date generated: 2023-09-22
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.
| x | |
|---|---|
| pol | 174.97945 | 
| env | 174.96945 | 
| tat | 161.28311 | 
| gag | 142.70074 | 
| nef | 124.22267 | 
| vif | 90.52759 | 
Here are some metrics about the input data profile:
| Profile metrics | |
|---|---|
| num_genesets | 2630 | 
| num_genes_in_profile | 10939 | 
| duplicated_genes_present | 0 | 
| num_profile_genes_in_sets | 6285 | 
| num_profile_genes_not_in_sets | 4654 | 
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_2023-09-20.gmt| Gene sets metrics | |
|---|---|
| num_genesets | 2630 | 
| num_genesets_excluded | 1330 | 
| num_genesets_included | 1300 | 
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
## Warning in kable_styling(., "hover", full_width = FALSE): Please specify format
## in kable. kableExtra can customize either HTML or LaTeX outputs. See
## https://haozhu233.github.io/kableExtra/ for details.| set | setSize | pANOVA | s.dist | p.adjustANOVA | 
|---|---|---|---|---|
| Eukaryotic Translation Termination | 90 | 2.34e-39 | -0.799 | 3.04e-37 | 
| Viral mRNA Translation | 87 | 1.30e-37 | -0.794 | 9.97e-36 | 
| Eukaryotic Translation Elongation | 90 | 7.27e-38 | -0.783 | 6.30e-36 | 
| Peptide chain elongation | 87 | 2.48e-36 | -0.780 | 1.79e-34 | 
| Formation of a pool of free 40S subunits | 98 | 4.92e-40 | -0.773 | 7.11e-38 | 
| SRP-dependent cotranslational protein targeting to membrane | 109 | 4.36e-44 | -0.771 | 1.42e-41 | 
| SARS-CoV-1 modulates host translation machinery | 36 | 1.67e-15 | -0.767 | 2.35e-14 | 
| Selenocysteine synthesis | 90 | 7.10e-36 | -0.761 | 4.86e-34 | 
| Folding of actin by CCT/TriC | 10 | 3.37e-05 | -0.757 | 2.05e-04 | 
| Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC) | 93 | 1.37e-35 | -0.746 | 8.46e-34 | 
| SARS-CoV-2 modulates host translation machinery | 47 | 8.64e-19 | -0.746 | 2.39e-17 | 
| Formation of ATP by chemiosmotic coupling | 18 | 6.58e-08 | -0.735 | 5.45e-07 | 
| GTP hydrolysis and joining of the 60S ribosomal subunit | 109 | 4.48e-39 | -0.724 | 5.30e-37 | 
| Formation of the ternary complex, and subsequently, the 43S complex | 50 | 1.00e-18 | -0.722 | 2.71e-17 | 
| Selenoamino acid metabolism | 101 | 2.25e-35 | -0.714 | 1.27e-33 | 
| L13a-mediated translational silencing of Ceruloplasmin expression | 108 | 1.11e-37 | -0.714 | 8.98e-36 | 
| Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding | 25 | 7.36e-10 | -0.711 | 6.69e-09 | 
| Response of EIF2AK4 (GCN2) to amino acid deficiency | 98 | 3.95e-34 | -0.711 | 1.97e-32 | 
| Regulation of activated PAK-2p34 by proteasome mediated degradation | 48 | 1.97e-17 | -0.708 | 4.42e-16 | 
| Regulation of expression of SLITs and ROBOs | 155 | 2.56e-52 | -0.707 | 1.11e-49 | 
| Regulation of ornithine decarboxylase (ODC) | 49 | 1.23e-17 | -0.706 | 2.92e-16 | 
| Mitochondrial translation elongation | 88 | 2.82e-30 | -0.705 | 1.18e-28 | 
| Prefoldin mediated transfer of substrate to CCT/TriC | 24 | 2.91e-09 | -0.700 | 2.54e-08 | 
| Cap-dependent Translation Initiation | 116 | 9.08e-39 | -0.699 | 8.43e-37 | 
| Eukaryotic Translation Initiation | 116 | 9.08e-39 | -0.699 | 8.43e-37 | 
| Vpu mediated degradation of CD4 | 50 | 1.86e-17 | -0.695 | 4.25e-16 | 
| FBXL7 down-regulates AURKA during mitotic entry and in early mitosis | 52 | 4.72e-18 | -0.694 | 1.18e-16 | 
| Negative regulation of NOTCH4 signaling | 53 | 3.73e-18 | -0.689 | 9.52e-17 | 
| Mitochondrial translation initiation | 88 | 5.03e-29 | -0.689 | 1.92e-27 | 
| Mitochondrial translation termination | 88 | 7.65e-29 | -0.687 | 2.84e-27 | 
| Ubiquitin-dependent degradation of Cyclin D | 50 | 4.94e-17 | -0.685 | 1.00e-15 | 
| Somitogenesis | 46 | 1.33e-15 | -0.681 | 1.92e-14 | 
| Ubiquitin Mediated Degradation of Phosphorylated Cdc25A | 49 | 1.63e-16 | -0.681 | 3.02e-15 | 
| p53-Independent DNA Damage Response | 49 | 1.63e-16 | -0.681 | 3.02e-15 | 
| p53-Independent G1/S DNA damage checkpoint | 49 | 1.63e-16 | -0.681 | 3.02e-15 | 
| Vif-mediated degradation of APOBEC3G | 53 | 1.49e-17 | -0.677 | 3.46e-16 | 
| Autodegradation of the E3 ubiquitin ligase COP1 | 49 | 3.92e-16 | -0.672 | 5.92e-15 | 
| SCF(Skp2)-mediated degradation of p27/p21 | 55 | 6.58e-18 | -0.672 | 1.61e-16 | 
| Mitochondrial translation | 94 | 2.43e-29 | -0.671 | 9.86e-28 | 
| Hh mutants are degraded by ERAD | 53 | 3.65e-17 | -0.669 | 7.85e-16 | 
| AUF1 (hnRNP D0) binds and destabilizes mRNA | 53 | 4.34e-17 | -0.667 | 9.10e-16 | 
| SCF-beta-TrCP mediated degradation of Emi1 | 51 | 1.95e-16 | -0.666 | 3.45e-15 | 
| GSK3B and BTRC:CUL1-mediated-degradation of NFE2L2 | 52 | 1.04e-16 | -0.665 | 2.01e-15 | 
| Cross-presentation of soluble exogenous antigens (endosomes) | 46 | 6.16e-15 | -0.665 | 8.17e-14 | 
| Regulation of Apoptosis | 51 | 2.89e-16 | -0.662 | 4.75e-15 | 
| Formation of tubulin folding intermediates by CCT/TriC | 18 | 1.21e-06 | -0.661 | 8.76e-06 | 
| The role of GTSE1 in G2/M progression after G2 checkpoint | 63 | 1.26e-19 | -0.660 | 3.56e-18 | 
| Metabolism of polyamines | 54 | 4.87e-17 | -0.660 | 1.00e-15 | 
| Defective CFTR causes cystic fibrosis | 57 | 1.24e-17 | -0.654 | 2.92e-16 | 
| Degradation of DVL | 52 | 3.80e-16 | -0.653 | 5.88e-15 | 
| set | setSize | pANOVA | s.dist | p.adjustANOVA | 
|---|---|---|---|---|
| Eukaryotic Translation Termination | 90 | 2.34e-39 | -0.799000 | 3.04e-37 | 
| Viral mRNA Translation | 87 | 1.30e-37 | -0.794000 | 9.97e-36 | 
| Eukaryotic Translation Elongation | 90 | 7.27e-38 | -0.783000 | 6.30e-36 | 
| Peptide chain elongation | 87 | 2.48e-36 | -0.780000 | 1.79e-34 | 
| Formation of a pool of free 40S subunits | 98 | 4.92e-40 | -0.773000 | 7.11e-38 | 
| SRP-dependent cotranslational protein targeting to membrane | 109 | 4.36e-44 | -0.771000 | 1.42e-41 | 
| SARS-CoV-1 modulates host translation machinery | 36 | 1.67e-15 | -0.767000 | 2.35e-14 | 
| Selenocysteine synthesis | 90 | 7.10e-36 | -0.761000 | 4.86e-34 | 
| Folding of actin by CCT/TriC | 10 | 3.37e-05 | -0.757000 | 2.05e-04 | 
| Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC) | 93 | 1.37e-35 | -0.746000 | 8.46e-34 | 
| SARS-CoV-2 modulates host translation machinery | 47 | 8.64e-19 | -0.746000 | 2.39e-17 | 
| Formation of ATP by chemiosmotic coupling | 18 | 6.58e-08 | -0.735000 | 5.45e-07 | 
| GTP hydrolysis and joining of the 60S ribosomal subunit | 109 | 4.48e-39 | -0.724000 | 5.30e-37 | 
| Formation of the ternary complex, and subsequently, the 43S complex | 50 | 1.00e-18 | -0.722000 | 2.71e-17 | 
| Selenoamino acid metabolism | 101 | 2.25e-35 | -0.714000 | 1.27e-33 | 
| L13a-mediated translational silencing of Ceruloplasmin expression | 108 | 1.11e-37 | -0.714000 | 8.98e-36 | 
| Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding | 25 | 7.36e-10 | -0.711000 | 6.69e-09 | 
| Response of EIF2AK4 (GCN2) to amino acid deficiency | 98 | 3.95e-34 | -0.711000 | 1.97e-32 | 
| Regulation of activated PAK-2p34 by proteasome mediated degradation | 48 | 1.97e-17 | -0.708000 | 4.42e-16 | 
| Regulation of expression of SLITs and ROBOs | 155 | 2.56e-52 | -0.707000 | 1.11e-49 | 
| Regulation of ornithine decarboxylase (ODC) | 49 | 1.23e-17 | -0.706000 | 2.92e-16 | 
| Mitochondrial translation elongation | 88 | 2.82e-30 | -0.705000 | 1.18e-28 | 
| Prefoldin mediated transfer of substrate to CCT/TriC | 24 | 2.91e-09 | -0.700000 | 2.54e-08 | 
| Cap-dependent Translation Initiation | 116 | 9.08e-39 | -0.699000 | 8.43e-37 | 
| Eukaryotic Translation Initiation | 116 | 9.08e-39 | -0.699000 | 8.43e-37 | 
| Vpu mediated degradation of CD4 | 50 | 1.86e-17 | -0.695000 | 4.25e-16 | 
| FBXL7 down-regulates AURKA during mitotic entry and in early mitosis | 52 | 4.72e-18 | -0.694000 | 1.18e-16 | 
| Negative regulation of NOTCH4 signaling | 53 | 3.73e-18 | -0.689000 | 9.52e-17 | 
| Mitochondrial translation initiation | 88 | 5.03e-29 | -0.689000 | 1.92e-27 | 
| Mitochondrial translation termination | 88 | 7.65e-29 | -0.687000 | 2.84e-27 | 
| Ubiquitin-dependent degradation of Cyclin D | 50 | 4.94e-17 | -0.685000 | 1.00e-15 | 
| Somitogenesis | 46 | 1.33e-15 | -0.681000 | 1.92e-14 | 
| Ubiquitin Mediated Degradation of Phosphorylated Cdc25A | 49 | 1.63e-16 | -0.681000 | 3.02e-15 | 
| p53-Independent DNA Damage Response | 49 | 1.63e-16 | -0.681000 | 3.02e-15 | 
| p53-Independent G1/S DNA damage checkpoint | 49 | 1.63e-16 | -0.681000 | 3.02e-15 | 
| Vif-mediated degradation of APOBEC3G | 53 | 1.49e-17 | -0.677000 | 3.46e-16 | 
| Autodegradation of the E3 ubiquitin ligase COP1 | 49 | 3.92e-16 | -0.672000 | 5.92e-15 | 
| SCF(Skp2)-mediated degradation of p27/p21 | 55 | 6.58e-18 | -0.672000 | 1.61e-16 | 
| Mitochondrial translation | 94 | 2.43e-29 | -0.671000 | 9.86e-28 | 
| Hh mutants are degraded by ERAD | 53 | 3.65e-17 | -0.669000 | 7.85e-16 | 
| AUF1 (hnRNP D0) binds and destabilizes mRNA | 53 | 4.34e-17 | -0.667000 | 9.10e-16 | 
| SCF-beta-TrCP mediated degradation of Emi1 | 51 | 1.95e-16 | -0.666000 | 3.45e-15 | 
| GSK3B and BTRC:CUL1-mediated-degradation of NFE2L2 | 52 | 1.04e-16 | -0.665000 | 2.01e-15 | 
| Cross-presentation of soluble exogenous antigens (endosomes) | 46 | 6.16e-15 | -0.665000 | 8.17e-14 | 
| Regulation of Apoptosis | 51 | 2.89e-16 | -0.662000 | 4.75e-15 | 
| Formation of tubulin folding intermediates by CCT/TriC | 18 | 1.21e-06 | -0.661000 | 8.76e-06 | 
| The role of GTSE1 in G2/M progression after G2 checkpoint | 63 | 1.26e-19 | -0.660000 | 3.56e-18 | 
| Metabolism of polyamines | 54 | 4.87e-17 | -0.660000 | 1.00e-15 | 
| Defective CFTR causes cystic fibrosis | 57 | 1.24e-17 | -0.654000 | 2.92e-16 | 
| Degradation of DVL | 52 | 3.80e-16 | -0.653000 | 5.88e-15 | 
| Translation | 265 | 2.66e-74 | -0.650000 | 3.46e-71 | 
| Asymmetric localization of PCP proteins | 50 | 1.91e-15 | -0.649000 | 2.67e-14 | 
| Ribosomal scanning and start codon recognition | 57 | 3.68e-17 | -0.645000 | 7.85e-16 | 
| Respiratory electron transport, ATP synthesis by chemiosmotic coupling, and heat production by uncoupling proteins. | 121 | 1.93e-34 | -0.644000 | 1.01e-32 | 
| Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC) | 113 | 3.49e-32 | -0.643000 | 1.62e-30 | 
| Nonsense-Mediated Decay (NMD) | 113 | 3.49e-32 | -0.643000 | 1.62e-30 | 
| Hh mutants abrogate ligand secretion | 54 | 4.79e-16 | -0.638000 | 7.16e-15 | 
| Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S | 58 | 7.75e-17 | -0.633000 | 1.53e-15 | 
| Glutathione conjugation | 19 | 2.01e-06 | -0.630000 | 1.42e-05 | 
| Complex I biogenesis | 57 | 2.03e-16 | -0.629000 | 3.52e-15 | 
| Translation initiation complex formation | 57 | 2.39e-16 | -0.628000 | 4.03e-15 | 
| Respiratory electron transport | 102 | 1.21e-27 | -0.624000 | 4.37e-26 | 
| Autodegradation of Cdh1 by Cdh1:APC/C | 62 | 5.21e-17 | -0.615000 | 1.04e-15 | 
| Regulation of RUNX3 expression and activity | 55 | 3.49e-15 | -0.614000 | 4.69e-14 | 
| Orc1 removal from chromatin | 60 | 2.27e-16 | -0.613000 | 3.88e-15 | 
| Post-chaperonin tubulin folding pathway | 14 | 7.69e-05 | -0.610000 | 4.38e-04 | 
| Cristae formation | 31 | 6.22e-09 | -0.603000 | 5.32e-08 | 
| Hedgehog ligand biogenesis | 57 | 3.50e-15 | -0.603000 | 4.69e-14 | 
| Mitochondrial protein import | 63 | 2.46e-16 | -0.597000 | 4.10e-15 | 
| Degradation of AXIN | 52 | 1.07e-13 | -0.596000 | 1.22e-12 | 
| rRNA processing in the nucleus and cytosol | 180 | 4.69e-43 | -0.594000 | 1.22e-40 | 
| NIK–>noncanonical NF-kB signaling | 57 | 8.54e-15 | -0.594000 | 1.12e-13 | 
| Erythropoietin activates Phosphoinositide-3-kinase (PI3K) | 11 | 6.48e-04 | 0.594000 | 3.24e-03 | 
| APC/C:Cdc20 mediated degradation of Securin | 63 | 3.90e-16 | -0.593000 | 5.92e-15 | 
| Major pathway of rRNA processing in the nucleolus and cytosol | 170 | 3.03e-40 | -0.590000 | 4.92e-38 | 
| CDK-mediated phosphorylation and removal of Cdc6 | 64 | 3.32e-16 | -0.590000 | 5.39e-15 | 
| APC:Cdc20 mediated degradation of cell cycle proteins prior to satisfation of the cell cycle checkpoint | 64 | 3.71e-16 | -0.589000 | 5.81e-15 | 
| Cdc20:Phospho-APC/C mediated degradation of Cyclin A | 64 | 3.71e-16 | -0.589000 | 5.81e-15 | 
| Oxygen-dependent proline hydroxylation of Hypoxia-inducible Factor Alpha | 60 | 3.22e-15 | -0.588000 | 4.45e-14 | 
| Stabilization of p53 | 54 | 7.61e-14 | -0.588000 | 8.91e-13 | 
| APC/C:Cdc20 mediated degradation of mitotic proteins | 66 | 1.67e-16 | -0.587000 | 3.02e-15 | 
| Activation of APC/C and APC/C:Cdc20 mediated degradation of mitotic proteins | 66 | 1.67e-16 | -0.587000 | 3.02e-15 | 
| Influenza Viral RNA Transcription and Replication | 133 | 4.39e-31 | -0.582000 | 1.97e-29 | 
| ER-Phagosome pathway | 83 | 7.12e-20 | -0.579000 | 2.06e-18 | 
| Degradation of GLI1 by the proteasome | 56 | 6.42e-14 | -0.579000 | 7.59e-13 | 
| Cohesin Loading onto Chromatin | 10 | 1.55e-03 | 0.578000 | 7.26e-03 | 
| Mitotic Telophase/Cytokinesis | 10 | 1.55e-03 | 0.578000 | 7.26e-03 | 
| Degradation of GLI2 by the proteasome | 56 | 8.48e-14 | -0.577000 | 9.76e-13 | 
| GLI3 is processed to GLI3R by the proteasome | 56 | 8.48e-14 | -0.577000 | 9.76e-13 | 
| Signaling by ROBO receptors | 186 | 1.48e-41 | -0.574000 | 2.75e-39 | 
| PCP/CE pathway | 69 | 1.97e-16 | -0.573000 | 3.45e-15 | 
| Gluconeogenesis | 23 | 2.12e-06 | -0.571000 | 1.48e-05 | 
| Dectin-1 mediated noncanonical NF-kB signaling | 59 | 5.68e-14 | -0.566000 | 6.83e-13 | 
| APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins in late mitosis/early G1 | 67 | 1.33e-15 | -0.565000 | 1.92e-14 | 
| Cell-extracellular matrix interactions | 13 | 4.26e-04 | -0.564000 | 2.21e-03 | 
| The citric acid (TCA) cycle and respiratory electron transport | 166 | 3.50e-35 | -0.557000 | 1.89e-33 | 
| ABC transporter disorders | 63 | 2.28e-14 | -0.556000 | 2.90e-13 | 
| Regulation of APC/C activators between G1/S and early anaphase | 69 | 1.66e-15 | -0.555000 | 2.35e-14 | 
| Cholesterol biosynthesis | 25 | 2.02e-06 | -0.549000 | 1.42e-05 | 
| TRAF6 mediated IRF7 activation in TLR7/8 or 9 signaling | 11 | 1.66e-03 | -0.548000 | 7.68e-03 | 
| Cellular response to starvation | 142 | 2.91e-29 | -0.546000 | 1.15e-27 | 
| Myogenesis | 15 | 2.55e-04 | 0.546000 | 1.35e-03 | 
| Regulation of PTEN mRNA translation | 11 | 1.77e-03 | 0.544000 | 8.07e-03 | 
| ROS and RNS production in phagocytes | 25 | 2.52e-06 | -0.544000 | 1.75e-05 | 
| p53-Dependent G1 DNA Damage Response | 58 | 1.03e-12 | -0.541000 | 1.11e-11 | 
| p53-Dependent G1/S DNA damage checkpoint | 58 | 1.03e-12 | -0.541000 | 1.11e-11 | 
| Influenza Infection | 152 | 1.26e-30 | -0.541000 | 5.48e-29 | 
| Gap junction assembly | 10 | 3.44e-03 | -0.534000 | 1.41e-02 | 
| Transport of connexons to the plasma membrane | 10 | 3.44e-03 | -0.534000 | 1.41e-02 | 
| Switching of origins to a post-replicative state | 77 | 9.55e-16 | -0.530000 | 1.41e-14 | 
| Josephin domain DUBs | 10 | 3.76e-03 | -0.529000 | 1.50e-02 | 
| Protein hydroxylation | 14 | 6.60e-04 | -0.526000 | 3.27e-03 | 
| Aggrephagy | 30 | 6.93e-07 | -0.524000 | 5.24e-06 | 
| G1/S DNA Damage Checkpoints | 59 | 5.18e-12 | -0.520000 | 5.22e-11 | 
| Citric acid cycle (TCA cycle) | 22 | 2.49e-05 | -0.519000 | 1.57e-04 | 
| Regulation of RUNX2 expression and activity | 63 | 1.71e-12 | -0.514000 | 1.79e-11 | 
| Detoxification of Reactive Oxygen Species | 28 | 2.56e-06 | -0.514000 | 1.77e-05 | 
| APC/C-mediated degradation of cell cycle proteins | 74 | 3.05e-14 | -0.511000 | 3.77e-13 | 
| Regulation of mitotic cell cycle | 74 | 3.05e-14 | -0.511000 | 3.77e-13 | 
| Assembly of the pre-replicative complex | 75 | 2.18e-14 | -0.510000 | 2.80e-13 | 
| rRNA processing | 201 | 1.66e-35 | -0.509000 | 9.83e-34 | 
| FGFR2 mutant receptor activation | 16 | 4.70e-04 | -0.505000 | 2.39e-03 | 
| Signaling by FGFR2 IIIa TM | 16 | 4.70e-04 | -0.505000 | 2.39e-03 | 
| NRAGE signals death through JNK | 36 | 1.62e-07 | 0.505000 | 1.30e-06 | 
| HDMs demethylate histones | 21 | 6.83e-05 | 0.502000 | 3.94e-04 | 
| Competing endogenous RNAs (ceRNAs) regulate PTEN translation | 10 | 6.01e-03 | 0.502000 | 2.21e-02 | 
| FOXO-mediated transcription of cell cycle genes | 11 | 3.96e-03 | 0.502000 | 1.57e-02 | 
| Transferrin endocytosis and recycling | 22 | 4.65e-05 | -0.502000 | 2.76e-04 | 
| Cellular response to hypoxia | 67 | 1.33e-12 | -0.501000 | 1.40e-11 | 
| Chk1/Chk2(Cds1) mediated inactivation of Cyclin B:Cdk1 complex | 10 | 6.16e-03 | -0.500000 | 2.24e-02 | 
| Antigen processing-Cross presentation | 97 | 2.38e-17 | -0.498000 | 5.23e-16 | 
| mRNA Splicing - Minor Pathway | 50 | 1.12e-09 | -0.498000 | 1.01e-08 | 
| Regulation of CDH11 Expression and Function | 15 | 8.50e-04 | 0.498000 | 4.09e-03 | 
| Regulation of RAS by GAPs | 61 | 1.88e-11 | -0.497000 | 1.84e-10 | 
| Activation of NF-kappaB in B cells | 64 | 6.71e-12 | -0.496000 | 6.71e-11 | 
| rRNA modification in the nucleus and cytosol | 55 | 2.13e-10 | -0.495000 | 1.99e-09 | 
| Formation of paraxial mesoderm | 55 | 2.61e-10 | -0.493000 | 2.43e-09 | 
| Synthesis of PIPs at the late endosome membrane | 10 | 6.97e-03 | 0.493000 | 2.48e-02 | 
| Regulation of PTEN stability and activity | 63 | 1.46e-11 | -0.492000 | 1.44e-10 | 
| Regulation of NPAS4 gene expression | 11 | 4.75e-03 | 0.492000 | 1.80e-02 | 
| SARS-CoV-2 targets host intracellular signalling and regulatory pathways | 10 | 7.25e-03 | -0.490000 | 2.56e-02 | 
| Insulin receptor recycling | 22 | 6.94e-05 | -0.490000 | 3.99e-04 | 
| Gap junction trafficking | 19 | 2.58e-04 | -0.484000 | 1.37e-03 | 
| UCH proteinases | 81 | 5.54e-14 | -0.484000 | 6.73e-13 | 
| Regulation of mRNA stability by proteins that bind AU-rich elements | 83 | 2.94e-14 | -0.483000 | 3.71e-13 | 
| ABC-family proteins mediated transport | 78 | 2.66e-13 | -0.479000 | 2.93e-12 | 
| Signaling by BMP | 14 | 2.17e-03 | 0.473000 | 9.52e-03 | 
| Degradation of cysteine and homocysteine | 10 | 9.69e-03 | -0.472000 | 3.27e-02 | 
| PIWI-interacting RNA (piRNA) biogenesis | 17 | 7.58e-04 | -0.472000 | 3.69e-03 | 
| Gene and protein expression by JAK-STAT signaling after Interleukin-12 stimulation | 32 | 3.98e-06 | -0.471000 | 2.66e-05 | 
| TNFR2 non-canonical NF-kB pathway | 77 | 9.02e-13 | -0.471000 | 9.85e-12 | 
| FCERI mediated NF-kB activation | 74 | 3.21e-12 | -0.469000 | 3.29e-11 | 
| Metabolism of amino acids and derivatives | 263 | 9.06e-39 | -0.468000 | 8.43e-37 | 
| LDL clearance | 15 | 1.74e-03 | -0.467000 | 8.02e-03 | 
| VLDLR internalisation and degradation | 15 | 1.81e-03 | -0.465000 | 8.19e-03 | 
| SARS-CoV-1-host interactions | 88 | 4.92e-14 | -0.465000 | 6.03e-13 | 
| PINK1-PRKN Mediated Mitophagy | 21 | 2.42e-04 | -0.463000 | 1.29e-03 | 
| Nuclear events mediated by NFE2L2 | 87 | 1.08e-13 | -0.461000 | 1.22e-12 | 
| DNA Replication Pre-Initiation | 85 | 2.12e-13 | -0.461000 | 2.37e-12 | 
| RUNX1 regulates transcription of genes involved in differentiation of HSCs | 61 | 5.13e-10 | -0.460000 | 4.73e-09 | 
| Synthesis of PIPs at the early endosome membrane | 15 | 2.17e-03 | 0.457000 | 9.52e-03 | 
| Hedgehog ‘on’ state | 65 | 2.02e-10 | -0.456000 | 1.91e-09 | 
| Pentose phosphate pathway | 13 | 4.48e-03 | -0.455000 | 1.74e-02 | 
| Synthesis of DNA | 96 | 1.83e-14 | -0.453000 | 2.38e-13 | 
| Signaling by NOTCH4 | 75 | 1.35e-11 | -0.452000 | 1.34e-10 | 
| SARS-CoV-1 targets host intracellular signalling and regulatory pathways | 13 | 5.09e-03 | -0.449000 | 1.91e-02 | 
| HSP90 chaperone cycle for steroid hormone receptors (SHR) in the presence of ligand | 41 | 7.00e-07 | -0.448000 | 5.26e-06 | 
| Cyclin E associated events during G1/S transition | 73 | 5.44e-11 | -0.444000 | 5.24e-10 | 
| Metabolism of steroid hormones | 16 | 2.18e-03 | -0.443000 | 9.52e-03 | 
| Cyclin A:Cdk2-associated events at S phase entry | 75 | 3.83e-11 | -0.442000 | 3.71e-10 | 
| Gap junction trafficking and regulation | 21 | 4.60e-04 | -0.442000 | 2.36e-03 | 
| Signaling by cytosolic FGFR1 fusion mutants | 17 | 1.77e-03 | 0.438000 | 8.07e-03 | 
| NRIF signals cell death from the nucleus | 14 | 5.22e-03 | -0.431000 | 1.96e-02 | 
| Purine catabolism | 13 | 7.63e-03 | -0.427000 | 2.68e-02 | 
| Nucleotide biosynthesis | 11 | 1.43e-02 | -0.427000 | 4.54e-02 | 
| Triglyceride catabolism | 13 | 7.76e-03 | -0.427000 | 2.72e-02 | 
| FGFR2 alternative splicing | 24 | 3.36e-04 | -0.423000 | 1.76e-03 | 
| DNA Replication | 101 | 2.44e-13 | -0.422000 | 2.71e-12 | 
| Mitophagy | 28 | 1.13e-04 | -0.422000 | 6.25e-04 | 
| Downstream signaling events of B Cell Receptor (BCR) | 77 | 1.68e-10 | -0.421000 | 1.60e-09 | 
| Synthesis of PIPs at the plasma membrane | 44 | 1.34e-06 | 0.421000 | 9.62e-06 | 
| Regulation of Expression and Function of Type II Classical Cadherins | 16 | 3.62e-03 | 0.420000 | 1.45e-02 | 
| Regulation of Homotypic Cell-Cell Adhesion | 16 | 3.62e-03 | 0.420000 | 1.45e-02 | 
| Abortive elongation of HIV-1 transcript in the absence of Tat | 23 | 5.77e-04 | -0.415000 | 2.90e-03 | 
| Trafficking and processing of endosomal TLR | 10 | 2.50e-02 | -0.409000 | 7.03e-02 | 
| Metabolism of cofactors | 16 | 4.62e-03 | -0.409000 | 1.76e-02 | 
| Plasma lipoprotein clearance | 29 | 1.57e-04 | -0.406000 | 8.62e-04 | 
| Chaperone Mediated Autophagy | 18 | 2.96e-03 | -0.405000 | 1.24e-02 | 
| RND3 GTPase cycle | 26 | 3.81e-04 | 0.403000 | 1.98e-03 | 
| Downstream TCR signaling | 84 | 1.93e-10 | -0.402000 | 1.83e-09 | 
| Interleukin-12 signaling | 37 | 2.71e-05 | -0.399000 | 1.69e-04 | 
| Transcriptional Regulation by NPAS4 | 24 | 7.41e-04 | 0.398000 | 3.62e-03 | 
| Signaling by FLT3 fusion proteins | 18 | 3.58e-03 | 0.397000 | 1.45e-02 | 
| MAPK6/MAPK4 signaling | 76 | 2.89e-09 | -0.394000 | 2.54e-08 | 
| Sema3A PAK dependent Axon repulsion | 13 | 1.46e-02 | -0.391000 | 4.63e-02 | 
| Signaling by WNT in cancer | 19 | 3.35e-03 | 0.389000 | 1.38e-02 | 
| PI3K Cascade | 18 | 4.31e-03 | 0.389000 | 1.69e-02 | 
| Protein localization | 149 | 3.49e-16 | -0.388000 | 5.60e-15 | 
| Phase II - Conjugation of compounds | 43 | 1.11e-05 | -0.387000 | 7.24e-05 | 
| Synthesis of Prostaglandins (PG) and Thromboxanes (TX) | 10 | 3.67e-02 | -0.382000 | 9.64e-02 | 
| TGF-beta receptor signaling in EMT (epithelial to mesenchymal transition) | 12 | 2.25e-02 | -0.381000 | 6.48e-02 | 
| APC truncation mutants have impaired AXIN binding | 12 | 2.37e-02 | 0.377000 | 6.71e-02 | 
| AXIN missense mutants destabilize the destruction complex | 12 | 2.37e-02 | 0.377000 | 6.71e-02 | 
| Signaling by AMER1 mutants | 12 | 2.37e-02 | 0.377000 | 6.71e-02 | 
| Signaling by APC mutants | 12 | 2.37e-02 | 0.377000 | 6.71e-02 | 
| Signaling by AXIN mutants | 12 | 2.37e-02 | 0.377000 | 6.71e-02 | 
| Truncations of AMER1 destabilize the destruction complex | 12 | 2.37e-02 | 0.377000 | 6.71e-02 | 
| Interleukin-6 signaling | 10 | 4.05e-02 | 0.374000 | 1.05e-01 | 
| FGFR1 mutant receptor activation | 20 | 3.98e-03 | 0.372000 | 1.57e-02 | 
| RHOB GTPase cycle | 47 | 1.07e-05 | 0.372000 | 6.96e-05 | 
| Suppression of phagosomal maturation | 12 | 2.68e-02 | -0.369000 | 7.47e-02 | 
| Beta-catenin phosphorylation cascade | 14 | 1.70e-02 | 0.368000 | 5.25e-02 | 
| Glycogen storage diseases | 11 | 3.47e-02 | -0.368000 | 9.24e-02 | 
| CTNNB1 S33 mutants aren’t phosphorylated | 13 | 2.22e-02 | 0.366000 | 6.42e-02 | 
| CTNNB1 S37 mutants aren’t phosphorylated | 13 | 2.22e-02 | 0.366000 | 6.42e-02 | 
| CTNNB1 S45 mutants aren’t phosphorylated | 13 | 2.22e-02 | 0.366000 | 6.42e-02 | 
| CTNNB1 T41 mutants aren’t phosphorylated | 13 | 2.22e-02 | 0.366000 | 6.42e-02 | 
| Signaling by CTNNB1 phospho-site mutants | 13 | 2.22e-02 | 0.366000 | 6.42e-02 | 
| Signaling by GSK3beta mutants | 13 | 2.22e-02 | 0.366000 | 6.42e-02 | 
| Regulation of beta-cell development | 16 | 1.18e-02 | 0.364000 | 3.86e-02 | 
| Sulfur amino acid metabolism | 19 | 6.11e-03 | -0.363000 | 2.23e-02 | 
| Activation of BAD and translocation to mitochondria | 14 | 1.88e-02 | -0.363000 | 5.67e-02 | 
| mRNA Splicing - Major Pathway | 200 | 1.29e-18 | -0.362000 | 3.34e-17 | 
| Insertion of tail-anchored proteins into the endoplasmic reticulum membrane | 19 | 6.43e-03 | -0.361000 | 2.33e-02 | 
| Hedgehog ‘off’ state | 89 | 4.25e-09 | -0.361000 | 3.66e-08 | 
| Host Interactions of HIV factors | 126 | 3.02e-12 | -0.361000 | 3.11e-11 | 
| PI Metabolism | 65 | 5.10e-07 | 0.361000 | 3.93e-06 | 
| RORA activates gene expression | 18 | 8.13e-03 | 0.360000 | 2.82e-02 | 
| Selective autophagy | 66 | 4.22e-07 | -0.360000 | 3.27e-06 | 
| Transcriptional regulation by RUNX2 | 90 | 3.63e-09 | -0.360000 | 3.15e-08 | 
| Activation of AMPK downstream of NMDARs | 16 | 1.30e-02 | -0.359000 | 4.24e-02 | 
| NF-kB is activated and signals survival | 11 | 3.97e-02 | -0.358000 | 1.03e-01 | 
| Generation of second messenger molecules | 18 | 8.53e-03 | -0.358000 | 2.95e-02 | 
| Diseases of carbohydrate metabolism | 23 | 2.96e-03 | -0.358000 | 1.24e-02 | 
| Interleukin-12 family signaling | 42 | 6.33e-05 | -0.357000 | 3.67e-04 | 
| TCR signaling | 98 | 1.09e-09 | -0.357000 | 9.84e-09 | 
| mRNA Splicing | 208 | 1.07e-18 | -0.356000 | 2.83e-17 | 
| HSF1 activation | 23 | 3.30e-03 | -0.354000 | 1.36e-02 | 
| Regulation of gene expression in late stage (branching morphogenesis) pancreatic bud precursor cells | 11 | 4.29e-02 | 0.353000 | 1.10e-01 | 
| Metabolism of RNA | 683 | 2.42e-54 | -0.352000 | 1.57e-51 | 
| Metabolic disorders of biological oxidation enzymes | 16 | 1.50e-02 | -0.351000 | 4.72e-02 | 
| Chondroitin sulfate biosynthesis | 10 | 5.62e-02 | 0.349000 | 1.35e-01 | 
| Pyruvate metabolism and Citric Acid (TCA) cycle | 49 | 2.60e-05 | -0.348000 | 1.63e-04 | 
| G2/M Checkpoints | 106 | 6.77e-10 | -0.347000 | 6.20e-09 | 
| APC/C:Cdc20 mediated degradation of Cyclin B | 20 | 7.43e-03 | -0.346000 | 2.62e-02 | 
| p75NTR recruits signalling complexes | 11 | 4.78e-02 | -0.345000 | 1.20e-01 | 
| G1/S Transition | 103 | 1.71e-09 | -0.344000 | 1.51e-08 | 
| G alpha (12/13) signalling events | 47 | 4.66e-05 | 0.344000 | 2.76e-04 | 
| Pre-NOTCH Transcription and Translation | 30 | 1.13e-03 | 0.344000 | 5.39e-03 | 
| Degradation of beta-catenin by the destruction complex | 75 | 2.85e-07 | -0.343000 | 2.23e-06 | 
| tRNA processing in the mitochondrion | 18 | 1.17e-02 | 0.343000 | 3.86e-02 | 
| Glyoxylate metabolism and glycine degradation | 19 | 9.70e-03 | -0.343000 | 3.27e-02 | 
| Formation of TC-NER Pre-Incision Complex | 53 | 1.87e-05 | -0.340000 | 1.19e-04 | 
| Inhibition of DNA recombination at telomere | 20 | 8.58e-03 | -0.340000 | 2.96e-02 | 
| Glycogen synthesis | 10 | 6.35e-02 | -0.339000 | 1.49e-01 | 
| Signaling by FGFR1 in disease | 26 | 2.78e-03 | 0.339000 | 1.19e-02 | 
