| Name |
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Septin and tuftelin interacting protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Septin and tuftelin interacting protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Tuftelin interacting protein, N-terminal domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Tuftelin interacting protein, N-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Tuftelin Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Tuftelin protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Aurora kinase A and ninein interacting protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Aurora kinase A and ninein interacting protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Janus kinase and microtubule-interacting protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Janus kinase and microtubule-interacting protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
SLP adapter and CSK-interacting membrane protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the SLP adapter and CSK-interacting membrane protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
ADP-ribosylation factor-like protein 6-interacting protein 6 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the ADP-ribosylation factor-like protein 6-interacting protein 6 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
G protein-coupled receptor kinase-interacting protein 1 C term Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the G protein-coupled receptor kinase-interacting protein 1 C term protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Growth arrest/ DNA-damage-inducible protein-interacting protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Growth arrest/ DNA-damage-inducible protein-interacting protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
ASF1-interacting protein complex Gene Setproteins in the ASF1-interacting protein complex protein complex from the CORUM Protein Complexes dataset. |
Immunodeficiency due to Defect in MAPBP-Interacting Protein Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Immunodeficiency due to Defect in MAPBP-Interacting Protein from the curated CTD Gene-Disease Associations dataset. |
Glutamate receptor-interacting protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Glutamate receptor-interacting protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Glutamate receptor-interacting protein 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Glutamate receptor-interacting protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
KRR1 interacting protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the KRR1 interacting protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Leucine-rich repeat flightless-interacting protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Leucine-rich repeat flightless-interacting protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Nuclear fragile X mental retardation-interacting protein 1, conserved domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Nuclear fragile X mental retardation-interacting protein 1, conserved domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Rab5-interacting protein family Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Rab5-interacting protein family protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Cdc42-interacting protein 4 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Cdc42-interacting protein 4 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Disabled homologue 2-interacting protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Disabled homologue 2-interacting protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
SKI-interacting protein SKIP, SNW domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the SKI-interacting protein SKIP, SNW domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Rab5-interacting protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Rab5-interacting protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Na,K-Atpase Interacting protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Na,K-Atpase Interacting protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
M-phase-specific PLK1-interacting protein-like, vertebrate Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the M-phase-specific PLK1-interacting protein-like, vertebrate protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Inositol 1,4,5-trisphosphate receptor-interacting protein family Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Inositol 1,4,5-trisphosphate receptor-interacting protein family protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
M-phase-specific PLK1-interacting protein-like Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the M-phase-specific PLK1-interacting protein-like protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
TATA-binding protein interacting (TIP20) Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the TATA-binding protein interacting (TIP20) protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Cip1-interacting zinc finger protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Cip1-interacting zinc finger protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
RPA-interacting protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the RPA-interacting protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ran-interacting Mog1 protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ran-interacting Mog1 protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Fibrous sheath-interacting protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Fibrous sheath-interacting protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Cyclin-dependent kinase 2-interacting protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Cyclin-dependent kinase 2-interacting protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Rad9, Rad1, Hus1-interacting nuclear orphan protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Rad9, Rad1, Hus1-interacting nuclear orphan protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
PDZK1-interacting protein 1 family Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the PDZK1-interacting protein 1 family protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Proline-serine-threonine phosphatase-interacting protein 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Proline-serine-threonine phosphatase-interacting protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
EPM2A-interacting protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the EPM2A-interacting protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
CB1 cannabinoid receptor-interacting protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the CB1 cannabinoid receptor-interacting protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Folliculin-interacting protein, C-terminal domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Folliculin-interacting protein, C-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
NEFA-interacting nuclear protein NIP30, N-terminal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the NEFA-interacting nuclear protein NIP30, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Folliculin-interacting protein family Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Folliculin-interacting protein family protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Receptor-interacting serine/threonine-protein kinase 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Receptor-interacting serine/threonine-protein kinase 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
LAR-interacting protein, Liprin Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the LAR-interacting protein, Liprin protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Activating transcription factor 7-interacting protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Activating transcription factor 7-interacting protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Tat binding protein 1-interacting Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Tat binding protein 1-interacting protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Nuclear pore complex interacting protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Nuclear pore complex interacting protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
RPA-interacting protein, C-terminal domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the RPA-interacting protein, C-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Phosphoinositide-interacting protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Phosphoinositide-interacting protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Hepatitis B X-interacting protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Hepatitis B X-interacting protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Muscular LMNA-interacting protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Muscular LMNA-interacting protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Siah interacting protein, N-terminal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Siah interacting protein, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
TRF2-interacting telomeric protein/Rap1, C-terminal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the TRF2-interacting telomeric protein/Rap1, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
RPA-interacting protein, N-terminal domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the RPA-interacting protein, N-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
RPA-interacting protein, central domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the RPA-interacting protein, central domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
WAS/WASL-interacting protein family member 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the WAS/WASL-interacting protein family member 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
WAS/WASL-interacting protein family member 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the WAS/WASL-interacting protein family member 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Kv channel-interacting protein 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Kv channel-interacting protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
TRAF3-interacting protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the TRAF3-interacting protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
PGAP2-interacting protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the PGAP2-interacting protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Rab interacting lysosomal protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Rab interacting lysosomal protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Folliculin-interacting protein, N-terminal domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Folliculin-interacting protein, N-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Activating transcription factor 7-interacting protein 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Activating transcription factor 7-interacting protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Inositol 1,4,5-trisphosphate receptor-interacting protein-like 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Inositol 1,4,5-trisphosphate receptor-interacting protein-like 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Inositol 1,4,5-trisphosphate receptor-interacting protein-like 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Inositol 1,4,5-trisphosphate receptor-interacting protein-like 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Inhibitor of nuclear factor kappa-B kinase-interacting protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Inhibitor of nuclear factor kappa-B kinase-interacting protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Folliculin-interacting protein, middle domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Folliculin-interacting protein, middle domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Nuclear receptor-interacting protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Nuclear receptor-interacting protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Schwannomin interacting protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Schwannomin interacting protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Arg/Abl-interacting protein 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Arg/Abl-interacting protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Inositol 1,4,5-trisphosphate receptor-interacting protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Inositol 1,4,5-trisphosphate receptor-interacting protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
SKI-interacting protein, SKIP Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the SKI-interacting protein, SKIP protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
TEL2-interacting protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the TEL2-interacting protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
PH-interacting protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the PH-interacting protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Bcl2-/adenovirus E1B 19kDa-interacting protein 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Bcl2-/adenovirus E1B 19kDa-interacting protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
immunodeficiency due to defect in mapbp-interacting protein Gene SetFrom OMIM Gene-Disease Associations genes associated with the immunodeficiency due to defect in mapbp-interacting protein phenotype from the curated OMIM Gene-Disease Associations dataset. |
LRR FLII-interacting protein 1 (LRRFIP1) activates type I IFN production Gene Setproteins participating in the LRR FLII-interacting protein 1 (LRRFIP1) activates type I IFN production pathway from the Reactome Pathways dataset. |
LRR FLII-interacting protein 1 (LRRFIP1) activates type I IFN production Gene Setproteins participating in the LRR FLII-interacting protein 1 (LRRFIP1) activates type I IFN production pathway from the Reactome Pathways 2024 dataset. |
septin cytoskeleton Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the septin cytoskeleton cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
septin complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the septin complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
septin filament array Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the septin filament array cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
septin cap Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the septin cap cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
septin cytoskeleton Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the septin cytoskeleton cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
mitotic septin complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the mitotic septin complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
septin complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the septin complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
septin collar Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the septin collar cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
septin ring Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the septin ring cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
