date generated: 2022-05-12
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.
## metric
## PSMB9 3.246776
## LTA 12.198286
## ZNF331 -4.472165
## HLA-F 4.071199
## TAP1 2.586892
## PHTF2 2.585173
Here are some metrics about the input data profile:
| Profile metrics | |
|---|---|
| num_genesets | 2546 |
| num_genes_in_profile | 10315 |
| duplicated_genes_present | 0 |
| num_profile_genes_in_sets | 5487 |
| num_profile_genes_not_in_sets | 4828 |
Here is a plot of the input profiles. Note the dynamic ranges.
Here is the contour plot of the profile including all detected genes.
| Gene sets metrics | |
|---|---|
| num_genesets | 2546 |
| num_genesets_excluded | 1354 |
| num_genesets_included | 1192 |
Significance is calculated by -log10(p-value). All points shown are FDR<0.05.
Significance is calculated by -log10(p-value). Top N sets shown irrespective of FDR.
| set | setSize | pANOVA | s.dist | p.adjustANOVA |
|---|---|---|---|---|
| Regulation of FZD by ubiquitination | 12 | 0.000444 | -0.585 | 0.0294 |
| RUNX2 regulates osteoblast differentiation | 13 | 0.000270 | -0.583 | 0.0230 |
| Glutamate Neurotransmitter Release Cycle | 11 | 0.002300 | -0.531 | 0.0830 |
| Assembly of collagen fibrils and other multimeric structures | 10 | 0.004600 | -0.517 | 0.1170 |
| Maturation of nucleoprotein | 11 | 0.004740 | 0.492 | 0.1170 |
| Voltage gated Potassium channels | 10 | 0.007600 | -0.487 | 0.1370 |
| Neurotransmitter release cycle | 18 | 0.000360 | -0.486 | 0.0266 |
| Regulation of pyruvate dehydrogenase (PDH) complex | 11 | 0.006980 | -0.470 | 0.1330 |
| Dopamine Neurotransmitter Release Cycle | 10 | 0.014300 | -0.447 | 0.1870 |
| Long-term potentiation | 11 | 0.010500 | -0.446 | 0.1620 |
| PKA activation | 10 | 0.017400 | -0.434 | 0.2170 |
| Signaling by Retinoic Acid | 17 | 0.002000 | -0.433 | 0.0770 |
| PKA-mediated phosphorylation of CREB | 11 | 0.013400 | -0.431 | 0.1790 |
| Negative regulation of NMDA receptor-mediated neuronal transmission | 12 | 0.010600 | -0.426 | 0.1620 |
| RUNX2 regulates bone development | 17 | 0.002530 | -0.423 | 0.0861 |
| Glycogen storage diseases | 10 | 0.021900 | -0.418 | 0.2360 |
| Ras activation upon Ca2+ influx through NMDA receptor | 10 | 0.027300 | -0.403 | 0.2450 |
| TNF receptor superfamily (TNFSF) members mediating non-canonical NF-kB pathway | 10 | 0.029600 | 0.397 | 0.2470 |
| Synthesis of Leukotrienes (LT) and Eoxins (EX) | 10 | 0.033400 | -0.388 | 0.2600 |
| Regulation of KIT signaling | 10 | 0.035000 | 0.385 | 0.2640 |
| CREB1 phosphorylation through NMDA receptor-mediated activation of RAS signaling | 16 | 0.008520 | -0.380 | 0.1450 |
| Purine catabolism | 10 | 0.040300 | 0.374 | 0.2810 |
| Synaptic adhesion-like molecules | 10 | 0.042300 | -0.371 | 0.2830 |
| Class I peroxisomal membrane protein import | 18 | 0.006470 | 0.371 | 0.1330 |
| Assembly and cell surface presentation of NMDA receptors | 13 | 0.023200 | -0.363 | 0.2380 |
| Signaling by Hippo | 11 | 0.039000 | -0.359 | 0.2810 |
| Cell-cell junction organization | 12 | 0.033300 | -0.355 | 0.2600 |
| Caspase activation via Death Receptors in the presence of ligand | 10 | 0.054600 | 0.351 | 0.3120 |
| Degradation of cysteine and homocysteine | 10 | 0.057300 | -0.347 | 0.3210 |
| Gastrin-CREB signalling pathway via PKC and MAPK | 11 | 0.047700 | -0.345 | 0.2990 |
| SARS-CoV-2 modulates autophagy | 11 | 0.050700 | 0.340 | 0.3050 |
| NOTCH4 Intracellular Domain Regulates Transcription | 14 | 0.028700 | 0.338 | 0.2470 |
| TP53 regulates transcription of additional cell cycle genes whose exact role in the p53 pathway remain uncertain | 16 | 0.021100 | 0.333 | 0.2290 |
| RUNX3 regulates NOTCH signaling | 11 | 0.058100 | 0.330 | 0.3230 |
| Potassium Channels | 26 | 0.003630 | -0.330 | 0.1060 |
| Leading Strand Synthesis | 12 | 0.049500 | 0.327 | 0.3000 |
| Polymerase switching | 12 | 0.049500 | 0.327 | 0.3000 |
| mRNA decay by 3’ to 5’ exoribonuclease | 14 | 0.036100 | 0.323 | 0.2680 |
| Heparan sulfate/heparin (HS-GAG) metabolism | 22 | 0.008890 | -0.322 | 0.1470 |
| Mucopolysaccharidoses | 10 | 0.080900 | -0.319 | 0.3750 |
| Arachidonic acid metabolism | 21 | 0.012200 | -0.316 | 0.1700 |
| Triglyceride catabolism | 11 | 0.070500 | -0.315 | 0.3430 |
| STING mediated induction of host immune responses | 10 | 0.088300 | -0.311 | 0.3750 |
| Rap1 signalling | 11 | 0.076500 | 0.308 | 0.3620 |
| Processing of Intronless Pre-mRNAs | 15 | 0.038800 | 0.308 | 0.2810 |
| RHO GTPases activate CIT | 14 | 0.049600 | 0.303 | 0.3000 |
| Tristetraprolin (TTP, ZFP36) binds and destabilizes mRNA | 15 | 0.043400 | 0.301 | 0.2860 |
| Josephin domain DUBs | 11 | 0.084500 | -0.300 | 0.3750 |
| Transcriptional regulation of granulopoiesis | 24 | 0.010900 | -0.300 | 0.1620 |
| E2F mediated regulation of DNA replication | 12 | 0.075800 | 0.296 | 0.3620 |
| set | setSize | pANOVA | s.dist | p.adjustANOVA |
|---|---|---|---|---|
| Regulation of FZD by ubiquitination | 12 | 4.44e-04 | -5.85e-01 | 0.029400 |
| RUNX2 regulates osteoblast differentiation | 13 | 2.70e-04 | -5.83e-01 | 0.023000 |
| Glutamate Neurotransmitter Release Cycle | 11 | 2.30e-03 | -5.31e-01 | 0.083000 |
| Assembly of collagen fibrils and other multimeric structures | 10 | 4.60e-03 | -5.17e-01 | 0.117000 |
| Maturation of nucleoprotein | 11 | 4.74e-03 | 4.92e-01 | 0.117000 |
| Voltage gated Potassium channels | 10 | 7.60e-03 | -4.87e-01 | 0.137000 |
| Neurotransmitter release cycle | 18 | 3.60e-04 | -4.86e-01 | 0.026600 |
| Regulation of pyruvate dehydrogenase (PDH) complex | 11 | 6.98e-03 | -4.70e-01 | 0.133000 |
| Dopamine Neurotransmitter Release Cycle | 10 | 1.43e-02 | -4.47e-01 | 0.187000 |
| Long-term potentiation | 11 | 1.05e-02 | -4.46e-01 | 0.162000 |
| PKA activation | 10 | 1.74e-02 | -4.34e-01 | 0.217000 |
| Signaling by Retinoic Acid | 17 | 2.00e-03 | -4.33e-01 | 0.077000 |
| PKA-mediated phosphorylation of CREB | 11 | 1.34e-02 | -4.31e-01 | 0.179000 |
| Negative regulation of NMDA receptor-mediated neuronal transmission | 12 | 1.06e-02 | -4.26e-01 | 0.162000 |
| RUNX2 regulates bone development | 17 | 2.53e-03 | -4.23e-01 | 0.086100 |
| Glycogen storage diseases | 10 | 2.19e-02 | -4.18e-01 | 0.236000 |
| Ras activation upon Ca2+ influx through NMDA receptor | 10 | 2.73e-02 | -4.03e-01 | 0.245000 |
| TNF receptor superfamily (TNFSF) members mediating non-canonical NF-kB pathway | 10 | 2.96e-02 | 3.97e-01 | 0.247000 |
| Synthesis of Leukotrienes (LT) and Eoxins (EX) | 10 | 3.34e-02 | -3.88e-01 | 0.260000 |
| Regulation of KIT signaling | 10 | 3.50e-02 | 3.85e-01 | 0.264000 |
| CREB1 phosphorylation through NMDA receptor-mediated activation of RAS signaling | 16 | 8.52e-03 | -3.80e-01 | 0.145000 |
| Purine catabolism | 10 | 4.03e-02 | 3.74e-01 | 0.281000 |
| Synaptic adhesion-like molecules | 10 | 4.23e-02 | -3.71e-01 | 0.283000 |
| Class I peroxisomal membrane protein import | 18 | 6.47e-03 | 3.71e-01 | 0.133000 |
| Assembly and cell surface presentation of NMDA receptors | 13 | 2.32e-02 | -3.63e-01 | 0.238000 |
| Signaling by Hippo | 11 | 3.90e-02 | -3.59e-01 | 0.281000 |
| Cell-cell junction organization | 12 | 3.33e-02 | -3.55e-01 | 0.260000 |
| Caspase activation via Death Receptors in the presence of ligand | 10 | 5.46e-02 | 3.51e-01 | 0.312000 |
| Degradation of cysteine and homocysteine | 10 | 5.73e-02 | -3.47e-01 | 0.321000 |
| Gastrin-CREB signalling pathway via PKC and MAPK | 11 | 4.77e-02 | -3.45e-01 | 0.299000 |
| SARS-CoV-2 modulates autophagy | 11 | 5.07e-02 | 3.40e-01 | 0.305000 |
| NOTCH4 Intracellular Domain Regulates Transcription | 14 | 2.87e-02 | 3.38e-01 | 0.247000 |
| TP53 regulates transcription of additional cell cycle genes whose exact role in the p53 pathway remain uncertain | 16 | 2.11e-02 | 3.33e-01 | 0.229000 |
| RUNX3 regulates NOTCH signaling | 11 | 5.81e-02 | 3.30e-01 | 0.323000 |
| Potassium Channels | 26 | 3.63e-03 | -3.30e-01 | 0.106000 |
| Leading Strand Synthesis | 12 | 4.95e-02 | 3.27e-01 | 0.300000 |
| Polymerase switching | 12 | 4.95e-02 | 3.27e-01 | 0.300000 |
| mRNA decay by 3’ to 5’ exoribonuclease | 14 | 3.61e-02 | 3.23e-01 | 0.268000 |
| Heparan sulfate/heparin (HS-GAG) metabolism | 22 | 8.89e-03 | -3.22e-01 | 0.147000 |
| Mucopolysaccharidoses | 10 | 8.09e-02 | -3.19e-01 | 0.375000 |
| Arachidonic acid metabolism | 21 | 1.22e-02 | -3.16e-01 | 0.170000 |
| Triglyceride catabolism | 11 | 7.05e-02 | -3.15e-01 | 0.343000 |
| STING mediated induction of host immune responses | 10 | 8.83e-02 | -3.11e-01 | 0.375000 |
| Rap1 signalling | 11 | 7.65e-02 | 3.08e-01 | 0.362000 |
| Processing of Intronless Pre-mRNAs | 15 | 3.88e-02 | 3.08e-01 | 0.281000 |
| RHO GTPases activate CIT | 14 | 4.96e-02 | 3.03e-01 | 0.300000 |
| Tristetraprolin (TTP, ZFP36) binds and destabilizes mRNA | 15 | 4.34e-02 | 3.01e-01 | 0.286000 |
| Josephin domain DUBs | 11 | 8.45e-02 | -3.00e-01 | 0.375000 |
| Transcriptional regulation of granulopoiesis | 24 | 1.09e-02 | -3.00e-01 | 0.162000 |
| E2F mediated regulation of DNA replication | 12 | 7.58e-02 | 2.96e-01 | 0.362000 |
| HDR through MMEJ (alt-NHEJ) | 11 | 8.93e-02 | 2.96e-01 | 0.375000 |
| Butyrate Response Factor 1 (BRF1) binds and destabilizes mRNA | 15 | 4.78e-02 | 2.95e-01 | 0.299000 |
| Cytochrome c-mediated apoptotic response | 11 | 9.03e-02 | -2.95e-01 | 0.375000 |
| The NLRP3 inflammasome | 12 | 7.88e-02 | -2.93e-01 | 0.368000 |
| Diseases of carbohydrate metabolism | 23 | 1.54e-02 | -2.92e-01 | 0.198000 |
| Cyclin A/B1/B2 associated events during G2/M transition | 22 | 1.84e-02 | 2.90e-01 | 0.217000 |
| HSP90 chaperone cycle for steroid hormone receptors (SHR) in the presence of ligand | 32 | 5.00e-03 | 2.87e-01 | 0.117000 |
| LDL clearance | 12 | 8.58e-02 | -2.86e-01 | 0.375000 |
| Pyruvate metabolism | 19 | 3.22e-02 | -2.84e-01 | 0.257000 |
| SLBP Dependent Processing of Replication-Dependent Histone Pre-mRNAs | 10 | 1.21e-01 | 2.83e-01 | 0.418000 |
| Processing of Capped Intronless Pre-mRNA | 23 | 1.89e-02 | 2.83e-01 | 0.217000 |
| Nicotinamide salvaging | 10 | 1.23e-01 | 2.82e-01 | 0.418000 |
| Depolymerisation of the Nuclear Lamina | 11 | 1.08e-01 | 2.80e-01 | 0.415000 |
| Activation of NMDA receptors and postsynaptic events | 44 | 1.37e-03 | -2.79e-01 | 0.062900 |
| SARS-CoV-2 targets host intracellular signalling and regulatory pathways | 11 | 1.12e-01 | 2.76e-01 | 0.418000 |
| Cell junction organization | 22 | 2.49e-02 | -2.76e-01 | 0.240000 |
| RHO GTPases activate PKNs | 26 | 1.79e-02 | 2.68e-01 | 0.217000 |
| Thrombin signalling through proteinase activated receptors (PARs) | 19 | 4.31e-02 | -2.68e-01 | 0.286000 |
| Triglyceride metabolism | 16 | 6.75e-02 | -2.64e-01 | 0.341000 |
| Initiation of Nuclear Envelope (NE) Reformation | 17 | 5.96e-02 | 2.64e-01 | 0.324000 |
| Transmission across Chemical Synapses | 97 | 7.50e-06 | -2.64e-01 | 0.001790 |
| Post NMDA receptor activation events | 38 | 5.02e-03 | -2.63e-01 | 0.117000 |
| Activation of kainate receptors upon glutamate binding | 16 | 6.99e-02 | -2.62e-01 | 0.343000 |
| Vitamin B5 (pantothenate) metabolism | 11 | 1.34e-01 | 2.61e-01 | 0.436000 |
| AKT phosphorylates targets in the cytosol | 13 | 1.03e-01 | 2.61e-01 | 0.406000 |
| Negative regulation of FGFR1 signaling | 17 | 6.26e-02 | -2.61e-01 | 0.329000 |
| Negative regulation of FGFR2 signaling | 17 | 6.26e-02 | -2.61e-01 | 0.329000 |
| Negative regulation of FGFR3 signaling | 17 | 6.26e-02 | -2.61e-01 | 0.329000 |
| Negative regulation of FGFR4 signaling | 17 | 6.26e-02 | -2.61e-01 | 0.329000 |
| Spry regulation of FGF signaling | 15 | 8.04e-02 | -2.61e-01 | 0.375000 |
| Apoptotic factor-mediated response | 16 | 7.16e-02 | -2.60e-01 | 0.347000 |
| SARS-CoV-2 modulates host translation machinery | 38 | 5.55e-03 | 2.60e-01 | 0.120000 |
| Metabolism of fat-soluble vitamins | 13 | 1.05e-01 | -2.59e-01 | 0.410000 |
| Regulation of ornithine decarboxylase (ODC) | 42 | 3.76e-03 | 2.59e-01 | 0.106000 |
| Membrane binding and targetting of GAG proteins | 11 | 1.38e-01 | -2.58e-01 | 0.436000 |
| Synthesis And Processing Of GAG, GAGPOL Polyproteins | 11 | 1.38e-01 | -2.58e-01 | 0.436000 |
| Carboxyterminal post-translational modifications of tubulin | 19 | 5.37e-02 | -2.56e-01 | 0.310000 |
| KSRP (KHSRP) binds and destabilizes mRNA | 15 | 8.66e-02 | 2.56e-01 | 0.375000 |
| ADP signalling through P2Y purinoceptor 1 | 15 | 8.70e-02 | -2.55e-01 | 0.375000 |
| Glucagon signaling in metabolic regulation | 17 | 7.03e-02 | -2.54e-01 | 0.343000 |
| Telomere Extension By Telomerase | 19 | 5.60e-02 | 2.53e-01 | 0.316000 |
| Signaling by ERBB4 | 29 | 1.88e-02 | -2.52e-01 | 0.217000 |
| Neurotransmitter receptors and postsynaptic signal transmission | 76 | 1.61e-04 | -2.51e-01 | 0.016500 |
| Nuclear signaling by ERBB4 | 14 | 1.07e-01 | -2.48e-01 | 0.415000 |
| RNA Polymerase III Transcription Initiation From Type 1 Promoter | 27 | 2.58e-02 | 2.48e-01 | 0.244000 |
| Activation of ATR in response to replication stress | 29 | 2.11e-02 | 2.47e-01 | 0.229000 |
| Plasma lipoprotein clearance | 23 | 4.14e-02 | -2.46e-01 | 0.281000 |
| Neuronal System | 132 | 1.38e-06 | -2.44e-01 | 0.000823 |
| Signaling by Leptin | 10 | 1.84e-01 | -2.42e-01 | 0.497000 |
| Metabolism of polyamines | 46 | 4.52e-03 | 2.42e-01 | 0.117000 |
| Activation of BAD and translocation to mitochondria | 14 | 1.17e-01 | 2.42e-01 | 0.418000 |
| Removal of the Flap Intermediate | 12 | 1.50e-01 | 2.40e-01 | 0.456000 |
| mRNA Capping | 26 | 3.53e-02 | 2.39e-01 | 0.265000 |
| Keratan sulfate biosynthesis | 14 | 1.23e-01 | -2.38e-01 | 0.418000 |
| Regulation of beta-cell development | 15 | 1.11e-01 | 2.38e-01 | 0.416000 |
| DNA Damage/Telomere Stress Induced Senescence | 24 | 4.46e-02 | 2.37e-01 | 0.291000 |
| Downregulation of ERBB2:ERBB3 signaling | 10 | 1.95e-01 | -2.37e-01 | 0.505000 |
| HDACs deacetylate histones | 28 | 3.10e-02 | 2.36e-01 | 0.253000 |
| RNA Polymerase III Transcription Initiation From Type 2 Promoter | 26 | 4.00e-02 | 2.33e-01 | 0.281000 |
| Signaling by WNT in cancer | 23 | 5.34e-02 | -2.33e-01 | 0.310000 |
| Defective pyroptosis | 10 | 2.05e-01 | 2.31e-01 | 0.521000 |
| GPVI-mediated activation cascade | 23 | 5.50e-02 | 2.31e-01 | 0.312000 |
| Cell recruitment (pro-inflammatory response) | 15 | 1.23e-01 | -2.30e-01 | 0.418000 |
| Purinergic signaling in leishmaniasis infection | 15 | 1.23e-01 | -2.30e-01 | 0.418000 |
| Keratan sulfate/keratin metabolism | 18 | 9.42e-02 | -2.28e-01 | 0.385000 |
| DARPP-32 events | 19 | 8.79e-02 | -2.26e-01 | 0.375000 |
| Retinoid metabolism and transport | 11 | 1.94e-01 | -2.26e-01 | 0.505000 |
| Meiotic recombination | 19 | 8.92e-02 | 2.25e-01 | 0.375000 |
| Regulation of RUNX1 Expression and Activity | 14 | 1.45e-01 | 2.25e-01 | 0.450000 |
| COPI-independent Golgi-to-ER retrograde traffic | 28 | 4.20e-02 | 2.22e-01 | 0.283000 |
| Inflammasomes | 16 | 1.29e-01 | -2.19e-01 | 0.426000 |
| Regulation of TP53 Activity through Acetylation | 27 | 4.90e-02 | 2.19e-01 | 0.300000 |
| RNA Pol II CTD phosphorylation and interaction with CE | 24 | 6.39e-02 | 2.19e-01 | 0.332000 |
| RNA Pol II CTD phosphorylation and interaction with CE during HIV infection | 24 | 6.39e-02 | 2.19e-01 | 0.332000 |
| Negative regulation of FLT3 | 13 | 1.73e-01 | 2.18e-01 | 0.490000 |
| Autodegradation of the E3 ubiquitin ligase COP1 | 43 | 1.36e-02 | 2.18e-01 | 0.181000 |
| Diseases associated with glycosylation precursor biosynthesis | 15 | 1.46e-01 | -2.17e-01 | 0.450000 |
| Viral mRNA Translation | 69 | 1.94e-03 | 2.16e-01 | 0.077000 |
| Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC) | 86 | 5.58e-04 | 2.16e-01 | 0.033200 |
| Nonsense-Mediated Decay (NMD) | 86 | 5.58e-04 | 2.16e-01 | 0.033200 |
| Regulation of BACH1 activity | 11 | 2.16e-01 | -2.16e-01 | 0.535000 |
| Chk1/Chk2(Cds1) mediated inactivation of Cyclin B:Cdk1 complex | 13 | 1.79e-01 | 2.15e-01 | 0.497000 |
| Negative regulation of NOTCH4 signaling | 47 | 1.07e-02 | 2.15e-01 | 0.162000 |
| Signaling by NODAL | 11 | 2.17e-01 | -2.15e-01 | 0.537000 |
| Amino acid transport across the plasma membrane | 16 | 1.38e-01 | -2.14e-01 | 0.436000 |
| Signaling by Activin | 11 | 2.21e-01 | -2.13e-01 | 0.541000 |
| Glycosaminoglycan metabolism | 63 | 3.49e-03 | -2.13e-01 | 0.104000 |
| Lagging Strand Synthesis | 17 | 1.29e-01 | 2.13e-01 | 0.426000 |
| HATs acetylate histones | 54 | 6.93e-03 | 2.13e-01 | 0.133000 |
| Regulation of gene expression in late stage (branching morphogenesis) pancreatic bud precursor cells | 11 | 2.23e-01 | 2.12e-01 | 0.542000 |
| Impaired BRCA2 binding to RAD51 | 30 | 4.54e-02 | 2.11e-01 | 0.292000 |
| NRIF signals cell death from the nucleus | 13 | 1.88e-01 | -2.11e-01 | 0.499000 |
| Assembly Of The HIV Virion | 13 | 1.89e-01 | -2.11e-01 | 0.500000 |
| Regulation of expression of SLITs and ROBOs | 122 | 6.19e-05 | 2.10e-01 | 0.009350 |
| Miscellaneous transport and binding events | 14 | 1.75e-01 | -2.09e-01 | 0.491000 |
| Stabilization of p53 | 48 | 1.23e-02 | 2.09e-01 | 0.170000 |
| FOXO-mediated transcription of cell death genes | 14 | 1.77e-01 | 2.09e-01 | 0.494000 |
| Ca-dependent events | 21 | 9.81e-02 | -2.09e-01 | 0.395000 |
| O-linked glycosylation | 39 | 2.49e-02 | -2.08e-01 | 0.240000 |
| A tetrasaccharide linker sequence is required for GAG synthesis | 10 | 2.56e-01 | -2.07e-01 | 0.581000 |
| RNA Polymerase II Transcription Termination | 38 | 2.72e-02 | 2.07e-01 | 0.245000 |
| Termination of O-glycan biosynthesis | 10 | 2.57e-01 | -2.07e-01 | 0.582000 |
| Polymerase switching on the C-strand of the telomere | 20 | 1.10e-01 | 2.07e-01 | 0.415000 |
| Condensation of Prometaphase Chromosomes | 10 | 2.63e-01 | 2.04e-01 | 0.586000 |
