date generated: 2024-04-16
Mitch performs unidimensional and multidimensional gene set enrichment analysis. The concept behind this dates to work by Cox and Mann (https://doi.org/10.1186/1471-2105-13-S16-S12). This implementation is suited to R based workflows of multi-omics datasets. This software was developed by Antony Kaspi and Mark Ziemann. Learn more about Mitch at the website: https://github.com/markziemann/Mitch
Here is the first few lines of the input profile.
rna | k9a | k36a | |
---|---|---|---|
CNNM2 | 0.5560970 | 0.6489925 | 1.4501024 |
CD81 | -0.7720398 | 0.5389497 | 1.0651607 |
DENND4C | 2.3051477 | 0.1649949 | 19.0693005 |
RP11-211G3.2 | 0.0682718 | 8.8137554 | -0.4796384 |
PRPF4 | 0.5968527 | 0.7500091 | 1.3103958 |
EIF3K | 1.3218972 | 1.6403949 | 4.1412992 |
Here are some metrics about the input data profile:
Profile metrics | |
---|---|
num_genes_in_profile | 12944 |
duplicated_genes_present | 0 |
num_profile_genes_in_sets | 6447 |
num_profile_genes_not_in_sets | 6497 |
Here is a plot of the input profiles. Note the dynamic ranges.
Here is the contour plot of the profile including all detected genes.
Here are some metrics about the gene sets used:
GMT file of genesets:Gene sets metrics | |
---|---|
num_genesets | 2263 |
num_genesets_excluded | 1068 |
num_genesets_included | 1195 |
rna | k9a | k36a | Count |
---|---|---|---|
-1 | -1 | -1 | 201 |
1 | -1 | -1 | 240 |
-1 | 1 | -1 | 929 |
0 | 1 | -1 | 1 |
1 | 1 | -1 | 1081 |
1 | 1 | 0 | 1 |
-1 | -1 | 1 | 978 |
1 | -1 | 1 | 1033 |
1 | 0 | 1 | 1 |
-1 | 1 | 1 | 4180 |
1 | 1 | 1 | 4299 |
All sets with FDR<0.05. Try hovering over the points.
Top N sets irrespective of FDR. Try hovering over the points.
Significance is the -log2(p.adjustMANOVA) and effect size is the s.dist which is the hypotenuse of the s scores.
set | setSize | pMANOVA | p.adjustMANOVA | s.dist | s.rna | s.k9a | s.k36a | p.rna | p.k9a | p.k36a |
---|---|---|---|---|---|---|---|---|---|---|
Signaling by NOTCH3 | 40 | 0.000643 | 0.769 | 0.384 | -0.2570 | -0.0563 | 0.2790 | 0.004950 | 0.53800 | 0.00226 |
TP53 Regulates Transcription of Genes Involved in G2 Cell Cycle Arrest | 13 | 0.002530 | 0.982 | 0.604 | 0.6000 | -0.0274 | 0.0612 | 0.000179 | 0.86400 | 0.70200 |
Visual phototransduction | 46 | 0.003360 | 0.982 | 0.317 | 0.1820 | -0.1380 | -0.2190 | 0.032400 | 0.10700 | 0.01010 |
Protein methylation | 14 | 0.003380 | 0.982 | 0.577 | -0.2660 | -0.4100 | 0.3070 | 0.085300 | 0.00793 | 0.04690 |
GPCR ligand binding | 106 | 0.004640 | 0.982 | 0.204 | 0.0619 | -0.0653 | -0.1830 | 0.272000 | 0.24600 | 0.00118 |
set | setSize | pMANOVA | p.adjustMANOVA | s.dist | s.rna | s.k9a | s.k36a | p.rna | p.k9a | p.k36a |
---|---|---|---|---|---|---|---|---|---|---|
Signaling by NOTCH3 | 40 | 0.000643 | 0.769 | 0.3840 | -2.57e-01 | -0.056300 | 2.79e-01 | 0.004950 | 0.53800 | 0.00226 |
TP53 Regulates Transcription of Genes Involved in G2 Cell Cycle Arrest | 13 | 0.002530 | 0.982 | 0.6040 | 6.00e-01 | -0.027400 | 6.12e-02 | 0.000179 | 0.86400 | 0.70200 |
Visual phototransduction | 46 | 0.003360 | 0.982 | 0.3170 | 1.82e-01 | -0.138000 | -2.19e-01 | 0.032400 | 0.10700 | 0.01010 |
Protein methylation | 14 | 0.003380 | 0.982 | 0.5770 | -2.66e-01 | -0.410000 | 3.07e-01 | 0.085300 | 0.00793 | 0.04690 |
GPCR ligand binding | 106 | 0.004640 | 0.982 | 0.2040 | 6.19e-02 | -0.065300 | -1.83e-01 | 0.272000 | 0.24600 | 0.00118 |
Class B/2 (Secretin family receptors) | 40 | 0.006240 | 0.982 | 0.3220 | 1.65e-01 | -0.171000 | -2.17e-01 | 0.070500 | 0.06130 | 0.01740 |
VEGFR2 mediated cell proliferation | 17 | 0.006980 | 0.982 | 0.4870 | 4.16e-01 | -0.240000 | -7.89e-02 | 0.002970 | 0.08740 | 0.57300 |
activated TAK1 mediates p38 MAPK activation | 18 | 0.008400 | 0.982 | 0.4640 | 3.74e-01 | -0.274000 | -7.82e-04 | 0.006020 | 0.04410 | 0.99500 |
NOTCH3 Intracellular Domain Regulates Transcription | 18 | 0.008510 | 0.982 | 0.4710 | -2.59e-01 | -0.181000 | 3.50e-01 | 0.057400 | 0.18500 | 0.01020 |
Deadenylation-dependent mRNA decay | 49 | 0.008690 | 0.982 | 0.2790 | -1.72e-01 | 0.042300 | -2.15e-01 | 0.037000 | 0.60800 | 0.00917 |
Constitutive Signaling by NOTCH1 HD Domain Mutants | 14 | 0.012000 | 0.982 | 0.5150 | -3.32e-01 | 0.103000 | 3.80e-01 | 0.031500 | 0.50300 | 0.01390 |
Signaling by NOTCH1 HD Domain Mutants in Cancer | 14 | 0.012000 | 0.982 | 0.5150 | -3.32e-01 | 0.103000 | 3.80e-01 | 0.031500 | 0.50300 | 0.01390 |
The phototransduction cascade | 16 | 0.013600 | 0.982 | 0.4730 | 2.65e-01 | -0.271000 | -2.83e-01 | 0.066500 | 0.06080 | 0.05040 |
Purine catabolism | 14 | 0.015100 | 0.982 | 0.4960 | 2.60e-01 | -0.396000 | 1.46e-01 | 0.091700 | 0.01040 | 0.34400 |
Diseases of carbohydrate metabolism | 27 | 0.017400 | 0.982 | 0.3560 | -3.11e-01 | 0.070800 | 1.59e-01 | 0.005200 | 0.52500 | 0.15300 |
Signaling by NOTCH1 | 65 | 0.018500 | 0.982 | 0.2290 | -1.57e-01 | -0.003750 | 1.67e-01 | 0.028800 | 0.95800 | 0.01970 |
Nitric oxide stimulates guanylate cyclase | 17 | 0.018700 | 0.982 | 0.4380 | -2.73e-01 | 0.029600 | -3.42e-01 | 0.051600 | 0.83300 | 0.01480 |
mRNA decay by 3’ to 5’ exoribonuclease | 12 | 0.020100 | 0.982 | 0.5170 | -4.25e-01 | 0.149000 | -2.54e-01 | 0.010800 | 0.37000 | 0.12700 |
G-protein beta:gamma signalling | 20 | 0.020400 | 0.982 | 0.4000 | 3.10e-01 | -0.196000 | 1.60e-01 | 0.016500 | 0.12800 | 0.21400 |
NCAM signaling for neurite out-growth | 40 | 0.020500 | 0.982 | 0.2850 | -2.83e-03 | 0.181000 | 2.21e-01 | 0.975000 | 0.04830 | 0.01570 |
Antiviral mechanism by IFN-stimulated genes | 75 | 0.022300 | 0.982 | 0.2100 | 1.52e-01 | 0.094100 | -1.10e-01 | 0.023000 | 0.15900 | 0.10100 |
Activation of the AP-1 family of transcription factors | 10 | 0.024300 | 0.982 | 0.5560 | 3.20e-01 | 0.219000 | 3.99e-01 | 0.080000 | 0.23100 | 0.02890 |
ISG15 antiviral mechanism | 69 | 0.025100 | 0.982 | 0.2150 | 1.66e-01 | 0.097600 | -9.68e-02 | 0.017300 | 0.16100 | 0.16500 |
Activated NOTCH1 Transmits Signal to the Nucleus | 26 | 0.026600 | 0.982 | 0.3450 | -1.66e-01 | 0.161000 | 2.56e-01 | 0.144000 | 0.15500 | 0.02370 |
NOTCH3 Activation and Transmission of Signal to the Nucleus | 23 | 0.027200 | 0.982 | 0.3680 | -2.64e-01 | 0.060800 | 2.48e-01 | 0.028300 | 0.61400 | 0.03930 |
Processing of DNA double-strand break ends | 52 | 0.031800 | 0.982 | 0.2390 | -2.25e-01 | -0.079200 | 1.02e-02 | 0.004950 | 0.32300 | 0.89900 |
Signaling by NOTCH | 153 | 0.032300 | 0.982 | 0.1410 | -1.09e-01 | -0.048600 | 7.50e-02 | 0.020400 | 0.30000 | 0.11000 |
Biosynthesis of the N-glycan precursor (dolichol lipid-linked oligosaccharide, LLO) and transfer to a nascent protein | 63 | 0.033000 | 0.982 | 0.2170 | 2.01e-01 | 0.006340 | -8.09e-02 | 0.005750 | 0.93100 | 0.26800 |
SUMOylation of transcription factors | 15 | 0.033400 | 0.982 | 0.4390 | -3.07e-01 | -0.274000 | -1.55e-01 | 0.039600 | 0.06650 | 0.29900 |
Ca2+ pathway | 46 | 0.034000 | 0.982 | 0.2490 | 1.72e-01 | -0.179000 | 2.29e-02 | 0.043100 | 0.03600 | 0.78800 |
Metabolism of porphyrins | 13 | 0.034300 | 0.982 | 0.4690 | -1.09e-01 | -0.285000 | -3.56e-01 | 0.495000 | 0.07510 | 0.02630 |
Mitochondrial translation | 65 | 0.035300 | 0.982 | 0.2090 | 1.95e-01 | 0.043300 | 6.34e-02 | 0.006630 | 0.54700 | 0.37700 |
Nucleobase catabolism | 26 | 0.035400 | 0.982 | 0.3300 | 2.63e-01 | -0.194000 | 4.44e-02 | 0.020500 | 0.08650 | 0.69600 |
mTORC1-mediated signalling | 21 | 0.035400 | 0.982 | 0.3710 | 1.42e-01 | 0.342000 | -8.85e-03 | 0.259000 | 0.00662 | 0.94400 |
Processing of SMDT1 | 14 | 0.035700 | 0.982 | 0.4510 | -7.56e-02 | 0.378000 | 2.35e-01 | 0.624000 | 0.01450 | 0.12800 |
Interferon Signaling | 146 | 0.036100 | 0.982 | 0.1420 | 7.53e-02 | 0.079400 | -9.06e-02 | 0.117000 | 0.09840 | 0.05940 |
HDR through Single Strand Annealing (SSA) | 30 | 0.039500 | 0.982 | 0.3070 | -2.39e-01 | -0.185000 | 5.36e-02 | 0.023300 | 0.07970 | 0.61100 |
Platelet degranulation | 84 | 0.040200 | 0.982 | 0.1840 | -9.99e-02 | -0.106000 | 1.13e-01 | 0.114000 | 0.09360 | 0.07410 |
Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks | 39 | 0.041700 | 0.982 | 0.2630 | -2.21e-01 | 0.017100 | -1.41e-01 | 0.016900 | 0.85300 | 0.12800 |
Regulation of TP53 Activity through Methylation | 16 | 0.042100 | 0.982 | 0.4150 | -2.49e-01 | 0.186000 | 2.75e-01 | 0.084200 | 0.19700 | 0.05710 |
Inactivation, recovery and regulation of the phototransduction cascade | 15 | 0.042700 | 0.982 | 0.4270 | 2.26e-01 | -0.226000 | -2.84e-01 | 0.129000 | 0.13000 | 0.05730 |
Apoptotic execution phase | 37 | 0.043200 | 0.982 | 0.2720 | 1.90e-01 | -0.149000 | -1.25e-01 | 0.045700 | 0.11800 | 0.18900 |
Signalling to RAS | 17 | 0.043500 | 0.982 | 0.3990 | 3.71e-01 | 0.130000 | 7.17e-02 | 0.008160 | 0.35500 | 0.60900 |
Striated Muscle Contraction | 30 | 0.044000 | 0.982 | 0.3030 | -1.98e-01 | -0.221000 | 6.20e-02 | 0.061000 | 0.03620 | 0.55700 |
Cell Cycle Checkpoints | 184 | 0.046600 | 0.982 | 0.1210 | -9.46e-02 | -0.073400 | -1.92e-02 | 0.027300 | 0.08690 | 0.65500 |
PTK6 Regulates RHO GTPases, RAS GTPase and MAP kinases | 13 | 0.046600 | 0.982 | 0.4510 | 7.03e-02 | 0.340000 | 2.88e-01 | 0.661000 | 0.03380 | 0.07270 |
Netrin-1 signaling | 38 | 0.046900 | 0.982 | 0.2630 | 1.72e-01 | -0.197000 | 2.58e-02 | 0.066500 | 0.03570 | 0.78300 |
Diseases associated with glycosylation precursor biosynthesis | 15 | 0.046900 | 0.982 | 0.4260 | 3.11e-01 | 0.059700 | -2.84e-01 | 0.036800 | 0.68900 | 0.05690 |
Anchoring of the basal body to the plasma membrane | 84 | 0.047000 | 0.982 | 0.1770 | 9.37e-02 | -0.133000 | 6.93e-02 | 0.138000 | 0.03530 | 0.27300 |
Fanconi Anemia Pathway | 26 | 0.048300 | 0.982 | 0.3220 | -1.72e-01 | -0.082400 | 2.60e-01 | 0.129000 | 0.46700 | 0.02200 |
G2/M DNA damage checkpoint | 49 | 0.048500 | 0.982 | 0.2330 | -1.69e-01 | -0.157000 | -3.22e-02 | 0.041100 | 0.05790 | 0.69700 |
Detoxification of Reactive Oxygen Species | 23 | 0.050600 | 0.982 | 0.3340 | 2.40e-01 | 0.122000 | 1.97e-01 | 0.046600 | 0.30900 | 0.10200 |
Estrogen-dependent gene expression | 79 | 0.051500 | 0.982 | 0.1830 | -1.09e-01 | 0.049800 | 1.38e-01 | 0.093800 | 0.44500 | 0.03470 |
RUNX3 regulates NOTCH signaling | 12 | 0.051700 | 0.982 | 0.4700 | -3.08e-01 | -0.206000 | 2.89e-01 | 0.064900 | 0.21600 | 0.08320 |
Signalling to ERKs | 30 | 0.052900 | 0.982 | 0.2930 | 2.82e-01 | 0.078800 | 7.90e-03 | 0.007470 | 0.45500 | 0.94000 |
DNA Double Strand Break Response | 40 | 0.055400 | 0.982 | 0.2500 | -2.23e-01 | 0.004320 | -1.13e-01 | 0.014800 | 0.96200 | 0.21800 |
Interleukin-37 signaling | 17 | 0.056600 | 0.982 | 0.3870 | 9.15e-02 | 0.201000 | -3.18e-01 | 0.514000 | 0.15100 | 0.02310 |
cGMP effects | 11 | 0.057400 | 0.982 | 0.4720 | -2.61e-01 | 0.177000 | -3.52e-01 | 0.134000 | 0.31000 | 0.04320 |
Mucopolysaccharidoses | 11 | 0.058900 | 0.982 | 0.4800 | -4.23e-01 | -0.071200 | 2.15e-01 | 0.015200 | 0.68300 | 0.21600 |
Pentose phosphate pathway | 11 | 0.060900 | 0.982 | 0.4740 | 2.14e-01 | -0.251000 | -3.41e-01 | 0.219000 | 0.15000 | 0.05050 |
Tristetraprolin (TTP, ZFP36) binds and destabilizes mRNA | 13 | 0.061000 | 0.982 | 0.4310 | -1.85e-01 | 0.060400 | -3.85e-01 | 0.248000 | 0.70600 | 0.01630 |
Unfolded Protein Response (UPR) | 69 | 0.061000 | 0.982 | 0.1870 | -1.48e-01 | 0.088200 | -7.27e-02 | 0.033200 | 0.20600 | 0.29700 |
IRF3-mediated induction of type I IFN | 10 | 0.064700 | 0.982 | 0.4960 | 3.24e-01 | 0.361000 | -1.03e-01 | 0.076200 | 0.04840 | 0.57100 |
Activation of kainate receptors upon glutamate binding | 19 | 0.065000 | 0.982 | 0.3540 | 1.87e-01 | -0.290000 | 8.06e-02 | 0.159000 | 0.02880 | 0.54300 |
ATF4 activates genes in response to endoplasmic reticulum stress | 19 | 0.065400 | 0.982 | 0.3520 | -2.86e-01 | 0.079000 | -1.89e-01 | 0.030700 | 0.55100 | 0.15400 |
Sphingolipid de novo biosynthesis | 31 | 0.066300 | 0.982 | 0.2760 | 1.44e-01 | 0.101000 | 2.13e-01 | 0.165000 | 0.33100 | 0.04060 |
NOTCH1 Intracellular Domain Regulates Transcription | 44 | 0.068000 | 0.982 | 0.2360 | -1.76e-01 | -0.069600 | 1.40e-01 | 0.043200 | 0.42500 | 0.10800 |
Pausing and recovery of Tat-mediated HIV elongation | 22 | 0.068100 | 0.982 | 0.3260 | 1.61e-01 | -0.231000 | 1.65e-01 | 0.192000 | 0.06070 | 0.18000 |
Tat-mediated HIV elongation arrest and recovery | 22 | 0.068100 | 0.982 | 0.3260 | 1.61e-01 | -0.231000 | 1.65e-01 | 0.192000 | 0.06070 | 0.18000 |
p38MAPK events | 13 | 0.068600 | 0.982 | 0.4250 | 4.18e-01 | 0.003110 | 7.82e-02 | 0.009060 | 0.98500 | 0.62600 |
Constitutive Signaling by NOTCH1 HD+PEST Domain Mutants | 52 | 0.068900 | 0.982 | 0.2160 | -1.61e-01 | -0.035800 | 1.40e-01 | 0.044500 | 0.65500 | 0.08200 |
Constitutive Signaling by NOTCH1 PEST Domain Mutants | 52 | 0.068900 | 0.982 | 0.2160 | -1.61e-01 | -0.035800 | 1.40e-01 | 0.044500 | 0.65500 | 0.08200 |
Signaling by NOTCH1 HD+PEST Domain Mutants in Cancer | 52 | 0.068900 | 0.982 | 0.2160 | -1.61e-01 | -0.035800 | 1.40e-01 | 0.044500 | 0.65500 | 0.08200 |
Signaling by NOTCH1 PEST Domain Mutants in Cancer | 52 | 0.068900 | 0.982 | 0.2160 | -1.61e-01 | -0.035800 | 1.40e-01 | 0.044500 | 0.65500 | 0.08200 |
Signaling by NOTCH1 in Cancer | 52 | 0.068900 | 0.982 | 0.2160 | -1.61e-01 | -0.035800 | 1.40e-01 | 0.044500 | 0.65500 | 0.08200 |
Regulation of gene expression in late stage (branching morphogenesis) pancreatic bud precursor cells | 11 | 0.069400 | 0.982 | 0.4690 | -3.53e-01 | -0.177000 | 2.53e-01 | 0.042500 | 0.30900 | 0.14700 |
Mitochondrial translation initiation | 60 | 0.069700 | 0.982 | 0.1970 | 1.64e-01 | 0.048800 | 9.74e-02 | 0.027800 | 0.51300 | 0.19200 |
Response to elevated platelet cytosolic Ca2+ | 87 | 0.070900 | 0.982 | 0.1670 | -8.17e-02 | -0.105000 | 9.97e-02 | 0.188000 | 0.08950 | 0.10800 |
HIV elongation arrest and recovery | 24 | 0.071500 | 0.982 | 0.3100 | 1.55e-01 | -0.151000 | 2.21e-01 | 0.189000 | 0.20000 | 0.06050 |
Pausing and recovery of HIV elongation | 24 | 0.071500 | 0.982 | 0.3100 | 1.55e-01 | -0.151000 | 2.21e-01 | 0.189000 | 0.20000 | 0.06050 |
HS-GAG biosynthesis | 17 | 0.071600 | 0.982 | 0.3700 | 2.02e-01 | -0.290000 | -1.11e-01 | 0.150000 | 0.03860 | 0.43000 |
Glutathione conjugation | 25 | 0.072200 | 0.982 | 0.3070 | -7.36e-02 | 0.017000 | 2.97e-01 | 0.524000 | 0.88300 | 0.01010 |
Metal ion SLC transporters | 14 | 0.073100 | 0.982 | 0.4040 | -1.72e-01 | 0.156000 | -3.31e-01 | 0.265000 | 0.31200 | 0.03220 |
SUMOylation | 147 | 0.074700 | 0.982 | 0.1270 | -1.17e-01 | -0.046000 | 1.33e-02 | 0.014400 | 0.33700 | 0.78100 |
Recruitment of NuMA to mitotic centrosomes | 67 | 0.075100 | 0.982 | 0.1840 | 1.11e-01 | -0.114000 | 9.22e-02 | 0.117000 | 0.10600 | 0.19200 |
CS/DS degradation | 10 | 0.075400 | 0.982 | 0.4820 | -3.44e-01 | 0.164000 | 2.96e-01 | 0.060000 | 0.36800 | 0.10500 |
Cilium Assembly | 154 | 0.075400 | 0.982 | 0.1220 | 8.58e-02 | -0.076300 | 4.06e-02 | 0.066700 | 0.10300 | 0.38600 |
TAK1 activates NFkB by phosphorylation and activation of IKKs complex | 21 | 0.078200 | 0.982 | 0.3300 | 2.12e-01 | -0.173000 | -1.84e-01 | 0.092300 | 0.17100 | 0.14400 |
Glycosaminoglycan metabolism | 78 | 0.078600 | 0.982 | 0.1730 | -1.04e-01 | -0.095800 | 9.95e-02 | 0.112000 | 0.14400 | 0.12900 |
SUMOylation of transcription cofactors | 39 | 0.079300 | 0.982 | 0.2420 | -1.95e-01 | -0.143000 | -7.25e-03 | 0.035000 | 0.12200 | 0.93800 |
NOTCH4 Intracellular Domain Regulates Transcription | 17 | 0.079500 | 0.982 | 0.3650 | -3.43e-01 | -0.121000 | -3.63e-02 | 0.014500 | 0.38800 | 0.79600 |
Presynaptic phase of homologous DNA pairing and strand exchange | 30 | 0.082100 | 0.982 | 0.2760 | -2.13e-01 | -0.160000 | 7.33e-02 | 0.043900 | 0.13100 | 0.48700 |
G beta:gamma signalling through CDC42 | 12 | 0.082800 | 0.982 | 0.4290 | 3.48e-01 | -0.250000 | -7.60e-04 | 0.036800 | 0.13400 | 0.99600 |
Regulation of TP53 Activity | 129 | 0.084300 | 0.982 | 0.1330 | -8.78e-02 | -0.019500 | 9.83e-02 | 0.085800 | 0.70300 | 0.05440 |
Signaling by Erythropoietin | 21 | 0.086600 | 0.982 | 0.3230 | -3.98e-03 | -0.120000 | -3.00e-01 | 0.975000 | 0.34300 | 0.01740 |
Synthesis of substrates in N-glycan biosythesis | 50 | 0.086800 | 0.982 | 0.2120 | 1.95e-01 | 0.041700 | -7.09e-02 | 0.017200 | 0.61000 | 0.38600 |
FRS-mediated FGFR4 signaling | 12 | 0.087000 | 0.982 | 0.4240 | 3.83e-01 | 0.025500 | 1.81e-01 | 0.021700 | 0.87900 | 0.27900 |
Asparagine N-linked glycosylation | 233 | 0.087500 | 0.982 | 0.0982 | 9.54e-02 | 0.019300 | -1.27e-02 | 0.012400 | 0.61200 | 0.74000 |
Mitochondrial tRNA aminoacylation | 20 | 0.089100 | 0.982 | 0.3290 | -3.29e-02 | 0.109000 | -3.09e-01 | 0.799000 | 0.39900 | 0.01670 |
trans-Golgi Network Vesicle Budding | 58 | 0.090800 | 0.982 | 0.1920 | 8.88e-02 | -0.168000 | 3.00e-02 | 0.243000 | 0.02710 | 0.69300 |
PKA-mediated phosphorylation of CREB | 17 | 0.092000 | 0.982 | 0.3520 | 2.31e-01 | 0.050300 | 2.61e-01 | 0.098700 | 0.71900 | 0.06280 |
MAP kinase activation | 60 | 0.092300 | 0.982 | 0.1870 | 1.30e-01 | -0.028900 | 1.32e-01 | 0.081400 | 0.69900 | 0.07800 |
G alpha (s) signalling events | 66 | 0.092300 | 0.982 | 0.1810 | 2.46e-03 | 0.121000 | -1.34e-01 | 0.972000 | 0.08820 | 0.05930 |
Phase II - Conjugation of compounds | 50 | 0.093600 | 0.982 | 0.2080 | -8.36e-02 | 0.031500 | 1.88e-01 | 0.307000 | 0.70000 | 0.02150 |
TRAF6 mediated induction of NFkB and MAP kinases upon TLR7/8 or 9 activation | 76 | 0.094100 | 0.982 | 0.1660 | 1.42e-01 | -0.054100 | 6.81e-02 | 0.032900 | 0.41500 | 0.30500 |
RHO GTPases Activate NADPH Oxidases | 12 | 0.095100 | 0.982 | 0.4180 | 2.99e-01 | 0.159000 | 2.45e-01 | 0.072900 | 0.34100 | 0.14200 |
Signaling by NOTCH2 | 27 | 0.096000 | 0.982 | 0.2830 | -2.34e-01 | -0.063500 | 1.47e-01 | 0.035600 | 0.56800 | 0.18600 |
FRS-mediated FGFR3 signaling | 10 | 0.096100 | 0.982 | 0.4570 | 4.37e-01 | 0.005880 | 1.34e-01 | 0.016700 | 0.97400 | 0.46300 |
Homologous DNA Pairing and Strand Exchange | 32 | 0.096300 | 0.982 | 0.2600 | -2.08e-01 | -0.139000 | 7.04e-02 | 0.042000 | 0.17300 | 0.49100 |
MyD88 cascade initiated on plasma membrane | 74 | 0.096500 | 0.982 | 0.1680 | 1.38e-01 | -0.056800 | 7.69e-02 | 0.040700 | 0.39900 | 0.25300 |
Toll Like Receptor 10 (TLR10) Cascade | 74 | 0.096500 | 0.982 | 0.1680 | 1.38e-01 | -0.056800 | 7.69e-02 | 0.040700 | 0.39900 | 0.25300 |
Toll Like Receptor 5 (TLR5) Cascade | 74 | 0.096500 | 0.982 | 0.1680 | 1.38e-01 | -0.056800 | 7.69e-02 | 0.040700 | 0.39900 | 0.25300 |
Peroxisomal protein import | 48 | 0.097700 | 0.982 | 0.2110 | -5.42e-02 | -0.036600 | 2.01e-01 | 0.516000 | 0.66100 | 0.01630 |
Interleukin-3, Interleukin-5 and GM-CSF signaling | 29 | 0.101000 | 0.982 | 0.2670 | -6.97e-02 | 0.016400 | -2.57e-01 | 0.516000 | 0.87900 | 0.01680 |
Class A/1 (Rhodopsin-like receptors) | 63 | 0.102000 | 0.982 | 0.1810 | -1.55e-02 | 0.000667 | -1.81e-01 | 0.832000 | 0.99300 | 0.01330 |
tRNA Aminoacylation | 39 | 0.103000 | 0.982 | 0.2310 | 1.19e-02 | 0.025900 | -2.29e-01 | 0.898000 | 0.78000 | 0.01350 |
FRS-mediated FGFR2 signaling | 12 | 0.104000 | 0.982 | 0.4100 | 3.56e-01 | 0.009180 | 2.03e-01 | 0.032700 | 0.95600 | 0.22200 |
Signaling by Non-Receptor Tyrosine Kinases | 44 | 0.104000 | 0.982 | 0.2180 | -1.70e-01 | 0.057200 | 1.24e-01 | 0.051500 | 0.51200 | 0.15600 |
Signaling by PTK6 | 44 | 0.104000 | 0.982 | 0.2180 | -1.70e-01 | 0.057200 | 1.24e-01 | 0.051500 | 0.51200 | 0.15600 |
ECM proteoglycans | 34 | 0.108000 | 0.982 | 0.2460 | -1.30e-01 | 0.041100 | 2.05e-01 | 0.191000 | 0.67800 | 0.03850 |
Transcriptional Regulation by MECP2 | 44 | 0.108000 | 0.982 | 0.2170 | -1.06e-01 | -0.067700 | 1.77e-01 | 0.226000 | 0.43700 | 0.04200 |
Regulation of TP53 Activity through Association with Co-factors | 11 | 0.108000 | 0.982 | 0.4250 | 2.33e-01 | 0.009160 | 3.55e-01 | 0.181000 | 0.95800 | 0.04160 |
Loss of Nlp from mitotic centrosomes | 59 | 0.109000 | 0.982 | 0.1840 | 1.08e-01 | -0.115000 | 9.37e-02 | 0.151000 | 0.12600 | 0.21400 |
Loss of proteins required for interphase microtubule organization from the centrosome | 59 | 0.109000 | 0.982 | 0.1840 | 1.08e-01 | -0.115000 | 9.37e-02 | 0.151000 | 0.12600 | 0.21400 |
Chondroitin sulfate/dermatan sulfate metabolism | 34 | 0.109000 | 0.982 | 0.2470 | -1.75e-01 | -0.028700 | 1.71e-01 | 0.077000 | 0.77200 | 0.08450 |
SHC-mediated cascade:FGFR4 | 10 | 0.111000 | 0.982 | 0.4460 | 4.21e-01 | 0.101000 | 1.06e-01 | 0.021000 | 0.57900 | 0.56200 |
The role of Nef in HIV-1 replication and disease pathogenesis | 20 | 0.112000 | 0.982 | 0.3180 | -2.97e-01 | -0.105000 | 4.21e-02 | 0.021500 | 0.41600 | 0.74500 |
Abortive elongation of HIV-1 transcript in the absence of Tat | 18 | 0.113000 | 0.982 | 0.3310 | 1.82e-01 | -0.254000 | 1.07e-01 | 0.181000 | 0.06190 | 0.43200 |
MyD88 dependent cascade initiated on endosome | 77 | 0.116000 | 0.982 | 0.1590 | 1.37e-01 | -0.052500 | 6.15e-02 | 0.038100 | 0.42600 | 0.35100 |
Toll Like Receptor 7/8 (TLR7/8) Cascade | 77 | 0.116000 | 0.982 | 0.1590 | 1.37e-01 | -0.052500 | 6.15e-02 | 0.038100 | 0.42600 | 0.35100 |
PKA activation | 15 | 0.117000 | 0.982 | 0.3590 | 2.36e-01 | 0.116000 | 2.45e-01 | 0.113000 | 0.43900 | 0.10100 |
SUMO E3 ligases SUMOylate target proteins | 141 | 0.117000 | 0.982 | 0.1190 | -1.07e-01 | -0.050800 | 1.20e-02 | 0.028200 | 0.29900 | 0.80600 |
Signaling by cytosolic FGFR1 fusion mutants | 18 | 0.119000 | 0.982 | 0.3280 | -3.23e-01 | -0.002120 | -5.86e-02 | 0.017800 | 0.98800 | 0.66700 |
Plasma lipoprotein assembly, remodeling, and clearance | 47 | 0.119000 | 0.982 | 0.2020 | -1.11e-01 | 0.108000 | -1.30e-01 | 0.189000 | 0.20100 | 0.12300 |
