 |
1.18e-01 |
| Mitochondrial calcium ion transport |
22 |
1.50e-02 |
3.82e-02 |
0.34700 |
0.333000 |
0.097400 |
6.77e-03 |
4.29e-01 |
| TRAF6 mediated NF-kB activation |
23 |
6.80e-02 |
1.26e-01 |
0.34700 |
0.218000 |
0.270000 |
6.98e-02 |
2.49e-02 |
| Regulation of TP53 Activity through Association with Co-factors |
12 |
2.47e-01 |
3.40e-01 |
0.34600 |
-0.270000 |
-0.217000 |
1.05e-01 |
1.93e-01 |
| Telomere C-strand (Lagging Strand) Synthesis |
34 |
1.14e-03 |
3.88e-03 |
0.34600 |
-0.085600 |
-0.336000 |
3.88e-01 |
7.08e-04 |
| Signaling by FGFR3 |
31 |
3.15e-02 |
6.77e-02 |
0.34500 |
0.239000 |
0.249000 |
2.15e-02 |
1.65e-02 |
| Deadenylation of mRNA |
22 |
8.32e-02 |
1.46e-01 |
0.34400 |
0.261000 |
0.224000 |
3.38e-02 |
6.91e-02 |
| Interconversion of nucleotide di- and triphosphates |
27 |
5.16e-03 |
1.51e-02 |
0.34300 |
0.332000 |
0.086300 |
2.79e-03 |
4.37e-01 |
| Mitophagy |
28 |
2.20e-02 |
5.08e-02 |
0.34300 |
0.301000 |
0.164000 |
5.83e-03 |
1.33e-01 |
| G beta:gamma signalling through PLC beta |
17 |
1.53e-01 |
2.35e-01 |
0.34300 |
0.248000 |
0.237000 |
7.72e-02 |
9.07e-02 |
| Presynaptic function of Kainate receptors |
17 |
1.53e-01 |
2.35e-01 |
0.34300 |
0.248000 |
0.237000 |
7.72e-02 |
9.07e-02 |
| RHO GTPases activate CIT |
18 |
5.43e-02 |
1.05e-01 |
0.34200 |
0.125000 |
0.318000 |
3.60e-01 |
1.94e-02 |
| Signaling by FGFR4 |
31 |
3.31e-02 |
7.07e-02 |
0.34200 |
0.250000 |
0.233000 |
1.59e-02 |
2.48e-02 |
| L1CAM interactions |
83 |
8.42e-06 |
4.57e-05 |
0.34200 |
0.154000 |
0.305000 |
1.52e-02 |
1.57e-06 |
| Cytosolic tRNA aminoacylation |
24 |
1.78e-03 |
5.85e-03 |
0.34200 |
0.341000 |
0.008680 |
3.79e-03 |
9.41e-01 |
| GPVI-mediated activation cascade |
31 |
1.47e-03 |
4.95e-03 |
0.34100 |
0.064600 |
0.335000 |
5.33e-01 |
1.26e-03 |
| Resolution of Abasic Sites (AP sites) |
37 |
2.25e-03 |
7.19e-03 |
0.34000 |
-0.118000 |
-0.319000 |
2.14e-01 |
7.81e-04 |
| Plasma lipoprotein clearance |
28 |
4.08e-02 |
8.36e-02 |
0.33900 |
0.203000 |
0.271000 |
6.27e-02 |
1.29e-02 |
| Thrombin signalling through proteinase activated receptors (PARs) |
27 |
4.43e-02 |
8.91e-02 |
0.33800 |
0.198000 |
0.274000 |
7.46e-02 |
1.36e-02 |
| Surfactant metabolism |
22 |
9.40e-02 |
1.60e-01 |
0.33700 |
0.250000 |
0.227000 |
4.24e-02 |
6.58e-02 |
| Glucagon signaling in metabolic regulation |
27 |
4.87e-02 |
9.61e-02 |
0.33700 |
0.206000 |
0.267000 |
6.41e-02 |
1.63e-02 |
| Rab regulation of trafficking |
120 |
7.18e-09 |
6.57e-08 |
0.33700 |
0.124000 |
0.314000 |
1.94e-02 |
2.93e-09 |
| p75NTR signals via NF-kB |
15 |
1.61e-01 |
2.45e-01 |
0.33700 |
0.285000 |
0.180000 |
5.62e-02 |
2.27e-01 |
| SHC-mediated cascade:FGFR4 |
10 |
1.17e-01 |
1.91e-01 |
0.33600 |
0.332000 |
0.052700 |
6.93e-02 |
7.73e-01 |
| Antigen activates B Cell Receptor (BCR) leading to generation of second messengers |
83 |
5.94e-11 |
1.04e-09 |
0.33600 |
0.022600 |
-0.335000 |
7.21e-01 |
1.29e-07 |
| N-Glycan antennae elongation |
13 |
2.55e-02 |
5.71e-02 |
0.33500 |
-0.334000 |
0.021700 |
3.68e-02 |
8.92e-01 |
| PPARA activates gene expression |
104 |
1.11e-07 |
8.72e-07 |
0.33500 |
0.123000 |
0.311000 |
2.96e-02 |
4.06e-08 |
| Costimulation by the CD28 family |
74 |
2.41e-04 |
9.61e-04 |
0.33500 |
-0.196000 |
-0.271000 |
3.52e-03 |
5.52e-05 |
| p38MAPK events |
13 |
2.35e-01 |
3.29e-01 |
0.33500 |
0.268000 |
0.201000 |
9.47e-02 |
2.10e-01 |
| TICAM1, RIP1-mediated IKK complex recruitment |
19 |
1.27e-01 |
2.01e-01 |
0.33400 |
0.261000 |
0.209000 |
4.86e-02 |
1.15e-01 |
| FCGR3A-mediated IL10 synthesis |
98 |
8.68e-14 |
2.75e-12 |
0.33400 |
0.052100 |
-0.330000 |
3.72e-01 |
1.69e-08 |
| Cyclin A:Cdk2-associated events at S phase entry |
85 |
3.17e-05 |
1.55e-04 |
0.33300 |
0.286000 |
0.172000 |
5.32e-06 |
6.07e-03 |
| Signaling by FGFR2 IIIa TM |
18 |
1.34e-01 |
2.12e-01 |
0.33200 |
0.270000 |
0.193000 |
4.71e-02 |
1.57e-01 |
| Beta-oxidation of very long chain fatty acids |
10 |
3.23e-01 |
4.18e-01 |
0.33100 |
0.187000 |
0.273000 |
3.05e-01 |
1.35e-01 |
| Uptake and actions of bacterial toxins |
27 |
6.00e-02 |
1.14e-01 |
0.33100 |
0.250000 |
0.217000 |
2.47e-02 |
5.07e-02 |
| Nuclear Events (kinase and transcription factor activation) |
53 |
2.26e-03 |
7.21e-03 |
0.33100 |
0.181000 |
0.276000 |
2.24e-02 |
4.98e-04 |
| Sphingolipid de novo biosynthesis |
42 |
1.09e-02 |
2.90e-02 |
0.33000 |
0.200000 |
0.263000 |
2.51e-02 |
3.20e-03 |
| Endosomal/Vacuolar pathway |
12 |
2.82e-01 |
3.80e-01 |
0.33000 |
-0.208000 |
-0.256000 |
2.12e-01 |
1.24e-01 |
| RA biosynthesis pathway |
13 |
1.86e-01 |
2.73e-01 |
0.33000 |
-0.152000 |
-0.293000 |
3.41e-01 |
6.77e-02 |
| Switching of origins to a post-replicative state |
89 |
2.22e-06 |
1.37e-05 |
0.33000 |
0.305000 |
0.126000 |
6.67e-07 |
4.06e-02 |
| Signalling to RAS |
18 |
8.88e-02 |
1.53e-01 |
0.32900 |
0.296000 |
0.142000 |
2.95e-02 |
2.96e-01 |
| Striated Muscle Contraction |
24 |
8.71e-02 |
1.51e-01 |
0.32800 |
0.244000 |
0.219000 |
3.85e-02 |
6.31e-02 |
| Estrogen-dependent nuclear events downstream of ESR-membrane signaling |
21 |
3.78e-02 |
7.87e-02 |
0.32800 |
0.110000 |
0.309000 |
3.83e-01 |
1.43e-02 |
| UCH proteinases |
86 |
1.71e-04 |
7.08e-04 |
0.32800 |
0.222000 |
0.241000 |
3.70e-04 |
1.13e-04 |
| Pre-NOTCH Expression and Processing |
65 |
4.84e-07 |
3.40e-06 |
0.32800 |
0.028700 |
0.326000 |
6.89e-01 |
5.36e-06 |
| Metabolism of steroid hormones |
19 |
1.01e-01 |
1.69e-01 |
0.32800 |
0.284000 |
0.163000 |
3.21e-02 |
2.18e-01 |
| Signaling by Non-Receptor Tyrosine Kinases |
47 |
3.38e-03 |
1.04e-02 |
0.32700 |
0.161000 |
0.284000 |
5.55e-02 |
7.49e-04 |
| Signaling by PTK6 |
47 |
3.38e-03 |
1.04e-02 |
0.32700 |
0.161000 |
0.284000 |
5.55e-02 |
7.49e-04 |
| Transcriptional regulation by RUNX2 |
99 |
2.91e-05 |
1.44e-04 |
0.32700 |
0.261000 |
0.197000 |
7.28e-06 |
7.17e-04 |
| Chondroitin sulfate biosynthesis |
12 |
2.33e-01 |
3.26e-01 |
0.32700 |
0.161000 |
0.284000 |
3.35e-01 |
8.80e-02 |
| Myogenesis |
21 |
6.49e-02 |
1.21e-01 |
0.32600 |
0.144000 |
0.292000 |
2.53e-01 |
2.04e-02 |
| Diseases of DNA repair |
10 |
3.48e-01 |
4.43e-01 |
0.32600 |
-0.261000 |
-0.195000 |
1.53e-01 |
2.86e-01 |
| Signaling by FGFR1 in disease |
30 |
4.32e-02 |
8.72e-02 |
0.32400 |
0.260000 |
0.194000 |
1.37e-02 |
6.61e-02 |
| COPI-dependent Golgi-to-ER retrograde traffic |
78 |
4.59e-04 |
1.74e-03 |
0.32400 |
0.224000 |
0.235000 |
6.32e-04 |
3.39e-04 |
| Acyl chain remodelling of PG |
11 |
3.21e-01 |
4.16e-01 |
0.32300 |
0.194000 |
0.258000 |
2.66e-01 |
1.39e-01 |
| Transcriptional regulation by RUNX3 |
90 |
6.99e-05 |
3.20e-04 |
0.32300 |
0.265000 |
0.184000 |
1.41e-05 |
2.50e-03 |
| A tetrasaccharide linker sequence is required for GAG synthesis |
17 |
1.85e-01 |
2.73e-01 |
0.32200 |
-0.207000 |
-0.247000 |
1.40e-01 |
7.85e-02 |
| ERBB2 Regulates Cell Motility |
10 |
3.33e-01 |
4.29e-01 |
0.32100 |
0.173000 |
0.271000 |
3.44e-01 |
1.39e-01 |
| XBP1(S) activates chaperone genes |
47 |
4.51e-03 |
1.34e-02 |
0.32100 |
0.162000 |
0.277000 |
5.44e-02 |
1.01e-03 |
| Acyl chain remodelling of PC |
19 |
1.52e-01 |
2.33e-01 |
0.32100 |
0.204000 |
0.248000 |
1.24e-01 |
6.15e-02 |
| Hedgehog ‘off’ state |
91 |
1.16e-04 |
4.99e-04 |
0.32100 |
0.250000 |
0.200000 |
3.63e-05 |
9.72e-04 |
| MET promotes cell motility |
26 |
3.65e-02 |
7.66e-02 |
0.32000 |
0.139000 |
0.289000 |
2.19e-01 |
1.09e-02 |
| Pre-NOTCH Transcription and Translation |
49 |
3.38e-05 |
1.65e-04 |
0.32000 |
0.032000 |
0.318000 |
6.98e-01 |
1.15e-04 |
| Homologous DNA Pairing and Strand Exchange |
42 |
2.28e-03 |
7.27e-03 |
0.32000 |
-0.112000 |
-0.300000 |
2.09e-01 |
7.81e-04 |
| FRS-mediated FGFR1 signaling |
14 |
2.25e-01 |
3.18e-01 |
0.32000 |
0.266000 |
0.178000 |
8.54e-02 |
2.48e-01 |
| PKA activation in glucagon signalling |
14 |
7.01e-02 |
1.29e-01 |
0.32000 |
0.055300 |
0.315000 |
7.20e-01 |
4.13e-02 |
| Senescence-Associated Secretory Phenotype (SASP) |
66 |
5.90e-04 |
2.18e-03 |
0.31900 |
0.164000 |
0.274000 |
2.16e-02 |
1.15e-04 |
| Purine salvage |
12 |
2.29e-01 |
3.22e-01 |
0.31900 |
0.285000 |
0.145000 |
8.77e-02 |
3.85e-01 |
| Formation of the cornified envelope |
21 |
1.13e-01 |
1.86e-01 |
0.31900 |
0.261000 |
0.183000 |
3.82e-02 |
1.47e-01 |
| Diseases of programmed cell death |
27 |
7.13e-02 |
1.30e-01 |
0.31900 |
0.203000 |
0.246000 |
6.85e-02 |
2.70e-02 |
| Selenocysteine synthesis |
91 |
1.16e-11 |
2.55e-10 |
0.31800 |
0.046600 |
-0.315000 |
4.43e-01 |
2.04e-07 |
| Metabolism of nucleotides |
86 |
1.33e-06 |
8.56e-06 |
0.31800 |
0.305000 |
0.092400 |
1.04e-06 |
1.38e-01 |
| Integration of energy metabolism |
86 |
1.53e-04 |
6.38e-04 |
0.31800 |
0.185000 |
0.259000 |
3.05e-03 |
3.34e-05 |
| FCERI mediated MAPK activation |
89 |
2.28e-14 |
7.96e-13 |
0.31800 |
0.152000 |
-0.279000 |
1.29e-02 |
5.51e-06 |
| PTEN Regulation |
138 |
1.41e-06 |
9.04e-06 |
0.31800 |
0.198000 |
0.248000 |
5.90e-05 |
4.75e-07 |
| Class C/3 (Metabotropic glutamate/pheromone receptors) |
11 |
1.84e-01 |
2.72e-01 |
0.31700 |
-0.094700 |
-0.302000 |
5.86e-01 |
8.27e-02 |
| RORA activates gene expression |
18 |
5.02e-03 |
1.47e-02 |
0.31600 |
-0.070800 |
0.308000 |
6.03e-01 |
2.36e-02 |
| Vesicle-mediated transport |
644 |
5.08e-27 |
8.66e-25 |
0.31600 |
0.200000 |
0.245000 |
4.78e-18 |
2.49e-26 |
| Eukaryotic Translation Elongation |
92 |
2.03e-12 |
5.22e-11 |
0.31600 |
0.070800 |
-0.308000 |
2.40e-01 |
3.33e-07 |
| Peptide chain elongation |
87 |
1.87e-11 |
3.76e-10 |
0.31500 |
0.061700 |
-0.309000 |
3.20e-01 |
6.31e-07 |
| SLBP Dependent Processing of Replication-Dependent Histone Pre-mRNAs |
11 |
5.80e-02 |
1.11e-01 |
0.31500 |
0.313000 |
-0.031900 |
7.21e-02 |
8.55e-01 |
| Downstream signaling of activated FGFR3 |
16 |
1.59e-01 |
2.43e-01 |
0.31400 |
0.276000 |
0.150000 |
5.58e-02 |
2.98e-01 |
| TBC/RABGAPs |
45 |
4.21e-04 |
1.61e-03 |
0.31400 |
0.067000 |
0.307000 |
4.37e-01 |
3.66e-04 |
| RNA Pol II CTD phosphorylation and interaction with CE |
27 |
6.08e-02 |
1.15e-01 |
0.31400 |
0.173000 |
0.262000 |
1.20e-01 |
1.83e-02 |
| RNA Pol II CTD phosphorylation and interaction with CE during HIV infection |
27 |
6.08e-02 |
1.15e-01 |
0.31400 |
0.173000 |
0.262000 |
1.20e-01 |
1.83e-02 |
| Intra-Golgi traffic |
43 |
9.12e-04 |
3.21e-03 |
0.31400 |
0.079100 |
0.304000 |
3.69e-01 |
5.64e-04 |
| Sema4D in semaphorin signaling |
22 |
2.53e-02 |
5.68e-02 |
0.31300 |
0.072500 |
0.305000 |
5.56e-01 |
1.34e-02 |
| Regulation of lipid metabolism by PPARalpha |
106 |
4.43e-07 |
3.15e-06 |
0.31200 |
0.109000 |
0.293000 |
5.23e-02 |
1.91e-07 |
| Metalloprotease DUBs |
21 |
1.32e-01 |
2.09e-01 |
0.31200 |
0.187000 |
0.249000 |
1.37e-01 |
4.79e-02 |
| SIRT1 negatively regulates rRNA expression |
24 |
9.33e-02 |
1.60e-01 |
0.31200 |
0.180000 |
0.254000 |
1.26e-01 |
3.10e-02 |
| Beta-catenin independent WNT signaling |
136 |
3.30e-06 |
1.96e-05 |
0.31100 |
0.197000 |
0.240000 |
7.20e-05 |
1.29e-06 |
| Mitochondrial biogenesis |
88 |
3.60e-04 |
1.39e-03 |
0.31000 |
0.221000 |
0.217000 |
3.29e-04 |
4.22e-04 |
| Diseases associated with O-glycosylation of proteins |
47 |
1.11e-02 |
2.95e-02 |
0.31000 |
-0.249000 |
-0.184000 |
3.13e-03 |
2.87e-02 |
| Inwardly rectifying K+ channels |
24 |
5.97e-02 |
1.14e-01 |
0.30900 |
0.278000 |
0.136000 |
1.86e-02 |
2.47e-01 |
| Elevation of cytosolic Ca2+ levels |
12 |
1.46e-02 |
3.73e-02 |
0.30900 |
-0.242000 |
0.192000 |
1.47e-01 |
2.49e-01 |
| NOD1/2 Signaling Pathway |
32 |
5.28e-02 |
1.02e-01 |
0.30900 |
0.239000 |
0.195000 |
1.93e-02 |
5.57e-02 |
| SARS-CoV-2 Infection |
63 |
1.82e-03 |
5.91e-03 |
0.30900 |
0.169000 |
0.258000 |
2.03e-02 |
3.95e-04 |
| Signaling by Hedgehog |
119 |
2.16e-05 |
1.10e-04 |
0.30800 |
0.234000 |
0.201000 |
1.07e-05 |
1.48e-04 |
| Regulation of cholesterol biosynthesis by SREBP (SREBF) |
55 |
6.02e-04 |
2.22e-03 |
0.30800 |
0.107000 |
0.289000 |
1.69e-01 |
2.10e-04 |
| Signaling by ERBB4 |
44 |
1.98e-02 |
4.67e-02 |
0.30800 |
0.213000 |
0.223000 |
1.45e-02 |
1.06e-02 |
| Rap1 signalling |
13 |
2.49e-01 |
3.42e-01 |
0.30700 |
0.152000 |
0.267000 |
3.42e-01 |
9.55e-02 |
| Peroxisomal lipid metabolism |
27 |
8.24e-02 |
1.45e-01 |
0.30600 |
0.243000 |
0.186000 |
2.88e-02 |
9.39e-02 |
| tRNA processing in the mitochondrion |
32 |
3.00e-04 |
1.18e-03 |
0.30600 |
-0.303000 |
0.041600 |
2.98e-03 |
6.84e-01 |
| IRE1alpha activates chaperones |
49 |
6.34e-03 |
1.80e-02 |
0.30600 |
0.157000 |
0.263000 |
5.77e-02 |
1.47e-03 |
| Carnitine metabolism |
10 |
4.16e-01 |
5.11e-01 |
0.30600 |
0.212000 |
0.220000 |
2.46e-01 |
2.28e-01 |
| RIPK1-mediated regulated necrosis |
29 |
1.97e-02 |
4.64e-02 |
0.30500 |
0.288000 |
0.102000 |
7.34e-03 |
3.44e-01 |
| Regulated Necrosis |
29 |
1.97e-02 |
4.64e-02 |
0.30500 |
0.288000 |
0.102000 |
7.34e-03 |
3.44e-01 |
| Regulation of necroptotic cell death |
29 |
1.97e-02 |
4.64e-02 |
0.30500 |
0.288000 |
0.102000 |
7.34e-03 |
3.44e-01 |
| CD28 dependent Vav1 pathway |
12 |
2.41e-01 |
3.34e-01 |
0.30400 |
0.277000 |
0.126000 |
9.69e-02 |
4.51e-01 |
| Interleukin-27 signaling |
11 |
3.83e-01 |
4.78e-01 |
0.30400 |
0.205000 |
0.224000 |
2.39e-01 |
1.98e-01 |
| VEGFA-VEGFR2 Pathway |
90 |
1.94e-05 |
9.96e-05 |
0.30400 |
0.121000 |
0.278000 |
4.65e-02 |
4.95e-06 |
| HIV Transcription Initiation |
45 |
1.89e-02 |
4.51e-02 |
0.30400 |
0.196000 |
0.232000 |
2.31e-02 |
7.04e-03 |
| RNA Polymerase II HIV Promoter Escape |
45 |
1.89e-02 |
4.51e-02 |
0.30400 |
0.196000 |
0.232000 |
2.31e-02 |
7.04e-03 |
| RNA Polymerase II Promoter Escape |
45 |
1.89e-02 |
4.51e-02 |
0.30400 |
0.196000 |
0.232000 |
2.31e-02 |
7.04e-03 |
| RNA Polymerase II Transcription Initiation |
45 |
1.89e-02 |
4.51e-02 |
0.30400 |
0.196000 |
0.232000 |
2.31e-02 |
7.04e-03 |
| RNA Polymerase II Transcription Initiation And Promoter Clearance |
45 |
1.89e-02 |
4.51e-02 |
0.30400 |
0.196000 |
0.232000 |
2.31e-02 |
7.04e-03 |
| RNA Polymerase II Transcription Pre-Initiation And Promoter Opening |
45 |
1.89e-02 |
4.51e-02 |
0.30400 |
0.196000 |
0.232000 |
2.31e-02 |
7.04e-03 |
| Sphingolipid metabolism |
78 |
3.46e-04 |
1.35e-03 |
0.30300 |
0.154000 |
0.261000 |
1.90e-02 |
6.55e-05 |
| Cyclin A/B1/B2 associated events during G2/M transition |
24 |
8.08e-02 |
1.43e-01 |
0.30100 |
0.264000 |
0.144000 |
2.52e-02 |
2.21e-01 |
| Initiation of Nuclear Envelope (NE) Reformation |
19 |
1.80e-01 |
2.69e-01 |
0.30100 |
0.180000 |
0.241000 |
1.75e-01 |
6.88e-02 |
| Regulation of signaling by CBL |
18 |
8.53e-02 |
1.48e-01 |
0.30100 |
0.092800 |
0.286000 |
4.96e-01 |
3.57e-02 |
| Opioid Signalling |
75 |
7.49e-04 |
2.72e-03 |
0.30100 |