septin band Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the septin band cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
Septin complex Gene Setproteins in the Septin complex protein complex from the CORUM Protein Complexes dataset. |
septin Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term septin in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
septin cytoskeleton organization Gene SetFrom GO Biological Process Annotations 2015 genes participating in the septin cytoskeleton organization biological process from the curated GO Biological Process Annotations 2015 dataset. |
septin ring organization Gene SetFrom GO Biological Process Annotations 2015 genes participating in the septin ring organization biological process from the curated GO Biological Process Annotations 2015 dataset. |
septin ring assembly Gene SetFrom GO Biological Process Annotations 2015 genes participating in the septin ring assembly biological process from the curated GO Biological Process Annotations 2015 dataset. |
septin complex Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the septin complex cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
Septin Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Septin protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Septin 7 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Septin 7 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Septin 3 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Septin 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Septin 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Septin 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Septin-type guanine nucleotide-binding (G) domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Septin-type guanine nucleotide-binding (G) domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
septin cytoskeleton organization Gene SetFrom GO Biological Process Annotations 2023 genes participating in the septin cytoskeleton organization biological process from the curated GO Biological Process Annotations 2023 dataset. |
septin ring assembly Gene SetFrom GO Biological Process Annotations 2023 genes participating in the septin ring assembly biological process from the curated GO Biological Process Annotations 2023 dataset. |
septin ring organization Gene SetFrom GO Biological Process Annotations 2023 genes participating in the septin ring organization biological process from the curated GO Biological Process Annotations 2023 dataset. |
septin ring Gene SetFrom GO Cellular Component Annotations 2023 proteins localized to the septin ring cellular component from the curated GO Cellular Component Annotations 2023 dataset. |
septin cytoskeleton Gene SetFrom GO Cellular Component Annotations 2023 proteins localized to the septin cytoskeleton cellular component from the curated GO Cellular Component Annotations 2023 dataset. |
postsynaptic septin cytoskeleton Gene SetFrom SynGO Synaptic Gene Annotations genes associated with the synaptic term postsynaptic septin cytoskeleton from the SynGO Synaptic Gene Annotations dataset. |
septin cytoskeleton organization Gene SetFrom GO Biological Process Annotations 2025 genes participating in the septin cytoskeleton organization biological process from the curated GO Biological Process Annotations 2025 dataset. |
septin ring assembly Gene SetFrom GO Biological Process Annotations 2025 genes participating in the septin ring assembly biological process from the curated GO Biological Process Annotations 2025 dataset. |
septin ring organization Gene SetFrom GO Biological Process Annotations 2025 genes participating in the septin ring organization biological process from the curated GO Biological Process Annotations 2025 dataset. |
septin ring Gene SetFrom GO Cellular Component Annotations 2025 proteins localized to the septin ring cellular component from the curated GO Cellular Component Annotations 2025 dataset. |
septin cytoskeleton Gene SetFrom GO Cellular Component Annotations 2025 proteins localized to the septin cytoskeleton cellular component from the curated GO Cellular Component Annotations 2025 dataset. |
Septin complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Septin complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Septin cytoskeleton Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Septin cytoskeleton cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Septin ring Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Septin ring cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Septin cytoskeleton Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Septin cytoskeleton cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Septin complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Septin complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Septin ring Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Septin ring cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Septin collar Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Septin collar cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Mitotic septin complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Mitotic septin complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Cleavage apparatus septin structure Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Cleavage apparatus septin structure cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Cellular bud neck septin ring Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Cellular bud neck septin ring cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Cellular bud neck septin structure Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Cellular bud neck septin structure cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Split septin rings Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Split septin rings cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Septin filament array Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Septin filament array cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Septin cap Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Septin cap cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Meiotic septin complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Meiotic septin complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Hyphal septin ring Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Hyphal septin ring cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Septin band Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Septin band cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Septin complex 1 Gene SetFrom CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Septin complex 1 assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset. |
Septin complex 2 Gene SetFrom CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Septin complex 2 assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset. |
Septin mediated cytoskeleton organization Gene SetFrom CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Septin mediated cytoskeleton organization assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset. |
interacting Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term interacting in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
Bcl-2-interacting killer Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Bcl-2-interacting killer protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Stress-activated map kinase interacting 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Stress-activated map kinase interacting 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Beta-catenin-interacting ICAT Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Beta-catenin-interacting ICAT protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Nuclear-interacting partner of ALK/Rsm1-like Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Nuclear-interacting partner of ALK/Rsm1-like protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Histone deacetylase interacting Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Histone deacetylase interacting protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Cytoplasmic FMR1-interacting Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Cytoplasmic FMR1-interacting protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Lck-interacting transmembrane adapter 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Lck-interacting transmembrane adapter 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
USP8 interacting Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the USP8 interacting protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Pre-mRNA splicing Prp18-interacting factor Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Pre-mRNA splicing Prp18-interacting factor protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
MHC class II-associated invariant chain/CLIP, MHC II-interacting Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the MHC class II-associated invariant chain/CLIP, MHC II-interacting protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Nitric oxide synthase-interacting Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Nitric oxide synthase-interacting protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Citron Rho-interacting kinase Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Citron Rho-interacting kinase protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
CBF1-interacting co-repressor CIR, N-terminal domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the CBF1-interacting co-repressor CIR, N-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
RNA helicase UPF1, UPF2-interacting domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the RNA helicase UPF1, UPF2-interacting domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ligand-dependent nuclear receptor-interacting factor 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ligand-dependent nuclear receptor-interacting factor 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
IP3R-interacting domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the IP3R-interacting domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Phosphorylated CTD interacting factor 1, WW domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Phosphorylated CTD interacting factor 1, WW domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Nucleoporin interacting component Nup93/Nic96 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Nucleoporin interacting component Nup93/Nic96 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Inhibitor of CDK interacting with cyclin A1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Inhibitor of CDK interacting with cyclin A1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Bicoid-interacting 3 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Bicoid-interacting 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
TERF1-interacting nuclear factor 2, N-terminal domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the TERF1-interacting nuclear factor 2, N-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Terminal deoxynucleotidyltransferase-interacting factor 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Terminal deoxynucleotidyltransferase-interacting factor 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
BH3-interacting domain death agonist Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the BH3-interacting domain death agonist protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
LSM-interacting domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the LSM-interacting domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Bcl-x interacting, BH3 domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Bcl-x interacting, BH3 domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
SRI, Set2 Rpb1 interacting Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the SRI, Set2 Rpb1 interacting protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
TRP-interacting helix, InaF motif Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the TRP-interacting helix, InaF motif protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
NLI interacting factor Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the NLI interacting factor protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ubiquitin interacting motif Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ubiquitin interacting motif protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
MKI67 FHA domain-interacting nucleolar phosphoprotein, FHA Ki67 binding Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the MKI67 FHA domain-interacting nucleolar phosphoprotein, FHA Ki67 binding protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
negative regulation of TCF-dependent signaling by DVL-interacting proteins Gene Setproteins participating in the negative regulation of TCF-dependent signaling by DVL-interacting proteins pathway from the Reactome Pathways dataset. |
PIWI-interacting RNA (piRNA) biogenesis Gene Setproteins participating in the PIWI-interacting RNA (piRNA) biogenesis pathway from the Reactome Pathways dataset. |
Negative regulation of TCF-dependent signaling by DVL-interacting proteins Gene Setproteins participating in the Negative regulation of TCF-dependent signaling by DVL-interacting proteins pathway from the Reactome Pathways 2024 dataset. |
PIWI-interacting RNA (piRNA) biogenesis Gene Setproteins participating in the PIWI-interacting RNA (piRNA) biogenesis pathway from the Reactome Pathways 2024 dataset. |
Regulation of endogenous retroelements by Piwi-interacting RNAs (piRNAs) Gene Setproteins participating in the Regulation of endogenous retroelements by Piwi-interacting RNAs (piRNAs) pathway from the Reactome Pathways 2024 dataset. |
Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds Gene Setproteins participating in the Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds pathway from the Reactome Pathways dataset. |
Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
50S ribosomal protein L18Ae/60S ribosomal protein L20 and L18a Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the 50S ribosomal protein L18Ae/60S ribosomal protein L20 and L18a protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Cleft lip and palate transmembrane protein 1-like protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Cleft lip and palate transmembrane protein 1-like protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
V-set and transmembrane domain-containing protein 2-like protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the V-set and transmembrane domain-containing protein 2-like protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Proline/serine-rich coiled-coil protein 1/G2 and S phase-expressed protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Proline/serine-rich coiled-coil protein 1/G2 and S phase-expressed protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
activated protein c resistance; blood coagulation disorders; liver diseases; protein c deficiency; protein s deficiency; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; blood coagulation disorders; liver diseases; protein c deficiency; protein s deficiency; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