| Golgi Cisternae Pericentriolar Stack Reorganization | 14 | 1.87e-01 | 2.04e-01 | 0.499000 |
| PCNA-Dependent Long Patch Base Excision Repair | 18 | 1.36e-01 | 2.03e-01 | 0.436000 |
| Sema4D induced cell migration and growth-cone collapse | 11 | 2.44e-01 | 2.03e-01 | 0.570000 |
| Class B/2 (Secretin family receptors) | 27 | 6.91e-02 | -2.02e-01 | 0.343000 |
| SRP-dependent cotranslational protein targeting to membrane | 88 | 1.07e-03 | 2.02e-01 | 0.058200 |
| G2/M DNA damage checkpoint | 51 | 1.28e-02 | 2.02e-01 | 0.174000 |
| CLEC7A (Dectin-1) induces NFAT activation | 11 | 2.49e-01 | 2.01e-01 | 0.575000 |
| AURKA Activation by TPX2 | 55 | 1.03e-02 | 2.00e-01 | 0.162000 |
| CD28 dependent PI3K/Akt signaling | 18 | 1.42e-01 | 2.00e-01 | 0.442000 |
| mRNA 3’-end processing | 30 | 5.85e-02 | 2.00e-01 | 0.323000 |
| Disorders of Developmental Biology | 10 | 2.75e-01 | -1.99e-01 | 0.593000 |
| Disorders of Nervous System Development | 10 | 2.75e-01 | -1.99e-01 | 0.593000 |
| Loss of function of MECP2 in Rett syndrome | 10 | 2.75e-01 | -1.99e-01 | 0.593000 |
| Pervasive developmental disorders | 10 | 2.75e-01 | -1.99e-01 | 0.593000 |
| HDMs demethylate histones | 15 | 1.84e-01 | 1.98e-01 | 0.497000 |
| Eukaryotic Translation Termination | 72 | 3.81e-03 | 1.97e-01 | 0.106000 |
| TNFs bind their physiological receptors | 10 | 2.80e-01 | 1.97e-01 | 0.602000 |
| Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC) | 74 | 3.46e-03 | 1.97e-01 | 0.104000 |
| Integrin signaling | 16 | 1.73e-01 | 1.97e-01 | 0.490000 |
| Platelet Aggregation (Plug Formation) | 16 | 1.73e-01 | 1.97e-01 | 0.490000 |
| Signaling by NOTCH4 | 67 | 5.55e-03 | 1.96e-01 | 0.120000 |
| RHO GTPases Activate NADPH Oxidases | 14 | 2.06e-01 | -1.95e-01 | 0.521000 |
| RNA polymerase II transcribes snRNA genes | 66 | 6.14e-03 | 1.95e-01 | 0.128000 |
| Regulation of IFNG signaling | 13 | 2.23e-01 | -1.95e-01 | 0.542000 |
| Attenuation phase | 19 | 1.42e-01 | 1.95e-01 | 0.442000 |
| PLC beta mediated events | 29 | 6.99e-02 | -1.95e-01 | 0.343000 |
| Cross-presentation of soluble exogenous antigens (endosomes) | 37 | 4.15e-02 | 1.94e-01 | 0.281000 |
| Diseases associated with N-glycosylation of proteins | 18 | 1.55e-01 | 1.94e-01 | 0.460000 |
| Formation of RNA Pol II elongation complex | 46 | 2.42e-02 | 1.92e-01 | 0.238000 |
| RNA Polymerase II Transcription Elongation | 46 | 2.42e-02 | 1.92e-01 | 0.238000 |
| TP53 Regulates Transcription of Cell Cycle Genes | 40 | 3.55e-02 | 1.92e-01 | 0.265000 |
| Formation of the ternary complex, and subsequently, the 43S complex | 40 | 3.69e-02 | 1.91e-01 | 0.271000 |
| Nuclear Pore Complex (NPC) Disassembly | 33 | 5.96e-02 | 1.90e-01 | 0.324000 |
| ROS and RNS production in phagocytes | 23 | 1.18e-01 | -1.88e-01 | 0.418000 |
| HCMV Early Events | 49 | 2.28e-02 | 1.88e-01 | 0.238000 |
| FOXO-mediated transcription of cell cycle genes | 12 | 2.59e-01 | 1.88e-01 | 0.584000 |
| Formation of a pool of free 40S subunits | 78 | 4.17e-03 | 1.88e-01 | 0.112000 |
| Signaling by ALK | 18 | 1.68e-01 | 1.88e-01 | 0.483000 |
| Loss of Nlp from mitotic centrosomes | 52 | 1.92e-02 | 1.88e-01 | 0.217000 |
| Loss of proteins required for interphase microtubule organization from the centrosome | 52 | 1.92e-02 | 1.88e-01 | 0.217000 |
| Sema3A PAK dependent Axon repulsion | 11 | 2.83e-01 | -1.87e-01 | 0.605000 |
| Transport of inorganic cations/anions and amino acids/oligopeptides | 40 | 4.09e-02 | -1.87e-01 | 0.281000 |
| G alpha (i) signalling events | 88 | 2.53e-03 | -1.87e-01 | 0.086100 |
| Methylation | 10 | 3.07e-01 | 1.87e-01 | 0.628000 |
| Constitutive Signaling by AKT1 E17K in Cancer | 23 | 1.22e-01 | 1.87e-01 | 0.418000 |
| Extension of Telomeres | 41 | 3.91e-02 | 1.86e-01 | 0.281000 |
| Cap-dependent Translation Initiation | 95 | 1.74e-03 | 1.86e-01 | 0.073400 |
| Eukaryotic Translation Initiation | 95 | 1.74e-03 | 1.86e-01 | 0.073400 |
| G alpha (s) signalling events | 44 | 3.27e-02 | -1.86e-01 | 0.258000 |
| G-protein activation | 12 | 2.64e-01 | -1.86e-01 | 0.586000 |
| Plasma lipoprotein assembly, remodeling, and clearance | 38 | 4.71e-02 | -1.86e-01 | 0.299000 |
| Gene and protein expression by JAK-STAT signaling after Interleukin-12 stimulation | 28 | 8.92e-02 | 1.86e-01 | 0.375000 |
| Peptide chain elongation | 69 | 8.02e-03 | 1.85e-01 | 0.143000 |
| Regulation of innate immune responses to cytosolic DNA | 11 | 2.89e-01 | -1.84e-01 | 0.607000 |
| G2/M Checkpoints | 108 | 9.62e-04 | 1.84e-01 | 0.054600 |
| p53-Dependent G1 DNA Damage Response | 55 | 1.82e-02 | 1.84e-01 | 0.217000 |
| p53-Dependent G1/S DNA damage checkpoint | 55 | 1.82e-02 | 1.84e-01 | 0.217000 |
| Eukaryotic Translation Elongation | 72 | 7.05e-03 | 1.84e-01 | 0.133000 |
| Recycling pathway of L1 | 15 | 2.20e-01 | -1.83e-01 | 0.541000 |
| FBXL7 down-regulates AURKA during mitotic entry and in early mitosis | 45 | 3.40e-02 | 1.83e-01 | 0.260000 |
| HSF1-dependent transactivation | 25 | 1.14e-01 | 1.83e-01 | 0.418000 |
| MicroRNA (miRNA) biogenesis | 18 | 1.81e-01 | 1.82e-01 | 0.497000 |
| Sema4D in semaphorin signaling | 13 | 2.55e-01 | 1.82e-01 | 0.581000 |
| GPER1 signaling | 24 | 1.23e-01 | -1.82e-01 | 0.418000 |
| Regulation of mRNA stability by proteins that bind AU-rich elements | 74 | 6.97e-03 | 1.82e-01 | 0.133000 |
| NOTCH3 Intracellular Domain Regulates Transcription | 15 | 2.24e-01 | 1.81e-01 | 0.542000 |
| G2/M Transition | 147 | 1.66e-04 | 1.80e-01 | 0.016500 |
| Translation initiation complex formation | 47 | 3.38e-02 | 1.79e-01 | 0.260000 |
| Transport of vitamins, nucleosides, and related molecules | 21 | 1.56e-01 | -1.79e-01 | 0.462000 |
| CaM pathway | 20 | 1.66e-01 | -1.79e-01 | 0.480000 |
| Calmodulin induced events | 20 | 1.66e-01 | -1.79e-01 | 0.480000 |
| Notch-HLH transcription pathway | 21 | 1.56e-01 | 1.79e-01 | 0.462000 |
| Elastic fibre formation | 16 | 2.17e-01 | -1.78e-01 | 0.537000 |
| Disassembly of the destruction complex and recruitment of AXIN to the membrane | 26 | 1.16e-01 | -1.78e-01 | 0.418000 |
| VLDLR internalisation and degradation | 11 | 3.07e-01 | -1.78e-01 | 0.628000 |
| Diseases associated with O-glycosylation of proteins | 20 | 1.68e-01 | -1.78e-01 | 0.484000 |
| Influenza Viral RNA Transcription and Replication | 112 | 1.18e-03 | 1.78e-01 | 0.060000 |
| RHO GTPases Activate ROCKs | 13 | 2.67e-01 | 1.78e-01 | 0.587000 |
| Nuclear Envelope Breakdown | 46 | 3.76e-02 | 1.77e-01 | 0.275000 |
| GABA receptor activation | 18 | 1.94e-01 | -1.77e-01 | 0.505000 |
| Protein-protein interactions at synapses | 32 | 8.36e-02 | -1.77e-01 | 0.375000 |
| Regulation of PLK1 Activity at G2/M Transition | 67 | 1.24e-02 | 1.77e-01 | 0.170000 |
| MTOR signalling | 32 | 8.38e-02 | 1.77e-01 | 0.375000 |
| Mitochondrial tRNA aminoacylation | 18 | 1.95e-01 | 1.77e-01 | 0.505000 |
| Oxygen-dependent proline hydroxylation of Hypoxia-inducible Factor Alpha | 51 | 2.94e-02 | 1.76e-01 | 0.247000 |
| Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S | 48 | 3.47e-02 | 1.76e-01 | 0.263000 |
| HDR through Single Strand Annealing (SSA) | 33 | 8.17e-02 | 1.75e-01 | 0.375000 |
| Diseases of DNA repair | 41 | 5.28e-02 | 1.75e-01 | 0.309000 |
| L13a-mediated translational silencing of Ceruloplasmin expression | 87 | 5.09e-03 | 1.74e-01 | 0.117000 |
| ADORA2B mediated anti-inflammatory cytokines production | 32 | 8.89e-02 | -1.74e-01 | 0.375000 |
| Stimuli-sensing channels | 35 | 7.60e-02 | -1.73e-01 | 0.362000 |
| Presynaptic phase of homologous DNA pairing and strand exchange | 32 | 8.99e-02 | 1.73e-01 | 0.375000 |
| Collagen formation | 19 | 1.91e-01 | -1.73e-01 | 0.504000 |
| Transport of the SLBP Dependant Mature mRNA | 32 | 9.01e-02 | 1.73e-01 | 0.375000 |
| TP53 Regulates Transcription of Genes Involved in G2 Cell Cycle Arrest | 15 | 2.46e-01 | 1.73e-01 | 0.572000 |
| Purine ribonucleoside monophosphate biosynthesis | 10 | 3.44e-01 | 1.73e-01 | 0.668000 |
| Meiosis | 39 | 6.23e-02 | 1.73e-01 | 0.329000 |
| Transport of Mature mRNAs Derived from Intronless Transcripts | 39 | 6.26e-02 | 1.72e-01 | 0.329000 |
| Amyloid fiber formation | 27 | 1.22e-01 | -1.72e-01 | 0.418000 |
| Mitotic G2-G2/M phases | 149 | 3.02e-04 | 1.72e-01 | 0.024000 |
| Cellular response to hypoxia | 58 | 2.37e-02 | 1.72e-01 | 0.238000 |
| Ubiquitin-dependent degradation of Cyclin D | 43 | 5.14e-02 | 1.72e-01 | 0.305000 |
| Aquaporin-mediated transport | 24 | 1.46e-01 | -1.72e-01 | 0.450000 |
| VxPx cargo-targeting to cilium | 16 | 2.35e-01 | -1.72e-01 | 0.553000 |
| Response of EIF2AK4 (GCN2) to amino acid deficiency | 77 | 9.69e-03 | 1.71e-01 | 0.158000 |
| ATF4 activates genes in response to endoplasmic reticulum stress | 23 | 1.56e-01 | 1.71e-01 | 0.462000 |
| Synthesis of PC | 22 | 1.66e-01 | 1.71e-01 | 0.480000 |
| Processive synthesis on the lagging strand | 13 | 2.88e-01 | 1.70e-01 | 0.607000 |
| Interleukin receptor SHC signaling | 15 | 2.54e-01 | 1.70e-01 | 0.581000 |
| Regulation of RUNX2 expression and activity | 56 | 2.85e-02 | 1.69e-01 | 0.247000 |
| Cell death signalling via NRAGE, NRIF and NADE | 40 | 6.44e-02 | -1.69e-01 | 0.332000 |
| Telomere Maintenance | 54 | 3.20e-02 | 1.69e-01 | 0.257000 |
| RNA Polymerase III Transcription Initiation | 35 | 8.41e-02 | 1.69e-01 | 0.375000 |
| Vif-mediated degradation of APOBEC3G | 42 | 5.90e-02 | 1.68e-01 | 0.324000 |
| Selenocysteine synthesis | 70 | 1.50e-02 | 1.68e-01 | 0.194000 |
| G1/S DNA Damage Checkpoints | 57 | 2.83e-02 | 1.68e-01 | 0.247000 |
| Metabolism of cofactors | 17 | 2.30e-01 | 1.68e-01 | 0.548000 |
| GPCR ligand binding | 75 | 1.22e-02 | -1.68e-01 | 0.170000 |
| GTP hydrolysis and joining of the 60S ribosomal subunit | 88 | 6.66e-03 | 1.68e-01 | 0.133000 |
| DNA strand elongation | 27 | 1.32e-01 | 1.67e-01 | 0.436000 |
| Translation of Structural Proteins | 27 | 1.33e-01 | 1.67e-01 | 0.436000 |
| Potential therapeutics for SARS | 65 | 2.06e-02 | 1.66e-01 | 0.229000 |
| Defective homologous recombination repair (HRR) due to BRCA2 loss of function | 33 | 9.98e-02 | 1.66e-01 | 0.398000 |
| Diseases of DNA Double-Strand Break Repair | 33 | 9.98e-02 | 1.66e-01 | 0.398000 |
| Signaling by FGFR2 IIIa TM | 15 | 2.67e-01 | 1.66e-01 | 0.587000 |
| Cytosolic sulfonation of small molecules | 10 | 3.67e-01 | -1.65e-01 | 0.681000 |
| Centrosome maturation | 60 | 2.76e-02 | 1.65e-01 | 0.245000 |
| Recruitment of mitotic centrosome proteins and complexes | 60 | 2.76e-02 | 1.65e-01 | 0.245000 |
| Chondroitin sulfate/dermatan sulfate metabolism | 27 | 1.39e-01 | -1.65e-01 | 0.436000 |
| Ribosomal scanning and start codon recognition | 47 | 5.12e-02 | 1.65e-01 | 0.305000 |
| SUMOylation of ubiquitinylation proteins | 36 | 8.78e-02 | 1.64e-01 | 0.375000 |
| FGFR2 mutant receptor activation | 16 | 2.55e-01 | 1.64e-01 | 0.581000 |
| RNA Polymerase II Pre-transcription Events | 64 | 2.34e-02 | 1.64e-01 | 0.238000 |
| G-protein mediated events | 32 | 1.09e-01 | -1.64e-01 | 0.415000 |
| AUF1 (hnRNP D0) binds and destabilizes mRNA | 45 | 5.73e-02 | 1.64e-01 | 0.321000 |
| Transport of Mature mRNA Derived from an Intronless Transcript | 38 | 8.18e-02 | 1.63e-01 | 0.375000 |
| Metabolic disorders of biological oxidation enzymes | 14 | 2.90e-01 | -1.63e-01 | 0.607000 |
| Regulation of activated PAK-2p34 by proteasome mediated degradation | 41 | 7.25e-02 | 1.62e-01 | 0.350000 |
| Transport of the SLBP independent Mature mRNA | 31 | 1.19e-01 | 1.62e-01 | 0.418000 |
| Signaling by BMP | 14 | 2.95e-01 | -1.62e-01 | 0.614000 |
| Azathioprine ADME | 15 | 2.80e-01 | 1.61e-01 | 0.602000 |
| Signaling by FGFR1 in disease | 23 | 1.81e-01 | -1.61e-01 | 0.497000 |
| tRNA modification in the nucleus and cytosol | 30 | 1.27e-01 | 1.61e-01 | 0.423000 |
| The role of GTSE1 in G2/M progression after G2 checkpoint | 51 | 4.79e-02 | 1.60e-01 | 0.299000 |
| Role of LAT2/NTAL/LAB on calcium mobilization | 10 | 3.80e-01 | 1.60e-01 | 0.701000 |
| Activation of NF-kappaB in B cells | 55 | 4.04e-02 | 1.60e-01 | 0.281000 |
| CTLA4 inhibitory signaling | 15 | 2.84e-01 | 1.60e-01 | 0.605000 |
| SLC-mediated transmembrane transport | 96 | 7.39e-03 | -1.59e-01 | 0.136000 |
| NR1H3 & NR1H2 regulate gene expression linked to cholesterol transport and efflux | 21 | 2.10e-01 | 1.58e-01 | 0.528000 |
| Activation of GABAB receptors | 17 | 2.61e-01 | -1.58e-01 | 0.584000 |
| GABA B receptor activation | 17 | 2.61e-01 | -1.58e-01 | 0.584000 |
| Apoptotic cleavage of cellular proteins | 24 | 1.82e-01 | 1.58e-01 | 0.497000 |
| Anchoring of the basal body to the plasma membrane | 74 | 1.93e-02 | 1.58e-01 | 0.217000 |
| Interleukin-6 family signaling | 13 | 3.26e-01 | -1.57e-01 | 0.648000 |
| Regulation of PTEN stability and activity | 55 | 4.36e-02 | 1.57e-01 | 0.286000 |
| TICAM1-dependent activation of IRF3/IRF7 | 12 | 3.46e-01 | -1.57e-01 | 0.668000 |
| Platelet calcium homeostasis | 17 | 2.62e-01 | -1.57e-01 | 0.585000 |
| Resolution of AP sites via the multiple-nucleotide patch replacement pathway | 20 | 2.26e-01 | 1.56e-01 | 0.542000 |
| TP53 Regulates Transcription of Genes Involved in Cytochrome C Release | 14 | 3.11e-01 | 1.56e-01 | 0.632000 |
| Formation of HIV elongation complex in the absence of HIV Tat | 33 | 1.23e-01 | 1.55e-01 | 0.418000 |
| RNA Polymerase I Transcription Termination | 25 | 1.80e-01 | 1.55e-01 | 0.497000 |
| Regulation of TP53 Activity through Phosphorylation | 77 | 1.92e-02 | 1.55e-01 | 0.217000 |
| Recruitment of NuMA to mitotic centrosomes | 59 | 4.03e-02 | 1.54e-01 | 0.281000 |
| RIP-mediated NFkB activation via ZBP1 | 13 | 3.35e-01 | 1.54e-01 | 0.660000 |
| G beta:gamma signalling through PLC beta | 12 | 3.55e-01 | -1.54e-01 | 0.673000 |
| Presynaptic function of Kainate receptors | 12 | 3.55e-01 | -1.54e-01 | 0.673000 |
| Mitotic Prophase | 72 | 2.41e-02 | 1.54e-01 | 0.238000 |
| NOD1/2 Signaling Pathway | 22 | 2.11e-01 | 1.54e-01 | 0.529000 |
| Orc1 removal from chromatin | 55 | 4.88e-02 | 1.54e-01 | 0.300000 |
| FOXO-mediated transcription | 45 | 7.68e-02 | 1.53e-01 | 0.362000 |
| Degradation of GLI2 by the proteasome | 49 | 6.50e-02 | 1.53e-01 | 0.332000 |
| GLI3 is processed to GLI3R by the proteasome | 49 | 6.50e-02 | 1.53e-01 | 0.332000 |
| Influenza Infection | 129 | 2.88e-03 | 1.52e-01 | 0.095400 |
| G alpha (q) signalling events | 74 | 2.38e-02 | -1.52e-01 | 0.238000 |
| Neurexins and neuroligins | 21 | 2.28e-01 | -1.52e-01 | 0.544000 |
| Opioid Signalling | 55 | 5.14e-02 | -1.52e-01 | 0.305000 |
| HCMV Infection | 68 | 3.06e-02 | 1.52e-01 | 0.252000 |
| Formation of HIV-1 elongation complex containing HIV-1 Tat | 32 | 1.38e-01 | 1.52e-01 | 0.436000 |
| HIV Transcription Elongation | 32 | 1.38e-01 | 1.52e-01 | 0.436000 |
| Tat-mediated elongation of the HIV-1 transcript | 32 | 1.38e-01 | 1.52e-01 | 0.436000 |
| Complex I biogenesis | 40 | 9.81e-02 | 1.51e-01 | 0.395000 |
| Inwardly rectifying K+ channels | 12 | 3.65e-01 | -1.51e-01 | 0.681000 |
| Ubiquitin Mediated Degradation of Phosphorylated Cdc25A | 43 | 8.73e-02 | 1.51e-01 | 0.375000 |
| p53-Independent DNA Damage Response | 43 | 8.73e-02 | 1.51e-01 | 0.375000 |
| p53-Independent G1/S DNA damage checkpoint | 43 | 8.73e-02 | 1.51e-01 | 0.375000 |
| TP53 Regulates Transcription of Genes Involved in G1 Cell Cycle Arrest | 12 | 3.67e-01 | 1.51e-01 | 0.681000 |
| Interleukin-12 signaling | 35 | 1.24e-01 | 1.50e-01 | 0.418000 |
| GSK3B and BTRC:CUL1-mediated-degradation of NFE2L2 | 45 | 8.11e-02 | 1.50e-01 | 0.375000 |
| Nucleotide biosynthesis | 12 | 3.68e-01 | 1.50e-01 | 0.681000 |
| Cargo concentration in the ER | 19 | 2.59e-01 | -1.50e-01 | 0.584000 |
| Downstream TCR signaling | 69 | 3.21e-02 | 1.49e-01 | 0.257000 |
| Nucleotide catabolism | 20 | 2.48e-01 | 1.49e-01 | 0.574000 |
| Sulfur amino acid metabolism | 17 | 2.87e-01 | -1.49e-01 | 0.607000 |
| SUMOylation of SUMOylation proteins | 31 | 1.53e-01 | 1.48e-01 | 0.460000 |
| Branched-chain amino acid catabolism | 20 | 2.51e-01 | -1.48e-01 | 0.578000 |
| RHOQ GTPase cycle | 36 | 1.24e-01 | -1.48e-01 | 0.418000 |
| RNA Polymerase III Abortive And Retractive Initiation | 39 | 1.10e-01 | 1.48e-01 | 0.415000 |
| RNA Polymerase III Transcription | 39 | 1.10e-01 | 1.48e-01 | 0.415000 |
| Listeria monocytogenes entry into host cells | 14 | 3.38e-01 | -1.48e-01 | 0.663000 |
| Activated NOTCH1 Transmits Signal to the Nucleus | 19 | 2.66e-01 | -1.47e-01 | 0.587000 |
| O-linked glycosylation of mucins | 26 | 1.95e-01 | -1.47e-01 | 0.505000 |
| BMAL1:CLOCK,NPAS2 activates circadian gene expression | 15 | 3.25e-01 | 1.47e-01 | 0.648000 |
| Vpu mediated degradation of CD4 | 43 | 9.61e-02 | 1.47e-01 | 0.390000 |
| Platelet homeostasis | 47 | 8.24e-02 | -1.47e-01 | 0.375000 |
| Cobalamin (Cbl, vitamin B12) transport and metabolism | 11 | 4.00e-01 | 1.47e-01 | 0.722000 |
| Activation of the pre-replicative complex | 23 | 2.26e-01 | 1.46e-01 | 0.542000 |
| Condensation of Prophase Chromosomes | 12 | 3.82e-01 | 1.46e-01 | 0.703000 |
| Selenoamino acid metabolism | 78 | 2.65e-02 | 1.45e-01 | 0.245000 |
| XBP1(S) activates chaperone genes | 39 | 1.17e-01 | 1.45e-01 | 0.418000 |
| Formation of the Early Elongation Complex | 26 | 2.01e-01 | 1.45e-01 | 0.517000 |
| Formation of the HIV-1 Early Elongation Complex | 26 | 2.01e-01 | 1.45e-01 | 0.517000 |
| Homologous DNA Pairing and Strand Exchange | 35 | 1.39e-01 | 1.45e-01 | 0.436000 |
| Transcription of the HIV genome | 53 | 6.90e-02 | 1.45e-01 | 0.343000 |
| Signaling by FGFR4 | 24 | 2.21e-01 | -1.44e-01 | 0.541000 |
| RHO GTPases activate PAKs | 13 | 3.68e-01 | 1.44e-01 | 0.681000 |
| Activation of G protein gated Potassium channels | 11 | 4.08e-01 | -1.44e-01 | 0.729000 |
