date generated: 2023-11-14
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.
| mean | |
|---|---|
| PRDM16 | 0.6501046 |
| CDH4 | 0.6997851 |
| SEPT9 | 0.6428529 |
| KCNQ1 | 0.5587846 |
| GNAS | 0.6544056 |
| SHANK2 | 0.4526450 |
Here are some metrics about the input data profile:
| Profile metrics | |
|---|---|
| num_genesets | 2630 |
| num_genes_in_profile | 25739 |
| duplicated_genes_present | 0 |
| num_profile_genes_in_sets | 10334 |
| num_profile_genes_not_in_sets | 15405 |
Here is a plot of the input profiles. Note the dynamic ranges.
Here is the contour plot of the profile including all detected genes.
Here are some metrics about the gene sets used:
GMT file of genesets: ReactomePathways.gmt| Gene sets metrics | |
|---|---|
| num_genesets | 2630 |
| num_genesets_excluded | 1044 |
| num_genesets_included | 1586 |
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.
Top N= 50 gene sets
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| set | setSize | pANOVA | s.dist | p.adjustANOVA |
|---|---|---|---|---|
| Chylomicron remodeling | 10 | 2.54e-03 | 0.551 | 4.82e-02 |
| TRAF6 mediated IRF7 activation in TLR7/8 or 9 signaling | 11 | 1.65e-03 | 0.548 | 3.59e-02 |
| SARS-CoV-1 modulates host translation machinery | 34 | 1.73e-07 | 0.518 | 9.79e-06 |
| Josephin domain DUBs | 11 | 5.49e-03 | 0.483 | 8.05e-02 |
| TRAF6 mediated IRF7 activation | 25 | 5.09e-05 | -0.468 | 1.72e-03 |
| Class C/3 (Metabotropic glutamate/pheromone receptors) | 39 | 6.08e-07 | -0.461 | 3.33e-05 |
| SUMOylation of immune response proteins | 11 | 8.67e-03 | 0.457 | 1.12e-01 |
| Pexophagy | 11 | 8.89e-03 | 0.455 | 1.14e-01 |
| Phase 4 - resting membrane potential | 19 | 1.10e-03 | 0.432 | 2.77e-02 |
| Interaction With Cumulus Cells And The Zona Pellucida | 11 | 1.43e-02 | -0.426 | 1.55e-01 |
| Regulation of CDH11 gene transcription | 10 | 2.08e-02 | 0.422 | 1.90e-01 |
| Expression and translocation of olfactory receptors | 358 | 3.01e-42 | -0.418 | 4.77e-39 |
| NF-kB is activated and signals survival | 12 | 1.25e-02 | 0.416 | 1.43e-01 |
| Peptide chain elongation | 84 | 6.63e-11 | 0.412 | 1.31e-08 |
| Regulation of NF-kappa B signaling | 17 | 3.41e-03 | 0.410 | 5.89e-02 |
| Olfactory Signaling Pathway | 365 | 3.28e-41 | -0.409 | 2.60e-38 |
| Viral mRNA Translation | 84 | 1.32e-10 | 0.405 | 2.12e-08 |
| APC/C:Cdc20 mediated degradation of Cyclin B | 24 | 6.62e-04 | 0.401 | 1.88e-02 |
| Eukaryotic Translation Termination | 87 | 1.35e-10 | 0.398 | 2.12e-08 |
| Eukaryotic Translation Elongation | 88 | 1.47e-10 | 0.395 | 2.12e-08 |
| NF-kB activation through FADD/RIP-1 pathway mediated by caspase-8 and -10 | 11 | 2.68e-02 | -0.385 | 2.25e-01 |
| Selenocysteine synthesis | 87 | 1.02e-09 | 0.378 | 1.29e-07 |
| Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC) | 89 | 1.18e-09 | 0.373 | 1.29e-07 |
| NRIF signals cell death from the nucleus | 16 | 1.00e-02 | 0.372 | 1.26e-01 |
| TICAM1,TRAF6-dependent induction of TAK1 complex | 10 | 4.44e-02 | 0.367 | 2.96e-01 |
| Intrinsic Pathway of Fibrin Clot Formation | 21 | 3.81e-03 | -0.365 | 6.36e-02 |
| Tandem pore domain potassium channels | 12 | 2.88e-02 | 0.365 | 2.36e-01 |
| Regulation of IFNA/IFNB signaling | 22 | 3.31e-03 | -0.362 | 5.84e-02 |
| Response of EIF2AK4 (GCN2) to amino acid deficiency | 95 | 1.17e-09 | 0.361 | 1.29e-07 |
| Formation of a pool of free 40S subunits | 94 | 1.71e-09 | 0.359 | 1.69e-07 |
| Signaling by cytosolic FGFR1 fusion mutants | 17 | 1.08e-02 | -0.357 | 1.31e-01 |
| Sensory perception of sweet, bitter, and umami (glutamate) taste | 41 | 7.68e-05 | -0.357 | 2.44e-03 |
| Pausing and recovery of Tat-mediated HIV elongation | 27 | 1.37e-03 | 0.356 | 3.11e-02 |
| Tat-mediated HIV elongation arrest and recovery | 27 | 1.37e-03 | 0.356 | 3.11e-02 |
| Caspase activation via Death Receptors in the presence of ligand | 16 | 1.42e-02 | -0.354 | 1.55e-01 |
| p75NTR recruits signalling complexes | 12 | 3.56e-02 | 0.350 | 2.58e-01 |
| HIV elongation arrest and recovery | 29 | 1.16e-03 | 0.348 | 2.81e-02 |
| Pausing and recovery of HIV elongation | 29 | 1.16e-03 | 0.348 | 2.81e-02 |
| Formation of the ternary complex, and subsequently, the 43S complex | 46 | 4.47e-05 | 0.348 | 1.58e-03 |
| NOTCH4 Activation and Transmission of Signal to the Nucleus | 11 | 4.67e-02 | 0.346 | 2.97e-01 |
| Interleukin-15 signaling | 13 | 3.08e-02 | -0.346 | 2.44e-01 |
| SARS-CoV-2 modulates host translation machinery | 46 | 6.31e-05 | 0.341 | 2.04e-03 |
| Selenoamino acid metabolism | 103 | 3.25e-09 | 0.337 | 2.72e-07 |
| Attenuation phase | 25 | 3.51e-03 | 0.337 | 5.93e-02 |
| Chylomicron assembly | 10 | 6.52e-02 | 0.337 | 3.38e-01 |
| L13a-mediated translational silencing of Ceruloplasmin expression | 103 | 4.02e-09 | 0.335 | 3.03e-07 |
| GTP hydrolysis and joining of the 60S ribosomal subunit | 104 | 3.93e-09 | 0.334 | 3.03e-07 |
| Biosynthesis of DHA-derived SPMs | 17 | 1.73e-02 | 0.334 | 1.72e-01 |
| Ribosomal scanning and start codon recognition | 53 | 2.82e-05 | 0.332 | 1.09e-03 |
| Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S | 54 | 2.39e-05 | 0.332 | 9.72e-04 |
| set | setSize | pANOVA | s.dist | p.adjustANOVA |
|---|---|---|---|---|
| Chylomicron remodeling | 10 | 2.54e-03 | 0.551000 | 4.82e-02 |
| TRAF6 mediated IRF7 activation in TLR7/8 or 9 signaling | 11 | 1.65e-03 | 0.548000 | 3.59e-02 |
| SARS-CoV-1 modulates host translation machinery | 34 | 1.73e-07 | 0.518000 | 9.79e-06 |
| Josephin domain DUBs | 11 | 5.49e-03 | 0.483000 | 8.05e-02 |
| TRAF6 mediated IRF7 activation | 25 | 5.09e-05 | -0.468000 | 1.72e-03 |
| Class C/3 (Metabotropic glutamate/pheromone receptors) | 39 | 6.08e-07 | -0.461000 | 3.33e-05 |
| SUMOylation of immune response proteins | 11 | 8.67e-03 | 0.457000 | 1.12e-01 |
| Pexophagy | 11 | 8.89e-03 | 0.455000 | 1.14e-01 |
| Phase 4 - resting membrane potential | 19 | 1.10e-03 | 0.432000 | 2.77e-02 |
| Interaction With Cumulus Cells And The Zona Pellucida | 11 | 1.43e-02 | -0.426000 | 1.55e-01 |
| Regulation of CDH11 gene transcription | 10 | 2.08e-02 | 0.422000 | 1.90e-01 |
| Expression and translocation of olfactory receptors | 358 | 3.01e-42 | -0.418000 | 4.77e-39 |
| NF-kB is activated and signals survival | 12 | 1.25e-02 | 0.416000 | 1.43e-01 |
| Peptide chain elongation | 84 | 6.63e-11 | 0.412000 | 1.31e-08 |
| Regulation of NF-kappa B signaling | 17 | 3.41e-03 | 0.410000 | 5.89e-02 |
| Olfactory Signaling Pathway | 365 | 3.28e-41 | -0.409000 | 2.60e-38 |
| Viral mRNA Translation | 84 | 1.32e-10 | 0.405000 | 2.12e-08 |
| APC/C:Cdc20 mediated degradation of Cyclin B | 24 | 6.62e-04 | 0.401000 | 1.88e-02 |
| Eukaryotic Translation Termination | 87 | 1.35e-10 | 0.398000 | 2.12e-08 |
| Eukaryotic Translation Elongation | 88 | 1.47e-10 | 0.395000 | 2.12e-08 |
| NF-kB activation through FADD/RIP-1 pathway mediated by caspase-8 and -10 | 11 | 2.68e-02 | -0.385000 | 2.25e-01 |
| Selenocysteine synthesis | 87 | 1.02e-09 | 0.378000 | 1.29e-07 |
| Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC) | 89 | 1.18e-09 | 0.373000 | 1.29e-07 |
| NRIF signals cell death from the nucleus | 16 | 1.00e-02 | 0.372000 | 1.26e-01 |
| TICAM1,TRAF6-dependent induction of TAK1 complex | 10 | 4.44e-02 | 0.367000 | 2.96e-01 |
| Intrinsic Pathway of Fibrin Clot Formation | 21 | 3.81e-03 | -0.365000 | 6.36e-02 |
| Tandem pore domain potassium channels | 12 | 2.88e-02 | 0.365000 | 2.36e-01 |
| Regulation of IFNA/IFNB signaling | 22 | 3.31e-03 | -0.362000 | 5.84e-02 |
| Response of EIF2AK4 (GCN2) to amino acid deficiency | 95 | 1.17e-09 | 0.361000 | 1.29e-07 |
| Formation of a pool of free 40S subunits | 94 | 1.71e-09 | 0.359000 | 1.69e-07 |
| Signaling by cytosolic FGFR1 fusion mutants | 17 | 1.08e-02 | -0.357000 | 1.31e-01 |
| Sensory perception of sweet, bitter, and umami (glutamate) taste | 41 | 7.68e-05 | -0.357000 | 2.44e-03 |
| Pausing and recovery of Tat-mediated HIV elongation | 27 | 1.37e-03 | 0.356000 | 3.11e-02 |
| Tat-mediated HIV elongation arrest and recovery | 27 | 1.37e-03 | 0.356000 | 3.11e-02 |
| Caspase activation via Death Receptors in the presence of ligand | 16 | 1.42e-02 | -0.354000 | 1.55e-01 |
| p75NTR recruits signalling complexes | 12 | 3.56e-02 | 0.350000 | 2.58e-01 |
| HIV elongation arrest and recovery | 29 | 1.16e-03 | 0.348000 | 2.81e-02 |
| Pausing and recovery of HIV elongation | 29 | 1.16e-03 | 0.348000 | 2.81e-02 |
| Formation of the ternary complex, and subsequently, the 43S complex | 46 | 4.47e-05 | 0.348000 | 1.58e-03 |
| NOTCH4 Activation and Transmission of Signal to the Nucleus | 11 | 4.67e-02 | 0.346000 | 2.97e-01 |
| Interleukin-15 signaling | 13 | 3.08e-02 | -0.346000 | 2.44e-01 |
| SARS-CoV-2 modulates host translation machinery | 46 | 6.31e-05 | 0.341000 | 2.04e-03 |
| Selenoamino acid metabolism | 103 | 3.25e-09 | 0.337000 | 2.72e-07 |
| Attenuation phase | 25 | 3.51e-03 | 0.337000 | 5.93e-02 |
| Chylomicron assembly | 10 | 6.52e-02 | 0.337000 | 3.38e-01 |
| L13a-mediated translational silencing of Ceruloplasmin expression | 103 | 4.02e-09 | 0.335000 | 3.03e-07 |
| GTP hydrolysis and joining of the 60S ribosomal subunit | 104 | 3.93e-09 | 0.334000 | 3.03e-07 |
| Biosynthesis of DHA-derived SPMs | 17 | 1.73e-02 | 0.334000 | 1.72e-01 |
| Ribosomal scanning and start codon recognition | 53 | 2.82e-05 | 0.332000 | 1.09e-03 |
| Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S | 54 | 2.39e-05 | 0.332000 | 9.72e-04 |
| Translation initiation complex formation | 53 | 3.12e-05 | 0.331000 | 1.17e-03 |
| Platelet Adhesion to exposed collagen | 15 | 2.66e-02 | -0.331000 | 2.25e-01 |
| IRAK1 recruits IKK complex | 12 | 4.76e-02 | 0.330000 | 2.97e-01 |
| IRAK1 recruits IKK complex upon TLR7/8 or 9 stimulation | 12 | 4.76e-02 | 0.330000 | 2.97e-01 |
| p75NTR signals via NF-kB | 15 | 2.70e-02 | 0.330000 | 2.26e-01 |
| Assembly Of The HIV Virion | 16 | 2.25e-02 | 0.330000 | 2.00e-01 |
| Downregulation of ERBB2:ERBB3 signaling | 13 | 4.02e-02 | 0.329000 | 2.80e-01 |
| Regulation of signaling by NODAL | 10 | 7.45e-02 | 0.326000 | 3.56e-01 |
| Metabolism of folate and pterines | 16 | 2.41e-02 | -0.326000 | 2.09e-01 |
| Cap-dependent Translation Initiation | 111 | 3.04e-09 | 0.326000 | 2.67e-07 |
| Eukaryotic Translation Initiation | 111 | 3.04e-09 | 0.326000 | 2.67e-07 |
| Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC) | 108 | 5.73e-09 | 0.324000 | 3.63e-07 |
| Nonsense-Mediated Decay (NMD) | 108 | 5.73e-09 | 0.324000 | 3.63e-07 |
| Membrane binding and targetting of GAG proteins | 14 | 3.60e-02 | 0.324000 | 2.58e-01 |
| Synthesis And Processing Of GAG, GAGPOL Polyproteins | 14 | 3.60e-02 | 0.324000 | 2.58e-01 |
| STAT5 activation downstream of FLT3 ITD mutants | 10 | 7.65e-02 | -0.323000 | 3.60e-01 |
| APC-Cdc20 mediated degradation of Nek2A | 26 | 4.39e-03 | 0.323000 | 6.96e-02 |
| SARS-CoV-1 targets host intracellular signalling and regulatory pathways | 16 | 2.81e-02 | 0.317000 | 2.33e-01 |
| HSF1 activation | 27 | 4.38e-03 | 0.317000 | 6.96e-02 |
| Major pathway of rRNA processing in the nucleolus and cytosol | 171 | 1.05e-12 | 0.315000 | 4.17e-10 |
| Recycling of bile acids and salts | 18 | 2.08e-02 | -0.315000 | 1.90e-01 |
| CYP2E1 reactions | 11 | 7.18e-02 | -0.313000 | 3.50e-01 |
| Alpha-protein kinase 1 signaling pathway | 10 | 8.69e-02 | 0.313000 | 3.88e-01 |
| TP53 Regulates Transcription of Genes Involved in G1 Cell Cycle Arrest | 14 | 4.35e-02 | 0.312000 | 2.91e-01 |
| Prednisone ADME | 10 | 8.79e-02 | -0.312000 | 3.90e-01 |
| HSF1-dependent transactivation | 35 | 1.50e-03 | 0.310000 | 3.30e-02 |
| Zinc influx into cells by the SLC39 gene family | 10 | 8.96e-02 | 0.310000 | 3.91e-01 |
| NPAS4 regulates expression of target genes | 21 | 1.51e-02 | 0.306000 | 1.59e-01 |
| Signal regulatory protein family interactions | 16 | 3.56e-02 | -0.303000 | 2.58e-01 |
| Synthesis of glycosylphosphatidylinositol (GPI) | 17 | 3.12e-02 | 0.302000 | 2.44e-01 |
| Role of LAT2/NTAL/LAB on calcium mobilization | 16 | 3.72e-02 | -0.301000 | 2.66e-01 |
| NOTCH2 Activation and Transmission of Signal to the Nucleus | 22 | 1.47e-02 | 0.301000 | 1.55e-01 |
| SRP-dependent cotranslational protein targeting to membrane | 105 | 1.14e-07 | 0.299000 | 6.72e-06 |
| SARS-CoV-2 targets host intracellular signalling and regulatory pathways | 12 | 7.31e-02 | 0.299000 | 3.53e-01 |
| Constitutive Signaling by NOTCH1 HD Domain Mutants | 15 | 4.51e-02 | 0.299000 | 2.97e-01 |
| Signaling by NOTCH1 HD Domain Mutants in Cancer | 15 | 4.51e-02 | 0.299000 | 2.97e-01 |
| rRNA processing in the nucleus and cytosol | 180 | 4.64e-12 | 0.299000 | 1.47e-09 |
| Golgi Cisternae Pericentriolar Stack Reorganization | 14 | 5.48e-02 | 0.296000 | 3.19e-01 |
| Cellular response to starvation | 147 | 1.22e-09 | 0.290000 | 1.29e-07 |
| Chemokine receptors bind chemokines | 56 | 1.81e-04 | -0.289000 | 5.61e-03 |
| rRNA processing | 186 | 1.48e-11 | 0.287000 | 3.35e-09 |
| Regulation of localization of FOXO transcription factors | 11 | 1.02e-01 | 0.285000 | 4.15e-01 |
| Cell-extracellular matrix interactions | 16 | 4.88e-02 | 0.285000 | 3.03e-01 |
| Negative regulation of activity of TFAP2 (AP-2) family transcription factors | 10 | 1.22e-01 | 0.283000 | 4.56e-01 |
| Cytosolic iron-sulfur cluster assembly | 10 | 1.22e-01 | 0.283000 | 4.56e-01 |
| mRNA Editing | 10 | 1.23e-01 | -0.282000 | 4.57e-01 |
| Synthesis of PIPs at the late endosome membrane | 10 | 1.24e-01 | -0.281000 | 4.59e-01 |
| Interleukin-2 family signaling | 40 | 2.17e-03 | -0.280000 | 4.35e-02 |
| Regulation of innate immune responses to cytosolic DNA | 14 | 6.99e-02 | 0.280000 | 3.43e-01 |
| Mitochondrial iron-sulfur cluster biogenesis | 12 | 9.53e-02 | 0.278000 | 4.03e-01 |
| HDL remodeling | 10 | 1.29e-01 | 0.277000 | 4.70e-01 |
| Conversion from APC/C:Cdc20 to APC/C:Cdh1 in late anaphase | 20 | 3.38e-02 | 0.274000 | 2.52e-01 |
| Diseases associated with glycosylation precursor biosynthesis | 15 | 6.63e-02 | 0.274000 | 3.38e-01 |
| Assembly of active LPL and LIPC lipase complexes | 17 | 5.16e-02 | 0.273000 | 3.13e-01 |
| Glutamate and glutamine metabolism | 12 | 1.03e-01 | 0.272000 | 4.15e-01 |
| Influenza Viral RNA Transcription and Replication | 129 | 9.45e-08 | 0.272000 | 5.77e-06 |
| SMAD2/SMAD3:SMAD4 heterotrimer regulates transcription | 36 | 4.83e-03 | 0.271000 | 7.44e-02 |
| Activation of PPARGC1A (PGC-1alpha) by phosphorylation | 10 | 1.41e-01 | 0.269000 | 4.94e-01 |
| NOTCH3 Activation and Transmission of Signal to the Nucleus | 25 | 2.00e-02 | 0.269000 | 1.87e-01 |
| Regulation of expression of SLITs and ROBOs | 159 | 4.83e-09 | 0.269000 | 3.33e-07 |
| Sensory Perception | 571 | 3.98e-28 | -0.268000 | 2.10e-25 |
| Glucuronidation | 25 | 2.03e-02 | -0.268000 | 1.89e-01 |
| TRAF3-dependent IRF activation pathway | 14 | 8.74e-02 | -0.264000 | 3.89e-01 |
| Pregnenolone biosynthesis | 10 | 1.49e-01 | 0.263000 | 5.06e-01 |
| Synthesis of PIPs at the early endosome membrane | 15 | 7.82e-02 | -0.263000 | 3.64e-01 |
| Spry regulation of FGF signaling | 16 | 6.96e-02 | 0.262000 | 3.43e-01 |
| Sensory perception of taste | 47 | 1.98e-03 | -0.261000 | 4.03e-02 |
| VLDLR internalisation and degradation | 16 | 7.47e-02 | 0.257000 | 3.56e-01 |
| Interleukin-6 signaling | 11 | 1.41e-01 | -0.256000 | 4.94e-01 |
| GRB2:SOS provides linkage to MAPK signaling for Integrins | 15 | 8.57e-02 | -0.256000 | 3.86e-01 |
| rRNA modification in the nucleus and cytosol | 55 | 1.06e-03 | 0.255000 | 2.70e-02 |
| XBP1(S) activates chaperone genes | 47 | 2.55e-03 | 0.254000 | 4.82e-02 |
| FGFR1 ligand binding and activation | 17 | 6.97e-02 | 0.254000 | 3.43e-01 |
| Formation of TC-NER Pre-Incision Complex | 51 | 1.70e-03 | 0.254000 | 3.64e-02 |
| Formation of HIV-1 elongation complex containing HIV-1 Tat | 38 | 6.79e-03 | 0.254000 | 9.05e-02 |
| HIV Transcription Elongation | 38 | 6.79e-03 | 0.254000 | 9.05e-02 |
| Tat-mediated elongation of the HIV-1 transcript | 38 | 6.79e-03 | 0.254000 | 9.05e-02 |
| ERKs are inactivated | 13 | 1.14e-01 | 0.253000 | 4.41e-01 |
| Formation of HIV elongation complex in the absence of HIV Tat | 40 | 5.53e-03 | 0.253000 | 8.05e-02 |
| Biosynthesis of specialized proresolving mediators (SPMs) | 19 | 5.59e-02 | 0.253000 | 3.23e-01 |
| Chk1/Chk2(Cds1) mediated inactivation of Cyclin B:Cdk1 complex | 13 | 1.14e-01 | 0.253000 | 4.41e-01 |
| Constitutive Signaling by Ligand-Responsive EGFR Cancer Variants | 19 | 5.82e-02 | 0.251000 | 3.25e-01 |
| Signaling by Ligand-Responsive EGFR Variants in Cancer | 19 | 5.82e-02 | 0.251000 | 3.25e-01 |
| IRE1alpha activates chaperones | 49 | 2.40e-03 | 0.251000 | 4.65e-02 |
| Phosphorylation of the APC/C | 20 | 5.26e-02 | 0.250000 | 3.14e-01 |
| Regulation of TLR by endogenous ligand | 20 | 5.28e-02 | -0.250000 | 3.14e-01 |
| Protein hydroxylation | 18 | 6.68e-02 | 0.250000 | 3.38e-01 |
| Gap-filling DNA repair synthesis and ligation in GG-NER | 25 | 3.11e-02 | 0.249000 | 2.44e-01 |
| SARS-CoV-1-host interactions | 90 | 4.85e-05 | 0.248000 | 1.67e-03 |
| Abortive elongation of HIV-1 transcript in the absence of Tat | 23 | 4.01e-02 | 0.247000 | 2.80e-01 |
| Diseases of mitotic cell cycle | 37 | 9.69e-03 | 0.246000 | 1.23e-01 |
| RNA Polymerase III Transcription Termination | 23 | 4.17e-02 | 0.245000 | 2.85e-01 |
| Defensins | 36 | 1.12e-02 | -0.244000 | 1.33e-01 |
| Signaling by EGFR in Cancer | 25 | 3.49e-02 | 0.244000 | 2.57e-01 |
| TICAM1-dependent activation of IRF3/IRF7 | 12 | 1.44e-01 | 0.244000 | 4.99e-01 |
| Synthesis, secretion, and inactivation of Glucagon-like Peptide-1 (GLP-1) | 20 | 5.99e-02 | -0.243000 | 3.28e-01 |
| Synthesis of bile acids and bile salts via 27-hydroxycholesterol | 15 | 1.03e-01 | -0.243000 | 4.17e-01 |
| RNA Polymerase III Chain Elongation | 18 | 7.51e-02 | 0.242000 | 3.56e-01 |
| Interleukin-2 signaling | 11 | 1.65e-01 | -0.242000 | 5.34e-01 |
| Regulated proteolysis of p75NTR | 11 | 1.65e-01 | 0.242000 | 5.34e-01 |
| RNA Pol II CTD phosphorylation and interaction with CE | 26 | 3.38e-02 | 0.240000 | 2.52e-01 |
| RNA Pol II CTD phosphorylation and interaction with CE during HIV infection | 26 | 3.38e-02 | 0.240000 | 2.52e-01 |
| mRNA Splicing - Minor Pathway | 51 | 3.06e-03 | 0.240000 | 5.59e-02 |
| Triglyceride catabolism | 23 | 4.68e-02 | -0.239000 | 2.97e-01 |
| Formation of RNA Pol II elongation complex | 52 | 2.92e-03 | 0.238000 | 5.39e-02 |
| RNA Polymerase II Transcription Elongation | 52 | 2.92e-03 | 0.238000 | 5.39e-02 |
| MyD88 deficiency (TLR2/4) | 16 | 1.01e-01 | -0.237000 | 4.14e-01 |
| Zinc transporters | 15 | 1.14e-01 | 0.236000 | 4.41e-01 |
| DAP12 interactions | 40 | 1.04e-02 | -0.234000 | 1.27e-01 |
| Bile acid and bile salt metabolism | 45 | 6.64e-03 | -0.234000 | 9.05e-02 |
| Aberrant regulation of mitotic exit in cancer due to RB1 defects | 20 | 7.26e-02 | 0.232000 | 3.52e-01 |
| Inactivation of APC/C via direct inhibition of the APC/C complex | 21 | 6.71e-02 | 0.231000 | 3.38e-01 |
| Inhibition of the proteolytic activity of APC/C required for the onset of anaphase by mitotic spindle checkpoint components | 21 | 6.71e-02 | 0.231000 | 3.38e-01 |
| Glycogen storage diseases | 14 | 1.35e-01 | 0.230000 | 4.85e-01 |
| Aberrant regulation of mitotic cell cycle due to RB1 defects | 36 | 1.67e-02 | 0.230000 | 1.69e-01 |
| Methylation | 14 | 1.37e-01 | 0.230000 | 4.87e-01 |
| Signaling by NODAL | 21 | 6.87e-02 | 0.229000 | 3.43e-01 |
| RNA Polymerase I Transcription Termination | 27 | 4.01e-02 | 0.228000 | 2.80e-01 |
| Translesion Synthesis by POLH | 19 | 8.80e-02 | 0.226000 | 3.90e-01 |
| Phospholipase C-mediated cascade: FGFR1 | 16 | 1.18e-01 | 0.226000 | 4.51e-01 |
| Insertion of tail-anchored proteins into the endoplasmic reticulum membrane | 18 | 9.86e-02 | 0.225000 | 4.11e-01 |
| Senescence-Associated Secretory Phenotype (SASP) | 53 | 4.91e-03 | 0.223000 | 7.45e-02 |
| Gap-filling DNA repair synthesis and ligation in TC-NER | 62 | 2.39e-03 | 0.223000 | 4.65e-02 |
| Formation of Fibrin Clot (Clotting Cascade) | 37 | 1.91e-02 | -0.223000 | 1.84e-01 |
| Negative regulation of FGFR1 signaling | 32 | 2.95e-02 | 0.222000 | 2.41e-01 |
| DNA Damage Recognition in GG-NER | 36 | 2.22e-02 | 0.220000 | 1.99e-01 |
| Influenza Infection | 148 | 3.83e-06 | 0.220000 | 1.79e-04 |
| FGFRL1 modulation of FGFR1 signaling | 13 | 1.71e-01 | 0.219000 | 5.46e-01 |
| Transcriptional Regulation by NPAS4 | 33 | 3.03e-02 | 0.218000 | 2.43e-01 |
| CASP8 activity is inhibited | 11 | 2.11e-01 | -0.218000 | 5.98e-01 |
| Dimerization of procaspase-8 | 11 | 2.11e-01 | -0.218000 | 5.98e-01 |
| Regulation by c-FLIP | 11 | 2.11e-01 | -0.218000 | 5.98e-01 |
| Mitochondrial translation initiation | 87 | 4.54e-04 | 0.217000 | 1.33e-02 |
| Signaling by Leptin | 11 | 2.14e-01 | -0.217000 | 5.99e-01 |
| Degradation of cysteine and homocysteine | 15 | 1.46e-01 | 0.217000 | 5.00e-01 |
| Hh mutants are degraded by ERAD | 54 | 5.96e-03 | 0.216000 | 8.52e-02 |
| TP53 Regulates Transcription of Genes Involved in G2 Cell Cycle Arrest | 18 | 1.13e-01 | 0.216000 | 4.41e-01 |
| Transcription-Coupled Nucleotide Excision Repair (TC-NER) | 76 | 1.17e-03 | 0.215000 | 2.81e-02 |
| Inhibition of DNA recombination at telomere | 20 | 9.59e-02 | 0.215000 | 4.04e-01 |
| Incretin synthesis, secretion, and inactivation | 23 | 7.49e-02 | -0.215000 | 3.56e-01 |
| Activation of RAC1 | 11 | 2.19e-01 | -0.214000 | 6.09e-01 |
| TAK1-dependent IKK and NF-kappa-B activation | 41 | 1.84e-02 | 0.213000 | 1.79e-01 |
| Lysine catabolism | 12 | 2.03e-01 | -0.212000 | 5.88e-01 |
| Activation of HOX genes during differentiation | 62 | 3.96e-03 | 0.211000 | 6.48e-02 |
| Activation of anterior HOX genes in hindbrain development during early embryogenesis | 62 | 3.96e-03 | 0.211000 | 6.48e-02 |
| Aspirin ADME | 44 | 1.54e-02 | -0.211000 | 1.59e-01 |
| mitochondrial fatty acid beta-oxidation of saturated fatty acids | 11 | 2.26e-01 | 0.211000 | 6.15e-01 |
| TP53 Regulates Transcription of DNA Repair Genes | 57 | 5.91e-03 | 0.211000 | 8.52e-02 |
| Autodegradation of Cdh1 by Cdh1:APC/C | 62 | 4.16e-03 | 0.210000 | 6.72e-02 |
| Translation | 262 | 4.37e-09 | 0.210000 | 3.15e-07 |
| Mitochondrial translation elongation | 87 | 6.92e-04 | 0.210000 | 1.93e-02 |
| NOTCH2 intracellular domain regulates transcription | 11 | 2.30e-01 | -0.209000 | 6.19e-01 |
| Interconversion of nucleotide di- and triphosphates | 29 | 5.13e-02 | 0.209000 | 3.13e-01 |
| Ketone body metabolism | 10 | 2.53e-01 | -0.209000 | 6.53e-01 |
| SCF(Skp2)-mediated degradation of p27/p21 | 58 | 6.02e-03 | 0.208000 | 8.53e-02 |
| Mitochondrial translation termination | 87 | 7.84e-04 | 0.208000 | 2.11e-02 |
| ER Quality Control Compartment (ERQC) | 20 | 1.09e-01 | 0.207000 | 4.30e-01 |
| Mitochondrial translation | 93 | 5.97e-04 | 0.206000 | 1.72e-02 |
| DAP12 signaling | 28 | 6.05e-02 | -0.205000 | 3.30e-01 |
| IRAK4 deficiency (TLR2/4) | 17 | 1.44e-01 | -0.204000 | 4.99e-01 |
| Chaperone Mediated Autophagy | 20 | 1.14e-01 | 0.204000 | 4.41e-01 |
| Formation of the Early Elongation Complex | 32 | 4.62e-02 | 0.204000 | 2.97e-01 |
| Formation of the HIV-1 Early Elongation Complex | 32 | 4.62e-02 | 0.204000 | 2.97e-01 |
| Plasma lipoprotein remodeling | 32 | 4.63e-02 | 0.203000 | 2.97e-01 |
| Beta defensins | 28 | 6.29e-02 | -0.203000 | 3.35e-01 |
| Regulation of FZD by ubiquitination | 21 | 1.08e-01 | 0.203000 | 4.28e-01 |
| RNA Polymerase III Transcription Initiation From Type 2 Promoter | 27 | 6.91e-02 | 0.202000 | 3.43e-01 |
| AUF1 (hnRNP D0) binds and destabilizes mRNA | 53 | 1.12e-02 | 0.201000 | 1.33e-01 |
| Hormone ligand-binding receptors | 13 | 2.09e-01 | -0.201000 | 5.98e-01 |
| Sema4D induced cell migration and growth-cone collapse | 20 | 1.19e-01 | 0.201000 | 4.52e-01 |
| CDK-mediated phosphorylation and removal of Cdc6 | 71 | 3.42e-03 | 0.201000 | 5.89e-02 |
| Cdc20:Phospho-APC/C mediated degradation of Cyclin A | 71 | 3.47e-03 | 0.201000 | 5.92e-02 |
| Deactivation of the beta-catenin transactivating complex | 39 | 3.03e-02 | 0.200000 | 2.43e-01 |
| APC:Cdc20 mediated degradation of cell cycle proteins prior to satisfation of the cell cycle checkpoint | 72 | 3.30e-03 | 0.200000 | 5.84e-02 |
| FGFR1c ligand binding and activation | 13 | 2.11e-01 | 0.200000 | 5.98e-01 |
| N-Glycan antennae elongation | 15 | 1.80e-01 | -0.200000 | 5.57e-01 |
| FCERI mediated Ca+2 mobilization | 30 | 5.92e-02 | -0.199000 | 3.27e-01 |
| Negative regulation of FGFR4 signaling | 30 | 5.98e-02 | 0.198000 | 3.28e-01 |
| APC/C:Cdc20 mediated degradation of Securin | 66 | 5.34e-03 | 0.198000 | 7.94e-02 |
| Tie2 Signaling | 18 | 1.46e-01 | -0.198000 | 5.00e-01 |
| SUMOylation of transcription factors | 20 | 1.25e-01 | 0.198000 | 4.60e-01 |
| RHO GTPases activate PKNs | 34 | 4.57e-02 | 0.198000 | 2.97e-01 |
| Specification of primordial germ cells | 12 | 2.39e-01 | 0.196000 | 6.32e-01 |
| Regulation of CDH11 mRNA translation by microRNAs | 10 | 2.82e-01 | -0.196000 | 6.87e-01 |
| AKT phosphorylates targets in the cytosol | 14 | 2.07e-01 | 0.195000 | 5.94e-01 |
| mRNA Capping | 28 | 7.43e-02 | 0.195000 | 3.56e-01 |
| Negative regulation of FGFR2 signaling | 33 | 5.30e-02 | 0.195000 | 3.14e-01 |
| Interleukin-20 family signaling | 24 | 9.89e-02 | -0.195000 | 4.11e-01 |
| Other interleukin signaling | 24 | 9.92e-02 | 0.194000 | 4.11e-01 |
| Formation of the posterior neural plate | 10 | 2.87e-01 | 0.194000 | 6.89e-01 |
| Estrogen-dependent nuclear events downstream of ESR-membrane signaling | 23 | 1.07e-01 | 0.194000 | 4.28e-01 |
| Hh mutants abrogate ligand secretion | 57 | 1.15e-02 | 0.193000 | 1.35e-01 |
| Signaling by FLT3 fusion proteins | 19 | 1.45e-01 | -0.193000 | 5.00e-01 |
| Constitutive Signaling by Overexpressed ERBB2 | 10 | 2.91e-01 | 0.193000 | 6.91e-01 |
| Pyroptosis | 26 | 8.86e-02 | -0.193000 | 3.90e-01 |
| LGI-ADAM interactions | 14 | 2.11e-01 | 0.193000 | 5.98e-01 |
| Synthesis of PE | 12 | 2.48e-01 | 0.192000 | 6.46e-01 |
| Signaling by FGFR1 | 51 | 1.76e-02 | 0.192000 | 1.73e-01 |
| Interleukin-10 signaling | 45 | 2.58e-02 | -0.192000 | 2.19e-01 |
| Eicosanoid ligand-binding receptors | 14 | 2.14e-01 | -0.192000 | 5.99e-01 |
| Dual incision in TC-NER | 63 | 8.40e-03 | 0.192000 | 1.09e-01 |
| RHOU GTPase cycle | 37 | 4.47e-02 | -0.191000 | 2.96e-01 |
| Signaling by ROBO receptors | 203 | 2.83e-06 | 0.190000 | 1.36e-04 |
| APC/C:Cdc20 mediated degradation of mitotic proteins | 74 | 4.63e-03 | 0.190000 | 7.28e-02 |
| Aberrant regulation of mitotic G1/S transition in cancer due to RB1 defects | 17 | 1.74e-01 | 0.190000 | 5.50e-01 |
| Defective binding of RB1 mutants to E2F1,(E2F2, E2F3) | 17 | 1.74e-01 | 0.190000 | 5.50e-01 |
| cGMP effects | 15 | 2.03e-01 | -0.190000 | 5.88e-01 |
| Signaling by Activin | 17 | 1.76e-01 | 0.190000 | 5.50e-01 |
| Synthesis of bile acids and bile salts via 7alpha-hydroxycholesterol | 24 | 1.09e-01 | -0.189000 | 4.29e-01 |
| Caspase activation via extrinsic apoptotic signalling pathway | 25 | 1.02e-01 | -0.189000 | 4.15e-01 |