Other interleukin signaling | 16 | 0.121000 | 0.982 | 0.3460 | 1.27e-01 | -0.277000 | 1.64e-01 | 0.381000 | 0.05470 | 0.25700 |
Class I peroxisomal membrane protein import | 14 | 0.123000 | 0.982 | 0.3700 | -4.99e-02 | 0.357000 | -8.51e-02 | 0.747000 | 0.02080 | 0.58200 |
Interleukin-17 signaling | 63 | 0.124000 | 0.982 | 0.1730 | 1.02e-01 | -0.019100 | 1.39e-01 | 0.163000 | 0.79300 | 0.05660 |
TCF dependent signaling in response to WNT | 136 | 0.125000 | 0.982 | 0.1200 | -4.89e-02 | -0.108000 | -1.77e-02 | 0.326000 | 0.03060 | 0.72300 |
Signaling by GPCR | 319 | 0.125000 | 0.982 | 0.0793 | 6.52e-02 | 0.013600 | -4.31e-02 | 0.046500 | 0.67800 | 0.18800 |
Toll Like Receptor 3 (TLR3) Cascade | 82 | 0.126000 | 0.982 | 0.1520 | 1.48e-01 | 0.004000 | 3.44e-02 | 0.020400 | 0.95000 | 0.59100 |
Competing endogenous RNAs (ceRNAs) regulate PTEN translation | 11 | 0.126000 | 0.982 | 0.4130 | 1.64e-01 | -0.141000 | 3.53e-01 | 0.348000 | 0.41800 | 0.04290 |
Assembly and cell surface presentation of NMDA receptors | 15 | 0.126000 | 0.982 | 0.3560 | -3.13e-01 | -0.128000 | -1.09e-01 | 0.035700 | 0.39000 | 0.46400 |
Centrosome maturation | 67 | 0.127000 | 0.982 | 0.1670 | 9.08e-02 | -0.097500 | 1.02e-01 | 0.199000 | 0.16800 | 0.15100 |
Recruitment of mitotic centrosome proteins and complexes | 67 | 0.127000 | 0.982 | 0.1670 | 9.08e-02 | -0.097500 | 1.02e-01 | 0.199000 | 0.16800 | 0.15100 |
Signaling by Insulin receptor | 47 | 0.127000 | 0.982 | 0.2030 | 1.65e-01 | 0.118000 | -1.78e-03 | 0.051000 | 0.16100 | 0.98300 |
FCERI mediated MAPK activation | 25 | 0.129000 | 0.982 | 0.2740 | 1.31e-01 | 0.209000 | 1.20e-01 | 0.255000 | 0.07100 | 0.29800 |
G beta:gamma signalling through PLC beta | 12 | 0.130000 | 0.982 | 0.3930 | 2.82e-01 | -0.241000 | 1.30e-01 | 0.091300 | 0.14800 | 0.43600 |
Presynaptic function of Kainate receptors | 12 | 0.130000 | 0.982 | 0.3930 | 2.82e-01 | -0.241000 | 1.30e-01 | 0.091300 | 0.14800 | 0.43600 |
Downregulation of ERBB2:ERBB3 signaling | 12 | 0.132000 | 0.982 | 0.3960 | -2.09e-01 | 0.216000 | 2.58e-01 | 0.210000 | 0.19500 | 0.12200 |
mRNA 3’-end processing | 46 | 0.134000 | 0.982 | 0.2020 | 5.46e-03 | 0.201000 | -8.31e-03 | 0.949000 | 0.01820 | 0.92200 |
G2/M Checkpoints | 102 | 0.134000 | 0.982 | 0.1360 | -8.02e-02 | -0.110000 | 3.94e-03 | 0.163000 | 0.05480 | 0.94500 |
Glycogen storage diseases | 13 | 0.134000 | 0.982 | 0.3780 | -3.08e-01 | 0.190000 | 1.08e-01 | 0.054400 | 0.23500 | 0.49800 |
Antigen activates B Cell Receptor (BCR) leading to generation of second messengers | 22 | 0.135000 | 0.982 | 0.2900 | -2.64e-01 | -0.106000 | -5.88e-02 | 0.032400 | 0.38800 | 0.63300 |
Regulation of actin dynamics for phagocytic cup formation | 49 | 0.136000 | 0.982 | 0.1950 | 2.17e-02 | 0.191000 | -3.06e-02 | 0.793000 | 0.02060 | 0.71200 |
Cellular hexose transport | 10 | 0.136000 | 0.982 | 0.4310 | -8.22e-02 | -0.003260 | 4.23e-01 | 0.653000 | 0.98600 | 0.02040 |
CREB1 phosphorylation through the activation of Adenylate Cyclase | 10 | 0.140000 | 0.982 | 0.4230 | 3.56e-01 | -0.048700 | 2.24e-01 | 0.051600 | 0.79000 | 0.21900 |
Branched-chain amino acid catabolism | 16 | 0.140000 | 0.982 | 0.3370 | -3.01e-01 | 0.149000 | 2.57e-02 | 0.037100 | 0.30100 | 0.85900 |
SUMOylation of DNA methylation proteins | 15 | 0.141000 | 0.982 | 0.3470 | 9.95e-02 | -0.324000 | 7.69e-02 | 0.505000 | 0.03000 | 0.60600 |
Diseases associated with the TLR signaling cascade | 18 | 0.142000 | 0.982 | 0.3170 | -1.29e-02 | -0.056100 | -3.12e-01 | 0.925000 | 0.68000 | 0.02200 |
Diseases of Immune System | 18 | 0.142000 | 0.982 | 0.3170 | -1.29e-02 | -0.056100 | -3.12e-01 | 0.925000 | 0.68000 | 0.02200 |
Mitochondrial translation elongation | 59 | 0.144000 | 0.982 | 0.1740 | 1.44e-01 | 0.056800 | 8.03e-02 | 0.056400 | 0.45100 | 0.28600 |
Toll Like Receptor 9 (TLR9) Cascade | 80 | 0.146000 | 0.982 | 0.1490 | 1.31e-01 | -0.050200 | 5.02e-02 | 0.043600 | 0.43800 | 0.43800 |
Iron uptake and transport | 41 | 0.147000 | 0.982 | 0.2090 | -2.61e-02 | 0.207000 | -8.06e-03 | 0.773000 | 0.02180 | 0.92900 |
Signaling by NOTCH4 | 71 | 0.147000 | 0.982 | 0.1600 | -1.23e-01 | -0.098700 | 2.93e-02 | 0.073300 | 0.15100 | 0.66900 |
Signaling by ERBB2 | 41 | 0.148000 | 0.982 | 0.2090 | -1.24e-02 | 0.208000 | -4.48e-03 | 0.891000 | 0.02100 | 0.96000 |
SHC-mediated cascade:FGFR2 | 10 | 0.149000 | 0.982 | 0.4200 | 3.89e-01 | 0.081800 | 1.33e-01 | 0.033000 | 0.65400 | 0.46600 |
Protein localization | 121 | 0.151000 | 0.982 | 0.1230 | -7.85e-02 | 0.001100 | 9.41e-02 | 0.137000 | 0.98300 | 0.07430 |
GABA receptor activation | 24 | 0.152000 | 0.982 | 0.2700 | 2.69e-02 | 0.143000 | 2.28e-01 | 0.820000 | 0.22600 | 0.05340 |
Mitochondrial translation termination | 60 | 0.152000 | 0.982 | 0.1710 | 1.48e-01 | 0.037300 | 7.72e-02 | 0.048300 | 0.61800 | 0.30100 |
Dectin-2 family | 10 | 0.152000 | 0.982 | 0.4180 | -4.13e-01 | 0.055100 | -3.56e-02 | 0.023700 | 0.76300 | 0.84500 |
CLEC7A (Dectin-1) induces NFAT activation | 11 | 0.154000 | 0.982 | 0.4010 | -1.60e-01 | -0.365000 | 4.81e-02 | 0.358000 | 0.03620 | 0.78200 |
Programmed Cell Death | 142 | 0.154000 | 0.982 | 0.1120 | 7.04e-02 | -0.072900 | -4.67e-02 | 0.148000 | 0.13500 | 0.33700 |
RNA Polymerase III Abortive And Retractive Initiation | 34 | 0.155000 | 0.982 | 0.2270 | 1.74e-01 | 0.128000 | 6.87e-02 | 0.079100 | 0.19700 | 0.48900 |
RNA Polymerase III Transcription | 34 | 0.155000 | 0.982 | 0.2270 | 1.74e-01 | 0.128000 | 6.87e-02 | 0.079100 | 0.19700 | 0.48900 |
Prolactin receptor signaling | 10 | 0.155000 | 0.982 | 0.4210 | 1.54e-01 | 0.009590 | -3.92e-01 | 0.400000 | 0.95800 | 0.03190 |
Pre-NOTCH Processing in Golgi | 15 | 0.159000 | 0.982 | 0.3420 | -2.63e-01 | 0.041000 | 2.16e-01 | 0.078300 | 0.78400 | 0.14800 |
AURKA Activation by TPX2 | 60 | 0.160000 | 0.982 | 0.1680 | 9.02e-02 | -0.101000 | 1.00e-01 | 0.228000 | 0.17700 | 0.17900 |
Transmission across Chemical Synapses | 139 | 0.160000 | 0.982 | 0.1110 | 8.32e-02 | 0.013200 | 7.20e-02 | 0.091100 | 0.78800 | 0.14400 |
Muscle contraction | 136 | 0.162000 | 0.982 | 0.1130 | -1.86e-02 | -0.094400 | 5.99e-02 | 0.708000 | 0.05780 | 0.22800 |
Rho GTPase cycle | 113 | 0.162000 | 0.982 | 0.1220 | 1.04e-01 | 0.001060 | 6.54e-02 | 0.057800 | 0.98400 | 0.23100 |
Mitochondrial calcium ion transport | 21 | 0.163000 | 0.982 | 0.2850 | -6.32e-02 | 0.269000 | 7.09e-02 | 0.616000 | 0.03320 | 0.57400 |
ZBP1(DAI) mediated induction of type I IFNs | 16 | 0.164000 | 0.982 | 0.3300 | 1.85e-01 | -0.010900 | -2.73e-01 | 0.201000 | 0.94000 | 0.05890 |
SUMOylation of intracellular receptors | 26 | 0.165000 | 0.982 | 0.2590 | -1.96e-01 | -0.012600 | 1.69e-01 | 0.084500 | 0.91100 | 0.13600 |
FRS-mediated FGFR1 signaling | 13 | 0.166000 | 0.982 | 0.3570 | 2.72e-01 | 0.027900 | 2.31e-01 | 0.090100 | 0.86200 | 0.15000 |
Diseases of signal transduction | 288 | 0.166000 | 0.982 | 0.0781 | -5.42e-02 | -0.055600 | 7.91e-03 | 0.115000 | 0.10600 | 0.81800 |
PKA activation in glucagon signalling | 15 | 0.169000 | 0.982 | 0.3320 | 1.84e-01 | 0.148000 | 2.34e-01 | 0.217000 | 0.32100 | 0.11700 |
Negative regulators of DDX58/IFIH1 signaling | 33 | 0.170000 | 0.982 | 0.2250 | -2.27e-02 | 0.224000 | -9.86e-03 | 0.822000 | 0.02610 | 0.92200 |
Formation of apoptosome | 11 | 0.171000 | 0.982 | 0.3920 | 3.61e-01 | 0.146000 | -5.09e-02 | 0.038300 | 0.40300 | 0.77000 |
Regulation of the apoptosome activity | 11 | 0.171000 | 0.982 | 0.3920 | 3.61e-01 | 0.146000 | -5.09e-02 | 0.038300 | 0.40300 | 0.77000 |
Interleukin-12 family signaling | 35 | 0.171000 | 0.982 | 0.2190 | -3.48e-02 | 0.002520 | 2.17e-01 | 0.722000 | 0.97900 | 0.02660 |
Synthesis of bile acids and bile salts via 24-hydroxycholesterol | 10 | 0.172000 | 0.982 | 0.4100 | -3.53e-01 | -0.209000 | -3.94e-03 | 0.053200 | 0.25300 | 0.98300 |
MyD88-independent TLR4 cascade | 84 | 0.173000 | 0.982 | 0.1410 | 1.39e-01 | -0.000722 | 2.20e-02 | 0.027900 | 0.99100 | 0.72800 |
TRIF(TICAM1)-mediated TLR4 signaling | 84 | 0.173000 | 0.982 | 0.1410 | 1.39e-01 | -0.000722 | 2.20e-02 | 0.027900 | 0.99100 | 0.72800 |
COPII-mediated vesicle transport | 55 | 0.173000 | 0.982 | 0.1750 | 1.58e-01 | -0.024300 | -7.10e-02 | 0.042600 | 0.75500 | 0.36300 |
Transferrin endocytosis and recycling | 20 | 0.174000 | 0.982 | 0.2900 | 1.70e-01 | 0.233000 | -2.46e-02 | 0.187000 | 0.07110 | 0.84900 |
Toll-like Receptor Cascades | 117 | 0.175000 | 0.982 | 0.1190 | 1.19e-01 | -0.005680 | -6.29e-03 | 0.026300 | 0.91600 | 0.90700 |
TP53 regulates transcription of additional cell cycle genes whose exact role in the p53 pathway remain uncertain | 19 | 0.175000 | 0.982 | 0.2940 | -2.48e-02 | -0.193000 | -2.21e-01 | 0.852000 | 0.14600 | 0.09580 |
Neuronal System | 195 | 0.176000 | 0.982 | 0.0921 | 6.94e-02 | 0.039600 | 4.58e-02 | 0.095800 | 0.34200 | 0.27200 |
Cell death signalling via NRAGE, NRIF and NADE | 58 | 0.178000 | 0.982 | 0.1690 | -3.75e-02 | 0.075300 | 1.46e-01 | 0.621000 | 0.32200 | 0.05440 |
Apoptotic cleavage of cellular proteins | 28 | 0.179000 | 0.982 | 0.2430 | 1.77e-01 | -0.110000 | -1.25e-01 | 0.105000 | 0.31500 | 0.25300 |
ESR-mediated signaling | 132 | 0.179000 | 0.982 | 0.1120 | -1.99e-02 | 0.037300 | 1.04e-01 | 0.694000 | 0.46000 | 0.04010 |
Hedgehog ‘off’ state | 88 | 0.179000 | 0.982 | 0.1350 | 1.06e-01 | -0.003840 | 8.45e-02 | 0.087500 | 0.95000 | 0.17100 |
Interleukin receptor SHC signaling | 15 | 0.180000 | 0.982 | 0.3300 | -1.35e-02 | 0.087500 | -3.18e-01 | 0.928000 | 0.55700 | 0.03310 |
HDR through Homologous Recombination (HRR) or Single Strand Annealing (SSA) | 75 | 0.182000 | 0.982 | 0.1480 | -1.32e-01 | -0.066300 | -7.40e-03 | 0.048300 | 0.32100 | 0.91200 |
Transport of Mature Transcript to Cytoplasm | 69 | 0.185000 | 0.982 | 0.1540 | 6.07e-02 | 0.140000 | -2.09e-02 | 0.384000 | 0.04460 | 0.76400 |
NOD1/2 Signaling Pathway | 29 | 0.185000 | 0.982 | 0.2350 | 1.13e-01 | -0.187000 | -8.74e-02 | 0.294000 | 0.08110 | 0.41600 |
Transport of Mature mRNA derived from an Intron-Containing Transcript | 61 | 0.186000 | 0.982 | 0.1640 | 9.90e-02 | 0.123000 | -4.45e-02 | 0.181000 | 0.09660 | 0.54900 |
Regulation of PLK1 Activity at G2/M Transition | 73 | 0.190000 | 0.982 | 0.1460 | 1.07e-01 | -0.060500 | 7.93e-02 | 0.114000 | 0.37200 | 0.24200 |
Regulation of HSF1-mediated heat shock response | 68 | 0.190000 | 0.982 | 0.1550 | 8.57e-02 | 0.078500 | -1.03e-01 | 0.222000 | 0.26300 | 0.14400 |
Formation of Incision Complex in GG-NER | 39 | 0.191000 | 0.982 | 0.2040 | -1.77e-01 | -0.017800 | 9.85e-02 | 0.055300 | 0.84700 | 0.28700 |
RNA Polymerase III Transcription Initiation | 29 | 0.193000 | 0.982 | 0.2330 | 1.15e-01 | 0.168000 | 1.14e-01 | 0.286000 | 0.11800 | 0.29000 |
XBP1(S) activates chaperone genes | 39 | 0.193000 | 0.982 | 0.2010 | -5.63e-02 | 0.177000 | -7.63e-02 | 0.543000 | 0.05630 | 0.41000 |
STING mediated induction of host immune responses | 12 | 0.193000 | 0.982 | 0.3650 | 2.33e-01 | 0.272000 | -7.31e-02 | 0.163000 | 0.10300 | 0.66100 |
KSRP (KHSRP) binds and destabilizes mRNA | 13 | 0.195000 | 0.982 | 0.3480 | -3.47e-01 | -0.024700 | 9.57e-03 | 0.030500 | 0.87700 | 0.95200 |
Formation of HIV elongation complex in the absence of HIV Tat | 33 | 0.196000 | 0.982 | 0.2160 | 1.44e-01 | 0.010500 | 1.60e-01 | 0.151000 | 0.91700 | 0.11200 |
ADP signalling through P2Y purinoceptor 1 | 14 | 0.196000 | 0.982 | 0.3330 | 1.49e-01 | -0.297000 | 7.68e-03 | 0.333000 | 0.05410 | 0.96000 |
RNA Polymerase III Transcription Initiation From Type 1 Promoter | 22 | 0.197000 | 0.982 | 0.2650 | 9.46e-02 | 0.178000 | 1.73e-01 | 0.442000 | 0.14900 | 0.16100 |
Pyruvate metabolism and Citric Acid (TCA) cycle | 48 | 0.198000 | 0.982 | 0.1800 | 1.51e-01 | -0.097100 | -9.69e-03 | 0.070900 | 0.24500 | 0.90800 |
Bile acid and bile salt metabolism | 24 | 0.198000 | 0.982 | 0.2560 | -2.31e-01 | -0.109000 | 4.93e-03 | 0.049900 | 0.35500 | 0.96700 |
Synthesis of bile acids and bile salts | 24 | 0.198000 | 0.982 | 0.2560 | -2.31e-01 | -0.109000 | 4.93e-03 | 0.049900 | 0.35500 | 0.96700 |
GPCR downstream signalling | 294 | 0.199000 | 0.982 | 0.0744 | 5.44e-02 | 0.036800 | -3.48e-02 | 0.110000 | 0.27900 | 0.30700 |
Infectious disease | 289 | 0.199000 | 0.982 | 0.0739 | 1.36e-02 | -0.051200 | 5.16e-02 | 0.693000 | 0.13600 | 0.13300 |
Beta-catenin independent WNT signaling | 114 | 0.200000 | 0.982 | 0.1160 | 5.05e-02 | -0.099100 | 3.44e-02 | 0.352000 | 0.06810 | 0.52700 |
Receptor-type tyrosine-protein phosphatases | 11 | 0.200000 | 0.982 | 0.3750 | 2.66e-02 | -0.141000 | 3.46e-01 | 0.879000 | 0.41700 | 0.04680 |
Regulation of beta-cell development | 17 | 0.202000 | 0.982 | 0.3050 | -2.13e-01 | -0.015900 | 2.17e-01 | 0.128000 | 0.90900 | 0.12200 |
Gastrin-CREB signalling pathway via PKC and MAPK | 13 | 0.202000 | 0.982 | 0.3450 | 3.04e-01 | 0.157000 | 4.00e-02 | 0.057400 | 0.32600 | 0.80300 |
MicroRNA (miRNA) biogenesis | 20 | 0.203000 | 0.982 | 0.2770 | 4.91e-03 | -0.032300 | 2.75e-01 | 0.970000 | 0.80200 | 0.03320 |
DNA Repair | 232 | 0.204000 | 0.982 | 0.0830 | -6.12e-02 | -0.027000 | 4.92e-02 | 0.110000 | 0.48000 | 0.19800 |
Neurexins and neuroligins | 29 | 0.204000 | 0.982 | 0.2320 | 2.17e-01 | 0.007610 | -8.04e-02 | 0.043200 | 0.94300 | 0.45400 |
Downregulation of ERBB2 signaling | 22 | 0.205000 | 0.982 | 0.2650 | -1.58e-01 | 0.140000 | 1.59e-01 | 0.200000 | 0.25500 | 0.19500 |
Metabolism of water-soluble vitamins and cofactors | 86 | 0.205000 | 0.982 | 0.1330 | 1.25e-01 | 0.020800 | 4.00e-02 | 0.044900 | 0.73900 | 0.52200 |
Interferon alpha/beta signaling | 41 | 0.205000 | 0.982 | 0.1940 | 3.45e-02 | 0.104000 | -1.60e-01 | 0.703000 | 0.24700 | 0.07590 |
Apoptosis | 140 | 0.206000 | 0.982 | 0.1050 | 7.24e-02 | -0.061400 | -4.47e-02 | 0.140000 | 0.21100 | 0.36200 |
IRE1alpha activates chaperones | 40 | 0.207000 | 0.982 | 0.1950 | -5.24e-02 | 0.173000 | -7.12e-02 | 0.567000 | 0.05790 | 0.43600 |
RHO GTPases Activate WASPs and WAVEs | 31 | 0.208000 | 0.982 | 0.2220 | 1.53e-01 | 0.159000 | 2.39e-02 | 0.140000 | 0.12600 | 0.81800 |
BMAL1:CLOCK,NPAS2 activates circadian gene expression | 23 | 0.208000 | 0.982 | 0.2570 | -2.56e-01 | 0.013100 | 6.72e-03 | 0.033300 | 0.91400 | 0.95600 |
Regulation of PTEN mRNA translation | 12 | 0.209000 | 0.982 | 0.3530 | 1.53e-01 | -0.195000 | 2.51e-01 | 0.358000 | 0.24300 | 0.13200 |
VxPx cargo-targeting to cilium | 15 | 0.210000 | 0.982 | 0.3160 | -3.57e-02 | -0.205000 | -2.39e-01 | 0.811000 | 0.17000 | 0.11000 |
Interleukin-2 family signaling | 26 | 0.210000 | 0.982 | 0.2390 | -1.08e-01 | 0.123000 | -1.74e-01 | 0.341000 | 0.27700 | 0.12400 |
Voltage gated Potassium channels | 10 | 0.211000 | 0.982 | 0.3880 | 3.08e-03 | 0.385000 | 4.61e-02 | 0.987000 | 0.03500 | 0.80100 |
Organelle biogenesis and maintenance | 221 | 0.211000 | 0.982 | 0.0825 | 4.18e-02 | -0.052300 | 4.82e-02 | 0.285000 | 0.18200 | 0.21800 |
Metabolism of non-coding RNA | 46 | 0.211000 | 0.982 | 0.1810 | 1.50e-01 | -0.083900 | -5.78e-02 | 0.078800 | 0.32500 | 0.49800 |
snRNP Assembly | 46 | 0.211000 | 0.982 | 0.1810 | 1.50e-01 | -0.083900 | -5.78e-02 | 0.078800 | 0.32500 | 0.49800 |
Chondroitin sulfate biosynthesis | 14 | 0.211000 | 0.982 | 0.3280 | -3.54e-02 | 0.051900 | 3.22e-01 | 0.818000 | 0.73700 | 0.03690 |
Metabolism of steroids | 100 | 0.211000 | 0.982 | 0.1230 | -5.51e-02 | -0.083800 | -7.05e-02 | 0.342000 | 0.14800 | 0.22400 |
Interleukin-1 signaling | 83 | 0.212000 | 0.982 | 0.1340 | 1.06e-01 | -0.078800 | 2.09e-02 | 0.094800 | 0.21500 | 0.74200 |
Sema3A PAK dependent Axon repulsion | 14 | 0.214000 | 0.982 | 0.3300 | -3.01e-01 | -0.048900 | 1.26e-01 | 0.051600 | 0.75100 | 0.41400 |
TP53 Regulates Transcription of Cell Cycle Genes | 37 | 0.214000 | 0.982 | 0.2020 | 1.45e-01 | -0.080200 | -1.15e-01 | 0.127000 | 0.39900 | 0.22600 |
NRAGE signals death through JNK | 44 | 0.215000 | 0.982 | 0.1840 | -2.00e-02 | 0.121000 | 1.37e-01 | 0.818000 | 0.16500 | 0.11600 |
MAPK targets/ Nuclear events mediated by MAP kinases | 29 | 0.216000 | 0.982 | 0.2250 | 7.06e-02 | -0.033300 | 2.11e-01 | 0.511000 | 0.75700 | 0.04890 |
DDX58/IFIH1-mediated induction of interferon-alpha/beta | 55 | 0.216000 | 0.982 | 0.1660 | 6.48e-02 | 0.152000 | -1.23e-02 | 0.406000 | 0.05160 | 0.87500 |
Glucagon signaling in metabolic regulation | 23 | 0.216000 | 0.982 | 0.2520 | 2.01e-01 | 0.001340 | 1.52e-01 | 0.095400 | 0.99100 | 0.20700 |
Signaling by WNT | 202 | 0.217000 | 0.982 | 0.0865 | -9.47e-03 | -0.085700 | 6.74e-03 | 0.817000 | 0.03620 | 0.86900 |
Activation of HOX genes during differentiation | 47 | 0.217000 | 0.982 | 0.1780 | -1.37e-01 | -0.103000 | -4.73e-02 | 0.104000 | 0.22300 | 0.57500 |
Activation of anterior HOX genes in hindbrain development during early embryogenesis | 47 | 0.217000 | 0.982 | 0.1780 | -1.37e-01 | -0.103000 | -4.73e-02 | 0.104000 | 0.22300 | 0.57500 |
MyD88:MAL(TIRAP) cascade initiated on plasma membrane | 79 | 0.218000 | 0.982 | 0.1360 | 1.12e-01 | -0.039600 | 6.66e-02 | 0.086900 | 0.54300 | 0.30700 |
Toll Like Receptor 2 (TLR2) Cascade | 79 | 0.218000 | 0.982 | 0.1360 | 1.12e-01 | -0.039600 | 6.66e-02 | 0.086900 | 0.54300 | 0.30700 |
Toll Like Receptor TLR1:TLR2 Cascade | 79 | 0.218000 | 0.982 | 0.1360 | 1.12e-01 | -0.039600 | 6.66e-02 | 0.086900 | 0.54300 | 0.30700 |
Toll Like Receptor TLR6:TLR2 Cascade | 79 | 0.218000 | 0.982 | 0.1360 | 1.12e-01 | -0.039600 | 6.66e-02 | 0.086900 | 0.54300 | 0.30700 |
Myogenesis | 25 | 0.218000 | 0.982 | 0.2410 | 2.22e-01 | -0.047100 | 8.09e-02 | 0.054200 | 0.68300 | 0.48400 |
FGFR1 mutant receptor activation | 24 | 0.219000 | 0.982 | 0.2470 | -2.45e-01 | 0.011100 | -3.19e-02 | 0.037800 | 0.92500 | 0.78700 |
Lysine catabolism | 10 | 0.222000 | 0.982 | 0.3830 | 2.24e-01 | 0.298000 | 9.01e-02 | 0.219000 | 0.10300 | 0.62200 |
Nuclear Events (kinase and transcription factor activation) | 23 | 0.222000 | 0.982 | 0.2520 | 4.85e-02 | -0.138000 | 2.05e-01 | 0.687000 | 0.25400 | 0.08840 |
Glutamate and glutamine metabolism | 11 | 0.224000 | 0.982 | 0.3600 | -2.31e-01 | 0.019700 | -2.76e-01 | 0.185000 | 0.91000 | 0.11300 |
G alpha (12/13) signalling events | 56 | 0.224000 | 0.982 | 0.1610 | 6.24e-02 | 0.088500 | 1.19e-01 | 0.420000 | 0.25200 | 0.12500 |
Synthesis of IP3 and IP4 in the cytosol | 22 | 0.224000 | 0.982 | 0.2570 | -1.00e-02 | -0.256000 | -2.63e-02 | 0.935000 | 0.03780 | 0.83100 |
Insertion of tail-anchored proteins into the endoplasmic reticulum membrane | 18 | 0.225000 | 0.982 | 0.2850 | -1.97e-02 | -0.095000 | 2.68e-01 | 0.885000 | 0.48500 | 0.04900 |
Signaling by Nuclear Receptors | 188 | 0.226000 | 0.982 | 0.0888 | -1.89e-02 | 0.017900 | 8.49e-02 | 0.656000 | 0.67300 | 0.04550 |
TP53 Regulates Transcription of DNA Repair Genes | 48 | 0.226000 | 0.982 | 0.1730 | 8.66e-02 | 0.056500 | 1.38e-01 | 0.300000 | 0.49800 | 0.09730 |
G beta:gamma signalling through PI3Kgamma | 14 | 0.226000 | 0.982 | 0.3190 | 2.56e-01 | -0.144000 | 1.24e-01 | 0.097000 | 0.35200 | 0.42200 |
Uptake and function of anthrax toxins | 11 | 0.227000 | 0.982 | 0.3640 | -5.06e-02 | -0.344000 | 1.07e-01 | 0.771000 | 0.04800 | 0.54000 |
NR1H2 and NR1H3-mediated signaling | 37 | 0.229000 | 0.982 | 0.2000 | -1.42e-01 | -0.089700 | 1.08e-01 | 0.134000 | 0.34500 | 0.25500 |
Zinc transporters | 10 | 0.229000 | 0.982 | 0.3800 | -2.99e-02 | 0.301000 | -2.29e-01 | 0.870000 | 0.09890 | 0.21000 |
The citric acid (TCA) cycle and respiratory electron transport | 118 | 0.229000 | 0.982 | 0.1110 | 9.39e-03 | -0.104000 | -3.56e-02 | 0.860000 | 0.05050 | 0.50500 |
Activation of ATR in response to replication stress | 26 | 0.230000 | 0.982 | 0.2370 | -7.70e-02 | -0.217000 | 5.60e-02 | 0.497000 | 0.05610 | 0.62100 |
MAP3K8 (TPL2)-dependent MAPK1/3 activation | 16 | 0.232000 | 0.982 | 0.2980 | 3.07e-02 | 0.241000 | 1.74e-01 | 0.832000 | 0.09580 | 0.22900 |
Role of LAT2/NTAL/LAB on calcium mobilization | 12 | 0.234000 | 0.982 | 0.3410 | -2.55e-01 | 0.153000 | -1.67e-01 | 0.126000 | 0.36000 | 0.31700 |
TGF-beta receptor signaling in EMT (epithelial to mesenchymal transition) | 12 | 0.234000 | 0.982 | 0.3470 | -1.16e-01 | -0.055700 | 3.22e-01 | 0.488000 | 0.73800 | 0.05310 |
Plasma lipoprotein remodeling | 15 | 0.234000 | 0.982 | 0.3060 | -1.05e-01 | 0.208000 | -1.99e-01 | 0.481000 | 0.16300 | 0.18200 |
Interferon gamma signaling | 60 | 0.234000 | 0.982 | 0.1540 | -4.04e-02 | 0.127000 | -7.69e-02 | 0.589000 | 0.08950 | 0.30400 |
DNA Damage Recognition in GG-NER | 34 | 0.235000 | 0.982 | 0.2050 | -3.92e-02 | 0.078100 | 1.85e-01 | 0.693000 | 0.43100 | 0.06190 |
SLC transporter disorders | 58 | 0.236000 | 0.982 | 0.1570 | 2.26e-02 | -0.065300 | -1.41e-01 | 0.766000 | 0.39000 | 0.06430 |
Cardiac conduction | 77 | 0.237000 | 0.982 | 0.1340 | 9.67e-02 | -0.069800 | 6.21e-02 | 0.143000 | 0.29000 | 0.34700 |
Cell surface interactions at the vascular wall | 75 | 0.239000 | 0.982 | 0.1370 | 1.16e-01 | 0.069600 | 2.32e-02 | 0.082500 | 0.29800 | 0.72800 |
Butyrate Response Factor 1 (BRF1) binds and destabilizes mRNA | 13 | 0.242000 | 0.982 | 0.3240 | -2.33e-01 | 0.026800 | -2.23e-01 | 0.145000 | 0.86700 | 0.16300 |
Formation of the beta-catenin:TCF transactivating complex | 29 | 0.243000 | 0.982 | 0.2210 | -1.96e-01 | -0.099900 | 1.50e-02 | 0.067600 | 0.35200 | 0.88900 |
G-protein activation | 15 | 0.243000 | 0.982 | 0.3080 | 2.73e-01 | 0.052000 | -1.33e-01 | 0.067600 | 0.72700 | 0.37100 |
Platelet Aggregation (Plug Formation) | 23 | 0.243000 | 0.982 | 0.2460 | -1.69e-01 | 0.166000 | 6.33e-02 | 0.160000 | 0.16800 | 0.60000 |