| G protein gated Potassium channels | 11 | 4.08e-01 | -1.44e-01 | 0.729000 |
| Inhibition of voltage gated Ca2+ channels via Gbeta/gamma subunits | 11 | 4.08e-01 | -1.44e-01 | 0.729000 |
| PERK regulates gene expression | 26 | 2.04e-01 | 1.44e-01 | 0.520000 |
| Gene Silencing by RNA | 57 | 6.02e-02 | 1.44e-01 | 0.326000 |
| Negative regulation of MET activity | 16 | 3.19e-01 | -1.44e-01 | 0.641000 |
| SARS-CoV Infections | 263 | 6.59e-05 | 1.44e-01 | 0.009350 |
| Downstream signaling events of B Cell Receptor (BCR) | 68 | 4.07e-02 | 1.44e-01 | 0.281000 |
| Heme signaling | 26 | 2.05e-01 | -1.44e-01 | 0.521000 |
| HIV Transcription Initiation | 39 | 1.21e-01 | 1.44e-01 | 0.418000 |
| RNA Polymerase II HIV Promoter Escape | 39 | 1.21e-01 | 1.44e-01 | 0.418000 |
| RNA Polymerase II Promoter Escape | 39 | 1.21e-01 | 1.44e-01 | 0.418000 |
| RNA Polymerase II Transcription Initiation | 39 | 1.21e-01 | 1.44e-01 | 0.418000 |
| RNA Polymerase II Transcription Initiation And Promoter Clearance | 39 | 1.21e-01 | 1.44e-01 | 0.418000 |
| RNA Polymerase II Transcription Pre-Initiation And Promoter Opening | 39 | 1.21e-01 | 1.44e-01 | 0.418000 |
| Chromatin modifying enzymes | 142 | 3.25e-03 | 1.43e-01 | 0.102000 |
| Chromatin organization | 142 | 3.25e-03 | 1.43e-01 | 0.102000 |
| Late endosomal microautophagy | 21 | 2.56e-01 | -1.43e-01 | 0.581000 |
| ER-Phagosome pathway | 67 | 4.29e-02 | 1.43e-01 | 0.286000 |
| Erythropoietin activates RAS | 10 | 4.33e-01 | -1.43e-01 | 0.754000 |
| MAPK6/MAPK4 signaling | 65 | 4.61e-02 | 1.43e-01 | 0.295000 |
| NOTCH2 Activation and Transmission of Signal to the Nucleus | 12 | 3.91e-01 | -1.43e-01 | 0.715000 |
| G1/S Transition | 106 | 1.14e-02 | 1.43e-01 | 0.168000 |
| Synthesis of very long-chain fatty acyl-CoAs | 12 | 3.93e-01 | 1.42e-01 | 0.717000 |
| Bile acid and bile salt metabolism | 14 | 3.57e-01 | -1.42e-01 | 0.673000 |
| Regulation of signaling by CBL | 14 | 3.58e-01 | 1.42e-01 | 0.673000 |
| N-Glycan antennae elongation | 11 | 4.15e-01 | -1.42e-01 | 0.738000 |
| Telomere C-strand (Lagging Strand) Synthesis | 27 | 2.03e-01 | 1.41e-01 | 0.520000 |
| Sphingolipid de novo biosynthesis | 18 | 2.99e-01 | 1.41e-01 | 0.621000 |
| Peptide ligand-binding receptors | 19 | 2.88e-01 | -1.41e-01 | 0.607000 |
| PIWI-interacting RNA (piRNA) biogenesis | 15 | 3.46e-01 | 1.41e-01 | 0.668000 |
| Glutamate binding, activation of AMPA receptors and synaptic plasticity | 12 | 3.99e-01 | -1.41e-01 | 0.722000 |
| Trafficking of AMPA receptors | 12 | 3.99e-01 | -1.41e-01 | 0.722000 |
| FCGR3A-mediated IL10 synthesis | 22 | 2.54e-01 | -1.41e-01 | 0.581000 |
| RHOC GTPase cycle | 45 | 1.03e-01 | 1.41e-01 | 0.406000 |
| Signaling by FGFR3 | 25 | 2.25e-01 | -1.40e-01 | 0.542000 |
| IRE1alpha activates chaperones | 40 | 1.27e-01 | 1.40e-01 | 0.423000 |
| Signalling to RAS | 12 | 4.03e-01 | 1.39e-01 | 0.726000 |
| Prostacyclin signalling through prostacyclin receptor | 11 | 4.24e-01 | -1.39e-01 | 0.748000 |
| PI3K/AKT Signaling in Cancer | 51 | 8.60e-02 | 1.39e-01 | 0.375000 |
| Energy dependent regulation of mTOR by LKB1-AMPK | 21 | 2.71e-01 | 1.39e-01 | 0.592000 |
| Polo-like kinase mediated events | 16 | 3.37e-01 | 1.39e-01 | 0.662000 |
| Caspase activation via extrinsic apoptotic signalling pathway | 15 | 3.53e-01 | 1.38e-01 | 0.672000 |
| Interleukin-12 family signaling | 41 | 1.27e-01 | 1.38e-01 | 0.423000 |
| Degradation of DVL | 47 | 1.03e-01 | 1.37e-01 | 0.406000 |
| Interleukin-4 and Interleukin-13 signaling | 48 | 1.00e-01 | 1.37e-01 | 0.398000 |
| Inhibition of DNA recombination at telomere | 18 | 3.14e-01 | 1.37e-01 | 0.635000 |
| SCF-beta-TrCP mediated degradation of Emi1 | 46 | 1.08e-01 | 1.37e-01 | 0.415000 |
| Inactivation of CSF3 (G-CSF) signaling | 20 | 2.89e-01 | -1.37e-01 | 0.607000 |
| Binding and Uptake of Ligands by Scavenger Receptors | 10 | 4.53e-01 | 1.37e-01 | 0.776000 |
| Unfolded Protein Response (UPR) | 72 | 4.50e-02 | 1.37e-01 | 0.292000 |
| Interactions of Vpr with host cellular proteins | 32 | 1.81e-01 | 1.37e-01 | 0.497000 |
| mRNA Splicing - Major Pathway | 131 | 7.13e-03 | 1.37e-01 | 0.133000 |
| Vasopressin regulates renal water homeostasis via Aquaporins | 22 | 2.68e-01 | -1.36e-01 | 0.588000 |
| Activation of IRF3/IRF7 mediated by TBK1/IKK epsilon | 13 | 3.99e-01 | -1.35e-01 | 0.722000 |
| Other interleukin signaling | 16 | 3.51e-01 | -1.35e-01 | 0.672000 |
| rRNA modification in the nucleus and cytosol | 46 | 1.15e-01 | 1.35e-01 | 0.418000 |
| PTEN Regulation | 107 | 1.66e-02 | 1.34e-01 | 0.210000 |
| Transcriptional regulation by RUNX3 | 73 | 4.86e-02 | 1.34e-01 | 0.300000 |
| TNFR2 non-canonical NF-kB pathway | 66 | 6.22e-02 | 1.33e-01 | 0.329000 |
| Transport of Mature Transcript to Cytoplasm | 56 | 8.60e-02 | 1.33e-01 | 0.375000 |
| Cyclin A:Cdk2-associated events at S phase entry | 72 | 5.19e-02 | 1.33e-01 | 0.305000 |
| Formation of the beta-catenin:TCF transactivating complex | 24 | 2.62e-01 | 1.32e-01 | 0.584000 |
| Signaling by ROBO receptors | 151 | 5.38e-03 | 1.32e-01 | 0.120000 |
| Signaling by ALK fusions and activated point mutants | 43 | 1.36e-01 | 1.32e-01 | 0.436000 |
| Signaling by ALK in cancer | 43 | 1.36e-01 | 1.32e-01 | 0.436000 |
| Nicotinate metabolism | 16 | 3.63e-01 | 1.31e-01 | 0.680000 |
| Platelet sensitization by LDL | 13 | 4.12e-01 | 1.31e-01 | 0.735000 |
| Mitochondrial protein import | 42 | 1.42e-01 | 1.31e-01 | 0.442000 |
| ABC transporters in lipid homeostasis | 10 | 4.73e-01 | 1.31e-01 | 0.793000 |
| S Phase | 129 | 1.04e-02 | 1.31e-01 | 0.162000 |
| RAF-independent MAPK1/3 activation | 20 | 3.11e-01 | -1.31e-01 | 0.632000 |
| Gap-filling DNA repair synthesis and ligation in TC-NER | 55 | 9.40e-02 | 1.31e-01 | 0.385000 |
| Cell Cycle | 492 | 1.05e-06 | 1.30e-01 | 0.000823 |
| Cell Cycle Checkpoints | 212 | 1.21e-03 | 1.30e-01 | 0.060000 |
| p75 NTR receptor-mediated signalling | 54 | 9.98e-02 | -1.30e-01 | 0.398000 |
| Mismatch Repair | 13 | 4.19e-01 | 1.29e-01 | 0.742000 |
| Antigen processing-Cross presentation | 72 | 5.82e-02 | 1.29e-01 | 0.323000 |
| Host Interactions of HIV factors | 104 | 2.30e-02 | 1.29e-01 | 0.238000 |
| TCR signaling | 84 | 4.15e-02 | 1.29e-01 | 0.281000 |
| Interleukin-2 family signaling | 28 | 2.39e-01 | 1.29e-01 | 0.561000 |
| Defective CFTR causes cystic fibrosis | 51 | 1.14e-01 | 1.28e-01 | 0.418000 |
| Constitutive Signaling by EGFRvIII | 10 | 4.85e-01 | 1.28e-01 | 0.800000 |
| Signaling by EGFRvIII in Cancer | 10 | 4.85e-01 | 1.28e-01 | 0.800000 |
| NIK–>noncanonical NF-kB signaling | 49 | 1.25e-01 | 1.27e-01 | 0.418000 |
| FCERI mediated NF-kB activation | 61 | 8.68e-02 | 1.27e-01 | 0.375000 |
| Class A/1 (Rhodopsin-like receptors) | 46 | 1.38e-01 | -1.27e-01 | 0.436000 |
| SARS-CoV-2 Infection | 207 | 1.79e-03 | 1.27e-01 | 0.073400 |
| TRAF6 mediated NF-kB activation | 19 | 3.40e-01 | 1.26e-01 | 0.666000 |
| Interferon alpha/beta signaling | 50 | 1.23e-01 | 1.26e-01 | 0.418000 |
| APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins in late mitosis/early G1 | 60 | 9.21e-02 | 1.26e-01 | 0.381000 |
| RNA Polymerase I Transcription Initiation | 40 | 1.70e-01 | 1.26e-01 | 0.485000 |
| Mitotic Prometaphase | 150 | 8.35e-03 | 1.25e-01 | 0.144000 |
| APC/C-mediated degradation of cell cycle proteins | 73 | 6.51e-02 | 1.25e-01 | 0.332000 |
| Regulation of mitotic cell cycle | 73 | 6.51e-02 | 1.25e-01 | 0.332000 |
| Regulation of RUNX3 expression and activity | 48 | 1.35e-01 | 1.25e-01 | 0.436000 |
| Chaperone Mediated Autophagy | 12 | 4.55e-01 | -1.24e-01 | 0.778000 |
| Activation of BH3-only proteins | 25 | 2.82e-01 | 1.24e-01 | 0.605000 |
| M Phase | 280 | 3.80e-04 | 1.24e-01 | 0.026600 |
| Regulation of Apoptosis | 44 | 1.54e-01 | 1.24e-01 | 0.460000 |
| DAP12 signaling | 19 | 3.50e-01 | 1.24e-01 | 0.672000 |
| APC-Cdc20 mediated degradation of Nek2A | 21 | 3.26e-01 | -1.24e-01 | 0.648000 |
| TNFR1-induced proapoptotic signaling | 12 | 4.58e-01 | 1.24e-01 | 0.780000 |
| mRNA Splicing | 141 | 1.21e-02 | 1.23e-01 | 0.170000 |
| alpha-linolenic (omega3) and linoleic (omega6) acid metabolism | 10 | 5.02e-01 | -1.23e-01 | 0.808000 |
| alpha-linolenic acid (ALA) metabolism | 10 | 5.02e-01 | -1.23e-01 | 0.808000 |
| GPCR downstream signalling | 185 | 4.21e-03 | -1.23e-01 | 0.112000 |
| TBC/RABGAPs | 39 | 1.87e-01 | 1.22e-01 | 0.499000 |
| NRAGE signals death through JNK | 25 | 2.90e-01 | -1.22e-01 | 0.607000 |
| Cyclin E associated events during G1/S transition | 70 | 7.78e-02 | 1.22e-01 | 0.365000 |
| Interleukin-20 family signaling | 13 | 4.46e-01 | -1.22e-01 | 0.767000 |
| ZBP1(DAI) mediated induction of type I IFNs | 16 | 3.99e-01 | 1.22e-01 | 0.722000 |
| Hh mutants are degraded by ERAD | 46 | 1.53e-01 | 1.22e-01 | 0.460000 |
| Cholesterol biosynthesis | 20 | 3.47e-01 | -1.21e-01 | 0.668000 |
| Cellular response to starvation | 112 | 2.69e-02 | 1.21e-01 | 0.245000 |
| Vpr-mediated nuclear import of PICs | 31 | 2.43e-01 | 1.21e-01 | 0.569000 |
| TP53 Regulates Transcription of DNA Repair Genes | 47 | 1.51e-01 | 1.21e-01 | 0.456000 |
| SARS-CoV-1 Infection | 44 | 1.65e-01 | 1.21e-01 | 0.480000 |
| RHOF GTPase cycle | 23 | 3.15e-01 | 1.21e-01 | 0.635000 |
| SCF(Skp2)-mediated degradation of p27/p21 | 51 | 1.36e-01 | 1.21e-01 | 0.436000 |
| tRNA processing | 87 | 5.20e-02 | 1.21e-01 | 0.305000 |
| Intraflagellar transport | 31 | 2.45e-01 | 1.21e-01 | 0.571000 |
| Metabolism of RNA | 521 | 3.30e-06 | 1.21e-01 | 0.000982 |
| Processing of Capped Intron-Containing Pre-mRNA | 181 | 5.72e-03 | 1.20e-01 | 0.122000 |
| Mitochondrial iron-sulfur cluster biogenesis | 12 | 4.74e-01 | 1.19e-01 | 0.793000 |
| Transport of Mature mRNA derived from an Intron-Containing Transcript | 47 | 1.57e-01 | 1.19e-01 | 0.462000 |
| RHOB GTPase cycle | 40 | 1.92e-01 | 1.19e-01 | 0.504000 |
| Elevation of cytosolic Ca2+ levels | 10 | 5.16e-01 | -1.19e-01 | 0.816000 |
| Downregulation of SMAD2/3:SMAD4 transcriptional activity | 23 | 3.26e-01 | -1.18e-01 | 0.648000 |
| Reproduction | 43 | 1.82e-01 | 1.18e-01 | 0.497000 |
| Signal transduction by L1 | 11 | 4.99e-01 | -1.18e-01 | 0.808000 |
| Resolution of Sister Chromatid Cohesion | 90 | 5.48e-02 | 1.17e-01 | 0.312000 |
| Cell Cycle, Mitotic | 398 | 7.06e-05 | 1.17e-01 | 0.009350 |
| Cardiac conduction | 42 | 1.92e-01 | -1.16e-01 | 0.504000 |
| Signal amplification | 19 | 3.80e-01 | -1.16e-01 | 0.701000 |
| PIP3 activates AKT signaling | 175 | 8.24e-03 | 1.16e-01 | 0.144000 |
| Sensory processing of sound by outer hair cells of the cochlea | 16 | 4.21e-01 | 1.16e-01 | 0.745000 |
| Translation | 237 | 2.20e-03 | 1.16e-01 | 0.081900 |
| Budding and maturation of HIV virion | 22 | 3.47e-01 | -1.16e-01 | 0.668000 |
| Viral Messenger RNA Synthesis | 40 | 2.05e-01 | 1.16e-01 | 0.521000 |
| Signaling by GPCR | 202 | 4.79e-03 | -1.16e-01 | 0.117000 |
| APC/C:Cdc20 mediated degradation of mitotic proteins | 61 | 1.20e-01 | 1.15e-01 | 0.418000 |
| Diseases associated with glycosaminoglycan metabolism | 16 | 4.26e-01 | -1.15e-01 | 0.748000 |
| Defective TPR may confer susceptibility towards thyroid papillary carcinoma (TPC) | 27 | 3.02e-01 | 1.15e-01 | 0.623000 |
| Regulation of Glucokinase by Glucokinase Regulatory Protein | 27 | 3.02e-01 | 1.15e-01 | 0.623000 |
| Chromosome Maintenance | 72 | 9.56e-02 | 1.14e-01 | 0.389000 |
| Infectious disease | 611 | 2.34e-06 | 1.14e-01 | 0.000930 |
| Metabolism of non-coding RNA | 46 | 1.84e-01 | 1.13e-01 | 0.497000 |
| snRNP Assembly | 46 | 1.84e-01 | 1.13e-01 | 0.497000 |
| Anti-inflammatory response favouring Leishmania parasite infection | 53 | 1.54e-01 | -1.13e-01 | 0.460000 |
| Leishmania parasite growth and survival | 53 | 1.54e-01 | -1.13e-01 | 0.460000 |
| Regulation of RAS by GAPs | 55 | 1.47e-01 | 1.13e-01 | 0.451000 |
| Glucagon-type ligand receptors | 13 | 4.80e-01 | -1.13e-01 | 0.798000 |
| Mitotic G1 phase and G1/S transition | 121 | 3.24e-02 | 1.13e-01 | 0.257000 |
| Autodegradation of Cdh1 by Cdh1:APC/C | 52 | 1.61e-01 | 1.13e-01 | 0.471000 |
| NEP/NS2 Interacts with the Cellular Export Machinery | 29 | 2.96e-01 | 1.12e-01 | 0.617000 |
| Transport of bile salts and organic acids, metal ions and amine compounds | 32 | 2.73e-01 | -1.12e-01 | 0.593000 |
| tRNA Aminoacylation | 23 | 3.53e-01 | 1.12e-01 | 0.672000 |
| L1CAM interactions | 40 | 2.21e-01 | -1.12e-01 | 0.541000 |
| Defects in vitamin and cofactor metabolism | 16 | 4.39e-01 | 1.12e-01 | 0.760000 |
| RIPK1-mediated regulated necrosis | 25 | 3.34e-01 | 1.12e-01 | 0.659000 |
| Regulation of necroptotic cell death | 25 | 3.34e-01 | 1.12e-01 | 0.659000 |
| RHOD GTPase cycle | 33 | 2.67e-01 | 1.12e-01 | 0.587000 |
| Cytoprotection by HMOX1 | 42 | 2.12e-01 | -1.11e-01 | 0.530000 |
| Interleukin-3, Interleukin-5 and GM-CSF signaling | 29 | 3.00e-01 | 1.11e-01 | 0.622000 |
| Dectin-1 mediated noncanonical NF-kB signaling | 50 | 1.75e-01 | 1.11e-01 | 0.491000 |
| Signaling by FGFR1 | 27 | 3.19e-01 | -1.11e-01 | 0.641000 |
| Estrogen-dependent gene expression | 68 | 1.16e-01 | 1.10e-01 | 0.418000 |
| UCH proteinases | 72 | 1.07e-01 | 1.10e-01 | 0.415000 |
| Costimulation by the CD28 family | 44 | 2.08e-01 | 1.10e-01 | 0.523000 |
| Signaling by the B Cell Receptor (BCR) | 88 | 7.62e-02 | 1.10e-01 | 0.362000 |
| Nuclear events mediated by NFE2L2 | 66 | 1.25e-01 | 1.09e-01 | 0.418000 |
| CD209 (DC-SIGN) signaling | 15 | 4.63e-01 | -1.09e-01 | 0.786000 |
| Mitotic Metaphase and Anaphase | 186 | 1.05e-02 | 1.09e-01 | 0.162000 |
| Post-translational modification: synthesis of GPI-anchored proteins | 30 | 3.01e-01 | -1.09e-01 | 0.623000 |
| ABC-family proteins mediated transport | 72 | 1.10e-01 | 1.09e-01 | 0.415000 |
| Synthesis of DNA | 95 | 6.71e-02 | 1.09e-01 | 0.341000 |
| APC:Cdc20 mediated degradation of cell cycle proteins prior to satisfation of the cell cycle checkpoint | 59 | 1.49e-01 | 1.09e-01 | 0.454000 |
| SARS-CoV-2-host interactions | 146 | 2.38e-02 | 1.09e-01 | 0.238000 |
| Separation of Sister Chromatids | 141 | 2.64e-02 | 1.09e-01 | 0.245000 |
| ECM proteoglycans | 11 | 5.33e-01 | -1.08e-01 | 0.829000 |
| Mitotic Anaphase | 185 | 1.18e-02 | 1.08e-01 | 0.170000 |
| tRNA processing in the nucleus | 53 | 1.75e-01 | 1.08e-01 | 0.491000 |
| SUMOylation of DNA methylation proteins | 14 | 4.85e-01 | -1.08e-01 | 0.800000 |
| Interleukin-10 signaling | 13 | 5.01e-01 | -1.08e-01 | 0.808000 |
| rRNA processing in the nucleus and cytosol | 156 | 2.11e-02 | 1.07e-01 | 0.229000 |
| Signaling by ERBB2 TMD/JMD mutants | 10 | 5.57e-01 | -1.07e-01 | 0.840000 |
| Export of Viral Ribonucleoproteins from Nucleus | 30 | 3.09e-01 | 1.07e-01 | 0.632000 |
| Activation of APC/C and APC/C:Cdc20 mediated degradation of mitotic proteins | 62 | 1.45e-01 | 1.07e-01 | 0.450000 |
| Transcriptional regulation by small RNAs | 42 | 2.31e-01 | 1.07e-01 | 0.548000 |
| Regulation of TP53 Activity | 133 | 3.41e-02 | 1.07e-01 | 0.260000 |
| NS1 Mediated Effects on Host Pathways | 37 | 2.62e-01 | 1.07e-01 | 0.584000 |
| DAG and IP3 signaling | 26 | 3.47e-01 | -1.07e-01 | 0.668000 |
| FGFR2 alternative splicing | 22 | 3.87e-01 | 1.07e-01 | 0.710000 |
| Deadenylation-dependent mRNA decay | 50 | 1.94e-01 | 1.06e-01 | 0.505000 |
| RHOU GTPase cycle | 29 | 3.22e-01 | 1.06e-01 | 0.645000 |
| Dual incision in TC-NER | 56 | 1.72e-01 | 1.06e-01 | 0.489000 |
| Downregulation of ERBB2 signaling | 17 | 4.53e-01 | -1.05e-01 | 0.776000 |
| KEAP1-NFE2L2 pathway | 85 | 9.42e-02 | 1.05e-01 | 0.385000 |
| Signaling by EGFR | 35 | 2.83e-01 | 1.05e-01 | 0.605000 |
| Removal of the Flap Intermediate from the C-strand | 15 | 4.83e-01 | 1.05e-01 | 0.799000 |
| Cdc20:Phospho-APC/C mediated degradation of Cyclin A | 58 | 1.69e-01 | 1.05e-01 | 0.484000 |
| Degradation of GLI1 by the proteasome | 50 | 2.02e-01 | 1.04e-01 | 0.518000 |
| APC/C:Cdc20 mediated degradation of Securin | 54 | 1.86e-01 | 1.04e-01 | 0.499000 |
| Insulin receptor recycling | 17 | 4.59e-01 | -1.04e-01 | 0.781000 |
| Hh mutants abrogate ligand secretion | 48 | 2.15e-01 | 1.04e-01 | 0.535000 |
| Major pathway of rRNA processing in the nucleolus and cytosol | 150 | 2.91e-02 | 1.04e-01 | 0.247000 |
| HCMV Late Events | 48 | 2.15e-01 | 1.03e-01 | 0.535000 |
| DNA Replication Pre-Initiation | 79 | 1.13e-01 | 1.03e-01 | 0.418000 |
| Mismatch repair (MMR) directed by MSH2:MSH3 (MutSbeta) | 12 | 5.36e-01 | 1.03e-01 | 0.829000 |
| Post-chaperonin tubulin folding pathway | 12 | 5.38e-01 | 1.03e-01 | 0.830000 |
| Mitochondrial calcium ion transport | 14 | 5.07e-01 | 1.02e-01 | 0.809000 |
| Integrin cell surface interactions | 24 | 3.85e-01 | 1.02e-01 | 0.708000 |
| FGFR1 mutant receptor activation | 19 | 4.40e-01 | -1.02e-01 | 0.761000 |
| Nuclear Envelope (NE) Reassembly | 56 | 1.86e-01 | 1.02e-01 | 0.499000 |
| NoRC negatively regulates rRNA expression | 42 | 2.54e-01 | 1.02e-01 | 0.581000 |
| Cellular responses to stress | 519 | 9.53e-05 | 1.01e-01 | 0.011400 |
| Glycogen synthesis | 11 | 5.60e-01 | -1.01e-01 | 0.840000 |
| CLEC7A (Dectin-1) signaling | 81 | 1.15e-01 | 1.01e-01 | 0.418000 |
| Transferrin endocytosis and recycling | 19 | 4.44e-01 | -1.01e-01 | 0.765000 |
| Fatty acid metabolism | 97 | 8.57e-02 | -1.01e-01 | 0.375000 |
| Homology Directed Repair | 84 | 1.10e-01 | 1.01e-01 | 0.415000 |
| CDK-mediated phosphorylation and removal of Cdc6 | 58 | 1.84e-01 | 1.01e-01 | 0.497000 |
| Inactivation of APC/C via direct inhibition of the APC/C complex | 16 | 4.88e-01 | -1.00e-01 | 0.802000 |
| Inhibition of the proteolytic activity of APC/C required for the onset of anaphase by mitotic spindle checkpoint components | 16 | 4.88e-01 | -1.00e-01 | 0.802000 |