activated protein c resistance; antithrombin iii deficiency; pregnancy complications, hematologic; protein c deficiency; protein s deficiency; puerperal disorders; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; antithrombin iii deficiency; pregnancy complications, hematologic; protein c deficiency; protein s deficiency; puerperal disorders; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
basic mechanism of action of ppara pparb(d) and pparg and effects on gene expression Gene SetFrom Biocarta Pathways proteins participating in the basic mechanism of action of ppara pparb(d) and pparg and effects on gene expression pathway from the Biocarta Pathways dataset. |
BRCA1 and BRCA2 Hereditary Breast and Ovarian Cancer Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the BRCA1 and BRCA2 Hereditary Breast and Ovarian Cancer phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Coloboma, uveal, with cleft lip and palate and mental retardation Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Coloboma, uveal, with cleft lip and palate and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hypomyelination with brainstem and spinal cord involvement and leg spasticity Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypomyelination with brainstem and spinal cord involvement and leg spasticity phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mental retardation and microcephaly with pontine and cerebellar hypoplasia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mental retardation and microcephaly with pontine and cerebellar hypoplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Diabetes mellitus AND insipidus with optic atrophy AND deafness Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Diabetes mellitus AND insipidus with optic atrophy AND deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH from the curated CTD Gene-Disease Associations dataset. |
Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation from the curated CTD Gene-Disease Associations dataset. |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities from the curated CTD Gene-Disease Associations dataset. |
Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia from the curated CTD Gene-Disease Associations dataset. |
Neuropathy, Hereditary Sensory And Autonomic, Type I, With Cough And Gastroesophageal Reflux Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, Hereditary Sensory And Autonomic, Type I, With Cough And Gastroesophageal Reflux from the curated CTD Gene-Disease Associations dataset. |
Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations from the curated CTD Gene-Disease Associations dataset. |
postheparin plasma lipase activities body fat and plasma lipid and lipoprotein concentrations Gene SetFrom GAD Gene-Disease Associations genes associated with the disease postheparin plasma lipase activities body fat and plasma lipid and lipoprotein concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anxiety and hostility and depression Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anxiety and hostility and depression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
charcot-marie-tooth disease; hereditary motor and sensory neuropathies; hereditary sensory and motor neuropathy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease charcot-marie-tooth disease; hereditary motor and sensory neuropathies; hereditary sensory and motor neuropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
frontotemporal dementia and pick-like 3r and 4r tauopathy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease frontotemporal dementia and pick-like 3r and 4r tauopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adipose tissue lipoprotein lipase activity and lipoprotein lipid and glucose concentrations Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adipose tissue lipoprotein lipase activity and lipoprotein lipid and glucose concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
squamous cell carcinomas of the head and neck (scchn) and breast cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease squamous cell carcinomas of the head and neck (scchn) and breast cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
vitamins and metabolites in pregnant women and neonates Gene SetFrom GAD Gene-Disease Associations genes associated with the disease vitamins and metabolites in pregnant women and neonates in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
racemase and epimerase activity, acting on amino acids and derivatives Gene SetFrom GO Molecular Function Annotations 2015 genes performing the racemase and epimerase activity, acting on amino acids and derivatives molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
racemase and epimerase activity, acting on carbohydrates and derivatives Gene SetFrom GO Molecular Function Annotations 2015 genes performing the racemase and epimerase activity, acting on carbohydrates and derivatives molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation Gene SetFrom OMIM Gene-Disease Associations genes associated with the leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation phenotype from the curated OMIM Gene-Disease Associations dataset. |
microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma Gene SetFrom OMIM Gene-Disease Associations genes associated with the microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma phenotype from the curated OMIM Gene-Disease Associations dataset. |
hypomyelination with brainstem and spinal cord involvement and leg spasticity Gene SetFrom OMIM Gene-Disease Associations genes associated with the hypomyelination with brainstem and spinal cord involvement and leg spasticity phenotype from the curated OMIM Gene-Disease Associations dataset. |
microcephaly, mental retardation, and distinctive facies, with cardiac and genitourinary malformations Gene SetFrom OMIM Gene-Disease Associations genes associated with the microcephaly, mental retardation, and distinctive facies, with cardiac and genitourinary malformations phenotype from the curated OMIM Gene-Disease Associations dataset. |
mental retardation and microcephaly with pontine and cerebellar hypoplasia Gene SetFrom OMIM Gene-Disease Associations genes associated with the mental retardation and microcephaly with pontine and cerebellar hypoplasia phenotype from the curated OMIM Gene-Disease Associations dataset. |
microcephaly, progressive, seizures, and cerebral and cerebellar atrophy Gene SetFrom OMIM Gene-Disease Associations genes associated with the microcephaly, progressive, seizures, and cerebral and cerebellar atrophy phenotype from the curated OMIM Gene-Disease Associations dataset. |
craniosynostosis with radiohumeral fusions and other skeletal and craniofacial anomalies Gene SetFrom OMIM Gene-Disease Associations genes associated with the craniosynostosis with radiohumeral fusions and other skeletal and craniofacial anomalies phenotype from the curated OMIM Gene-Disease Associations dataset. |
Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S Gene Setproteins participating in the Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S pathway from the Reactome Pathways dataset. |
Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding Gene Setproteins participating in the Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding pathway from the Reactome Pathways dataset. |
PI and PC transport between ER and Golgi membranes Gene Setproteins participating in the PI and PC transport between ER and Golgi membranes pathway from the Reactome Pathways dataset. |
Orexin and neuropeptides FF and QRFP bind to their respective receptors Gene Setproteins participating in the Orexin and neuropeptides FF and QRFP bind to their respective receptors pathway from the Reactome Pathways dataset. |
FGFR1c and Klotho ligand binding and activation Gene Setproteins participating in the FGFR1c and Klotho ligand binding and activation pathway from the Reactome Pathways dataset. |
Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane Gene Setproteins participating in the Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane pathway from the Reactome Pathways dataset. |
Synthesis and processing of ENV and VPU Gene Setproteins participating in the Synthesis and processing of ENV and VPU pathway from the Reactome Pathways dataset. |
Synthesis and interconversion of nucleotide di- and triphosphates Gene Setproteins participating in the Synthesis and interconversion of nucleotide di- and triphosphates pathway from the Reactome Pathways dataset. |
SREBF and miR33 in cholesterol and lipid homeostasis(Homo sapiens) Gene SetFrom WikiPathways Pathways 2014 proteins participating in the SREBF and miR33 in cholesterol and lipid homeostasis(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset. |
SREBF and miR33 in cholesterol and lipid homeostasis(Mus musculus) Gene SetFrom WikiPathways Pathways 2014 proteins participating in the SREBF and miR33 in cholesterol and lipid homeostasis(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset. |
SRF and miRs in Smooth Muscle Differentiation and Proliferation(Homo sapiens) Gene SetFrom WikiPathways Pathways 2014 proteins participating in the SRF and miRs in Smooth Muscle Differentiation and Proliferation(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset. |
High-Grade B-Cell Lymphoma, With Myc And Bcl2 And/Or Bcl6 Rearrangements Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease High-Grade B-Cell Lymphoma, With Myc And Bcl2 And/Or Bcl6 Rearrangements in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Toe Syndactyly, Telecanthus, And Anogenital And Renal Malformations Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Toe Syndactyly, Telecanthus, And Anogenital And Renal Malformations in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hypomyelination With Brain Stem And Spinal Cord Involvement And Leg Spasticity Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hypomyelination With Brain Stem And Spinal Cord Involvement And Leg Spasticity in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Growth And Mental Retardation, Mandibulofacial Dysostosis, Microcephaly, And Cleft Palate Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Growth And Mental Retardation, Mandibulofacial Dysostosis, Microcephaly, And Cleft Palate in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Contractures Of The Limbs And Face, Hypotonia, And Developmental Delay Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Contractures Of The Limbs And Face, Hypotonia, And Developmental Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Microspherophakia And/Or Megalocornea, With Ectopia Lentis And With Or Without Secondary Glaucoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Microspherophakia And/Or Megalocornea, With Ectopia Lentis And With Or Without Secondary Glaucoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Anal Intraepithelial Neoplasia I And Ii (Ain I And Ii) (Histologically Confirmed) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Anal Intraepithelial Neoplasia I And Ii (Ain I And Ii) (Histologically Confirmed) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pierre Robin Sequence With Pectus Excavatum And Rib And Scapular Anomalies Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pierre Robin Sequence With Pectus Excavatum And Rib And Scapular Anomalies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
racemase and epimerase activity, acting on carbohydrates and derivatives Gene SetFrom GO Molecular Function Annotations 2023 genes performing the racemase and epimerase activity, acting on carbohydrates and derivatives molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
SRF and miRs in smooth muscle differentiation and proliferation Gene SetFrom WikiPathways Pathways 2024 proteins participating in the SRF and miRs in smooth muscle differentiation and proliferation pathway from the WikiPathways Pathways 2024 dataset. |
SREBF and miR33 in cholesterol and lipid homeostasis Gene SetFrom WikiPathways Pathways 2024 proteins participating in the SREBF and miR33 in cholesterol and lipid homeostasis pathway from the WikiPathways Pathways 2024 dataset. |
RIOK1 and RIOK2 in EGFR and PI3K mediated tumorigenesis Gene SetFrom WikiPathways Pathways 2024 proteins participating in the RIOK1 and RIOK2 in EGFR and PI3K mediated tumorigenesis pathway from the WikiPathways Pathways 2024 dataset. |
ApoE and miR 146 in inflammation and atherosclerosis Gene SetFrom WikiPathways Pathways 2024 proteins participating in the ApoE and miR 146 in inflammation and atherosclerosis pathway from the WikiPathways Pathways 2024 dataset. |
Biosynthesis and regeneration of tetrahydrobiopterin and catabolism of phenylalanine Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Biosynthesis and regeneration of tetrahydrobiopterin and catabolism of phenylalanine pathway from the WikiPathways Pathways 2024 dataset. |
Somatroph axis GH and its relationship to dietary restriction and aging Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Somatroph axis GH and its relationship to dietary restriction and aging pathway from the WikiPathways Pathways 2024 dataset. |
Mechanoregulation and pathology of YAP TAZ via Hippo and non Hippo mechanisms Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Mechanoregulation and pathology of YAP TAZ via Hippo and non Hippo mechanisms pathway from the WikiPathways Pathways 2024 dataset. |
GLP 1 from intestine and pancreas and role in glucose homeostasis Gene SetFrom WikiPathways Pathways 2024 proteins participating in the GLP 1 from intestine and pancreas and role in glucose homeostasis pathway from the WikiPathways Pathways 2024 dataset. |
Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S Gene Setproteins participating in the Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S pathway from the Reactome Pathways 2024 dataset. |
Biosynthesis of protectin and resolvin conjugates in tissue regeneration (PCTR and RCTR) Gene Setproteins participating in the Biosynthesis of protectin and resolvin conjugates in tissue regeneration (PCTR and RCTR) pathway from the Reactome Pathways 2024 dataset. |
Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding Gene Setproteins participating in the Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding pathway from the Reactome Pathways 2024 dataset. |
FGFR1c and Klotho ligand binding and activation Gene Setproteins participating in the FGFR1c and Klotho ligand binding and activation pathway from the Reactome Pathways 2024 dataset. |
MLL4 and MLL3 complexes regulate expression of PPARG target genes in adipogenesis and hepatic steatosis Gene Setproteins participating in the MLL4 and MLL3 complexes regulate expression of PPARG target genes in adipogenesis and hepatic steatosis pathway from the Reactome Pathways 2024 dataset. |
Orexin and neuropeptides FF and QRFP bind to their respective receptors Gene Setproteins participating in the Orexin and neuropeptides FF and QRFP bind to their respective receptors pathway from the Reactome Pathways 2024 dataset. |
PI and PC transport between ER and Golgi membranes Gene Setproteins participating in the PI and PC transport between ER and Golgi membranes pathway from the Reactome Pathways 2024 dataset. |
PTK6 Regulates RTKs and Their Effectors AKT1 and DOK1 Gene Setproteins participating in the PTK6 Regulates RTKs and Their Effectors AKT1 and DOK1 pathway from the Reactome Pathways 2024 dataset. |
Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks Gene Setproteins participating in the Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks pathway from the Reactome Pathways 2024 dataset. |
Synthesis and processing of ENV and VPU Gene Setproteins participating in the Synthesis and processing of ENV and VPU pathway from the Reactome Pathways 2024 dataset. |
Transcriptional and post-translational regulation of MITF-M expression and activity Gene Setproteins participating in the Transcriptional and post-translational regulation of MITF-M expression and activity pathway from the Reactome Pathways 2024 dataset. |
Transport of bile salts and organic acids, metal ions and amine compounds Gene Setproteins participating in the Transport of bile salts and organic acids, metal ions and amine compounds pathway from the Reactome Pathways 2024 dataset. |
Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane Gene Setproteins participating in the Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane pathway from the Reactome Pathways 2024 dataset. |
racemase and epimerase activity, acting on carbohydrates and derivatives Gene SetFrom GO Molecular Function Annotations 2025 genes performing the racemase and epimerase activity, acting on carbohydrates and derivatives molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
Vertebral anomalies and variable endocrine and T-cell dysfunction Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Vertebral anomalies and variable endocrine and T-cell dysfunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Vertebral anomalies and variable endocrine and T-cell dysfunction Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Vertebral anomalies and variable endocrine and T-cell dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Regulation of gene expression and signal transduction in immune and stress responses Gene SetFrom CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Regulation of gene expression and signal transduction in immune and stress responses assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset. |
Gastroesophageal reflux disease, peptic ulcer disease and/or corresponding medications and treatment Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Gastroesophageal reflux disease, peptic ulcer disease and/or corresponding medications and treatment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
estrogen responsive protein efp controls cell cycle and breast tumors growth Gene SetFrom Biocarta Pathways proteins participating in the estrogen responsive protein efp controls cell cycle and breast tumors growth pathway from the Biocarta Pathways dataset. |
Trifunctional protein deficiency with myopathy and neuropathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Trifunctional protein deficiency with myopathy and neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
calcium- and calmodulin-dependent protein kinase complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the calcium- and calmodulin-dependent protein kinase complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
calcium- and calmodulin-dependent protein kinase complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the calcium- and calmodulin-dependent protein kinase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
Apoptosis- and splicing-associated protein complex (ASAP-L), SAP18-RNPS1-Acinus-L Gene Setproteins in the Apoptosis- and splicing-associated protein complex (ASAP-L), SAP18-RNPS1-Acinus-L protein complex from the CORUM Protein Complexes dataset. |
Apoptosis- and splicing-associated protein complex (ASAP-S), SAP18-RNPS1-Acinus-S Gene Setproteins in the Apoptosis- and splicing-associated protein complex (ASAP-S), SAP18-RNPS1-Acinus-S protein complex from the CORUM Protein Complexes dataset. |
20S methylosome and RG-containing Sm protein complex Gene Setproteins in the 20S methylosome and RG-containing Sm protein complex protein complex from the CORUM Protein Complexes dataset. |
Trifunctional Protein Deficiency With Myopathy And Neuropathy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Trifunctional Protein Deficiency With Myopathy And Neuropathy from the curated CTD Gene-Disease Associations dataset. |
circulating protein c levels and thrombotic risk Gene SetFrom GAD Gene-Disease Associations genes associated with the disease circulating protein c levels and thrombotic risk in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
plasma protein c levels and thrombotic risk Gene SetFrom GAD Gene-Disease Associations genes associated with the disease plasma protein c levels and thrombotic risk in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
plasma triglyceride and c-reactive protein, fasting glucose Gene SetFrom GAD Gene-Disease Associations genes associated with the disease plasma triglyceride and c-reactive protein, fasting glucose in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
thrombosis and resistance to activated protein c Gene SetFrom GAD Gene-Disease Associations genes associated with the disease thrombosis and resistance to activated protein c in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
antigen processing and presentation of exogenous protein antigen via mhc class ib, tap-dependent Gene SetFrom GO Biological Process Annotations 2015 genes participating in the antigen processing and presentation of exogenous protein antigen via mhc class ib, tap-dependent biological process from the curated GO Biological Process Annotations 2015 dataset. |
calcium- and calmodulin-dependent protein kinase complex Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the calcium- and calmodulin-dependent protein kinase complex cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced iron-sulfur protein as one donor, and incorporation of one atom of oxygen Gene SetFrom GO Molecular Function Annotations 2015 genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced iron-sulfur protein as one donor, and incorporation of one atom of oxygen molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
C-reactive protein and white blood cell count Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the C-reactive protein and white blood cell count phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
decreased beta-glucocerebrosidase protein and activity Gene SetFrom HPO Gene-Disease Associations genes associated with the decreased beta-glucocerebrosidase protein and activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Transmembrane and coiled-coil domain-containing protein 2/5 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Transmembrane and coiled-coil domain-containing protein 2/5 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Fasciculation and elongation protein zeta, FEZ Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Fasciculation and elongation protein zeta, FEZ protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
LIM and senescent cell antigen-like-containing domain protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the LIM and senescent cell antigen-like-containing domain protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Membrane-associated guanylate kinase, WW and PDZ domain-containing protein 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Membrane-associated guanylate kinase, WW and PDZ domain-containing protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
V-set and immunoglobulin domain-containing protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the V-set and immunoglobulin domain-containing protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Prostate and testis expressed protein 4 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Prostate and testis expressed protein 4 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Prostate and testis expressed protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Prostate and testis expressed protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Prostate and testis expressed protein 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Prostate and testis expressed protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Prostate and testis expressed protein 3 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Prostate and testis expressed protein 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
G2 and S phase-expressed protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the G2 and S phase-expressed protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
DNA recombination and repair protein RecA-like, ATP-binding domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the DNA recombination and repair protein RecA-like, ATP-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Growth arrest and DNA damage-inducible protein GADD45 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Growth arrest and DNA damage-inducible protein GADD45 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Neuropilin and tolloid-like protein 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Neuropilin and tolloid-like protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
LIM domain and actin-binding protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the LIM domain and actin-binding protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Neuropilin and tolloid-like protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Neuropilin and tolloid-like protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
FERM and PDZ domain-containing protein 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the FERM and PDZ domain-containing protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Centrosome and spindle pole associated protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Centrosome and spindle pole associated protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Methylmalonic aciduria and homocystinuria type D protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Methylmalonic aciduria and homocystinuria type D protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Cattle cerebrum and skeletal muscle-specific protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Cattle cerebrum and skeletal muscle-specific protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Cell cycle and apoptosis regulator protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Cell cycle and apoptosis regulator protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Hematological and neurological expressed 1 protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Hematological and neurological expressed 1 protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Myelin and lymphocyte (MAL) protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Myelin and lymphocyte (MAL) protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Leucine-rich repeat and fibronectin type-III domain-containing protein 5 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Leucine-rich repeat and fibronectin type-III domain-containing protein 5 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Cysteine and tyrosine-rich protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Cysteine and tyrosine-rich protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
PDZ and LIM domain protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the PDZ and LIM domain protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
EGF-like repeat and discoidin I-like domain-containing protein 3 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the EGF-like repeat and discoidin I-like domain-containing protein 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Membrane-associated guanylate kinase, WW and PDZ domain-containing protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Membrane-associated guanylate kinase, WW and PDZ domain-containing protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Membrane-associated guanylate kinase, WW and PDZ domain-containing protein 3 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Membrane-associated guanylate kinase, WW and PDZ domain-containing protein 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
WD repeat-containing and planar cell polarity effector protein Fritz Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the WD repeat-containing and planar cell polarity effector protein Fritz protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
CUB and zona pellucida-like domain-containing protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the CUB and zona pellucida-like domain-containing protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger and BTB domain-containing protein 22 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger and BTB domain-containing protein 22 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Disintegrin and metalloproteinase domain-containing protein 10 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Disintegrin and metalloproteinase domain-containing protein 10 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
TRIO and F-actin-binding protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the TRIO and F-actin-binding protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Spindle and kinetochore-associated protein 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Spindle and kinetochore-associated protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Fasciculation and elongation protein zeta 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Fasciculation and elongation protein zeta 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger and BTB domain-containing protein 40 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger and BTB domain-containing protein 40 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Calcium-binding and spermatid-specific protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Calcium-binding and spermatid-specific protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
DNA recombination and repair protein, RecA-like Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the DNA recombination and repair protein, RecA-like protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
DNA recombination and repair protein Rad51, C-terminal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the DNA recombination and repair protein Rad51, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
DNA recombination and repair protein RecA, monomer-monomer interface Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the DNA recombination and repair protein RecA, monomer-monomer interface protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
LIM and calponin homology domains-containing protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the LIM and calponin homology domains-containing protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Vacuole morphology and inheritance protein 14 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuole morphology and inheritance protein 14 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
von Willebrand factor C and EGF domain-containing protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the von Willebrand factor C and EGF domain-containing protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Kelch repeat and BTB domain-containing protein 8 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Kelch repeat and BTB domain-containing protein 8 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Nucleolar and spindle-associated protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Nucleolar and spindle-associated protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Testis and ovary-specific PAZ domain-containing protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Testis and ovary-specific PAZ domain-containing protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