| RHO GTPases activate IQGAPs | 22 | 5.95e-03 | -0.339000 | 2.20e-02 | 
| APC-Cdc20 mediated degradation of Nek2A | 20 | 8.99e-03 | -0.338000 | 3.07e-02 | 
| Insulin processing | 16 | 1.95e-02 | 0.337000 | 5.83e-02 | 
| NR1H3 & NR1H2 regulate gene expression linked to cholesterol transport and efflux | 34 | 6.65e-04 | 0.337000 | 3.27e-03 | 
| Sealing of the nuclear envelope (NE) by ESCRT-III | 22 | 6.17e-03 | -0.337000 | 2.24e-02 | 
| WNT5A-dependent internalization of FZD4 | 12 | 4.32e-02 | -0.337000 | 1.11e-01 | 
| Notch-HLH transcription pathway | 26 | 3.01e-03 | 0.336000 | 1.26e-02 | 
| NOTCH4 Intracellular Domain Regulates Transcription | 14 | 2.94e-02 | 0.336000 | 8.06e-02 | 
| Regulation of BACH1 activity | 11 | 5.38e-02 | -0.336000 | 1.32e-01 | 
| Disassembly of the destruction complex and recruitment of AXIN to the membrane | 18 | 1.39e-02 | 0.335000 | 4.44e-02 | 
| mRNA decay by 3’ to 5’ exoribonuclease | 12 | 4.47e-02 | -0.335000 | 1.14e-01 | 
| Regulation of RUNX1 Expression and Activity | 17 | 1.75e-02 | 0.333000 | 5.36e-02 | 
| KEAP1-NFE2L2 pathway | 112 | 1.29e-09 | -0.333000 | 1.15e-08 | 
| Nef-mediates down modulation of cell surface receptors by recruiting them to clathrin adapters | 18 | 1.48e-02 | -0.332000 | 4.68e-02 | 
| RAS processing | 20 | 1.05e-02 | -0.331000 | 3.50e-02 | 
| Interleukin-6 family signaling | 11 | 5.91e-02 | 0.329000 | 1.40e-01 | 
| RNA Pol II CTD phosphorylation and interaction with CE | 27 | 3.19e-03 | -0.328000 | 1.33e-02 | 
| RNA Pol II CTD phosphorylation and interaction with CE during HIV infection | 27 | 3.19e-03 | -0.328000 | 1.33e-02 | 
| Diseases associated with glycosylation precursor biosynthesis | 15 | 2.82e-02 | -0.327000 | 7.76e-02 | 
| IRS-related events triggered by IGF1R | 23 | 6.71e-03 | 0.327000 | 2.42e-02 | 
| Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell | 59 | 1.47e-05 | -0.327000 | 9.49e-05 | 
| Interconversion of nucleotide di- and triphosphates | 23 | 6.79e-03 | -0.326000 | 2.44e-02 | 
| Pyroptosis | 22 | 8.14e-03 | -0.326000 | 2.82e-02 | 
| Endosomal Sorting Complex Required For Transport (ESCRT) | 30 | 2.04e-03 | -0.326000 | 9.08e-03 | 
| CLEC7A (Dectin-1) signaling | 93 | 7.11e-08 | -0.324000 | 5.78e-07 | 
| Formation of the Early Elongation Complex | 33 | 1.32e-03 | -0.323000 | 6.22e-03 | 
| Formation of the HIV-1 Early Elongation Complex | 33 | 1.32e-03 | -0.323000 | 6.22e-03 | 
| NR1H2 and NR1H3-mediated signaling | 39 | 4.82e-04 | 0.323000 | 2.45e-03 | 
| BMAL1:CLOCK,NPAS2 activates circadian gene expression | 22 | 8.91e-03 | 0.322000 | 3.05e-02 | 
| Pausing and recovery of Tat-mediated HIV elongation | 31 | 1.91e-03 | -0.322000 | 8.57e-03 | 
| Tat-mediated HIV elongation arrest and recovery | 31 | 1.91e-03 | -0.322000 | 8.57e-03 | 
| Cellular response to chemical stress | 187 | 5.88e-14 | -0.319000 | 7.01e-13 | 
| Attenuation phase | 19 | 1.60e-02 | -0.319000 | 4.99e-02 | 
| Heme signaling | 38 | 6.70e-04 | 0.319000 | 3.29e-03 | 
| HIV elongation arrest and recovery | 32 | 1.79e-03 | -0.319000 | 8.13e-03 | 
| Pausing and recovery of HIV elongation | 32 | 1.79e-03 | -0.319000 | 8.13e-03 | 
| Chemokine receptors bind chemokines | 10 | 8.11e-02 | -0.319000 | 1.83e-01 | 
| Iron uptake and transport | 45 | 2.25e-04 | -0.318000 | 1.21e-03 | 
| NPAS4 regulates expression of target genes | 13 | 4.72e-02 | 0.318000 | 1.19e-01 | 
| PKMTs methylate histone lysines | 37 | 8.30e-04 | 0.318000 | 4.03e-03 | 
| Axon guidance | 358 | 1.15e-24 | -0.317000 | 3.75e-23 | 
| DNA Damage Recognition in GG-NER | 37 | 8.50e-04 | -0.317000 | 4.09e-03 | 
| Neutrophil degranulation | 378 | 1.50e-25 | -0.315000 | 5.00e-24 | 
| mRNA Capping | 29 | 3.57e-03 | -0.313000 | 1.45e-02 | 
| Nephrin family interactions | 15 | 3.63e-02 | 0.312000 | 9.58e-02 | 
| Lysosome Vesicle Biogenesis | 32 | 2.25e-03 | -0.312000 | 9.79e-03 | 
| Nervous system development | 370 | 1.93e-24 | -0.311000 | 6.13e-23 | 
| RNA Polymerase III Chain Elongation | 17 | 2.69e-02 | -0.310000 | 7.48e-02 | 
| IRS-mediated signalling | 22 | 1.22e-02 | 0.309000 | 4.00e-02 | 
| Platelet degranulation | 76 | 3.44e-06 | -0.308000 | 2.34e-05 | 
| RHO GTPases activate PAKs | 18 | 2.35e-02 | -0.308000 | 6.71e-02 | 
| Interleukin-1 signaling | 103 | 6.86e-08 | -0.308000 | 5.61e-07 | 
| TP53 Regulates Transcription of Caspase Activators and Caspases | 10 | 9.16e-02 | 0.308000 | 2.02e-01 | 
| Ca2+ pathway | 36 | 1.40e-03 | 0.308000 | 6.60e-03 | 
| Pyruvate metabolism | 25 | 7.91e-03 | -0.307000 | 2.76e-02 | 
| SUMOylation of immune response proteins | 11 | 7.87e-02 | -0.306000 | 1.79e-01 | 
| Role of LAT2/NTAL/LAB on calcium mobilization | 14 | 4.74e-02 | 0.306000 | 1.19e-01 | 
| The NLRP3 inflammasome | 15 | 4.13e-02 | -0.304000 | 1.06e-01 | 
| FOXO-mediated transcription of cell death genes | 14 | 4.87e-02 | 0.304000 | 1.21e-01 | 
| mTORC1-mediated signalling | 24 | 1.00e-02 | -0.304000 | 3.37e-02 | 
| RNA Polymerase II Transcription Termination | 62 | 3.75e-05 | -0.303000 | 2.27e-04 | 
| Gastrulation | 68 | 1.65e-05 | -0.302000 | 1.06e-04 | 
| Translesion Synthesis by POLH | 17 | 3.12e-02 | -0.302000 | 8.45e-02 | 
| Diseases associated with N-glycosylation of proteins | 19 | 2.32e-02 | -0.301000 | 6.66e-02 | 
| Metabolism of porphyrins | 19 | 2.36e-02 | -0.300000 | 6.71e-02 | 
| Recycling pathway of L1 | 33 | 2.88e-03 | -0.300000 | 1.22e-02 | 
| NOTCH2 Activation and Transmission of Signal to the Nucleus | 16 | 3.84e-02 | -0.299000 | 1.00e-01 | 
| Signaling by Erythropoietin | 23 | 1.35e-02 | 0.298000 | 4.35e-02 | 
| p75NTR signals via NF-kB | 14 | 5.51e-02 | -0.296000 | 1.34e-01 | 
| ALK mutants bind TKIs | 12 | 7.63e-02 | 0.296000 | 1.76e-01 | 
| Translocation of ZAP-70 to Immunological synapse | 10 | 1.06e-01 | -0.295000 | 2.27e-01 | 
| Basigin interactions | 17 | 3.62e-02 | -0.294000 | 9.56e-02 | 
| RHOJ GTPase cycle | 45 | 6.63e-04 | 0.294000 | 3.27e-03 | 
| RNA Polymerase I Transcription Termination | 23 | 1.52e-02 | -0.292000 | 4.78e-02 | 
| Arachidonic acid metabolism | 22 | 1.82e-02 | -0.291000 | 5.51e-02 | 
| TP53 Regulates Transcription of Death Receptors and Ligands | 10 | 1.12e-01 | 0.290000 | 2.37e-01 | 
| IGF1R signaling cascade | 24 | 1.39e-02 | 0.290000 | 4.44e-02 | 
| Signaling by Type 1 Insulin-like Growth Factor 1 Receptor (IGF1R) | 24 | 1.39e-02 | 0.290000 | 4.44e-02 | 
| MHC class II antigen presentation | 92 | 1.61e-06 | -0.290000 | 1.14e-05 | 
| Cooperation of PDCL (PhLP1) and TRiC/CCT in G-protein beta folding | 27 | 9.33e-03 | -0.289000 | 3.17e-02 | 
| Response of Mtb to phagocytosis | 21 | 2.20e-02 | -0.289000 | 6.42e-02 | 
| FCERI mediated Ca+2 mobilization | 24 | 1.48e-02 | 0.288000 | 4.68e-02 | 
| Response to elevated platelet cytosolic Ca2+ | 80 | 9.18e-06 | -0.287000 | 6.06e-05 | 
| Disorders of transmembrane transporters | 119 | 6.85e-08 | -0.287000 | 5.61e-07 | 
| PRC2 methylates histones and DNA | 13 | 7.73e-02 | 0.283000 | 1.78e-01 | 
| SARS-CoV-1 Infection | 131 | 2.61e-08 | -0.282000 | 2.17e-07 | 
| N-glycan trimming in the ER and Calnexin/Calreticulin cycle | 34 | 4.43e-03 | -0.282000 | 1.73e-02 | 
| Dual incision in TC-NER | 62 | 1.25e-04 | -0.282000 | 6.89e-04 | 
| Gap-filling DNA repair synthesis and ligation in GG-NER | 22 | 2.22e-02 | -0.282000 | 6.42e-02 | 
| MyD88 deficiency (TLR2/4) | 14 | 6.98e-02 | -0.280000 | 1.62e-01 | 
| RUNX1 interacts with co-factors whose precise effect on RUNX1 targets is not known | 34 | 4.77e-03 | 0.280000 | 1.80e-02 | 
| Beta-catenin independent WNT signaling | 104 | 8.59e-07 | -0.280000 | 6.31e-06 | 
| alpha-linolenic (omega3) and linoleic (omega6) acid metabolism | 11 | 1.08e-01 | -0.280000 | 2.30e-01 | 
| alpha-linolenic acid (ALA) metabolism | 11 | 1.08e-01 | -0.280000 | 2.30e-01 | 
| Cell recruitment (pro-inflammatory response) | 21 | 2.68e-02 | -0.279000 | 7.46e-02 | 
| Purinergic signaling in leishmaniasis infection | 21 | 2.68e-02 | -0.279000 | 7.46e-02 | 
| RND1 GTPase cycle | 27 | 1.20e-02 | 0.279000 | 3.94e-02 | 
| RNA Polymerase I Promoter Escape | 25 | 1.57e-02 | -0.279000 | 4.92e-02 | 
| Protein folding | 70 | 5.59e-05 | -0.279000 | 3.29e-04 | 
| Plasma lipoprotein assembly | 12 | 9.56e-02 | -0.278000 | 2.08e-01 | 
| Processing of Capped Intron-Containing Pre-mRNA | 274 | 3.41e-15 | -0.278000 | 4.67e-14 | 
| Signaling by the B Cell Receptor (BCR) | 101 | 1.49e-06 | -0.278000 | 1.06e-05 | 
| MicroRNA (miRNA) biogenesis | 24 | 1.90e-02 | -0.277000 | 5.72e-02 | 
| Mitotic G1 phase and G1/S transition | 116 | 2.79e-07 | -0.277000 | 2.20e-06 | 
| Cytosolic iron-sulfur cluster assembly | 11 | 1.15e-01 | -0.275000 | 2.40e-01 | 
| Gap-filling DNA repair synthesis and ligation in TC-NER | 61 | 2.17e-04 | -0.274000 | 1.17e-03 | 
| tRNA Aminoacylation | 21 | 2.97e-02 | -0.274000 | 8.11e-02 | 
| HIV Infection | 219 | 3.66e-12 | -0.274000 | 3.72e-11 | 
| Signaling by Hedgehog | 111 | 7.54e-07 | -0.272000 | 5.57e-06 | 
| Calnexin/calreticulin cycle | 25 | 1.86e-02 | -0.272000 | 5.62e-02 | 
| VxPx cargo-targeting to cilium | 17 | 5.25e-02 | 0.272000 | 1.29e-01 | 
| Late endosomal microautophagy | 30 | 1.04e-02 | -0.270000 | 3.50e-02 | 
| Heme biosynthesis | 12 | 1.05e-01 | -0.270000 | 2.25e-01 | 
| COPI-mediated anterograde transport | 81 | 2.75e-05 | -0.270000 | 1.71e-04 | 
| FASTK family proteins regulate processing and stability of mitochondrial RNAs | 17 | 5.44e-02 | 0.270000 | 1.33e-01 | 
| Transcription-Coupled Nucleotide Excision Repair (TC-NER) | 75 | 6.16e-05 | -0.268000 | 3.60e-04 | 
| Insulin receptor signalling cascade | 27 | 1.65e-02 | 0.267000 | 5.11e-02 | 
| Mitochondrial iron-sulfur cluster biogenesis | 13 | 9.76e-02 | -0.265000 | 2.12e-01 | 
| RUNX3 regulates NOTCH signaling | 13 | 9.86e-02 | 0.265000 | 2.14e-01 | 
| Formation of HIV-1 elongation complex containing HIV-1 Tat | 43 | 2.80e-03 | -0.264000 | 1.19e-02 | 
| HIV Transcription Elongation | 43 | 2.80e-03 | -0.264000 | 1.19e-02 | 
| Tat-mediated elongation of the HIV-1 transcript | 43 | 2.80e-03 | -0.264000 | 1.19e-02 | 
| PD-1 signaling | 14 | 8.82e-02 | -0.263000 | 1.96e-01 | 
| Formation of HIV elongation complex in the absence of HIV Tat | 44 | 2.59e-03 | -0.263000 | 1.12e-02 | 
| E3 ubiquitin ligases ubiquitinate target proteins | 41 | 3.74e-03 | -0.262000 | 1.50e-02 | 
| S Phase | 130 | 2.75e-07 | -0.262000 | 2.18e-06 | 
| Transcriptional regulation by RUNX3 | 87 | 2.62e-05 | -0.261000 | 1.64e-04 | 
| Biological oxidations | 85 | 3.33e-05 | -0.261000 | 2.04e-04 | 
| Binding and Uptake of Ligands by Scavenger Receptors | 20 | 4.47e-02 | -0.259000 | 1.14e-01 | 
| N-Glycan antennae elongation | 11 | 1.37e-01 | 0.259000 | 2.74e-01 | 
| Nuclear Receptor transcription pathway | 29 | 1.62e-02 | 0.258000 | 5.06e-02 | 
| Termination of translesion DNA synthesis | 27 | 2.06e-02 | -0.258000 | 6.12e-02 | 
| Mismatch repair (MMR) directed by MSH2:MSH3 (MutSbeta) | 13 | 1.09e-01 | -0.257000 | 2.31e-01 | 
| Plasma lipoprotein assembly, remodeling, and clearance | 48 | 2.15e-03 | -0.256000 | 9.52e-03 | 
| Separation of Sister Chromatids | 145 | 1.10e-07 | -0.256000 | 8.90e-07 | 
| Interleukin-1 family signaling | 122 | 1.10e-06 | -0.256000 | 8.02e-06 | 
| Recognition of DNA damage by PCNA-containing replication complex | 26 | 2.42e-02 | -0.256000 | 6.82e-02 | 
| RHOC GTPase cycle | 55 | 1.08e-03 | 0.255000 | 5.17e-03 | 
| C-type lectin receptors (CLRs) | 112 | 3.56e-06 | -0.254000 | 2.41e-05 | 
| Signaling by PDGFR in disease | 19 | 5.55e-02 | 0.254000 | 1.35e-01 | 
| HIV Transcription Initiation | 42 | 4.56e-03 | -0.253000 | 1.74e-02 | 
| RNA Polymerase II HIV Promoter Escape | 42 | 4.56e-03 | -0.253000 | 1.74e-02 | 
| RNA Polymerase II Promoter Escape | 42 | 4.56e-03 | -0.253000 | 1.74e-02 | 
| RNA Polymerase II Transcription Initiation | 42 | 4.56e-03 | -0.253000 | 1.74e-02 | 
| RNA Polymerase II Transcription Initiation And Promoter Clearance | 42 | 4.56e-03 | -0.253000 | 1.74e-02 | 
| RNA Polymerase II Transcription Pre-Initiation And Promoter Opening | 42 | 4.56e-03 | -0.253000 | 1.74e-02 | 
| Acyl chain remodelling of PC | 10 | 1.66e-01 | 0.253000 | 3.13e-01 | 
| IRAK1 recruits IKK complex | 13 | 1.16e-01 | -0.252000 | 2.41e-01 | 
| IRAK1 recruits IKK complex upon TLR7/8 or 9 stimulation | 13 | 1.16e-01 | -0.252000 | 2.41e-01 | 
| Inositol phosphate metabolism | 29 | 1.93e-02 | 0.251000 | 5.78e-02 | 
| Cellular responses to stress | 623 | 5.36e-26 | -0.251000 | 1.88e-24 | 
| Chaperonin-mediated protein folding | 65 | 4.92e-04 | -0.250000 | 2.49e-03 | 
| FOXO-mediated transcription of oxidative stress, metabolic and neuronal genes | 16 | 8.35e-02 | 0.250000 | 1.87e-01 | 
| Smooth Muscle Contraction | 26 | 2.77e-02 | -0.250000 | 7.66e-02 | 
| RAC1 GTPase cycle | 133 | 7.17e-07 | 0.250000 | 5.36e-06 | 
| TP53 Regulates Metabolic Genes | 82 | 1.00e-04 | -0.249000 | 5.61e-04 | 
| Cellular responses to stimuli | 631 | 6.06e-26 | -0.249000 | 2.07e-24 | 
| CDC42 GTPase cycle | 110 | 7.03e-06 | 0.248000 | 4.69e-05 | 
| RHOQ GTPase cycle | 46 | 3.63e-03 | 0.248000 | 1.45e-02 | 
| Class I peroxisomal membrane protein import | 18 | 6.92e-02 | -0.247000 | 1.61e-01 | 
| Impaired BRCA2 binding to PALB2 | 19 | 6.25e-02 | 0.247000 | 1.47e-01 | 
| Infection with Mycobacterium tuberculosis | 24 | 3.66e-02 | -0.247000 | 9.63e-02 | 
| Telomere Maintenance | 53 | 1.93e-03 | -0.246000 | 8.63e-03 | 
| Metabolism of nucleotides | 76 | 2.10e-04 | -0.246000 | 1.14e-03 | 
| Retrograde neurotrophin signalling | 10 | 1.78e-01 | -0.246000 | 3.28e-01 | 
| ATF6 (ATF6-alpha) activates chaperone genes | 10 | 1.78e-01 | -0.246000 | 3.29e-01 | 
| Amyloid fiber formation | 34 | 1.32e-02 | -0.246000 | 4.28e-02 | 
| Regulation of MECP2 expression and activity | 27 | 2.77e-02 | 0.245000 | 7.66e-02 | 
| Prolonged ERK activation events | 12 | 1.42e-01 | 0.245000 | 2.82e-01 | 
| Nucleotide Excision Repair | 105 | 1.56e-05 | -0.245000 | 1.00e-04 | 
| SARS-CoV-1 activates/modulates innate immune responses | 36 | 1.12e-02 | -0.244000 | 3.71e-02 | 
| PCNA-Dependent Long Patch Base Excision Repair | 17 | 8.29e-02 | -0.243000 | 1.86e-01 | 
| Dual Incision in GG-NER | 38 | 9.60e-03 | -0.243000 | 3.26e-02 | 
| Regulation of innate immune responses to cytosolic DNA | 11 | 1.64e-01 | -0.242000 | 3.10e-01 | 
| Signaling by FLT3 ITD and TKD mutants | 14 | 1.17e-01 | 0.242000 | 2.43e-01 | 
| Miscellaneous transport and binding events | 16 | 9.40e-02 | 0.242000 | 2.05e-01 | 
| Nicotinamide salvaging | 13 | 1.32e-01 | 0.242000 | 2.66e-01 | 
| IRAK4 deficiency (TLR2/4) | 15 | 1.05e-01 | -0.242000 | 2.25e-01 | 
| RNA Polymerase III Transcription Termination | 20 | 6.17e-02 | -0.241000 | 1.46e-01 | 
| Downregulation of ERBB2 signaling | 18 | 7.66e-02 | -0.241000 | 1.76e-01 | 
| Collagen degradation | 21 | 5.61e-02 | -0.241000 | 1.35e-01 | 
| Azathioprine ADME | 17 | 8.67e-02 | -0.240000 | 1.93e-01 | 
| Mitotic Anaphase | 185 | 2.01e-08 | -0.240000 | 1.69e-07 | 
| Mitotic Metaphase and Anaphase | 185 | 2.01e-08 | -0.240000 | 1.69e-07 | 
| Translesion synthesis by Y family DNA polymerases bypasses lesions on DNA template | 33 | 1.71e-02 | -0.240000 | 5.27e-02 | 
| mRNA decay by 5’ to 3’ exoribonuclease | 15 | 1.09e-01 | -0.239000 | 2.31e-01 | 
| Cell-cell junction organization | 33 | 1.76e-02 | 0.239000 | 5.37e-02 | 
| mRNA 3’-end processing | 55 | 2.30e-03 | -0.238000 | 9.95e-03 | 
| Viral Infection Pathways | 613 | 3.07e-23 | -0.238000 | 9.50e-22 | 
| Interleukin receptor SHC signaling | 17 | 8.97e-02 | 0.238000 | 1.99e-01 | 
| HDR through MMEJ (alt-NHEJ) | 10 | 1.93e-01 | 0.238000 | 3.51e-01 | 
| Gamma carboxylation, hypusinylation, hydroxylation, and arylsulfatase activation | 41 | 8.73e-03 | -0.237000 | 2.99e-02 | 
| DNA Damage/Telomere Stress Induced Senescence | 22 | 5.48e-02 | 0.237000 | 1.33e-01 | 
| Metabolism of nitric oxide: NOS3 activation and regulation | 10 | 1.97e-01 | -0.236000 | 3.56e-01 | 
| TICAM1, RIP1-mediated IKK complex recruitment | 18 | 8.39e-02 | -0.235000 | 1.88e-01 | 
| TP53 Regulates Transcription of Genes Involved in G2 Cell Cycle Arrest | 15 | 1.17e-01 | -0.234000 | 2.42e-01 | 
| Formation of the beta-catenin:TCF transactivating complex | 24 | 4.74e-02 | 0.234000 | 1.19e-01 | 
| Signaling by FGFR2 | 49 | 4.69e-03 | -0.234000 | 1.78e-02 | 
| G2/M Transition | 159 | 4.21e-07 | -0.233000 | 3.27e-06 | 
| Mismatch repair (MMR) directed by MSH2:MSH6 (MutSalpha) | 13 | 1.47e-01 | -0.233000 | 2.87e-01 | 
| Peroxisomal lipid metabolism | 24 | 4.91e-02 | -0.232000 | 1.22e-01 | 
| Downstream signaling of activated FGFR1 | 13 | 1.50e-01 | 0.231000 | 2.88e-01 | 
| Response of EIF2AK1 (HRI) to heme deficiency | 14 | 1.36e-01 | -0.230000 | 2.73e-01 | 
| Rap1 signalling | 12 | 1.68e-01 | -0.230000 | 3.16e-01 | 
| CD28 dependent PI3K/Akt signaling | 19 | 8.35e-02 | 0.229000 | 1.87e-01 | 
| RUNX1 regulates genes involved in megakaryocyte differentiation and platelet function | 30 | 2.98e-02 | 0.229000 | 8.11e-02 | 
| Signaling by FGFR2 in disease | 25 | 4.74e-02 | -0.229000 | 1.19e-01 | 
| Constitutive Signaling by Ligand-Responsive EGFR Cancer Variants | 16 | 1.13e-01 | -0.229000 | 2.37e-01 | 
| Signaling by Ligand-Responsive EGFR Variants in Cancer | 16 | 1.13e-01 | -0.229000 | 2.37e-01 | 
| Mitotic G2-G2/M phases | 160 | 6.68e-07 | -0.228000 | 5.08e-06 | 
| Resolution of D-Loop Structures | 23 | 5.86e-02 | 0.228000 | 1.40e-01 | 
| Resolution of D-loop Structures through Holliday Junction Intermediates | 23 | 5.86e-02 | 0.228000 | 1.40e-01 | 
| Programmed Cell Death | 176 | 2.08e-07 | -0.228000 | 1.66e-06 | 
| Receptor Mediated Mitophagy | 11 | 1.91e-01 | -0.228000 | 3.49e-01 | 
| Metalloprotease DUBs | 16 | 1.15e-01 | -0.228000 | 2.40e-01 | 
| TNF receptor superfamily (TNFSF) members mediating non-canonical NF-kB pathway | 12 | 1.73e-01 | -0.227000 | 3.21e-01 | 
| Defective Intrinsic Pathway for Apoptosis | 20 | 7.91e-02 | -0.227000 | 1.80e-01 | 
| KSRP (KHSRP) binds and destabilizes mRNA | 15 | 1.31e-01 | -0.225000 | 2.65e-01 | 
| rRNA processing in the mitochondrion | 21 | 7.42e-02 | 0.225000 | 1.72e-01 | 
| Synthesis of IP3 and IP4 in the cytosol | 14 | 1.46e-01 | 0.225000 | 2.87e-01 | 
| Interleukin-20 family signaling | 14 | 1.46e-01 | 0.224000 | 2.87e-01 | 
| SARS-CoV-2-host interactions | 169 | 5.50e-07 | -0.224000 | 4.20e-06 | 
| TICAM1-dependent activation of IRF3/IRF7 | 11 | 1.98e-01 | -0.224000 | 3.59e-01 | 
| Phospholipid metabolism | 144 | 3.87e-06 | 0.224000 | 2.61e-05 | 
| Intra-Golgi traffic | 39 | 1.64e-02 | 0.222000 | 5.10e-02 | 
| Global Genome Nucleotide Excision Repair (GG-NER) | 79 | 6.52e-04 | -0.222000 | 3.25e-03 | 
| Apoptosis | 149 | 3.08e-06 | -0.222000 | 2.12e-05 | 
| Metabolism | 1410 | 9.63e-42 | -0.222000 | 2.09e-39 | 
| RHO GTPases activate CIT | 14 | 1.52e-01 | -0.221000 | 2.90e-01 | 
| Collagen formation | 31 | 3.34e-02 | -0.221000 | 8.96e-02 | 
| RNA Polymerase III Transcription Initiation From Type 2 Promoter | 26 | 5.24e-02 | -0.220000 | 1.29e-01 | 
| Interleukin-2 family signaling | 29 | 4.09e-02 | 0.219000 | 1.06e-01 | 
| Regulated Necrosis | 51 | 6.99e-03 | -0.219000 | 2.48e-02 | 
| Translesion synthesis by REV1 | 15 | 1.43e-01 | -0.218000 | 2.83e-01 | 
| Triglyceride metabolism | 19 | 9.96e-02 | -0.218000 | 2.15e-01 | 
| Phosphorylation of the APC/C | 16 | 1.31e-01 | -0.218000 | 2.65e-01 | 
| Nucleotide catabolism | 25 | 5.96e-02 | -0.218000 | 1.41e-01 | 
| Signaling by EGFR in Cancer | 17 | 1.21e-01 | -0.217000 | 2.50e-01 | 
| Synthesis of PIPs at the Golgi membrane | 14 | 1.60e-01 | 0.217000 | 3.03e-01 | 
| RNA Polymerase III Transcription Initiation From Type 1 Promoter | 27 | 5.16e-02 | -0.217000 | 1.27e-01 | 
| Adherens junctions interactions | 25 | 6.10e-02 | 0.217000 | 1.44e-01 | 
| Carnitine metabolism | 11 | 2.14e-01 | 0.216000 | 3.79e-01 | 
| Resolution of Abasic Sites (AP sites) | 32 | 3.44e-02 | -0.216000 | 9.19e-02 | 
| RHO GTPases activate PKNs | 26 | 5.77e-02 | -0.215000 | 1.39e-01 | 
| HSF1-dependent transactivation | 26 | 5.83e-02 | -0.215000 | 1.40e-01 | 
| Spry regulation of FGF signaling | 16 | 1.37e-01 | -0.215000 | 2.74e-01 | 
| NOTCH3 Intracellular Domain Regulates Transcription | 16 | 1.37e-01 | 0.215000 | 2.74e-01 | 
| Telomere Extension By Telomerase | 16 | 1.38e-01 | -0.215000 | 2.74e-01 | 
| Macroautophagy | 118 | 6.17e-05 | -0.214000 | 3.60e-04 | 
| Resolution of AP sites via the multiple-nucleotide patch replacement pathway | 20 | 1.00e-01 | -0.212000 | 2.16e-01 | 
| Circadian Clock | 59 | 4.85e-03 | 0.212000 | 1.83e-02 | 
| EPH-Ephrin signaling | 62 | 3.92e-03 | -0.212000 | 1.56e-02 | 
| Signal regulatory protein family interactions | 11 | 2.24e-01 | -0.212000 | 3.90e-01 | 
| Maturation of nucleoprotein 9683610 | 11 | 2.25e-01 | 0.211000 | 3.91e-01 | 
| Fc epsilon receptor (FCERI) signaling | 118 | 8.09e-05 | -0.211000 | 4.57e-04 | 
| Metabolism of proteins | 1348 | 1.25e-35 | -0.209000 | 8.13e-34 | 
| Interleukin-15 signaling | 11 | 2.32e-01 | 0.208000 | 4.01e-01 | 
| The role of Nef in HIV-1 replication and disease pathogenesis | 24 | 7.76e-02 | -0.208000 | 1.78e-01 | 
| EPH-ephrin mediated repulsion of cells | 28 | 5.68e-02 | -0.208000 | 1.37e-01 | 
| Sphingolipid de novo biosynthesis | 24 | 7.83e-02 | 0.208000 | 1.79e-01 | 
| Inactivation of APC/C via direct inhibition of the APC/C complex | 16 | 1.50e-01 | -0.208000 | 2.88e-01 | 
| Inhibition of the proteolytic activity of APC/C required for the onset of anaphase by mitotic spindle checkpoint components | 16 | 1.50e-01 | -0.208000 | 2.88e-01 | 
| Post-translational modification: synthesis of GPI-anchored proteins | 37 | 2.90e-02 | -0.208000 | 7.96e-02 | 
| RHOA GTPase cycle | 104 | 3.14e-04 | 0.205000 | 1.65e-03 | 
| COPI-independent Golgi-to-ER retrograde traffic | 40 | 2.50e-02 | -0.205000 | 7.03e-02 | 
| Fatty acyl-CoA biosynthesis | 24 | 8.24e-02 | -0.205000 | 1.86e-01 | 
| NOTCH3 Activation and Transmission of Signal to the Nucleus | 18 | 1.34e-01 | -0.204000 | 2.70e-01 | 
| Cell death signalling via NRAGE, NRIF and NADE | 53 | 1.02e-02 | 0.204000 | 3.44e-02 | 
| Paracetamol ADME | 10 | 2.65e-01 | -0.204000 | 4.36e-01 | 
| L1CAM interactions | 63 | 5.38e-03 | -0.203000 | 2.01e-02 | 
| Infectious disease | 747 | 1.51e-20 | -0.203000 | 4.56e-19 | 
| Diseases of metabolism | 129 | 7.23e-05 | -0.203000 | 4.14e-04 | 
| Maternal to zygotic transition (MZT) | 50 | 1.33e-02 | 0.203000 | 4.28e-02 | 
| IRE1alpha activates chaperones | 43 | 2.18e-02 | -0.202000 | 6.42e-02 | 
| Pre-NOTCH Expression and Processing | 45 | 1.99e-02 | 0.201000 | 5.95e-02 | 
| Mitochondrial calcium ion transport | 20 | 1.21e-01 | -0.201000 | 2.49e-01 | 
| Activated NOTCH1 Transmits Signal to the Nucleus | 22 | 1.04e-01 | -0.200000 | 2.24e-01 | 
| Innate Immune System | 749 | 4.69e-20 | -0.200000 | 1.39e-18 | 
| Negative regulation of FLT3 | 11 | 2.51e-01 | -0.200000 | 4.21e-01 | 
| Maturation of nucleoprotein 9694631 | 15 | 1.81e-01 | 0.200000 | 3.32e-01 | 
| Formation of Incision Complex in GG-NER | 42 | 2.58e-02 | -0.199000 | 7.23e-02 | 
| Mismatch Repair | 14 | 2.01e-01 | -0.197000 | 3.62e-01 | 
| Pexophagy | 11 | 2.58e-01 | -0.197000 | 4.27e-01 | 
| Downstream signaling of activated FGFR2 | 11 | 2.58e-01 | 0.197000 | 4.27e-01 | 
| Downstream signaling of activated FGFR3 | 11 | 2.58e-01 | 0.197000 | 4.27e-01 | 
| Downstream signaling of activated FGFR4 | 11 | 2.58e-01 | 0.197000 | 4.27e-01 | 
| MAP2K and MAPK activation | 32 | 5.39e-02 | -0.197000 | 1.32e-01 | 
| Transcriptional Regulation by MECP2 | 39 | 3.36e-02 | 0.197000 | 8.98e-02 | 
| ER to Golgi Anterograde Transport | 125 | 1.61e-04 | -0.196000 | 8.81e-04 | 
| FLT3 signaling in disease | 25 | 9.02e-02 | 0.196000 | 1.99e-01 | 
| Signaling by ERBB2 TMD/JMD mutants | 10 | 2.84e-01 | -0.196000 | 4.56e-01 | 
| Signaling by NODAL | 12 | 2.42e-01 | 0.195000 | 4.12e-01 | 
| Negative regulation of the PI3K/AKT network | 57 | 1.09e-02 | 0.195000 | 3.60e-02 | 
| Collagen biosynthesis and modifying enzymes | 19 | 1.41e-01 | -0.195000 | 2.80e-01 | 
| Cell Cycle Checkpoints | 193 | 3.38e-06 | -0.195000 | 2.31e-05 | 
| MECP2 regulates neuronal receptors and channels | 10 | 2.87e-01 | 0.194000 | 4.60e-01 | 
| RHO GTPases Activate WASPs and WAVEs | 34 | 5.03e-02 | -0.194000 | 1.25e-01 | 
| Processing of Capped Intronless Pre-mRNA | 27 | 8.11e-02 | -0.194000 | 1.83e-01 | 
| NOTCH1 Intracellular Domain Regulates Transcription | 41 | 3.21e-02 | 0.194000 | 8.68e-02 | 
| PI3K/AKT Signaling in Cancer | 50 | 1.80e-02 | 0.194000 | 5.49e-02 | 
| COPI-dependent Golgi-to-ER retrograde traffic | 66 | 6.72e-03 | -0.193000 | 2.42e-02 | 
| PKR-mediated signaling | 59 | 1.05e-02 | -0.193000 | 3.50e-02 | 
| Caspase activation via extrinsic apoptotic signalling pathway | 21 | 1.27e-01 | 0.193000 | 2.59e-01 | 
| ADP signalling through P2Y purinoceptor 12 | 12 | 2.50e-01 | -0.192000 | 4.20e-01 | 
| CTLA4 inhibitory signaling | 17 | 1.71e-01 | 0.192000 | 3.19e-01 | 
| Deregulated CDK5 triggers multiple neurodegenerative pathways in Alzheimer’s disease models | 17 | 1.71e-01 | -0.192000 | 3.19e-01 | 
| Neurodegenerative Diseases | 17 | 1.71e-01 | -0.192000 | 3.19e-01 | 
| Signaling by FGFR | 56 | 1.32e-02 | -0.192000 | 4.28e-02 | 
| Chromosome Maintenance | 70 | 5.71e-03 | -0.191000 | 2.12e-02 | 
| Fatty acid metabolism | 113 | 4.56e-04 | -0.191000 | 2.35e-03 | 
| RND2 GTPase cycle | 26 | 9.20e-02 | 0.191000 | 2.02e-01 | 
| Autophagy | 130 | 1.80e-04 | -0.191000 | 9.77e-04 | 
| RHOV GTPase cycle | 28 | 8.26e-02 | 0.190000 | 1.86e-01 | 
| NF-kB activation through FADD/RIP-1 pathway mediated by caspase-8 and -10 | 12 | 2.56e-01 | 0.190000 | 4.27e-01 | 
| Constitutive Signaling by NOTCH1 HD Domain Mutants | 10 | 3.00e-01 | -0.189000 | 4.70e-01 | 
| Signaling by NOTCH1 HD Domain Mutants in Cancer | 10 | 3.00e-01 | -0.189000 | 4.70e-01 | 
| PTEN Regulation | 128 | 2.32e-04 | -0.189000 | 1.24e-03 | 
| Transport of Mature mRNA derived from an Intron-Containing Transcript | 69 | 6.93e-03 | -0.188000 | 2.47e-02 | 
| RET signaling | 22 | 1.28e-01 | 0.188000 | 2.61e-01 | 
| Defective HDR through Homologous Recombination Repair (HRR) due to PALB2 loss of BRCA1 binding function | 20 | 1.47e-01 | 0.187000 | 2.87e-01 | 
| Defective HDR through Homologous Recombination Repair (HRR) due to PALB2 loss of BRCA2/RAD51/RAD51C binding function | 20 | 1.47e-01 | 0.187000 | 2.87e-01 | 
| Defective homologous recombination repair (HRR) due to BRCA1 loss of function | 20 | 1.47e-01 | 0.187000 | 2.87e-01 | 
| Defective homologous recombination repair (HRR) due to PALB2 loss of function | 20 | 1.47e-01 | 0.187000 | 2.87e-01 | 