| rRNA processing | 160 | 3.01e-02 | 9.97e-02 | 0.249000 |
| Cellular Senescence | 99 | 8.79e-02 | 9.95e-02 | 0.375000 |
| Hedgehog ligand biogenesis | 51 | 2.20e-01 | 9.95e-02 | 0.541000 |
| Nuclear events stimulated by ALK signaling in cancer | 13 | 5.36e-01 | 9.90e-02 | 0.829000 |
| Metalloprotease DUBs | 16 | 4.93e-01 | -9.89e-02 | 0.807000 |
| Regulation of APC/C activators between G1/S and early anaphase | 66 | 1.66e-01 | 9.87e-02 | 0.480000 |
| Degradation of AXIN | 46 | 2.48e-01 | 9.85e-02 | 0.575000 |
| ABC transporter disorders | 58 | 1.96e-01 | 9.83e-02 | 0.506000 |
| Insulin processing | 15 | 5.11e-01 | 9.81e-02 | 0.810000 |
| Inactivation, recovery and regulation of the phototransduction cascade | 16 | 5.02e-01 | 9.70e-02 | 0.808000 |
| The phototransduction cascade | 16 | 5.02e-01 | 9.70e-02 | 0.808000 |
| Mismatch repair (MMR) directed by MSH2:MSH6 (MutSalpha) | 12 | 5.61e-01 | 9.69e-02 | 0.840000 |
| HIV Infection | 182 | 2.47e-02 | 9.69e-02 | 0.240000 |
| Cellular responses to stimuli | 524 | 1.90e-04 | 9.66e-02 | 0.017400 |
| Switching of origins to a post-replicative state | 71 | 1.60e-01 | 9.65e-02 | 0.471000 |
| Cargo recognition for clathrin-mediated endocytosis | 64 | 1.84e-01 | -9.61e-02 | 0.497000 |
| Processing of DNA double-strand break ends | 52 | 2.31e-01 | 9.61e-02 | 0.548000 |
| GAB1 signalosome | 10 | 5.99e-01 | 9.60e-02 | 0.850000 |
| Neddylation | 183 | 2.58e-02 | 9.59e-02 | 0.244000 |
| RET signaling | 23 | 4.26e-01 | -9.59e-02 | 0.748000 |
| Intra-Golgi traffic | 38 | 3.07e-01 | 9.58e-02 | 0.628000 |
| Collagen biosynthesis and modifying enzymes | 13 | 5.51e-01 | -9.55e-02 | 0.838000 |
| Cell-Cell communication | 44 | 2.75e-01 | -9.52e-02 | 0.593000 |
| mTORC1-mediated signalling | 17 | 4.98e-01 | 9.49e-02 | 0.808000 |
| Ion homeostasis | 26 | 4.03e-01 | -9.47e-02 | 0.726000 |
| Regulation of PTEN gene transcription | 44 | 2.84e-01 | 9.35e-02 | 0.605000 |
| Ephrin signaling | 12 | 5.75e-01 | -9.35e-02 | 0.842000 |
| MAP3K8 (TPL2)-dependent MAPK1/3 activation | 13 | 5.60e-01 | -9.34e-02 | 0.840000 |
| HDR through Homologous Recombination (HRR) | 55 | 2.32e-01 | 9.33e-02 | 0.549000 |
| Golgi-to-ER retrograde transport | 94 | 1.19e-01 | 9.32e-02 | 0.418000 |
| Synthesis of bile acids and bile salts | 13 | 5.62e-01 | -9.29e-02 | 0.840000 |
| Signaling by cytosolic FGFR1 fusion mutants | 16 | 5.25e-01 | -9.19e-02 | 0.826000 |
| EML4 and NUDC in mitotic spindle formation | 85 | 1.47e-01 | 9.12e-02 | 0.451000 |
| FCGR3A-mediated phagocytosis | 41 | 3.15e-01 | 9.07e-02 | 0.635000 |
| Leishmania phagocytosis | 41 | 3.15e-01 | 9.07e-02 | 0.635000 |
| Parasite infection | 41 | 3.15e-01 | 9.07e-02 | 0.635000 |
| Myogenesis | 13 | 5.72e-01 | 9.05e-02 | 0.842000 |
| Insertion of tail-anchored proteins into the endoplasmic reticulum membrane | 14 | 5.58e-01 | -9.04e-02 | 0.840000 |
| Intracellular signaling by second messengers | 200 | 2.92e-02 | 8.99e-02 | 0.247000 |
| Regulation of TP53 Expression and Degradation | 34 | 3.65e-01 | 8.99e-02 | 0.681000 |
| Synthesis of PIPs at the Golgi membrane | 12 | 5.90e-01 | 8.98e-02 | 0.847000 |
| DNA Replication | 102 | 1.18e-01 | 8.97e-02 | 0.418000 |
| Unwinding of DNA | 10 | 6.24e-01 | 8.96e-02 | 0.864000 |
| Signaling by Insulin receptor | 41 | 3.21e-01 | -8.95e-02 | 0.644000 |
| Beta-catenin phosphorylation cascade | 15 | 5.48e-01 | -8.95e-02 | 0.838000 |
| Transcription of E2F targets under negative control by DREAM complex | 17 | 5.25e-01 | -8.90e-02 | 0.826000 |
| Cilium Assembly | 140 | 6.98e-02 | 8.90e-02 | 0.343000 |
| RHOBTB2 GTPase cycle | 20 | 4.92e-01 | 8.87e-02 | 0.806000 |
| Metabolism of nitric oxide: NOS3 activation and regulation | 12 | 5.95e-01 | 8.87e-02 | 0.849000 |
| CD28 co-stimulation | 27 | 4.27e-01 | 8.83e-02 | 0.749000 |
| G beta:gamma signalling through BTK | 10 | 6.31e-01 | -8.78e-02 | 0.864000 |
| Respiratory electron transport, ATP synthesis by chemiosmotic coupling, and heat production by uncoupling proteins. | 76 | 1.87e-01 | 8.77e-02 | 0.499000 |
| Diseases of programmed cell death | 37 | 3.56e-01 | 8.77e-02 | 0.673000 |
| RUNX3 regulates p14-ARF | 10 | 6.32e-01 | -8.75e-02 | 0.864000 |
| Infection with Mycobacterium tuberculosis | 22 | 4.78e-01 | -8.73e-02 | 0.798000 |
| RUNX1 regulates transcription of genes involved in differentiation of HSCs | 55 | 2.68e-01 | 8.65e-02 | 0.587000 |
| TRAF3-dependent IRF activation pathway | 14 | 5.76e-01 | -8.64e-02 | 0.842000 |
| RAB geranylgeranylation | 39 | 3.51e-01 | -8.63e-02 | 0.672000 |
| Glycogen metabolism | 17 | 5.41e-01 | -8.57e-02 | 0.832000 |
| RHO GTPases Activate WASPs and WAVEs | 28 | 4.34e-01 | 8.55e-02 | 0.754000 |
| Fanconi Anemia Pathway | 29 | 4.26e-01 | -8.55e-02 | 0.748000 |
| Nucleotide salvage | 18 | 5.33e-01 | -8.49e-02 | 0.829000 |
| FLT3 Signaling | 32 | 4.07e-01 | 8.47e-02 | 0.729000 |
| Gamma carboxylation, hypusine formation and arylsulfatase activation | 21 | 5.02e-01 | 8.47e-02 | 0.808000 |
| Citric acid cycle (TCA cycle) | 19 | 5.23e-01 | 8.46e-02 | 0.826000 |
| Insulin receptor signalling cascade | 25 | 4.64e-01 | -8.45e-02 | 0.786000 |
| Interleukin-1 signaling | 75 | 2.07e-01 | 8.45e-02 | 0.521000 |
| Base Excision Repair | 39 | 3.65e-01 | 8.39e-02 | 0.681000 |
| Ion channel transport | 76 | 2.07e-01 | -8.39e-02 | 0.521000 |
| Collagen degradation | 10 | 6.47e-01 | 8.35e-02 | 0.870000 |
| Organelle biogenesis and maintenance | 193 | 4.70e-02 | 8.33e-02 | 0.299000 |
| Resolution of Abasic Sites (AP sites) | 32 | 4.15e-01 | 8.32e-02 | 0.738000 |
| Peptide hormone metabolism | 28 | 4.46e-01 | 8.32e-02 | 0.767000 |
| COPI-mediated anterograde transport | 69 | 2.33e-01 | 8.32e-02 | 0.550000 |
| Apoptotic execution phase | 32 | 4.16e-01 | 8.31e-02 | 0.738000 |
| Regulation of actin dynamics for phagocytic cup formation | 43 | 3.52e-01 | 8.21e-02 | 0.672000 |
| Uptake and actions of bacterial toxins | 18 | 5.47e-01 | -8.20e-02 | 0.838000 |
| Signaling by CSF3 (G-CSF) | 25 | 4.79e-01 | -8.19e-02 | 0.798000 |
| Sphingolipid metabolism | 43 | 3.54e-01 | 8.18e-02 | 0.672000 |
| SUMOylation of DNA replication proteins | 42 | 3.60e-01 | 8.17e-02 | 0.675000 |
| Diseases of metabolism | 125 | 1.17e-01 | -8.14e-02 | 0.418000 |
| ERCC6 (CSB) and EHMT2 (G9a) positively regulate rRNA expression | 15 | 5.85e-01 | 8.14e-02 | 0.847000 |
| Protein localization | 115 | 1.33e-01 | 8.13e-02 | 0.436000 |
| Base-Excision Repair, AP Site Formation | 16 | 5.74e-01 | -8.13e-02 | 0.842000 |
| mRNA Splicing - Minor Pathway | 45 | 3.47e-01 | 8.11e-02 | 0.668000 |
| Intra-Golgi and retrograde Golgi-to-ER traffic | 155 | 8.35e-02 | 8.08e-02 | 0.375000 |
| RHO GTPases Activate Formins | 100 | 1.64e-01 | 8.08e-02 | 0.478000 |
| G0 and Early G1 | 24 | 4.95e-01 | -8.05e-02 | 0.808000 |
| Gap-filling DNA repair synthesis and ligation in GG-NER | 23 | 5.04e-01 | 8.05e-02 | 0.809000 |
| RNA Polymerase III Chain Elongation | 17 | 5.66e-01 | 8.04e-02 | 0.840000 |
| RHOV GTPase cycle | 27 | 4.72e-01 | 8.00e-02 | 0.792000 |
| Apoptosis | 129 | 1.19e-01 | 7.97e-02 | 0.418000 |
| Transport of Ribonucleoproteins into the Host Nucleus | 29 | 4.58e-01 | 7.96e-02 | 0.780000 |
| HDR through Homologous Recombination (HRR) or Single Strand Annealing (SSA) | 78 | 2.25e-01 | 7.96e-02 | 0.542000 |
| Regulation of TP53 Degradation | 33 | 4.30e-01 | 7.94e-02 | 0.751000 |
| Assembly of the pre-replicative complex | 66 | 2.66e-01 | 7.92e-02 | 0.587000 |
| RAF/MAP kinase cascade | 152 | 9.30e-02 | 7.92e-02 | 0.384000 |
| FCERI mediated Ca+2 mobilization | 23 | 5.12e-01 | 7.90e-02 | 0.810000 |
| Disease | 1053 | 2.66e-05 | 7.88e-02 | 0.005290 |
| Basigin interactions | 14 | 6.10e-01 | 7.87e-02 | 0.860000 |
| Sialic acid metabolism | 22 | 5.24e-01 | -7.86e-02 | 0.826000 |
| Suppression of phagosomal maturation | 12 | 6.38e-01 | -7.85e-02 | 0.865000 |
| MAPK family signaling cascades | 181 | 7.00e-02 | 7.84e-02 | 0.343000 |
| Fatty acyl-CoA biosynthesis | 22 | 5.27e-01 | 7.80e-02 | 0.826000 |
| Amplification of signal from unattached kinetochores via a MAD2 inhibitory signal | 81 | 2.26e-01 | 7.79e-02 | 0.542000 |
| Amplification of signal from the kinetochores | 81 | 2.26e-01 | 7.79e-02 | 0.542000 |
| Signaling by MET | 40 | 3.95e-01 | -7.78e-02 | 0.720000 |
| Regulation of TP53 Activity through Methylation | 16 | 5.91e-01 | 7.77e-02 | 0.847000 |
| Fc epsilon receptor (FCERI) signaling | 103 | 1.75e-01 | 7.75e-02 | 0.491000 |
| Sealing of the nuclear envelope (NE) by ESCRT-III | 16 | 5.92e-01 | 7.75e-02 | 0.848000 |
| Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding | 18 | 5.71e-01 | 7.72e-02 | 0.842000 |
| Diseases of glycosylation | 68 | 2.72e-01 | -7.71e-02 | 0.593000 |
| Plasma lipoprotein remodeling | 11 | 6.59e-01 | -7.68e-02 | 0.876000 |
| Respiratory electron transport | 75 | 2.51e-01 | 7.68e-02 | 0.578000 |
| Asymmetric localization of PCP proteins | 51 | 3.43e-01 | 7.68e-02 | 0.668000 |
| Iron uptake and transport | 38 | 4.13e-01 | -7.67e-02 | 0.736000 |
| Transcriptional Regulation by TP53 | 280 | 2.91e-02 | 7.63e-02 | 0.247000 |
| Diseases of signal transduction by growth factor receptors and second messengers | 293 | 2.61e-02 | 7.61e-02 | 0.245000 |
| Processive synthesis on the C-strand of the telomere | 17 | 5.88e-01 | 7.59e-02 | 0.847000 |
| Response of Mtb to phagocytosis | 20 | 5.58e-01 | -7.57e-02 | 0.840000 |
| HIV elongation arrest and recovery | 23 | 5.30e-01 | 7.56e-02 | 0.829000 |
| Pausing and recovery of HIV elongation | 23 | 5.30e-01 | 7.56e-02 | 0.829000 |
| Cytokine Signaling in Immune system | 416 | 8.90e-03 | 7.55e-02 | 0.147000 |
| Prolonged ERK activation events | 13 | 6.37e-01 | -7.55e-02 | 0.865000 |
| Ca2+ pathway | 36 | 4.34e-01 | -7.54e-02 | 0.754000 |
| MAPK1/MAPK3 signaling | 157 | 1.05e-01 | 7.53e-02 | 0.409000 |
| APC/C:Cdc20 mediated degradation of Cyclin B | 19 | 5.70e-01 | -7.52e-02 | 0.842000 |
| Recognition of DNA damage by PCNA-containing replication complex | 26 | 5.07e-01 | 7.52e-02 | 0.809000 |
| SUMO E3 ligases SUMOylate target proteins | 131 | 1.39e-01 | 7.51e-02 | 0.436000 |
| Transcription of E2F targets under negative control by p107 (RBL1) and p130 (RBL2) in complex with HDAC1 | 15 | 6.16e-01 | 7.48e-02 | 0.864000 |
| Death Receptor Signalling | 88 | 2.26e-01 | -7.48e-02 | 0.542000 |
| Abortive elongation of HIV-1 transcript in the absence of Tat | 18 | 5.84e-01 | 7.45e-02 | 0.847000 |
| DNA Double-Strand Break Repair | 109 | 1.82e-01 | 7.42e-02 | 0.497000 |
| Signaling by ERBB2 KD Mutants | 12 | 6.57e-01 | -7.40e-02 | 0.875000 |
| Clathrin-mediated endocytosis | 89 | 2.29e-01 | -7.40e-02 | 0.545000 |
| Cleavage of the damaged pyrimidine | 14 | 6.33e-01 | -7.36e-02 | 0.864000 |
| Depyrimidination | 14 | 6.33e-01 | -7.36e-02 | 0.864000 |
| Recognition and association of DNA glycosylase with site containing an affected pyrimidine | 14 | 6.33e-01 | -7.36e-02 | 0.864000 |
| JNK (c-Jun kinases) phosphorylation and activation mediated by activated human TAK1 | 10 | 6.88e-01 | 7.33e-02 | 0.891000 |
| Disorders of transmembrane transporters | 107 | 1.92e-01 | 7.32e-02 | 0.504000 |
| Circadian Clock | 51 | 3.68e-01 | -7.29e-02 | 0.681000 |
| RHOG GTPase cycle | 45 | 3.99e-01 | -7.28e-02 | 0.722000 |
| Degradation of beta-catenin by the destruction complex | 67 | 3.04e-01 | 7.27e-02 | 0.625000 |
| Glyoxylate metabolism and glycine degradation | 19 | 5.84e-01 | -7.27e-02 | 0.847000 |
| Metabolism of nucleotides | 68 | 3.04e-01 | 7.22e-02 | 0.625000 |
| Fcgamma receptor (FCGR) dependent phagocytosis | 61 | 3.36e-01 | 7.14e-02 | 0.660000 |
| Frs2-mediated activation | 11 | 6.82e-01 | 7.13e-02 | 0.891000 |
| Signaling by NOTCH3 | 30 | 5.00e-01 | 7.11e-02 | 0.808000 |
| Metabolism of carbohydrates | 178 | 1.04e-01 | -7.10e-02 | 0.407000 |
| RUNX1 regulates genes involved in megakaryocyte differentiation and platelet function | 22 | 5.66e-01 | 7.07e-02 | 0.840000 |
| Aggrephagy | 19 | 5.94e-01 | -7.07e-02 | 0.849000 |
| Constitutive Signaling by Aberrant PI3K in Cancer | 27 | 5.26e-01 | 7.05e-02 | 0.826000 |
| Transport of small molecules | 338 | 2.78e-02 | -7.02e-02 | 0.245000 |
| Synthesis of PIPs at the plasma membrane | 36 | 4.69e-01 | 6.97e-02 | 0.792000 |
| Translocation of SLC2A4 (GLUT4) to the plasma membrane | 44 | 4.25e-01 | 6.96e-02 | 0.748000 |
| Transcriptional regulation by RUNX1 | 125 | 1.83e-01 | 6.91e-02 | 0.497000 |
| Deactivation of the beta-catenin transactivating complex | 27 | 5.38e-01 | -6.84e-02 | 0.830000 |
| ERKs are inactivated | 11 | 6.94e-01 | -6.84e-02 | 0.894000 |
| Cooperation of PDCL (PhLP1) and TRiC/CCT in G-protein beta folding | 22 | 5.80e-01 | -6.82e-02 | 0.846000 |
| Programmed Cell Death | 150 | 1.51e-01 | 6.82e-02 | 0.456000 |
| Hyaluronan metabolism | 10 | 7.09e-01 | -6.80e-02 | 0.901000 |
| Role of phospholipids in phagocytosis | 16 | 6.38e-01 | 6.79e-02 | 0.865000 |
| Transcriptional Regulation by MECP2 | 28 | 5.36e-01 | 6.75e-02 | 0.829000 |
| Negative regulators of DDX58/IFIH1 signaling | 34 | 4.96e-01 | 6.75e-02 | 0.808000 |
| SUMOylation of immune response proteins | 10 | 7.13e-01 | -6.73e-02 | 0.901000 |
| SUMOylation of DNA damage response and repair proteins | 66 | 3.46e-01 | 6.71e-02 | 0.668000 |
| Meiotic synapsis | 22 | 5.86e-01 | 6.71e-02 | 0.847000 |
| SUMOylation | 136 | 1.81e-01 | 6.66e-02 | 0.497000 |
| SUMOylation of RNA binding proteins | 41 | 4.61e-01 | 6.66e-02 | 0.782000 |
| FCERI mediated MAPK activation | 22 | 5.89e-01 | -6.66e-02 | 0.847000 |
| Pausing and recovery of Tat-mediated HIV elongation | 22 | 5.90e-01 | 6.64e-02 | 0.847000 |
| Tat-mediated HIV elongation arrest and recovery | 22 | 5.90e-01 | 6.64e-02 | 0.847000 |
| Senescence-Associated Secretory Phenotype (SASP) | 39 | 4.75e-01 | -6.61e-02 | 0.794000 |
| p75NTR signals via NF-kB | 11 | 7.04e-01 | -6.61e-02 | 0.901000 |
| TGF-beta receptor signaling in EMT (epithelial to mesenchymal transition) | 13 | 6.80e-01 | -6.61e-02 | 0.891000 |
| Mitochondrial biogenesis | 53 | 4.06e-01 | 6.60e-02 | 0.729000 |
| Formation of tubulin folding intermediates by CCT/TriC | 13 | 6.83e-01 | 6.55e-02 | 0.891000 |
| TNFR1-induced NFkappaB signaling pathway | 19 | 6.21e-01 | 6.55e-02 | 0.864000 |
| Signaling by NOTCH | 130 | 2.01e-01 | 6.51e-02 | 0.517000 |
| Pre-NOTCH Processing in Golgi | 16 | 6.52e-01 | 6.50e-02 | 0.873000 |
| DAP12 interactions | 21 | 6.06e-01 | 6.50e-02 | 0.856000 |
| C-type lectin receptors (CLRs) | 97 | 2.71e-01 | 6.48e-02 | 0.592000 |
| Signaling by Interleukins | 258 | 7.54e-02 | 6.47e-02 | 0.362000 |
| Deregulated CDK5 triggers multiple neurodegenerative pathways in Alzheimer’s disease models | 20 | 6.17e-01 | -6.46e-02 | 0.864000 |
| Neurodegenerative Diseases | 20 | 6.17e-01 | -6.46e-02 | 0.864000 |
| Interleukin-35 Signalling | 11 | 7.12e-01 | -6.44e-02 | 0.901000 |
| Pyruvate metabolism and Citric Acid (TCA) cycle | 40 | 4.82e-01 | -6.43e-02 | 0.799000 |
| Interleukin-1 family signaling | 93 | 2.86e-01 | 6.41e-02 | 0.607000 |
| Pre-NOTCH Transcription and Translation | 27 | 5.65e-01 | 6.39e-02 | 0.840000 |
| Nuclear import of Rev protein | 30 | 5.45e-01 | 6.39e-02 | 0.837000 |
| Mitotic Spindle Checkpoint | 93 | 2.91e-01 | 6.35e-02 | 0.607000 |
| RHO GTPase Effectors | 185 | 1.39e-01 | 6.34e-02 | 0.436000 |
| Metal ion SLC transporters | 15 | 6.71e-01 | -6.33e-02 | 0.885000 |
| Molecules associated with elastic fibres | 11 | 7.16e-01 | -6.33e-02 | 0.901000 |
| NF-kB activation through FADD/RIP-1 pathway mediated by caspase-8 and -10 | 11 | 7.18e-01 | -6.29e-02 | 0.902000 |
| Metabolism of amino acids and derivatives | 219 | 1.11e-01 | 6.28e-02 | 0.416000 |
| RNA Polymerase I Promoter Clearance | 44 | 4.71e-01 | 6.28e-02 | 0.792000 |
| RNA Polymerase I Transcription | 44 | 4.71e-01 | 6.28e-02 | 0.792000 |
| Signaling by NTRK3 (TRKC) | 10 | 7.32e-01 | -6.26e-02 | 0.904000 |
| Cellular response to heat stress | 77 | 3.44e-01 | 6.24e-02 | 0.668000 |
| Leishmania infection | 109 | 2.62e-01 | -6.24e-02 | 0.584000 |
| Signaling by FLT3 ITD and TKD mutants | 12 | 7.09e-01 | -6.23e-02 | 0.901000 |
| Visual phototransduction | 32 | 5.46e-01 | -6.17e-02 | 0.838000 |
| G beta:gamma signalling through PI3Kgamma | 16 | 6.70e-01 | 6.16e-02 | 0.885000 |
| Deposition of new CENPA-containing nucleosomes at the centromere | 20 | 6.34e-01 | -6.15e-02 | 0.864000 |
| Nucleosome assembly | 20 | 6.34e-01 | -6.15e-02 | 0.864000 |
| Glucagon-like Peptide-1 (GLP1) regulates insulin secretion | 21 | 6.28e-01 | -6.12e-02 | 0.864000 |
| Protein methylation | 10 | 7.39e-01 | -6.08e-02 | 0.904000 |
| BBSome-mediated cargo-targeting to cilium | 18 | 6.57e-01 | 6.05e-02 | 0.875000 |
| RNA Polymerase III Transcription Initiation From Type 3 Promoter | 27 | 5.87e-01 | 6.04e-02 | 0.847000 |
| NGF-stimulated transcription | 25 | 6.01e-01 | 6.04e-02 | 0.852000 |
| Metabolism of water-soluble vitamins and cofactors | 78 | 3.58e-01 | 6.03e-02 | 0.674000 |
| Zinc transporters | 11 | 7.30e-01 | -6.01e-02 | 0.904000 |
| Regulation of IFNA/IFNB signaling | 12 | 7.19e-01 | 6.00e-02 | 0.902000 |
| Cleavage of the damaged purine | 10 | 7.43e-01 | 5.99e-02 | 0.904000 |
| Depurination | 10 | 7.43e-01 | 5.99e-02 | 0.904000 |
| Recognition and association of DNA glycosylase with site containing an affected purine | 10 | 7.43e-01 | 5.99e-02 | 0.904000 |
| Smooth Muscle Contraction | 19 | 6.54e-01 | 5.95e-02 | 0.873000 |
| Post-translational protein phosphorylation | 34 | 5.49e-01 | 5.95e-02 | 0.838000 |
| Regulated Necrosis | 42 | 5.06e-01 | 5.94e-02 | 0.809000 |
| Negative epigenetic regulation of rRNA expression | 44 | 5.00e-01 | 5.88e-02 | 0.808000 |