p75NTR recruits signalling complexes | 11 | 0.243000 | 0.982 | 0.3550 | 3.13e-02 | -0.027900 | 3.53e-01 | 0.858000 | 0.87300 | 0.04290 |
HDR through Homologous Recombination (HRR) | 49 | 0.245000 | 0.982 | 0.1700 | -1.22e-01 | -0.094300 | 7.18e-02 | 0.139000 | 0.25400 | 0.38500 |
Activated NTRK2 signals through FRS2 and FRS3 | 10 | 0.246000 | 0.982 | 0.3710 | 3.20e-01 | 0.158000 | 1.03e-01 | 0.079800 | 0.38800 | 0.57100 |
Inositol phosphate metabolism | 39 | 0.246000 | 0.982 | 0.1900 | -6.18e-02 | -0.175000 | 3.75e-02 | 0.505000 | 0.05850 | 0.68500 |
RNA Polymerase III Transcription Initiation From Type 3 Promoter | 22 | 0.247000 | 0.982 | 0.2500 | 1.66e-01 | 0.167000 | 8.62e-02 | 0.179000 | 0.17600 | 0.48400 |
Mitotic Prometaphase | 131 | 0.248000 | 0.982 | 0.1030 | 3.89e-02 | -0.092000 | 2.32e-02 | 0.443000 | 0.06950 | 0.64800 |
Cellular response to heat stress | 84 | 0.248000 | 0.982 | 0.1290 | 2.77e-02 | 0.082000 | -9.60e-02 | 0.661000 | 0.19400 | 0.12900 |
Reproduction | 47 | 0.249000 | 0.982 | 0.1700 | -1.52e-01 | 0.077400 | -6.44e-03 | 0.072300 | 0.35900 | 0.93900 |
Long-term potentiation | 13 | 0.251000 | 0.982 | 0.3230 | -2.47e-01 | -0.148000 | -1.45e-01 | 0.123000 | 0.35500 | 0.36400 |
DAP12 signaling | 20 | 0.252000 | 0.982 | 0.2610 | -4.42e-02 | 0.254000 | -4.10e-02 | 0.732000 | 0.04940 | 0.75100 |
Transcription of E2F targets under negative control by p107 (RBL1) and p130 (RBL2) in complex with HDAC1 | 11 | 0.253000 | 0.982 | 0.3540 | 2.34e-01 | -0.135000 | -2.28e-01 | 0.179000 | 0.43700 | 0.19100 |
Triglyceride catabolism | 16 | 0.254000 | 0.982 | 0.2930 | -6.27e-02 | -0.140000 | 2.50e-01 | 0.664000 | 0.33300 | 0.08310 |
Golgi Associated Vesicle Biogenesis | 44 | 0.256000 | 0.982 | 0.1750 | 4.81e-02 | -0.165000 | 3.23e-02 | 0.581000 | 0.05820 | 0.71100 |
Negative regulation of FGFR4 signaling | 21 | 0.256000 | 0.982 | 0.2530 | 2.38e-01 | 0.063600 | 5.72e-02 | 0.058800 | 0.61400 | 0.65000 |
SHC-mediated cascade:FGFR1 | 11 | 0.256000 | 0.982 | 0.3480 | 2.86e-01 | 0.097300 | 1.72e-01 | 0.100000 | 0.57600 | 0.32400 |
CASP8 activity is inhibited | 10 | 0.257000 | 0.982 | 0.3690 | 1.06e-01 | 0.345000 | -7.56e-02 | 0.562000 | 0.05860 | 0.67900 |
Dimerization of procaspase-8 | 10 | 0.257000 | 0.982 | 0.3690 | 1.06e-01 | 0.345000 | -7.56e-02 | 0.562000 | 0.05860 | 0.67900 |
Regulation by c-FLIP | 10 | 0.257000 | 0.982 | 0.3690 | 1.06e-01 | 0.345000 | -7.56e-02 | 0.562000 | 0.05860 | 0.67900 |
Platelet homeostasis | 61 | 0.258000 | 0.982 | 0.1490 | -8.32e-02 | -0.121000 | -2.59e-02 | 0.262000 | 0.10300 | 0.72600 |
COPI-dependent Golgi-to-ER retrograde traffic | 58 | 0.260000 | 0.982 | 0.1520 | 7.32e-02 | 0.119000 | 6.00e-02 | 0.335000 | 0.11700 | 0.43000 |
Fcgamma receptor (FCGR) dependent phagocytosis | 69 | 0.261000 | 0.982 | 0.1410 | 5.66e-02 | 0.099900 | -8.15e-02 | 0.417000 | 0.15200 | 0.24200 |
Regulation of PTEN gene transcription | 56 | 0.262000 | 0.982 | 0.1530 | 9.15e-02 | -0.083100 | 9.02e-02 | 0.237000 | 0.28300 | 0.24300 |
G alpha (i) signalling events | 160 | 0.264000 | 0.982 | 0.0923 | 7.13e-02 | -0.013400 | -5.71e-02 | 0.121000 | 0.77000 | 0.21400 |
Negative regulation of MAPK pathway | 39 | 0.265000 | 0.982 | 0.1860 | -1.13e-01 | -0.126000 | 7.80e-02 | 0.221000 | 0.17400 | 0.39900 |
Oxidative Stress Induced Senescence | 63 | 0.266000 | 0.982 | 0.1440 | 1.04e-01 | -0.057900 | 7.97e-02 | 0.152000 | 0.42700 | 0.27400 |
NOTCH2 Activation and Transmission of Signal to the Nucleus | 20 | 0.267000 | 0.982 | 0.2580 | -2.33e-01 | 0.035600 | 1.06e-01 | 0.071700 | 0.78300 | 0.41000 |
Adherens junctions interactions | 14 | 0.267000 | 0.982 | 0.3060 | 3.04e-01 | -0.011300 | 3.25e-02 | 0.049000 | 0.94200 | 0.83300 |
SRP-dependent cotranslational protein targeting to membrane | 76 | 0.268000 | 0.982 | 0.1330 | -8.12e-02 | -0.005300 | 1.06e-01 | 0.221000 | 0.93600 | 0.11200 |
Smooth Muscle Contraction | 35 | 0.268000 | 0.982 | 0.1960 | -1.51e-01 | -0.105000 | 6.82e-02 | 0.122000 | 0.28400 | 0.48500 |
Synthesis of bile acids and bile salts via 7alpha-hydroxycholesterol | 15 | 0.268000 | 0.982 | 0.2980 | -2.12e-01 | -0.209000 | 1.76e-02 | 0.156000 | 0.16100 | 0.90600 |
MECP2 regulates neuronal receptors and channels | 11 | 0.269000 | 0.982 | 0.3460 | -1.79e-01 | 0.215000 | 2.03e-01 | 0.305000 | 0.21600 | 0.24300 |
G alpha (q) signalling events | 78 | 0.270000 | 0.982 | 0.1290 | 1.20e-01 | -0.046900 | 5.40e-03 | 0.066500 | 0.47500 | 0.93400 |
Platelet calcium homeostasis | 19 | 0.270000 | 0.982 | 0.2650 | -1.26e-01 | -0.186000 | 1.41e-01 | 0.342000 | 0.16100 | 0.28700 |
Tie2 Signaling | 14 | 0.272000 | 0.982 | 0.3080 | 2.38e-01 | 0.164000 | -1.06e-01 | 0.123000 | 0.28800 | 0.49100 |
Cargo trafficking to the periciliary membrane | 38 | 0.272000 | 0.982 | 0.1850 | 5.42e-02 | -0.158000 | -7.91e-02 | 0.564000 | 0.09180 | 0.39900 |
N-glycan trimming in the ER and Calnexin/Calreticulin cycle | 32 | 0.272000 | 0.982 | 0.2020 | -1.55e-01 | 0.097300 | 8.67e-02 | 0.130000 | 0.34100 | 0.39600 |
Neutrophil degranulation | 310 | 0.274000 | 0.982 | 0.0651 | 1.98e-02 | -0.033600 | 5.21e-02 | 0.551000 | 0.31200 | 0.11600 |
HSF1 activation | 22 | 0.278000 | 0.982 | 0.2390 | -1.34e-01 | 0.063000 | -1.88e-01 | 0.275000 | 0.60900 | 0.12700 |
Toll Like Receptor 4 (TLR4) Cascade | 103 | 0.278000 | 0.982 | 0.1120 | 1.11e-01 | 0.009400 | 5.77e-03 | 0.051000 | 0.86900 | 0.92000 |
Processing of Intronless Pre-mRNAs | 17 | 0.280000 | 0.982 | 0.2730 | -1.41e-01 | 0.233000 | -1.25e-02 | 0.314000 | 0.09590 | 0.92900 |
mTOR signalling | 37 | 0.280000 | 0.982 | 0.1860 | 8.29e-02 | 0.162000 | 3.94e-02 | 0.383000 | 0.08810 | 0.67800 |
Negative regulation of FGFR3 signaling | 19 | 0.283000 | 0.982 | 0.2590 | 2.52e-01 | 0.057300 | 1.96e-02 | 0.057600 | 0.66500 | 0.88200 |
FOXO-mediated transcription | 51 | 0.283000 | 0.982 | 0.1590 | 1.51e-01 | 0.038500 | -3.41e-02 | 0.063000 | 0.63500 | 0.67400 |
Aquaporin-mediated transport | 31 | 0.283000 | 0.982 | 0.2000 | 1.61e-01 | -0.023600 | 1.17e-01 | 0.121000 | 0.82000 | 0.26000 |
Neddylation | 190 | 0.286000 | 0.982 | 0.0822 | -8.15e-02 | -0.011000 | 2.41e-03 | 0.053600 | 0.79400 | 0.95500 |
CaM pathway | 29 | 0.287000 | 0.982 | 0.2070 | 7.76e-02 | 0.099300 | 1.65e-01 | 0.470000 | 0.35500 | 0.12500 |
Calmodulin induced events | 29 | 0.287000 | 0.982 | 0.2070 | 7.76e-02 | 0.099300 | 1.65e-01 | 0.470000 | 0.35500 | 0.12500 |
Activation of GABAB receptors | 22 | 0.287000 | 0.982 | 0.2380 | 1.13e-01 | 0.128000 | 1.66e-01 | 0.358000 | 0.29900 | 0.17900 |
GABA B receptor activation | 22 | 0.287000 | 0.982 | 0.2380 | 1.13e-01 | 0.128000 | 1.66e-01 | 0.358000 | 0.29900 | 0.17900 |
Regulation of TP53 Activity through Phosphorylation | 71 | 0.290000 | 0.982 | 0.1350 | -9.86e-02 | -0.048200 | 7.81e-02 | 0.151000 | 0.48300 | 0.25600 |
Protein ubiquitination | 57 | 0.291000 | 0.982 | 0.1480 | -9.96e-02 | 0.093400 | 5.76e-02 | 0.194000 | 0.22300 | 0.45200 |
Homology Directed Repair | 80 | 0.292000 | 0.982 | 0.1260 | -1.13e-01 | -0.054500 | -4.16e-03 | 0.080900 | 0.40000 | 0.94900 |
Ca-dependent events | 30 | 0.292000 | 0.982 | 0.2020 | 9.79e-02 | 0.089300 | 1.53e-01 | 0.354000 | 0.39700 | 0.14700 |
Cell Cycle | 424 | 0.292000 | 0.982 | 0.0550 | 4.97e-03 | -0.054700 | -3.47e-03 | 0.862000 | 0.05510 | 0.90300 |
HDMs demethylate histones | 21 | 0.292000 | 0.982 | 0.2430 | 3.59e-02 | -0.050900 | 2.35e-01 | 0.776000 | 0.68600 | 0.06270 |
Resolution of D-Loop Structures | 21 | 0.293000 | 0.982 | 0.2450 | -2.28e-01 | 0.022500 | 8.72e-02 | 0.071200 | 0.85800 | 0.48900 |
Resolution of D-loop Structures through Holliday Junction Intermediates | 21 | 0.293000 | 0.982 | 0.2450 | -2.28e-01 | 0.022500 | 8.72e-02 | 0.071200 | 0.85800 | 0.48900 |
Transport of Ribonucleoproteins into the Host Nucleus | 30 | 0.294000 | 0.982 | 0.2060 | 1.61e-01 | 0.014300 | -1.27e-01 | 0.127000 | 0.89200 | 0.22900 |
Adenylate cyclase inhibitory pathway | 12 | 0.296000 | 0.982 | 0.3200 | 9.04e-02 | 0.260000 | 1.62e-01 | 0.588000 | 0.11800 | 0.33100 |
Synthesis of PE | 10 | 0.297000 | 0.982 | 0.3470 | 2.54e-01 | -0.141000 | 1.90e-01 | 0.165000 | 0.44000 | 0.29700 |
Intracellular signaling by second messengers | 246 | 0.298000 | 0.982 | 0.0711 | 1.42e-02 | -0.040600 | 5.67e-02 | 0.702000 | 0.27500 | 0.12700 |
Mitotic Metaphase and Anaphase | 133 | 0.299000 | 0.982 | 0.0973 | -6.30e-02 | -0.071400 | 2.00e-02 | 0.210000 | 0.15600 | 0.69100 |
ERKs are inactivated | 12 | 0.299000 | 0.982 | 0.3220 | -6.96e-02 | -0.258000 | 1.79e-01 | 0.677000 | 0.12200 | 0.28200 |
ERK/MAPK targets | 20 | 0.300000 | 0.982 | 0.2480 | 1.80e-03 | -0.112000 | 2.21e-01 | 0.989000 | 0.38600 | 0.08740 |
Negative regulation of FGFR2 signaling | 21 | 0.301000 | 0.982 | 0.2400 | 2.23e-01 | 0.054300 | 7.02e-02 | 0.076900 | 0.66700 | 0.57800 |
Mitotic Spindle Checkpoint | 73 | 0.302000 | 0.982 | 0.1290 | -1.14e-01 | -0.051200 | -3.26e-02 | 0.092400 | 0.45000 | 0.63000 |
Retinoid metabolism and transport | 23 | 0.303000 | 0.982 | 0.2320 | 1.34e-01 | -0.055500 | -1.81e-01 | 0.266000 | 0.64500 | 0.13400 |
Post-chaperonin tubulin folding pathway | 15 | 0.303000 | 0.982 | 0.2830 | 1.13e-01 | -0.222000 | 1.35e-01 | 0.449000 | 0.13700 | 0.36600 |
Metabolism of nucleotides | 77 | 0.304000 | 0.982 | 0.1250 | 1.14e-01 | -0.041200 | 3.12e-02 | 0.085100 | 0.53200 | 0.63700 |
Transport to the Golgi and subsequent modification | 134 | 0.305000 | 0.982 | 0.0959 | 9.21e-02 | -0.000099 | -2.68e-02 | 0.066200 | 0.99800 | 0.59300 |
Nucleotide salvage | 18 | 0.305000 | 0.982 | 0.2620 | 1.71e-01 | -0.000189 | -1.98e-01 | 0.209000 | 0.99900 | 0.14600 |
Respiratory electron transport, ATP synthesis by chemiosmotic coupling, and heat production by uncoupling proteins. | 74 | 0.306000 | 0.982 | 0.1280 | -6.27e-02 | -0.087800 | -6.80e-02 | 0.351000 | 0.19200 | 0.31200 |
PI3K events in ERBB2 signaling | 12 | 0.306000 | 0.982 | 0.3160 | -3.14e-01 | 0.012300 | -3.76e-02 | 0.060000 | 0.94100 | 0.82200 |
tRNA modification in the nucleus and cytosol | 30 | 0.307000 | 0.982 | 0.2020 | -9.94e-02 | -0.171000 | 4.10e-02 | 0.346000 | 0.10500 | 0.69800 |
Signaling by FGFR4 | 31 | 0.307000 | 0.982 | 0.1970 | 1.81e-01 | 0.070400 | 3.37e-02 | 0.081300 | 0.49800 | 0.74500 |
Signaling by Rho GTPases | 282 | 0.307000 | 0.982 | 0.0654 | 3.36e-02 | -0.000491 | 5.61e-02 | 0.334000 | 0.98900 | 0.10600 |
NCAM1 interactions | 21 | 0.308000 | 0.982 | 0.2390 | -1.03e-01 | 0.162000 | 1.44e-01 | 0.416000 | 0.20000 | 0.25400 |
PIP3 activates AKT signaling | 212 | 0.309000 | 0.982 | 0.0758 | 3.65e-03 | -0.053200 | 5.39e-02 | 0.927000 | 0.18300 | 0.17700 |
Reduction of cytosolic Ca++ levels | 10 | 0.309000 | 0.982 | 0.3460 | -3.56e-03 | -0.028600 | 3.45e-01 | 0.984000 | 0.87500 | 0.05900 |
Amplification of signal from unattached kinetochores via a MAD2 inhibitory signal | 59 | 0.309000 | 0.982 | 0.1430 | -1.09e-01 | -0.082900 | -4.01e-02 | 0.148000 | 0.27100 | 0.59400 |
Amplification of signal from the kinetochores | 59 | 0.309000 | 0.982 | 0.1430 | -1.09e-01 | -0.082900 | -4.01e-02 | 0.148000 | 0.27100 | 0.59400 |
CRMPs in Sema3A signaling | 13 | 0.310000 | 0.982 | 0.3030 | -1.46e-01 | 0.209000 | 1.64e-01 | 0.361000 | 0.19300 | 0.30500 |
VEGFA-VEGFR2 Pathway | 78 | 0.310000 | 0.982 | 0.1230 | 1.01e-01 | 0.002010 | 7.04e-02 | 0.124000 | 0.97600 | 0.28300 |
RAF-independent MAPK1/3 activation | 21 | 0.311000 | 0.982 | 0.2390 | -1.03e-01 | -0.216000 | -8.32e-03 | 0.415000 | 0.08670 | 0.94700 |
TP53 Regulates Transcription of Caspase Activators and Caspases | 11 | 0.311000 | 0.982 | 0.3270 | 1.61e-01 | -0.271000 | 8.89e-02 | 0.355000 | 0.12000 | 0.61000 |
Phase 2 - plateau phase | 13 | 0.311000 | 0.982 | 0.3000 | 2.41e-01 | 0.000434 | 1.78e-01 | 0.132000 | 0.99800 | 0.26600 |
PERK regulates gene expression | 23 | 0.312000 | 0.982 | 0.2260 | -2.17e-01 | -0.005300 | -6.51e-02 | 0.072000 | 0.96500 | 0.58900 |
mRNA decay by 5’ to 3’ exoribonuclease | 13 | 0.312000 | 0.982 | 0.3020 | -4.12e-02 | -0.060700 | -2.93e-01 | 0.797000 | 0.70500 | 0.06780 |
O-linked glycosylation | 62 | 0.313000 | 0.982 | 0.1400 | 5.21e-02 | -0.013100 | -1.29e-01 | 0.479000 | 0.85900 | 0.07950 |
FGFR2 mutant receptor activation | 16 | 0.313000 | 0.982 | 0.2720 | 6.88e-02 | -0.172000 | 1.98e-01 | 0.634000 | 0.23300 | 0.17000 |
Complement cascade | 19 | 0.313000 | 0.982 | 0.2480 | -9.60e-02 | -0.022300 | -2.28e-01 | 0.469000 | 0.86600 | 0.08580 |
HDACs deacetylate histones | 32 | 0.317000 | 0.982 | 0.1920 | -1.36e-01 | -0.125000 | -5.17e-02 | 0.183000 | 0.22200 | 0.61300 |
Export of Viral Ribonucleoproteins from Nucleus | 30 | 0.319000 | 0.982 | 0.2000 | 1.45e-01 | 0.061900 | -1.24e-01 | 0.170000 | 0.55700 | 0.24100 |
NEP/NS2 Interacts with the Cellular Export Machinery | 30 | 0.319000 | 0.982 | 0.2000 | 1.45e-01 | 0.061900 | -1.24e-01 | 0.170000 | 0.55700 | 0.24100 |
Mitotic Anaphase | 132 | 0.321000 | 0.982 | 0.0952 | -6.80e-02 | -0.065000 | 1.48e-02 | 0.179000 | 0.19800 | 0.77000 |
Regulation of pyruvate dehydrogenase (PDH) complex | 15 | 0.322000 | 0.982 | 0.2770 | 1.28e-01 | -0.226000 | 9.60e-02 | 0.392000 | 0.13000 | 0.52000 |
Lysosome Vesicle Biogenesis | 26 | 0.322000 | 0.982 | 0.2120 | -8.99e-03 | -0.185000 | 1.04e-01 | 0.937000 | 0.10300 | 0.36100 |
Signaling by FGFR3 in disease | 12 | 0.323000 | 0.982 | 0.3110 | 3.07e-01 | 0.038000 | 3.27e-02 | 0.065800 | 0.82000 | 0.84500 |
Signaling by FGFR3 point mutants in cancer | 12 | 0.323000 | 0.982 | 0.3110 | 3.07e-01 | 0.038000 | 3.27e-02 | 0.065800 | 0.82000 | 0.84500 |
ER to Golgi Anterograde Transport | 112 | 0.324000 | 0.982 | 0.1030 | 9.37e-02 | 0.010700 | -4.16e-02 | 0.087400 | 0.84600 | 0.44800 |
Signaling by WNT in cancer | 27 | 0.324000 | 0.982 | 0.2070 | -1.44e-02 | -0.207000 | -1.82e-03 | 0.897000 | 0.06290 | 0.98700 |
Formation of HIV-1 elongation complex containing HIV-1 Tat | 31 | 0.325000 | 0.982 | 0.1910 | 1.48e-01 | -0.035900 | 1.16e-01 | 0.155000 | 0.72900 | 0.26400 |
HIV Transcription Elongation | 31 | 0.325000 | 0.982 | 0.1910 | 1.48e-01 | -0.035900 | 1.16e-01 | 0.155000 | 0.72900 | 0.26400 |
Tat-mediated elongation of the HIV-1 transcript | 31 | 0.325000 | 0.982 | 0.1910 | 1.48e-01 | -0.035900 | 1.16e-01 | 0.155000 | 0.72900 | 0.26400 |
Activation of SMO | 13 | 0.327000 | 0.982 | 0.3010 | 1.53e-01 | 0.104000 | -2.38e-01 | 0.340000 | 0.51500 | 0.13800 |
Separation of Sister Chromatids | 122 | 0.329000 | 0.982 | 0.0981 | -7.93e-02 | -0.057000 | 8.91e-03 | 0.131000 | 0.27800 | 0.86500 |
Nucleobase biosynthesis | 15 | 0.329000 | 0.982 | 0.2750 | 2.46e-01 | 0.052200 | 1.10e-01 | 0.099000 | 0.72700 | 0.45900 |
Sphingolipid metabolism | 64 | 0.330000 | 0.982 | 0.1330 | 9.18e-02 | 0.025400 | 9.25e-02 | 0.205000 | 0.72500 | 0.20100 |
NS1 Mediated Effects on Host Pathways | 38 | 0.330000 | 0.982 | 0.1750 | 1.58e-01 | -0.019900 | -7.13e-02 | 0.091500 | 0.83200 | 0.44700 |
Downstream TCR signaling | 76 | 0.331000 | 0.982 | 0.1230 | 4.41e-02 | -0.042200 | -1.07e-01 | 0.507000 | 0.52500 | 0.10700 |
Signaling by FGFR4 in disease | 11 | 0.331000 | 0.982 | 0.3230 | 2.24e-01 | 0.230000 | 3.85e-02 | 0.199000 | 0.18700 | 0.82500 |
Nephrin family interactions | 17 | 0.332000 | 0.982 | 0.2580 | -2.54e-01 | 0.000196 | -4.56e-02 | 0.070000 | 0.99900 | 0.74500 |
Cell Cycle, Mitotic | 351 | 0.334000 | 0.982 | 0.0575 | 1.13e-02 | -0.055900 | -7.42e-03 | 0.717000 | 0.07370 | 0.81200 |
Signaling by MET | 56 | 0.335000 | 0.982 | 0.1420 | -2.55e-02 | 0.111000 | 8.59e-02 | 0.742000 | 0.15300 | 0.26700 |
Metabolism of fat-soluble vitamins | 26 | 0.335000 | 0.982 | 0.2100 | 1.18e-01 | -0.085800 | -1.51e-01 | 0.299000 | 0.44900 | 0.18300 |
Pre-NOTCH Expression and Processing | 46 | 0.336000 | 0.982 | 0.1590 | -1.23e-01 | -0.037800 | 9.34e-02 | 0.150000 | 0.65700 | 0.27400 |
Retrograde transport at the Trans-Golgi-Network | 44 | 0.337000 | 0.982 | 0.1590 | 1.31e-01 | -0.069200 | 5.73e-02 | 0.134000 | 0.42700 | 0.51100 |
Trafficking of GluR2-containing AMPA receptors | 12 | 0.337000 | 0.982 | 0.3040 | 1.55e-01 | 0.132000 | 2.26e-01 | 0.352000 | 0.42900 | 0.17600 |
Signaling by FGFR3 | 29 | 0.338000 | 0.982 | 0.1980 | 1.86e-01 | 0.066700 | 7.45e-03 | 0.083400 | 0.53400 | 0.94500 |
Beta-catenin phosphorylation cascade | 16 | 0.339000 | 0.982 | 0.2640 | 7.31e-02 | -0.230000 | 1.07e-01 | 0.613000 | 0.11100 | 0.46000 |
Transport of the SLBP Dependant Mature mRNA | 33 | 0.340000 | 0.982 | 0.1860 | 1.51e-01 | 0.054300 | -9.45e-02 | 0.133000 | 0.58900 | 0.34800 |
Transport of the SLBP independent Mature mRNA | 33 | 0.340000 | 0.982 | 0.1860 | 1.51e-01 | 0.054300 | -9.45e-02 | 0.133000 | 0.58900 | 0.34800 |
rRNA modification in the nucleus and cytosol | 46 | 0.341000 | 0.982 | 0.1550 | -6.28e-02 | 0.128000 | -6.23e-02 | 0.462000 | 0.13500 | 0.46500 |
Translocation of SLC2A4 (GLUT4) to the plasma membrane | 46 | 0.341000 | 0.982 | 0.1560 | -2.95e-03 | -0.110000 | -1.10e-01 | 0.972000 | 0.19700 | 0.19700 |
G alpha (z) signalling events | 30 | 0.342000 | 0.982 | 0.1940 | 1.10e-01 | 0.159000 | 1.55e-02 | 0.298000 | 0.13300 | 0.88300 |
Biological oxidations | 107 | 0.342000 | 0.982 | 0.1040 | -7.49e-02 | -0.017900 | 6.94e-02 | 0.182000 | 0.75000 | 0.21600 |
Disease | 750 | 0.343000 | 0.982 | 0.0399 | -1.81e-02 | -0.034700 | 8.24e-03 | 0.406000 | 0.11100 | 0.70400 |
RNA Polymerase I Transcription | 46 | 0.343000 | 0.982 | 0.1550 | 3.90e-02 | 0.132000 | 7.15e-02 | 0.648000 | 0.12100 | 0.40200 |
Metabolism of vitamins and cofactors | 128 | 0.344000 | 0.982 | 0.0935 | 9.24e-02 | -0.012200 | -6.86e-03 | 0.071500 | 0.81200 | 0.89400 |
Interconversion of nucleotide di- and triphosphates | 20 | 0.345000 | 0.982 | 0.2360 | -2.06e-01 | 0.053400 | 1.02e-01 | 0.110000 | 0.68000 | 0.42800 |
Cytosolic tRNA aminoacylation | 22 | 0.346000 | 0.982 | 0.2240 | -2.14e-02 | 0.016300 | -2.22e-01 | 0.862000 | 0.89500 | 0.07140 |
Growth hormone receptor signaling | 15 | 0.348000 | 0.982 | 0.2680 | -1.96e-01 | 0.070800 | -1.68e-01 | 0.188000 | 0.63500 | 0.26000 |
Signaling by FGFR1 | 38 | 0.348000 | 0.982 | 0.1700 | 1.64e-01 | 0.026000 | 3.45e-02 | 0.080000 | 0.78200 | 0.71300 |
Lagging Strand Synthesis | 20 | 0.350000 | 0.982 | 0.2320 | -1.62e-01 | -0.061000 | -1.55e-01 | 0.210000 | 0.63700 | 0.23200 |
RIP-mediated NFkB activation via ZBP1 | 13 | 0.350000 | 0.982 | 0.2920 | 1.57e-01 | -0.109000 | -2.20e-01 | 0.327000 | 0.49600 | 0.16900 |
Cyclin A/B1/B2 associated events during G2/M transition | 17 | 0.350000 | 0.982 | 0.2520 | -1.42e-01 | 0.164000 | -1.27e-01 | 0.309000 | 0.24200 | 0.36600 |
Glucagon-type ligand receptors | 14 | 0.352000 | 0.982 | 0.2790 | 1.03e-01 | -0.164000 | -2.02e-01 | 0.505000 | 0.28800 | 0.19200 |
Frs2-mediated activation | 10 | 0.353000 | 0.982 | 0.3330 | 2.85e-01 | 0.034800 | -1.69e-01 | 0.119000 | 0.84900 | 0.35400 |
Signaling by FGFR | 60 | 0.353000 | 0.982 | 0.1340 | 1.21e-01 | 0.012900 | 5.67e-02 | 0.106000 | 0.86300 | 0.44800 |
Caspase activation via Death Receptors in the presence of ligand | 13 | 0.353000 | 0.982 | 0.2910 | 5.12e-02 | 0.239000 | -1.58e-01 | 0.749000 | 0.13600 | 0.32500 |
Regulation of IFNG signaling | 11 | 0.356000 | 0.982 | 0.3100 | -2.21e-01 | 0.144000 | -1.64e-01 | 0.205000 | 0.41000 | 0.34700 |
Neurotransmitter receptors and postsynaptic signal transmission | 103 | 0.357000 | 0.982 | 0.1020 | 6.20e-02 | -0.013100 | 7.95e-02 | 0.278000 | 0.81800 | 0.16400 |
Interleukin-1 family signaling | 103 | 0.357000 | 0.982 | 0.1030 | 8.16e-02 | -0.022000 | -5.96e-02 | 0.153000 | 0.70000 | 0.29700 |
Nicotinate metabolism | 23 | 0.358000 | 0.982 | 0.2160 | 5.07e-02 | 0.187000 | 9.54e-02 | 0.674000 | 0.12000 | 0.42800 |
RNA Polymerase III Transcription Termination | 18 | 0.358000 | 0.982 | 0.2440 | 2.35e-01 | 0.049900 | 4.19e-02 | 0.084000 | 0.71400 | 0.75800 |
Senescence-Associated Secretory Phenotype (SASP) | 43 | 0.358000 | 0.982 | 0.1570 | -1.26e-01 | 0.092300 | -1.68e-02 | 0.152000 | 0.29500 | 0.84900 |
Deactivation of the beta-catenin transactivating complex | 36 | 0.360000 | 0.982 | 0.1740 | -1.61e-01 | -0.040400 | 5.30e-02 | 0.095000 | 0.67500 | 0.58200 |
SLC-mediated transmembrane transport | 131 | 0.361000 | 0.982 | 0.0909 | -6.82e-02 | -0.058500 | -1.38e-02 | 0.178000 | 0.24800 | 0.78600 |
DAP12 interactions | 21 | 0.362000 | 0.982 | 0.2250 | -2.56e-02 | 0.224000 | -1.25e-02 | 0.839000 | 0.07630 | 0.92100 |
Sulfur amino acid metabolism | 21 | 0.362000 | 0.982 | 0.2270 | 2.13e-01 | -0.024800 | -7.25e-02 | 0.090800 | 0.84400 | 0.56600 |
Nef-mediates down modulation of cell surface receptors by recruiting them to clathrin adapters | 16 | 0.363000 | 0.982 | 0.2600 | -2.01e-01 | -0.160000 | 4.00e-02 | 0.163000 | 0.26900 | 0.78200 |
Signal amplification | 19 | 0.364000 | 0.982 | 0.2370 | 2.01e-01 | -0.083200 | -9.46e-02 | 0.129000 | 0.53000 | 0.47600 |
Transcriptional regulation of pluripotent stem cells | 11 | 0.365000 | 0.982 | 0.3090 | 1.06e-01 | -0.267000 | 1.14e-01 | 0.544000 | 0.12500 | 0.51300 |
Citric acid cycle (TCA cycle) | 21 | 0.365000 | 0.982 | 0.2250 | 1.60e-01 | -0.110000 | -1.14e-01 | 0.204000 | 0.38500 | 0.36500 |
PPARA activates gene expression | 95 | 0.370000 | 0.982 | 0.1060 | -3.59e-02 | 0.065400 | 7.46e-02 | 0.546000 | 0.27100 | 0.20900 |
Role of phospholipids in phagocytosis | 16 | 0.370000 | 0.982 | 0.2570 | 1.05e-01 | -0.126000 | -1.98e-01 | 0.469000 | 0.38200 | 0.17100 |
RNA Polymerase III Transcription Initiation From Type 2 Promoter | 21 | 0.370000 | 0.982 | 0.2230 | 5.66e-02 | 0.154000 | 1.50e-01 | 0.654000 | 0.22100 | 0.23400 |