0.162000 |
0.253000 |
1.50e-02 |
1.52e-04 |
| FCERI mediated NF-kB activation |
136 |
3.65e-17 |
1.89e-15 |
0.30000 |
0.288000 |
-0.086100 |
6.79e-09 |
8.32e-02 |
| Telomere C-strand synthesis initiation |
13 |
2.25e-01 |
3.18e-01 |
0.29900 |
-0.124000 |
-0.272000 |
4.39e-01 |
8.92e-02 |
| Viral mRNA Translation |
87 |
5.41e-11 |
9.57e-10 |
0.29800 |
0.081200 |
-0.287000 |
1.90e-01 |
3.71e-06 |
| Cholesterol biosynthesis |
24 |
1.35e-01 |
2.14e-01 |
0.29800 |
0.211000 |
0.210000 |
7.30e-02 |
7.48e-02 |
| Signaling by ERBB2 in Cancer |
21 |
1.63e-01 |
2.48e-01 |
0.29800 |
0.233000 |
0.186000 |
6.47e-02 |
1.41e-01 |
| Oxidative Stress Induced Senescence |
79 |
1.79e-04 |
7.36e-04 |
0.29800 |
0.130000 |
0.268000 |
4.59e-02 |
3.88e-05 |
| GABA receptor activation |
36 |
4.44e-02 |
8.91e-02 |
0.29800 |
0.234000 |
0.184000 |
1.51e-02 |
5.64e-02 |
| Plasma lipoprotein assembly, remodeling, and clearance |
52 |
8.22e-03 |
2.29e-02 |
0.29700 |
0.165000 |
0.247000 |
3.95e-02 |
2.02e-03 |
| Condensation of Prophase Chromosomes |
29 |
4.96e-02 |
9.70e-02 |
0.29700 |
0.139000 |
0.262000 |
1.94e-01 |
1.46e-02 |
| Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell |
181 |
5.13e-12 |
1.21e-10 |
0.29600 |
-0.075100 |
-0.286000 |
8.15e-02 |
2.92e-11 |
| Eukaryotic Translation Termination |
91 |
9.00e-11 |
1.50e-09 |
0.29600 |
0.062800 |
-0.289000 |
3.01e-01 |
1.85e-06 |
| Glycerophospholipid biosynthesis |
106 |
1.72e-04 |
7.10e-04 |
0.29600 |
0.213000 |
0.205000 |
1.50e-04 |
2.67e-04 |
| Listeria monocytogenes entry into host cells |
17 |
2.47e-01 |
3.40e-01 |
0.29600 |
0.201000 |
0.217000 |
1.51e-01 |
1.22e-01 |
| Mitochondrial protein import |
64 |
5.86e-05 |
2.75e-04 |
0.29500 |
0.288000 |
0.063100 |
6.57e-05 |
3.83e-01 |
| Synthesis of bile acids and bile salts via 7alpha-hydroxycholesterol |
16 |
2.45e-01 |
3.38e-01 |
0.29500 |
0.173000 |
0.239000 |
2.32e-01 |
9.73e-02 |
| Activation of GABAB receptors |
31 |
7.43e-02 |
1.33e-01 |
0.29500 |
0.228000 |
0.187000 |
2.81e-02 |
7.14e-02 |
| GABA B receptor activation |
31 |
7.43e-02 |
1.33e-01 |
0.29500 |
0.228000 |
0.187000 |
2.81e-02 |
7.14e-02 |
| NOTCH1 Intracellular Domain Regulates Transcription |
44 |
2.31e-02 |
5.28e-02 |
0.29500 |
0.179000 |
0.234000 |
3.98e-02 |
7.18e-03 |
| Mitochondrial translation |
97 |
4.02e-07 |
2.90e-06 |
0.29500 |
0.288000 |
0.062300 |
9.55e-07 |
2.89e-01 |
| Metabolism of folate and pterines |
16 |
2.11e-01 |
3.03e-01 |
0.29400 |
0.255000 |
0.148000 |
7.79e-02 |
3.07e-01 |
| mRNA Capping |
29 |
9.17e-02 |
1.57e-01 |
0.29400 |
0.193000 |
0.222000 |
7.28e-02 |
3.81e-02 |
| Leading Strand Synthesis |
14 |
4.72e-02 |
9.39e-02 |
0.29300 |
0.021200 |
-0.293000 |
8.91e-01 |
5.80e-02 |
| Polymerase switching |
14 |
4.72e-02 |
9.39e-02 |
0.29300 |
0.021200 |
-0.293000 |
8.91e-01 |
5.80e-02 |
| rRNA processing in the mitochondrion |
29 |
9.05e-03 |
2.48e-02 |
0.29300 |
-0.289000 |
-0.046200 |
7.09e-03 |
6.67e-01 |
| Interleukin-3, Interleukin-5 and GM-CSF signaling |
40 |
3.06e-02 |
6.65e-02 |
0.29300 |
0.168000 |
0.239000 |
6.52e-02 |
8.87e-03 |
| Signaling by NTRK2 (TRKB) |
20 |
1.63e-01 |
2.48e-01 |
0.29200 |
0.245000 |
0.158000 |
5.74e-02 |
2.21e-01 |
| NS1 Mediated Effects on Host Pathways |
40 |
1.92e-02 |
4.58e-02 |
0.29200 |
-0.139000 |
-0.256000 |
1.27e-01 |
5.03e-03 |
| Rev-mediated nuclear export of HIV RNA |
35 |
1.30e-02 |
3.37e-02 |
0.29100 |
-0.096000 |
-0.275000 |
3.26e-01 |
4.87e-03 |
| Sema4D induced cell migration and growth-cone collapse |
19 |
1.01e-01 |
1.69e-01 |
0.29100 |
0.101000 |
0.273000 |
4.47e-01 |
3.93e-02 |
| Interactions of Rev with host cellular proteins |
37 |
6.24e-03 |
1.77e-02 |
0.29100 |
-0.077000 |
-0.281000 |
4.18e-01 |
3.13e-03 |
| Cleavage of the damaged pyrimidine |
29 |
1.79e-02 |
4.42e-02 |
0.29100 |
0.074900 |
0.281000 |
4.85e-01 |
8.76e-03 |
| Depyrimidination |
29 |
1.79e-02 |
4.42e-02 |
0.29100 |
0.074900 |
0.281000 |
4.85e-01 |
8.76e-03 |
| Recognition and association of DNA glycosylase with site containing an affected pyrimidine |
29 |
1.79e-02 |
4.42e-02 |
0.29100 |
0.074900 |
0.281000 |
4.85e-01 |
8.76e-03 |
| PIWI-interacting RNA (piRNA) biogenesis |
24 |
8.71e-03 |
2.39e-02 |
0.29100 |
0.291000 |
-0.000729 |
1.37e-02 |
9.95e-01 |
| rRNA modification in the nucleus and cytosol |
59 |
2.54e-06 |
1.56e-05 |
0.29000 |
0.027300 |
-0.289000 |
7.17e-01 |
1.22e-04 |
| Zinc transporters |
14 |
2.92e-01 |
3.89e-01 |
0.28900 |
0.242000 |
0.159000 |
1.18e-01 |
3.03e-01 |
| Glucagon-like Peptide-1 (GLP1) regulates insulin secretion |
32 |
6.26e-02 |
1.17e-01 |
0.28900 |
0.162000 |
0.239000 |
1.13e-01 |
1.91e-02 |
| Phosphorylation of the APC/C |
20 |
9.46e-02 |
1.61e-01 |
0.28800 |
0.270000 |
0.101000 |
3.65e-02 |
4.36e-01 |
| Nuclear import of Rev protein |
34 |
1.30e-02 |
3.37e-02 |
0.28800 |
-0.085200 |
-0.275000 |
3.90e-01 |
5.52e-03 |
| Signaling by Receptor Tyrosine Kinases |
408 |
6.64e-17 |
3.23e-15 |
0.28800 |
0.144000 |
0.249000 |
5.50e-07 |
6.16e-18 |
| Metabolism of cofactors |
19 |
2.03e-01 |
2.95e-01 |
0.28700 |
0.235000 |
0.165000 |
7.66e-02 |
2.13e-01 |
| Presynaptic phase of homologous DNA pairing and strand exchange |
39 |
5.52e-03 |
1.60e-02 |
0.28700 |
-0.075800 |
-0.277000 |
4.13e-01 |
2.79e-03 |
| Peptide hormone metabolism |
49 |
1.33e-03 |
4.50e-03 |
0.28700 |
0.277000 |
0.072500 |
7.88e-04 |
3.80e-01 |
| Degradation of the extracellular matrix |
78 |
2.80e-04 |
1.11e-03 |
0.28600 |
0.118000 |
0.261000 |
7.11e-02 |
6.87e-05 |
| APC/C:Cdc20 mediated degradation of Cyclin B |
24 |
4.91e-02 |
9.65e-02 |
0.28600 |
0.273000 |
0.085400 |
2.07e-02 |
4.69e-01 |
| Signaling by NOTCH1 |
66 |
3.25e-03 |
1.00e-02 |
0.28600 |
0.154000 |
0.241000 |
3.01e-02 |
7.25e-04 |
| Defective TPR may confer susceptibility towards thyroid papillary carcinoma (TPC) |
31 |
3.08e-02 |
6.66e-02 |
0.28500 |
-0.105000 |
-0.265000 |
3.13e-01 |
1.05e-02 |
| Regulation of Glucokinase by Glucokinase Regulatory Protein |
31 |
3.08e-02 |
6.66e-02 |
0.28500 |
-0.105000 |
-0.265000 |
3.13e-01 |
1.05e-02 |
| Retrograde transport at the Trans-Golgi-Network |
49 |
5.65e-03 |
1.63e-02 |
0.28500 |
0.115000 |
0.261000 |
1.64e-01 |
1.59e-03 |
| Activation of gene expression by SREBF (SREBP) |
42 |
5.03e-03 |
1.47e-02 |
0.28500 |
0.083100 |
0.273000 |
3.51e-01 |
2.24e-03 |
| Chaperonin-mediated protein folding |
84 |
1.54e-03 |
5.14e-03 |
0.28500 |
0.186000 |
0.216000 |
3.20e-03 |
6.34e-04 |
| SUMOylation of transcription factors |
16 |
1.66e-01 |
2.52e-01 |
0.28500 |
0.104000 |
0.265000 |
4.72e-01 |
6.65e-02 |
| Protein methylation |
15 |
3.20e-01 |
4.16e-01 |
0.28400 |
0.205000 |
0.197000 |
1.69e-01 |
1.87e-01 |
| Synthesis of very long-chain fatty acyl-CoAs |
21 |
2.00e-01 |
2.92e-01 |
0.28400 |
0.213000 |
0.188000 |
9.08e-02 |
1.36e-01 |
| Mitochondrial translation termination |
91 |
1.20e-06 |
7.90e-06 |
0.28400 |
0.280000 |
0.048600 |
3.93e-06 |
4.23e-01 |
| Biosynthesis of DHA-derived SPMs |
14 |
2.74e-01 |
3.71e-01 |
0.28400 |
0.248000 |
0.138000 |
1.08e-01 |
3.72e-01 |
| Vasopressin regulates renal water homeostasis via Aquaporins |
34 |
7.54e-02 |
1.35e-01 |
0.28300 |
0.189000 |
0.211000 |
5.66e-02 |
3.29e-02 |
| FGFR2 alternative splicing |
25 |
9.80e-02 |
1.66e-01 |
0.28300 |
0.249000 |
0.136000 |
3.15e-02 |
2.39e-01 |
| Ub-specific processing proteases |
169 |
2.78e-06 |
1.67e-05 |
0.28300 |
0.213000 |
0.186000 |
1.70e-06 |
3.02e-05 |
| p75NTR recruits signalling complexes |
12 |
3.53e-01 |
4.48e-01 |
0.28200 |
0.241000 |
0.148000 |
1.49e-01 |
3.75e-01 |
| Transport of bile salts and organic acids, metal ions and amine compounds |
55 |
1.17e-02 |
3.09e-02 |
0.28200 |
0.163000 |
0.230000 |
3.60e-02 |
3.15e-03 |
| Nuclear signaling by ERBB4 |
24 |
1.15e-01 |
1.89e-01 |
0.28200 |
0.140000 |
0.245000 |
2.36e-01 |
3.75e-02 |
| Formation of the Early Elongation Complex |
33 |
5.78e-02 |
1.11e-01 |
0.28200 |
0.148000 |
0.240000 |
1.41e-01 |
1.70e-02 |
| Formation of the HIV-1 Early Elongation Complex |
33 |
5.78e-02 |
1.11e-01 |
0.28200 |
0.148000 |
0.240000 |
1.41e-01 |
1.70e-02 |
| TNFs bind their physiological receptors |
25 |
1.50e-03 |
5.03e-03 |
0.28200 |
0.102000 |
-0.263000 |
3.76e-01 |
2.30e-02 |
| Aquaporin-mediated transport |
38 |
5.95e-02 |
1.14e-01 |
0.28100 |
0.194000 |
0.204000 |
3.89e-02 |
2.96e-02 |
| TICAM1,TRAF6-dependent induction of TAK1 complex |
11 |
4.35e-01 |
5.28e-01 |
0.28100 |
0.215000 |
0.182000 |
2.18e-01 |
2.97e-01 |
| Regulation of insulin secretion |
60 |
1.13e-02 |
2.98e-02 |
0.28100 |
0.186000 |
0.210000 |
1.26e-02 |
4.81e-03 |
| Vpr-mediated nuclear import of PICs |
34 |
9.98e-03 |
2.69e-02 |
0.28000 |
-0.062700 |
-0.273000 |
5.27e-01 |
5.81e-03 |
| Mitochondrial translation elongation |
91 |
1.30e-06 |
8.38e-06 |
0.28000 |
0.277000 |
0.043700 |
5.00e-06 |
4.71e-01 |
| Downstream signaling of activated FGFR4 |
17 |
1.85e-01 |
2.73e-01 |
0.27900 |
0.254000 |
0.117000 |
7.02e-02 |
4.05e-01 |
| RNA Polymerase I Promoter Escape |
44 |
3.77e-02 |
7.87e-02 |
0.27900 |
0.180000 |
0.213000 |
3.92e-02 |
1.43e-02 |
| rRNA processing in the nucleus and cytosol |
189 |
1.34e-19 |
9.59e-18 |
0.27900 |
0.066100 |
-0.271000 |
1.17e-01 |
1.30e-10 |
| Metabolism of amine-derived hormones |
10 |
7.95e-02 |
1.40e-01 |
0.27800 |
0.102000 |
-0.258000 |
5.77e-01 |
1.57e-01 |
| Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC) |
93 |
1.52e-10 |
2.25e-09 |
0.27800 |
0.087300 |
-0.263000 |
1.46e-01 |
1.13e-05 |
| EPHA-mediated growth cone collapse |
13 |
3.20e-01 |
4.16e-01 |
0.27700 |
0.136000 |
0.242000 |
3.96e-01 |
1.31e-01 |
| Mitochondrial translation initiation |
91 |
2.72e-06 |
1.64e-05 |
0.27700 |
0.273000 |
0.050000 |
6.89e-06 |
4.10e-01 |
| Apoptotic execution phase |
45 |
1.87e-02 |
4.51e-02 |
0.27700 |
0.134000 |
0.243000 |
1.20e-01 |
4.85e-03 |
| Glycosphingolipid metabolism |
36 |
2.09e-02 |
4.88e-02 |
0.27700 |
0.099200 |
0.259000 |
3.03e-01 |
7.22e-03 |
| Platelet homeostasis |
67 |
7.04e-04 |
2.57e-03 |
0.27600 |
0.096400 |
0.259000 |
1.72e-01 |
2.45e-04 |
| Major pathway of rRNA processing in the nucleolus and cytosol |
179 |
2.42e-18 |
1.38e-16 |
0.27600 |
0.066800 |
-0.268000 |
1.23e-01 |
6.03e-10 |
| Signaling by ERBB2 TMD/JMD mutants |
17 |
2.39e-01 |
3.33e-01 |
0.27600 |
0.237000 |
0.142000 |
9.06e-02 |
3.12e-01 |
| Competing endogenous RNAs (ceRNAs) regulate PTEN translation |
11 |
1.82e-01 |
2.70e-01 |
0.27500 |
-0.274000 |
-0.028400 |
1.16e-01 |
8.70e-01 |
| Heme biosynthesis |
14 |
3.23e-01 |
4.18e-01 |
0.27500 |
0.147000 |
0.232000 |
3.40e-01 |
1.33e-01 |
| RHO GTPase Effectors |
248 |
4.73e-10 |
6.08e-09 |
0.27400 |
0.131000 |
0.241000 |
3.86e-04 |
6.23e-11 |
| Cohesin Loading onto Chromatin |
10 |
2.85e-01 |
3.84e-01 |
0.27400 |
0.066500 |
0.265000 |
7.16e-01 |
1.46e-01 |
| HIV Infection |
224 |
6.15e-08 |
4.93e-07 |
0.27400 |
0.220000 |
0.162000 |
1.38e-08 |
2.80e-05 |
| N-glycan antennae elongation in the medial/trans-Golgi |
21 |
1.77e-02 |
4.40e-02 |
0.27300 |
-0.272000 |
0.023600 |
3.08e-02 |
8.51e-01 |
| Formation of a pool of free 40S subunits |
99 |
7.31e-12 |
1.66e-10 |
0.27200 |
0.130000 |
-0.240000 |
2.59e-02 |
3.76e-05 |
| Diseases of signal transduction by growth factor receptors and second messengers |
339 |
1.99e-11 |
3.94e-10 |
0.27200 |
0.163000 |
0.218000 |
2.35e-07 |
5.31e-12 |
| Chemokine receptors bind chemokines |
39 |
2.01e-02 |
4.72e-02 |
0.27200 |
-0.103000 |
-0.252000 |
2.67e-01 |
6.52e-03 |
| Misspliced GSK3beta mutants stabilize beta-catenin |
15 |
1.25e-01 |
2.00e-01 |
0.27200 |
0.045400 |
0.268000 |
7.61e-01 |
7.23e-02 |
| S33 mutants of beta-catenin aren’t phosphorylated |
15 |
1.25e-01 |
2.00e-01 |
0.27200 |
0.045400 |
0.268000 |
7.61e-01 |
7.23e-02 |
| S37 mutants of beta-catenin aren’t phosphorylated |
15 |
1.25e-01 |
2.00e-01 |
0.27200 |
0.045400 |
0.268000 |
7.61e-01 |
7.23e-02 |
| S45 mutants of beta-catenin aren’t phosphorylated |
15 |
1.25e-01 |
2.00e-01 |
0.27200 |
0.045400 |
0.268000 |
7.61e-01 |
7.23e-02 |
| T41 mutants of beta-catenin aren’t phosphorylated |
15 |
1.25e-01 |
2.00e-01 |
0.27200 |
0.045400 |
0.268000 |
7.61e-01 |
7.23e-02 |
| phosphorylation site mutants of CTNNB1 are not targeted to the proteasome by the destruction complex |
15 |
1.25e-01 |
2.00e-01 |
0.27200 |
0.045400 |
0.268000 |
7.61e-01 |
7.23e-02 |
| Interleukin-6 family signaling |
18 |
2.13e-01 |
3.05e-01 |
0.27100 |
0.239000 |
0.128000 |
7.97e-02 |
3.47e-01 |
| EPH-ephrin mediated repulsion of cells |
39 |
7.00e-02 |
1.29e-01 |
0.26900 |
0.197000 |
0.184000 |
3.33e-02 |
4.73e-02 |
| Regulation of IFNA signaling |
12 |
3.17e-01 |
4.15e-01 |
0.26900 |
0.106000 |
0.247000 |
5.25e-01 |
1.38e-01 |
| Interactions of Vpr with host cellular proteins |
37 |
1.12e-02 |
2.98e-02 |
0.26900 |
-0.064500 |
-0.261000 |
4.97e-01 |
6.04e-03 |
| Protein folding |
90 |
1.90e-03 |
6.14e-03 |
0.26900 |
0.169000 |
0.209000 |
5.54e-03 |
6.22e-04 |
| Response of EIF2AK4 (GCN2) to amino acid deficiency |
99 |
6.63e-11 |
1.13e-09 |
0.26900 |
0.099500 |
-0.249000 |
8.70e-02 |
1.79e-05 |
| Plasma lipoprotein assembly |
10 |
3.41e-01 |
4.38e-01 |
0.26900 |
0.085500 |
0.255000 |
6.39e-01 |
1.63e-01 |
| Base-Excision Repair, AP Site Formation |
31 |
2.38e-02 |
5.45e-02 |
0.26800 |
0.065000 |
0.260000 |
5.31e-01 |
1.22e-02 |
| Signaling by ERBB2 ECD mutants |
15 |
3.19e-01 |
4.15e-01 |
0.26800 |
0.225000 |
0.146000 |
1.31e-01 |
3.28e-01 |
| PLC beta mediated events |
43 |
1.73e-02 |
4.33e-02 |
0.26800 |
0.107000 |
0.246000 |
2.26e-01 |
5.26e-03 |
| Constitutive Signaling by NOTCH1 HD+PEST Domain Mutants |
53 |
2.54e-02 |
5.68e-02 |
0.26800 |
0.169000 |
0.208000 |
3.33e-02 |
8.85e-03 |
| Constitutive Signaling by NOTCH1 PEST Domain Mutants |
53 |
2.54e-02 |
5.68e-02 |
0.26800 |
0.169000 |
0.208000 |
3.33e-02 |
8.85e-03 |
| Signaling by NOTCH1 HD+PEST Domain Mutants in Cancer |
53 |
2.54e-02 |
5.68e-02 |
0.26800 |
0.169000 |
0.208000 |
3.33e-02 |
8.85e-03 |
| Signaling by NOTCH1 PEST Domain Mutants in Cancer |
53 |
2.54e-02 |
5.68e-02 |
0.26800 |
0.169000 |
0.208000 |
3.33e-02 |
8.85e-03 |
| Signaling by NOTCH1 in Cancer |
53 |
2.54e-02 |
5.68e-02 |
0.26800 |
0.169000 |
0.208000 |
3.33e-02 |
8.85e-03 |
| Transport of Ribonucleoproteins into the Host Nucleus |
32 |
3.66e-02 |
7.67e-02 |
0.26700 |
-0.089600 |
-0.252000 |
3.81e-01 |
1.38e-02 |
| SLBP independent Processing of Histone Pre-mRNAs |
10 |
1.13e-01 |
1.86e-01 |
0.26600 |
0.256000 |
-0.073300 |
1.61e-01 |
6.88e-01 |
| NGF-stimulated transcription |
31 |
1.15e-01 |
1.89e-01 |
0.26600 |
0.162000 |
0.211000 |
1.19e-01 |