| p38MAPK events | 13 | 2.40e-01 | 0.188000 | 6.33e-01 |
| RNA Polymerase I Promoter Escape | 28 | 8.51e-02 | 0.188000 | 3.86e-01 |
| Defects of contact activation system (CAS) and kallikrein/kinin system (KKS) | 14 | 2.26e-01 | -0.187000 | 6.15e-01 |
| Diseases of hemostasis | 14 | 2.26e-01 | -0.187000 | 6.15e-01 |
| FGFR2 mutant receptor activation | 32 | 6.78e-02 | 0.187000 | 3.40e-01 |
| PI3K events in ERBB4 signaling | 10 | 3.09e-01 | -0.186000 | 7.00e-01 |
| Phenylalanine and tyrosine metabolism | 10 | 3.10e-01 | 0.185000 | 7.00e-01 |
| N-glycan trimming in the ER and Calnexin/Calreticulin cycle | 34 | 6.17e-02 | 0.185000 | 3.32e-01 |
| GPVI-mediated activation cascade | 34 | 6.19e-02 | -0.185000 | 3.32e-01 |
| Activated NOTCH1 Transmits Signal to the Nucleus | 31 | 7.50e-02 | 0.185000 | 3.56e-01 |
| Defective CFTR causes cystic fibrosis | 59 | 1.46e-02 | 0.184000 | 1.55e-01 |
| Regulation of APC/C activators between G1/S and early anaphase | 79 | 4.93e-03 | 0.183000 | 7.45e-02 |
| Erythropoietin activates Phosphoinositide-3-kinase (PI3K) | 12 | 2.74e-01 | -0.182000 | 6.75e-01 |
| Synthesis of bile acids and bile salts | 34 | 6.63e-02 | -0.182000 | 3.38e-01 |
| Keratan sulfate degradation | 15 | 2.23e-01 | -0.182000 | 6.12e-01 |
| Activation of APC/C and APC/C:Cdc20 mediated degradation of mitotic proteins | 75 | 6.57e-03 | 0.181000 | 9.05e-02 |
| Retinoid metabolism and transport | 42 | 4.19e-02 | 0.181000 | 2.85e-01 |
| RNA Polymerase I Transcription | 47 | 3.14e-02 | 0.181000 | 2.44e-01 |
| p130Cas linkage to MAPK signaling for integrins | 15 | 2.25e-01 | -0.181000 | 6.15e-01 |
| SCF-beta-TrCP mediated degradation of Emi1 | 53 | 2.28e-02 | 0.181000 | 2.02e-01 |
| Type I hemidesmosome assembly | 11 | 3.01e-01 | 0.180000 | 6.96e-01 |
| p53-Dependent G1 DNA Damage Response | 64 | 1.29e-02 | 0.180000 | 1.45e-01 |
| p53-Dependent G1/S DNA damage checkpoint | 64 | 1.29e-02 | 0.180000 | 1.45e-01 |
| Ubiquitin-dependent degradation of Cyclin D | 50 | 2.82e-02 | 0.179000 | 2.33e-01 |
| Common Pathway of Fibrin Clot Formation | 21 | 1.56e-01 | -0.179000 | 5.17e-01 |
| Negative regulation of FGFR3 signaling | 28 | 1.02e-01 | 0.178000 | 4.15e-01 |
| Regulation of commissural axon pathfinding by SLIT and ROBO | 10 | 3.32e-01 | -0.177000 | 7.23e-01 |
| Translesion synthesis by Y family DNA polymerases bypasses lesions on DNA template | 38 | 5.90e-02 | 0.177000 | 3.27e-01 |
| Gluconeogenesis | 33 | 7.89e-02 | 0.177000 | 3.66e-01 |
| G1/S DNA Damage Checkpoints | 66 | 1.34e-02 | 0.176000 | 1.50e-01 |
| RHO GTPases activate CIT | 19 | 1.85e-01 | 0.176000 | 5.60e-01 |
| Phospholipase C-mediated cascade; FGFR4 | 14 | 2.56e-01 | 0.175000 | 6.56e-01 |
| Induction of Cell-Cell Fusion | 12 | 2.93e-01 | 0.175000 | 6.92e-01 |
| RNA Polymerase III Transcription Initiation From Type 1 Promoter | 28 | 1.08e-01 | 0.175000 | 4.29e-01 |
| Regulation of PTEN mRNA translation | 25 | 1.29e-01 | 0.175000 | 4.70e-01 |
| Folding of actin by CCT/TriC | 10 | 3.39e-01 | -0.175000 | 7.26e-01 |
| Nucleotide Excision Repair | 107 | 1.81e-03 | 0.175000 | 3.82e-02 |
| Androgen biosynthesis | 11 | 3.17e-01 | -0.174000 | 7.05e-01 |
| Endosomal Sorting Complex Required For Transport (ESCRT) | 31 | 9.34e-02 | 0.174000 | 3.97e-01 |
| Pyrimidine salvage | 10 | 3.41e-01 | -0.174000 | 7.26e-01 |
| mRNA Splicing | 199 | 2.39e-05 | 0.174000 | 9.72e-04 |
| APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins in late mitosis/early G1 | 72 | 1.10e-02 | 0.173000 | 1.32e-01 |
| Acyl chain remodelling of PE | 24 | 1.43e-01 | 0.173000 | 4.98e-01 |
| RNA Polymerase I Promoter Clearance | 46 | 4.26e-02 | 0.173000 | 2.88e-01 |
| Signaling by KIT in disease | 20 | 1.82e-01 | -0.172000 | 5.57e-01 |
| Signaling by phosphorylated juxtamembrane, extracellular and kinase domain KIT mutants | 20 | 1.82e-01 | -0.172000 | 5.57e-01 |
| Translesion synthesis by POLI | 17 | 2.19e-01 | 0.172000 | 6.09e-01 |
| MECP2 regulates neuronal receptors and channels | 17 | 2.20e-01 | -0.172000 | 6.09e-01 |
| Phospholipase C-mediated cascade; FGFR2 | 17 | 2.20e-01 | 0.172000 | 6.09e-01 |
| Telomere C-strand synthesis initiation | 11 | 3.25e-01 | -0.171000 | 7.17e-01 |
| RNA Polymerase II Pre-transcription Events | 72 | 1.20e-02 | 0.171000 | 1.39e-01 |
| RMTs methylate histone arginines | 30 | 1.05e-01 | 0.171000 | 4.23e-01 |
| SHC-mediated cascade:FGFR1 | 21 | 1.76e-01 | 0.171000 | 5.50e-01 |
| Na+/Cl- dependent neurotransmitter transporters | 18 | 2.10e-01 | 0.171000 | 5.98e-01 |
| Calnexin/calreticulin cycle | 25 | 1.40e-01 | 0.171000 | 4.94e-01 |
| Striated Muscle Contraction | 35 | 8.09e-02 | 0.170000 | 3.72e-01 |
| Transcriptional regulation by the AP-2 (TFAP2) family of transcription factors | 34 | 8.56e-02 | 0.170000 | 3.86e-01 |
| Hedgehog ligand biogenesis | 63 | 1.94e-02 | 0.170000 | 1.86e-01 |
| activated TAK1 mediates p38 MAPK activation | 20 | 1.88e-01 | 0.170000 | 5.66e-01 |
| Mitotic Telophase/Cytokinesis | 10 | 3.52e-01 | -0.170000 | 7.34e-01 |
| N-glycan antennae elongation in the medial/trans-Golgi | 26 | 1.34e-01 | -0.170000 | 4.83e-01 |
| Autodegradation of the E3 ubiquitin ligase COP1 | 50 | 3.77e-02 | 0.170000 | 2.68e-01 |
| Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell | 126 | 9.91e-04 | -0.170000 | 2.58e-02 |
| RHOV GTPase cycle | 36 | 7.81e-02 | -0.170000 | 3.64e-01 |
| Formation of axial mesoderm | 13 | 2.90e-01 | 0.170000 | 6.91e-01 |
| Dectin-1 mediated noncanonical NF-kB signaling | 60 | 2.33e-02 | 0.169000 | 2.05e-01 |
| Fertilization | 26 | 1.36e-01 | -0.169000 | 4.86e-01 |
| Signaling by NOTCH3 | 48 | 4.30e-02 | 0.169000 | 2.89e-01 |
| Transport of organic anions | 10 | 3.57e-01 | -0.168000 | 7.40e-01 |
| Signaling by FGFR | 87 | 6.79e-03 | 0.168000 | 9.05e-02 |
| Signaling by NTRK3 (TRKC) | 17 | 2.31e-01 | 0.168000 | 6.20e-01 |
| mTORC1-mediated signalling | 23 | 1.66e-01 | 0.167000 | 5.34e-01 |
| Keratinization | 213 | 2.66e-05 | -0.167000 | 1.06e-03 |
| Transcription of the HIV genome | 62 | 2.33e-02 | 0.167000 | 2.05e-01 |
| Positive epigenetic regulation of rRNA expression | 43 | 5.95e-02 | 0.166000 | 3.27e-01 |
| Sema4D in semaphorin signaling | 24 | 1.60e-01 | 0.166000 | 5.24e-01 |
| Recognition of DNA damage by PCNA-containing replication complex | 29 | 1.22e-01 | 0.166000 | 4.57e-01 |
| Organic cation transport | 10 | 3.65e-01 | -0.165000 | 7.45e-01 |
| Aggrephagy | 42 | 6.36e-02 | 0.165000 | 3.35e-01 |
| CD209 (DC-SIGN) signaling | 20 | 2.01e-01 | -0.165000 | 5.87e-01 |
| Fanconi Anemia Pathway | 36 | 8.64e-02 | 0.165000 | 3.87e-01 |
| Neurotoxicity of clostridium toxins | 10 | 3.66e-01 | 0.165000 | 7.45e-01 |
| Other semaphorin interactions | 18 | 2.26e-01 | -0.165000 | 6.15e-01 |
| B-WICH complex positively regulates rRNA expression | 29 | 1.24e-01 | 0.165000 | 4.59e-01 |
| ABC transporter disorders | 75 | 1.37e-02 | 0.165000 | 1.51e-01 |
| Negative regulation of TCF-dependent signaling by WNT ligand antagonists | 15 | 2.72e-01 | 0.164000 | 6.73e-01 |
| Prolactin receptor signaling | 15 | 2.72e-01 | -0.164000 | 6.73e-01 |
| TBC/RABGAPs | 42 | 6.63e-02 | 0.164000 | 3.38e-01 |
| Signaling by BMP | 30 | 1.22e-01 | -0.163000 | 4.56e-01 |
| Signaling by FLT3 ITD and TKD mutants | 16 | 2.59e-01 | -0.163000 | 6.56e-01 |
| Vpu mediated degradation of CD4 | 50 | 4.62e-02 | 0.163000 | 2.97e-01 |
| Cyclin D associated events in G1 | 46 | 5.62e-02 | 0.163000 | 3.23e-01 |
| G1 Phase | 46 | 5.62e-02 | 0.163000 | 3.23e-01 |
| Regulation of signaling by CBL | 22 | 1.86e-01 | 0.163000 | 5.62e-01 |
| NIK–>noncanonical NF-kB signaling | 57 | 3.37e-02 | 0.163000 | 2.52e-01 |
| Nucleotide biosynthesis | 14 | 2.93e-01 | 0.162000 | 6.92e-01 |
| Signaling by FGFR4 | 40 | 7.64e-02 | 0.162000 | 3.60e-01 |
| Activation of the AP-1 family of transcription factors | 10 | 3.75e-01 | 0.162000 | 7.48e-01 |
| Translation of Replicase and Assembly of the Replication Transcription Complex 9679504 | 13 | 3.13e-01 | -0.162000 | 7.04e-01 |
| Activation of BAD and translocation to mitochondria | 15 | 2.80e-01 | 0.161000 | 6.85e-01 |
| Budding and maturation of HIV virion | 28 | 1.40e-01 | 0.161000 | 4.94e-01 |
| FGFR4 ligand binding and activation | 13 | 3.15e-01 | 0.161000 | 7.04e-01 |
| SARS-CoV-1 Infection | 134 | 1.35e-03 | 0.160000 | 3.11e-02 |
| Synaptic adhesion-like molecules | 19 | 2.27e-01 | 0.160000 | 6.16e-01 |
| Termination of translesion DNA synthesis | 31 | 1.23e-01 | 0.160000 | 4.58e-01 |
| Activated point mutants of FGFR2 | 16 | 2.69e-01 | 0.160000 | 6.70e-01 |
| Amino acids regulate mTORC1 | 52 | 4.75e-02 | 0.159000 | 2.97e-01 |
| Condensation of Prometaphase Chromosomes | 11 | 3.62e-01 | 0.159000 | 7.42e-01 |
| IRF3-mediated induction of type I IFN | 11 | 3.63e-01 | -0.158000 | 7.42e-01 |
| Regulation of activated PAK-2p34 by proteasome mediated degradation | 48 | 5.80e-02 | 0.158000 | 3.25e-01 |
| Regulation of RUNX3 expression and activity | 53 | 4.66e-02 | 0.158000 | 2.97e-01 |
| Ubiquitin Mediated Degradation of Phosphorylated Cdc25A | 50 | 5.34e-02 | 0.158000 | 3.14e-01 |
| p53-Independent DNA Damage Response | 50 | 5.34e-02 | 0.158000 | 3.14e-01 |
| p53-Independent G1/S DNA damage checkpoint | 50 | 5.34e-02 | 0.158000 | 3.14e-01 |
| Signaling by FGFR2 IIIa TM | 19 | 2.34e-01 | 0.158000 | 6.24e-01 |
| Metabolism of fat-soluble vitamins | 46 | 6.56e-02 | 0.157000 | 3.38e-01 |
| Biosynthesis of the N-glycan precursor (dolichol lipid-linked oligosaccharide, LLO) and transfer to a nascent protein | 74 | 1.97e-02 | 0.157000 | 1.87e-01 |
| KSRP (KHSRP) binds and destabilizes mRNA | 17 | 2.64e-01 | 0.157000 | 6.65e-01 |
| mRNA Splicing - Major Pathway | 189 | 2.15e-04 | 0.156000 | 6.57e-03 |
| Advanced glycosylation endproduct receptor signaling | 13 | 3.31e-01 | 0.156000 | 7.21e-01 |
| Antimicrobial peptides | 78 | 1.75e-02 | -0.156000 | 1.73e-01 |
| POU5F1 (OCT4), SOX2, NANOG repress genes related to differentiation | 10 | 3.96e-01 | 0.155000 | 7.65e-01 |
| Negative regulation of NOTCH4 signaling | 52 | 5.35e-02 | 0.155000 | 3.14e-01 |
| TP53 Regulates Transcription of Cell Cycle Genes | 49 | 6.14e-02 | 0.154000 | 3.32e-01 |
| G beta:gamma signalling through BTK | 17 | 2.72e-01 | -0.154000 | 6.73e-01 |
| Initial triggering of complement | 21 | 2.22e-01 | 0.154000 | 6.11e-01 |
| Transcriptional regulation of testis differentiation | 12 | 3.59e-01 | -0.153000 | 7.40e-01 |
| PINK1-PRKN Mediated Mitophagy | 21 | 2.25e-01 | 0.153000 | 6.15e-01 |
| Synthesis of substrates in N-glycan biosythesis | 60 | 4.16e-02 | 0.152000 | 2.85e-01 |
| Metabolism of RNA | 678 | 1.36e-11 | 0.152000 | 3.35e-09 |
| MicroRNA (miRNA) biogenesis | 26 | 1.81e-01 | 0.152000 | 5.57e-01 |
| mRNA decay by 5’ to 3’ exoribonuclease | 15 | 3.09e-01 | 0.152000 | 7.00e-01 |
| Metabolism of amino acids and derivatives | 345 | 1.31e-06 | 0.151000 | 6.72e-05 |
| Synthesis of active ubiquitin: roles of E1 and E2 enzymes | 27 | 1.74e-01 | 0.151000 | 5.50e-01 |
| APC/C-mediated degradation of cell cycle proteins | 86 | 1.54e-02 | 0.151000 | 1.59e-01 |
| Regulation of mitotic cell cycle | 86 | 1.54e-02 | 0.151000 | 1.59e-01 |
| FGFR2 alternative splicing | 26 | 1.82e-01 | 0.151000 | 5.57e-01 |
| Signaling by NOTCH2 | 32 | 1.41e-01 | 0.150000 | 4.94e-01 |
| Xenobiotics | 24 | 2.02e-01 | -0.150000 | 5.87e-01 |
| Signaling by NOTCH4 | 79 | 2.11e-02 | 0.150000 | 1.91e-01 |
| Receptor Mediated Mitophagy | 10 | 4.12e-01 | 0.150000 | 7.77e-01 |
| MTOR signalling | 40 | 1.01e-01 | 0.150000 | 4.14e-01 |
| Initiation of Nuclear Envelope (NE) Reformation | 18 | 2.73e-01 | 0.149000 | 6.74e-01 |
| Regulation of mRNA stability by proteins that bind AU-rich elements | 87 | 1.62e-02 | 0.149000 | 1.65e-01 |
| MAP2K and MAPK activation | 38 | 1.12e-01 | -0.149000 | 4.38e-01 |
| Butyrate Response Factor 1 (BRF1) binds and destabilizes mRNA | 17 | 2.88e-01 | 0.149000 | 6.89e-01 |
| Insulin receptor recycling | 29 | 1.66e-01 | 0.149000 | 5.34e-01 |
| Glutathione synthesis and recycling | 12 | 3.73e-01 | 0.148000 | 7.48e-01 |
| Cyclin E associated events during G1/S transition | 81 | 2.14e-02 | 0.148000 | 1.93e-01 |
| ABC transporters in lipid homeostasis | 17 | 2.92e-01 | 0.148000 | 6.91e-01 |
| Organic anion transporters | 10 | 4.20e-01 | 0.147000 | 7.82e-01 |
| Cyclin A:Cdk2-associated events at S phase entry | 83 | 2.04e-02 | 0.147000 | 1.89e-01 |
| Metabolism of Angiotensinogen to Angiotensins | 15 | 3.25e-01 | -0.147000 | 7.17e-01 |
| Signaling by FGFR2 in disease | 42 | 1.00e-01 | 0.147000 | 4.13e-01 |
| Transport of vitamins, nucleosides, and related molecules | 38 | 1.18e-01 | 0.146000 | 4.51e-01 |
| Heme degradation | 16 | 3.11e-01 | -0.146000 | 7.00e-01 |
| Interleukin-37 signaling | 20 | 2.57e-01 | -0.146000 | 6.56e-01 |
| Transcriptional Regulation by MECP2 | 60 | 4.99e-02 | -0.146000 | 3.07e-01 |
| Processing of Capped Intron-Containing Pre-mRNA | 263 | 4.45e-05 | 0.146000 | 1.58e-03 |
| DNA Damage Bypass | 46 | 8.86e-02 | 0.145000 | 3.90e-01 |
| Dectin-2 family | 28 | 1.84e-01 | -0.145000 | 5.59e-01 |
| Reactions specific to the complex N-glycan synthesis pathway | 10 | 4.28e-01 | -0.145000 | 7.84e-01 |
| Stabilization of p53 | 55 | 6.34e-02 | 0.145000 | 3.35e-01 |
| Telomere Maintenance | 62 | 4.89e-02 | 0.145000 | 3.03e-01 |
| Regulation of TP53 Activity through Methylation | 18 | 2.88e-01 | 0.145000 | 6.89e-01 |
| Metabolism of polyamines | 55 | 6.48e-02 | 0.144000 | 3.38e-01 |
| Negative epigenetic regulation of rRNA expression | 45 | 9.49e-02 | 0.144000 | 4.02e-01 |
| Signaling by FGFR2 | 72 | 3.48e-02 | 0.144000 | 2.57e-01 |
| Plasma lipoprotein assembly, remodeling, and clearance | 73 | 3.36e-02 | 0.144000 | 2.52e-01 |
| Signaling by FGFR3 | 39 | 1.21e-01 | 0.144000 | 4.55e-01 |
| TICAM1, RIP1-mediated IKK complex recruitment | 18 | 2.92e-01 | 0.143000 | 6.91e-01 |
| Global Genome Nucleotide Excision Repair (GG-NER) | 81 | 2.57e-02 | 0.143000 | 2.19e-01 |
| Attachment and Entry 9694614 | 16 | 3.24e-01 | 0.142000 | 7.17e-01 |
| RHO GTPases Activate ROCKs | 19 | 2.83e-01 | 0.142000 | 6.88e-01 |
| HS-GAG degradation | 21 | 2.60e-01 | 0.142000 | 6.56e-01 |
| NoRC negatively regulates rRNA expression | 43 | 1.08e-01 | 0.142000 | 4.28e-01 |
| Selective autophagy | 78 | 3.13e-02 | 0.141000 | 2.44e-01 |
| PTK6 Regulates RHO GTPases, RAS GTPase and MAP kinases | 14 | 3.62e-01 | 0.141000 | 7.42e-01 |
| Cooperation of PDCL (PhLP1) and TRiC/CCT in G-protein beta folding | 38 | 1.34e-01 | -0.140000 | 4.83e-01 |
| Interleukin-7 signaling | 21 | 2.67e-01 | -0.140000 | 6.68e-01 |
| SHC1 events in ERBB2 signaling | 22 | 2.56e-01 | -0.140000 | 6.56e-01 |
| Activation of NF-kappaB in B cells | 64 | 5.31e-02 | 0.140000 | 3.14e-01 |
| Regulation of ornithine decarboxylase (ODC) | 49 | 9.15e-02 | 0.139000 | 3.94e-01 |
| Signaling by activated point mutants of FGFR1 | 11 | 4.24e-01 | 0.139000 | 7.83e-01 |
| PI3K events in ERBB2 signaling | 16 | 3.35e-01 | -0.139000 | 7.26e-01 |
| Acetylcholine regulates insulin secretion | 10 | 4.48e-01 | -0.139000 | 7.86e-01 |
| Laminin interactions | 28 | 2.05e-01 | 0.138000 | 5.92e-01 |
| Heme signaling | 45 | 1.09e-01 | -0.138000 | 4.29e-01 |
| Receptor-type tyrosine-protein phosphatases | 16 | 3.39e-01 | 0.138000 | 7.26e-01 |
| Interleukin-35 Signalling | 12 | 4.08e-01 | -0.138000 | 7.74e-01 |
| Plasma lipoprotein clearance | 37 | 1.48e-01 | 0.137000 | 5.02e-01 |
| InlB-mediated entry of Listeria monocytogenes into host cell | 14 | 3.74e-01 | 0.137000 | 7.48e-01 |
| Transcriptional activity of SMAD2/SMAD3:SMAD4 heterotrimer | 49 | 9.71e-02 | 0.137000 | 4.07e-01 |
| RNA Polymerase I Transcription Initiation | 42 | 1.25e-01 | 0.137000 | 4.60e-01 |
| Homology Directed Repair | 99 | 1.88e-02 | 0.137000 | 1.82e-01 |
| Erythrocytes take up carbon dioxide and release oxygen | 12 | 4.13e-01 | 0.136000 | 7.77e-01 |
| O2/CO2 exchange in erythrocytes | 12 | 4.13e-01 | 0.136000 | 7.77e-01 |
| Scavenging by Class A Receptors | 19 | 3.04e-01 | -0.136000 | 6.98e-01 |
| FGFR1 mutant receptor activation | 30 | 1.97e-01 | -0.136000 | 5.80e-01 |
| Regulation of TP53 Degradation | 36 | 1.58e-01 | 0.136000 | 5.20e-01 |
| Citric acid cycle (TCA cycle) | 21 | 2.81e-01 | 0.136000 | 6.85e-01 |
| Maturation of spike protein 9694548 | 35 | 1.65e-01 | -0.136000 | 5.34e-01 |
| Glycogen synthesis | 13 | 3.98e-01 | 0.135000 | 7.65e-01 |
| Plasma lipoprotein assembly | 19 | 3.07e-01 | 0.135000 | 7.00e-01 |
| RNA Polymerase II Transcription Termination | 62 | 6.69e-02 | 0.135000 | 3.38e-01 |
| Reversible hydration of carbon dioxide | 11 | 4.40e-01 | -0.134000 | 7.84e-01 |
| Assembly of the pre-replicative complex | 82 | 3.56e-02 | 0.134000 | 2.58e-01 |
| HSP90 chaperone cycle for steroid hormone receptors (SHR) in the presence of ligand | 55 | 8.54e-02 | 0.134000 | 3.86e-01 |
| Nef-mediates down modulation of cell surface receptors by recruiting them to clathrin adapters | 20 | 3.00e-01 | 0.134000 | 6.96e-01 |
| RORA activates gene expression | 17 | 3.40e-01 | -0.134000 | 7.26e-01 |
| Cleavage of the damaged purine | 11 | 4.43e-01 | -0.134000 | 7.84e-01 |
| Depurination | 11 | 4.43e-01 | -0.134000 | 7.84e-01 |
| Recognition and association of DNA glycosylase with site containing an affected purine | 11 | 4.43e-01 | -0.134000 | 7.84e-01 |
| Phosphorylation of CD3 and TCR zeta chains | 20 | 3.01e-01 | -0.134000 | 6.96e-01 |
| RAS processing | 23 | 2.68e-01 | 0.133000 | 6.69e-01 |
| Sulfur amino acid metabolism | 28 | 2.22e-01 | 0.133000 | 6.11e-01 |
| Regulation of RAS by GAPs | 65 | 6.32e-02 | 0.133000 | 3.35e-01 |
| G alpha (i) signalling events | 305 | 6.24e-05 | -0.133000 | 2.04e-03 |
| Regulation of gene expression by Hypoxia-inducible Factor | 11 | 4.45e-01 | 0.133000 | 7.85e-01 |
| Ribavirin ADME | 11 | 4.46e-01 | 0.133000 | 7.86e-01 |
| Constitutive Signaling by NOTCH1 HD+PEST Domain Mutants | 54 | 9.22e-02 | 0.132000 | 3.94e-01 |
| Constitutive Signaling by NOTCH1 PEST Domain Mutants | 54 | 9.22e-02 | 0.132000 | 3.94e-01 |
| Signaling by NOTCH1 HD+PEST Domain Mutants in Cancer | 54 | 9.22e-02 | 0.132000 | 3.94e-01 |
| Signaling by NOTCH1 PEST Domain Mutants in Cancer | 54 | 9.22e-02 | 0.132000 | 3.94e-01 |
| Signaling by NOTCH1 in Cancer | 54 | 9.22e-02 | 0.132000 | 3.94e-01 |
| Signaling by ERBB2 ECD mutants | 15 | 3.75e-01 | 0.132000 | 7.48e-01 |
| Suppression of phagosomal maturation | 13 | 4.09e-01 | 0.132000 | 7.76e-01 |
| G beta:gamma signalling through PLC beta | 20 | 3.07e-01 | -0.132000 | 7.00e-01 |
| MET activates RAP1 and RAC1 | 11 | 4.49e-01 | -0.132000 | 7.86e-01 |
| Unfolded Protein Response (UPR) | 91 | 2.97e-02 | 0.132000 | 2.41e-01 |
| Degradation of DVL | 55 | 9.07e-02 | 0.132000 | 3.94e-01 |
| The role of GTSE1 in G2/M progression after G2 checkpoint | 76 | 4.70e-02 | 0.132000 | 2.97e-01 |
| Translesion synthesis by REV1 | 16 | 3.62e-01 | 0.132000 | 7.42e-01 |
| SHC-mediated cascade:FGFR2 | 22 | 2.86e-01 | 0.131000 | 6.89e-01 |
| Diseases of carbohydrate metabolism | 30 | 2.13e-01 | 0.131000 | 5.99e-01 |
| Defective B4GALT7 causes EDS, progeroid type | 17 | 3.49e-01 | 0.131000 | 7.33e-01 |
| Regulation of pyruvate dehydrogenase (PDH) complex | 14 | 3.96e-01 | 0.131000 | 7.65e-01 |
| Switching of origins to a post-replicative state | 90 | 3.15e-02 | 0.131000 | 2.44e-01 |
| Purine salvage | 12 | 4.32e-01 | 0.131000 | 7.84e-01 |
| RNA Polymerase III Abortive And Retractive Initiation | 41 | 1.47e-01 | 0.131000 | 5.00e-01 |
| RNA Polymerase III Transcription | 41 | 1.47e-01 | 0.131000 | 5.00e-01 |
| Cytosolic sensors of pathogen-associated DNA | 60 | 7.96e-02 | 0.131000 | 3.67e-01 |
| Scavenging of heme from plasma | 12 | 4.33e-01 | -0.131000 | 7.84e-01 |
| Downregulation of ERBB2 signaling | 28 | 2.32e-01 | 0.130000 | 6.20e-01 |
| mRNA 3’-end processing | 53 | 1.00e-01 | 0.130000 | 4.13e-01 |
| DNA Replication | 125 | 1.17e-02 | 0.130000 | 1.37e-01 |
| ERCC6 (CSB) and EHMT2 (G9a) positively regulate rRNA expression | 16 | 3.68e-01 | 0.130000 | 7.47e-01 |
| Synthesis of DNA | 118 | 1.46e-02 | 0.130000 | 1.55e-01 |
| Glyoxylate metabolism and glycine degradation | 30 | 2.18e-01 | 0.130000 | 6.09e-01 |
| Processing of DNA double-strand break ends | 61 | 7.92e-02 | 0.130000 | 3.66e-01 |
| A tetrasaccharide linker sequence is required for GAG synthesis | 23 | 2.81e-01 | 0.130000 | 6.85e-01 |
| Elastic fibre formation | 44 | 1.37e-01 | 0.130000 | 4.87e-01 |
| G beta:gamma signalling through CDC42 | 19 | 3.29e-01 | -0.129000 | 7.20e-01 |
| Intra-Golgi traffic | 43 | 1.43e-01 | -0.129000 | 4.98e-01 |
| FBXL7 down-regulates AURKA during mitotic entry and in early mitosis | 53 | 1.04e-01 | 0.129000 | 4.20e-01 |
| HDR through Homologous Recombination (HRR) | 64 | 7.44e-02 | 0.129000 | 3.56e-01 |
| Regulation of NPAS4 gene expression | 13 | 4.21e-01 | 0.129000 | 7.82e-01 |
| Maturation of nucleoprotein 9683610 | 11 | 4.61e-01 | 0.128000 | 7.91e-01 |
| Association of TriC/CCT with target proteins during biosynthesis | 36 | 1.83e-01 | -0.128000 | 5.57e-01 |
| Vif-mediated degradation of APOBEC3G | 50 | 1.18e-01 | 0.128000 | 4.51e-01 |
| SHC-mediated cascade:FGFR4 | 19 | 3.35e-01 | 0.128000 | 7.26e-01 |
| Triglyceride metabolism | 35 | 1.93e-01 | -0.127000 | 5.69e-01 |
| SHC1 events in ERBB4 signaling | 14 | 4.10e-01 | -0.127000 | 7.76e-01 |
| Early Phase of HIV Life Cycle | 14 | 4.10e-01 | 0.127000 | 7.76e-01 |
| ADP signalling through P2Y purinoceptor 12 | 22 | 3.06e-01 | -0.126000 | 7.00e-01 |
| Resolution of Abasic Sites (AP sites) | 37 | 1.86e-01 | 0.126000 | 5.60e-01 |
| Detoxification of Reactive Oxygen Species | 35 | 1.98e-01 | 0.126000 | 5.81e-01 |
| DCC mediated attractive signaling | 14 | 4.15e-01 | -0.126000 | 7.80e-01 |
| Interleukin receptor SHC signaling | 24 | 2.87e-01 | -0.125000 | 6.89e-01 |
| Mitophagy | 27 | 2.59e-01 | 0.125000 | 6.56e-01 |
| Signal attenuation | 10 | 4.94e-01 | 0.125000 | 8.17e-01 |
| Phase 2 - plateau phase | 14 | 4.18e-01 | 0.125000 | 7.82e-01 |
| Phospholipase C-mediated cascade; FGFR3 | 12 | 4.54e-01 | 0.125000 | 7.90e-01 |
| Miscellaneous transport and binding events | 23 | 3.00e-01 | -0.125000 | 6.96e-01 |
| Uptake and actions of bacterial toxins | 29 | 2.45e-01 | 0.125000 | 6.39e-01 |
| Dual Incision in GG-NER | 39 | 1.78e-01 | 0.125000 | 5.55e-01 |
| HDR through Homologous Recombination (HRR) or Single Strand Annealing (SSA) | 93 | 3.84e-02 | 0.124000 | 2.72e-01 |
| DNA Double Strand Break Response | 42 | 1.66e-01 | 0.124000 | 5.34e-01 |
| Frs2-mediated activation | 12 | 4.60e-01 | 0.123000 | 7.91e-01 |
| Signalling to ERKs | 34 | 2.14e-01 | 0.123000 | 5.99e-01 |
| Regulation of TNFR1 signaling | 45 | 1.53e-01 | 0.123000 | 5.12e-01 |
| VEGFR2 mediated cell proliferation | 19 | 3.54e-01 | 0.123000 | 7.36e-01 |
| Defective B3GAT3 causes JDSSDHD | 17 | 3.82e-01 | 0.123000 | 7.52e-01 |
| FCERI mediated MAPK activation | 32 | 2.30e-01 | -0.123000 | 6.19e-01 |
| Sodium/Calcium exchangers | 11 | 4.82e-01 | -0.122000 | 8.07e-01 |
| TGF-beta receptor signaling in EMT (epithelial to mesenchymal transition) | 16 | 3.98e-01 | 0.122000 | 7.65e-01 |
| GSK3B and BTRC:CUL1-mediated-degradation of NFE2L2 | 50 | 1.35e-01 | 0.122000 | 4.85e-01 |
| SARS-CoV-2 activates/modulates innate and adaptive immune responses | 113 | 2.52e-02 | -0.122000 | 2.17e-01 |
| CREB1 phosphorylation through the activation of Adenylate Cyclase | 11 | 4.86e-01 | -0.121000 | 8.10e-01 |
| Glycosphingolipid biosynthesis | 10 | 5.08e-01 | 0.121000 | 8.18e-01 |
| TNFR1-induced NF-kappa-B signaling pathway | 29 | 2.60e-01 | 0.121000 | 6.56e-01 |
| Constitutive Signaling by AKT1 E17K in Cancer | 25 | 2.96e-01 | 0.121000 | 6.93e-01 |
| RNA polymerase II transcribes snRNA genes | 77 | 6.72e-02 | 0.121000 | 3.38e-01 |
| GP1b-IX-V activation signalling | 11 | 4.89e-01 | -0.121000 | 8.12e-01 |
| ERK/MAPK targets | 20 | 3.52e-01 | 0.120000 | 7.34e-01 |
| Transport of Ribonucleoproteins into the Host Nucleus | 30 | 2.55e-01 | -0.120000 | 6.56e-01 |
| Cross-presentation of soluble exogenous antigens (endosomes) | 46 | 1.60e-01 | 0.120000 | 5.24e-01 |
| Translation of Structural Proteins 9683701 | 29 | 2.65e-01 | 0.120000 | 6.68e-01 |
| Regulation of Apoptosis | 51 | 1.41e-01 | 0.119000 | 4.94e-01 |
| FGFR2c ligand binding and activation | 12 | 4.75e-01 | 0.119000 | 8.02e-01 |
| Tetrahydrobiopterin (BH4) synthesis, recycling, salvage and regulation | 10 | 5.14e-01 | 0.119000 | 8.20e-01 |
| Downstream signaling events of B Cell Receptor (BCR) | 78 | 6.92e-02 | 0.119000 | 3.43e-01 |
| Passive transport by Aquaporins | 13 | 4.59e-01 | 0.119000 | 7.91e-01 |
| DNA Double-Strand Break Repair | 129 | 1.99e-02 | 0.119000 | 1.87e-01 |
| Regulation of TP53 Activity through Phosphorylation | 88 | 5.49e-02 | 0.118000 | 3.19e-01 |
| Class I peroxisomal membrane protein import | 19 | 3.72e-01 | 0.118000 | 7.48e-01 |
| BBSome-mediated cargo-targeting to cilium | 23 | 3.26e-01 | -0.118000 | 7.18e-01 |
| RAC1 GTPase cycle | 170 | 7.82e-03 | -0.118000 | 1.03e-01 |
| UCH proteinases | 81 | 6.67e-02 | 0.118000 | 3.38e-01 |
| Interactions of Vpr with host cellular proteins | 33 | 2.45e-01 | -0.117000 | 6.39e-01 |
| ERBB2 Regulates Cell Motility | 15 | 4.33e-01 | -0.117000 | 7.84e-01 |
| Cobalamin (Cbl, vitamin B12) transport and metabolism | 20 | 3.66e-01 | 0.117000 | 7.45e-01 |
| Regulation of TP53 Expression and Degradation | 37 | 2.19e-01 | 0.117000 | 6.09e-01 |
| Generation of second messenger molecules | 30 | 2.70e-01 | -0.116000 | 6.72e-01 |
| Resolution of D-loop Structures through Synthesis-Dependent Strand Annealing (SDSA) | 25 | 3.14e-01 | 0.116000 | 7.04e-01 |
| Activation of the TFAP2 (AP-2) family of transcription factors | 11 | 5.04e-01 | 0.116000 | 8.18e-01 |
| Metabolism of nucleotides | 95 | 5.02e-02 | 0.116000 | 3.07e-01 |
| Downregulation of TGF-beta receptor signaling | 26 | 3.05e-01 | 0.116000 | 6.99e-01 |
| Defective pyroptosis | 11 | 5.05e-01 | -0.116000 | 8.18e-01 |
| HIV Life Cycle | 139 | 1.80e-02 | 0.116000 | 1.76e-01 |
| Insulin processing | 24 | 3.25e-01 | -0.116000 | 7.17e-01 |
| Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks | 41 | 1.99e-01 | 0.116000 | 5.83e-01 |
| Erythropoietin activates RAS | 14 | 4.53e-01 | 0.116000 | 7.90e-01 |
| NS1 Mediated Effects on Host Pathways | 39 | 2.11e-01 | -0.116000 | 5.98e-01 |
| PIWI-interacting RNA (piRNA) biogenesis | 29 | 2.81e-01 | 0.116000 | 6.85e-01 |
| Processive synthesis on the lagging strand | 14 | 4.54e-01 | 0.116000 | 7.90e-01 |
| Respiratory electron transport, ATP synthesis by chemiosmotic coupling, and heat production by uncoupling proteins. | 95 | 5.20e-02 | 0.115000 | 3.14e-01 |
| DNA Replication Pre-Initiation | 97 | 4.96e-02 | 0.115000 | 3.06e-01 |
| HIV Transcription Initiation | 43 | 1.92e-01 | 0.115000 | 5.68e-01 |
| RNA Polymerase II HIV Promoter Escape | 43 | 1.92e-01 | 0.115000 | 5.68e-01 |
| RNA Polymerase II Promoter Escape | 43 | 1.92e-01 | 0.115000 | 5.68e-01 |