Transport of vitamins, nucleosides, and related molecules | 25 | 0.373000 | 0.982 | 0.2070 | -1.35e-01 | -0.112000 | 1.09e-01 | 0.241000 | 0.33300 | 0.34500 |
PLC beta mediated events | 43 | 0.375000 | 0.982 | 0.1540 | 1.23e-01 | 0.041100 | 8.38e-02 | 0.163000 | 0.64100 | 0.34200 |
PTEN Regulation | 126 | 0.375000 | 0.982 | 0.0905 | 3.48e-02 | -0.043500 | 7.14e-02 | 0.501000 | 0.40000 | 0.16700 |
ROS and RNS production in phagocytes | 23 | 0.375000 | 0.982 | 0.2120 | -1.14e-01 | 0.174000 | 3.64e-02 | 0.343000 | 0.14800 | 0.76300 |
Glyoxylate metabolism and glycine degradation | 20 | 0.376000 | 0.982 | 0.2280 | -2.60e-02 | -0.036800 | 2.24e-01 | 0.841000 | 0.77600 | 0.08310 |
Resolution of D-loop Structures through Synthesis-Dependent Strand Annealing (SDSA) | 17 | 0.376000 | 0.982 | 0.2480 | -2.35e-01 | 0.046600 | 6.35e-02 | 0.094000 | 0.73900 | 0.65000 |
Integrin alphaIIb beta3 signaling | 20 | 0.378000 | 0.982 | 0.2280 | -1.75e-01 | 0.076800 | 1.25e-01 | 0.175000 | 0.55200 | 0.33500 |
Integrin signaling | 20 | 0.378000 | 0.982 | 0.2280 | -1.75e-01 | 0.076800 | 1.25e-01 | 0.175000 | 0.55200 | 0.33500 |
O-linked glycosylation of mucins | 29 | 0.379000 | 0.982 | 0.1910 | 1.46e-01 | 0.033500 | -1.18e-01 | 0.173000 | 0.75500 | 0.27200 |
Unblocking of NMDA receptors, glutamate binding and activation | 12 | 0.380000 | 0.982 | 0.2940 | -2.27e-01 | -0.185000 | -2.26e-02 | 0.173000 | 0.26800 | 0.89200 |
Termination of O-glycan biosynthesis | 13 | 0.380000 | 0.982 | 0.2780 | -1.51e-01 | 0.152000 | -1.78e-01 | 0.347000 | 0.34400 | 0.26600 |
Formation of TC-NER Pre-Incision Complex | 44 | 0.380000 | 0.982 | 0.1520 | 2.75e-02 | 0.056000 | 1.39e-01 | 0.753000 | 0.52000 | 0.11100 |
Meiotic recombination | 19 | 0.383000 | 0.982 | 0.2300 | -2.06e-01 | 0.039400 | -9.29e-02 | 0.120000 | 0.76600 | 0.48400 |
Downstream signaling of activated FGFR3 | 15 | 0.383000 | 0.982 | 0.2620 | 2.56e-01 | 0.006050 | -5.30e-02 | 0.085600 | 0.96800 | 0.72300 |
Transcriptional regulation by RUNX3 | 82 | 0.384000 | 0.982 | 0.1120 | -5.08e-02 | -0.099900 | 7.14e-03 | 0.427000 | 0.11800 | 0.91100 |
Rev-mediated nuclear export of HIV RNA | 33 | 0.386000 | 0.982 | 0.1770 | 6.36e-02 | 0.051300 | -1.57e-01 | 0.528000 | 0.61100 | 0.11900 |
Cell-cell junction organization | 24 | 0.386000 | 0.982 | 0.2040 | 1.81e-01 | -0.092600 | 1.89e-02 | 0.125000 | 0.43200 | 0.87300 |
Interleukin-7 signaling | 12 | 0.386000 | 0.982 | 0.2890 | -3.61e-02 | -0.196000 | -2.10e-01 | 0.829000 | 0.24100 | 0.20700 |
Cytochrome P450 - arranged by substrate type | 25 | 0.387000 | 0.982 | 0.1990 | -1.79e-01 | -0.002390 | -8.87e-02 | 0.122000 | 0.98300 | 0.44300 |
WNT ligand biogenesis and trafficking | 12 | 0.387000 | 0.982 | 0.2920 | 8.01e-02 | -0.004900 | -2.80e-01 | 0.631000 | 0.97700 | 0.09260 |
Defective TPR may confer susceptibility towards thyroid papillary carcinoma (TPC) | 28 | 0.389000 | 0.982 | 0.1920 | 1.41e-01 | 0.034800 | -1.25e-01 | 0.195000 | 0.75000 | 0.25200 |
Regulation of Glucokinase by Glucokinase Regulatory Protein | 28 | 0.389000 | 0.982 | 0.1920 | 1.41e-01 | 0.034800 | -1.25e-01 | 0.195000 | 0.75000 | 0.25200 |
Removal of the Flap Intermediate | 14 | 0.389000 | 0.982 | 0.2660 | -2.38e-01 | -0.026100 | -1.16e-01 | 0.123000 | 0.86600 | 0.45400 |
mRNA Splicing - Major Pathway | 154 | 0.391000 | 0.982 | 0.0810 | 6.46e-03 | 0.007650 | 8.03e-02 | 0.890000 | 0.87000 | 0.08610 |
Insulin receptor signalling cascade | 31 | 0.391000 | 0.982 | 0.1800 | 1.68e-01 | 0.053300 | 3.56e-02 | 0.106000 | 0.60800 | 0.73100 |
Plasma lipoprotein clearance | 25 | 0.392000 | 0.982 | 0.1980 | -1.13e-01 | 0.122000 | -1.08e-01 | 0.327000 | 0.29200 | 0.34800 |
Processive synthesis on the lagging strand | 15 | 0.392000 | 0.982 | 0.2560 | -1.86e-01 | -0.076300 | -1.58e-01 | 0.211000 | 0.60900 | 0.28800 |
Regulation of lipid metabolism by Peroxisome proliferator-activated receptor alpha (PPARalpha) | 97 | 0.393000 | 0.982 | 0.1020 | -2.37e-02 | 0.075700 | 6.37e-02 | 0.688000 | 0.19800 | 0.27900 |
Cap-dependent Translation Initiation | 86 | 0.394000 | 0.982 | 0.1080 | -1.59e-03 | -0.037000 | 1.02e-01 | 0.980000 | 0.55400 | 0.10400 |
Eukaryotic Translation Initiation | 86 | 0.394000 | 0.982 | 0.1080 | -1.59e-03 | -0.037000 | 1.02e-01 | 0.980000 | 0.55400 | 0.10400 |
Signaling by FGFR2 IIIa TM | 13 | 0.395000 | 0.982 | 0.2770 | 1.87e-02 | -0.191000 | 1.99e-01 | 0.907000 | 0.23400 | 0.21300 |
Negative regulation of FGFR1 signaling | 22 | 0.395000 | 0.982 | 0.2110 | 1.79e-01 | 0.063300 | 9.24e-02 | 0.146000 | 0.60700 | 0.45300 |
Signaling by Receptor Tyrosine Kinases | 331 | 0.395000 | 0.982 | 0.0553 | 8.81e-03 | -0.013600 | 5.29e-02 | 0.784000 | 0.67100 | 0.10000 |
Thrombin signalling through proteinase activated receptors (PARs) | 18 | 0.399000 | 0.982 | 0.2330 | 2.03e-01 | -0.113000 | 1.14e-02 | 0.136000 | 0.40600 | 0.93300 |
Downstream signaling of activated FGFR4 | 17 | 0.402000 | 0.982 | 0.2400 | 2.39e-01 | 0.019900 | 1.96e-03 | 0.087700 | 0.88700 | 0.98900 |
Processing and activation of SUMO | 10 | 0.402000 | 0.982 | 0.3120 | -2.66e-01 | -0.129000 | -1.01e-01 | 0.146000 | 0.48000 | 0.58200 |
Insulin processing | 15 | 0.402000 | 0.982 | 0.2560 | 3.24e-02 | 0.236000 | -9.56e-02 | 0.828000 | 0.11400 | 0.52100 |
Synthesis of glycosylphosphatidylinositol (GPI) | 14 | 0.404000 | 0.982 | 0.2670 | -2.16e-01 | -0.003630 | 1.57e-01 | 0.162000 | 0.98100 | 0.31100 |
IGF1R signaling cascade | 30 | 0.405000 | 0.982 | 0.1800 | 1.73e-01 | 0.048600 | 1.29e-02 | 0.101000 | 0.64500 | 0.90200 |
DNA Double-Strand Break Repair | 106 | 0.407000 | 0.982 | 0.0968 | -8.39e-02 | -0.044300 | 1.88e-02 | 0.136000 | 0.43100 | 0.73900 |
Constitutive Signaling by EGFRvIII | 15 | 0.409000 | 0.982 | 0.2570 | 1.67e-01 | 0.102000 | -1.66e-01 | 0.262000 | 0.49300 | 0.26600 |
Signaling by EGFRvIII in Cancer | 15 | 0.409000 | 0.982 | 0.2570 | 1.67e-01 | 0.102000 | -1.66e-01 | 0.262000 | 0.49300 | 0.26600 |
Developmental Biology | 570 | 0.410000 | 0.982 | 0.0423 | -1.08e-02 | -0.028200 | 2.97e-02 | 0.663000 | 0.25500 | 0.23000 |
Early Phase of HIV Life Cycle | 13 | 0.411000 | 0.982 | 0.2720 | 1.55e-02 | -0.157000 | 2.21e-01 | 0.923000 | 0.32600 | 0.16700 |
Ephrin signaling | 15 | 0.411000 | 0.982 | 0.2530 | -3.50e-02 | -0.250000 | -2.21e-02 | 0.815000 | 0.09410 | 0.88200 |
Molecules associated with elastic fibres | 23 | 0.411000 | 0.982 | 0.2040 | 6.22e-02 | 0.161000 | 1.08e-01 | 0.606000 | 0.18100 | 0.37000 |
Translesion Synthesis by POLH | 18 | 0.415000 | 0.982 | 0.2290 | -1.81e-01 | 0.133000 | 4.51e-02 | 0.184000 | 0.32700 | 0.74000 |
Deadenylation of mRNA | 24 | 0.415000 | 0.982 | 0.1970 | -1.16e-01 | 0.044400 | -1.53e-01 | 0.325000 | 0.70700 | 0.19500 |
Synthesis of PA | 21 | 0.416000 | 0.982 | 0.2140 | 1.70e-01 | 0.129000 | 9.18e-03 | 0.177000 | 0.30600 | 0.94200 |
MET activates RAP1 and RAC1 | 10 | 0.416000 | 0.982 | 0.3060 | -2.63e-01 | 0.157000 | -1.41e-02 | 0.151000 | 0.38900 | 0.93900 |
Telomere C-strand (Lagging Strand) Synthesis | 22 | 0.417000 | 0.982 | 0.2060 | -9.94e-02 | -0.089000 | -1.57e-01 | 0.420000 | 0.47000 | 0.20200 |
Purine salvage | 13 | 0.417000 | 0.982 | 0.2720 | 1.21e-01 | 0.016900 | -2.43e-01 | 0.451000 | 0.91600 | 0.12900 |
O-glycosylation of TSR domain-containing proteins | 26 | 0.418000 | 0.982 | 0.1890 | -7.48e-02 | -0.027600 | -1.72e-01 | 0.509000 | 0.80700 | 0.13000 |
Resolution of Sister Chromatid Cohesion | 68 | 0.419000 | 0.982 | 0.1190 | -9.08e-02 | -0.076400 | 6.85e-03 | 0.196000 | 0.27700 | 0.92200 |
G1/S-Specific Transcription | 17 | 0.419000 | 0.982 | 0.2350 | 1.47e-01 | -0.166000 | -7.72e-02 | 0.294000 | 0.23500 | 0.58200 |
RNA Polymerase I Promoter Clearance | 45 | 0.420000 | 0.982 | 0.1440 | 4.12e-02 | 0.120000 | 6.87e-02 | 0.633000 | 0.16300 | 0.42600 |
NR1H3 & NR1H2 regulate gene expression linked to cholesterol transport and efflux | 31 | 0.420000 | 0.982 | 0.1770 | -1.28e-01 | -0.082100 | 8.94e-02 | 0.217000 | 0.42900 | 0.38900 |
Signal transduction by L1 | 17 | 0.420000 | 0.982 | 0.2340 | -1.22e-01 | 0.200000 | 1.22e-02 | 0.384000 | 0.15400 | 0.93100 |
mRNA Splicing | 159 | 0.421000 | 0.982 | 0.0771 | 7.68e-03 | 0.006290 | 7.65e-02 | 0.868000 | 0.89100 | 0.09680 |
Ion homeostasis | 42 | 0.421000 | 0.982 | 0.1490 | 4.25e-02 | -0.119000 | 7.95e-02 | 0.634000 | 0.18300 | 0.37300 |
Metabolism of carbohydrates | 202 | 0.422000 | 0.982 | 0.0692 | -3.25e-02 | -0.055100 | 2.66e-02 | 0.428000 | 0.17900 | 0.51600 |
Regulation of RUNX1 Expression and Activity | 17 | 0.422000 | 0.982 | 0.2340 | 1.98e-02 | -0.179000 | -1.50e-01 | 0.888000 | 0.20100 | 0.28500 |
Signaling by NTRK3 (TRKC) | 15 | 0.424000 | 0.982 | 0.2490 | 2.47e-01 | 0.025600 | 2.51e-02 | 0.098400 | 0.86400 | 0.86600 |
Pyruvate metabolism | 26 | 0.424000 | 0.982 | 0.1880 | 1.21e-01 | -0.090300 | 1.12e-01 | 0.287000 | 0.42600 | 0.32400 |
Interleukin-20 family signaling | 13 | 0.424000 | 0.982 | 0.2680 | -1.63e-01 | -0.196000 | -8.27e-02 | 0.309000 | 0.22200 | 0.60600 |
Assembly Of The HIV Virion | 14 | 0.425000 | 0.982 | 0.2560 | 9.53e-02 | -0.042700 | 2.34e-01 | 0.537000 | 0.78200 | 0.13000 |
RUNX1 regulates transcription of genes involved in differentiation of HSCs | 62 | 0.425000 | 0.982 | 0.1220 | -8.17e-02 | -0.048300 | -7.66e-02 | 0.266000 | 0.51100 | 0.29800 |
Peptide chain elongation | 59 | 0.426000 | 0.982 | 0.1270 | -5.86e-02 | -0.017500 | 1.11e-01 | 0.436000 | 0.81700 | 0.14000 |
NF-kB is activated and signals survival | 11 | 0.426000 | 0.982 | 0.2910 | -1.27e-01 | 0.189000 | 1.82e-01 | 0.467000 | 0.27900 | 0.29700 |
Basigin interactions | 17 | 0.427000 | 0.982 | 0.2320 | 1.06e-01 | -0.052300 | 1.99e-01 | 0.451000 | 0.70900 | 0.15500 |
RA biosynthesis pathway | 13 | 0.427000 | 0.982 | 0.2700 | 1.98e-01 | 0.138000 | -1.21e-01 | 0.216000 | 0.38900 | 0.44900 |
GTP hydrolysis and joining of the 60S ribosomal subunit | 79 | 0.428000 | 0.982 | 0.1090 | -2.08e-03 | -0.018500 | 1.07e-01 | 0.975000 | 0.77600 | 0.10000 |
Peroxisomal lipid metabolism | 20 | 0.428000 | 0.982 | 0.2170 | -5.53e-02 | -0.134000 | 1.61e-01 | 0.669000 | 0.30100 | 0.21200 |
G-protein mediated events | 44 | 0.429000 | 0.982 | 0.1440 | 1.07e-01 | 0.029000 | 9.14e-02 | 0.220000 | 0.74000 | 0.29400 |
IRS-related events triggered by IGF1R | 29 | 0.429000 | 0.982 | 0.1780 | 1.69e-01 | 0.038500 | 4.24e-02 | 0.116000 | 0.72000 | 0.69300 |
E3 ubiquitin ligases ubiquitinate target proteins | 38 | 0.429000 | 0.982 | 0.1560 | -7.50e-02 | 0.114000 | 7.57e-02 | 0.424000 | 0.22500 | 0.42000 |
RHO GTPases activate CIT | 18 | 0.434000 | 0.982 | 0.2240 | 8.86e-02 | 0.141000 | 1.50e-01 | 0.516000 | 0.30100 | 0.27000 |
Nuclear Pore Complex (NPC) Disassembly | 32 | 0.434000 | 0.982 | 0.1710 | 1.44e-01 | 0.041300 | -8.29e-02 | 0.160000 | 0.68600 | 0.41700 |
JNK (c-Jun kinases) phosphorylation and activation mediated by activated human TAK1 | 17 | 0.436000 | 0.982 | 0.2310 | 1.28e-01 | -0.171000 | -8.82e-02 | 0.361000 | 0.22300 | 0.52900 |
Prostacyclin signalling through prostacyclin receptor | 10 | 0.437000 | 0.982 | 0.3000 | 1.63e-01 | -0.250000 | 2.42e-02 | 0.371000 | 0.17100 | 0.89500 |
Gap junction trafficking | 13 | 0.439000 | 0.982 | 0.2630 | -2.30e-01 | 0.120000 | 4.02e-02 | 0.150000 | 0.45300 | 0.80200 |
Regulation of TNFR1 signaling | 31 | 0.440000 | 0.982 | 0.1710 | 4.22e-02 | 0.162000 | 3.35e-02 | 0.684000 | 0.11800 | 0.74700 |
Vasopressin regulates renal water homeostasis via Aquaporins | 30 | 0.441000 | 0.982 | 0.1720 | 1.40e-01 | 0.005140 | 9.93e-02 | 0.185000 | 0.96100 | 0.34700 |
Diseases associated with N-glycosylation of proteins | 14 | 0.443000 | 0.982 | 0.2530 | 6.66e-02 | -0.170000 | -1.75e-01 | 0.666000 | 0.27000 | 0.25800 |
Plasma lipoprotein assembly | 12 | 0.443000 | 0.982 | 0.2700 | -1.47e-01 | 0.082900 | -2.12e-01 | 0.379000 | 0.61900 | 0.20400 |
Vpr-mediated nuclear import of PICs | 32 | 0.444000 | 0.982 | 0.1690 | 1.20e-01 | 0.027200 | -1.16e-01 | 0.241000 | 0.79000 | 0.25500 |
Regulation of signaling by CBL | 14 | 0.444000 | 0.982 | 0.2510 | -6.41e-02 | 0.027600 | -2.41e-01 | 0.678000 | 0.85800 | 0.11800 |
IRS-mediated signalling | 26 | 0.444000 | 0.982 | 0.1860 | 1.74e-01 | 0.063100 | 1.41e-02 | 0.125000 | 0.57800 | 0.90100 |
Synthesis of active ubiquitin: roles of E1 and E2 enzymes | 29 | 0.446000 | 0.982 | 0.1760 | -1.52e-01 | 0.050500 | 7.23e-02 | 0.156000 | 0.63800 | 0.50000 |
COPI-independent Golgi-to-ER retrograde traffic | 28 | 0.446000 | 0.982 | 0.1800 | -1.21e-01 | -0.132000 | 1.24e-02 | 0.266000 | 0.22800 | 0.90900 |
Defective B3GALTL causes Peters-plus syndrome (PpS) | 25 | 0.446000 | 0.982 | 0.1870 | -7.06e-02 | -0.058800 | -1.63e-01 | 0.541000 | 0.61100 | 0.15800 |
Mismatch repair (MMR) directed by MSH2:MSH3 (MutSbeta) | 12 | 0.446000 | 0.982 | 0.2730 | 7.78e-02 | -0.074900 | -2.51e-01 | 0.641000 | 0.65400 | 0.13300 |
SUMOylation of SUMOylation proteins | 32 | 0.446000 | 0.982 | 0.1680 | 6.84e-02 | -0.022800 | -1.52e-01 | 0.503000 | 0.82400 | 0.13800 |
Formation of the cornified envelope | 12 | 0.447000 | 0.982 | 0.2710 | -1.25e-02 | -0.230000 | -1.44e-01 | 0.940000 | 0.16800 | 0.38900 |
p75 NTR receptor-mediated signalling | 73 | 0.448000 | 0.982 | 0.1110 | -1.73e-02 | 0.032200 | 1.04e-01 | 0.799000 | 0.63500 | 0.12400 |
TNF signaling | 39 | 0.448000 | 0.982 | 0.1520 | 7.47e-02 | 0.118000 | -6.13e-02 | 0.420000 | 0.20400 | 0.50800 |
AKT phosphorylates targets in the nucleus | 10 | 0.449000 | 0.982 | 0.2990 | -7.64e-02 | 0.010400 | 2.89e-01 | 0.676000 | 0.95500 | 0.11400 |
Dopamine Neurotransmitter Release Cycle | 12 | 0.450000 | 0.982 | 0.2740 | -1.52e-01 | -0.161000 | 1.63e-01 | 0.363000 | 0.33500 | 0.32900 |
Kinesins | 23 | 0.450000 | 0.982 | 0.1960 | -7.07e-02 | 0.166000 | 7.64e-02 | 0.557000 | 0.17000 | 0.52600 |
Nuclear Envelope Breakdown | 47 | 0.450000 | 0.982 | 0.1380 | 1.07e-01 | -0.026300 | -8.37e-02 | 0.206000 | 0.75500 | 0.32100 |
Vesicle-mediated transport | 496 | 0.452000 | 0.982 | 0.0428 | 3.47e-02 | -0.023100 | -9.93e-03 | 0.190000 | 0.38300 | 0.70700 |
Regulation of glycolysis by fructose 2,6-bisphosphate metabolism | 11 | 0.452000 | 0.982 | 0.2820 | -2.74e-01 | -0.063300 | -2.73e-02 | 0.116000 | 0.71600 | 0.87500 |
Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell | 37 | 0.453000 | 0.982 | 0.1530 | 4.02e-02 | -0.038500 | 1.43e-01 | 0.673000 | 0.68600 | 0.13300 |
Membrane Trafficking | 473 | 0.454000 | 0.982 | 0.0437 | 3.87e-02 | -0.019600 | -4.74e-03 | 0.152000 | 0.46900 | 0.86100 |
Complex I biogenesis | 36 | 0.456000 | 0.982 | 0.1560 | -1.51e-01 | -0.032300 | -1.84e-02 | 0.117000 | 0.73800 | 0.84900 |
Chaperone Mediated Autophagy | 18 | 0.458000 | 0.982 | 0.2210 | -1.79e-01 | 0.051400 | 1.19e-01 | 0.189000 | 0.70600 | 0.38100 |
Signaling by Hippo | 19 | 0.458000 | 0.982 | 0.2130 | -6.13e-02 | -0.117000 | -1.67e-01 | 0.644000 | 0.37900 | 0.20800 |
RNA Polymerase I Promoter Escape | 26 | 0.459000 | 0.982 | 0.1820 | -3.09e-03 | 0.151000 | 1.01e-01 | 0.978000 | 0.18200 | 0.37200 |
CLEC7A (Dectin-1) signaling | 83 | 0.460000 | 0.982 | 0.1020 | 1.59e-02 | -0.072500 | -7.02e-02 | 0.802000 | 0.25400 | 0.26900 |
DNA Damage/Telomere Stress Induced Senescence | 23 | 0.462000 | 0.982 | 0.1940 | -1.80e-01 | -0.071700 | 9.49e-03 | 0.135000 | 0.55200 | 0.93700 |
Ion channel transport | 102 | 0.463000 | 0.982 | 0.0924 | 5.61e-02 | 0.073100 | 6.84e-03 | 0.328000 | 0.20300 | 0.90500 |
Gene and protein expression by JAK-STAT signaling after Interleukin-12 stimulation | 24 | 0.463000 | 0.982 | 0.1890 | -2.32e-02 | 0.028800 | 1.86e-01 | 0.844000 | 0.80700 | 0.11500 |
TICAM1-dependent activation of IRF3/IRF7 | 11 | 0.463000 | 0.982 | 0.2800 | 5.54e-02 | 0.273000 | -2.68e-02 | 0.750000 | 0.11700 | 0.87800 |
Peptide hormone metabolism | 41 | 0.465000 | 0.982 | 0.1440 | -2.57e-02 | 0.139000 | 2.96e-02 | 0.776000 | 0.12500 | 0.74300 |
BBSome-mediated cargo-targeting to cilium | 18 | 0.466000 | 0.982 | 0.2180 | -2.42e-02 | -0.216000 | 7.28e-03 | 0.859000 | 0.11200 | 0.95700 |
S Phase | 129 | 0.466000 | 0.982 | 0.0820 | -6.67e-02 | -0.047700 | 8.96e-04 | 0.192000 | 0.35100 | 0.98600 |
tRNA processing in the nucleus | 50 | 0.469000 | 0.982 | 0.1320 | 9.28e-02 | -0.006750 | -9.29e-02 | 0.257000 | 0.93400 | 0.25600 |
Phosphorylation of CD3 and TCR zeta chains | 12 | 0.472000 | 0.982 | 0.2660 | 6.55e-02 | 0.053400 | -2.53e-01 | 0.694000 | 0.74900 | 0.13000 |
TCR signaling | 90 | 0.472000 | 0.982 | 0.0973 | 4.81e-02 | -0.041500 | -7.37e-02 | 0.431000 | 0.49700 | 0.22800 |
Caspase-mediated cleavage of cytoskeletal proteins | 11 | 0.473000 | 0.982 | 0.2750 | -2.12e-03 | -0.166000 | -2.19e-01 | 0.990000 | 0.34000 | 0.20800 |
Downstream signaling of activated FGFR2 | 17 | 0.475000 | 0.982 | 0.2210 | 2.20e-01 | 0.008360 | 1.80e-02 | 0.116000 | 0.95200 | 0.89800 |
Estrogen-dependent nuclear events downstream of ESR-membrane signaling | 20 | 0.477000 | 0.982 | 0.2030 | 5.44e-02 | 0.119000 | 1.55e-01 | 0.674000 | 0.35500 | 0.23100 |
Misspliced GSK3beta mutants stabilize beta-catenin | 15 | 0.477000 | 0.982 | 0.2340 | 1.17e-01 | -0.193000 | 6.01e-02 | 0.433000 | 0.19500 | 0.68700 |
S33 mutants of beta-catenin aren’t phosphorylated | 15 | 0.477000 | 0.982 | 0.2340 | 1.17e-01 | -0.193000 | 6.01e-02 | 0.433000 | 0.19500 | 0.68700 |
S37 mutants of beta-catenin aren’t phosphorylated | 15 | 0.477000 | 0.982 | 0.2340 | 1.17e-01 | -0.193000 | 6.01e-02 | 0.433000 | 0.19500 | 0.68700 |
S45 mutants of beta-catenin aren’t phosphorylated | 15 | 0.477000 | 0.982 | 0.2340 | 1.17e-01 | -0.193000 | 6.01e-02 | 0.433000 | 0.19500 | 0.68700 |
T41 mutants of beta-catenin aren’t phosphorylated | 15 | 0.477000 | 0.982 | 0.2340 | 1.17e-01 | -0.193000 | 6.01e-02 | 0.433000 | 0.19500 | 0.68700 |
phosphorylation site mutants of CTNNB1 are not targeted to the proteasome by the destruction complex | 15 | 0.477000 | 0.982 | 0.2340 | 1.17e-01 | -0.193000 | 6.01e-02 | 0.433000 | 0.19500 | 0.68700 |
Viral mRNA Translation | 58 | 0.478000 | 0.982 | 0.1210 | -5.03e-02 | -0.011500 | 1.09e-01 | 0.508000 | 0.88000 | 0.15000 |
Negative regulation of NMDA receptor-mediated neuronal transmission | 12 | 0.478000 | 0.982 | 0.2630 | -2.41e-01 | -0.097600 | -3.76e-02 | 0.148000 | 0.55800 | 0.82200 |
Transport of small molecules | 444 | 0.479000 | 0.982 | 0.0436 | -2.35e-02 | 0.032600 | -1.69e-02 | 0.399000 | 0.24300 | 0.54400 |
Signaling by FGFR2 in disease | 26 | 0.480000 | 0.982 | 0.1760 | 1.11e-01 | -0.043200 | 1.30e-01 | 0.326000 | 0.70300 | 0.25200 |
Chromatin modifying enzymes | 183 | 0.482000 | 0.982 | 0.0674 | -4.03e-02 | 0.045000 | 3.01e-02 | 0.349000 | 0.29600 | 0.48400 |
Chromatin organization | 183 | 0.482000 | 0.982 | 0.0674 | -4.03e-02 | 0.045000 | 3.01e-02 | 0.349000 | 0.29600 | 0.48400 |
HS-GAG degradation | 13 | 0.484000 | 0.982 | 0.2520 | -1.08e-01 | -0.226000 | 2.87e-02 | 0.500000 | 0.15800 | 0.85800 |
Amino acids regulate mTORC1 | 40 | 0.484000 | 0.982 | 0.1430 | -7.82e-03 | 0.139000 | -3.36e-02 | 0.932000 | 0.12900 | 0.71300 |
Elastic fibre formation | 33 | 0.485000 | 0.982 | 0.1560 | 6.94e-02 | 0.038500 | 1.34e-01 | 0.490000 | 0.70200 | 0.18100 |
Diseases of glycosylation | 97 | 0.487000 | 0.982 | 0.0920 | 8.99e-03 | 0.014100 | -9.05e-02 | 0.879000 | 0.81100 | 0.12400 |
ADP signalling through P2Y purinoceptor 12 | 12 | 0.490000 | 0.982 | 0.2610 | 2.44e-01 | -0.018900 | -8.99e-02 | 0.143000 | 0.91000 | 0.59000 |
Signaling by NODAL | 11 | 0.491000 | 0.982 | 0.2700 | -8.82e-02 | -0.212000 | -1.42e-01 | 0.612000 | 0.22400 | 0.41500 |
Signaling by VEGF | 85 | 0.493000 | 0.982 | 0.0965 | 6.63e-02 | 0.023000 | 6.64e-02 | 0.292000 | 0.71500 | 0.29100 |
Transcriptional regulation by RUNX1 | 145 | 0.493000 | 0.982 | 0.0746 | -2.32e-02 | -0.063700 | -3.11e-02 | 0.631000 | 0.18600 | 0.51900 |
Cleavage of the damaged purine | 10 | 0.493000 | 0.982 | 0.2800 | -2.24e-01 | -0.001220 | -1.68e-01 | 0.220000 | 0.99500 | 0.35700 |
Depurination | 10 | 0.493000 | 0.982 | 0.2800 | -2.24e-01 | -0.001220 | -1.68e-01 | 0.220000 | 0.99500 | 0.35700 |
Recognition and association of DNA glycosylase with site containing an affected purine | 10 | 0.493000 | 0.982 | 0.2800 | -2.24e-01 | -0.001220 | -1.68e-01 | 0.220000 | 0.99500 | 0.35700 |
Cargo concentration in the ER | 23 | 0.495000 | 0.982 | 0.1870 | 1.52e-01 | -0.081000 | -7.27e-02 | 0.208000 | 0.50100 | 0.54600 |
Cholesterol biosynthesis | 19 | 0.496000 | 0.982 | 0.2050 | 1.68e-01 | -0.102000 | -5.76e-02 | 0.205000 | 0.44200 | 0.66400 |
Regulation of MECP2 expression and activity | 28 | 0.499000 | 0.982 | 0.1700 | -8.91e-02 | -0.117000 | 8.55e-02 | 0.414000 | 0.28400 | 0.43400 |
RNA Polymerase I Transcription Termination | 23 | 0.499000 | 0.982 | 0.1860 | 7.52e-02 | 0.163000 | 4.76e-02 | 0.533000 | 0.17600 | 0.69300 |
N-glycan antennae elongation in the medial/trans-Golgi | 17 | 0.499000 | 0.982 | 0.2140 | 1.88e-01 | -0.036000 | 9.42e-02 | 0.179000 | 0.79700 | 0.50100 |
Depolymerisation of the Nuclear Lamina | 12 | 0.501000 | 0.982 | 0.2570 | 1.43e-01 | -0.150000 | -1.51e-01 | 0.391000 | 0.36800 | 0.36400 |
Cell junction organization | 47 | 0.503000 | 0.982 | 0.1290 | 6.42e-02 | -0.111000 | 4.93e-03 | 0.447000 | 0.18600 | 0.95300 |
Axon guidance | 378 | 0.503000 | 0.982 | 0.0460 | 8.60e-03 | -0.014400 | 4.29e-02 | 0.775000 | 0.63300 | 0.15500 |
Degradation of beta-catenin by the destruction complex | 73 | 0.504000 | 0.982 | 0.1040 | 4.29e-03 | -0.094900 | 4.19e-02 | 0.950000 | 0.16100 | 0.53600 |