WASP homologue-associated protein with actin, membranes and microtubules Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the WASP homologue-associated protein with actin, membranes and microtubules protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Centriole, cilia and spindle-associated protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Centriole, cilia and spindle-associated protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Cell cycle and apoptosis regulator protein 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Cell cycle and apoptosis regulator protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Fasciculation and elongation protein zeta 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Fasciculation and elongation protein zeta 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Heterotrimeric G-protein signaling pathway-Gi alpha and Gs alpha mediated pathway Gene SetFrom PANTHER Pathways proteins participating in the Heterotrimeric G-protein signaling pathway-Gi alpha and Gs alpha mediated pathway pathway from the PANTHER Pathways dataset. |
Heterotrimeric G-protein signaling pathway-Gq alpha and Go alpha mediated pathway Gene SetFrom PANTHER Pathways proteins participating in the Heterotrimeric G-protein signaling pathway-Gq alpha and Go alpha mediated pathway pathway from the PANTHER Pathways dataset. |
protein-interaction-domains-and-motifs Gene SetFrom Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term protein-interaction-domains-and-motifs in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset. |
Activation and oligomerization of BAK protein Gene Setproteins participating in the Activation and oligomerization of BAK protein pathway from the Reactome Pathways dataset. |
Biosynthesis of the N-glycan precursor (dolichol lipid-linked oligosaccharide, LLO) and transfer to a nascent protein Gene Setproteins participating in the Biosynthesis of the N-glycan precursor (dolichol lipid-linked oligosaccharide, LLO) and transfer to a nascent protein pathway from the Reactome Pathways dataset. |
Trifunctional Protein Deficiency With Myopathy And Neuropathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Trifunctional Protein Deficiency With Myopathy And Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Complement Hyperactivation, Angiopathic Thrombosis, And Protein-Losing Enteropathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Complement Hyperactivation, Angiopathic Thrombosis, And Protein-Losing Enteropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Caused By Mutation In The Zinc Finger- And Btb Domain-Containing Protein-42 (Zbtb42, 613915.0001) Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Caused By Mutation In The Zinc Finger- And Btb Domain-Containing Protein-42 (Zbtb42, 613915.0001) in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced iron-sulfur protein as one donor, and incorporation of one atom of oxygen Gene SetFrom GO Molecular Function Annotations 2023 genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced iron-sulfur protein as one donor, and incorporation of one atom of oxygen molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
Bone morphogenic protein signaling and regulation Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Bone morphogenic protein signaling and regulation pathway from the WikiPathways Pathways 2024 dataset. |
mRNA protein and metabolite inducation pathway by cyclosporin A Gene SetFrom WikiPathways Pathways 2024 proteins participating in the mRNA protein and metabolite inducation pathway by cyclosporin A pathway from the WikiPathways Pathways 2024 dataset. |
Transcription co factors SKI and SKIL protein partners Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Transcription co factors SKI and SKIL protein partners pathway from the WikiPathways Pathways 2024 dataset. |
Activation and oligomerization of BAK protein Gene Setproteins participating in the Activation and oligomerization of BAK protein pathway from the Reactome Pathways 2024 dataset. |
Biosynthesis of the N-glycan precursor (dolichol lipid-linked oligosaccharide, LLO) and transfer to a nascent protein Gene Setproteins participating in the Biosynthesis of the N-glycan precursor (dolichol lipid-linked oligosaccharide, LLO) and transfer to a nascent protein pathway from the Reactome Pathways 2024 dataset. |
Cooperation of PDCL (PhLP1) and TRiC/CCT in G-protein beta folding Gene Setproteins participating in the Cooperation of PDCL (PhLP1) and TRiC/CCT in G-protein beta folding pathway from the Reactome Pathways 2024 dataset. |
Gene and protein expression by JAK-STAT signaling after Interleukin-12 stimulation Gene Setproteins participating in the Gene and protein expression by JAK-STAT signaling after Interleukin-12 stimulation pathway from the Reactome Pathways 2024 dataset. |
oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced iron-sulfur protein as one donor, and incorporation of one atom of oxygen Gene SetFrom GO Molecular Function Annotations 2025 genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced iron-sulfur protein as one donor, and incorporation of one atom of oxygen molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
calcium- and calmodulin-dependent protein kinase complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the calcium- and calmodulin-dependent protein kinase complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
calcium- and calmodulin-dependent protein kinase complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the calcium- and calmodulin-dependent protein kinase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Myopathy due to calsequestrin and SERCA1 protein overload Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Myopathy due to calsequestrin and SERCA1 protein overload phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Intracellular protein transport and DNA repair Gene SetFrom CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Intracellular protein transport and DNA repair assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset. |
Protein quality control and ubiquitin-proteasome system regulation Gene SetFrom CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Protein quality control and ubiquitin-proteasome system regulation assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset. |
Protein folding and complex assembly regulation Gene SetFrom CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Protein folding and complex assembly regulation assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset. |
Protein quality control and DNA repair Gene SetFrom CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Protein quality control and DNA repair assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset. |
Mitochondrial biogenesis and protein quality control Gene SetFrom CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Mitochondrial biogenesis and protein quality control assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset. |
Protein folding and stress response regulation Gene SetFrom CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Protein folding and stress response regulation assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset. |
Regulation of gene expression and protein quality control Gene SetFrom CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Regulation of gene expression and protein quality control assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset. |
Regulation of gene expression and protein modification Gene SetFrom CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Regulation of gene expression and protein modification assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset. |
Protein processing and intracellular signaling Gene SetFrom CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Protein processing and intracellular signaling assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset. |
Protein quality control and DNA repair complex Gene SetFrom CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Protein quality control and DNA repair complex assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset. |
Regulation of mRNA processing and protein ubiquitination Gene SetFrom CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Regulation of mRNA processing and protein ubiquitination assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset. |
G-protein signaling and cell cycle regulation Gene SetFrom CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising G-protein signaling and cell cycle regulation assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset. |
Mitochondrial metabolism and protein regulation Gene SetFrom CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Mitochondrial metabolism and protein regulation assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset. |
Regulation of Gene Expression and Protein Ubiquitination Gene SetFrom CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Regulation of Gene Expression and Protein Ubiquitination assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset. |
Protein Stability and Turnover Regulation Gene SetFrom CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Protein Stability and Turnover Regulation assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset. |
C-reactive protein and white blood cell count Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the C-reactive protein and white blood cell count phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Multiple sclerosis and C-reactive protein levels (pleiotropy) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Multiple sclerosis and C-reactive protein levels (pleiotropy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Viral protein interaction with cytokine and cytokine receptor Gene SetFrom KEGG Pathways 2026 proteins participating in the Viral protein interaction with cytokine and cytokine receptor pathway from the KEGG Pathways 2026 dataset. |
Protein digestion and absorption Gene SetFrom KEGG Pathways 2026 proteins participating in the Protein digestion and absorption pathway from the KEGG Pathways 2026 dataset. |
eclampsia; pre-eclampsia; protein c deficiency; protein s deficiency; thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease eclampsia; pre-eclampsia; protein c deficiency; protein s deficiency; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
blood coagulation disorders, inherited; protein c deficiency; protein s deficiency; thrombophilia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease blood coagulation disorders, inherited; protein c deficiency; protein s deficiency; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
blood coagulation disorders; protein c deficiency; protein s deficiency; pulmonary embolism; pulmonary embolisms; thrombosis; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease blood coagulation disorders; protein c deficiency; protein s deficiency; pulmonary embolism; pulmonary embolisms; thrombosis; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
factor v deficiency; hypoprothrombinemias; protein c deficiency; protein s deficiency; pulmonary embolism; thrombophilia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease factor v deficiency; hypoprothrombinemias; protein c deficiency; protein s deficiency; pulmonary embolism; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
activated protein c resistance; protein s deficiency; thrombophilia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; protein s deficiency; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
protein c deficiency; protein s deficiency; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease protein c deficiency; protein s deficiency; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
neoplasms; protein c deficiency; protein s deficiency; venous thromboembolism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease neoplasms; protein c deficiency; protein s deficiency; venous thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
antithrombin iii deficiency; gastrointestinal hemorrhage; protein c deficiency; protein s deficiency; splenomegaly; thrombophilia; turner syndrome; venous thrombosis; xo syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease antithrombin iii deficiency; gastrointestinal hemorrhage; protein c deficiency; protein s deficiency; splenomegaly; thrombophilia; turner syndrome; venous thrombosis; xo syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
negative regulation of protein ubiquitination involved in ubiquitin-dependent protein catabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of protein ubiquitination involved in ubiquitin-dependent protein catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
protein modification by small protein conjugation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the protein modification by small protein conjugation biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of g-protein coupled receptor protein signaling pathway Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of g-protein coupled receptor protein signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset. |
protein maturation by protein folding Gene SetFrom GO Biological Process Annotations 2015 genes participating in the protein maturation by protein folding biological process from the curated GO Biological Process Annotations 2015 dataset. |
protein targeting to vacuole involved in ubiquitin-dependent protein catabolic process via the multivesicular body sorting pathway Gene SetFrom GO Biological Process Annotations 2015 genes participating in the protein targeting to vacuole involved in ubiquitin-dependent protein catabolic process via the multivesicular body sorting pathway biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of protein modification by small protein conjugation or removal Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of protein modification by small protein conjugation or removal biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of protein kinase activity by regulation of protein phosphorylation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of protein kinase activity by regulation of protein phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of protein processing involved in protein targeting to mitochondrion Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of protein processing involved in protein targeting to mitochondrion biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of g-protein coupled receptor protein signaling pathway Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of g-protein coupled receptor protein signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of protein processing involved in protein targeting to mitochondrion Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of protein processing involved in protein targeting to mitochondrion biological process from the curated GO Biological Process Annotations 2015 dataset. |