| Immune System | 1114 | 1.37e-03 | 5.86e-02 | 0.062900 |
| Late Phase of HIV Life Cycle | 110 | 2.90e-01 | 5.85e-02 | 0.607000 |
| RNA Polymerase III Transcription Termination | 21 | 6.43e-01 | 5.85e-02 | 0.867000 |
| RHOBTB1 GTPase cycle | 18 | 6.68e-01 | -5.85e-02 | 0.883000 |
| Transcriptional regulation by the AP-2 (TFAP2) family of transcription factors | 21 | 6.46e-01 | -5.79e-02 | 0.869000 |
| Thromboxane signalling through TP receptor | 14 | 7.09e-01 | -5.75e-02 | 0.901000 |
| Innate Immune System | 593 | 1.87e-02 | 5.74e-02 | 0.217000 |
| ADP signalling through P2Y purinoceptor 12 | 12 | 7.31e-01 | -5.74e-02 | 0.904000 |
| Heme biosynthesis | 10 | 7.54e-01 | 5.73e-02 | 0.910000 |
| NR1H2 and NR1H3-mediated signaling | 25 | 6.22e-01 | 5.70e-02 | 0.864000 |
| EPH-ephrin mediated repulsion of cells | 24 | 6.31e-01 | -5.67e-02 | 0.864000 |
| Prefoldin mediated transfer of substrate to CCT/TriC | 16 | 6.95e-01 | 5.65e-02 | 0.894000 |
| Synthesis of active ubiquitin: roles of E1 and E2 enzymes | 25 | 6.26e-01 | -5.64e-02 | 0.864000 |
| Peroxisomal lipid metabolism | 20 | 6.63e-01 | -5.63e-02 | 0.880000 |
| Interferon Signaling | 138 | 2.57e-01 | 5.61e-02 | 0.582000 |
| NCAM signaling for neurite out-growth | 23 | 6.42e-01 | -5.59e-02 | 0.867000 |
| HSF1 activation | 21 | 6.59e-01 | 5.57e-02 | 0.876000 |
| Sensory processing of sound | 25 | 6.31e-01 | 5.55e-02 | 0.864000 |
| Sensory processing of sound by inner hair cells of the cochlea | 25 | 6.31e-01 | 5.55e-02 | 0.864000 |
| Hedgehog ‘on’ state | 62 | 4.54e-01 | 5.51e-02 | 0.776000 |
| DNA Damage Recognition in GG-NER | 35 | 5.76e-01 | -5.47e-02 | 0.842000 |
| Ovarian tumor domain proteases | 29 | 6.16e-01 | -5.39e-02 | 0.864000 |
| Ub-specific processing proteases | 132 | 2.87e-01 | 5.38e-02 | 0.607000 |
| RNA Polymerase I Promoter Escape | 27 | 6.30e-01 | 5.36e-02 | 0.864000 |
| ESR-mediated signaling | 112 | 3.29e-01 | 5.36e-02 | 0.651000 |
| Integration of energy metabolism | 58 | 4.81e-01 | -5.35e-02 | 0.799000 |
| Epigenetic regulation of gene expression | 74 | 4.29e-01 | 5.33e-02 | 0.751000 |
| Activation of HOX genes during differentiation | 37 | 5.76e-01 | 5.32e-02 | 0.842000 |
| Activation of anterior HOX genes in hindbrain development during early embryogenesis | 37 | 5.76e-01 | 5.32e-02 | 0.842000 |
| Interactions of Rev with host cellular proteins | 33 | 5.98e-01 | 5.31e-02 | 0.850000 |
| PINK1-PRKN Mediated Mitophagy | 20 | 6.82e-01 | 5.30e-02 | 0.891000 |
| Detoxification of Reactive Oxygen Species | 22 | 6.67e-01 | -5.29e-02 | 0.883000 |
| Regulation of HSF1-mediated heat shock response | 64 | 4.66e-01 | 5.28e-02 | 0.787000 |
| Transcriptional activation of mitochondrial biogenesis | 39 | 5.69e-01 | 5.27e-02 | 0.842000 |
| Signaling by VEGF | 72 | 4.41e-01 | 5.26e-02 | 0.761000 |
| Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell | 30 | 6.18e-01 | 5.26e-02 | 0.864000 |
| Signaling by RAF1 mutants | 25 | 6.50e-01 | -5.24e-02 | 0.872000 |
| SEMA3A-Plexin repulsion signaling by inhibiting Integrin adhesion | 10 | 7.74e-01 | -5.24e-02 | 0.919000 |
| Constitutive Signaling by NOTCH1 HD+PEST Domain Mutants | 41 | 5.64e-01 | 5.21e-02 | 0.840000 |
| Constitutive Signaling by NOTCH1 PEST Domain Mutants | 41 | 5.64e-01 | 5.21e-02 | 0.840000 |
| Signaling by NOTCH1 HD+PEST Domain Mutants in Cancer | 41 | 5.64e-01 | 5.21e-02 | 0.840000 |
| Signaling by NOTCH1 PEST Domain Mutants in Cancer | 41 | 5.64e-01 | 5.21e-02 | 0.840000 |
| Signaling by NOTCH1 in Cancer | 41 | 5.64e-01 | 5.21e-02 | 0.840000 |
| activated TAK1 mediates p38 MAPK activation | 12 | 7.55e-01 | 5.20e-02 | 0.910000 |
| Hedgehog ‘off’ state | 74 | 4.40e-01 | 5.19e-02 | 0.761000 |
| Estrogen-dependent nuclear events downstream of ESR-membrane signaling | 16 | 7.20e-01 | 5.18e-02 | 0.902000 |
| Synthesis of PA | 17 | 7.12e-01 | -5.17e-02 | 0.901000 |
| HIV Life Cycle | 122 | 3.29e-01 | 5.14e-02 | 0.651000 |
| G beta:gamma signalling through CDC42 | 12 | 7.58e-01 | -5.13e-02 | 0.910000 |
| Positive epigenetic regulation of rRNA expression | 40 | 5.75e-01 | 5.12e-02 | 0.842000 |
| Metabolism of steroid hormones | 13 | 7.49e-01 | 5.12e-02 | 0.907000 |
| Deadenylation of mRNA | 22 | 6.78e-01 | 5.11e-02 | 0.890000 |
| Synthesis of substrates in N-glycan biosythesis | 46 | 5.54e-01 | -5.04e-02 | 0.840000 |
| Oxidative Stress Induced Senescence | 51 | 5.35e-01 | 5.02e-02 | 0.829000 |
| Retrograde transport at the Trans-Golgi-Network | 43 | 5.69e-01 | 5.02e-02 | 0.842000 |
| Adaptive Immune System | 464 | 6.92e-02 | 4.98e-02 | 0.343000 |
| Signaling by Erythropoietin | 19 | 7.08e-01 | -4.96e-02 | 0.901000 |
| Downstream signal transduction | 20 | 7.01e-01 | -4.95e-02 | 0.900000 |
| Muscle contraction | 66 | 4.89e-01 | -4.93e-02 | 0.803000 |
| Platelet degranulation | 47 | 5.59e-01 | -4.93e-02 | 0.840000 |
| Interleukin-17 signaling | 49 | 5.51e-01 | -4.93e-02 | 0.838000 |
| Rev-mediated nuclear export of HIV RNA | 32 | 6.30e-01 | 4.92e-02 | 0.864000 |
| Purine salvage | 11 | 7.78e-01 | 4.92e-02 | 0.919000 |
| RHOJ GTPase cycle | 34 | 6.20e-01 | -4.92e-02 | 0.864000 |
| Axon guidance | 290 | 1.54e-01 | 4.91e-02 | 0.460000 |
| Generation of second messenger molecules | 16 | 7.34e-01 | 4.90e-02 | 0.904000 |
| VEGFA-VEGFR2 Pathway | 70 | 4.80e-01 | 4.89e-02 | 0.798000 |
| SMAD2/SMAD3:SMAD4 heterotrimer regulates transcription | 25 | 6.74e-01 | 4.86e-02 | 0.888000 |
| Nervous system development | 301 | 1.50e-01 | 4.86e-02 | 0.456000 |
| Interleukin-6 signaling | 10 | 7.91e-01 | -4.84e-02 | 0.919000 |
| G alpha (12/13) signalling events | 35 | 6.21e-01 | -4.84e-02 | 0.864000 |
| The role of Nef in HIV-1 replication and disease pathogenesis | 19 | 7.15e-01 | 4.83e-02 | 0.901000 |
| Activation of gene expression by SREBF (SREBP) | 35 | 6.22e-01 | -4.82e-02 | 0.864000 |
| Cytosolic sensors of pathogen-associated DNA | 52 | 5.50e-01 | -4.80e-02 | 0.838000 |
| Kinesins | 32 | 6.44e-01 | 4.72e-02 | 0.867000 |
| MAPK targets/ Nuclear events mediated by MAP kinases | 22 | 7.02e-01 | -4.71e-02 | 0.900000 |
| MyD88:MAL(TIRAP) cascade initiated on plasma membrane | 66 | 5.11e-01 | -4.69e-02 | 0.810000 |
| Toll Like Receptor 2 (TLR2) Cascade | 66 | 5.11e-01 | -4.69e-02 | 0.810000 |
| Toll Like Receptor TLR1:TLR2 Cascade | 66 | 5.11e-01 | -4.69e-02 | 0.810000 |
| Toll Like Receptor TLR6:TLR2 Cascade | 66 | 5.11e-01 | -4.69e-02 | 0.810000 |
| Downstream signaling of activated FGFR1 | 11 | 7.88e-01 | 4.69e-02 | 0.919000 |
| Downstream signaling of activated FGFR2 | 11 | 7.88e-01 | 4.69e-02 | 0.919000 |
| Downstream signaling of activated FGFR3 | 11 | 7.88e-01 | 4.69e-02 | 0.919000 |
| Downstream signaling of activated FGFR4 | 11 | 7.88e-01 | 4.69e-02 | 0.919000 |
| G alpha (z) signalling events | 24 | 6.92e-01 | -4.68e-02 | 0.894000 |
| Antigen processing: Ubiquitination & Proteasome degradation | 233 | 2.22e-01 | 4.67e-02 | 0.542000 |
| Translation of Replicase and Assembly of the Replication Transcription Complex | 10 | 7.99e-01 | 4.66e-02 | 0.919000 |
| Transcription-Coupled Nucleotide Excision Repair (TC-NER) | 69 | 5.05e-01 | 4.65e-02 | 0.809000 |
| Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs) | 35 | 6.35e-01 | 4.65e-02 | 0.864000 |
| TICAM1, RIP1-mediated IKK complex recruitment | 17 | 7.40e-01 | 4.64e-02 | 0.904000 |
| Mitophagy | 25 | 6.88e-01 | -4.64e-02 | 0.891000 |
| Antigen Presentation: Folding, assembly and peptide loading of class I MHC | 25 | 6.94e-01 | 4.54e-02 | 0.894000 |
| Biological oxidations | 78 | 4.90e-01 | -4.53e-02 | 0.804000 |
| Signaling by ERBB2 ECD mutants | 10 | 8.04e-01 | 4.52e-02 | 0.921000 |
| Ion transport by P-type ATPases | 27 | 6.86e-01 | 4.50e-02 | 0.891000 |
| DDX58/IFIH1-mediated induction of interferon-alpha/beta | 58 | 5.54e-01 | 4.49e-02 | 0.840000 |
| RHOH GTPase cycle | 27 | 6.87e-01 | 4.49e-02 | 0.891000 |
| Nonhomologous End-Joining (NHEJ) | 27 | 6.87e-01 | 4.48e-02 | 0.891000 |
| NOTCH1 Intracellular Domain Regulates Transcription | 37 | 6.42e-01 | 4.42e-02 | 0.867000 |
| Interconversion of nucleotide di- and triphosphates | 21 | 7.31e-01 | 4.34e-02 | 0.904000 |
| Growth hormone receptor signaling | 17 | 7.59e-01 | -4.30e-02 | 0.910000 |
| PKMTs methylate histone lysines | 24 | 7.16e-01 | 4.30e-02 | 0.901000 |
| Signaling by PDGF | 24 | 7.17e-01 | -4.28e-02 | 0.901000 |
| SLC transporter disorders | 49 | 6.06e-01 | 4.27e-02 | 0.856000 |
| Regulation of TNFR1 signaling | 30 | 6.88e-01 | 4.24e-02 | 0.891000 |
| Adrenaline,noradrenaline inhibits insulin secretion | 13 | 7.93e-01 | 4.20e-02 | 0.919000 |
| RHOA GTPase cycle | 86 | 5.07e-01 | 4.15e-02 | 0.809000 |
| Class I MHC mediated antigen processing & presentation | 277 | 2.39e-01 | 4.14e-02 | 0.561000 |
| CTNNB1 S33 mutants aren’t phosphorylated | 13 | 7.97e-01 | -4.12e-02 | 0.919000 |
| CTNNB1 S37 mutants aren’t phosphorylated | 13 | 7.97e-01 | -4.12e-02 | 0.919000 |
| CTNNB1 S45 mutants aren’t phosphorylated | 13 | 7.97e-01 | -4.12e-02 | 0.919000 |
| CTNNB1 T41 mutants aren’t phosphorylated | 13 | 7.97e-01 | -4.12e-02 | 0.919000 |
| Signaling by CTNNB1 phospho-site mutants | 13 | 7.97e-01 | -4.12e-02 | 0.919000 |
| Signaling by GSK3beta mutants | 13 | 7.97e-01 | -4.12e-02 | 0.919000 |
| InlB-mediated entry of Listeria monocytogenes into host cell | 11 | 8.14e-01 | -4.10e-02 | 0.922000 |
| IKK complex recruitment mediated by RIP1 | 17 | 7.71e-01 | 4.08e-02 | 0.919000 |
| Resolution of D-loop Structures through Holliday Junction Intermediates | 24 | 7.30e-01 | 4.07e-02 | 0.904000 |
| Nef-mediates down modulation of cell surface receptors by recruiting them to clathrin adapters | 14 | 7.96e-01 | -4.00e-02 | 0.919000 |
| PPARA activates gene expression | 82 | 5.34e-01 | 3.98e-02 | 0.829000 |
| Transcriptional Regulation by E2F6 | 28 | 7.16e-01 | -3.98e-02 | 0.901000 |
| Formation of Incision Complex in GG-NER | 36 | 6.80e-01 | -3.97e-02 | 0.891000 |
| Regulation of lipid metabolism by PPARalpha | 84 | 5.31e-01 | 3.96e-02 | 0.829000 |
| RHOBTB GTPase Cycle | 29 | 7.14e-01 | 3.94e-02 | 0.901000 |
| NOTCH3 Activation and Transmission of Signal to the Nucleus | 15 | 7.93e-01 | -3.92e-02 | 0.919000 |
| Signaling by FGFR2 in disease | 23 | 7.46e-01 | 3.90e-02 | 0.905000 |
| Glycosphingolipid metabolism | 25 | 7.38e-01 | 3.86e-02 | 0.904000 |
| trans-Golgi Network Vesicle Budding | 50 | 6.37e-01 | 3.86e-02 | 0.865000 |
| Signalling to ERKs | 25 | 7.39e-01 | -3.85e-02 | 0.904000 |
| RND1 GTPase cycle | 29 | 7.22e-01 | 3.82e-02 | 0.903000 |
| Response to elevated platelet cytosolic Ca2+ | 51 | 6.39e-01 | -3.80e-02 | 0.865000 |
| COPI-dependent Golgi-to-ER retrograde traffic | 66 | 5.95e-01 | 3.78e-02 | 0.849000 |
| TP53 Regulates Metabolic Genes | 61 | 6.10e-01 | 3.78e-02 | 0.860000 |
| Sensory Perception | 64 | 6.03e-01 | -3.77e-02 | 0.853000 |
| PCP/CE pathway | 70 | 5.86e-01 | 3.77e-02 | 0.847000 |
| Interleukin-7 signaling | 14 | 8.08e-01 | 3.75e-02 | 0.922000 |
| Gene expression (Transcription) | 981 | 5.38e-02 | 3.74e-02 | 0.310000 |
| Regulation of insulin secretion | 38 | 6.93e-01 | -3.70e-02 | 0.894000 |
| Autophagy | 95 | 5.35e-01 | -3.69e-02 | 0.829000 |
| FOXO-mediated transcription of oxidative stress, metabolic and neuronal genes | 14 | 8.13e-01 | 3.65e-02 | 0.922000 |
| Peroxisomal protein import | 46 | 6.71e-01 | 3.63e-02 | 0.885000 |
| VEGFR2 mediated cell proliferation | 16 | 8.02e-01 | -3.62e-02 | 0.920000 |
| Metabolism of proteins | 1205 | 4.10e-02 | 3.61e-02 | 0.281000 |
| N-glycan trimming in the ER and Calnexin/Calreticulin cycle | 32 | 7.25e-01 | 3.60e-02 | 0.904000 |
| B-WICH complex positively regulates rRNA expression | 27 | 7.47e-01 | 3.59e-02 | 0.905000 |
| Synthesis of PIPs at the early endosome membrane | 12 | 8.30e-01 | -3.59e-02 | 0.931000 |
| Nuclear Receptor transcription pathway | 26 | 7.54e-01 | -3.55e-02 | 0.910000 |
| Cellular response to chemical stress | 141 | 4.70e-01 | 3.54e-02 | 0.792000 |
| Cytochrome P450 - arranged by substrate type | 14 | 8.19e-01 | -3.53e-02 | 0.926000 |
| Negative regulation of MAPK pathway | 36 | 7.15e-01 | -3.52e-02 | 0.901000 |
| Transcriptional regulation by RUNX2 | 82 | 5.83e-01 | 3.51e-02 | 0.847000 |
| Netrin-1 signaling | 24 | 7.69e-01 | -3.47e-02 | 0.917000 |
| Signaling by KIT in disease | 16 | 8.10e-01 | -3.46e-02 | 0.922000 |
| Signaling by phosphorylated juxtamembrane, extracellular and kinase domain KIT mutants | 16 | 8.10e-01 | -3.46e-02 | 0.922000 |
| RAB GEFs exchange GTP for GDP on RABs | 56 | 6.55e-01 | -3.45e-02 | 0.874000 |
| Metabolism of vitamins and cofactors | 107 | 5.41e-01 | 3.43e-02 | 0.832000 |
| RAC1 GTPase cycle | 103 | 5.49e-01 | 3.43e-02 | 0.838000 |
| PI Metabolism | 60 | 6.51e-01 | 3.38e-02 | 0.872000 |
| RUNX1 interacts with co-factors whose precise effect on RUNX1 targets is not known | 33 | 7.41e-01 | -3.33e-02 | 0.904000 |
| PI5P, PP2A and IER3 Regulate PI3K/AKT Signaling | 49 | 6.87e-01 | 3.33e-02 | 0.891000 |
| PI3K Cascade | 18 | 8.07e-01 | 3.32e-02 | 0.922000 |
| Paradoxical activation of RAF signaling by kinase inactive BRAF | 29 | 7.57e-01 | 3.32e-02 | 0.910000 |
| Signaling by RAS mutants | 29 | 7.57e-01 | 3.32e-02 | 0.910000 |
| Signaling by moderate kinase activity BRAF mutants | 29 | 7.57e-01 | 3.32e-02 | 0.910000 |
| Signaling downstream of RAS mutants | 29 | 7.57e-01 | 3.32e-02 | 0.910000 |
| Nephrin family interactions | 14 | 8.30e-01 | 3.32e-02 | 0.931000 |
| VEGFR2 mediated vascular permeability | 21 | 7.93e-01 | -3.30e-02 | 0.919000 |
| Pexophagy | 11 | 8.51e-01 | -3.27e-02 | 0.946000 |
| Antigen activates B Cell Receptor (BCR) leading to generation of second messengers | 21 | 7.95e-01 | -3.27e-02 | 0.919000 |
| Developmental Biology | 448 | 2.43e-01 | 3.25e-02 | 0.569000 |
| Signaling by Non-Receptor Tyrosine Kinases | 35 | 7.40e-01 | -3.24e-02 | 0.904000 |
| Signaling by PTK6 | 35 | 7.40e-01 | -3.24e-02 | 0.904000 |
| Neutrophil degranulation | 292 | 3.45e-01 | 3.23e-02 | 0.668000 |
| Transcriptional regulation of white adipocyte differentiation | 56 | 6.77e-01 | 3.22e-02 | 0.890000 |
| Signaling by FGFR in disease | 38 | 7.32e-01 | -3.21e-02 | 0.904000 |
| Translesion synthesis by Y family DNA polymerases bypasses lesions on DNA template | 34 | 7.46e-01 | 3.21e-02 | 0.905000 |
| Defective Intrinsic Pathway for Apoptosis | 23 | 7.90e-01 | -3.20e-02 | 0.919000 |
| Signaling by BRAF and RAF1 fusions | 42 | 7.22e-01 | -3.18e-02 | 0.903000 |
| IRS-mediated signalling | 20 | 8.10e-01 | -3.11e-02 | 0.922000 |
| DNA Damage Bypass | 41 | 7.33e-01 | 3.08e-02 | 0.904000 |
| Asparagine N-linked glycosylation | 219 | 4.35e-01 | 3.08e-02 | 0.755000 |
| Factors involved in megakaryocyte development and platelet production | 85 | 6.25e-01 | 3.07e-02 | 0.864000 |
| Chaperonin-mediated protein folding | 55 | 6.97e-01 | -3.04e-02 | 0.895000 |
| SHC1 events in ERBB2 signaling | 11 | 8.62e-01 | -3.03e-02 | 0.951000 |
| Antiviral mechanism by IFN-stimulated genes | 74 | 6.53e-01 | 3.03e-02 | 0.873000 |
| Hemostasis | 297 | 3.76e-01 | -3.01e-02 | 0.695000 |
| ER to Golgi Anterograde Transport | 103 | 5.99e-01 | 3.00e-02 | 0.850000 |
| Downregulation of TGF-beta receptor signaling | 26 | 7.92e-01 | -3.00e-02 | 0.919000 |
| G1/S-Specific Transcription | 24 | 8.00e-01 | -2.99e-02 | 0.919000 |
| DNA Repair | 238 | 4.30e-01 | 2.99e-02 | 0.751000 |
| The citric acid (TCA) cycle and respiratory electron transport | 113 | 5.84e-01 | 2.99e-02 | 0.847000 |
| Nuclear Events (kinase and transcription factor activation) | 42 | 7.38e-01 | 2.99e-02 | 0.904000 |
| TCF dependent signaling in response to WNT | 117 | 5.78e-01 | 2.98e-02 | 0.845000 |
| Syndecan interactions | 10 | 8.74e-01 | -2.90e-02 | 0.951000 |
| Degradation of the extracellular matrix | 28 | 7.91e-01 | 2.89e-02 | 0.919000 |
| Intrinsic Pathway for Apoptosis | 45 | 7.38e-01 | 2.88e-02 | 0.904000 |
| Termination of translesion DNA synthesis | 28 | 7.98e-01 | 2.79e-02 | 0.919000 |
| Nucleotide Excision Repair | 99 | 6.33e-01 | 2.79e-02 | 0.864000 |
| Cargo trafficking to the periciliary membrane | 39 | 7.65e-01 | -2.77e-02 | 0.916000 |
| Transport to the Golgi and subsequent modification | 126 | 5.93e-01 | 2.76e-02 | 0.849000 |
| Non-integrin membrane-ECM interactions | 13 | 8.64e-01 | -2.74e-02 | 0.951000 |
| RND3 GTPase cycle | 29 | 7.99e-01 | 2.74e-02 | 0.919000 |
| Dual Incision in GG-NER | 35 | 7.81e-01 | 2.72e-02 | 0.919000 |
| Transcriptional activity of SMAD2/SMAD3:SMAD4 heterotrimer | 37 | 7.75e-01 | -2.71e-02 | 0.919000 |
| IRS-related events triggered by IGF1R | 21 | 8.31e-01 | -2.69e-02 | 0.931000 |
| Negative regulation of the PI3K/AKT network | 54 | 7.33e-01 | 2.69e-02 | 0.904000 |
| RNA Polymerase II Transcription | 873 | 1.88e-01 | 2.69e-02 | 0.500000 |
| Diseases of mitotic cell cycle | 30 | 7.99e-01 | 2.68e-02 | 0.919000 |
| Metabolism of porphyrins | 15 | 8.59e-01 | -2.65e-02 | 0.951000 |
| Signaling by Rho GTPases | 421 | 3.57e-01 | 2.64e-02 | 0.673000 |
| Translesion synthesis by POLK | 15 | 8.61e-01 | -2.61e-02 | 0.951000 |
| Transcriptional Regulation by VENTX | 25 | 8.23e-01 | 2.59e-02 | 0.928000 |
| Golgi Associated Vesicle Biogenesis | 37 | 7.86e-01 | -2.58e-02 | 0.919000 |
| TAK1-dependent IKK and NF-kappa-B activation | 17 | 8.55e-01 | 2.57e-02 | 0.948000 |
| RMTs methylate histone arginines | 25 | 8.26e-01 | 2.54e-02 | 0.929000 |
| Semaphorin interactions | 36 | 7.93e-01 | 2.53e-02 | 0.919000 |
| mRNA decay by 5’ to 3’ exoribonuclease | 14 | 8.71e-01 | -2.50e-02 | 0.951000 |
| Aberrant regulation of mitotic G1/S transition in cancer due to RB1 defects | 15 | 8.68e-01 | 2.48e-02 | 0.951000 |