Metabolism of steroid hormones | 15 | 0.504000 | 0.982 | 0.2270 | -4.15e-02 | -0.101000 | -1.99e-01 | 0.781000 | 0.49800 | 0.18100 |
Formation of the Early Elongation Complex | 25 | 0.507000 | 0.982 | 0.1750 | 1.58e-01 | -0.012100 | 7.41e-02 | 0.172000 | 0.91700 | 0.52200 |
Formation of the HIV-1 Early Elongation Complex | 25 | 0.507000 | 0.982 | 0.1750 | 1.58e-01 | -0.012100 | 7.41e-02 | 0.172000 | 0.91700 | 0.52200 |
SHC1 events in ERBB4 signaling | 10 | 0.508000 | 0.982 | 0.2780 | -7.97e-02 | 0.217000 | 1.55e-01 | 0.662000 | 0.23500 | 0.39600 |
Collagen biosynthesis and modifying enzymes | 44 | 0.508000 | 0.982 | 0.1340 | 4.06e-02 | 0.122000 | -3.56e-02 | 0.641000 | 0.16100 | 0.68300 |
APC/C:Cdc20 mediated degradation of Cyclin B | 19 | 0.508000 | 0.982 | 0.2020 | -9.49e-02 | 0.132000 | 1.20e-01 | 0.474000 | 0.32000 | 0.36500 |
Glycogen breakdown (glycogenolysis) | 13 | 0.508000 | 0.982 | 0.2450 | 1.64e-01 | -0.131000 | -1.26e-01 | 0.306000 | 0.41400 | 0.43200 |
RUNX1 interacts with co-factors whose precise effect on RUNX1 targets is not known | 34 | 0.509000 | 0.982 | 0.1500 | 9.06e-02 | -0.117000 | 2.41e-02 | 0.361000 | 0.23800 | 0.80800 |
MAPK family signaling cascades | 211 | 0.511000 | 0.982 | 0.0615 | -2.55e-02 | -0.017600 | 5.31e-02 | 0.525000 | 0.66100 | 0.18500 |
Interleukin-6 signaling | 10 | 0.511000 | 0.982 | 0.2760 | 2.07e-01 | -0.182000 | -1.10e-02 | 0.256000 | 0.31900 | 0.95200 |
Degradation of GLI2 by the proteasome | 51 | 0.513000 | 0.982 | 0.1220 | 6.43e-02 | -0.068000 | 7.78e-02 | 0.427000 | 0.40100 | 0.33700 |
Caspase activation via extrinsic apoptotic signalling pathway | 21 | 0.514000 | 0.982 | 0.1930 | 1.25e-01 | 0.030000 | -1.44e-01 | 0.322000 | 0.81200 | 0.25300 |
RAB geranylgeranylation | 41 | 0.516000 | 0.982 | 0.1370 | -3.51e-02 | -0.130000 | -2.16e-02 | 0.697000 | 0.14900 | 0.81100 |
Signaling by Type 1 Insulin-like Growth Factor 1 Receptor (IGF1R) | 31 | 0.516000 | 0.982 | 0.1570 | 1.55e-01 | 0.020500 | -1.74e-02 | 0.135000 | 0.84300 | 0.86700 |
Extra-nuclear estrogen signaling | 56 | 0.516000 | 0.982 | 0.1160 | 1.13e-01 | 0.018400 | 2.36e-02 | 0.146000 | 0.81200 | 0.76000 |
Mitotic Telophase/Cytokinesis | 10 | 0.517000 | 0.982 | 0.2790 | -1.83e-01 | -0.109000 | 1.81e-01 | 0.316000 | 0.55200 | 0.32300 |
Degradation of the extracellular matrix | 58 | 0.517000 | 0.982 | 0.1150 | -5.83e-02 | -0.099300 | -2.21e-03 | 0.443000 | 0.19100 | 0.97700 |
Telomere Maintenance | 34 | 0.517000 | 0.982 | 0.1480 | -8.98e-02 | -0.049900 | -1.07e-01 | 0.365000 | 0.61500 | 0.28100 |
G2/M Transition | 146 | 0.518000 | 0.982 | 0.0718 | 5.87e-02 | -0.035500 | 2.10e-02 | 0.222000 | 0.46000 | 0.66200 |
Eukaryotic Translation Elongation | 62 | 0.519000 | 0.982 | 0.1120 | -7.06e-02 | -0.007870 | 8.64e-02 | 0.337000 | 0.91500 | 0.24000 |
Gap junction degradation | 10 | 0.519000 | 0.982 | 0.2740 | -2.25e-01 | 0.152000 | 4.06e-02 | 0.219000 | 0.40600 | 0.82400 |
Endosomal Sorting Complex Required For Transport (ESCRT) | 26 | 0.520000 | 0.982 | 0.1690 | 5.42e-02 | -0.072200 | 1.43e-01 | 0.633000 | 0.52400 | 0.20600 |
Neurotransmitter release cycle | 26 | 0.523000 | 0.982 | 0.1690 | 5.36e-02 | -0.145000 | 6.87e-02 | 0.636000 | 0.20100 | 0.54400 |
Regulation of Complement cascade | 16 | 0.524000 | 0.982 | 0.2140 | -1.14e-01 | 0.014000 | -1.81e-01 | 0.431000 | 0.92300 | 0.21100 |
Potassium Channels | 33 | 0.524000 | 0.982 | 0.1500 | -8.30e-02 | 0.124000 | -1.49e-02 | 0.409000 | 0.21900 | 0.88200 |
SHC1 events in ERBB2 signaling | 18 | 0.526000 | 0.982 | 0.2040 | 7.36e-02 | 0.185000 | 4.40e-02 | 0.589000 | 0.17500 | 0.74700 |
WNT5A-dependent internalization of FZD2, FZD5 and ROR2 | 11 | 0.527000 | 0.982 | 0.2610 | -2.87e-02 | -0.225000 | 1.28e-01 | 0.869000 | 0.19600 | 0.46100 |
Glycerophospholipid biosynthesis | 83 | 0.528000 | 0.982 | 0.0940 | 4.41e-02 | 0.020100 | 8.05e-02 | 0.488000 | 0.75200 | 0.20500 |
Insulin receptor recycling | 17 | 0.528000 | 0.982 | 0.2110 | 9.24e-02 | 0.175000 | -7.12e-02 | 0.510000 | 0.21100 | 0.61200 |
Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC) | 84 | 0.529000 | 0.982 | 0.0937 | -5.66e-02 | 0.072200 | 1.93e-02 | 0.370000 | 0.25300 | 0.76000 |
Nonsense-Mediated Decay (NMD) | 84 | 0.529000 | 0.982 | 0.0937 | -5.66e-02 | 0.072200 | 1.93e-02 | 0.370000 | 0.25300 | 0.76000 |
Association of TriC/CCT with target proteins during biosynthesis | 32 | 0.530000 | 0.982 | 0.1530 | -9.75e-02 | -0.113000 | 3.35e-02 | 0.340000 | 0.26700 | 0.74300 |
Diseases associated with O-glycosylation of proteins | 41 | 0.531000 | 0.982 | 0.1330 | -5.44e-02 | 0.047300 | -1.12e-01 | 0.547000 | 0.60000 | 0.21500 |
Interleukin-12 signaling | 30 | 0.533000 | 0.982 | 0.1570 | -2.74e-02 | -0.012800 | 1.54e-01 | 0.795000 | 0.90300 | 0.14500 |
Nicotinamide salvaging | 12 | 0.534000 | 0.982 | 0.2460 | -7.29e-03 | 0.228000 | 9.35e-02 | 0.965000 | 0.17200 | 0.57500 |
Deubiquitination | 209 | 0.535000 | 0.982 | 0.0597 | -4.58e-02 | 0.022500 | 3.11e-02 | 0.255000 | 0.57600 | 0.44000 |
Factors involved in megakaryocyte development and platelet production | 84 | 0.536000 | 0.982 | 0.0930 | -2.38e-02 | 0.080200 | -4.07e-02 | 0.707000 | 0.20500 | 0.51900 |
Carboxyterminal post-translational modifications of tubulin | 22 | 0.537000 | 0.982 | 0.1810 | -2.79e-02 | -0.148000 | -1.01e-01 | 0.821000 | 0.23000 | 0.41200 |
RUNX2 regulates osteoblast differentiation | 20 | 0.538000 | 0.982 | 0.1900 | -2.57e-02 | 0.172000 | -7.62e-02 | 0.843000 | 0.18200 | 0.55500 |
Recycling pathway of L1 | 22 | 0.538000 | 0.982 | 0.1800 | 7.09e-02 | 0.002620 | 1.65e-01 | 0.565000 | 0.98300 | 0.17900 |
Signaling by NTRK1 (TRKA) | 69 | 0.539000 | 0.982 | 0.1010 | 8.30e-02 | -0.031800 | 4.90e-02 | 0.234000 | 0.64800 | 0.48200 |
Synaptic adhesion-like molecules | 11 | 0.540000 | 0.982 | 0.2590 | -1.61e-01 | -0.146000 | 1.41e-01 | 0.354000 | 0.40200 | 0.41900 |
Transport of Mature mRNA Derived from an Intronless Transcript | 40 | 0.540000 | 0.982 | 0.1360 | 6.81e-02 | 0.106000 | -5.06e-02 | 0.457000 | 0.24700 | 0.58000 |
Transport of Mature mRNAs Derived from Intronless Transcripts | 40 | 0.540000 | 0.982 | 0.1360 | 6.81e-02 | 0.106000 | -5.06e-02 | 0.457000 | 0.24700 | 0.58000 |
Assembly of active LPL and LIPC lipase complexes | 10 | 0.542000 | 0.982 | 0.2650 | -1.63e-01 | 0.090900 | -1.88e-01 | 0.372000 | 0.61900 | 0.30400 |
Signaling by BMP | 24 | 0.543000 | 0.982 | 0.1720 | 4.28e-02 | -0.167000 | 5.28e-03 | 0.716000 | 0.15700 | 0.96400 |
Repression of WNT target genes | 12 | 0.545000 | 0.982 | 0.2440 | -2.24e-01 | -0.096800 | -1.31e-02 | 0.179000 | 0.56200 | 0.93700 |
Protein-protein interactions at synapses | 46 | 0.546000 | 0.982 | 0.1230 | 1.09e-01 | -0.036000 | 4.60e-02 | 0.203000 | 0.67300 | 0.59000 |
G0 and Early G1 | 17 | 0.546000 | 0.982 | 0.2040 | -1.37e-02 | -0.181000 | -9.36e-02 | 0.922000 | 0.19700 | 0.50400 |
Uptake and actions of bacterial toxins | 22 | 0.546000 | 0.982 | 0.1810 | -4.55e-02 | -0.149000 | 9.16e-02 | 0.712000 | 0.22600 | 0.45700 |
Signaling by NTRKs | 83 | 0.547000 | 0.982 | 0.0917 | 5.69e-02 | -0.038500 | 6.07e-02 | 0.371000 | 0.54400 | 0.33900 |
Host Interactions with Influenza Factors | 40 | 0.548000 | 0.982 | 0.1340 | 1.16e-01 | -0.009400 | -6.74e-02 | 0.206000 | 0.91800 | 0.46100 |
Mitotic G2-G2/M phases | 147 | 0.549000 | 0.982 | 0.0690 | 5.79e-02 | -0.032800 | 1.83e-02 | 0.226000 | 0.49400 | 0.70200 |
Mitotic G1-G1/S phases | 114 | 0.550000 | 0.982 | 0.0788 | 7.00e-03 | -0.071200 | -3.29e-02 | 0.897000 | 0.19000 | 0.54500 |
Protein folding | 71 | 0.550000 | 0.982 | 0.0993 | 4.13e-02 | -0.088700 | 1.71e-02 | 0.547000 | 0.19700 | 0.80300 |
Defective B3GAT3 causes JDSSDHD | 12 | 0.550000 | 0.982 | 0.2400 | 1.57e-01 | -0.177000 | 4.13e-02 | 0.345000 | 0.28900 | 0.80400 |
RNA Polymerase II Transcription Termination | 53 | 0.550000 | 0.982 | 0.1150 | 2.82e-02 | 0.101000 | 4.77e-02 | 0.723000 | 0.20400 | 0.54800 |
Intraflagellar transport | 33 | 0.551000 | 0.982 | 0.1450 | 6.23e-02 | 0.098000 | 8.76e-02 | 0.536000 | 0.33000 | 0.38400 |
Glutamate binding, activation of AMPA receptors and synaptic plasticity | 22 | 0.552000 | 0.982 | 0.1770 | 1.15e-01 | 0.085100 | 1.05e-01 | 0.349000 | 0.49000 | 0.39600 |
Trafficking of AMPA receptors | 22 | 0.552000 | 0.982 | 0.1770 | 1.15e-01 | 0.085100 | 1.05e-01 | 0.349000 | 0.49000 | 0.39600 |
Signaling by Interleukins | 291 | 0.554000 | 0.982 | 0.0492 | 1.71e-02 | -0.028800 | 3.61e-02 | 0.618000 | 0.40000 | 0.29200 |
Removal of the Flap Intermediate from the C-strand | 10 | 0.555000 | 0.982 | 0.2650 | -2.42e-01 | -0.107000 | 3.42e-03 | 0.184000 | 0.55900 | 0.98500 |
Eukaryotic Translation Termination | 62 | 0.555000 | 0.982 | 0.1070 | -4.60e-02 | 0.013700 | 9.55e-02 | 0.532000 | 0.85200 | 0.19400 |
Signaling by FGFR2 | 51 | 0.556000 | 0.982 | 0.1160 | 1.03e-01 | 0.003550 | 5.28e-02 | 0.203000 | 0.96500 | 0.51500 |
Negative regulation of the PI3K/AKT network | 73 | 0.557000 | 0.982 | 0.0985 | -3.53e-02 | -0.031200 | 8.65e-02 | 0.603000 | 0.64500 | 0.20200 |
TP53 Regulates Transcription of Cell Death Genes | 36 | 0.560000 | 0.982 | 0.1380 | 1.30e-01 | -0.044200 | 9.72e-03 | 0.177000 | 0.64600 | 0.92000 |
PCNA-Dependent Long Patch Base Excision Repair | 18 | 0.560000 | 0.982 | 0.1950 | 2.51e-02 | -0.155000 | -1.16e-01 | 0.854000 | 0.25500 | 0.39500 |
Calnexin/calreticulin cycle | 23 | 0.561000 | 0.982 | 0.1730 | -3.38e-02 | 0.147000 | 8.44e-02 | 0.779000 | 0.22400 | 0.48400 |
Glycogen synthesis | 13 | 0.563000 | 0.982 | 0.2280 | -2.09e-01 | 0.091100 | -1.52e-03 | 0.192000 | 0.57000 | 0.99200 |
M Phase | 248 | 0.564000 | 0.982 | 0.0526 | 2.11e-02 | -0.047600 | 7.77e-03 | 0.568000 | 0.19900 | 0.83400 |
Processive synthesis on the C-strand of the telomere | 11 | 0.564000 | 0.982 | 0.2490 | -1.71e-01 | -0.168000 | -6.59e-02 | 0.325000 | 0.33500 | 0.70500 |
Vitamin B5 (pantothenate) metabolism | 13 | 0.566000 | 0.982 | 0.2280 | 4.92e-02 | -0.141000 | 1.72e-01 | 0.759000 | 0.38000 | 0.28200 |
TNFR1-induced proapoptotic signaling | 12 | 0.566000 | 0.982 | 0.2370 | 1.00e-02 | 0.216000 | 9.78e-02 | 0.952000 | 0.19500 | 0.55700 |
Diseases of metabolism | 64 | 0.567000 | 0.982 | 0.1040 | -4.53e-02 | 0.031800 | 8.75e-02 | 0.531000 | 0.66100 | 0.22600 |
Transcription of E2F targets under negative control by DREAM complex | 15 | 0.568000 | 0.982 | 0.2120 | 1.04e-01 | -0.137000 | -1.25e-01 | 0.488000 | 0.35900 | 0.40200 |
Death Receptor Signalling | 114 | 0.568000 | 0.982 | 0.0773 | 2.66e-02 | 0.070800 | 1.57e-02 | 0.624000 | 0.19200 | 0.77300 |
HIV Life Cycle | 123 | 0.571000 | 0.982 | 0.0736 | 7.02e-02 | -0.010000 | 1.99e-02 | 0.180000 | 0.84800 | 0.70400 |
Regulation of TP53 Degradation | 28 | 0.572000 | 0.982 | 0.1550 | -4.88e-02 | 0.014100 | 1.47e-01 | 0.655000 | 0.89700 | 0.17900 |
Regulation of TP53 Expression and Degradation | 28 | 0.572000 | 0.982 | 0.1550 | -4.88e-02 | 0.014100 | 1.47e-01 | 0.655000 | 0.89700 | 0.17900 |
RAF/MAP kinase cascade | 174 | 0.573000 | 0.982 | 0.0631 | -4.34e-02 | -0.021600 | 4.04e-02 | 0.325000 | 0.62400 | 0.35900 |
Recognition of DNA damage by PCNA-containing replication complex | 27 | 0.573000 | 0.982 | 0.1590 | -1.07e-01 | -0.081200 | 8.55e-02 | 0.336000 | 0.46600 | 0.44200 |
PI5P, PP2A and IER3 Regulate PI3K/AKT Signaling | 67 | 0.574000 | 0.982 | 0.1000 | -1.84e-02 | -0.033300 | 9.29e-02 | 0.794000 | 0.63800 | 0.18900 |
SUMOylation of DNA replication proteins | 39 | 0.574000 | 0.982 | 0.1320 | 7.25e-02 | 0.026300 | -1.07e-01 | 0.434000 | 0.77600 | 0.24600 |
SUMOylation of RNA binding proteins | 45 | 0.574000 | 0.982 | 0.1220 | 7.18e-02 | -0.084100 | -5.05e-02 | 0.405000 | 0.33000 | 0.55800 |
Regulation of RUNX2 expression and activity | 59 | 0.575000 | 0.982 | 0.1060 | 5.40e-03 | 0.029500 | 1.02e-01 | 0.943000 | 0.69500 | 0.17700 |
Other semaphorin interactions | 15 | 0.576000 | 0.982 | 0.2110 | -1.12e-01 | -0.179000 | -5.65e-03 | 0.453000 | 0.23100 | 0.97000 |
Negative epigenetic regulation of rRNA expression | 42 | 0.577000 | 0.982 | 0.1270 | 9.91e-02 | -0.014900 | -7.72e-02 | 0.267000 | 0.86800 | 0.38700 |
GAB1 signalosome | 13 | 0.578000 | 0.982 | 0.2230 | -1.82e-01 | 0.055500 | -1.15e-01 | 0.256000 | 0.72900 | 0.47100 |
AMER1 mutants destabilize the destruction complex | 14 | 0.580000 | 0.982 | 0.2150 | 9.41e-02 | -0.194000 | -2.33e-03 | 0.542000 | 0.20900 | 0.98800 |
APC truncation mutants have impaired AXIN binding | 14 | 0.580000 | 0.982 | 0.2150 | 9.41e-02 | -0.194000 | -2.33e-03 | 0.542000 | 0.20900 | 0.98800 |
AXIN missense mutants destabilize the destruction complex | 14 | 0.580000 | 0.982 | 0.2150 | 9.41e-02 | -0.194000 | -2.33e-03 | 0.542000 | 0.20900 | 0.98800 |
AXIN mutants destabilize the destruction complex, activating WNT signaling | 14 | 0.580000 | 0.982 | 0.2150 | 9.41e-02 | -0.194000 | -2.33e-03 | 0.542000 | 0.20900 | 0.98800 |
Truncations of AMER1 destabilize the destruction complex | 14 | 0.580000 | 0.982 | 0.2150 | 9.41e-02 | -0.194000 | -2.33e-03 | 0.542000 | 0.20900 | 0.98800 |
truncated APC mutants destabilize the destruction complex | 14 | 0.580000 | 0.982 | 0.2150 | 9.41e-02 | -0.194000 | -2.33e-03 | 0.542000 | 0.20900 | 0.98800 |
Regulation of FZD by ubiquitination | 14 | 0.582000 | 0.982 | 0.2140 | -1.80e-01 | 0.065500 | -9.41e-02 | 0.243000 | 0.67100 | 0.54200 |
VEGFR2 mediated vascular permeability | 21 | 0.583000 | 0.982 | 0.1750 | 1.42e-01 | -0.097000 | 2.91e-02 | 0.259000 | 0.44200 | 0.81700 |
FCERI mediated NF-kB activation | 67 | 0.585000 | 0.982 | 0.0984 | 9.84e-03 | -0.078800 | -5.81e-02 | 0.889000 | 0.26500 | 0.41100 |
Signal Transduction | 1457 | 0.585000 | 0.982 | 0.0225 | -3.97e-03 | -0.014000 | 1.71e-02 | 0.805000 | 0.38200 | 0.28600 |
TP53 Regulates Transcription of Death Receptors and Ligands | 10 | 0.586000 | 0.982 | 0.2530 | 2.14e-01 | 0.067800 | 1.16e-01 | 0.241000 | 0.71000 | 0.52700 |
Disassembly of the destruction complex and recruitment of AXIN to the membrane | 25 | 0.586000 | 0.982 | 0.1590 | 7.77e-02 | -0.096600 | 1.00e-01 | 0.502000 | 0.40400 | 0.38500 |
Defects in vitamin and cofactor metabolism | 18 | 0.586000 | 0.982 | 0.1880 | 1.67e-01 | 0.035300 | 7.99e-02 | 0.221000 | 0.79600 | 0.55800 |
RAB GEFs exchange GTP for GDP on RABs | 76 | 0.586000 | 0.982 | 0.0918 | 6.24e-02 | -0.066900 | 6.91e-03 | 0.348000 | 0.31400 | 0.91700 |
Cobalamin (Cbl, vitamin B12) transport and metabolism | 11 | 0.588000 | 0.982 | 0.2440 | 1.91e-01 | 0.014700 | -1.52e-01 | 0.274000 | 0.93300 | 0.38200 |
Cytosolic sensors of pathogen-associated DNA | 48 | 0.589000 | 0.982 | 0.1170 | 8.44e-02 | 0.079200 | -1.32e-02 | 0.312000 | 0.34300 | 0.87500 |
Nuclear import of Rev protein | 32 | 0.590000 | 0.982 | 0.1430 | 1.29e-01 | 0.012100 | -6.06e-02 | 0.208000 | 0.90600 | 0.55300 |
Effects of PIP2 hydrolysis | 20 | 0.590000 | 0.982 | 0.1800 | 1.58e-01 | -0.019600 | -8.48e-02 | 0.222000 | 0.87900 | 0.51200 |
Interleukin-6 family signaling | 18 | 0.590000 | 0.982 | 0.1880 | 6.49e-02 | -0.164000 | 6.51e-02 | 0.634000 | 0.23000 | 0.63300 |
Downregulation of SMAD2/3:SMAD4 transcriptional activity | 23 | 0.590000 | 0.982 | 0.1670 | -1.04e-01 | -0.129000 | -2.36e-02 | 0.390000 | 0.28400 | 0.84500 |
Prolonged ERK activation events | 12 | 0.591000 | 0.982 | 0.2340 | 1.78e-01 | 0.090600 | -1.21e-01 | 0.285000 | 0.58700 | 0.47000 |
Formation of RNA Pol II elongation complex | 43 | 0.591000 | 0.982 | 0.1210 | 1.05e-01 | 0.017500 | 5.84e-02 | 0.236000 | 0.84300 | 0.50800 |
RNA Polymerase II Transcription Elongation | 43 | 0.591000 | 0.982 | 0.1210 | 1.05e-01 | 0.017500 | 5.84e-02 | 0.236000 | 0.84300 | 0.50800 |
Formation of a pool of free 40S subunits | 69 | 0.592000 | 0.982 | 0.0968 | -2.61e-02 | 0.003710 | 9.31e-02 | 0.708000 | 0.95800 | 0.18200 |
MAPK1/MAPK3 signaling | 179 | 0.592000 | 0.982 | 0.0607 | -3.03e-02 | -0.029000 | 4.39e-02 | 0.486000 | 0.50500 | 0.31300 |
Triglyceride metabolism | 23 | 0.594000 | 0.982 | 0.1680 | -7.38e-02 | -0.107000 | 1.06e-01 | 0.540000 | 0.37500 | 0.37800 |
RET signaling | 27 | 0.595000 | 0.982 | 0.1550 | 1.28e-01 | 0.020000 | -8.45e-02 | 0.249000 | 0.85700 | 0.44700 |
Gamma carboxylation, hypusine formation and arylsulfatase activation | 27 | 0.595000 | 0.982 | 0.1540 | -1.20e-01 | -0.096500 | 1.17e-02 | 0.283000 | 0.38600 | 0.91600 |
Dual Incision in GG-NER | 36 | 0.596000 | 0.982 | 0.1330 | -3.77e-02 | 0.010900 | 1.27e-01 | 0.696000 | 0.91000 | 0.18700 |
MHC class II antigen presentation | 75 | 0.601000 | 0.982 | 0.0924 | 6.57e-02 | 0.013900 | -6.33e-02 | 0.325000 | 0.83500 | 0.34300 |
Regulation of necroptotic cell death | 13 | 0.603000 | 0.982 | 0.2200 | 8.72e-02 | 0.127000 | -1.58e-01 | 0.586000 | 0.43000 | 0.32400 |
SUMOylation of chromatin organization proteins | 55 | 0.603000 | 0.982 | 0.1060 | 2.30e-02 | -0.103000 | -1.42e-02 | 0.769000 | 0.18900 | 0.85600 |
HIV Infection | 187 | 0.604000 | 0.982 | 0.0575 | 2.59e-02 | -0.042600 | 2.86e-02 | 0.543000 | 0.31600 | 0.50100 |
N-Glycan antennae elongation | 11 | 0.604000 | 0.982 | 0.2360 | 2.26e-01 | 0.051000 | 4.90e-02 | 0.195000 | 0.77000 | 0.77800 |
Heparan sulfate/heparin (HS-GAG) metabolism | 31 | 0.605000 | 0.982 | 0.1420 | -2.91e-02 | -0.138000 | 6.25e-03 | 0.779000 | 0.18300 | 0.95200 |
PKMTs methylate histone lysines | 35 | 0.609000 | 0.982 | 0.1330 | -3.82e-02 | 0.035200 | 1.22e-01 | 0.696000 | 0.71800 | 0.21200 |
TGF-beta receptor signaling activates SMADs | 30 | 0.610000 | 0.982 | 0.1430 | -3.34e-02 | -0.133000 | 3.96e-02 | 0.752000 | 0.20600 | 0.70700 |
PD-1 signaling | 13 | 0.611000 | 0.982 | 0.2160 | -1.12e-02 | 0.034900 | -2.13e-01 | 0.944000 | 0.82700 | 0.18400 |
Respiratory electron transport | 70 | 0.612000 | 0.982 | 0.0927 | -4.65e-02 | -0.059100 | -5.42e-02 | 0.502000 | 0.39300 | 0.43300 |
Regulation of IFNA signaling | 10 | 0.613000 | 0.982 | 0.2460 | 2.96e-02 | 0.242000 | -3.62e-02 | 0.871000 | 0.18600 | 0.84300 |
HIV Transcription Initiation | 34 | 0.614000 | 0.982 | 0.1330 | -1.28e-02 | 0.127000 | 3.63e-02 | 0.897000 | 0.19900 | 0.71500 |
RNA Polymerase II HIV Promoter Escape | 34 | 0.614000 | 0.982 | 0.1330 | -1.28e-02 | 0.127000 | 3.63e-02 | 0.897000 | 0.19900 | 0.71500 |
RNA Polymerase II Promoter Escape | 34 | 0.614000 | 0.982 | 0.1330 | -1.28e-02 | 0.127000 | 3.63e-02 | 0.897000 | 0.19900 | 0.71500 |
RNA Polymerase II Transcription Initiation | 34 | 0.614000 | 0.982 | 0.1330 | -1.28e-02 | 0.127000 | 3.63e-02 | 0.897000 | 0.19900 | 0.71500 |
RNA Polymerase II Transcription Initiation And Promoter Clearance | 34 | 0.614000 | 0.982 | 0.1330 | -1.28e-02 | 0.127000 | 3.63e-02 | 0.897000 | 0.19900 | 0.71500 |
RNA Polymerase II Transcription Pre-Initiation And Promoter Opening | 34 | 0.614000 | 0.982 | 0.1330 | -1.28e-02 | 0.127000 | 3.63e-02 | 0.897000 | 0.19900 | 0.71500 |
Late Phase of HIV Life Cycle | 111 | 0.618000 | 0.982 | 0.0736 | 7.30e-02 | 0.007850 | 4.74e-03 | 0.185000 | 0.88700 | 0.93100 |
RNA Polymerase III Chain Elongation | 13 | 0.620000 | 0.982 | 0.2120 | 1.26e-01 | 0.108000 | 1.32e-01 | 0.431000 | 0.49900 | 0.41000 |
Cellular responses to external stimuli | 333 | 0.621000 | 0.982 | 0.0425 | -1.36e-02 | 0.032100 | -2.43e-02 | 0.672000 | 0.31600 | 0.44900 |
Rap1 signalling | 13 | 0.624000 | 0.982 | 0.2140 | -1.92e-01 | 0.008410 | 9.36e-02 | 0.230000 | 0.95800 | 0.55900 |
Innate Immune System | 639 | 0.624000 | 0.982 | 0.0308 | 2.57e-02 | 0.005730 | 1.59e-02 | 0.272000 | 0.80700 | 0.49600 |
Adrenaline,noradrenaline inhibits insulin secretion | 18 | 0.624000 | 0.982 | 0.1820 | 1.55e-01 | 0.091400 | -2.81e-02 | 0.256000 | 0.50200 | 0.83700 |
Platelet sensitization by LDL | 15 | 0.624000 | 0.982 | 0.1980 | 8.82e-04 | -0.196000 | 2.40e-02 | 0.995000 | 0.18800 | 0.87200 |
Transcription of the HIV genome | 52 | 0.625000 | 0.982 | 0.1050 | 7.80e-02 | 0.024400 | 6.64e-02 | 0.331000 | 0.76100 | 0.40800 |
Activation of IRF3/IRF7 mediated by TBK1/IKK epsilon | 14 | 0.626000 | 0.982 | 0.2050 | 6.30e-02 | 0.187000 | -5.76e-02 | 0.683000 | 0.22600 | 0.70900 |
Keratan sulfate/keratin metabolism | 22 | 0.627000 | 0.982 | 0.1640 | -1.42e-01 | -0.071800 | 3.98e-02 | 0.248000 | 0.56000 | 0.74700 |
TBC/RABGAPs | 38 | 0.627000 | 0.982 | 0.1250 | -1.14e-01 | -0.011600 | 4.92e-02 | 0.223000 | 0.90100 | 0.60000 |
Regulation of innate immune responses to cytosolic DNA | 11 | 0.628000 | 0.982 | 0.2280 | -1.38e-01 | 0.180000 | -2.10e-02 | 0.428000 | 0.30000 | 0.90400 |
Signaling by NTRK2 (TRKB) | 19 | 0.629000 | 0.982 | 0.1760 | 7.05e-02 | 0.157000 | -3.56e-02 | 0.595000 | 0.23600 | 0.78800 |
Degradation of cysteine and homocysteine | 11 | 0.631000 | 0.982 | 0.2310 | 2.11e-01 | 0.008880 | -9.33e-02 | 0.226000 | 0.95900 | 0.59200 |
Transport of bile salts and organic acids, metal ions and amine compounds | 32 | 0.633000 | 0.982 | 0.1330 | -7.30e-02 | -0.026100 | -1.08e-01 | 0.475000 | 0.79800 | 0.29200 |
Semaphorin interactions | 55 | 0.634000 | 0.982 | 0.1030 | -7.10e-02 | 0.016100 | 7.29e-02 | 0.363000 | 0.83700 | 0.35000 |
Purine ribonucleoside monophosphate biosynthesis | 12 | 0.634000 | 0.982 | 0.2170 | 1.85e-01 | 0.080000 | 8.21e-02 | 0.268000 | 0.63100 | 0.62200 |
Post-translational protein modification | 1009 | 0.635000 | 0.982 | 0.0249 | -2.01e-02 | -0.014500 | 2.22e-03 | 0.288000 | 0.44300 | 0.90700 |
TNFR1-induced NFkappaB signaling pathway | 24 | 0.635000 | 0.982 | 0.1550 | 1.06e-01 | -0.080000 | -7.87e-02 | 0.368000 | 0.49800 | 0.50400 |
Endogenous sterols | 17 | 0.637000 | 0.982 | 0.1810 | -1.31e-01 | 0.021100 | -1.23e-01 | 0.351000 | 0.88100 | 0.38000 |