| Resolution of D-loop Structures through Synthesis-Dependent Strand Annealing (SDSA) | 20 | 1.47e-01 | 0.187000 | 2.87e-01 | 
| Glycosphingolipid catabolism | 24 | 1.13e-01 | -0.187000 | 2.37e-01 | 
| HS-GAG biosynthesis | 16 | 1.96e-01 | 0.187000 | 3.56e-01 | 
| RAF/MAP kinase cascade | 168 | 3.25e-05 | -0.186000 | 2.00e-04 | 
| XBP1(S) activates chaperone genes | 41 | 4.09e-02 | -0.185000 | 1.06e-01 | 
| M-decay: degradation of maternal mRNAs by maternally stored factors | 37 | 5.29e-02 | 0.184000 | 1.30e-01 | 
| Transcription of the HIV genome | 65 | 1.08e-02 | -0.183000 | 3.58e-02 | 
| Cytosolic sensors of pathogen-associated DNA | 56 | 1.79e-02 | -0.183000 | 5.46e-02 | 
| Neddylation | 198 | 1.00e-05 | -0.183000 | 6.57e-05 | 
| Metabolism of steroids | 100 | 1.64e-03 | -0.183000 | 7.61e-03 | 
| Aberrant regulation of mitotic G1/S transition in cancer due to RB1 defects | 12 | 2.74e-01 | 0.182000 | 4.46e-01 | 
| Defective binding of RB1 mutants to E2F1,(E2F2, E2F3) | 12 | 2.74e-01 | 0.182000 | 4.46e-01 | 
| Nuclear Envelope (NE) Reassembly | 62 | 1.31e-02 | -0.182000 | 4.26e-02 | 
| Inhibition of replication initiation of damaged DNA by RB1/E2F1 | 12 | 2.76e-01 | 0.182000 | 4.49e-01 | 
| Asparagine N-linked glycosylation | 249 | 9.54e-07 | -0.181000 | 6.96e-06 | 
| G beta:gamma signalling through BTK | 11 | 3.00e-01 | -0.180000 | 4.70e-01 | 
| DNA Damage Bypass | 41 | 4.59e-02 | -0.180000 | 1.16e-01 | 
| Aberrant regulation of mitotic exit in cancer due to RB1 defects | 18 | 1.86e-01 | -0.180000 | 3.41e-01 | 
| Deadenylation of mRNA | 22 | 1.44e-01 | 0.180000 | 2.84e-01 | 
| Regulation of TP53 Activity through Association with Co-factors | 10 | 3.26e-01 | 0.179000 | 4.96e-01 | 
| Constitutive Signaling by AKT1 E17K in Cancer | 23 | 1.37e-01 | 0.179000 | 2.74e-01 | 
| Glucose metabolism | 74 | 7.78e-03 | -0.179000 | 2.72e-02 | 
| Glycosphingolipid metabolism | 30 | 9.20e-02 | -0.178000 | 2.02e-01 | 
| Oxidative Stress Induced Senescence | 56 | 2.16e-02 | 0.178000 | 6.38e-02 | 
| Translesion synthesis by POLK | 16 | 2.19e-01 | -0.178000 | 3.84e-01 | 
| Transport of Mature Transcript to Cytoplasm | 78 | 6.84e-03 | -0.177000 | 2.45e-02 | 
| Nef mediated downregulation of MHC class I complex cell surface expression | 10 | 3.32e-01 | -0.177000 | 5.00e-01 | 
| Nucleotide salvage | 20 | 1.70e-01 | -0.177000 | 3.18e-01 | 
| Cargo concentration in the ER | 24 | 1.37e-01 | -0.176000 | 2.74e-01 | 
| Constitutive Signaling by Aberrant PI3K in Cancer | 26 | 1.22e-01 | 0.175000 | 2.51e-01 | 
| Antimicrobial peptides | 15 | 2.40e-01 | -0.175000 | 4.11e-01 | 
| MAPK1/MAPK3 signaling | 172 | 7.89e-05 | -0.175000 | 4.48e-04 | 
| Post-translational protein phosphorylation | 44 | 4.49e-02 | -0.175000 | 1.14e-01 | 
| Cytoprotection by HMOX1 | 58 | 2.15e-02 | -0.175000 | 6.37e-02 | 
| Mitochondrial Fatty Acid Beta-Oxidation | 31 | 9.28e-02 | -0.175000 | 2.04e-01 | 
| Chromatin modifying enzymes | 189 | 3.87e-05 | 0.174000 | 2.32e-04 | 
| Chromatin organization | 189 | 3.87e-05 | 0.174000 | 2.32e-04 | 
| RNA Polymerase III Transcription Initiation From Type 3 Promoter | 26 | 1.24e-01 | -0.174000 | 2.55e-01 | 
| Cargo recognition for clathrin-mediated endocytosis | 71 | 1.13e-02 | -0.174000 | 3.73e-02 | 
| Frs2-mediated activation | 10 | 3.41e-01 | 0.174000 | 5.09e-01 | 
| Activation of G protein gated Potassium channels | 11 | 3.20e-01 | -0.173000 | 4.89e-01 | 
| G protein gated Potassium channels | 11 | 3.20e-01 | -0.173000 | 4.89e-01 | 
| Inhibition of voltage gated Ca2+ channels via Gbeta/gamma subunits | 11 | 3.20e-01 | -0.173000 | 4.89e-01 | 
| Synthesis of very long-chain fatty acyl-CoAs | 15 | 2.46e-01 | -0.173000 | 4.18e-01 | 
| RHO GTPases Activate NADPH Oxidases | 19 | 1.92e-01 | -0.173000 | 3.50e-01 | 
| NCAM signaling for neurite out-growth | 25 | 1.35e-01 | 0.173000 | 2.73e-01 | 
| Assembly of collagen fibrils and other multimeric structures | 19 | 1.93e-01 | -0.172000 | 3.51e-01 | 
| Metabolism of non-coding RNA | 50 | 3.56e-02 | -0.172000 | 9.44e-02 | 
| snRNP Assembly | 50 | 3.56e-02 | -0.172000 | 9.44e-02 | 
| Base Excision Repair | 38 | 6.84e-02 | -0.171000 | 1.60e-01 | 
| Translesion synthesis by POLI | 16 | 2.37e-01 | -0.171000 | 4.07e-01 | 
| Amino acids regulate mTORC1 | 44 | 5.07e-02 | -0.170000 | 1.25e-01 | 
| TRAF3-dependent IRF activation pathway | 13 | 2.88e-01 | 0.170000 | 4.61e-01 | 
| RHOF GTPase cycle | 29 | 1.13e-01 | 0.170000 | 2.37e-01 | 
| Base-Excision Repair, AP Site Formation | 15 | 2.57e-01 | -0.169000 | 4.27e-01 | 
| MTOR signalling | 39 | 6.96e-02 | -0.168000 | 1.62e-01 | 
| PKA-mediated phosphorylation of CREB | 14 | 2.78e-01 | 0.168000 | 4.51e-01 | 
| Cytochrome c-mediated apoptotic response | 12 | 3.16e-01 | 0.167000 | 4.86e-01 | 
| Scavenging by Class A Receptors | 10 | 3.61e-01 | -0.167000 | 5.30e-01 | 
| B-WICH complex positively regulates rRNA expression | 24 | 1.59e-01 | -0.166000 | 3.02e-01 | 
| MAPK targets/ Nuclear events mediated by MAP kinases | 28 | 1.29e-01 | 0.166000 | 2.62e-01 | 
| InlB-mediated entry of Listeria monocytogenes into host cell | 12 | 3.22e-01 | -0.165000 | 4.91e-01 | 
| Synthesis of bile acids and bile salts via 7alpha-hydroxycholesterol | 11 | 3.44e-01 | -0.165000 | 5.13e-01 | 
| Gastrin-CREB signalling pathway via PKC and MAPK | 14 | 2.87e-01 | 0.164000 | 4.60e-01 | 
| Protein ubiquitination | 60 | 2.87e-02 | -0.164000 | 7.89e-02 | 
| HDACs deacetylate histones | 32 | 1.10e-01 | 0.163000 | 2.33e-01 | 
| RHOU GTPase cycle | 34 | 1.00e-01 | 0.163000 | 2.16e-01 | 
| Endogenous sterols | 13 | 3.11e-01 | -0.162000 | 4.83e-01 | 
| Activation of GABAB receptors | 17 | 2.47e-01 | -0.162000 | 4.18e-01 | 
| GABA B receptor activation | 17 | 2.47e-01 | -0.162000 | 4.18e-01 | 
| Nuclear events stimulated by ALK signaling in cancer | 19 | 2.22e-01 | -0.162000 | 3.87e-01 | 
| Golgi-to-ER retrograde transport | 97 | 6.07e-03 | -0.162000 | 2.23e-02 | 
| Peroxisomal protein import | 54 | 4.03e-02 | -0.161000 | 1.05e-01 | 
| Synthesis of PC | 19 | 2.23e-01 | 0.161000 | 3.90e-01 | 
| Formation of RNA Pol II elongation complex | 56 | 3.77e-02 | -0.161000 | 9.86e-02 | 
| RNA Polymerase II Transcription Elongation | 56 | 3.77e-02 | -0.161000 | 9.86e-02 | 
| RHO GTPase cycle | 328 | 7.30e-07 | 0.160000 | 5.42e-06 | 
| Uptake and actions of bacterial toxins | 17 | 2.53e-01 | -0.160000 | 4.24e-01 | 
| Retrograde transport at the Trans-Golgi-Network | 48 | 5.57e-02 | 0.160000 | 1.35e-01 | 
| TRAF6 mediated IRF7 activation | 15 | 2.85e-01 | 0.159000 | 4.58e-01 | 
| Viral Messenger RNA Synthesis | 43 | 7.25e-02 | -0.158000 | 1.68e-01 | 
| Transcriptional regulation of granulopoiesis | 21 | 2.10e-01 | 0.158000 | 3.76e-01 | 
| Synthesis of glycosylphosphatidylinositol (GPI) | 15 | 2.91e-01 | -0.158000 | 4.62e-01 | 
| ERK/MAPK targets | 20 | 2.24e-01 | 0.157000 | 3.90e-01 | 
| Complement cascade | 19 | 2.36e-01 | -0.157000 | 4.05e-01 | 
| Extension of Telomeres | 38 | 9.70e-02 | -0.156000 | 2.11e-01 | 
| Signal transduction by L1 | 16 | 2.81e-01 | -0.156000 | 4.55e-01 | 
| Protein methylation | 14 | 3.14e-01 | -0.155000 | 4.86e-01 | 
| PI5P, PP2A and IER3 Regulate PI3K/AKT Signaling | 50 | 5.78e-02 | 0.155000 | 1.39e-01 | 
| Growth hormone receptor signaling | 15 | 2.98e-01 | 0.155000 | 4.70e-01 | 
| Membrane binding and targetting of GAG proteins | 14 | 3.16e-01 | -0.155000 | 4.86e-01 | 
| Synthesis And Processing Of GAG, GAGPOL Polyproteins | 14 | 3.16e-01 | -0.155000 | 4.86e-01 | 
| Synthesis of active ubiquitin: roles of E1 and E2 enzymes | 29 | 1.50e-01 | -0.155000 | 2.88e-01 | 
| Unfolded Protein Response (UPR) | 79 | 1.81e-02 | -0.154000 | 5.49e-02 | 
| Regulation of TLR by endogenous ligand | 13 | 3.38e-01 | -0.153000 | 5.06e-01 | 
| Senescence-Associated Secretory Phenotype (SASP) | 44 | 7.89e-02 | -0.153000 | 1.80e-01 | 
| Regulated proteolysis of p75NTR | 10 | 4.04e-01 | -0.153000 | 5.70e-01 | 
| Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs) | 45 | 7.71e-02 | -0.152000 | 1.77e-01 | 
| Translocation of SLC2A4 (GLUT4) to the plasma membrane | 58 | 4.50e-02 | -0.152000 | 1.14e-01 | 
| Initiation of Nuclear Envelope (NE) Reformation | 17 | 2.82e-01 | -0.151000 | 4.55e-01 | 
| Integrin cell surface interactions | 35 | 1.28e-01 | -0.149000 | 2.60e-01 | 
| Synthesis of PA | 24 | 2.07e-01 | 0.149000 | 3.71e-01 | 
| G beta:gamma signalling through CDC42 | 13 | 3.53e-01 | -0.149000 | 5.21e-01 | 
| SUMOylation | 150 | 1.76e-03 | 0.148000 | 8.07e-03 | 
| IKK complex recruitment mediated by RIP1 | 23 | 2.18e-01 | -0.148000 | 3.84e-01 | 
| Negative regulation of FGFR2 signaling | 17 | 2.90e-01 | -0.148000 | 4.62e-01 | 
| Negative regulation of FGFR3 signaling | 17 | 2.90e-01 | -0.148000 | 4.62e-01 | 
| Negative regulation of FGFR4 signaling | 17 | 2.90e-01 | -0.148000 | 4.62e-01 | 
| TCF dependent signaling in response to WNT | 117 | 5.82e-03 | -0.148000 | 2.16e-02 | 
| Conversion from APC/C:Cdc20 to APC/C:Cdh1 in late anaphase | 17 | 2.92e-01 | -0.148000 | 4.63e-01 | 
| SUMOylation of transcription cofactors | 40 | 1.07e-01 | 0.148000 | 2.27e-01 | 
| Interleukin-7 signaling | 11 | 3.98e-01 | 0.147000 | 5.65e-01 | 
| Defective pyroptosis | 13 | 3.60e-01 | 0.147000 | 5.28e-01 | 
| Assembly and cell surface presentation of NMDA receptors | 21 | 2.45e-01 | -0.147000 | 4.16e-01 | 
| Carboxyterminal post-translational modifications of tubulin | 22 | 2.34e-01 | -0.147000 | 4.03e-01 | 
| Constitutive Signaling by Overexpressed ERBB2 | 10 | 4.23e-01 | -0.146000 | 5.88e-01 | 
| Sensory processing of sound | 30 | 1.66e-01 | -0.146000 | 3.14e-01 | 
| SARS-CoV-2 Infection | 246 | 8.90e-05 | -0.146000 | 5.01e-04 | 
| Transport to the Golgi and subsequent modification | 146 | 2.47e-03 | -0.146000 | 1.07e-02 | 
| FOXO-mediated transcription | 45 | 9.24e-02 | 0.145000 | 2.03e-01 | 
| DARPP-32 events | 21 | 2.50e-01 | 0.145000 | 4.20e-01 | 
| Interleukin-10 signaling | 24 | 2.20e-01 | -0.145000 | 3.85e-01 | 
| Signaling by Hippo | 15 | 3.32e-01 | 0.145000 | 5.00e-01 | 
| SUMO E3 ligases SUMOylate target proteins | 144 | 2.90e-03 | 0.144000 | 1.22e-02 | 
| RNA Polymerase II Pre-transcription Events | 74 | 3.27e-02 | -0.144000 | 8.81e-02 | 
| COPII-mediated vesicle transport | 58 | 5.85e-02 | -0.144000 | 1.40e-01 | 
| Formation of Fibrin Clot (Clotting Cascade) | 10 | 4.34e-01 | -0.143000 | 6.00e-01 | 
| Potassium Channels | 21 | 2.57e-01 | -0.143000 | 4.27e-01 | 
| Signaling by NTRK3 (TRKC) | 12 | 3.92e-01 | -0.143000 | 5.60e-01 | 
| RNA Polymerase III Transcription Initiation | 34 | 1.53e-01 | -0.142000 | 2.92e-01 | 
| Signaling by high-kinase activity BRAF mutants | 29 | 1.87e-01 | -0.142000 | 3.42e-01 | 
| Signaling by KIT in disease | 16 | 3.27e-01 | 0.142000 | 4.96e-01 | 
| Signaling by phosphorylated juxtamembrane, extracellular and kinase domain KIT mutants | 16 | 3.27e-01 | 0.142000 | 4.96e-01 | 
| Antigen activates B Cell Receptor (BCR) leading to generation of second messengers | 25 | 2.21e-01 | 0.141000 | 3.87e-01 | 
| Drug ADME | 40 | 1.22e-01 | -0.141000 | 2.51e-01 | 
| p38MAPK events | 11 | 4.17e-01 | -0.141000 | 5.85e-01 | 
| Signaling by Interleukins | 307 | 2.35e-05 | -0.141000 | 1.49e-04 | 
| Ub-specific processing proteases | 140 | 4.20e-03 | -0.141000 | 1.65e-02 | 
| Downregulation of TGF-beta receptor signaling | 24 | 2.34e-01 | -0.140000 | 4.03e-01 | 
| Diseases of glycosylation | 66 | 4.88e-02 | -0.140000 | 1.21e-01 | 
| Developmental Biology | 592 | 9.97e-09 | -0.140000 | 8.48e-08 | 
| Cobalamin (Cbl, vitamin B12) transport and metabolism | 11 | 4.23e-01 | -0.140000 | 5.88e-01 | 
| Endosomal/Vacuolar pathway | 10 | 4.45e-01 | -0.140000 | 6.03e-01 | 
| tRNA modification in the nucleus and cytosol | 36 | 1.48e-01 | -0.139000 | 2.87e-01 | 
| activated TAK1 mediates p38 MAPK activation | 21 | 2.70e-01 | -0.139000 | 4.44e-01 | 
| Apoptotic cleavage of cellular proteins | 27 | 2.12e-01 | 0.139000 | 3.77e-01 | 
| ER Quality Control Compartment (ERQC) | 20 | 2.82e-01 | -0.139000 | 4.55e-01 | 
| Formation of WDR5-containing histone-modifying complexes | 40 | 1.29e-01 | 0.139000 | 2.62e-01 | 
| Beta-oxidation of very long chain fatty acids | 10 | 4.49e-01 | -0.138000 | 6.07e-01 | 
| Netrin-1 signaling | 21 | 2.73e-01 | 0.138000 | 4.46e-01 | 
| tRNA processing in the nucleus | 55 | 7.75e-02 | -0.138000 | 1.78e-01 | 
| Signaling by NTRK2 (TRKB) | 18 | 3.12e-01 | 0.138000 | 4.84e-01 | 
| Paradoxical activation of RAF signaling by kinase inactive BRAF | 37 | 1.48e-01 | -0.137000 | 2.87e-01 | 
| Signaling by RAS mutants | 37 | 1.48e-01 | -0.137000 | 2.87e-01 | 
| Signaling by moderate kinase activity BRAF mutants | 37 | 1.48e-01 | -0.137000 | 2.87e-01 | 
| Signaling downstream of RAS mutants | 37 | 1.48e-01 | -0.137000 | 2.87e-01 | 
| Signaling by NOTCH | 148 | 4.36e-03 | -0.136000 | 1.71e-02 | 
| RIPK1-mediated regulated necrosis | 29 | 2.05e-01 | -0.136000 | 3.69e-01 | 
| Regulation of necroptotic cell death | 29 | 2.05e-01 | -0.136000 | 3.69e-01 | 
| Estrogen-dependent nuclear events downstream of ESR-membrane signaling | 17 | 3.32e-01 | 0.136000 | 5.00e-01 | 
| Diseases associated with the TLR signaling cascade | 26 | 2.32e-01 | -0.136000 | 4.01e-01 | 
| Diseases of Immune System | 26 | 2.32e-01 | -0.136000 | 4.01e-01 | 
| CREB1 phosphorylation through NMDA receptor-mediated activation of RAS signaling | 18 | 3.22e-01 | 0.135000 | 4.91e-01 | 
| PLC beta mediated events | 34 | 1.74e-01 | 0.135000 | 3.23e-01 | 
| Acyl chain remodelling of PE | 10 | 4.61e-01 | 0.135000 | 6.18e-01 | 
| EGFR downregulation | 20 | 2.98e-01 | -0.134000 | 4.70e-01 | 
| Mitochondrial biogenesis | 82 | 3.59e-02 | -0.134000 | 9.51e-02 | 
| Inflammasomes | 19 | 3.12e-01 | -0.134000 | 4.84e-01 | 
| PERK regulates gene expression | 28 | 2.21e-01 | -0.134000 | 3.87e-01 | 
| EPHB-mediated forward signaling | 33 | 1.85e-01 | -0.133000 | 3.40e-01 | 
| GPER1 signaling | 29 | 2.16e-01 | -0.133000 | 3.81e-01 | 
| Regulation of Complement cascade | 17 | 3.47e-01 | -0.132000 | 5.16e-01 | 
| PKA activation in glucagon signalling | 11 | 4.49e-01 | 0.132000 | 6.07e-01 | 
| Biosynthesis of the N-glycan precursor (dolichol lipid-linked oligosaccharide, LLO) and transfer to a nascent protein | 64 | 6.91e-02 | -0.132000 | 1.61e-01 | 
| Removal of the Flap Intermediate | 12 | 4.32e-01 | -0.131000 | 5.98e-01 | 
| Platelet activation, signaling and aggregation | 167 | 3.59e-03 | -0.131000 | 1.45e-02 | 
| M Phase | 291 | 1.33e-04 | -0.131000 | 7.34e-04 | 
| Processing of SMDT1 | 14 | 3.98e-01 | -0.131000 | 5.65e-01 | 
| DCC mediated attractive signaling | 10 | 4.75e-01 | 0.131000 | 6.28e-01 | 
| HIV Life Cycle | 144 | 7.05e-03 | -0.130000 | 2.50e-02 | 
| Transcriptional Regulation by E2F6 | 30 | 2.17e-01 | 0.130000 | 3.82e-01 | 
| SARS-CoV Infections | 345 | 3.69e-05 | -0.130000 | 2.24e-04 | 
| Phase I - Functionalization of compounds | 39 | 1.61e-01 | -0.130000 | 3.04e-01 | 
| IRAK2 mediated activation of TAK1 complex | 10 | 4.77e-01 | -0.130000 | 6.30e-01 | 
| MAPK family signaling cascades | 201 | 1.60e-03 | -0.130000 | 7.45e-03 | 
| RAB GEFs exchange GTP for GDP on RABs | 81 | 4.40e-02 | 0.130000 | 1.12e-01 | 
| SUMOylation of intracellular receptors | 22 | 2.93e-01 | 0.130000 | 4.63e-01 | 
| Signaling by CSF1 (M-CSF) in myeloid cells | 28 | 2.41e-01 | 0.128000 | 4.12e-01 | 
| Processing and activation of SUMO | 10 | 4.84e-01 | -0.128000 | 6.35e-01 | 
| NoRC negatively regulates rRNA expression | 39 | 1.68e-01 | -0.128000 | 3.16e-01 | 
| GAB1 signalosome | 10 | 4.85e-01 | 0.127000 | 6.36e-01 | 
| Positive epigenetic regulation of rRNA expression | 39 | 1.75e-01 | -0.126000 | 3.24e-01 | 
| TP53 regulates transcription of additional cell cycle genes whose exact role in the p53 pathway remain uncertain | 17 | 3.72e-01 | 0.125000 | 5.39e-01 | 
| ERKs are inactivated | 12 | 4.54e-01 | -0.125000 | 6.10e-01 | 
| Syndecan interactions | 15 | 4.02e-01 | -0.125000 | 5.69e-01 | 
| Negative epigenetic regulation of rRNA expression | 41 | 1.69e-01 | -0.124000 | 3.16e-01 | 
| G0 and Early G1 | 14 | 4.21e-01 | 0.124000 | 5.87e-01 | 
| TP53 regulates transcription of several additional cell death genes whose specific roles in p53-dependent apoptosis remain uncertain | 11 | 4.75e-01 | 0.124000 | 6.28e-01 | 
| Late Phase of HIV Life Cycle | 132 | 1.43e-02 | -0.124000 | 4.56e-02 | 
| Signaling by NOTCH1 | 58 | 1.03e-01 | 0.124000 | 2.22e-01 | 
| GABA receptor activation | 19 | 3.51e-01 | -0.124000 | 5.19e-01 | 
| TICAM1,TRAF6-dependent induction of TAK1 complex | 10 | 4.99e-01 | -0.123000 | 6.44e-01 | 
| Nicotinate metabolism | 22 | 3.18e-01 | 0.123000 | 4.87e-01 | 
| Disease | 1215 | 2.38e-12 | -0.123000 | 2.48e-11 | 
| Cellular Senescence | 106 | 2.97e-02 | 0.122000 | 8.11e-02 | 
| Cell surface interactions at the vascular wall | 74 | 6.93e-02 | -0.122000 | 1.61e-01 | 
| Association of TriC/CCT with target proteins during biosynthesis | 31 | 2.40e-01 | -0.122000 | 4.11e-01 | 
| RUNX2 regulates bone development | 16 | 4.03e-01 | 0.121000 | 5.69e-01 | 
| Mitochondrial tRNA aminoacylation | 15 | 4.18e-01 | -0.121000 | 5.86e-01 | 
| SEMA3A-Plexin repulsion signaling by inhibiting Integrin adhesion | 11 | 4.88e-01 | -0.121000 | 6.36e-01 | 
| Processive synthesis on the lagging strand | 13 | 4.52e-01 | -0.121000 | 6.09e-01 | 
| RHO GTPases Activate ROCKs | 17 | 3.91e-01 | -0.120000 | 5.59e-01 | 
| Sensory processing of sound by inner hair cells of the cochlea | 28 | 2.72e-01 | -0.120000 | 4.45e-01 | 
| Transcriptional activation of mitochondrial biogenesis | 47 | 1.56e-01 | 0.120000 | 2.97e-01 | 
| Removal of the Flap Intermediate from the C-strand | 14 | 4.40e-01 | -0.119000 | 6.03e-01 | 
| Meiosis | 34 | 2.30e-01 | 0.119000 | 4.00e-01 | 
| Interleukin-3, Interleukin-5 and GM-CSF signaling | 37 | 2.12e-01 | 0.119000 | 3.77e-01 | 
| FLT3 Signaling | 32 | 2.46e-01 | 0.119000 | 4.18e-01 | 
| RNA Polymerase III Abortive And Retractive Initiation | 37 | 2.14e-01 | -0.118000 | 3.79e-01 | 
| RNA Polymerase III Transcription | 37 | 2.14e-01 | -0.118000 | 3.79e-01 | 
| Regulation of signaling by CBL | 20 | 3.61e-01 | 0.118000 | 5.29e-01 | 
| Immune System | 1374 | 1.28e-12 | -0.118000 | 1.36e-11 | 
| Other interleukin signaling | 16 | 4.17e-01 | -0.117000 | 5.85e-01 | 
| JNK (c-Jun kinases) phosphorylation and activation mediated by activated human TAK1 | 20 | 3.66e-01 | -0.117000 | 5.35e-01 | 
| Meiotic synapsis | 19 | 3.80e-01 | 0.117000 | 5.46e-01 | 
| RNA Polymerase I Transcription Initiation | 39 | 2.10e-01 | -0.116000 | 3.76e-01 | 
| Sialic acid metabolism | 23 | 3.36e-01 | 0.116000 | 5.05e-01 | 
| Amino acid transport across the plasma membrane | 18 | 3.95e-01 | 0.116000 | 5.63e-01 | 
| EPHA-mediated growth cone collapse | 11 | 5.06e-01 | -0.116000 | 6.50e-01 | 
| Clathrin-mediated endocytosis | 106 | 4.05e-02 | -0.115000 | 1.05e-01 | 
| DAG and IP3 signaling | 28 | 2.91e-01 | 0.115000 | 4.62e-01 | 
| Cleavage of the damaged pyrimidine | 13 | 4.72e-01 | -0.115000 | 6.28e-01 | 
| Depyrimidination | 13 | 4.72e-01 | -0.115000 | 6.28e-01 | 
| Recognition and association of DNA glycosylase with site containing an affected pyrimidine | 13 | 4.72e-01 | -0.115000 | 6.28e-01 | 
| TP53 Regulates Transcription of DNA Repair Genes | 60 | 1.23e-01 | -0.115000 | 2.53e-01 | 
| HCMV Infection | 88 | 6.24e-02 | -0.115000 | 1.47e-01 | 
| Transcriptional regulation by small RNAs | 47 | 1.73e-01 | -0.115000 | 3.21e-01 | 
| E2F mediated regulation of DNA replication | 18 | 4.00e-01 | 0.115000 | 5.66e-01 | 
| NFE2L2 regulating anti-oxidant/detoxification enzymes | 16 | 4.30e-01 | -0.114000 | 5.96e-01 | 
| RIP-mediated NFkB activation via ZBP1 | 15 | 4.45e-01 | -0.114000 | 6.03e-01 | 
| Cytokine Signaling in Immune system | 533 | 9.14e-06 | -0.114000 | 6.06e-05 | 
| p75 NTR receptor-mediated signalling | 73 | 9.36e-02 | 0.114000 | 2.05e-01 | 
| Chondroitin sulfate/dermatan sulfate metabolism | 28 | 3.00e-01 | 0.113000 | 4.70e-01 | 
| STAT3 nuclear events downstream of ALK signaling | 10 | 5.36e-01 | 0.113000 | 6.77e-01 | 
| Reproduction | 45 | 1.91e-01 | 0.113000 | 3.49e-01 | 
| Negative regulation of FGFR1 signaling | 19 | 3.96e-01 | -0.113000 | 5.64e-01 | 
| Class A/1 (Rhodopsin-like receptors) | 55 | 1.52e-01 | -0.112000 | 2.90e-01 | 
| Signaling by SCF-KIT | 33 | 2.67e-01 | 0.112000 | 4.39e-01 | 
| RHOBTB2 GTPase cycle | 23 | 3.54e-01 | -0.112000 | 5.21e-01 | 
| TGF-beta receptor signaling activates SMADs | 35 | 2.54e-01 | -0.112000 | 4.24e-01 | 
| Deubiquitination | 205 | 6.11e-03 | -0.112000 | 2.23e-02 | 
| Fanconi Anemia Pathway | 27 | 3.17e-01 | -0.111000 | 4.86e-01 | 
| Presynaptic phase of homologous DNA pairing and strand exchange | 32 | 2.79e-01 | 0.111000 | 4.52e-01 | 
| RAC3 GTPase cycle | 69 | 1.13e-01 | 0.111000 | 2.37e-01 | 
| Antiviral mechanism by IFN-stimulated genes | 129 | 3.08e-02 | -0.110000 | 8.37e-02 | 
| Disorders of Developmental Biology | 11 | 5.27e-01 | 0.110000 | 6.68e-01 | 
| Disorders of Nervous System Development | 11 | 5.27e-01 | 0.110000 | 6.68e-01 | 
| Loss of function of MECP2 in Rett syndrome | 11 | 5.27e-01 | 0.110000 | 6.68e-01 | 
| Pervasive developmental disorders | 11 | 5.27e-01 | 0.110000 | 6.68e-01 | 
| DNA strand elongation | 20 | 3.96e-01 | -0.110000 | 5.64e-01 | 
| Semaphorin interactions | 46 | 1.99e-01 | -0.110000 | 3.59e-01 | 
| RNA Polymerase I Promoter Clearance | 43 | 2.14e-01 | -0.110000 | 3.79e-01 | 
| RNA Polymerase I Transcription | 43 | 2.14e-01 | -0.110000 | 3.79e-01 | 
| Keratan sulfate biosynthesis | 14 | 4.78e-01 | 0.110000 | 6.30e-01 | 
| Bacterial Infection Pathways | 53 | 1.69e-01 | -0.109000 | 3.16e-01 | 
| CD209 (DC-SIGN) signaling | 17 | 4.36e-01 | 0.109000 | 6.01e-01 | 
| N-glycan antennae elongation in the medial/trans-Golgi | 16 | 4.52e-01 | 0.109000 | 6.09e-01 | 
| Oncogene Induced Senescence | 26 | 3.38e-01 | 0.109000 | 5.06e-01 | 
| ATF6 (ATF6-alpha) activates chaperones | 12 | 5.15e-01 | -0.109000 | 6.58e-01 | 
| Signaling by Retinoic Acid | 25 | 3.48e-01 | -0.109000 | 5.16e-01 | 
| Glycolysis | 59 | 1.50e-01 | -0.108000 | 2.88e-01 | 
| Phosphorylation of CD3 and TCR zeta chains | 14 | 4.85e-01 | -0.108000 | 6.36e-01 | 
| Glycerophospholipid biosynthesis | 80 | 9.76e-02 | 0.107000 | 2.12e-01 | 
| O-linked glycosylation | 36 | 2.67e-01 | 0.107000 | 4.39e-01 | 
| Meiotic recombination | 17 | 4.47e-01 | 0.107000 | 6.05e-01 | 
| Peptide ligand-binding receptors | 32 | 2.97e-01 | -0.107000 | 4.69e-01 | 
| SUMOylation of DNA damage response and repair proteins | 73 | 1.16e-01 | 0.106000 | 2.41e-01 | 
| Signaling by ERBB4 | 33 | 2.90e-01 | -0.106000 | 4.62e-01 | 
| Sensory processing of sound by outer hair cells of the cochlea | 23 | 3.77e-01 | -0.106000 | 5.44e-01 | 
| Role of phospholipids in phagocytosis | 18 | 4.35e-01 | 0.106000 | 6.01e-01 | 
| Transport of small molecules | 395 | 3.41e-04 | -0.106000 | 1.78e-03 | 
| Regulation of pyruvate dehydrogenase (PDH) complex | 14 | 4.93e-01 | -0.106000 | 6.40e-01 | 
| Formation of apoptosome | 10 | 5.64e-01 | 0.106000 | 7.00e-01 | 
| Regulation of the apoptosome activity | 10 | 5.64e-01 | 0.106000 | 7.00e-01 | 
| AKT phosphorylates targets in the cytosol | 14 | 4.95e-01 | 0.105000 | 6.41e-01 | 
| Nuclear signaling by ERBB4 | 18 | 4.39e-01 | -0.105000 | 6.03e-01 | 
| Signalling to RAS | 14 | 4.95e-01 | -0.105000 | 6.41e-01 | 
| RAF-independent MAPK1/3 activation | 18 | 4.40e-01 | 0.105000 | 6.03e-01 | 
| trans-Golgi Network Vesicle Budding | 67 | 1.38e-01 | -0.105000 | 2.75e-01 | 
| RHOH GTPase cycle | 28 | 3.37e-01 | 0.105000 | 5.06e-01 | 
| RHOD GTPase cycle | 39 | 2.59e-01 | 0.104000 | 4.28e-01 | 
| Laminin interactions | 10 | 5.68e-01 | 0.104000 | 7.02e-01 | 
| Budding and maturation of HIV virion | 31 | 3.16e-01 | -0.104000 | 4.86e-01 | 
| Factors involved in megakaryocyte development and platelet production | 91 | 8.75e-02 | 0.104000 | 1.95e-01 | 
| RHO GTPases Activate Formins | 96 | 8.03e-02 | -0.104000 | 1.82e-01 | 
| Polymerase switching on the C-strand of the telomere | 21 | 4.12e-01 | -0.103000 | 5.81e-01 | 
| Tristetraprolin (TTP, ZFP36) binds and destabilizes mRNA | 16 | 4.74e-01 | -0.103000 | 6.28e-01 | 
| Energy dependent regulation of mTOR by LKB1-AMPK | 27 | 3.53e-01 | -0.103000 | 5.21e-01 | 
| Death Receptor Signaling | 123 | 4.97e-02 | 0.103000 | 1.23e-01 | 
| Transcription of E2F targets under negative control by DREAM complex | 12 | 5.40e-01 | 0.102000 | 6.79e-01 | 
| Glycogen metabolism | 19 | 4.43e-01 | -0.102000 | 6.03e-01 | 
| Regulation of NF-kappa B signaling | 18 | 4.56e-01 | -0.101000 | 6.13e-01 | 
| Regulation of KIT signaling | 12 | 5.44e-01 | 0.101000 | 6.83e-01 | 
| Intraflagellar transport | 38 | 2.82e-01 | -0.101000 | 4.55e-01 | 
| Regulation of actin dynamics for phagocytic cup formation | 56 | 1.92e-01 | -0.101000 | 3.50e-01 | 
| G-protein mediated events | 36 | 2.96e-01 | 0.101000 | 4.67e-01 | 
| Adaptive Immune System | 566 | 5.30e-05 | -0.101000 | 3.13e-04 | 
| CRMPs in Sema3A signaling | 11 | 5.65e-01 | -0.100000 | 7.00e-01 | 
| Activation of BH3-only proteins | 27 | 3.68e-01 | -0.100000 | 5.36e-01 | 
| Processive synthesis on the C-strand of the telomere | 16 | 4.89e-01 | -0.099900 | 6.37e-01 | 
| Metabolism of carbohydrates | 194 | 1.73e-02 | -0.099600 | 5.32e-02 | 
| Activation of gene expression by SREBF (SREBP) | 41 | 2.71e-01 | -0.099500 | 4.44e-01 | 
| Zinc transporters | 10 | 5.88e-01 | -0.098900 | 7.23e-01 | 
| GRB2:SOS provides linkage to MAPK signaling for Integrins | 11 | 5.71e-01 | 0.098700 | 7.03e-01 | 
| Signaling by RAF1 mutants | 33 | 3.29e-01 | -0.098300 | 4.97e-01 | 
| Synthesis of substrates in N-glycan biosythesis | 50 | 2.33e-01 | -0.097600 | 4.02e-01 | 
| Adrenaline,noradrenaline inhibits insulin secretion | 12 | 5.61e-01 | -0.097000 | 6.99e-01 | 
| Constitutive Signaling by NOTCH1 HD+PEST Domain Mutants | 47 | 2.50e-01 | 0.097000 | 4.20e-01 | 
| Constitutive Signaling by NOTCH1 PEST Domain Mutants | 47 | 2.50e-01 | 0.097000 | 4.20e-01 | 
| Signaling by NOTCH1 HD+PEST Domain Mutants in Cancer | 47 | 2.50e-01 | 0.097000 | 4.20e-01 | 
| Signaling by NOTCH1 PEST Domain Mutants in Cancer | 47 | 2.50e-01 | 0.097000 | 4.20e-01 | 
| Signaling by NOTCH1 in Cancer | 47 | 2.50e-01 | 0.097000 | 4.20e-01 | 
| Extracellular matrix organization | 106 | 8.79e-02 | -0.096200 | 1.95e-01 | 
| Cargo trafficking to the periciliary membrane | 39 | 2.99e-01 | 0.096100 | 4.70e-01 | 
| RHO GTPase Effectors | 193 | 2.20e-02 | -0.096000 | 6.42e-02 | 