| RNA Polymerase II Transcription Initiation | 43 | 1.92e-01 | 0.115000 | 5.68e-01 |
| RNA Polymerase II Transcription Initiation And Promoter Clearance | 43 | 1.92e-01 | 0.115000 | 5.68e-01 |
| RNA Polymerase II Transcription Pre-Initiation And Promoter Opening | 43 | 1.92e-01 | 0.115000 | 5.68e-01 |
| Late Phase of HIV Life Cycle | 126 | 2.58e-02 | 0.115000 | 2.19e-01 |
| IL-6-type cytokine receptor ligand interactions | 17 | 4.12e-01 | 0.115000 | 7.77e-01 |
| MyD88 cascade initiated on plasma membrane | 91 | 5.80e-02 | 0.115000 | 3.25e-01 |
| Toll Like Receptor 10 (TLR10) Cascade | 91 | 5.80e-02 | 0.115000 | 3.25e-01 |
| Toll Like Receptor 5 (TLR5) Cascade | 91 | 5.80e-02 | 0.115000 | 3.25e-01 |
| PCNA-Dependent Long Patch Base Excision Repair | 21 | 3.65e-01 | 0.114000 | 7.45e-01 |
| Meiotic recombination | 26 | 3.15e-01 | -0.114000 | 7.04e-01 |
| Trafficking and processing of endosomal TLR | 11 | 5.14e-01 | 0.114000 | 8.20e-01 |
| RNA Polymerase III Transcription Initiation | 36 | 2.38e-01 | 0.114000 | 6.32e-01 |
| Gamma carboxylation, hypusinylation, hydroxylation, and arylsulfatase activation | 52 | 1.57e-01 | 0.113000 | 5.20e-01 |
| Iron uptake and transport | 57 | 1.40e-01 | 0.113000 | 4.94e-01 |
| Synthesis of bile acids and bile salts via 24-hydroxycholesterol | 14 | 4.64e-01 | -0.113000 | 7.93e-01 |
| Cellular response to heat stress | 95 | 5.72e-02 | 0.113000 | 3.25e-01 |
| Retrograde transport at the Trans-Golgi-Network | 47 | 1.81e-01 | -0.113000 | 5.57e-01 |
| Regulation of MECP2 expression and activity | 30 | 2.86e-01 | -0.113000 | 6.89e-01 |
| Antigen Presentation: Folding, assembly and peptide loading of class I MHC | 29 | 2.95e-01 | -0.112000 | 6.92e-01 |
| Nitric oxide stimulates guanylate cyclase | 22 | 3.62e-01 | -0.112000 | 7.42e-01 |
| Asymmetric localization of PCP proteins | 62 | 1.26e-01 | 0.112000 | 4.60e-01 |
| Translesion synthesis by POLK | 17 | 4.24e-01 | 0.112000 | 7.83e-01 |
| RNA Polymerase III Transcription Initiation From Type 3 Promoter | 28 | 3.06e-01 | 0.112000 | 7.00e-01 |
| Mitochondrial RNA degradation | 10 | 5.43e-01 | 0.111000 | 8.38e-01 |
| Late endosomal microautophagy | 33 | 2.74e-01 | 0.110000 | 6.75e-01 |
| mRNA decay by 3’ to 5’ exoribonuclease | 13 | 4.94e-01 | 0.110000 | 8.17e-01 |
| EPH-ephrin mediated repulsion of cells | 50 | 1.81e-01 | 0.109000 | 5.57e-01 |
| Degradation of GLI2 by the proteasome | 58 | 1.51e-01 | 0.109000 | 5.07e-01 |
| G2/M Checkpoints | 129 | 3.25e-02 | 0.109000 | 2.49e-01 |
| Cell Cycle Checkpoints | 248 | 3.10e-03 | 0.109000 | 5.59e-02 |
| Defective B3GALT6 causes EDSP2 and SEMDJL1 | 17 | 4.38e-01 | 0.109000 | 7.84e-01 |
| Cell recruitment (pro-inflammatory response) | 26 | 3.38e-01 | -0.109000 | 7.26e-01 |
| Purinergic signaling in leishmaniasis infection | 26 | 3.38e-01 | -0.109000 | 7.26e-01 |
| Formation of Incision Complex in GG-NER | 40 | 2.36e-01 | 0.108000 | 6.28e-01 |
| Prolonged ERK activation events | 14 | 4.83e-01 | 0.108000 | 8.07e-01 |
| Chromosome Maintenance | 86 | 8.31e-02 | 0.108000 | 3.80e-01 |
| Signaling by FGFR1 in disease | 37 | 2.57e-01 | -0.108000 | 6.56e-01 |
| Somitogenesis | 53 | 1.76e-01 | 0.107000 | 5.50e-01 |
| TNF signaling | 53 | 1.77e-01 | 0.107000 | 5.51e-01 |
| GRB2 events in ERBB2 signaling | 16 | 4.58e-01 | -0.107000 | 7.91e-01 |
| FGFR2 ligand binding and activation | 19 | 4.21e-01 | 0.107000 | 7.82e-01 |
| MAPK6/MAPK4 signaling | 89 | 8.25e-02 | 0.106000 | 3.78e-01 |
| Epigenetic regulation of gene expression | 118 | 4.57e-02 | 0.106000 | 2.97e-01 |
| Metabolic disorders of biological oxidation enzymes | 32 | 2.98e-01 | 0.106000 | 6.96e-01 |
| Cellular responses to stress | 714 | 1.22e-06 | 0.106000 | 6.46e-05 |
| Muscle contraction | 197 | 1.03e-02 | 0.106000 | 1.27e-01 |
| G0 and Early G1 | 27 | 3.41e-01 | 0.106000 | 7.26e-01 |
| Leading Strand Synthesis | 13 | 5.10e-01 | 0.106000 | 8.19e-01 |
| Polymerase switching | 13 | 5.10e-01 | 0.106000 | 8.19e-01 |
| Glycogen metabolism | 22 | 3.94e-01 | 0.105000 | 7.65e-01 |
| Regulation of cholesterol biosynthesis by SREBP (SREBF) | 54 | 1.82e-01 | 0.105000 | 5.57e-01 |
| Cell surface interactions at the vascular wall | 129 | 3.95e-02 | -0.105000 | 2.79e-01 |
| G-protein activation | 24 | 3.76e-01 | -0.104000 | 7.48e-01 |
| Signalling to RAS | 20 | 4.20e-01 | 0.104000 | 7.82e-01 |
| Estrogen-dependent gene expression | 91 | 8.62e-02 | 0.104000 | 3.87e-01 |
| FOXO-mediated transcription | 65 | 1.47e-01 | 0.104000 | 5.00e-01 |
| Phase 0 - rapid depolarisation | 31 | 3.18e-01 | 0.104000 | 7.06e-01 |
| Adenylate cyclase inhibitory pathway | 14 | 5.02e-01 | 0.104000 | 8.18e-01 |
| MET receptor recycling | 10 | 5.71e-01 | 0.104000 | 8.52e-01 |
| Cellular responses to stimuli | 728 | 1.83e-06 | 0.104000 | 9.06e-05 |
| Interleukin-1 signaling | 109 | 6.19e-02 | 0.103000 | 3.32e-01 |
| NCAM1 interactions | 41 | 2.53e-01 | 0.103000 | 6.53e-01 |
| Binding and Uptake of Ligands by Scavenger Receptors | 41 | 2.53e-01 | -0.103000 | 6.53e-01 |
| G beta:gamma signalling through PI3Kgamma | 25 | 3.73e-01 | -0.103000 | 7.48e-01 |
| EGFR downregulation | 30 | 3.29e-01 | 0.103000 | 7.20e-01 |
| FGFR3 mutant receptor activation | 11 | 5.55e-01 | 0.103000 | 8.43e-01 |
| Signaling by activated point mutants of FGFR3 | 11 | 5.55e-01 | 0.103000 | 8.43e-01 |
| CD28 dependent Vav1 pathway | 11 | 5.55e-01 | -0.103000 | 8.43e-01 |
| PTEN Regulation | 150 | 2.98e-02 | 0.103000 | 2.41e-01 |
| Oncogene Induced Senescence | 35 | 2.94e-01 | 0.102000 | 6.92e-01 |
| Depolymerization of the Nuclear Lamina | 14 | 5.07e-01 | 0.102000 | 8.18e-01 |
| Cellular response to hypoxia | 71 | 1.35e-01 | 0.102000 | 4.85e-01 |
| FGFR3 ligand binding and activation | 12 | 5.43e-01 | 0.101000 | 8.38e-01 |
| FGFR3c ligand binding and activation | 12 | 5.43e-01 | 0.101000 | 8.38e-01 |
| Degradation of AXIN | 53 | 2.02e-01 | 0.101000 | 5.87e-01 |
| Acyl chain remodelling of PI | 16 | 4.83e-01 | 0.101000 | 8.07e-01 |
| Signaling by PDGFR in disease | 20 | 4.34e-01 | -0.101000 | 7.84e-01 |
| Acyl chain remodelling of PC | 26 | 3.74e-01 | 0.101000 | 7.48e-01 |
| Transferrin endocytosis and recycling | 30 | 3.41e-01 | 0.100000 | 7.26e-01 |
| CLEC7A (Dectin-1) signaling | 96 | 8.94e-02 | 0.100000 | 3.91e-01 |
| ADP signalling through P2Y purinoceptor 1 | 25 | 3.86e-01 | -0.100000 | 7.55e-01 |
| MAP3K8 (TPL2)-dependent MAPK1/3 activation | 15 | 5.02e-01 | 0.100000 | 8.18e-01 |
| Amino acid transport across the plasma membrane | 30 | 3.43e-01 | 0.100000 | 7.27e-01 |
| VxPx cargo-targeting to cilium | 20 | 4.39e-01 | 0.099900 | 7.84e-01 |
| Sphingolipid de novo biosynthesis | 32 | 3.29e-01 | -0.099600 | 7.20e-01 |
| PKR-mediated signaling | 72 | 1.44e-01 | 0.099600 | 4.99e-01 |
| Defective TPR may confer susceptibility towards thyroid papillary carcinoma (TPC) | 30 | 3.46e-01 | -0.099500 | 7.29e-01 |
| Regulation of Glucokinase by Glucokinase Regulatory Protein | 30 | 3.46e-01 | -0.099500 | 7.29e-01 |
| RUNX1 regulates transcription of genes involved in differentiation of HSCs | 68 | 1.56e-01 | 0.099500 | 5.17e-01 |
| Presynaptic depolarization and calcium channel opening | 12 | 5.51e-01 | 0.099400 | 8.43e-01 |
| S Phase | 157 | 3.16e-02 | 0.099300 | 2.44e-01 |
| Cytosolic sulfonation of small molecules | 21 | 4.32e-01 | 0.099100 | 7.84e-01 |
| TP53 Regulates Transcription of Death Receptors and Ligands | 12 | 5.52e-01 | -0.099000 | 8.43e-01 |
| TP53 Regulates Metabolic Genes | 83 | 1.19e-01 | 0.098900 | 4.52e-01 |
| TGF-beta receptor signaling activates SMADs | 47 | 2.42e-01 | 0.098700 | 6.35e-01 |
| FOXO-mediated transcription of cell death genes | 15 | 5.09e-01 | 0.098500 | 8.19e-01 |
| Molecules associated with elastic fibres | 37 | 3.00e-01 | 0.098400 | 6.96e-01 |
| FOXO-mediated transcription of cell cycle genes | 16 | 4.96e-01 | 0.098400 | 8.17e-01 |
| Respiratory electron transport | 90 | 1.07e-01 | 0.098200 | 4.28e-01 |
| Myogenesis | 29 | 3.60e-01 | -0.098200 | 7.42e-01 |
| Gastrulation | 113 | 7.20e-02 | 0.097900 | 3.50e-01 |
| Smooth Muscle Contraction | 43 | 2.66e-01 | 0.097900 | 6.68e-01 |
| Neddylation | 232 | 1.03e-02 | 0.097700 | 1.27e-01 |
| G1/S Transition | 126 | 5.82e-02 | 0.097700 | 3.25e-01 |
| Oxygen-dependent proline hydroxylation of Hypoxia-inducible Factor Alpha | 62 | 1.83e-01 | 0.097700 | 5.57e-01 |
| Inflammasomes | 21 | 4.39e-01 | -0.097500 | 7.84e-01 |
| Vpr-mediated nuclear import of PICs | 32 | 3.40e-01 | -0.097400 | 7.26e-01 |
| HIV Infection | 216 | 1.36e-02 | 0.097300 | 1.51e-01 |
| Tryptophan catabolism | 12 | 5.60e-01 | -0.097300 | 8.48e-01 |
| COPII-mediated vesicle transport | 66 | 1.73e-01 | 0.097000 | 5.49e-01 |
| Signaling by ALK fusions and activated point mutants | 51 | 2.31e-01 | -0.097000 | 6.19e-01 |
| Signaling by ALK in cancer | 51 | 2.31e-01 | -0.097000 | 6.19e-01 |
| Regulation of CDH11 Expression and Function | 28 | 3.75e-01 | 0.096900 | 7.48e-01 |
| Energy dependent regulation of mTOR by LKB1-AMPK | 28 | 3.75e-01 | 0.096800 | 7.48e-01 |
| RUNX2 regulates osteoblast differentiation | 22 | 4.33e-01 | 0.096600 | 7.84e-01 |
| Formation of the anterior neural plate | 11 | 5.79e-01 | 0.096500 | 8.56e-01 |
| Activation of kainate receptors upon glutamate binding | 29 | 3.69e-01 | -0.096400 | 7.48e-01 |
| Transcriptional regulation by RUNX3 | 93 | 1.08e-01 | 0.096400 | 4.28e-01 |
| Vitamin B5 (pantothenate) metabolism | 19 | 4.68e-01 | -0.096100 | 7.98e-01 |
| Degradation of GLI1 by the proteasome | 58 | 2.06e-01 | 0.096100 | 5.92e-01 |
| DNA Repair | 276 | 6.08e-03 | 0.095900 | 8.53e-02 |
| ERBB2 Activates PTK6 Signaling | 13 | 5.50e-01 | -0.095800 | 8.43e-01 |
| SUMOylation of intracellular receptors | 29 | 3.72e-01 | -0.095700 | 7.48e-01 |
| RHOJ GTPase cycle | 51 | 2.37e-01 | -0.095700 | 6.30e-01 |
| Surfactant metabolism | 28 | 3.81e-01 | 0.095600 | 7.52e-01 |
| Presynaptic function of Kainate receptors | 21 | 4.49e-01 | -0.095500 | 7.86e-01 |
| Downstream signaling of activated FGFR1 | 31 | 3.58e-01 | 0.095300 | 7.40e-01 |
| Antigen activates B Cell Receptor (BCR) leading to generation of second messengers | 28 | 3.83e-01 | -0.095200 | 7.54e-01 |
| Deadenylation of mRNA | 25 | 4.10e-01 | -0.095100 | 7.76e-01 |
| LDL clearance | 19 | 4.75e-01 | 0.094700 | 8.02e-01 |
| Activation of IRF3, IRF7 mediated by TBK1, IKBKE | 17 | 5.01e-01 | -0.094200 | 8.18e-01 |
| Nuclear events mediated by NFE2L2 | 94 | 1.15e-01 | 0.094100 | 4.42e-01 |
| SUMOylation of DNA damage response and repair proteins | 71 | 1.71e-01 | -0.094000 | 5.46e-01 |
| Regulation of HSF1-mediated heat shock response | 78 | 1.51e-01 | 0.094000 | 5.07e-01 |
| Peptide hormone metabolism | 81 | 1.44e-01 | -0.093800 | 4.99e-01 |
| Constitutive Signaling by EGFRvIII | 15 | 5.30e-01 | 0.093600 | 8.31e-01 |
| Signaling by EGFRvIII in Cancer | 15 | 5.30e-01 | 0.093600 | 8.31e-01 |
| O-glycosylation of TSR domain-containing proteins | 37 | 3.26e-01 | 0.093400 | 7.17e-01 |
| Regulation of Complement cascade | 45 | 2.80e-01 | -0.093100 | 6.85e-01 |
| Mitotic G1 phase and G1/S transition | 144 | 5.38e-02 | 0.093000 | 3.15e-01 |
| TNFs bind their physiological receptors | 25 | 4.21e-01 | -0.093000 | 7.82e-01 |
| Mitotic Spindle Checkpoint | 106 | 9.80e-02 | 0.093000 | 4.10e-01 |
| Mitotic Metaphase and Anaphase | 222 | 1.69e-02 | 0.092900 | 1.70e-01 |
| Protein methylation | 16 | 5.20e-01 | 0.092900 | 8.21e-01 |
| Drug ADME | 106 | 9.86e-02 | -0.092800 | 4.11e-01 |
| GLI3 is processed to GLI3R by the proteasome | 58 | 2.21e-01 | 0.092800 | 6.11e-01 |
| SARS-CoV-2 modulates autophagy | 11 | 5.94e-01 | -0.092800 | 8.64e-01 |
| Germ layer formation at gastrulation | 16 | 5.22e-01 | -0.092500 | 8.23e-01 |
| Defective HDR through Homologous Recombination Repair (HRR) due to PALB2 loss of BRCA1 binding function | 23 | 4.42e-01 | 0.092500 | 7.84e-01 |
| Defective HDR through Homologous Recombination Repair (HRR) due to PALB2 loss of BRCA2/RAD51/RAD51C binding function | 23 | 4.42e-01 | 0.092500 | 7.84e-01 |
| Defective homologous recombination repair (HRR) due to BRCA1 loss of function | 23 | 4.42e-01 | 0.092500 | 7.84e-01 |
| Defective homologous recombination repair (HRR) due to PALB2 loss of function | 23 | 4.42e-01 | 0.092500 | 7.84e-01 |
| Impaired BRCA2 binding to PALB2 | 23 | 4.42e-01 | 0.092500 | 7.84e-01 |
| Glucagon-like Peptide-1 (GLP1) regulates insulin secretion | 42 | 3.00e-01 | -0.092400 | 6.96e-01 |
| Formation of tubulin folding intermediates by CCT/TriC | 26 | 4.15e-01 | -0.092300 | 7.80e-01 |
| NEP/NS2 Interacts with the Cellular Export Machinery | 30 | 3.82e-01 | -0.092300 | 7.52e-01 |
| Signaling by TGF-beta Receptor Complex | 92 | 1.26e-01 | 0.092300 | 4.60e-01 |
| Formation of annular gap junctions | 11 | 5.96e-01 | 0.092300 | 8.64e-01 |
| DDX58/IFIH1-mediated induction of interferon-alpha/beta | 74 | 1.70e-01 | -0.092200 | 5.46e-01 |
| Regulation of RUNX2 expression and activity | 71 | 1.79e-01 | 0.092100 | 5.57e-01 |
| Butyrophilin (BTN) family interactions | 12 | 5.81e-01 | -0.092000 | 8.56e-01 |
| RAC2 GTPase cycle | 80 | 1.56e-01 | -0.091800 | 5.17e-01 |
| DAG and IP3 signaling | 39 | 3.22e-01 | -0.091600 | 7.15e-01 |
| Regulation of TP53 Activity through Acetylation | 29 | 3.94e-01 | 0.091500 | 7.65e-01 |
| Disorders of transmembrane transporters | 167 | 4.23e-02 | 0.091000 | 2.86e-01 |
| Separation of Sister Chromatids | 179 | 3.56e-02 | 0.091000 | 2.58e-01 |
| ABC-family proteins mediated transport | 98 | 1.20e-01 | 0.090900 | 4.52e-01 |
| RHOG GTPase cycle | 69 | 1.92e-01 | -0.090800 | 5.68e-01 |
| Thromboxane signalling through TP receptor | 24 | 4.41e-01 | -0.090800 | 7.84e-01 |
| CDC42 GTPase cycle | 143 | 6.09e-02 | -0.090700 | 3.31e-01 |
| Ca-dependent events | 35 | 3.54e-01 | -0.090600 | 7.36e-01 |
| Transcriptional regulation by RUNX2 | 116 | 9.28e-02 | 0.090300 | 3.96e-01 |
| Mitotic Anaphase | 221 | 2.08e-02 | 0.090200 | 1.90e-01 |
| Nuclear Events (kinase and transcription factor activation) | 60 | 2.27e-01 | 0.090100 | 6.16e-01 |
| Cytochrome c-mediated apoptotic response | 12 | 5.89e-01 | -0.090100 | 8.60e-01 |
| Killing mechanisms | 11 | 6.05e-01 | 0.090000 | 8.66e-01 |
| WNT5:FZD7-mediated leishmania damping | 11 | 6.05e-01 | 0.090000 | 8.66e-01 |
| Uptake and function of anthrax toxins | 11 | 6.06e-01 | -0.089900 | 8.66e-01 |
| PI-3K cascade:FGFR1 | 21 | 4.76e-01 | 0.089800 | 8.03e-01 |
| RHO GTPases activate KTN1 | 11 | 6.06e-01 | 0.089800 | 8.66e-01 |
| Orc1 removal from chromatin | 69 | 1.98e-01 | 0.089600 | 5.81e-01 |
| Signaling by SCF-KIT | 43 | 3.11e-01 | -0.089300 | 7.00e-01 |
| Lysosome Vesicle Biogenesis | 33 | 3.76e-01 | 0.089100 | 7.48e-01 |
| Regulation of glycolysis by fructose 2,6-bisphosphate metabolism | 11 | 6.11e-01 | -0.088600 | 8.70e-01 |
| TP53 Regulates Transcription of Caspase Activators and Caspases | 12 | 5.97e-01 | -0.088200 | 8.64e-01 |
| Prostacyclin signalling through prostacyclin receptor | 19 | 5.06e-01 | -0.088100 | 8.18e-01 |
| Branched-chain amino acid catabolism | 20 | 4.95e-01 | 0.088100 | 8.17e-01 |
| Mismatch repair (MMR) directed by MSH2:MSH6 (MutSalpha) | 14 | 5.68e-01 | 0.088100 | 8.52e-01 |
| NFE2L2 regulating anti-oxidant/detoxification enzymes | 19 | 5.06e-01 | -0.088000 | 8.18e-01 |
| Triglyceride biosynthesis | 12 | 5.98e-01 | 0.088000 | 8.65e-01 |
| Transport of bile salts and organic acids, metal ions and amine compounds | 82 | 1.69e-01 | 0.087800 | 5.43e-01 |
| Signaling by Non-Receptor Tyrosine Kinases | 55 | 2.60e-01 | 0.087800 | 6.56e-01 |
| Signaling by PTK6 | 55 | 2.60e-01 | 0.087800 | 6.56e-01 |
| FRS-mediated FGFR1 signaling | 23 | 4.66e-01 | 0.087700 | 7.95e-01 |
| Regulation of PTEN gene transcription | 59 | 2.44e-01 | 0.087600 | 6.39e-01 |
| Regulation of TP53 Activity through Association with Co-factors | 14 | 5.71e-01 | 0.087400 | 8.52e-01 |
| PLC beta mediated events | 47 | 3.01e-01 | -0.087300 | 6.96e-01 |
| G2/M DNA damage checkpoint | 58 | 2.51e-01 | 0.087100 | 6.51e-01 |
| SHC1 events in EGFR signaling | 14 | 5.74e-01 | 0.086800 | 8.54e-01 |
| Voltage gated Potassium channels | 42 | 3.31e-01 | 0.086700 | 7.21e-01 |
| TNFR2 non-canonical NF-kB pathway | 94 | 1.47e-01 | 0.086500 | 5.00e-01 |
| Azathioprine ADME | 22 | 4.83e-01 | 0.086400 | 8.07e-01 |
| NCAM signaling for neurite out-growth | 62 | 2.40e-01 | 0.086300 | 6.33e-01 |
| CLEC7A (Dectin-1) induces NFAT activation | 11 | 6.20e-01 | -0.086300 | 8.76e-01 |
| Translation of Replicase and Assembly of the Replication Transcription Complex 9694676 | 14 | 5.76e-01 | -0.086300 | 8.56e-01 |
| SHC-mediated cascade:FGFR3 | 17 | 5.38e-01 | 0.086200 | 8.36e-01 |
| Homologous DNA Pairing and Strand Exchange | 41 | 3.40e-01 | 0.086200 | 7.26e-01 |
| GPCR ligand binding | 443 | 1.84e-03 | -0.086200 | 3.85e-02 |
| Maturation of nucleoprotein 9694631 | 15 | 5.64e-01 | 0.086100 | 8.48e-01 |
| Cardiac conduction | 125 | 9.66e-02 | 0.086000 | 4.06e-01 |
| Hedgehog ‘on’ state | 83 | 1.77e-01 | 0.085800 | 5.51e-01 |
| The citric acid (TCA) cycle and respiratory electron transport | 143 | 7.67e-02 | 0.085700 | 3.60e-01 |
| Tristetraprolin (TTP, ZFP36) binds and destabilizes mRNA | 17 | 5.41e-01 | 0.085700 | 8.37e-01 |
| RHO GTPases activate PAKs | 19 | 5.18e-01 | 0.085700 | 8.21e-01 |
| YAP1- and WWTR1 (TAZ)-stimulated gene expression | 15 | 5.66e-01 | 0.085600 | 8.50e-01 |
| WNT ligand biogenesis and trafficking | 25 | 4.59e-01 | 0.085500 | 7.91e-01 |
| TP53 regulates transcription of several additional cell death genes whose specific roles in p53-dependent apoptosis remain uncertain | 13 | 5.94e-01 | 0.085500 | 8.64e-01 |
| Synthesis of IP3 and IP4 in the cytosol | 25 | 4.62e-01 | 0.085000 | 7.91e-01 |
| RHOQ GTPase cycle | 57 | 2.67e-01 | -0.085000 | 6.68e-01 |
| Netrin-1 signaling | 49 | 3.04e-01 | -0.084900 | 6.98e-01 |
| Signaling by high-kinase activity BRAF mutants | 34 | 3.93e-01 | -0.084700 | 7.65e-01 |
| Acyl chain remodelling of PS | 21 | 5.04e-01 | 0.084300 | 8.18e-01 |
| KEAP1-NFE2L2 pathway | 126 | 1.02e-01 | 0.084300 | 4.15e-01 |
| Negative regulators of DDX58/IFIH1 signaling | 33 | 4.03e-01 | 0.084100 | 7.69e-01 |
| Formation of paraxial mesoderm | 65 | 2.42e-01 | 0.083900 | 6.35e-01 |
| RHOBTB1 GTPase cycle | 22 | 4.96e-01 | -0.083900 | 8.17e-01 |
| Axon guidance | 526 | 9.80e-04 | 0.083800 | 2.58e-02 |
| Glycerophospholipid biosynthesis | 114 | 1.23e-01 | 0.083600 | 4.57e-01 |
| GRB2 events in EGFR signaling | 13 | 6.02e-01 | 0.083600 | 8.66e-01 |
| RHOBTB2 GTPase cycle | 22 | 4.98e-01 | -0.083500 | 8.17e-01 |
| FLT3 signaling in disease | 28 | 4.45e-01 | -0.083300 | 7.85e-01 |
| Potassium Channels | 102 | 1.46e-01 | 0.083200 | 5.00e-01 |
| RIP-mediated NFkB activation via ZBP1 | 16 | 5.66e-01 | 0.083000 | 8.50e-01 |
| Transcriptional Regulation by TP53 | 346 | 8.00e-03 | 0.082900 | 1.05e-01 |
| Sensory processing of sound by inner hair cells of the cochlea | 64 | 2.51e-01 | 0.082900 | 6.52e-01 |
| Metabolism of cofactors | 19 | 5.32e-01 | 0.082800 | 8.31e-01 |
| Heparan sulfate/heparin (HS-GAG) metabolism | 52 | 3.03e-01 | 0.082500 | 6.98e-01 |
| MyD88 dependent cascade initiated on endosome | 96 | 1.62e-01 | 0.082500 | 5.30e-01 |
| Toll Like Receptor 7/8 (TLR7/8) Cascade | 96 | 1.62e-01 | 0.082500 | 5.30e-01 |
| Translocation of SLC2A4 (GLUT4) to the plasma membrane | 71 | 2.29e-01 | 0.082500 | 6.19e-01 |
| Complement cascade | 56 | 2.87e-01 | -0.082300 | 6.89e-01 |
| Ion transport by P-type ATPases | 51 | 3.09e-01 | -0.082300 | 7.00e-01 |
| Metal ion SLC transporters | 23 | 4.95e-01 | 0.082200 | 8.17e-01 |
| Signaling by ERBB2 | 49 | 3.20e-01 | 0.082100 | 7.11e-01 |
| Unwinding of DNA | 12 | 6.23e-01 | 0.082000 | 8.76e-01 |
| MAPK3 (ERK1) activation | 10 | 6.53e-01 | -0.082000 | 8.94e-01 |
| Activation of gene expression by SREBF (SREBP) | 42 | 3.59e-01 | 0.081800 | 7.40e-01 |
| ROS and RNS production in phagocytes | 35 | 4.03e-01 | 0.081700 | 7.69e-01 |
| G-protein beta:gamma signalling | 30 | 4.40e-01 | -0.081500 | 7.84e-01 |
| Glutamate Neurotransmitter Release Cycle | 23 | 4.99e-01 | 0.081400 | 8.18e-01 |
| Regulation of gene expression in beta cells | 21 | 5.19e-01 | 0.081300 | 8.21e-01 |
| Mitochondrial Fatty Acid Beta-Oxidation | 35 | 4.05e-01 | 0.081300 | 7.71e-01 |
| Metabolism of amine-derived hormones | 17 | 5.62e-01 | 0.081100 | 8.48e-01 |
| NGF-stimulated transcription | 39 | 3.82e-01 | 0.080900 | 7.52e-01 |
| Activation of BH3-only proteins | 30 | 4.43e-01 | 0.080900 | 7.84e-01 |
| SUMOylation of ubiquitinylation proteins | 37 | 3.95e-01 | -0.080800 | 7.65e-01 |
| ESR-mediated signaling | 161 | 7.79e-02 | 0.080500 | 3.64e-01 |
| ATF6 (ATF6-alpha) activates chaperones | 11 | 6.44e-01 | 0.080400 | 8.89e-01 |
| Inactivation of CSF3 (G-CSF) signaling | 23 | 5.05e-01 | 0.080300 | 8.18e-01 |
| GPCR downstream signalling | 604 | 7.50e-04 | -0.080100 | 2.05e-02 |
| Nervous system development | 550 | 1.32e-03 | 0.079900 | 3.11e-02 |
| Nuclear Pore Complex (NPC) Disassembly | 34 | 4.23e-01 | -0.079400 | 7.83e-01 |
| Signaling by NOTCH | 183 | 6.57e-02 | 0.078800 | 3.38e-01 |
| Assembly of the ORC complex at the origin of replication | 10 | 6.67e-01 | -0.078500 | 9.04e-01 |
| JNK (c-Jun kinases) phosphorylation and activation mediated by activated human TAK1 | 19 | 5.54e-01 | 0.078500 | 8.43e-01 |
| NOD1/2 Signaling Pathway | 33 | 4.36e-01 | 0.078400 | 7.84e-01 |
| Transport of the SLBP independent Mature mRNA | 33 | 4.37e-01 | -0.078200 | 7.84e-01 |
| DNA strand elongation | 31 | 4.52e-01 | 0.078100 | 7.89e-01 |
| Keratan sulfate/keratin metabolism | 36 | 4.17e-01 | -0.078100 | 7.81e-01 |
| Transcription of E2F targets under negative control by p107 (RBL1) and p130 (RBL2) in complex with HDAC1 | 16 | 5.89e-01 | 0.078100 | 8.60e-01 |
| Defective homologous recombination repair (HRR) due to BRCA2 loss of function | 39 | 4.02e-01 | 0.077500 | 7.69e-01 |
| Diseases of DNA Double-Strand Break Repair | 39 | 4.02e-01 | 0.077500 | 7.69e-01 |
| Fatty acids | 15 | 6.03e-01 | -0.077500 | 8.66e-01 |
| Diseases of metabolism | 234 | 4.11e-02 | 0.077400 | 2.84e-01 |
| Beta-catenin phosphorylation cascade | 16 | 5.94e-01 | -0.077000 | 8.64e-01 |
| SUMOylation of chromatin organization proteins | 54 | 3.28e-01 | -0.076900 | 7.19e-01 |
| Formation of WDR5-containing histone-modifying complexes | 37 | 4.19e-01 | 0.076800 | 7.82e-01 |
| eNOS activation | 10 | 6.75e-01 | 0.076600 | 9.06e-01 |
| Ethanol oxidation | 12 | 6.46e-01 | 0.076500 | 8.90e-01 |
| Defective B3GALTL causes PpS | 36 | 4.27e-01 | 0.076500 | 7.84e-01 |
| Metabolism of porphyrins | 27 | 4.92e-01 | -0.076400 | 8.17e-01 |
| Resolution of D-Loop Structures | 31 | 4.62e-01 | 0.076300 | 7.91e-01 |
| Beta-oxidation of very long chain fatty acids | 10 | 6.76e-01 | -0.076300 | 9.06e-01 |
| RHO GTPases Activate NADPH Oxidases | 22 | 5.36e-01 | -0.076200 | 8.36e-01 |
| SUMOylation of RNA binding proteins | 45 | 3.78e-01 | -0.075900 | 7.51e-01 |
| Transport of Mature mRNA Derived from an Intronless Transcript | 40 | 4.06e-01 | -0.075900 | 7.72e-01 |
| Diseases associated with the TLR signaling cascade | 29 | 4.79e-01 | -0.075900 | 8.07e-01 |
| Diseases of Immune System | 29 | 4.79e-01 | -0.075900 | 8.07e-01 |
| Base Excision Repair | 45 | 3.79e-01 | 0.075800 | 7.52e-01 |
| Lagging Strand Synthesis | 19 | 5.68e-01 | 0.075600 | 8.52e-01 |
| Peroxisomal protein import | 62 | 3.03e-01 | 0.075600 | 6.98e-01 |
| Acyl chain remodelling of PG | 18 | 5.80e-01 | 0.075300 | 8.56e-01 |
| Signaling by EGFR | 49 | 3.63e-01 | 0.075100 | 7.42e-01 |
| CTNNB1 S33 mutants aren’t phosphorylated | 14 | 6.27e-01 | -0.075100 | 8.76e-01 |
| CTNNB1 S37 mutants aren’t phosphorylated | 14 | 6.27e-01 | -0.075100 | 8.76e-01 |
| CTNNB1 S45 mutants aren’t phosphorylated | 14 | 6.27e-01 | -0.075100 | 8.76e-01 |
| CTNNB1 T41 mutants aren’t phosphorylated | 14 | 6.27e-01 | -0.075100 | 8.76e-01 |
| Signaling by CTNNB1 phospho-site mutants | 14 | 6.27e-01 | -0.075100 | 8.76e-01 |
| Signaling by GSK3beta mutants | 14 | 6.27e-01 | -0.075100 | 8.76e-01 |
| Regulation of Expression and Function of Type II Classical Cadherins | 31 | 4.70e-01 | 0.074900 | 7.99e-01 |
| Regulation of Homotypic Cell-Cell Adhesion | 31 | 4.70e-01 | 0.074900 | 7.99e-01 |
| CaM pathway | 33 | 4.57e-01 | -0.074900 | 7.91e-01 |
| Calmodulin induced events | 33 | 4.57e-01 | -0.074900 | 7.91e-01 |
| Cellular response to chemical stress | 207 | 6.32e-02 | 0.074800 | 3.35e-01 |
| TRAF6 mediated induction of NFkB and MAP kinases upon TLR7/8 or 9 activation | 95 | 2.08e-01 | 0.074800 | 5.96e-01 |
| Regulation of PTEN stability and activity | 66 | 2.94e-01 | 0.074600 | 6.92e-01 |
| Class A/1 (Rhodopsin-like receptors) | 311 | 2.38e-02 | -0.074500 | 2.07e-01 |
| Protein localization | 147 | 1.20e-01 | 0.074300 | 4.52e-01 |
| RHOH GTPase cycle | 36 | 4.41e-01 | -0.074300 | 7.84e-01 |
| RNA Polymerase II Transcription | 1282 | 7.13e-06 | 0.074300 | 3.23e-04 |
| Downregulation of SMAD2/3:SMAD4 transcriptional activity | 29 | 4.89e-01 | 0.074200 | 8.12e-01 |
| Tight junction interactions | 28 | 4.97e-01 | -0.074100 | 8.17e-01 |
| Signaling by NTRK1 (TRKA) | 114 | 1.72e-01 | 0.074100 | 5.47e-01 |
| Metabolism of nitric oxide: NOS3 activation and regulation | 14 | 6.33e-01 | 0.073700 | 8.82e-01 |
| Regulation of BACH1 activity | 15 | 6.23e-01 | 0.073400 | 8.76e-01 |
| Processing of Capped Intronless Pre-mRNA | 28 | 5.02e-01 | 0.073200 | 8.18e-01 |
| FCERI mediated NF-kB activation | 77 | 2.66e-01 | 0.073200 | 6.68e-01 |
| Glutathione conjugation | 36 | 4.47e-01 | 0.073200 | 7.86e-01 |
| Effects of PIP2 hydrolysis | 26 | 5.19e-01 | -0.073100 | 8.21e-01 |
| Metabolism of non-coding RNA | 50 | 3.71e-01 | -0.073100 | 7.48e-01 |
| snRNP Assembly | 50 | 3.71e-01 | -0.073100 | 7.48e-01 |
| Highly calcium permeable postsynaptic nicotinic acetylcholine receptors | 11 | 6.76e-01 | 0.072900 | 9.06e-01 |
| Pyrimidine catabolism | 12 | 6.62e-01 | -0.072800 | 8.98e-01 |
| Regulation of TP53 Activity | 154 | 1.19e-01 | 0.072700 | 4.52e-01 |
| Generic Transcription Pathway | 1162 | 3.18e-05 | 0.072100 | 1.17e-03 |
| Inactivation, recovery and regulation of the phototransduction cascade | 31 | 4.88e-01 | -0.072000 | 8.12e-01 |
| Keratan sulfate biosynthesis | 28 | 5.10e-01 | -0.071900 | 8.19e-01 |
| Asparagine N-linked glycosylation | 296 | 3.38e-02 | 0.071700 | 2.52e-01 |
| Aspartate and asparagine metabolism | 11 | 6.81e-01 | -0.071500 | 9.08e-01 |
| Signaling by NOTCH1 | 70 | 3.01e-01 | 0.071400 | 6.96e-01 |
| Resolution of AP sites via the multiple-nucleotide patch replacement pathway | 24 | 5.46e-01 | 0.071200 | 8.40e-01 |
| Toll Like Receptor 3 (TLR3) Cascade | 99 | 2.22e-01 | 0.071000 | 6.11e-01 |
| Transcriptional Regulation by VENTX | 41 | 4.31e-01 | 0.071000 | 7.84e-01 |
| NOTCH3 Intracellular Domain Regulates Transcription | 24 | 5.47e-01 | 0.071000 | 8.40e-01 |
| Purine ribonucleoside monophosphate biosynthesis | 11 | 6.85e-01 | 0.070700 | 9.08e-01 |
| Reduction of cytosolic Ca++ levels | 11 | 6.85e-01 | 0.070700 | 9.08e-01 |