activation of signaling protein activity involved in unfolded protein response Gene SetFrom GO Biological Process Annotations 2015 genes participating in the activation of signaling protein activity involved in unfolded protein response biological process from the curated GO Biological Process Annotations 2015 dataset. |
desensitization of g-protein coupled receptor protein signaling pathway Gene SetFrom GO Biological Process Annotations 2015 genes participating in the desensitization of g-protein coupled receptor protein signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of protein modification by small protein conjugation or removal Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of protein modification by small protein conjugation or removal biological process from the curated GO Biological Process Annotations 2015 dataset. |
protein ubiquitination involved in ubiquitin-dependent protein catabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the protein ubiquitination involved in ubiquitin-dependent protein catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of protein ubiquitination involved in ubiquitin-dependent protein catabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of protein ubiquitination involved in ubiquitin-dependent protein catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
protein deubiquitination involved in ubiquitin-dependent protein catabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the protein deubiquitination involved in ubiquitin-dependent protein catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of g-protein coupled receptor protein signaling pathway Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of g-protein coupled receptor protein signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of protein ubiquitination involved in ubiquitin-dependent protein catabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of protein ubiquitination involved in ubiquitin-dependent protein catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
protein processing involved in protein targeting to mitochondrion Gene SetFrom GO Biological Process Annotations 2015 genes participating in the protein processing involved in protein targeting to mitochondrion biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of protein modification by small protein conjugation or removal Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of protein modification by small protein conjugation or removal biological process from the curated GO Biological Process Annotations 2015 dataset. |
protein kinase c-activating g-protein coupled receptor signaling pathway Gene SetFrom GO Biological Process Annotations 2015 genes participating in the protein kinase c-activating g-protein coupled receptor signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset. |
desensitization of g-protein coupled receptor protein signaling pathway by arrestin Gene SetFrom GO Biological Process Annotations 2015 genes participating in the desensitization of g-protein coupled receptor protein signaling pathway by arrestin biological process from the curated GO Biological Process Annotations 2015 dataset. |
protein modification by small protein removal Gene SetFrom GO Biological Process Annotations 2015 genes participating in the protein modification by small protein removal biological process from the curated GO Biological Process Annotations 2015 dataset. |
protein modification by small protein conjugation or removal Gene SetFrom GO Biological Process Annotations 2015 genes participating in the protein modification by small protein conjugation or removal biological process from the curated GO Biological Process Annotations 2015 dataset. |
protein binding involved in protein folding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the protein binding involved in protein folding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
Vacuolar protein sorting-associated protein 54 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuolar protein sorting-associated protein 54 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Myelin protein zero-like protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Myelin protein zero-like protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Myelin protein zero-like protein 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Myelin protein zero-like protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Myelin protein zero-like protein 3 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Myelin protein zero-like protein 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Tumour protein p53-inducible nuclear protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Tumour protein p53-inducible nuclear protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Dyslexia-associated protein KIAA0319-like protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Dyslexia-associated protein KIAA0319-like protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small proline-rich protein/late cornified envelope protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small proline-rich protein/late cornified envelope protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Protein kinase A anchor protein, RI-RII subunit-binding domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Protein kinase A anchor protein, RI-RII subunit-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Guanine nucleotide binding protein (G-protein), alpha subunit Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Guanine nucleotide binding protein (G-protein), alpha subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Protein transport protein SecG/Sec61-beta/Sbh Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Protein transport protein SecG/Sec61-beta/Sbh protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Protein of unknown function DUF3669, zinc finger protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Protein of unknown function DUF3669, zinc finger protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Pre-rRNA-processing protein IPI1/Testis-expressed sequence 10 protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Pre-rRNA-processing protein IPI1/Testis-expressed sequence 10 protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Tumor protein p53-inducible protein 11 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Tumor protein p53-inducible protein 11 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Actin-related protein 2/3 complex subunit 5-like protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Actin-related protein 2/3 complex subunit 5-like protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
GTP-binding protein TrmE/Glycine cleavage system T protein, domain 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the GTP-binding protein TrmE/Glycine cleavage system T protein, domain 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Insulin-like growth factor binding protein-related protein (IGFBP-rP), MAC25 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Insulin-like growth factor binding protein-related protein (IGFBP-rP), MAC25 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Vacuolar protein sorting-associated protein 13 domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuolar protein sorting-associated protein 13 domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
EH domain-binding protein 1-like protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the EH domain-binding protein 1-like protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
SWR1-complex protein 5/Craniofacial development protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the SWR1-complex protein 5/Craniofacial development protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
DMRT/protein doublesex/protein male abnormal 3 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the DMRT/protein doublesex/protein male abnormal 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Vacuolar protein sorting protein 36, GLUE domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuolar protein sorting protein 36, GLUE domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ribosomal protein L7/L12, C-terminal/adaptor protein ClpS-like Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ribosomal protein L7/L12, C-terminal/adaptor protein ClpS-like protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
UV radiation resistance protein/autophagy-related protein 14 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the UV radiation resistance protein/autophagy-related protein 14 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Four-jointed box protein 1/four-jointed protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Four-jointed box protein 1/four-jointed protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Coiled-coil domain-containing protein 18/Cytoskeletal protein Sojo Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Coiled-coil domain-containing protein 18/Cytoskeletal protein Sojo protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ribosomal RNA-processing protein 14/surfeit locus protein 6, C-terminal domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ribosomal RNA-processing protein 14/surfeit locus protein 6, C-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Kinetochore protein Cenp-F/LEK1, Rb protein-binding domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Kinetochore protein Cenp-F/LEK1, Rb protein-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Vacuolar protein sorting-associated protein 13A N-terminal domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuolar protein sorting-associated protein 13A N-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
SWR1-complex protein 4/DNA methyltransferase 1-associated protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the SWR1-complex protein 4/DNA methyltransferase 1-associated protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Vacuolar protein sorting protein 26 related Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuolar protein sorting protein 26 related protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Tumor protein p53-inducible nuclear protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Tumor protein p53-inducible nuclear protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Vacuolar protein sorting-associated protein 41 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuolar protein sorting-associated protein 41 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Bone morphogenetic protein 1/tolloid-like protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Bone morphogenetic protein 1/tolloid-like protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Synaptonemal complex protein 2/protein 2-like Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Synaptonemal complex protein 2/protein 2-like protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Sterol regulatory element-binding protein cleavage-activating protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Sterol regulatory element-binding protein cleavage-activating protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Polyadenylate-binding protein/Hyperplastic disc protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Polyadenylate-binding protein/Hyperplastic disc protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Uncharacterised protein family WW domain-binding protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Uncharacterised protein family WW domain-binding protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Receptor-transporting protein/CXXC-type zinc finger protein 11 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Receptor-transporting protein/CXXC-type zinc finger protein 11 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Receptor tyrosine-protein phosphatase C-associated protein CD45-AP Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Receptor tyrosine-protein phosphatase C-associated protein CD45-AP protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Vacuolar protein sorting-associated protein 8, central domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuolar protein sorting-associated protein 8, central domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Vacuolar protein sorting-associated protein 16 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuolar protein sorting-associated protein 16 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Vacuolar protein sorting-associate protein Vta1/Callose synthase, N-terminal domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuolar protein sorting-associate protein Vta1/Callose synthase, N-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Probable cytosolic iron-sulfur protein assembly protein, CIAO1/Cia1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Probable cytosolic iron-sulfur protein assembly protein, CIAO1/Cia1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Outer membrane protein Iml2/Tetratricopeptide repeat protein 39 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Outer membrane protein Iml2/Tetratricopeptide repeat protein 39 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Vesicle-associated membrane protein-associated protein B Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Vesicle-associated membrane protein-associated protein B protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Vesicle-associated membrane protein-associated protein A Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Vesicle-associated membrane protein-associated protein A protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Protein LIN-9/Protein ALWAYS EARLY Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Protein LIN-9/Protein ALWAYS EARLY protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Steroid receptor RNA activator-protein/coat protein complex II, Sec31 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Steroid receptor RNA activator-protein/coat protein complex II, Sec31 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Vacuolar protein sorting-associated protein 35, Vps35 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuolar protein sorting-associated protein 35, Vps35 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Tumor protein p53-inducible nuclear protein 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Tumor protein p53-inducible nuclear protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Protein of unknown function DUF3697, ubiquitin-associated protein 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Protein of unknown function DUF3697, ubiquitin-associated protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Retinoic acid-induced protein 2/sine oculis-binding protein homologue Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Retinoic acid-induced protein 2/sine oculis-binding protein homologue protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Tetracycline resistance protein, TetA/multidrug resistance protein MdtG Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Tetracycline resistance protein, TetA/multidrug resistance protein MdtG protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