| Defective binding of RB1 mutants to E2F1,(E2F2, E2F3) | 15 | 8.68e-01 | 2.48e-02 | 0.951000 |
| TNF signaling | 35 | 8.00e-01 | 2.48e-02 | 0.919000 |
| TP53 Regulates Transcription of Cell Death Genes | 30 | 8.15e-01 | -2.47e-02 | 0.922000 |
| Early Phase of HIV Life Cycle | 13 | 8.78e-01 | 2.45e-02 | 0.951000 |
| Signaling by Rho GTPases, Miro GTPases and RHOBTB3 | 433 | 3.90e-01 | 2.44e-02 | 0.714000 |
| MyD88 dependent cascade initiated on endosome | 63 | 7.43e-01 | -2.39e-02 | 0.904000 |
| Toll Like Receptor 7/8 (TLR7/8) Cascade | 63 | 7.43e-01 | -2.39e-02 | 0.904000 |
| Glucose metabolism | 70 | 7.30e-01 | 2.39e-02 | 0.904000 |
| Interleukin-15 signaling | 11 | 8.91e-01 | 2.39e-02 | 0.956000 |
| Association of TriC/CCT with target proteins during biosynthesis | 29 | 8.25e-01 | -2.37e-02 | 0.929000 |
| Signaling by WNT | 171 | 5.97e-01 | 2.35e-02 | 0.850000 |
| Signaling by TGFB family members | 82 | 7.13e-01 | -2.35e-02 | 0.901000 |
| Macroautophagy | 87 | 7.06e-01 | -2.35e-02 | 0.901000 |
| DNA Double Strand Break Response | 34 | 8.13e-01 | 2.34e-02 | 0.922000 |
| Selective autophagy | 50 | 7.75e-01 | 2.34e-02 | 0.919000 |
| TGF-beta receptor signaling activates SMADs | 37 | 8.07e-01 | -2.32e-02 | 0.922000 |
| Glycolysis | 55 | 7.68e-01 | 2.30e-02 | 0.917000 |
| DCC mediated attractive signaling | 11 | 8.95e-01 | 2.30e-02 | 0.958000 |
| Rab regulation of trafficking | 85 | 7.15e-01 | 2.30e-02 | 0.901000 |
| Synthesis of IP3 and IP4 in the cytosol | 16 | 8.77e-01 | -2.23e-02 | 0.951000 |
| Platelet activation, signaling and aggregation | 128 | 6.66e-01 | 2.21e-02 | 0.883000 |
| PRC2 methylates histones and DNA | 11 | 9.00e-01 | 2.18e-02 | 0.960000 |
| MAP kinase activation | 46 | 7.98e-01 | -2.18e-02 | 0.919000 |
| Gap junction trafficking and regulation | 10 | 9.06e-01 | -2.16e-02 | 0.961000 |
| Phase II - Conjugation of compounds | 45 | 8.05e-01 | -2.13e-02 | 0.921000 |
| Pre-NOTCH Expression and Processing | 42 | 8.11e-01 | 2.13e-02 | 0.922000 |
| Resolution of D-loop Structures through Synthesis-Dependent Strand Annealing (SDSA) | 21 | 8.68e-01 | -2.09e-02 | 0.951000 |
| Signaling by NOTCH2 | 18 | 8.79e-01 | -2.08e-02 | 0.951000 |
| Phospholipid metabolism | 131 | 6.84e-01 | 2.06e-02 | 0.891000 |
| RHO GTPase cycle | 280 | 5.55e-01 | 2.06e-02 | 0.840000 |
| Post-translational protein modification | 882 | 3.10e-01 | 2.06e-02 | 0.632000 |
| FLT3 signaling in disease | 24 | 8.61e-01 | 2.06e-02 | 0.951000 |
| Cyclin D associated events in G1 | 40 | 8.22e-01 | 2.06e-02 | 0.928000 |
| G1 Phase | 40 | 8.22e-01 | 2.06e-02 | 0.928000 |
| CDC42 GTPase cycle | 90 | 7.37e-01 | -2.06e-02 | 0.904000 |
| Defective HDR through Homologous Recombination (HRR) due to BRCA1 loss-of-function | 19 | 8.78e-01 | 2.04e-02 | 0.951000 |
| Defective HDR through Homologous Recombination (HRR) due to PALB2 loss of function | 19 | 8.78e-01 | 2.04e-02 | 0.951000 |
| Defective HDR through Homologous Recombination Repair (HRR) due to PALB2 loss of BRCA1 binding function | 19 | 8.78e-01 | 2.04e-02 | 0.951000 |
| Defective HDR through Homologous Recombination Repair (HRR) due to PALB2 loss of BRCA2/RAD51/RAD51C binding function | 19 | 8.78e-01 | 2.04e-02 | 0.951000 |
| Impaired BRCA2 binding to PALB2 | 19 | 8.78e-01 | 2.04e-02 | 0.951000 |
| Oncogenic MAPK signaling | 56 | 7.94e-01 | -2.02e-02 | 0.919000 |
| SUMOylation of transcription factors | 13 | 9.01e-01 | -2.00e-02 | 0.960000 |
| ERK/MAPK targets | 16 | 8.91e-01 | -1.98e-02 | 0.956000 |
| Interferon gamma signaling | 54 | 8.01e-01 | 1.98e-02 | 0.920000 |
| RORA activates gene expression | 11 | 9.10e-01 | 1.97e-02 | 0.962000 |
| Interleukin-37 signaling | 16 | 8.92e-01 | 1.96e-02 | 0.956000 |
| IGF1R signaling cascade | 22 | 8.74e-01 | 1.95e-02 | 0.951000 |
| Signaling by Type 1 Insulin-like Growth Factor 1 Receptor (IGF1R) | 22 | 8.74e-01 | 1.95e-02 | 0.951000 |
| Deubiquitination | 194 | 6.41e-01 | 1.95e-02 | 0.867000 |
| Signaling by PDGFR in disease | 15 | 8.99e-01 | -1.90e-02 | 0.959000 |
| RND2 GTPase cycle | 33 | 8.52e-01 | -1.87e-02 | 0.947000 |
| Mitochondrial translation | 88 | 7.66e-01 | 1.84e-02 | 0.916000 |
| Pyroptosis | 17 | 8.99e-01 | -1.78e-02 | 0.959000 |
| Extracellular matrix organization | 78 | 7.86e-01 | -1.78e-02 | 0.919000 |
| RAF activation | 28 | 8.72e-01 | 1.76e-02 | 0.951000 |
| Toll Like Receptor 9 (TLR9) Cascade | 65 | 8.06e-01 | -1.76e-02 | 0.922000 |
| EGFR downregulation | 20 | 8.92e-01 | 1.75e-02 | 0.956000 |
| Cell surface interactions at the vascular wall | 56 | 8.23e-01 | 1.73e-02 | 0.928000 |
| MAP2K and MAPK activation | 22 | 8.89e-01 | -1.73e-02 | 0.956000 |
| Signaling by high-kinase activity BRAF mutants | 22 | 8.89e-01 | -1.73e-02 | 0.956000 |
| Toll-like Receptor Cascades | 100 | 7.66e-01 | 1.72e-02 | 0.916000 |
| Formation of TC-NER Pre-Incision Complex | 46 | 8.41e-01 | 1.71e-02 | 0.938000 |
| Aberrant regulation of mitotic exit in cancer due to RB1 defects | 15 | 9.11e-01 | 1.67e-02 | 0.962000 |
| Calnexin/calreticulin cycle | 23 | 8.90e-01 | -1.67e-02 | 0.956000 |
| Postmitotic nuclear pore complex (NPC) reformation | 25 | 8.86e-01 | 1.65e-02 | 0.956000 |
| Signaling by FLT3 fusion proteins | 16 | 9.09e-01 | -1.64e-02 | 0.962000 |
| Translesion synthesis by POLI | 15 | 9.13e-01 | -1.63e-02 | 0.963000 |
| RAC2 GTPase cycle | 52 | 8.42e-01 | -1.60e-02 | 0.938000 |
| Synthesis of glycosylphosphatidylinositol (GPI) | 14 | 9.19e-01 | -1.57e-02 | 0.965000 |
| MyD88 cascade initiated on plasma membrane | 61 | 8.35e-01 | -1.55e-02 | 0.933000 |
| Toll Like Receptor 10 (TLR10) Cascade | 61 | 8.35e-01 | -1.55e-02 | 0.933000 |
| Toll Like Receptor 5 (TLR5) Cascade | 61 | 8.35e-01 | -1.55e-02 | 0.933000 |
| Mitochondrial Fatty Acid Beta-Oxidation | 25 | 8.94e-01 | -1.54e-02 | 0.958000 |
| Inositol phosphate metabolism | 29 | 8.89e-01 | 1.50e-02 | 0.956000 |
| MET promotes cell motility | 12 | 9.29e-01 | 1.49e-02 | 0.973000 |
| Conversion from APC/C:Cdc20 to APC/C:Cdh1 in late anaphase | 15 | 9.21e-01 | -1.48e-02 | 0.965000 |
| COPII-mediated vesicle transport | 48 | 8.64e-01 | 1.43e-02 | 0.951000 |
| Protein folding | 61 | 8.50e-01 | -1.40e-02 | 0.946000 |
| G-protein beta:gamma signalling | 20 | 9.15e-01 | 1.38e-02 | 0.963000 |
| RAS processing | 13 | 9.31e-01 | -1.38e-02 | 0.974000 |
| EPH-Ephrin signaling | 54 | 8.61e-01 | 1.38e-02 | 0.951000 |
| Drug ADME | 27 | 9.02e-01 | -1.37e-02 | 0.960000 |
| Signaling by NOTCH1 | 51 | 8.67e-01 | -1.36e-02 | 0.951000 |
| Glutathione conjugation | 21 | 9.16e-01 | -1.34e-02 | 0.963000 |
| Signaling by Nuclear Receptors | 148 | 7.88e-01 | -1.29e-02 | 0.919000 |
| Beta-catenin independent WNT signaling | 101 | 8.27e-01 | 1.26e-02 | 0.929000 |
| EPHB-mediated forward signaling | 25 | 9.14e-01 | 1.25e-02 | 0.963000 |
| SUMOylation of chromatin organization proteins | 48 | 8.86e-01 | -1.20e-02 | 0.956000 |
| Vesicle-mediated transport | 434 | 6.76e-01 | 1.18e-02 | 0.889000 |
| EGR2 and SOX10-mediated initiation of Schwann cell myelination | 12 | 9.45e-01 | 1.16e-02 | 0.982000 |
| Metabolism of lipids | 420 | 6.94e-01 | -1.13e-02 | 0.894000 |
| Amino acids regulate mTORC1 | 35 | 9.09e-01 | 1.12e-02 | 0.962000 |
| Global Genome Nucleotide Excision Repair (GG-NER) | 76 | 8.68e-01 | 1.10e-02 | 0.951000 |
| Glycerophospholipid biosynthesis | 72 | 8.72e-01 | 1.10e-02 | 0.951000 |
| Phase I - Functionalization of compounds | 30 | 9.18e-01 | -1.08e-02 | 0.964000 |
| Signaling by EGFR in Cancer | 16 | 9.42e-01 | -1.06e-02 | 0.981000 |
| Metabolism of folate and pterines | 11 | 9.52e-01 | -1.05e-02 | 0.982000 |
| Gluconeogenesis | 24 | 9.30e-01 | -1.03e-02 | 0.974000 |
| Signaling by NTRK1 (TRKA) | 79 | 8.75e-01 | 1.03e-02 | 0.951000 |
| Regulation of cholesterol biosynthesis by SREBP (SREBF) | 47 | 9.05e-01 | -1.01e-02 | 0.961000 |
| Membrane Trafficking | 426 | 7.41e-01 | 9.45e-03 | 0.904000 |
| Effects of PIP2 hydrolysis | 18 | 9.46e-01 | 9.27e-03 | 0.982000 |
| Translesion synthesis by REV1 | 14 | 9.53e-01 | -9.19e-03 | 0.982000 |
| Phosphorylation of the APC/C | 15 | 9.52e-01 | 9.05e-03 | 0.982000 |
| Signaling by TGF-beta Receptor Complex | 69 | 8.97e-01 | -9.03e-03 | 0.959000 |
| APC truncation mutants have impaired AXIN binding | 12 | 9.57e-01 | 9.03e-03 | 0.982000 |
| AXIN missense mutants destabilize the destruction complex | 12 | 9.57e-01 | 9.03e-03 | 0.982000 |
| Signaling by AMER1 mutants | 12 | 9.57e-01 | 9.03e-03 | 0.982000 |
| Signaling by APC mutants | 12 | 9.57e-01 | 9.03e-03 | 0.982000 |
| Signaling by AXIN mutants | 12 | 9.57e-01 | 9.03e-03 | 0.982000 |
| Truncations of AMER1 destabilize the destruction complex | 12 | 9.57e-01 | 9.03e-03 | 0.982000 |
| Protein ubiquitination | 56 | 9.07e-01 | 8.99e-03 | 0.961000 |
| Metabolism | 1204 | 6.11e-01 | 8.99e-03 | 0.860000 |
| TRAF6 mediated induction of NFkB and MAP kinases upon TLR7/8 or 9 activation | 62 | 9.03e-01 | -8.95e-03 | 0.960000 |
| Oncogene Induced Senescence | 27 | 9.37e-01 | 8.84e-03 | 0.979000 |
| Response of EIF2AK1 (HRI) to heme deficiency | 14 | 9.55e-01 | 8.74e-03 | 0.982000 |
| Signaling by Hedgehog | 98 | 8.82e-01 | -8.69e-03 | 0.954000 |
| SUMOylation of intracellular receptors | 19 | 9.51e-01 | -8.09e-03 | 0.982000 |
| TRAF6 mediated IRF7 activation | 16 | 9.59e-01 | 7.49e-03 | 0.982000 |
| Signaling by NTRKs | 86 | 9.07e-01 | 7.32e-03 | 0.961000 |
| Nucleotide-binding domain, leucine rich repeat containing receptor (NLR) signaling pathways | 37 | 9.39e-01 | 7.27e-03 | 0.979000 |
| Mitochondrial translation initiation | 83 | 9.17e-01 | 6.62e-03 | 0.964000 |
| Signaling by Receptor Tyrosine Kinases | 286 | 8.50e-01 | -6.56e-03 | 0.946000 |
| E3 ubiquitin ligases ubiquitinate target proteins | 40 | 9.46e-01 | 6.18e-03 | 0.982000 |
| Translesion Synthesis by POLH | 16 | 9.66e-01 | -6.14e-03 | 0.985000 |
| Resolution of D-Loop Structures | 25 | 9.58e-01 | 6.13e-03 | 0.982000 |
| Striated Muscle Contraction | 10 | 9.75e-01 | -5.82e-03 | 0.985000 |
| Signaling by FGFR | 51 | 9.43e-01 | 5.80e-03 | 0.982000 |
| Generic Transcription Pathway | 784 | 7.95e-01 | 5.58e-03 | 0.919000 |
| Signal Transduction | 1305 | 7.50e-01 | 5.45e-03 | 0.907000 |
| Constitutive Signaling by Ligand-Responsive EGFR Cancer Variants | 14 | 9.73e-01 | -5.28e-03 | 0.985000 |
| Signaling by Ligand-Responsive EGFR Variants in Cancer | 14 | 9.73e-01 | -5.28e-03 | 0.985000 |
| Signaling by NTRK2 (TRKB) | 15 | 9.72e-01 | -5.25e-03 | 0.985000 |
| Diseases associated with the TLR signaling cascade | 16 | 9.71e-01 | -5.20e-03 | 0.985000 |
| Diseases of Immune System | 16 | 9.71e-01 | -5.20e-03 | 0.985000 |
| Mitochondrial translation elongation | 83 | 9.38e-01 | -4.95e-03 | 0.979000 |
| Signaling by SCF-KIT | 32 | 9.63e-01 | 4.70e-03 | 0.985000 |
| Toll Like Receptor 3 (TLR3) Cascade | 71 | 9.49e-01 | 4.42e-03 | 0.982000 |
| Extra-nuclear estrogen signaling | 48 | 9.58e-01 | -4.36e-03 | 0.982000 |
| N-glycan antennae elongation in the medial/trans-Golgi | 18 | 9.76e-01 | -4.14e-03 | 0.985000 |
| Lysosome Vesicle Biogenesis | 24 | 9.73e-01 | -3.98e-03 | 0.985000 |
| ER Quality Control Compartment (ERQC) | 18 | 9.77e-01 | -3.90e-03 | 0.985000 |
| Mitochondrial translation termination | 82 | 9.57e-01 | -3.48e-03 | 0.982000 |
| Signaling by FGFR2 | 47 | 9.71e-01 | -3.09e-03 | 0.985000 |
| ISG15 antiviral mechanism | 68 | 9.67e-01 | -2.92e-03 | 0.985000 |
| MHC class II antigen presentation | 66 | 9.68e-01 | 2.85e-03 | 0.985000 |
| Metabolism of steroids | 83 | 9.65e-01 | -2.82e-03 | 0.985000 |
| Biosynthesis of the N-glycan precursor (dolichol lipid-linked oligosaccharide, LLO) and transfer to a nascent protein | 59 | 9.75e-01 | 2.40e-03 | 0.985000 |
| Toll Like Receptor 4 (TLR4) Cascade | 89 | 9.70e-01 | -2.31e-03 | 0.985000 |
| SARS-CoV-2 activates/modulates innate and adaptive immune responses | 85 | 9.76e-01 | -1.91e-03 | 0.985000 |
| Signaling by ERBB2 | 33 | 9.85e-01 | -1.87e-03 | 0.993000 |
| SUMOylation of transcription cofactors | 35 | 9.89e-01 | 1.39e-03 | 0.994000 |
| RAC3 GTPase cycle | 55 | 9.88e-01 | 1.13e-03 | 0.994000 |
| Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks | 33 | 9.91e-01 | -1.09e-03 | 0.996000 |
| MyD88-independent TLR4 cascade | 71 | 9.92e-01 | 6.67e-04 | 0.996000 |
| TRIF(TICAM1)-mediated TLR4 signaling | 71 | 9.92e-01 | 6.67e-04 | 0.996000 |
| Regulation of MECP2 expression and activity | 20 | 9.97e-01 | 5.15e-04 | 0.998000 |
| Aberrant regulation of mitotic cell cycle due to RB1 defects | 29 | 9.97e-01 | 4.32e-04 | 0.998000 |
| Endosomal Sorting Complex Required For Transport (ESCRT) | 25 | 9.99e-01 | -1.09e-04 | 1.000000 |
| Signaling by ERBB2 in Cancer | 13 | 1.00e+00 | -3.73e-05 | 1.000000 |
Regulation of FZD by ubiquitination
| 829 | |
|---|---|
| set | Regulation of FZD by ubiquitination |
| setSize | 12 |
| pANOVA | 0.000444 |
| s.dist | -0.585 |
| p.adjustANOVA | 0.0294 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| WNT3A | -2845.5 |
| FZD6 | -2804.5 |
| FZD8 | -2633.5 |
| USP8 | -1926.5 |
| LRP5 | -1748.5 |
| UBC | -1150.5 |
| LRP6 | -1006.5 |
| UBB | -759.5 |
| FZD5 | 0.5 |
| ZNRF3 | 0.5 |
| RPS27A | 759.5 |
| UBA52 | 2326.5 |
| GeneID | Gene Rank |
|---|---|
| WNT3A | -2845.5 |
| FZD6 | -2804.5 |
| FZD8 | -2633.5 |
| USP8 | -1926.5 |
| LRP5 | -1748.5 |
| UBC | -1150.5 |
| LRP6 | -1006.5 |
| UBB | -759.5 |
| FZD5 | 0.5 |
| ZNRF3 | 0.5 |
| RPS27A | 759.5 |
| UBA52 | 2326.5 |
RUNX2 regulates osteoblast differentiation
| 812 | |
|---|---|
| set | RUNX2 regulates osteoblast differentiation |
| setSize | 13 |
| pANOVA | 0.00027 |
| s.dist | -0.583 |
| p.adjustANOVA | 0.023 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| COL1A1 | -3049.5 |
| SATB2 | -3016.5 |
| MAPK1 | -2100.5 |
| MAF | -2089.5 |
| MAPK3 | -1898.5 |
| HDAC3 | -1869.5 |
| CBFB | -1581.5 |
| SRC | -960.5 |
| ABL1 | -636.5 |
| RUNX2 | -591.5 |
| HEY2 | 0.5 |
| YES1 | 0.5 |
| RB1 | 5174.5 |
| GeneID | Gene Rank |
|---|---|
| COL1A1 | -3049.5 |
| SATB2 | -3016.5 |
| MAPK1 | -2100.5 |
| MAF | -2089.5 |
| MAPK3 | -1898.5 |
| HDAC3 | -1869.5 |
| CBFB | -1581.5 |
| SRC | -960.5 |
| ABL1 | -636.5 |
| RUNX2 | -591.5 |
| HEY2 | 0.5 |
| YES1 | 0.5 |
| RB1 | 5174.5 |
Glutamate Neurotransmitter Release Cycle
| 379 | |
|---|---|
| set | Glutamate Neurotransmitter Release Cycle |
| setSize | 11 |
| pANOVA | 0.0023 |
| s.dist | -0.531 |
| p.adjustANOVA | 0.083 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RAB3A | -2880.5 |
| SLC1A1 | -2820.5 |
| ARL6IP5 | -2479.5 |
| PPFIA3 | -2011.5 |
| UNC13B | -1625.5 |
| PPFIA1 | -1416.5 |
| GLS | 0.5 |
| STXBP1 | 0.5 |
| VAMP2 | 1077.5 |
| STX1A | 2039.5 |
| SLC38A2 | 2409.5 |
| GeneID | Gene Rank |
|---|---|
| RAB3A | -2880.5 |
| SLC1A1 | -2820.5 |
| ARL6IP5 | -2479.5 |
| PPFIA3 | -2011.5 |
| UNC13B | -1625.5 |
| PPFIA1 | -1416.5 |
| GLS | 0.5 |
| STXBP1 | 0.5 |
| VAMP2 | 1077.5 |
| STX1A | 2039.5 |
| SLC38A2 | 2409.5 |
Assembly of collagen fibrils and other multimeric structures
| 65 | |
|---|---|
| set | Assembly of collagen fibrils and other multimeric structures |
| setSize | 10 |
| pANOVA | 0.0046 |
| s.dist | -0.517 |
| p.adjustANOVA | 0.117 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| COL1A1 | -3049.5 |
| TLL2 | -2649.5 |
| COL9A2 | -2271.5 |
| ITGB4 | -1798.5 |
| DST | -1406.5 |
| LOXL1 | -929.5 |
| CTSB | 0.5 |
| LOXL3 | 0.5 |
| BMP1 | 0.5 |
| ITGA6 | 5782.5 |
| GeneID | Gene Rank |
|---|---|
| COL1A1 | -3049.5 |
| TLL2 | -2649.5 |
| COL9A2 | -2271.5 |
| ITGB4 | -1798.5 |
| DST | -1406.5 |
| LOXL1 | -929.5 |
| CTSB | 0.5 |
| LOXL3 | 0.5 |
| BMP1 | 0.5 |
| ITGA6 | 5782.5 |
Maturation of nucleoprotein
| 526 | |
|---|---|
| set | Maturation of nucleoprotein |
| setSize | 11 |
| pANOVA | 0.00474 |
| s.dist | 0.492 |
| p.adjustANOVA | 0.117 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| PARP10 | 7119.5 |
| GSK3A | 7077.5 |
| PARP4 | 6643.5 |
| UBE2I | 6548.5 |
| PARP9 | 6421.0 |
| GSK3B | 6022.5 |
| PARP14 | 5632.5 |
| PARP16 | 4566.5 |
| PARP6 | 2945.5 |
| PARP8 | 0.5 |
| SUMO1 | -2748.5 |
| GeneID | Gene Rank |
|---|---|
| PARP10 | 7119.5 |
| GSK3A | 7077.5 |
| PARP4 | 6643.5 |
| UBE2I | 6548.5 |
| PARP9 | 6421.0 |
| GSK3B | 6022.5 |
| PARP14 | 5632.5 |
| PARP16 | 4566.5 |
| PARP6 | 2945.5 |
| PARP8 | 0.5 |
| SUMO1 | -2748.5 |
Voltage gated Potassium channels
| 1160 | |
|---|---|
| set | Voltage gated Potassium channels |
| setSize | 10 |
| pANOVA | 0.0076 |
| s.dist | -0.487 |
| p.adjustANOVA | 0.137 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| KCNS1 | -2978.5 |
| KCNH4 | -2826.5 |
| KCNQ1 | -2806.0 |
| KCNQ5 | -2456.5 |
| KCNAB2 | -1568.5 |
| KCNC4 | 0.5 |
| KCNG3 | 0.5 |
| KCNH2 | 0.5 |
| KCNQ4 | 1090.5 |
| KCNA3 | 6769.5 |
| GeneID | Gene Rank |
|---|---|
| KCNS1 | -2978.5 |
| KCNH4 | -2826.5 |
| KCNQ1 | -2806.0 |
| KCNQ5 | -2456.5 |
| KCNAB2 | -1568.5 |
| KCNC4 | 0.5 |
| KCNG3 | 0.5 |
| KCNH2 | 0.5 |
| KCNQ4 | 1090.5 |
| KCNA3 | 6769.5 |
Neurotransmitter release cycle
| 625 | |
|---|---|
| set | Neurotransmitter release cycle |
| setSize | 18 |
| pANOVA | 0.00036 |
| s.dist | -0.486 |
| p.adjustANOVA | 0.0266 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| ABAT | -2940.5 |
| RAB3A | -2880.5 |
| SLC1A1 | -2820.5 |
| ARL6IP5 | -2479.5 |
| DNAJC5 | -2219.5 |
| APBA1 | -2019.5 |
| PPFIA3 | -2011.5 |
| UNC13B | -1625.5 |
| PPFIA1 | -1416.5 |
| LIN7B | -991.5 |
| ALDH5A1 | 0.5 |
| GLS | 0.5 |
| STXBP1 | 0.5 |
| VAMP2 | 1077.5 |
| STX1A | 2039.5 |
| NAAA | 2366.5 |
| SLC38A2 | 2409.5 |
| LIN7C | 5109.0 |
| GeneID | Gene Rank |
|---|---|
| ABAT | -2940.5 |
| RAB3A | -2880.5 |
| SLC1A1 | -2820.5 |
| ARL6IP5 | -2479.5 |
| DNAJC5 | -2219.5 |
| APBA1 | -2019.5 |
| PPFIA3 | -2011.5 |
| UNC13B | -1625.5 |