| Macroautophagy | 130 | 1.65e-01 | 0.070500 | 5.34e-01 |
| Listeria monocytogenes entry into host cells | 19 | 5.95e-01 | 0.070400 | 8.64e-01 |
| Activation of G protein gated Potassium channels | 29 | 5.12e-01 | -0.070400 | 8.19e-01 |
| G protein gated Potassium channels | 29 | 5.12e-01 | -0.070400 | 8.19e-01 |
| Inhibition of voltage gated Ca2+ channels via Gbeta/gamma subunits | 29 | 5.12e-01 | -0.070400 | 8.19e-01 |
| Eicosanoids | 12 | 6.73e-01 | 0.070300 | 9.06e-01 |
| EPHA-mediated growth cone collapse | 29 | 5.13e-01 | 0.070200 | 8.20e-01 |
| Nicotinamide salvaging | 17 | 6.16e-01 | 0.070200 | 8.74e-01 |
| Signaling by GPCR | 671 | 1.97e-03 | -0.069900 | 4.03e-02 |
| Gene expression (Transcription) | 1441 | 8.39e-06 | 0.069700 | 3.69e-04 |
| Defective Intrinsic Pathway for Apoptosis | 25 | 5.46e-01 | 0.069700 | 8.40e-01 |
| Diseases associated with O-glycosylation of proteins | 66 | 3.28e-01 | 0.069600 | 7.19e-01 |
| Viral Infection Pathways | 662 | 2.21e-03 | 0.069600 | 4.38e-02 |
| G alpha (q) signalling events | 206 | 8.50e-02 | -0.069600 | 3.86e-01 |
| Regulation of CDH11 function | 10 | 7.04e-01 | -0.069500 | 9.10e-01 |
| Cargo recognition for clathrin-mediated endocytosis | 98 | 2.34e-01 | 0.069500 | 6.25e-01 |
| Thrombin signalling through proteinase activated receptors (PARs) | 32 | 4.96e-01 | -0.069500 | 8.17e-01 |
| RHO GTPase Effectors | 250 | 5.85e-02 | 0.069400 | 3.25e-01 |
| Autophagy | 144 | 1.50e-01 | 0.069400 | 5.06e-01 |
| RUNX1 interacts with co-factors whose precise effect on RUNX1 targets is not known | 37 | 4.66e-01 | -0.069300 | 7.95e-01 |
| Signaling by BRAF and RAF1 fusions | 62 | 3.45e-01 | -0.069300 | 7.29e-01 |
| CTLA4 inhibitory signaling | 21 | 5.83e-01 | -0.069200 | 8.56e-01 |
| Sensory processing of sound | 71 | 3.14e-01 | 0.069100 | 7.04e-01 |
| Signaling by Insulin receptor | 80 | 2.86e-01 | 0.069000 | 6.89e-01 |
| Adenylate cyclase activating pathway | 10 | 7.07e-01 | 0.068700 | 9.10e-01 |
| Signaling by FGFR4 in disease | 11 | 6.94e-01 | 0.068500 | 9.09e-01 |
| The phototransduction cascade | 32 | 5.03e-01 | -0.068400 | 8.18e-01 |
| Transcriptional regulation by small RNAs | 46 | 4.23e-01 | 0.068200 | 7.83e-01 |
| Removal of the Flap Intermediate | 13 | 6.71e-01 | 0.068000 | 9.06e-01 |
| Transcriptional Regulation by E2F6 | 32 | 5.07e-01 | -0.067800 | 8.18e-01 |
| RHO GTPases Activate Formins | 132 | 1.80e-01 | 0.067500 | 5.57e-01 |
| HDACs deacetylate histones | 29 | 5.30e-01 | 0.067400 | 8.31e-01 |
| Interleukin-27 signaling | 11 | 6.99e-01 | -0.067300 | 9.10e-01 |
| Cell Cycle | 601 | 4.80e-03 | 0.067200 | 7.44e-02 |
| RAB geranylgeranylation | 57 | 3.80e-01 | 0.067200 | 7.52e-01 |
| Regulated Necrosis | 56 | 3.84e-01 | -0.067200 | 7.54e-01 |
| FOXO-mediated transcription of oxidative stress, metabolic and neuronal genes | 29 | 5.31e-01 | 0.067200 | 8.31e-01 |
| Defects in cobalamin (B12) metabolism | 12 | 6.87e-01 | 0.067100 | 9.08e-01 |
| Host Interactions of HIV factors | 122 | 2.01e-01 | 0.066900 | 5.87e-01 |
| Organic cation/anion/zwitterion transport | 15 | 6.55e-01 | 0.066600 | 8.95e-01 |
| Activated NTRK2 signals through FRS2 and FRS3 | 11 | 7.02e-01 | -0.066600 | 9.10e-01 |
| Potential therapeutics for SARS | 92 | 2.70e-01 | 0.066500 | 6.72e-01 |
| Adrenaline,noradrenaline inhibits insulin secretion | 28 | 5.43e-01 | 0.066400 | 8.38e-01 |
| ADORA2B mediated anti-inflammatory cytokines production | 42 | 4.60e-01 | -0.065800 | 7.91e-01 |
| NOTCH1 Intracellular Domain Regulates Transcription | 44 | 4.51e-01 | 0.065700 | 7.88e-01 |
| Regulation of PLK1 Activity at G2/M Transition | 83 | 3.01e-01 | 0.065600 | 6.96e-01 |
| Mucopolysaccharidoses | 10 | 7.21e-01 | 0.065200 | 9.11e-01 |
| Formation of the beta-catenin:TCF transactivating complex | 32 | 5.24e-01 | 0.065200 | 8.24e-01 |
| Resolution of D-loop Structures through Holliday Junction Intermediates | 30 | 5.38e-01 | 0.064900 | 8.36e-01 |
| PCP/CE pathway | 90 | 2.87e-01 | 0.064900 | 6.89e-01 |
| Hedgehog ‘off’ state | 110 | 2.40e-01 | 0.064900 | 6.33e-01 |
| Export of Viral Ribonucleoproteins from Nucleus | 31 | 5.32e-01 | -0.064900 | 8.31e-01 |
| Disassembly of the destruction complex and recruitment of AXIN to the membrane | 30 | 5.39e-01 | -0.064900 | 8.36e-01 |
| Inositol phosphate metabolism | 45 | 4.53e-01 | 0.064600 | 7.90e-01 |
| Regulation of beta-cell development | 41 | 4.74e-01 | 0.064600 | 8.02e-01 |
| Degradation of beta-catenin by the destruction complex | 81 | 3.16e-01 | 0.064500 | 7.04e-01 |
| BMAL1:CLOCK,NPAS2 activates circadian gene expression | 27 | 5.63e-01 | -0.064400 | 8.48e-01 |
| p75 NTR receptor-mediated signalling | 90 | 2.92e-01 | 0.064200 | 6.91e-01 |
| Complex I biogenesis | 49 | 4.37e-01 | 0.064100 | 7.84e-01 |
| Synthesis, secretion, and inactivation of Glucose-dependent Insulinotropic Polypeptide (GIP) | 12 | 7.01e-01 | -0.064000 | 9.10e-01 |
| ATF4 activates genes in response to endoplasmic reticulum stress | 28 | 5.58e-01 | 0.063900 | 8.46e-01 |
| Disorders of Developmental Biology | 11 | 7.14e-01 | 0.063800 | 9.11e-01 |
| Disorders of Nervous System Development | 11 | 7.14e-01 | 0.063800 | 9.11e-01 |
| Loss of function of MECP2 in Rett syndrome | 11 | 7.14e-01 | 0.063800 | 9.11e-01 |
| Pervasive developmental disorders | 11 | 7.14e-01 | 0.063800 | 9.11e-01 |
| Antiviral mechanism by IFN-stimulated genes | 143 | 1.88e-01 | 0.063700 | 5.66e-01 |
| Transport of Mature mRNAs Derived from Intronless Transcripts | 41 | 4.80e-01 | -0.063700 | 8.07e-01 |
| Nephrin family interactions | 22 | 6.05e-01 | -0.063600 | 8.66e-01 |
| Gene and protein expression by JAK-STAT signaling after Interleukin-12 stimulation | 35 | 5.15e-01 | 0.063600 | 8.20e-01 |
| Signaling by Nuclear Receptors | 238 | 9.12e-02 | 0.063500 | 3.94e-01 |
| MyD88:MAL(TIRAP) cascade initiated on plasma membrane | 106 | 2.59e-01 | 0.063500 | 6.56e-01 |
| Toll Like Receptor TLR6:TLR2 Cascade | 106 | 2.59e-01 | 0.063500 | 6.56e-01 |
| Transport of the SLBP Dependant Mature mRNA | 34 | 5.23e-01 | -0.063300 | 8.23e-01 |
| ATF6 (ATF6-alpha) activates chaperone genes | 10 | 7.30e-01 | 0.062900 | 9.14e-01 |
| TCF dependent signaling in response to WNT | 168 | 1.60e-01 | 0.062800 | 5.24e-01 |
| Signaling by FGFR3 in disease | 21 | 6.18e-01 | 0.062800 | 8.76e-01 |
| Factors involved in megakaryocyte development and platelet production | 147 | 1.89e-01 | -0.062800 | 5.66e-01 |
| Thyroxine biosynthesis | 10 | 7.31e-01 | -0.062700 | 9.14e-01 |
| MAPK targets/ Nuclear events mediated by MAP kinases | 29 | 5.61e-01 | 0.062300 | 8.48e-01 |
| Hemostasis | 575 | 1.07e-02 | -0.062200 | 1.30e-01 |
| Endogenous sterols | 26 | 5.84e-01 | 0.062100 | 8.56e-01 |
| PKA-mediated phosphorylation of CREB | 19 | 6.39e-01 | -0.062100 | 8.85e-01 |
| G-protein mediated events | 52 | 4.40e-01 | -0.061900 | 7.84e-01 |
| DARPP-32 events | 24 | 6.00e-01 | 0.061800 | 8.66e-01 |
| Regulation of gene expression in late stage (branching morphogenesis) pancreatic bud precursor cells | 15 | 6.79e-01 | 0.061800 | 9.08e-01 |
| Post-translational modification: synthesis of GPI-anchored proteins | 89 | 3.14e-01 | 0.061800 | 7.04e-01 |
| RUNX3 regulates NOTCH signaling | 13 | 7.00e-01 | 0.061700 | 9.10e-01 |
| Clathrin-mediated endocytosis | 137 | 2.12e-01 | 0.061700 | 5.99e-01 |
| O-linked glycosylation of mucins | 62 | 4.04e-01 | -0.061200 | 7.71e-01 |
| Diseases associated with visual transduction | 11 | 7.25e-01 | -0.061200 | 9.11e-01 |
| Diseases of the neuronal system | 11 | 7.25e-01 | -0.061200 | 9.11e-01 |
| Retinoid cycle disease events | 11 | 7.25e-01 | -0.061200 | 9.11e-01 |
| NR1H3 & NR1H2 regulate gene expression linked to cholesterol transport and efflux | 43 | 4.88e-01 | 0.061200 | 8.12e-01 |
| SEMA3A-Plexin repulsion signaling by inhibiting Integrin adhesion | 13 | 7.03e-01 | 0.061200 | 9.10e-01 |
| Signaling by Hedgehog | 146 | 2.02e-01 | 0.061100 | 5.87e-01 |
| TP53 regulates transcription of additional cell cycle genes whose exact role in the p53 pathway remain uncertain | 21 | 6.28e-01 | 0.061100 | 8.77e-01 |
| Downstream signaling of activated FGFR2 | 29 | 5.70e-01 | 0.060900 | 8.52e-01 |
| Post-translational protein phosphorylation | 100 | 2.94e-01 | -0.060700 | 6.92e-01 |
| Constitutive Signaling by Aberrant PI3K in Cancer | 77 | 3.58e-01 | -0.060600 | 7.40e-01 |
| MAP kinase activation | 58 | 4.25e-01 | 0.060600 | 7.83e-01 |
| Nuclear events stimulated by ALK signaling in cancer | 18 | 6.57e-01 | -0.060500 | 8.95e-01 |
| Presynaptic phase of homologous DNA pairing and strand exchange | 38 | 5.19e-01 | 0.060500 | 8.21e-01 |
| RAB GEFs exchange GTP for GDP on RABs | 82 | 3.45e-01 | -0.060400 | 7.29e-01 |
| Signaling by the B Cell Receptor (BCR) | 105 | 2.86e-01 | 0.060300 | 6.89e-01 |
| Peptide ligand-binding receptors | 190 | 1.52e-01 | -0.060200 | 5.08e-01 |
| Transcriptional activation of mitochondrial biogenesis | 51 | 4.58e-01 | 0.060100 | 7.91e-01 |
| ER to Golgi Anterograde Transport | 152 | 2.04e-01 | 0.059700 | 5.89e-01 |
| Digestion and absorption | 23 | 6.21e-01 | -0.059600 | 8.76e-01 |
| Regulation of KIT signaling | 16 | 6.81e-01 | -0.059300 | 9.08e-01 |
| Cell death signalling via NRAGE, NRIF and NADE | 69 | 3.97e-01 | 0.058900 | 7.65e-01 |
| Toll Like Receptor 9 (TLR9) Cascade | 100 | 3.09e-01 | 0.058900 | 7.00e-01 |
| PECAM1 interactions | 12 | 7.24e-01 | -0.058800 | 9.11e-01 |
| Extra-nuclear estrogen signaling | 74 | 3.83e-01 | 0.058600 | 7.54e-01 |
| Neutrophil degranulation | 456 | 3.18e-02 | -0.058600 | 2.45e-01 |
| Synthesis of Prostaglandins (PG) and Thromboxanes (TX) | 14 | 7.05e-01 | 0.058400 | 9.10e-01 |
| Signal amplification | 33 | 5.62e-01 | -0.058300 | 8.48e-01 |
| Amplification of signal from unattached kinetochores via a MAD2 inhibitory signal | 89 | 3.42e-01 | 0.058300 | 7.26e-01 |
| Amplification of signal from the kinetochores | 89 | 3.42e-01 | 0.058300 | 7.26e-01 |
| Metabolism of steroids | 148 | 2.22e-01 | -0.058100 | 6.11e-01 |
| Cellular hexose transport | 21 | 6.45e-01 | 0.058000 | 8.90e-01 |
| Metabolism of vitamins and cofactors | 184 | 1.75e-01 | 0.058000 | 5.50e-01 |
| Metabolism | 1969 | 1.98e-05 | 0.057800 | 8.48e-04 |
| Diseases of glycosylation | 137 | 2.43e-01 | 0.057700 | 6.37e-01 |
| Chondroitin sulfate biosynthesis | 18 | 6.73e-01 | -0.057500 | 9.06e-01 |
| FCGR3A-mediated IL10 synthesis | 37 | 5.47e-01 | -0.057300 | 8.40e-01 |
| M Phase | 335 | 7.13e-02 | 0.057300 | 3.49e-01 |
| Synthesis of Leukotrienes (LT) and Eoxins (EX) | 21 | 6.50e-01 | 0.057200 | 8.92e-01 |
| GAB1 signalosome | 17 | 6.85e-01 | 0.056900 | 9.08e-01 |
| SLBP Dependent Processing of Replication-Dependent Histone Pre-mRNAs | 11 | 7.44e-01 | 0.056900 | 9.18e-01 |
| Mismatch Repair | 15 | 7.03e-01 | 0.056800 | 9.10e-01 |
| Signaling by ERBB4 | 57 | 4.58e-01 | 0.056800 | 7.91e-01 |
| Mitochondrial biogenesis | 69 | 4.16e-01 | 0.056600 | 7.80e-01 |
| The role of Nef in HIV-1 replication and disease pathogenesis | 27 | 6.11e-01 | 0.056500 | 8.70e-01 |
| Activation of the pre-replicative complex | 31 | 5.86e-01 | -0.056400 | 8.59e-01 |
| Glucose metabolism | 89 | 3.58e-01 | 0.056400 | 7.40e-01 |
| Signaling by PDGFRA extracellular domain mutants | 12 | 7.35e-01 | -0.056300 | 9.16e-01 |
| Signaling by PDGFRA transmembrane, juxtamembrane and kinase domain mutants | 12 | 7.35e-01 | -0.056300 | 9.16e-01 |
| Norepinephrine Neurotransmitter Release Cycle | 16 | 6.97e-01 | 0.056300 | 9.09e-01 |
| Trafficking of GluR2-containing AMPA receptors | 15 | 7.07e-01 | -0.056100 | 9.10e-01 |
| Bicarbonate transporters | 10 | 7.59e-01 | -0.056100 | 9.22e-01 |
| Amyloid fiber formation | 53 | 4.82e-01 | 0.055900 | 8.07e-01 |
| Signaling by ALK | 26 | 6.22e-01 | 0.055900 | 8.76e-01 |
| Signaling by Erythropoietin | 25 | 6.29e-01 | -0.055900 | 8.77e-01 |
| Synthesis of PIPs at the plasma membrane | 48 | 5.04e-01 | -0.055700 | 8.18e-01 |
| Creation of C4 and C2 activators | 14 | 7.18e-01 | 0.055700 | 9.11e-01 |
| Regulation of actin dynamics for phagocytic cup formation | 59 | 4.61e-01 | 0.055400 | 7.91e-01 |
| Platelet activation, signaling and aggregation | 247 | 1.34e-01 | -0.055300 | 4.83e-01 |
| Mitochondrial calcium ion transport | 22 | 6.54e-01 | -0.055200 | 8.94e-01 |
| FRS-mediated FGFR2 signaling | 24 | 6.40e-01 | 0.055200 | 8.85e-01 |
| Defective GALNT3 causes HFTC | 18 | 6.86e-01 | 0.055000 | 9.08e-01 |
| Negative regulation of NMDA receptor-mediated neuronal transmission | 20 | 6.71e-01 | -0.054900 | 9.06e-01 |
| Acetylcholine binding and downstream events | 14 | 7.22e-01 | 0.054900 | 9.11e-01 |
| Postsynaptic nicotinic acetylcholine receptors | 14 | 7.22e-01 | 0.054900 | 9.11e-01 |
| Defective EXT1 causes exostoses 1, TRPS2 and CHDS | 12 | 7.42e-01 | 0.054900 | 9.18e-01 |
| Defective EXT2 causes exostoses 2 | 12 | 7.42e-01 | 0.054900 | 9.18e-01 |
| Nuclear Envelope Breakdown | 50 | 5.03e-01 | -0.054700 | 8.18e-01 |
| Cell Cycle, Mitotic | 476 | 4.09e-02 | 0.054600 | 2.83e-01 |
| Antigen processing-Cross presentation | 100 | 3.46e-01 | 0.054500 | 7.29e-01 |
| Signaling by NTRKs | 133 | 2.77e-01 | 0.054500 | 6.81e-01 |
| PKMTs methylate histone lysines | 36 | 5.73e-01 | -0.054300 | 8.53e-01 |
| ALK mutants bind TKIs | 12 | 7.45e-01 | -0.054300 | 9.18e-01 |
| PI-3K cascade:FGFR2 | 22 | 6.59e-01 | 0.054300 | 8.96e-01 |
| COPI-mediated anterograde transport | 101 | 3.47e-01 | 0.054200 | 7.29e-01 |
| Competing endogenous RNAs (ceRNAs) regulate PTEN translation | 16 | 7.08e-01 | 0.054100 | 9.10e-01 |
| HDR through MMEJ (alt-NHEJ) | 11 | 7.56e-01 | -0.054000 | 9.21e-01 |
| Extension of Telomeres | 48 | 5.20e-01 | 0.053700 | 8.21e-01 |
| SLC-mediated transmembrane transport | 236 | 1.56e-01 | 0.053600 | 5.17e-01 |
| Processing and activation of SUMO | 10 | 7.70e-01 | 0.053500 | 9.27e-01 |
| Cargo concentration in the ER | 32 | 6.01e-01 | 0.053400 | 8.66e-01 |
| Protein folding | 94 | 3.73e-01 | -0.053200 | 7.48e-01 |
| Vasopressin regulates renal water homeostasis via Aquaporins | 42 | 5.52e-01 | -0.053000 | 8.43e-01 |
| EPH-Ephrin signaling | 90 | 3.86e-01 | 0.052900 | 7.55e-01 |
| Adaptive Immune System | 733 | 1.46e-02 | -0.052800 | 1.55e-01 |
| Integration of energy metabolism | 105 | 3.51e-01 | 0.052600 | 7.34e-01 |
| Unblocking of NMDA receptors, glutamate binding and activation | 19 | 6.91e-01 | -0.052600 | 9.08e-01 |
| Post-chaperonin tubulin folding pathway | 23 | 6.63e-01 | -0.052400 | 8.99e-01 |
| Response of Mtb to phagocytosis | 22 | 6.72e-01 | 0.052200 | 9.06e-01 |
| Formation of apoptosome | 10 | 7.75e-01 | -0.052200 | 9.27e-01 |
| Regulation of the apoptosome activity | 10 | 7.75e-01 | -0.052200 | 9.27e-01 |
| Transport of Mature Transcript to Cytoplasm | 76 | 4.32e-01 | 0.052200 | 7.84e-01 |
| Toll Like Receptor 2 (TLR2) Cascade | 109 | 3.51e-01 | 0.051700 | 7.34e-01 |
| Toll Like Receptor TLR1:TLR2 Cascade | 109 | 3.51e-01 | 0.051700 | 7.34e-01 |
| Apoptotic factor-mediated response | 17 | 7.13e-01 | -0.051600 | 9.11e-01 |
| IKK complex recruitment mediated by RIP1 | 22 | 6.75e-01 | -0.051600 | 9.06e-01 |
| Cardiogenesis | 25 | 6.57e-01 | 0.051300 | 8.95e-01 |
| WNT5A-dependent internalization of FZD4 | 15 | 7.31e-01 | -0.051200 | 9.14e-01 |
| Caspase-mediated cleavage of cytoskeletal proteins | 12 | 7.59e-01 | 0.051000 | 9.22e-01 |
| COPI-dependent Golgi-to-ER retrograde traffic | 99 | 3.81e-01 | 0.050900 | 7.52e-01 |
| Downstream TCR signaling | 92 | 3.99e-01 | 0.050900 | 7.66e-01 |
| Transport of Mature mRNA derived from an Intron-Containing Transcript | 67 | 4.72e-01 | 0.050800 | 8.01e-01 |
| Signaling by TGFB family members | 121 | 3.36e-01 | 0.050600 | 7.26e-01 |
| Infectious disease | 848 | 1.22e-02 | 0.050500 | 1.40e-01 |
| Cyclin A/B1/B2 associated events during G2/M transition | 24 | 6.69e-01 | 0.050500 | 9.05e-01 |
| Ras activation upon Ca2+ influx through NMDA receptor | 19 | 7.05e-01 | 0.050100 | 9.10e-01 |
| Downstream signaling of activated FGFR4 | 26 | 6.59e-01 | 0.050000 | 8.96e-01 |
| Elevation of cytosolic Ca2+ levels | 16 | 7.29e-01 | -0.050000 | 9.14e-01 |
| Transcriptional regulation of pluripotent stem cells | 30 | 6.36e-01 | 0.050000 | 8.84e-01 |
| Metabolism of carbohydrates | 281 | 1.50e-01 | 0.049900 | 5.06e-01 |
| GABA receptor activation | 57 | 5.16e-01 | -0.049800 | 8.21e-01 |
| Signaling by CSF1 (M-CSF) in myeloid cells | 30 | 6.40e-01 | -0.049300 | 8.85e-01 |
| Immune System | 1921 | 3.52e-04 | -0.048900 | 1.05e-02 |
| Phase I - Functionalization of compounds | 100 | 3.98e-01 | 0.048900 | 7.65e-01 |
| RHO GTPase cycle | 419 | 8.88e-02 | -0.048400 | 3.90e-01 |
| Paradoxical activation of RAF signaling by kinase inactive BRAF | 43 | 5.83e-01 | -0.048300 | 8.56e-01 |
| Signaling by RAS mutants | 43 | 5.83e-01 | -0.048300 | 8.56e-01 |
| Signaling by moderate kinase activity BRAF mutants | 43 | 5.83e-01 | -0.048300 | 8.56e-01 |
| Signaling downstream of RAS mutants | 43 | 5.83e-01 | -0.048300 | 8.56e-01 |
| RHOBTB GTPase Cycle | 34 | 6.27e-01 | -0.048100 | 8.76e-01 |
| Signaling by VEGF | 103 | 4.00e-01 | 0.048000 | 7.66e-01 |
| Visual phototransduction | 93 | 4.24e-01 | 0.047900 | 7.83e-01 |
| Signaling by Receptor Tyrosine Kinases | 511 | 6.42e-02 | 0.047800 | 3.37e-01 |
| Nuclear Envelope (NE) Reassembly | 73 | 4.83e-01 | 0.047500 | 8.07e-01 |
| CS/DS degradation | 12 | 7.76e-01 | 0.047500 | 9.27e-01 |
| Signal transduction by L1 | 20 | 7.16e-01 | 0.047100 | 9.11e-01 |
| SUMOylation of transcription cofactors | 43 | 5.98e-01 | 0.046400 | 8.65e-01 |
| STING mediated induction of host immune responses | 13 | 7.73e-01 | -0.046300 | 9.27e-01 |
| Regulation of lipid metabolism by PPARalpha | 116 | 3.89e-01 | 0.046300 | 7.61e-01 |
| Golgi-to-ER retrograde transport | 133 | 3.58e-01 | 0.046200 | 7.40e-01 |
| Deregulated CDK5 triggers multiple neurodegenerative pathways in Alzheimer’s disease models | 22 | 7.08e-01 | 0.046100 | 9.10e-01 |
| Neurodegenerative Diseases | 22 | 7.08e-01 | 0.046100 | 9.10e-01 |
| Platelet homeostasis | 85 | 4.62e-01 | -0.046100 | 7.91e-01 |
| Condensation of Prophase Chromosomes | 12 | 7.82e-01 | -0.046100 | 9.30e-01 |
| Nuclear import of Rev protein | 32 | 6.53e-01 | -0.045900 | 8.94e-01 |
| NRAGE signals death through JNK | 53 | 5.64e-01 | -0.045900 | 8.48e-01 |
| Reproduction | 94 | 4.44e-01 | -0.045700 | 7.84e-01 |
| Activation of Matrix Metalloproteinases | 31 | 6.60e-01 | 0.045600 | 8.96e-01 |
| Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs) | 117 | 3.96e-01 | -0.045400 | 7.65e-01 |
| Metabolism of proteins | 1777 | 1.40e-03 | 0.045300 | 3.12e-02 |
| GABA synthesis, release, reuptake and degradation | 19 | 7.33e-01 | 0.045300 | 9.15e-01 |
| Stimuli-sensing channels | 101 | 4.33e-01 | 0.045100 | 7.84e-01 |
| POU5F1 (OCT4), SOX2, NANOG activate genes related to proliferation | 12 | 7.87e-01 | 0.045000 | 9.30e-01 |
| Mitotic G2-G2/M phases | 191 | 2.85e-01 | 0.044800 | 6.89e-01 |
| Innate Immune System | 999 | 1.66e-02 | -0.044600 | 1.69e-01 |
| G2/M Transition | 189 | 2.91e-01 | 0.044600 | 6.91e-01 |
| Negative regulation of MAPK pathway | 41 | 6.24e-01 | 0.044300 | 8.76e-01 |
| Glutamate binding, activation of AMPA receptors and synaptic plasticity | 29 | 6.80e-01 | 0.044300 | 9.08e-01 |
| Trafficking of AMPA receptors | 29 | 6.80e-01 | 0.044300 | 9.08e-01 |
| Cell junction organization | 107 | 4.32e-01 | 0.044000 | 7.84e-01 |
| Sensory processing of sound by outer hair cells of the cochlea | 51 | 5.89e-01 | 0.043800 | 8.60e-01 |
| G alpha (12/13) signalling events | 74 | 5.17e-01 | -0.043600 | 8.21e-01 |
| RUNX1 regulates genes involved in megakaryocyte differentiation and platelet function | 37 | 6.47e-01 | -0.043500 | 8.90e-01 |
| Activation of the phototransduction cascade | 11 | 8.03e-01 | 0.043400 | 9.30e-01 |
| CREB1 phosphorylation through NMDA receptor-mediated activation of RAS signaling | 25 | 7.08e-01 | 0.043300 | 9.10e-01 |
| Collagen degradation | 61 | 5.64e-01 | -0.042700 | 8.48e-01 |
| PPARA activates gene expression | 114 | 4.31e-01 | 0.042700 | 7.84e-01 |
| RAF activation | 33 | 6.72e-01 | 0.042600 | 9.06e-01 |
| Formation of definitive endoderm | 15 | 7.76e-01 | 0.042500 | 9.27e-01 |
| Arachidonic acid metabolism | 56 | 5.83e-01 | 0.042500 | 8.56e-01 |
| Protein-protein interactions at synapses | 78 | 5.17e-01 | 0.042400 | 8.21e-01 |
| Resolution of Sister Chromatid Cohesion | 116 | 4.31e-01 | 0.042300 | 7.84e-01 |
| Z-decay: degradation of maternal mRNAs by zygotically expressed factors | 12 | 8.00e-01 | -0.042200 | 9.30e-01 |
| Synthesis of PIPs at the Golgi membrane | 17 | 7.64e-01 | -0.042100 | 9.26e-01 |
| Chaperonin-mediated protein folding | 88 | 4.96e-01 | -0.042000 | 8.17e-01 |
| RIPK1-mediated regulated necrosis | 30 | 6.91e-01 | 0.041900 | 9.08e-01 |
| Regulation of necroptotic cell death | 30 | 6.91e-01 | 0.041900 | 9.08e-01 |
| Synthesis of IP2, IP, and Ins in the cytosol | 13 | 7.94e-01 | 0.041800 | 9.30e-01 |
| Disease | 1584 | 5.35e-03 | 0.041700 | 7.94e-02 |
| TP53 Regulates Transcription of Cell Death Genes | 42 | 6.40e-01 | -0.041700 | 8.85e-01 |
| MASTL Facilitates Mitotic Progression | 10 | 8.20e-01 | 0.041500 | 9.36e-01 |
| WNT5A-dependent internalization of FZD2, FZD5 and ROR2 | 13 | 7.96e-01 | -0.041300 | 9.30e-01 |
| Signaling by RAF1 mutants | 39 | 6.57e-01 | -0.041100 | 8.95e-01 |
| CD28 co-stimulation | 32 | 6.88e-01 | -0.041000 | 9.08e-01 |
| FRS-mediated FGFR4 signaling | 21 | 7.45e-01 | 0.040900 | 9.18e-01 |
| Oncogenic MAPK signaling | 78 | 5.32e-01 | -0.040900 | 8.31e-01 |
| NFE2L2 regulating tumorigenic genes | 11 | 8.14e-01 | 0.040900 | 9.33e-01 |
| Pyruvate metabolism and Citric Acid (TCA) cycle | 52 | 6.10e-01 | 0.040900 | 8.70e-01 |
| Meiotic synapsis | 32 | 6.90e-01 | 0.040700 | 9.08e-01 |
| Insulin receptor signalling cascade | 53 | 6.08e-01 | 0.040700 | 8.68e-01 |
| Peroxisomal lipid metabolism | 28 | 7.09e-01 | 0.040700 | 9.11e-01 |
| Ca2+ pathway | 62 | 5.80e-01 | -0.040600 | 8.56e-01 |
| PIP3 activates AKT signaling | 276 | 2.47e-01 | 0.040500 | 6.43e-01 |
| Nuclear signaling by ERBB4 | 32 | 6.92e-01 | -0.040400 | 9.08e-01 |
| Paracetamol ADME | 27 | 7.16e-01 | -0.040400 | 9.11e-01 |
| Phospholipid metabolism | 192 | 3.35e-01 | 0.040300 | 7.26e-01 |
| Postmitotic nuclear pore complex (NPC) reformation | 26 | 7.22e-01 | 0.040300 | 9.11e-01 |
| Blood group systems biosynthesis | 22 | 7.44e-01 | -0.040200 | 9.18e-01 |
| TNFR1-induced proapoptotic signaling | 24 | 7.33e-01 | 0.040200 | 9.15e-01 |
| Meiosis | 56 | 6.03e-01 | -0.040200 | 8.66e-01 |
| Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding | 32 | 6.95e-01 | 0.040000 | 9.09e-01 |
| Rev-mediated nuclear export of HIV RNA | 33 | 6.92e-01 | -0.039800 | 9.08e-01 |
| Defective GALNT12 causes CRCS1 | 18 | 7.70e-01 | 0.039700 | 9.27e-01 |
| Formation of the cornified envelope | 127 | 4.41e-01 | -0.039600 | 7.84e-01 |
| FLT3 Signaling | 38 | 6.73e-01 | -0.039500 | 9.06e-01 |
| Interaction between L1 and Ankyrins | 30 | 7.08e-01 | 0.039500 | 9.10e-01 |
| Negative regulation of the PI3K/AKT network | 111 | 4.72e-01 | -0.039500 | 8.01e-01 |
| Phase II - Conjugation of compounds | 106 | 4.82e-01 | -0.039500 | 8.07e-01 |
| Anti-inflammatory response favouring Leishmania parasite infection | 75 | 5.55e-01 | -0.039400 | 8.43e-01 |
| Leishmania parasite growth and survival | 75 | 5.55e-01 | -0.039400 | 8.43e-01 |
| Biotin transport and metabolism | 10 | 8.30e-01 | 0.039300 | 9.40e-01 |
| Heme biosynthesis | 13 | 8.06e-01 | -0.039300 | 9.30e-01 |
| Nucleotide catabolism | 35 | 6.90e-01 | 0.039000 | 9.08e-01 |
| PKA activation | 18 | 7.76e-01 | -0.038700 | 9.27e-01 |
| Costimulation by the CD28 family | 65 | 5.91e-01 | -0.038500 | 8.62e-01 |
| Fatty acid metabolism | 168 | 3.90e-01 | 0.038400 | 7.62e-01 |
| APC truncation mutants have impaired AXIN binding | 13 | 8.11e-01 | -0.038400 | 9.30e-01 |
| AXIN missense mutants destabilize the destruction complex | 13 | 8.11e-01 | -0.038400 | 9.30e-01 |
| Signaling by AMER1 mutants | 13 | 8.11e-01 | -0.038400 | 9.30e-01 |
| Signaling by APC mutants | 13 | 8.11e-01 | -0.038400 | 9.30e-01 |
| Signaling by AXIN mutants | 13 | 8.11e-01 | -0.038400 | 9.30e-01 |
| Truncations of AMER1 destabilize the destruction complex | 13 | 8.11e-01 | -0.038400 | 9.30e-01 |
| Purine catabolism | 17 | 7.84e-01 | 0.038400 | 9.30e-01 |
| PI-3K cascade:FGFR4 | 19 | 7.72e-01 | 0.038300 | 9.27e-01 |
| Interleukin-17 signaling | 66 | 5.90e-01 | 0.038300 | 8.61e-01 |
| Response to metal ions | 14 | 8.04e-01 | -0.038300 | 9.30e-01 |
| Transcriptional regulation of white adipocyte differentiation | 81 | 5.53e-01 | 0.038100 | 8.43e-01 |
| ER-Phagosome pathway | 87 | 5.40e-01 | 0.038000 | 8.37e-01 |
| Regulation of insulin secretion | 77 | 5.69e-01 | 0.037500 | 8.52e-01 |
| HS-GAG biosynthesis | 28 | 7.32e-01 | 0.037400 | 9.14e-01 |
| Opioid Signalling | 88 | 5.45e-01 | -0.037300 | 8.40e-01 |
| Regulation of RUNX1 Expression and Activity | 25 | 7.47e-01 | -0.037300 | 9.19e-01 |
| Extracellular matrix organization | 292 | 2.74e-01 | 0.037200 | 6.75e-01 |
| tRNA processing in the nucleus | 55 | 6.34e-01 | 0.037100 | 8.82e-01 |
| Hyaluronan uptake and degradation | 12 | 8.24e-01 | 0.037100 | 9.37e-01 |
| Golgi Associated Vesicle Biogenesis | 51 | 6.48e-01 | -0.036900 | 8.90e-01 |
| ECM proteoglycans | 73 | 5.87e-01 | -0.036800 | 8.59e-01 |
| RHOF GTPase cycle | 40 | 6.88e-01 | -0.036700 | 9.08e-01 |
| VEGFA-VEGFR2 Pathway | 95 | 5.38e-01 | 0.036600 | 8.36e-01 |
| Signaling by MET | 78 | 5.78e-01 | 0.036400 | 8.56e-01 |
| Chromatin modifying enzymes | 185 | 3.96e-01 | 0.036200 | 7.65e-01 |
| Chromatin organization | 185 | 3.96e-01 | 0.036200 | 7.65e-01 |
| Glucagon signaling in metabolic regulation | 32 | 7.23e-01 | -0.036200 | 9.11e-01 |
| Sialic acid metabolism | 33 | 7.20e-01 | -0.036100 | 9.11e-01 |
| TFAP2 (AP-2) family regulates transcription of growth factors and their receptors | 12 | 8.29e-01 | -0.036100 | 9.39e-01 |
| Class B/2 (Secretin family receptors) | 93 | 5.48e-01 | 0.036000 | 8.41e-01 |
| Serotonin Neurotransmitter Release Cycle | 16 | 8.05e-01 | 0.035700 | 9.30e-01 |
| Transport of small molecules | 694 | 1.10e-01 | 0.035500 | 4.30e-01 |
| G alpha (s) signalling events | 154 | 4.47e-01 | -0.035500 | 7.86e-01 |
| Amine ligand-binding receptors | 41 | 6.95e-01 | 0.035400 | 9.09e-01 |
| Prefoldin mediated transfer of substrate to CCT/TriC | 27 | 7.50e-01 | 0.035400 | 9.20e-01 |
| Interferon alpha/beta signaling | 74 | 5.99e-01 | -0.035300 | 8.65e-01 |
| Circadian Clock | 69 | 6.12e-01 | 0.035300 | 8.70e-01 |
| Hyaluronan metabolism | 17 | 8.02e-01 | 0.035200 | 9.30e-01 |
| TRP channels | 27 | 7.54e-01 | 0.034800 | 9.20e-01 |
| Death Receptor Signaling | 143 | 4.73e-01 | 0.034800 | 8.01e-01 |
| Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane | 10 | 8.50e-01 | 0.034600 | 9.51e-01 |
| Pre-NOTCH Transcription and Translation | 45 | 6.89e-01 | 0.034500 | 9.08e-01 |
| Assembly and cell surface presentation of NMDA receptors | 41 | 7.02e-01 | -0.034500 | 9.10e-01 |