TYRO protein tyrosine kinase-binding protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the TYRO protein tyrosine kinase-binding protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Usher syndrome type-1C protein-binding protein 1, PDZ domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Usher syndrome type-1C protein-binding protein 1, PDZ domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ribosomal protein L1/ribosomal biogenesis protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ribosomal protein L1/ribosomal biogenesis protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Actin-related protein 8/Plant actin-related protein 9 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Actin-related protein 8/Plant actin-related protein 9 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Regulator of G-protein signalling 9-binding protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Regulator of G-protein signalling 9-binding protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Vacuolar protein sorting-associated protein 11 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuolar protein sorting-associated protein 11 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Vacuolar protein sorting-associated protein 13 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuolar protein sorting-associated protein 13 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Vesicle-associated membrane-protein-associated protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Vesicle-associated membrane-protein-associated protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Vacuolar protein sorting protein 11, C-terminal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuolar protein sorting protein 11, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
cAMP-responsive element-binding protein 3-like protein 4 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the cAMP-responsive element-binding protein 3-like protein 4 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
cAMP-responsive element-binding protein 3-like protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the cAMP-responsive element-binding protein 3-like protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
cAMP-responsive element-binding protein 3-like protein 3 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the cAMP-responsive element-binding protein 3-like protein 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
cAMP-responsive element-binding protein 3-like protein 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the cAMP-responsive element-binding protein 3-like protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Vacuolar protein sorting-associated protein 33 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuolar protein sorting-associated protein 33 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Protein kinase A anchor protein, nuclear localisation signal domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Protein kinase A anchor protein, nuclear localisation signal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Spermatogenesis-associated protein 2-like protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Spermatogenesis-associated protein 2-like protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
A-kinase anchor protein 6/Centrosomal protein of 68kDa Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the A-kinase anchor protein 6/Centrosomal protein of 68kDa protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
PodNet: protein-protein interactions in the podocyte(Mus musculus) Gene SetFrom WikiPathways Pathways 2014 proteins participating in the PodNet: protein-protein interactions in the podocyte(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset. |
XPodNet - protein-protein interactions in the podocyte expanded by STRING(Mus musculus) Gene SetFrom WikiPathways Pathways 2014 proteins participating in the XPodNet - protein-protein interactions in the podocyte expanded by STRING(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset. |
protein transport to vacuole involved in ubiquitin-dependent protein catabolic process via the multivesicular body sorting pathway Gene SetFrom GO Biological Process Annotations 2023 genes participating in the protein transport to vacuole involved in ubiquitin-dependent protein catabolic process via the multivesicular body sorting pathway biological process from the curated GO Biological Process Annotations 2023 dataset. |
protein kinase C-activating G protein-coupled receptor signaling pathway Gene SetFrom GO Biological Process Annotations 2023 genes participating in the protein kinase C-activating G protein-coupled receptor signaling pathway biological process from the curated GO Biological Process Annotations 2023 dataset. |
protein modification by small protein conjugation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the protein modification by small protein conjugation biological process from the curated GO Biological Process Annotations 2023 dataset. |
protein processing involved in protein targeting to mitochondrion Gene SetFrom GO Biological Process Annotations 2023 genes participating in the protein processing involved in protein targeting to mitochondrion biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of protein kinase activity by regulation of protein phosphorylation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of protein kinase activity by regulation of protein phosphorylation biological process from the curated GO Biological Process Annotations 2023 dataset. |
protein initiator methionine removal involved in protein maturation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the protein initiator methionine removal involved in protein maturation biological process from the curated GO Biological Process Annotations 2023 dataset. |
protein deubiquitination involved in ubiquitin-dependent protein catabolic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the protein deubiquitination involved in ubiquitin-dependent protein catabolic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of protein processing involved in protein targeting to mitochondrion Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of protein processing involved in protein targeting to mitochondrion biological process from the curated GO Biological Process Annotations 2023 dataset. |
membrane protein proteolysis involved in retrograde protein transport, ER to cytosol Gene SetFrom GO Biological Process Annotations 2023 genes participating in the membrane protein proteolysis involved in retrograde protein transport, ER to cytosol biological process from the curated GO Biological Process Annotations 2023 dataset. |
protein modification by small protein removal Gene SetFrom GO Biological Process Annotations 2023 genes participating in the protein modification by small protein removal biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of protein modification by small protein conjugation or removal Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of protein modification by small protein conjugation or removal biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of protein modification by small protein conjugation or removal Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of protein modification by small protein conjugation or removal biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of protein modification by small protein conjugation or removal Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of protein modification by small protein conjugation or removal biological process from the curated GO Biological Process Annotations 2023 dataset. |
protein modification by small protein conjugation or removal Gene SetFrom GO Biological Process Annotations 2023 genes participating in the protein modification by small protein conjugation or removal biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of protein processing involved in protein targeting to mitochondrion Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of protein processing involved in protein targeting to mitochondrion biological process from the curated GO Biological Process Annotations 2023 dataset. |
Protein-protein interactions at synapses Gene Setproteins participating in the Protein-protein interactions at synapses pathway from the Reactome Pathways 2024 dataset. |
protein transport to vacuole involved in ubiquitin-dependent protein catabolic process via the multivesicular body sorting pathway Gene SetFrom GO Biological Process Annotations 2025 genes participating in the protein transport to vacuole involved in ubiquitin-dependent protein catabolic process via the multivesicular body sorting pathway biological process from the curated GO Biological Process Annotations 2025 dataset. |
protein modification by small protein conjugation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the protein modification by small protein conjugation biological process from the curated GO Biological Process Annotations 2025 dataset. |
protein processing involved in protein targeting to mitochondrion Gene SetFrom GO Biological Process Annotations 2025 genes participating in the protein processing involved in protein targeting to mitochondrion biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of protein kinase activity by regulation of protein phosphorylation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of protein kinase activity by regulation of protein phosphorylation biological process from the curated GO Biological Process Annotations 2025 dataset. |
protein deubiquitination involved in ubiquitin-dependent protein catabolic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the protein deubiquitination involved in ubiquitin-dependent protein catabolic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of protein processing involved in protein targeting to mitochondrion Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of protein processing involved in protein targeting to mitochondrion biological process from the curated GO Biological Process Annotations 2025 dataset. |
membrane protein proteolysis involved in retrograde protein transport, ER to cytosol Gene SetFrom GO Biological Process Annotations 2025 genes participating in the membrane protein proteolysis involved in retrograde protein transport, ER to cytosol biological process from the curated GO Biological Process Annotations 2025 dataset. |
protein modification by small protein removal Gene SetFrom GO Biological Process Annotations 2025 genes participating in the protein modification by small protein removal biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of protein modification by small protein conjugation or removal Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of protein modification by small protein conjugation or removal biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of protein modification by small protein conjugation or removal Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of protein modification by small protein conjugation or removal biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of protein modification by small protein conjugation or removal Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of protein modification by small protein conjugation or removal biological process from the curated GO Biological Process Annotations 2025 dataset. |
protein modification by small protein conjugation or removal Gene SetFrom GO Biological Process Annotations 2025 genes participating in the protein modification by small protein conjugation or removal biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of protein processing involved in protein targeting to mitochondrion Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of protein processing involved in protein targeting to mitochondrion biological process from the curated GO Biological Process Annotations 2025 dataset. |
Basic cell groups and regions Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Basic cell groups and regions relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
head and face region of M1 Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in head and face region of M1 relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
telomeres telomerase cellular aging and immortality Gene SetFrom Biocarta Pathways proteins participating in the telomeres telomerase cellular aging and immortality pathway from the Biocarta Pathways dataset. |
mcalpain and friends in cell motility Gene SetFrom Biocarta Pathways proteins participating in the mcalpain and friends in cell motility pathway from the Biocarta Pathways dataset. |
role of ppar-gamma coactivators in obesity and thermogenesis Gene SetFrom Biocarta Pathways proteins participating in the role of ppar-gamma coactivators in obesity and thermogenesis pathway from the Biocarta Pathways dataset. |
il12 and stat4 dependent signaling pathway in th1 development Gene SetFrom Biocarta Pathways proteins participating in the il12 and stat4 dependent signaling pathway in th1 development pathway from the Biocarta Pathways dataset. |
hypoxia and p53 in the cardiovascular system Gene SetFrom Biocarta Pathways proteins participating in the hypoxia and p53 in the cardiovascular system pathway from the Biocarta Pathways dataset. |
lissencephaly gene (lis1) in neuronal migration and development Gene SetFrom Biocarta Pathways proteins participating in the lissencephaly gene (lis1) in neuronal migration and development pathway from the Biocarta Pathways dataset. |
role of erbb2 in signal transduction and oncology Gene SetFrom Biocarta Pathways proteins participating in the role of erbb2 in signal transduction and oncology pathway from the Biocarta Pathways dataset. |
corticosteroids and cardioprotection Gene SetFrom Biocarta Pathways proteins participating in the corticosteroids and cardioprotection pathway from the Biocarta Pathways dataset. |
cyclins and cell cycle regulation Gene SetFrom Biocarta Pathways proteins participating in the cyclins and cell cycle regulation pathway from the Biocarta Pathways dataset. |
mechanism of acetaminophen activity and toxicity Gene SetFrom Biocarta Pathways proteins participating in the mechanism of acetaminophen activity and toxicity pathway from the Biocarta Pathways dataset. |
nfat and hypertrophy of the heart Gene SetFrom Biocarta Pathways proteins participating in the nfat and hypertrophy of the heart pathway from the Biocarta Pathways dataset. |
acetylation and deacetylation of rela in nucleus Gene SetFrom Biocarta Pathways proteins participating in the acetylation and deacetylation of rela in nucleus pathway from the Biocarta Pathways dataset. |
thrombin signaling and protease-activated receptors Gene SetFrom Biocarta Pathways proteins participating in the thrombin signaling and protease-activated receptors pathway from the Biocarta Pathways dataset. |
antigen processing and presentation Gene SetFrom Biocarta Pathways proteins participating in the antigen processing and presentation pathway from the Biocarta Pathways dataset. |
stathmin and breast cancer resistance to antimicrotubule agents Gene SetFrom Biocarta Pathways proteins participating in the stathmin and breast cancer resistance to antimicrotubule agents pathway from the Biocarta Pathways dataset. |
role of ß-arrestins in the activation and targeting of map kinases Gene SetFrom Biocarta Pathways proteins participating in the role of ß-arrestins in the activation and targeting of map kinases pathway from the Biocarta Pathways dataset. |