4.18e-02 |
| Signaling by FGFR in disease |
50 |
2.30e-02 |
5.28e-02 |
0.26600 |
0.224000 |
0.142000 |
6.07e-03 |
8.16e-02 |
| Disorders of transmembrane transporters |
144 |
2.81e-05 |
1.40e-04 |
0.26600 |
0.220000 |
0.149000 |
5.23e-06 |
2.02e-03 |
| NRIF signals cell death from the nucleus |
15 |
2.86e-01 |
3.84e-01 |
0.26600 |
0.235000 |
0.124000 |
1.15e-01 |
4.07e-01 |
| SARS-CoV-1 Infection |
47 |
2.33e-02 |
5.33e-02 |
0.26500 |
0.131000 |
0.231000 |
1.21e-01 |
6.15e-03 |
| Signaling by Hippo |
18 |
2.02e-01 |
2.94e-01 |
0.26500 |
0.112000 |
0.240000 |
4.11e-01 |
7.75e-02 |
| Abortive elongation of HIV-1 transcript in the absence of Tat |
23 |
2.07e-01 |
3.00e-01 |
0.26500 |
0.164000 |
0.208000 |
1.75e-01 |
8.39e-02 |
| Translesion synthesis by REV1 |
16 |
7.84e-02 |
1.39e-01 |
0.26500 |
-0.005550 |
-0.264000 |
9.69e-01 |
6.70e-02 |
| Prostacyclin signalling through prostacyclin receptor |
16 |
3.19e-01 |
4.15e-01 |
0.26400 |
0.217000 |
0.152000 |
1.34e-01 |
2.94e-01 |
| BMAL1:CLOCK,NPAS2 activates circadian gene expression |
25 |
2.75e-03 |
8.62e-03 |
0.26400 |
-0.110000 |
0.240000 |
3.43e-01 |
3.77e-02 |
| NEP/NS2 Interacts with the Cellular Export Machinery |
32 |
2.27e-02 |
5.23e-02 |
0.26400 |
-0.061600 |
-0.257000 |
5.47e-01 |
1.20e-02 |
| Tie2 Signaling |
16 |
3.33e-01 |
4.29e-01 |
0.26300 |
0.157000 |
0.211000 |
2.77e-01 |
1.45e-01 |
| Cytosolic iron-sulfur cluster assembly |
13 |
1.75e-01 |
2.62e-01 |
0.26300 |
-0.260000 |
-0.036900 |
1.04e-01 |
8.18e-01 |
| Formation of RNA Pol II elongation complex |
57 |
7.07e-03 |
1.97e-02 |
0.26200 |
0.111000 |
0.238000 |
1.48e-01 |
1.90e-03 |
| RNA Polymerase II Transcription Elongation |
57 |
7.07e-03 |
1.97e-02 |
0.26200 |
0.111000 |
0.238000 |
1.48e-01 |
1.90e-03 |
| GP1b-IX-V activation signalling |
10 |
4.14e-01 |
5.10e-01 |
0.26200 |
0.108000 |
0.239000 |
5.53e-01 |
1.91e-01 |
| Transcriptional regulation of white adipocyte differentiation |
77 |
2.08e-04 |
8.43e-04 |
0.26200 |
0.070500 |
0.252000 |
2.85e-01 |
1.30e-04 |
| Metal ion SLC transporters |
21 |
2.53e-01 |
3.47e-01 |
0.26000 |
0.201000 |
0.165000 |
1.10e-01 |
1.90e-01 |
| Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S |
59 |
6.94e-06 |
3.89e-05 |
0.26000 |
0.253000 |
-0.061800 |
7.78e-04 |
4.12e-01 |
| Semaphorin interactions |
57 |
1.38e-02 |
3.55e-02 |
0.26000 |
0.132000 |
0.224000 |
8.37e-02 |
3.43e-03 |
| ERCC6 (CSB) and EHMT2 (G9a) positively regulate rRNA expression |
32 |
5.98e-03 |
1.71e-02 |
0.26000 |
-0.003330 |
0.260000 |
9.74e-01 |
1.09e-02 |
| Signaling by ERBB2 KD Mutants |
20 |
2.51e-01 |
3.45e-01 |
0.26000 |
0.213000 |
0.148000 |
9.89e-02 |
2.50e-01 |
| PI3K events in ERBB2 signaling |
11 |
4.93e-01 |
5.82e-01 |
0.26000 |
0.170000 |
0.196000 |
3.28e-01 |
2.60e-01 |
| DNA Replication Pre-Initiation |
82 |
6.89e-05 |
3.16e-04 |
0.26000 |
0.253000 |
0.056800 |
7.26e-05 |
3.74e-01 |
| Assembly of active LPL and LIPC lipase complexes |
10 |
2.02e-01 |
2.94e-01 |
0.25900 |
-0.004810 |
0.259000 |
9.79e-01 |
1.56e-01 |
| Post-chaperonin tubulin folding pathway |
19 |
2.10e-01 |
3.02e-01 |
0.25900 |
0.114000 |
0.232000 |
3.89e-01 |
7.99e-02 |
| MHC class II antigen presentation |
101 |
9.23e-04 |
3.24e-03 |
0.25800 |
0.143000 |
0.214000 |
1.31e-02 |
1.96e-04 |
| Signaling by FGFR1 |
38 |
7.73e-02 |
1.37e-01 |
0.25700 |
0.149000 |
0.210000 |
1.13e-01 |
2.49e-02 |
| Translation initiation complex formation |
58 |
7.17e-06 |
4.01e-05 |
0.25700 |
0.246000 |
-0.074100 |
1.20e-03 |
3.29e-01 |
| NOTCH3 Activation and Transmission of Signal to the Nucleus |
23 |
2.16e-01 |
3.08e-01 |
0.25500 |
0.146000 |
0.209000 |
2.25e-01 |
8.22e-02 |
| Selenoamino acid metabolism |
113 |
2.35e-11 |
4.45e-10 |
0.25500 |
0.100000 |
-0.235000 |
6.63e-02 |
1.62e-05 |
| Acetylcholine Neurotransmitter Release Cycle |
11 |
2.97e-01 |
3.94e-01 |
0.25500 |
-0.059800 |
-0.248000 |
7.31e-01 |
1.55e-01 |
| Peroxisomal protein import |
57 |
2.77e-02 |
6.12e-02 |
0.25500 |
0.199000 |
0.159000 |
9.48e-03 |
3.73e-02 |
| The role of Nef in HIV-1 replication and disease pathogenesis |
28 |
1.75e-01 |
2.62e-01 |
0.25500 |
0.163000 |
0.196000 |
1.36e-01 |
7.30e-02 |
| Insulin processing |
20 |
2.93e-01 |
3.90e-01 |
0.25500 |
0.190000 |
0.169000 |
1.41e-01 |
1.90e-01 |
| NCAM1 interactions |
23 |
1.16e-01 |
1.90e-01 |
0.25400 |
-0.085900 |
-0.240000 |
4.76e-01 |
4.67e-02 |
| Protein localization |
157 |
1.36e-05 |
7.18e-05 |
0.25400 |
0.219000 |
0.129000 |
2.21e-06 |
5.18e-03 |
| Formation of TC-NER Pre-Incision Complex |
53 |
3.44e-02 |
7.26e-02 |
0.25400 |
0.155000 |
0.202000 |
5.14e-02 |
1.11e-02 |
| Formation of the ternary complex, and subsequently, the 43S complex |
51 |
6.50e-06 |
3.68e-05 |
0.25400 |
0.209000 |
-0.144000 |
9.78e-03 |
7.49e-02 |
| ESR-mediated signaling |
159 |
8.53e-06 |
4.61e-05 |
0.25400 |
0.124000 |
0.222000 |
7.19e-03 |
1.40e-06 |
| Sialic acid metabolism |
28 |
1.63e-01 |
2.48e-01 |
0.25400 |
0.149000 |
0.205000 |
1.73e-01 |
5.99e-02 |
| Aflatoxin activation and detoxification |
14 |
2.01e-01 |
2.93e-01 |
0.25300 |
0.248000 |
0.050500 |
1.08e-01 |
7.44e-01 |
| RNA polymerase II transcribes snRNA genes |
72 |
8.53e-03 |
2.35e-02 |
0.25300 |
0.142000 |
0.209000 |
3.76e-02 |
2.13e-03 |
| Signaling by PDGFR in disease |
19 |
3.01e-01 |
3.97e-01 |
0.25300 |
0.152000 |
0.202000 |
2.50e-01 |
1.28e-01 |
| Prolactin receptor signaling |
11 |
2.31e-01 |
3.24e-01 |
0.25100 |
0.250000 |
0.019700 |
1.51e-01 |
9.10e-01 |
| Signaling by WNT |
253 |
4.40e-09 |
4.32e-08 |
0.25100 |
0.112000 |
0.225000 |
2.23e-03 |
7.51e-10 |
| Signaling by VEGF |
97 |
1.87e-04 |
7.64e-04 |
0.25000 |
0.087300 |
0.234000 |
1.37e-01 |
6.63e-05 |
| G-protein mediated events |
44 |
2.45e-02 |
5.56e-02 |
0.25000 |
0.095000 |
0.231000 |
2.75e-01 |
7.98e-03 |
| SHC-mediated cascade:FGFR1 |
12 |
3.67e-01 |
4.62e-01 |
0.24900 |
0.230000 |
0.095700 |
1.67e-01 |
5.66e-01 |
| Extra-nuclear estrogen signaling |
65 |
2.29e-02 |
5.27e-02 |
0.24900 |
0.173000 |
0.179000 |
1.59e-02 |
1.25e-02 |
| Extension of Telomeres |
51 |
3.11e-03 |
9.65e-03 |
0.24900 |
-0.045500 |
-0.245000 |
5.74e-01 |
2.50e-03 |
| TCF dependent signaling in response to WNT |
165 |
1.85e-05 |
9.58e-05 |
0.24800 |
0.131000 |
0.211000 |
3.56e-03 |
3.07e-06 |
| Ribosomal scanning and start codon recognition |
58 |
1.35e-05 |
7.15e-05 |
0.24800 |
0.236000 |
-0.076000 |
1.85e-03 |
3.17e-01 |
| RUNX1 regulates genes involved in megakaryocyte differentiation and platelet function |
53 |
1.79e-04 |
7.36e-04 |
0.24700 |
-0.031200 |
0.245000 |
6.94e-01 |
2.07e-03 |
| Postmitotic nuclear pore complex (NPC) reformation |
27 |
7.26e-02 |
1.31e-01 |
0.24600 |
-0.067000 |
-0.237000 |
5.46e-01 |
3.30e-02 |
| Cellular responses to external stimuli |
503 |
1.05e-13 |
3.19e-12 |
0.24600 |
0.198000 |
0.146000 |
2.49e-14 |
2.30e-08 |
| Purine catabolism |
16 |
2.68e-01 |
3.64e-01 |
0.24500 |
0.228000 |
0.091600 |
1.15e-01 |
5.26e-01 |
| RNA Polymerase II Pre-transcription Events |
78 |
5.95e-03 |
1.70e-02 |
0.24500 |
0.128000 |
0.210000 |
5.11e-02 |
1.37e-03 |
| L13a-mediated translational silencing of Ceruloplasmin expression |
109 |
2.64e-11 |
4.87e-10 |
0.24500 |
0.174000 |
-0.173000 |
1.66e-03 |
1.86e-03 |
| Deubiquitination |
240 |
1.26e-06 |
8.19e-06 |
0.24500 |
0.162000 |
0.184000 |
1.60e-05 |
8.53e-07 |
| GTP hydrolysis and joining of the 60S ribosomal subunit |
110 |
2.25e-11 |
4.33e-10 |
0.24500 |
0.172000 |
-0.174000 |
1.80e-03 |
1.60e-03 |
| Intrinsic Pathway for Apoptosis |
53 |
3.00e-02 |
6.54e-02 |
0.24500 |
0.210000 |
0.126000 |
8.08e-03 |
1.14e-01 |
| Hemostasis |
542 |
1.02e-13 |
3.17e-12 |
0.24500 |
0.166000 |
0.180000 |
4.31e-11 |
6.88e-13 |
| IRAK2 mediated activation of TAK1 complex |
10 |
5.64e-01 |
6.42e-01 |
0.24500 |
0.158000 |
0.187000 |
3.87e-01 |
3.06e-01 |
| NoRC negatively regulates rRNA expression |
59 |
2.08e-02 |
4.88e-02 |
0.24400 |
0.125000 |
0.209000 |
9.64e-02 |
5.39e-03 |
| Polymerase switching on the C-strand of the telomere |
26 |
8.24e-02 |
1.45e-01 |
0.24400 |
-0.064900 |
-0.235000 |
5.66e-01 |
3.81e-02 |
| SUMOylation of intracellular receptors |
25 |
2.69e-02 |
5.98e-02 |
0.24300 |
-0.009510 |
0.243000 |
9.34e-01 |
3.53e-02 |
| B-WICH complex positively regulates rRNA expression |
44 |
8.75e-02 |
1.51e-01 |
0.24300 |
0.175000 |
0.169000 |
4.51e-02 |
5.23e-02 |
| Cellular responses to stress |
497 |
3.13e-13 |
9.09e-12 |
0.24200 |
0.196000 |
0.142000 |
6.60e-14 |
5.74e-08 |
| rRNA processing |
218 |
9.52e-15 |
3.71e-13 |
0.24200 |
0.018600 |
-0.241000 |
6.36e-01 |
7.96e-10 |
| Translation |
294 |
4.72e-20 |
3.78e-18 |
0.24200 |
0.241000 |
-0.024300 |
1.16e-12 |
4.74e-01 |
| TP53 Regulates Transcription of Genes Involved in G2 Cell Cycle Arrest |
17 |
1.36e-01 |
2.16e-01 |
0.24200 |
0.240000 |
0.029200 |
8.62e-02 |
8.35e-01 |
| Glutathione synthesis and recycling |
10 |
3.61e-01 |
4.56e-01 |
0.24200 |
0.236000 |
0.052500 |
1.96e-01 |
7.74e-01 |
| Regulation of pyruvate dehydrogenase (PDH) complex |
15 |
4.32e-01 |
5.27e-01 |
0.24200 |
0.184000 |
0.157000 |
2.17e-01 |
2.92e-01 |
| AMER1 mutants destabilize the destruction complex |
14 |
2.09e-01 |
3.00e-01 |
0.24200 |
0.036700 |
0.239000 |
8.12e-01 |
1.21e-01 |
| APC truncation mutants have impaired AXIN binding |
14 |
2.09e-01 |
3.00e-01 |
0.24200 |
0.036700 |
0.239000 |
8.12e-01 |
1.21e-01 |
| AXIN missense mutants destabilize the destruction complex |
14 |
2.09e-01 |
3.00e-01 |
0.24200 |
0.036700 |
0.239000 |
8.12e-01 |
1.21e-01 |
| AXIN mutants destabilize the destruction complex, activating WNT signaling |
14 |
2.09e-01 |
3.00e-01 |
0.24200 |
0.036700 |
0.239000 |
8.12e-01 |
1.21e-01 |
| Truncations of AMER1 destabilize the destruction complex |
14 |
2.09e-01 |
3.00e-01 |
0.24200 |
0.036700 |
0.239000 |
8.12e-01 |
1.21e-01 |
| truncated APC mutants destabilize the destruction complex |
14 |
2.09e-01 |
3.00e-01 |
0.24200 |
0.036700 |
0.239000 |
8.12e-01 |
1.21e-01 |
| Synthesis, secretion, and deacylation of Ghrelin |
11 |
1.05e-01 |
1.75e-01 |
0.24100 |
0.211000 |
-0.118000 |
2.26e-01 |
4.99e-01 |
| Platelet calcium homeostasis |
21 |
1.08e-02 |
2.90e-02 |
0.24100 |
-0.155000 |
0.185000 |
2.19e-01 |
1.43e-01 |
| Metabolism of nitric oxide: NOS3 activation and regulation |
12 |
5.18e-01 |
6.05e-01 |
0.24100 |
0.163000 |
0.177000 |
3.27e-01 |
2.88e-01 |
| Immune System |
1885 |
3.55e-42 |
1.61e-39 |
0.24100 |
0.182000 |
0.158000 |
3.38e-39 |
8.29e-30 |
| Host Interactions of HIV factors |
129 |
6.55e-05 |
3.02e-04 |
0.24100 |
0.220000 |
0.097800 |
1.62e-05 |
5.52e-02 |
| Triglyceride metabolism |
25 |
2.46e-01 |
3.39e-01 |
0.24100 |
0.151000 |
0.187000 |
1.91e-01 |
1.05e-01 |
| TGF-beta receptor signaling activates SMADs |
32 |
1.06e-01 |
1.77e-01 |
0.24000 |
0.107000 |
0.215000 |
2.95e-01 |
3.55e-02 |
| FOXO-mediated transcription of cell cycle genes |
15 |
2.73e-01 |
3.70e-01 |
0.24000 |
-0.228000 |
-0.074700 |
1.27e-01 |
6.16e-01 |
| Activated NOTCH1 Transmits Signal to the Nucleus |
27 |
1.47e-01 |
2.29e-01 |
0.23900 |
0.104000 |
0.215000 |
3.49e-01 |
5.26e-02 |
| SRP-dependent cotranslational protein targeting to membrane |
110 |
8.81e-11 |
1.48e-09 |
0.23900 |
0.187000 |
-0.149000 |
6.95e-04 |
6.94e-03 |
| Negative regulation of NMDA receptor-mediated neuronal transmission |
14 |
3.51e-01 |
4.46e-01 |
0.23900 |
-0.095200 |
-0.219000 |
5.38e-01 |
1.56e-01 |
| SARS-CoV Infections |
140 |
2.03e-04 |
8.29e-04 |
0.23900 |
0.128000 |
0.202000 |
9.11e-03 |
3.80e-05 |
| PKA activation |
15 |
1.06e-01 |
1.77e-01 |
0.23800 |
-0.025900 |
0.237000 |
8.62e-01 |
1.12e-01 |
| Regulation of PTEN gene transcription |
59 |
1.45e-02 |
3.73e-02 |
0.23800 |
0.101000 |
0.216000 |
1.81e-01 |
4.10e-03 |
| Transport of small molecules |
554 |
2.73e-13 |
8.08e-12 |
0.23800 |
0.160000 |
0.176000 |
1.31e-10 |
1.22e-12 |
| Dectin-2 family |
19 |
3.39e-01 |
4.35e-01 |
0.23800 |
0.139000 |
0.193000 |
2.94e-01 |
1.46e-01 |
| Fc epsilon receptor (FCERI) signaling |
189 |
2.09e-11 |
4.07e-10 |
0.23700 |
0.237000 |
0.000690 |
1.79e-08 |
9.87e-01 |
| CD209 (DC-SIGN) signaling |
20 |
3.03e-01 |
3.99e-01 |
0.23700 |
0.199000 |
0.129000 |
1.23e-01 |
3.18e-01 |
| Synthesis of PE |
12 |
2.96e-01 |
3.93e-01 |
0.23700 |
-0.045600 |
-0.232000 |
7.85e-01 |
1.63e-01 |
| Negative regulation of FGFR2 signaling |
23 |
3.02e-01 |
3.98e-01 |
0.23500 |
0.159000 |
0.173000 |
1.87e-01 |
1.51e-01 |
| Metabolism of steroids |
116 |
7.26e-04 |
2.65e-03 |
0.23500 |
0.116000 |
0.204000 |
3.10e-02 |
1.45e-04 |
| Resolution of D-loop Structures through Synthesis-Dependent Strand Annealing (SDSA) |
26 |
2.14e-01 |
3.06e-01 |
0.23400 |
-0.124000 |
-0.199000 |
2.73e-01 |
7.93e-02 |
| Class I MHC mediated antigen processing & presentation |
347 |
1.92e-08 |
1.63e-07 |
0.23400 |
0.155000 |
0.175000 |
6.89e-07 |
1.99e-08 |
| Arachidonic acid metabolism |
42 |
1.12e-01 |
1.85e-01 |
0.23400 |
0.178000 |
0.152000 |
4.62e-02 |
8.85e-02 |
| Regulation of PTEN mRNA translation |
13 |
1.81e-01 |
2.69e-01 |
0.23400 |
-0.233000 |
0.006950 |
1.45e-01 |
9.65e-01 |
| Influenza Viral RNA Transcription and Replication |
134 |
3.86e-10 |
5.10e-09 |
0.23300 |
0.056100 |
-0.227000 |
2.62e-01 |
5.91e-06 |
| Estrogen-dependent gene expression |
98 |
7.81e-04 |
2.82e-03 |
0.23300 |
0.089200 |
0.216000 |
1.27e-01 |
2.27e-04 |
| Downstream TCR signaling |
100 |
7.56e-05 |
3.45e-04 |
0.23300 |
0.228000 |
0.049500 |
8.29e-05 |
3.92e-01 |
| Disassembly of the destruction complex and recruitment of AXIN to the membrane |
29 |
1.18e-01 |
1.92e-01 |
0.23200 |
0.086800 |
0.215000 |
4.19e-01 |
4.46e-02 |
| Integrin cell surface interactions |
52 |
4.51e-02 |
9.05e-02 |
0.23200 |
0.118000 |
0.200000 |
1.42e-01 |
1.28e-02 |
| Serotonin Neurotransmitter Release Cycle |
14 |
4.74e-01 |
5.64e-01 |
0.23200 |
-0.139000 |
-0.185000 |
3.68e-01 |
2.30e-01 |
| STING mediated induction of host immune responses |
15 |
2.40e-01 |
3.33e-01 |
0.23200 |
0.227000 |
0.047500 |
1.29e-01 |
7.50e-01 |
| Export of Viral Ribonucleoproteins from Nucleus |
33 |
3.39e-02 |
7.17e-02 |
0.23100 |
-0.034600 |
-0.229000 |
7.31e-01 |
2.30e-02 |
| Aberrant regulation of mitotic exit in cancer due to RB1 defects |
20 |
2.87e-01 |
3.85e-01 |
0.23100 |
0.204000 |
0.110000 |
1.15e-01 |
3.96e-01 |
| Fatty acid metabolism |
150 |
5.50e-04 |
2.06e-03 |
0.23100 |
0.170000 |
0.156000 |
3.20e-04 |
9.61e-04 |
| Neddylation |
217 |
1.43e-05 |
7.51e-05 |
0.23100 |
0.144000 |
0.180000 |
2.52e-04 |
4.64e-06 |
| TNF receptor superfamily (TNFSF) members mediating non-canonical NF-kB pathway |
17 |
7.92e-02 |
1.40e-01 |