Cyclin D associated events in G1 | 38 | 0.638000 | 0.982 | 0.1230 | 3.83e-02 | -0.023400 | -1.14e-01 | 0.683000 | 0.80300 | 0.22300 |
G1 Phase | 38 | 0.638000 | 0.982 | 0.1230 | 3.83e-02 | -0.023400 | -1.14e-01 | 0.683000 | 0.80300 | 0.22300 |
Chemokine receptors bind chemokines | 12 | 0.640000 | 0.982 | 0.2160 | -1.20e-01 | 0.177000 | 3.06e-02 | 0.472000 | 0.28900 | 0.85400 |
Sialic acid metabolism | 26 | 0.642000 | 0.982 | 0.1470 | 1.45e-01 | 0.007590 | -2.63e-02 | 0.201000 | 0.94700 | 0.81700 |
Post-translational protein phosphorylation | 64 | 0.642000 | 0.982 | 0.0945 | 8.56e-02 | 0.005360 | -3.97e-02 | 0.237000 | 0.94100 | 0.58300 |
Interactions of Rev with host cellular proteins | 35 | 0.643000 | 0.982 | 0.1280 | 6.14e-02 | 0.025700 | -1.09e-01 | 0.530000 | 0.79200 | 0.26400 |
DCC mediated attractive signaling | 12 | 0.643000 | 0.982 | 0.2140 | -1.51e-01 | 0.148000 | -3.57e-02 | 0.367000 | 0.37500 | 0.83100 |
TNFR2 non-canonical NF-kB pathway | 62 | 0.645000 | 0.982 | 0.0944 | 6.19e-02 | -0.070900 | -8.00e-03 | 0.400000 | 0.33500 | 0.91300 |
Glucagon-like Peptide-1 (GLP1) regulates insulin secretion | 27 | 0.646000 | 0.982 | 0.1420 | 1.27e-01 | -0.060800 | 1.90e-02 | 0.252000 | 0.58500 | 0.86400 |
TP53 Regulates Metabolic Genes | 70 | 0.646000 | 0.982 | 0.0887 | 4.82e-02 | -0.074400 | 3.38e-03 | 0.486000 | 0.28300 | 0.96100 |
IRAK1 recruits IKK complex | 10 | 0.648000 | 0.982 | 0.2340 | 2.12e-01 | -0.098800 | -7.41e-03 | 0.246000 | 0.58900 | 0.96800 |
IRAK1 recruits IKK complex upon TLR7/8 or 9 stimulation | 10 | 0.648000 | 0.982 | 0.2340 | 2.12e-01 | -0.098800 | -7.41e-03 | 0.246000 | 0.58900 | 0.96800 |
Signaling by Hedgehog | 114 | 0.648000 | 0.982 | 0.0692 | 6.34e-02 | -0.022600 | 1.62e-02 | 0.243000 | 0.67700 | 0.76600 |
Arachidonic acid metabolism | 23 | 0.649000 | 0.982 | 0.1530 | -1.26e-01 | 0.066200 | -5.76e-02 | 0.297000 | 0.58300 | 0.63300 |
Defective B3GALT6 causes EDSP2 and SEMDJL1 | 11 | 0.650000 | 0.982 | 0.2220 | 1.45e-01 | -0.158000 | 5.66e-02 | 0.406000 | 0.36500 | 0.74500 |
Listeria monocytogenes entry into host cells | 16 | 0.650000 | 0.982 | 0.1840 | 5.82e-02 | -0.016200 | 1.74e-01 | 0.687000 | 0.91100 | 0.22900 |
Interleukin-4 and Interleukin-13 signaling | 63 | 0.651000 | 0.982 | 0.0944 | -6.75e-02 | -0.044600 | 4.88e-02 | 0.355000 | 0.54100 | 0.50400 |
VLDLR internalisation and degradation | 11 | 0.652000 | 0.982 | 0.2240 | -1.81e-01 | 0.061900 | 1.17e-01 | 0.300000 | 0.72200 | 0.50200 |
FCERI mediated Ca+2 mobilization | 21 | 0.653000 | 0.982 | 0.1610 | -1.10e-01 | -0.114000 | -2.94e-02 | 0.383000 | 0.36600 | 0.81600 |
Synthesis of PIPs at the early endosome membrane | 16 | 0.654000 | 0.982 | 0.1830 | 4.22e-02 | 0.098800 | 1.48e-01 | 0.770000 | 0.49400 | 0.30500 |
Biotin transport and metabolism | 10 | 0.654000 | 0.982 | 0.2310 | 1.25e-01 | 0.040900 | 1.89e-01 | 0.492000 | 0.82300 | 0.30100 |
SHC1 events in EGFR signaling | 10 | 0.655000 | 0.982 | 0.2320 | 1.36e-01 | 0.172000 | 7.84e-02 | 0.457000 | 0.34800 | 0.66800 |
GPVI-mediated activation cascade | 19 | 0.655000 | 0.982 | 0.1690 | 4.71e-03 | 0.149000 | -7.93e-02 | 0.972000 | 0.26000 | 0.55000 |
Cellular responses to stress | 328 | 0.655000 | 0.982 | 0.0410 | -8.31e-03 | 0.035200 | -1.94e-02 | 0.797000 | 0.27600 | 0.54700 |
C-type lectin receptors (CLRs) | 102 | 0.656000 | 0.982 | 0.0728 | -3.20e-03 | -0.069000 | -2.29e-02 | 0.956000 | 0.22900 | 0.68900 |
Mismatch repair (MMR) directed by MSH2:MSH6 (MutSalpha) | 12 | 0.657000 | 0.982 | 0.2110 | 1.47e-02 | -0.148000 | -1.50e-01 | 0.930000 | 0.37400 | 0.36900 |
Pre-NOTCH Transcription and Translation | 33 | 0.658000 | 0.982 | 0.1280 | -1.24e-01 | -0.022600 | 2.31e-02 | 0.218000 | 0.82200 | 0.81900 |
L13a-mediated translational silencing of Ceruloplasmin expression | 78 | 0.658000 | 0.982 | 0.0833 | -1.25e-02 | 0.006730 | 8.20e-02 | 0.849000 | 0.91800 | 0.21100 |
RMTs methylate histone arginines | 27 | 0.660000 | 0.982 | 0.1410 | 5.67e-02 | 0.129000 | -1.26e-02 | 0.610000 | 0.24700 | 0.91000 |
Membrane binding and targetting of GAG proteins | 12 | 0.661000 | 0.982 | 0.2080 | 1.51e-01 | -0.018800 | 1.42e-01 | 0.365000 | 0.91000 | 0.39400 |
Synthesis And Processing Of GAG, GAGPOL Polyproteins | 12 | 0.661000 | 0.982 | 0.2080 | 1.51e-01 | -0.018800 | 1.42e-01 | 0.365000 | 0.91000 | 0.39400 |
CD209 (DC-SIGN) signaling | 16 | 0.661000 | 0.982 | 0.1830 | -6.03e-02 | 0.021500 | 1.72e-01 | 0.676000 | 0.88200 | 0.23400 |
Erythropoietin activates RAS | 12 | 0.662000 | 0.982 | 0.2110 | 9.13e-02 | -0.105000 | -1.58e-01 | 0.584000 | 0.52900 | 0.34300 |
DAG and IP3 signaling | 35 | 0.665000 | 0.982 | 0.1210 | 8.02e-02 | 0.009070 | 9.08e-02 | 0.412000 | 0.92600 | 0.35300 |
NRIF signals cell death from the nucleus | 12 | 0.665000 | 0.982 | 0.2090 | -1.30e-01 | 0.158000 | 3.98e-02 | 0.435000 | 0.34300 | 0.81200 |
Mitochondrial protein import | 44 | 0.665000 | 0.982 | 0.1090 | -1.09e-01 | -0.000955 | -6.45e-03 | 0.211000 | 0.99100 | 0.94100 |
HSP90 chaperone cycle for steroid hormone receptors (SHR) | 31 | 0.665000 | 0.982 | 0.1300 | -1.38e-02 | 0.093900 | -8.91e-02 | 0.894000 | 0.36600 | 0.39100 |
Transcriptional regulation of white adipocyte differentiation | 68 | 0.665000 | 0.982 | 0.0889 | -7.44e-02 | -0.043900 | 2.07e-02 | 0.289000 | 0.53200 | 0.76800 |
Costimulation by the CD28 family | 45 | 0.667000 | 0.982 | 0.1080 | -2.69e-03 | -0.099300 | -4.17e-02 | 0.975000 | 0.25000 | 0.62900 |
Leading Strand Synthesis | 14 | 0.668000 | 0.982 | 0.1920 | -7.33e-02 | -0.015900 | -1.76e-01 | 0.635000 | 0.91800 | 0.25400 |
Polymerase switching | 14 | 0.668000 | 0.982 | 0.1920 | -7.33e-02 | -0.015900 | -1.76e-01 | 0.635000 | 0.91800 | 0.25400 |
Polymerase switching on the C-strand of the telomere | 14 | 0.668000 | 0.982 | 0.1920 | -7.33e-02 | -0.015900 | -1.76e-01 | 0.635000 | 0.91800 | 0.25400 |
Mismatch Repair | 13 | 0.668000 | 0.982 | 0.2000 | 3.47e-02 | -0.084600 | -1.78e-01 | 0.828000 | 0.59700 | 0.26600 |
Activation of RAC1 | 10 | 0.669000 | 0.982 | 0.2270 | 7.11e-02 | -0.103000 | 1.89e-01 | 0.697000 | 0.57300 | 0.30000 |
Chromosome Maintenance | 49 | 0.669000 | 0.982 | 0.1030 | -5.72e-02 | -0.057800 | -6.25e-02 | 0.489000 | 0.48500 | 0.44900 |
Nuclear Receptor transcription pathway | 41 | 0.670000 | 0.982 | 0.1130 | -4.87e-02 | 0.067700 | 7.57e-02 | 0.590000 | 0.45300 | 0.40200 |
Transcriptional regulation of granulopoiesis | 25 | 0.671000 | 0.982 | 0.1440 | -4.35e-02 | -0.135000 | -2.41e-02 | 0.707000 | 0.24200 | 0.83500 |
Thromboxane signalling through TP receptor | 13 | 0.671000 | 0.982 | 0.1990 | 1.56e-01 | -0.118000 | -3.38e-02 | 0.330000 | 0.46100 | 0.83300 |
Phase I - Functionalization of compounds | 55 | 0.672000 | 0.982 | 0.0973 | -4.70e-02 | -0.084900 | -6.96e-03 | 0.547000 | 0.27600 | 0.92900 |
Processing of Capped Intron-Containing Pre-mRNA | 203 | 0.673000 | 0.982 | 0.0504 | 1.35e-02 | 0.020000 | 4.42e-02 | 0.740000 | 0.62400 | 0.27900 |
Inflammasomes | 14 | 0.675000 | 0.982 | 0.1910 | -6.42e-02 | 0.173000 | 4.79e-02 | 0.678000 | 0.26300 | 0.75600 |
Hyaluronan metabolism | 11 | 0.676000 | 0.982 | 0.2160 | -1.28e-01 | 0.090800 | 1.49e-01 | 0.463000 | 0.60200 | 0.39300 |
Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding | 21 | 0.677000 | 0.982 | 0.1550 | 9.77e-02 | -0.118000 | 2.08e-02 | 0.439000 | 0.35000 | 0.86900 |
Interleukin-15 signaling | 11 | 0.677000 | 0.982 | 0.2170 | 1.09e-01 | 0.176000 | -6.36e-02 | 0.532000 | 0.31200 | 0.71500 |
Retrograde neurotrophin signalling | 10 | 0.678000 | 0.982 | 0.2260 | -9.32e-02 | 0.070800 | 1.94e-01 | 0.610000 | 0.69800 | 0.28900 |
Mitochondrial biogenesis | 67 | 0.679000 | 0.982 | 0.0879 | -5.95e-02 | 0.003720 | 6.46e-02 | 0.400000 | 0.95800 | 0.36100 |
Activation of G protein gated Potassium channels | 10 | 0.679000 | 0.982 | 0.2220 | 1.40e-01 | -0.031300 | 1.70e-01 | 0.442000 | 0.86400 | 0.35300 |
G protein gated Potassium channels | 10 | 0.679000 | 0.982 | 0.2220 | 1.40e-01 | -0.031300 | 1.70e-01 | 0.442000 | 0.86400 | 0.35300 |
Inhibition of voltage gated Ca2+ channels via Gbeta/gamma subunits | 10 | 0.679000 | 0.982 | 0.2220 | 1.40e-01 | -0.031300 | 1.70e-01 | 0.442000 | 0.86400 | 0.35300 |
Keratinization | 13 | 0.681000 | 0.982 | 0.1960 | -5.48e-02 | -0.161000 | -9.83e-02 | 0.732000 | 0.31600 | 0.54000 |
Transcriptional regulation by the AP-2 (TFAP2) family of transcription factors | 25 | 0.681000 | 0.982 | 0.1410 | 3.91e-02 | -0.136000 | 8.79e-03 | 0.735000 | 0.24100 | 0.93900 |
PI-3K cascade:FGFR4 | 10 | 0.681000 | 0.982 | 0.2260 | 2.08e-01 | 0.000402 | -8.70e-02 | 0.254000 | 0.99800 | 0.63400 |
Spry regulation of FGF signaling | 16 | 0.682000 | 0.982 | 0.1780 | 1.29e-01 | 0.121000 | -2.67e-02 | 0.373000 | 0.40400 | 0.85300 |
Diseases associated with glycosaminoglycan metabolism | 27 | 0.683000 | 0.982 | 0.1370 | -9.30e-02 | 0.033600 | 9.49e-02 | 0.403000 | 0.76300 | 0.39400 |
RORA activates gene expression | 17 | 0.683000 | 0.982 | 0.1720 | -1.61e-01 | -0.059400 | 5.53e-03 | 0.249000 | 0.67200 | 0.96900 |
Signaling by ROBO receptors | 159 | 0.684000 | 0.982 | 0.0559 | 1.91e-02 | -0.023100 | 4.72e-02 | 0.678000 | 0.61600 | 0.30600 |
Hedgehog ‘on’ state | 71 | 0.685000 | 0.982 | 0.0837 | 3.57e-02 | -0.067300 | -3.46e-02 | 0.604000 | 0.32700 | 0.61500 |
Nuclear signaling by ERBB4 | 21 | 0.686000 | 0.982 | 0.1530 | -1.37e-01 | -0.058600 | -3.65e-02 | 0.277000 | 0.64200 | 0.77200 |
Major pathway of rRNA processing in the nucleolus and cytosol | 129 | 0.686000 | 0.982 | 0.0616 | -4.99e-02 | 0.022200 | -2.84e-02 | 0.329000 | 0.66300 | 0.57900 |
Degradation of DVL | 48 | 0.687000 | 0.982 | 0.1010 | 1.54e-02 | -0.099200 | 1.45e-02 | 0.853000 | 0.23500 | 0.86200 |
Metabolism of nitric oxide: eNOS activation and regulation | 14 | 0.687000 | 0.982 | 0.1870 | 5.97e-02 | -0.177000 | -1.68e-02 | 0.699000 | 0.25300 | 0.91300 |
Ribosomal scanning and start codon recognition | 43 | 0.689000 | 0.982 | 0.1060 | 3.77e-02 | -0.007290 | 9.91e-02 | 0.669000 | 0.93400 | 0.26100 |
EPHA-mediated growth cone collapse | 14 | 0.689000 | 0.982 | 0.1860 | 7.97e-02 | 0.065400 | 1.55e-01 | 0.606000 | 0.67200 | 0.31600 |
Josephin domain DUBs | 11 | 0.689000 | 0.982 | 0.2110 | -3.86e-02 | 0.133000 | 1.59e-01 | 0.824000 | 0.44500 | 0.36100 |
Metabolism | 1392 | 0.690000 | 0.982 | 0.0197 | 9.67e-03 | -0.016500 | 4.78e-03 | 0.555000 | 0.31400 | 0.77000 |
Microautophagy | 26 | 0.690000 | 0.982 | 0.1370 | 1.44e-02 | -0.019200 | 1.35e-01 | 0.899000 | 0.86600 | 0.23400 |
Negative regulation of MET activity | 18 | 0.691000 | 0.982 | 0.1640 | -4.11e-02 | 0.126000 | 9.69e-02 | 0.763000 | 0.35400 | 0.47700 |
Transport of inorganic cations/anions and amino acids/oligopeptides | 65 | 0.692000 | 0.982 | 0.0863 | -2.40e-02 | -0.049000 | -6.69e-02 | 0.739000 | 0.49500 | 0.35200 |
Regulation of ornithine decarboxylase (ODC) | 40 | 0.694000 | 0.982 | 0.1100 | 3.80e-02 | -0.101000 | -2.16e-02 | 0.678000 | 0.27000 | 0.81300 |
Cytochrome c-mediated apoptotic response | 13 | 0.694000 | 0.982 | 0.1920 | 1.90e-01 | -0.014300 | 2.27e-02 | 0.235000 | 0.92900 | 0.88700 |
Interaction between L1 and Ankyrins | 16 | 0.695000 | 0.982 | 0.1750 | 1.20e-01 | -0.056300 | -1.14e-01 | 0.405000 | 0.69700 | 0.43200 |
Interactions of Vpr with host cellular proteins | 34 | 0.696000 | 0.982 | 0.1200 | 9.14e-02 | 0.020100 | -7.57e-02 | 0.357000 | 0.83900 | 0.44500 |
TP53 Regulates Transcription of Genes Involved in Cytochrome C Release | 15 | 0.698000 | 0.982 | 0.1800 | -3.33e-02 | -0.156000 | 8.23e-02 | 0.823000 | 0.29600 | 0.58100 |
FOXO-mediated transcription of oxidative stress, metabolic and neuronal genes | 22 | 0.698000 | 0.982 | 0.1470 | 9.51e-02 | 0.068900 | 8.76e-02 | 0.440000 | 0.57600 | 0.47700 |
The NLRP3 inflammasome | 10 | 0.700000 | 0.982 | 0.2160 | -9.75e-02 | 0.131000 | -1.42e-01 | 0.593000 | 0.47200 | 0.43800 |
Circadian Clock | 62 | 0.700000 | 0.982 | 0.0888 | -5.40e-02 | -0.019200 | 6.78e-02 | 0.463000 | 0.79400 | 0.35600 |
RNA Polymerase II Pre-transcription Events | 60 | 0.701000 | 0.982 | 0.0886 | 7.42e-02 | 0.035500 | 3.29e-02 | 0.321000 | 0.63500 | 0.65900 |
Extracellular matrix organization | 189 | 0.702000 | 0.982 | 0.0499 | 4.41e-02 | -0.013000 | 1.94e-02 | 0.298000 | 0.75900 | 0.64600 |
Constitutive Signaling by Ligand-Responsive EGFR Cancer Variants | 19 | 0.702000 | 0.982 | 0.1590 | 8.52e-02 | 0.130000 | -3.08e-02 | 0.520000 | 0.32500 | 0.81600 |
Signaling by Ligand-Responsive EGFR Variants in Cancer | 19 | 0.702000 | 0.982 | 0.1590 | 8.52e-02 | 0.130000 | -3.08e-02 | 0.520000 | 0.32500 | 0.81600 |
Nucleotide-binding domain, leucine rich repeat containing receptor (NLR) signaling pathways | 42 | 0.703000 | 0.982 | 0.1060 | 7.74e-02 | -0.068500 | -2.26e-02 | 0.386000 | 0.44300 | 0.80000 |
EPH-Ephrin signaling | 68 | 0.703000 | 0.982 | 0.0827 | 3.14e-02 | -0.003880 | 7.64e-02 | 0.654000 | 0.95600 | 0.27600 |
Transcriptional activation of mitochondrial biogenesis | 49 | 0.704000 | 0.982 | 0.0976 | -7.46e-02 | 0.062400 | 7.66e-03 | 0.367000 | 0.45000 | 0.92600 |
Generic Transcription Pathway | 895 | 0.705000 | 0.982 | 0.0237 | 1.05e-03 | -0.017200 | 1.63e-02 | 0.958000 | 0.38900 | 0.41600 |
Translesion synthesis by POLI | 17 | 0.709000 | 0.982 | 0.1660 | -1.61e-01 | -0.013100 | 3.62e-02 | 0.250000 | 0.92500 | 0.79600 |
GRB2 events in ERBB2 signaling | 12 | 0.710000 | 0.982 | 0.1960 | -2.55e-02 | 0.081700 | 1.76e-01 | 0.879000 | 0.62400 | 0.29000 |
RHO GTPase Effectors | 178 | 0.710000 | 0.982 | 0.0511 | 2.68e-03 | 0.008360 | 5.04e-02 | 0.951000 | 0.84800 | 0.24800 |
Transcriptional Regulation by E2F6 | 31 | 0.710000 | 0.982 | 0.1230 | -7.03e-02 | -0.093400 | 3.87e-02 | 0.498000 | 0.36900 | 0.71000 |
SIRT1 negatively regulates rRNA expression | 10 | 0.711000 | 0.982 | 0.2170 | 1.65e-01 | 0.040400 | -1.35e-01 | 0.366000 | 0.82500 | 0.45900 |
Activation of NMDA receptors and postsynaptic events | 52 | 0.711000 | 0.982 | 0.0939 | 2.25e-02 | -0.086400 | 2.92e-02 | 0.779000 | 0.28200 | 0.71600 |
Extension of Telomeres | 27 | 0.711000 | 0.982 | 0.1300 | -6.57e-02 | -0.054800 | -9.73e-02 | 0.555000 | 0.62200 | 0.38200 |
Inhibition of replication initiation of damaged DNA by RB1/E2F1 | 12 | 0.712000 | 0.982 | 0.1940 | -8.73e-02 | 0.082600 | -1.52e-01 | 0.601000 | 0.62100 | 0.36200 |
FLT3 Signaling | 187 | 0.712000 | 0.982 | 0.0503 | -4.09e-02 | -0.024800 | 1.56e-02 | 0.336000 | 0.55900 | 0.71400 |
GLI3 is processed to GLI3R by the proteasome | 51 | 0.713000 | 0.982 | 0.0939 | 5.40e-02 | -0.055500 | 5.31e-02 | 0.505000 | 0.49300 | 0.51200 |
Formation of the ternary complex, and subsequently, the 43S complex | 37 | 0.714000 | 0.982 | 0.1110 | -4.28e-03 | -0.037800 | 1.05e-01 | 0.964000 | 0.69100 | 0.27100 |
Metabolism of polyamines | 47 | 0.714000 | 0.982 | 0.0978 | 7.44e-02 | -0.061100 | 1.69e-02 | 0.378000 | 0.46900 | 0.84100 |
Adaptive Immune System | 507 | 0.715000 | 0.982 | 0.0303 | 1.45e-02 | -0.026500 | 2.99e-03 | 0.579000 | 0.31200 | 0.90900 |
Laminin interactions | 20 | 0.715000 | 0.982 | 0.1520 | -3.99e-02 | -0.036900 | 1.42e-01 | 0.758000 | 0.77500 | 0.27300 |
Mitotic Prophase | 76 | 0.715000 | 0.982 | 0.0784 | 5.87e-02 | 0.021900 | -4.71e-02 | 0.377000 | 0.74100 | 0.47800 |
Cell-extracellular matrix interactions | 15 | 0.716000 | 0.982 | 0.1760 | -1.33e-01 | -0.048600 | 1.04e-01 | 0.373000 | 0.74500 | 0.48500 |
tRNA processing | 85 | 0.717000 | 0.982 | 0.0729 | 9.48e-03 | -0.063600 | -3.44e-02 | 0.880000 | 0.31200 | 0.58400 |
Signaling by FGFR in disease | 45 | 0.718000 | 0.982 | 0.1010 | -5.62e-02 | 0.030600 | 7.76e-02 | 0.514000 | 0.72300 | 0.36800 |
SEMA3A-Plexin repulsion signaling by inhibiting Integrin adhesion | 12 | 0.721000 | 0.982 | 0.1910 | -1.66e-01 | 0.047900 | -8.13e-02 | 0.320000 | 0.77400 | 0.62600 |
Metalloprotease DUBs | 16 | 0.721000 | 0.982 | 0.1680 | -1.57e-01 | 0.022700 | 5.48e-02 | 0.278000 | 0.87500 | 0.70400 |
Cyclin A:Cdk2-associated events at S phase entry | 70 | 0.722000 | 0.982 | 0.0799 | -6.40e-02 | -0.044700 | -1.72e-02 | 0.355000 | 0.51900 | 0.80400 |
Sema4D induced cell migration and growth-cone collapse | 19 | 0.722000 | 0.982 | 0.1520 | 1.19e-01 | 0.058400 | 7.46e-02 | 0.370000 | 0.65900 | 0.57400 |
Immune System | 1295 | 0.723000 | 0.982 | 0.0194 | 1.92e-02 | -0.001040 | 2.80e-03 | 0.257000 | 0.95100 | 0.86800 |
rRNA processing in the nucleus and cytosol | 135 | 0.725000 | 0.982 | 0.0569 | -4.88e-02 | 0.028800 | -5.66e-03 | 0.329000 | 0.56400 | 0.91000 |
Binding and Uptake of Ligands by Scavenger Receptors | 24 | 0.728000 | 0.982 | 0.1340 | -6.00e-02 | -0.045900 | -1.10e-01 | 0.611000 | 0.69700 | 0.34900 |
Downstream signal transduction | 27 | 0.728000 | 0.982 | 0.1280 | 8.59e-02 | -0.006890 | -9.51e-02 | 0.440000 | 0.95100 | 0.39300 |
Assembly of collagen fibrils and other multimeric structures | 41 | 0.729000 | 0.982 | 0.1020 | 5.42e-02 | -0.084700 | 1.88e-02 | 0.549000 | 0.34800 | 0.83500 |
Conversion from APC/C:Cdc20 to APC/C:Cdh1 in late anaphase | 16 | 0.730000 | 0.982 | 0.1640 | -1.62e-01 | 0.027700 | 1.01e-02 | 0.263000 | 0.84800 | 0.94400 |
APC-Cdc20 mediated degradation of Nek2A | 20 | 0.731000 | 0.982 | 0.1480 | -1.14e-01 | 0.050000 | 8.00e-02 | 0.380000 | 0.69900 | 0.53600 |
SUMOylation of ubiquitinylation proteins | 37 | 0.734000 | 0.982 | 0.1070 | -2.04e-02 | 0.013800 | -1.04e-01 | 0.830000 | 0.88400 | 0.27300 |
Activation of BAD and translocation to mitochondria | 13 | 0.736000 | 0.982 | 0.1800 | 5.63e-02 | 0.055200 | 1.61e-01 | 0.725000 | 0.73100 | 0.31400 |
InlB-mediated entry of Listeria monocytogenes into host cell | 13 | 0.736000 | 0.982 | 0.1820 | -5.26e-02 | -0.033100 | 1.71e-01 | 0.743000 | 0.83600 | 0.28600 |
Cellular Senescence | 113 | 0.738000 | 0.982 | 0.0621 | -4.50e-02 | -0.030300 | 3.03e-02 | 0.410000 | 0.57900 | 0.57900 |
Signal regulatory protein family interactions | 11 | 0.738000 | 0.982 | 0.1980 | 1.40e-01 | -0.014300 | -1.38e-01 | 0.420000 | 0.93400 | 0.42700 |
Activation of gene expression by SREBF (SREBP) | 37 | 0.738000 | 0.982 | 0.1070 | -1.48e-02 | -0.101000 | -3.17e-02 | 0.876000 | 0.28900 | 0.73900 |
CDT1 association with the CDC6:ORC:origin complex | 46 | 0.739000 | 0.982 | 0.0957 | 8.87e-03 | -0.089300 | 3.32e-02 | 0.917000 | 0.29500 | 0.69700 |
Cargo recognition for clathrin-mediated endocytosis | 76 | 0.739000 | 0.982 | 0.0742 | 1.93e-02 | 0.046300 | 5.46e-02 | 0.771000 | 0.48600 | 0.41100 |
EPHB-mediated forward signaling | 29 | 0.740000 | 0.982 | 0.1200 | 9.78e-02 | 0.068400 | 1.65e-02 | 0.362000 | 0.52400 | 0.87800 |
ABC transporters in lipid homeostasis | 11 | 0.741000 | 0.982 | 0.1950 | -1.03e-01 | 0.126000 | 1.07e-01 | 0.553000 | 0.47000 | 0.53800 |
Gap-filling DNA repair synthesis and ligation in GG-NER | 23 | 0.741000 | 0.982 | 0.1360 | 6.99e-02 | -0.024500 | -1.14e-01 | 0.562000 | 0.83900 | 0.34600 |
PI3K Cascade | 22 | 0.743000 | 0.982 | 0.1380 | 1.25e-01 | 0.008360 | -5.88e-02 | 0.310000 | 0.94600 | 0.63300 |
Chaperonin-mediated protein folding | 65 | 0.745000 | 0.982 | 0.0793 | 3.96e-02 | -0.068700 | 9.68e-05 | 0.581000 | 0.33800 | 0.99900 |
Ubiquitin-dependent degradation of Cyclin D | 44 | 0.745000 | 0.982 | 0.0972 | -2.77e-02 | -0.092000 | 1.49e-02 | 0.751000 | 0.29100 | 0.86500 |
Acyl chain remodelling of PE | 11 | 0.746000 | 0.982 | 0.1950 | 9.18e-02 | 0.159000 | -6.44e-02 | 0.598000 | 0.36100 | 0.71200 |
Prefoldin mediated transfer of substrate to CCT/TriC | 20 | 0.747000 | 0.982 | 0.1420 | 7.05e-02 | -0.109000 | 5.77e-02 | 0.585000 | 0.40000 | 0.65500 |
Antigen processing-Cross presentation | 74 | 0.748000 | 0.982 | 0.0749 | -2.41e-02 | -0.006540 | 7.06e-02 | 0.720000 | 0.92300 | 0.29400 |
Interleukin-10 signaling | 15 | 0.749000 | 0.982 | 0.1640 | -1.16e-01 | -0.075600 | -8.68e-02 | 0.435000 | 0.61200 | 0.56100 |
Gene Silencing by RNA | 64 | 0.750000 | 0.982 | 0.0795 | 6.32e-02 | 0.040700 | 2.60e-02 | 0.383000 | 0.57400 | 0.72000 |
IL-6-type cytokine receptor ligand interactions | 12 | 0.751000 | 0.982 | 0.1830 | 2.12e-02 | -0.129000 | 1.29e-01 | 0.899000 | 0.43900 | 0.44000 |
CD28 co-stimulation | 22 | 0.752000 | 0.982 | 0.1350 | 7.02e-02 | -0.099200 | -5.89e-02 | 0.569000 | 0.42100 | 0.63200 |
HATs acetylate histones | 73 | 0.754000 | 0.982 | 0.0740 | -1.27e-02 | 0.072800 | -2.25e-03 | 0.851000 | 0.28300 | 0.97400 |
CTLA4 inhibitory signaling | 17 | 0.757000 | 0.982 | 0.1540 | -6.65e-02 | -0.099500 | 9.71e-02 | 0.635000 | 0.47800 | 0.48800 |
Opioid Signalling | 68 | 0.757000 | 0.982 | 0.0756 | 6.17e-02 | -0.014000 | 4.13e-02 | 0.379000 | 0.84200 | 0.55600 |
Cyclin E associated events during G1/S transition | 68 | 0.758000 | 0.982 | 0.0764 | -6.20e-02 | -0.042100 | -1.47e-02 | 0.377000 | 0.54800 | 0.83400 |
Regulation of Apoptosis | 45 | 0.758000 | 0.982 | 0.0943 | -3.00e-02 | -0.079300 | 4.14e-02 | 0.728000 | 0.35800 | 0.63100 |
DNA strand elongation | 28 | 0.758000 | 0.982 | 0.1170 | -9.35e-02 | 0.008890 | -7.03e-02 | 0.392000 | 0.93500 | 0.52000 |
Hedgehog ligand biogenesis | 49 | 0.758000 | 0.982 | 0.0902 | -6.52e-02 | -0.062200 | 3.67e-03 | 0.430000 | 0.45200 | 0.96500 |
Fatty acyl-CoA biosynthesis | 19 | 0.760000 | 0.982 | 0.1430 | 1.22e-01 | -0.074700 | -4.70e-03 | 0.359000 | 0.57300 | 0.97200 |
Gap junction trafficking and regulation | 15 | 0.761000 | 0.982 | 0.1600 | -1.47e-01 | 0.008090 | -6.19e-02 | 0.324000 | 0.95700 | 0.67800 |
Cell-Cell communication | 74 | 0.762000 | 0.982 | 0.0724 | 1.04e-02 | -0.060000 | -3.93e-02 | 0.878000 | 0.37300 | 0.56000 |