| PPFIA1 | -1416.5 |
| LIN7B | -991.5 |
| ALDH5A1 | 0.5 |
| GLS | 0.5 |
| STXBP1 | 0.5 |
| VAMP2 | 1077.5 |
| STX1A | 2039.5 |
| NAAA | 2366.5 |
| SLC38A2 | 2409.5 |
| LIN7C | 5109.0 |
Regulation of pyruvate dehydrogenase (PDH) complex
| 864 | |
|---|---|
| set | Regulation of pyruvate dehydrogenase (PDH) complex |
| setSize | 11 |
| pANOVA | 0.00698 |
| s.dist | -0.47 |
| p.adjustANOVA | 0.133 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| PDK2 | -2904.5 |
| PPARD | -2865.5 |
| DLD | -2338.5 |
| PDK1 | -1431.5 |
| PDHX | -1067.0 |
| PDHB | -1037.5 |
| PDP2 | -785.5 |
| PDP1 | 0.5 |
| PDPR | 0.5 |
| DLAT | 2227.5 |
| GSTZ1 | 5956.0 |
| GeneID | Gene Rank |
|---|---|
| PDK2 | -2904.5 |
| PPARD | -2865.5 |
| DLD | -2338.5 |
| PDK1 | -1431.5 |
| PDHX | -1067.0 |
| PDHB | -1037.5 |
| PDP2 | -785.5 |
| PDP1 | 0.5 |
| PDPR | 0.5 |
| DLAT | 2227.5 |
| GSTZ1 | 5956.0 |
Dopamine Neurotransmitter Release Cycle
| 250 | |
|---|---|
| set | Dopamine Neurotransmitter Release Cycle |
| setSize | 10 |
| pANOVA | 0.0143 |
| s.dist | -0.447 |
| p.adjustANOVA | 0.187 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RAB3A | -2880.5 |
| APBA1 | -2019.5 |
| PPFIA3 | -2011.5 |
| UNC13B | -1625.5 |
| PPFIA1 | -1416.5 |
| LIN7B | -991.5 |
| STXBP1 | 0.5 |
| VAMP2 | 1077.5 |
| STX1A | 2039.5 |
| LIN7C | 5109.0 |
| GeneID | Gene Rank |
|---|---|
| RAB3A | -2880.5 |
| APBA1 | -2019.5 |
| PPFIA3 | -2011.5 |
| UNC13B | -1625.5 |
| PPFIA1 | -1416.5 |
| LIN7B | -991.5 |
| STXBP1 | 0.5 |
| VAMP2 | 1077.5 |
| STX1A | 2039.5 |
| LIN7C | 5109.0 |
Long-term potentiation
| 508 | |
|---|---|
| set | Long-term potentiation |
| setSize | 11 |
| pANOVA | 0.0105 |
| s.dist | -0.446 |
| p.adjustANOVA | 0.162 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| GRIN2C | -2550.5 |
| DLG4 | -2233.5 |
| GRIN1 | -1884.5 |
| CAMK2G | -1756.5 |
| NRGN | -1152.5 |
| SRC | -960.5 |
| DLG1 | -938.5 |
| CALM1 | -730.5 |
| GRIN2D | 0.5 |
| DLG2 | 2819.5 |
| CAMK2D | 6506.5 |
| GeneID | Gene Rank |
|---|---|
| GRIN2C | -2550.5 |
| DLG4 | -2233.5 |
| GRIN1 | -1884.5 |
| CAMK2G | -1756.5 |
| NRGN | -1152.5 |
| SRC | -960.5 |
| DLG1 | -938.5 |
| CALM1 | -730.5 |
| GRIN2D | 0.5 |
| DLG2 | 2819.5 |
| CAMK2D | 6506.5 |
PKA activation
| 672 | |
|---|---|
| set | PKA activation |
| setSize | 10 |
| pANOVA | 0.0174 |
| s.dist | -0.434 |
| p.adjustANOVA | 0.217 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| PRKAR1B | -2946.5 |
| ADCY7 | -2888.5 |
| PRKAR2A | -2465.5 |
| ADCY4 | -2358.5 |
| NBEA | -1930.5 |
| PRKACA | -1900.5 |
| CALM1 | -730.5 |
| PRKACB | 3457.5 |
| ADCY9 | 3676.5 |
| PRKAR1A | 6053.5 |
| GeneID | Gene Rank |
|---|---|
| PRKAR1B | -2946.5 |
| ADCY7 | -2888.5 |
| PRKAR2A | -2465.5 |
| ADCY4 | -2358.5 |
| NBEA | -1930.5 |
| PRKACA | -1900.5 |
| CALM1 | -730.5 |
| PRKACB | 3457.5 |
| ADCY9 | 3676.5 |
| PRKAR1A | 6053.5 |
Signaling by Retinoic Acid
| 1001 | |
|---|---|
| set | Signaling by Retinoic Acid |
| setSize | 17 |
| pANOVA | 0.002 |
| s.dist | -0.433 |
| p.adjustANOVA | 0.077 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RDH13 | -3072.5 |
| PDK2 | -2904.5 |
| PPARD | -2865.5 |
| CPT1A | -2545.5 |
| DLD | -2338.5 |
| RARA | -1605.5 |
| PDK1 | -1431.5 |
| RDH14 | -1330.5 |
| PDHX | -1067.0 |
| PDHB | -1037.5 |
| DHRS4 | -679.0 |
| DHRS3 | -642.5 |
| FABP5 | 1514.5 |
| DLAT | 2227.5 |
| RDH11 | 3929.5 |
| RDH10 | 5166.0 |
| RARG | 5371.5 |
| GeneID | Gene Rank |
|---|---|
| RDH13 | -3072.5 |
| PDK2 | -2904.5 |
| PPARD | -2865.5 |
| CPT1A | -2545.5 |
| DLD | -2338.5 |
| RARA | -1605.5 |
| PDK1 | -1431.5 |
| RDH14 | -1330.5 |
| PDHX | -1067.0 |
| PDHB | -1037.5 |
| DHRS4 | -679.0 |
| DHRS3 | -642.5 |
| FABP5 | 1514.5 |
| DLAT | 2227.5 |
| RDH11 | 3929.5 |
| RDH10 | 5166.0 |
| RARG | 5371.5 |
PKA-mediated phosphorylation of CREB
| 673 | |
|---|---|
| set | PKA-mediated phosphorylation of CREB |
| setSize | 11 |
| pANOVA | 0.0134 |
| s.dist | -0.431 |
| p.adjustANOVA | 0.179 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| PRKAR1B | -2946.5 |
| ADCY7 | -2888.5 |
| PRKAR2A | -2465.5 |
| ADCY4 | -2358.5 |
| NBEA | -1930.5 |
| PRKACA | -1900.5 |
| CALM1 | -730.5 |
| CREB1 | 0.5 |
| PRKACB | 3457.5 |
| ADCY9 | 3676.5 |
| PRKAR1A | 6053.5 |
| GeneID | Gene Rank |
|---|---|
| PRKAR1B | -2946.5 |
| ADCY7 | -2888.5 |
| PRKAR2A | -2465.5 |
| ADCY4 | -2358.5 |
| NBEA | -1930.5 |
| PRKACA | -1900.5 |
| CALM1 | -730.5 |
| CREB1 | 0.5 |
| PRKACB | 3457.5 |
| ADCY9 | 3676.5 |
| PRKAR1A | 6053.5 |
Negative regulation of NMDA receptor-mediated neuronal transmission
| 614 | |
|---|---|
| set | Negative regulation of NMDA receptor-mediated neuronal transmission |
| setSize | 12 |
| pANOVA | 0.0106 |
| s.dist | -0.426 |
| p.adjustANOVA | 0.162 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| CAMK1 | -2846.5 |
| GRIN2C | -2550.5 |
| DLG4 | -2233.5 |
| GRIN1 | -1884.5 |
| CAMK2G | -1756.5 |
| PPM1F | -1618.5 |
| DLG1 | -938.5 |
| CALM1 | -730.5 |
| GRIN2D | 0.5 |
| DLG2 | 2819.5 |
| CAMK4 | 3291.5 |
| CAMK2D | 6506.5 |
| GeneID | Gene Rank |
|---|---|
| CAMK1 | -2846.5 |
| GRIN2C | -2550.5 |
| DLG4 | -2233.5 |
| GRIN1 | -1884.5 |
| CAMK2G | -1756.5 |
| PPM1F | -1618.5 |
| DLG1 | -938.5 |
| CALM1 | -730.5 |
| GRIN2D | 0.5 |
| DLG2 | 2819.5 |
| CAMK4 | 3291.5 |
| CAMK2D | 6506.5 |
RUNX2 regulates bone development
| 811 | |
|---|---|
| set | RUNX2 regulates bone development |
| setSize | 17 |
| pANOVA | 0.00253 |
| s.dist | -0.423 |
| p.adjustANOVA | 0.0861 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| COL1A1 | -3049.5 |
| SATB2 | -3016.5 |
| MAPK1 | -2100.5 |
| MAF | -2089.5 |
| MAPK3 | -1898.5 |
| HDAC3 | -1869.5 |
| CBFB | -1581.5 |
| SRC | -960.5 |
| ABL1 | -636.5 |
| RUNX2 | -591.5 |
| SMAD1 | 0.5 |
| HEY2 | 0.5 |
| YES1 | 0.5 |
| HDAC4 | 936.5 |
| RBM14 | 3736.5 |
| RB1 | 5174.5 |
| SMAD6 | 5490.5 |
| GeneID | Gene Rank |
|---|---|
| COL1A1 | -3049.5 |
| SATB2 | -3016.5 |
| MAPK1 | -2100.5 |
| MAF | -2089.5 |
| MAPK3 | -1898.5 |
| HDAC3 | -1869.5 |
| CBFB | -1581.5 |
| SRC | -960.5 |
| ABL1 | -636.5 |
| RUNX2 | -591.5 |
| SMAD1 | 0.5 |
| HEY2 | 0.5 |
| YES1 | 0.5 |
| HDAC4 | 936.5 |
| RBM14 | 3736.5 |
| RB1 | 5174.5 |
| SMAD6 | 5490.5 |
Glycogen storage diseases
| 384 | |
|---|---|
| set | Glycogen storage diseases |
| setSize | 10 |
| pANOVA | 0.0219 |
| s.dist | -0.418 |
| p.adjustANOVA | 0.236 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| NHLRC1 | -3113.5 |
| GAA | -2232.5 |
| SLC37A4 | -1738.5 |
| UBC | -1150.5 |
| UBB | -759.5 |
| G6PC3 | 0.5 |
| RPS27A | 759.5 |
| GYS1 | 1609.0 |
| UBA52 | 2326.5 |
| GYG1 | 3078.5 |
| GeneID | Gene Rank |
|---|---|
| NHLRC1 | -3113.5 |
| GAA | -2232.5 |
| SLC37A4 | -1738.5 |
| UBC | -1150.5 |
| UBB | -759.5 |
| G6PC3 | 0.5 |
| RPS27A | 759.5 |
| GYS1 | 1609.0 |
| UBA52 | 2326.5 |
| GYG1 | 3078.5 |
Ras activation upon Ca2+ influx through NMDA receptor
| 817 | |
|---|---|
| set | Ras activation upon Ca2+ influx through NMDA receptor |
| setSize | 10 |
| pANOVA | 0.0273 |
| s.dist | -0.403 |
| p.adjustANOVA | 0.245 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| DLG4 | -2233.5 |
| HRAS | -2214.5 |
| GRIN1 | -1884.5 |
| CAMK2G | -1756.5 |
| DLG1 | -938.5 |
| CALM1 | -730.5 |
| KRAS | 0.5 |
| GRIN2D | 0.5 |
| DLG2 | 2819.5 |
| CAMK2D | 6506.5 |
| GeneID | Gene Rank |
|---|---|
| DLG4 | -2233.5 |
| HRAS | -2214.5 |
| GRIN1 | -1884.5 |
| CAMK2G | -1756.5 |
| DLG1 | -938.5 |
| CALM1 | -730.5 |
| KRAS | 0.5 |
| GRIN2D | 0.5 |
| DLG2 | 2819.5 |
| CAMK2D | 6506.5 |
TNF receptor superfamily (TNFSF) members mediating non-canonical NF-kB pathway
| 1053 | |
|---|---|
| set | TNF receptor superfamily (TNFSF) members mediating non-canonical NF-kB pathway |
| setSize | 10 |
| pANOVA | 0.0296 |
| s.dist | 0.397 |
| p.adjustANOVA | 0.247 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| LTA | 7190.5 |
| TRAF2 | 6559.5 |
| MAP3K14 | 6503.5 |
| BIRC2 | 5397.5 |
| TNFSF13B | 4242.5 |
| LTB | 4157.5 |
| TNFSF14 | 3919.5 |
| TNFRSF12A | 1489.5 |
| BIRC3 | 1338.5 |
| TRAF3 | 0.5 |
| GeneID | Gene Rank |
|---|---|
| LTA | 7190.5 |
| TRAF2 | 6559.5 |
| MAP3K14 | 6503.5 |
| BIRC2 | 5397.5 |
| TNFSF13B | 4242.5 |
| LTB | 4157.5 |
| TNFSF14 | 3919.5 |
| TNFRSF12A | 1489.5 |
| BIRC3 | 1338.5 |
| TRAF3 | 0.5 |
Synthesis of Leukotrienes (LT) and Eoxins (EX)
| 1034 | |
|---|---|
| set | Synthesis of Leukotrienes (LT) and Eoxins (EX) |
| setSize | 10 |
| pANOVA | 0.0334 |
| s.dist | -0.388 |
| p.adjustANOVA | 0.26 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| LTC4S | -3024.5 |
| DPEP2 | -2574.5 |
| ALOX5 | -2511.5 |
| GGT1 | -2500.5 |
| PTGR1 | -2332.5 |
| ALOX5AP | 0.5 |
| ABCC1 | 946.5 |
| MAPKAPK2 | 2344.5 |
| LTA4H | 4840.5 |
| CYP4F22 | 5134.5 |
| GeneID | Gene Rank |
|---|---|
| LTC4S | -3024.5 |
| DPEP2 | -2574.5 |
| ALOX5 | -2511.5 |
| GGT1 | -2500.5 |
| PTGR1 | -2332.5 |
| ALOX5AP | 0.5 |
| ABCC1 | 946.5 |
| MAPKAPK2 | 2344.5 |
| LTA4H | 4840.5 |
| CYP4F22 | 5134.5 |
Regulation of KIT signaling
| 835 | |
|---|---|
| set | Regulation of KIT signaling |
| setSize | 10 |
| pANOVA | 0.035 |
| s.dist | 0.385 |
| p.adjustANOVA | 0.264 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| LCK | 7188.5 |
| SH2B3 | 7069.5 |
| FYN | 7012.5 |
| CBL | 5685.5 |
| PTPN6 | 5311.5 |
| SOCS1 | 4142.5 |
| PRKCA | 3492.5 |
| GRB2 | 1224.5 |
| YES1 | 0.5 |
| SRC | -960.5 |
| GeneID | Gene Rank |
|---|---|
| LCK | 7188.5 |
| SH2B3 | 7069.5 |
| FYN | 7012.5 |
| CBL | 5685.5 |
| PTPN6 | 5311.5 |
| SOCS1 | 4142.5 |
| PRKCA | 3492.5 |
| GRB2 | 1224.5 |
| YES1 | 0.5 |
| SRC | -960.5 |
CREB1 phosphorylation through NMDA receptor-mediated activation of RAS signaling
| 102 | |
|---|---|
| set | CREB1 phosphorylation through NMDA receptor-mediated activation of RAS signaling |
| setSize | 16 |
| pANOVA | 0.00852 |
| s.dist | -0.38 |
| p.adjustANOVA | 0.145 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPS6KA1 | -2359.5 |
| DLG4 | -2233.5 |
| HRAS | -2214.5 |
| MAPK1 | -2100.5 |
| MAPK3 | -1898.5 |
| GRIN1 | -1884.5 |
| CAMK2G | -1756.5 |
| DLG1 | -938.5 |
| CALM1 | -730.5 |
| KRAS | 0.5 |
| CREB1 | 0.5 |
| GRIN2D | 0.5 |
| DLG2 | 2819.5 |
| PDPK1 | 3609.5 |
| RPS6KA2 | 4422.5 |
| CAMK2D | 6506.5 |
| GeneID | Gene Rank |
|---|---|
| RPS6KA1 | -2359.5 |
| DLG4 | -2233.5 |
| HRAS | -2214.5 |
| MAPK1 | -2100.5 |
| MAPK3 | -1898.5 |
| GRIN1 | -1884.5 |
| CAMK2G | -1756.5 |
| DLG1 | -938.5 |
| CALM1 | -730.5 |
| KRAS | 0.5 |
| CREB1 | 0.5 |
| GRIN2D | 0.5 |
| DLG2 | 2819.5 |
| PDPK1 | 3609.5 |
| RPS6KA2 | 4422.5 |
| CAMK2D | 6506.5 |
Purine catabolism
| 735 | |
|---|---|
| set | Purine catabolism |
| setSize | 10 |
| pANOVA | 0.0403 |
| s.dist | 0.374 |
| p.adjustANOVA | 0.281 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| PNP | 6872.5 |
| NUDT15 | 6697.5 |
| NUDT18 | 6513.5 |
| NUDT5 | 5439.5 |
| NT5C | 5181.5 |
| NT5C2 | 3361.5 |
| NUDT9 | 3153.5 |
| NUDT1 | 3114.0 |
| ITPA | 1350.5 |
| NUDT16 | -2058.5 |
| GeneID | Gene Rank |
|---|---|
| PNP | 6872.5 |
| NUDT15 | 6697.5 |
| NUDT18 | 6513.5 |
| NUDT5 | 5439.5 |
| NT5C | 5181.5 |
| NT5C2 | 3361.5 |
| NUDT9 | 3153.5 |
| NUDT1 | 3114.0 |
| ITPA | 1350.5 |
| NUDT16 | -2058.5 |
Synaptic adhesion-like molecules
| 1029 | |
|---|---|
| set | Synaptic adhesion-like molecules |
| setSize | 10 |
| pANOVA | 0.0423 |
| s.dist | -0.371 |
| p.adjustANOVA | 0.283 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| GRIN2C | -2550.5 |
| DLG4 | -2233.5 |
| FLOT1 | -1952.5 |
| GRIN1 | -1884.5 |
| DLG1 | -938.5 |
| GRIN2D | 0.5 |
| RTN3 | 620.5 |
| LRFN4 | 1872.5 |
| FLOT2 | 3639.5 |
| LRFN3 | 4660.5 |
| GeneID | Gene Rank |
|---|---|
| GRIN2C | -2550.5 |
| DLG4 | -2233.5 |
| FLOT1 | -1952.5 |
| GRIN1 | -1884.5 |
| DLG1 | -938.5 |
| GRIN2D | 0.5 |
| RTN3 | 620.5 |
| LRFN4 | 1872.5 |
| FLOT2 | 3639.5 |
| LRFN3 | 4660.5 |
Class I peroxisomal membrane protein import
| 153 | |
|---|---|
| set | Class I peroxisomal membrane protein import |
| setSize | 18 |
| pANOVA | 0.00647 |
| s.dist | 0.371 |
| p.adjustANOVA | 0.133 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| PEX12 | 6938.5 |
| PEX19 | 6814.5 |
| SLC25A17 | 6189.5 |
| ALDH3A2 | 6154.5 |
| PEX16 | 6019.5 |
| PEX3 | 5678.0 |
| PEX11B | 5616.0 |
| PEX13 | 5516.0 |
| ATAD1 | 5259.0 |
| PEX14 | 4380.5 |
| PEX26 | 4152.5 |
| ABCD3 | 4148.5 |
| ABCD2 | 3557.5 |
| PXMP2 | 2961.0 |
| FIS1 | 2517.5 |
| PXMP4 | -1026.5 |
| ACBD5 | -1507.5 |
| GDAP1 | -2413.5 |
| GeneID | Gene Rank |
|---|---|
| PEX12 | 6938.5 |
| PEX19 | 6814.5 |
| SLC25A17 | 6189.5 |
| ALDH3A2 | 6154.5 |
| PEX16 | 6019.5 |
| PEX3 | 5678.0 |
| PEX11B | 5616.0 |
| PEX13 | 5516.0 |
| ATAD1 | 5259.0 |
| PEX14 | 4380.5 |
| PEX26 | 4152.5 |
| ABCD3 | 4148.5 |
| ABCD2 | 3557.5 |
| PXMP2 | 2961.0 |
| FIS1 | 2517.5 |
| PXMP4 | -1026.5 |
| ACBD5 | -1507.5 |
| GDAP1 | -2413.5 |
Assembly and cell surface presentation of NMDA receptors
| 64 | |
|---|---|
| set | Assembly and cell surface presentation of NMDA receptors |
| setSize | 13 |
| pANOVA | 0.0232 |
| s.dist | -0.363 |
| p.adjustANOVA | 0.238 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| GRIN2C | -2550.5 |
| DLG4 | -2233.5 |
| APBA1 | -2019.5 |
| NBEA | -1930.5 |
| GRIN1 | -1884.5 |
| CAMK2G | -1756.5 |
| LIN7B | -991.5 |
| DLG1 | -938.5 |
| GRIN2D | 0.5 |
| KIF17 | 1967.5 |
| DLG2 | 2819.5 |
| LIN7C | 5109.0 |
| CAMK2D | 6506.5 |
| GeneID | Gene Rank |
|---|---|
| GRIN2C | -2550.5 |
| DLG4 | -2233.5 |
| APBA1 | -2019.5 |
| NBEA | -1930.5 |
| GRIN1 | -1884.5 |
| CAMK2G | -1756.5 |
| LIN7B | -991.5 |
| DLG1 | -938.5 |
| GRIN2D | 0.5 |
| KIF17 | 1967.5 |
| DLG2 | 2819.5 |
| LIN7C | 5109.0 |
| CAMK2D | 6506.5 |
Signaling by Hippo
| 972 | |
|---|---|
| set | Signaling by Hippo |
| setSize | 11 |
| pANOVA | 0.039 |
| s.dist | -0.359 |
| p.adjustANOVA | 0.281 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| YWHAE | -2505.5 |
| LATS2 | -2066.5 |
| SAV1 | -2060.5 |
| LATS1 | -2050.5 |
| STK4 | -1186.5 |
| DVL2 | -578.5 |
| NPHP4 | 0.5 |
| TJP2 | 503.5 |
| CASP3 | 1673.0 |
| YWHAB | 3617.5 |
| STK3 | 6660.5 |
| GeneID | Gene Rank |
|---|---|
| YWHAE | -2505.5 |
| LATS2 | -2066.5 |
| SAV1 | -2060.5 |
| LATS1 | -2050.5 |
| STK4 | -1186.5 |
| DVL2 | -578.5 |
| NPHP4 | 0.5 |
| TJP2 | 503.5 |
| CASP3 | 1673.0 |
| YWHAB | 3617.5 |
| STK3 | 6660.5 |
Cell-cell junction organization
| 130 | |
|---|---|
| set | Cell-cell junction organization |
| setSize | 12 |
| pANOVA | 0.0333 |
| s.dist | -0.355 |
| p.adjustANOVA | 0.26 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| F11R | -2581.5 |
| MPP5 | -2141.5 |
| CDH24 | -2124.5 |
| CLDN12 | -1720.5 |
| CTNNB1 | -1282.5 |
| CTNND1 | 0.5 |
| SDK2 | 0.5 |
| PRKCI | 1714.5 |
| CLDN1 | 1954.5 |
| PARD6A | 2560.0 |
| PARD6B | 2676.5 |
| ANG | 3418.0 |
| GeneID | Gene Rank |
|---|---|
| F11R | -2581.5 |
| MPP5 | -2141.5 |
| CDH24 | -2124.5 |
| CLDN12 | -1720.5 |
| CTNNB1 | -1282.5 |
| CTNND1 | 0.5 |
| SDK2 | 0.5 |
| PRKCI | 1714.5 |
| CLDN1 | 1954.5 |
| PARD6A | 2560.0 |
| PARD6B | 2676.5 |
| ANG | 3418.0 |
Caspase activation via Death Receptors in the presence of ligand
| 119 | |
|---|---|
| set | Caspase activation via Death Receptors in the presence of ligand |
| setSize | 10 |
| pANOVA | 0.0546 |
| s.dist | 0.351 |
| p.adjustANOVA | 0.312 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| CFLAR | 6851.5 |
| CASP8 | 6625.5 |
| TRAF2 | 6559.5 |
| TRADD | 6244.0 |
| TICAM1 | 4987.5 |
| FAS | 4179.0 |
| TNFRSF10B | 3315.5 |
| TNFSF10 | 2395.5 |
| TNFRSF10A | 0.5 |
| FADD | -2742.5 |
| GeneID | Gene Rank |
|---|---|
| CFLAR | 6851.5 |
| CASP8 | 6625.5 |
| TRAF2 | 6559.5 |
| TRADD | 6244.0 |
| TICAM1 | 4987.5 |
| FAS | 4179.0 |
| TNFRSF10B | 3315.5 |
| TNFSF10 | 2395.5 |
| TNFRSF10A | 0.5 |
| FADD | -2742.5 |
Degradation of cysteine and homocysteine
| 221 | |
|---|---|
| set | Degradation of cysteine and homocysteine |
| setSize | 10 |
| pANOVA | 0.0573 |
| s.dist | -0.347 |
| p.adjustANOVA | 0.321 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| TXN2 | -2579.5 |
| TSTD1 | -2220.5 |
| ETHE1 | -1964.5 |
| MPST | -1906.0 |
| TST | -1906.0 |
| GOT2 | -1326.5 |
| CSAD | 1538.0 |
| SQRDL | 2542.5 |
| CTH | 4092.5 |
| ADO | 6179.5 |
| GeneID | Gene Rank |
|---|---|
| TXN2 | -2579.5 |
| TSTD1 | -2220.5 |
| ETHE1 | -1964.5 |
| MPST | -1906.0 |
| TST | -1906.0 |
| GOT2 | -1326.5 |
| CSAD | 1538.0 |
| SQRDL | 2542.5 |
| CTH | 4092.5 |
| ADO | 6179.5 |
Gastrin-CREB signalling pathway via PKC and MAPK
| 367 | |
|---|---|
| set | Gastrin-CREB signalling pathway via PKC and MAPK |
| setSize | 11 |
| pANOVA | 0.0477 |
| s.dist | -0.345 |
| p.adjustANOVA | 0.299 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| HBEGF | -2841.5 |
| RPS6KA1 | -2359.5 |
| HRAS | -2214.5 |
| MAPK1 | -2100.5 |
| MAPK3 | -1898.5 |
| KRAS | 0.5 |
| CREB1 | 0.5 |
| GRB2 | 1224.5 |
| PRKCA | 3492.5 |
| RPS6KA2 | 4422.5 |
| MAPK7 | 5103.5 |
| GeneID | Gene Rank |
|---|---|
| HBEGF | -2841.5 |
| RPS6KA1 | -2359.5 |
| HRAS | -2214.5 |
| MAPK1 | -2100.5 |
| MAPK3 | -1898.5 |
| KRAS | 0.5 |
| CREB1 | 0.5 |
| GRB2 | 1224.5 |
| PRKCA | 3492.5 |
| RPS6KA2 | 4422.5 |
| MAPK7 | 5103.5 |
SARS-CoV-2 modulates autophagy
| 892 | |
|---|---|
| set | SARS-CoV-2 modulates autophagy |
| setSize | 11 |
| pANOVA | 0.0507 |
| s.dist | 0.34 |
| p.adjustANOVA | 0.305 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| UVRAG | 7162.5 |
| VPS16 | 7008.0 |
| VPS39 | 6378.5 |
| VPS11 | 5765.5 |
| TUFM | 4632.5 |
| MAP1LC3B | 4083.5 |
| VPS33B | 3798.5 |
| VPS45 | 3521.5 |
| VPS18 | 2469.5 |
| VPS33A | -784.5 |
| VPS41 | -2387.5 |
| GeneID | Gene Rank |
|---|---|
| UVRAG | 7162.5 |
| VPS16 | 7008.0 |
| VPS39 | 6378.5 |
| VPS11 | 5765.5 |
| TUFM | 4632.5 |
| MAP1LC3B | 4083.5 |
| VPS33B | 3798.5 |
| VPS45 | 3521.5 |