0.23100 |
0.039600 |
-0.227000 |
7.77e-01 |
1.05e-01 |
| Formation of HIV-1 elongation complex containing HIV-1 Tat |
42 |
6.50e-02 |
1.21e-01 |
0.23000 |
0.102000 |
0.207000 |
2.53e-01 |
2.04e-02 |
| HIV Transcription Elongation |
42 |
6.50e-02 |
1.21e-01 |
0.23000 |
0.102000 |
0.207000 |
2.53e-01 |
2.04e-02 |
| Tat-mediated elongation of the HIV-1 transcript |
42 |
6.50e-02 |
1.21e-01 |
0.23000 |
0.102000 |
0.207000 |
2.53e-01 |
2.04e-02 |
| Oncogene Induced Senescence |
33 |
4.55e-02 |
9.11e-02 |
0.23000 |
0.047900 |
0.225000 |
6.34e-01 |
2.50e-02 |
| Unfolded Protein Response (UPR) |
87 |
1.35e-02 |
3.47e-02 |
0.23000 |
0.164000 |
0.161000 |
8.20e-03 |
9.27e-03 |
| Regulation of RUNX1 Expression and Activity |
18 |
1.42e-01 |
2.24e-01 |
0.23000 |
-0.229000 |
-0.023600 |
9.28e-02 |
8.62e-01 |
| Vitamin B5 (pantothenate) metabolism |
17 |
4.30e-01 |
5.25e-01 |
0.23000 |
0.162000 |
0.163000 |
2.48e-01 |
2.43e-01 |
| Gap-filling DNA repair synthesis and ligation in GG-NER |
25 |
3.11e-02 |
6.71e-02 |
0.23000 |
0.024400 |
-0.229000 |
8.33e-01 |
4.78e-02 |
| Glyoxylate metabolism and glycine degradation |
24 |
9.84e-02 |
1.66e-01 |
0.23000 |
0.226000 |
0.042100 |
5.54e-02 |
7.21e-01 |
| Cellular Senescence |
144 |
5.04e-05 |
2.40e-04 |
0.22900 |
0.090500 |
0.210000 |
6.09e-02 |
1.33e-05 |
| Cap-dependent Translation Initiation |
117 |
1.50e-10 |
2.24e-09 |
0.22900 |
0.174000 |
-0.149000 |
1.17e-03 |
5.42e-03 |
| Eukaryotic Translation Initiation |
117 |
1.50e-10 |
2.24e-09 |
0.22900 |
0.174000 |
-0.149000 |
1.17e-03 |
5.42e-03 |
| Signaling by FGFR4 in disease |
11 |
3.80e-01 |
4.76e-01 |
0.22900 |
0.222000 |
0.054900 |
2.03e-01 |
7.53e-01 |
| mRNA decay by 3’ to 5’ exoribonuclease |
16 |
9.95e-02 |
1.68e-01 |
0.22800 |
0.035900 |
-0.226000 |
8.04e-01 |
1.18e-01 |
| RUNX1 interacts with co-factors whose precise effect on RUNX1 targets is not known |
36 |
1.51e-03 |
5.05e-03 |
0.22700 |
-0.108000 |
0.200000 |
2.61e-01 |
3.81e-02 |
| Ca-dependent events |
29 |
1.69e-01 |
2.55e-01 |
0.22700 |
0.105000 |
0.201000 |
3.29e-01 |
6.04e-02 |
| HDR through Single Strand Annealing (SSA) |
37 |
6.49e-02 |
1.21e-01 |
0.22700 |
-0.077300 |
-0.213000 |
4.16e-01 |
2.48e-02 |
| Translesion synthesis by POLI |
17 |
9.03e-02 |
1.55e-01 |
0.22700 |
0.034600 |
-0.224000 |
8.05e-01 |
1.10e-01 |
| Metabolism of lipids |
619 |
8.44e-15 |
3.38e-13 |
0.22600 |
0.124000 |
0.189000 |
1.28e-07 |
9.92e-16 |
| NR1H3 & NR1H2 regulate gene expression linked to cholesterol transport and efflux |
32 |
4.87e-03 |
1.44e-02 |
0.22600 |
-0.080400 |
0.211000 |
4.31e-01 |
3.86e-02 |
| cGMP effects |
12 |
3.19e-01 |
4.15e-01 |
0.22600 |
0.038000 |
0.223000 |
8.20e-01 |
1.82e-01 |
| Separation of Sister Chromatids |
167 |
1.07e-04 |
4.75e-04 |
0.22600 |
0.192000 |
0.119000 |
1.92e-05 |
7.95e-03 |
| Elastic fibre formation |
31 |
1.58e-01 |
2.41e-01 |
0.22500 |
0.106000 |
0.199000 |
3.06e-01 |
5.56e-02 |
| G alpha (z) signalling events |
36 |
7.26e-02 |
1.31e-01 |
0.22400 |
0.075700 |
0.211000 |
4.32e-01 |
2.82e-02 |
| Formation of HIV elongation complex in the absence of HIV Tat |
44 |
5.83e-02 |
1.12e-01 |
0.22400 |
0.092500 |
0.204000 |
2.89e-01 |
1.90e-02 |
| Synthesis of Prostaglandins (PG) and Thromboxanes (TX) |
12 |
5.67e-01 |
6.45e-01 |
0.22400 |
0.153000 |
0.164000 |
3.60e-01 |
3.26e-01 |
| Metabolism |
1758 |
1.93e-34 |
5.26e-32 |
0.22400 |
0.170000 |
0.145000 |
1.72e-32 |
4.24e-24 |
| Phase 2 - plateau phase |
11 |
5.86e-01 |
6.62e-01 |
0.22400 |
-0.140000 |
-0.175000 |
4.23e-01 |
3.16e-01 |
| CASP8 activity is inhibited |
11 |
1.51e-01 |
2.33e-01 |
0.22400 |
0.098500 |
-0.201000 |
5.72e-01 |
2.49e-01 |
| Dimerization of procaspase-8 |
11 |
1.51e-01 |
2.33e-01 |
0.22400 |
0.098500 |
-0.201000 |
5.72e-01 |
2.49e-01 |
| Regulation by c-FLIP |
11 |
1.51e-01 |
2.33e-01 |
0.22400 |
0.098500 |
-0.201000 |
5.72e-01 |
2.49e-01 |
| Termination of translesion DNA synthesis |
32 |
4.09e-03 |
1.22e-02 |
0.22300 |
0.100000 |
-0.199000 |
3.26e-01 |
5.09e-02 |
| Signaling by Rho GTPases |
364 |
1.72e-11 |
3.61e-10 |
0.22300 |
0.080900 |
0.208000 |
8.05e-03 |
9.52e-12 |
| TICAM1-dependent activation of IRF3/IRF7 |
12 |
2.29e-01 |
3.22e-01 |
0.22300 |
0.222000 |
-0.011500 |
1.82e-01 |
9.45e-01 |
| Signaling by Nuclear Receptors |
214 |
7.27e-06 |
4.04e-05 |
0.22200 |
0.111000 |
0.193000 |
5.17e-03 |
1.16e-06 |
| Adenylate cyclase inhibitory pathway |
11 |
2.61e-01 |
3.57e-01 |
0.22200 |
-0.011300 |
0.222000 |
9.48e-01 |
2.03e-01 |
| Plasma lipoprotein remodeling |
18 |
2.71e-01 |
3.68e-01 |
0.22100 |
0.070800 |
0.209000 |
6.03e-01 |
1.24e-01 |
| Signaling by FGFR2 |
60 |
4.59e-02 |
9.17e-02 |
0.22100 |
0.185000 |
0.121000 |
1.33e-02 |
1.06e-01 |
| TP53 Regulates Transcription of Cell Death Genes |
43 |
2.52e-02 |
5.68e-02 |
0.22100 |
0.216000 |
0.046200 |
1.44e-02 |
6.00e-01 |
| PERK regulates gene expression |
31 |
3.38e-02 |
7.17e-02 |
0.22100 |
0.220000 |
0.006650 |
3.36e-02 |
9.49e-01 |
| Signaling by FGFR3 in disease |
13 |
2.40e-01 |
3.33e-01 |
0.22000 |
0.220000 |
0.005200 |
1.70e-01 |
9.74e-01 |
| Signaling by FGFR3 point mutants in cancer |
13 |
2.40e-01 |
3.33e-01 |
0.22000 |
0.220000 |
0.005200 |
1.70e-01 |
9.74e-01 |
| Mitotic Anaphase |
223 |
2.11e-05 |
1.08e-04 |
0.21900 |
0.178000 |
0.128000 |
4.43e-06 |
1.01e-03 |
| Interferon gamma signaling |
83 |
7.98e-04 |
2.86e-03 |
0.21900 |
-0.043000 |
-0.215000 |
4.98e-01 |
7.15e-04 |
| Pausing and recovery of Tat-mediated HIV elongation |
30 |
1.26e-01 |
2.00e-01 |
0.21900 |
0.074400 |
0.206000 |
4.81e-01 |
5.08e-02 |
| Tat-mediated HIV elongation arrest and recovery |
30 |
1.26e-01 |
2.00e-01 |
0.21900 |
0.074400 |
0.206000 |
4.81e-01 |
5.08e-02 |
| PIP3 activates AKT signaling |
239 |
3.01e-06 |
1.80e-05 |
0.21900 |
0.110000 |
0.189000 |
3.42e-03 |
4.62e-07 |
| MAPK1/MAPK3 signaling |
233 |
3.13e-05 |
1.54e-04 |
0.21800 |
0.148000 |
0.161000 |
1.03e-04 |
2.35e-05 |
| Processive synthesis on the C-strand of the telomere |
19 |
9.57e-02 |
1.63e-01 |
0.21800 |
0.021100 |
-0.217000 |
8.73e-01 |
1.02e-01 |
| Transport of the SLBP independent Mature mRNA |
35 |
3.38e-02 |
7.17e-02 |
0.21700 |
-0.022100 |
-0.216000 |
8.21e-01 |
2.68e-02 |
| Metabolism of proteins |
1706 |
2.40e-31 |
5.44e-29 |
0.21600 |
0.164000 |
0.141000 |
1.35e-29 |
3.77e-22 |
| Mitotic Metaphase and Anaphase |
224 |
2.43e-05 |
1.21e-04 |
0.21600 |
0.177000 |
0.123000 |
4.70e-06 |
1.52e-03 |
| VEGFR2 mediated cell proliferation |
18 |
2.60e-01 |
3.56e-01 |
0.21500 |
0.057000 |
0.207000 |
6.75e-01 |
1.28e-01 |
| APC-Cdc20 mediated degradation of Nek2A |
26 |
7.81e-02 |
1.39e-01 |
0.21500 |
0.214000 |
0.016100 |
5.85e-02 |
8.87e-01 |
| GABA synthesis, release, reuptake and degradation |
13 |
1.17e-01 |
1.91e-01 |
0.21500 |
0.182000 |
-0.113000 |
2.55e-01 |
4.81e-01 |
| Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC) |
113 |
6.37e-08 |
5.05e-07 |
0.21400 |
0.071000 |
-0.202000 |
1.93e-01 |
2.03e-04 |
| Nonsense-Mediated Decay (NMD) |
113 |
6.37e-08 |
5.05e-07 |
0.21400 |
0.071000 |
-0.202000 |
1.93e-01 |
2.03e-04 |
| PKMTs methylate histone lysines |
44 |
9.46e-03 |
2.58e-02 |
0.21400 |
-0.214000 |
-0.001080 |
1.41e-02 |
9.90e-01 |
| Long-term potentiation |
14 |
2.17e-01 |
3.09e-01 |
0.21400 |
0.004190 |
-0.214000 |
9.78e-01 |
1.66e-01 |
| PRC2 methylates histones and DNA |
29 |
9.82e-02 |
1.66e-01 |
0.21400 |
0.045400 |
0.209000 |
6.72e-01 |
5.16e-02 |
| Mismatch repair (MMR) directed by MSH2:MSH6 (MutSalpha) |
14 |
1.77e-01 |
2.65e-01 |
0.21400 |
0.029300 |
-0.212000 |
8.49e-01 |
1.70e-01 |
| Nephrin family interactions |
18 |
2.90e-01 |
3.88e-01 |
0.21300 |
-0.203000 |
-0.066200 |
1.36e-01 |
6.27e-01 |
| p75 NTR receptor-mediated signalling |
88 |
1.23e-02 |
3.21e-02 |
0.21300 |
0.110000 |
0.183000 |
7.50e-02 |
3.01e-03 |
| Activation of HOX genes during differentiation |
69 |
1.05e-04 |
4.69e-04 |
0.21300 |
-0.046300 |
0.208000 |
5.06e-01 |
2.78e-03 |
| Activation of anterior HOX genes in hindbrain development during early embryogenesis |
69 |
1.05e-04 |
4.69e-04 |
0.21300 |
-0.046300 |
0.208000 |
5.06e-01 |
2.78e-03 |
| tRNA processing in the nucleus |
59 |
2.35e-03 |
7.48e-03 |
0.21300 |
-0.005320 |
-0.213000 |
9.44e-01 |
4.64e-03 |
| Synthesis of DNA |
118 |
1.63e-06 |
1.03e-05 |
0.21300 |
0.213000 |
-0.012700 |
6.56e-05 |
8.12e-01 |
| Inactivation of APC/C via direct inhibition of the APC/C complex |
21 |
1.47e-01 |
2.28e-01 |
0.21300 |
0.211000 |
0.023900 |
9.35e-02 |
8.50e-01 |
| Inhibition of the proteolytic activity of APC/C required for the onset of anaphase by mitotic spindle checkpoint components |
21 |
1.47e-01 |
2.28e-01 |
0.21300 |
0.211000 |
0.023900 |
9.35e-02 |
8.50e-01 |
| Downstream signaling of activated FGFR1 |
20 |
3.81e-01 |
4.76e-01 |
0.21300 |
0.179000 |
0.115000 |
1.65e-01 |
3.75e-01 |
| G beta:gamma signalling through PI3Kgamma |
22 |
2.23e-01 |
3.16e-01 |
0.21300 |
0.066100 |
0.202000 |
5.91e-01 |
1.01e-01 |
| Repression of WNT target genes |
14 |
5.49e-01 |
6.29e-01 |
0.21300 |
-0.141000 |
-0.159000 |
3.61e-01 |
3.03e-01 |
| HIV elongation arrest and recovery |
32 |
1.08e-01 |
1.80e-01 |
0.21200 |
0.063100 |
0.203000 |
5.37e-01 |
4.71e-02 |
| Pausing and recovery of HIV elongation |
32 |
1.08e-01 |
1.80e-01 |
0.21200 |
0.063100 |
0.203000 |
5.37e-01 |
4.71e-02 |
| Translesion synthesis by POLK |
17 |
1.07e-01 |
1.78e-01 |
0.21200 |
0.045700 |
-0.207000 |
7.44e-01 |
1.39e-01 |
| HCMV Late Events |
69 |
4.91e-02 |
9.65e-02 |
0.21200 |
0.131000 |
0.166000 |
5.92e-02 |
1.70e-02 |
| Maturation of nucleoprotein |
10 |
6.42e-01 |
7.11e-01 |
0.21200 |
-0.128000 |
-0.168000 |
4.83e-01 |
3.56e-01 |
| Regulation of expression of SLITs and ROBOs |
158 |
2.12e-09 |
2.28e-08 |
0.21200 |
0.208000 |
-0.039300 |
6.50e-06 |
3.94e-01 |
| DNA Damage/Telomere Stress Induced Senescence |
44 |
2.82e-02 |
6.20e-02 |
0.21100 |
0.039700 |
0.208000 |
6.48e-01 |
1.72e-02 |
| Biosynthesis of the N-glycan precursor (dolichol lipid-linked oligosaccharide, LLO) and transfer to a nascent protein |
73 |
1.33e-02 |
3.44e-02 |
0.21000 |
0.194000 |
0.080700 |
4.14e-03 |
2.33e-01 |
| FRS-mediated FGFR2 signaling |
14 |
2.54e-01 |
3.47e-01 |
0.21000 |
0.210000 |
0.008100 |
1.74e-01 |
9.58e-01 |
| Sema3A PAK dependent Axon repulsion |
16 |
3.74e-01 |
4.69e-01 |
0.21000 |
0.196000 |
0.075500 |
1.75e-01 |
6.01e-01 |
| mRNA Splicing - Minor Pathway |
52 |
7.44e-02 |
1.33e-01 |
0.20900 |
0.183000 |
0.103000 |
2.28e-02 |
2.01e-01 |
| MAPK family signaling cascades |
267 |
1.71e-05 |
8.96e-05 |
0.20900 |
0.139000 |
0.157000 |
9.23e-05 |
1.05e-05 |
| Defective B3GALT6 causes EDSP2 and SEMDJL1 |
11 |
5.16e-01 |
6.03e-01 |
0.20900 |
-0.077000 |
-0.194000 |
6.58e-01 |
2.64e-01 |
| PI-3K cascade:FGFR4 |
10 |
6.19e-01 |
6.92e-01 |
0.20900 |
0.179000 |
0.107000 |
3.28e-01 |
5.56e-01 |
| Post-translational protein modification |
1183 |
1.18e-21 |
1.15e-19 |
0.20800 |
0.126000 |
0.166000 |
2.77e-13 |
6.39e-22 |
| Transcription of the HIV genome |
67 |
4.93e-02 |
9.67e-02 |
0.20800 |
0.116000 |
0.173000 |
1.01e-01 |
1.46e-02 |
| Cytosolic sulfonation of small molecules |
18 |
2.21e-01 |
3.14e-01 |
0.20700 |
0.028500 |
0.205000 |
8.34e-01 |
1.31e-01 |
| Cellular hexose transport |
15 |
5.42e-01 |
6.23e-01 |
0.20700 |
-0.136000 |
-0.156000 |
3.61e-01 |
2.95e-01 |
| Phase II - Conjugation of compounds |
66 |
7.03e-02 |
1.29e-01 |
0.20700 |
0.150000 |
0.143000 |
3.52e-02 |
4.46e-02 |
| Signaling by FGFR2 in disease |
32 |
1.11e-01 |
1.84e-01 |
0.20700 |
0.199000 |
0.055700 |
5.12e-02 |
5.85e-01 |
| RAS processing |
19 |
4.67e-01 |
5.58e-01 |
0.20700 |
0.148000 |
0.144000 |
2.64e-01 |
2.76e-01 |
| Regulation of actin dynamics for phagocytic cup formation |
122 |
1.16e-07 |
9.04e-07 |
0.20700 |
0.199000 |
-0.057500 |
1.52e-04 |
2.73e-01 |
| Depolymerisation of the Nuclear Lamina |
15 |
5.07e-01 |
5.96e-01 |
0.20600 |
0.112000 |
0.173000 |
4.53e-01 |
2.45e-01 |
| Insulin receptor signalling cascade |
39 |
1.86e-01 |
2.73e-01 |
0.20600 |
0.120000 |
0.168000 |
1.96e-01 |
6.92e-02 |
| Phospholipid metabolism |
184 |
2.33e-04 |
9.30e-04 |
0.20600 |
0.109000 |
0.175000 |
1.05e-02 |
4.35e-05 |
| FLT3 Signaling |
242 |
6.00e-05 |
2.81e-04 |
0.20600 |
0.132000 |
0.157000 |
3.90e-04 |
2.44e-05 |
| DNA Replication |
125 |
4.26e-06 |
2.48e-05 |
0.20500 |
0.205000 |
-0.002080 |
7.42e-05 |
9.68e-01 |
| RAF/MAP kinase cascade |
228 |
1.27e-04 |
5.41e-04 |
0.20500 |
0.137000 |
0.153000 |
3.79e-04 |
7.13e-05 |
| DAP12 interactions |
39 |
2.16e-01 |
3.08e-01 |
0.20500 |
0.141000 |
0.149000 |
1.29e-01 |
1.08e-01 |
| Formation of Incision Complex in GG-NER |
43 |
1.85e-01 |
2.73e-01 |
0.20500 |
0.147000 |
0.142000 |
9.56e-02 |
1.06e-01 |
| Intracellular signaling by second messengers |
271 |
1.90e-06 |
1.19e-05 |
0.20400 |
0.095800 |
0.181000 |
6.62e-03 |
3.13e-07 |
| tRNA modification in the nucleus and cytosol |
43 |
3.08e-03 |
9.58e-03 |
0.20400 |
0.070100 |
-0.192000 |
4.27e-01 |
2.96e-02 |
| Disorders of Developmental Biology |
12 |
3.18e-01 |
4.15e-01 |
0.20400 |
0.002910 |
0.204000 |
9.86e-01 |
2.21e-01 |
| Disorders of Nervous System Development |
12 |
3.18e-01 |
4.15e-01 |
0.20400 |
0.002910 |
0.204000 |
9.86e-01 |
2.21e-01 |
| Loss of function of MECP2 in Rett syndrome |
12 |
3.18e-01 |
4.15e-01 |
0.20400 |
0.002910 |
0.204000 |
9.86e-01 |
2.21e-01 |
| Pervasive developmental disorders |
12 |
3.18e-01 |
4.15e-01 |
0.20400 |
0.002910 |
0.204000 |
9.86e-01 |
2.21e-01 |
| Miscellaneous transport and binding events |
20 |
2.71e-01 |
3.68e-01 |
0.20400 |
0.058400 |
0.195000 |
6.51e-01 |
1.30e-01 |
| Regulation of FOXO transcriptional activity by acetylation |
10 |
2.23e-01 |
3.16e-01 |
0.20400 |
-0.170000 |
0.113000 |
3.53e-01 |
5.37e-01 |
| HDR through Homologous Recombination (HRR) |
66 |
9.87e-03 |
2.67e-02 |
0.20300 |
-0.047800 |
-0.198000 |
5.02e-01 |
5.47e-03 |
| Glucose metabolism |
83 |
3.81e-02 |
7.94e-02 |
0.20300 |
0.155000 |
0.132000 |
1.48e-02 |
3.80e-02 |
| G1/S Transition |
130 |
7.63e-06 |
4.16e-05 |
0.20300 |
0.203000 |
0.009170 |
6.42e-05 |
8.57e-01 |
| Unblocking of NMDA receptors, glutamate binding and activation |
12 |
5.09e-01 |
5.97e-01 |
0.20300 |
-0.076100 |
-0.188000 |
6.48e-01 |
2.59e-01 |
| G2/M Checkpoints |
138 |
3.55e-04 |
1.38e-03 |
0.20300 |
0.189000 |
0.071600 |
1.21e-04 |
1.47e-01 |
| Extracellular matrix organization |
215 |
2.23e-05 |
1.13e-04 |
0.20100 |
0.087500 |
0.181000 |
2.70e-02 |
4.61e-06 |
| Synthesis of substrates in N-glycan biosythesis |
58 |
6.25e-02 |
1.17e-01 |
0.20100 |
0.178000 |
0.093800 |
1.90e-02 |
2.17e-01 |