| Class B/2 (Secretin family receptors) | 20 | 4.59e-01 | 0.095800 | 6.15e-01 | 
| Golgi Cisternae Pericentriolar Stack Reorganization | 12 | 5.66e-01 | -0.095700 | 7.01e-01 | 
| VEGFA-VEGFR2 Pathway | 81 | 1.39e-01 | 0.095200 | 2.77e-01 | 
| Antigen Presentation: Folding, assembly and peptide loading of class I MHC | 28 | 3.84e-01 | -0.095100 | 5.51e-01 | 
| Inwardly rectifying K+ channels | 12 | 5.69e-01 | -0.095000 | 7.02e-01 | 
| Nonhomologous End-Joining (NHEJ) | 30 | 3.70e-01 | 0.094600 | 5.38e-01 | 
| Platelet sensitization by LDL | 14 | 5.40e-01 | 0.094600 | 6.79e-01 | 
| Uptake and function of anthrax toxins | 10 | 6.06e-01 | 0.094200 | 7.38e-01 | 
| Activation of the pre-replicative complex | 19 | 4.79e-01 | -0.093900 | 6.31e-01 | 
| Cardiac conduction | 42 | 2.93e-01 | 0.093900 | 4.63e-01 | 
| Interferon Signaling | 209 | 2.00e-02 | -0.093800 | 5.96e-02 | 
| O-linked glycosylation of mucins | 26 | 4.08e-01 | 0.093800 | 5.75e-01 | 
| Cell Cycle | 474 | 5.56e-04 | -0.093600 | 2.80e-03 | 
| IRAK2 mediated activation of TAK1 complex upon TLR7/8 or 9 stimulation | 15 | 5.32e-01 | -0.093200 | 6.72e-01 | 
| Downregulation of SMAD2/3:SMAD4 transcriptional activity | 29 | 3.85e-01 | 0.093200 | 5.52e-01 | 
| HS-GAG degradation | 14 | 5.46e-01 | -0.093200 | 6.85e-01 | 
| Signaling by WNT | 179 | 3.33e-02 | -0.092600 | 8.94e-02 | 
| Interferon alpha/beta signaling | 56 | 2.32e-01 | -0.092500 | 4.01e-01 | 
| Cell Cycle, Mitotic | 386 | 2.19e-03 | -0.091600 | 9.55e-03 | 
| ATF4 activates genes in response to endoplasmic reticulum stress | 23 | 4.48e-01 | -0.091500 | 6.06e-01 | 
| Homologous DNA Pairing and Strand Exchange | 34 | 3.56e-01 | 0.091500 | 5.24e-01 | 
| TAK1-dependent IKK and NF-kappa-B activation | 39 | 3.25e-01 | -0.091100 | 4.95e-01 | 
| Synthesis of bile acids and bile salts | 17 | 5.16e-01 | 0.091000 | 6.59e-01 | 
| Regulation of IFNA/IFNB signaling | 12 | 5.85e-01 | 0.091000 | 7.20e-01 | 
| Anchoring of the basal body to the plasma membrane | 82 | 1.58e-01 | 0.090400 | 3.00e-01 | 
| Cellular response to heat stress | 84 | 1.55e-01 | -0.089900 | 2.96e-01 | 
| Metabolism of vitamins and cofactors | 124 | 8.65e-02 | -0.089400 | 1.93e-01 | 
| Diseases of programmed cell death | 40 | 3.29e-01 | -0.089300 | 4.97e-01 | 
| Glycogen breakdown (glycogenolysis) | 11 | 6.09e-01 | 0.089100 | 7.41e-01 | 
| Transport of bile salts and organic acids, metal ions and amine compounds | 34 | 3.70e-01 | 0.089000 | 5.38e-01 | 
| Signaling by ERBB2 | 35 | 3.63e-01 | -0.089000 | 5.31e-01 | 
| Butyrate Response Factor 1 (BRF1) binds and destabilizes mRNA | 16 | 5.40e-01 | -0.088400 | 6.79e-01 | 
| Signaling by ALK | 20 | 4.95e-01 | 0.088200 | 6.41e-01 | 
| Regulation of HSF1-mediated heat shock response | 69 | 2.07e-01 | -0.088000 | 3.71e-01 | 
| Interleukin-4 and Interleukin-13 signaling | 60 | 2.42e-01 | -0.087500 | 4.12e-01 | 
| Transcriptional Regulation by TP53 | 317 | 8.61e-03 | -0.086400 | 2.96e-02 | 
| RUNX3 regulates p14-ARF | 10 | 6.36e-01 | 0.086400 | 7.61e-01 | 
| GPCR downstream signalling | 211 | 3.29e-02 | 0.085600 | 8.85e-02 | 
| Vitamin B5 (pantothenate) metabolism | 13 | 5.94e-01 | -0.085500 | 7.27e-01 | 
| Interferon gamma signaling | 72 | 2.11e-01 | -0.085400 | 3.76e-01 | 
| Signaling by Insulin receptor | 48 | 3.07e-01 | -0.085400 | 4.78e-01 | 
| Signaling by GPCR | 226 | 2.79e-02 | 0.085300 | 7.69e-02 | 
| GPVI-mediated activation cascade | 27 | 4.44e-01 | 0.085200 | 6.03e-01 | 
| MET promotes cell motility | 18 | 5.32e-01 | 0.085100 | 6.72e-01 | 
| Regulation of lipid metabolism by PPARalpha | 98 | 1.47e-01 | 0.085000 | 2.87e-01 | 
| Regulation of insulin secretion | 37 | 3.78e-01 | 0.083900 | 5.44e-01 | 
| Signaling by Non-Receptor Tyrosine Kinases | 38 | 3.73e-01 | -0.083600 | 5.39e-01 | 
| Signaling by PTK6 | 38 | 3.73e-01 | -0.083600 | 5.39e-01 | 
| Cytochrome P450 - arranged by substrate type | 18 | 5.39e-01 | -0.083600 | 6.79e-01 | 
| SMAD2/SMAD3:SMAD4 heterotrimer regulates transcription | 32 | 4.15e-01 | -0.083300 | 5.83e-01 | 
| Rab regulation of trafficking | 113 | 1.27e-01 | 0.083200 | 2.60e-01 | 
| Signaling by Rho GTPases, Miro GTPases and RHOBTB3 | 480 | 2.09e-03 | 0.082900 | 9.26e-03 | 
| RUNX2 regulates osteoblast differentiation | 12 | 6.23e-01 | 0.081900 | 7.52e-01 | 
| Stimuli-sensing channels | 44 | 3.50e-01 | 0.081500 | 5.18e-01 | 
| RHOG GTPase cycle | 58 | 2.84e-01 | 0.081500 | 4.56e-01 | 
| Opioid Signalling | 61 | 2.72e-01 | 0.081400 | 4.45e-01 | 
| Glutamate binding, activation of AMPA receptors and synaptic plasticity | 17 | 5.62e-01 | 0.081200 | 6.99e-01 | 
| Trafficking of AMPA receptors | 17 | 5.62e-01 | 0.081200 | 6.99e-01 | 
| VEGFR2 mediated vascular permeability | 23 | 5.02e-01 | 0.081000 | 6.46e-01 | 
| SUMOylation of DNA methylation proteins | 13 | 6.17e-01 | 0.080100 | 7.47e-01 | 
| Signaling by Rho GTPases | 467 | 3.40e-03 | 0.080000 | 1.40e-02 | 
| Lagging Strand Synthesis | 17 | 5.68e-01 | -0.080000 | 7.02e-01 | 
| PPARA activates gene expression | 96 | 1.78e-01 | 0.079800 | 3.28e-01 | 
| HCMV Late Events | 53 | 3.16e-01 | -0.079800 | 4.86e-01 | 
| Telomere C-strand (Lagging Strand) Synthesis | 27 | 4.74e-01 | -0.079600 | 6.28e-01 | 
| Transcriptional regulation by RUNX1 | 143 | 1.02e-01 | -0.079500 | 2.19e-01 | 
| Biotin transport and metabolism | 11 | 6.52e-01 | 0.078600 | 7.76e-01 | 
| Kinesins | 28 | 4.72e-01 | -0.078600 | 6.28e-01 | 
| STING mediated induction of host immune responses | 12 | 6.38e-01 | -0.078500 | 7.62e-01 | 
| Extra-nuclear estrogen signaling | 50 | 3.38e-01 | -0.078400 | 5.06e-01 | 
| Downstream signal transduction | 25 | 5.02e-01 | 0.077700 | 6.46e-01 | 
| Regulation of TNFR1 signaling | 44 | 3.77e-01 | -0.077100 | 5.44e-01 | 
| Golgi Associated Vesicle Biogenesis | 52 | 3.40e-01 | -0.076600 | 5.08e-01 | 
| FCGR3A-mediated IL10 synthesis | 27 | 4.94e-01 | 0.076100 | 6.41e-01 | 
| Apoptotic execution phase | 34 | 4.44e-01 | 0.075900 | 6.03e-01 | 
| Negative regulation of MAPK pathway | 37 | 4.27e-01 | -0.075500 | 5.94e-01 | 
| Hemostasis | 348 | 1.68e-02 | -0.075200 | 5.20e-02 | 
| Nucleotide-binding domain, leucine rich repeat containing receptor (NLR) signaling pathways | 51 | 3.53e-01 | -0.075200 | 5.21e-01 | 
| Activation of IRF3, IRF7 mediated by TBK1, IKBKE | 17 | 5.92e-01 | -0.075100 | 7.26e-01 | 
| DNA Repair | 241 | 4.59e-02 | -0.075100 | 1.16e-01 | 
| Post-translational protein modification | 985 | 1.02e-04 | -0.074900 | 5.67e-04 | 
| Deadenylation-dependent mRNA decay | 49 | 3.66e-01 | -0.074700 | 5.35e-01 | 
| Attachment and Entry 9694614 | 11 | 6.69e-01 | -0.074600 | 7.90e-01 | 
| Protein-protein interactions at synapses | 33 | 4.62e-01 | 0.074000 | 6.18e-01 | 
| Transcription of E2F targets under negative control by p107 (RBL1) and p130 (RBL2) in complex with HDAC1 | 10 | 6.87e-01 | 0.073500 | 8.01e-01 | 
| Signaling by MET | 51 | 3.64e-01 | 0.073500 | 5.33e-01 | 
| Defective homologous recombination repair (HRR) due to BRCA2 loss of function | 33 | 4.74e-01 | 0.072100 | 6.28e-01 | 
| Diseases of DNA Double-Strand Break Repair | 33 | 4.74e-01 | 0.072100 | 6.28e-01 | 
| Integrin signaling | 22 | 5.64e-01 | -0.071100 | 7.00e-01 | 
| The phototransduction cascade | 18 | 6.02e-01 | 0.071100 | 7.34e-01 | 
| HCMV Early Events | 65 | 3.28e-01 | -0.070200 | 4.97e-01 | 
| Listeria monocytogenes entry into host cells | 17 | 6.17e-01 | -0.070200 | 7.47e-01 | 
| SUMOylation of chromatin organization proteins | 53 | 3.78e-01 | 0.070100 | 5.44e-01 | 
| Purine salvage | 12 | 6.74e-01 | -0.070100 | 7.94e-01 | 
| Caspase-mediated cleavage of cytoskeletal proteins | 10 | 7.02e-01 | -0.070000 | 8.08e-01 | 
| RAC2 GTPase cycle | 71 | 3.09e-01 | 0.070000 | 4.80e-01 | 
| Inactivation, recovery and regulation of the phototransduction cascade | 17 | 6.20e-01 | 0.069400 | 7.50e-01 | 
| ZBP1(DAI) mediated induction of type I IFNs | 18 | 6.11e-01 | -0.069300 | 7.42e-01 | 
| G beta:gamma signalling through PLC beta | 12 | 6.78e-01 | -0.069300 | 7.94e-01 | 
| Presynaptic function of Kainate receptors | 12 | 6.78e-01 | -0.069300 | 7.94e-01 | 
| Tie2 Signaling | 13 | 6.70e-01 | 0.068200 | 7.91e-01 | 
| Post NMDA receptor activation events | 47 | 4.19e-01 | -0.068200 | 5.86e-01 | 
| Nuclear Events (kinase and transcription factor activation) | 45 | 4.31e-01 | 0.068000 | 5.97e-01 | 
| Signaling by PDGF | 35 | 4.91e-01 | 0.067400 | 6.38e-01 | 
| HDR through Single Strand Annealing (SSA) | 30 | 5.25e-01 | 0.067100 | 6.68e-01 | 
| DAP12 interactions | 30 | 5.25e-01 | -0.067100 | 6.68e-01 | 
| Erythropoietin activates RAS | 13 | 6.76e-01 | 0.067000 | 7.94e-01 | 
| Bile acid and bile salt metabolism | 18 | 6.23e-01 | 0.066900 | 7.52e-01 | 
| Aberrant regulation of mitotic cell cycle due to RB1 defects | 29 | 5.37e-01 | -0.066200 | 6.78e-01 | 
| CD28 co-stimulation | 27 | 5.52e-01 | 0.066200 | 6.90e-01 | 
| Activation of HOX genes during differentiation | 45 | 4.45e-01 | -0.065900 | 6.03e-01 | 
| Activation of anterior HOX genes in hindbrain development during early embryogenesis | 45 | 4.45e-01 | -0.065900 | 6.03e-01 | 
| Alpha-protein kinase 1 signaling pathway | 11 | 7.08e-01 | -0.065300 | 8.14e-01 | 
| Degradation of the extracellular matrix | 51 | 4.21e-01 | -0.065300 | 5.87e-01 | 
| Neurexins and neuroligins | 22 | 5.97e-01 | 0.065200 | 7.30e-01 | 
| Recruitment of NuMA to mitotic centrosomes | 74 | 3.36e-01 | -0.064800 | 5.05e-01 | 
| Glucagon-type ligand receptors | 11 | 7.12e-01 | -0.064300 | 8.17e-01 | 
| Prostacyclin signalling through prostacyclin receptor | 11 | 7.12e-01 | -0.064300 | 8.17e-01 | 
| Toll Like Receptor 9 (TLR9) Cascade | 95 | 2.84e-01 | 0.063800 | 4.56e-01 | 
| Caspase activation via Death Receptors in the presence of ligand | 14 | 6.82e-01 | 0.063200 | 7.96e-01 | 
| TNFR1-induced proapoptotic signaling | 23 | 6.00e-01 | 0.063200 | 7.33e-01 | 
| Signaling by ALK fusions and activated point mutants | 50 | 4.41e-01 | 0.063000 | 6.03e-01 | 
| Signaling by ALK in cancer | 50 | 4.41e-01 | 0.063000 | 6.03e-01 | 
| NOD1/2 Signaling Pathway | 33 | 5.31e-01 | -0.063000 | 6.72e-01 | 
| NS1 Mediated Effects on Host Pathways | 39 | 4.97e-01 | 0.062900 | 6.42e-01 | 
| Signaling by BRAF and RAF1 fusions | 54 | 4.28e-01 | 0.062500 | 5.94e-01 | 
| Plasma lipoprotein remodeling | 13 | 6.97e-01 | -0.062400 | 8.06e-01 | 
| Regulation of glycolysis by fructose 2,6-bisphosphate metabolism | 10 | 7.35e-01 | 0.061900 | 8.29e-01 | 
| Vpr-mediated nuclear import of PICs | 35 | 5.27e-01 | 0.061800 | 6.68e-01 | 
| SARS-CoV-2 modulates autophagy | 11 | 7.26e-01 | 0.061100 | 8.26e-01 | 
| Cell-Cell communication | 74 | 3.68e-01 | 0.060700 | 5.36e-01 | 
| tRNA processing | 111 | 2.73e-01 | -0.060300 | 4.46e-01 | 
| Neurotransmitter release cycle | 21 | 6.33e-01 | 0.060300 | 7.59e-01 | 
| Glucagon-like Peptide-1 (GLP1) regulates insulin secretion | 22 | 6.25e-01 | 0.060300 | 7.53e-01 | 
| Class I MHC mediated antigen processing & presentation | 321 | 6.72e-02 | -0.059900 | 1.58e-01 | 
| Leishmania infection | 120 | 2.59e-01 | -0.059800 | 4.28e-01 | 
| Parasitic Infection Pathways | 120 | 2.59e-01 | -0.059800 | 4.28e-01 | 
| Cilium Assembly | 153 | 2.10e-01 | 0.058900 | 3.76e-01 | 
| Condensation of Prophase Chromosomes | 10 | 7.47e-01 | 0.058900 | 8.35e-01 | 
| MyD88 cascade initiated on plasma membrane | 86 | 3.48e-01 | 0.058700 | 5.16e-01 | 
| Toll Like Receptor 10 (TLR10) Cascade | 86 | 3.48e-01 | 0.058700 | 5.16e-01 | 
| Toll Like Receptor 5 (TLR5) Cascade | 86 | 3.48e-01 | 0.058700 | 5.16e-01 | 
| RAB geranylgeranylation | 47 | 4.87e-01 | -0.058600 | 6.36e-01 | 
| Activation of kainate receptors upon glutamate binding | 15 | 6.95e-01 | -0.058500 | 8.06e-01 | 
| Diseases associated with O-glycosylation of proteins | 15 | 6.98e-01 | 0.057900 | 8.06e-01 | 
| Interactions of Rev with host cellular proteins | 35 | 5.56e-01 | -0.057500 | 6.94e-01 | 
| Glycosaminoglycan metabolism | 68 | 4.14e-01 | 0.057400 | 5.82e-01 | 
| Generic Transcription Pathway | 858 | 5.35e-03 | 0.057200 | 2.00e-02 | 
| Intrinsic Pathway for Apoptosis | 50 | 4.87e-01 | -0.056800 | 6.36e-01 | 
| PIP3 activates AKT signaling | 198 | 1.72e-01 | -0.056500 | 3.20e-01 | 
| GPCR ligand binding | 75 | 3.98e-01 | -0.056500 | 5.65e-01 | 
| Sema4D in semaphorin signaling | 18 | 6.79e-01 | -0.056400 | 7.94e-01 | 
| MAP kinase activation | 59 | 4.59e-01 | 0.055800 | 6.15e-01 | 
| Epigenetic regulation of gene expression | 115 | 3.04e-01 | 0.055600 | 4.75e-01 | 
| Transport of the SLBP Dependant Mature mRNA | 35 | 5.71e-01 | -0.055300 | 7.03e-01 | 
| PKA activation | 12 | 7.40e-01 | 0.055300 | 8.32e-01 | 
| Depolymerization of the Nuclear Lamina | 12 | 7.40e-01 | 0.055300 | 8.32e-01 | 
| Gene Silencing by RNA | 67 | 4.36e-01 | -0.055100 | 6.01e-01 | 
| Ion channel transport | 89 | 3.71e-01 | -0.055000 | 5.39e-01 | 
| SLC-mediated transmembrane transport | 112 | 3.17e-01 | 0.054900 | 4.86e-01 | 
| Regulation of cholesterol biosynthesis by SREBP (SREBF) | 54 | 4.87e-01 | -0.054800 | 6.36e-01 | 
| Postmitotic nuclear pore complex (NPC) reformation | 25 | 6.38e-01 | -0.054400 | 7.62e-01 | 
| Signal Transduction | 1459 | 9.09e-04 | 0.053900 | 4.36e-03 | 
| Interleukin-17 signaling | 61 | 4.69e-01 | 0.053700 | 6.26e-01 | 
| Signaling by VEGF | 86 | 4.02e-01 | 0.052400 | 5.69e-01 | 
| TNFR1-induced NF-kappa-B signaling pathway | 31 | 6.15e-01 | -0.052300 | 7.46e-01 | 
| RNA polymerase II transcribes snRNA genes | 68 | 4.57e-01 | -0.052200 | 6.14e-01 | 
| Fcgamma receptor (FCGR) dependent phagocytosis | 75 | 4.38e-01 | -0.051900 | 6.03e-01 | 
| Activation of NMDA receptors and postsynaptic events | 54 | 5.10e-01 | -0.051900 | 6.54e-01 | 
| Impaired BRCA2 binding to RAD51 | 28 | 6.36e-01 | 0.051700 | 7.61e-01 | 
| Retinoid metabolism and transport | 19 | 7.00e-01 | -0.051100 | 8.08e-01 | 
| Signaling by FGFR3 | 25 | 6.59e-01 | -0.051000 | 7.83e-01 | 
| Signaling by FGFR4 | 25 | 6.59e-01 | -0.051000 | 7.83e-01 | 
| MAP3K8 (TPL2)-dependent MAPK1/3 activation | 16 | 7.26e-01 | -0.050700 | 8.26e-01 | 
| MyD88-independent TLR4 cascade | 100 | 3.84e-01 | 0.050500 | 5.51e-01 | 
| TRIF(TICAM1)-mediated TLR4 signaling | 100 | 3.84e-01 | 0.050500 | 5.51e-01 | 
| Regulation of PTEN gene transcription | 54 | 5.26e-01 | 0.050000 | 6.68e-01 | 
| Metabolism of folate and pterines | 15 | 7.39e-01 | -0.049700 | 8.32e-01 | 
| Processing of DNA double-strand break ends | 51 | 5.47e-01 | -0.048800 | 6.86e-01 | 
| Toll Like Receptor 3 (TLR3) Cascade | 95 | 4.19e-01 | 0.048100 | 5.86e-01 | 
| Neurotransmitter receptors and postsynaptic signal transmission | 87 | 4.40e-01 | -0.048000 | 6.03e-01 | 
| Signalling to ERKs | 27 | 6.67e-01 | 0.047900 | 7.90e-01 | 
| TRAF6 mediated induction of NFkB and MAP kinases upon TLR7/8 or 9 activation | 90 | 4.35e-01 | 0.047700 | 6.01e-01 | 
| RHOBTB1 GTPase cycle | 23 | 6.95e-01 | 0.047200 | 8.06e-01 | 
| Sensory Perception | 77 | 4.75e-01 | -0.047200 | 6.28e-01 | 
| TNFs bind their physiological receptors | 11 | 7.88e-01 | -0.046800 | 8.62e-01 | 
| Leading Strand Synthesis | 13 | 7.71e-01 | -0.046700 | 8.49e-01 | 
| Polymerase switching | 13 | 7.71e-01 | -0.046700 | 8.49e-01 | 
| Translation of Replicase and Assembly of the Replication Transcription Complex 9679504 | 13 | 7.72e-01 | -0.046500 | 8.49e-01 | 
| ECM proteoglycans | 18 | 7.34e-01 | 0.046300 | 8.29e-01 | 
| Transcriptional regulation of white adipocyte differentiation | 68 | 5.12e-01 | 0.046100 | 6.55e-01 | 
| CaM pathway | 24 | 6.97e-01 | 0.045900 | 8.06e-01 | 
| Calmodulin induced events | 24 | 6.97e-01 | 0.045900 | 8.06e-01 | 
| Inactivation of CSF3 (G-CSF) signaling | 24 | 6.99e-01 | -0.045700 | 8.07e-01 | 
| Transcriptional activity of SMAD2/SMAD3:SMAD4 heterotrimer | 46 | 5.94e-01 | 0.045500 | 7.27e-01 | 
| Signal amplification | 21 | 7.20e-01 | -0.045300 | 8.22e-01 | 
| SUMOylation of DNA replication proteins | 39 | 6.29e-01 | -0.044800 | 7.55e-01 | 
| Transport of Ribonucleoproteins into the Host Nucleus | 31 | 6.68e-01 | 0.044600 | 7.90e-01 | 
| Deactivation of the beta-catenin transactivating complex | 30 | 6.73e-01 | -0.044500 | 7.94e-01 | 
| G2/M DNA damage checkpoint | 49 | 5.91e-01 | -0.044500 | 7.25e-01 | 
| EML4 and NUDC in mitotic spindle formation | 77 | 5.06e-01 | -0.043900 | 6.50e-01 | 
| G1/S-Specific Transcription | 15 | 7.71e-01 | 0.043500 | 8.49e-01 | 
| BBSome-mediated cargo-targeting to cilium | 18 | 7.50e-01 | -0.043400 | 8.35e-01 | 
| TRAF6 mediated NF-kB activation | 20 | 7.39e-01 | 0.043000 | 8.32e-01 | 
| TRAF6-mediated induction of TAK1 complex within TLR4 complex | 16 | 7.67e-01 | -0.042800 | 8.49e-01 | 
| G-protein activation | 14 | 7.82e-01 | -0.042700 | 8.59e-01 | 
| Toll Like Receptor 7/8 (TLR7/8) Cascade | 92 | 4.80e-01 | 0.042700 | 6.32e-01 | 
| Regulation of TP53 Expression and Degradation | 34 | 6.67e-01 | 0.042600 | 7.90e-01 | 
| Gene expression (Transcription) | 1109 | 2.00e-02 | 0.042500 | 5.96e-02 | 
| EGR2 and SOX10-mediated initiation of Schwann cell myelination | 14 | 7.85e-01 | -0.042200 | 8.60e-01 | 
| Apoptotic factor-mediated response | 19 | 7.52e-01 | -0.041900 | 8.35e-01 | 
| Ca-dependent events | 26 | 7.12e-01 | 0.041800 | 8.17e-01 | 
| Metabolism of water-soluble vitamins and cofactors | 87 | 5.02e-01 | -0.041700 | 6.47e-01 | 
| Oncogenic MAPK signaling | 68 | 5.54e-01 | 0.041600 | 6.92e-01 | 
| Nuclear Envelope Breakdown | 48 | 6.23e-01 | 0.041100 | 7.52e-01 | 
| Signaling by PDGFRA extracellular domain mutants | 12 | 8.06e-01 | 0.040900 | 8.75e-01 | 
| Signaling by PDGFRA transmembrane, juxtamembrane and kinase domain mutants | 12 | 8.06e-01 | 0.040900 | 8.75e-01 | 
| Signaling by NTRKs | 97 | 4.87e-01 | 0.040900 | 6.36e-01 | 
| Metabolism of fat-soluble vitamins | 22 | 7.43e-01 | -0.040400 | 8.33e-01 | 
| Activation of ATR in response to replication stress | 21 | 7.49e-01 | -0.040300 | 8.35e-01 | 
| ISG15 antiviral mechanism | 70 | 5.62e-01 | -0.040200 | 6.99e-01 | 
| MyD88 dependent cascade initiated on endosome | 91 | 5.10e-01 | 0.040100 | 6.54e-01 | 
| Transport of inorganic cations/anions and amino acids/oligopeptides | 48 | 6.34e-01 | 0.039700 | 7.60e-01 | 
| RNA Polymerase II Transcription | 971 | 4.27e-02 | 0.039300 | 1.10e-01 | 
| Intracellular signaling by second messengers | 225 | 3.16e-01 | -0.039000 | 4.86e-01 | 
| Transcriptional Regulation by VENTX | 34 | 6.95e-01 | 0.038900 | 8.06e-01 | 
| Signaling by NOTCH2 | 24 | 7.42e-01 | -0.038900 | 8.32e-01 | 
| Ribavirin ADME | 10 | 8.33e-01 | -0.038600 | 8.94e-01 | 
| G alpha (q) signalling events | 74 | 5.67e-01 | 0.038600 | 7.01e-01 | 
| Transcriptional regulation by the AP-2 (TFAP2) family of transcription factors | 19 | 7.77e-01 | 0.037600 | 8.54e-01 | 
| Vesicle-mediated transport | 517 | 1.49e-01 | -0.037600 | 2.88e-01 | 
| Early Phase of HIV Life Cycle | 17 | 7.89e-01 | 0.037400 | 8.62e-01 | 
| RHOBTB GTPase Cycle | 35 | 7.04e-01 | -0.037200 | 8.10e-01 | 
| Defective TPR may confer susceptibility towards thyroid papillary carcinoma (TPC) | 29 | 7.30e-01 | 0.037000 | 8.29e-01 | 
| Regulation of Glucokinase by Glucokinase Regulatory Protein | 29 | 7.30e-01 | 0.037000 | 8.29e-01 | 
| Formation of the cornified envelope | 14 | 8.12e-01 | 0.036700 | 8.80e-01 | 
| Keratinization | 14 | 8.12e-01 | 0.036700 | 8.80e-01 | 
| Integration of energy metabolism | 59 | 6.27e-01 | 0.036700 | 7.54e-01 | 
| Toll Like Receptor 4 (TLR4) Cascade | 126 | 4.82e-01 | 0.036300 | 6.34e-01 | 
| Signaling by ERBB2 in Cancer | 14 | 8.14e-01 | 0.036300 | 8.81e-01 | 
| Telomere C-strand synthesis initiation | 12 | 8.29e-01 | -0.036000 | 8.94e-01 | 
| Cell junction organization | 49 | 6.67e-01 | 0.035600 | 7.90e-01 | 
| Platelet homeostasis | 46 | 6.77e-01 | -0.035500 | 7.94e-01 | 
| Platelet Aggregation (Plug Formation) | 23 | 7.69e-01 | -0.035400 | 8.49e-01 | 
| Maturation of spike protein 9694548 | 34 | 7.21e-01 | -0.035400 | 8.23e-01 | 
| Intra-Golgi and retrograde Golgi-to-ER traffic | 160 | 4.42e-01 | -0.035400 | 6.03e-01 | 
| TP53 Regulates Transcription of Genes Involved in Cytochrome C Release | 17 | 8.01e-01 | -0.035300 | 8.74e-01 | 
| SUMOylation of RNA binding proteins | 44 | 6.88e-01 | 0.035000 | 8.01e-01 | 
| Regulation of TP53 Activity | 135 | 4.84e-01 | 0.035000 | 6.35e-01 | 
| Mitotic Prophase | 76 | 5.99e-01 | 0.034900 | 7.32e-01 | 
| Regulation of TP53 Activity through Acetylation | 29 | 7.51e-01 | 0.034100 | 8.35e-01 | 
| Nuclear Pore Complex (NPC) Disassembly | 34 | 7.33e-01 | 0.033800 | 8.29e-01 | 
| Diseases of mitotic cell cycle | 31 | 7.45e-01 | -0.033700 | 8.35e-01 | 
| Transport of the SLBP independent Mature mRNA | 34 | 7.35e-01 | -0.033600 | 8.29e-01 | 
| TP53 Regulates Transcription of Cell Death Genes | 37 | 7.28e-01 | 0.033100 | 8.28e-01 | 
| FCGR3A-mediated phagocytosis | 53 | 6.79e-01 | -0.032900 | 7.94e-01 | 
| Leishmania phagocytosis | 53 | 6.79e-01 | -0.032900 | 7.94e-01 | 
| Parasite infection | 53 | 6.79e-01 | -0.032900 | 7.94e-01 | 
| Muscle contraction | 72 | 6.33e-01 | -0.032600 | 7.59e-01 | 
| Nuclear import of Rev protein | 32 | 7.50e-01 | -0.032500 | 8.35e-01 | 
| SHC1 events in ERBB2 signaling | 11 | 8.52e-01 | -0.032500 | 9.07e-01 | 
| Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks | 38 | 7.30e-01 | 0.032400 | 8.29e-01 | 
| Translation of Replicase and Assembly of the Replication Transcription Complex 9694676 | 14 | 8.35e-01 | -0.032200 | 8.94e-01 | 
| Ovarian tumor domain proteases | 32 | 7.55e-01 | 0.031900 | 8.37e-01 | 
| Mitochondrial RNA degradation | 23 | 7.92e-01 | 0.031800 | 8.65e-01 | 
| Platelet calcium homeostasis | 15 | 8.32e-01 | -0.031700 | 8.94e-01 | 
| SUMOylation of SUMOylation proteins | 34 | 7.51e-01 | -0.031500 | 8.35e-01 | 
| HDR through Homologous Recombination (HRR) or Single Strand Annealing (SSA) | 75 | 6.45e-01 | -0.030800 | 7.70e-01 | 
| Diseases associated with glycosaminoglycan metabolism | 18 | 8.21e-01 | 0.030700 | 8.88e-01 | 
| Signaling by EGFR | 36 | 7.51e-01 | -0.030600 | 8.35e-01 | 
| Molecules associated with elastic fibres | 11 | 8.62e-01 | 0.030300 | 9.13e-01 | 
| RAF activation | 32 | 7.74e-01 | -0.029400 | 8.51e-01 | 
| SUMOylation of ubiquitinylation proteins | 38 | 7.60e-01 | 0.028600 | 8.42e-01 | 
| Translation of Structural Proteins 9694635 | 54 | 7.20e-01 | -0.028200 | 8.22e-01 | 
| Deposition of new CENPA-containing nucleosomes at the centromere | 19 | 8.33e-01 | -0.028000 | 8.94e-01 | 
| Nucleosome assembly | 19 | 8.33e-01 | -0.028000 | 8.94e-01 | 
| Signaling by NOTCH3 | 33 | 7.86e-01 | -0.027400 | 8.60e-01 | 
| Sema4D induced cell migration and growth-cone collapse | 15 | 8.55e-01 | -0.027400 | 9.09e-01 | 
| Membrane Trafficking | 499 | 3.04e-01 | -0.027200 | 4.75e-01 | 
| Mitotic Spindle Checkpoint | 79 | 6.78e-01 | -0.027100 | 7.94e-01 | 
| Homology Directed Repair | 79 | 6.80e-01 | -0.026900 | 7.95e-01 | 
| Cyclin A/B1/B2 associated events during G2/M transition | 17 | 8.50e-01 | 0.026500 | 9.06e-01 | 
| Transport of Mature mRNAs Derived from Intronless Transcripts | 42 | 7.69e-01 | -0.026200 | 8.49e-01 | 
| VEGFR2 mediated cell proliferation | 15 | 8.61e-01 | 0.026000 | 9.13e-01 | 
| Loss of Nlp from mitotic centrosomes | 59 | 7.34e-01 | 0.025600 | 8.29e-01 | 
| Loss of proteins required for interphase microtubule organization from the centrosome | 59 | 7.34e-01 | 0.025600 | 8.29e-01 | 
| Negative regulation of MET activity | 16 | 8.60e-01 | -0.025600 | 9.13e-01 | 
| ESR-mediated signaling | 124 | 6.27e-01 | -0.025400 | 7.54e-01 | 
| Neuronal System | 141 | 6.04e-01 | -0.025400 | 7.36e-01 | 
| Signaling by NTRK1 (TRKA) | 85 | 6.88e-01 | 0.025200 | 8.01e-01 | 
| Transport of vitamins, nucleosides, and related molecules | 25 | 8.28e-01 | -0.025100 | 8.94e-01 | 
| Glucagon signaling in metabolic regulation | 19 | 8.51e-01 | -0.024900 | 9.07e-01 | 
| Rev-mediated nuclear export of HIV RNA | 33 | 8.05e-01 | -0.024900 | 8.75e-01 | 
| Metal ion SLC transporters | 16 | 8.64e-01 | -0.024700 | 9.13e-01 | 
| Transmission across Chemical Synapses | 108 | 6.59e-01 | -0.024600 | 7.83e-01 | 
| Toll-like Receptor Cascades | 143 | 6.17e-01 | 0.024300 | 7.47e-01 | 
| Antigen processing: Ubiquitination & Proteasome degradation | 255 | 5.12e-01 | -0.024000 | 6.55e-01 | 
| p130Cas linkage to MAPK signaling for integrins | 11 | 8.92e-01 | 0.023500 | 9.36e-01 | 
| AURKA Activation by TPX2 | 60 | 7.55e-01 | 0.023300 | 8.37e-01 | 
| G alpha (z) signalling events | 25 | 8.42e-01 | -0.023100 | 9.00e-01 | 
| HDR through Homologous Recombination (HRR) | 51 | 7.85e-01 | -0.022100 | 8.60e-01 | 
| NGF-stimulated transcription | 25 | 8.49e-01 | -0.022000 | 9.06e-01 | 
| Signaling by TGFB family members | 82 | 7.32e-01 | 0.021900 | 8.29e-01 | 
| Heparan sulfate/heparin (HS-GAG) metabolism | 28 | 8.41e-01 | -0.021900 | 9.00e-01 | 
| Processing of Intronless Pre-mRNAs | 20 | 8.66e-01 | 0.021800 | 9.13e-01 | 
| Signaling by TGF-beta Receptor Complex | 73 | 7.48e-01 | -0.021800 | 8.35e-01 | 
| Regulation of TP53 Activity through Phosphorylation | 73 | 7.48e-01 | -0.021800 | 8.35e-01 | 
| A tetrasaccharide linker sequence is required for GAG synthesis | 12 | 8.99e-01 | -0.021200 | 9.38e-01 | 
| MyD88:MAL(TIRAP) cascade initiated on plasma membrane | 100 | 7.15e-01 | 0.021200 | 8.18e-01 | 
| Toll Like Receptor 2 (TLR2) Cascade | 100 | 7.15e-01 | 0.021200 | 8.18e-01 | 
| Toll Like Receptor TLR1:TLR2 Cascade | 100 | 7.15e-01 | 0.021200 | 8.18e-01 | 
| Toll Like Receptor TLR6:TLR2 Cascade | 100 | 7.15e-01 | 0.021200 | 8.18e-01 | 
| Peptide hormone metabolism | 35 | 8.30e-01 | 0.021000 | 8.94e-01 | 
| Constitutive Signaling by EGFRvIII | 12 | 9.06e-01 | -0.019700 | 9.41e-01 | 
| Signaling by EGFRvIII in Cancer | 12 | 9.06e-01 | -0.019700 | 9.41e-01 | 
| Thromboxane signalling through TP receptor | 15 | 8.95e-01 | 0.019600 | 9.37e-01 | 
| Ion homeostasis | 27 | 8.62e-01 | -0.019400 | 9.13e-01 | 
| SLC transporter disorders | 56 | 8.05e-01 | 0.019100 | 8.75e-01 | 
| Diseases of DNA repair | 41 | 8.34e-01 | 0.019000 | 8.94e-01 | 
| ADP signalling through P2Y purinoceptor 1 | 17 | 8.94e-01 | -0.018700 | 9.37e-01 | 
| HATs acetylate histones | 75 | 7.83e-01 | 0.018400 | 8.59e-01 | 
| Vasopressin regulates renal water homeostasis via Aquaporins | 23 | 8.80e-01 | 0.018300 | 9.24e-01 | 
| Cytosolic sulfonation of small molecules | 11 | 9.19e-01 | 0.017800 | 9.47e-01 | 
| Ras activation upon Ca2+ influx through NMDA receptor | 11 | 9.20e-01 | -0.017500 | 9.47e-01 | 
| Signaling by FGFR in disease | 42 | 8.46e-01 | 0.017300 | 9.04e-01 | 
| Signaling by FGFR1 | 32 | 8.66e-01 | -0.017200 | 9.13e-01 | 