ERBB2 Regulates Cell Motility | 11 | 0.763000 | 0.982 | 0.1890 | -1.54e-01 | 0.042400 | 1.01e-01 | 0.377000 | 0.80800 | 0.56200 |
Golgi Cisternae Pericentriolar Stack Reorganization | 10 | 0.763000 | 0.982 | 0.1960 | 7.88e-02 | 0.147000 | 1.02e-01 | 0.666000 | 0.41900 | 0.57500 |
PECAM1 interactions | 10 | 0.763000 | 0.982 | 0.1970 | 3.00e-02 | -0.010700 | -1.95e-01 | 0.869000 | 0.95300 | 0.28700 |
Transcriptional regulation by small RNAs | 44 | 0.763000 | 0.982 | 0.0941 | 9.30e-02 | -0.003290 | -1.40e-02 | 0.286000 | 0.97000 | 0.87300 |
Sema4D in semaphorin signaling | 23 | 0.765000 | 0.982 | 0.1290 | 6.21e-02 | 0.109000 | 3.14e-02 | 0.607000 | 0.36500 | 0.79500 |
Cytosolic sulfonation of small molecules | 11 | 0.765000 | 0.982 | 0.1880 | -4.87e-02 | -0.088700 | 1.59e-01 | 0.780000 | 0.61100 | 0.36200 |
Synthesis of IP2, IP, and Ins in the cytosol | 13 | 0.767000 | 0.982 | 0.1720 | -1.06e-01 | -0.135000 | 1.78e-03 | 0.507000 | 0.39800 | 0.99100 |
ER Quality Control Compartment (ERQC) | 19 | 0.773000 | 0.982 | 0.1390 | 3.34e-02 | 0.081600 | 1.08e-01 | 0.801000 | 0.53800 | 0.41600 |
Collagen formation | 61 | 0.776000 | 0.982 | 0.0787 | 5.58e-02 | 0.050200 | -2.36e-02 | 0.451000 | 0.49800 | 0.75000 |
SUMOylation of DNA damage response and repair proteins | 70 | 0.779000 | 0.982 | 0.0726 | -5.17e-02 | -0.050800 | -4.96e-03 | 0.455000 | 0.46300 | 0.94300 |
rRNA processing | 141 | 0.779000 | 0.982 | 0.0507 | -4.22e-02 | 0.026700 | -8.72e-03 | 0.388000 | 0.58500 | 0.85800 |
CDK-mediated phosphorylation and removal of Cdc6 | 57 | 0.779000 | 0.982 | 0.0806 | -6.46e-02 | -0.047700 | 6.06e-03 | 0.399000 | 0.53300 | 0.93700 |
Vif-mediated degradation of APOBEC3G | 43 | 0.780000 | 0.982 | 0.0922 | 7.39e-05 | -0.076000 | 5.22e-02 | 0.999000 | 0.38900 | 0.55400 |
Oncogene Induced Senescence | 30 | 0.780000 | 0.982 | 0.1100 | 1.53e-03 | -0.025800 | 1.07e-01 | 0.988000 | 0.80700 | 0.31100 |
Ubiquitin Mediated Degradation of Phosphorylated Cdc25A | 43 | 0.781000 | 0.982 | 0.0927 | -3.80e-02 | -0.071600 | 4.50e-02 | 0.666000 | 0.41700 | 0.61000 |
p53-Independent DNA Damage Response | 43 | 0.781000 | 0.982 | 0.0927 | -3.80e-02 | -0.071600 | 4.50e-02 | 0.666000 | 0.41700 | 0.61000 |
p53-Independent G1/S DNA damage checkpoint | 43 | 0.781000 | 0.982 | 0.0927 | -3.80e-02 | -0.071600 | 4.50e-02 | 0.666000 | 0.41700 | 0.61000 |
Signaling by EGFR in Cancer | 21 | 0.781000 | 0.982 | 0.1320 | 4.18e-02 | 0.125000 | 2.07e-03 | 0.740000 | 0.32300 | 0.98700 |
Hemostasis | 367 | 0.782000 | 0.982 | 0.0318 | -1.11e-02 | 0.023200 | 1.86e-02 | 0.717000 | 0.44700 | 0.54300 |
Signaling by the B Cell Receptor (BCR) | 88 | 0.782000 | 0.982 | 0.0647 | -4.53e-02 | -0.043300 | 1.62e-02 | 0.463000 | 0.48400 | 0.79200 |
Dual incision in TC-NER | 55 | 0.785000 | 0.982 | 0.0813 | -2.12e-02 | -0.044200 | 6.48e-02 | 0.786000 | 0.57100 | 0.40600 |
FOXO-mediated transcription of cell cycle genes | 15 | 0.785000 | 0.982 | 0.1540 | 8.90e-02 | -0.111000 | -5.95e-02 | 0.551000 | 0.45800 | 0.69000 |
RHO GTPases activate PAKs | 20 | 0.787000 | 0.982 | 0.1320 | 3.52e-02 | -0.034200 | 1.23e-01 | 0.785000 | 0.79100 | 0.34100 |
Signaling by FGFR1 in disease | 31 | 0.787000 | 0.982 | 0.1070 | -9.23e-02 | 0.045700 | 2.89e-02 | 0.374000 | 0.66000 | 0.78100 |
Processing of Capped Intronless Pre-mRNA | 24 | 0.787000 | 0.982 | 0.1220 | -4.83e-02 | 0.002680 | 1.12e-01 | 0.682000 | 0.98200 | 0.34100 |
Transcriptional Regulation by TP53 | 291 | 0.791000 | 0.982 | 0.0348 | 7.99e-03 | -0.003290 | 3.37e-02 | 0.815000 | 0.92300 | 0.32500 |
PI-3K cascade:FGFR2 | 10 | 0.792000 | 0.982 | 0.1870 | 1.76e-01 | -0.019100 | -5.97e-02 | 0.335000 | 0.91700 | 0.74400 |
Metabolism of cofactors | 16 | 0.793000 | 0.982 | 0.1470 | -1.28e-01 | -0.068900 | -2.33e-02 | 0.376000 | 0.63300 | 0.87200 |
Regulation of TP53 Activity through Acetylation | 29 | 0.794000 | 0.982 | 0.1100 | -5.96e-02 | -0.058300 | 7.22e-02 | 0.578000 | 0.58700 | 0.50100 |
Downstream signaling of activated FGFR1 | 21 | 0.794000 | 0.982 | 0.1270 | 1.12e-01 | -0.059300 | 1.05e-02 | 0.374000 | 0.63800 | 0.93400 |
Nucleotide Excision Repair | 96 | 0.794000 | 0.982 | 0.0606 | -2.30e-02 | -0.045800 | 3.23e-02 | 0.697000 | 0.43900 | 0.58500 |
Hh mutants abrogate ligand secretion | 46 | 0.798000 | 0.982 | 0.0867 | -5.62e-02 | -0.060200 | 2.69e-02 | 0.510000 | 0.48000 | 0.75200 |
Hh mutants that don’t undergo autocatalytic processing are degraded by ERAD | 46 | 0.798000 | 0.982 | 0.0867 | -5.62e-02 | -0.060200 | 2.69e-02 | 0.510000 | 0.48000 | 0.75200 |
Meiosis | 40 | 0.801000 | 0.982 | 0.0920 | -7.59e-02 | 0.027300 | 4.42e-02 | 0.406000 | 0.76600 | 0.62900 |
Platelet activation, signaling and aggregation | 168 | 0.802000 | 0.982 | 0.0452 | -2.41e-02 | -0.004790 | 3.80e-02 | 0.592000 | 0.91500 | 0.39700 |
Regulation of activated PAK-2p34 by proteasome mediated degradation | 42 | 0.802000 | 0.982 | 0.0896 | -2.66e-02 | -0.079400 | 3.19e-02 | 0.765000 | 0.37400 | 0.72100 |
PRC2 methylates histones and DNA | 15 | 0.805000 | 0.982 | 0.1480 | -2.20e-02 | 0.121000 | -8.20e-02 | 0.883000 | 0.41700 | 0.58300 |
ER-Phagosome pathway | 65 | 0.806000 | 0.982 | 0.0718 | -2.85e-02 | -0.052300 | 4.02e-02 | 0.691000 | 0.46700 | 0.57600 |
RAF activation | 30 | 0.806000 | 0.982 | 0.1040 | 4.64e-02 | -0.090500 | -2.29e-02 | 0.660000 | 0.39100 | 0.82800 |
Constitutive Signaling by AKT1 E17K in Cancer | 23 | 0.808000 | 0.982 | 0.1190 | 1.91e-03 | -0.115000 | -2.94e-02 | 0.987000 | 0.34000 | 0.80700 |
The role of GTSE1 in G2/M progression after G2 checkpoint | 49 | 0.809000 | 0.982 | 0.0813 | 1.00e-02 | -0.070800 | 3.87e-02 | 0.903000 | 0.39200 | 0.63900 |
Translesion synthesis by REV1 | 16 | 0.809000 | 0.982 | 0.1420 | -1.28e-01 | 0.046000 | 4.19e-02 | 0.375000 | 0.75000 | 0.77200 |
DNA Damage Bypass | 42 | 0.811000 | 0.982 | 0.0880 | -8.01e-02 | 0.008060 | 3.54e-02 | 0.369000 | 0.92800 | 0.69100 |
Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S | 44 | 0.812000 | 0.982 | 0.0848 | 1.91e-02 | 0.004590 | 8.25e-02 | 0.827000 | 0.95800 | 0.34400 |
Signaling by TGF-beta Receptor Complex | 66 | 0.812000 | 0.982 | 0.0701 | -1.59e-02 | -0.054700 | 4.08e-02 | 0.824000 | 0.44300 | 0.56700 |
Influenza Infection | 115 | 0.812000 | 0.982 | 0.0526 | 1.06e-02 | -0.011400 | 5.02e-02 | 0.844000 | 0.83200 | 0.35300 |
Notch-HLH transcription pathway | 28 | 0.813000 | 0.982 | 0.1070 | -9.95e-02 | -0.037000 | 1.54e-02 | 0.363000 | 0.73500 | 0.88800 |
TRAF6 mediated IRF7 activation | 13 | 0.814000 | 0.982 | 0.1560 | -2.28e-02 | 0.148000 | 4.27e-02 | 0.887000 | 0.35600 | 0.79000 |
Defects in cobalamin (B12) metabolism | 10 | 0.814000 | 0.982 | 0.1790 | 1.59e-01 | -0.015000 | -8.05e-02 | 0.383000 | 0.93500 | 0.65900 |
LDL clearance | 16 | 0.814000 | 0.982 | 0.1410 | -2.76e-03 | 0.103000 | -9.61e-02 | 0.985000 | 0.47600 | 0.50600 |
Epigenetic regulation of gene expression | 78 | 0.818000 | 0.982 | 0.0641 | 3.49e-02 | 0.021300 | -4.93e-02 | 0.594000 | 0.74600 | 0.45200 |
Signaling by TGF-beta family members | 90 | 0.818000 | 0.982 | 0.0593 | -2.00e-02 | -0.047700 | 2.91e-02 | 0.744000 | 0.43400 | 0.63400 |
Phospholipid metabolism | 153 | 0.819000 | 0.982 | 0.0449 | 1.46e-02 | 0.020200 | 3.74e-02 | 0.756000 | 0.66600 | 0.42600 |
MET promotes cell motility | 24 | 0.820000 | 0.982 | 0.1130 | -3.66e-02 | 0.092500 | 5.40e-02 | 0.756000 | 0.43300 | 0.64700 |
Synthesis of DNA | 94 | 0.822000 | 0.982 | 0.0571 | -3.37e-02 | -0.042400 | -1.82e-02 | 0.573000 | 0.47800 | 0.76100 |
Energy dependent regulation of mTOR by LKB1-AMPK | 26 | 0.822000 | 0.982 | 0.1080 | -1.46e-02 | 0.107000 | -6.79e-03 | 0.898000 | 0.34500 | 0.95200 |
Integrin cell surface interactions | 43 | 0.822000 | 0.982 | 0.0841 | 1.23e-02 | -0.083200 | 7.30e-04 | 0.889000 | 0.34600 | 0.99300 |
Regulation of KIT signaling | 14 | 0.823000 | 0.982 | 0.1480 | 4.34e-02 | 0.004850 | -1.41e-01 | 0.778000 | 0.97500 | 0.36000 |
Synthesis of PC | 21 | 0.824000 | 0.982 | 0.1210 | -6.46e-02 | 0.027000 | 9.86e-02 | 0.609000 | 0.83100 | 0.43400 |
Antigen Presentation: Folding, assembly and peptide loading of class I MHC | 19 | 0.824000 | 0.982 | 0.1270 | 2.88e-02 | 0.122000 | -1.56e-02 | 0.828000 | 0.35600 | 0.90600 |
Post NMDA receptor activation events | 45 | 0.824000 | 0.982 | 0.0815 | 6.15e-02 | -0.053000 | 6.63e-03 | 0.475000 | 0.53800 | 0.93900 |
Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC) | 65 | 0.825000 | 0.982 | 0.0683 | -3.56e-02 | 0.037000 | 4.51e-02 | 0.620000 | 0.60700 | 0.53000 |
NIK–>noncanonical NF-kB signaling | 50 | 0.826000 | 0.982 | 0.0770 | 4.99e-02 | -0.056800 | 1.45e-02 | 0.542000 | 0.48800 | 0.85900 |
Golgi-to-ER retrograde transport | 86 | 0.826000 | 0.982 | 0.0590 | 9.77e-03 | 0.037300 | 4.46e-02 | 0.876000 | 0.55000 | 0.47500 |
CREB1 phosphorylation through NMDA receptor-mediated activation of RAS signaling | 22 | 0.827000 | 0.982 | 0.1160 | 7.83e-02 | -0.070900 | -4.90e-02 | 0.525000 | 0.56500 | 0.69100 |
Signaling by Retinoic Acid | 32 | 0.828000 | 0.982 | 0.0953 | 7.46e-02 | -0.017600 | 5.66e-02 | 0.466000 | 0.86400 | 0.58000 |
Budding and maturation of HIV virion | 23 | 0.829000 | 0.982 | 0.1130 | 3.73e-02 | -0.038800 | 9.90e-02 | 0.757000 | 0.74800 | 0.41100 |
Loss of function of MECP2 in Rett syndrome | 11 | 0.830000 | 0.982 | 0.1630 | -1.48e-01 | 0.065500 | 2.21e-02 | 0.396000 | 0.70700 | 0.89900 |
Pervasive developmental disorders | 11 | 0.830000 | 0.982 | 0.1630 | -1.48e-01 | 0.065500 | 2.21e-02 | 0.396000 | 0.70700 | 0.89900 |
Metabolism of lipids | 500 | 0.831000 | 0.982 | 0.0246 | 4.18e-03 | 0.017200 | 1.71e-02 | 0.874000 | 0.51500 | 0.51600 |
Viral Messenger RNA Synthesis | 38 | 0.831000 | 0.982 | 0.0885 | 7.64e-02 | -0.009280 | -4.37e-02 | 0.415000 | 0.92100 | 0.64100 |
RNA Polymerase II Transcription | 995 | 0.832000 | 0.982 | 0.0178 | 1.85e-03 | -0.012700 | 1.23e-02 | 0.923000 | 0.50400 | 0.51900 |
Phase 0 - rapid depolarisation | 25 | 0.833000 | 0.982 | 0.1070 | 5.62e-02 | -0.055700 | 7.17e-02 | 0.627000 | 0.63000 | 0.53500 |
ABC transporter disorders | 60 | 0.834000 | 0.982 | 0.0697 | -3.77e-02 | 0.039500 | 4.33e-02 | 0.614000 | 0.59700 | 0.56200 |
Disorders of transmembrane transporters | 118 | 0.834000 | 0.982 | 0.0495 | -8.08e-03 | -0.012100 | -4.73e-02 | 0.880000 | 0.82100 | 0.37600 |
Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs) | 70 | 0.837000 | 0.982 | 0.0643 | 5.98e-02 | 0.022900 | -5.39e-03 | 0.388000 | 0.74100 | 0.93800 |
Orc1 removal from chromatin | 54 | 0.838000 | 0.982 | 0.0719 | 4.53e-02 | -0.038200 | 4.07e-02 | 0.565000 | 0.62700 | 0.60600 |
Peptide ligand-binding receptors | 38 | 0.838000 | 0.982 | 0.0862 | -1.53e-02 | -0.070700 | -4.69e-02 | 0.871000 | 0.45100 | 0.61700 |
Meiotic synapsis | 24 | 0.838000 | 0.982 | 0.1090 | -1.33e-02 | -0.011900 | 1.07e-01 | 0.910000 | 0.92000 | 0.36300 |
Downstream signaling events of B Cell Receptor (BCR) | 67 | 0.838000 | 0.982 | 0.0646 | 2.65e-02 | -0.036600 | 4.62e-02 | 0.708000 | 0.60500 | 0.51400 |
Import of palmitoyl-CoA into the mitochondrial matrix | 11 | 0.839000 | 0.982 | 0.1590 | -6.82e-02 | 0.140000 | -3.49e-02 | 0.696000 | 0.42300 | 0.84100 |
Signaling by ERBB4 | 40 | 0.841000 | 0.982 | 0.0834 | -5.19e-02 | 0.059000 | 2.81e-02 | 0.570000 | 0.51900 | 0.75900 |
Ub-specific processing proteases | 144 | 0.841000 | 0.982 | 0.0444 | -2.91e-02 | 0.018100 | 2.82e-02 | 0.547000 | 0.70800 | 0.56000 |
RNA Polymerase I Transcription Initiation | 39 | 0.842000 | 0.982 | 0.0842 | 2.22e-02 | 0.063500 | 5.05e-02 | 0.810000 | 0.49300 | 0.58500 |
Synthesis of PIPs at the plasma membrane | 46 | 0.842000 | 0.982 | 0.0774 | -6.64e-02 | -0.028700 | -2.77e-02 | 0.436000 | 0.73600 | 0.74600 |
Amyloid fiber formation | 33 | 0.842000 | 0.982 | 0.0912 | -6.98e-02 | 0.058700 | 3.36e-03 | 0.488000 | 0.56000 | 0.97300 |
p75NTR signals via NF-kB | 14 | 0.843000 | 0.982 | 0.1410 | -5.37e-02 | 0.021600 | 1.29e-01 | 0.728000 | 0.88900 | 0.40400 |
Attenuation phase | 17 | 0.844000 | 0.982 | 0.1290 | 1.04e-01 | 0.031500 | -6.93e-02 | 0.459000 | 0.82200 | 0.62100 |
Cytokine Signaling in Immune system | 548 | 0.846000 | 0.982 | 0.0228 | 2.25e-02 | -0.003070 | -2.03e-03 | 0.373000 | 0.90300 | 0.93600 |
ERCC6 (CSB) and EHMT2 (G9a) positively regulate rRNA expression | 19 | 0.846000 | 0.982 | 0.1190 | -3.11e-02 | 0.088900 | -7.31e-02 | 0.814000 | 0.50200 | 0.58100 |
MET activates PTK2 signaling | 14 | 0.847000 | 0.982 | 0.1390 | 6.95e-02 | 0.104000 | 6.02e-02 | 0.653000 | 0.50100 | 0.69700 |
PCP/CE pathway | 74 | 0.847000 | 0.982 | 0.0608 | -6.34e-03 | -0.056600 | 2.11e-02 | 0.925000 | 0.40000 | 0.75400 |
MAPK6/MAPK4 signaling | 73 | 0.847000 | 0.982 | 0.0612 | -7.31e-03 | -0.013700 | 5.91e-02 | 0.914000 | 0.83900 | 0.38300 |
Inwardly rectifying K+ channels | 15 | 0.850000 | 0.982 | 0.1330 | 3.12e-02 | -0.107000 | 7.29e-02 | 0.834000 | 0.47500 | 0.62500 |
B-WICH complex positively regulates rRNA expression | 28 | 0.850000 | 0.982 | 0.0973 | 6.49e-03 | -0.092500 | -2.96e-02 | 0.953000 | 0.39700 | 0.78700 |
SMAD2/SMAD3:SMAD4 heterotrimer regulates transcription | 31 | 0.851000 | 0.982 | 0.0922 | 1.80e-02 | 0.017600 | 8.87e-02 | 0.862000 | 0.86500 | 0.39300 |
Formation of Senescence-Associated Heterochromatin Foci (SAHF) | 10 | 0.852000 | 0.982 | 0.1610 | 1.10e-01 | -0.100000 | 6.27e-02 | 0.549000 | 0.58400 | 0.73200 |
Signaling by high-kinase activity BRAF mutants | 27 | 0.853000 | 0.982 | 0.0983 | 7.60e-02 | 0.049000 | 3.86e-02 | 0.495000 | 0.65900 | 0.72900 |
Base-Excision Repair, AP Site Formation | 17 | 0.853000 | 0.982 | 0.1240 | -1.22e-01 | -0.014000 | -1.90e-02 | 0.386000 | 0.92000 | 0.89200 |
Nonhomologous End-Joining (NHEJ) | 32 | 0.854000 | 0.982 | 0.0910 | -4.72e-02 | 0.010200 | 7.71e-02 | 0.644000 | 0.92100 | 0.45100 |
Non-integrin membrane-ECM interactions | 33 | 0.854000 | 0.982 | 0.0879 | 6.20e-02 | -0.025900 | 5.66e-02 | 0.538000 | 0.79700 | 0.57400 |
TRAF3-dependent IRF activation pathway | 11 | 0.856000 | 0.982 | 0.1540 | 6.83e-02 | 0.136000 | -2.09e-02 | 0.695000 | 0.43400 | 0.90500 |
Ion transport by P-type ATPases | 36 | 0.857000 | 0.982 | 0.0839 | 3.40e-02 | 0.022400 | 7.33e-02 | 0.724000 | 0.81700 | 0.44700 |
RIPK1-mediated regulated necrosis | 14 | 0.857000 | 0.982 | 0.1360 | 2.76e-02 | 0.059300 | -1.19e-01 | 0.858000 | 0.70100 | 0.43900 |
Regulated Necrosis | 14 | 0.857000 | 0.982 | 0.1360 | 2.76e-02 | 0.059300 | -1.19e-01 | 0.858000 | 0.70100 | 0.43900 |
mRNA Splicing - Minor Pathway | 39 | 0.858000 | 0.982 | 0.0802 | 6.66e-02 | -0.028300 | 3.46e-02 | 0.472000 | 0.76000 | 0.70900 |
Collagen degradation | 18 | 0.858000 | 0.982 | 0.1190 | -2.10e-02 | -0.117000 | -1.27e-02 | 0.877000 | 0.39200 | 0.92500 |
FGFR2 alternative splicing | 20 | 0.858000 | 0.982 | 0.1130 | -2.12e-03 | -0.090200 | 6.84e-02 | 0.987000 | 0.48500 | 0.59700 |
NoRC negatively regulates rRNA expression | 39 | 0.859000 | 0.982 | 0.0814 | 5.58e-02 | -0.013100 | -5.78e-02 | 0.547000 | 0.88700 | 0.53200 |
EPH-ephrin mediated repulsion of cells | 31 | 0.859000 | 0.982 | 0.0913 | -3.57e-02 | -0.009480 | 8.35e-02 | 0.731000 | 0.92700 | 0.42200 |
Formation of tubulin folding intermediates by CCT/TriC | 16 | 0.860000 | 0.982 | 0.1250 | 2.43e-02 | -0.093800 | 7.94e-02 | 0.866000 | 0.51600 | 0.58200 |
Condensation of Prophase Chromosomes | 14 | 0.861000 | 0.982 | 0.1340 | 5.75e-02 | 0.093000 | 7.67e-02 | 0.710000 | 0.54700 | 0.62000 |
Fatty acid metabolism | 102 | 0.861000 | 0.982 | 0.0501 | -4.76e-02 | -0.006620 | 1.41e-02 | 0.407000 | 0.90800 | 0.80600 |
PI3K/AKT Signaling in Cancer | 65 | 0.863000 | 0.982 | 0.0619 | 2.83e-02 | -0.045100 | -3.17e-02 | 0.693000 | 0.53000 | 0.65900 |
Degradation of GLI1 by the proteasome | 50 | 0.864000 | 0.982 | 0.0698 | 3.20e-02 | -0.016000 | 6.00e-02 | 0.696000 | 0.84500 | 0.46400 |
DNA Replication | 97 | 0.864000 | 0.982 | 0.0507 | -2.92e-02 | -0.040900 | -6.75e-03 | 0.620000 | 0.48700 | 0.90900 |
IRAK2 mediated activation of TAK1 complex | 10 | 0.865000 | 0.982 | 0.1550 | 9.04e-02 | -0.031100 | 1.22e-01 | 0.621000 | 0.86500 | 0.50500 |
Selenocysteine synthesis | 63 | 0.870000 | 0.982 | 0.0622 | -4.52e-02 | 0.008510 | 4.19e-02 | 0.536000 | 0.90700 | 0.56500 |
Assembly of the pre-replicative complex | 53 | 0.870000 | 0.982 | 0.0667 | 2.45e-02 | -0.048500 | 3.86e-02 | 0.757000 | 0.54200 | 0.62700 |
Post-translational modification: synthesis of GPI-anchored proteins | 41 | 0.873000 | 0.982 | 0.0752 | 2.34e-02 | -0.053900 | 4.69e-02 | 0.796000 | 0.55100 | 0.60300 |
Cooperation of PDCL (PhLP1) and TRiC/CCT in G-protein beta folding | 26 | 0.875000 | 0.982 | 0.0953 | 6.68e-02 | 0.064000 | -2.30e-02 | 0.556000 | 0.57300 | 0.83900 |
APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins in late mitosis/early G1 | 57 | 0.875000 | 0.982 | 0.0641 | -5.07e-02 | -0.039200 | 1.40e-03 | 0.509000 | 0.60900 | 0.98500 |
Scavenging by Class A Receptors | 11 | 0.875000 | 0.982 | 0.1450 | -1.41e-01 | 0.030100 | 1.53e-02 | 0.419000 | 0.86300 | 0.93000 |
Influenza Life Cycle | 105 | 0.876000 | 0.982 | 0.0466 | 1.36e-02 | -0.004820 | 4.43e-02 | 0.810000 | 0.93200 | 0.43400 |
Downregulation of TGF-beta receptor signaling | 25 | 0.876000 | 0.982 | 0.0960 | -2.45e-02 | -0.092800 | 2.78e-03 | 0.832000 | 0.42200 | 0.98100 |
Gene expression (Transcription) | 1109 | 0.877000 | 0.982 | 0.0149 | 1.26e-02 | -0.006830 | 3.78e-03 | 0.486000 | 0.70600 | 0.83500 |
G1/S Transition | 100 | 0.878000 | 0.982 | 0.0478 | -8.91e-03 | -0.046700 | -4.62e-03 | 0.878000 | 0.42000 | 0.93600 |
Rab regulation of trafficking | 102 | 0.879000 | 0.982 | 0.0470 | 1.68e-02 | -0.038800 | 2.03e-02 | 0.769000 | 0.49900 | 0.72300 |
alpha-linolenic (omega3) and linoleic (omega6) acid metabolism | 10 | 0.880000 | 0.982 | 0.1490 | 2.18e-02 | -0.103000 | -1.06e-01 | 0.905000 | 0.57400 | 0.56100 |
alpha-linolenic acid (ALA) metabolism | 10 | 0.880000 | 0.982 | 0.1490 | 2.18e-02 | -0.103000 | -1.06e-01 | 0.905000 | 0.57400 | 0.56100 |
Apoptotic factor-mediated response | 16 | 0.881000 | 0.982 | 0.1170 | 8.59e-02 | -0.079100 | 1.06e-02 | 0.552000 | 0.58400 | 0.94200 |
TRAF6 mediated NF-kB activation | 18 | 0.881000 | 0.982 | 0.1120 | 1.06e-01 | -0.008810 | -3.57e-02 | 0.438000 | 0.94800 | 0.79300 |
Alpha-protein kinase 1 signaling pathway | 11 | 0.882000 | 0.982 | 0.1410 | -1.20e-01 | -0.056100 | -4.79e-02 | 0.490000 | 0.74700 | 0.78300 |
Translesion synthesis by POLK | 17 | 0.883000 | 0.982 | 0.1130 | -8.18e-02 | 0.077500 | 8.38e-03 | 0.559000 | 0.58000 | 0.95200 |
TICAM1, RIP1-mediated IKK complex recruitment | 18 | 0.884000 | 0.982 | 0.1110 | 6.56e-02 | 0.006230 | -8.96e-02 | 0.630000 | 0.96400 | 0.51100 |
RHO GTPases Activate Formins | 83 | 0.884000 | 0.982 | 0.0519 | -3.46e-02 | -0.034400 | 1.78e-02 | 0.587000 | 0.58800 | 0.78000 |
E2F mediated regulation of DNA replication | 17 | 0.884000 | 0.982 | 0.1140 | 2.73e-02 | -0.018000 | -1.09e-01 | 0.845000 | 0.89800 | 0.43700 |
Deregulated CDK5 triggers multiple neurodegenerative pathways in Alzheimer’s disease models | 17 | 0.885000 | 0.982 | 0.1120 | 6.10e-02 | -0.057500 | 7.43e-02 | 0.663000 | 0.68100 | 0.59600 |
Neurodegenerative Diseases | 17 | 0.885000 | 0.982 | 0.1120 | 6.10e-02 | -0.057500 | 7.43e-02 | 0.663000 | 0.68100 | 0.59600 |
SCF-beta-TrCP mediated degradation of Emi1 | 46 | 0.885000 | 0.982 | 0.0684 | 2.95e-02 | -0.057800 | 2.17e-02 | 0.729000 | 0.49800 | 0.79900 |
Regulation of RAS by GAPs | 58 | 0.886000 | 0.982 | 0.0607 | 2.42e-02 | -0.047800 | 2.86e-02 | 0.750000 | 0.53000 | 0.70700 |
Signaling by SCF-KIT | 34 | 0.886000 | 0.982 | 0.0795 | -2.67e-03 | -0.074800 | -2.68e-02 | 0.979000 | 0.45100 | 0.78700 |
Defective B4GALT7 causes EDS, progeroid type | 12 | 0.888000 | 0.982 | 0.1330 | 1.02e-01 | -0.084600 | -6.10e-03 | 0.541000 | 0.61200 | 0.97100 |
Keratan sulfate biosynthesis | 18 | 0.889000 | 0.982 | 0.1090 | -6.86e-02 | 0.005720 | 8.47e-02 | 0.614000 | 0.96700 | 0.53400 |
Deposition of new CENPA-containing nucleosomes at the centromere | 18 | 0.890000 | 0.982 | 0.1080 | 3.46e-02 | -0.092400 | -4.30e-02 | 0.799000 | 0.49700 | 0.75200 |
Nucleosome assembly | 18 | 0.890000 | 0.982 | 0.1080 | 3.46e-02 | -0.092400 | -4.30e-02 | 0.799000 | 0.49700 | 0.75200 |
Ovarian tumor domain proteases | 33 | 0.890000 | 0.982 | 0.0802 | -6.89e-02 | 0.011600 | 3.94e-02 | 0.494000 | 0.90800 | 0.69500 |
EGFR downregulation | 25 | 0.893000 | 0.982 | 0.0896 | 6.74e-02 | -0.040600 | 4.29e-02 | 0.560000 | 0.72600 | 0.71100 |
HSF1-dependent transactivation | 26 | 0.893000 | 0.982 | 0.0899 | 6.28e-02 | 0.041600 | -4.90e-02 | 0.579000 | 0.71400 | 0.66600 |
RHO GTPases Activate ROCKs | 19 | 0.893000 | 0.982 | 0.1040 | 9.17e-03 | -0.013200 | 1.02e-01 | 0.945000 | 0.92100 | 0.44000 |
Cleavage of the damaged pyrimidine | 15 | 0.896000 | 0.982 | 0.1150 | -1.10e-01 | -0.029200 | -2.00e-02 | 0.461000 | 0.84500 | 0.89300 |
Depyrimidination | 15 | 0.896000 | 0.982 | 0.1150 | -1.10e-01 | -0.029200 | -2.00e-02 | 0.461000 | 0.84500 | 0.89300 |
Recognition and association of DNA glycosylase with site containing an affected pyrimidine | 15 | 0.896000 | 0.982 | 0.1150 | -1.10e-01 | -0.029200 | -2.00e-02 | 0.461000 | 0.84500 | 0.89300 |
Regulation of RUNX3 expression and activity | 46 | 0.898000 | 0.982 | 0.0657 | 2.37e-02 | -0.052500 | -3.16e-02 | 0.781000 | 0.53800 | 0.71100 |
Autodegradation of the E3 ubiquitin ligase COP1 | 44 | 0.898000 | 0.982 | 0.0675 | -1.13e-02 | -0.063800 | 1.88e-02 | 0.897000 | 0.46400 | 0.82900 |