| NF-kB is activated and signals survival |
12 |
6.02e-01 |
6.77e-01 |
0.20100 |
0.167000 |
0.111000 |
3.15e-01 |
5.06e-01 |
| Meiotic synapsis |
45 |
4.21e-02 |
8.58e-02 |
0.20100 |
0.043100 |
0.196000 |
6.17e-01 |
2.28e-02 |
| Nef-mediates down modulation of cell surface receptors by recruiting them to clathrin adapters |
21 |
4.52e-01 |
5.43e-01 |
0.20100 |
0.143000 |
0.140000 |
2.55e-01 |
2.66e-01 |
| Transport of the SLBP Dependant Mature mRNA |
36 |
3.33e-02 |
7.08e-02 |
0.20000 |
0.003040 |
-0.200000 |
9.75e-01 |
3.82e-02 |
| Metabolism of carbohydrates |
241 |
6.81e-05 |
3.13e-04 |
0.20000 |
0.117000 |
0.162000 |
1.80e-03 |
1.49e-05 |
| Signaling by NOTCH3 |
42 |
1.07e-01 |
1.78e-01 |
0.20000 |
0.077200 |
0.184000 |
3.87e-01 |
3.91e-02 |
| Negative epigenetic regulation of rRNA expression |
62 |
6.08e-02 |
1.15e-01 |
0.19900 |
0.097900 |
0.174000 |
1.83e-01 |
1.80e-02 |
| Defective B4GALT7 causes EDS, progeroid type |
11 |
5.19e-01 |
6.05e-01 |
0.19900 |
-0.062700 |
-0.189000 |
7.19e-01 |
2.77e-01 |
| Eicosanoid ligand-binding receptors |
13 |
2.77e-01 |
3.74e-01 |
0.19900 |
0.011200 |
-0.199000 |
9.44e-01 |
2.14e-01 |
| NR1H2 and NR1H3-mediated signaling |
38 |
9.32e-03 |
2.55e-02 |
0.19900 |
-0.057800 |
0.191000 |
5.38e-01 |
4.21e-02 |
| HCMV Infection |
96 |
2.17e-02 |
5.04e-02 |
0.19900 |
0.116000 |
0.162000 |
4.94e-02 |
6.20e-03 |
| Metabolism of fat-soluble vitamins |
28 |
1.44e-01 |
2.26e-01 |
0.19900 |
0.042000 |
0.194000 |
7.01e-01 |
7.55e-02 |
| Lysosphingolipid and LPA receptors |
11 |
5.29e-01 |
6.12e-01 |
0.19800 |
-0.064800 |
-0.188000 |
7.10e-01 |
2.82e-01 |
| HSF1 activation |
26 |
8.93e-02 |
1.54e-01 |
0.19800 |
0.198000 |
-0.002720 |
8.05e-02 |
9.81e-01 |
| NOTCH3 Intracellular Domain Regulates Transcription |
20 |
1.06e-01 |
1.77e-01 |
0.19800 |
-0.039500 |
0.194000 |
7.60e-01 |
1.34e-01 |
| Acyl chain remodelling of PE |
20 |
4.81e-01 |
5.71e-01 |
0.19700 |
0.136000 |
0.143000 |
2.93e-01 |
2.68e-01 |
| Anti-inflammatory response favouring Leishmania parasite infection |
167 |
2.24e-09 |
2.35e-08 |
0.19700 |
0.055900 |
-0.189000 |
2.13e-01 |
2.51e-05 |
| Leishmania parasite growth and survival |
167 |
2.24e-09 |
2.35e-08 |
0.19700 |
0.055900 |
-0.189000 |
2.13e-01 |
2.51e-05 |
| Ion channel transport |
133 |
3.91e-03 |
1.18e-02 |
0.19600 |
0.103000 |
0.167000 |
3.97e-02 |
8.72e-04 |
| Interferon Signaling |
177 |
2.10e-05 |
1.07e-04 |
0.19600 |
-0.054700 |
-0.189000 |
2.10e-01 |
1.48e-05 |
| Metabolism of non-coding RNA |
53 |
1.56e-03 |
5.18e-03 |
0.19600 |
0.062000 |
-0.186000 |
4.35e-01 |
1.89e-02 |
| snRNP Assembly |
53 |
1.56e-03 |
5.18e-03 |
0.19600 |
0.062000 |
-0.186000 |
4.35e-01 |
1.89e-02 |
| MicroRNA (miRNA) biogenesis |
24 |
4.11e-01 |
5.08e-01 |
0.19600 |
0.124000 |
0.152000 |
2.93e-01 |
1.99e-01 |
| Diseases associated with N-glycosylation of proteins |
17 |
4.52e-01 |
5.43e-01 |
0.19600 |
0.175000 |
0.087200 |
2.11e-01 |
5.34e-01 |
| Formation of the beta-catenin:TCF transactivating complex |
46 |
1.93e-02 |
4.60e-02 |
0.19500 |
0.004610 |
0.195000 |
9.57e-01 |
2.24e-02 |
| SHC-mediated cascade:FGFR2 |
12 |
1.96e-01 |
2.88e-01 |
0.19500 |
0.165000 |
-0.103000 |
3.22e-01 |
5.38e-01 |
| G1/S-Specific Transcription |
29 |
1.78e-02 |
4.42e-02 |
0.19400 |
0.120000 |
-0.152000 |
2.62e-01 |
1.56e-01 |
| Influenza Infection |
153 |
6.30e-09 |
5.80e-08 |
0.19400 |
0.072300 |
-0.180000 |
1.23e-01 |
1.20e-04 |
| Signaling by the B Cell Receptor (BCR) |
161 |
1.28e-08 |
1.14e-07 |
0.19400 |
0.187000 |
-0.049900 |
4.15e-05 |
2.75e-01 |
| Potential therapeutics for SARS |
78 |
4.23e-02 |
8.60e-02 |
0.19300 |
0.101000 |
0.165000 |
1.21e-01 |
1.19e-02 |
| Phase 4 - resting membrane potential |
10 |
5.40e-01 |
6.23e-01 |
0.19300 |
0.187000 |
0.049200 |
3.06e-01 |
7.88e-01 |
| ABC transporters in lipid homeostasis |
14 |
3.57e-01 |
4.53e-01 |
0.19300 |
-0.025000 |
-0.191000 |
8.71e-01 |
2.15e-01 |
| Keratan sulfate/keratin metabolism |
25 |
1.41e-01 |
2.22e-01 |
0.19300 |
0.015900 |
0.192000 |
8.91e-01 |
9.60e-02 |
| Glutamate binding, activation of AMPA receptors and synaptic plasticity |
20 |
1.45e-01 |
2.27e-01 |
0.19300 |
-0.018400 |
0.192000 |
8.86e-01 |
1.37e-01 |
| Trafficking of AMPA receptors |
20 |
1.45e-01 |
2.27e-01 |
0.19300 |
-0.018400 |
0.192000 |
8.86e-01 |
1.37e-01 |
| Signaling by TGFB family members |
91 |
1.87e-02 |
4.51e-02 |
0.19200 |
0.089300 |
0.170000 |
1.41e-01 |
4.96e-03 |
| Metabolic disorders of biological oxidation enzymes |
23 |
4.28e-01 |
5.22e-01 |
0.19200 |
0.155000 |
0.115000 |
2.00e-01 |
3.42e-01 |
| RUNX3 regulates p14-ARF |
10 |
3.78e-01 |
4.73e-01 |
0.19200 |
-0.022000 |
0.190000 |
9.04e-01 |
2.97e-01 |
| Retinoid metabolism and transport |
24 |
1.79e-01 |
2.67e-01 |
0.19100 |
0.024800 |
0.189000 |
8.33e-01 |
1.09e-01 |
| Laminin interactions |
21 |
3.53e-01 |
4.49e-01 |
0.19000 |
0.071200 |
0.177000 |
5.72e-01 |
1.61e-01 |
| Fatty acyl-CoA biosynthesis |
33 |
3.18e-01 |
4.15e-01 |
0.19000 |
0.121000 |
0.146000 |
2.28e-01 |
1.46e-01 |
| Signaling by ERBB2 |
44 |
1.80e-01 |
2.68e-01 |
0.19000 |
0.099800 |
0.161000 |
2.52e-01 |
6.40e-02 |
| Neurotransmitter receptors and postsynaptic signal transmission |
123 |
6.53e-03 |
1.85e-02 |
0.19000 |
0.092700 |
0.165000 |
7.59e-02 |
1.53e-03 |
| Conversion from APC/C:Cdc20 to APC/C:Cdh1 in late anaphase |
20 |
2.98e-01 |
3.94e-01 |
0.18900 |
0.184000 |
0.045100 |
1.54e-01 |
7.27e-01 |
| Transcriptional regulation by RUNX1 |
184 |
1.27e-04 |
5.41e-04 |
0.18900 |
0.070400 |
0.176000 |
9.97e-02 |
3.90e-05 |
| RIP-mediated NFkB activation via ZBP1 |
17 |
5.45e-01 |
6.26e-01 |
0.18900 |
0.113000 |
0.152000 |
4.19e-01 |
2.79e-01 |
| Defects in vitamin and cofactor metabolism |
21 |
4.26e-01 |
5.20e-01 |
0.18900 |
-0.093600 |
-0.165000 |
4.58e-01 |
1.92e-01 |
| Signaling by TGF-beta Receptor Complex |
72 |
1.34e-02 |
3.46e-02 |
0.18900 |
0.044900 |
0.183000 |
5.10e-01 |
7.17e-03 |
| ZBP1(DAI) mediated induction of type I IFNs |
20 |
4.63e-01 |
5.54e-01 |
0.18800 |
0.098600 |
0.160000 |
4.45e-01 |
2.15e-01 |
| Translesion Synthesis by POLH |
18 |
9.42e-02 |
1.60e-01 |
0.18800 |
0.122000 |
-0.143000 |
3.69e-01 |
2.94e-01 |
| Mitotic G1 phase and G1/S transition |
148 |
4.73e-05 |
2.26e-04 |
0.18800 |
0.186000 |
0.028400 |
9.54e-05 |
5.51e-01 |
| Signaling by WNT in cancer |
30 |
2.09e-02 |
4.88e-02 |
0.18800 |
-0.152000 |
0.111000 |
1.51e-01 |
2.94e-01 |
| Resolution of D-Loop Structures |
33 |
3.38e-01 |
4.34e-01 |
0.18700 |
-0.131000 |
-0.134000 |
1.94e-01 |
1.83e-01 |
| Cell surface interactions at the vascular wall |
172 |
1.95e-08 |
1.64e-07 |
0.18700 |
0.182000 |
-0.044300 |
3.98e-05 |
3.16e-01 |
| Early Phase of HIV Life Cycle |
14 |
1.65e-01 |
2.51e-01 |
0.18700 |
0.147000 |
-0.116000 |
3.42e-01 |
4.54e-01 |
| Nitric oxide stimulates guanylate cyclase |
14 |
5.68e-01 |
6.45e-01 |
0.18600 |
0.088200 |
0.164000 |
5.68e-01 |
2.89e-01 |
| FCGR3A-mediated phagocytosis |
120 |
7.02e-07 |
4.78e-06 |
0.18600 |
0.167000 |
-0.081300 |
1.55e-03 |
1.24e-01 |
| Leishmania phagocytosis |
120 |
7.02e-07 |
4.78e-06 |
0.18600 |
0.167000 |
-0.081300 |
1.55e-03 |
1.24e-01 |
| Parasite infection |
120 |
7.02e-07 |
4.78e-06 |
0.18600 |
0.167000 |
-0.081300 |
1.55e-03 |
1.24e-01 |
| Stimuli-sensing channels |
72 |
9.65e-02 |
1.64e-01 |
0.18600 |
0.126000 |
0.137000 |
6.48e-02 |
4.48e-02 |
| Factors involved in megakaryocyte development and platelet production |
116 |
1.22e-02 |
3.20e-02 |
0.18600 |
0.094800 |
0.160000 |
7.78e-02 |
2.98e-03 |
| Negative regulation of MAPK pathway |
42 |
2.25e-01 |
3.18e-01 |
0.18600 |
0.105000 |
0.153000 |
2.40e-01 |
8.59e-02 |
| Activation of RAC1 |
11 |
7.00e-01 |
7.61e-01 |
0.18600 |
0.125000 |
0.137000 |
4.72e-01 |
4.32e-01 |
| Downregulation of ERBB2 signaling |
24 |
3.50e-01 |
4.45e-01 |
0.18500 |
0.077400 |
0.168000 |
5.12e-01 |
1.53e-01 |
| Interleukin-20 family signaling |
17 |
5.12e-01 |
6.00e-01 |
0.18500 |
0.162000 |
0.090200 |
2.48e-01 |
5.19e-01 |
| Removal of the Flap Intermediate from the C-strand |
17 |
1.83e-01 |
2.71e-01 |
0.18500 |
0.039400 |
-0.181000 |
7.79e-01 |
1.96e-01 |
| Mitotic G2-G2/M phases |
180 |
1.05e-03 |
3.59e-03 |
0.18500 |
0.160000 |
0.092900 |
2.12e-04 |
3.16e-02 |
| RET signaling |
32 |
3.16e-01 |
4.14e-01 |
0.18500 |
0.101000 |
0.155000 |
3.23e-01 |
1.30e-01 |
| G2/M Transition |
178 |
9.22e-04 |
3.24e-03 |
0.18400 |
0.162000 |
0.087600 |
1.92e-04 |
4.38e-02 |
| Downstream signal transduction |
27 |
3.10e-01 |
4.08e-01 |
0.18400 |
0.076300 |
0.167000 |
4.92e-01 |
1.32e-01 |
| Antiviral mechanism by IFN-stimulated genes |
80 |
3.14e-02 |
6.76e-02 |
0.18400 |
-0.075600 |
-0.167000 |
2.42e-01 |
9.65e-03 |
| Glycolysis |
66 |
1.02e-01 |
1.71e-01 |
0.18300 |
0.151000 |
0.104000 |
3.36e-02 |
1.45e-01 |
| TCR signaling |
121 |
1.97e-03 |
6.35e-03 |
0.18300 |
0.175000 |
0.054500 |
8.85e-04 |
3.00e-01 |
| Resolution of D-loop Structures through Holliday Junction Intermediates |
32 |
3.48e-01 |
4.43e-01 |
0.18300 |
-0.112000 |
-0.145000 |
2.73e-01 |
1.56e-01 |
| TP53 Regulates Transcription of Genes Involved in Cytochrome C Release |
19 |
5.33e-01 |
6.16e-01 |
0.18300 |
-0.110000 |
-0.146000 |
4.05e-01 |
2.71e-01 |
| Inhibition of replication initiation of damaged DNA by RB1/E2F1 |
13 |
3.26e-01 |
4.21e-01 |
0.18200 |
0.182000 |
-0.016800 |
2.57e-01 |
9.17e-01 |
| Constitutive Signaling by AKT1 E17K in Cancer |
26 |
4.36e-02 |
8.78e-02 |
0.18100 |
-0.109000 |
0.145000 |
3.36e-01 |
2.02e-01 |
| Potassium Channels |
63 |
1.40e-01 |
2.20e-01 |
0.18100 |
0.137000 |
0.118000 |
5.91e-02 |
1.06e-01 |
| Metabolism of amino acids and derivatives |
323 |
1.32e-11 |
2.82e-10 |
0.18100 |
0.181000 |
-0.004500 |
2.29e-08 |
8.89e-01 |
| Regulation of TP53 Activity through Methylation |
19 |
5.41e-01 |
6.23e-01 |
0.18100 |
-0.109000 |
-0.144000 |
4.11e-01 |
2.77e-01 |
| Axon guidance |
451 |
6.55e-07 |
4.53e-06 |
0.18000 |
0.144000 |
0.109000 |
1.68e-07 |
7.16e-05 |
| Late Phase of HIV Life Cycle |
131 |
1.85e-02 |
4.51e-02 |
0.18000 |
0.134000 |
0.120000 |
8.17e-03 |
1.75e-02 |
| BBSome-mediated cargo-targeting to cilium |
22 |
7.24e-02 |
1.31e-01 |
0.18000 |
0.115000 |
-0.138000 |
3.51e-01 |
2.63e-01 |
| Synthesis of Leukotrienes (LT) and Eoxins (EX) |
15 |
5.95e-01 |
6.71e-01 |
0.17900 |
0.094000 |
0.152000 |
5.28e-01 |
3.09e-01 |
| Tight junction interactions |
18 |
1.22e-01 |
1.97e-01 |
0.17800 |
0.107000 |
-0.143000 |
4.31e-01 |
2.94e-01 |
| TP53 Regulates Transcription of Death Receptors and Ligands |
12 |
2.96e-01 |
3.93e-01 |
0.17800 |
0.168000 |
-0.058100 |
3.12e-01 |
7.28e-01 |
| E2F mediated regulation of DNA replication |
22 |
7.51e-02 |
1.34e-01 |
0.17800 |
0.119000 |
-0.132000 |
3.34e-01 |
2.83e-01 |
| Xenobiotics |
11 |
5.47e-01 |
6.27e-01 |
0.17800 |
0.174000 |
0.039100 |
3.19e-01 |
8.22e-01 |
| FGFR2 mutant receptor activation |
22 |
2.89e-01 |
3.87e-01 |
0.17700 |
0.174000 |
0.034500 |
1.59e-01 |
7.79e-01 |
| Processing of Capped Intronless Pre-mRNA |
28 |
3.45e-01 |
4.40e-01 |
0.17700 |
0.158000 |
0.079200 |
1.47e-01 |
4.68e-01 |
| Assembly and cell surface presentation of NMDA receptors |
18 |
1.71e-01 |
2.57e-01 |
0.17700 |
0.054400 |
-0.168000 |
6.90e-01 |
2.17e-01 |
| Transport of vitamins, nucleosides, and related molecules |
32 |
1.76e-01 |
2.65e-01 |
0.17600 |
0.038200 |
0.172000 |
7.09e-01 |
9.17e-02 |
| Cargo trafficking to the periciliary membrane |
47 |
2.04e-01 |
2.96e-01 |
0.17600 |
0.150000 |
0.092400 |
7.47e-02 |
2.73e-01 |
| Apoptotic cleavage of cellular proteins |
34 |
2.76e-01 |
3.74e-01 |
0.17600 |
0.078700 |
0.158000 |
4.27e-01 |
1.11e-01 |
| Infectious disease |
773 |
8.59e-13 |
2.25e-11 |
0.17500 |
0.156000 |
0.078700 |
1.33e-13 |
1.97e-04 |
| CLEC7A (Dectin-1) induces NFAT activation |
11 |
3.26e-01 |
4.21e-01 |
0.17500 |
-0.162000 |
0.067100 |
3.53e-01 |
7.00e-01 |
| Nuclear Pore Complex (NPC) Disassembly |
36 |
9.50e-02 |
1.61e-01 |
0.17500 |
-0.012400 |
-0.175000 |
8.97e-01 |
6.97e-02 |
| PI-3K cascade:FGFR1 |
12 |
6.92e-01 |
7.57e-01 |
0.17500 |
0.103000 |
0.141000 |
5.38e-01 |
3.97e-01 |
| Recognition of DNA damage by PCNA-containing replication complex |
30 |
4.35e-02 |
8.77e-02 |
0.17500 |
0.076500 |
-0.157000 |
4.68e-01 |
1.37e-01 |
| Glutamate Neurotransmitter Release Cycle |
20 |
1.16e-01 |
1.89e-01 |
0.17300 |
0.092500 |
-0.147000 |
4.74e-01 |
2.56e-01 |
| FOXO-mediated transcription of cell death genes |
16 |
3.61e-01 |
4.56e-01 |
0.17300 |
0.013300 |
0.173000 |
9.26e-01 |
2.31e-01 |
| ATF4 activates genes in response to endoplasmic reticulum stress |
26 |
8.51e-02 |
1.48e-01 |
0.17300 |
0.164000 |
-0.054900 |
1.48e-01 |
6.28e-01 |
| Degradation of cysteine and homocysteine |
12 |
7.08e-01 |
7.67e-01 |
0.17300 |
0.109000 |
0.134000 |
5.12e-01 |
4.23e-01 |
| MECP2 regulates neuronal receptors and channels |
13 |
2.67e-01 |
3.64e-01 |
0.17300 |
-0.073900 |
0.156000 |
6.45e-01 |
3.30e-01 |
| Nuclear Receptor transcription pathway |
37 |
1.39e-01 |
2.20e-01 |
0.17200 |
-0.169000 |
-0.033900 |
7.53e-02 |
7.21e-01 |
| Glycosaminoglycan metabolism |
92 |
6.76e-03 |
1.91e-02 |
0.17200 |
0.030100 |
0.169000 |
6.18e-01 |
5.10e-03 |
| Signaling by FGFR |
69 |
1.50e-01 |
2.33e-01 |
0.17100 |
0.126000 |
0.116000 |
7.13e-02 |
9.57e-02 |
| Olfactory Signaling Pathway |
55 |
1.12e-01 |
1.85e-01 |
0.17100 |
0.159000 |
0.063700 |
4.20e-02 |
4.14e-01 |
| Interleukin-37 signaling |
19 |
1.30e-01 |
2.07e-01 |
0.17100 |
-0.105000 |
0.135000 |
4.29e-01 |
3.09e-01 |
| SUMOylation of SUMOylation proteins |
35 |
1.88e-01 |
2.75e-01 |
0.17000 |
-0.043300 |
-0.165000 |
6.58e-01 |
9.14e-02 |
| mRNA Splicing |
187 |
2.22e-03 |
7.12e-03 |
0.17000 |
0.148000 |
0.084100 |
4.77e-04 |
4.75e-02 |
| Nervous system development |
470 |
2.58e-06 |
1.57e-05 |
0.16900 |
0.133000 |
0.105000 |
8.19e-07 |
9.50e-05 |
| NOTCH4 Intracellular Domain Regulates Transcription |
17 |
2.45e-01 |
3.39e-01 |
0.16900 |
-0.165000 |
0.035700 |
2.40e-01 |
7.99e-01 |
| Activation of kainate receptors upon glutamate binding |
25 |
4.89e-01 |
5.78e-01 |
0.16800 |
0.097900 |
0.137000 |
3.97e-01 |
2.37e-01 |
| Transcriptional Regulation by E2F6 |
34 |
2.37e-01 |
3.31e-01 |
0.16800 |
-0.052700 |
-0.160000 |
5.95e-01 |
1.07e-01 |
| Phase I - Functionalization of compounds |
61 |
1.46e-01 |
2.28e-01 |
0.16800 |
0.145000 |
0.083900 |
4.99e-02 |
2.57e-01 |
| Neurexins and neuroligins |
35 |
3.81e-01 |
4.76e-01 |
0.16700 |
-0.102000 |
-0.133000 |
2.97e-01 |
1.74e-01 |
| Circadian Clock |
67 |
1.87e-02 |
4.51e-02 |
0.16700 |
0.012300 |
0.167000 |
8.62e-01 |
1.82e-02 |
| Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks |
46 |
1.61e-02 |
4.06e-02 |
0.16700 |
-0.056500 |
0.157000 |
5.07e-01 |
6.49e-02 |
| HIV Life Cycle |
144 |
1.76e-02 |
4.38e-02 |
0.16700 |
0.136000 |
0.097200 |
4.92e-03 |
4.41e-02 |
| CaM pathway |
27 |
4.16e-01 |
5.11e-01 |
0.16600 |
0.078500 |
0.147000 |
4.80e-01 |
1.87e-01 |
| Calmodulin induced events |
27 |
4.16e-01 |
5.11e-01 |
0.16600 |
0.078500 |
0.147000 |
4.80e-01 |
1.87e-01 |
| TRAF3-dependent IRF activation pathway |
13 |
6.41e-01 |
7.11e-01 |
0.16600 |
0.150000 |
0.072600 |
3.50e-01 |
6.51e-01 |
| Mismatch repair (MMR) directed by MSH2:MSH3 (MutSbeta) |
14 |
3.34e-01 |
4.30e-01 |
0.16600 |
0.030400 |
-0.163000 |
8.44e-01 |
2.90e-01 |
| Keratinization |
33 |
2.63e-01 |
3.59e-01 |
0.16600 |
0.157000 |
0.054600 |
1.19e-01 |
5.87e-01 |
| Polo-like kinase mediated events |
15 |
6.66e-01 |
7.34e-01 |
0.16600 |
0.101000 |
0.132000 |
4.98e-01 |
3.78e-01 |
| TP53 Regulates Transcription of Caspase Activators and Caspases |
12 |
2.95e-01 |
3.92e-01 |
0.16500 |
0.111000 |
-0.122000 |
5.04e-01 |
4.64e-01 |
| mRNA Splicing - Major Pathway |
179 |
3.91e-03 |
1.18e-02 |
0.16500 |
0.144000 |
0.080900 |
8.79e-04 |
6.20e-02 |
| Mitotic Prophase |
98 |
8.23e-02 |
1.45e-01 |
0.16500 |
0.116000 |
0.118000 |
4.77e-02 |
4.39e-02 |
| Signaling by PDGF |
44 |
2.25e-01 |
3.18e-01 |
0.16500 |
0.071100 |
0.149000 |
4.14e-01 |
8.75e-02 |
| Synthesis of IP2, IP, and Ins in the cytosol |
13 |
7.14e-01 |
7.72e-01 |
0.16500 |
0.125000 |
0.107000 |
4.35e-01 |
5.03e-01 |
| Signaling by Activin |
10 |
5.21e-01 |
6.06e-01 |
0.16500 |
0.004660 |
-0.164000 |
9.80e-01 |
3.68e-01 |
| Rho GTPase cycle |
125 |
3.76e-04 |
1.45e-03 |
0.16400 |
-0.000755 |
0.164000 |
9.88e-01 |
1.50e-03 |
| Establishment of Sister Chromatid Cohesion |
11 |
7.52e-01 |
8.02e-01 |
0.16400 |
0.126000 |
0.106000 |
4.70e-01 |
5.44e-01 |
| Transport of Mature mRNA Derived from an Intronless Transcript |
42 |
1.49e-01 |
2.31e-01 |
0.16300 |
-0.038100 |
-0.159000 |
6.69e-01 |
7.48e-02 |
| Mitochondrial tRNA aminoacylation |
21 |
4.85e-01 |
5.74e-01 |
0.16300 |
-0.066600 |
-0.149000 |
5.97e-01 |
2.37e-01 |
| Defective B3GAT3 causes JDSSDHD |
11 |
6.35e-01 |
7.07e-01 |
0.16300 |
-0.047900 |
-0.156000 |
7.83e-01 |
3.71e-01 |
| Fcgamma receptor (FCGR) dependent phagocytosis |
146 |
1.93e-05 |
9.94e-05 |
0.16200 |
0.160000 |
-0.029700 |
8.62e-04 |
5.36e-01 |
| Collagen formation |
64 |
3.21e-02 |
6.89e-02 |
0.16200 |
0.016400 |
0.161000 |
8.21e-01 |
2.58e-02 |
| Antigen processing: Ubiquitination & Proteasome degradation |
286 |
7.83e-04 |
2.82e-03 |
0.16200 |
0.102000 |
0.126000 |
2.98e-03 |
2.60e-04 |
| Biological oxidations |
132 |
2.60e-02 |
5.78e-02 |
0.16200 |
0.136000 |
0.087600 |
6.98e-03 |
8.21e-02 |
| Regulation of MECP2 expression and activity |
28 |
7.55e-02 |
1.35e-01 |
0.16100 |
-0.081900 |
0.139000 |
4.53e-01 |
2.03e-01 |
| PKA-mediated phosphorylation of CREB |
17 |
2.96e-01 |
3.93e-01 |
0.16100 |
-0.025200 |
0.159000 |
8.57e-01 |
2.56e-01 |
| DNA Double Strand Break Response |
47 |
1.83e-02 |
4.50e-02 |
0.16100 |
-0.059400 |
0.150000 |
4.81e-01 |
7.58e-02 |
| Glutamate and glutamine metabolism |
12 |
3.21e-01 |
4.16e-01 |
0.16100 |
0.129000 |
-0.095400 |
4.37e-01 |
5.67e-01 |
| Collagen chain trimerization |
27 |
1.23e-01 |
1.98e-01 |
0.16000 |
-0.155000 |
0.041000 |
1.63e-01 |
7.13e-01 |
| Disease |
1339 |
2.57e-14 |
8.76e-13 |
0.16000 |
0.125000 |
0.101000 |
1.99e-14 |
6.27e-10 |
| M Phase |
359 |
1.68e-04 |
6.97e-04 |
0.16000 |
0.123000 |
0.103000 |
6.58e-05 |
7.98e-04 |
| tRNA processing |
136 |
4.70e-03 |
1.39e-02 |
0.16000 |
-0.046700 |
-0.153000 |
3.47e-01 |
2.09e-03 |
| Transmission across Chemical Synapses |
170 |
1.69e-02 |
4.23e-02 |
0.16000 |
0.105000 |
0.120000 |
1.79e-02 |
6.97e-03 |
| Mismatch Repair |
15 |
2.89e-01 |
3.86e-01 |
0.15900 |
0.057700 |
-0.148000 |
6.99e-01 |
3.20e-01 |
| Signaling by ROBO receptors |
198 |
7.49e-06 |
4.11e-05 |
0.15900 |
0.159000 |
-0.002830 |
1.17e-04 |
9.45e-01 |
| Carboxyterminal post-translational modifications of tubulin |
26 |
4.56e-01 |
5.46e-01 |
0.15900 |
0.072300 |
0.141000 |
5.23e-01 |
2.13e-01 |
| Intraflagellar transport |
39 |
3.61e-01 |
4.56e-01 |
0.15900 |
-0.131000 |
-0.088800 |
1.56e-01 |
3.37e-01 |
| Attenuation phase |
23 |
5.41e-01 |
6.23e-01 |
0.15800 |
0.133000 |
0.084900 |
2.68e-01 |
4.81e-01 |
| Amino acid transport across the plasma membrane |
23 |
5.00e-01 |
5.88e-01 |
0.15800 |
0.141000 |
0.070800 |
2.42e-01 |
5.57e-01 |
| Transcriptional activation of mitochondrial biogenesis |
51 |
2.22e-01 |
3.16e-01 |
0.15700 |
0.072000 |
0.140000 |
3.74e-01 |
8.46e-02 |
| Downstream signaling of activated FGFR2 |
19 |
3.70e-01 |
4.65e-01 |
0.15700 |
0.157000 |
0.011700 |
2.37e-01 |
9.29e-01 |
| WNT ligand biogenesis and trafficking |
21 |
5.20e-01 |
6.06e-01 |
0.15600 |
0.065600 |
0.142000 |
6.03e-01 |
2.60e-01 |
| TGF-beta receptor signaling in EMT (epithelial to mesenchymal transition) |
16 |
4.84e-01 |
5.73e-01 |
0.15600 |
0.027200 |
0.154000 |
8.51e-01 |
2.86e-01 |
| CTLA4 inhibitory signaling |
21 |
3.84e-01 |
4.78e-01 |
0.15600 |
-0.154000 |
-0.026500 |
2.22e-01 |
8.34e-01 |
| Death Receptor Signalling |
131 |
5.02e-02 |
9.80e-02 |
0.15600 |
0.113000 |
0.107000 |
2.50e-02 |
3.36e-02 |
| Dopamine Neurotransmitter Release Cycle |
19 |
4.98e-01 |
5.87e-01 |
0.15600 |
-0.048600 |
-0.148000 |
7.14e-01 |
2.63e-01 |
| Ion transport by P-type ATPases |
43 |
3.41e-02 |
7.20e-02 |
0.15600 |
-0.146000 |
0.054700 |
9.83e-02 |
5.35e-01 |
| Cytochrome P450 - arranged by substrate type |
32 |
3.83e-01 |
4.77e-01 |
0.15600 |
0.140000 |
0.067600 |
1.70e-01 |
5.08e-01 |
| Signal Transduction |
1869 |
7.70e-23 |
9.58e-21 |
0.15600 |
0.068400 |
0.140000 |
9.87e-07 |
1.51e-23 |
| TP53 Regulates Transcription of Cell Cycle Genes |
47 |
4.86e-02 |
9.61e-02 |
0.15500 |
0.154000 |
-0.018800 |
6.73e-02 |
8.23e-01 |
| Translesion synthesis by Y family DNA polymerases bypasses lesions on DNA template |
38 |
3.36e-02 |
7.15e-02 |
0.15500 |
0.119000 |
-0.099700 |
2.04e-01 |
2.88e-01 |
| RUNX2 regulates osteoblast differentiation |
17 |
4.25e-01 |
5.20e-01 |
0.15500 |
-0.154000 |
-0.013200 |
2.71e-01 |
9.25e-01 |
| Nuclear Envelope (NE) Reassembly |
69 |
2.12e-01 |
3.04e-01 |
0.15400 |
0.117000 |
0.099200 |
9.24e-02 |
1.54e-01 |
| Deadenylation-dependent mRNA decay |
53 |
1.17e-01 |
1.91e-01 |
0.15300 |
0.150000 |
0.034600 |
5.97e-02 |
6.63e-01 |
| SUMOylation of transcription cofactors |
44 |
2.14e-02 |
4.97e-02 |
0.15300 |
-0.115000 |
0.102000 |
1.87e-01 |
2.43e-01 |
| Synthesis of PIPs at the plasma membrane |
52 |
3.25e-02 |
6.95e-02 |
0.15300 |
-0.026900 |
0.151000 |
7.38e-01 |
5.99e-02 |
| Mitochondrial Fatty Acid Beta-Oxidation |
36 |
4.34e-01 |
5.28e-01 |
0.15300 |
0.122000 |
0.091800 |
2.04e-01 |
3.41e-01 |
| Developmental Biology |
726 |
1.49e-07 |
1.14e-06 |
0.15100 |
0.093700 |
0.119000 |
1.73e-05 |
4.86e-08 |
| tRNA Aminoacylation |
42 |
3.03e-02 |
6.59e-02 |
0.15100 |
0.124000 |
-0.086900 |
1.65e-01 |
3.30e-01 |
| Defective EXT1 causes exostoses 1, TRPS2 and CHDS |
10 |
6.94e-01 |
7.58e-01 |
0.15100 |
-0.041300 |
-0.145000 |
8.21e-01 |
4.26e-01 |
| Defective EXT2 causes exostoses 2 |
10 |
6.94e-01 |
7.58e-01 |
0.15100 |
-0.041300 |
-0.145000 |
8.21e-01 |
4.26e-01 |
| Nonhomologous End-Joining (NHEJ) |
42 |
2.22e-01 |
3.15e-01 |
0.15100 |
0.042500 |
0.145000 |
6.33e-01 |
1.05e-01 |
| Association of TriC/CCT with target proteins during biosynthesis |
37 |
4.54e-01 |
5.45e-01 |
0.15100 |
0.110000 |
0.103000 |
2.49e-01 |
2.76e-01 |
| RNA Polymerase III Transcription Initiation From Type 1 Promoter |
28 |
5.51e-01 |
6.31e-01 |
0.15000 |
-0.111000 |
-0.101000 |
3.08e-01 |
3.56e-01 |
| IRF3-mediated induction of type I IFN |
12 |
4.33e-01 |
5.27e-01 |
0.15000 |
0.144000 |
-0.042800 |
3.88e-01 |
7.97e-01 |
| TP53 regulates transcription of several additional cell death genes whose specific roles in p53-dependent apoptosis remain uncertain |
14 |
3.35e-01 |
4.30e-01 |
0.15000 |
0.133000 |
-0.069200 |
3.88e-01 |
6.54e-01 |
| RNA Polymerase III Transcription Initiation From Type 2 Promoter |
27 |
5.41e-01 |
6.23e-01 |
0.15000 |
-0.122000 |
-0.087400 |
2.73e-01 |
4.32e-01 |
| Regulation of localization of FOXO transcription factors |
12 |
3.67e-01 |
4.62e-01 |
0.15000 |
-0.101000 |
0.111000 |
5.45e-01 |
5.06e-01 |
| Tetrahydrobiopterin (BH4) synthesis, recycling, salvage and regulation |
10 |
6.84e-01 |
7.50e-01 |
0.14900 |
0.145000 |
0.034300 |
4.27e-01 |
8.51e-01 |
| S Phase |
160 |
2.05e-04 |
8.36e-04 |
0.14900 |
0.149000 |
-0.003830 |
1.14e-03 |
9.33e-01 |
| Receptor-type tyrosine-protein phosphatases |
11 |
6.89e-01 |
7.55e-01 |
0.14900 |
-0.142000 |
-0.045200 |
4.15e-01 |
7.95e-01 |
| KSRP (KHSRP) binds and destabilizes mRNA |
17 |
4.23e-01 |
5.19e-01 |
0.14900 |
0.149000 |
0.002520 |
2.88e-01 |
9.86e-01 |
| RAF-independent MAPK1/3 activation |
21 |
5.77e-01 |
6.55e-01 |
0.14800 |
0.131000 |
0.068300 |
2.97e-01 |
5.88e-01 |
| Muscle contraction |
135 |
2.43e-02 |
5.52e-02 |
0.14800 |
0.062700 |
0.134000 |
2.09e-01 |
7.11e-03 |
| Collagen biosynthesis and modifying enzymes |
46 |
4.24e-02 |
8.60e-02 |
0.14800 |
-0.045600 |
0.141000 |
5.92e-01 |
9.90e-02 |
| Transport of Mature mRNAs Derived from Intronless Transcripts |
43 |
1.53e-01 |
2.35e-01 |
0.14700 |
-0.016700 |
-0.146000 |
8.50e-01 |
9.69e-02 |
| Regulation of TNFR1 signaling |
34 |
1.80e-01 |
2.68e-01 |
0.14600 |
0.002050 |
-0.146000 |
9.83e-01 |
1.41e-01 |
| RNA Polymerase I Promoter Clearance |
63 |
1.99e-01 |
2.91e-01 |
0.14600 |
0.065800 |
0.130000 |
3.66e-01 |
7.43e-02 |
| RNA Polymerase I Transcription |
63 |
1.99e-01 |
2.91e-01 |
0.14600 |
0.065800 |
0.130000 |
3.66e-01 |
7.43e-02 |
| Meiotic recombination |
38 |
3.71e-01 |
4.65e-01 |
0.14400 |
0.061600 |
0.130000 |
5.11e-01 |
1.64e-01 |
| Formation of Senescence-Associated Heterochromatin Foci (SAHF) |
13 |
5.26e-01 |
6.10e-01 |
0.14400 |
-0.002710 |
0.144000 |
9.87e-01 |
3.69e-01 |
| Cytokine Signaling in Immune system |
733 |
1.39e-07 |
1.07e-06 |
0.14400 |
0.122000 |
0.076400 |
1.95e-08 |
4.32e-04 |
| ECM proteoglycans |
34 |
1.84e-01 |
2.73e-01 |
0.14300 |
-0.004800 |
0.143000 |
9.61e-01 |
1.48e-01 |
| Processing of Intronless Pre-mRNAs |
19 |
6.95e-01 |
7.58e-01 |
0.14300 |
0.100000 |
0.102000 |
4.50e-01 |
4.42e-01 |
| Transcriptional regulation of pluripotent stem cells |
20 |
2.33e-01 |
3.26e-01 |
0.14300 |
-0.075300 |
0.121000 |
5.60e-01 |
3.48e-01 |
| RNA Polymerase II Transcription Termination |
65 |
1.43e-01 |
2.25e-01 |
0.14200 |
0.134000 |
0.045400 |
6.08e-02 |
5.27e-01 |
| Methylation |
12 |
6.13e-01 |
6.85e-01 |
0.14200 |
0.141000 |
0.015600 |
3.98e-01 |
9.25e-01 |
| Leishmania infection |
243 |
2.10e-05 |
1.07e-04 |
0.14100 |
0.141000 |
0.003820 |
1.56e-04 |
9.18e-01 |
| Transcriptional Regulation by MECP2 |
47 |
7.44e-02 |
1.33e-01 |
0.14100 |
-0.023700 |
0.139000 |
7.78e-01 |
9.99e-02 |
| Molecules associated with elastic fibres |
21 |
5.43e-01 |
6.25e-01 |
0.14100 |
0.046100 |
0.133000 |
7.15e-01 |
2.92e-01 |
| CD28 co-stimulation |
33 |
3.91e-01 |
4.86e-01 |
0.14000 |
-0.132000 |
-0.046800 |
1.90e-01 |
6.42e-01 |
| Regulation of KIT signaling |
15 |
6.30e-01 |
7.02e-01 |
0.14000 |
0.039500 |
0.134000 |
7.91e-01 |
3.69e-01 |
| TP53 regulates transcription of additional cell cycle genes whose exact role in the p53 pathway remain uncertain |
19 |
2.62e-01 |
3.58e-01 |
0.14000 |
0.116000 |
-0.077800 |
3.82e-01 |
5.57e-01 |
| SUMOylation of RNA binding proteins |
47 |
1.81e-01 |
2.69e-01 |
0.13900 |
-0.022500 |
-0.137000 |
7.90e-01 |
1.04e-01 |
| Nicotinamide salvaging |
14 |
3.95e-01 |
4.90e-01 |
0.13900 |
0.061700 |
-0.124000 |
6.89e-01 |
4.20e-01 |
| Post-translational modification: synthesis of GPI-anchored proteins |
56 |
2.41e-01 |
3.34e-01 |
0.13900 |
0.128000 |
0.054800 |
9.86e-02 |
4.78e-01 |
| Constitutive Signaling by NOTCH1 HD Domain Mutants |
14 |
7.42e-01 |
7.94e-01 |
0.13800 |
-0.119000 |
-0.070000 |
4.39e-01 |
6.50e-01 |
| Signaling by NOTCH1 HD Domain Mutants in Cancer |
14 |
7.42e-01 |
7.94e-01 |
0.13800 |
-0.119000 |
-0.070000 |
4.39e-01 |
6.50e-01 |
| Acyl chain remodelling of PS |
14 |
7.74e-01 |
8.21e-01 |
0.13800 |
0.089700 |
0.105000 |
5.61e-01 |
4.95e-01 |
| Chromatin modifying enzymes |
217 |
2.26e-07 |
1.67e-06 |
0.13800 |
-0.097700 |
0.097800 |
1.32e-02 |
1.31e-02 |
| Chromatin organization |
217 |
2.26e-07 |
1.67e-06 |
0.13800 |
-0.097700 |
0.097800 |
1.32e-02 |
1.31e-02 |
| Regulation of gene expression in late stage (branching morphogenesis) pancreatic bud precursor cells |
14 |
6.90e-01 |
7.56e-01 |
0.13800 |
0.049800 |
0.129000 |
7.47e-01 |
4.05e-01 |
| ISG15 antiviral mechanism |
72 |
1.09e-01 |
1.81e-01 |
0.13800 |
-0.036400 |
-0.133000 |
5.93e-01 |
5.10e-02 |
| Synthesis of IP3 and IP4 in the cytosol |
22 |
2.31e-01 |
3.24e-01 |
0.13700 |
-0.068900 |
0.119000 |
5.76e-01 |
3.35e-01 |
| Defects in cobalamin (B12) metabolism |
13 |
4.17e-01 |
5.12e-01 |
0.13700 |
0.072900 |
-0.116000 |
6.49e-01 |
4.69e-01 |
| DNA Damage Bypass |
47 |
4.21e-02 |
8.59e-02 |
0.13700 |
0.115000 |
-0.074600 |
1.74e-01 |
3.76e-01 |
| Signaling by NODAL |
13 |
7.85e-01 |
8.29e-01 |
0.13600 |
-0.110000 |
-0.080500 |
4.92e-01 |
6.15e-01 |
| O-linked glycosylation of mucins |
46 |
4.49e-01 |
5.41e-01 |
0.13600 |
0.092600 |
0.099600 |
2.77e-01 |
2.43e-01 |
| Positive epigenetic regulation of rRNA expression |
59 |
3.10e-01 |
4.08e-01 |
0.13600 |
0.072200 |
0.115000 |
3.37e-01 |
1.26e-01 |
| Synthesis of PIPs at the early endosome membrane |
16 |
3.64e-01 |
4.59e-01 |
0.13600 |
-0.059100 |
0.122000 |
6.83e-01 |
3.97e-01 |
| PI5P, PP2A and IER3 Regulate PI3K/AKT Signaling |
79 |
7.10e-02 |
1.30e-01 |
0.13500 |
0.024700 |
0.133000 |
7.04e-01 |
4.08e-02 |
| Fertilization |
12 |
7.06e-01 |
7.66e-01 |
0.13500 |
0.130000 |
0.036900 |
4.37e-01 |
8.25e-01 |
| RUNX3 regulates NOTCH signaling |
14 |
4.73e-01 |
5.63e-01 |
0.13400 |
-0.031700 |
0.130000 |
8.37e-01 |
3.98e-01 |
| TRAF6 mediated IRF7 activation |
15 |
7.75e-01 |
8.21e-01 |
0.13400 |
0.099400 |
0.090000 |
5.05e-01 |
5.46e-01 |
| Negative regulators of DDX58/IFIH1 signaling |
34 |
1.70e-01 |
2.56e-01 |
0.13400 |
0.131000 |
-0.028200 |
1.86e-01 |
7.76e-01 |
| EGR2 and SOX10-mediated initiation of Schwann cell myelination |
22 |
2.39e-01 |
3.33e-01 |
0.13400 |
-0.109000 |
0.077500 |
3.77e-01 |
5.29e-01 |
| Keratan sulfate biosynthesis |
20 |
2.86e-01 |
3.84e-01 |
0.13300 |
-0.116000 |
0.065600 |
3.69e-01 |
6.12e-01 |
| Downregulation of TGF-beta receptor signaling |