| SUMOylation of transcription factors | 14 | 9.11e-01 | 0.017200 | 9.43e-01 | 
| G-protein beta:gamma signalling | 24 | 8.85e-01 | -0.017100 | 9.28e-01 | 
| FCERI mediated MAPK activation | 27 | 8.78e-01 | 0.017100 | 9.23e-01 | 
| Costimulation by the CD28 family | 51 | 8.34e-01 | -0.017000 | 8.94e-01 | 
| DNA Double Strand Break Response | 39 | 8.64e-01 | 0.015900 | 9.13e-01 | 
| G beta:gamma signalling through PI3Kgamma | 18 | 9.07e-01 | 0.015900 | 9.41e-01 | 
| Effects of PIP2 hydrolysis | 18 | 9.08e-01 | -0.015800 | 9.41e-01 | 
| Potential therapeutics for SARS | 82 | 8.05e-01 | -0.015800 | 8.75e-01 | 
| Regulation of TP53 Degradation | 33 | 8.77e-01 | 0.015600 | 9.23e-01 | 
| Signaling by Receptor Tyrosine Kinases | 333 | 6.50e-01 | -0.014600 | 7.74e-01 | 
| Mitotic Prometaphase | 151 | 7.60e-01 | 0.014500 | 8.42e-01 | 
| G alpha (i) signalling events | 104 | 8.03e-01 | -0.014200 | 8.75e-01 | 
| TBC/RABGAPs | 44 | 8.75e-01 | -0.013700 | 9.21e-01 | 
| TRP channels | 12 | 9.36e-01 | -0.013400 | 9.59e-01 | 
| Translation of Structural Proteins 9683701 | 29 | 9.02e-01 | 0.013200 | 9.40e-01 | 
| Late SARS-CoV-2 Infection Events | 58 | 8.62e-01 | 0.013200 | 9.13e-01 | 
| Ion transport by P-type ATPases | 29 | 9.03e-01 | 0.013000 | 9.40e-01 | 
| Interleukin-37 signaling | 15 | 9.31e-01 | -0.013000 | 9.57e-01 | 
| SARS-CoV-2 activates/modulates innate and adaptive immune responses | 99 | 8.27e-01 | -0.012800 | 8.92e-01 | 
| Non-integrin membrane-ECM interactions | 23 | 9.16e-01 | 0.012700 | 9.46e-01 | 
| Export of Viral Ribonucleoproteins from Nucleus | 32 | 9.03e-01 | -0.012400 | 9.40e-01 | 
| Amplification of signal from unattached kinetochores via a MAD2 inhibitory signal | 64 | 8.67e-01 | 0.012100 | 9.13e-01 | 
| Amplification of signal from the kinetochores | 64 | 8.67e-01 | 0.012100 | 9.13e-01 | 
| Signaling by CSF3 (G-CSF) | 29 | 9.13e-01 | -0.011700 | 9.45e-01 | 
| Negative regulators of DDX58/IFIH1 signaling | 34 | 9.09e-01 | 0.011400 | 9.41e-01 | 
| Keratan sulfate/keratin metabolism | 19 | 9.35e-01 | -0.010900 | 9.59e-01 | 
| PTK6 Regulates RHO GTPases, RAS GTPase and MAP kinases | 13 | 9.47e-01 | -0.010700 | 9.68e-01 | 
| Regulation of TP53 Activity through Methylation | 19 | 9.36e-01 | -0.010700 | 9.59e-01 | 
| Metabolism of lipids | 491 | 6.91e-01 | -0.010600 | 8.04e-01 | 
| Anti-inflammatory response favouring Leishmania parasite infection | 48 | 8.99e-01 | 0.010600 | 9.38e-01 | 
| Leishmania parasite growth and survival | 48 | 8.99e-01 | 0.010600 | 9.38e-01 | 
| Visual phototransduction | 43 | 9.16e-01 | 0.009320 | 9.46e-01 | 
| Ephrin signaling | 13 | 9.55e-01 | 0.009010 | 9.72e-01 | 
| DDX58/IFIH1-mediated induction of interferon-alpha/beta | 63 | 9.02e-01 | -0.008950 | 9.40e-01 | 
| Organelle biogenesis and maintenance | 235 | 8.16e-01 | -0.008850 | 8.83e-01 | 
| Regulation of PLK1 Activity at G2/M Transition | 75 | 8.96e-01 | -0.008750 | 9.37e-01 | 
| ERCC6 (CSB) and EHMT2 (G9a) positively regulate rRNA expression | 17 | 9.51e-01 | 0.008580 | 9.70e-01 | 
| Elastic fibre formation | 14 | 9.56e-01 | 0.008510 | 9.72e-01 | 
| Other semaphorin interactions | 12 | 9.63e-01 | 0.007840 | 9.76e-01 | 
| Aquaporin-mediated transport | 24 | 9.49e-01 | -0.007590 | 9.69e-01 | 
| Transport of Mature mRNA Derived from an Intronless Transcript | 41 | 9.35e-01 | -0.007400 | 9.59e-01 | 
| Cyclin D associated events in G1 | 38 | 9.37e-01 | -0.007380 | 9.59e-01 | 
| G1 Phase | 38 | 9.37e-01 | -0.007380 | 9.59e-01 | 
| RMTs methylate histone arginines | 30 | 9.46e-01 | -0.007160 | 9.68e-01 | 
| Centrosome maturation | 70 | 9.19e-01 | -0.007030 | 9.47e-01 | 
| Recruitment of mitotic centrosome proteins and complexes | 70 | 9.19e-01 | -0.007030 | 9.47e-01 | 
| Z-decay: degradation of maternal mRNAs by zygotically expressed factors | 10 | 9.71e-01 | -0.006620 | 9.80e-01 | 
| Defects in vitamin and cofactor metabolism | 17 | 9.64e-01 | -0.006260 | 9.76e-01 | 
| Signaling by ERBB2 ECD mutants | 12 | 9.71e-01 | 0.006160 | 9.80e-01 | 
| Thrombin signalling through proteinase activated receptors (PARs) | 20 | 9.62e-01 | 0.006140 | 9.76e-01 | 
| DAP12 signaling | 24 | 9.61e-01 | -0.005830 | 9.76e-01 | 
| Diseases of signal transduction by growth factor receptors and second messengers | 324 | 8.61e-01 | -0.005720 | 9.13e-01 | 
| G alpha (s) signalling events | 50 | 9.50e-01 | -0.005130 | 9.69e-01 | 
| Pre-NOTCH Processing in Golgi | 16 | 9.72e-01 | 0.005060 | 9.80e-01 | 
| Early SARS-CoV-2 Infection Events | 29 | 9.63e-01 | 0.004980 | 9.76e-01 | 
| TNF signaling | 52 | 9.55e-01 | -0.004490 | 9.72e-01 | 
| Signaling by ERBB2 KD Mutants | 13 | 9.83e-01 | 0.003410 | 9.88e-01 | 
| NEP/NS2 Interacts with the Cellular Export Machinery | 31 | 9.75e-01 | -0.003260 | 9.83e-01 | 
| ADORA2B mediated anti-inflammatory cytokines production | 26 | 9.78e-01 | 0.003190 | 9.84e-01 | 
| Branched-chain amino acid catabolism | 21 | 9.81e-01 | -0.003040 | 9.87e-01 | 
| DNA Double-Strand Break Repair | 104 | 9.59e-01 | -0.002930 | 9.75e-01 | 
| Resolution of Sister Chromatid Cohesion | 84 | 9.65e-01 | -0.002790 | 9.76e-01 | 
| Assembly Of The HIV Virion | 19 | 9.83e-01 | -0.002780 | 9.88e-01 | 
| Interactions of Vpr with host cellular proteins | 38 | 9.84e-01 | -0.001910 | 9.88e-01 | 
| Signaling by Nuclear Receptors | 174 | 9.71e-01 | -0.001600 | 9.80e-01 | 
| Integration of provirus | 11 | 9.93e-01 | 0.001480 | 9.95e-01 | 
| Sphingolipid metabolism | 61 | 9.85e-01 | -0.001440 | 9.88e-01 | 
| Regulation of IFNG signaling | 13 | 9.94e-01 | -0.001140 | 9.95e-01 | 
| Estrogen-dependent gene expression | 77 | 9.88e-01 | 0.001010 | 9.90e-01 | 
| TP53 Regulates Transcription of Cell Cycle Genes | 35 | 9.99e-01 | 0.000162 | 9.99e-01 | 
  Eukaryotic Translation Termination 
| 317 | |
|---|---|
| set | Eukaryotic Translation Termination | 
| setSize | 90 | 
| pANOVA | 2.34e-39 | 
| s.dist | -0.799 | 
| p.adjustANOVA | 3.04e-37 | 
Top enriched genes
| GeneID | Gene Rank | 
|---|---|
| RPS28 | -3265 | 
| RPL36 | -3263 | 
| RPL35 | -3250 | 
| RPS29 | -3247 | 
| RPS21 | -3244 | 
| RPL32 | -3239 | 
| RPL19 | -3232 | 
| RPL39 | -3228 | 
| UBA52 | -3224 | 
| RPS18 | -3220 | 
| RPS26 | -3215 | 
| RPLP2 | -3212 | 
| FAU | -3209 | 
| RPS15 | -3207 | 
| RPLP1 | -3206 | 
| RPL41 | -3204 | 
| RPL38 | -3177 | 
| RPS12 | -3173 | 
| RPL34 | -3171 | 
| RPS24 | -3160 | 
| GeneID | Gene Rank | 
|---|---|
| RPS28 | -3265 | 
| RPL36 | -3263 | 
| RPL35 | -3250 | 
| RPS29 | -3247 | 
| RPS21 | -3244 | 
| RPL32 | -3239 | 
| RPL19 | -3232 | 
| RPL39 | -3228 | 
| UBA52 | -3224 | 
| RPS18 | -3220 | 
| RPS26 | -3215 | 
| RPLP2 | -3212 | 
| FAU | -3209 | 
| RPS15 | -3207 | 
| RPLP1 | -3206 | 
| RPL41 | -3204 | 
| RPL38 | -3177 | 
| RPS12 | -3173 | 
| RPL34 | -3171 | 
| RPS24 | -3160 | 
| RPL13 | -3154 | 
| RPL18A | -3141 | 
| RPL37A | -3140 | 
| RPSA | -3139 | 
| RPS9 | -3133 | 
| RPL35A | -3125 | 
| RPL37 | -3121 | 
| RPL11 | -3116 | 
| RPS5 | -3098 | 
| RPS14 | -3088 | 
| RPS7 | -3072 | 
| RPL30 | -3071 | 
| RPL10A | -3051 | 
| RPL14 | -3046 | 
| RPS16 | -3045 | 
| RPS15A | -3005 | 
| RPS27 | -2985 | 
| RPL24 | -2957 | 
| RPL8 | -2956 | 
| RPS8 | -2950 | 
| RPL10 | -2947 | 
| RPL21 | -2945 | 
| RPL28 | -2926 | 
| RPL27 | -2923 | 
| RPS25 | -2902 | 
| RPS3 | -2869 | 
| RPL36A | -2858 | 
| TRMT112 | -2848 | 
| RPS27A | -2821 | 
| RPL22 | -2796 | 
| RPL23A | -2793 | 
| RPS23 | -2783 | 
| RPL3 | -2782 | 
| RPL26 | -2774 | 
| RPS4Y1 | -2771 | 
| RPL7A | -2766 | 
| RPS10 | -2749 | 
| RPS3A | -2745 | 
| RPS19 | -2714 | 
| RPL36AL | -2703 | 
| RPL18 | -2699 | 
| RPL6 | -2665 | 
| RPS27L | -2611 | 
| RPL26L1 | -2572 | 
| RPL29 | -2433 | 
| RPL4 | -2374 | 
| RPL27A | -2238 | 
| RPS13 | -2162 | 
| RPS6 | -2137 | 
| RPL15 | -2045 | 
| RPL17 | -1968 | 
| RPLP0 | -1966 | 
| GSPT2 | -1653 | 
| APEH | -1444 | 
| RPL22L1 | -985 | 
| RPL5 | -485 | 
| RPL12 | -443 | 
| GSPT1 | -159 | 
| RPS17 | 7 | 
| RPL31 | 20 | 
| RPL7 | 108 | 
| RPS2 | 319 | 
| ETF1 | 467 | 
| RPS4X | 1068 | 
| RPL9 | 1356 | 
| RPS11 | 1556 | 
| RPL23 | 1657 | 
| RPL39L | 3853 | 
| RPL13A | 5851 | 
| RPS20 | 6819 | 
 Viral mRNA Translation 
| 1259 | |
|---|---|
| set | Viral mRNA Translation | 
| setSize | 87 | 
| pANOVA | 1.3e-37 | 
| s.dist | -0.794 | 
| p.adjustANOVA | 9.97e-36 | 
Top enriched genes
| GeneID | Gene Rank | 
|---|---|
| RPS28 | -3265 | 
| RPL36 | -3263 | 
| RPL35 | -3250 | 
| RPS29 | -3247 | 
| RPS21 | -3244 | 
| RPL32 | -3239 | 
| RPL19 | -3232 | 
| RPL39 | -3228 | 
| UBA52 | -3224 | 
| RPS18 | -3220 | 
| RPS26 | -3215 | 
| RPLP2 | -3212 | 
| FAU | -3209 | 
| RPS15 | -3207 | 
| RPLP1 | -3206 | 
| RPL41 | -3204 | 
| RPL38 | -3177 | 
| RPS12 | -3173 | 
| RPL34 | -3171 | 
| RPS24 | -3160 | 
| GeneID | Gene Rank | 
|---|---|
| RPS28 | -3265 | 
| RPL36 | -3263 | 
| RPL35 | -3250 | 
| RPS29 | -3247 | 
| RPS21 | -3244 | 
| RPL32 | -3239 | 
| RPL19 | -3232 | 
| RPL39 | -3228 | 
| UBA52 | -3224 | 
| RPS18 | -3220 | 
| RPS26 | -3215 | 
| RPLP2 | -3212 | 
| FAU | -3209 | 
| RPS15 | -3207 | 
| RPLP1 | -3206 | 
| RPL41 | -3204 | 
| RPL38 | -3177 | 
| RPS12 | -3173 | 
| RPL34 | -3171 | 
| RPS24 | -3160 | 
| RPL13 | -3154 | 
| RPL18A | -3141 | 
| RPL37A | -3140 | 
| RPSA | -3139 | 
| RPS9 | -3133 | 
| RPL35A | -3125 | 
| RPL37 | -3121 | 
| RPL11 | -3116 | 
| RPS5 | -3098 | 
| RPS14 | -3088 | 
| RPS7 | -3072 | 
| RPL30 | -3071 | 
| RPL10A | -3051 | 
| RPL14 | -3046 | 
| RPS16 | -3045 | 
| RPS15A | -3005 | 
| RPS27 | -2985 | 
| RPL24 | -2957 | 
| RPL8 | -2956 | 
| RPS8 | -2950 | 
| RPL10 | -2947 | 
| RPL21 | -2945 | 
| RPL28 | -2926 | 
| RPL27 | -2923 | 
| RPS25 | -2902 | 
| RPS3 | -2869 | 
| RPL36A | -2858 | 
| RPS27A | -2821 | 
| RPL22 | -2796 | 
| RPL23A | -2793 | 
| RPS23 | -2783 | 
| RPL3 | -2782 | 
| RPL26 | -2774 | 
| RPS4Y1 | -2771 | 
| RPL7A | -2766 | 
| RPS10 | -2749 | 
| RPS3A | -2745 | 
| RPS19 | -2714 | 
| RPL36AL | -2703 | 
| RPL18 | -2699 | 
| RPL6 | -2665 | 
| RPS27L | -2611 | 
| RPL26L1 | -2572 | 
| RPL29 | -2433 | 
| RPL4 | -2374 | 
| RPL27A | -2238 | 
| RPS13 | -2162 | 
| RPS6 | -2137 | 
| RPL15 | -2045 | 
| RPL17 | -1968 | 
| RPLP0 | -1966 | 
| RPL22L1 | -985 | 
| RPL5 | -485 | 
| GRSF1 | -475 | 
| RPL12 | -443 | 
| RPS17 | 7 | 
| RPL31 | 20 | 
| RPL7 | 108 | 
| RPS2 | 319 | 
| RPS4X | 1068 | 
| RPL9 | 1356 | 
| RPS11 | 1556 | 
| RPL23 | 1657 | 
| DNAJC3 | 3683 | 
| RPL39L | 3853 | 
| RPL13A | 5851 | 
| RPS20 | 6819 | 
 Eukaryotic Translation Elongation 
| 315 | |
|---|---|
| set | Eukaryotic Translation Elongation | 
| setSize | 90 | 
| pANOVA | 7.27e-38 | 
| s.dist | -0.783 | 
| p.adjustANOVA | 6.3e-36 | 
Top enriched genes
| GeneID | Gene Rank | 
|---|---|
| RPS28 | -3265 | 
| RPL36 | -3263 | 
| RPL35 | -3250 | 
| RPS29 | -3247 | 
| RPS21 | -3244 | 
| RPL32 | -3239 | 
| RPL19 | -3232 | 
| RPL39 | -3228 | 
| UBA52 | -3224 | 
| RPS18 | -3220 | 
| RPS26 | -3215 | 
| RPLP2 | -3212 | 
| FAU | -3209 | 
| RPS15 | -3207 | 
| RPLP1 | -3206 | 
| RPL41 | -3204 | 
| RPL38 | -3177 | 
| RPS12 | -3173 | 
| RPL34 | -3171 | 
| RPS24 | -3160 | 
| GeneID | Gene Rank | 
|---|---|
| RPS28 | -3265 | 
| RPL36 | -3263 | 
| RPL35 | -3250 | 
| RPS29 | -3247 | 
| RPS21 | -3244 | 
| RPL32 | -3239 | 
| RPL19 | -3232 | 
| RPL39 | -3228 | 
| UBA52 | -3224 | 
| RPS18 | -3220 | 
| RPS26 | -3215 | 
| RPLP2 | -3212 | 
| FAU | -3209 | 
| RPS15 | -3207 | 
| RPLP1 | -3206 | 
| RPL41 | -3204 | 
| RPL38 | -3177 | 
| RPS12 | -3173 | 
| RPL34 | -3171 | 
| RPS24 | -3160 | 
| RPL13 | -3154 | 
| RPL18A | -3141 | 
| RPL37A | -3140 | 
| RPSA | -3139 | 
| RPS9 | -3133 | 
| RPL35A | -3125 | 
| RPL37 | -3121 | 
| RPL11 | -3116 | 
| RPS5 | -3098 | 
| EEF1B2 | -3090 | 
| RPS14 | -3088 | 
| RPS7 | -3072 | 
| RPL30 | -3071 | 
| RPL10A | -3051 | 
| RPL14 | -3046 | 
| RPS16 | -3045 | 
| RPS15A | -3005 | 
| RPS27 | -2985 | 
| RPL24 | -2957 | 
| RPL8 | -2956 | 
| RPS8 | -2950 | 
| RPL10 | -2947 | 
| RPL21 | -2945 | 
| RPL28 | -2926 | 
| RPL27 | -2923 | 
| RPS25 | -2902 | 
| RPS3 | -2869 | 
| RPL36A | -2858 | 
| RPS27A | -2821 | 
| EEF1D | -2810 | 
| RPL22 | -2796 | 
| RPL23A | -2793 | 
| RPS23 | -2783 | 
| RPL3 | -2782 | 
| RPL26 | -2774 | 
| RPS4Y1 | -2771 | 
| RPL7A | -2766 | 
| RPS10 | -2749 | 
| RPS3A | -2745 | 
| RPS19 | -2714 | 
| RPL36AL | -2703 | 
| RPL18 | -2699 | 
| RPL6 | -2665 | 
| RPS27L | -2611 | 
| RPL26L1 | -2572 | 
| RPL29 | -2433 | 
| RPL4 | -2374 | 
| RPL27A | -2238 | 
| RPS13 | -2162 | 
| RPS6 | -2137 | 
| RPL15 | -2045 | 
| RPL17 | -1968 | 
| RPLP0 | -1966 | 
| EEF1G | -1871 | 
| RPL22L1 | -985 | 
| RPL5 | -485 | 
| RPL12 | -443 | 
| RPS17 | 7 | 
| RPL31 | 20 | 
| RPL7 | 108 | 
| RPS2 | 319 | 
| RPS4X | 1068 | 
| RPL9 | 1356 | 
| RPS11 | 1556 | 
| RPL23 | 1657 | 
| EEF2 | 2708 | 
| RPL39L | 3853 | 
| RPL13A | 5851 | 
| RPS20 | 6819 | 
| EEF1A1 | 7185 | 
 Peptide chain elongation 
| 745 | |
|---|---|
| set | Peptide chain elongation | 
| setSize | 87 | 
| pANOVA | 2.48e-36 | 
| s.dist | -0.78 | 
| p.adjustANOVA | 1.79e-34 | 
Top enriched genes
| GeneID | Gene Rank | 
|---|---|
| RPS28 | -3265 | 
| RPL36 | -3263 | 
| RPL35 | -3250 | 
| RPS29 | -3247 | 
| RPS21 | -3244 | 
| RPL32 | -3239 | 
| RPL19 | -3232 | 
| RPL39 | -3228 | 
| UBA52 | -3224 | 
| RPS18 | -3220 | 
| RPS26 | -3215 | 
| RPLP2 | -3212 | 
| FAU | -3209 | 
| RPS15 | -3207 | 
| RPLP1 | -3206 | 
| RPL41 | -3204 | 
| RPL38 | -3177 | 
| RPS12 | -3173 | 
| RPL34 | -3171 | 
| RPS24 | -3160 | 
| GeneID | Gene Rank | 
|---|---|
| RPS28 | -3265 | 
| RPL36 | -3263 | 
| RPL35 | -3250 | 
| RPS29 | -3247 | 
| RPS21 | -3244 | 
| RPL32 | -3239 | 
| RPL19 | -3232 | 
| RPL39 | -3228 | 
| UBA52 | -3224 | 
| RPS18 | -3220 | 
| RPS26 | -3215 | 
| RPLP2 | -3212 | 
| FAU | -3209 | 
| RPS15 | -3207 | 
| RPLP1 | -3206 | 
| RPL41 | -3204 | 
| RPL38 | -3177 | 
| RPS12 | -3173 | 
| RPL34 | -3171 | 
| RPS24 | -3160 | 
| RPL13 | -3154 | 
| RPL18A | -3141 | 
| RPL37A | -3140 | 
| RPSA | -3139 | 
| RPS9 | -3133 | 
| RPL35A | -3125 | 
| RPL37 | -3121 | 
| RPL11 | -3116 | 
| RPS5 | -3098 | 
| RPS14 | -3088 | 
| RPS7 | -3072 | 
| RPL30 | -3071 | 
| RPL10A | -3051 | 
| RPL14 | -3046 | 
| RPS16 | -3045 | 
| RPS15A | -3005 | 
| RPS27 | -2985 | 
| RPL24 | -2957 | 
| RPL8 | -2956 | 
| RPS8 | -2950 | 
| RPL10 | -2947 | 
| RPL21 | -2945 | 
| RPL28 | -2926 | 
| RPL27 | -2923 | 
| RPS25 | -2902 | 
| RPS3 | -2869 | 
| RPL36A | -2858 | 
| RPS27A | -2821 | 
| RPL22 | -2796 | 
| RPL23A | -2793 | 
| RPS23 | -2783 | 
| RPL3 | -2782 | 
| RPL26 | -2774 | 
| RPS4Y1 | -2771 | 
| RPL7A | -2766 | 
| RPS10 | -2749 | 
| RPS3A | -2745 | 
| RPS19 | -2714 | 
| RPL36AL | -2703 | 
| RPL18 | -2699 | 
| RPL6 | -2665 | 
| RPS27L | -2611 | 
| RPL26L1 | -2572 | 
| RPL29 | -2433 | 
| RPL4 | -2374 | 
| RPL27A | -2238 | 
| RPS13 | -2162 | 
| RPS6 | -2137 | 
| RPL15 | -2045 | 
| RPL17 | -1968 | 
| RPLP0 | -1966 | 
| RPL22L1 | -985 | 
| RPL5 | -485 | 
| RPL12 | -443 | 
| RPS17 | 7 | 
| RPL31 | 20 | 
| RPL7 | 108 | 
| RPS2 | 319 | 
| RPS4X | 1068 | 
| RPL9 | 1356 | 
| RPS11 | 1556 | 
| RPL23 | 1657 | 
| EEF2 | 2708 | 
| RPL39L | 3853 | 
| RPL13A | 5851 | 
| RPS20 | 6819 | 
| EEF1A1 | 7185 | 
 Formation of a pool of free 40S subunits 
| 353 | |
|---|---|
| set | Formation of a pool of free 40S subunits | 
| setSize | 98 | 
| pANOVA | 4.92e-40 | 
| s.dist | -0.773 | 
| p.adjustANOVA | 7.11e-38 | 
Top enriched genes
| GeneID | Gene Rank | 
|---|---|
| RPS28 | -3265 | 
| RPL36 | -3263 | 
| RPL35 | -3250 | 
| RPS29 | -3247 | 
| RPS21 | -3244 | 
| RPL32 | -3239 | 
| RPL19 | -3232 | 
| RPL39 | -3228 | 
| UBA52 | -3224 | 
| RPS18 | -3220 | 
| RPS26 | -3215 | 
| RPLP2 | -3212 | 
| FAU | -3209 | 
| RPS15 | -3207 | 
| RPLP1 | -3206 | 
| RPL41 | -3204 | 
| RPL38 | -3177 | 
| RPS12 | -3173 | 
| RPL34 | -3171 | 
| RPS24 | -3160 | 
| GeneID | Gene Rank | 
|---|---|
| RPS28 | -3265 | 
| RPL36 | -3263 | 
| RPL35 | -3250 | 
| RPS29 | -3247 | 
| RPS21 | -3244 | 
| RPL32 | -3239 | 
| RPL19 | -3232 | 
| RPL39 | -3228 | 
| UBA52 | -3224 | 
| RPS18 | -3220 | 
| RPS26 | -3215 | 
| RPLP2 | -3212 | 
| FAU | -3209 | 
| RPS15 | -3207 | 
| RPLP1 | -3206 | 
| RPL41 | -3204 | 
| RPL38 | -3177 | 
| RPS12 | -3173 | 
| RPL34 | -3171 | 
| RPS24 | -3160 | 
| RPL13 | -3154 | 
| RPL18A | -3141 | 
| RPL37A | -3140 | 
| RPSA | -3139 | 
| RPS9 | -3133 | 
| RPL35A | -3125 | 
| RPL37 | -3121 | 
| RPL11 | -3116 | 
| RPS5 | -3098 | 
| EIF3K | -3095 | 
| RPS14 | -3088 | 
| RPS7 | -3072 | 
| RPL30 | -3071 | 
| RPL10A | -3051 | 
| RPL14 | -3046 | 
| RPS16 | -3045 | 
| RPS15A | -3005 | 
| RPS27 | -2985 | 
| RPL24 | -2957 | 
| RPL8 | -2956 | 
| RPS8 | -2950 | 
| RPL10 | -2947 | 
| RPL21 | -2945 | 
| RPL28 | -2926 | 
| RPL27 | -2923 | 
| RPS25 | -2902 | 
| RPS3 | -2869 | 
| RPL36A | -2858 | 
| RPS27A | -2821 | 
| RPL22 | -2796 | 
| RPL23A | -2793 | 
| RPS23 | -2783 | 
| RPL3 | -2782 | 
| RPL26 | -2774 | 
| RPS4Y1 | -2771 | 
| RPL7A | -2766 | 
| RPS10 | -2749 | 
| RPS3A | -2745 | 
| RPS19 | -2714 | 
| RPL36AL | -2703 | 
| RPL18 | -2699 | 
| RPL6 | -2665 | 
| EIF3I | -2640 | 
| RPS27L | -2611 | 
| RPL26L1 | -2572 | 
| RPL29 | -2433 | 
| EIF3J | -2427 | 
| RPL4 | -2374 | 
| RPL27A | -2238 | 
| EIF3D | -2163 | 
| RPS13 | -2162 | 
| RPS6 | -2137 | 
| RPL15 | -2045 | 
| EIF3G | -2009 | 
| EIF3M | -1989 | 
| RPL17 | -1968 | 
| RPLP0 | -1966 | 
| RPL22L1 | -985 | 
| EIF1AX | -952 | 
| RPL5 | -485 | 
| RPL12 | -443 | 
| RPS17 | 7 | 
| RPL31 | 20 | 
| EIF3F | 71 | 
| RPL7 | 108 | 
| EIF3L | 121 | 
| EIF3E | 252 | 
| RPS2 | 319 | 
| EIF3H | 376 | 
| RPS4X | 1068 | 
| RPL9 | 1356 | 
| RPS11 | 1556 | 
| RPL23 | 1657 | 
| EIF3A | 2251 | 
| EIF3B | 3737 | 
| RPL39L | 3853 | 
| RPL13A | 5851 | 
| RPS20 | 6819 | 
 SRP-dependent cotranslational protein targeting to membrane 
| 986 | |
|---|---|
| set | SRP-dependent cotranslational protein targeting to membrane | 
| setSize | 109 | 
| pANOVA | 4.36e-44 | 
| s.dist | -0.771 | 
| p.adjustANOVA | 1.42e-41 | 
Top enriched genes
| GeneID | Gene Rank | 
|---|---|
| RPS28 | -3265 | 
| RPL36 | -3263 | 
| RPL35 | -3250 | 
| RPS29 | -3247 | 
| RPS21 | -3244 | 
| RPL32 | -3239 | 
| RPL19 | -3232 | 
| RPL39 | -3228 | 
| UBA52 | -3224 | 
| RPS18 | -3220 | 
| RPS26 | -3215 | 
| RPLP2 | -3212 | 
| FAU | -3209 | 
| RPS15 | -3207 | 
| RPLP1 | -3206 | 
| RPL41 | -3204 | 
| RPL38 | -3177 | 
| RPS12 | -3173 | 
| RPL34 | -3171 | 
| RPS24 | -3160 | 
| GeneID | Gene Rank | 
|---|---|
| RPS28 | -3265 | 
| RPL36 | -3263 | 
| RPL35 | -3250 | 
| RPS29 | -3247 | 
| RPS21 | -3244 | 
| RPL32 | -3239 | 
| RPL19 | -3232 | 
| RPL39 | -3228 | 
| UBA52 | -3224 | 
| RPS18 | -3220 | 
| RPS26 | -3215 | 
| RPLP2 | -3212 | 
| FAU | -3209 | 
| RPS15 | -3207 | 
| RPLP1 | -3206 | 
| RPL41 | -3204 | 
| RPL38 | -3177 | 
| RPS12 | -3173 | 
| RPL34 | -3171 | 
| RPS24 | -3160 | 
| RPL13 | -3154 | 
| RPL18A | -3141 | 
| RPL37A | -3140 | 
| RPSA | -3139 | 
| SPCS2 | -3137 | 
| RPS9 | -3133 | 
| RPL35A | -3125 | 
| RPL37 | -3121 | 
| RPL11 | -3116 | 
| RPS5 | -3098 | 
| RPS14 | -3088 | 
| SEC61G | -3077 | 
| RPS7 | -3072 | 
| RPL30 | -3071 | 
| RPL10A | -3051 | 
| RPL14 | -3046 | 
| RPS16 | -3045 | 
| RPS15A | -3005 | 
| SSR4 | -2999 | 
| RPS27 | -2985 | 
| SRP14 | -2976 | 
| RPL24 | -2957 | 
| RPL8 | -2956 | 
| RPS8 | -2950 | 
| RPL10 | -2947 | 
| RPL21 | -2945 | 
| SSR3 | -2931 | 
| SEC61B | -2927 | 
| RPL28 | -2926 | 
| RPL27 | -2923 | 
| RPS25 | -2902 | 
| RPS3 | -2869 | 
| RPL36A | -2858 | 
| SSR2 | -2823 | 
| RPS27A | -2821 | 
| RPL22 | -2796 | 
| RPL23A | -2793 | 
| RPS23 | -2783 | 
| RPL3 | -2782 | 
| RPL26 | -2774 | 
| RPS4Y1 | -2771 | 
| RPL7A | -2766 | 
| RPS10 | -2749 | 
| RPS3A | -2745 | 
| SPCS3 | -2728 | 
| RPS19 | -2714 | 
| RPL36AL | -2703 | 
| RPL18 | -2699 | 
| SEC11C | -2673 | 
| RPL6 | -2665 | 
| RPS27L | -2611 | 
| RPL26L1 | -2572 | 
| SRPRB | -2462 | 
| RPL29 | -2433 | 
| DDOST | -2414 | 
| RPL4 | -2374 | 
| RPL27A | -2238 | 
| RPN2 | -2180 | 
| RPS13 | -2162 | 
| SEC11A | -2141 | 
| RPS6 | -2137 | 
| SRP9 | -2106 | 
| RPL15 | -2045 | 
| RPL17 | -1968 | 
| RPLP0 | -1966 | 
| SRPRA | -1035 | 
| RPL22L1 | -985 | 
| SRP68 | -746 | 
| SEC61A1 | -605 | 
| RPL5 | -485 | 
| RPL12 | -443 | 
| SRP19 | -235 | 
| RPS17 | 7 | 
| RPL31 | 20 | 
| RPL7 | 108 | 
| RPN1 | 204 | 
| RPS2 | 319 | 
| SPCS1 | 403 | 
| TRAM1 | 581 | 
| RPS4X | 1068 | 
| RPL9 | 1356 | 
| RPS11 | 1556 | 
| SRP72 | 1654 | 
| RPL23 | 1657 | 
| RPL39L | 3853 | 
| SSR1 | 3991 | 
| SRP54 | 4755 | 
| RPL13A | 5851 | 
| RPS20 | 6819 | 
 SARS-CoV-1 modulates host translation machinery 
| 970 | |
|---|---|
| set | SARS-CoV-1 modulates host translation machinery | 
| setSize | 36 | 
| pANOVA | 1.67e-15 | 
| s.dist | -0.767 | 
| p.adjustANOVA | 2.35e-14 | 
Top enriched genes
| GeneID | Gene Rank | 
|---|---|
| RPS28 | -3265 | 
| RPS29 | -3247 | 
| RPS21 | -3244 | 
| RPS18 | -3220 | 
| RPS26 | -3215 | 
| FAU | -3209 | 
| RPS15 | -3207 | 
| RPS12 | -3173 | 
| RPS24 | -3160 | 
| RPSA | -3139 | 
| RPS9 | -3133 | 
| RPS5 | -3098 | 
| RPS14 | -3088 | 
| RPS7 | -3072 | 
| RPS16 | -3045 | 
| RPS15A | -3005 | 
| RPS27 | -2985 | 
| RPS8 | -2950 | 
| RPS25 | -2902 | 
| RPS3 | -2869 | 
| GeneID | Gene Rank | 
|---|---|
| RPS28 | -3265 | 
| RPS29 | -3247 | 
| RPS21 | -3244 | 
| RPS18 | -3220 | 
| RPS26 | -3215 | 
| FAU | -3209 | 
| RPS15 | -3207 | 
| RPS12 | -3173 | 
| RPS24 | -3160 | 
| RPSA | -3139 | 
| RPS9 | -3133 | 
| RPS5 | -3098 | 
| RPS14 | -3088 | 
| RPS7 | -3072 | 
| RPS16 | -3045 | 
| RPS15A | -3005 | 
| RPS27 | -2985 | 
| RPS8 | -2950 | 
| RPS25 | -2902 | 
| RPS3 | -2869 | 
| RPS27A | -2821 | 
| RPS23 | -2783 | 
| RPS4Y1 | -2771 | 
| RPS10 | -2749 | 
| RPS3A | -2745 | 
| RPS19 | -2714 | 
| RPS27L | -2611 | 
| HNRNPA1 | -2478 | 
| RPS13 | -2162 | 
| RPS6 | -2137 | 
| RPS17 | 7 | 
| RPS2 | 319 | 
| RPS4X | 1068 | 
| RPS11 | 1556 | 
| RPS20 | 6819 | 
| EEF1A1 | 7185 | 
 Selenocysteine synthesis 
| 1006 | |
|---|---|
| set | Selenocysteine synthesis | 
| setSize | 90 | 
| pANOVA | 7.1e-36 | 
| s.dist | -0.761 | 
| p.adjustANOVA | 4.86e-34 | 
Top enriched genes
| GeneID | Gene Rank | 
|---|---|
| RPS28 | -3265 | 
| RPL36 | -3263 | 
| RPL35 | -3250 | 
| RPS29 | -3247 | 
| RPS21 | -3244 | 
| RPL32 | -3239 | 
| RPL19 | -3232 | 
| RPL39 | -3228 | 
| UBA52 | -3224 | 
| RPS18 | -3220 | 
| RPS26 | -3215 | 
| RPLP2 | -3212 | 
| FAU | -3209 | 
| RPS15 | -3207 | 
| RPLP1 | -3206 | 
| RPL41 | -3204 | 
| RPL38 | -3177 | 
| RPS12 | -3173 | 
| RPL34 | -3171 | 
| RPS24 | -3160 | 
| GeneID | Gene Rank | 
|---|---|
| RPS28 | -3265 | 
| RPL36 | -3263 | 
| RPL35 | -3250 | 
| RPS29 | -3247 | 
| RPS21 | -3244 | 
| RPL32 | -3239 | 
| RPL19 | -3232 | 
| RPL39 | -3228 | 
| UBA52 | -3224 | 
| RPS18 | -3220 | 
| RPS26 | -3215 | 
| RPLP2 | -3212 | 
| FAU | -3209 | 
| RPS15 | -3207 | 
| RPLP1 | -3206 | 
| RPL41 | -3204 | 
| RPL38 | -3177 | 
| RPS12 | -3173 | 
| RPL34 | -3171 | 
| RPS24 | -3160 | 
| RPL13 | -3154 | 
| RPL18A | -3141 | 
| RPL37A | -3140 | 
| RPSA | -3139 | 
| RPS9 | -3133 | 
| RPL35A | -3125 | 
| RPL37 | -3121 | 
| RPL11 | -3116 | 
| RPS5 | -3098 | 
| RPS14 | -3088 | 
| RPS7 | -3072 | 
| RPL30 | -3071 | 
| RPL10A | -3051 | 
| RPL14 | -3046 | 
| RPS16 | -3045 | 
| RPS15A | -3005 | 
| RPS27 | -2985 | 
| RPL24 | -2957 | 
| RPL8 | -2956 | 
| RPS8 | -2950 | 
| RPL10 | -2947 | 
| RPL21 | -2945 | 
| RPL28 | -2926 | 
| RPL27 | -2923 | 
| RPS25 | -2902 | 
| RPS3 | -2869 | 
| RPL36A | -2858 | 
| RPS27A | -2821 | 
| RPL22 | -2796 | 
| RPL23A | -2793 | 
| RPS23 | -2783 | 
| RPL3 | -2782 | 
| RPL26 | -2774 | 
| RPS4Y1 | -2771 | 
| RPL7A | -2766 | 
| RPS10 | -2749 | 
| RPS3A | -2745 | 
| RPS19 | -2714 | 
| RPL36AL | -2703 | 
| RPL18 | -2699 | 
| RPL6 | -2665 | 
| RPS27L | -2611 | 
| RPL26L1 | -2572 | 
| RPL29 | -2433 | 
| RPL4 | -2374 | 
| RPL27A | -2238 | 
| RPS13 | -2162 | 
| RPS6 | -2137 | 
| RPL15 | -2045 | 
| RPL17 | -1968 | 
| RPLP0 | -1966 | 
| RPL22L1 | -985 | 
| RPL5 | -485 | 
| RPL12 | -443 | 
| RPS17 | 7 | 
| RPL31 | 20 | 
| RPL7 | 108 | 
| RPS2 | 319 | 
| SEPSECS | 448 | 
| RPS4X | 1068 | 
| SEPHS2 | 1328 | 
| RPL9 | 1356 | 
| RPS11 | 1556 | 
| RPL23 | 1657 | 
| PSTK | 1750 | 
| EEFSEC | 3673 | 
| RPL39L | 3853 | 
| SECISBP2 | 5516 | 
| RPL13A | 5851 | 
| RPS20 | 6819 | 
 Folding of actin by CCT/TriC 
| 344 | |
|---|---|
| set | Folding of actin by CCT/TriC | 
| setSize | 10 | 
| pANOVA | 3.37e-05 | 
| s.dist | -0.757 | 
| p.adjustANOVA | 0.000205 | 
Top enriched genes
| GeneID | Gene Rank | 
|---|---|
| ACTB | -3267 | 
| CCT8 | -2762 | 
| CCT7 | -2743 | 
| CCT4 | -2649 | 
| CCT3 | -2593 | 
| CCT2 | -2573 | 
| CCT5 | -2406 | 
| TCP1 | -1872 | 
| CCT6A | 139 | 
| CCT6B | 1343 | 
| GeneID | Gene Rank | 
|---|---|
| ACTB | -3267 | 
| CCT8 | -2762 | 
| CCT7 | -2743 | 
| CCT4 | -2649 | 
| CCT3 | -2593 | 
| CCT2 | -2573 | 
| CCT5 | -2406 | 
| TCP1 | -1872 | 
| CCT6A | 139 | 
| CCT6B | 1343 | 
 Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC) 
| 687 | |
|---|---|
| set | Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC) | 
| setSize | 93 | 
| pANOVA | 1.37e-35 | 
| s.dist | -0.746 | 
| p.adjustANOVA | 8.46e-34 | 
Top enriched genes
| GeneID | Gene Rank | 
|---|---|
| RPS28 | -3265 | 
| RPL36 | -3263 | 
| RPL35 | -3250 | 
| RPS29 | -3247 | 
| RPS21 | -3244 | 
| RPL32 | -3239 | 
| RPL19 | -3232 | 
| RPL39 | -3228 | 
| UBA52 | -3224 | 
| RPS18 | -3220 | 
| RPS26 | -3215 | 
| RPLP2 | -3212 | 
| FAU | -3209 | 
| RPS15 | -3207 | 
| RPLP1 | -3206 | 
| RPL41 | -3204 | 
| RPL38 | -3177 | 
| RPS12 | -3173 | 
| RPL34 | -3171 | 
| RPS24 | -3160 | 
| GeneID | Gene Rank | 
|---|---|
| RPS28 | -3265 | 
| RPL36 | -3263 | 
| RPL35 | -3250 | 
| RPS29 | -3247 | 
| RPS21 | -3244 | 
| RPL32 | -3239 | 
| RPL19 | -3232 | 
| RPL39 | -3228 | 
| UBA52 | -3224 | 
| RPS18 | -3220 | 
| RPS26 | -3215 | 
| RPLP2 | -3212 | 
| FAU | -3209 | 
| RPS15 | -3207 | 
| RPLP1 | -3206 | 
| RPL41 | -3204 | 
| RPL38 | -3177 | 
| RPS12 | -3173 | 
| RPL34 | -3171 | 
| RPS24 | -3160 | 
| RPL13 | -3154 | 
| RPL18A | -3141 | 
| RPL37A | -3140 | 
| RPSA | -3139 | 
| RPS9 | -3133 | 
| RPL35A | -3125 | 
| RPL37 | -3121 | 
| RPL11 | -3116 | 
| RPS5 | -3098 | 
| RPS14 | -3088 | 
| RPS7 | -3072 | 
| RPL30 | -3071 | 
| RPL10A | -3051 | 
| RPL14 | -3046 | 
| RPS16 | -3045 | 
| RPS15A | -3005 | 
| RPS27 | -2985 | 
| RPL24 | -2957 | 
| RPL8 | -2956 | 
| RPS8 | -2950 | 
| RPL10 | -2947 | 
| RPL21 | -2945 | 
| RPL28 | -2926 | 
| RPL27 | -2923 | 
| RPS25 | -2902 | 
| RPS3 | -2869 | 
| RPL36A | -2858 | 
| RPS27A | -2821 | 
| RPL22 | -2796 | 
| RPL23A | -2793 | 
| RPS23 | -2783 | 
| RPL3 | -2782 | 
| RPL26 | -2774 | 
| RPS4Y1 | -2771 | 
| RPL7A | -2766 | 
| RPS10 | -2749 | 
| RPS3A | -2745 | 
| RPS19 | -2714 | 
| RPL36AL | -2703 | 
| RPL18 | -2699 | 
| RPL6 | -2665 | 
| RPS27L | -2611 | 