| VPS18 | 2469.5 |
| VPS33A | -784.5 |
| VPS41 | -2387.5 |
NOTCH4 Intracellular Domain Regulates Transcription
| 598 | |
|---|---|
| set | NOTCH4 Intracellular Domain Regulates Transcription |
| setSize | 14 |
| pANOVA | 0.0287 |
| s.dist | 0.338 |
| p.adjustANOVA | 0.247 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| NOTCH4 | 6823.5 |
| SMAD3 | 6606.5 |
| NOTCH1 | 6546.5 |
| RBPJ | 5433.5 |
| EP300 | 5031.5 |
| SNW1 | 4685.0 |
| MAML1 | 4626.5 |
| ACTA2 | 4179.0 |
| MAML3 | 3119.5 |
| KAT2B | 2854.5 |
| KAT2A | 2000.5 |
| MAML2 | 903.5 |
| HEY2 | 0.5 |
| CREBBP | 0.5 |
| GeneID | Gene Rank |
|---|---|
| NOTCH4 | 6823.5 |
| SMAD3 | 6606.5 |
| NOTCH1 | 6546.5 |
| RBPJ | 5433.5 |
| EP300 | 5031.5 |
| SNW1 | 4685.0 |
| MAML1 | 4626.5 |
| ACTA2 | 4179.0 |
| MAML3 | 3119.5 |
| KAT2B | 2854.5 |
| KAT2A | 2000.5 |
| MAML2 | 903.5 |
| HEY2 | 0.5 |
| CREBBP | 0.5 |
TP53 regulates transcription of additional cell cycle genes whose exact role in the p53 pathway remain uncertain
| 1066 | |
|---|---|
| set | TP53 regulates transcription of additional cell cycle genes whose exact role in the p53 pathway remain uncertain |
| setSize | 16 |
| pANOVA | 0.0211 |
| s.dist | 0.333 |
| p.adjustANOVA | 0.229 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| CNOT4 | 7117.5 |
| PLK3 | 7090.5 |
| CENPJ | 6944.5 |
| BTG2 | 6562.5 |
| TP53 | 6276.0 |
| PLK2 | 4871.5 |
| CNOT6L | 4374.5 |
| CDC25C | 4156.5 |
| CNOT10 | 3255.5 |
| CNOT3 | 3169.5 |
| CNOT8 | 2744.5 |
| CNOT7 | 1626.0 |
| PLAGL1 | 1176.5 |
| TNKS1BP1 | 888.5 |
| CNOT1 | 884.5 |
| CNOT6 | -1158.5 |
| GeneID | Gene Rank |
|---|---|
| CNOT4 | 7117.5 |
| PLK3 | 7090.5 |
| CENPJ | 6944.5 |
| BTG2 | 6562.5 |
| TP53 | 6276.0 |
| PLK2 | 4871.5 |
| CNOT6L | 4374.5 |
| CDC25C | 4156.5 |
| CNOT10 | 3255.5 |
| CNOT3 | 3169.5 |
| CNOT8 | 2744.5 |
| CNOT7 | 1626.0 |
| PLAGL1 | 1176.5 |
| TNKS1BP1 | 888.5 |
| CNOT1 | 884.5 |
| CNOT6 | -1158.5 |
RUNX3 regulates NOTCH signaling
| 813 | |
|---|---|
| set | RUNX3 regulates NOTCH signaling |
| setSize | 11 |
| pANOVA | 0.0581 |
| s.dist | 0.33 |
| p.adjustANOVA | 0.323 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| NOTCH1 | 6546.5 |
| RUNX3 | 5866.5 |
| RBPJ | 5433.5 |
| EP300 | 5031.5 |
| SNW1 | 4685.0 |
| MAML1 | 4626.5 |
| MAML3 | 3119.5 |
| KAT2B | 2854.5 |
| KAT2A | 2000.5 |
| MAML2 | 903.5 |
| CREBBP | 0.5 |
| GeneID | Gene Rank |
|---|---|
| NOTCH1 | 6546.5 |
| RUNX3 | 5866.5 |
| RBPJ | 5433.5 |
| EP300 | 5031.5 |
| SNW1 | 4685.0 |
| MAML1 | 4626.5 |
| MAML3 | 3119.5 |
| KAT2B | 2854.5 |
| KAT2A | 2000.5 |
| MAML2 | 903.5 |
| CREBBP | 0.5 |
Potassium Channels
| 713 | |
|---|---|
| set | Potassium Channels |
| setSize | 26 |
| pANOVA | 0.00363 |
| s.dist | -0.33 |
| p.adjustANOVA | 0.106 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| KCNK6 | -3011.5 |
| KCNS1 | -2978.5 |
| KCNH4 | -2826.5 |
| KCNQ1 | -2806.0 |
| KCNQ5 | -2456.5 |
| KCNMB4 | -1890.5 |
| GABBR1 | -1610.5 |
| KCNAB2 | -1568.5 |
| GNB1 | -1307.5 |
| GNB4 | -1252.5 |
| KCNC4 | 0.5 |
| KCNG3 | 0.5 |
| GNG12 | 0.5 |
| KCNH2 | 0.5 |
| GNGT2 | 0.5 |
| KCNJ11 | 860.5 |
| KCNQ4 | 1090.5 |
| GNG4 | 1378.5 |
| GNG5 | 1544.0 |
| HCN3 | 1610.5 |
| GeneID | Gene Rank |
|---|---|
| KCNK6 | -3011.5 |
| KCNS1 | -2978.5 |
| KCNH4 | -2826.5 |
| KCNQ1 | -2806.0 |
| KCNQ5 | -2456.5 |
| KCNMB4 | -1890.5 |
| GABBR1 | -1610.5 |
| KCNAB2 | -1568.5 |
| GNB1 | -1307.5 |
| GNB4 | -1252.5 |
| KCNC4 | 0.5 |
| KCNG3 | 0.5 |
| GNG12 | 0.5 |
| KCNH2 | 0.5 |
| GNGT2 | 0.5 |
| KCNJ11 | 860.5 |
| KCNQ4 | 1090.5 |
| GNG4 | 1378.5 |
| GNG5 | 1544.0 |
| HCN3 | 1610.5 |
| KCNN4 | 1791.5 |
| GNG2 | 2385.5 |
| GNB5 | 2733.5 |
| GNG3 | 4284.5 |
| GNB2 | 6046.5 |
| KCNA3 | 6769.5 |
Leading Strand Synthesis
| 503 | |
|---|---|
| set | Leading Strand Synthesis |
| setSize | 12 |
| pANOVA | 0.0495 |
| s.dist | 0.327 |
| p.adjustANOVA | 0.3 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| PRIM1 | 6923.5 |
| POLD1 | 6531.5 |
| RFC5 | 6225.5 |
| RFC3 | 5827.5 |
| RFC4 | 5458.5 |
| PRIM2 | 5131.5 |
| POLD4 | 4972.5 |
| POLA2 | 3956.5 |
| POLD3 | 3647.5 |
| PCNA | -693.5 |
| POLD2 | -1204.5 |
| RFC2 | -2131.5 |
| GeneID | Gene Rank |
|---|---|
| PRIM1 | 6923.5 |
| POLD1 | 6531.5 |
| RFC5 | 6225.5 |
| RFC3 | 5827.5 |
| RFC4 | 5458.5 |
| PRIM2 | 5131.5 |
| POLD4 | 4972.5 |
| POLA2 | 3956.5 |
| POLD3 | 3647.5 |
| PCNA | -693.5 |
| POLD2 | -1204.5 |
| RFC2 | -2131.5 |
Polymerase switching
| 704 | |
|---|---|
| set | Polymerase switching |
| setSize | 12 |
| pANOVA | 0.0495 |
| s.dist | 0.327 |
| p.adjustANOVA | 0.3 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| PRIM1 | 6923.5 |
| POLD1 | 6531.5 |
| RFC5 | 6225.5 |
| RFC3 | 5827.5 |
| RFC4 | 5458.5 |
| PRIM2 | 5131.5 |
| POLD4 | 4972.5 |
| POLA2 | 3956.5 |
| POLD3 | 3647.5 |
| PCNA | -693.5 |
| POLD2 | -1204.5 |
| RFC2 | -2131.5 |
| GeneID | Gene Rank |
|---|---|
| PRIM1 | 6923.5 |
| POLD1 | 6531.5 |
| RFC5 | 6225.5 |
| RFC3 | 5827.5 |
| RFC4 | 5458.5 |
| PRIM2 | 5131.5 |
| POLD4 | 4972.5 |
| POLA2 | 3956.5 |
| POLD3 | 3647.5 |
| PCNA | -693.5 |
| POLD2 | -1204.5 |
| RFC2 | -2131.5 |
mRNA decay by 3’ to 5’ exoribonuclease
| 1175 | |
|---|---|
| set | mRNA decay by 3’ to 5’ exoribonuclease |
| setSize | 14 |
| pANOVA | 0.0361 |
| s.dist | 0.323 |
| p.adjustANOVA | 0.268 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| EXOSC8 | 6532.5 |
| DIS3 | 6495.0 |
| TTC37 | 6365.0 |
| WDR61 | 5590.5 |
| HBS1L | 4774.5 |
| EXOSC7 | 4446.0 |
| DCPS | 4198.5 |
| EXOSC4 | 3970.5 |
| SKIV2L | 3282.0 |
| EXOSC2 | 3110.5 |
| EXOSC5 | 2336.0 |
| EXOSC3 | 1535.5 |
| EXOSC6 | 542.5 |
| EXOSC1 | -1392.0 |
| GeneID | Gene Rank |
|---|---|
| EXOSC8 | 6532.5 |
| DIS3 | 6495.0 |
| TTC37 | 6365.0 |
| WDR61 | 5590.5 |
| HBS1L | 4774.5 |
| EXOSC7 | 4446.0 |
| DCPS | 4198.5 |
| EXOSC4 | 3970.5 |
| SKIV2L | 3282.0 |
| EXOSC2 | 3110.5 |
| EXOSC5 | 2336.0 |
| EXOSC3 | 1535.5 |
| EXOSC6 | 542.5 |
| EXOSC1 | -1392.0 |
Heparan sulfate/heparin (HS-GAG) metabolism
| 418 | |
|---|---|
| set | Heparan sulfate/heparin (HS-GAG) metabolism |
| setSize | 22 |
| pANOVA | 0.00889 |
| s.dist | -0.322 |
| p.adjustANOVA | 0.147 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| B3GAT2 | -2982.5 |
| B4GALT7 | -2710.5 |
| SDC4 | -2692.5 |
| XYLT1 | -2258.5 |
| NAGLU | -1491.5 |
| GLB1 | -1468.0 |
| GUSB | -1433.5 |
| IDUA | -1266.0 |
| HS6ST1 | -1250.5 |
| BCAN | -1170.5 |
| EXT2 | -1062.5 |
| HS3ST3B1 | -912.5 |
| HPSE2 | 0.5 |
| EXT1 | 558.5 |
| GPC2 | 627.0 |
| SGSH | 2006.0 |
| NDST2 | 2124.5 |
| B3GALT6 | 2174.0 |
| GLCE | 2804.0 |
| AGRN | 4937.5 |
| GeneID | Gene Rank |
|---|---|
| B3GAT2 | -2982.5 |
| B4GALT7 | -2710.5 |
| SDC4 | -2692.5 |
| XYLT1 | -2258.5 |
| NAGLU | -1491.5 |
| GLB1 | -1468.0 |
| GUSB | -1433.5 |
| IDUA | -1266.0 |
| HS6ST1 | -1250.5 |
| BCAN | -1170.5 |
| EXT2 | -1062.5 |
| HS3ST3B1 | -912.5 |
| HPSE2 | 0.5 |
| EXT1 | 558.5 |
| GPC2 | 627.0 |
| SGSH | 2006.0 |
| NDST2 | 2124.5 |
| B3GALT6 | 2174.0 |
| GLCE | 2804.0 |
| AGRN | 4937.5 |
| XYLT2 | 6721.5 |
| B3GAT3 | 7000.5 |
Mucopolysaccharidoses
| 578 | |
|---|---|
| set | Mucopolysaccharidoses |
| setSize | 10 |
| pANOVA | 0.0809 |
| s.dist | -0.319 |
| p.adjustANOVA | 0.375 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| NAGLU | -1491.5 |
| GLB1 | -1468.0 |
| GUSB | -1433.5 |
| IDUA | -1266.0 |
| ARSB | -1012.5 |
| HYAL1 | 0.5 |
| GALNS | 1340.0 |
| SGSH | 2006.0 |
| GNS | 3478.5 |
| HGSNAT | 3759.5 |
| GeneID | Gene Rank |
|---|---|
| NAGLU | -1491.5 |
| GLB1 | -1468.0 |
| GUSB | -1433.5 |
| IDUA | -1266.0 |
| ARSB | -1012.5 |
| HYAL1 | 0.5 |
| GALNS | 1340.0 |
| SGSH | 2006.0 |
| GNS | 3478.5 |
| HGSNAT | 3759.5 |
Arachidonic acid metabolism
| 61 | |
|---|---|
| set | Arachidonic acid metabolism |
| setSize | 21 |
| pANOVA | 0.0122 |
| s.dist | -0.316 |
| p.adjustANOVA | 0.17 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| LTC4S | -3024.5 |
| TBXAS1 | -2619.5 |
| DPEP2 | -2574.5 |
| ALOX5 | -2511.5 |
| GGT1 | -2500.5 |
| PTGR1 | -2332.5 |
| EPHX2 | -2264.5 |
| HPGD | -1600.5 |
| PON2 | -1276.5 |
| PTGR2 | -1124.5 |
| GPX1 | 0.5 |
| ALOX5AP | 0.5 |
| CYP2U1 | 0.5 |
| ALOXE3 | 637.5 |
| ABCC1 | 946.5 |
| MAPKAPK2 | 2344.5 |
| GPX4 | 3488.5 |
| LTA4H | 4840.5 |
| CYP4F22 | 5134.5 |
| PTGES2 | 5886.0 |
| GeneID | Gene Rank |
|---|---|
| LTC4S | -3024.5 |
| TBXAS1 | -2619.5 |
| DPEP2 | -2574.5 |
| ALOX5 | -2511.5 |
| GGT1 | -2500.5 |
| PTGR1 | -2332.5 |
| EPHX2 | -2264.5 |
| HPGD | -1600.5 |
| PON2 | -1276.5 |
| PTGR2 | -1124.5 |
| GPX1 | 0.5 |
| ALOX5AP | 0.5 |
| CYP2U1 | 0.5 |
| ALOXE3 | 637.5 |
| ABCC1 | 946.5 |
| MAPKAPK2 | 2344.5 |
| GPX4 | 3488.5 |
| LTA4H | 4840.5 |
| CYP4F22 | 5134.5 |
| PTGES2 | 5886.0 |
| PTGES3 | 7088.5 |
Triglyceride catabolism
| 1138 | |
|---|---|
| set | Triglyceride catabolism |
| setSize | 11 |
| pANOVA | 0.0705 |
| s.dist | -0.315 |
| p.adjustANOVA | 0.343 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| GPD2 | -2825.5 |
| ABHD5 | -2549.5 |
| PRKACA | -1900.5 |
| PPP1CB | -1620.5 |
| PLIN3 | -905.5 |
| PPP1CC | 746.5 |
| PPP1CA | 862.5 |
| LIPE | 1070.5 |
| FABP5 | 1514.5 |
| PRKACB | 3457.5 |
| CAV1 | 6670.5 |
| GeneID | Gene Rank |
|---|---|
| GPD2 | -2825.5 |
| ABHD5 | -2549.5 |
| PRKACA | -1900.5 |
| PPP1CB | -1620.5 |
| PLIN3 | -905.5 |
| PPP1CC | 746.5 |
| PPP1CA | 862.5 |
| LIPE | 1070.5 |
| FABP5 | 1514.5 |
| PRKACB | 3457.5 |
| CAV1 | 6670.5 |
STING mediated induction of host immune responses
| 905 | |
|---|---|
| set | STING mediated induction of host immune responses |
| setSize | 10 |
| pANOVA | 0.0883 |
| s.dist | -0.311 |
| p.adjustANOVA | 0.375 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| TREX1 | -2563.5 |
| XRCC6 | -1940.0 |
| TRIM21 | -1321.5 |
| STAT6 | -1239.5 |
| IRF3 | 1327.0 |
| DTX4 | 1629.5 |
| XRCC5 | 1787.5 |
| PRKDC | 1830.0 |
| DDX41 | 1951.5 |
| TBK1 | 2839.5 |
| GeneID | Gene Rank |
|---|---|
| TREX1 | -2563.5 |
| XRCC6 | -1940.0 |
| TRIM21 | -1321.5 |
| STAT6 | -1239.5 |
| IRF3 | 1327.0 |
| DTX4 | 1629.5 |
| XRCC5 | 1787.5 |
| PRKDC | 1830.0 |
| DDX41 | 1951.5 |
| TBK1 | 2839.5 |
Rap1 signalling
| 816 | |
|---|---|
| set | Rap1 signalling |
| setSize | 11 |
| pANOVA | 0.0765 |
| s.dist | 0.308 |
| p.adjustANOVA | 0.362 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| YWHAZ | 7122.5 |
| RAP1A | 6705.5 |
| RAP1B | 6500.5 |
| RASGRP1 | 4429.5 |
| YWHAB | 3617.5 |
| PRKACB | 3457.5 |
| RAF1 | 3305.5 |
| SIPA1 | 2974.5 |
| RASGRP2 | 1940.5 |
| RAP1GAP2 | 1691.5 |
| PRKACA | -1900.5 |
| GeneID | Gene Rank |
|---|---|
| YWHAZ | 7122.5 |
| RAP1A | 6705.5 |
| RAP1B | 6500.5 |
| RASGRP1 | 4429.5 |
| YWHAB | 3617.5 |
| PRKACB | 3457.5 |
| RAF1 | 3305.5 |
| SIPA1 | 2974.5 |
| RASGRP2 | 1940.5 |
| RAP1GAP2 | 1691.5 |
| PRKACA | -1900.5 |
Processing of Intronless Pre-mRNAs
| 724 | |
|---|---|
| set | Processing of Intronless Pre-mRNAs |
| setSize | 15 |
| pANOVA | 0.0388 |
| s.dist | 0.308 |
| p.adjustANOVA | 0.281 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| NCBP1 | 6538.0 |
| NUDT21 | 6498.0 |
| CSTF1 | 6459.0 |
| CPSF4 | 5462.0 |
| CPSF2 | 5140.0 |
| CLP1 | 4722.5 |
| WDR33 | 3344.5 |
| CPSF6 | 3239.5 |
| PABPN1 | 3193.5 |
| NCBP2 | 2447.0 |
| FIP1L1 | 2354.5 |
| CPSF1 | 1547.5 |
| CPSF3 | 1363.0 |
| SYMPK | 1072.5 |
| PAPOLA | 928.5 |
| GeneID | Gene Rank |
|---|---|
| NCBP1 | 6538.0 |
| NUDT21 | 6498.0 |
| CSTF1 | 6459.0 |
| CPSF4 | 5462.0 |
| CPSF2 | 5140.0 |
| CLP1 | 4722.5 |
| WDR33 | 3344.5 |
| CPSF6 | 3239.5 |
| PABPN1 | 3193.5 |
| NCBP2 | 2447.0 |
| FIP1L1 | 2354.5 |
| CPSF1 | 1547.5 |
| CPSF3 | 1363.0 |
| SYMPK | 1072.5 |
| PAPOLA | 928.5 |
RHO GTPases activate CIT
| 758 | |
|---|---|
| set | RHO GTPases activate CIT |
| setSize | 14 |
| pANOVA | 0.0496 |
| s.dist | 0.303 |
| p.adjustANOVA | 0.3 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| CIT | 6951.5 |
| RHOB | 6666.5 |
| PPP1R12A | 6450.5 |
| KIF14 | 5548.5 |
| MYH9 | 5448.5 |
| MYL6 | 5389.5 |
| CDKN1B | 5388.5 |
| RHOA | 4771.0 |
| PPP1R12B | 4546.5 |
| MYH10 | 2703.5 |
| RAC1 | 1104.5 |
| PRC1 | -792.5 |
| PPP1CB | -1620.5 |
| DLG4 | -2233.5 |
| GeneID | Gene Rank |
|---|---|
| CIT | 6951.5 |
| RHOB | 6666.5 |
| PPP1R12A | 6450.5 |
| KIF14 | 5548.5 |
| MYH9 | 5448.5 |
| MYL6 | 5389.5 |
| CDKN1B | 5388.5 |
| RHOA | 4771.0 |
| PPP1R12B | 4546.5 |
| MYH10 | 2703.5 |
| RAC1 | 1104.5 |
| PRC1 | -792.5 |
| PPP1CB | -1620.5 |
| DLG4 | -2233.5 |
Tristetraprolin (TTP, ZFP36) binds and destabilizes mRNA
| 1140 | |
|---|---|
| set | Tristetraprolin (TTP, ZFP36) binds and destabilizes mRNA |
| setSize | 15 |
| pANOVA | 0.0434 |
| s.dist | 0.301 |
| p.adjustANOVA | 0.286 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| EXOSC8 | 6532.5 |
| DIS3 | 6495.0 |
| TNPO1 | 6058.5 |
| DCP2 | 5890.5 |
| ZFP36 | 5773.5 |
| EXOSC7 | 4446.0 |
| EXOSC4 | 3970.5 |
| YWHAB | 3617.5 |
| EXOSC2 | 3110.5 |
| DCP1A | 2507.5 |
| MAPKAPK2 | 2344.5 |
| EXOSC5 | 2336.0 |
| EXOSC3 | 1535.5 |
| EXOSC6 | 542.5 |
| EXOSC1 | -1392.0 |
| GeneID | Gene Rank |
|---|---|
| EXOSC8 | 6532.5 |
| DIS3 | 6495.0 |
| TNPO1 | 6058.5 |
| DCP2 | 5890.5 |
| ZFP36 | 5773.5 |
| EXOSC7 | 4446.0 |
| EXOSC4 | 3970.5 |
| YWHAB | 3617.5 |
| EXOSC2 | 3110.5 |
| DCP1A | 2507.5 |
| MAPKAPK2 | 2344.5 |
| EXOSC5 | 2336.0 |
| EXOSC3 | 1535.5 |
| EXOSC6 | 542.5 |
| EXOSC1 | -1392.0 |
Josephin domain DUBs
| 491 | |
|---|---|
| set | Josephin domain DUBs |
| setSize | 11 |
| pANOVA | 0.0845 |
| s.dist | -0.3 |
| p.adjustANOVA | 0.375 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RAD23A | -2240.5 |
| PARK2 | -2181.0 |
| UBC | -1150.5 |
| VCP | -1134.5 |
| UBB | -759.5 |
| JOSD2 | -583.5 |
| RPS27A | 759.5 |
| JOSD1 | 1411.5 |
| UBA52 | 2326.5 |
| ATXN3 | 3481.5 |
| RAD23B | 5416.5 |
| GeneID | Gene Rank |
|---|---|
| RAD23A | -2240.5 |
| PARK2 | -2181.0 |
| UBC | -1150.5 |
| VCP | -1134.5 |
| UBB | -759.5 |
| JOSD2 | -583.5 |
| RPS27A | 759.5 |
| JOSD1 | 1411.5 |
| UBA52 | 2326.5 |
| ATXN3 | 3481.5 |
| RAD23B | 5416.5 |
Transcriptional regulation of granulopoiesis
| 1112 | |
|---|---|
| set | Transcriptional regulation of granulopoiesis |
| setSize | 24 |
| pANOVA | 0.0109 |
| s.dist | -0.3 |
| p.adjustANOVA | 0.162 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| SPI1 | -3114.5 |
| CEBPE | -3094.5 |
| CEBPA | -2827.5 |
| CSF3R | -2702.5 |
| TFDP1 | -2179.5 |
| IL6R | -1698.5 |
| RARA | -1605.5 |
| CBFB | -1581.5 |
| H2AFX | -1571.5 |
| RUNX1 | -1540.5 |
| DEK | -1480.5 |
| KLF5 | -676.5 |
| CREB1 | 0.5 |
| CDKN1A | 0.5 |
| CDK2 | 1826.0 |
| CDK4 | 1926.5 |
| E2F1 | 1992.5 |
| FLI1 | 2126.5 |
| STAT3 | 2532.5 |
| MYB | 3698.5 |
| GeneID | Gene Rank |
|---|---|
| SPI1 | -3114.5 |
| CEBPE | -3094.5 |
| CEBPA | -2827.5 |
| CSF3R | -2702.5 |
| TFDP1 | -2179.5 |
| IL6R | -1698.5 |
| RARA | -1605.5 |
| CBFB | -1581.5 |
| H2AFX | -1571.5 |
| RUNX1 | -1540.5 |
| DEK | -1480.5 |
| KLF5 | -676.5 |
| CREB1 | 0.5 |
| CDKN1A | 0.5 |
| CDK2 | 1826.0 |
| CDK4 | 1926.5 |
| E2F1 | 1992.5 |
| FLI1 | 2126.5 |
| STAT3 | 2532.5 |
| MYB | 3698.5 |
| GFI1 | 4968.5 |
| EP300 | 5031.5 |
| CEBPB | 5379.5 |
| PML | 6318.5 |
E2F mediated regulation of DNA replication
| 265 | |
|---|---|
| set | E2F mediated regulation of DNA replication |
| setSize | 12 |
| pANOVA | 0.0758 |
| s.dist | 0.296 |
| p.adjustANOVA | 0.362 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| PRIM1 | 6923.5 |
| CCNB1 | 6075.5 |
| PPP2CA | 5524.5 |
| RB1 | 5174.5 |
| PRIM2 | 5131.5 |
| PPP2CB | 4601.5 |
| POLA2 | 3956.5 |
| MCM8 | 3343.0 |
| CDK1 | 2828.0 |
| E2F1 | 1992.5 |
| PPP2R1B | -675.5 |
| TFDP1 | -2179.5 |
| GeneID | Gene Rank |
|---|---|
| PRIM1 | 6923.5 |
| CCNB1 | 6075.5 |
| PPP2CA | 5524.5 |
| RB1 | 5174.5 |
| PRIM2 | 5131.5 |
| PPP2CB | 4601.5 |
| POLA2 | 3956.5 |
| MCM8 | 3343.0 |
| CDK1 | 2828.0 |
| E2F1 | 1992.5 |
| PPP2R1B | -675.5 |
| TFDP1 | -2179.5 |
Here is the session info with all the versions of packages used.
sessionInfo()
## R version 4.2.0 (2022-04-22)
## Platform: x86_64-pc-linux-gnu (64-bit)
## Running under: Ubuntu 20.04.4 LTS
##
## Matrix products: default
## BLAS: /usr/lib/x86_64-linux-gnu/blas/libblas.so.3.9.0
## LAPACK: /usr/lib/x86_64-linux-gnu/lapack/liblapack.so.3.9.0
##
## 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
##
## attached base packages:
## [1] parallel stats graphics grDevices utils datasets methods
## [8] base
##
## other attached packages:
## [1] pkgload_1.2.4 GGally_2.1.2 ggplot2_3.3.5 reshape2_1.4.4
## [5] beeswarm_0.4.0 gplots_3.1.1 gtools_3.9.2 tibble_3.1.6
## [9] echarts4r_0.4.3 mitch_1.4.1 eulerr_6.1.1 kableExtra_1.3.4
## [13] dplyr_1.0.8
##
## loaded via a namespace (and not attached):
## [1] httr_1.4.2 sass_0.4.1 jsonlite_1.8.0 viridisLite_0.4.0
## [5] brio_1.1.3 bslib_0.3.1 shiny_1.7.1 assertthat_0.2.1
## [9] highr_0.9 yaml_2.3.5 pillar_1.7.0 glue_1.6.2
## [13] digest_0.6.29 RColorBrewer_1.1-3 promises_1.2.0.1 rvest_1.0.2
## [17] colorspace_2.0-3 htmltools_0.5.2 httpuv_1.6.5 plyr_1.8.7
## [21] pkgconfig_2.0.3 purrr_0.3.4 xtable_1.8-4 scales_1.1.1
## [25] webshot_0.5.2 svglite_2.1.0 later_1.3.0 generics_0.1.2
## [29] ellipsis_0.3.2 withr_2.5.0 cli_3.2.0 magrittr_2.0.3
## [33] crayon_1.5.1 mime_0.12 evaluate_0.15 fansi_1.0.3
## [37] MASS_7.3-57 xml2_1.3.3 tools_4.2.0 lifecycle_1.0.1
## [41] stringr_1.4.0 munsell_0.5.0 compiler_4.2.0 jquerylib_0.1.4
## [45] caTools_1.18.2 systemfonts_1.0.4 rlang_1.0.2 grid_4.2.0
## [49] rstudioapi_0.13 htmlwidgets_1.5.4 bitops_1.0-7 rmarkdown_2.13
## [53] testthat_3.1.3 gtable_0.3.0 DBI_1.1.2 reshape_0.8.8
## [57] R6_2.5.1 gridExtra_2.3 knitr_1.38 fastmap_1.1.0
## [61] utf8_1.2.2 rprojroot_2.0.3 KernSmooth_2.23-20 desc_1.4.1
## [65] stringi_1.7.6 Rcpp_1.0.8.3 vctrs_0.4.0 tidyselect_1.1.2
## [69] xfun_0.30
END of report