26 |
4.68e-01 |
5.60e-01 |
0.13300 |
0.034000 |
0.129000 |
7.64e-01 |
2.56e-01 |
| Activation of NMDA receptors and postsynaptic events |
58 |
3.58e-01 |
4.53e-01 |
0.13200 |
0.076600 |
0.108000 |
3.13e-01 |
1.56e-01 |
| Synthesis of PIPs at the Golgi membrane |
16 |
6.12e-01 |
6.85e-01 |
0.13200 |
0.028000 |
0.129000 |
8.46e-01 |
3.71e-01 |
| PI Metabolism |
79 |
1.85e-02 |
4.51e-02 |
0.13200 |
-0.028000 |
0.129000 |
6.67e-01 |
4.76e-02 |
| Basigin interactions |
22 |
6.93e-01 |
7.58e-01 |
0.13100 |
0.083000 |
0.102000 |
5.00e-01 |
4.09e-01 |
| Cobalamin (Cbl, vitamin B12) transport and metabolism |
17 |
5.15e-01 |
6.03e-01 |
0.13100 |
-0.002820 |
-0.131000 |
9.84e-01 |
3.50e-01 |
| Signaling by NTRK3 (TRKC) |
15 |
6.81e-01 |
7.47e-01 |
0.13000 |
0.124000 |
0.040300 |
4.07e-01 |
7.87e-01 |
| Antigen Presentation: Folding, assembly and peptide loading of class I MHC |
25 |
6.05e-01 |
6.80e-01 |
0.13000 |
0.115000 |
0.059600 |
3.19e-01 |
6.06e-01 |
| Ca2+ pathway |
57 |
3.10e-01 |
4.08e-01 |
0.12900 |
0.056900 |
0.116000 |
4.57e-01 |
1.29e-01 |
| G alpha (12/13) signalling events |
68 |
8.27e-02 |
1.45e-01 |
0.12800 |
0.003830 |
0.128000 |
9.56e-01 |
6.84e-02 |
| Caspase-mediated cleavage of cytoskeletal proteins |
12 |
7.53e-01 |
8.02e-01 |
0.12700 |
0.042200 |
0.120000 |
8.00e-01 |
4.71e-01 |
| Processing of Capped Intron-Containing Pre-mRNA |
238 |
2.56e-03 |
8.10e-03 |
0.12700 |
0.122000 |
0.035600 |
1.24e-03 |
3.44e-01 |
| Assembly of collagen fibrils and other multimeric structures |
42 |
1.68e-01 |
2.54e-01 |
0.12700 |
-0.014800 |
0.126000 |
8.69e-01 |
1.59e-01 |
| Lysine catabolism |
11 |
5.64e-01 |
6.42e-01 |
0.12600 |
-0.118000 |
0.045600 |
4.99e-01 |
7.93e-01 |
| IL-6-type cytokine receptor ligand interactions |
12 |
4.98e-01 |
5.87e-01 |
0.12600 |
0.102000 |
-0.074200 |
5.42e-01 |
6.56e-01 |
| Metabolism of RNA |
686 |
1.94e-14 |
6.96e-13 |
0.12600 |
0.122000 |
-0.030900 |
5.16e-08 |
1.67e-01 |
| Post NMDA receptor activation events |
48 |
4.13e-01 |
5.10e-01 |
0.12600 |
0.059800 |
0.111000 |
4.73e-01 |
1.85e-01 |
| RNA Polymerase I Transcription Termination |
27 |
4.17e-01 |
5.12e-01 |
0.12500 |
0.124000 |
0.011700 |
2.63e-01 |
9.16e-01 |
| SUMOylation of ubiquitinylation proteins |
39 |
3.44e-01 |
4.40e-01 |
0.12500 |
-0.026400 |
-0.122000 |
7.76e-01 |
1.87e-01 |
| Ephrin signaling |
17 |
7.51e-01 |
8.02e-01 |
0.12500 |
0.066100 |
0.106000 |
6.37e-01 |
4.50e-01 |
| HS-GAG biosynthesis |
20 |
6.24e-01 |
6.95e-01 |
0.12400 |
0.036700 |
0.118000 |
7.76e-01 |
3.60e-01 |
| Tristetraprolin (TTP, ZFP36) binds and destabilizes mRNA |
17 |
3.86e-01 |
4.80e-01 |
0.12300 |
0.081800 |
-0.091500 |
5.59e-01 |
5.14e-01 |
| Downregulation of SMAD2/3:SMAD4 transcriptional activity |
23 |
2.82e-01 |
3.80e-01 |
0.12300 |
-0.072100 |
0.099200 |
5.50e-01 |
4.10e-01 |
| NOTCH2 Activation and Transmission of Signal to the Nucleus |
20 |
6.95e-01 |
7.58e-01 |
0.12200 |
0.109000 |
0.053900 |
3.98e-01 |
6.76e-01 |
| Aberrant regulation of mitotic G1/S transition in cancer due to RB1 defects |
17 |
5.83e-01 |
6.59e-01 |
0.12100 |
-0.121000 |
-0.007780 |
3.87e-01 |
9.56e-01 |
| Defective binding of RB1 mutants to E2F1,(E2F2, E2F3) |
17 |
5.83e-01 |
6.59e-01 |
0.12100 |
-0.121000 |
-0.007780 |
3.87e-01 |
9.56e-01 |
| Cell Cycle Checkpoints |
258 |
3.20e-03 |
9.92e-03 |
0.12100 |
0.116000 |
0.036800 |
1.37e-03 |
3.09e-01 |
| Butyrate Response Factor 1 (BRF1) binds and destabilizes mRNA |
17 |
4.74e-01 |
5.64e-01 |
0.12100 |
0.029500 |
-0.118000 |
8.33e-01 |
4.01e-01 |
| mRNA 3’-end processing |
56 |
3.42e-01 |
4.38e-01 |
0.12100 |
0.111000 |
0.047600 |
1.52e-01 |
5.38e-01 |
| Cyclin D associated events in G1 |
47 |
5.24e-01 |
6.08e-01 |
0.12000 |
0.091500 |
0.077800 |
2.78e-01 |
3.56e-01 |
| G1 Phase |
47 |
5.24e-01 |
6.08e-01 |
0.12000 |
0.091500 |
0.077800 |
2.78e-01 |
3.56e-01 |
| TNFR1-induced NFkappaB signaling pathway |
25 |
2.71e-01 |
3.68e-01 |
0.12000 |
0.070200 |
-0.096800 |
5.43e-01 |
4.02e-01 |
| RMTs methylate histone arginines |
37 |
1.47e-01 |
2.28e-01 |
0.11900 |
-0.097700 |
0.068600 |
3.04e-01 |
4.70e-01 |
| Inositol phosphate metabolism |
42 |
2.13e-01 |
3.05e-01 |
0.11900 |
-0.011100 |
0.119000 |
9.01e-01 |
1.83e-01 |
| Termination of O-glycan biosynthesis |
16 |
4.84e-01 |
5.73e-01 |
0.11800 |
-0.111000 |
0.040900 |
4.42e-01 |
7.77e-01 |
| Interleukin-2 family signaling |
38 |
5.64e-01 |
6.42e-01 |
0.11800 |
0.100000 |
0.061500 |
2.84e-01 |
5.12e-01 |
| PECAM1 interactions |
12 |
5.90e-01 |
6.67e-01 |
0.11700 |
-0.110000 |
0.039900 |
5.11e-01 |
8.11e-01 |
| Interleukin receptor SHC signaling |
23 |
7.39e-01 |
7.94e-01 |
0.11600 |
0.090500 |
0.073300 |
4.53e-01 |
5.43e-01 |
| Regulation of innate immune responses to cytosolic DNA |
14 |
5.06e-01 |
5.94e-01 |
0.11600 |
0.062800 |
-0.098000 |
6.84e-01 |
5.26e-01 |
| Protein-protein interactions at synapses |
55 |
4.76e-01 |
5.65e-01 |
0.11600 |
-0.093700 |
-0.068800 |
2.29e-01 |
3.78e-01 |
| Norepinephrine Neurotransmitter Release Cycle |
14 |
7.25e-01 |
7.82e-01 |
0.11600 |
-0.026800 |
-0.113000 |
8.62e-01 |
4.64e-01 |
| Adrenaline,noradrenaline inhibits insulin secretion |
24 |
7.29e-01 |
7.86e-01 |
0.11600 |
0.091600 |
0.070700 |
4.37e-01 |
5.49e-01 |
| Nef mediated downregulation of MHC class I complex cell surface expression |
10 |
8.79e-01 |
9.08e-01 |
0.11500 |
0.071300 |
0.090300 |
6.96e-01 |
6.21e-01 |
| Defective C1GALT1C1 causes Tn polyagglutination syndrome (TNPS) |
10 |
6.23e-01 |
6.95e-01 |
0.11500 |
0.096800 |
-0.061400 |
5.96e-01 |
7.37e-01 |
| Transport of Mature mRNA derived from an Intron-Containing Transcript |
72 |
7.11e-02 |
1.30e-01 |
0.11400 |
0.020000 |
-0.113000 |
7.69e-01 |
9.84e-02 |
| NCAM signaling for neurite out-growth |
43 |
4.51e-01 |
5.43e-01 |
0.11400 |
-0.039900 |
-0.107000 |
6.51e-01 |
2.24e-01 |
| Cell death signalling via NRAGE, NRIF and NADE |
69 |
2.32e-01 |
3.25e-01 |
0.11400 |
0.029900 |
0.110000 |
6.68e-01 |
1.13e-01 |
| Transcriptional regulation by small RNAs |
63 |
4.02e-01 |
4.98e-01 |
0.11300 |
0.056800 |
0.098300 |
4.36e-01 |
1.77e-01 |
| Neuronal System |
253 |
3.56e-02 |
7.47e-02 |
0.11300 |
0.062500 |
0.094000 |
8.68e-02 |
1.01e-02 |
| SUMOylation of DNA damage response and repair proteins |
77 |
3.44e-01 |
4.40e-01 |
0.11300 |
-0.058500 |
-0.096200 |
3.75e-01 |
1.44e-01 |
| Regulation of TP53 Activity |
152 |
1.51e-01 |
2.33e-01 |
0.11300 |
-0.089600 |
-0.068100 |
5.67e-02 |
1.47e-01 |
| Other semaphorin interactions |
16 |
6.36e-01 |
7.07e-01 |
0.11200 |
0.002910 |
0.112000 |
9.84e-01 |
4.39e-01 |
| SUMOylation of chromatin organization proteins |
57 |
3.06e-01 |
4.03e-01 |
0.11200 |
-0.027700 |
-0.108000 |
7.18e-01 |
1.57e-01 |
| Regulation of beta-cell development |
19 |
4.70e-01 |
5.61e-01 |
0.11200 |
-0.106000 |
0.036300 |
4.26e-01 |
7.84e-01 |
| mRNA decay by 5’ to 3’ exoribonuclease |
15 |
7.55e-01 |
8.04e-01 |
0.11100 |
0.106000 |
0.034600 |
4.77e-01 |
8.17e-01 |
| Adherens junctions interactions |
18 |
5.26e-01 |
6.10e-01 |
0.11100 |
-0.109000 |
0.023100 |
4.25e-01 |
8.65e-01 |
| Bile acid and bile salt metabolism |
28 |
4.38e-01 |
5.30e-01 |
0.11100 |
-0.002730 |
0.111000 |
9.80e-01 |
3.10e-01 |
| DDX58/IFIH1-mediated induction of interferon-alpha/beta |
63 |
4.25e-01 |
5.20e-01 |
0.11100 |
0.095300 |
0.056500 |
1.91e-01 |
4.38e-01 |
| Ion homeostasis |
41 |
2.06e-01 |
2.99e-01 |
0.11000 |
-0.104000 |
0.035300 |
2.48e-01 |
6.95e-01 |
| Ras activation upon Ca2+ influx through NMDA receptor |
15 |
5.44e-01 |
6.25e-01 |
0.11000 |
0.044900 |
-0.100000 |
7.63e-01 |
5.02e-01 |
| Synaptic adhesion-like molecules |
15 |
5.93e-01 |
6.69e-01 |
0.10900 |
-0.106000 |
0.024100 |
4.76e-01 |
8.71e-01 |
| NOTCH2 intracellular domain regulates transcription |
11 |
7.15e-01 |
7.73e-01 |
0.10900 |
-0.009380 |
0.108000 |
9.57e-01 |
5.34e-01 |
| SUMOylation of DNA replication proteins |
46 |
2.97e-01 |
3.94e-01 |
0.10900 |
-0.003620 |
-0.109000 |
9.66e-01 |
2.03e-01 |
| Dual incision in TC-NER |
65 |
4.39e-01 |
5.30e-01 |
0.10800 |
0.092100 |
0.056000 |
1.99e-01 |
4.35e-01 |
| Blood group systems biosynthesis |
17 |
8.13e-01 |
8.51e-01 |
0.10700 |
0.089900 |
0.058200 |
5.21e-01 |
6.78e-01 |
| DAG and IP3 signaling |
33 |
4.14e-01 |
5.10e-01 |
0.10700 |
-0.000912 |
0.107000 |
9.93e-01 |
2.89e-01 |
| SEMA3A-Plexin repulsion signaling by inhibiting Integrin adhesion |
14 |
8.08e-01 |
8.47e-01 |
0.10700 |
-0.098300 |
-0.041200 |
5.24e-01 |
7.90e-01 |
| IGF1R signaling cascade |
36 |
6.56e-01 |
7.25e-01 |
0.10700 |
0.060100 |
0.087900 |
5.32e-01 |
3.61e-01 |
| CREB1 phosphorylation through NMDA receptor-mediated activation of RAS signaling |
23 |
7.41e-01 |
7.94e-01 |
0.10500 |
0.049800 |
0.092900 |
6.79e-01 |
4.40e-01 |
| MET activates PTK2 signaling |
15 |
7.19e-01 |
7.76e-01 |
0.10500 |
0.012100 |
0.104000 |
9.36e-01 |
4.86e-01 |
| Transcription of E2F targets under negative control by DREAM complex |
19 |
5.79e-01 |
6.56e-01 |
0.10400 |
0.104000 |
-0.011600 |
4.34e-01 |
9.30e-01 |
| O-linked glycosylation |
81 |
4.38e-01 |
5.30e-01 |
0.10400 |
-0.078500 |
-0.067600 |
2.22e-01 |
2.93e-01 |
| Transcriptional activity of SMAD2/SMAD3:SMAD4 heterotrimer |
43 |
2.14e-01 |
3.06e-01 |
0.10300 |
-0.041300 |
0.094900 |
6.39e-01 |
2.82e-01 |
| Transcription-Coupled Nucleotide Excision Repair (TC-NER) |
78 |
4.39e-01 |
5.30e-01 |
0.10300 |
0.082500 |
0.062200 |
2.08e-01 |
3.43e-01 |
| Neurotransmitter release cycle |
38 |
2.93e-01 |
3.90e-01 |
0.10300 |
0.099700 |
-0.026900 |
2.88e-01 |
7.74e-01 |
| RNA Polymerase I Transcription Initiation |
44 |
6.34e-01 |
7.06e-01 |
0.10200 |
-0.062100 |
-0.081400 |
4.76e-01 |
3.50e-01 |
| Synthesis of bile acids and bile salts |
24 |
6.72e-01 |
7.39e-01 |
0.10200 |
0.028600 |
0.098200 |
8.08e-01 |
4.05e-01 |
| Negative regulation of the PI3K/AKT network |
86 |
8.59e-02 |
1.49e-01 |
0.10200 |
-0.015100 |
0.101000 |
8.09e-01 |
1.05e-01 |
| HATs acetylate histones |
93 |
6.04e-02 |
1.15e-01 |
0.10200 |
-0.099400 |
0.022100 |
9.77e-02 |
7.13e-01 |
| SLC-mediated transmembrane transport |
178 |
1.18e-01 |
1.92e-01 |
0.10200 |
0.048100 |
0.089600 |
2.68e-01 |
3.93e-02 |
| Sulfur amino acid metabolism |
22 |
8.05e-01 |
8.45e-01 |
0.10200 |
0.076800 |
0.066600 |
5.33e-01 |
5.88e-01 |
| RUNX2 regulates bone development |
22 |
4.35e-01 |
5.28e-01 |
0.10100 |
-0.080000 |
0.062300 |
5.16e-01 |
6.13e-01 |
| Cell junction organization |
59 |
5.56e-01 |
6.35e-01 |
0.09980 |
0.059100 |
0.080400 |
4.33e-01 |
2.85e-01 |
| SUMOylation of DNA methylation proteins |
16 |
7.38e-01 |
7.93e-01 |
0.09900 |
-0.098000 |
-0.014300 |
4.97e-01 |
9.21e-01 |
| RNA Polymerase III Transcription Termination |
23 |
7.37e-01 |
7.92e-01 |
0.09840 |
0.091400 |
0.036400 |
4.48e-01 |
7.62e-01 |
| G0 and Early G1 |
27 |
4.40e-01 |
5.31e-01 |
0.09840 |
0.093700 |
-0.030100 |
3.99e-01 |
7.87e-01 |
| Translation of structural proteins |
28 |
4.37e-01 |
5.30e-01 |
0.09790 |
-0.027600 |
0.093900 |
8.01e-01 |
3.90e-01 |
| Signaling by Retinoic Acid |
31 |
7.00e-01 |
7.61e-01 |
0.09780 |
0.087100 |
0.044300 |
4.01e-01 |
6.69e-01 |
| Nucleotide Excision Repair |
110 |
3.76e-01 |
4.71e-01 |
0.09700 |
0.064100 |
0.072800 |
2.46e-01 |
1.87e-01 |
| Interaction between L1 and Ankyrins |
20 |
7.56e-01 |
8.04e-01 |
0.09690 |
-0.091800 |
-0.031100 |
4.77e-01 |
8.10e-01 |
| NF-kB activation through FADD/RIP-1 pathway mediated by caspase-8 and -10 |
12 |
8.32e-01 |
8.67e-01 |
0.09680 |
0.024800 |
0.093500 |
8.82e-01 |
5.75e-01 |
| Non-integrin membrane-ECM interactions |
37 |
5.18e-01 |
6.05e-01 |
0.09620 |
0.014300 |
0.095100 |
8.80e-01 |
3.17e-01 |
| Cell-Cell communication |
88 |
3.70e-01 |
4.65e-01 |
0.09500 |
0.040600 |
0.085900 |
5.11e-01 |
1.64e-01 |
| Transcriptional Regulation by TP53 |
351 |
4.86e-02 |
9.61e-02 |
0.09480 |
0.074200 |
0.059000 |
1.70e-02 |
5.76e-02 |
| TP53 Regulates Transcription of Genes Involved in G1 Cell Cycle Arrest |
14 |
6.38e-01 |
7.08e-01 |
0.09400 |
0.053900 |
-0.077000 |
7.27e-01 |
6.18e-01 |
| Regulation of FZD by ubiquitination |
15 |
8.33e-01 |
8.68e-01 |
0.09360 |
-0.033800 |
-0.087300 |
8.20e-01 |
5.58e-01 |
| DCC mediated attractive signaling |
13 |
7.88e-01 |
8.31e-01 |
0.09320 |
-0.092900 |
-0.007350 |
5.62e-01 |
9.63e-01 |
| Signaling by KIT in disease |
20 |
5.25e-01 |
6.09e-01 |
0.09300 |
0.064100 |
-0.067400 |
6.20e-01 |
6.02e-01 |
| Signaling by phosphorylated juxtamembrane, extracellular and kinase domain KIT mutants |
20 |
5.25e-01 |
6.09e-01 |
0.09300 |
0.064100 |
-0.067400 |
6.20e-01 |
6.02e-01 |
| IRS-related events triggered by IGF1R |
35 |
7.34e-01 |
7.91e-01 |
0.09270 |
0.052700 |
0.076200 |
5.90e-01 |
4.35e-01 |
| VEGFR2 mediated vascular permeability |
26 |
4.50e-01 |
5.42e-01 |
0.09230 |
-0.049900 |
0.077700 |
6.60e-01 |
4.93e-01 |
| Deactivation of the beta-catenin transactivating complex |
36 |
4.35e-01 |
5.28e-01 |
0.09000 |
-0.088300 |
0.017300 |
3.59e-01 |
8.57e-01 |
| Cardiac conduction |
86 |
1.88e-01 |
2.75e-01 |
0.08970 |
-0.089600 |
0.003050 |
1.51e-01 |
9.61e-01 |
| Viral Messenger RNA Synthesis |
44 |
3.60e-01 |
4.56e-01 |
0.08960 |
0.018500 |
-0.087600 |
8.32e-01 |
3.14e-01 |
| G alpha (q) signalling events |
132 |
3.91e-02 |
8.11e-02 |
0.08950 |
-0.025000 |
0.085900 |
6.19e-01 |
8.82e-02 |
| Condensation of Prometaphase Chromosomes |
11 |
8.68e-01 |
9.00e-01 |
0.08840 |
0.022400 |
0.085500 |
8.97e-01 |
6.23e-01 |
| Class I peroxisomal membrane protein import |
20 |
6.03e-01 |
6.78e-01 |
0.08790 |
-0.081900 |
0.031900 |
5.26e-01 |
8.05e-01 |
| Regulation of HSF1-mediated heat shock response |
79 |
1.34e-01 |
2.13e-01 |
0.08770 |
0.033400 |
-0.081100 |
6.08e-01 |
2.13e-01 |
| Signaling by NOTCH2 |
30 |
8.05e-01 |
8.45e-01 |
0.08750 |
0.064800 |
0.058900 |
5.39e-01 |
5.77e-01 |
| IRS-mediated signalling |
34 |
7.77e-01 |
8.23e-01 |
0.08740 |
0.054700 |
0.068100 |
5.81e-01 |
4.92e-01 |
| Voltage gated Potassium channels |
24 |
6.54e-01 |
7.24e-01 |
0.08690 |
-0.000413 |
0.086900 |
9.97e-01 |
4.61e-01 |
| NRAGE signals death through JNK |
52 |
2.40e-01 |
3.33e-01 |
0.08610 |
-0.066000 |
0.055300 |
4.10e-01 |
4.90e-01 |
| Generic Transcription Pathway |
1078 |
7.38e-04 |
2.68e-03 |
0.08580 |
-0.055800 |
-0.065300 |
2.00e-03 |
2.98e-04 |
| Dual Incision in GG-NER |
41 |
4.25e-01 |
5.20e-01 |
0.08540 |
0.016800 |
-0.083700 |
8.52e-01 |
3.54e-01 |
| Global Genome Nucleotide Excision Repair (GG-NER) |
84 |
5.68e-01 |
6.45e-01 |
0.08410 |
0.063900 |
0.054700 |
3.11e-01 |
3.86e-01 |
| Cellular response to heat stress |
93 |
1.27e-01 |
2.02e-01 |
0.08320 |
0.027900 |
-0.078500 |