| RPL26L1 | -2572 | 
| RPL29 | -2433 | 
| RPL4 | -2374 | 
| RPL27A | -2238 | 
| RPS13 | -2162 | 
| RPS6 | -2137 | 
| RPL15 | -2045 | 
| RPL17 | -1968 | 
| RPLP0 | -1966 | 
| GSPT2 | -1653 | 
| RPL22L1 | -985 | 
| RPL5 | -485 | 
| RPL12 | -443 | 
| NCBP2 | -191 | 
| GSPT1 | -159 | 
| RPS17 | 7 | 
| RPL31 | 20 | 
| RPL7 | 108 | 
| RPS2 | 319 | 
| ETF1 | 467 | 
| RPS4X | 1068 | 
| RPL9 | 1356 | 
| RPS11 | 1556 | 
| RPL23 | 1657 | 
| UPF1 | 2667 | 
| EIF4G1 | 2728 | 
| NCBP1 | 3424 | 
| RPL39L | 3853 | 
| RPL13A | 5851 | 
| RPS20 | 6819 | 
| PABPC1 | 7504 | 
 SARS-CoV-2 modulates host translation machinery 
| 976 | |
|---|---|
| set | SARS-CoV-2 modulates host translation machinery | 
| setSize | 47 | 
| pANOVA | 8.64e-19 | 
| s.dist | -0.746 | 
| p.adjustANOVA | 2.39e-17 | 
Top enriched genes
| GeneID | Gene Rank | 
|---|---|
| RPS28 | -3265 | 
| RPS29 | -3247 | 
| RPS21 | -3244 | 
| RPS18 | -3220 | 
| RPS26 | -3215 | 
| FAU | -3209 | 
| RPS15 | -3207 | 
| RPS12 | -3173 | 
| RPS24 | -3160 | 
| RPSA | -3139 | 
| RPS9 | -3133 | 
| RPS5 | -3098 | 
| RPS14 | -3088 | 
| RPS7 | -3072 | 
| RPS16 | -3045 | 
| RPS15A | -3005 | 
| SNRPD1 | -2998 | 
| RPS27 | -2985 | 
| SNRPD2 | -2978 | 
| RPS8 | -2950 | 
| GeneID | Gene Rank | 
|---|---|
| RPS28 | -3265 | 
| RPS29 | -3247 | 
| RPS21 | -3244 | 
| RPS18 | -3220 | 
| RPS26 | -3215 | 
| FAU | -3209 | 
| RPS15 | -3207 | 
| RPS12 | -3173 | 
| RPS24 | -3160 | 
| RPSA | -3139 | 
| RPS9 | -3133 | 
| RPS5 | -3098 | 
| RPS14 | -3088 | 
| RPS7 | -3072 | 
| RPS16 | -3045 | 
| RPS15A | -3005 | 
| SNRPD1 | -2998 | 
| RPS27 | -2985 | 
| SNRPD2 | -2978 | 
| RPS8 | -2950 | 
| SNRPF | -2934 | 
| RPS25 | -2902 | 
| SNRPG | -2874 | 
| RPS3 | -2869 | 
| SNRPB | -2830 | 
| RPS27A | -2821 | 
| RPS23 | -2783 | 
| SNRPE | -2776 | 
| RPS4Y1 | -2771 | 
| RPS10 | -2749 | 
| RPS3A | -2745 | 
| RPS19 | -2714 | 
| RPS27L | -2611 | 
| RPS13 | -2162 | 
| RPS6 | -2137 | 
| GEMIN6 | -1391 | 
| GEMIN7 | -870 | 
| SNRPD3 | -150 | 
| RPS17 | 7 | 
| RPS2 | 319 | 
| RPS4X | 1068 | 
| GEMIN5 | 1449 | 
| RPS11 | 1556 | 
| DDX20 | 1757 | 
| GEMIN8 | 2496 | 
| GEMIN2 | 2558 | 
| RPS20 | 6819 | 
 Formation of ATP by chemiosmotic coupling 
| 345 | |
|---|---|
| set | Formation of ATP by chemiosmotic coupling | 
| setSize | 18 | 
| pANOVA | 6.58e-08 | 
| s.dist | -0.735 | 
| p.adjustANOVA | 5.45e-07 | 
Top enriched genes
| GeneID | Gene Rank | 
|---|---|
| ATP5MF | -3261 | 
| ATP5F1E | -3260 | 
| ATP5ME | -3233 | 
| ATP5MC3 | -3201 | 
| ATP5MG | -3168 | 
| ATP5PD | -3162 | 
| ATP5MC2 | -3158 | 
| ATP5PF | -3132 | 
| ATP5MC1 | -3120 | 
| ATP5F1D | -3106 | 
| ATP5F1B | -3039 | 
| ATP5PO | -2940 | 
| ATP5PB | -2817 | 
| ATP5F1C | -2738 | 
| ATP5F1A | -2508 | 
| DMAC2L | -1795 | 
| MT-ATP6 | 7354 | 
| MT-ATP8 | 7606 | 
| GeneID | Gene Rank | 
|---|---|
| ATP5MF | -3261 | 
| ATP5F1E | -3260 | 
| ATP5ME | -3233 | 
| ATP5MC3 | -3201 | 
| ATP5MG | -3168 | 
| ATP5PD | -3162 | 
| ATP5MC2 | -3158 | 
| ATP5PF | -3132 | 
| ATP5MC1 | -3120 | 
| ATP5F1D | -3106 | 
| ATP5F1B | -3039 | 
| ATP5PO | -2940 | 
| ATP5PB | -2817 | 
| ATP5F1C | -2738 | 
| ATP5F1A | -2508 | 
| DMAC2L | -1795 | 
| MT-ATP6 | 7354 | 
| MT-ATP8 | 7606 | 
 GTP hydrolysis and joining of the 60S ribosomal subunit 
| 394 | |
|---|---|
| set | GTP hydrolysis and joining of the 60S ribosomal subunit | 
| setSize | 109 | 
| pANOVA | 4.48e-39 | 
| s.dist | -0.724 | 
| p.adjustANOVA | 5.3e-37 | 
Top enriched genes
| GeneID | Gene Rank | 
|---|---|
| RPS28 | -3265 | 
| RPL36 | -3263 | 
| RPL35 | -3250 | 
| RPS29 | -3247 | 
| RPS21 | -3244 | 
| RPL32 | -3239 | 
| RPL19 | -3232 | 
| RPL39 | -3228 | 
| UBA52 | -3224 | 
| RPS18 | -3220 | 
| RPS26 | -3215 | 
| RPLP2 | -3212 | 
| FAU | -3209 | 
| RPS15 | -3207 | 
| RPLP1 | -3206 | 
| RPL41 | -3204 | 
| RPL38 | -3177 | 
| RPS12 | -3173 | 
| RPL34 | -3171 | 
| RPS24 | -3160 | 
| GeneID | Gene Rank | 
|---|---|
| RPS28 | -3265 | 
| RPL36 | -3263 | 
| RPL35 | -3250 | 
| RPS29 | -3247 | 
| RPS21 | -3244 | 
| RPL32 | -3239 | 
| RPL19 | -3232 | 
| RPL39 | -3228 | 
| UBA52 | -3224 | 
| RPS18 | -3220 | 
| RPS26 | -3215 | 
| RPLP2 | -3212 | 
| FAU | -3209 | 
| RPS15 | -3207 | 
| RPLP1 | -3206 | 
| RPL41 | -3204 | 
| RPL38 | -3177 | 
| RPS12 | -3173 | 
| RPL34 | -3171 | 
| RPS24 | -3160 | 
| RPL13 | -3154 | 
| RPL18A | -3141 | 
| RPL37A | -3140 | 
| RPSA | -3139 | 
| RPS9 | -3133 | 
| EIF4A1 | -3130 | 
| RPL35A | -3125 | 
| RPL37 | -3121 | 
| RPL11 | -3116 | 
| RPS5 | -3098 | 
| EIF3K | -3095 | 
| RPS14 | -3088 | 
| RPS7 | -3072 | 
| RPL30 | -3071 | 
| RPL10A | -3051 | 
| RPL14 | -3046 | 
| RPS16 | -3045 | 
| RPS15A | -3005 | 
| RPS27 | -2985 | 
| RPL24 | -2957 | 
| RPL8 | -2956 | 
| RPS8 | -2950 | 
| RPL10 | -2947 | 
| RPL21 | -2945 | 
| RPL28 | -2926 | 
| RPL27 | -2923 | 
| RPS25 | -2902 | 
| RPS3 | -2869 | 
| RPL36A | -2858 | 
| RPS27A | -2821 | 
| RPL22 | -2796 | 
| RPL23A | -2793 | 
| RPS23 | -2783 | 
| RPL3 | -2782 | 
| RPL26 | -2774 | 
| RPS4Y1 | -2771 | 
| RPL7A | -2766 | 
| RPS10 | -2749 | 
| RPS3A | -2745 | 
| RPS19 | -2714 | 
| RPL36AL | -2703 | 
| RPL18 | -2699 | 
| RPL6 | -2665 | 
| EIF3I | -2640 | 
| RPS27L | -2611 | 
| EIF4E | -2583 | 
| RPL26L1 | -2572 | 
| EIF5B | -2440 | 
| RPL29 | -2433 | 
| EIF3J | -2427 | 
| RPL4 | -2374 | 
| RPL27A | -2238 | 
| EIF3D | -2163 | 
| RPS13 | -2162 | 
| RPS6 | -2137 | 
| RPL15 | -2045 | 
| EIF3G | -2009 | 
| EIF3M | -1989 | 
| RPL17 | -1968 | 
| RPLP0 | -1966 | 
| EIF2S1 | -1641 | 
| RPL22L1 | -985 | 
| EIF1AX | -952 | 
| EIF2S2 | -901 | 
| RPL5 | -485 | 
| RPL12 | -443 | 
| RPS17 | 7 | 
| RPL31 | 20 | 
| EIF3F | 71 | 
| RPL7 | 108 | 
| EIF3L | 121 | 
| EIF3E | 252 | 
| RPS2 | 319 | 
| EIF4H | 357 | 
| EIF3H | 376 | 
| EIF2S3 | 459 | 
| RPS4X | 1068 | 
| RPL9 | 1356 | 
| RPS11 | 1556 | 
| RPL23 | 1657 | 
| EIF3A | 2251 | 
| EIF5 | 2257 | 
| EIF4G1 | 2728 | 
| EIF3B | 3737 | 
| RPL39L | 3853 | 
| EIF4A2 | 4936 | 
| RPL13A | 5851 | 
| RPS20 | 6819 | 
| EIF4B | 7359 | 
 Formation of the ternary complex, and subsequently, the 43S complex 
| 360 | |
|---|---|
| set | Formation of the ternary complex, and subsequently, the 43S complex | 
| setSize | 50 | 
| pANOVA | 1e-18 | 
| s.dist | -0.722 | 
| p.adjustANOVA | 2.71e-17 | 
Top enriched genes
| GeneID | Gene Rank | 
|---|---|
| RPS28 | -3265 | 
| RPS29 | -3247 | 
| RPS21 | -3244 | 
| RPS18 | -3220 | 
| RPS26 | -3215 | 
| FAU | -3209 | 
| RPS15 | -3207 | 
| RPS12 | -3173 | 
| RPS24 | -3160 | 
| RPSA | -3139 | 
| RPS9 | -3133 | 
| RPS5 | -3098 | 
| EIF3K | -3095 | 
| RPS14 | -3088 | 
| RPS7 | -3072 | 
| RPS16 | -3045 | 
| RPS15A | -3005 | 
| RPS27 | -2985 | 
| RPS8 | -2950 | 
| RPS25 | -2902 | 
| GeneID | Gene Rank | 
|---|---|
| RPS28 | -3265 | 
| RPS29 | -3247 | 
| RPS21 | -3244 | 
| RPS18 | -3220 | 
| RPS26 | -3215 | 
| FAU | -3209 | 
| RPS15 | -3207 | 
| RPS12 | -3173 | 
| RPS24 | -3160 | 
| RPSA | -3139 | 
| RPS9 | -3133 | 
| RPS5 | -3098 | 
| EIF3K | -3095 | 
| RPS14 | -3088 | 
| RPS7 | -3072 | 
| RPS16 | -3045 | 
| RPS15A | -3005 | 
| RPS27 | -2985 | 
| RPS8 | -2950 | 
| RPS25 | -2902 | 
| RPS3 | -2869 | 
| RPS27A | -2821 | 
| RPS23 | -2783 | 
| RPS4Y1 | -2771 | 
| RPS10 | -2749 | 
| RPS3A | -2745 | 
| RPS19 | -2714 | 
| EIF3I | -2640 | 
| RPS27L | -2611 | 
| EIF3J | -2427 | 
| EIF3D | -2163 | 
| RPS13 | -2162 | 
| RPS6 | -2137 | 
| EIF3G | -2009 | 
| EIF3M | -1989 | 
| EIF2S1 | -1641 | 
| EIF1AX | -952 | 
| EIF2S2 | -901 | 
| RPS17 | 7 | 
| EIF3F | 71 | 
| EIF3L | 121 | 
| EIF3E | 252 | 
| RPS2 | 319 | 
| EIF3H | 376 | 
| EIF2S3 | 459 | 
| RPS4X | 1068 | 
| RPS11 | 1556 | 
| EIF3A | 2251 | 
| EIF3B | 3737 | 
| RPS20 | 6819 | 
 Selenoamino acid metabolism 
| 1005 | |
|---|---|
| set | Selenoamino acid metabolism | 
| setSize | 101 | 
| pANOVA | 2.25e-35 | 
| s.dist | -0.714 | 
| p.adjustANOVA | 1.27e-33 | 
Top enriched genes
| GeneID | Gene Rank | 
|---|---|
| RPS28 | -3265 | 
| RPL36 | -3263 | 
| RPL35 | -3250 | 
| RPS29 | -3247 | 
| RPS21 | -3244 | 
| RPL32 | -3239 | 
| RPL19 | -3232 | 
| RPL39 | -3228 | 
| UBA52 | -3224 | 
| RPS18 | -3220 | 
| RPS26 | -3215 | 
| RPLP2 | -3212 | 
| FAU | -3209 | 
| RPS15 | -3207 | 
| RPLP1 | -3206 | 
| RPL41 | -3204 | 
| RPL38 | -3177 | 
| RPS12 | -3173 | 
| RPL34 | -3171 | 
| RPS24 | -3160 | 
| GeneID | Gene Rank | 
|---|---|
| RPS28 | -3265 | 
| RPL36 | -3263 | 
| RPL35 | -3250 | 
| RPS29 | -3247 | 
| RPS21 | -3244 | 
| RPL32 | -3239 | 
| RPL19 | -3232 | 
| RPL39 | -3228 | 
| UBA52 | -3224 | 
| RPS18 | -3220 | 
| RPS26 | -3215 | 
| RPLP2 | -3212 | 
| FAU | -3209 | 
| RPS15 | -3207 | 
| RPLP1 | -3206 | 
| RPL41 | -3204 | 
| RPL38 | -3177 | 
| RPS12 | -3173 | 
| RPL34 | -3171 | 
| RPS24 | -3160 | 
| RPL13 | -3154 | 
| RPL18A | -3141 | 
| RPL37A | -3140 | 
| RPSA | -3139 | 
| RPS9 | -3133 | 
| RPL35A | -3125 | 
| RPL37 | -3121 | 
| RPL11 | -3116 | 
| RPS5 | -3098 | 
| RPS14 | -3088 | 
| RPS7 | -3072 | 
| RPL30 | -3071 | 
| RPL10A | -3051 | 
| RPL14 | -3046 | 
| RPS16 | -3045 | 
| RPS15A | -3005 | 
| RPS27 | -2985 | 
| RPL24 | -2957 | 
| RPL8 | -2956 | 
| RPS8 | -2950 | 
| RPL10 | -2947 | 
| RPL21 | -2945 | 
| RPL28 | -2926 | 
| RPL27 | -2923 | 
| RPS25 | -2902 | 
| RPS3 | -2869 | 
| RPL36A | -2858 | 
| RPS27A | -2821 | 
| RPL22 | -2796 | 
| RPL23A | -2793 | 
| RPS23 | -2783 | 
| RPL3 | -2782 | 
| RPL26 | -2774 | 
| RPS4Y1 | -2771 | 
| RPL7A | -2766 | 
| RPS10 | -2749 | 
| RPS3A | -2745 | 
| RPS19 | -2714 | 
| RPL36AL | -2703 | 
| RPL18 | -2699 | 
| RPL6 | -2665 | 
| RPS27L | -2611 | 
| RPL26L1 | -2572 | 
| RPL29 | -2433 | 
| RPL4 | -2374 | 
| AHCY | -2293 | 
| RPL27A | -2238 | 
| RPS13 | -2162 | 
| RPS6 | -2137 | 
| AIMP1 | -2119 | 
| RPL15 | -2045 | 
| HNMT | -1976 | 
| RPL17 | -1968 | 
| RPLP0 | -1966 | 
| RPL22L1 | -985 | 
| PAPSS1 | -774 | 
| AIMP2 | -550 | 
| EEF1E1 | -535 | 
| RPL5 | -485 | 
| RPL12 | -443 | 
| GSR | -417 | 
| RPS17 | 7 | 
| RPL31 | 20 | 
| RPL7 | 108 | 
| RPS2 | 319 | 
| SEPSECS | 448 | 
| CTH | 706 | 
| RPS4X | 1068 | 
| SEPHS2 | 1328 | 
| RPL9 | 1356 | 
| RPS11 | 1556 | 
| RPL23 | 1657 | 
| PSTK | 1750 | 
| TXNRD1 | 1901 | 
| EEFSEC | 3673 | 
| RPL39L | 3853 | 
| SCLY | 3855 | 
| SECISBP2 | 5516 | 
| RPL13A | 5851 | 
| RPS20 | 6819 | 
| PAPSS2 | 7415 | 
 L13a-mediated translational silencing of Ceruloplasmin expression 
| 541 | |
|---|---|
| set | L13a-mediated translational silencing of Ceruloplasmin expression | 
| setSize | 108 | 
| pANOVA | 1.11e-37 | 
| s.dist | -0.714 | 
| p.adjustANOVA | 8.98e-36 | 
Top enriched genes
| GeneID | Gene Rank | 
|---|---|
| RPS28 | -3265 | 
| RPL36 | -3263 | 
| RPL35 | -3250 | 
| RPS29 | -3247 | 
| RPS21 | -3244 | 
| RPL32 | -3239 | 
| RPL19 | -3232 | 
| RPL39 | -3228 | 
| UBA52 | -3224 | 
| RPS18 | -3220 | 
| RPS26 | -3215 | 
| RPLP2 | -3212 | 
| FAU | -3209 | 
| RPS15 | -3207 | 
| RPLP1 | -3206 | 
| RPL41 | -3204 | 
| RPL38 | -3177 | 
| RPS12 | -3173 | 
| RPL34 | -3171 | 
| RPS24 | -3160 | 
| GeneID | Gene Rank | 
|---|---|
| RPS28 | -3265 | 
| RPL36 | -3263 | 
| RPL35 | -3250 | 
| RPS29 | -3247 | 
| RPS21 | -3244 | 
| RPL32 | -3239 | 
| RPL19 | -3232 | 
| RPL39 | -3228 | 
| UBA52 | -3224 | 
| RPS18 | -3220 | 
| RPS26 | -3215 | 
| RPLP2 | -3212 | 
| FAU | -3209 | 
| RPS15 | -3207 | 
| RPLP1 | -3206 | 
| RPL41 | -3204 | 
| RPL38 | -3177 | 
| RPS12 | -3173 | 
| RPL34 | -3171 | 
| RPS24 | -3160 | 
| RPL13 | -3154 | 
| RPL18A | -3141 | 
| RPL37A | -3140 | 
| RPSA | -3139 | 
| RPS9 | -3133 | 
| EIF4A1 | -3130 | 
| RPL35A | -3125 | 
| RPL37 | -3121 | 
| RPL11 | -3116 | 
| RPS5 | -3098 | 
| EIF3K | -3095 | 
| RPS14 | -3088 | 
| RPS7 | -3072 | 
| RPL30 | -3071 | 
| RPL10A | -3051 | 
| RPL14 | -3046 | 
| RPS16 | -3045 | 
| RPS15A | -3005 | 
| RPS27 | -2985 | 
| RPL24 | -2957 | 
| RPL8 | -2956 | 
| RPS8 | -2950 | 
| RPL10 | -2947 | 
| RPL21 | -2945 | 
| RPL28 | -2926 | 
| RPL27 | -2923 | 
| RPS25 | -2902 | 
| RPS3 | -2869 | 
| RPL36A | -2858 | 
| RPS27A | -2821 | 
| RPL22 | -2796 | 
| RPL23A | -2793 | 
| RPS23 | -2783 | 
| RPL3 | -2782 | 
| RPL26 | -2774 | 
| RPS4Y1 | -2771 | 
| RPL7A | -2766 | 
| RPS10 | -2749 | 
| RPS3A | -2745 | 
| RPS19 | -2714 | 
| RPL36AL | -2703 | 
| RPL18 | -2699 | 
| RPL6 | -2665 | 
| EIF3I | -2640 | 
| RPS27L | -2611 | 
| EIF4E | -2583 | 
| RPL26L1 | -2572 | 
| RPL29 | -2433 | 
| EIF3J | -2427 | 
| RPL4 | -2374 | 
| RPL27A | -2238 | 
| EIF3D | -2163 | 
| RPS13 | -2162 | 
| RPS6 | -2137 | 
| RPL15 | -2045 | 
| EIF3G | -2009 | 
| EIF3M | -1989 | 
| RPL17 | -1968 | 
| RPLP0 | -1966 | 
| EIF2S1 | -1641 | 
| RPL22L1 | -985 | 
| EIF1AX | -952 | 
| EIF2S2 | -901 | 
| RPL5 | -485 | 
| RPL12 | -443 | 
| RPS17 | 7 | 
| RPL31 | 20 | 
| EIF3F | 71 | 
| RPL7 | 108 | 
| EIF3L | 121 | 
| EIF3E | 252 | 
| RPS2 | 319 | 
| EIF4H | 357 | 
| EIF3H | 376 | 
| EIF2S3 | 459 | 
| RPS4X | 1068 | 
| RPL9 | 1356 | 
| RPS11 | 1556 | 
| RPL23 | 1657 | 
| EIF3A | 2251 | 
| EIF4G1 | 2728 | 
| EIF3B | 3737 | 
| RPL39L | 3853 | 
| EIF4A2 | 4936 | 
| RPL13A | 5851 | 
| RPS20 | 6819 | 
| EIF4B | 7359 | 
| PABPC1 | 7504 | 
 Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding 
| 192 | |
|---|---|
| set | Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding | 
| setSize | 25 | 
| pANOVA | 7.36e-10 | 
| s.dist | -0.711 | 
| p.adjustANOVA | 6.69e-09 | 
Top enriched genes
| GeneID | Gene Rank | 
|---|---|
| ACTB | -3267 | 
| PFDN5 | -3192 | 
| TUBA1B | -3174 | 
| PFDN2 | -3122 | 
| PFDN6 | -2895 | 
| TUBB4B | -2873 | 
| CCT8 | -2762 | 
| CCT7 | -2743 | 
| TUBA1A | -2711 | 
| CCT4 | -2649 | 
| CCT3 | -2593 | 
| CCT2 | -2573 | 
| VBP1 | -2454 | 
| CCT5 | -2406 | 
| TUBB2A | -2354 | 
| PFDN4 | -2166 | 
| TUBA1C | -1994 | 
| TCP1 | -1872 | 
| TUBB3 | -1433 | 
| TUBB6 | -1363 | 
| GeneID | Gene Rank | 
|---|---|
| ACTB | -3267 | 
| PFDN5 | -3192 | 
| TUBA1B | -3174 | 
| PFDN2 | -3122 | 
| PFDN6 | -2895 | 
| TUBB4B | -2873 | 
| CCT8 | -2762 | 
| CCT7 | -2743 | 
| TUBA1A | -2711 | 
| CCT4 | -2649 | 
| CCT3 | -2593 | 
| CCT2 | -2573 | 
| VBP1 | -2454 | 
| CCT5 | -2406 | 
| TUBB2A | -2354 | 
| PFDN4 | -2166 | 
| TUBA1C | -1994 | 
| TCP1 | -1872 | 
| TUBB3 | -1433 | 
| TUBB6 | -1363 | 
| CCT6A | 139 | 
| PFDN1 | 390 | 
| CCT6B | 1343 | 
| TUBA4A | 2254 | 
| TUBB4A | 4421 | 
 Response of EIF2AK4 (GCN2) to amino acid deficiency 
| 955 | |
|---|---|
| set | Response of EIF2AK4 (GCN2) to amino acid deficiency | 
| setSize | 98 | 
| pANOVA | 3.95e-34 | 
| s.dist | -0.711 | 
| p.adjustANOVA | 1.97e-32 | 
Top enriched genes
| GeneID | Gene Rank | 
|---|---|
| RPS28 | -3265 | 
| RPL36 | -3263 | 
| RPL35 | -3250 | 
| RPS29 | -3247 | 
| RPS21 | -3244 | 
| RPL32 | -3239 | 
| RPL19 | -3232 | 
| RPL39 | -3228 | 
| UBA52 | -3224 | 
| RPS18 | -3220 | 
| RPS26 | -3215 | 
| RPLP2 | -3212 | 
| FAU | -3209 | 
| RPS15 | -3207 | 
| RPLP1 | -3206 | 
| RPL41 | -3204 | 
| RPL38 | -3177 | 
| RPS12 | -3173 | 
| RPL34 | -3171 | 
| RPS24 | -3160 | 
| GeneID | Gene Rank | 
|---|---|
| RPS28 | -3265 | 
| RPL36 | -3263 | 
| RPL35 | -3250 | 
| RPS29 | -3247 | 
| RPS21 | -3244 | 
| RPL32 | -3239 | 
| RPL19 | -3232 | 
| RPL39 | -3228 | 
| UBA52 | -3224 | 
| RPS18 | -3220 | 
| RPS26 | -3215 | 
| RPLP2 | -3212 | 
| FAU | -3209 | 
| RPS15 | -3207 | 
| RPLP1 | -3206 | 
| RPL41 | -3204 | 
| RPL38 | -3177 | 
| RPS12 | -3173 | 
| RPL34 | -3171 | 
| RPS24 | -3160 | 
| RPL13 | -3154 | 
| RPL18A | -3141 | 
| RPL37A | -3140 | 
| RPSA | -3139 | 
| RPS9 | -3133 | 
| RPL35A | -3125 | 
| RPL37 | -3121 | 
| RPL11 | -3116 | 
| RPS5 | -3098 | 
| RPS14 | -3088 | 
| RPS7 | -3072 | 
| RPL30 | -3071 | 
| RPL10A | -3051 | 
| RPL14 | -3046 | 
| RPS16 | -3045 | 
| RPS15A | -3005 | 
| RPS27 | -2985 | 
| RPL24 | -2957 | 
| RPL8 | -2956 | 
| RPS8 | -2950 | 
| RPL10 | -2947 | 
| RPL21 | -2945 | 
| RPL28 | -2926 | 
| RPL27 | -2923 | 
| RPS25 | -2902 | 
| RPS3 | -2869 | 
| RPL36A | -2858 | 
| RPS27A | -2821 | 
| RPL22 | -2796 | 
| RPL23A | -2793 | 
| RPS23 | -2783 | 
| RPL3 | -2782 | 
| RPL26 | -2774 | 
| RPS4Y1 | -2771 | 
| RPL7A | -2766 | 
| RPS10 | -2749 | 
| RPS3A | -2745 | 
| RPS19 | -2714 | 
| RPL36AL | -2703 | 
| RPL18 | -2699 | 
| RPL6 | -2665 | 
| RPS27L | -2611 | 
| RPL26L1 | -2572 | 
| RPL29 | -2433 | 
| RPL4 | -2374 | 
| RPL27A | -2238 | 
| RPS13 | -2162 | 
| RPS6 | -2137 | 
| RPL15 | -2045 | 
| RPL17 | -1968 | 
| RPLP0 | -1966 | 
| EIF2S1 | -1641 | 
| RPL22L1 | -985 | 
| EIF2S2 | -901 | 
| RPL5 | -485 | 
| RPL12 | -443 | 
| RPS17 | 7 | 
| RPL31 | 20 | 
| DDIT3 | 76 | 
| TRIB3 | 100 | 
| RPL7 | 108 | 
| CEBPB | 164 | 
| RPS2 | 319 | 
| ATF3 | 359 | 
| EIF2S3 | 459 | 
| IMPACT | 782 | 
| RPS4X | 1068 | 
| RPL9 | 1356 | 
| RPS11 | 1556 | 
| RPL23 | 1657 | 
| CEBPG | 3027 | 
| GCN1 | 3507 | 
| RPL39L | 3853 | 
| EIF2AK4 | 5654 | 
| RPL13A | 5851 | 
| ATF2 | 5852 | 
| ATF4 | 6813 | 
| RPS20 | 6819 | 
 Regulation of activated PAK-2p34 by proteasome mediated degradation 
| 927 | |
|---|---|
| set | Regulation of activated PAK-2p34 by proteasome mediated degradation | 
| setSize | 48 | 
| pANOVA | 1.97e-17 | 
| s.dist | -0.708 | 
| p.adjustANOVA | 4.42e-16 | 
Top enriched genes
| GeneID | Gene Rank | 
|---|---|
| UBA52 | -3224 | 
| PSMB6 | -3105 | 
| PSMA7 | -3028 | 
| PSMB3 | -3012 | 
| PSMD8 | -3008 | 
| PSMB1 | -2979 | 
| SEM1 | -2968 | 
| PSMA4 | -2929 | 
| UBC | -2887 | 
| PSMD7 | -2885 | 
| PSMB7 | -2865 | 
| PSMB10 | -2849 | 
| RPS27A | -2821 | 
| PSMA2 | -2803 | 
| PSMA3 | -2787 | 
| PSMB8 | -2753 | 
| PSMA5 | -2655 | 
| PSMB2 | -2644 | 
| PSMD9 | -2638 | 
| PSMA1 | -2401 | 
| GeneID | Gene Rank | 
|---|---|
| UBA52 | -3224 | 
| PSMB6 | -3105 | 
| PSMA7 | -3028 | 
| PSMB3 | -3012 | 
| PSMD8 | -3008 | 
| PSMB1 | -2979 | 
| SEM1 | -2968 | 
| PSMA4 | -2929 | 
| UBC | -2887 | 
| PSMD7 | -2885 | 
| PSMB7 | -2865 | 
| PSMB10 | -2849 | 
| RPS27A | -2821 | 
| PSMA2 | -2803 | 
| PSMA3 | -2787 | 
| PSMB8 | -2753 | 
| PSMA5 | -2655 | 
| PSMB2 | -2644 | 
| PSMD9 | -2638 | 
| PSMA1 | -2401 | 
| PSME2 | -2323 | 
| PSMD4 | -2233 | 
| PSME1 | -2223 | 
| PSMC4 | -2206 | 
| PSMC1 | -2176 | 
| PSMD13 | -2161 | 
| PSMA6 | -2159 | 
| PSMC3 | -2144 | 
| PSMC5 | -2073 | 
| PSMC6 | -2047 | 
| PSMD1 | -2012 | 
| PSMD2 | -1923 | 
| PSMC2 | -1899 | 
| PSMD6 | -1878 | 
| PSMD14 | -1585 | 
| PSMB4 | -1579 | 
| UBB | -975 | 
| PSMD10 | -847 | 
| PSMB9 | -715 | 
| PSMF1 | -455 | 
| PSMD3 | -416 | 
| PSMD11 | -307 | 
| PSME3 | -153 | 
| PSMB5 | 486 | 
| PSMD12 | 1198 | 
| PAK2 | 1997 | 
| PSMD5 | 4230 | 
| PSME4 | 6251 | 
 Regulation of expression of SLITs and ROBOs 
| 930 | |
|---|---|
| set | Regulation of expression of SLITs and ROBOs | 
| setSize | 155 | 
| pANOVA | 2.56e-52 | 
| s.dist | -0.707 | 
| p.adjustANOVA | 1.11e-49 | 
Top enriched genes
| GeneID | Gene Rank | 
|---|---|
| RPS28 | -3265 | 
| RPL36 | -3263 | 
| RPL35 | -3250 | 
| RPS29 | -3247 | 
| RPS21 | -3244 | 
| RPL32 | -3239 | 
| RPL19 | -3232 | 
| RPL39 | -3228 | 
| UBA52 | -3224 | 
| RPS18 | -3220 | 
| RPS26 | -3215 | 
| RPLP2 | -3212 | 
| FAU | -3209 | 
| RPS15 | -3207 | 
| RPLP1 | -3206 | 
| RPL41 | -3204 | 
| RPL38 | -3177 | 
| RPS12 | -3173 | 
| RPL34 | -3171 | 
| RPS24 | -3160 | 
| GeneID | Gene Rank | 
|---|---|
| RPS28 | -3265 | 
| RPL36 | -3263 | 
| RPL35 | -3250 | 
| RPS29 | -3247 | 
| RPS21 | -3244 | 
| RPL32 | -3239 | 
| RPL19 | -3232 | 
| RPL39 | -3228 | 
| UBA52 | -3224 | 
| RPS18 | -3220 | 
| RPS26 | -3215 | 
| RPLP2 | -3212 | 
| FAU | -3209 | 
| RPS15 | -3207 | 
| RPLP1 | -3206 | 
| RPL41 | -3204 | 
| RPL38 | -3177 | 
| RPS12 | -3173 | 
| RPL34 | -3171 | 
| RPS24 | -3160 | 
| RPL13 | -3154 | 
| RPL18A | -3141 | 
| RPL37A | -3140 | 
| RPSA | -3139 | 
| RPS9 | -3133 | 
| RPL35A | -3125 | 
| RPL37 | -3121 | 
| RPL11 | -3116 | 
| PSMB6 | -3105 | 
| RPS5 | -3098 | 
| RPS14 | -3088 | 
| RBX1 | -3082 | 
| RPS7 | -3072 | 
| RPL30 | -3071 | 
| ELOB | -3061 | 
| RPL10A | -3051 | 
| RPL14 | -3046 | 
| RPS16 | -3045 | 
| PSMA7 | -3028 | 
| PSMB3 | -3012 | 
| PSMD8 | -3008 | 
| RPS15A | -3005 | 
| ELOC | -2992 | 
| RPS27 | -2985 | 
| PSMB1 | -2979 | 
| SEM1 | -2968 | 
| RPL24 | -2957 | 
| RPL8 | -2956 | 
| RPS8 | -2950 | 
| RPL10 | -2947 | 
| RPL21 | -2945 | 
| PSMA4 | -2929 | 
| RPL28 | -2926 | 
| RPL27 | -2923 | 
| MAGOH | -2915 | 
| RPS25 | -2902 | 
| UBC | -2887 | 
| PSMD7 | -2885 | 
| RPS3 | -2869 | 
| PSMB7 | -2865 | 
| RPL36A | -2858 | 
| PSMB10 | -2849 | 
| RPS27A | -2821 | 
| PSMA2 | -2803 | 
| RPL22 | -2796 | 
| RPL23A | -2793 | 
| PSMA3 | -2787 | 
| RPS23 | -2783 | 
| RPL3 | -2782 | 
| RPL26 | -2774 | 
| RPS4Y1 | -2771 | 
| RPL7A | -2766 | 
| PSMB8 | -2753 | 
| RPS10 | -2749 | 
| RPS3A | -2745 | 
| RPS19 | -2714 | 
| RPL36AL | -2703 | 
| RPL18 | -2699 | 
| RPL6 | -2665 | 
| PSMA5 | -2655 | 
| PSMB2 | -2644 | 
| PSMD9 | -2638 | 
| RBM8A | -2629 | 
| RPS27L | -2611 | 
| RPL26L1 | -2572 | 
| RPL29 | -2433 | 
| EIF4A3 | -2404 | 
| PSMA1 | -2401 | 
| RPL4 | -2374 | 
| PSME2 | -2323 | 
| RPL27A | -2238 | 
| PSMD4 | -2233 | 
| MAGOHB | -2230 | 
| PSME1 | -2223 | 
| PSMC4 | -2206 | 
| PSMC1 | -2176 | 
| RPS13 | -2162 | 
| PSMD13 | -2161 | 
| PSMA6 | -2159 | 
| PSMC3 | -2144 | 
| RPS6 | -2137 | 
| PSMC5 | -2073 | 
| PSMC6 | -2047 | 
| RPL15 | -2045 | 
| PSMD1 | -2012 | 
| RNPS1 | -1986 | 
| RPL17 | -1968 | 
| RPLP0 | -1966 | 
| PSMD2 | -1923 | 
| PSMC2 | -1899 | 
| PSMD6 | -1878 | 
| GSPT2 | -1653 | 
| PSMD14 | -1585 | 
| PSMB4 | -1579 | 
| RPL22L1 | -985 | 
| UPF2 | -976 | 
| UBB | -975 | 
| PSMD10 | -847 | 
| PSMB9 | -715 | 
| RPL5 | -485 | 
| PSMF1 | -455 | 
| RPL12 | -443 | 
| PSMD3 | -416 | 
| UPF3A | -359 | 
| PSMD11 | -307 | 
| NCBP2 | -191 | 
| GSPT1 | -159 | 
| PSME3 | -153 | 
| ZSWIM8 | -145 | 
| RPS17 | 7 | 
| RPL31 | 20 | 
| RPL7 | 108 | 
| RPS2 | 319 | 
| ETF1 | 467 | 
| PSMB5 | 486 | 
| DAG1 | 830 | 
| CASC3 | 968 | 
| RPS4X | 1068 | 
| PSMD12 | 1198 | 
| RPL9 | 1356 | 
| RPS11 | 1556 | 
| RPL23 | 1657 | 
| CUL2 | 1764 | 
| EIF4G1 | 2728 | 
| NCBP1 | 3424 | 
| RPL39L | 3853 | 
| PSMD5 | 4230 | 
| UPF3B | 4280 | 
| ROBO3 | 4727 | 
| LDB1 | 4935 | 
| USP33 | 5060 | 
| RPL13A | 5851 | 
| PSME4 | 6251 | 
| RPS20 | 6819 | 
| PABPC1 | 7504 | 
 Regulation of ornithine decarboxylase (ODC) 
| 939 | |
|---|---|
| set | Regulation of ornithine decarboxylase (ODC) | 
| setSize | 49 | 
| pANOVA | 1.23e-17 | 
| s.dist | -0.706 | 
| p.adjustANOVA | 2.92e-16 | 
Top enriched genes
| GeneID | Gene Rank | 
|---|---|
| PSMB6 | -3105 | 
| PSMA7 | -3028 | 
| PSMB3 | -3012 | 
| PSMD8 | -3008 | 
| PSMB1 | -2979 | 
| SEM1 | -2968 | 
| PSMA4 | -2929 | 
| OAZ1 | -2912 | 
| PSMD7 | -2885 | 
| PSMB7 | -2865 | 
| PSMB10 | -2849 | 
| PSMA2 | -2803 | 
| PSMA3 | -2787 | 
| PSMB8 | -2753 | 
| PSMA5 | -2655 | 
| PSMB2 | -2644 | 
| PSMD9 | -2638 | 
| PSMA1 | -2401 | 
| PSME2 | -2323 | 
| PSMD4 | -2233 | 
| GeneID | Gene Rank | 
|---|---|
| PSMB6 | -3105 | 
| PSMA7 | -3028 | 
| PSMB3 | -3012 | 
| PSMD8 | -3008 | 
| PSMB1 | -2979 | 
| SEM1 | -2968 | 
| PSMA4 | -2929 | 
| OAZ1 | -2912 | 
| PSMD7 | -2885 | 
| PSMB7 | -2865 | 
| PSMB10 | -2849 | 
| PSMA2 | -2803 | 
| PSMA3 | -2787 | 
| PSMB8 | -2753 | 
| PSMA5 | -2655 | 
| PSMB2 | -2644 | 
| PSMD9 | -2638 | 
| PSMA1 | -2401 | 
| PSME2 | -2323 | 
| PSMD4 | -2233 | 
| PSME1 | -2223 | 
| PSMC4 | -2206 | 
| PSMC1 | -2176 | 
| PSMD13 | -2161 | 
| PSMA6 | -2159 | 
| PSMC3 | -2144 | 
| NQO1 | -2131 | 
| PSMC5 | -2073 | 
| PSMC6 | -2047 | 
| PSMD1 | -2012 | 
| OAZ2 | -1964 | 
| PSMD2 | -1923 | 
| PSMC2 | -1899 | 
| PSMD6 | -1878 | 
| OAZ3 | -1610 | 
| PSMD14 | -1585 | 
| PSMB4 | -1579 | 
| PSMD10 | -847 | 
| PSMB9 | -715 | 
| PSMF1 | -455 | 
| PSMD3 | -416 | 
| ODC1 | -336 | 
| PSMD11 | -307 | 
| PSME3 | -153 | 
| AZIN1 | 129 | 
| PSMB5 | 486 | 
| PSMD12 | 1198 | 
| PSMD5 | 4230 | 
| PSME4 | 6251 | 
 Mitochondrial translation elongation 
| 616 | |
|---|---|
| set | Mitochondrial translation elongation | 
| setSize | 88 | 
| pANOVA | 2.82e-30 | 
| s.dist | -0.705 | 
| p.adjustANOVA | 1.18e-28 | 
Top enriched genes
| GeneID | Gene Rank | 
|---|---|
| MRPS36 | -3096 | 
| MRPS34 | -3052 | 
| MRPL41 | -3040 | 
| MRPL54 | -3016 | 
| MRPL52 | -2988 | 
| MRPS24 | -2986 | 
| GADD45GIP1 | -2980 | 
| MRPS12 | -2910 | 
| MRPS7 | -2883 | 
| MRPL47 | -2881 | 
| MRPS18C | -2864 | 
| AURKAIP1 | -2856 | 
| MRPL20 | -2854 | 
| MRPS6 | -2853 | 
| MRPL12 | -2852 | 
| MRPL36 | -2818 | 
| MRPL57 | -2811 | 
| MRPL11 | -2801 | 
| MRPL33 | -2799 | 
| MRPL34 | -2778 | 
| GeneID | Gene Rank | 
|---|---|
| MRPS36 | -3096 | 
| MRPS34 | -3052 | 
| MRPL41 | -3040 | 
| MRPL54 | -3016 | 
| MRPL52 | -2988 | 
| MRPS24 | -2986 | 
| GADD45GIP1 | -2980 | 
| MRPS12 | -2910 | 
| MRPS7 | -2883 | 
| MRPL47 | -2881 | 
| MRPS18C | -2864 | 
| AURKAIP1 | -2856 | 
| MRPL20 | -2854 | 
| MRPS6 | -2853 | 
| MRPL12 | -2852 | 
| MRPL36 | -2818 | 
| MRPL57 | -2811 | 
| MRPL11 | -2801 | 
| MRPL33 | -2799 | 
| MRPL34 | -2778 | 
| MRPL14 | -2769 | 
| MRPS25 | -2756 | 
| MRPL51 | -2741 | 
| MRPL35 | -2735 | 
| MRPL2 | -2723 | 
| MRPL22 | -2715 | 
| MRPL21 | -2709 | 
| CHCHD1 | -2708 | 
| TUFM | -2698 | 
| MRPL28 | -2672 | 
| MRPL27 | -2643 | 
| MRPS17 | -2596 | 
| MRPL40 | -2570 | 
| MRPL13 | -2561 | 
| MRPS21 | -2525 | 
| MRPL23 | -2523 | 
| MRPS16 | -2512 | 
| MRPL55 | -2507 | 
| MRPL4 | -2468 | 
| MRPS11 | -2464 | 
| MRPL16 | -2435 | 
| MRPS15 | -2368 | 
| MRPS18A | -2341 | 
| MRPS33 | -2327 | 
| MRPS18B | -2282 | 
| MRPS35 | -2221 | 
| MRPS23 | -2202 | 
| MRPL50 | -2192 | 
| MRPL17 | -2143 | 
| MRPL15 | -2128 | 
| MRPS22 | -2108 | 
| MRPL24 | -2101 | 
| MRPL38 | -2001 | 
| MRPL39 | -1804 | 
| MRPL10 | -1715 | 
| MRPS10 | -1709 | 
| MRPS26 | -1707 | 
| GFM1 | -1632 | 
| MRPS2 | -1506 | 
| ERAL1 | -1319 | 
| MRPL32 | -1269 | 
| MRPL53 | -1256 | 
| MRPL42 | -1112 | 
| MRPL48 | -829 | 
| MRPL19 | -796 | 
| MRPL58 | -782 | 
| MRPL46 | -706 | 
| MRPS14 | -687 | 
| MRPS5 | -640 | 
| MRPS28 | -495 | 
| MRPL30 | -283 | 
| MRPL45 | -173 | 
| MRPL44 | -137 | 
| MRPL18 | -55 | 
| MRPL37 | 44 | 
| MRPL43 | 46 | 
| MRPL3 | 115 | 
| DAP3 | 242 | 
| TSFM | 243 | 
| MRPL1 | 323 | 
| MRPS31 | 441 | 
| MRPS30 | 475 | 
| MRPS27 | 1255 | 
| MRPL9 | 1287 | 
| OXA1L | 1294 | 
| MRPL49 | 3110 | 
| MRPS9 | 4099 | 
| PTCD3 | 4414 | 
 Prefoldin mediated transfer of substrate to CCT/TriC 
| 781 | |
|---|---|
| set | Prefoldin mediated transfer of substrate to CCT/TriC | 
| setSize | 24 | 
| pANOVA | 2.91e-09 | 
| s.dist | -0.7 | 
| p.adjustANOVA | 2.54e-08 | 
Top enriched genes
| GeneID | Gene Rank | 
|---|---|
| ACTB | -3267 | 
| PFDN5 | -3192 | 
| PFDN2 | -3122 | 
| PFDN6 | -2895 | 
| TUBB4B | -2873 | 
| CCT8 | -2762 | 
| CCT7 | -2743 | 
| TUBA1A | -2711 | 
| CCT4 | -2649 | 
| CCT3 | -2593 | 
| CCT2 | -2573 | 
| VBP1 | -2454 | 
| CCT5 | -2406 | 
| TUBB2A | -2354 | 
| PFDN4 | -2166 | 
| TUBA1C | -1994 | 
| TCP1 | -1872 | 
| TUBB3 | -1433 | 
| TUBB6 | -1363 | 
| CCT6A | 139 | 
| GeneID | Gene Rank | 
|---|---|