| Centrosome maturation | 76 | 6.05e-01 | -0.034300 | 8.66e-01 |
| Recruitment of mitotic centrosome proteins and complexes | 76 | 6.05e-01 | -0.034300 | 8.66e-01 |
| tRNA Aminoacylation | 24 | 7.72e-01 | -0.034200 | 9.27e-01 |
| Platelet sensitization by LDL | 17 | 8.07e-01 | -0.034100 | 9.30e-01 |
| Endosomal/Vacuolar pathway | 12 | 8.40e-01 | 0.033600 | 9.45e-01 |
| RAF-independent MAPK1/3 activation | 22 | 7.87e-01 | 0.033300 | 9.30e-01 |
| Synthesis, secretion, and deacylation of Ghrelin | 19 | 8.01e-01 | 0.033300 | 9.30e-01 |
| Oxidative Stress Induced Senescence | 66 | 6.40e-01 | -0.033200 | 8.85e-01 |
| Repression of WNT target genes | 13 | 8.36e-01 | 0.033200 | 9.43e-01 |
| Processing of Intronless Pre-mRNAs | 19 | 8.03e-01 | 0.033000 | 9.30e-01 |
| Signaling by FGFR in disease | 61 | 6.57e-01 | 0.032900 | 8.95e-01 |
| Mitochondrial tRNA aminoacylation | 18 | 8.10e-01 | 0.032700 | 9.30e-01 |
| Diseases of DNA repair | 49 | 6.92e-01 | 0.032700 | 9.08e-01 |
| G alpha (z) signalling events | 48 | 6.97e-01 | -0.032500 | 9.09e-01 |
| RHOC GTPase cycle | 69 | 6.41e-01 | -0.032400 | 8.86e-01 |
| Membrane Trafficking | 605 | 1.74e-01 | 0.032300 | 5.50e-01 |
| Signaling by Hippo | 19 | 8.09e-01 | -0.032100 | 9.30e-01 |
| Transport of connexons to the plasma membrane | 20 | 8.04e-01 | -0.032000 | 9.30e-01 |
| Transcriptional regulation by RUNX1 | 182 | 4.60e-01 | 0.031700 | 7.91e-01 |
| HDR through Single Strand Annealing (SSA) | 36 | 7.42e-01 | 0.031700 | 9.18e-01 |
| Glycolysis | 70 | 6.48e-01 | 0.031500 | 8.90e-01 |
| Developmental Biology | 1158 | 6.99e-02 | 0.031500 | 3.43e-01 |
| Glycogen breakdown (glycogenolysis) | 11 | 8.57e-01 | 0.031400 | 9.52e-01 |
| NOTCH4 Intracellular Domain Regulates Transcription | 19 | 8.13e-01 | 0.031300 | 9.32e-01 |
| Deposition of new CENPA-containing nucleosomes at the centromere | 26 | 7.82e-01 | 0.031300 | 9.30e-01 |
| Nucleosome assembly | 26 | 7.82e-01 | 0.031300 | 9.30e-01 |
| Acetylcholine Neurotransmitter Release Cycle | 16 | 8.28e-01 | 0.031300 | 9.39e-01 |
| SLC transporter disorders | 92 | 6.12e-01 | 0.030600 | 8.70e-01 |
| C-type lectin receptors (CLRs) | 137 | 5.37e-01 | 0.030500 | 8.36e-01 |
| PERK regulates gene expression | 32 | 7.67e-01 | 0.030200 | 9.27e-01 |
| Interleukin-6 family signaling | 24 | 7.98e-01 | -0.030100 | 9.30e-01 |
| Cholesterol biosynthesis | 24 | 7.99e-01 | -0.030000 | 9.30e-01 |
| SARS-CoV Infections | 386 | 3.11e-01 | 0.030000 | 7.00e-01 |
| Serotonin receptors | 11 | 8.63e-01 | -0.030000 | 9.52e-01 |
| Notch-HLH transcription pathway | 24 | 7.99e-01 | -0.030000 | 9.30e-01 |
| Negative regulation of FLT3 | 15 | 8.42e-01 | 0.029700 | 9.47e-01 |
| Diseases associated with glycosaminoglycan metabolism | 38 | 7.52e-01 | -0.029600 | 9.20e-01 |
| alpha-linolenic (omega3) and linoleic (omega6) acid metabolism | 12 | 8.60e-01 | 0.029500 | 9.52e-01 |
| alpha-linolenic acid (ALA) metabolism | 12 | 8.60e-01 | 0.029500 | 9.52e-01 |
| Synthesis of very long-chain fatty acyl-CoAs | 23 | 8.07e-01 | -0.029400 | 9.30e-01 |
| tRNA modification in the nucleus and cytosol | 38 | 7.55e-01 | -0.029300 | 9.20e-01 |
| Pyruvate metabolism | 29 | 7.86e-01 | -0.029100 | 9.30e-01 |
| Nonhomologous End-Joining (NHEJ) | 32 | 7.76e-01 | 0.029000 | 9.27e-01 |
| RHOB GTPase cycle | 66 | 6.84e-01 | -0.029000 | 9.08e-01 |
| Response of EIF2AK1 (HRI) to heme deficiency | 14 | 8.52e-01 | 0.028700 | 9.51e-01 |
| M-decay: degradation of maternal mRNAs by maternally stored factors | 45 | 7.39e-01 | 0.028700 | 9.18e-01 |
| EGR2 and SOX10-mediated initiation of Schwann cell myelination | 27 | 7.97e-01 | -0.028700 | 9.30e-01 |
| Ovarian tumor domain proteases | 35 | 7.69e-01 | -0.028600 | 9.27e-01 |
| Retrograde neurotrophin signalling | 14 | 8.53e-01 | -0.028600 | 9.51e-01 |
| Neuronal System | 389 | 3.35e-01 | 0.028400 | 7.26e-01 |
| Intrinsic Pathway for Apoptosis | 52 | 7.25e-01 | 0.028200 | 9.11e-01 |
| Neurotransmitter receptors and postsynaptic signal transmission | 193 | 5.01e-01 | -0.028100 | 8.18e-01 |
| Nicotinate metabolism | 29 | 7.94e-01 | 0.028000 | 9.30e-01 |
| Cargo trafficking to the periciliary membrane | 49 | 7.35e-01 | -0.027900 | 9.16e-01 |
| The NLRP3 inflammasome | 16 | 8.47e-01 | -0.027900 | 9.51e-01 |
| The canonical retinoid cycle in rods (twilight vision) | 23 | 8.17e-01 | 0.027900 | 9.35e-01 |
| Adherens junctions interactions | 52 | 7.28e-01 | 0.027900 | 9.14e-01 |
| MyD88-independent TLR4 cascade | 103 | 6.27e-01 | 0.027700 | 8.76e-01 |
| TRIF(TICAM1)-mediated TLR4 signaling | 103 | 6.27e-01 | 0.027700 | 8.76e-01 |
| Signaling by WNT | 263 | 4.39e-01 | 0.027700 | 7.84e-01 |
| trans-Golgi Network Vesicle Budding | 67 | 6.97e-01 | -0.027500 | 9.09e-01 |
| Viral Messenger RNA Synthesis | 42 | 7.58e-01 | 0.027400 | 9.22e-01 |
| HuR (ELAVL1) binds and stabilizes mRNA | 10 | 8.81e-01 | -0.027400 | 9.56e-01 |
| Glucagon-type ligand receptors | 32 | 7.89e-01 | 0.027400 | 9.30e-01 |
| Signaling by PDGF | 57 | 7.22e-01 | -0.027200 | 9.11e-01 |
| Rap1 signalling | 16 | 8.51e-01 | 0.027100 | 9.51e-01 |
| SUMOylation of SUMOylation proteins | 33 | 7.88e-01 | -0.027100 | 9.30e-01 |
| Semaphorin interactions | 61 | 7.15e-01 | 0.027100 | 9.11e-01 |
| SUMOylation of DNA methylation proteins | 16 | 8.54e-01 | -0.026600 | 9.51e-01 |
| Interleukin-1 family signaling | 145 | 5.80e-01 | 0.026600 | 8.56e-01 |
| Platelet degranulation | 115 | 6.23e-01 | -0.026500 | 8.76e-01 |
| Cilium Assembly | 185 | 5.38e-01 | -0.026300 | 8.36e-01 |
| Leishmania infection | 157 | 5.71e-01 | -0.026200 | 8.52e-01 |
| Parasitic Infection Pathways | 157 | 5.71e-01 | -0.026200 | 8.52e-01 |
| Crosslinking of collagen fibrils | 16 | 8.56e-01 | 0.026100 | 9.52e-01 |
| PI Metabolism | 79 | 6.88e-01 | -0.026100 | 9.08e-01 |
| Ephrin signaling | 17 | 8.53e-01 | 0.026000 | 9.51e-01 |
| Aquaporin-mediated transport | 51 | 7.48e-01 | -0.026000 | 9.19e-01 |
| EML4 and NUDC in mitotic spindle formation | 111 | 6.39e-01 | 0.025800 | 8.85e-01 |
| RND2 GTPase cycle | 41 | 7.75e-01 | -0.025800 | 9.27e-01 |
| Nucleotide-binding domain, leucine rich repeat containing receptor (NLR) signaling pathways | 53 | 7.46e-01 | 0.025700 | 9.19e-01 |
| Intracellular signaling by second messengers | 314 | 4.33e-01 | 0.025700 | 7.84e-01 |
| Regulation of IFNG signaling | 14 | 8.69e-01 | 0.025500 | 9.52e-01 |
| Physiological factors | 14 | 8.70e-01 | 0.025300 | 9.52e-01 |
| Anchoring of the basal body to the plasma membrane | 92 | 6.76e-01 | -0.025200 | 9.06e-01 |
| TP53 Regulates Transcription of Genes Involved in Cytochrome C Release | 19 | 8.49e-01 | -0.025200 | 9.51e-01 |
| Deadenylation-dependent mRNA decay | 53 | 7.53e-01 | 0.025000 | 9.20e-01 |
| SUMOylation | 165 | 5.80e-01 | -0.024900 | 8.56e-01 |
| RHO GTPases Activate WASPs and WAVEs | 34 | 8.03e-01 | 0.024700 | 9.30e-01 |
| Post-translational protein modification | 1313 | 1.31e-01 | 0.024700 | 4.76e-01 |
| Signaling by Type 1 Insulin-like Growth Factor 1 Receptor (IGF1R) | 52 | 7.59e-01 | 0.024600 | 9.22e-01 |
| Interactions of Rev with host cellular proteins | 35 | 8.01e-01 | -0.024600 | 9.30e-01 |
| Microtubule-dependent trafficking of connexons from Golgi to the plasma membrane | 19 | 8.53e-01 | -0.024500 | 9.51e-01 |
| Mismatch repair (MMR) directed by MSH2:MSH3 (MutSbeta) | 14 | 8.74e-01 | 0.024500 | 9.54e-01 |
| Integrin signaling | 27 | 8.26e-01 | -0.024500 | 9.38e-01 |
| Recycling pathway of L1 | 43 | 7.82e-01 | -0.024400 | 9.30e-01 |
| Response to elevated platelet cytosolic Ca2+ | 120 | 6.47e-01 | -0.024200 | 8.90e-01 |
| Interferon gamma signaling | 93 | 6.87e-01 | -0.024200 | 9.08e-01 |
| DSCAM interactions | 11 | 8.90e-01 | -0.024100 | 9.62e-01 |
| RUNX2 regulates bone development | 29 | 8.23e-01 | 0.024000 | 9.37e-01 |
| FCGR3A-mediated phagocytosis | 57 | 7.55e-01 | 0.023900 | 9.20e-01 |
| Leishmania phagocytosis | 57 | 7.55e-01 | 0.023900 | 9.20e-01 |
| Parasite infection | 57 | 7.55e-01 | 0.023900 | 9.20e-01 |
| SUMOylation of DNA replication proteins | 44 | 7.84e-01 | 0.023900 | 9.30e-01 |
| Digestion | 18 | 8.61e-01 | -0.023800 | 9.52e-01 |
| HDMs demethylate histones | 18 | 8.64e-01 | -0.023400 | 9.52e-01 |
| PD-1 signaling | 21 | 8.55e-01 | 0.023100 | 9.51e-01 |
| Anchoring fibril formation | 13 | 8.86e-01 | 0.022900 | 9.61e-01 |
| Bacterial Infection Pathways | 68 | 7.44e-01 | 0.022900 | 9.18e-01 |
| Processing of SMDT1 | 15 | 8.78e-01 | -0.022800 | 9.56e-01 |
| Sphingolipid metabolism | 83 | 7.19e-01 | -0.022800 | 9.11e-01 |
| Downstream signal transduction | 29 | 8.31e-01 | 0.022800 | 9.41e-01 |
| Transport to the Golgi and subsequent modification | 183 | 5.95e-01 | 0.022800 | 8.64e-01 |
| TNF receptor superfamily (TNFSF) members mediating non-canonical NF-kB pathway | 16 | 8.75e-01 | -0.022700 | 9.55e-01 |
| Vitamin D (calciferol) metabolism | 12 | 8.92e-01 | -0.022700 | 9.62e-01 |
| Carnitine metabolism | 13 | 8.89e-01 | 0.022400 | 9.62e-01 |
| IGF1R signaling cascade | 51 | 7.83e-01 | 0.022300 | 9.30e-01 |
| Glycosphingolipid metabolism | 42 | 8.06e-01 | 0.021900 | 9.30e-01 |
| Aflatoxin activation and detoxification | 19 | 8.69e-01 | 0.021800 | 9.52e-01 |
| TRAF6 mediated NF-kB activation | 23 | 8.57e-01 | 0.021800 | 9.52e-01 |
| ZBP1(DAI) mediated induction of type I IFNs | 20 | 8.66e-01 | -0.021700 | 9.52e-01 |
| Vesicle-mediated transport | 643 | 3.46e-01 | 0.021700 | 7.29e-01 |
| Neurexins and neuroligins | 52 | 7.87e-01 | -0.021700 | 9.30e-01 |
| Activation of ATR in response to replication stress | 37 | 8.21e-01 | 0.021500 | 9.37e-01 |
| SUMO E3 ligases SUMOylate target proteins | 159 | 6.40e-01 | -0.021500 | 8.85e-01 |
| Fcgamma receptor (FCGR) dependent phagocytosis | 82 | 7.38e-01 | 0.021400 | 9.17e-01 |
| Chondroitin sulfate/dermatan sulfate metabolism | 45 | 8.05e-01 | 0.021200 | 9.30e-01 |
| Translocation of ZAP-70 to Immunological synapse | 17 | 8.80e-01 | -0.021200 | 9.56e-01 |
| GPER1 signaling | 45 | 8.07e-01 | 0.021000 | 9.30e-01 |
| Pre-NOTCH Expression and Processing | 61 | 7.78e-01 | 0.020900 | 9.28e-01 |
| PI3K/AKT Signaling in Cancer | 103 | 7.14e-01 | -0.020900 | 9.11e-01 |
| Collagen biosynthesis and modifying enzymes | 65 | 7.71e-01 | 0.020900 | 9.27e-01 |
| Gastrin-CREB signalling pathway via PKC and MAPK | 17 | 8.82e-01 | 0.020700 | 9.57e-01 |
| Collagen formation | 88 | 7.37e-01 | 0.020700 | 9.17e-01 |
| Collagen chain trimerization | 42 | 8.20e-01 | -0.020300 | 9.36e-01 |
| Telomere Extension By Telomerase | 22 | 8.70e-01 | 0.020200 | 9.52e-01 |
| NR1H2 and NR1H3-mediated signaling | 53 | 7.99e-01 | 0.020200 | 9.30e-01 |
| IRS-related events triggered by IGF1R | 50 | 8.05e-01 | 0.020200 | 9.30e-01 |
| Signaling by Retinoic Acid | 41 | 8.23e-01 | 0.020200 | 9.37e-01 |
| Non-integrin membrane-ECM interactions | 55 | 7.96e-01 | 0.020100 | 9.30e-01 |
| Interleukin-12 family signaling | 53 | 8.00e-01 | -0.020100 | 9.30e-01 |
| Rab regulation of trafficking | 113 | 7.13e-01 | 0.020100 | 9.11e-01 |
| SLBP independent Processing of Histone Pre-mRNAs | 10 | 9.13e-01 | 0.020000 | 9.69e-01 |
| SARS-CoV-1 activates/modulates innate immune responses | 36 | 8.36e-01 | 0.020000 | 9.43e-01 |
| Long-term potentiation | 22 | 8.71e-01 | -0.020000 | 9.52e-01 |
| Growth hormone receptor signaling | 24 | 8.68e-01 | 0.019700 | 9.52e-01 |
| Defects in vitamin and cofactor metabolism | 20 | 8.81e-01 | 0.019400 | 9.56e-01 |
| SARS-CoV-2-host interactions | 185 | 6.51e-01 | 0.019200 | 8.93e-01 |
| PKA activation in glucagon signalling | 17 | 8.91e-01 | 0.019200 | 9.62e-01 |
| HCMV Late Events | 54 | 8.07e-01 | -0.019200 | 9.30e-01 |
| Beta-catenin independent WNT signaling | 144 | 6.94e-01 | 0.019000 | 9.09e-01 |
| TRAF6-mediated induction of TAK1 complex within TLR4 complex | 15 | 9.01e-01 | -0.018600 | 9.65e-01 |
| Integrin cell surface interactions | 83 | 7.70e-01 | -0.018500 | 9.27e-01 |
| FGFR2b ligand binding and activation | 10 | 9.20e-01 | 0.018400 | 9.69e-01 |
| Early SARS-CoV-2 Infection Events | 34 | 8.54e-01 | 0.018200 | 9.51e-01 |
| PI5P, PP2A and IER3 Regulate PI3K/AKT Signaling | 104 | 7.50e-01 | -0.018100 | 9.20e-01 |
| Basigin interactions | 24 | 8.80e-01 | 0.017900 | 9.56e-01 |
| Metalloprotease DUBs | 19 | 8.95e-01 | 0.017500 | 9.62e-01 |
| Nucleotide-like (purinergic) receptors | 13 | 9.13e-01 | -0.017400 | 9.69e-01 |
| RND1 GTPase cycle | 41 | 8.48e-01 | -0.017300 | 9.51e-01 |
| Late SARS-CoV-2 Infection Events | 67 | 8.07e-01 | 0.017300 | 9.30e-01 |
| Dermatan sulfate biosynthesis | 10 | 9.25e-01 | 0.017300 | 9.69e-01 |
| Translation of Structural Proteins 9694635 | 55 | 8.25e-01 | -0.017300 | 9.37e-01 |
| Apoptotic execution phase | 43 | 8.45e-01 | -0.017200 | 9.49e-01 |
| Peptide hormone biosynthesis | 11 | 9.22e-01 | 0.017000 | 9.69e-01 |
| Ub-specific processing proteases | 152 | 7.18e-01 | 0.017000 | 9.11e-01 |
| AURKA Activation by TPX2 | 68 | 8.14e-01 | 0.016500 | 9.32e-01 |
| Toll-like Receptor Cascades | 157 | 7.24e-01 | -0.016300 | 9.11e-01 |
| Defective C1GALT1C1 causes TNPS | 18 | 9.05e-01 | 0.016300 | 9.68e-01 |
| RHOA GTPase cycle | 140 | 7.42e-01 | -0.016100 | 9.18e-01 |
| Ion channel transport | 173 | 7.15e-01 | 0.016100 | 9.11e-01 |
| Synthesis of PA | 35 | 8.70e-01 | -0.016000 | 9.52e-01 |
| Metallothioneins bind metals | 11 | 9.27e-01 | -0.016000 | 9.70e-01 |
| Inwardly rectifying K+ channels | 35 | 8.70e-01 | -0.016000 | 9.52e-01 |
| Mitotic Prometaphase | 188 | 7.06e-01 | 0.016000 | 9.10e-01 |
| Signaling by ERBB2 in Cancer | 25 | 8.90e-01 | -0.016000 | 9.62e-01 |
| Free fatty acids regulate insulin secretion | 10 | 9.31e-01 | -0.015800 | 9.70e-01 |
| E3 ubiquitin ligases ubiquitinate target proteins | 42 | 8.61e-01 | -0.015600 | 9.52e-01 |
| Polo-like kinase mediated events | 16 | 9.14e-01 | 0.015600 | 9.69e-01 |
| Toll Like Receptor 4 (TLR4) Cascade | 138 | 7.52e-01 | -0.015600 | 9.20e-01 |
| Cellular Senescence | 130 | 7.63e-01 | 0.015300 | 9.25e-01 |
| Infection with Mycobacterium tuberculosis | 25 | 8.95e-01 | 0.015200 | 9.62e-01 |
| Chromatin modifications during the maternal to zygotic transition (MZT) | 11 | 9.31e-01 | -0.015100 | 9.70e-01 |
| Metabolism of water-soluble vitamins and cofactors | 121 | 7.75e-01 | 0.015000 | 9.27e-01 |
| MET activates RAS signaling | 11 | 9.31e-01 | -0.015000 | 9.70e-01 |
| Dopamine Neurotransmitter Release Cycle | 20 | 9.08e-01 | 0.015000 | 9.69e-01 |
| Fc epsilon receptor (FCERI) signaling | 126 | 7.72e-01 | 0.014900 | 9.27e-01 |
| Mitochondrial protein import | 54 | 8.49e-01 | -0.014900 | 9.51e-01 |
| FCGR activation | 12 | 9.29e-01 | -0.014900 | 9.70e-01 |
| Presynaptic nicotinic acetylcholine receptors | 12 | 9.29e-01 | -0.014800 | 9.70e-01 |
| Signaling by CSF3 (G-CSF) | 28 | 8.93e-01 | 0.014700 | 9.62e-01 |
| Glycosaminoglycan metabolism | 120 | 7.83e-01 | 0.014600 | 9.30e-01 |
| Apoptosis | 164 | 7.48e-01 | 0.014500 | 9.19e-01 |
| Activation of AMPK downstream of NMDARs | 28 | 8.95e-01 | 0.014400 | 9.62e-01 |
| Diseases of programmed cell death | 43 | 8.71e-01 | -0.014400 | 9.52e-01 |
| VEGFR2 mediated vascular permeability | 26 | 8.99e-01 | -0.014300 | 9.65e-01 |
| Downstream signaling of activated FGFR3 | 24 | 9.04e-01 | 0.014200 | 9.68e-01 |
| Formation of Senescence-Associated Heterochromatin Foci (SAHF) | 11 | 9.36e-01 | -0.013900 | 9.71e-01 |
| ISG15 antiviral mechanism | 71 | 8.40e-01 | 0.013900 | 9.45e-01 |
| Activation of GABAB receptors | 43 | 8.76e-01 | -0.013700 | 9.55e-01 |
| GABA B receptor activation | 43 | 8.76e-01 | -0.013700 | 9.55e-01 |
| DNA Damage/Telomere Stress Induced Senescence | 28 | 9.00e-01 | 0.013700 | 9.65e-01 |
| PI-3K cascade:FGFR3 | 17 | 9.23e-01 | -0.013600 | 9.69e-01 |
| IRS-mediated signalling | 47 | 8.74e-01 | 0.013300 | 9.54e-01 |
| RAC3 GTPase cycle | 84 | 8.34e-01 | -0.013200 | 9.42e-01 |
| Interleukin-4 and Interleukin-13 signaling | 104 | 8.20e-01 | -0.012900 | 9.36e-01 |
| Transcription of E2F targets under negative control by DREAM complex | 19 | 9.24e-01 | 0.012700 | 9.69e-01 |
| Diseases associated with N-glycosylation of proteins | 19 | 9.24e-01 | -0.012700 | 9.69e-01 |
| Signaling by NTRK2 (TRKB) | 25 | 9.15e-01 | -0.012400 | 9.69e-01 |
| Nucleotide salvage | 21 | 9.22e-01 | -0.012400 | 9.69e-01 |
| Cytochrome P450 - arranged by substrate type | 64 | 8.65e-01 | -0.012300 | 9.52e-01 |
| HATs acetylate histones | 71 | 8.60e-01 | 0.012100 | 9.52e-01 |
| O-linked glycosylation | 107 | 8.32e-01 | 0.011800 | 9.41e-01 |
| EPHB-mediated forward signaling | 41 | 8.98e-01 | -0.011600 | 9.64e-01 |
| HCMV Early Events | 73 | 8.65e-01 | -0.011500 | 9.52e-01 |
| Maternal to zygotic transition (MZT) | 76 | 8.65e-01 | 0.011300 | 9.52e-01 |
| Metabolism of lipids | 697 | 6.14e-01 | 0.011200 | 8.71e-01 |
| Activation of SMO | 17 | 9.36e-01 | -0.011200 | 9.71e-01 |
| L1CAM interactions | 112 | 8.38e-01 | 0.011200 | 9.45e-01 |
| Syndecan interactions | 26 | 9.23e-01 | 0.010900 | 9.69e-01 |
| Sealing of the nuclear envelope (NE) by ESCRT-III | 31 | 9.17e-01 | 0.010800 | 9.69e-01 |
| Transcriptional regulation of granulopoiesis | 31 | 9.17e-01 | -0.010700 | 9.69e-01 |
| Termination of O-glycan biosynthesis | 25 | 9.26e-01 | 0.010700 | 9.70e-01 |
| Apoptotic cleavage of cellular proteins | 35 | 9.14e-01 | -0.010500 | 9.69e-01 |
| Class I MHC mediated antigen processing & presentation | 361 | 7.31e-01 | -0.010500 | 9.14e-01 |
| Platelet Aggregation (Plug Formation) | 39 | 9.10e-01 | -0.010500 | 9.69e-01 |
| Transmission across Chemical Synapses | 255 | 7.74e-01 | -0.010400 | 9.27e-01 |
| Impaired BRCA2 binding to RAD51 | 33 | 9.17e-01 | 0.010400 | 9.69e-01 |
| Programmed Cell Death | 195 | 8.03e-01 | -0.010300 | 9.30e-01 |
| Cytoprotection by HMOX1 | 58 | 8.93e-01 | 0.010200 | 9.62e-01 |
| tRNA processing | 98 | 8.62e-01 | -0.010100 | 9.52e-01 |
| Cell-Cell communication | 144 | 8.34e-01 | -0.010100 | 9.42e-01 |
| Pentose phosphate pathway | 12 | 9.53e-01 | 0.009810 | 9.82e-01 |
| TCR signaling | 112 | 8.60e-01 | -0.009630 | 9.52e-01 |
| Signaling by Rho GTPases, Miro GTPases and RHOBTB3 | 619 | 6.90e-01 | -0.009360 | 9.08e-01 |
| CRMPs in Sema3A signaling | 15 | 9.51e-01 | -0.009200 | 9.81e-01 |
| Glycosphingolipid catabolism | 32 | 9.29e-01 | -0.009150 | 9.70e-01 |
| Gene Silencing by RNA | 80 | 8.89e-01 | 0.009050 | 9.62e-01 |
| Signaling by ERBB2 KD Mutants | 24 | 9.39e-01 | -0.009000 | 9.74e-01 |
| Mitotic Prophase | 78 | 8.92e-01 | -0.008930 | 9.62e-01 |
| G1/S-Specific Transcription | 28 | 9.36e-01 | -0.008830 | 9.71e-01 |
| Nuclear Receptor transcription pathway | 51 | 9.14e-01 | -0.008700 | 9.69e-01 |
| Kinesins | 60 | 9.08e-01 | -0.008640 | 9.69e-01 |
| Neurotransmitter release cycle | 47 | 9.19e-01 | -0.008520 | 9.69e-01 |
| Metabolism of steroid hormones | 33 | 9.33e-01 | 0.008410 | 9.71e-01 |
| Signaling by WNT in cancer | 32 | 9.34e-01 | 0.008410 | 9.71e-01 |
| COPI-independent Golgi-to-ER retrograde traffic | 52 | 9.19e-01 | 0.008140 | 9.69e-01 |
| Miscellaneous substrates | 12 | 9.61e-01 | 0.008070 | 9.87e-01 |
| Gap junction degradation | 12 | 9.62e-01 | 0.007980 | 9.87e-01 |
| CD28 dependent PI3K/Akt signaling | 22 | 9.49e-01 | -0.007920 | 9.80e-01 |
| Ion homeostasis | 52 | 9.22e-01 | -0.007870 | 9.69e-01 |
| Signal Transduction | 2447 | 5.23e-01 | -0.007840 | 8.23e-01 |
| Inhibition of replication initiation of damaged DNA by RB1/E2F1 | 11 | 9.64e-01 | -0.007820 | 9.88e-01 |
| Gap junction trafficking and regulation | 49 | 9.25e-01 | 0.007780 | 9.69e-01 |
| Signaling by ERBB2 TMD/JMD mutants | 21 | 9.51e-01 | -0.007710 | 9.81e-01 |
| SARS-CoV-2 Infection | 275 | 8.26e-01 | 0.007700 | 9.38e-01 |
| Loss of Nlp from mitotic centrosomes | 65 | 9.16e-01 | -0.007600 | 9.69e-01 |
| Loss of proteins required for interphase microtubule organization from the centrosome | 65 | 9.16e-01 | -0.007600 | 9.69e-01 |
| MAPK family signaling cascades | 313 | 8.24e-01 | 0.007320 | 9.37e-01 |
| Cell-cell junction organization | 82 | 9.09e-01 | -0.007300 | 9.69e-01 |
| Diseases of signal transduction by growth factor receptors and second messengers | 412 | 7.99e-01 | 0.007290 | 9.30e-01 |
| RAF/MAP kinase cascade | 266 | 8.39e-01 | 0.007240 | 9.45e-01 |
| Signaling by Rho GTPases | 605 | 7.61e-01 | -0.007240 | 9.23e-01 |
| Cytokine Signaling in Immune system | 728 | 7.39e-01 | -0.007220 | 9.18e-01 |
| Recruitment of NuMA to mitotic centrosomes | 89 | 9.06e-01 | -0.007220 | 9.69e-01 |
| Synthesis of PC | 27 | 9.50e-01 | 0.007020 | 9.81e-01 |
| Intraflagellar transport | 47 | 9.36e-01 | 0.006730 | 9.71e-01 |
| RHOD GTPase cycle | 48 | 9.36e-01 | -0.006690 | 9.71e-01 |
| Calcitonin-like ligand receptors | 10 | 9.71e-01 | 0.006680 | 9.88e-01 |
| Sema3A PAK dependent Axon repulsion | 14 | 9.66e-01 | -0.006580 | 9.88e-01 |
| Removal of the Flap Intermediate from the C-strand | 17 | 9.63e-01 | -0.006540 | 9.88e-01 |
| Transport of inorganic cations/anions and amino acids/oligopeptides | 101 | 9.10e-01 | 0.006510 | 9.69e-01 |
| Carboxyterminal post-translational modifications of tubulin | 44 | 9.41e-01 | -0.006430 | 9.75e-01 |
| RUNX3 regulates p14-ARF | 10 | 9.72e-01 | -0.006310 | 9.88e-01 |
| PRC2 methylates histones and DNA | 13 | 9.70e-01 | -0.006060 | 9.88e-01 |
| MAPK1/MAPK3 signaling | 272 | 8.66e-01 | 0.005950 | 9.52e-01 |
| PI3K Cascade | 43 | 9.47e-01 | 0.005890 | 9.79e-01 |
| IRAK2 mediated activation of TAK1 complex upon TLR7/8 or 9 stimulation | 14 | 9.70e-01 | 0.005710 | 9.88e-01 |
| Dissolution of Fibrin Clot | 13 | 9.72e-01 | 0.005590 | 9.88e-01 |
| Intra-Golgi and retrograde Golgi-to-ER traffic | 199 | 8.94e-01 | -0.005470 | 9.62e-01 |
| Glucocorticoid biosynthesis | 10 | 9.76e-01 | -0.005440 | 9.89e-01 |
| MHC class II antigen presentation | 122 | 9.19e-01 | 0.005340 | 9.69e-01 |
| FRS-mediated FGFR3 signaling | 19 | 9.68e-01 | -0.005260 | 9.88e-01 |
| RND3 GTPase cycle | 41 | 9.56e-01 | 0.005020 | 9.84e-01 |
| Base-Excision Repair, AP Site Formation | 18 | 9.71e-01 | 0.004990 | 9.88e-01 |
| Processive synthesis on the C-strand of the telomere | 19 | 9.70e-01 | -0.004990 | 9.88e-01 |
| Interleukin-3, Interleukin-5 and GM-CSF signaling | 45 | 9.58e-01 | -0.004530 | 9.85e-01 |
| Activation of NMDA receptors and postsynaptic events | 87 | 9.43e-01 | -0.004430 | 9.76e-01 |
| RET signaling | 41 | 9.63e-01 | -0.004150 | 9.88e-01 |
| RA biosynthesis pathway | 22 | 9.74e-01 | 0.003980 | 9.89e-01 |
| MET promotes cell motility | 41 | 9.66e-01 | -0.003850 | 9.88e-01 |
| Gap junction assembly | 36 | 9.68e-01 | 0.003820 | 9.88e-01 |
| Pre-NOTCH Processing in Golgi | 18 | 9.78e-01 | -0.003780 | 9.90e-01 |
| Organelle biogenesis and maintenance | 254 | 9.19e-01 | -0.003680 | 9.69e-01 |
| Antigen processing: Ubiquitination & Proteasome degradation | 293 | 9.18e-01 | 0.003490 | 9.69e-01 |
| Cleavage of the damaged pyrimidine | 16 | 9.82e-01 | 0.003250 | 9.91e-01 |
| Depyrimidination | 16 | 9.82e-01 | 0.003250 | 9.91e-01 |
| Recognition and association of DNA glycosylase with site containing an affected pyrimidine | 16 | 9.82e-01 | 0.003250 | 9.91e-01 |
| Protein ubiquitination | 60 | 9.66e-01 | 0.003150 | 9.88e-01 |
| RHO GTPases activate IQGAPs | 31 | 9.76e-01 | 0.003070 | 9.89e-01 |
| Polymerase switching on the C-strand of the telomere | 24 | 9.79e-01 | -0.003040 | 9.90e-01 |
| HCMV Infection | 97 | 9.61e-01 | 0.002890 | 9.87e-01 |
| Post NMDA receptor activation events | 76 | 9.68e-01 | -0.002700 | 9.88e-01 |
| Lewis blood group biosynthesis | 18 | 9.86e-01 | -0.002450 | 9.92e-01 |
| Interferon Signaling | 256 | 9.47e-01 | 0.002420 | 9.79e-01 |
| Deubiquitination | 225 | 9.52e-01 | -0.002310 | 9.81e-01 |
| Interleukin-12 signaling | 43 | 9.80e-01 | -0.002240 | 9.90e-01 |
| Role of phospholipids in phagocytosis | 23 | 9.86e-01 | -0.002180 | 9.92e-01 |
| E2F mediated regulation of DNA replication | 20 | 9.87e-01 | 0.002150 | 9.92e-01 |
| Zygotic genome activation (ZGA) | 15 | 9.90e-01 | -0.001800 | 9.94e-01 |
| Apoptotic cleavage of cell adhesion proteins | 11 | 9.92e-01 | -0.001740 | 9.94e-01 |
| Telomere C-strand (Lagging Strand) Synthesis | 32 | 9.87e-01 | 0.001690 | 9.92e-01 |
| Degradation of the extracellular matrix | 135 | 9.74e-01 | -0.001650 | 9.88e-01 |
| MET activates PTK2 signaling | 30 | 9.88e-01 | -0.001590 | 9.93e-01 |
| CaMK IV-mediated phosphorylation of CREB | 10 | 9.94e-01 | 0.001340 | 9.94e-01 |
| Fatty acyl-CoA biosynthesis | 36 | 9.90e-01 | -0.001180 | 9.94e-01 |
| Negative regulation of MET activity | 20 | 9.93e-01 | -0.001070 | 9.94e-01 |
| Biological oxidations | 213 | 9.79e-01 | 0.001050 | 9.90e-01 |
| Platelet calcium homeostasis | 27 | 9.94e-01 | -0.000833 | 9.94e-01 |
| Gap junction trafficking | 47 | 9.94e-01 | 0.000658 | 9.94e-01 |
| Assembly of collagen fibrils and other multimeric structures | 59 | 9.93e-01 | 0.000635 | 9.94e-01 |
| Signaling by Interleukins | 434 | 9.84e-01 | 0.000548 | 9.92e-01 |
Chylomicron remodeling
| 210 | |
|---|---|
| set | Chylomicron remodeling |
| setSize | 10 |
| pANOVA | 0.00254 |
| s.dist | 0.551 |
| p.adjustANOVA | 0.0482 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| APOA2 | 17615 |
| LPL | 17101 |
| APOC3 | 15561 |
| APOC2 | 14895 |
| APOA5 | 14684 |
| APOA1 | 12062 |
| GPIHBP1 | 10408 |
| APOA4 | 10060 |
| APOE | 9123 |
| APOB | 3390 |
| GeneID | Gene Rank |
|---|---|
| APOA2 | 17615 |
| LPL | 17101 |
| APOC3 | 15561 |
| APOC2 | 14895 |
| APOA5 | 14684 |
| APOA1 | 12062 |
| GPIHBP1 | 10408 |
| APOA4 | 10060 |
| APOE | 9123 |
| APOB | 3390 |
TRAF6 mediated IRF7 activation in TLR7/8 or 9 signaling
| 1419 | |
|---|---|
| set | TRAF6 mediated IRF7 activation in TLR7/8 or 9 signaling |
| setSize | 11 |
| pANOVA | 0.00165 |
| s.dist | 0.548 |
| p.adjustANOVA | 0.0359 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPS27A | 17623 |
| UBC | 17042 |
| IRF7 | 15832 |
| UBA52 | 15146 |
| UBB | 15063 |
| UBE2V1 | 14282 |
| MYD88 | 10379 |
| TRAF6 | 9524 |
| IRAK4 | 9466 |
| TLR9 | 8295 |
| UBE2N | 4251 |
| GeneID | Gene Rank |
|---|---|
| RPS27A | 17623 |
| UBC | 17042 |
| IRF7 | 15832 |
| UBA52 | 15146 |
| UBB | 15063 |
| UBE2V1 | 14282 |
| MYD88 | 10379 |
| TRAF6 | 9524 |
| IRAK4 | 9466 |
| TLR9 | 8295 |
| UBE2N | 4251 |
SARS-CoV-1 modulates host translation machinery
| 1194 | |
|---|---|
| set | SARS-CoV-1 modulates host translation machinery |
| setSize | 34 |
| pANOVA | 1.73e-07 |
| s.dist | 0.518 |
| p.adjustANOVA | 9.79e-06 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPS17 | 17998 |
| RPS27A | 17623 |
| RPS14 | 17460 |
| RPSA | 16750 |
| RPS27 | 16701 |
| RPS28 | 16547 |
| RPS16 | 16394 |
| RPS10 | 16101 |
| HNRNPA1 | 16020 |
| RPS21 | 15733 |
| RPS24 | 15434 |
| RPS11 | 15381 |
| RPS26 | 15184 |
| RPS23 | 15084 |
| RPS25 | 14869 |
| RPS6 | 14761 |
| RPS9 | 14415 |
| RPS29 | 14234 |
| RPS2 | 12789 |
| RPS7 | 12370 |
| GeneID | Gene Rank |
|---|---|
| RPS17 | 17998 |
| RPS27A | 17623 |
| RPS14 | 17460 |
| RPSA | 16750 |
| RPS27 | 16701 |
| RPS28 | 16547 |
| RPS16 | 16394 |
| RPS10 | 16101 |