6.43e-01 |
1.91e-01 |
| Nuclear Envelope Breakdown |
53 |
3.93e-01 |
4.88e-01 |
0.08230 |
0.008170 |
-0.081900 |
9.18e-01 |
3.03e-01 |
| Gamma carboxylation, hypusine formation and arylsulfatase activation |
34 |
7.52e-01 |
8.02e-01 |
0.08120 |
0.073800 |
0.033900 |
4.57e-01 |
7.32e-01 |
| Heparan sulfate/heparin (HS-GAG) metabolism |
37 |
4.70e-01 |
5.61e-01 |
0.08110 |
-0.023700 |
0.077500 |
8.03e-01 |
4.14e-01 |
| Transport of Mature Transcript to Cytoplasm |
81 |
1.82e-01 |
2.70e-01 |
0.08060 |
0.028200 |
-0.075600 |
6.61e-01 |
2.40e-01 |
| Cell Cycle, Mitotic |
500 |
1.33e-02 |
3.44e-02 |
0.08050 |
0.074600 |
0.030200 |
4.27e-03 |
2.48e-01 |
| Signaling by Type 1 Insulin-like Growth Factor 1 Receptor (IGF1R) |
37 |
7.98e-01 |
8.39e-01 |
0.08010 |
0.052700 |
0.060300 |
5.79e-01 |
5.26e-01 |
| Gap-filling DNA repair synthesis and ligation in TC-NER |
64 |
6.26e-01 |
6.97e-01 |
0.07960 |
0.069900 |
0.038200 |
3.34e-01 |
5.97e-01 |
| PI3K/AKT Signaling in Cancer |
80 |
1.90e-01 |
2.79e-01 |
0.07840 |
-0.032500 |
0.071400 |
6.15e-01 |
2.70e-01 |
| Recruitment of NuMA to mitotic centrosomes |
79 |
6.12e-01 |
6.85e-01 |
0.07830 |
-0.045400 |
-0.063800 |
4.85e-01 |
3.27e-01 |
| Epigenetic regulation of gene expression |
100 |
2.87e-01 |
3.85e-01 |
0.07800 |
0.007610 |
0.077600 |
8.95e-01 |
1.80e-01 |
| DNA Damage Recognition in GG-NER |
38 |
6.01e-01 |
6.77e-01 |
0.07710 |
0.002130 |
0.077100 |
9.82e-01 |
4.11e-01 |
| Centrosome maturation |
80 |
6.12e-01 |
6.85e-01 |
0.07570 |
-0.040300 |
-0.064100 |
5.33e-01 |
3.22e-01 |
| Recruitment of mitotic centrosome proteins and complexes |
80 |
6.12e-01 |
6.85e-01 |
0.07570 |
-0.040300 |
-0.064100 |
5.33e-01 |
3.22e-01 |
| TRP channels |
17 |
8.99e-01 |
9.23e-01 |
0.07570 |
-0.064700 |
-0.039200 |
6.44e-01 |
7.80e-01 |
| Peptide ligand-binding receptors |
95 |
5.15e-01 |
6.02e-01 |
0.07560 |
0.067800 |
0.033300 |
2.53e-01 |
5.75e-01 |
| Synthesis of PA |
32 |
7.13e-01 |
7.72e-01 |
0.07480 |
0.012000 |
0.073800 |
9.06e-01 |
4.70e-01 |
| Cytosolic sensors of pathogen-associated DNA |
62 |
6.68e-01 |
7.36e-01 |
0.07450 |
0.065700 |
0.035000 |
3.71e-01 |
6.33e-01 |
| Gene Silencing by RNA |
88 |
4.82e-01 |
5.71e-01 |
0.07330 |
0.070100 |
0.021500 |
2.56e-01 |
7.27e-01 |
| Metabolism of vitamins and cofactors |
156 |
4.55e-01 |
5.45e-01 |
0.07290 |
0.055600 |
0.047100 |
2.31e-01 |
3.10e-01 |
| Activation of BH3-only proteins |
30 |
7.80e-01 |
8.25e-01 |
0.07230 |
0.069500 |
0.020300 |
5.10e-01 |
8.48e-01 |
| Organelle biogenesis and maintenance |
268 |
2.66e-01 |
3.62e-01 |
0.07210 |
0.055600 |
0.045800 |
1.17e-01 |
1.97e-01 |
| Ovarian tumor domain proteases |
37 |
7.47e-01 |
7.99e-01 |
0.07180 |
0.068400 |
0.021600 |
4.71e-01 |
8.20e-01 |
| Meiosis |
68 |
5.00e-01 |
5.88e-01 |
0.07120 |
0.008090 |
0.070700 |
9.08e-01 |
3.13e-01 |
| TP53 Regulates Transcription of DNA Repair Genes |
61 |
3.24e-01 |
4.18e-01 |
0.07090 |
-0.055500 |
0.044100 |
4.54e-01 |
5.51e-01 |
| Reproduction |
80 |
5.79e-01 |
6.56e-01 |
0.07080 |
0.026400 |
0.065700 |
6.83e-01 |
3.10e-01 |
| Chromosome Maintenance |
105 |
1.72e-01 |
2.59e-01 |
0.07040 |
0.029800 |
-0.063700 |
5.98e-01 |
2.59e-01 |
| Lewis blood group biosynthesis |
13 |
8.69e-01 |
9.00e-01 |
0.06990 |
-0.069800 |
-0.003170 |
6.63e-01 |
9.84e-01 |
| Glucagon-type ligand receptors |
20 |
7.30e-01 |
7.87e-01 |
0.06960 |
0.065100 |
-0.024500 |
6.14e-01 |
8.50e-01 |
| Nucleotide-like (purinergic) receptors |
13 |
8.94e-01 |
9.20e-01 |
0.06950 |
-0.068100 |
-0.013900 |
6.71e-01 |
9.31e-01 |
| PI-3K cascade:FGFR2 |
12 |
8.16e-01 |
8.53e-01 |
0.06850 |
0.037700 |
-0.057200 |
8.21e-01 |
7.32e-01 |
| Adaptive Immune System |
753 |
2.04e-02 |
4.78e-02 |
0.06830 |
0.059700 |
0.033300 |
5.32e-03 |
1.20e-01 |
| SUMO E3 ligases SUMOylate target proteins |
159 |
3.47e-01 |
4.43e-01 |
0.06820 |
-0.064200 |
-0.023200 |
1.63e-01 |
6.13e-01 |
| Nicotinate metabolism |
25 |
6.50e-01 |
7.20e-01 |
0.06800 |
0.046200 |
-0.049900 |
6.89e-01 |
6.66e-01 |
| Deposition of new CENPA-containing nucleosomes at the centromere |
40 |
8.46e-01 |
8.79e-01 |
0.06650 |
0.049800 |
0.044100 |
5.86e-01 |
6.29e-01 |
| Nucleosome assembly |
40 |
8.46e-01 |
8.79e-01 |
0.06650 |
0.049800 |
0.044100 |
5.86e-01 |
6.29e-01 |
| Gene expression (Transcription) |
1325 |
3.24e-03 |
1.00e-02 |
0.06600 |
-0.036000 |
-0.055300 |
2.78e-02 |
7.28e-04 |
| Anchoring of the basal body to the plasma membrane |
96 |
6.77e-01 |
7.44e-01 |
0.06470 |
-0.040200 |
-0.050700 |
4.96e-01 |
3.91e-01 |
| Transcriptional regulation by the AP-2 (TFAP2) family of transcription factors |
27 |
6.78e-01 |
7.45e-01 |
0.06470 |
-0.058100 |
0.028500 |
6.01e-01 |
7.97e-01 |
| SUMOylation |
165 |
4.03e-01 |
4.99e-01 |
0.06370 |
-0.059100 |
-0.023700 |
1.90e-01 |
5.99e-01 |
| G alpha (i) signalling events |
243 |
4.00e-01 |
4.96e-01 |
0.06340 |
0.042100 |
0.047400 |
2.58e-01 |
2.04e-01 |
| PI3K Cascade |
30 |
7.62e-01 |
8.09e-01 |
0.06280 |
0.000823 |
0.062800 |
9.94e-01 |
5.52e-01 |
| HSF1-dependent transactivation |
29 |
8.13e-01 |
8.51e-01 |
0.06240 |
0.061400 |
0.011400 |
5.67e-01 |
9.15e-01 |
| RNA Polymerase III Chain Elongation |
18 |
9.08e-01 |
9.29e-01 |
0.06130 |
-0.021000 |
-0.057600 |
8.77e-01 |
6.72e-01 |
| Cell Cycle |
622 |
1.57e-02 |
3.97e-02 |
0.06130 |
0.060300 |
0.011200 |
1.03e-02 |
6.32e-01 |
| Synthesis of glycosylphosphatidylinositol (GPI) |
17 |
9.32e-01 |
9.49e-01 |
0.06080 |
-0.030300 |
-0.052700 |
8.29e-01 |
7.07e-01 |
| TNF signaling |
43 |
5.76e-01 |
6.54e-01 |
0.06070 |
0.053400 |
-0.028700 |
5.44e-01 |
7.45e-01 |
| Loss of Nlp from mitotic centrosomes |
68 |
7.90e-01 |
8.31e-01 |
0.06060 |
-0.044700 |
-0.041000 |
5.24e-01 |
5.59e-01 |
| Loss of proteins required for interphase microtubule organization from the centrosome |
68 |
7.90e-01 |
8.31e-01 |
0.06060 |
-0.044700 |
-0.041000 |
5.24e-01 |
5.59e-01 |
| CDC6 association with the ORC:origin complex |
11 |
8.64e-01 |
8.97e-01 |
0.06020 |
0.048600 |
-0.035600 |
7.80e-01 |
8.38e-01 |
| Telomere Maintenance |
80 |
4.85e-01 |
5.74e-01 |
0.05810 |
0.057700 |
-0.007370 |
3.73e-01 |
9.09e-01 |
| Diseases associated with glycosaminoglycan metabolism |
25 |
7.43e-01 |
7.95e-01 |
0.05800 |
-0.028800 |
0.050300 |
8.03e-01 |
6.63e-01 |
| DNA Double-Strand Break Repair |
135 |
6.70e-01 |
7.38e-01 |
0.05610 |
-0.037400 |
-0.041800 |
4.53e-01 |
4.02e-01 |
| RNA Polymerase II Transcription |
1197 |
3.31e-02 |
7.06e-02 |
0.05580 |
-0.035100 |
-0.043400 |
4.11e-02 |
1.16e-02 |
| DAP12 signaling |
28 |
7.56e-01 |
8.04e-01 |
0.05220 |
-0.042000 |
0.030900 |
7.00e-01 |
7.77e-01 |
| Pregnenolone biosynthesis |
10 |
9.19e-01 |
9.39e-01 |
0.05210 |
0.049600 |
-0.015700 |
7.86e-01 |
9.31e-01 |
| Diseases of metabolism |
185 |
6.05e-01 |
6.80e-01 |
0.05150 |
0.042500 |
0.029200 |
3.19e-01 |
4.94e-01 |
| Other interleukin signaling |
18 |
9.06e-01 |
9.29e-01 |
0.05080 |
0.050700 |
0.003900 |
7.10e-01 |
9.77e-01 |
| FOXO-mediated transcription |
59 |
7.35e-01 |
7.91e-01 |
0.04880 |
0.002470 |
0.048800 |
9.74e-01 |
5.17e-01 |
| Downregulation of ERBB2:ERBB3 signaling |
12 |
9.73e-01 |
9.81e-01 |
0.04860 |
0.030500 |
0.037800 |
8.55e-01 |
8.20e-01 |
| Branched-chain amino acid catabolism |
21 |
9.22e-01 |
9.41e-01 |
0.04760 |
0.010900 |
0.046300 |
9.31e-01 |
7.13e-01 |
| Cilium Assembly |
180 |
6.66e-01 |
7.34e-01 |
0.04690 |
-0.026300 |
-0.038800 |
5.43e-01 |
3.69e-01 |
| RNA Polymerase III Transcription Initiation |
36 |
8.93e-01 |
9.20e-01 |
0.04630 |
-0.043700 |
-0.015200 |
6.50e-01 |
8.74e-01 |
| Homology Directed Repair |
110 |
7.88e-01 |
8.31e-01 |
0.04630 |
-0.026800 |
-0.037700 |
6.27e-01 |
4.94e-01 |
| Interleukin-2 signaling |
11 |
9.77e-01 |
9.83e-01 |
0.04570 |
0.027600 |
0.036500 |
8.74e-01 |
8.34e-01 |
| Visual phototransduction |
59 |
6.59e-01 |
7.28e-01 |
0.04560 |
-0.019400 |
0.041300 |
7.97e-01 |
5.84e-01 |
| Signaling by GPCR |
534 |
6.64e-02 |
1.23e-01 |
0.04530 |
-0.003380 |
0.045100 |
8.94e-01 |
7.44e-02 |
| Base Excision Repair |
58 |
8.64e-01 |
8.97e-01 |
0.04480 |
-0.019100 |
-0.040600 |
8.02e-01 |
5.93e-01 |
| The phototransduction cascade |
26 |
9.39e-01 |
9.52e-01 |
0.04470 |
-0.039900 |
-0.020100 |
7.25e-01 |
8.59e-01 |
| Kinesins |
39 |
9.01e-01 |
9.25e-01 |
0.04430 |
-0.041100 |
-0.016700 |
6.57e-01 |
8.57e-01 |
| GPCR downstream signalling |
489 |
1.11e-01 |
1.84e-01 |
0.04360 |
-0.001320 |
0.043600 |
9.60e-01 |
9.88e-02 |
| Interleukin-35 Signalling |
12 |
9.79e-01 |
9.84e-01 |
0.04340 |
-0.031500 |
-0.029800 |
8.50e-01 |
8.58e-01 |
| G2/M DNA damage checkpoint |
67 |
7.58e-01 |
8.05e-01 |
0.04300 |
0.043000 |
0.001350 |
5.43e-01 |
9.85e-01 |
| Interleukin-7 signaling |
21 |
9.59e-01 |
9.68e-01 |
0.04270 |
0.022200 |
0.036500 |
8.60e-01 |
7.72e-01 |
| Regulation of TP53 Expression and Degradation |
36 |
9.28e-01 |
9.46e-01 |
0.04260 |
-0.037200 |
-0.020800 |
6.99e-01 |
8.29e-01 |
| Aberrant regulation of mitotic cell cycle due to RB1 defects |
36 |
9.42e-01 |
9.53e-01 |
0.04210 |
0.028800 |
0.030700 |
7.65e-01 |
7.50e-01 |
| Diseases of mitotic cell cycle |
36 |
9.42e-01 |
9.53e-01 |
0.04210 |
0.028800 |
0.030700 |
7.65e-01 |
7.50e-01 |
| Regulation of TP53 Activity through Phosphorylation |
88 |
6.98e-01 |
7.60e-01 |
0.04170 |
0.000461 |
-0.041700 |
9.94e-01 |
4.99e-01 |
| G alpha (s) signalling events |
137 |
7.87e-01 |
8.31e-01 |
0.04150 |
0.034000 |
0.023800 |
4.92e-01 |
6.30e-01 |
| Signaling by BMP |
21 |
8.98e-01 |
9.23e-01 |
0.04100 |
0.039500 |
-0.011000 |
7.54e-01 |
9.30e-01 |
| AURKA Activation by TPX2 |
71 |
8.91e-01 |
9.19e-01 |
0.04040 |
-0.032600 |
-0.023900 |
6.35e-01 |
7.27e-01 |
| RNA Polymerase III Abortive And Retractive Initiation |
41 |
9.37e-01 |
9.52e-01 |
0.03920 |
0.022200 |
0.032400 |
8.06e-01 |
7.20e-01 |
| RNA Polymerase III Transcription |
41 |
9.37e-01 |
9.52e-01 |
0.03920 |
0.022200 |
0.032400 |
8.06e-01 |
7.20e-01 |
| GPCR ligand binding |
231 |
5.53e-01 |
6.32e-01 |
0.03850 |
-0.008240 |
-0.037600 |
8.29e-01 |
3.25e-01 |
| Class A/1 (Rhodopsin-like receptors) |
166 |
5.46e-01 |
6.27e-01 |
0.03830 |
0.002260 |
-0.038300 |
9.60e-01 |
3.95e-01 |
| Processing of DNA double-strand break ends |
71 |
8.75e-01 |
9.05e-01 |
0.03810 |
0.034800 |
0.015500 |
6.12e-01 |
8.21e-01 |
| Transcriptional Regulation by VENTX |
38 |
8.38e-01 |
8.73e-01 |
0.03580 |
-0.029900 |
0.019700 |
7.50e-01 |
8.33e-01 |
| Regulation of TP53 Degradation |
35 |
9.09e-01 |
9.30e-01 |
0.03570 |
-0.035600 |
-0.002490 |
7.16e-01 |
9.80e-01 |
| SMAD2/SMAD3:SMAD4 heterotrimer regulates transcription |
31 |
8.73e-01 |
9.03e-01 |
0.03510 |
-0.018400 |
0.029900 |
8.60e-01 |
7.73e-01 |
| CRMPs in Sema3A signaling |
14 |
9.39e-01 |
9.52e-01 |
0.03500 |
0.021800 |
-0.027400 |
8.88e-01 |
8.59e-01 |
| HCMV Early Events |
74 |
7.90e-01 |
8.31e-01 |
0.03480 |
-0.003830 |
0.034600 |
9.55e-01 |
6.07e-01 |
| Metabolism of water-soluble vitamins and cofactors |
110 |
7.03e-01 |
7.64e-01 |
0.03470 |
0.034400 |
-0.004330 |
5.33e-01 |
9.37e-01 |
| Cell-cell junction organization |
38 |
8.89e-01 |
9.18e-01 |
0.03450 |
0.003410 |
-0.034300 |
9.71e-01 |
7.15e-01 |
| RHO GTPases Activate Formins |
117 |
7.06e-01 |
7.66e-01 |
0.03380 |
-0.003390 |
0.033700 |
9.49e-01 |
5.29e-01 |
| Transcription of E2F targets under negative control by p107 (RBL1) and p130 (RBL2) in complex with HDAC1 |
16 |
9.58e-01 |
9.68e-01 |
0.03230 |
0.002400 |
-0.032300 |
9.87e-01 |
8.23e-01 |
| Mitotic Spindle Checkpoint |
108 |
7.71e-01 |
8.17e-01 |
0.03190 |
0.031900 |
-0.000500 |
5.66e-01 |
9.93e-01 |
| ADORA2B mediated anti-inflammatory cytokines production |
72 |
8.23e-01 |
8.59e-01 |
0.03150 |
0.031200 |
-0.004490 |
6.47e-01 |
9.47e-01 |
| RNA Polymerase III Transcription Initiation From Type 3 Promoter |
28 |
9.74e-01 |
9.81e-01 |
0.03120 |
0.023400 |
0.020700 |
8.30e-01 |
8.50e-01 |
| FOXO-mediated transcription of oxidative stress, metabolic and neuronal genes |
25 |
9.25e-01 |
9.43e-01 |
0.03120 |
-0.010400 |
0.029400 |
9.28e-01 |
7.99e-01 |
| Mitotic Prometaphase |
184 |
8.18e-01 |
8.55e-01 |
0.03010 |
-0.013600 |
-0.026900 |
7.51e-01 |
5.29e-01 |
| Diseases of glycosylation |
106 |
9.14e-01 |
9.35e-01 |
0.02990 |
-0.022200 |
-0.020100 |
6.93e-01 |
7.21e-01 |
| SLC transporter disorders |
75 |
8.09e-01 |
8.47e-01 |
0.02970 |
0.028000 |
-0.010000 |
6.75e-01 |
8.81e-01 |
| Resolution of Sister Chromatid Cohesion |
104 |
8.93e-01 |
9.20e-01 |
0.02870 |
0.026400 |
0.011100 |
6.42e-01 |
8.45e-01 |
| HS-GAG degradation |
16 |
9.89e-01 |
9.92e-01 |
0.02710 |
0.017100 |
0.020900 |
9.05e-01 |
8.85e-01 |
| Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane |
11 |
9.93e-01 |
9.95e-01 |
0.02570 |
0.019000 |
0.017300 |
9.13e-01 |
9.21e-01 |
| Constitutive Signaling by Aberrant PI3K in Cancer |
53 |
9.06e-01 |
9.29e-01 |
0.02300 |
-0.011400 |
0.020000 |
8.86e-01 |
8.01e-01 |
| DNA Repair |
289 |
8.67e-01 |
8.99e-01 |
0.02230 |
-0.018100 |
-0.013000 |
5.97e-01 |
7.04e-01 |
| Netrin-1 signaling |
40 |
9.55e-01 |
9.66e-01 |
0.02140 |
-0.001390 |
0.021400 |
9.88e-01 |
8.15e-01 |
| Amplification of signal from unattached kinetochores via a MAD2 inhibitory signal |
91 |
9.38e-01 |
9.52e-01 |
0.02130 |
-0.006200 |
-0.020300 |
9.19e-01 |
7.37e-01 |
| Amplification of signal from the kinetochores |
91 |
9.38e-01 |
9.52e-01 |
0.02130 |
-0.006200 |
-0.020300 |
9.19e-01 |
7.37e-01 |
| Activation of SMO |
13 |
9.91e-01 |
9.94e-01 |
0.02090 |
-0.019900 |
-0.006400 |
9.01e-01 |
9.68e-01 |
| Regulation of PLK1 Activity at G2/M Transition |
86 |
8.99e-01 |
9.23e-01 |
0.02020 |
0.005360 |
-0.019500 |
9.32e-01 |
7.55e-01 |
| Transport of inorganic cations/anions and amino acids/oligopeptides |
79 |
9.69e-01 |
9.77e-01 |
0.01990 |
0.016300 |
0.011500 |
8.03e-01 |
8.59e-01 |
| Class B/2 (Secretin family receptors) |
55 |
9.39e-01 |
9.52e-01 |
0.01910 |
-0.018200 |
0.005820 |
8.16e-01 |
9.41e-01 |
| Telomere Extension By Telomerase |
23 |
9.81e-01 |
9.85e-01 |
0.01530 |
0.012300 |
-0.008970 |
9.18e-01 |
9.41e-01 |
| Inactivation, recovery and regulation of the phototransduction cascade |
25 |
9.96e-01 |
9.97e-01 |
0.01180 |
-0.009970 |
-0.006340 |
9.31e-01 |
9.56e-01 |
| HDR through Homologous Recombination (HRR) or Single Strand Annealing (SSA) |
104 |
9.75e-01 |
9.81e-01 |
0.01010 |
0.000370 |
-0.010100 |
9.95e-01 |
8.59e-01 |
| EML4 and NUDC in mitotic spindle formation |
95 |
9.93e-01 |
9.95e-01 |
0.00464 |
0.001970 |
-0.004190 |
9.73e-01 |
9.44e-01 |
| Chondroitin sulfate/dermatan sulfate metabolism |
38 |
9.99e-01 |
9.99e-01 |
0.00279 |
-0.002730 |
-0.000567 |
9.77e-01 |
9.95e-01 |