| ACTB | -3267 | 
| PFDN5 | -3192 | 
| PFDN2 | -3122 | 
| PFDN6 | -2895 | 
| TUBB4B | -2873 | 
| CCT8 | -2762 | 
| CCT7 | -2743 | 
| TUBA1A | -2711 | 
| CCT4 | -2649 | 
| CCT3 | -2593 | 
| CCT2 | -2573 | 
| VBP1 | -2454 | 
| CCT5 | -2406 | 
| TUBB2A | -2354 | 
| PFDN4 | -2166 | 
| TUBA1C | -1994 | 
| TCP1 | -1872 | 
| TUBB3 | -1433 | 
| TUBB6 | -1363 | 
| CCT6A | 139 | 
| PFDN1 | 390 | 
| CCT6B | 1343 | 
| TUBA4A | 2254 | 
| TUBB4A | 4421 | 
 Cap-dependent Translation Initiation 
| 125 | |
|---|---|
| set | Cap-dependent Translation Initiation | 
| setSize | 116 | 
| pANOVA | 9.08e-39 | 
| s.dist | -0.699 | 
| p.adjustANOVA | 8.43e-37 | 
Top enriched genes
| GeneID | Gene Rank | 
|---|---|
| RPS28 | -3265 | 
| RPL36 | -3263 | 
| RPL35 | -3250 | 
| RPS29 | -3247 | 
| RPS21 | -3244 | 
| RPL32 | -3239 | 
| RPL19 | -3232 | 
| RPL39 | -3228 | 
| UBA52 | -3224 | 
| RPS18 | -3220 | 
| RPS26 | -3215 | 
| RPLP2 | -3212 | 
| FAU | -3209 | 
| RPS15 | -3207 | 
| RPLP1 | -3206 | 
| RPL41 | -3204 | 
| RPL38 | -3177 | 
| RPS12 | -3173 | 
| RPL34 | -3171 | 
| RPS24 | -3160 | 
| GeneID | Gene Rank | 
|---|---|
| RPS28 | -3265 | 
| RPL36 | -3263 | 
| RPL35 | -3250 | 
| RPS29 | -3247 | 
| RPS21 | -3244 | 
| RPL32 | -3239 | 
| RPL19 | -3232 | 
| RPL39 | -3228 | 
| UBA52 | -3224 | 
| RPS18 | -3220 | 
| RPS26 | -3215 | 
| RPLP2 | -3212 | 
| FAU | -3209 | 
| RPS15 | -3207 | 
| RPLP1 | -3206 | 
| RPL41 | -3204 | 
| RPL38 | -3177 | 
| RPS12 | -3173 | 
| RPL34 | -3171 | 
| RPS24 | -3160 | 
| RPL13 | -3154 | 
| RPL18A | -3141 | 
| RPL37A | -3140 | 
| RPSA | -3139 | 
| RPS9 | -3133 | 
| EIF4A1 | -3130 | 
| RPL35A | -3125 | 
| RPL37 | -3121 | 
| RPL11 | -3116 | 
| RPS5 | -3098 | 
| EIF3K | -3095 | 
| RPS14 | -3088 | 
| RPS7 | -3072 | 
| RPL30 | -3071 | 
| RPL10A | -3051 | 
| RPL14 | -3046 | 
| RPS16 | -3045 | 
| RPS15A | -3005 | 
| RPS27 | -2985 | 
| RPL24 | -2957 | 
| RPL8 | -2956 | 
| RPS8 | -2950 | 
| RPL10 | -2947 | 
| RPL21 | -2945 | 
| RPL28 | -2926 | 
| RPL27 | -2923 | 
| RPS25 | -2902 | 
| RPS3 | -2869 | 
| RPL36A | -2858 | 
| RPS27A | -2821 | 
| RPL22 | -2796 | 
| RPL23A | -2793 | 
| RPS23 | -2783 | 
| RPL3 | -2782 | 
| RPL26 | -2774 | 
| RPS4Y1 | -2771 | 
| RPL7A | -2766 | 
| RPS10 | -2749 | 
| RPS3A | -2745 | 
| RPS19 | -2714 | 
| RPL36AL | -2703 | 
| RPL18 | -2699 | 
| EIF4EBP1 | -2694 | 
| RPL6 | -2665 | 
| EIF3I | -2640 | 
| RPS27L | -2611 | 
| EIF4E | -2583 | 
| RPL26L1 | -2572 | 
| EIF5B | -2440 | 
| RPL29 | -2433 | 
| EIF3J | -2427 | 
| RPL4 | -2374 | 
| RPL27A | -2238 | 
| EIF3D | -2163 | 
| RPS13 | -2162 | 
| RPS6 | -2137 | 
| RPL15 | -2045 | 
| EIF3G | -2009 | 
| EIF3M | -1989 | 
| RPL17 | -1968 | 
| RPLP0 | -1966 | 
| EIF2S1 | -1641 | 
| RPL22L1 | -985 | 
| EIF1AX | -952 | 
| EIF2S2 | -901 | 
| EIF2B4 | -772 | 
| EIF2B1 | -660 | 
| EIF2B5 | -615 | 
| RPL5 | -485 | 
| RPL12 | -443 | 
| RPS17 | 7 | 
| RPL31 | 20 | 
| EIF3F | 71 | 
| RPL7 | 108 | 
| EIF3L | 121 | 
| EIF3E | 252 | 
| EIF2B3 | 278 | 
| RPS2 | 319 | 
| EIF4H | 357 | 
| EIF3H | 376 | 
| EIF2S3 | 459 | 
| EIF2B2 | 792 | 
| RPS4X | 1068 | 
| RPL9 | 1356 | 
| RPS11 | 1556 | 
| RPL23 | 1657 | 
| EIF3A | 2251 | 
| EIF5 | 2257 | 
| EIF4G1 | 2728 | 
| EIF3B | 3737 | 
| RPL39L | 3853 | 
| EIF4A2 | 4936 | 
| RPL13A | 5851 | 
| RPS20 | 6819 | 
| EIF4B | 7359 | 
| PABPC1 | 7504 | 
 Eukaryotic Translation Initiation 
| 316 | |
|---|---|
| set | Eukaryotic Translation Initiation | 
| setSize | 116 | 
| pANOVA | 9.08e-39 | 
| s.dist | -0.699 | 
| p.adjustANOVA | 8.43e-37 | 
Top enriched genes
| GeneID | Gene Rank | 
|---|---|
| RPS28 | -3265 | 
| RPL36 | -3263 | 
| RPL35 | -3250 | 
| RPS29 | -3247 | 
| RPS21 | -3244 | 
| RPL32 | -3239 | 
| RPL19 | -3232 | 
| RPL39 | -3228 | 
| UBA52 | -3224 | 
| RPS18 | -3220 | 
| RPS26 | -3215 | 
| RPLP2 | -3212 | 
| FAU | -3209 | 
| RPS15 | -3207 | 
| RPLP1 | -3206 | 
| RPL41 | -3204 | 
| RPL38 | -3177 | 
| RPS12 | -3173 | 
| RPL34 | -3171 | 
| RPS24 | -3160 | 
| GeneID | Gene Rank | 
|---|---|
| RPS28 | -3265 | 
| RPL36 | -3263 | 
| RPL35 | -3250 | 
| RPS29 | -3247 | 
| RPS21 | -3244 | 
| RPL32 | -3239 | 
| RPL19 | -3232 | 
| RPL39 | -3228 | 
| UBA52 | -3224 | 
| RPS18 | -3220 | 
| RPS26 | -3215 | 
| RPLP2 | -3212 | 
| FAU | -3209 | 
| RPS15 | -3207 | 
| RPLP1 | -3206 | 
| RPL41 | -3204 | 
| RPL38 | -3177 | 
| RPS12 | -3173 | 
| RPL34 | -3171 | 
| RPS24 | -3160 | 
| RPL13 | -3154 | 
| RPL18A | -3141 | 
| RPL37A | -3140 | 
| RPSA | -3139 | 
| RPS9 | -3133 | 
| EIF4A1 | -3130 | 
| RPL35A | -3125 | 
| RPL37 | -3121 | 
| RPL11 | -3116 | 
| RPS5 | -3098 | 
| EIF3K | -3095 | 
| RPS14 | -3088 | 
| RPS7 | -3072 | 
| RPL30 | -3071 | 
| RPL10A | -3051 | 
| RPL14 | -3046 | 
| RPS16 | -3045 | 
| RPS15A | -3005 | 
| RPS27 | -2985 | 
| RPL24 | -2957 | 
| RPL8 | -2956 | 
| RPS8 | -2950 | 
| RPL10 | -2947 | 
| RPL21 | -2945 | 
| RPL28 | -2926 | 
| RPL27 | -2923 | 
| RPS25 | -2902 | 
| RPS3 | -2869 | 
| RPL36A | -2858 | 
| RPS27A | -2821 | 
| RPL22 | -2796 | 
| RPL23A | -2793 | 
| RPS23 | -2783 | 
| RPL3 | -2782 | 
| RPL26 | -2774 | 
| RPS4Y1 | -2771 | 
| RPL7A | -2766 | 
| RPS10 | -2749 | 
| RPS3A | -2745 | 
| RPS19 | -2714 | 
| RPL36AL | -2703 | 
| RPL18 | -2699 | 
| EIF4EBP1 | -2694 | 
| RPL6 | -2665 | 
| EIF3I | -2640 | 
| RPS27L | -2611 | 
| EIF4E | -2583 | 
| RPL26L1 | -2572 | 
| EIF5B | -2440 | 
| RPL29 | -2433 | 
| EIF3J | -2427 | 
| RPL4 | -2374 | 
| RPL27A | -2238 | 
| EIF3D | -2163 | 
| RPS13 | -2162 | 
| RPS6 | -2137 | 
| RPL15 | -2045 | 
| EIF3G | -2009 | 
| EIF3M | -1989 | 
| RPL17 | -1968 | 
| RPLP0 | -1966 | 
| EIF2S1 | -1641 | 
| RPL22L1 | -985 | 
| EIF1AX | -952 | 
| EIF2S2 | -901 | 
| EIF2B4 | -772 | 
| EIF2B1 | -660 | 
| EIF2B5 | -615 | 
| RPL5 | -485 | 
| RPL12 | -443 | 
| RPS17 | 7 | 
| RPL31 | 20 | 
| EIF3F | 71 | 
| RPL7 | 108 | 
| EIF3L | 121 | 
| EIF3E | 252 | 
| EIF2B3 | 278 | 
| RPS2 | 319 | 
| EIF4H | 357 | 
| EIF3H | 376 | 
| EIF2S3 | 459 | 
| EIF2B2 | 792 | 
| RPS4X | 1068 | 
| RPL9 | 1356 | 
| RPS11 | 1556 | 
| RPL23 | 1657 | 
| EIF3A | 2251 | 
| EIF5 | 2257 | 
| EIF4G1 | 2728 | 
| EIF3B | 3737 | 
| RPL39L | 3853 | 
| EIF4A2 | 4936 | 
| RPL13A | 5851 | 
| RPS20 | 6819 | 
| EIF4B | 7359 | 
| PABPC1 | 7504 | 
 Vpu mediated degradation of CD4 
| 1263 | |
|---|---|
| set | Vpu mediated degradation of CD4 | 
| setSize | 50 | 
| pANOVA | 1.86e-17 | 
| s.dist | -0.695 | 
| p.adjustANOVA | 4.25e-16 | 
Top enriched genes
| GeneID | Gene Rank | 
|---|---|
| UBA52 | -3224 | 
| PSMB6 | -3105 | 
| PSMA7 | -3028 | 
| SKP1 | -3020 | 
| PSMB3 | -3012 | 
| PSMD8 | -3008 | 
| PSMB1 | -2979 | 
| SEM1 | -2968 | 
| PSMA4 | -2929 | 
| UBC | -2887 | 
| PSMD7 | -2885 | 
| PSMB7 | -2865 | 
| PSMB10 | -2849 | 
| RPS27A | -2821 | 
| PSMA2 | -2803 | 
| PSMA3 | -2787 | 
| PSMB8 | -2753 | 
| PSMA5 | -2655 | 
| PSMB2 | -2644 | 
| PSMD9 | -2638 | 
| GeneID | Gene Rank | 
|---|---|
| UBA52 | -3224 | 
| PSMB6 | -3105 | 
| PSMA7 | -3028 | 
| SKP1 | -3020 | 
| PSMB3 | -3012 | 
| PSMD8 | -3008 | 
| PSMB1 | -2979 | 
| SEM1 | -2968 | 
| PSMA4 | -2929 | 
| UBC | -2887 | 
| PSMD7 | -2885 | 
| PSMB7 | -2865 | 
| PSMB10 | -2849 | 
| RPS27A | -2821 | 
| PSMA2 | -2803 | 
| PSMA3 | -2787 | 
| PSMB8 | -2753 | 
| PSMA5 | -2655 | 
| PSMB2 | -2644 | 
| PSMD9 | -2638 | 
| PSMA1 | -2401 | 
| PSME2 | -2323 | 
| PSMD4 | -2233 | 
| PSME1 | -2223 | 
| PSMC4 | -2206 | 
| PSMC1 | -2176 | 
| PSMD13 | -2161 | 
| PSMA6 | -2159 | 
| PSMC3 | -2144 | 
| PSMC5 | -2073 | 
| PSMC6 | -2047 | 
| PSMD1 | -2012 | 
| PSMD2 | -1923 | 
| PSMC2 | -1899 | 
| PSMD6 | -1878 | 
| PSMD14 | -1585 | 
| PSMB4 | -1579 | 
| CD4 | -1497 | 
| UBB | -975 | 
| PSMD10 | -847 | 
| PSMB9 | -715 | 
| PSMF1 | -455 | 
| PSMD3 | -416 | 
| PSMD11 | -307 | 
| PSME3 | -153 | 
| PSMB5 | 486 | 
| PSMD12 | 1198 | 
| PSMD5 | 4230 | 
| PSME4 | 6251 | 
| BTRC | 6965 | 
 FBXL7 down-regulates AURKA during mitotic entry and in early mitosis 
| 323 | |
|---|---|
| set | FBXL7 down-regulates AURKA during mitotic entry and in early mitosis | 
| setSize | 52 | 
| pANOVA | 4.72e-18 | 
| s.dist | -0.694 | 
| p.adjustANOVA | 1.18e-16 | 
Top enriched genes
| GeneID | Gene Rank | 
|---|---|
| UBA52 | -3224 | 
| PSMB6 | -3105 | 
| RBX1 | -3082 | 
| PSMA7 | -3028 | 
| SKP1 | -3020 | 
| PSMB3 | -3012 | 
| PSMD8 | -3008 | 
| PSMB1 | -2979 | 
| SEM1 | -2968 | 
| PSMA4 | -2929 | 
| UBC | -2887 | 
| PSMD7 | -2885 | 
| PSMB7 | -2865 | 
| PSMB10 | -2849 | 
| RPS27A | -2821 | 
| PSMA2 | -2803 | 
| PSMA3 | -2787 | 
| PSMB8 | -2753 | 
| PSMA5 | -2655 | 
| PSMB2 | -2644 | 
| GeneID | Gene Rank | 
|---|---|
| UBA52 | -3224 | 
| PSMB6 | -3105 | 
| RBX1 | -3082 | 
| PSMA7 | -3028 | 
| SKP1 | -3020 | 
| PSMB3 | -3012 | 
| PSMD8 | -3008 | 
| PSMB1 | -2979 | 
| SEM1 | -2968 | 
| PSMA4 | -2929 | 
| UBC | -2887 | 
| PSMD7 | -2885 | 
| PSMB7 | -2865 | 
| PSMB10 | -2849 | 
| RPS27A | -2821 | 
| PSMA2 | -2803 | 
| PSMA3 | -2787 | 
| PSMB8 | -2753 | 
| PSMA5 | -2655 | 
| PSMB2 | -2644 | 
| PSMD9 | -2638 | 
| PSMA1 | -2401 | 
| PSME2 | -2323 | 
| PSMD4 | -2233 | 
| PSME1 | -2223 | 
| PSMC4 | -2206 | 
| PSMC1 | -2176 | 
| PSMD13 | -2161 | 
| PSMA6 | -2159 | 
| PSMC3 | -2144 | 
| PSMC5 | -2073 | 
| PSMC6 | -2047 | 
| PSMD1 | -2012 | 
| PSMD2 | -1923 | 
| PSMC2 | -1899 | 
| PSMD6 | -1878 | 
| PSMD14 | -1585 | 
| PSMB4 | -1579 | 
| FBXL18 | -1423 | 
| UBB | -975 | 
| PSMD10 | -847 | 
| PSMB9 | -715 | 
| PSMF1 | -455 | 
| PSMD3 | -416 | 
| PSMD11 | -307 | 
| PSME3 | -153 | 
| PSMB5 | 486 | 
| PSMD12 | 1198 | 
| AURKA | 1590 | 
| PSMD5 | 4230 | 
| CUL1 | 5483 | 
| PSME4 | 6251 | 
 Negative regulation of NOTCH4 signaling 
| 669 | |
|---|---|
| set | Negative regulation of NOTCH4 signaling | 
| setSize | 53 | 
| pANOVA | 3.73e-18 | 
| s.dist | -0.689 | 
| p.adjustANOVA | 9.52e-17 | 
Top enriched genes
| GeneID | Gene Rank | 
|---|---|
| UBA52 | -3224 | 
| PSMB6 | -3105 | 
| RBX1 | -3082 | 
| PSMA7 | -3028 | 
| SKP1 | -3020 | 
| PSMB3 | -3012 | 
| PSMD8 | -3008 | 
| PSMB1 | -2979 | 
| SEM1 | -2968 | 
| PSMA4 | -2929 | 
| UBC | -2887 | 
| PSMD7 | -2885 | 
| PSMB7 | -2865 | 
| PSMB10 | -2849 | 
| RPS27A | -2821 | 
| PSMA2 | -2803 | 
| PSMA3 | -2787 | 
| PSMB8 | -2753 | 
| PSMA5 | -2655 | 
| PSMB2 | -2644 | 
| GeneID | Gene Rank | 
|---|---|
| UBA52 | -3224 | 
| PSMB6 | -3105 | 
| RBX1 | -3082 | 
| PSMA7 | -3028 | 
| SKP1 | -3020 | 
| PSMB3 | -3012 | 
| PSMD8 | -3008 | 
| PSMB1 | -2979 | 
| SEM1 | -2968 | 
| PSMA4 | -2929 | 
| UBC | -2887 | 
| PSMD7 | -2885 | 
| PSMB7 | -2865 | 
| PSMB10 | -2849 | 
| RPS27A | -2821 | 
| PSMA2 | -2803 | 
| PSMA3 | -2787 | 
| PSMB8 | -2753 | 
| PSMA5 | -2655 | 
| PSMB2 | -2644 | 
| PSMD9 | -2638 | 
| YWHAZ | -2463 | 
| PSMA1 | -2401 | 
| PSME2 | -2323 | 
| PSMD4 | -2233 | 
| PSME1 | -2223 | 
| PSMC4 | -2206 | 
| PSMC1 | -2176 | 
| PSMD13 | -2161 | 
| PSMA6 | -2159 | 
| PSMC3 | -2144 | 
| PSMC5 | -2073 | 
| PSMC6 | -2047 | 
| PSMD1 | -2012 | 
| PSMD2 | -1923 | 
| PSMC2 | -1899 | 
| PSMD6 | -1878 | 
| PSMD14 | -1585 | 
| PSMB4 | -1579 | 
| AKT1 | -1013 | 
| UBB | -975 | 
| PSMD10 | -847 | 
| PSMB9 | -715 | 
| PSMF1 | -455 | 
| PSMD3 | -416 | 
| PSMD11 | -307 | 
| PSME3 | -153 | 
| PSMB5 | 486 | 
| PSMD12 | 1198 | 
| TACC3 | 2670 | 
| PSMD5 | 4230 | 
| CUL1 | 5483 | 
| FBXW7 | 6947 | 
 Mitochondrial translation initiation 
| 617 | |
|---|---|
| set | Mitochondrial translation initiation | 
| setSize | 88 | 
| pANOVA | 5.03e-29 | 
| s.dist | -0.689 | 
| p.adjustANOVA | 1.92e-27 | 
Top enriched genes
| GeneID | Gene Rank | 
|---|---|
| MRPS36 | -3096 | 
| MRPS34 | -3052 | 
| MRPL41 | -3040 | 
| MRPL54 | -3016 | 
| MRPL52 | -2988 | 
| MRPS24 | -2986 | 
| GADD45GIP1 | -2980 | 
| MRPS12 | -2910 | 
| MRPS7 | -2883 | 
| MRPL47 | -2881 | 
| MRPS18C | -2864 | 
| AURKAIP1 | -2856 | 
| MRPL20 | -2854 | 
| MRPS6 | -2853 | 
| MRPL12 | -2852 | 
| MRPL36 | -2818 | 
| MRPL57 | -2811 | 
| MRPL11 | -2801 | 
| MRPL33 | -2799 | 
| MRPL34 | -2778 | 
| GeneID | Gene Rank | 
|---|---|
| MRPS36 | -3096 | 
| MRPS34 | -3052 | 
| MRPL41 | -3040 | 
| MRPL54 | -3016 | 
| MRPL52 | -2988 | 
| MRPS24 | -2986 | 
| GADD45GIP1 | -2980 | 
| MRPS12 | -2910 | 
| MRPS7 | -2883 | 
| MRPL47 | -2881 | 
| MRPS18C | -2864 | 
| AURKAIP1 | -2856 | 
| MRPL20 | -2854 | 
| MRPS6 | -2853 | 
| MRPL12 | -2852 | 
| MRPL36 | -2818 | 
| MRPL57 | -2811 | 
| MRPL11 | -2801 | 
| MRPL33 | -2799 | 
| MRPL34 | -2778 | 
| MRPL14 | -2769 | 
| MRPS25 | -2756 | 
| MRPL51 | -2741 | 
| MRPL35 | -2735 | 
| MRPL2 | -2723 | 
| MRPL22 | -2715 | 
| MRPL21 | -2709 | 
| CHCHD1 | -2708 | 
| MRPL28 | -2672 | 
| MRPL27 | -2643 | 
| MRPS17 | -2596 | 
| MRPL40 | -2570 | 
| MRPL13 | -2561 | 
| MRPS21 | -2525 | 
| MRPL23 | -2523 | 
| MRPS16 | -2512 | 
| MRPL55 | -2507 | 
| MRPL4 | -2468 | 
| MRPS11 | -2464 | 
| MRPL16 | -2435 | 
| MRPS15 | -2368 | 
| MRPS18A | -2341 | 
| MRPS33 | -2327 | 
| MRPS18B | -2282 | 
| MRPS35 | -2221 | 
| MRPS23 | -2202 | 
| MRPL50 | -2192 | 
| MRPL17 | -2143 | 
| MRPL15 | -2128 | 
| MRPS22 | -2108 | 
| MRPL24 | -2101 | 
| MRPL38 | -2001 | 
| MRPL39 | -1804 | 
| MRPL10 | -1715 | 
| MRPS10 | -1709 | 
| MRPS26 | -1707 | 
| MRPS2 | -1506 | 
| ERAL1 | -1319 | 
| MRPL32 | -1269 | 
| MRPL53 | -1256 | 
| MTIF3 | -1168 | 
| MRPL42 | -1112 | 
| MRPL48 | -829 | 
| MRPL19 | -796 | 
| MRPL58 | -782 | 
| MRPL46 | -706 | 
| MRPS14 | -687 | 
| MRPS5 | -640 | 
| MRPS28 | -495 | 
| MRPL30 | -283 | 
| MRPL45 | -173 | 
| MRPL44 | -137 | 
| MRPL18 | -55 | 
| MRPL37 | 44 | 
| MRPL43 | 46 | 
| MRPL3 | 115 | 
| DAP3 | 242 | 
| MRPL1 | 323 | 
| MRPS31 | 441 | 
| MRPS30 | 475 | 
| MRPS27 | 1255 | 
| MTFMT | 1275 | 
| MRPL9 | 1287 | 
| OXA1L | 1294 | 
| MRPL49 | 3110 | 
| MTIF2 | 3204 | 
| MRPS9 | 4099 | 
| PTCD3 | 4414 | 
 Mitochondrial translation termination 
| 618 | |
|---|---|
| set | Mitochondrial translation termination | 
| setSize | 88 | 
| pANOVA | 7.65e-29 | 
| s.dist | -0.687 | 
| p.adjustANOVA | 2.84e-27 | 
Top enriched genes
| GeneID | Gene Rank | 
|---|---|
| MRPS36 | -3096 | 
| MRPS34 | -3052 | 
| MRPL41 | -3040 | 
| MRPL54 | -3016 | 
| MRPL52 | -2988 | 
| MRPS24 | -2986 | 
| GADD45GIP1 | -2980 | 
| MRPS12 | -2910 | 
| MRPS7 | -2883 | 
| MRPL47 | -2881 | 
| MRPS18C | -2864 | 
| AURKAIP1 | -2856 | 
| MRPL20 | -2854 | 
| MRPS6 | -2853 | 
| MRPL12 | -2852 | 
| MRPL36 | -2818 | 
| MRPL57 | -2811 | 
| MRPL11 | -2801 | 
| MRPL33 | -2799 | 
| MRPL34 | -2778 | 
| GeneID | Gene Rank | 
|---|---|
| MRPS36 | -3096 | 
| MRPS34 | -3052 | 
| MRPL41 | -3040 | 
| MRPL54 | -3016 | 
| MRPL52 | -2988 | 
| MRPS24 | -2986 | 
| GADD45GIP1 | -2980 | 
| MRPS12 | -2910 | 
| MRPS7 | -2883 | 
| MRPL47 | -2881 | 
| MRPS18C | -2864 | 
| AURKAIP1 | -2856 | 
| MRPL20 | -2854 | 
| MRPS6 | -2853 | 
| MRPL12 | -2852 | 
| MRPL36 | -2818 | 
| MRPL57 | -2811 | 
| MRPL11 | -2801 | 
| MRPL33 | -2799 | 
| MRPL34 | -2778 | 
| MRPL14 | -2769 | 
| MRPS25 | -2756 | 
| MRPL51 | -2741 | 
| MRPL35 | -2735 | 
| MRPL2 | -2723 | 
| MRPL22 | -2715 | 
| MRPL21 | -2709 | 
| CHCHD1 | -2708 | 
| MRPL28 | -2672 | 
| MRPL27 | -2643 | 
| MRPS17 | -2596 | 
| MRPL40 | -2570 | 
| MRPL13 | -2561 | 
| MRPS21 | -2525 | 
| MRPL23 | -2523 | 
| MRPS16 | -2512 | 
| MRPL55 | -2507 | 
| MRPL4 | -2468 | 
| MRPS11 | -2464 | 
| MRPL16 | -2435 | 
| MRPS15 | -2368 | 
| MRPS18A | -2341 | 
| MRPS33 | -2327 | 
| MRPS18B | -2282 | 
| MRPS35 | -2221 | 
| MRPS23 | -2202 | 
| MRPL50 | -2192 | 
| MRPL17 | -2143 | 
| MRPL15 | -2128 | 
| MRPS22 | -2108 | 
| MRPL24 | -2101 | 
| MRPL38 | -2001 | 
| MRPL39 | -1804 | 
| MRPL10 | -1715 | 
| MRPS10 | -1709 | 
| MRPS26 | -1707 | 
| MRPS2 | -1506 | 
| ERAL1 | -1319 | 
| MRPL32 | -1269 | 
| MRPL53 | -1256 | 
| MRRF | -1231 | 
| MRPL42 | -1112 | 
| MRPL48 | -829 | 
| MRPL19 | -796 | 
| MRPL58 | -782 | 
| MRPL46 | -706 | 
| MRPS14 | -687 | 
| MRPS5 | -640 | 
| MRPS28 | -495 | 
| MRPL30 | -283 | 
| MRPL45 | -173 | 
| MRPL44 | -137 | 
| MRPL18 | -55 | 
| MRPL37 | 44 | 
| MRPL43 | 46 | 
| MRPL3 | 115 | 
| DAP3 | 242 | 
| MRPL1 | 323 | 
| MRPS31 | 441 | 
| MRPS30 | 475 | 
| MRPS27 | 1255 | 
| MRPL9 | 1287 | 
| OXA1L | 1294 | 
| MTRF1L | 1940 | 
| MRPL49 | 3110 | 
| GFM2 | 3694 | 
| MRPS9 | 4099 | 
| PTCD3 | 4414 | 
 Ubiquitin-dependent degradation of Cyclin D 
| 1246 | |
|---|---|
| set | Ubiquitin-dependent degradation of Cyclin D | 
| setSize | 50 | 
| pANOVA | 4.94e-17 | 
| s.dist | -0.685 | 
| p.adjustANOVA | 1e-15 | 
Top enriched genes
| GeneID | Gene Rank | 
|---|---|
| UBA52 | -3224 | 
| PSMB6 | -3105 | 
| PSMA7 | -3028 | 
| PSMB3 | -3012 | 
| PSMD8 | -3008 | 
| PSMB1 | -2979 | 
| SEM1 | -2968 | 
| PSMA4 | -2929 | 
| UBC | -2887 | 
| PSMD7 | -2885 | 
| PSMB7 | -2865 | 
| PSMB10 | -2849 | 
| RPS27A | -2821 | 
| PSMA2 | -2803 | 
| PSMA3 | -2787 | 
| PSMB8 | -2753 | 
| PSMA5 | -2655 | 
| PSMB2 | -2644 | 
| PSMD9 | -2638 | 
| PSMA1 | -2401 | 
| GeneID | Gene Rank | 
|---|---|
| UBA52 | -3224 | 
| PSMB6 | -3105 | 
| PSMA7 | -3028 | 
| PSMB3 | -3012 | 
| PSMD8 | -3008 | 
| PSMB1 | -2979 | 
| SEM1 | -2968 | 
| PSMA4 | -2929 | 
| UBC | -2887 | 
| PSMD7 | -2885 | 
| PSMB7 | -2865 | 
| PSMB10 | -2849 | 
| RPS27A | -2821 | 
| PSMA2 | -2803 | 
| PSMA3 | -2787 | 
| PSMB8 | -2753 | 
| PSMA5 | -2655 | 
| PSMB2 | -2644 | 
| PSMD9 | -2638 | 
| PSMA1 | -2401 | 
| CDK4 | -2345 | 
| PSME2 | -2323 | 
| PSMD4 | -2233 | 
| PSME1 | -2223 | 
| PSMC4 | -2206 | 
| PSMC1 | -2176 | 
| PSMD13 | -2161 | 
| PSMA6 | -2159 | 
| PSMC3 | -2144 | 
| PSMC5 | -2073 | 
| PSMC6 | -2047 | 
| PSMD1 | -2012 | 
| PSMD2 | -1923 | 
| PSMC2 | -1899 | 
| PSMD6 | -1878 | 
| PSMD14 | -1585 | 
| PSMB4 | -1579 | 
| UBB | -975 | 
| PSMD10 | -847 | 
| PSMB9 | -715 | 
| PSMF1 | -455 | 
| PSMD3 | -416 | 
| PSMD11 | -307 | 
| CCND1 | -163 | 
| PSME3 | -153 | 
| PSMB5 | 486 | 
| PSMD12 | 1198 | 
| PSMD5 | 4230 | 
| PSME4 | 6251 | 
| GSK3B | 7481 | 
 Somitogenesis 
| 1107 | |
|---|---|
| set | Somitogenesis | 
| setSize | 46 | 
| pANOVA | 1.33e-15 | 
| s.dist | -0.681 | 
| p.adjustANOVA | 1.92e-14 | 
Top enriched genes
| GeneID | Gene Rank | 
|---|---|
| PSMB6 | -3105 | 
| PSMA7 | -3028 | 
| PSMB3 | -3012 | 
| PSMD8 | -3008 | 
| PSMB1 | -2979 | 
| SEM1 | -2968 | 
| PSMA4 | -2929 | 
| PSMD7 | -2885 | 
| PSMB7 | -2865 | 
| PSMB10 | -2849 | 
| PSMA2 | -2803 | 
| PSMA3 | -2787 | 
| PSMB8 | -2753 | 
| PSMA5 | -2655 | 
| PSMB2 | -2644 | 
| PSMD9 | -2638 | 
| PSMA1 | -2401 | 
| PSME2 | -2323 | 
| PSMD4 | -2233 | 
| PSME1 | -2223 | 
| GeneID | Gene Rank | 
|---|---|
| PSMB6 | -3105 | 
| PSMA7 | -3028 | 
| PSMB3 | -3012 | 
| PSMD8 | -3008 | 
| PSMB1 | -2979 | 
| SEM1 | -2968 | 
| PSMA4 | -2929 | 
| PSMD7 | -2885 | 
| PSMB7 | -2865 | 
| PSMB10 | -2849 | 
| PSMA2 | -2803 | 
| PSMA3 | -2787 | 
| PSMB8 | -2753 | 
| PSMA5 | -2655 | 
| PSMB2 | -2644 | 
| PSMD9 | -2638 | 
| PSMA1 | -2401 | 
| PSME2 | -2323 | 
| PSMD4 | -2233 | 
| PSME1 | -2223 | 
| PSMC4 | -2206 | 
| PSMC1 | -2176 | 
| PSMD13 | -2161 | 
| PSMA6 | -2159 | 
| PSMC3 | -2144 | 
| PSMC5 | -2073 | 
| PSMC6 | -2047 | 
| PSMD1 | -2012 | 
| PSMD2 | -1923 | 
| PSMC2 | -1899 | 
| PSMD6 | -1878 | 
| PSMD14 | -1585 | 
| PSMB4 | -1579 | 
| PSMD10 | -847 | 
| PSMB9 | -715 | 
| PSMF1 | -455 | 
| PSMD3 | -416 | 
| PSMD11 | -307 | 
| LFNG | -176 | 
| PSME3 | -153 | 
| PSMB5 | 486 | 
| NOTCH1 | 1058 | 
| PSMD12 | 1198 | 
| CTNNB1 | 3498 | 
| RBPJ | 4158 | 
| PSMD5 | 4230 | 
 Ubiquitin Mediated Degradation of Phosphorylated Cdc25A 
| 1245 | |
|---|---|
| set | Ubiquitin Mediated Degradation of Phosphorylated Cdc25A | 
| setSize | 49 | 
| pANOVA | 1.63e-16 | 
| s.dist | -0.681 | 
| p.adjustANOVA | 3.02e-15 | 
Top enriched genes
| GeneID | Gene Rank | 
|---|---|
| UBA52 | -3224 | 
| PSMB6 | -3105 | 
| PSMA7 | -3028 | 
| PSMB3 | -3012 | 
| PSMD8 | -3008 | 
| PSMB1 | -2979 | 
| SEM1 | -2968 | 
| PSMA4 | -2929 | 
| UBC | -2887 | 
| PSMD7 | -2885 | 
| PSMB7 | -2865 | 
| PSMB10 | -2849 | 
| RPS27A | -2821 | 
| PSMA2 | -2803 | 
| PSMA3 | -2787 | 
| PSMB8 | -2753 | 
| PSMA5 | -2655 | 
| PSMB2 | -2644 | 
| PSMD9 | -2638 | 
| PSMA1 | -2401 | 
| GeneID | Gene Rank | 
|---|---|
| UBA52 | -3224 | 
| PSMB6 | -3105 | 
| PSMA7 | -3028 | 
| PSMB3 | -3012 | 
| PSMD8 | -3008 | 
| PSMB1 | -2979 | 
| SEM1 | -2968 | 
| PSMA4 | -2929 | 
| UBC | -2887 | 
| PSMD7 | -2885 | 
| PSMB7 | -2865 | 
| PSMB10 | -2849 | 
| RPS27A | -2821 | 
| PSMA2 | -2803 | 
| PSMA3 | -2787 | 
| PSMB8 | -2753 | 
| PSMA5 | -2655 | 
| PSMB2 | -2644 | 
| PSMD9 | -2638 | 
| PSMA1 | -2401 | 
| PSME2 | -2323 | 
| PSMD4 | -2233 | 
| PSME1 | -2223 | 
| PSMC4 | -2206 | 
| PSMC1 | -2176 | 
| PSMD13 | -2161 | 
| PSMA6 | -2159 | 
| PSMC3 | -2144 | 
| PSMC5 | -2073 | 
| PSMC6 | -2047 | 
| PSMD1 | -2012 | 
| PSMD2 | -1923 | 
| PSMC2 | -1899 | 
| PSMD6 | -1878 | 
| PSMD14 | -1585 | 
| PSMB4 | -1579 | 
| UBB | -975 | 
| PSMD10 | -847 | 
| PSMB9 | -715 | 
| PSMF1 | -455 | 
| PSMD3 | -416 | 
| PSMD11 | -307 | 
| PSME3 | -153 | 
| PSMB5 | 486 | 
| PSMD12 | 1198 | 
| CHEK2 | 1574 | 
| PSMD5 | 4230 | 
| CHEK1 | 6178 | 
| PSME4 | 6251 | 
 p53-Independent DNA Damage Response 
| 1285 | |
|---|---|
| set | p53-Independent DNA Damage Response | 
| setSize | 49 | 
| pANOVA | 1.63e-16 | 
| s.dist | -0.681 | 
| p.adjustANOVA | 3.02e-15 | 
Top enriched genes
| GeneID | Gene Rank | 
|---|---|
| UBA52 | -3224 | 
| PSMB6 | -3105 | 
| PSMA7 | -3028 | 
| PSMB3 | -3012 | 
| PSMD8 | -3008 | 
| PSMB1 | -2979 | 
| SEM1 | -2968 | 
| PSMA4 | -2929 | 
| UBC | -2887 | 
| PSMD7 | -2885 | 
| PSMB7 | -2865 | 
| PSMB10 | -2849 | 
| RPS27A | -2821 | 
| PSMA2 | -2803 | 
| PSMA3 | -2787 | 
| PSMB8 | -2753 | 
| PSMA5 | -2655 | 
| PSMB2 | -2644 | 
| PSMD9 | -2638 | 
| PSMA1 | -2401 | 
| GeneID | Gene Rank | 
|---|---|
| UBA52 | -3224 | 
| PSMB6 | -3105 | 
| PSMA7 | -3028 | 
| PSMB3 | -3012 | 
| PSMD8 | -3008 | 
| PSMB1 | -2979 | 
| SEM1 | -2968 | 
| PSMA4 | -2929 | 
| UBC | -2887 | 
| PSMD7 | -2885 | 
| PSMB7 | -2865 | 
| PSMB10 | -2849 | 
| RPS27A | -2821 | 
| PSMA2 | -2803 | 
| PSMA3 | -2787 | 
| PSMB8 | -2753 | 
| PSMA5 | -2655 | 
| PSMB2 | -2644 | 
| PSMD9 | -2638 | 
| PSMA1 | -2401 | 
| PSME2 | -2323 | 
| PSMD4 | -2233 | 
| PSME1 | -2223 | 
| PSMC4 | -2206 | 
| PSMC1 | -2176 | 
| PSMD13 | -2161 | 
| PSMA6 | -2159 | 
| PSMC3 | -2144 | 
| PSMC5 | -2073 | 
| PSMC6 | -2047 | 
| PSMD1 | -2012 | 
| PSMD2 | -1923 | 
| PSMC2 | -1899 | 
| PSMD6 | -1878 | 
| PSMD14 | -1585 | 
| PSMB4 | -1579 | 
| UBB | -975 | 
| PSMD10 | -847 | 
| PSMB9 | -715 | 
| PSMF1 | -455 | 
| PSMD3 | -416 | 
| PSMD11 | -307 | 
| PSME3 | -153 | 
| PSMB5 | 486 | 
| PSMD12 | 1198 | 
| CHEK2 | 1574 | 
| PSMD5 | 4230 | 
| CHEK1 | 6178 | 
| PSME4 | 6251 | 
 p53-Independent G1/S DNA damage checkpoint 
| 1286 | |
|---|---|
| set | p53-Independent G1/S DNA damage checkpoint | 
| setSize | 49 | 
| pANOVA | 1.63e-16 | 
| s.dist | -0.681 | 
| p.adjustANOVA | 3.02e-15 | 
Top enriched genes
| GeneID | Gene Rank | 
|---|---|
| UBA52 | -3224 | 
| PSMB6 | -3105 | 
| PSMA7 | -3028 | 
| PSMB3 | -3012 | 
| PSMD8 | -3008 | 
| PSMB1 | -2979 | 
| SEM1 | -2968 | 
| PSMA4 | -2929 | 
| UBC | -2887 | 
| PSMD7 | -2885 | 
| PSMB7 | -2865 | 
| PSMB10 | -2849 | 
| RPS27A | -2821 | 
| PSMA2 | -2803 | 
| PSMA3 | -2787 | 
| PSMB8 | -2753 | 
| PSMA5 | -2655 | 
| PSMB2 | -2644 | 
| PSMD9 | -2638 | 
| PSMA1 | -2401 | 
| GeneID | Gene Rank | 
|---|---|
| UBA52 | -3224 | 
| PSMB6 | -3105 | 
| PSMA7 | -3028 | 
| PSMB3 | -3012 | 
| PSMD8 | -3008 | 
| PSMB1 | -2979 | 
| SEM1 | -2968 | 
| PSMA4 | -2929 | 
| UBC | -2887 | 
| PSMD7 | -2885 | 
| PSMB7 | -2865 | 
| PSMB10 | -2849 | 
| RPS27A | -2821 | 
| PSMA2 | -2803 | 
| PSMA3 | -2787 | 
| PSMB8 | -2753 | 
| PSMA5 | -2655 | 
| PSMB2 | -2644 | 
| PSMD9 | -2638 | 
| PSMA1 | -2401 | 
| PSME2 | -2323 | 
| PSMD4 | -2233 | 
| PSME1 | -2223 | 
| PSMC4 | -2206 | 
| PSMC1 | -2176 | 
| PSMD13 | -2161 | 
| PSMA6 | -2159 | 
| PSMC3 | -2144 | 
| PSMC5 | -2073 | 
| PSMC6 | -2047 | 
| PSMD1 | -2012 | 
| PSMD2 | -1923 | 
| PSMC2 | -1899 | 
| PSMD6 | -1878 | 
| PSMD14 | -1585 | 
| PSMB4 | -1579 | 
| UBB | -975 | 
| PSMD10 | -847 | 
| PSMB9 | -715 | 
| PSMF1 | -455 | 
| PSMD3 | -416 | 
| PSMD11 | -307 | 
| PSME3 | -153 | 
| PSMB5 | 486 | 
| PSMD12 | 1198 | 
| CHEK2 | 1574 | 
| PSMD5 | 4230 | 
| CHEK1 | 6178 | 
| PSME4 | 6251 | 
 Vif-mediated degradation of APOBEC3G 
| 1256 | |
|---|---|
| set | Vif-mediated degradation of APOBEC3G | 
| setSize | 53 | 
| pANOVA | 1.49e-17 | 
| s.dist | -0.677 | 
| p.adjustANOVA | 3.46e-16 | 
Top enriched genes
| GeneID | Gene Rank | 
|---|---|
| UBA52 | -3224 | 
| PSMB6 | -3105 | 
| RBX1 | -3082 | 
| ELOB | -3061 | 
| PSMA7 | -3028 | 
| PSMB3 | -3012 | 
| PSMD8 | -3008 | 
| ELOC | -2992 | 
| PSMB1 | -2979 | 
| SEM1 | -2968 | 
| PSMA4 | -2929 | 
| UBC | -2887 | 
| PSMD7 | -2885 | 
| PSMB7 | -2865 | 
| PSMB10 | -2849 | 
| RPS27A | -2821 | 
| PSMA2 | -2803 | 
| PSMA3 | -2787 | 
| PSMB8 | -2753 | 
| PSMA5 | -2655 | 
| GeneID | Gene Rank | 
|---|---|
| UBA52 | -3224 | 
| PSMB6 | -3105 | 
| RBX1 | -3082 | 
| ELOB | -3061 | 
| PSMA7 | -3028 | 
| PSMB3 | -3012 | 
| PSMD8 | -3008 | 
| ELOC | -2992 | 
| PSMB1 | -2979 | 
| SEM1 | -2968 | 
| PSMA4 | -2929 | 
| UBC | -2887 | 
| PSMD7 | -2885 | 
| PSMB7 | -2865 | 
| PSMB10 | -2849 | 
| RPS27A | -2821 | 
| PSMA2 | -2803 | 
| PSMA3 | -2787 | 
| PSMB8 | -2753 | 
| PSMA5 | -2655 | 
| PSMB2 | -2644 | 
| PSMD9 | -2638 | 
| PSMA1 | -2401 | 
| PSME2 | -2323 | 
| PSMD4 | -2233 | 
| PSME1 | -2223 | 
| PSMC4 | -2206 | 
| PSMC1 | -2176 | 
| PSMD13 | -2161 | 
| PSMA6 | -2159 | 
| PSMC3 | -2144 | 
| PSMC5 | -2073 | 
| PSMC6 | -2047 | 
| PSMD1 | -2012 | 
| PSMD2 | -1923 | 
| PSMC2 | -1899 | 
| PSMD6 | -1878 | 
| PSMD14 | -1585 | 
| PSMB4 | -1579 | 
| APOBEC3G | -1522 | 
| UBB | -975 | 
| PSMD10 | -847 | 
| PSMB9 | -715 | 
| PSMF1 | -455 | 
| PSMD3 | -416 | 
| PSMD11 | -307 | 
| PSME3 | -153 | 
| PSMB5 | 486 | 
| PSMD12 | 1198 | 
| PSMD5 | 4230 | 
| CUL5 | 5887 | 
| PSME4 | 6251 | 
| vif | 7664 | 
 Autodegradation of the E3 ubiquitin ligase COP1 
| 80 | |
|---|---|
| set | Autodegradation of the E3 ubiquitin ligase COP1 | 
| setSize | 49 | 
| pANOVA | 3.92e-16 | 
| s.dist | -0.672 | 
| p.adjustANOVA | 5.92e-15 | 
Top enriched genes
| GeneID | Gene Rank | 
|---|---|
| UBA52 | -3224 | 
| PSMB6 | -3105 | 
| PSMA7 | -3028 | 
| PSMB3 | -3012 | 
| PSMD8 | -3008 | 
| PSMB1 | -2979 | 
| SEM1 | -2968 | 
| PSMA4 | -2929 | 
| UBC | -2887 | 
| PSMD7 | -2885 | 
| PSMB7 | -2865 | 
| PSMB10 | -2849 | 
| RPS27A | -2821 | 
| PSMA2 | -2803 | 
| PSMA3 | -2787 | 
| PSMB8 | -2753 | 
| PSMA5 | -2655 | 
| PSMB2 | -2644 | 
| PSMD9 | -2638 | 
| PSMA1 | -2401 | 
| GeneID | Gene Rank | 
|---|---|
| UBA52 | -3224 | 
| PSMB6 | -3105 | 
| PSMA7 | -3028 | 
| PSMB3 | -3012 | 
| PSMD8 | -3008 | 
| PSMB1 | -2979 | 
| SEM1 | -2968 | 
| PSMA4 | -2929 | 
| UBC | -2887 | 
| PSMD7 | -2885 | 
| PSMB7 | -2865 | 
| PSMB10 | -2849 | 
| RPS27A | -2821 | 
| PSMA2 | -2803 | 
| PSMA3 | -2787 | 