| HNRNPA1 | 16020 |
| RPS21 | 15733 |
| RPS24 | 15434 |
| RPS11 | 15381 |
| RPS26 | 15184 |
| RPS23 | 15084 |
| RPS25 | 14869 |
| RPS6 | 14761 |
| RPS9 | 14415 |
| RPS29 | 14234 |
| RPS2 | 12789 |
| RPS7 | 12370 |
| RPS5 | 11632 |
| RPS18 | 11410 |
| RPS3A | 11123 |
| RPS19 | 10890 |
| RPS8 | 10296 |
| RPS27L | 9869 |
| EEF1A1 | 9096 |
| RPS13 | 7369 |
| RPS20 | 7077 |
| RPS3 | 5505 |
| RPS15A | 3120 |
| RPS12 | 2257 |
| RPS15 | -220 |
| FAU | -1469 |
Josephin domain DUBs
| 669 | |
|---|---|
| set | Josephin domain DUBs |
| setSize | 11 |
| pANOVA | 0.00549 |
| s.dist | 0.483 |
| p.adjustANOVA | 0.0805 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPS27A | 17623 |
| JOSD2 | 17047 |
| UBC | 17042 |
| RAD23A | 15562 |
| UBA52 | 15146 |
| UBB | 15063 |
| JOSD1 | 12720 |
| VCP | 11557 |
| RAD23B | 4991 |
| ATXN3 | 3743 |
| PARK2 | -2692 |
| GeneID | Gene Rank |
|---|---|
| RPS27A | 17623 |
| JOSD2 | 17047 |
| UBC | 17042 |
| RAD23A | 15562 |
| UBA52 | 15146 |
| UBB | 15063 |
| JOSD1 | 12720 |
| VCP | 11557 |
| RAD23B | 4991 |
| ATXN3 | 3743 |
| PARK2 | -2692 |
TRAF6 mediated IRF7 activation
| 1418 | |
|---|---|
| set | TRAF6 mediated IRF7 activation |
| setSize | 25 |
| pANOVA | 5.09e-05 |
| s.dist | -0.468 |
| p.adjustANOVA | 0.00172 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| IFNA6 | -7454 |
| IFNA16 | -7423 |
| IFNA2 | -7251 |
| IFNA21 | -7180 |
| IFNA14 | -7099 |
| IFNB1 | -7088 |
| IFNA1 | -7038 |
| TRIM4 | -6652 |
| IFNA5 | -5828 |
| TANK | -5660 |
| IFNA7 | -4450 |
| SIKE1 | -4057 |
| IFNA8 | -2780 |
| TBK1 | -2417 |
| TRIM25 | -1856 |
| EP300 | 381 |
| CREBBP | 955 |
| IRF3 | 3496 |
| RNF135 | 4528 |
| IFIH1 | 5240 |
| GeneID | Gene Rank |
|---|---|
| IFNA6 | -7454 |
| IFNA16 | -7423 |
| IFNA2 | -7251 |
| IFNA21 | -7180 |
| IFNA14 | -7099 |
| IFNB1 | -7088 |
| IFNA1 | -7038 |
| TRIM4 | -6652 |
| IFNA5 | -5828 |
| TANK | -5660 |
| IFNA7 | -4450 |
| SIKE1 | -4057 |
| IFNA8 | -2780 |
| TBK1 | -2417 |
| TRIM25 | -1856 |
| EP300 | 381 |
| CREBBP | 955 |
| IRF3 | 3496 |
| RNF135 | 4528 |
| IFIH1 | 5240 |
| MAVS | 5384 |
| TRAF2 | 8353 |
| TRAF6 | 9524 |
| IKBKE | 15091 |
| IRF7 | 15832 |
Class C/3 (Metabotropic glutamate/pheromone receptors)
| 216 | |
|---|---|
| set | Class C/3 (Metabotropic glutamate/pheromone receptors) |
| setSize | 39 |
| pANOVA | 6.08e-07 |
| s.dist | -0.461 |
| p.adjustANOVA | 3.33e-05 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| TAS2R46 | -7339 |
| TAS2R10 | -7306 |
| TAS2R4 | -7233 |
| TAS2R14 | -6983 |
| TAS2R50 | -6656 |
| TAS2R8 | -6601 |
| TAS2R43 | -6600 |
| TAS2R39 | -6469 |
| TAS2R13 | -6411 |
| TAS2R3 | -6389 |
| TAS2R60 | -5931 |
| TAS2R31 | -5781 |
| TAS2R30 | -5769 |
| TAS2R5 | -5318 |
| TAS2R42 | -5043 |
| GRM5 | -4895 |
| TAS2R19 | -4787 |
| TAS2R7 | -4436 |
| TAS2R16 | -4099 |
| TAS2R1 | -3267 |
| GeneID | Gene Rank |
|---|---|
| TAS2R46 | -7339 |
| TAS2R10 | -7306 |
| TAS2R4 | -7233 |
| TAS2R14 | -6983 |
| TAS2R50 | -6656 |
| TAS2R8 | -6601 |
| TAS2R43 | -6600 |
| TAS2R39 | -6469 |
| TAS2R13 | -6411 |
| TAS2R3 | -6389 |
| TAS2R60 | -5931 |
| TAS2R31 | -5781 |
| TAS2R30 | -5769 |
| TAS2R5 | -5318 |
| TAS2R42 | -5043 |
| GRM5 | -4895 |
| TAS2R19 | -4787 |
| TAS2R7 | -4436 |
| TAS2R16 | -4099 |
| TAS2R1 | -3267 |
| TAS2R38 | -2766 |
| TAS1R2 | -767 |
| TAS2R20 | -749 |
| TAS2R9 | 481 |
| GRM7 | 954 |
| CASR | 1209 |
| GRM8 | 1491 |
| GRM1 | 2427 |
| GABBR1 | 5279 |
| TAS1R3 | 5729 |
| GRM2 | 5849 |
| GABBR2 | 6454 |
| TAS2R40 | 7295 |
| GRM6 | 7787 |
| GRM4 | 8862 |
| GPRC6A | 9013 |
| TAS2R41 | 9019 |
| GRM3 | 12208 |
| TAS1R1 | 16838 |
SUMOylation of immune response proteins
| 1229 | |
|---|---|
| set | SUMOylation of immune response proteins |
| setSize | 11 |
| pANOVA | 0.00867 |
| s.dist | 0.457 |
| p.adjustANOVA | 0.112 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| PIAS3 | 16789 |
| SUMO1 | 15514 |
| NFKBIA | 15415 |
| IKBKE | 15091 |
| NFKB2 | 13895 |
| RELA | 12906 |
| TOPORS | 11451 |
| UBE2I | 10454 |
| PIAS4 | 9746 |
| SUMO3 | 3785 |
| EIF2AK2 | -993 |
| GeneID | Gene Rank |
|---|---|
| PIAS3 | 16789 |
| SUMO1 | 15514 |
| NFKBIA | 15415 |
| IKBKE | 15091 |
| NFKB2 | 13895 |
| RELA | 12906 |
| TOPORS | 11451 |
| UBE2I | 10454 |
| PIAS4 | 9746 |
| SUMO3 | 3785 |
| EIF2AK2 | -993 |
Pexophagy
| 934 | |
|---|---|
| set | Pexophagy |
| setSize | 11 |
| pANOVA | 0.00889 |
| s.dist | 0.455 |
| p.adjustANOVA | 0.114 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPS27A | 17623 |
| UBC | 17042 |
| PEX5 | 17036 |
| MAP1LC3B | 15762 |
| UBA52 | 15146 |
| UBB | 15063 |
| NBR1 | 14839 |
| ATM | 10689 |
| SQSTM1 | 5152 |
| EPAS1 | -2163 |
| USP30 | -2346 |
| GeneID | Gene Rank |
|---|---|
| RPS27A | 17623 |
| UBC | 17042 |
| PEX5 | 17036 |
| MAP1LC3B | 15762 |
| UBA52 | 15146 |
| UBB | 15063 |
| NBR1 | 14839 |
| ATM | 10689 |
| SQSTM1 | 5152 |
| EPAS1 | -2163 |
| USP30 | -2346 |
Phase 4 - resting membrane potential
| 937 | |
|---|---|
| set | Phase 4 - resting membrane potential |
| setSize | 19 |
| pANOVA | 0.0011 |
| s.dist | 0.432 |
| p.adjustANOVA | 0.0277 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| KCNK16 | 17421 |
| KCNJ4 | 16930 |
| KCNK18 | 16819 |
| KCNJ12 | 16370 |
| KCNK15 | 15074 |
| KCNK6 | 14501 |
| KCNK7 | 13732 |
| KCNJ14 | 12733 |
| KCNK17 | 12557 |
| KCNK10 | 11671 |
| KCNK4 | 10547 |
| KCNK12 | 9301 |
| KCNK3 | 9192 |
| KCNK5 | 8778 |
| KCNK9 | 8381 |
| KCNJ2 | 7972 |
| KCNK1 | 4007 |
| KCNK13 | 1366 |
| KCNK2 | 866 |
| GeneID | Gene Rank |
|---|---|
| KCNK16 | 17421 |
| KCNJ4 | 16930 |
| KCNK18 | 16819 |
| KCNJ12 | 16370 |
| KCNK15 | 15074 |
| KCNK6 | 14501 |
| KCNK7 | 13732 |
| KCNJ14 | 12733 |
| KCNK17 | 12557 |
| KCNK10 | 11671 |
| KCNK4 | 10547 |
| KCNK12 | 9301 |
| KCNK3 | 9192 |
| KCNK5 | 8778 |
| KCNK9 | 8381 |
| KCNJ2 | 7972 |
| KCNK1 | 4007 |
| KCNK13 | 1366 |
| KCNK2 | 866 |
Interaction With Cumulus Cells And The Zona Pellucida
| 630 | |
|---|---|
| set | Interaction With Cumulus Cells And The Zona Pellucida |
| setSize | 11 |
| pANOVA | 0.0143 |
| s.dist | -0.426 |
| p.adjustANOVA | 0.155 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| ADAM20 | -6401 |
| SPAM1 | -6352 |
| ADAM2 | -4855 |
| ADAM21 | -4386 |
| B4GALT1 | -1620 |
| ZP4 | -1539 |
| OVGP1 | -444 |
| ZP2 | 2669 |
| ADAM30 | 3126 |
| ZP3 | 7641 |
| ZP1 | 11219 |
| GeneID | Gene Rank |
|---|---|
| ADAM20 | -6401 |
| SPAM1 | -6352 |
| ADAM2 | -4855 |
| ADAM21 | -4386 |
| B4GALT1 | -1620 |
| ZP4 | -1539 |
| OVGP1 | -444 |
| ZP2 | 2669 |
| ADAM30 | 3126 |
| ZP3 | 7641 |
| ZP1 | 11219 |
Regulation of CDH11 gene transcription
| 1109 | |
|---|---|
| set | Regulation of CDH11 gene transcription |
| setSize | 10 |
| pANOVA | 0.0208 |
| s.dist | 0.422 |
| p.adjustANOVA | 0.19 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| HOXC8 | 17775 |
| SP1 | 16404 |
| BHLHE22 | 16156 |
| PRDM8 | 15535 |
| FOXF1 | 14246 |
| HEYL | 13939 |
| ILF3 | 7799 |
| SNAI1 | 4808 |
| ZEB2 | 3623 |
| CDH11 | -1980 |
| GeneID | Gene Rank |
|---|---|
| HOXC8 | 17775 |
| SP1 | 16404 |
| BHLHE22 | 16156 |
| PRDM8 | 15535 |
| FOXF1 | 14246 |
| HEYL | 13939 |
| ILF3 | 7799 |
| SNAI1 | 4808 |
| ZEB2 | 3623 |
| CDH11 | -1980 |
Expression and translocation of olfactory receptors
| 403 | |
|---|---|
| set | Expression and translocation of olfactory receptors |
| setSize | 358 |
| pANOVA | 3.01e-42 |
| s.dist | -0.418 |
| p.adjustANOVA | 4.77e-39 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| OR2A12 | -7381 |
| OR7E24 | -7370 |
| OR8U1 | -7368 |
| OR52A5 | -7357 |
| OR52D1 | -7353 |
| OR4Q3 | -7352 |
| OR13C8 | -7292 |
| OR10H3 | -7285 |
| OR52E4 | -7279 |
| OR5K1 | -7254 |
| OR8B2 | -7245 |
| OR4N4 | -7225 |
| OR8H1 | -7216 |
| OR6C1 | -7212 |
| OR2G6 | -7211 |
| OR5AC2 | -7206 |
| OR51G2 | -7199 |
| OR5T2 | -7182 |
| OR4D5 | -7160 |
| OR2W3 | -7151 |
| GeneID | Gene Rank |
|---|---|
| OR2A12 | -7381.0 |
| OR7E24 | -7370.0 |
| OR8U1 | -7368.0 |
| OR52A5 | -7357.0 |
| OR52D1 | -7353.0 |
| OR4Q3 | -7352.0 |
| OR13C8 | -7292.0 |
| OR10H3 | -7285.0 |
| OR52E4 | -7279.0 |
| OR5K1 | -7254.0 |
| OR8B2 | -7245.0 |
| OR4N4 | -7225.0 |
| OR8H1 | -7216.0 |
| OR6C1 | -7212.0 |
| OR2G6 | -7211.0 |
| OR5AC2 | -7206.0 |
| OR51G2 | -7199.0 |
| OR5T2 | -7182.0 |
| OR4D5 | -7160.0 |
| OR2W3 | -7151.0 |
| OR1J2 | -7147.0 |
| OR2G3 | -7137.0 |
| OR8D1 | -7128.0 |
| OR5K2 | -7124.0 |
| OR5P2 | -7115.0 |
| OR5K4 | -7106.0 |
| OR2T33 | -7059.0 |
| OR5B12 | -7058.0 |
| OR4F15 | -7048.0 |
| OR4E2 | -7013.0 |
| OR2B6 | -7012.0 |
| OR6Q1 | -7011.0 |
| OR7G2 | -6985.0 |
| OR52H1 | -6976.0 |
| OR6M1 | -6975.0 |
| OR11G2 | -6970.0 |
| OR13F1 | -6959.0 |
| OR10G9 | -6944.0 |
| OR52I2 | -6940.0 |
| OR8I2 | -6922.0 |
| OR51I1 | -6895.0 |
| OR2K2 | -6891.0 |
| OR7D4 | -6884.0 |
| OR5K3 | -6882.0 |
| OR5AP2 | -6877.0 |
| OR6C2 | -6858.0 |
| OR9G1 | -6835.5 |
| OR9G9 | -6835.5 |
| OR4C45 | -6834.0 |
| OR5D18 | -6810.0 |
| OR13C4 | -6790.0 |
| OR14A16 | -6781.0 |
| OR12D2 | -6765.0 |
| OR51B6 | -6753.0 |
| OR5F1 | -6736.0 |
| OR2B3 | -6721.0 |
| OR8D2 | -6714.0 |
| OR52I1 | -6682.0 |
| OR10K2 | -6671.0 |
| OR5AK2 | -6666.0 |
| OR1S1 | -6615.0 |
| OR13C2 | -6588.0 |
| OR6K6 | -6556.0 |
| OR2A2 | -6552.0 |
| OR5AN1 | -6525.0 |
| OR10J1 | -6509.0 |
| OR4K14 | -6507.0 |
| OR6C75 | -6488.0 |
| OR10J5 | -6486.0 |
| OR10G8 | -6474.0 |
| OR56A1 | -6409.0 |
| OR8K3 | -6403.0 |
| OR13G1 | -6377.0 |
| OR1Q1 | -6372.0 |
| OR2T10 | -6350.0 |
| OR2M5 | -6345.0 |
| OR13C3 | -6339.0 |
| OR5P3 | -6333.0 |
| OR10W1 | -6317.0 |
| OR4N5 | -6306.0 |
| OR5AS1 | -6278.0 |
| OR5H1 | -6252.0 |
| OR10G4 | -6218.0 |
| OR6C6 | -6213.0 |
| OR6N2 | -6200.0 |
| OR10Q1 | -6180.0 |
| OR8U8 | -6153.0 |
| OR51V1 | -6140.0 |
| OR8H2 | -6098.0 |
| OR5M9 | -6090.0 |
| OR6C3 | -6089.0 |
| OR4B1 | -6088.0 |
| OR1J1 | -6071.0 |
| OR5D14 | -6062.0 |
| OR5L2 | -6055.0 |
| OR4C46 | -5996.0 |
| OR6B1 | -5960.0 |
| OR2A14 | -5920.0 |
| OR52E6 | -5900.0 |
| OR4D10 | -5889.0 |
| OR11A1 | -5871.0 |
| OR6C74 | -5838.0 |
| OR6C4 | -5836.0 |
| OR5W2 | -5825.0 |
| OR2W1 | -5811.0 |
| OR8H3 | -5790.0 |
| OR3A2 | -5776.0 |
| OR7A10 | -5772.0 |
| OR2M4 | -5748.0 |
| OR5M11 | -5726.0 |
| OR51I2 | -5649.0 |
| OR51A7 | -5647.0 |
| OR5M10 | -5630.0 |
| OR5H2 | -5605.0 |
| OR9G4 | -5594.0 |
| OR5D16 | -5563.0 |
| OR2D3 | -5546.0 |
| OR1K1 | -5497.0 |
| OR6F1 | -5459.0 |
| OR1L3 | -5413.0 |
| OR11H4 | -5359.0 |
| OR4A16 | -5356.0 |
| OR52N2 | -5327.0 |
| OR51B5 | -5325.0 |
| OR5B3 | -5286.0 |
| OR2AK2 | -5177.0 |
| OR4P4 | -5158.0 |
| OR4M1 | -5143.0 |
| OR8J3 | -5140.0 |
| OR10A6 | -5124.0 |
| OR8J1 | -5121.0 |
| OR1A2 | -5098.0 |
| OR4C13 | -5097.0 |
| OR2T1 | -5034.0 |
| OR2J2 | -5002.0 |
| OR1A1 | -4982.0 |
| OR1N2 | -4924.0 |
| OR4K13 | -4922.0 |
| OR4D1 | -4911.0 |
| OR8A1 | -4865.0 |
| OR52M1 | -4652.0 |
| OR2T8 | -4611.0 |
| OR10A4 | -4558.0 |
| OR10AD1 | -4545.0 |
| OR52E8 | -4542.0 |
| OR4A47 | -4495.0 |
| OR6B3 | -4493.0 |
| OR5M8 | -4482.0 |
| OR1E1 | -4435.0 |
| OR6A2 | -4158.0 |
| OR2Y1 | -4123.0 |
| OR5M3 | -4106.0 |
| OR52A1 | -4101.0 |
| OR52B6 | -4041.0 |
| OR9A2 | -4028.0 |
| OR5T3 | -3979.0 |
| OR5M1 | -3966.0 |
| OR7G1 | -3955.0 |
| OR4C12 | -3940.0 |
| OR6C70 | -3937.0 |
| OR10A7 | -3934.0 |
| OR2T34 | -3916.0 |
| OR6C76 | -3912.0 |
| OR6T1 | -3825.0 |
| OR8S1 | -3730.0 |
| OR2L8 | -3715.0 |
| OR2H1 | -3700.0 |
| OR2AG1 | -3691.0 |
| OR3A1 | -3664.0 |
| OR5H6 | -3651.0 |
| OR10G3 | -3640.0 |
| OR52K2 | -3629.0 |
| OR1I1 | -3613.0 |
| OR4C6 | -3499.0 |
| OR51L1 | -3475.0 |
| OR10G7 | -3459.0 |
| OR51E2 | -3430.0 |
| OR4K17 | -3422.0 |
| OR2L5 | -3421.0 |
| OR2B2 | -3311.0 |
| OR10G2 | -3176.0 |
| OR8K1 | -3167.0 |
| OR51A2 | -3135.0 |
| OR8G1 | -3112.0 |
| OR10H1 | -3075.0 |
| OR51F2 | -3040.0 |
| OR2L13 | -2985.0 |
| OR2T6 | -2956.0 |
| OR52N1 | -2928.0 |
| OR4D11 | -2894.0 |
| OR4N2 | -2891.0 |
| OR10AG1 | -2553.0 |
| OR52R1 | -2519.0 |
| OR1B1 | -2477.0 |
| OR2J3 | -2412.0 |
| OR5V1 | -2284.0 |
| OR51T1 | -2207.0 |
| OR51B4 | -2171.0 |
| OR4K1 | -2153.0 |
| OR14C36 | -2066.0 |
| OR4D9 | -1979.0 |
| OR2G2 | -1911.0 |
| OR51B2 | -1813.0 |
| OR4X2 | -1674.0 |
| OR5B2 | -1670.0 |
| OR2M3 | -1627.0 |
| OR10S1 | -1558.0 |
| OR2T3 | -1489.0 |
| OR5H15 | -1427.0 |
| OR6P1 | -1408.0 |
| OR7A5 | -1357.0 |
| OR4F6 | -1282.0 |
| OR5C1 | -1268.0 |
| OR10A3 | -1203.0 |
| OR9Q1 | -1199.0 |
| OR6C65 | -1188.0 |
| OR1J4 | -1182.0 |
| OR2T4 | -1063.0 |
| OR56A3 | -1024.0 |
| OR2F1 | -957.0 |
| OR5T1 | -950.0 |
| OR6S1 | -839.0 |
| OR5R1 | -770.0 |
| OR6X1 | -670.0 |
| OR7C1 | -596.0 |
| OR1C1 | -469.0 |
| OR10H4 | -416.0 |
| OR7D2 | -245.0 |
| OR10C1 | 189.0 |
| REEP1 | 222.0 |
| OR51D1 | 350.0 |
| OR4D6 | 393.0 |
| OR14I1 | 439.0 |
| OR52E2 | 529.0 |
| OR5AU1 | 826.0 |
| OR1L6 | 884.0 |
| OR5A1 | 981.0 |
| OR56A4 | 1233.0 |
| OR12D3 | 1425.0 |
| OR52N5 | 1434.0 |
| OR4K15 | 1581.0 |
| OR1M1 | 1617.0 |
| OR5I1 | 1930.0 |
| OR52K1 | 2152.0 |
| OR7A17 | 2227.0 |
| OR52J3 | 2294.0 |
| OR8B12 | 2362.0 |
| OR4S2 | 2386.0 |
| OR6Y1 | 2477.0 |
| OR4K2 | 2788.0 |
| OR9K2 | 2795.0 |
| OR2L3 | 2808.0 |
| OR7C2 | 2904.0 |
| OR14J1 | 2966.0 |
| OR10T2 | 3085.0 |
| OR2C1 | 3091.0 |
| OR6V1 | 3199.0 |
| OR4D2 | 3275.0 |
| OR13C9 | 3403.0 |
| OR1E2 | 3635.0 |
| OR11L1 | 3856.0 |
| OR2AG2 | 3965.0 |
| OR11H6 | 3984.0 |
| OR8D4 | 4764.0 |
| OR1L8 | 4766.0 |
| OR4L1 | 4792.0 |
| OR8G5 | 4800.0 |
| OR6B2 | 5006.0 |
| EBF1 | 5132.0 |
| OR2A25 | 5362.0 |
| OR5D13 | 5440.0 |
| OR5B17 | 5595.0 |
| OR4C3 | 5647.0 |
| OR56A5 | 5830.0 |
| OR13J1 | 5895.0 |
| OR2Z1 | 6091.0 |
| OR9Q2 | 6260.0 |
| OR9I1 | 6545.0 |
| OR4K5 | 6553.0 |
| OR2M7 | 6606.0 |
| OR51M1 | 6711.0 |
| OR6K2 | 6910.0 |
| OR2D2 | 6931.0 |
| OR2AT4 | 7019.0 |
| RTP1 | 7037.0 |
| OR2H2 | 7205.0 |
| OR4M2 | 7432.0 |
| OR51S1 | 7615.0 |
| OR2T27 | 7636.0 |
| OR4C15 | 7930.0 |
| OR10A5 | 8093.0 |
| OR51E1 | 8132.0 |
| OR2T11 | 8306.0 |
| OR1L4 | 8788.0 |
| OR2W5 | 8872.0 |
| OR10K1 | 8931.0 |
| OR1D2 | 9324.0 |
| OR10X1 | 9650.0 |
| OR4X1 | 10189.0 |
| OR8K5 | 10313.0 |
| OR1N1 | 10825.0 |
| OR2S2 | 10832.0 |
| OR10A2 | 10874.0 |
| OR52L1 | 11054.0 |
| OR1L1 | 11223.0 |
| OR2V2 | 11274.0 |
| OR2F2 | 11301.0 |
| OR1F1 | 11439.0 |
| OR5J2 | 11629.0 |
| OR2AE1 | 11641.0 |
| OR5A2 | 12082.0 |
| LHX2 | 12100.0 |
| OR11H2 | 12259.0 |
| OR9A4 | 12413.0 |
| OR51G1 | 12446.0 |
| OR1G1 | 12459.0 |
| OR4S1 | 12547.0 |
| OR3A3 | 12685.0 |
| LDB1 | 12794.0 |
| OR8B4 | 12984.0 |
| OR10H5 | 13076.0 |
| OR4A15 | 13189.0 |
| OR13A1 | 13331.0 |
| OR10Z1 | 13351.0 |
| OR2B11 | 13393.0 |
| OR52W1 | 13423.0 |
| OR5B21 | 13461.0 |
| OR10J3 | 13598.0 |
| OR2C3 | 13675.0 |
| OR6N1 | 13782.0 |
| OR4A5 | 14912.0 |
| OR4C16 | 14952.0 |
| OR10P1 | 15124.0 |
| OR2L2 | 15471.0 |
| OR1S2 | 15520.0 |
| OR5L1 | 15697.0 |
| OR51A4 | 15799.0 |
| OR6K3 | 15979.0 |
| OR5AR1 | 16000.0 |
| OR56B1 | 16282.0 |
| OR2V1 | 16351.0 |
| OR10R2 | 16396.0 |
| OR52B2 | 16410.0 |
| OR2M2 | 16490.0 |
| OR10H2 | 16512.0 |
| OR10V1 | 16587.0 |
| OR51F1 | 16686.0 |
| OR8B8 | 16831.0 |
| OR51Q1 | 16994.0 |
| OR2AP1 | 17117.0 |
| RTP2 | 17287.0 |
| OR6C68 | 17620.0 |
| OR56B4 | 17811.0 |
| OR2A5 | 17820.0 |
| OR8G2 | 18086.0 |
| OR13D1 | 18192.0 |
| OR4C11 | 18210.0 |
| OR7G3 | 18227.0 |
NF-kB is activated and signals survival
| 798 | |
|---|---|
| set | NF-kB is activated and signals survival |
| setSize | 12 |
| pANOVA | 0.0125 |
| s.dist | 0.416 |
| p.adjustANOVA | 0.143 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPS27A | 17623 |
| UBC | 17042 |
| NFKBIA | 15415 |
| UBA52 | 15146 |
| UBB | 15063 |
| RELA | 12906 |
| TRAF6 | 9524 |
| NGF | 8768 |
| NGFR | 7653 |
| IKBKB | 7359 |
| SQSTM1 | 5152 |
| NFKB1 | -2596 |
| GeneID | Gene Rank |
|---|---|
| RPS27A | 17623 |
| UBC | 17042 |
| NFKBIA | 15415 |
| UBA52 | 15146 |
| UBB | 15063 |
| RELA | 12906 |
| TRAF6 | 9524 |
| NGF | 8768 |
| NGFR | 7653 |
| IKBKB | 7359 |
| SQSTM1 | 5152 |
| NFKB1 | -2596 |
Peptide chain elongation
| 927 | |
|---|---|
| set | Peptide chain elongation |
| setSize | 84 |
| pANOVA | 6.63e-11 |
| s.dist | 0.412 |
| p.adjustANOVA | 1.31e-08 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPS17 | 17998 |
| RPL35A | 17964 |
| RPS27A | 17623 |
| RPL34 | 17570 |
| RPS14 | 17460 |
| RPL27 | 17419 |
| RPL18A | 17406 |
| RPSA | 16750 |
| RPS27 | 16701 |
| RPS28 | 16547 |
| RPL32 | 16401 |
| RPS16 | 16394 |
| RPL28 | 16373 |
| RPS10 | 16101 |
| EEF2 | 15877 |
| RPL7 | 15788 |
| RPS21 | 15733 |
| RPL29 | 15716 |
| RPL10L | 15577 |
| RPL17 | 15487 |
| GeneID | Gene Rank |
|---|---|
| RPS17 | 17998.0 |
| RPL35A | 17964.0 |
| RPS27A | 17623.0 |
| RPL34 | 17570.0 |
| RPS14 | 17460.0 |
| RPL27 | 17419.0 |
| RPL18A | 17406.0 |
| RPSA | 16750.0 |
| RPS27 | 16701.0 |
| RPS28 | 16547.0 |
| RPL32 | 16401.0 |
| RPS16 | 16394.0 |
| RPL28 | 16373.0 |
| RPS10 | 16101.0 |
| EEF2 | 15877.0 |
| RPL7 | 15788.0 |
| RPS21 | 15733.0 |
| RPL29 | 15716.0 |
| RPL10L | 15577.0 |
| RPL17 | 15487.0 |
| RPS24 | 15434.0 |
| RPL23 | 15404.0 |
| RPS11 | 15381.0 |
| RPL38 | 15324.0 |
| RPS26 | 15184.0 |
| UBA52 | 15146.0 |
| RPS23 | 15084.0 |
| RPL24 | 14927.0 |
| RPS25 | 14869.0 |
| RPS6 | 14761.0 |
| RPL9 | 14519.0 |
| RPS9 | 14415.0 |
| RPS29 | 14234.0 |
| RPL26L1 | 14132.0 |
| RPL30 | 13945.0 |
| RPL14 | 13883.0 |
| RPL26 | 13496.0 |
| RPL7A | 13425.0 |
| RPS2 | 12789.0 |
| RPL12 | 12744.0 |
| RPL41 | 12555.0 |
| RPS7 | 12370.0 |
| RPL37A | 11838.0 |
| RPL3L | 11730.0 |
| RPS5 | 11632.0 |
| RPS18 | 11410.0 |
| RPL13A | 11201.5 |
| RPS3A | 11123.0 |
| RPL19 | 10992.0 |
| RPS19 | 10890.0 |
| RPL13 | 10808.0 |
| RPS8 | 10296.0 |
| RPS27L | 9869.0 |
| RPL39L | 9655.0 |
| RPL18 | 9621.0 |
| EEF1A1 | 9096.0 |
| RPL23A | 8852.0 |
| RPLP1 | 8689.0 |
| RPLP2 | 8239.0 |
| RPL37 | 7695.0 |
| RPS13 | 7369.0 |
| RPL36AL | 7147.0 |
| RPS20 | 7077.0 |
| RPL4 | 6779.0 |
| RPL36 | 6145.0 |
| RPS3 | 5505.0 |
| RPL8 | 5310.0 |
| RPL10A | 5072.0 |
| RPL15 | 4446.0 |
| RPL3 | 4267.0 |
| RPLP0 | 3455.0 |
| RPS15A | 3120.0 |
| RPL11 | 2419.0 |
| RPS12 | 2257.0 |
| RPL27A | 1306.0 |
| RPL22 | 1272.0 |
| RPL5 | 852.0 |
| RPL31 | 733.0 |
| RPL35 | 467.0 |
| RPS15 | -220.0 |
| RPL21 | -682.0 |
| FAU | -1469.0 |
| RPL22L1 | -1702.0 |
| RPL6 | -4235.0 |
Regulation of NF-kappa B signaling
| 1122 | |
|---|---|
| set | Regulation of NF-kappa B signaling |
| setSize | 17 |
| pANOVA | 0.00341 |
| s.dist | 0.41 |
| p.adjustANOVA | 0.0589 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPS27A | 17623 |
| UBC | 17042 |
| UBA52 | 15146 |
| LRRC14 | 15139 |
| UBB | 15063 |
| USP18 | 14882 |
| IKBIP | 12610 |
| NLRX1 | 12126 |
| TP53 | 11464 |
| NLRC5 | 9936 |
| TRAF6 | 9524 |
| USP14 | 8938 |
| TRAF2 | 8353 |
| IKBKB | 7359 |
| CASP8 | 7096 |
| N4BP1 | 1599 |
| CHUK | -2452 |
| GeneID | Gene Rank |
|---|---|
| RPS27A | 17623 |
| UBC | 17042 |
| UBA52 | 15146 |
| LRRC14 | 15139 |
| UBB | 15063 |
| USP18 | 14882 |
| IKBIP | 12610 |
| NLRX1 | 12126 |
| TP53 | 11464 |
| NLRC5 | 9936 |
| TRAF6 | 9524 |
| USP14 | 8938 |
| TRAF2 | 8353 |
| IKBKB | 7359 |
| CASP8 | 7096 |
| N4BP1 | 1599 |
| CHUK | -2452 |
Olfactory Signaling Pathway
| 875 | |
|---|---|
| set | Olfactory Signaling Pathway |
| setSize | 365 |
| pANOVA | 3.28e-41 |
| s.dist | -0.409 |
| p.adjustANOVA | 2.6e-38 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| OR2A12 | -7381 |
| OR7E24 | -7370 |
| OR8U1 | -7368 |
| OR52A5 | -7357 |
| OR52D1 | -7353 |
| OR4Q3 | -7352 |
| OR13C8 | -7292 |
| OR10H3 | -7285 |
| OR52E4 | -7279 |
| OR5K1 | -7254 |
| OR8B2 | -7245 |
| OR4N4 | -7225 |
| OR8H1 | -7216 |
| OR6C1 | -7212 |
| OR2G6 | -7211 |
| OR5AC2 | -7206 |
| OR51G2 | -7199 |
| OR5T2 | -7182 |
| OR4D5 | -7160 |
| OR2W3 | -7151 |
| GeneID | Gene Rank |
|---|---|
| OR2A12 | -7381.0 |
| OR7E24 | -7370.0 |
| OR8U1 | -7368.0 |
| OR52A5 | -7357.0 |
| OR52D1 | -7353.0 |
| OR4Q3 | -7352.0 |
| OR13C8 | -7292.0 |
| OR10H3 | -7285.0 |
| OR52E4 | -7279.0 |
| OR5K1 | -7254.0 |
| OR8B2 | -7245.0 |
| OR4N4 | -7225.0 |
| OR8H1 | -7216.0 |
| OR6C1 | -7212.0 |
| OR2G6 | -7211.0 |
| OR5AC2 | -7206.0 |
| OR51G2 | -7199.0 |
| OR5T2 | -7182.0 |
| OR4D5 | -7160.0 |
| OR2W3 | -7151.0 |
| OR1J2 | -7147.0 |
| OR2G3 | -7137.0 |
| OR8D1 | -7128.0 |
| OR5K2 | -7124.0 |
| OR5P2 | -7115.0 |
| OR5K4 | -7106.0 |
| OR2T33 | -7059.0 |
| OR5B12 | -7058.0 |
| OR4F15 | -7048.0 |
| OR4E2 | -7013.0 |
| OR2B6 | -7012.0 |
| OR6Q1 | -7011.0 |
| OR7G2 | -6985.0 |
| OR52H1 | -6976.0 |
| OR6M1 | -6975.0 |
| OR11G2 | -6970.0 |
| OR13F1 | -6959.0 |
| OR10G9 | -6944.0 |
| OR52I2 | -6940.0 |
| OR8I2 | -6922.0 |
| OR51I1 | -6895.0 |
| OR2K2 | -6891.0 |
| OR7D4 | -6884.0 |
| OR5K3 | -6882.0 |
| OR5AP2 | -6877.0 |
| OR6C2 | -6858.0 |
| OR9G1 | -6835.5 |
| OR9G9 | -6835.5 |
| OR4C45 | -6834.0 |
| OR5D18 | -6810.0 |
| OR13C4 | -6790.0 |
| OR14A16 | -6781.0 |
| OR12D2 | -6765.0 |
| OR51B6 | -6753.0 |
| OR5F1 | -6736.0 |
| OR2B3 | -6721.0 |
| OR8D2 | -6714.0 |
| OR52I1 | -6682.0 |
| OR10K2 | -6671.0 |
| OR5AK2 | -6666.0 |
| OR1S1 | -6615.0 |
| OR13C2 | -6588.0 |
| OR6K6 | -6556.0 |
| OR2A2 | -6552.0 |
| OR5AN1 | -6525.0 |
| OR10J1 | -6509.0 |
| OR4K14 | -6507.0 |
| OR6C75 | -6488.0 |
| OR10J5 | -6486.0 |
| OR10G8 | -6474.0 |
| OR56A1 | -6409.0 |
| OR8K3 | -6403.0 |
| OR13G1 | -6377.0 |
| OR1Q1 | -6372.0 |
| OR2T10 | -6350.0 |
| OR2M5 | -6345.0 |
| OR13C3 | -6339.0 |
| OR5P3 | -6333.0 |
| OR10W1 | -6317.0 |
| OR4N5 | -6306.0 |
| OR5AS1 | -6278.0 |
| OR5H1 | -6252.0 |
| OR10G4 | -6218.0 |
| OR6C6 | -6213.0 |
| OR6N2 | -6200.0 |
| OR10Q1 | -6180.0 |
| OR8U8 | -6153.0 |
| OR51V1 | -6140.0 |
| OR8H2 | -6098.0 |
| OR5M9 | -6090.0 |
| OR6C3 | -6089.0 |
| OR4B1 | -6088.0 |
| OR1J1 | -6071.0 |
| OR5D14 | -6062.0 |
| OR5L2 | -6055.0 |
| OR4C46 | -5996.0 |
| OR6B1 | -5960.0 |
| OR2A14 | -5920.0 |
| OR52E6 | -5900.0 |
| OR4D10 | -5889.0 |
| OR11A1 | -5871.0 |
| OR6C74 | -5838.0 |
| OR6C4 | -5836.0 |
| OR5W2 | -5825.0 |
| OR2W1 | -5811.0 |
| OR8H3 | -5790.0 |
| OR3A2 | -5776.0 |
| OR7A10 | -5772.0 |
| OR2M4 | -5748.0 |
| OR5M11 | -5726.0 |
| OR51I2 | -5649.0 |
| OR51A7 | -5647.0 |
| OR5M10 | -5630.0 |
| OR5H2 | -5605.0 |
| OR9G4 | -5594.0 |
| OR5D16 | -5563.0 |
| OR2D3 | -5546.0 |
| OR1K1 | -5497.0 |
| OR6F1 | -5459.0 |
| OR1L3 | -5413.0 |
| OR11H4 | -5359.0 |
| OR4A16 | -5356.0 |
| OR52N2 | -5327.0 |
| OR51B5 | -5325.0 |
| OR5B3 | -5286.0 |
| OR2AK2 | -5177.0 |
| OR4P4 | -5158.0 |
| OR4M1 | -5143.0 |
| OR8J3 | -5140.0 |
| OR10A6 | -5124.0 |
| OR8J1 | -5121.0 |
| OR1A2 | -5098.0 |
| OR4C13 | -5097.0 |
| OR2T1 | -5034.0 |
| OR2J2 | -5002.0 |
| OR1A1 | -4982.0 |
| OR1N2 | -4924.0 |
| OR4K13 | -4922.0 |
| OR4D1 | -4911.0 |
| OR8A1 | -4865.0 |
| OR52M1 | -4652.0 |
| OR2T8 | -4611.0 |
| OR10A4 | -4558.0 |
| OR10AD1 | -4545.0 |
| OR52E8 | -4542.0 |
| OR4A47 | -4495.0 |
| OR6B3 | -4493.0 |
| OR5M8 | -4482.0 |
| OR1E1 | -4435.0 |
| OR6A2 | -4158.0 |
| OR2Y1 | -4123.0 |
| OR5M3 | -4106.0 |
| OR52A1 | -4101.0 |
| GNG13 | -4054.0 |
| OR52B6 | -4041.0 |
| OR9A2 | -4028.0 |
| OR5T3 | -3979.0 |
| OR5M1 | -3966.0 |
| OR7G1 | -3955.0 |
| OR4C12 | -3940.0 |
| OR6C70 | -3937.0 |
| OR10A7 | -3934.0 |
| OR2T34 | -3916.0 |
| OR6C76 | -3912.0 |
| OR6T1 | -3825.0 |
| OR8S1 | -3730.0 |
| OR2L8 | -3715.0 |
| OR2H1 | -3700.0 |
| OR2AG1 | -3691.0 |
| OR3A1 | -3664.0 |
| OR5H6 | -3651.0 |
| OR10G3 | -3640.0 |
| OR52K2 | -3629.0 |
| OR1I1 | -3613.0 |
| OR4C6 | -3499.0 |
| OR51L1 | -3475.0 |
| OR10G7 | -3459.0 |
| OR51E2 | -3430.0 |
| OR4K17 | -3422.0 |
| OR2L5 | -3421.0 |
| OR2B2 | -3311.0 |
| OR10G2 | -3176.0 |
| OR8K1 | -3167.0 |
| OR51A2 | -3135.0 |
| OR8G1 | -3112.0 |
| OR10H1 | -3075.0 |
| OR51F2 | -3040.0 |
| OR2L13 | -2985.0 |
| OR2T6 | -2956.0 |
| OR52N1 | -2928.0 |
| OR4D11 | -2894.0 |
| OR4N2 | -2891.0 |
| OR10AG1 | -2553.0 |
| OR52R1 | -2519.0 |
| OR1B1 | -2477.0 |
| OR2J3 | -2412.0 |
| OR5V1 | -2284.0 |
| OR51T1 | -2207.0 |
| OR51B4 | -2171.0 |
| OR4K1 | -2153.0 |
| OR14C36 | -2066.0 |
| OR4D9 | -1979.0 |
| OR2G2 | -1911.0 |
| OR51B2 | -1813.0 |
| OR4X2 | -1674.0 |
| OR5B2 | -1670.0 |
| OR2M3 | -1627.0 |
| OR10S1 | -1558.0 |
| OR2T3 | -1489.0 |
| OR5H15 | -1427.0 |
| OR6P1 | -1408.0 |
| OR7A5 | -1357.0 |
| OR4F6 | -1282.0 |
| OR5C1 | -1268.0 |
| OR10A3 | -1203.0 |
| OR9Q1 | -1199.0 |
| OR6C65 | -1188.0 |
| OR1J4 | -1182.0 |
| OR2T4 | -1063.0 |
| OR56A3 | -1024.0 |
| OR2F1 | -957.0 |
| OR5T1 | -950.0 |
| OR6S1 | -839.0 |
| OR5R1 | -770.0 |
| OR6X1 | -670.0 |
| OR7C1 | -596.0 |
| OR1C1 | -469.0 |
| OR10H4 | -416.0 |
| OR7D2 | -245.0 |
| OR10C1 | 189.0 |
| REEP1 | 222.0 |
| OR51D1 | 350.0 |
| OR4D6 | 393.0 |
| OR14I1 | 439.0 |
| OR52E2 | 529.0 |
| OR5AU1 | 826.0 |
| OR1L6 | 884.0 |
| OR5A1 | 981.0 |
| OR56A4 | 1233.0 |
| OR12D3 | 1425.0 |
| OR52N5 | 1434.0 |
| OR4K15 | 1581.0 |
| OR1M1 | 1617.0 |
| OR5I1 | 1930.0 |
| ANO2 | 2111.0 |
| OR52K1 | 2152.0 |
| OR7A17 | 2227.0 |
| OR52J3 | 2294.0 |
| OR8B12 | 2362.0 |
| OR4S2 | 2386.0 |
| OR6Y1 | 2477.0 |
| GNB1 | 2634.0 |
| OR4K2 | 2788.0 |
| OR9K2 | 2795.0 |
| OR2L3 | 2808.0 |
| OR7C2 | 2904.0 |
| OR14J1 | 2966.0 |
| OR10T2 | 3085.0 |
| OR2C1 | 3091.0 |
| OR6V1 | 3199.0 |
| OR4D2 | 3275.0 |
| OR13C9 | 3403.0 |
| OR1E2 | 3635.0 |
| OR11L1 | 3856.0 |
| OR2AG2 | 3965.0 |
| OR11H6 | 3984.0 |
| OR8D4 | 4764.0 |
| OR1L8 | 4766.0 |
| OR4L1 | 4792.0 |
| OR8G5 | 4800.0 |
| OR6B2 | 5006.0 |
| EBF1 | 5132.0 |
| OR2A25 | 5362.0 |
| OR5D13 | 5440.0 |
| OR5B17 | 5595.0 |
| OR4C3 | 5647.0 |
| OR56A5 | 5830.0 |
| OR13J1 | 5895.0 |
| OR2Z1 | 6091.0 |
| OR9Q2 | 6260.0 |
| OR9I1 | 6545.0 |
| OR4K5 | 6553.0 |
| OR2M7 | 6606.0 |
| OR51M1 | 6711.0 |
| OR6K2 | 6910.0 |
| GNAL | 6927.0 |
| OR2D2 | 6931.0 |
| OR2AT4 | 7019.0 |
| RTP1 | 7037.0 |
| OR2H2 | 7205.0 |
| OR4M2 | 7432.0 |
| OR51S1 | 7615.0 |
| OR2T27 | 7636.0 |
| OR4C15 | 7930.0 |
| OR10A5 | 8093.0 |
| OR51E1 | 8132.0 |
| OR2T11 | 8306.0 |
| OR1L4 | 8788.0 |
| OR2W5 | 8872.0 |
| OR10K1 | 8931.0 |
| OR1D2 | 9324.0 |
| OR10X1 | 9650.0 |
| ADCY3 | 9770.0 |
| OR4X1 | 10189.0 |
| OR8K5 | 10313.0 |
| OR1N1 | 10825.0 |
| OR2S2 | 10832.0 |
| OR10A2 | 10874.0 |
| OR52L1 | 11054.0 |
| OR1L1 | 11223.0 |
| OR2V2 | 11274.0 |
| OR2F2 | 11301.0 |
| OR1F1 | 11439.0 |
| OR5J2 | 11629.0 |
| OR2AE1 | 11641.0 |
| OR5A2 | 12082.0 |
| LHX2 | 12100.0 |
| CNGA4 | 12115.0 |
| OR11H2 | 12259.0 |
| OR9A4 | 12413.0 |
| OR51G1 | 12446.0 |
| OR1G1 | 12459.0 |
| OR4S1 | 12547.0 |
| OR3A3 | 12685.0 |
| LDB1 | 12794.0 |
| OR8B4 | 12984.0 |
| OR10H5 | 13076.0 |
| OR4A15 | 13189.0 |
| OR13A1 | 13331.0 |
| OR10Z1 | 13351.0 |
| OR2B11 | 13393.0 |
| OR52W1 | 13423.0 |
| OR5B21 | 13461.0 |
| OR10J3 | 13598.0 |
| OR2C3 | 13675.0 |
| OR6N1 | 13782.0 |
| CNGB1 | 14697.0 |
| OR4A5 | 14912.0 |
| OR4C16 | 14952.0 |
| OR10P1 | 15124.0 |
| OR2L2 | 15471.0 |
| OR1S2 | 15520.0 |
| OR5L1 | 15697.0 |
| OR51A4 | 15799.0 |
| OR6K3 | 15979.0 |
| OR5AR1 | 16000.0 |
| OR56B1 | 16282.0 |
| OR2V1 | 16351.0 |
| OR10R2 | 16396.0 |
| OR52B2 | 16410.0 |
| OR2M2 | 16490.0 |
| OR10H2 | 16512.0 |
| OR10V1 | 16587.0 |
| OR51F1 | 16686.0 |
| OR8B8 | 16831.0 |
| OR51Q1 | 16994.0 |
| OR2AP1 | 17117.0 |
| RTP2 | 17287.0 |
| OR6C68 | 17620.0 |
| OR56B4 | 17811.0 |
| OR2A5 | 17820.0 |
| OR8G2 | 18086.0 |
| OR13D1 | 18192.0 |
| OR4C11 | 18210.0 |
| OR7G3 | 18227.0 |