Integration of energy metabolism | 75 | 0.898000 | 0.982 | 0.0511 | 2.33e-02 | 0.014900 | 4.30e-02 | 0.728000 | 0.82400 | 0.52000 |
DNA Replication Pre-Initiation | 63 | 0.898000 | 0.982 | 0.0562 | -1.86e-03 | -0.056000 | -3.21e-03 | 0.980000 | 0.44200 | 0.96500 |
Metabolic disorders of biological oxidation enzymes | 17 | 0.898000 | 0.982 | 0.1080 | 1.02e-01 | -0.024600 | -2.33e-02 | 0.465000 | 0.86000 | 0.86800 |
Initiation of Nuclear Envelope Reformation | 12 | 0.899000 | 0.982 | 0.1280 | 2.16e-02 | -0.110000 | 6.16e-02 | 0.897000 | 0.51000 | 0.71200 |
Nuclear Envelope Reassembly | 12 | 0.899000 | 0.982 | 0.1280 | 2.16e-02 | -0.110000 | 6.16e-02 | 0.897000 | 0.51000 | 0.71200 |
Translation | 219 | 0.903000 | 0.982 | 0.0295 | 2.55e-02 | 0.001340 | 1.49e-02 | 0.518000 | 0.97300 | 0.70500 |
Generation of second messenger molecules | 18 | 0.904000 | 0.982 | 0.1020 | 9.78e-02 | 0.008420 | 2.73e-02 | 0.473000 | 0.95100 | 0.84100 |
G1/S DNA Damage Checkpoints | 54 | 0.905000 | 0.982 | 0.0596 | -3.66e-02 | -0.044500 | 1.53e-02 | 0.642000 | 0.57200 | 0.84600 |
Translation initiation complex formation | 43 | 0.905000 | 0.982 | 0.0659 | 5.51e-03 | 0.016800 | 6.35e-02 | 0.950000 | 0.84900 | 0.47100 |
Paradoxical activation of RAF signaling by kinase inactive BRAF | 36 | 0.905000 | 0.982 | 0.0717 | 6.11e-02 | 0.016800 | 3.35e-02 | 0.526000 | 0.86100 | 0.72800 |
Signaling by RAS mutants | 36 | 0.905000 | 0.982 | 0.0717 | 6.11e-02 | 0.016800 | 3.35e-02 | 0.526000 | 0.86100 | 0.72800 |
Signaling by moderate kinase activity BRAF mutants | 36 | 0.905000 | 0.982 | 0.0717 | 6.11e-02 | 0.016800 | 3.35e-02 | 0.526000 | 0.86100 | 0.72800 |
Signaling downstream of RAS mutants | 36 | 0.905000 | 0.982 | 0.0717 | 6.11e-02 | 0.016800 | 3.35e-02 | 0.526000 | 0.86100 | 0.72800 |
MAP2K and MAPK activation | 30 | 0.906000 | 0.982 | 0.0791 | 2.88e-02 | 0.071900 | 1.57e-02 | 0.785000 | 0.49500 | 0.88200 |
RUNX1 regulates genes involved in megakaryocyte differentiation and platelet function | 33 | 0.906000 | 0.982 | 0.0746 | 5.11e-02 | 0.033600 | 4.28e-02 | 0.612000 | 0.73900 | 0.67000 |
Clathrin-mediated endocytosis | 110 | 0.908000 | 0.982 | 0.0406 | 1.86e-02 | 0.007530 | 3.53e-02 | 0.736000 | 0.89200 | 0.52300 |
Translesion synthesis by Y family DNA polymerases bypasses lesions on DNA template | 34 | 0.908000 | 0.982 | 0.0727 | -5.67e-02 | 0.038600 | -2.43e-02 | 0.568000 | 0.69700 | 0.80600 |
Gap-filling DNA repair synthesis and ligation in TC-NER | 54 | 0.909000 | 0.982 | 0.0576 | 3.59e-02 | -0.035800 | 2.74e-02 | 0.648000 | 0.64900 | 0.72800 |
NF-kB activation through FADD/RIP-1 pathway mediated by caspase-8 and -10 | 12 | 0.909000 | 0.982 | 0.1220 | 1.16e-01 | 0.010700 | 3.63e-02 | 0.485000 | 0.94900 | 0.82800 |
Signaling by PDGF | 44 | 0.910000 | 0.982 | 0.0639 | 2.32e-02 | -0.059300 | -5.28e-03 | 0.790000 | 0.49600 | 0.95200 |
RNA polymerase II transcribes snRNA genes | 62 | 0.910000 | 0.982 | 0.0537 | 2.84e-02 | -0.039200 | 2.32e-02 | 0.700000 | 0.59400 | 0.75200 |
Influenza Viral RNA Transcription and Replication | 98 | 0.910000 | 0.982 | 0.0430 | 4.97e-03 | -0.016200 | 3.95e-02 | 0.932000 | 0.78200 | 0.50000 |
Stimuli-sensing channels | 52 | 0.912000 | 0.982 | 0.0586 | 3.22e-02 | 0.048700 | 5.00e-03 | 0.688000 | 0.54400 | 0.95000 |
APC:Cdc20 mediated degradation of cell cycle proteins prior to satisfation of the cell cycle checkpoint | 57 | 0.912000 | 0.982 | 0.0562 | -3.47e-02 | -0.042500 | 1.24e-02 | 0.651000 | 0.57900 | 0.87200 |
Cdc20:Phospho-APC/C mediated degradation of Cyclin A | 57 | 0.912000 | 0.982 | 0.0562 | -3.47e-02 | -0.042500 | 1.24e-02 | 0.651000 | 0.57900 | 0.87200 |
UCH proteinases | 75 | 0.913000 | 0.982 | 0.0488 | -2.51e-02 | 0.004080 | 4.17e-02 | 0.707000 | 0.95100 | 0.53300 |
TP53 regulates transcription of several additional cell death genes whose specific roles in p53-dependent apoptosis remain uncertain | 11 | 0.914000 | 0.982 | 0.1260 | 1.11e-01 | -0.043100 | -4.21e-02 | 0.524000 | 0.80500 | 0.80900 |
Transcriptional regulation by RUNX2 | 96 | 0.914000 | 0.982 | 0.0427 | 9.32e-04 | 0.003980 | 4.25e-02 | 0.987000 | 0.94600 | 0.47200 |
Macroautophagy | 76 | 0.916000 | 0.982 | 0.0476 | 4.14e-03 | -0.031300 | 3.57e-02 | 0.950000 | 0.63800 | 0.59100 |
Phosphorylation of the APC/C | 16 | 0.916000 | 0.982 | 0.1030 | -6.86e-02 | 0.076300 | 9.19e-03 | 0.635000 | 0.59800 | 0.94900 |
Resolution of AP sites via the multiple-nucleotide patch replacement pathway | 22 | 0.917000 | 0.982 | 0.0876 | 3.11e-02 | -0.077400 | 2.66e-02 | 0.801000 | 0.53000 | 0.82900 |
Mitophagy | 23 | 0.917000 | 0.982 | 0.0857 | 3.68e-02 | -0.072600 | -2.68e-02 | 0.760000 | 0.54700 | 0.82400 |
Glycolysis | 58 | 0.917000 | 0.982 | 0.0544 | 4.34e-02 | -0.015900 | -2.87e-02 | 0.568000 | 0.83400 | 0.70500 |
Signaling by EGFR | 41 | 0.918000 | 0.982 | 0.0641 | 5.55e-02 | 0.025700 | 1.92e-02 | 0.539000 | 0.77600 | 0.83100 |
Host Interactions of HIV factors | 109 | 0.918000 | 0.982 | 0.0398 | -2.14e-02 | -0.031800 | 1.09e-02 | 0.700000 | 0.56700 | 0.84400 |
Regulation of cholesterol biosynthesis by SREBP (SREBF) | 49 | 0.921000 | 0.982 | 0.0577 | 2.86e-03 | -0.030700 | -4.87e-02 | 0.972000 | 0.71000 | 0.55600 |
COPI-mediated anterograde transport | 70 | 0.922000 | 0.982 | 0.0483 | 4.70e-02 | 0.011000 | -1.26e-03 | 0.497000 | 0.87300 | 0.98500 |
TRAF6-mediated induction of TAK1 complex within TLR4 complex | 14 | 0.923000 | 0.982 | 0.1060 | 9.10e-02 | -0.047100 | 2.74e-02 | 0.555000 | 0.76000 | 0.85900 |
FBXL7 down-regulates AURKA during mitotic entry and in early mitosis | 46 | 0.924000 | 0.982 | 0.0583 | 4.04e-02 | -0.033300 | 2.59e-02 | 0.636000 | 0.69700 | 0.76200 |
SCF(Skp2)-mediated degradation of p27/p21 | 47 | 0.924000 | 0.982 | 0.0583 | -4.27e-02 | -0.037400 | -1.31e-02 | 0.612000 | 0.65800 | 0.87700 |
APC/C:Cdc20 mediated degradation of Securin | 55 | 0.925000 | 0.982 | 0.0543 | -4.51e-02 | -0.024000 | 1.82e-02 | 0.563000 | 0.75800 | 0.81500 |
Regulation of insulin secretion | 49 | 0.925000 | 0.982 | 0.0563 | 2.63e-02 | 0.025900 | 4.25e-02 | 0.750000 | 0.75400 | 0.60700 |
APC/C-mediated degradation of cell cycle proteins | 65 | 0.925000 | 0.982 | 0.0492 | 4.37e-03 | -0.041300 | 2.64e-02 | 0.951000 | 0.56500 | 0.71300 |
Regulation of mitotic cell cycle | 65 | 0.925000 | 0.982 | 0.0492 | 4.37e-03 | -0.041300 | 2.64e-02 | 0.951000 | 0.56500 | 0.71300 |
Negative regulation of NOTCH4 signaling | 48 | 0.926000 | 0.982 | 0.0577 | -2.71e-02 | -0.045400 | 2.30e-02 | 0.746000 | 0.58600 | 0.78300 |
Collagen chain trimerization | 28 | 0.927000 | 0.982 | 0.0742 | -2.61e-03 | 0.072300 | 1.68e-02 | 0.981000 | 0.50800 | 0.87800 |
Synthesis of PIPs at the late endosome membrane | 11 | 0.927000 | 0.982 | 0.1180 | -8.72e-03 | 0.082700 | 8.39e-02 | 0.960000 | 0.63500 | 0.63000 |
IKK complex recruitment mediated by RIP1 | 20 | 0.929000 | 0.982 | 0.0877 | 4.75e-02 | -0.010600 | -7.30e-02 | 0.713000 | 0.93400 | 0.57200 |
Transcription-Coupled Nucleotide Excision Repair (TC-NER) | 67 | 0.929000 | 0.982 | 0.0471 | 3.65e-02 | -0.007240 | 2.88e-02 | 0.605000 | 0.91900 | 0.68400 |
AUF1 (hnRNP D0) binds and destabilizes mRNA | 46 | 0.930000 | 0.982 | 0.0571 | 2.53e-03 | -0.041800 | 3.89e-02 | 0.976000 | 0.62400 | 0.64900 |
Activation of BH3-only proteins | 24 | 0.930000 | 0.982 | 0.0789 | -3.88e-02 | -0.065400 | -2.11e-02 | 0.742000 | 0.57900 | 0.85800 |
RNA Pol II CTD phosphorylation and interaction with CE | 20 | 0.930000 | 0.982 | 0.0862 | -7.65e-03 | 0.077100 | 3.77e-02 | 0.953000 | 0.55000 | 0.77100 |
RNA Pol II CTD phosphorylation and interaction with CE during HIV infection | 20 | 0.930000 | 0.982 | 0.0862 | -7.65e-03 | 0.077100 | 3.77e-02 | 0.953000 | 0.55000 | 0.77100 |
TICAM1,TRAF6-dependent induction of TAK1 complex | 11 | 0.932000 | 0.982 | 0.1160 | 7.42e-02 | -0.059500 | -6.59e-02 | 0.670000 | 0.73300 | 0.70500 |
Regulation of mRNA stability by proteins that bind AU-rich elements | 75 | 0.933000 | 0.982 | 0.0441 | 4.01e-03 | -0.043500 | -6.04e-03 | 0.952000 | 0.51600 | 0.92800 |
Defective CFTR causes cystic fibrosis | 49 | 0.933000 | 0.982 | 0.0543 | -5.33e-02 | 0.010600 | 1.44e-03 | 0.519000 | 0.89700 | 0.98600 |
Oxygen-dependent proline hydroxylation of Hypoxia-inducible Factor Alpha | 55 | 0.933000 | 0.982 | 0.0518 | -4.51e-02 | -0.002480 | 2.53e-02 | 0.563000 | 0.97500 | 0.74600 |
eNOS activation | 11 | 0.935000 | 0.982 | 0.1130 | 3.62e-02 | -0.107000 | 7.77e-03 | 0.835000 | 0.53800 | 0.96400 |
CD28 dependent PI3K/Akt signaling | 14 | 0.935000 | 0.982 | 0.1000 | 6.79e-02 | -0.072900 | 1.09e-02 | 0.660000 | 0.63700 | 0.94400 |
Glycosphingolipid metabolism | 33 | 0.935000 | 0.982 | 0.0654 | 4.20e-02 | -0.045700 | -2.08e-02 | 0.677000 | 0.65000 | 0.83700 |
Activation of the pre-replicative complex | 21 | 0.935000 | 0.982 | 0.0819 | 2.51e-02 | -0.067000 | -3.98e-02 | 0.842000 | 0.59500 | 0.75200 |
Vpu mediated degradation of CD4 | 44 | 0.936000 | 0.982 | 0.0564 | 1.35e-02 | -0.052700 | 1.49e-02 | 0.877000 | 0.54500 | 0.86500 |
PIWI-interacting RNA (piRNA) biogenesis | 15 | 0.937000 | 0.982 | 0.0961 | -2.67e-02 | 0.081200 | 4.40e-02 | 0.858000 | 0.58600 | 0.76800 |
Metabolism of proteins | 1398 | 0.939000 | 0.982 | 0.0105 | -9.99e-03 | -0.002530 | 1.89e-03 | 0.541000 | 0.87700 | 0.90800 |
Cellular response to hypoxia | 60 | 0.940000 | 0.982 | 0.0475 | -4.71e-02 | -0.005240 | 2.58e-03 | 0.528000 | 0.94400 | 0.97200 |
Intra-Golgi traffic | 35 | 0.940000 | 0.982 | 0.0622 | 1.65e-02 | -0.001640 | -5.99e-02 | 0.866000 | 0.98700 | 0.54000 |
Dectin-1 mediated noncanonical NF-kB signaling | 51 | 0.941000 | 0.982 | 0.0506 | 3.21e-02 | -0.039000 | 4.00e-03 | 0.692000 | 0.63000 | 0.96100 |
Activation of NF-kappaB in B cells | 54 | 0.942000 | 0.982 | 0.0495 | 3.53e-02 | -0.024400 | -2.47e-02 | 0.654000 | 0.75600 | 0.75400 |
Selenoamino acid metabolism | 82 | 0.943000 | 0.982 | 0.0397 | 3.69e-02 | -0.013800 | -4.63e-03 | 0.564000 | 0.82900 | 0.94200 |
Activation of APC/C and APC/C:Cdc20 mediated degradation of mitotic proteins | 59 | 0.943000 | 0.982 | 0.0471 | -2.01e-02 | -0.040000 | 1.46e-02 | 0.790000 | 0.59600 | 0.84600 |
Inactivation of APC/C via direct inhibition of the APC/C complex | 16 | 0.944000 | 0.982 | 0.0885 | -8.64e-02 | 0.003590 | -1.92e-02 | 0.550000 | 0.98000 | 0.89400 |
Inhibition of the proteolytic activity of APC/C required for the onset of anaphase by mitotic spindle checkpoint components | 16 | 0.944000 | 0.982 | 0.0885 | -8.64e-02 | 0.003590 | -1.92e-02 | 0.550000 | 0.98000 | 0.89400 |
Intrinsic Pathway of Fibrin Clot Formation | 11 | 0.945000 | 0.982 | 0.1070 | 4.00e-02 | -0.097200 | -1.88e-02 | 0.818000 | 0.57700 | 0.91400 |
Gluconeogenesis | 22 | 0.945000 | 0.982 | 0.0754 | -2.92e-02 | 0.069500 | 1.26e-03 | 0.813000 | 0.57300 | 0.99200 |
Resolution of Abasic Sites (AP sites) | 35 | 0.945000 | 0.982 | 0.0598 | 3.61e-02 | -0.046700 | -9.40e-03 | 0.712000 | 0.63300 | 0.92300 |
Base Excision Repair | 42 | 0.946000 | 0.982 | 0.0544 | -3.36e-04 | -0.044100 | -3.19e-02 | 0.997000 | 0.62100 | 0.72100 |
Formation of Fibrin Clot (Clotting Cascade) | 17 | 0.947000 | 0.982 | 0.0849 | -1.48e-02 | 0.067400 | -4.95e-02 | 0.916000 | 0.63100 | 0.72400 |
A tetrasaccharide linker sequence is required for GAG synthesis | 15 | 0.947000 | 0.982 | 0.0909 | -1.22e-02 | -0.075700 | 4.89e-02 | 0.935000 | 0.61200 | 0.74300 |
Regulation of APC/C activators between G1/S and early anaphase | 64 | 0.948000 | 0.982 | 0.0435 | 1.19e-02 | -0.039700 | 1.33e-02 | 0.869000 | 0.58300 | 0.85400 |
Regulation of localization of FOXO transcription factors | 11 | 0.948000 | 0.982 | 0.1060 | 4.98e-02 | 0.068300 | -6.43e-02 | 0.775000 | 0.69500 | 0.71200 |
Cristae formation | 10 | 0.949000 | 0.982 | 0.1100 | -1.05e-01 | 0.004380 | 3.05e-02 | 0.564000 | 0.98100 | 0.86800 |
Synthesis of very long-chain fatty acyl-CoAs | 12 | 0.949000 | 0.982 | 0.0998 | 8.69e-02 | -0.032300 | -3.69e-02 | 0.602000 | 0.84600 | 0.82500 |
Autodegradation of Cdh1 by Cdh1:APC/C | 55 | 0.950000 | 0.982 | 0.0466 | -3.84e-02 | -0.026400 | -1.00e-04 | 0.622000 | 0.73500 | 0.99900 |
Antigen processing: Ubiquitination & Proteasome degradation | 258 | 0.950000 | 0.982 | 0.0215 | 1.48e-02 | -0.012800 | -9.05e-03 | 0.684000 | 0.72400 | 0.80300 |
Mitochondrial Fatty Acid Beta-Oxidation | 27 | 0.951000 | 0.982 | 0.0654 | -4.43e-02 | 0.042300 | 2.28e-02 | 0.690000 | 0.70400 | 0.83800 |
Intra-Golgi and retrograde Golgi-to-ER traffic | 143 | 0.952000 | 0.982 | 0.0282 | 2.30e-02 | -0.014900 | 6.37e-03 | 0.635000 | 0.75900 | 0.89600 |
Switching of origins to a post-replicative state | 70 | 0.952000 | 0.982 | 0.0406 | -9.26e-03 | -0.032900 | 2.19e-02 | 0.894000 | 0.63400 | 0.75200 |
RUNX2 regulates bone development | 26 | 0.952000 | 0.982 | 0.0660 | -4.71e-02 | 0.041200 | 2.08e-02 | 0.678000 | 0.71600 | 0.85400 |
Cross-presentation of soluble exogenous antigens (endosomes) | 39 | 0.953000 | 0.982 | 0.0540 | -3.20e-03 | -0.053800 | 3.31e-03 | 0.972000 | 0.56200 | 0.97100 |
Metabolism of amino acids and derivatives | 249 | 0.953000 | 0.982 | 0.0216 | 1.92e-02 | 0.005600 | -8.23e-03 | 0.603000 | 0.88000 | 0.82400 |
DARPP-32 events | 21 | 0.953000 | 0.982 | 0.0735 | -6.99e-02 | 0.006180 | 2.18e-02 | 0.579000 | 0.96100 | 0.86300 |
Glutamate Neurotransmitter Release Cycle | 14 | 0.955000 | 0.982 | 0.0893 | -6.74e-02 | -0.054900 | 2.03e-02 | 0.662000 | 0.72200 | 0.89600 |
Oncogenic MAPK signaling | 58 | 0.955000 | 0.982 | 0.0433 | -4.43e-03 | 0.031000 | -2.99e-02 | 0.953000 | 0.68300 | 0.69400 |
AKT phosphorylates targets in the cytosol | 13 | 0.955000 | 0.982 | 0.0903 | -5.35e-02 | 0.032200 | -6.53e-02 | 0.739000 | 0.84100 | 0.68400 |
Signaling by Activin | 12 | 0.956000 | 0.982 | 0.0939 | -8.17e-02 | 0.039100 | -2.48e-02 | 0.624000 | 0.81500 | 0.88200 |
RHO GTPases activate PKNs | 33 | 0.957000 | 0.982 | 0.0569 | -5.02e-03 | -0.024800 | 5.10e-02 | 0.960000 | 0.80600 | 0.61200 |
APC/C:Cdc20 mediated degradation of mitotic proteins | 58 | 0.957000 | 0.982 | 0.0431 | -1.72e-02 | -0.034700 | 1.88e-02 | 0.820000 | 0.64800 | 0.80400 |
Asymmetric localization of PCP proteins | 53 | 0.957000 | 0.982 | 0.0445 | 1.83e-02 | -0.039100 | -1.09e-02 | 0.818000 | 0.62300 | 0.89100 |
Fc epsilon receptor (FCERI) signaling | 109 | 0.958000 | 0.982 | 0.0311 | -5.17e-03 | -0.030700 | -3.44e-04 | 0.926000 | 0.58100 | 0.99500 |
Intrinsic Pathway for Apoptosis | 44 | 0.958000 | 0.982 | 0.0487 | 7.32e-03 | -0.046900 | 1.08e-02 | 0.933000 | 0.59100 | 0.90200 |
Degradation of AXIN | 46 | 0.958000 | 0.982 | 0.0475 | -7.03e-03 | -0.041400 | -2.23e-02 | 0.934000 | 0.62800 | 0.79400 |
Signaling by BRAF and RAF fusions | 54 | 0.959000 | 0.982 | 0.0433 | -1.90e-02 | 0.016600 | -3.52e-02 | 0.810000 | 0.83300 | 0.65400 |
Regulation of PTEN stability and activity | 58 | 0.959000 | 0.982 | 0.0415 | -3.72e-02 | 0.000859 | -1.85e-02 | 0.625000 | 0.99100 | 0.80700 |
mRNA Capping | 22 | 0.960000 | 0.982 | 0.0675 | 9.76e-03 | 0.056300 | 3.60e-02 | 0.937000 | 0.64800 | 0.77000 |
WNT5A-dependent internalization of FZD4 | 12 | 0.960000 | 0.982 | 0.0907 | 2.83e-02 | 0.041500 | 7.55e-02 | 0.865000 | 0.80400 | 0.65100 |
Acyl chain remodelling of PC | 13 | 0.961000 | 0.982 | 0.0872 | -5.95e-02 | 0.055500 | 3.14e-02 | 0.710000 | 0.72900 | 0.84500 |
Syndecan interactions | 15 | 0.962000 | 0.982 | 0.0807 | 1.84e-02 | 0.046900 | -6.30e-02 | 0.902000 | 0.75300 | 0.67300 |
PI-3K cascade:FGFR1 | 11 | 0.963000 | 0.982 | 0.0929 | 9.26e-02 | 0.005550 | -3.49e-03 | 0.595000 | 0.97500 | 0.98400 |
Positive epigenetic regulation of rRNA expression | 43 | 0.965000 | 0.982 | 0.0461 | -1.44e-02 | -0.036600 | -2.41e-02 | 0.870000 | 0.67900 | 0.78500 |
Ras activation upon Ca2+ influx through NMDA receptor | 15 | 0.965000 | 0.982 | 0.0769 | -4.46e-02 | -0.004980 | -6.25e-02 | 0.765000 | 0.97300 | 0.67500 |
Miscellaneous transport and binding events | 19 | 0.965000 | 0.982 | 0.0692 | -4.77e-02 | -0.049700 | -6.12e-03 | 0.719000 | 0.70800 | 0.96300 |
Glucose metabolism | 72 | 0.967000 | 0.982 | 0.0351 | 1.55e-02 | -0.022800 | -2.19e-02 | 0.821000 | 0.73900 | 0.74900 |
Stabilization of p53 | 47 | 0.967000 | 0.982 | 0.0434 | -1.62e-02 | -0.037300 | 1.53e-02 | 0.848000 | 0.65900 | 0.85600 |
Termination of translesion DNA synthesis | 27 | 0.968000 | 0.982 | 0.0561 | -2.25e-02 | -0.007530 | -5.09e-02 | 0.840000 | 0.94600 | 0.64700 |
Constitutive Signaling by Aberrant PI3K in Cancer | 41 | 0.968000 | 0.982 | 0.0462 | 4.27e-02 | 0.012400 | -1.24e-02 | 0.636000 | 0.89100 | 0.89000 |
Synthesis of PIPs at the Golgi membrane | 15 | 0.968000 | 0.982 | 0.0753 | 1.77e-02 | -0.014100 | 7.18e-02 | 0.905000 | 0.92500 | 0.63000 |
Transcriptional activity of SMAD2/SMAD3:SMAD4 heterotrimer | 43 | 0.969000 | 0.982 | 0.0447 | -2.47e-02 | -0.012500 | 3.51e-02 | 0.779000 | 0.88800 | 0.69100 |
p53-Dependent G1 DNA Damage Response | 52 | 0.972000 | 0.983 | 0.0391 | -1.79e-02 | -0.034700 | -1.87e-03 | 0.824000 | 0.66600 | 0.98100 |
p53-Dependent G1/S DNA damage checkpoint | 52 | 0.972000 | 0.983 | 0.0391 | -1.79e-02 | -0.034700 | -1.87e-03 | 0.824000 | 0.66600 | 0.98100 |
Amino acid transport across the plasma membrane | 21 | 0.973000 | 0.983 | 0.0609 | 3.37e-02 | 0.019500 | -4.69e-02 | 0.790000 | 0.87700 | 0.71000 |
Autophagy | 94 | 0.973000 | 0.983 | 0.0287 | -8.75e-03 | -0.024000 | 1.31e-02 | 0.884000 | 0.68800 | 0.82700 |
PI Metabolism | 71 | 0.974000 | 0.983 | 0.0320 | -2.00e-02 | 0.024900 | -1.38e-03 | 0.771000 | 0.71700 | 0.98400 |
Class I MHC mediated antigen processing & presentation | 300 | 0.979000 | 0.988 | 0.0146 | 1.45e-02 | -0.001600 | 9.94e-04 | 0.667000 | 0.96200 | 0.97600 |
Glycogen metabolism | 24 | 0.981000 | 0.989 | 0.0492 | -4.66e-02 | -0.001090 | -1.57e-02 | 0.693000 | 0.99300 | 0.89400 |
IRAK2 mediated activation of TAK1 complex upon TLR7/8 or 9 stimulation | 13 | 0.983000 | 0.990 | 0.0643 | 3.91e-02 | -0.050700 | -5.65e-03 | 0.807000 | 0.75200 | 0.97200 |
FOXO-mediated transcription of cell death genes | 12 | 0.984000 | 0.990 | 0.0666 | 7.80e-03 | 0.034400 | -5.65e-02 | 0.963000 | 0.83700 | 0.73500 |
Regulation of expression of SLITs and ROBOs | 121 | 0.985000 | 0.990 | 0.0206 | 4.74e-04 | -0.005610 | 1.98e-02 | 0.993000 | 0.91500 | 0.70700 |
Metabolism of folate and pterines | 13 | 0.986000 | 0.990 | 0.0619 | 4.59e-02 | 0.025000 | -3.32e-02 | 0.775000 | 0.87600 | 0.83600 |
L1CAM interactions | 69 | 0.989000 | 0.992 | 0.0246 | -1.65e-02 | 0.012600 | 1.32e-02 | 0.813000 | 0.85600 | 0.85000 |
Global Genome Nucleotide Excision Repair (GG-NER) | 75 | 0.990000 | 0.992 | 0.0229 | -1.45e-02 | 0.016300 | 6.94e-03 | 0.829000 | 0.80700 | 0.91700 |
ABC-family proteins mediated transport | 79 | 0.995000 | 0.996 | 0.0177 | -6.29e-03 | 0.008380 | -1.42e-02 | 0.923000 | 0.89800 | 0.82700 |
Metabolism of RNA | 534 | 0.998000 | 0.998 | 0.0049 | -2.64e-03 | -0.003850 | 1.50e-03 | 0.918000 | 0.88000 | 0.95300 |
Pink/Parkin Mediated Mitophagy | 17 | 0.998000 | 0.998 | 0.0264 | 1.74e-02 | -0.016800 | -1.06e-02 | 0.901000 | 0.90500 | 0.94000 |
Signaling by NOTCH3
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TP53 Regulates Transcription of Genes Involved in G2 Cell Cycle Arrest
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Visual phototransduction
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Protein methylation
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GPCR ligand binding
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Here is the session info with all the versions of packages used.
sessionInfo()
## R version 4.3.3 (2024-02-29)
## Platform: x86_64-pc-linux-gnu (64-bit)
## Running under: Ubuntu 22.04.4 LTS
##
## Matrix products: default
## BLAS: /usr/lib/x86_64-linux-gnu/blas/libblas.so.3.10.0
## LAPACK: /usr/lib/x86_64-linux-gnu/lapack/liblapack.so.3.10.0
##
## locale:
## [1] LC_CTYPE=en_US.UTF-8 LC_NUMERIC=C
## [3] LC_TIME=en_US.UTF-8 LC_COLLATE=en_US.UTF-8
## [5] LC_MONETARY=en_US.UTF-8 LC_MESSAGES=en_US.UTF-8
## [7] LC_PAPER=en_US.UTF-8 LC_NAME=C
## [9] LC_ADDRESS=C LC_TELEPHONE=C
## [11] LC_MEASUREMENT=en_US.UTF-8 LC_IDENTIFICATION=C
##
## time zone: Australia/Melbourne
## tzcode source: system (glibc)
##
## attached base packages:
## [1] stats graphics grDevices utils datasets methods base
##
## other attached packages:
## [1] kableExtra_1.4.0 pkgload_1.3.4 GGally_2.2.1 ggplot2_3.5.0
## [5] reshape2_1.4.4 beeswarm_0.4.0 gplots_3.1.3.1 gtools_3.9.5
## [9] tibble_3.2.1 dplyr_1.1.4 echarts4r_0.4.5 mitch_1.15.3
##
## loaded via a namespace (and not attached):
## [1] gtable_0.3.4 xfun_0.43 bslib_0.7.0 htmlwidgets_1.6.4
## [5] caTools_1.18.2 vctrs_0.6.5 tools_4.3.3 bitops_1.0-7
## [9] generics_0.1.3 parallel_4.3.3 fansi_1.0.6 highr_0.10
## [13] pkgconfig_2.0.3 KernSmooth_2.23-22 RColorBrewer_1.1-3 lifecycle_1.0.4
## [17] compiler_4.3.3 farver_2.1.1 stringr_1.5.1 munsell_0.5.1
## [21] httpuv_1.6.15 sass_0.4.9 htmltools_0.5.8.1 yaml_2.3.8
## [25] later_1.3.2 pillar_1.9.0 crayon_1.5.2 jquerylib_0.1.4
## [29] tidyr_1.3.1 MASS_7.3-60.0.1 cachem_1.0.8 mime_0.12
## [33] ggstats_0.6.0 tidyselect_1.2.1 digest_0.6.35 stringi_1.8.3
## [37] purrr_1.0.2 labeling_0.4.3 fastmap_1.1.1 grid_4.3.3
## [41] colorspace_2.1-0 cli_3.6.2 magrittr_2.0.3 utf8_1.2.4
## [45] withr_3.0.0 scales_1.3.0 promises_1.3.0 rmarkdown_2.26
## [49] gridExtra_2.3 shiny_1.8.1.1 evaluate_0.23 knitr_1.46
## [53] viridisLite_0.4.2 rlang_1.1.3 Rcpp_1.0.12 xtable_1.8-4
## [57] glue_1.7.0 xml2_1.3.6 jsonlite_1.8.8 svglite_2.1.3
## [61] rstudioapi_0.16.0 R6_2.5.1 plyr_1.8.9 systemfonts_1.0.6
END of report