| PSMB8 | -2753 | 
| PSMA5 | -2655 | 
| PSMB2 | -2644 | 
| PSMD9 | -2638 | 
| PSMA1 | -2401 | 
| PSME2 | -2323 | 
| PSMD4 | -2233 | 
| PSME1 | -2223 | 
| PSMC4 | -2206 | 
| PSMC1 | -2176 | 
| PSMD13 | -2161 | 
| PSMA6 | -2159 | 
| PSMC3 | -2144 | 
| PSMC5 | -2073 | 
| PSMC6 | -2047 | 
| PSMD1 | -2012 | 
| PSMD2 | -1923 | 
| PSMC2 | -1899 | 
| PSMD6 | -1878 | 
| PSMD14 | -1585 | 
| PSMB4 | -1579 | 
| UBB | -975 | 
| PSMD10 | -847 | 
| PSMB9 | -715 | 
| PSMF1 | -455 | 
| PSMD3 | -416 | 
| PSMD11 | -307 | 
| PSME3 | -153 | 
| PSMB5 | 486 | 
| PSMD12 | 1198 | 
| TP53 | 2656 | 
| PSMD5 | 4230 | 
| PSME4 | 6251 | 
| ATM | 7406 | 
 SCF(Skp2)-mediated degradation of p27/p21 
| 979 | |
|---|---|
| set | SCF(Skp2)-mediated degradation of p27/p21 | 
| setSize | 55 | 
| pANOVA | 6.58e-18 | 
| s.dist | -0.672 | 
| p.adjustANOVA | 1.61e-16 | 
Top enriched genes
| GeneID | Gene Rank | 
|---|---|
| UBA52 | -3224 | 
| PSMB6 | -3105 | 
| PSMA7 | -3028 | 
| SKP1 | -3020 | 
| PSMB3 | -3012 | 
| PSMD8 | -3008 | 
| PSMB1 | -2979 | 
| SEM1 | -2968 | 
| PSMA4 | -2929 | 
| UBC | -2887 | 
| PSMD7 | -2885 | 
| PSMB7 | -2865 | 
| PSMB10 | -2849 | 
| RPS27A | -2821 | 
| PSMA2 | -2803 | 
| PSMA3 | -2787 | 
| PSMB8 | -2753 | 
| PSMA5 | -2655 | 
| PSMB2 | -2644 | 
| PSMD9 | -2638 | 
| GeneID | Gene Rank | 
|---|---|
| UBA52 | -3224 | 
| PSMB6 | -3105 | 
| PSMA7 | -3028 | 
| SKP1 | -3020 | 
| PSMB3 | -3012 | 
| PSMD8 | -3008 | 
| PSMB1 | -2979 | 
| SEM1 | -2968 | 
| PSMA4 | -2929 | 
| UBC | -2887 | 
| PSMD7 | -2885 | 
| PSMB7 | -2865 | 
| PSMB10 | -2849 | 
| RPS27A | -2821 | 
| PSMA2 | -2803 | 
| PSMA3 | -2787 | 
| PSMB8 | -2753 | 
| PSMA5 | -2655 | 
| PSMB2 | -2644 | 
| PSMD9 | -2638 | 
| PSMA1 | -2401 | 
| CDK4 | -2345 | 
| PSME2 | -2323 | 
| PSMD4 | -2233 | 
| PSME1 | -2223 | 
| PSMC4 | -2206 | 
| PSMC1 | -2176 | 
| PSMD13 | -2161 | 
| PSMA6 | -2159 | 
| PSMC3 | -2144 | 
| PSMC5 | -2073 | 
| PSMC6 | -2047 | 
| PSMD1 | -2012 | 
| PSMD2 | -1923 | 
| PSMC2 | -1899 | 
| PSMD6 | -1878 | 
| SKP2 | -1749 | 
| PSMD14 | -1585 | 
| PSMB4 | -1579 | 
| CKS1B | -1198 | 
| UBB | -975 | 
| PSMD10 | -847 | 
| PSMB9 | -715 | 
| PSMF1 | -455 | 
| PSMD3 | -416 | 
| PSMD11 | -307 | 
| CCND1 | -163 | 
| PSME3 | -153 | 
| CCNA1 | 377 | 
| PSMB5 | 486 | 
| PSMD12 | 1198 | 
| CDKN1B | 3342 | 
| PSMD5 | 4230 | 
| CUL1 | 5483 | 
| CDKN1A | 6998 | 
 Mitochondrial translation 
| 615 | |
|---|---|
| set | Mitochondrial translation | 
| setSize | 94 | 
| pANOVA | 2.43e-29 | 
| s.dist | -0.671 | 
| p.adjustANOVA | 9.86e-28 | 
Top enriched genes
| GeneID | Gene Rank | 
|---|---|
| MRPS36 | -3096 | 
| MRPS34 | -3052 | 
| MRPL41 | -3040 | 
| MRPL54 | -3016 | 
| MRPL52 | -2988 | 
| MRPS24 | -2986 | 
| GADD45GIP1 | -2980 | 
| MRPS12 | -2910 | 
| MRPS7 | -2883 | 
| MRPL47 | -2881 | 
| MRPS18C | -2864 | 
| AURKAIP1 | -2856 | 
| MRPL20 | -2854 | 
| MRPS6 | -2853 | 
| MRPL12 | -2852 | 
| MRPL36 | -2818 | 
| MRPL57 | -2811 | 
| MRPL11 | -2801 | 
| MRPL33 | -2799 | 
| MRPL34 | -2778 | 
| GeneID | Gene Rank | 
|---|---|
| MRPS36 | -3096 | 
| MRPS34 | -3052 | 
| MRPL41 | -3040 | 
| MRPL54 | -3016 | 
| MRPL52 | -2988 | 
| MRPS24 | -2986 | 
| GADD45GIP1 | -2980 | 
| MRPS12 | -2910 | 
| MRPS7 | -2883 | 
| MRPL47 | -2881 | 
| MRPS18C | -2864 | 
| AURKAIP1 | -2856 | 
| MRPL20 | -2854 | 
| MRPS6 | -2853 | 
| MRPL12 | -2852 | 
| MRPL36 | -2818 | 
| MRPL57 | -2811 | 
| MRPL11 | -2801 | 
| MRPL33 | -2799 | 
| MRPL34 | -2778 | 
| MRPL14 | -2769 | 
| MRPS25 | -2756 | 
| MRPL51 | -2741 | 
| MRPL35 | -2735 | 
| MRPL2 | -2723 | 
| MRPL22 | -2715 | 
| MRPL21 | -2709 | 
| CHCHD1 | -2708 | 
| TUFM | -2698 | 
| MRPL28 | -2672 | 
| MRPL27 | -2643 | 
| MRPS17 | -2596 | 
| MRPL40 | -2570 | 
| MRPL13 | -2561 | 
| MRPS21 | -2525 | 
| MRPL23 | -2523 | 
| MRPS16 | -2512 | 
| MRPL55 | -2507 | 
| MRPL4 | -2468 | 
| MRPS11 | -2464 | 
| MRPL16 | -2435 | 
| MRPS15 | -2368 | 
| MRPS18A | -2341 | 
| MRPS33 | -2327 | 
| MRPS18B | -2282 | 
| MRPS35 | -2221 | 
| MRPS23 | -2202 | 
| MRPL50 | -2192 | 
| MRPL17 | -2143 | 
| MRPL15 | -2128 | 
| MRPS22 | -2108 | 
| MRPL24 | -2101 | 
| MRPL38 | -2001 | 
| MRPL39 | -1804 | 
| MRPL10 | -1715 | 
| MRPS10 | -1709 | 
| MRPS26 | -1707 | 
| GFM1 | -1632 | 
| MRPS2 | -1506 | 
| ERAL1 | -1319 | 
| MRPL32 | -1269 | 
| MRPL53 | -1256 | 
| MRRF | -1231 | 
| MTIF3 | -1168 | 
| MRPL42 | -1112 | 
| MRPL48 | -829 | 
| MRPL19 | -796 | 
| MRPL58 | -782 | 
| MRPL46 | -706 | 
| MRPS14 | -687 | 
| MRPS5 | -640 | 
| MRPS28 | -495 | 
| MRPL30 | -283 | 
| MRPL45 | -173 | 
| MRPL44 | -137 | 
| MRPL18 | -55 | 
| MRPL37 | 44 | 
| MRPL43 | 46 | 
| MRPL3 | 115 | 
| DAP3 | 242 | 
| TSFM | 243 | 
| MRPL1 | 323 | 
| MRPS31 | 441 | 
| MRPS30 | 475 | 
| MRPS27 | 1255 | 
| MTFMT | 1275 | 
| MRPL9 | 1287 | 
| OXA1L | 1294 | 
| MTRF1L | 1940 | 
| MRPL49 | 3110 | 
| MTIF2 | 3204 | 
| GFM2 | 3694 | 
| MRPS9 | 4099 | 
| PTCD3 | 4414 | 
 Hh mutants are degraded by ERAD 
| 458 | |
|---|---|
| set | Hh mutants are degraded by ERAD | 
| setSize | 53 | 
| pANOVA | 3.65e-17 | 
| s.dist | -0.669 | 
| p.adjustANOVA | 7.85e-16 | 
Top enriched genes
| GeneID | Gene Rank | 
|---|---|
| UBA52 | -3224 | 
| PSMB6 | -3105 | 
| PSMA7 | -3028 | 
| PSMB3 | -3012 | 
| PSMD8 | -3008 | 
| PSMB1 | -2979 | 
| SEM1 | -2968 | 
| PSMA4 | -2929 | 
| UBC | -2887 | 
| PSMD7 | -2885 | 
| PSMB7 | -2865 | 
| PSMB10 | -2849 | 
| RPS27A | -2821 | 
| PSMA2 | -2803 | 
| PSMA3 | -2787 | 
| PSMB8 | -2753 | 
| PSMA5 | -2655 | 
| PSMB2 | -2644 | 
| PSMD9 | -2638 | 
| DERL2 | -2405 | 
| GeneID | Gene Rank | 
|---|---|
| UBA52 | -3224 | 
| PSMB6 | -3105 | 
| PSMA7 | -3028 | 
| PSMB3 | -3012 | 
| PSMD8 | -3008 | 
| PSMB1 | -2979 | 
| SEM1 | -2968 | 
| PSMA4 | -2929 | 
| UBC | -2887 | 
| PSMD7 | -2885 | 
| PSMB7 | -2865 | 
| PSMB10 | -2849 | 
| RPS27A | -2821 | 
| PSMA2 | -2803 | 
| PSMA3 | -2787 | 
| PSMB8 | -2753 | 
| PSMA5 | -2655 | 
| PSMB2 | -2644 | 
| PSMD9 | -2638 | 
| DERL2 | -2405 | 
| PSMA1 | -2401 | 
| PSME2 | -2323 | 
| PSMD4 | -2233 | 
| PSME1 | -2223 | 
| PSMC4 | -2206 | 
| PSMC1 | -2176 | 
| PSMD13 | -2161 | 
| PSMA6 | -2159 | 
| PSMC3 | -2144 | 
| PSMC5 | -2073 | 
| PSMC6 | -2047 | 
| PSMD1 | -2012 | 
| PSMD2 | -1923 | 
| PSMC2 | -1899 | 
| PSMD6 | -1878 | 
| PSMD14 | -1585 | 
| PSMB4 | -1579 | 
| UBB | -975 | 
| PSMD10 | -847 | 
| PSMB9 | -715 | 
| VCP | -549 | 
| PSMF1 | -455 | 
| PSMD3 | -416 | 
| PSMD11 | -307 | 
| PSME3 | -153 | 
| ERLEC1 | 432 | 
| PSMB5 | 486 | 
| SYVN1 | 1083 | 
| PSMD12 | 1198 | 
| SEL1L | 3218 | 
| OS9 | 3492 | 
| PSMD5 | 4230 | 
| PSME4 | 6251 | 
 AUF1 (hnRNP D0) binds and destabilizes mRNA 
| 20 | |
|---|---|
| set | AUF1 (hnRNP D0) binds and destabilizes mRNA | 
| setSize | 53 | 
| pANOVA | 4.34e-17 | 
| s.dist | -0.667 | 
| p.adjustANOVA | 9.1e-16 | 
Top enriched genes
| GeneID | Gene Rank | 
|---|---|
| UBA52 | -3224 | 
| HSPA8 | -3128 | 
| PSMB6 | -3105 | 
| PSMA7 | -3028 | 
| PSMB3 | -3012 | 
| PSMD8 | -3008 | 
| PSMB1 | -2979 | 
| SEM1 | -2968 | 
| PSMA4 | -2929 | 
| UBC | -2887 | 
| PSMD7 | -2885 | 
| PSMB7 | -2865 | 
| PSMB10 | -2849 | 
| RPS27A | -2821 | 
| PSMA2 | -2803 | 
| PSMA3 | -2787 | 
| PSMB8 | -2753 | 
| PSMA5 | -2655 | 
| PSMB2 | -2644 | 
| PSMD9 | -2638 | 
| GeneID | Gene Rank | 
|---|---|
| UBA52 | -3224 | 
| HSPA8 | -3128 | 
| PSMB6 | -3105 | 
| PSMA7 | -3028 | 
| PSMB3 | -3012 | 
| PSMD8 | -3008 | 
| PSMB1 | -2979 | 
| SEM1 | -2968 | 
| PSMA4 | -2929 | 
| UBC | -2887 | 
| PSMD7 | -2885 | 
| PSMB7 | -2865 | 
| PSMB10 | -2849 | 
| RPS27A | -2821 | 
| PSMA2 | -2803 | 
| PSMA3 | -2787 | 
| PSMB8 | -2753 | 
| PSMA5 | -2655 | 
| PSMB2 | -2644 | 
| PSMD9 | -2638 | 
| PSMA1 | -2401 | 
| PSME2 | -2323 | 
| PSMD4 | -2233 | 
| PSME1 | -2223 | 
| PSMC4 | -2206 | 
| PSMC1 | -2176 | 
| PSMD13 | -2161 | 
| PSMA6 | -2159 | 
| PSMC3 | -2144 | 
| PSMC5 | -2073 | 
| PSMC6 | -2047 | 
| PSMD1 | -2012 | 
| PSMD2 | -1923 | 
| PSMC2 | -1899 | 
| PSMD6 | -1878 | 
| PSMD14 | -1585 | 
| PSMB4 | -1579 | 
| HSPB1 | -1553 | 
| UBB | -975 | 
| PSMD10 | -847 | 
| PSMB9 | -715 | 
| PSMF1 | -455 | 
| PSMD3 | -416 | 
| HNRNPD | -395 | 
| PSMD11 | -307 | 
| PSME3 | -153 | 
| PSMB5 | 486 | 
| HSPA1A | 580 | 
| PSMD12 | 1198 | 
| EIF4G1 | 2728 | 
| PSMD5 | 4230 | 
| PSME4 | 6251 | 
| PABPC1 | 7504 | 
 SCF-beta-TrCP mediated degradation of Emi1 
| 980 | |
|---|---|
| set | SCF-beta-TrCP mediated degradation of Emi1 | 
| setSize | 51 | 
| pANOVA | 1.95e-16 | 
| s.dist | -0.666 | 
| p.adjustANOVA | 3.45e-15 | 
Top enriched genes
| GeneID | Gene Rank | 
|---|---|
| UBA52 | -3224 | 
| PSMB6 | -3105 | 
| PSMA7 | -3028 | 
| SKP1 | -3020 | 
| PSMB3 | -3012 | 
| PSMD8 | -3008 | 
| PSMB1 | -2979 | 
| SEM1 | -2968 | 
| PSMA4 | -2929 | 
| UBC | -2887 | 
| PSMD7 | -2885 | 
| PSMB7 | -2865 | 
| PSMB10 | -2849 | 
| RPS27A | -2821 | 
| PSMA2 | -2803 | 
| PSMA3 | -2787 | 
| PSMB8 | -2753 | 
| PSMA5 | -2655 | 
| PSMB2 | -2644 | 
| PSMD9 | -2638 | 
| GeneID | Gene Rank | 
|---|---|
| UBA52 | -3224 | 
| PSMB6 | -3105 | 
| PSMA7 | -3028 | 
| SKP1 | -3020 | 
| PSMB3 | -3012 | 
| PSMD8 | -3008 | 
| PSMB1 | -2979 | 
| SEM1 | -2968 | 
| PSMA4 | -2929 | 
| UBC | -2887 | 
| PSMD7 | -2885 | 
| PSMB7 | -2865 | 
| PSMB10 | -2849 | 
| RPS27A | -2821 | 
| PSMA2 | -2803 | 
| PSMA3 | -2787 | 
| PSMB8 | -2753 | 
| PSMA5 | -2655 | 
| PSMB2 | -2644 | 
| PSMD9 | -2638 | 
| PSMA1 | -2401 | 
| PSME2 | -2323 | 
| PSMD4 | -2233 | 
| PSME1 | -2223 | 
| PSMC4 | -2206 | 
| PSMC1 | -2176 | 
| PSMD13 | -2161 | 
| PSMA6 | -2159 | 
| PSMC3 | -2144 | 
| PSMC5 | -2073 | 
| PSMC6 | -2047 | 
| PSMD1 | -2012 | 
| PSMD2 | -1923 | 
| PSMC2 | -1899 | 
| PSMD6 | -1878 | 
| PSMD14 | -1585 | 
| PSMB4 | -1579 | 
| UBB | -975 | 
| PSMD10 | -847 | 
| PSMB9 | -715 | 
| PSMF1 | -455 | 
| FZR1 | -449 | 
| PSMD3 | -416 | 
| PSMD11 | -307 | 
| PSME3 | -153 | 
| PSMB5 | 486 | 
| PSMD12 | 1198 | 
| PSMD5 | 4230 | 
| CUL1 | 5483 | 
| PSME4 | 6251 | 
| BTRC | 6965 | 
 GSK3B and BTRC:CUL1-mediated-degradation of NFE2L2 
| 393 | |
|---|---|
| set | GSK3B and BTRC:CUL1-mediated-degradation of NFE2L2 | 
| setSize | 52 | 
| pANOVA | 1.04e-16 | 
| s.dist | -0.665 | 
| p.adjustANOVA | 2.01e-15 | 
Top enriched genes
| GeneID | Gene Rank | 
|---|---|
| UBA52 | -3224 | 
| PSMB6 | -3105 | 
| RBX1 | -3082 | 
| PSMA7 | -3028 | 
| SKP1 | -3020 | 
| PSMB3 | -3012 | 
| PSMD8 | -3008 | 
| PSMB1 | -2979 | 
| SEM1 | -2968 | 
| PSMA4 | -2929 | 
| UBC | -2887 | 
| PSMD7 | -2885 | 
| PSMB7 | -2865 | 
| PSMB10 | -2849 | 
| RPS27A | -2821 | 
| PSMA2 | -2803 | 
| PSMA3 | -2787 | 
| PSMB8 | -2753 | 
| PSMA5 | -2655 | 
| PSMB2 | -2644 | 
| GeneID | Gene Rank | 
|---|---|
| UBA52 | -3224 | 
| PSMB6 | -3105 | 
| RBX1 | -3082 | 
| PSMA7 | -3028 | 
| SKP1 | -3020 | 
| PSMB3 | -3012 | 
| PSMD8 | -3008 | 
| PSMB1 | -2979 | 
| SEM1 | -2968 | 
| PSMA4 | -2929 | 
| UBC | -2887 | 
| PSMD7 | -2885 | 
| PSMB7 | -2865 | 
| PSMB10 | -2849 | 
| RPS27A | -2821 | 
| PSMA2 | -2803 | 
| PSMA3 | -2787 | 
| PSMB8 | -2753 | 
| PSMA5 | -2655 | 
| PSMB2 | -2644 | 
| PSMD9 | -2638 | 
| PSMA1 | -2401 | 
| PSME2 | -2323 | 
| PSMD4 | -2233 | 
| PSME1 | -2223 | 
| PSMC4 | -2206 | 
| PSMC1 | -2176 | 
| PSMD13 | -2161 | 
| PSMA6 | -2159 | 
| PSMC3 | -2144 | 
| PSMC5 | -2073 | 
| PSMC6 | -2047 | 
| PSMD1 | -2012 | 
| PSMD2 | -1923 | 
| PSMC2 | -1899 | 
| PSMD6 | -1878 | 
| PSMD14 | -1585 | 
| PSMB4 | -1579 | 
| UBB | -975 | 
| PSMD10 | -847 | 
| PSMB9 | -715 | 
| PSMF1 | -455 | 
| PSMD3 | -416 | 
| PSMD11 | -307 | 
| PSME3 | -153 | 
| NFE2L2 | 102 | 
| PSMB5 | 486 | 
| PSMD12 | 1198 | 
| PSMD5 | 4230 | 
| CUL1 | 5483 | 
| BTRC | 6965 | 
| GSK3B | 7481 | 
 Cross-presentation of soluble exogenous antigens (endosomes) 
| 195 | |
|---|---|
| set | Cross-presentation of soluble exogenous antigens (endosomes) | 
| setSize | 46 | 
| pANOVA | 6.16e-15 | 
| s.dist | -0.665 | 
| p.adjustANOVA | 8.17e-14 | 
Top enriched genes
| GeneID | Gene Rank | 
|---|---|
| PSMB6 | -3105 | 
| PSMA7 | -3028 | 
| PSMB3 | -3012 | 
| PSMD8 | -3008 | 
| PSMB1 | -2979 | 
| SEM1 | -2968 | 
| PSMA4 | -2929 | 
| PSMD7 | -2885 | 
| PSMB7 | -2865 | 
| PSMB10 | -2849 | 
| PSMA2 | -2803 | 
| PSMA3 | -2787 | 
| PSMB8 | -2753 | 
| PSMA5 | -2655 | 
| PSMB2 | -2644 | 
| PSMD9 | -2638 | 
| PSMA1 | -2401 | 
| PSME2 | -2323 | 
| PSMD4 | -2233 | 
| PSME1 | -2223 | 
| GeneID | Gene Rank | 
|---|---|
| PSMB6 | -3105 | 
| PSMA7 | -3028 | 
| PSMB3 | -3012 | 
| PSMD8 | -3008 | 
| PSMB1 | -2979 | 
| SEM1 | -2968 | 
| PSMA4 | -2929 | 
| PSMD7 | -2885 | 
| PSMB7 | -2865 | 
| PSMB10 | -2849 | 
| PSMA2 | -2803 | 
| PSMA3 | -2787 | 
| PSMB8 | -2753 | 
| PSMA5 | -2655 | 
| PSMB2 | -2644 | 
| PSMD9 | -2638 | 
| PSMA1 | -2401 | 
| PSME2 | -2323 | 
| PSMD4 | -2233 | 
| PSME1 | -2223 | 
| PSMC4 | -2206 | 
| PSMC1 | -2176 | 
| PSMD13 | -2161 | 
| PSMA6 | -2159 | 
| PSMC3 | -2144 | 
| PSMC5 | -2073 | 
| PSMC6 | -2047 | 
| PSMD1 | -2012 | 
| PSMD2 | -1923 | 
| PSMC2 | -1899 | 
| PSMD6 | -1878 | 
| PSMD14 | -1585 | 
| PSMB4 | -1579 | 
| PSMD10 | -847 | 
| PSMB9 | -715 | 
| FCGR1A | -493 | 
| PSMF1 | -455 | 
| PSMD3 | -416 | 
| PSMD11 | -307 | 
| PSME3 | -153 | 
| PSMB5 | 486 | 
| PSMD12 | 1198 | 
| MRC2 | 1445 | 
| PSMD5 | 4230 | 
| MRC1 | 5400 | 
| PSME4 | 6251 | 
 Regulation of Apoptosis 
| 894 | |
|---|---|
| set | Regulation of Apoptosis | 
| setSize | 51 | 
| pANOVA | 2.89e-16 | 
| s.dist | -0.662 | 
| p.adjustANOVA | 4.75e-15 | 
Top enriched genes
| GeneID | Gene Rank | 
|---|---|
| UBA52 | -3224 | 
| PSMB6 | -3105 | 
| PSMA7 | -3028 | 
| PSMB3 | -3012 | 
| PSMD8 | -3008 | 
| PSMB1 | -2979 | 
| SEM1 | -2968 | 
| PSMA4 | -2929 | 
| UBC | -2887 | 
| PSMD7 | -2885 | 
| PSMB7 | -2865 | 
| PSMB10 | -2849 | 
| RPS27A | -2821 | 
| PSMA2 | -2803 | 
| PSMA3 | -2787 | 
| PSMB8 | -2753 | 
| PSMA5 | -2655 | 
| PSMB2 | -2644 | 
| PSMD9 | -2638 | 
| PSMA1 | -2401 | 
| GeneID | Gene Rank | 
|---|---|
| UBA52 | -3224 | 
| PSMB6 | -3105 | 
| PSMA7 | -3028 | 
| PSMB3 | -3012 | 
| PSMD8 | -3008 | 
| PSMB1 | -2979 | 
| SEM1 | -2968 | 
| PSMA4 | -2929 | 
| UBC | -2887 | 
| PSMD7 | -2885 | 
| PSMB7 | -2865 | 
| PSMB10 | -2849 | 
| RPS27A | -2821 | 
| PSMA2 | -2803 | 
| PSMA3 | -2787 | 
| PSMB8 | -2753 | 
| PSMA5 | -2655 | 
| PSMB2 | -2644 | 
| PSMD9 | -2638 | 
| PSMA1 | -2401 | 
| PSME2 | -2323 | 
| PSMD4 | -2233 | 
| PSME1 | -2223 | 
| PSMC4 | -2206 | 
| PSMC1 | -2176 | 
| PSMD13 | -2161 | 
| PSMA6 | -2159 | 
| PSMC3 | -2144 | 
| PSMC5 | -2073 | 
| PSMC6 | -2047 | 
| PSMD1 | -2012 | 
| OMA1 | -1996 | 
| PSMD2 | -1923 | 
| PSMC2 | -1899 | 
| PSMD6 | -1878 | 
| PSMD14 | -1585 | 
| PSMB4 | -1579 | 
| UBB | -975 | 
| PSMD10 | -847 | 
| PSMB9 | -715 | 
| PSMF1 | -455 | 
| PSMD3 | -416 | 
| PSMD11 | -307 | 
| PSME3 | -153 | 
| PSMB5 | 486 | 
| PSMD12 | 1198 | 
| PAK2 | 1997 | 
| ARHGAP10 | 4001 | 
| PSMD5 | 4230 | 
| OPA1 | 6032 | 
| PSME4 | 6251 | 
 Formation of tubulin folding intermediates by CCT/TriC 
| 361 | |
|---|---|
| set | Formation of tubulin folding intermediates by CCT/TriC | 
| setSize | 18 | 
| pANOVA | 1.21e-06 | 
| s.dist | -0.661 | 
| p.adjustANOVA | 8.76e-06 | 
Top enriched genes
| GeneID | Gene Rank | 
|---|---|
| TUBA1B | -3174 | 
| TUBB4B | -2873 | 
| CCT8 | -2762 | 
| CCT7 | -2743 | 
| TUBA1A | -2711 | 
| CCT4 | -2649 | 
| CCT3 | -2593 | 
| CCT2 | -2573 | 
| CCT5 | -2406 | 
| TUBB2A | -2354 | 
| TUBA1C | -1994 | 
| TCP1 | -1872 | 
| TUBB3 | -1433 | 
| TUBB6 | -1363 | 
| CCT6A | 139 | 
| CCT6B | 1343 | 
| TUBA4A | 2254 | 
| TUBB4A | 4421 | 
| GeneID | Gene Rank | 
|---|---|
| TUBA1B | -3174 | 
| TUBB4B | -2873 | 
| CCT8 | -2762 | 
| CCT7 | -2743 | 
| TUBA1A | -2711 | 
| CCT4 | -2649 | 
| CCT3 | -2593 | 
| CCT2 | -2573 | 
| CCT5 | -2406 | 
| TUBB2A | -2354 | 
| TUBA1C | -1994 | 
| TCP1 | -1872 | 
| TUBB3 | -1433 | 
| TUBB6 | -1363 | 
| CCT6A | 139 | 
| CCT6B | 1343 | 
| TUBA4A | 2254 | 
| TUBB4A | 4421 | 
 The role of GTSE1 in G2/M progression after G2 checkpoint 
| 1176 | |
|---|---|
| set | The role of GTSE1 in G2/M progression after G2 checkpoint | 
| setSize | 63 | 
| pANOVA | 1.26e-19 | 
| s.dist | -0.66 | 
| p.adjustANOVA | 3.56e-18 | 
Top enriched genes
| GeneID | Gene Rank | 
|---|---|
| UBA52 | -3224 | 
| TUBA1B | -3174 | 
| PSMB6 | -3105 | 
| PSMA7 | -3028 | 
| PSMB3 | -3012 | 
| PSMD8 | -3008 | 
| PSMB1 | -2979 | 
| SEM1 | -2968 | 
| PSMA4 | -2929 | 
| UBC | -2887 | 
| PSMD7 | -2885 | 
| HSP90AA1 | -2884 | 
| TUBB4B | -2873 | 
| PSMB7 | -2865 | 
| PSMB10 | -2849 | 
| RPS27A | -2821 | 
| PSMA2 | -2803 | 
| HSP90AB1 | -2802 | 
| PSMA3 | -2787 | 
| PSMB8 | -2753 | 
| GeneID | Gene Rank | 
|---|---|
| UBA52 | -3224 | 
| TUBA1B | -3174 | 
| PSMB6 | -3105 | 
| PSMA7 | -3028 | 
| PSMB3 | -3012 | 
| PSMD8 | -3008 | 
| PSMB1 | -2979 | 
| SEM1 | -2968 | 
| PSMA4 | -2929 | 
| UBC | -2887 | 
| PSMD7 | -2885 | 
| HSP90AA1 | -2884 | 
| TUBB4B | -2873 | 
| PSMB7 | -2865 | 
| PSMB10 | -2849 | 
| RPS27A | -2821 | 
| PSMA2 | -2803 | 
| HSP90AB1 | -2802 | 
| PSMA3 | -2787 | 
| PSMB8 | -2753 | 
| TUBA1A | -2711 | 
| PSMA5 | -2655 | 
| PSMB2 | -2644 | 
| PSMD9 | -2638 | 
| PSMA1 | -2401 | 
| TUBB2A | -2354 | 
| PSME2 | -2323 | 
| PSMD4 | -2233 | 
| PSME1 | -2223 | 
| PSMC4 | -2206 | 
| PSMC1 | -2176 | 
| PSMD13 | -2161 | 
| PSMA6 | -2159 | 
| PSMC3 | -2144 | 
| PSMC5 | -2073 | 
| PSMC6 | -2047 | 
| PSMD1 | -2012 | 
| TUBA1C | -1994 | 
| PSMD2 | -1923 | 
| PSMC2 | -1899 | 
| PSMD6 | -1878 | 
| PSMD14 | -1585 | 
| PSMB4 | -1579 | 
| TUBB3 | -1433 | 
| TUBB6 | -1363 | 
| MAPRE1 | -1068 | 
| CCNB1 | -1019 | 
| UBB | -975 | 
| PSMD10 | -847 | 
| PSMB9 | -715 | 
| PSMF1 | -455 | 
| PSMD3 | -416 | 
| PSMD11 | -307 | 
| PSME3 | -153 | 
| PSMB5 | 486 | 
| PSMD12 | 1198 | 
| CCNB2 | 1383 | 
| TUBA4A | 2254 | 
| TP53 | 2656 | 
| PSMD5 | 4230 | 
| TUBB4A | 4421 | 
| PSME4 | 6251 | 
| CDKN1A | 6998 | 
 Metabolism of polyamines 
| 594 | |
|---|---|
| set | Metabolism of polyamines | 
| setSize | 54 | 
| pANOVA | 4.87e-17 | 
| s.dist | -0.66 | 
| p.adjustANOVA | 1e-15 | 
Top enriched genes
| GeneID | Gene Rank | 
|---|---|
| PSMB6 | -3105 | 
| SMS | -3097 | 
| PSMA7 | -3028 | 
| PSMB3 | -3012 | 
| PSMD8 | -3008 | 
| PSMB1 | -2979 | 
| SEM1 | -2968 | 
| PSMA4 | -2929 | 
| OAZ1 | -2912 | 
| PSMD7 | -2885 | 
| PSMB7 | -2865 | 
| PSMB10 | -2849 | 
| PSMA2 | -2803 | 
| PSMA3 | -2787 | 
| PSMB8 | -2753 | 
| SRM | -2748 | 
| PSMA5 | -2655 | 
| PSMB2 | -2644 | 
| PSMD9 | -2638 | 
| PSMA1 | -2401 | 
| GeneID | Gene Rank | 
|---|---|
| PSMB6 | -3105 | 
| SMS | -3097 | 
| PSMA7 | -3028 | 
| PSMB3 | -3012 | 
| PSMD8 | -3008 | 
| PSMB1 | -2979 | 
| SEM1 | -2968 | 
| PSMA4 | -2929 | 
| OAZ1 | -2912 | 
| PSMD7 | -2885 | 
| PSMB7 | -2865 | 
| PSMB10 | -2849 | 
| PSMA2 | -2803 | 
| PSMA3 | -2787 | 
| PSMB8 | -2753 | 
| SRM | -2748 | 
| PSMA5 | -2655 | 
| PSMB2 | -2644 | 
| PSMD9 | -2638 | 
| PSMA1 | -2401 | 
| PSME2 | -2323 | 
| PSMD4 | -2233 | 
| PSME1 | -2223 | 
| PSMC4 | -2206 | 
| PSMC1 | -2176 | 
| PSMD13 | -2161 | 
| PSMA6 | -2159 | 
| PSMC3 | -2144 | 
| NQO1 | -2131 | 
| PSMC5 | -2073 | 
| PSMC6 | -2047 | 
| PSMD1 | -2012 | 
| OAZ2 | -1964 | 
| PSMD2 | -1923 | 
| PSMC2 | -1899 | 
| PSMD6 | -1878 | 
| OAZ3 | -1610 | 
| PSMD14 | -1585 | 
| PSMB4 | -1579 | 
| PAOX | -1015 | 
| PSMD10 | -847 | 
| PSMB9 | -715 | 
| PSMF1 | -455 | 
| PSMD3 | -416 | 
| ODC1 | -336 | 
| PSMD11 | -307 | 
| PSME3 | -153 | 
| AZIN1 | 129 | 
| PSMB5 | 486 | 
| PSMD12 | 1198 | 
| PSMD5 | 4230 | 
| AMD1 | 5905 | 
| PSME4 | 6251 | 
| SAT1 | 6324 | 
 Defective CFTR causes cystic fibrosis 
| 227 | |
|---|---|
| set | Defective CFTR causes cystic fibrosis | 
| setSize | 57 | 
| pANOVA | 1.24e-17 | 
| s.dist | -0.654 | 
| p.adjustANOVA | 2.92e-16 | 
Top enriched genes
| GeneID | Gene Rank | 
|---|---|
| UBA52 | -3224 | 
| PSMB6 | -3105 | 
| PSMA7 | -3028 | 
| PSMB3 | -3012 | 
| PSMD8 | -3008 | 
| PSMB1 | -2979 | 
| SEM1 | -2968 | 
| PSMA4 | -2929 | 
| UBC | -2887 | 
| PSMD7 | -2885 | 
| PSMB7 | -2865 | 
| PSMB10 | -2849 | 
| RPS27A | -2821 | 
| PSMA2 | -2803 | 
| PSMA3 | -2787 | 
| PSMB8 | -2753 | 
| PSMA5 | -2655 | 
| PSMB2 | -2644 | 
| PSMD9 | -2638 | 
| DERL2 | -2405 | 
| GeneID | Gene Rank | 
|---|---|
| UBA52 | -3224 | 
| PSMB6 | -3105 | 
| PSMA7 | -3028 | 
| PSMB3 | -3012 | 
| PSMD8 | -3008 | 
| PSMB1 | -2979 | 
| SEM1 | -2968 | 
| PSMA4 | -2929 | 
| UBC | -2887 | 
| PSMD7 | -2885 | 
| PSMB7 | -2865 | 
| PSMB10 | -2849 | 
| RPS27A | -2821 | 
| PSMA2 | -2803 | 
| PSMA3 | -2787 | 
| PSMB8 | -2753 | 
| PSMA5 | -2655 | 
| PSMB2 | -2644 | 
| PSMD9 | -2638 | 
| DERL2 | -2405 | 
| PSMA1 | -2401 | 
| DERL1 | -2387 | 
| PSME2 | -2323 | 
| PSMD4 | -2233 | 
| PSME1 | -2223 | 
| PSMC4 | -2206 | 
| PSMC1 | -2176 | 
| PSMD13 | -2161 | 
| PSMA6 | -2159 | 
| PSMC3 | -2144 | 
| PSMC5 | -2073 | 
| PSMC6 | -2047 | 
| PSMD1 | -2012 | 
| PSMD2 | -1923 | 
| PSMC2 | -1899 | 
| PSMD6 | -1878 | 
| PSMD14 | -1585 | 
| PSMB4 | -1579 | 
| UBB | -975 | 
| PSMD10 | -847 | 
| ERLIN2 | -837 | 
| PSMB9 | -715 | 
| VCP | -549 | 
| PSMF1 | -455 | 
| RNF5 | -422 | 
| PSMD3 | -416 | 
| PSMD11 | -307 | 
| PSME3 | -153 | 
| RNF185 | 257 | 
| ERLEC1 | 432 | 
| PSMB5 | 486 | 
| PSMD12 | 1198 | 
| ERLIN1 | 3183 | 
| SEL1L | 3218 | 
| OS9 | 3492 | 
| PSMD5 | 4230 | 
| PSME4 | 6251 | 
 Degradation of DVL 
| 239 | |
|---|---|
| set | Degradation of DVL | 
| setSize | 52 | 
| pANOVA | 3.8e-16 | 
| s.dist | -0.653 | 
| p.adjustANOVA | 5.88e-15 | 
Top enriched genes
| GeneID | Gene Rank | 
|---|---|
| UBA52 | -3224 | 
| PSMB6 | -3105 | 
| RBX1 | -3082 | 
| PSMA7 | -3028 | 
| PSMB3 | -3012 | 
| PSMD8 | -3008 | 
| PSMB1 | -2979 | 
| SEM1 | -2968 | 
| PSMA4 | -2929 | 
| UBC | -2887 | 
| PSMD7 | -2885 | 
| PSMB7 | -2865 | 
| PSMB10 | -2849 | 
| RPS27A | -2821 | 
| PSMA2 | -2803 | 
| PSMA3 | -2787 | 
| PSMB8 | -2753 | 
| PSMA5 | -2655 | 
| PSMB2 | -2644 | 
| PSMD9 | -2638 | 
| GeneID | Gene Rank | 
|---|---|
| UBA52 | -3224 | 
| PSMB6 | -3105 | 
| RBX1 | -3082 | 
| PSMA7 | -3028 | 
| PSMB3 | -3012 | 
| PSMD8 | -3008 | 
| PSMB1 | -2979 | 
| SEM1 | -2968 | 
| PSMA4 | -2929 | 
| UBC | -2887 | 
| PSMD7 | -2885 | 
| PSMB7 | -2865 | 
| PSMB10 | -2849 | 
| RPS27A | -2821 | 
| PSMA2 | -2803 | 
| PSMA3 | -2787 | 
| PSMB8 | -2753 | 
| PSMA5 | -2655 | 
| PSMB2 | -2644 | 
| PSMD9 | -2638 | 
| PSMA1 | -2401 | 
| PSME2 | -2323 | 
| PSMD4 | -2233 | 
| PSME1 | -2223 | 
| PSMC4 | -2206 | 
| PSMC1 | -2176 | 
| PSMD13 | -2161 | 
| PSMA6 | -2159 | 
| PSMC3 | -2144 | 
| PSMC5 | -2073 | 
| PSMC6 | -2047 | 
| PSMD1 | -2012 | 
| PSMD2 | -1923 | 
| PSMC2 | -1899 | 
| PSMD6 | -1878 | 
| PSMD14 | -1585 | 
| PSMB4 | -1579 | 
| UBB | -975 | 
| PSMD10 | -847 | 
| PSMB9 | -715 | 
| PSMF1 | -455 | 
| PSMD3 | -416 | 
| PSMD11 | -307 | 
| PSME3 | -153 | 
| PSMB5 | 486 | 
| PSMD12 | 1198 | 
| DVL3 | 2041 | 
| DVL2 | 2265 | 
| KLHL12 | 2360 | 
| PSMD5 | 4230 | 
| PSME4 | 6251 | 
| CUL3 | 7612 | 
Here is the session info with all the versions of packages used.
sessionInfo()## R version 4.3.1 (2023-06-16)
## 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] stats     graphics  grDevices utils     datasets  methods   base     
## 
## other attached packages:
##  [1] stringr_1.5.0        harmony_0.1.1        Rcpp_1.0.11         
##  [4] tidyr_1.3.0          SeuratWrappers_0.3.1 SeuratObject_4.1.3  
##  [7] Seurat_4.3.0.1       pkgload_1.3.2.1      GGally_2.1.2        
## [10] ggplot2_3.4.3        reshape2_1.4.4       beeswarm_0.4.0      
## [13] gtools_3.9.4         tibble_3.2.1         dplyr_1.1.3         
## [16] echarts4r_0.4.5      kableExtra_1.3.4     gplots_3.1.3        
## [19] mitch_1.12.0        
## 
## loaded via a namespace (and not attached):
##   [1] RColorBrewer_1.1-3     rstudioapi_0.15.0      jsonlite_1.8.7        
##   [4] magrittr_2.0.3         spatstat.utils_3.0-3   farver_2.1.1          
##   [7] rmarkdown_2.25         vctrs_0.6.3            ROCR_1.0-11           
##  [10] spatstat.explore_3.2-3 webshot_0.5.5          htmltools_0.5.6       
##  [13] sass_0.4.7             sctransform_0.3.5      parallelly_1.36.0     
##  [16] KernSmooth_2.23-22     bslib_0.5.1            htmlwidgets_1.6.2     
##  [19] ica_1.0-3              plyr_1.8.8             plotly_4.10.2         
##  [22] zoo_1.8-12             cachem_1.0.8           igraph_1.5.1          
##  [25] mime_0.12              lifecycle_1.0.3        pkgconfig_2.0.3       
##  [28] rsvd_1.0.5             Matrix_1.6-1.1         R6_2.5.1              
##  [31] fastmap_1.1.1          fitdistrplus_1.1-11    future_1.33.0         
##  [34] shiny_1.7.5            digest_0.6.33          colorspace_2.1-0      
##  [37] reshape_0.8.9          patchwork_1.1.3        tensor_1.5            
##  [40] irlba_2.3.5.1          labeling_0.4.3         progressr_0.14.0      
##  [43] fansi_1.0.4            spatstat.sparse_3.0-2  httr_1.4.7            
##  [46] polyclip_1.10-4        abind_1.4-5            compiler_4.3.1        
##  [49] remotes_2.4.2.1        withr_2.5.0            highr_0.10            
##  [52] R.utils_2.12.2         MASS_7.3-60            caTools_1.18.2        
##  [55] tools_4.3.1            lmtest_0.9-40          httpuv_1.6.11         
##  [58] future.apply_1.11.0    goftest_1.2-3          R.oo_1.25.0           
##  [61] glue_1.6.2             nlme_3.1-163           promises_1.2.1        
##  [64] grid_4.3.1             Rtsne_0.16             cluster_2.1.4         
##  [67] generics_0.1.3         gtable_0.3.4           spatstat.data_3.0-1   
##  [70] R.methodsS3_1.8.2      data.table_1.14.8      sp_2.0-0              
##  [73] xml2_1.3.5             utf8_1.2.3             spatstat.geom_3.2-5   
##  [76] RcppAnnoy_0.0.21       ggrepel_0.9.3          RANN_2.6.1            
##  [79] pillar_1.9.0           later_1.3.1            splines_4.3.1         
##  [82] lattice_0.21-8         survival_3.5-7         deldir_1.0-9          
##  [85] tidyselect_1.2.0       miniUI_0.1.1.1         pbapply_1.7-2         
##  [88] knitr_1.44             gridExtra_2.3          svglite_2.1.1         
##  [91] scattermore_1.2        xfun_0.40              matrixStats_1.0.0     
##  [94] stringi_1.7.12         lazyeval_0.2.2         yaml_2.3.7            
##  [97] evaluate_0.21          codetools_0.2-19       BiocManager_1.30.22   
## [100] cli_3.6.1              uwot_0.1.16            xtable_1.8-4          
## [103] reticulate_1.32.0      systemfonts_1.0.4      munsell_0.5.0         
## [106] jquerylib_0.1.4        globals_0.16.2         spatstat.random_3.1-6 
## [109] png_0.1-8              parallel_4.3.1         ellipsis_0.3.2        
## [112] bitops_1.0-7           listenv_0.9.0          viridisLite_0.4.2     
## [115] scales_1.2.1           ggridges_0.5.4         leiden_0.4.3          
## [118] purrr_1.0.2            rlang_1.1.1            cowplot_1.1.1         
## [121] rvest_1.0.3END of report