Viral mRNA Translation
| 1534 | |
|---|---|
| set | Viral mRNA Translation |
| setSize | 84 |
| pANOVA | 1.32e-10 |
| s.dist | 0.405 |
| p.adjustANOVA | 2.12e-08 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPS17 | 17998 |
| RPL35A | 17964 |
| RPS27A | 17623 |
| RPL34 | 17570 |
| RPS14 | 17460 |
| RPL27 | 17419 |
| RPL18A | 17406 |
| RPSA | 16750 |
| RPS27 | 16701 |
| RPS28 | 16547 |
| RPL32 | 16401 |
| RPS16 | 16394 |
| RPL28 | 16373 |
| RPS10 | 16101 |
| RPL7 | 15788 |
| RPS21 | 15733 |
| RPL29 | 15716 |
| RPL10L | 15577 |
| RPL17 | 15487 |
| RPS24 | 15434 |
| GeneID | Gene Rank |
|---|---|
| RPS17 | 17998.0 |
| RPL35A | 17964.0 |
| RPS27A | 17623.0 |
| RPL34 | 17570.0 |
| RPS14 | 17460.0 |
| RPL27 | 17419.0 |
| RPL18A | 17406.0 |
| RPSA | 16750.0 |
| RPS27 | 16701.0 |
| RPS28 | 16547.0 |
| RPL32 | 16401.0 |
| RPS16 | 16394.0 |
| RPL28 | 16373.0 |
| RPS10 | 16101.0 |
| RPL7 | 15788.0 |
| RPS21 | 15733.0 |
| RPL29 | 15716.0 |
| RPL10L | 15577.0 |
| RPL17 | 15487.0 |
| RPS24 | 15434.0 |
| RPL23 | 15404.0 |
| RPS11 | 15381.0 |
| RPL38 | 15324.0 |
| RPS26 | 15184.0 |
| UBA52 | 15146.0 |
| RPS23 | 15084.0 |
| RPL24 | 14927.0 |
| RPS25 | 14869.0 |
| RPS6 | 14761.0 |
| RPL9 | 14519.0 |
| RPS9 | 14415.0 |
| RPS29 | 14234.0 |
| RPL26L1 | 14132.0 |
| RPL30 | 13945.0 |
| RPL14 | 13883.0 |
| RPL26 | 13496.0 |
| RPL7A | 13425.0 |
| RPS2 | 12789.0 |
| RPL12 | 12744.0 |
| RPL41 | 12555.0 |
| RPS7 | 12370.0 |
| RPL37A | 11838.0 |
| RPL3L | 11730.0 |
| RPS5 | 11632.0 |
| RPS18 | 11410.0 |
| RPL13A | 11201.5 |
| RPS3A | 11123.0 |
| RPL19 | 10992.0 |
| RPS19 | 10890.0 |
| RPL13 | 10808.0 |
| RPS8 | 10296.0 |
| RPS27L | 9869.0 |
| RPL39L | 9655.0 |
| RPL18 | 9621.0 |
| GRSF1 | 9256.0 |
| RPL23A | 8852.0 |
| RPLP1 | 8689.0 |
| DNAJC3 | 8665.0 |
| RPLP2 | 8239.0 |
| RPL37 | 7695.0 |
| RPS13 | 7369.0 |
| RPL36AL | 7147.0 |
| RPS20 | 7077.0 |
| RPL4 | 6779.0 |
| RPL36 | 6145.0 |
| RPS3 | 5505.0 |
| RPL8 | 5310.0 |
| RPL10A | 5072.0 |
| RPL15 | 4446.0 |
| RPL3 | 4267.0 |
| RPLP0 | 3455.0 |
| RPS15A | 3120.0 |
| RPL11 | 2419.0 |
| RPS12 | 2257.0 |
| RPL27A | 1306.0 |
| RPL22 | 1272.0 |
| RPL5 | 852.0 |
| RPL31 | 733.0 |
| RPL35 | 467.0 |
| RPS15 | -220.0 |
| RPL21 | -682.0 |
| FAU | -1469.0 |
| RPL22L1 | -1702.0 |
| RPL6 | -4235.0 |
APC/C:Cdc20 mediated degradation of Cyclin B
| 13 | |
|---|---|
| set | APC/C:Cdc20 mediated degradation of Cyclin B |
| setSize | 24 |
| pANOVA | 0.000662 |
| s.dist | 0.401 |
| p.adjustANOVA | 0.0188 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPS27A | 17623 |
| UBC | 17042 |
| ANAPC15 | 16288 |
| UBE2S | 15864 |
| CDC20 | 15528 |
| UBA52 | 15146 |
| UBB | 15063 |
| CDK1 | 14620 |
| ANAPC7 | 13840 |
| ANAPC11 | 13372 |
| ANAPC10 | 12673 |
| CDC23 | 12635 |
| ANAPC1 | 12119 |
| ANAPC2 | 11107 |
| ANAPC4 | 10052 |
| UBE2C | 7012 |
| CCNB1 | 6871 |
| CDC16 | 5961 |
| ANAPC16 | 5542 |
| UBE2D1 | 4603 |
| GeneID | Gene Rank |
|---|---|
| RPS27A | 17623 |
| UBC | 17042 |
| ANAPC15 | 16288 |
| UBE2S | 15864 |
| CDC20 | 15528 |
| UBA52 | 15146 |
| UBB | 15063 |
| CDK1 | 14620 |
| ANAPC7 | 13840 |
| ANAPC11 | 13372 |
| ANAPC10 | 12673 |
| CDC23 | 12635 |
| ANAPC1 | 12119 |
| ANAPC2 | 11107 |
| ANAPC4 | 10052 |
| UBE2C | 7012 |
| CCNB1 | 6871 |
| CDC16 | 5961 |
| ANAPC16 | 5542 |
| UBE2D1 | 4603 |
| ANAPC5 | 3493 |
| UBE2E1 | 2742 |
| CDC26 | 2559 |
| CDC27 | 1689 |
Eukaryotic Translation Termination
| 401 | |
|---|---|
| set | Eukaryotic Translation Termination |
| setSize | 87 |
| pANOVA | 1.35e-10 |
| s.dist | 0.398 |
| p.adjustANOVA | 2.12e-08 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPS17 | 17998 |
| RPL35A | 17964 |
| APEH | 17849 |
| RPS27A | 17623 |
| RPL34 | 17570 |
| RPS14 | 17460 |
| RPL27 | 17419 |
| RPL18A | 17406 |
| RPSA | 16750 |
| RPS27 | 16701 |
| RPS28 | 16547 |
| RPL32 | 16401 |
| RPS16 | 16394 |
| RPL28 | 16373 |
| RPS10 | 16101 |
| RPL7 | 15788 |
| RPS21 | 15733 |
| RPL29 | 15716 |
| RPL10L | 15577 |
| RPL17 | 15487 |
| GeneID | Gene Rank |
|---|---|
| RPS17 | 17998.0 |
| RPL35A | 17964.0 |
| APEH | 17849.0 |
| RPS27A | 17623.0 |
| RPL34 | 17570.0 |
| RPS14 | 17460.0 |
| RPL27 | 17419.0 |
| RPL18A | 17406.0 |
| RPSA | 16750.0 |
| RPS27 | 16701.0 |
| RPS28 | 16547.0 |
| RPL32 | 16401.0 |
| RPS16 | 16394.0 |
| RPL28 | 16373.0 |
| RPS10 | 16101.0 |
| RPL7 | 15788.0 |
| RPS21 | 15733.0 |
| RPL29 | 15716.0 |
| RPL10L | 15577.0 |
| RPL17 | 15487.0 |
| RPS24 | 15434.0 |
| RPL23 | 15404.0 |
| RPS11 | 15381.0 |
| RPL38 | 15324.0 |
| RPS26 | 15184.0 |
| UBA52 | 15146.0 |
| RPS23 | 15084.0 |
| RPL24 | 14927.0 |
| RPS25 | 14869.0 |
| RPS6 | 14761.0 |
| RPL9 | 14519.0 |
| RPS9 | 14415.0 |
| RPS29 | 14234.0 |
| RPL26L1 | 14132.0 |
| RPL30 | 13945.0 |
| RPL14 | 13883.0 |
| RPL26 | 13496.0 |
| RPL7A | 13425.0 |
| RPS2 | 12789.0 |
| RPL12 | 12744.0 |
| RPL41 | 12555.0 |
| RPS7 | 12370.0 |
| RPL37A | 11838.0 |
| RPL3L | 11730.0 |
| N6AMT1 | 11698.0 |
| RPS5 | 11632.0 |
| RPS18 | 11410.0 |
| RPL13A | 11201.5 |
| RPS3A | 11123.0 |
| RPL19 | 10992.0 |
| RPS19 | 10890.0 |
| RPL13 | 10808.0 |
| RPS8 | 10296.0 |
| RPS27L | 9869.0 |
| RPL39L | 9655.0 |
| RPL18 | 9621.0 |
| RPL23A | 8852.0 |
| RPLP1 | 8689.0 |
| RPLP2 | 8239.0 |
| RPL37 | 7695.0 |
| RPS13 | 7369.0 |
| RPL36AL | 7147.0 |
| RPS20 | 7077.0 |
| RPL4 | 6779.0 |
| RPL36 | 6145.0 |
| RPS3 | 5505.0 |
| RPL8 | 5310.0 |
| RPL10A | 5072.0 |
| ETF1 | 4788.0 |
| RPL15 | 4446.0 |
| RPL3 | 4267.0 |
| GSPT1 | 4234.0 |
| RPLP0 | 3455.0 |
| RPS15A | 3120.0 |
| TRMT112 | 3046.0 |
| RPL11 | 2419.0 |
| RPS12 | 2257.0 |
| RPL27A | 1306.0 |
| RPL22 | 1272.0 |
| RPL5 | 852.0 |
| RPL31 | 733.0 |
| RPL35 | 467.0 |
| RPS15 | -220.0 |
| RPL21 | -682.0 |
| FAU | -1469.0 |
| RPL22L1 | -1702.0 |
| RPL6 | -4235.0 |
Eukaryotic Translation Elongation
| 399 | |
|---|---|
| set | Eukaryotic Translation Elongation |
| setSize | 88 |
| pANOVA | 1.47e-10 |
| s.dist | 0.395 |
| p.adjustANOVA | 2.12e-08 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPS17 | 17998 |
| RPL35A | 17964 |
| RPS27A | 17623 |
| RPL34 | 17570 |
| RPS14 | 17460 |
| RPL27 | 17419 |
| RPL18A | 17406 |
| RPSA | 16750 |
| RPS27 | 16701 |
| RPS28 | 16547 |
| RPL32 | 16401 |
| RPS16 | 16394 |
| RPL28 | 16373 |
| RPS10 | 16101 |
| EEF2 | 15877 |
| RPL7 | 15788 |
| RPS21 | 15733 |
| RPL29 | 15716 |
| RPL10L | 15577 |
| RPL17 | 15487 |
| GeneID | Gene Rank |
|---|---|
| RPS17 | 17998.0 |
| RPL35A | 17964.0 |
| RPS27A | 17623.0 |
| RPL34 | 17570.0 |
| RPS14 | 17460.0 |
| RPL27 | 17419.0 |
| RPL18A | 17406.0 |
| RPSA | 16750.0 |
| RPS27 | 16701.0 |
| RPS28 | 16547.0 |
| RPL32 | 16401.0 |
| RPS16 | 16394.0 |
| RPL28 | 16373.0 |
| RPS10 | 16101.0 |
| EEF2 | 15877.0 |
| RPL7 | 15788.0 |
| RPS21 | 15733.0 |
| RPL29 | 15716.0 |
| RPL10L | 15577.0 |
| RPL17 | 15487.0 |
| RPS24 | 15434.0 |
| RPL23 | 15404.0 |
| RPS11 | 15381.0 |
| RPL38 | 15324.0 |
| RPS26 | 15184.0 |
| UBA52 | 15146.0 |
| RPS23 | 15084.0 |
| RPL24 | 14927.0 |
| RPS25 | 14869.0 |
| RPS6 | 14761.0 |
| RPL9 | 14519.0 |
| RPS9 | 14415.0 |
| RPS29 | 14234.0 |
| RPL26L1 | 14132.0 |
| RPL30 | 13945.0 |
| RPL14 | 13883.0 |
| RPL26 | 13496.0 |
| RPL7A | 13425.0 |
| RPS2 | 12789.0 |
| RPL12 | 12744.0 |
| RPL41 | 12555.0 |
| RPS7 | 12370.0 |
| RPL37A | 11838.0 |
| RPL3L | 11730.0 |
| RPS5 | 11632.0 |
| RPS18 | 11410.0 |
| RPL13A | 11201.5 |
| RPS3A | 11123.0 |
| RPL19 | 10992.0 |
| RPS19 | 10890.0 |
| RPL13 | 10808.0 |
| RPS8 | 10296.0 |
| RPS27L | 9869.0 |
| RPL39L | 9655.0 |
| RPL18 | 9621.0 |
| EEF1A1 | 9096.0 |
| EEF1D | 8934.0 |
| RPL23A | 8852.0 |
| RPLP1 | 8689.0 |
| EEF1A2 | 8347.0 |
| RPLP2 | 8239.0 |
| EEF1G | 8025.0 |
| RPL37 | 7695.0 |
| RPS13 | 7369.0 |
| RPL36AL | 7147.0 |
| RPS20 | 7077.0 |
| RPL4 | 6779.0 |
| RPL36 | 6145.0 |
| RPS3 | 5505.0 |
| RPL8 | 5310.0 |
| RPL10A | 5072.0 |
| RPL15 | 4446.0 |
| RPL3 | 4267.0 |
| RPLP0 | 3455.0 |
| RPS15A | 3120.0 |
| RPL11 | 2419.0 |
| RPS12 | 2257.0 |
| RPL27A | 1306.0 |
| RPL22 | 1272.0 |
| RPL5 | 852.0 |
| RPL31 | 733.0 |
| RPL35 | 467.0 |
| RPS15 | -220.0 |
| RPL21 | -682.0 |
| FAU | -1469.0 |
| EEF1B2 | -1647.0 |
| RPL22L1 | -1702.0 |
| RPL6 | -4235.0 |
NF-kB activation through FADD/RIP-1 pathway mediated by caspase-8 and -10
| 797 | |
|---|---|
| set | NF-kB activation through FADD/RIP-1 pathway mediated by caspase-8 and -10 |
| setSize | 11 |
| pANOVA | 0.0268 |
| s.dist | -0.385 |
| p.adjustANOVA | 0.225 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| TRIM4 | -6652 |
| RIPK1 | -5245 |
| FADD | -4998 |
| CASP10 | -3558 |
| CHUK | -2452 |
| TRIM25 | -1856 |
| RNF135 | 4528 |
| IFIH1 | 5240 |
| MAVS | 5384 |
| CASP8 | 7096 |
| IKBKB | 7359 |
| GeneID | Gene Rank |
|---|---|
| TRIM4 | -6652 |
| RIPK1 | -5245 |
| FADD | -4998 |
| CASP10 | -3558 |
| CHUK | -2452 |
| TRIM25 | -1856 |
| RNF135 | 4528 |
| IFIH1 | 5240 |
| MAVS | 5384 |
| CASP8 | 7096 |
| IKBKB | 7359 |
Selenocysteine synthesis
| 1239 | |
|---|---|
| set | Selenocysteine synthesis |
| setSize | 87 |
| pANOVA | 1.02e-09 |
| s.dist | 0.378 |
| p.adjustANOVA | 1.29e-07 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPS17 | 17998 |
| RPL35A | 17964 |
| RPS27A | 17623 |
| RPL34 | 17570 |
| RPS14 | 17460 |
| RPL27 | 17419 |
| RPL18A | 17406 |
| RPSA | 16750 |
| RPS27 | 16701 |
| RPS28 | 16547 |
| RPL32 | 16401 |
| RPS16 | 16394 |
| RPL28 | 16373 |
| RPS10 | 16101 |
| RPL7 | 15788 |
| RPS21 | 15733 |
| RPL29 | 15716 |
| RPL10L | 15577 |
| RPL17 | 15487 |
| RPS24 | 15434 |
| GeneID | Gene Rank |
|---|---|
| RPS17 | 17998.0 |
| RPL35A | 17964.0 |
| RPS27A | 17623.0 |
| RPL34 | 17570.0 |
| RPS14 | 17460.0 |
| RPL27 | 17419.0 |
| RPL18A | 17406.0 |
| RPSA | 16750.0 |
| RPS27 | 16701.0 |
| RPS28 | 16547.0 |
| RPL32 | 16401.0 |
| RPS16 | 16394.0 |
| RPL28 | 16373.0 |
| RPS10 | 16101.0 |
| RPL7 | 15788.0 |
| RPS21 | 15733.0 |
| RPL29 | 15716.0 |
| RPL10L | 15577.0 |
| RPL17 | 15487.0 |
| RPS24 | 15434.0 |
| RPL23 | 15404.0 |
| RPS11 | 15381.0 |
| RPL38 | 15324.0 |
| RPS26 | 15184.0 |
| UBA52 | 15146.0 |
| RPS23 | 15084.0 |
| RPL24 | 14927.0 |
| RPS25 | 14869.0 |
| RPS6 | 14761.0 |
| RPL9 | 14519.0 |
| RPS9 | 14415.0 |
| RPS29 | 14234.0 |
| RPL26L1 | 14132.0 |
| RPL30 | 13945.0 |
| RPL14 | 13883.0 |
| RPL26 | 13496.0 |
| RPL7A | 13425.0 |
| RPS2 | 12789.0 |
| RPL12 | 12744.0 |
| RPL41 | 12555.0 |
| RPS7 | 12370.0 |
| RPL37A | 11838.0 |
| RPL3L | 11730.0 |
| RPS5 | 11632.0 |
| RPS18 | 11410.0 |
| RPL13A | 11201.5 |
| RPS3A | 11123.0 |
| RPL19 | 10992.0 |
| RPS19 | 10890.0 |
| RPL13 | 10808.0 |
| RPS8 | 10296.0 |
| RPS27L | 9869.0 |
| RPL39L | 9655.0 |
| RPL18 | 9621.0 |
| RPL23A | 8852.0 |
| RPLP1 | 8689.0 |
| RPLP2 | 8239.0 |
| RPL37 | 7695.0 |
| RPS13 | 7369.0 |
| RPL36AL | 7147.0 |
| RPS20 | 7077.0 |
| EEFSEC | 6881.0 |
| RPL4 | 6779.0 |
| RPL36 | 6145.0 |
| RPS3 | 5505.0 |
| RPL8 | 5310.0 |
| RPL10A | 5072.0 |
| RPL15 | 4446.0 |
| SEPHS2 | 4404.0 |
| RPL3 | 4267.0 |
| SECISBP2 | 4184.0 |
| RPLP0 | 3455.0 |
| SEPSECS | 3124.0 |
| RPS15A | 3120.0 |
| RPL11 | 2419.0 |
| RPS12 | 2257.0 |
| RPL27A | 1306.0 |
| RPL22 | 1272.0 |
| PSTK | 1189.0 |
| RPL5 | 852.0 |
| RPL31 | 733.0 |
| RPL35 | 467.0 |
| RPS15 | -220.0 |
| RPL21 | -682.0 |
| FAU | -1469.0 |
| RPL22L1 | -1702.0 |
| RPL6 | -4235.0 |
Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC)
| 851 | |
|---|---|
| set | Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC) |
| setSize | 89 |
| pANOVA | 1.18e-09 |
| s.dist | 0.373 |
| p.adjustANOVA | 1.29e-07 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPS17 | 17998 |
| RPL35A | 17964 |
| RPS27A | 17623 |
| RPL34 | 17570 |
| RPS14 | 17460 |
| RPL27 | 17419 |
| RPL18A | 17406 |
| RPSA | 16750 |
| RPS27 | 16701 |
| RPS28 | 16547 |
| RPL32 | 16401 |
| RPS16 | 16394 |
| RPL28 | 16373 |
| RPS10 | 16101 |
| RPL7 | 15788 |
| RPS21 | 15733 |
| RPL29 | 15716 |
| RPL10L | 15577 |
| RPL17 | 15487 |
| RPS24 | 15434 |
| GeneID | Gene Rank |
|---|---|
| RPS17 | 17998.0 |
| RPL35A | 17964.0 |
| RPS27A | 17623.0 |
| RPL34 | 17570.0 |
| RPS14 | 17460.0 |
| RPL27 | 17419.0 |
| RPL18A | 17406.0 |
| RPSA | 16750.0 |
| RPS27 | 16701.0 |
| RPS28 | 16547.0 |
| RPL32 | 16401.0 |
| RPS16 | 16394.0 |
| RPL28 | 16373.0 |
| RPS10 | 16101.0 |
| RPL7 | 15788.0 |
| RPS21 | 15733.0 |
| RPL29 | 15716.0 |
| RPL10L | 15577.0 |
| RPL17 | 15487.0 |
| RPS24 | 15434.0 |
| RPL23 | 15404.0 |
| RPS11 | 15381.0 |
| RPL38 | 15324.0 |
| RPS26 | 15184.0 |
| UBA52 | 15146.0 |
| RPS23 | 15084.0 |
| RPL24 | 14927.0 |
| RPS25 | 14869.0 |
| RPS6 | 14761.0 |
| RPL9 | 14519.0 |
| RPS9 | 14415.0 |
| RPS29 | 14234.0 |
| RPL26L1 | 14132.0 |
| RPL30 | 13945.0 |
| RPL14 | 13883.0 |
| RPL26 | 13496.0 |
| RPL7A | 13425.0 |
| EIF4G1 | 13114.0 |
| RPS2 | 12789.0 |
| RPL12 | 12744.0 |
| RPL41 | 12555.0 |
| RPS7 | 12370.0 |
| RPL37A | 11838.0 |
| RPL3L | 11730.0 |
| RPS5 | 11632.0 |
| RPS18 | 11410.0 |
| RPL13A | 11201.5 |
| RPS3A | 11123.0 |
| RPL19 | 10992.0 |
| RPS19 | 10890.0 |
| RPL13 | 10808.0 |
| RPS8 | 10296.0 |
| RPS27L | 9869.0 |
| RPL39L | 9655.0 |
| RPL18 | 9621.0 |
| UPF1 | 9418.0 |
| RPL23A | 8852.0 |
| RPLP1 | 8689.0 |
| RPLP2 | 8239.0 |
| RPL37 | 7695.0 |
| RPS13 | 7369.0 |
| RPL36AL | 7147.0 |
| RPS20 | 7077.0 |
| RPL4 | 6779.0 |
| RPL36 | 6145.0 |
| RPS3 | 5505.0 |
| RPL8 | 5310.0 |
| RPL10A | 5072.0 |
| ETF1 | 4788.0 |
| RPL15 | 4446.0 |
| RPL3 | 4267.0 |
| GSPT1 | 4234.0 |
| RPLP0 | 3455.0 |
| RPS15A | 3120.0 |
| RPL11 | 2419.0 |
| RPS12 | 2257.0 |
| PABPC1 | 1667.0 |
| NCBP1 | 1531.0 |
| RPL27A | 1306.0 |
| RPL22 | 1272.0 |
| RPL5 | 852.0 |
| RPL31 | 733.0 |
| RPL35 | 467.0 |
| RPS15 | -220.0 |
| RPL21 | -682.0 |
| NCBP2 | -975.0 |
| FAU | -1469.0 |
| RPL22L1 | -1702.0 |
| RPL6 | -4235.0 |
NRIF signals cell death from the nucleus
| 815 | |
|---|---|
| set | NRIF signals cell death from the nucleus |
| setSize | 16 |
| pANOVA | 0.01 |
| s.dist | 0.372 |
| p.adjustANOVA | 0.126 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPS27A | 17623 |
| APH1B | 17290 |
| UBC | 17042 |
| UBA52 | 15146 |
| UBB | 15063 |
| APH1A | 14609 |
| PSEN2 | 13707 |
| TRAF6 | 9524 |
| NGF | 8768 |
| PSEN1 | 8681 |
| PSENEN | 8537 |
| NGFR | 7653 |
| ITGB3BP | 5286 |
| SQSTM1 | 5152 |
| NCSTN | 2113 |
| MAPK8 | -3330 |
| GeneID | Gene Rank |
|---|---|
| RPS27A | 17623 |
| APH1B | 17290 |
| UBC | 17042 |
| UBA52 | 15146 |
| UBB | 15063 |
| APH1A | 14609 |
| PSEN2 | 13707 |
| TRAF6 | 9524 |
| NGF | 8768 |
| PSEN1 | 8681 |
| PSENEN | 8537 |
| NGFR | 7653 |
| ITGB3BP | 5286 |
| SQSTM1 | 5152 |
| NCSTN | 2113 |
| MAPK8 | -3330 |
TICAM1,TRAF6-dependent induction of TAK1 complex
| 1398 | |
|---|---|
| set | TICAM1,TRAF6-dependent induction of TAK1 complex |
| setSize | 10 |
| pANOVA | 0.0444 |
| s.dist | 0.367 |
| p.adjustANOVA | 0.296 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPS27A | 17623 |
| UBC | 17042 |
| MAP3K7 | 16345 |
| UBA52 | 15146 |
| UBB | 15063 |
| TLR3 | 11133 |
| TRAF6 | 9524 |
| TAB1 | 2822 |
| TICAM1 | 812 |
| TAB2 | -4298 |
| GeneID | Gene Rank |
|---|---|
| RPS27A | 17623 |
| UBC | 17042 |
| MAP3K7 | 16345 |
| UBA52 | 15146 |
| UBB | 15063 |
| TLR3 | 11133 |
| TRAF6 | 9524 |
| TAB1 | 2822 |
| TICAM1 | 812 |
| TAB2 | -4298 |
Intrinsic Pathway of Fibrin Clot Formation
| 662 | |
|---|---|
| set | Intrinsic Pathway of Fibrin Clot Formation |
| setSize | 21 |
| pANOVA | 0.00381 |
| s.dist | -0.365 |
| p.adjustANOVA | 0.0636 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| PROS1 | -6679 |
| GP5 | -5879 |
| SERPINC1 | -5768 |
| A2M | -4977 |
| F11 | -3879 |
| SERPIND1 | -3063 |
| SERPINE2 | -2989 |
| GP1BA | -2009 |
| PROC | -1021 |
| KNG1 | -830 |
| GP9 | 213 |
| F12 | 293 |
| F10 | 1817 |
| PRCP | 2075 |
| VWF | 4332 |
| SERPINA5 | 4505 |
| GP1BB | 5527 |
| SERPING1 | 5568 |
| KLKB1 | 5924 |
| C1QBP | 7179 |
| GeneID | Gene Rank |
|---|---|
| PROS1 | -6679 |
| GP5 | -5879 |
| SERPINC1 | -5768 |
| A2M | -4977 |
| F11 | -3879 |
| SERPIND1 | -3063 |
| SERPINE2 | -2989 |
| GP1BA | -2009 |
| PROC | -1021 |
| KNG1 | -830 |
| GP9 | 213 |
| F12 | 293 |
| F10 | 1817 |
| PRCP | 2075 |
| VWF | 4332 |
| SERPINA5 | 4505 |
| GP1BB | 5527 |
| SERPING1 | 5568 |
| KLKB1 | 5924 |
| C1QBP | 7179 |
| F2 | 14563 |
Tandem pore domain potassium channels
| 1425 | |
|---|---|
| set | Tandem pore domain potassium channels |
| setSize | 12 |
| pANOVA | 0.0288 |
| s.dist | 0.365 |
| p.adjustANOVA | 0.236 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| KCNK16 | 17421 |
| KCNK18 | 16819 |
| KCNK6 | 14501 |
| KCNK7 | 13732 |
| KCNK17 | 12557 |
| KCNK10 | 11671 |
| KCNK4 | 10547 |
| KCNK3 | 9192 |
| KCNK9 | 8381 |
| KCNK1 | 4007 |
| KCNK13 | 1366 |
| KCNK2 | 866 |
| GeneID | Gene Rank |
|---|---|
| KCNK16 | 17421 |
| KCNK18 | 16819 |
| KCNK6 | 14501 |
| KCNK7 | 13732 |
| KCNK17 | 12557 |
| KCNK10 | 11671 |
| KCNK4 | 10547 |
| KCNK3 | 9192 |
| KCNK9 | 8381 |
| KCNK1 | 4007 |
| KCNK13 | 1366 |
| KCNK2 | 866 |
Regulation of IFNA/IFNB signaling
| 1117 | |
|---|---|
| set | Regulation of IFNA/IFNB signaling |
| setSize | 22 |
| pANOVA | 0.00331 |
| s.dist | -0.362 |
| p.adjustANOVA | 0.0584 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| IFNA6 | -7454 |
| IFNA16 | -7423 |
| IFNA2 | -7251 |
| IFNA21 | -7180 |
| IFNA14 | -7099 |
| IFNB1 | -7088 |
| IFNA1 | -7038 |
| IFNA5 | -5828 |
| PTPN11 | -5020 |
| IFNA7 | -4450 |
| STAT1 | -4154 |
| IFNA8 | -2780 |
| JAK1 | -1659 |
| STAT2 | 4463 |
| IFNAR2 | 5854 |
| TYK2 | 6414 |
| SOCS3 | 7430 |
| PTPN1 | 10443 |
| PTPN6 | 11736 |
| IFNAR1 | 13771 |
| GeneID | Gene Rank |
|---|---|
| IFNA6 | -7454 |
| IFNA16 | -7423 |
| IFNA2 | -7251 |
| IFNA21 | -7180 |
| IFNA14 | -7099 |
| IFNB1 | -7088 |
| IFNA1 | -7038 |
| IFNA5 | -5828 |
| PTPN11 | -5020 |
| IFNA7 | -4450 |
| STAT1 | -4154 |
| IFNA8 | -2780 |
| JAK1 | -1659 |
| STAT2 | 4463 |
| IFNAR2 | 5854 |
| TYK2 | 6414 |
| SOCS3 | 7430 |
| PTPN1 | 10443 |
| PTPN6 | 11736 |
| IFNAR1 | 13771 |
| USP18 | 14882 |
| SOCS1 | 15898 |
Response of EIF2AK4 (GCN2) to amino acid deficiency
| 1176 | |
|---|---|
| set | Response of EIF2AK4 (GCN2) to amino acid deficiency |
| setSize | 95 |
| pANOVA | 1.17e-09 |
| s.dist | 0.361 |
| p.adjustANOVA | 1.29e-07 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPS17 | 17998 |
| RPL35A | 17964 |
| RPS27A | 17623 |
| RPL34 | 17570 |
| RPS14 | 17460 |
| RPL27 | 17419 |
| RPL18A | 17406 |
| RPSA | 16750 |
| RPS27 | 16701 |
| RPS28 | 16547 |
| RPL32 | 16401 |
| RPS16 | 16394 |
| RPL28 | 16373 |
| RPS10 | 16101 |
| RPL7 | 15788 |
| RPS21 | 15733 |
| RPL29 | 15716 |
| RPL10L | 15577 |
| RPL17 | 15487 |
| RPS24 | 15434 |
| GeneID | Gene Rank |
|---|---|
| RPS17 | 17998.0 |
| RPL35A | 17964.0 |
| RPS27A | 17623.0 |
| RPL34 | 17570.0 |
| RPS14 | 17460.0 |
| RPL27 | 17419.0 |
| RPL18A | 17406.0 |
| RPSA | 16750.0 |
| RPS27 | 16701.0 |
| RPS28 | 16547.0 |
| RPL32 | 16401.0 |
| RPS16 | 16394.0 |
| RPL28 | 16373.0 |
| RPS10 | 16101.0 |
| RPL7 | 15788.0 |
| RPS21 | 15733.0 |
| RPL29 | 15716.0 |
| RPL10L | 15577.0 |
| RPL17 | 15487.0 |
| RPS24 | 15434.0 |
| RPL23 | 15404.0 |
| ATF2 | 15388.0 |
| RPS11 | 15381.0 |
| RPL38 | 15324.0 |
| RPS26 | 15184.0 |
| UBA52 | 15146.0 |
| RPS23 | 15084.0 |
| RPL24 | 14927.0 |
| RPS25 | 14869.0 |
| RPS6 | 14761.0 |
| RPL9 | 14519.0 |
| RPS9 | 14415.0 |
| RPS29 | 14234.0 |
| RPL26L1 | 14132.0 |
| RPL30 | 13945.0 |
| RPL14 | 13883.0 |
| RPL26 | 13496.0 |
| RPL7A | 13425.0 |
| DDIT3 | 13284.0 |
| GCN1 | 13237.0 |
| RPS2 | 12789.0 |
| RPL12 | 12744.0 |
| RPL41 | 12555.0 |
| RPS7 | 12370.0 |
| CEBPG | 12189.0 |
| RPL37A | 11838.0 |
| RPL3L | 11730.0 |
| RPS5 | 11632.0 |
| EIF2AK4 | 11475.0 |
| RPS18 | 11410.0 |
| RPL13A | 11201.5 |
| RPS3A | 11123.0 |
| RPL19 | 10992.0 |
| RPS19 | 10890.0 |
| RPL13 | 10808.0 |
| RPS8 | 10296.0 |
| RPS27L | 9869.0 |
| RPL39L | 9655.0 |
| RPL18 | 9621.0 |
| RPL23A | 8852.0 |
| RPLP1 | 8689.0 |
| RPLP2 | 8239.0 |
| ASNS | 7915.0 |
| RPL37 | 7695.0 |
| RPS13 | 7369.0 |
| RPL36AL | 7147.0 |
| RPS20 | 7077.0 |
| RPL4 | 6779.0 |
| RPL36 | 6145.0 |
| RPS3 | 5505.0 |
| RPL8 | 5310.0 |
| RPL10A | 5072.0 |
| ATF4 | 4664.0 |
| RPL15 | 4446.0 |
| RPL3 | 4267.0 |
| RPLP0 | 3455.0 |
| RPS15A | 3120.0 |
| CEBPB | 2992.0 |
| RPL11 | 2419.0 |
| RPS12 | 2257.0 |
| EIF2S1 | 1847.0 |
| ATF3 | 1514.0 |
| RPL27A | 1306.0 |
| RPL22 | 1272.0 |
| RPL5 | 852.0 |
| RPL31 | 733.0 |
| TRIB3 | 530.0 |
| RPL35 | 467.0 |
| RPS15 | -220.0 |
| RPL21 | -682.0 |
| EIF2S2 | -941.0 |
| FAU | -1469.0 |
| RPL22L1 | -1702.0 |
| IMPACT | -3793.0 |
| RPL6 | -4235.0 |
Formation of a pool of free 40S subunits
| 454 | |
|---|---|
| set | Formation of a pool of free 40S subunits |
| setSize | 94 |
| pANOVA | 1.71e-09 |
| s.dist | 0.359 |
| p.adjustANOVA | 1.69e-07 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPS17 | 17998 |
| RPL35A | 17964 |
| EIF3G | 17865 |
| RPS27A | 17623 |
| RPL34 | 17570 |
| RPS14 | 17460 |
| RPL27 | 17419 |
| RPL18A | 17406 |
| RPSA | 16750 |
| RPS27 | 16701 |
| RPS28 | 16547 |
| RPL32 | 16401 |
| RPS16 | 16394 |
| RPL28 | 16373 |
| RPS10 | 16101 |
| RPL7 | 15788 |
| RPS21 | 15733 |
| RPL29 | 15716 |
| RPL10L | 15577 |
| RPL17 | 15487 |
| GeneID | Gene Rank |
|---|---|
| RPS17 | 17998.0 |
| RPL35A | 17964.0 |
| EIF3G | 17865.0 |
| RPS27A | 17623.0 |
| RPL34 | 17570.0 |
| RPS14 | 17460.0 |
| RPL27 | 17419.0 |
| RPL18A | 17406.0 |
| RPSA | 16750.0 |
| RPS27 | 16701.0 |
| RPS28 | 16547.0 |
| RPL32 | 16401.0 |
| RPS16 | 16394.0 |
| RPL28 | 16373.0 |
| RPS10 | 16101.0 |
| RPL7 | 15788.0 |
| RPS21 | 15733.0 |
| RPL29 | 15716.0 |
| RPL10L | 15577.0 |
| RPL17 | 15487.0 |
| RPS24 | 15434.0 |
| RPL23 | 15404.0 |
| RPS11 | 15381.0 |
| RPL38 | 15324.0 |
| RPS26 | 15184.0 |
| UBA52 | 15146.0 |
| RPS23 | 15084.0 |
| RPL24 | 14927.0 |
| RPS25 | 14869.0 |
| RPS6 | 14761.0 |
| EIF3D | 14542.0 |
| RPL9 | 14519.0 |
| RPS9 | 14415.0 |
| RPS29 | 14234.0 |
| RPL26L1 | 14132.0 |
| RPL30 | 13945.0 |
| RPL14 | 13883.0 |
| RPL26 | 13496.0 |
| RPL7A | 13425.0 |
| EIF3I | 12960.0 |
| RPS2 | 12789.0 |
| RPL12 | 12744.0 |
| RPL41 | 12555.0 |
| RPS7 | 12370.0 |
| RPL37A | 11838.0 |
| RPL3L | 11730.0 |
| RPS5 | 11632.0 |
| RPS18 | 11410.0 |
| RPL13A | 11201.5 |
| RPS3A | 11123.0 |
| RPL19 | 10992.0 |
| RPS19 | 10890.0 |
| RPL13 | 10808.0 |
| RPS8 | 10296.0 |
| RPS27L | 9869.0 |
| RPL39L | 9655.0 |
| RPL18 | 9621.0 |
| RPL23A | 8852.0 |
| RPLP1 | 8689.0 |
| RPLP2 | 8239.0 |
| RPL37 | 7695.0 |
| EIF3B | 7424.0 |
| RPS13 | 7369.0 |
| RPL36AL | 7147.0 |
| RPS20 | 7077.0 |
| RPL4 | 6779.0 |
| EIF3J | 6721.0 |
| EIF3E | 6441.0 |
| RPL36 | 6145.0 |
| RPS3 | 5505.0 |
| RPL8 | 5310.0 |
| RPL10A | 5072.0 |
| EIF3K | 4535.0 |
| RPL15 | 4446.0 |
| RPL3 | 4267.0 |
| EIF3L | 3545.0 |
| RPLP0 | 3455.0 |
| EIF3F | 3217.0 |
| RPS15A | 3120.0 |
| RPL11 | 2419.0 |
| RPS12 | 2257.0 |
| RPL27A | 1306.0 |
| RPL22 | 1272.0 |
| RPL5 | 852.0 |
| RPL31 | 733.0 |
| RPL35 | 467.0 |
| RPS15 | -220.0 |
| RPL21 | -682.0 |
| FAU | -1469.0 |
| EIF3H | -1690.0 |
| RPL22L1 | -1702.0 |
| EIF3A | -3383.0 |
| EIF3M | -3931.0 |
| RPL6 | -4235.0 |
Signaling by cytosolic FGFR1 fusion mutants
| 1342 | |
|---|---|
| set | Signaling by cytosolic FGFR1 fusion mutants |
| setSize | 17 |
| pANOVA | 0.0108 |
| s.dist | -0.357 |
| p.adjustANOVA | 0.131 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| ZMYM2 | -5435 |
| STAT1 | -4154 |
| TRIM24 | -3939 |
| STAT5A | -3538 |
| STAT5B | -2708 |
| GAB2 | -2592 |
| CNTRL | -974 |
| CUX1 | -850 |
| STAT3 | 454 |
| LRRFIP1 | 987 |
| FGFR1OP2 | 1031 |
| GRB2 | 3241 |
| CPSF6 | 3376 |
| PIK3CA | 5249 |
| BCR | 7309 |
| MYO18A | 7475 |
| PIK3R1 | 8833 |
| GeneID | Gene Rank |
|---|---|
| ZMYM2 | -5435 |
| STAT1 | -4154 |
| TRIM24 | -3939 |
| STAT5A | -3538 |
| STAT5B | -2708 |
| GAB2 | -2592 |
| CNTRL | -974 |
| CUX1 | -850 |
| STAT3 | 454 |
| LRRFIP1 | 987 |
| FGFR1OP2 | 1031 |
| GRB2 | 3241 |
| CPSF6 | 3376 |
| PIK3CA | 5249 |
| BCR | 7309 |
| MYO18A | 7475 |
| PIK3R1 | 8833 |
Sensory perception of sweet, bitter, and umami (glutamate) taste
| 1246 | |
|---|---|
| set | Sensory perception of sweet, bitter, and umami (glutamate) taste |
| setSize | 41 |
| pANOVA | 7.68e-05 |
| s.dist | -0.357 |
| p.adjustANOVA | 0.00244 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| TAS2R46 | -7339 |
| TAS2R10 | -7306 |
| TAS2R4 | -7233 |
| TAS2R14 | -6983 |
| TAS2R50 | -6656 |
| TAS2R8 | -6601 |
| TAS2R43 | -6600 |
| TAS2R39 | -6469 |
| TAS2R13 | -6411 |
| TAS2R3 | -6389 |
| TAS2R31 | -5781 |
| TAS2R30 | -5769 |
| TAS2R5 | -5318 |
| GNAT3 | -4554 |
| TAS2R7 | -4436 |
| TAS2R16 | -4099 |
| GNG13 | -4054 |
| TAS2R1 | -3267 |
| TAS2R38 | -2766 |
| SCN3A | -1615 |
| GeneID | Gene Rank |
|---|---|
| TAS2R46 | -7339 |
| TAS2R10 | -7306 |
| TAS2R4 | -7233 |
| TAS2R14 | -6983 |
| TAS2R50 | -6656 |
| TAS2R8 | -6601 |
| TAS2R43 | -6600 |
| TAS2R39 | -6469 |
| TAS2R13 | -6411 |
| TAS2R3 | -6389 |
| TAS2R31 | -5781 |
| TAS2R30 | -5769 |
| TAS2R5 | -5318 |
| GNAT3 | -4554 |
| TAS2R7 | -4436 |
| TAS2R16 | -4099 |
| GNG13 | -4054 |
| TAS2R1 | -3267 |
| TAS2R38 | -2766 |
| SCN3A | -1615 |
| TAS1R2 | -767 |
| TAS2R20 | -749 |
| GRM1 | 2427 |
| GNB1 | 2634 |
| SCN9A | 2744 |
| CALHM1 | 2907 |
| PLCB2 | 3318 |
| SCN2B | 3609 |
| CALHM3 | 4068 |
| TAS1R3 | 5729 |
| TAS2R40 | 7295 |
| SCN2A | 7350 |
| GNB3 | 7987 |
| SCN4B | 8832 |
| GRM4 | 8862 |
| TAS2R41 | 9019 |
| ITPR3 | 10927 |
| TRPM5 | 11997 |
| TRPM4 | 13148 |
| SCN1B | 14870 |
| TAS1R1 | 16838 |
Pausing and recovery of Tat-mediated HIV elongation
| 925 | |
|---|---|
| set | Pausing and recovery of Tat-mediated HIV elongation |
| setSize | 27 |
| pANOVA | 0.00137 |
| s.dist | 0.356 |
| p.adjustANOVA | 0.0311 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| POLR2K | 18005 |
| SUPT5H | 17546 |
| POLR2J | 17537 |
| NELFB | 17306 |
| CDK9 | 16364 |
| TCEA1 | 16072 |
| POLR2E | 15351 |
| SUPT4H1 | 15226 |
| POLR2D | 15138 |
| SSRP1 | 14710 |
| CCNT1 | 13227 |
| POLR2H | 11868 |
| POLR2L | 11588 |
| POLR2F | 11205 |
| POLR2I | 10571 |
| ELL | 9284 |
| NELFA | 7707 |
| POLR2A | 7258 |
| POLR2B | 5067 |
| NELFE | 5043 |
| GeneID | Gene Rank |
|---|---|
| POLR2K | 18005 |
| SUPT5H | 17546 |
| POLR2J | 17537 |
| NELFB | 17306 |
| CDK9 | 16364 |
| TCEA1 | 16072 |
| POLR2E | 15351 |
| SUPT4H1 | 15226 |
| POLR2D | 15138 |
| SSRP1 | 14710 |
| CCNT1 | 13227 |
| POLR2H | 11868 |
| POLR2L | 11588 |
| POLR2F | 11205 |
| POLR2I | 10571 |
| ELL | 9284 |
| NELFA | 7707 |
| POLR2A | 7258 |
| POLR2B | 5067 |
| NELFE | 5043 |
| POLR2C | 4753 |
| POLR2G | 3709 |
| SUPT16H | 2892 |
| CTDP1 | 2574 |
| NELFCD | 1651 |
| GTF2F1 | 269 |
| GTF2F2 | -2649 |
Tat-mediated HIV elongation arrest and recovery
| 1426 | |
|---|---|
| set | Tat-mediated HIV elongation arrest and recovery |
| setSize | 27 |
| pANOVA | 0.00137 |
| s.dist | 0.356 |
| p.adjustANOVA | 0.0311 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| POLR2K | 18005 |
| SUPT5H | 17546 |
| POLR2J | 17537 |
| NELFB | 17306 |
| CDK9 | 16364 |
| TCEA1 | 16072 |
| POLR2E | 15351 |
| SUPT4H1 | 15226 |
| POLR2D | 15138 |
| SSRP1 | 14710 |
| CCNT1 | 13227 |
| POLR2H | 11868 |
| POLR2L | 11588 |
| POLR2F | 11205 |
| POLR2I | 10571 |
| ELL | 9284 |
| NELFA | 7707 |
| POLR2A | 7258 |
| POLR2B | 5067 |
| NELFE | 5043 |
| GeneID | Gene Rank |
|---|---|
| POLR2K | 18005 |
| SUPT5H | 17546 |
| POLR2J | 17537 |
| NELFB | 17306 |
| CDK9 | 16364 |
| TCEA1 | 16072 |
| POLR2E | 15351 |
| SUPT4H1 | 15226 |
| POLR2D | 15138 |
| SSRP1 | 14710 |
| CCNT1 | 13227 |
| POLR2H | 11868 |
| POLR2L | 11588 |
| POLR2F | 11205 |
| POLR2I | 10571 |
| ELL | 9284 |
| NELFA | 7707 |
| POLR2A | 7258 |
| POLR2B | 5067 |
| NELFE | 5043 |
| POLR2C | 4753 |
| POLR2G | 3709 |
| SUPT16H | 2892 |
| CTDP1 | 2574 |
| NELFCD | 1651 |
| GTF2F1 | 269 |
| GTF2F2 | -2649 |
Caspase activation via Death Receptors in the presence of ligand
| 175 | |
|---|---|
| set | Caspase activation via Death Receptors in the presence of ligand |
| setSize | 16 |
| pANOVA | 0.0142 |
| s.dist | -0.354 |
| p.adjustANOVA | 0.155 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| LY96 | -6864 |
| CD14 | -5904 |
| FASLG | -5653 |
| RIPK1 | -5245 |
| FADD | -4998 |
| TLR4 | -1575 |
| TICAM2 | -1504 |
| TNFRSF10A | -1218 |
| TNFRSF10B | 716 |
| TICAM1 | 812 |
| TNFSF10 | 1565 |
| CFLAR | 4199 |
| CASP8 | 7096 |
| FAS | 7842 |
| TRAF2 | 8353 |
| TRADD | 15909 |
| GeneID | Gene Rank |
|---|---|
| LY96 | -6864 |
| CD14 | -5904 |
| FASLG | -5653 |
| RIPK1 | -5245 |
| FADD | -4998 |
| TLR4 | -1575 |
| TICAM2 | -1504 |
| TNFRSF10A | -1218 |
| TNFRSF10B | 716 |
| TICAM1 | 812 |
| TNFSF10 | 1565 |
| CFLAR | 4199 |
| CASP8 | 7096 |
| FAS | 7842 |
| TRAF2 | 8353 |
| TRADD | 15909 |
p75NTR recruits signalling complexes
| 1576 | |
|---|---|
| set | p75NTR recruits signalling complexes |
| setSize | 12 |
| pANOVA | 0.0356 |
| s.dist | 0.35 |
| p.adjustANOVA | 0.258 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPS27A | 17623 |
| UBC | 17042 |
| UBA52 | 15146 |
| UBB | 15063 |
| MYD88 | 10379 |
| TRAF6 | 9524 |
| NGF | 8768 |
| NGFR | 7653 |
| IKBKB | 7359 |
| PRKCI | 5995 |
| SQSTM1 | 5152 |
| RIPK2 | -840 |
| GeneID | Gene Rank |
|---|---|
| RPS27A | 17623 |
| UBC | 17042 |
| UBA52 | 15146 |
| UBB | 15063 |
| MYD88 | 10379 |
| TRAF6 | 9524 |
| NGF | 8768 |
| NGFR | 7653 |
| IKBKB | 7359 |
| PRKCI | 5995 |
| SQSTM1 | 5152 |
| RIPK2 | -840 |
HIV elongation arrest and recovery
| 564 | |
|---|---|
| set | HIV elongation arrest and recovery |
| setSize | 29 |
| pANOVA | 0.00116 |
| s.dist | 0.348 |
| p.adjustANOVA | 0.0281 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| POLR2K | 18005 |
| SUPT5H | 17546 |
| POLR2J | 17537 |
| NELFB | 17306 |
| CDK9 | 16364 |
| TCEA1 | 16072 |
| POLR2E | 15351 |
| SUPT4H1 | 15226 |
| POLR2D | 15138 |
| SSRP1 | 14710 |
| CCNT1 | 13227 |
| POLR2H | 11868 |
| CCNK | 11598 |
| POLR2L | 11588 |
| POLR2F | 11205 |
| POLR2I | 10571 |
| ELL | 9284 |
| NELFA | 7707 |
| POLR2A | 7258 |
| CCNT2 | 5581 |
| GeneID | Gene Rank |
|---|---|
| POLR2K | 18005 |
| SUPT5H | 17546 |
| POLR2J | 17537 |
| NELFB | 17306 |
| CDK9 | 16364 |
| TCEA1 | 16072 |
| POLR2E | 15351 |
| SUPT4H1 | 15226 |
| POLR2D | 15138 |
| SSRP1 | 14710 |
| CCNT1 | 13227 |
| POLR2H | 11868 |
| CCNK | 11598 |
| POLR2L | 11588 |
| POLR2F | 11205 |
| POLR2I | 10571 |
| ELL | 9284 |
| NELFA | 7707 |
| POLR2A | 7258 |
| CCNT2 | 5581 |
| POLR2B | 5067 |
| NELFE | 5043 |
| POLR2C | 4753 |
| POLR2G | 3709 |
| SUPT16H | 2892 |
| CTDP1 | 2574 |
| NELFCD | 1651 |
| GTF2F1 | 269 |
| GTF2F2 | -2649 |
Pausing and recovery of HIV elongation
| 924 | |
|---|---|
| set | Pausing and recovery of HIV elongation |
| setSize | 29 |
| pANOVA | 0.00116 |
| s.dist | 0.348 |
| p.adjustANOVA | 0.0281 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| POLR2K | 18005 |
| SUPT5H | 17546 |
| POLR2J | 17537 |
| NELFB | 17306 |
| CDK9 | 16364 |
| TCEA1 | 16072 |
| POLR2E | 15351 |
| SUPT4H1 | 15226 |
| POLR2D | 15138 |
| SSRP1 | 14710 |
| CCNT1 | 13227 |
| POLR2H | 11868 |
| CCNK | 11598 |
| POLR2L | 11588 |
| POLR2F | 11205 |
| POLR2I | 10571 |
| ELL | 9284 |
| NELFA | 7707 |
| POLR2A | 7258 |
| CCNT2 | 5581 |
| GeneID | Gene Rank |
|---|---|
| POLR2K | 18005 |
| SUPT5H | 17546 |
| POLR2J | 17537 |
| NELFB | 17306 |
| CDK9 | 16364 |
| TCEA1 | 16072 |
| POLR2E | 15351 |
| SUPT4H1 | 15226 |
| POLR2D | 15138 |
| SSRP1 | 14710 |
| CCNT1 | 13227 |
| POLR2H | 11868 |
| CCNK | 11598 |
| POLR2L | 11588 |
| POLR2F | 11205 |
| POLR2I | 10571 |
| ELL | 9284 |
| NELFA | 7707 |
| POLR2A | 7258 |
| CCNT2 | 5581 |
| POLR2B | 5067 |
| NELFE | 5043 |
| POLR2C | 4753 |
| POLR2G | 3709 |
| SUPT16H | 2892 |
| CTDP1 | 2574 |
| NELFCD | 1651 |
| GTF2F1 | 269 |
| GTF2F2 | -2649 |
Formation of the ternary complex, and subsequently, the 43S complex
| 466 | |
|---|---|
| set | Formation of the ternary complex, and subsequently, the 43S complex |
| setSize | 46 |
| pANOVA | 4.47e-05 |
| s.dist | 0.348 |
| p.adjustANOVA | 0.00158 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPS17 | 17998 |
| EIF3G | 17865 |
| RPS27A | 17623 |
| RPS14 | 17460 |
| RPSA | 16750 |
| RPS27 | 16701 |
| RPS28 | 16547 |
| RPS16 | 16394 |
| RPS10 | 16101 |
| RPS21 | 15733 |
| RPS24 | 15434 |
| RPS11 | 15381 |
| RPS26 | 15184 |
| RPS23 | 15084 |
| RPS25 | 14869 |
| RPS6 | 14761 |
| EIF3D | 14542 |
| RPS9 | 14415 |
| RPS29 | 14234 |
| EIF3I | 12960 |
| GeneID | Gene Rank |
|---|---|
| RPS17 | 17998 |
| EIF3G | 17865 |
| RPS27A | 17623 |
| RPS14 | 17460 |
| RPSA | 16750 |
| RPS27 | 16701 |
| RPS28 | 16547 |
| RPS16 | 16394 |
| RPS10 | 16101 |
| RPS21 | 15733 |
| RPS24 | 15434 |
| RPS11 | 15381 |
| RPS26 | 15184 |
| RPS23 | 15084 |
| RPS25 | 14869 |
| RPS6 | 14761 |
| EIF3D | 14542 |
| RPS9 | 14415 |
| RPS29 | 14234 |
| EIF3I | 12960 |
| RPS2 | 12789 |
| RPS7 | 12370 |
| RPS5 | 11632 |
| RPS18 | 11410 |
| RPS3A | 11123 |
| RPS19 | 10890 |
| RPS8 | 10296 |
| RPS27L | 9869 |
| EIF3B | 7424 |
| RPS13 | 7369 |
| RPS20 | 7077 |
| EIF3J | 6721 |
| EIF3E | 6441 |
| RPS3 | 5505 |
| EIF3K | 4535 |
| EIF3L | 3545 |
| EIF3F | 3217 |
| RPS15A | 3120 |
| RPS12 | 2257 |
| EIF2S1 | 1847 |
| RPS15 | -220 |
| EIF2S2 | -941 |
| FAU | -1469 |
| EIF3H | -1690 |
| EIF3A | -3383 |
| EIF3M | -3931 |
NOTCH4 Activation and Transmission of Signal to the Nucleus
| 809 | |
|---|---|
| set | NOTCH4 Activation and Transmission of Signal to the Nucleus |
| setSize | 11 |
| pANOVA | 0.0467 |
| s.dist | 0.346 |
| p.adjustANOVA | 0.297 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| APH1B | 17290 |
| YWHAZ | 15102 |
| APH1A | 14609 |
| DLL4 | 13911 |
| PSEN2 | 13707 |
| PSEN1 | 8681 |
| PSENEN | 8537 |
| JAG1 | 7042 |
| NOTCH4 | 4531 |
| ADAM10 | 2882 |
| NCSTN | 2113 |
| GeneID | Gene Rank |
|---|---|
| APH1B | 17290 |
| YWHAZ | 15102 |
| APH1A | 14609 |
| DLL4 | 13911 |
| PSEN2 | 13707 |
| PSEN1 | 8681 |
| PSENEN | 8537 |
| JAG1 | 7042 |
| NOTCH4 | 4531 |
| ADAM10 | 2882 |
| NCSTN | 2113 |
Interleukin-15 signaling
| 644 | |
|---|---|
| set | Interleukin-15 signaling |
| setSize | 13 |
| pANOVA | 0.0308 |
| s.dist | -0.346 |
| p.adjustANOVA | 0.244 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| STAT5A | -3538 |
| SOS2 | -3122 |
| STAT5B | -2708 |
| GAB2 | -2592 |
| SOS1 | -2269 |
| JAK1 | -1659 |
| IL15 | -1584 |
| STAT3 | 454 |
| GRB2 | 3241 |
| IL15RA | 3385 |
| IL2RB | 6203 |
| SHC1 | 7057 |
| JAK3 | 9478 |
| GeneID | Gene Rank |
|---|---|
| STAT5A | -3538 |
| SOS2 | -3122 |
| STAT5B | -2708 |
| GAB2 | -2592 |
| SOS1 | -2269 |
| JAK1 | -1659 |
| IL15 | -1584 |
| STAT3 | 454 |
| GRB2 | 3241 |
| IL15RA | 3385 |
| IL2RB | 6203 |
| SHC1 | 7057 |
| JAK3 | 9478 |
SARS-CoV-2 modulates host translation machinery
| 1200 | |
|---|---|
| set | SARS-CoV-2 modulates host translation machinery |
| setSize | 46 |
| pANOVA | 6.31e-05 |
| s.dist | 0.341 |
| p.adjustANOVA | 0.00204 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPS17 | 17998 |
| RPS27A | 17623 |
| RPS14 | 17460 |
| GEMIN4 | 17233 |
| GEMIN6 | 17215 |
| RPSA | 16750 |
| RPS27 | 16701 |
| RPS28 | 16547 |
| RPS16 | 16394 |
| RPS10 | 16101 |
| RPS21 | 15733 |
| RPS24 | 15434 |
| RPS11 | 15381 |
| RPS26 | 15184 |
| RPS23 | 15084 |
| RPS25 | 14869 |
| RPS6 | 14761 |
| RPS9 | 14415 |
| RPS29 | 14234 |
| RPS2 | 12789 |
| GeneID | Gene Rank |
|---|---|
| RPS17 | 17998.0 |
| RPS27A | 17623.0 |
| RPS14 | 17460.0 |
| GEMIN4 | 17233.0 |
| GEMIN6 | 17215.0 |
| RPSA | 16750.0 |
| RPS27 | 16701.0 |
| RPS28 | 16547.0 |
| RPS16 | 16394.0 |
| RPS10 | 16101.0 |
| RPS21 | 15733.0 |
| RPS24 | 15434.0 |
| RPS11 | 15381.0 |
| RPS26 | 15184.0 |
| RPS23 | 15084.0 |
| RPS25 | 14869.0 |
| RPS6 | 14761.0 |
| RPS9 | 14415.0 |
| RPS29 | 14234.0 |
| RPS2 | 12789.0 |
| RPS7 | 12370.0 |
| SNRPE | 11674.0 |
| RPS5 | 11632.0 |
| RPS18 | 11410.0 |
| RPS3A | 11123.0 |
| RPS19 | 10890.0 |
| RPS8 | 10296.0 |
| SNRPD2 | 9917.0 |
| RPS27L | 9869.0 |
| SNRPB | 7901.0 |
| SNRPD1 | 7756.0 |
| RPS13 | 7369.0 |
| RPS20 | 7077.0 |
| SNRPF | 6044.0 |
| RPS3 | 5505.0 |
| SNRPG | 4432.0 |
| RPS15A | 3120.0 |
| SNRPD3 | 2542.0 |
| RPS12 | 2257.0 |
| GEMIN5 | 544.0 |
| RPS15 | -220.0 |
| FAU | -1469.0 |
| DDX20 | -2110.0 |
| GEMIN2 | -4722.0 |
| GEMIN7 | -5985.0 |
| SMN1 | -7354.5 |
Selenoamino acid metabolism
| 1238 | |
|---|---|
| set | Selenoamino acid metabolism |
| setSize | 103 |
| pANOVA | 3.25e-09 |
| s.dist | 0.337 |
| p.adjustANOVA | 2.72e-07 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPS17 | 17998 |
| RPL35A | 17964 |
| RPS27A | 17623 |
| RPL34 | 17570 |
| RPS14 | 17460 |
| RPL27 | 17419 |
| RPL18A | 17406 |
| RPSA | 16750 |
| RPS27 | 16701 |
| RPS28 | 16547 |
| RPL32 | 16401 |
| RPS16 | 16394 |
| RPL28 | 16373 |
| RPS10 | 16101 |
| RPL7 | 15788 |
| RPS21 | 15733 |
| RPL29 | 15716 |
| RPL10L | 15577 |
| RPL17 | 15487 |
| RPS24 | 15434 |
| GeneID | Gene Rank |
|---|---|
| RPS17 | 17998.0 |
| RPL35A | 17964.0 |
| RPS27A | 17623.0 |
| RPL34 | 17570.0 |
| RPS14 | 17460.0 |
| RPL27 | 17419.0 |
| RPL18A | 17406.0 |
| RPSA | 16750.0 |
| RPS27 | 16701.0 |
| RPS28 | 16547.0 |
| RPL32 | 16401.0 |
| RPS16 | 16394.0 |
| RPL28 | 16373.0 |
| RPS10 | 16101.0 |
| RPL7 | 15788.0 |
| RPS21 | 15733.0 |
| RPL29 | 15716.0 |
| RPL10L | 15577.0 |
| RPL17 | 15487.0 |
| RPS24 | 15434.0 |
| RPL23 | 15404.0 |
| RPS11 | 15381.0 |
| RPL38 | 15324.0 |
| RPS26 | 15184.0 |
| UBA52 | 15146.0 |
| RPS23 | 15084.0 |
| GSR | 15015.0 |
| RPL24 | 14927.0 |
| RPS25 | 14869.0 |
| RPS6 | 14761.0 |
| GNMT | 14576.0 |
| RPL9 | 14519.0 |
| RPS9 | 14415.0 |
| RPS29 | 14234.0 |
| RPL26L1 | 14132.0 |
| RPL30 | 13945.0 |
| RPL14 | 13883.0 |
| RPL26 | 13496.0 |
| RPL7A | 13425.0 |
| MAT1A | 13366.0 |
| RPS2 | 12789.0 |
| RPL12 | 12744.0 |
| RPL41 | 12555.0 |
| RPS7 | 12370.0 |
| RPL37A | 11838.0 |
| RPL3L | 11730.0 |
| RPS5 | 11632.0 |
| RPS18 | 11410.0 |
| RPL13A | 11201.5 |
| RPS3A | 11123.0 |
| RPL19 | 10992.0 |
| RPS19 | 10890.0 |
| RPL13 | 10808.0 |
| RPS8 | 10296.0 |
| TXNRD1 | 10171.0 |
| AHCY | 10121.0 |
| CTH | 10038.0 |
| PAPSS2 | 9945.0 |
| RPS27L | 9869.0 |
| RPL39L | 9655.0 |
| RPL18 | 9621.0 |
| RPL23A | 8852.0 |
| RPLP1 | 8689.0 |
| RPLP2 | 8239.0 |
| NNMT | 7725.0 |
| RPL37 | 7695.0 |
| RPS13 | 7369.0 |
| RPL36AL | 7147.0 |
| RPS20 | 7077.0 |
| PAPSS1 | 7051.0 |
| EEFSEC | 6881.0 |
| RPL4 | 6779.0 |
| CBS | 6598.0 |
| RPL36 | 6145.0 |
| RPS3 | 5505.0 |
| RPL8 | 5310.0 |
| RPL10A | 5072.0 |
| RPL15 | 4446.0 |
| SEPHS2 | 4404.0 |
| INMT | 4311.0 |
| RPL3 | 4267.0 |
| SECISBP2 | 4184.0 |
| RPLP0 | 3455.0 |
| HNMT | 3216.0 |
| SEPSECS | 3124.0 |
| RPS15A | 3120.0 |
| RPL11 | 2419.0 |
| RPS12 | 2257.0 |
| AIMP1 | 1642.0 |
| RPL27A | 1306.0 |
| RPL22 | 1272.0 |
| PSTK | 1189.0 |
| RPL5 | 852.0 |
| RPL31 | 733.0 |
| RPL35 | 467.0 |
| RPS15 | -220.0 |
| RPL21 | -682.0 |
| AIMP2 | -702.0 |
| FAU | -1469.0 |
| EEF1E1 | -1527.0 |
| RPL22L1 | -1702.0 |
| SCLY | -2228.0 |
| RPL6 | -4235.0 |
Attenuation phase
| 106 | |
|---|---|
| set | Attenuation phase |
| setSize | 25 |
| pANOVA | 0.00351 |
| s.dist | 0.337 |
| p.adjustANOVA | 0.0593 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| HSPA1B | 17619 |
| DNAJB1 | 17407 |
| RLN1 | 16258 |
| SERPINH1 | 15956 |
| HSPA6 | 15776 |
| HSPA1A | 15149 |
| UBB | 15063 |
| HSBP1 | 14924 |
| HSPA2 | 14666 |
| HSP90AA1 | 14304 |
| PTGES3 | 13287 |
| CRYBA4 | 13066 |
| FKBP4 | 12309 |
| HSF1 | 10287 |
| HSPA8 | 10210 |
| HSPA1L | 7148 |
| GML | 5432 |
| DEDD2 | 4935 |
| HSPH1 | 4283 |
| MRPL18 | 3284 |
| GeneID | Gene Rank |
|---|---|
| HSPA1B | 17619 |
| DNAJB1 | 17407 |
| RLN1 | 16258 |
| SERPINH1 | 15956 |
| HSPA6 | 15776 |
| HSPA1A | 15149 |
| UBB | 15063 |
| HSBP1 | 14924 |
| HSPA2 | 14666 |
| HSP90AA1 | 14304 |
| PTGES3 | 13287 |
| CRYBA4 | 13066 |
| FKBP4 | 12309 |
| HSF1 | 10287 |
| HSPA8 | 10210 |
| HSPA1L | 7148 |
| GML | 5432 |
| DEDD2 | 4935 |
| HSPH1 | 4283 |
| MRPL18 | 3284 |
| TNFRSF21 | 2226 |
| CREBBP | 955 |
| HSP90AB1 | 555 |
| EP300 | 381 |
| DNAJB6 | -2121 |
Chylomicron assembly
| 209 | |
|---|---|
| set | Chylomicron assembly |
| setSize | 10 |
| pANOVA | 0.0652 |
| s.dist | 0.337 |
| p.adjustANOVA | 0.338 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| APOA2 | 17615 |
| APOC3 | 15561 |
| APOC2 | 14895 |
| APOA1 | 12062 |
| APOA4 | 10060 |
| APOE | 9123 |
| MTTP | 9001 |
| SAR1B | 7480 |
| APOB | 3390 |
| P4HB | -1886 |
| GeneID | Gene Rank |
|---|---|
| APOA2 | 17615 |
| APOC3 | 15561 |
| APOC2 | 14895 |
| APOA1 | 12062 |
| APOA4 | 10060 |
| APOE | 9123 |
| MTTP | 9001 |
| SAR1B | 7480 |
| APOB | 3390 |
| P4HB | -1886 |
L13a-mediated translational silencing of Ceruloplasmin expression
| 679 | |
|---|---|
| set | L13a-mediated translational silencing of Ceruloplasmin expression |
| setSize | 103 |
| pANOVA | 4.02e-09 |
| s.dist | 0.335 |
| p.adjustANOVA | 3.03e-07 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPS17 | 17998 |
| RPL35A | 17964 |
| EIF3G | 17865 |
| RPS27A | 17623 |
| RPL34 | 17570 |
| RPS14 | 17460 |
| RPL27 | 17419 |
| RPL18A | 17406 |
| RPSA | 16750 |
| RPS27 | 16701 |
| RPS28 | 16547 |
| RPL32 | 16401 |
| RPS16 | 16394 |
| RPL28 | 16373 |
| RPS10 | 16101 |
| RPL7 | 15788 |
| RPS21 | 15733 |
| RPL29 | 15716 |
| RPL10L | 15577 |
| RPL17 | 15487 |
| GeneID | Gene Rank |
|---|---|
| RPS17 | 17998.0 |
| RPL35A | 17964.0 |
| EIF3G | 17865.0 |
| RPS27A | 17623.0 |
| RPL34 | 17570.0 |
| RPS14 | 17460.0 |
| RPL27 | 17419.0 |
| RPL18A | 17406.0 |
| RPSA | 16750.0 |
| RPS27 | 16701.0 |
| RPS28 | 16547.0 |
| RPL32 | 16401.0 |
| RPS16 | 16394.0 |
| RPL28 | 16373.0 |
| RPS10 | 16101.0 |
| RPL7 | 15788.0 |
| RPS21 | 15733.0 |
| RPL29 | 15716.0 |
| RPL10L | 15577.0 |
| RPL17 | 15487.0 |
| RPS24 | 15434.0 |
| RPL23 | 15404.0 |
| RPS11 | 15381.0 |
| RPL38 | 15324.0 |
| RPS26 | 15184.0 |
| UBA52 | 15146.0 |
| RPS23 | 15084.0 |
| RPL24 | 14927.0 |
| RPS25 | 14869.0 |
| RPS6 | 14761.0 |
| EIF3D | 14542.0 |
| RPL9 | 14519.0 |
| RPS9 | 14415.0 |
| EIF4A2 | 14275.0 |
| RPS29 | 14234.0 |
| RPL26L1 | 14132.0 |
| RPL30 | 13945.0 |
| RPL14 | 13883.0 |
| RPL26 | 13496.0 |
| RPL7A | 13425.0 |
| EIF4G1 | 13114.0 |
| EIF4E | 13005.0 |
| EIF3I | 12960.0 |
| RPS2 | 12789.0 |
| RPL12 | 12744.0 |
| RPL41 | 12555.0 |
| RPS7 | 12370.0 |
| RPL37A | 11838.0 |
| RPL3L | 11730.0 |
| RPS5 | 11632.0 |
| RPS18 | 11410.0 |
| RPL13A | 11201.5 |
| RPS3A | 11123.0 |
| RPL19 | 10992.0 |
| RPS19 | 10890.0 |
| RPL13 | 10808.0 |
| RPS8 | 10296.0 |
| RPS27L | 9869.0 |
| RPL39L | 9655.0 |
| RPL18 | 9621.0 |
| RPL23A | 8852.0 |
| RPLP1 | 8689.0 |
| RPLP2 | 8239.0 |
| RPL37 | 7695.0 |
| EIF3B | 7424.0 |
| RPS13 | 7369.0 |
| RPL36AL | 7147.0 |
| RPS20 | 7077.0 |
| RPL4 | 6779.0 |
| EIF4B | 6741.0 |
| EIF3J | 6721.0 |
| EIF3E | 6441.0 |
| RPL36 | 6145.0 |
| EIF4H | 6065.0 |
| RPS3 | 5505.0 |
| RPL8 | 5310.0 |
| RPL10A | 5072.0 |
| EIF3K | 4535.0 |
| RPL15 | 4446.0 |
| RPL3 | 4267.0 |
| EIF3L | 3545.0 |
| RPLP0 | 3455.0 |
| EIF3F | 3217.0 |
| RPS15A | 3120.0 |
| EIF4A1 | 2463.0 |
| RPL11 | 2419.0 |
| RPS12 | 2257.0 |
| EIF2S1 | 1847.0 |
| PABPC1 | 1667.0 |
| RPL27A | 1306.0 |
| RPL22 | 1272.0 |
| RPL5 | 852.0 |
| RPL31 | 733.0 |
| RPL35 | 467.0 |
| RPS15 | -220.0 |
| RPL21 | -682.0 |
| EIF2S2 | -941.0 |
| FAU | -1469.0 |
| EIF3H | -1690.0 |
| RPL22L1 | -1702.0 |
| EIF3A | -3383.0 |
| EIF3M | -3931.0 |
| RPL6 | -4235.0 |
GTP hydrolysis and joining of the 60S ribosomal subunit
| 505 | |
|---|---|
| set | GTP hydrolysis and joining of the 60S ribosomal subunit |
| setSize | 104 |
| pANOVA | 3.93e-09 |
| s.dist | 0.334 |
| p.adjustANOVA | 3.03e-07 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPS17 | 17998 |
| RPL35A | 17964 |
| EIF3G | 17865 |
| RPS27A | 17623 |
| RPL34 | 17570 |
| RPS14 | 17460 |
| RPL27 | 17419 |
| RPL18A | 17406 |
| RPSA | 16750 |
| RPS27 | 16701 |
| RPS28 | 16547 |
| RPL32 | 16401 |
| RPS16 | 16394 |
| RPL28 | 16373 |
| RPS10 | 16101 |
| RPL7 | 15788 |
| RPS21 | 15733 |
| RPL29 | 15716 |
| RPL10L | 15577 |
| RPL17 | 15487 |
| GeneID | Gene Rank |
|---|---|
| RPS17 | 17998.0 |
| RPL35A | 17964.0 |
| EIF3G | 17865.0 |
| RPS27A | 17623.0 |
| RPL34 | 17570.0 |
| RPS14 | 17460.0 |
| RPL27 | 17419.0 |
| RPL18A | 17406.0 |
| RPSA | 16750.0 |
| RPS27 | 16701.0 |
| RPS28 | 16547.0 |
| RPL32 | 16401.0 |
| RPS16 | 16394.0 |
| RPL28 | 16373.0 |
| RPS10 | 16101.0 |
| RPL7 | 15788.0 |
| RPS21 | 15733.0 |
| RPL29 | 15716.0 |
| RPL10L | 15577.0 |
| RPL17 | 15487.0 |
| RPS24 | 15434.0 |
| RPL23 | 15404.0 |
| RPS11 | 15381.0 |
| RPL38 | 15324.0 |
| RPS26 | 15184.0 |
| UBA52 | 15146.0 |
| RPS23 | 15084.0 |
| RPL24 | 14927.0 |
| RPS25 | 14869.0 |
| RPS6 | 14761.0 |
| EIF3D | 14542.0 |
| RPL9 | 14519.0 |
| RPS9 | 14415.0 |
| EIF4A2 | 14275.0 |
| RPS29 | 14234.0 |
| RPL26L1 | 14132.0 |
| RPL30 | 13945.0 |
| RPL14 | 13883.0 |
| RPL26 | 13496.0 |
| RPL7A | 13425.0 |
| EIF4G1 | 13114.0 |
| EIF4E | 13005.0 |
| EIF3I | 12960.0 |
| RPS2 | 12789.0 |
| RPL12 | 12744.0 |
| RPL41 | 12555.0 |
| RPS7 | 12370.0 |
| RPL37A | 11838.0 |
| RPL3L | 11730.0 |
| RPS5 | 11632.0 |
| RPS18 | 11410.0 |
| RPL13A | 11201.5 |
| RPS3A | 11123.0 |
| RPL19 | 10992.0 |
| RPS19 | 10890.0 |
| RPL13 | 10808.0 |
| RPS8 | 10296.0 |
| RPS27L | 9869.0 |
| RPL39L | 9655.0 |
| RPL18 | 9621.0 |
| RPL23A | 8852.0 |
| RPLP1 | 8689.0 |
| RPLP2 | 8239.0 |
| RPL37 | 7695.0 |
| EIF3B | 7424.0 |
| RPS13 | 7369.0 |
| RPL36AL | 7147.0 |
| RPS20 | 7077.0 |
| RPL4 | 6779.0 |
| EIF4B | 6741.0 |
| EIF3J | 6721.0 |
| EIF5B | 6601.0 |
| EIF3E | 6441.0 |
| RPL36 | 6145.0 |
| EIF4H | 6065.0 |
| RPS3 | 5505.0 |
| RPL8 | 5310.0 |
| RPL10A | 5072.0 |
| EIF3K | 4535.0 |
| RPL15 | 4446.0 |
| RPL3 | 4267.0 |
| EIF3L | 3545.0 |
| RPLP0 | 3455.0 |
| EIF3F | 3217.0 |
| RPS15A | 3120.0 |
| EIF5 | 2884.0 |
| EIF4A1 | 2463.0 |
| RPL11 | 2419.0 |
| RPS12 | 2257.0 |
| EIF2S1 | 1847.0 |
| RPL27A | 1306.0 |
| RPL22 | 1272.0 |
| RPL5 | 852.0 |
| RPL31 | 733.0 |
| RPL35 | 467.0 |
| RPS15 | -220.0 |
| RPL21 | -682.0 |
| EIF2S2 | -941.0 |
| FAU | -1469.0 |
| EIF3H | -1690.0 |
| RPL22L1 | -1702.0 |
| EIF3A | -3383.0 |
| EIF3M | -3931.0 |
| RPL6 | -4235.0 |
Biosynthesis of DHA-derived SPMs
| 127 | |
|---|---|
| set | Biosynthesis of DHA-derived SPMs |
| setSize | 17 |
| pANOVA | 0.0173 |
| s.dist | 0.334 |
| p.adjustANOVA | 0.172 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| PTGS2 | 17868 |
| CYP2E1 | 17310 |
| ALOX12 | 17279 |
| CYP1A2 | 15894 |
| CYP2D6 | 14012 |
| GPX4 | 12680 |
| CYP3A4 | 11967 |
| LTC4S | 10798 |
| GSTM4 | 10453 |
| ALOX5 | 9755 |
| HPGD | 9371 |
| LTA4H | 8036 |
| ALOX15 | 7416 |
| CYP1A1 | 7088 |
| EPHX2 | 5655 |
| CYP2C8 | -5402 |
| CYP2C9 | -5476 |
| GeneID | Gene Rank |
|---|---|
| PTGS2 | 17868 |
| CYP2E1 | 17310 |
| ALOX12 | 17279 |
| CYP1A2 | 15894 |
| CYP2D6 | 14012 |
| GPX4 | 12680 |
| CYP3A4 | 11967 |
| LTC4S | 10798 |
| GSTM4 | 10453 |
| ALOX5 | 9755 |
| HPGD | 9371 |
| LTA4H | 8036 |
| ALOX15 | 7416 |
| CYP1A1 | 7088 |
| EPHX2 | 5655 |
| CYP2C8 | -5402 |
| CYP2C9 | -5476 |
Ribosomal scanning and start codon recognition
| 1187 | |
|---|---|
| set | Ribosomal scanning and start codon recognition |
| setSize | 53 |
| pANOVA | 2.82e-05 |
| s.dist | 0.332 |
| p.adjustANOVA | 0.00109 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPS17 | 17998 |
| EIF3G | 17865 |
| RPS27A | 17623 |
| RPS14 | 17460 |
| RPSA | 16750 |
| RPS27 | 16701 |
| RPS28 | 16547 |
| RPS16 | 16394 |
| RPS10 | 16101 |
| RPS21 | 15733 |
| RPS24 | 15434 |
| RPS11 | 15381 |
| RPS26 | 15184 |
| RPS23 | 15084 |
| RPS25 | 14869 |
| RPS6 | 14761 |
| EIF3D | 14542 |
| RPS9 | 14415 |
| EIF4A2 | 14275 |
| RPS29 | 14234 |
| GeneID | Gene Rank |
|---|---|
| RPS17 | 17998 |
| EIF3G | 17865 |
| RPS27A | 17623 |
| RPS14 | 17460 |
| RPSA | 16750 |
| RPS27 | 16701 |
| RPS28 | 16547 |
| RPS16 | 16394 |
| RPS10 | 16101 |
| RPS21 | 15733 |
| RPS24 | 15434 |
| RPS11 | 15381 |
| RPS26 | 15184 |
| RPS23 | 15084 |
| RPS25 | 14869 |
| RPS6 | 14761 |
| EIF3D | 14542 |
| RPS9 | 14415 |
| EIF4A2 | 14275 |
| RPS29 | 14234 |
| EIF4G1 | 13114 |
| EIF4E | 13005 |
| EIF3I | 12960 |
| RPS2 | 12789 |
| RPS7 | 12370 |
| RPS5 | 11632 |
| RPS18 | 11410 |
| RPS3A | 11123 |
| RPS19 | 10890 |
| RPS8 | 10296 |
| RPS27L | 9869 |
| EIF3B | 7424 |
| RPS13 | 7369 |
| RPS20 | 7077 |
| EIF4B | 6741 |
| EIF3J | 6721 |
| EIF3E | 6441 |
| EIF4H | 6065 |
| RPS3 | 5505 |
| EIF3K | 4535 |
| EIF3L | 3545 |
| EIF3F | 3217 |
| RPS15A | 3120 |
| EIF5 | 2884 |
| EIF4A1 | 2463 |
| RPS12 | 2257 |
| EIF2S1 | 1847 |
| RPS15 | -220 |
| EIF2S2 | -941 |
| FAU | -1469 |
| EIF3H | -1690 |
| EIF3A | -3383 |
| EIF3M | -3931 |
Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S
| 54 | |
|---|---|
| set | Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S |
| setSize | 54 |
| pANOVA | 2.39e-05 |
| s.dist | 0.332 |
| p.adjustANOVA | 0.000972 |
Top enriched genes
| GeneID | Gene Rank |
|---|---|
| RPS17 | 17998 |
| EIF3G | 17865 |
| RPS27A | 17623 |
| RPS14 | 17460 |
| RPSA | 16750 |
| RPS27 | 16701 |
| RPS28 | 16547 |
| RPS16 | 16394 |
| RPS10 | 16101 |
| RPS21 | 15733 |
| RPS24 | 15434 |
| RPS11 | 15381 |
| RPS26 | 15184 |
| RPS23 | 15084 |
| RPS25 | 14869 |
| RPS6 | 14761 |
| EIF3D | 14542 |
| RPS9 | 14415 |
| EIF4A2 | 14275 |
| RPS29 | 14234 |
| GeneID | Gene Rank |
|---|---|
| RPS17 | 17998 |
| EIF3G | 17865 |
| RPS27A | 17623 |
| RPS14 | 17460 |
| RPSA | 16750 |
| RPS27 | 16701 |
| RPS28 | 16547 |
| RPS16 | 16394 |
| RPS10 | 16101 |
| RPS21 | 15733 |
| RPS24 | 15434 |
| RPS11 | 15381 |
| RPS26 | 15184 |
| RPS23 | 15084 |
| RPS25 | 14869 |
| RPS6 | 14761 |
| EIF3D | 14542 |
| RPS9 | 14415 |
| EIF4A2 | 14275 |
| RPS29 | 14234 |
| EIF4G1 | 13114 |
| EIF4E | 13005 |
| EIF3I | 12960 |
| RPS2 | 12789 |
| RPS7 | 12370 |
| RPS5 | 11632 |
| RPS18 | 11410 |
| RPS3A | 11123 |
| RPS19 | 10890 |
| EIF4EBP1 | 10805 |
| RPS8 | 10296 |
| RPS27L | 9869 |
| EIF3B | 7424 |
| RPS13 | 7369 |
| RPS20 | 7077 |
| EIF4B | 6741 |
| EIF3J | 6721 |
| EIF3E | 6441 |
| EIF4H | 6065 |
| RPS3 | 5505 |
| EIF3K | 4535 |
| EIF3L | 3545 |
| EIF3F | 3217 |
| RPS15A | 3120 |
| EIF4A1 | 2463 |
| RPS12 | 2257 |
| EIF2S1 | 1847 |
| PABPC1 | 1667 |
| RPS15 | -220 |
| EIF2S2 | -941 |
| FAU | -1469 |
| EIF3H | -1690 |
| EIF3A | -3383 |
| EIF3M | -3931 |
Here is the session info with all the versions of packages used.
sessionInfo()
## R version 4.3.2 (2023-10-31)
## Platform: x86_64-pc-linux-gnu (64-bit)
## Running under: Ubuntu 22.04.3 LTS
##
## Matrix products: default
## BLAS: /usr/lib/x86_64-linux-gnu/blas/libblas.so.3.10.0
## LAPACK: /usr/lib/x86_64-linux-gnu/lapack/liblapack.so.3.10.0
##
## locale:
## [1] LC_CTYPE=en_US.UTF-8 LC_NUMERIC=C
## [3] LC_TIME=en_US.UTF-8 LC_COLLATE=en_US.UTF-8
## [5] LC_MONETARY=en_US.UTF-8 LC_MESSAGES=en_US.UTF-8
## [7] LC_PAPER=en_US.UTF-8 LC_NAME=C
## [9] LC_ADDRESS=C LC_TELEPHONE=C
## [11] LC_MEASUREMENT=en_US.UTF-8 LC_IDENTIFICATION=C
##
## time zone: Australia/Melbourne
## tzcode source: system (glibc)
##
## attached base packages:
## [1] stats4 parallel stats graphics grDevices utils datasets
## [8] methods base
##
## other attached packages:
## [1] pkgload_1.3.3
## [2] GGally_2.1.2
## [3] ggplot2_3.4.4
## [4] reshape2_1.4.4
## [5] beeswarm_0.4.0
## [6] gplots_3.1.3
## [7] gtools_3.9.4
## [8] tibble_3.2.1
## [9] dplyr_1.1.3
## [10] echarts4r_0.4.5
## [11] eulerr_7.0.0
## [12] kableExtra_1.3.4
## [13] data.table_1.14.8
## [14] IlluminaHumanMethylationEPICanno.ilm10b4.hg19_0.6.0
## [15] minfi_1.48.0
## [16] bumphunter_1.44.0
## [17] locfit_1.5-9.8
## [18] iterators_1.0.14
## [19] foreach_1.5.2
## [20] Biostrings_2.70.1
## [21] XVector_0.42.0
## [22] SummarizedExperiment_1.32.0
## [23] Biobase_2.62.0
## [24] MatrixGenerics_1.14.0
## [25] matrixStats_1.1.0
## [26] GenomicRanges_1.54.1
## [27] GenomeInfoDb_1.38.1
## [28] IRanges_2.36.0
## [29] S4Vectors_0.40.1
## [30] BiocGenerics_0.48.1
## [31] mitch_1.14.0
## [32] limma_3.58.1
##
## loaded via a namespace (and not attached):
## [1] splines_4.3.2 later_1.3.1
## [3] BiocIO_1.12.0 bitops_1.0-7
## [5] filelock_1.0.2 preprocessCore_1.64.0
## [7] XML_3.99-0.15 lifecycle_1.0.4
## [9] lattice_0.22-5 MASS_7.3-60
## [11] base64_2.0.1 scrime_1.3.5
## [13] magrittr_2.0.3 sass_0.4.7
## [15] rmarkdown_2.25 jquerylib_0.1.4
## [17] yaml_2.3.7 httpuv_1.6.12
## [19] doRNG_1.8.6 askpass_1.2.0
## [21] DBI_1.1.3 RColorBrewer_1.1-3
## [23] abind_1.4-5 zlibbioc_1.48.0
## [25] rvest_1.0.3 quadprog_1.5-8
## [27] purrr_1.0.2 RCurl_1.98-1.13
## [29] rappdirs_0.3.3 GenomeInfoDbData_1.2.11
## [31] genefilter_1.84.0 annotate_1.80.0
## [33] svglite_2.1.2 DelayedMatrixStats_1.24.0
## [35] codetools_0.2-19 DelayedArray_0.28.0
## [37] xml2_1.3.5 tidyselect_1.2.0
## [39] beanplot_1.3.1 BiocFileCache_2.10.1
## [41] illuminaio_0.44.0 webshot_0.5.5
## [43] GenomicAlignments_1.38.0 jsonlite_1.8.7
## [45] multtest_2.58.0 ellipsis_0.3.2
## [47] survival_3.5-7 systemfonts_1.0.5
## [49] tools_4.3.2 progress_1.2.2
## [51] Rcpp_1.0.11 glue_1.6.2
## [53] gridExtra_2.3 SparseArray_1.2.2
## [55] xfun_0.41 HDF5Array_1.30.0
## [57] withr_2.5.2 fastmap_1.1.1
## [59] rhdf5filters_1.14.1 fansi_1.0.5
## [61] openssl_2.1.1 caTools_1.18.2
## [63] digest_0.6.33 R6_2.5.1
## [65] mime_0.12 colorspace_2.1-0
## [67] biomaRt_2.58.0 RSQLite_2.3.3
## [69] tidyr_1.3.0 utf8_1.2.4
## [71] generics_0.1.3 rtracklayer_1.62.0
## [73] prettyunits_1.2.0 httr_1.4.7
## [75] htmlwidgets_1.6.2 S4Arrays_1.2.0
## [77] pkgconfig_2.0.3 gtable_0.3.4
## [79] blob_1.2.4 siggenes_1.76.0
## [81] htmltools_0.5.7 scales_1.2.1
## [83] png_0.1-8 knitr_1.45
## [85] rstudioapi_0.15.0 tzdb_0.4.0
## [87] rjson_0.2.21 nlme_3.1-163
## [89] curl_5.1.0 cachem_1.0.8
## [91] rhdf5_2.46.0 stringr_1.5.0
## [93] KernSmooth_2.23-22 AnnotationDbi_1.64.1
## [95] restfulr_0.0.15 GEOquery_2.70.0
## [97] pillar_1.9.0 grid_4.3.2
## [99] reshape_0.8.9 vctrs_0.6.4
## [101] promises_1.2.1 dbplyr_2.4.0
## [103] xtable_1.8-4 evaluate_0.23
## [105] readr_2.1.4 GenomicFeatures_1.54.1
## [107] cli_3.6.1 compiler_4.3.2
## [109] Rsamtools_2.18.0 rlang_1.1.2
## [111] crayon_1.5.2 rngtools_1.5.2
## [113] nor1mix_1.3-0 mclust_6.0.0
## [115] plyr_1.8.9 stringi_1.7.12
## [117] viridisLite_0.4.2 BiocParallel_1.36.0
## [119] munsell_0.5.0 Matrix_1.6-2
## [121] hms_1.1.3 sparseMatrixStats_1.14.0
## [123] bit64_4.0.5 Rhdf5lib_1.24.0
## [125] KEGGREST_1.42.0 statmod_1.5.0
## [127] shiny_1.7.5.1 highr_0.10
## [129] memoise_2.0.1 bslib_0.5.1
## [131] bit_4.0.5
END of report