cystic fibrosis transmembrane conductance regulator (cftr) and beta 2 adrenergic receptor (b2ar) pathway Gene SetFrom Biocarta Pathways proteins participating in the cystic fibrosis transmembrane conductance regulator (cftr) and beta 2 adrenergic receptor (b2ar) pathway pathway from the Biocarta Pathways dataset. |
role of pi3k subunit p85 in regulation of actin organization and cell migration Gene SetFrom Biocarta Pathways proteins participating in the role of pi3k subunit p85 in regulation of actin organization and cell migration pathway from the Biocarta Pathways dataset. |
btg family proteins and cell cycle regulation Gene SetFrom Biocarta Pathways proteins participating in the btg family proteins and cell cycle regulation pathway from the Biocarta Pathways dataset. |
control of skeletal myogenesis by hdac and calcium/calmodulin-dependent kinase (camk) Gene SetFrom Biocarta Pathways proteins participating in the control of skeletal myogenesis by hdac and calcium/calmodulin-dependent kinase (camk) pathway from the Biocarta Pathways dataset. |
endocytotic role of ndk phosphins and dynamin Gene SetFrom Biocarta Pathways proteins participating in the endocytotic role of ndk phosphins and dynamin pathway from the Biocarta Pathways dataset. |
regulation of eif-4e and p70s6 kinase Gene SetFrom Biocarta Pathways proteins participating in the regulation of eif-4e and p70s6 kinase pathway from the Biocarta Pathways dataset. |
vegf hypoxia and angiogenesis Gene SetFrom Biocarta Pathways proteins participating in the vegf hypoxia and angiogenesis pathway from the Biocarta Pathways dataset. |
yaci and bcma stimulation of b cell immune responses Gene SetFrom Biocarta Pathways proteins participating in the yaci and bcma stimulation of b cell immune responses pathway from the Biocarta Pathways dataset. |
lck and fyn tyrosine kinases in initiation of tcr activation Gene SetFrom Biocarta Pathways proteins participating in the lck and fyn tyrosine kinases in initiation of tcr activation pathway from the Biocarta Pathways dataset. |
hiv-1 nef: negative effector of fas and tnf Gene SetFrom Biocarta Pathways proteins participating in the hiv-1 nef: negative effector of fas and tnf pathway from the Biocarta Pathways dataset. |
nuclear receptors coordinate the activities of chromatin remodeling complexes and coactivators to facilitate initiation of transcription in carcinoma cells Gene SetFrom Biocarta Pathways proteins participating in the nuclear receptors coordinate the activities of chromatin remodeling complexes and coactivators to facilitate initiation of transcription in carcinoma cells pathway from the Biocarta Pathways dataset. |
ucalpain and friends in cell spread Gene SetFrom Biocarta Pathways proteins participating in the ucalpain and friends in cell spread pathway from the Biocarta Pathways dataset. |
ionomycin and phorbal ester signaling pathway Gene SetFrom Biocarta Pathways proteins participating in the ionomycin and phorbal ester signaling pathway pathway from the Biocarta Pathways dataset. |
carm1 and regulation of the estrogen receptor Gene SetFrom Biocarta Pathways proteins participating in the carm1 and regulation of the estrogen receptor pathway from the Biocarta Pathways dataset. |
phosphoinositides and their downstream targets Gene SetFrom Biocarta Pathways proteins participating in the phosphoinositides and their downstream targets pathway from the Biocarta Pathways dataset. |
melanocyte development and pigmentation pathway Gene SetFrom Biocarta Pathways proteins participating in the melanocyte development and pigmentation pathway pathway from the Biocarta Pathways dataset. |
akap95 role in mitosis and chromosome dynamics Gene SetFrom Biocarta Pathways proteins participating in the akap95 role in mitosis and chromosome dynamics pathway from the Biocarta Pathways dataset. |
transcription factor creb and its extracellular signals Gene SetFrom Biocarta Pathways proteins participating in the transcription factor creb and its extracellular signals pathway from the Biocarta Pathways dataset. |
visceral fat deposits and the metabolic syndrome Gene SetFrom Biocarta Pathways proteins participating in the visceral fat deposits and the metabolic syndrome pathway from the Biocarta Pathways dataset. |
the igf-1 receptor and longevity Gene SetFrom Biocarta Pathways proteins participating in the the igf-1 receptor and longevity pathway from the Biocarta Pathways dataset. |
cdc25 and chk1 regulatory pathway in response to dna damage Gene SetFrom Biocarta Pathways proteins participating in the cdc25 and chk1 regulatory pathway in response to dna damage pathway from the Biocarta Pathways dataset. |
human cytomegalovirus and map kinase pathways Gene SetFrom Biocarta Pathways proteins participating in the human cytomegalovirus and map kinase pathways pathway from the Biocarta Pathways dataset. |
influence of ras and rho proteins on g1 to s transition Gene SetFrom Biocarta Pathways proteins participating in the influence of ras and rho proteins on g1 to s transition pathway from the Biocarta Pathways dataset. |
proteolysis and signaling pathway of notch Gene SetFrom Biocarta Pathways proteins participating in the proteolysis and signaling pathway of notch pathway from the Biocarta Pathways dataset. |
apoptotic dna-fragmentation and tissue homeostasis Gene SetFrom Biocarta Pathways proteins participating in the apoptotic dna-fragmentation and tissue homeostasis pathway from the Biocarta Pathways dataset. |
ion channels and their functional role in vascular endothelium Gene SetFrom Biocarta Pathways proteins participating in the ion channels and their functional role in vascular endothelium pathway from the Biocarta Pathways dataset. |
alpha-synuclein and parkin-mediated proteolysis in parkinson`s disease Gene SetFrom Biocarta Pathways proteins participating in the alpha-synuclein and parkin-mediated proteolysis in parkinson`s disease pathway from the Biocarta Pathways dataset. |
fosb gene expression and drug abuse Gene SetFrom Biocarta Pathways proteins participating in the fosb gene expression and drug abuse pathway from the Biocarta Pathways dataset. |
links between pyk2 and map kinases Gene SetFrom Biocarta Pathways proteins participating in the links between pyk2 and map kinases pathway from the Biocarta Pathways dataset. |
opposing roles of aif in apoptosis and cell survival Gene SetFrom Biocarta Pathways proteins participating in the opposing roles of aif in apoptosis and cell survival pathway from the Biocarta Pathways dataset. |
degradation of the rar and rxr by the proteasome Gene SetFrom Biocarta Pathways proteins participating in the degradation of the rar and rxr by the proteasome pathway from the Biocarta Pathways dataset. |
cadmium induces dna synthesis and proliferation in macrophages Gene SetFrom Biocarta Pathways proteins participating in the cadmium induces dna synthesis and proliferation in macrophages pathway from the Biocarta Pathways dataset. |
erk and pi-3 kinase are necessary for collagen binding in corneal epithelia Gene SetFrom Biocarta Pathways proteins participating in the erk and pi-3 kinase are necessary for collagen binding in corneal epithelia pathway from the Biocarta Pathways dataset. |
role of brca1 brca2 and atr in cancer susceptibility Gene SetFrom Biocarta Pathways proteins participating in the role of brca1 brca2 and atr in cancer susceptibility pathway from the Biocarta Pathways dataset. |
chrebp regulation by carbohydrates and camp Gene SetFrom Biocarta Pathways proteins participating in the chrebp regulation by carbohydrates and camp pathway from the Biocarta Pathways dataset. |
pten dependent cell cycle arrest and apoptosis Gene SetFrom Biocarta Pathways proteins participating in the pten dependent cell cycle arrest and apoptosis pathway from the Biocarta Pathways dataset. |
induction of apoptosis through dr3 and dr4/5 death receptors Gene SetFrom Biocarta Pathways proteins participating in the induction of apoptosis through dr3 and dr4/5 death receptors pathway from the Biocarta Pathways dataset. |
CIITA-18437201-Raji B cells and iDC-human Gene SetFrom ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the CIITA-18437201-Raji B cells and iDC-human transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset. |
FOXP2-23625967-PFSK-1 AND SK-N-MC-HUMAN Gene SetFrom ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the FOXP2-23625967-PFSK-1 AND SK-N-MC-HUMAN transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset. |
VDR-23401126-LCL-AND-THP1-HUMAN Gene SetFrom ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the VDR-23401126-LCL-AND-THP1-HUMAN transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset. |
YY1-23942234-MYOBLASTS AND MYOTUBES-MOUSE Gene SetFrom ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the YY1-23942234-MYOBLASTS AND MYOTUBES-MOUSE transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset. |
BACH1-22875853-HELA-AND-SCP4-HUMAN Gene SetFrom ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the BACH1-22875853-HELA-AND-SCP4-HUMAN transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset. |
EZH2-23942234-MYOBLASTS AND MYOTUBES-MOUSE Gene SetFrom ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the EZH2-23942234-MYOBLASTS AND MYOTUBES-MOUSE transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset. |
Hypothyroidism, central, and testicular enlargement Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypothyroidism, central, and testicular enlargement phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Retinal dystrophy, juvenile cataracts, and short stature syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Retinal dystrophy, juvenile cataracts, and short stature syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Holoprosencephaly, ectrodactyly, and bilateral cleft lip/palate Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Holoprosencephaly, ectrodactyly, and bilateral cleft lip/palate phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Foveal hypoplasia and presenile cataract syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Foveal hypoplasia and presenile cataract syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Arthrogryposis, mental retardation, and seizures Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Arthrogryposis, mental retardation, and seizures phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Vater association with macrocephaly and ventriculomegaly Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Vater association with macrocephaly and ventriculomegaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Renal hamartomas nephroblastomatosis and fetal gigantism Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Renal hamartomas nephroblastomatosis and fetal gigantism phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopathy, lactic acidosis, and sideroblastic anemia 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myopathy, lactic acidosis, and sideroblastic anemia 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microtia, hearing impairment, and cleft palate Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microtia, hearing impairment, and cleft palate phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ichthyosis, spastic quadriplegia, and mental retardation Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ichthyosis, spastic quadriplegia, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hypermanganesemia with dystonia, polycythemia and cirrhosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypermanganesemia with dystonia, polycythemia and cirrhosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Combined cellular and humoral immune defects with granulomas Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Combined cellular and humoral immune defects with granulomas phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Combined d-2- and l-2-hydroxyglutaric aciduria Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Combined d-2- and l-2-hydroxyglutaric aciduria phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Sinoatrial node dysfunction and deafness Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Sinoatrial node dysfunction and deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ectodermal dysplasia, anhidrotic, with immunodeficiency, osteopetrosis, and lymphedema Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ectodermal dysplasia, anhidrotic, with immunodeficiency, osteopetrosis, and lymphedema phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
T-cell immunodeficiency, recurrent infections, and autoimmunity with or without cardiac malformations Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the T-cell immunodeficiency, recurrent infections, and autoimmunity with or without cardiac malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mental retardation with language impairment and autistic features Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mental retardation with language impairment and autistic features phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Warts, hypogammaglobulinemia, infections, and myelokathexis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Warts, hypogammaglobulinemia, infections, and myelokathexis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Fibular hypoplasia and complex brachydactyly Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Fibular hypoplasia and complex brachydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Autoinflammation, antibody deficiency, and immune dysregulation, plcg2-associated Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Autoinflammation, antibody deficiency, and immune dysregulation, plcg2-associated phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mental retardation, anterior maxillary protrusion, and strabismus Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, anterior maxillary protrusion, and strabismus phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Infantile convulsions and paroxysmal choreoathetosis, familial Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Infantile convulsions and paroxysmal choreoathetosis, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Short stature, optic nerve atrophy, and pelger-huet anomaly Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Short stature, optic nerve atrophy, and pelger-huet anomaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Alzheimer disease, familial, 3, with spastic paraparesis and apraxia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Alzheimer disease, familial, 3, with spastic paraparesis and apraxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Insulin-resistant diabetes mellitus AND acanthosis nigricans Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Insulin-resistant diabetes mellitus AND acanthosis nigricans phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hypertelorism, severe, with midface prominence, myopia, mental retardation, and bone fragility Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypertelorism, severe, with midface prominence, myopia, mental retardation, and bone fragility phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myasthenic syndrome, congenital, with pre- and postsynaptic defects Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myasthenic syndrome, congenital, with pre- and postsynaptic defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Craniofacial anomalies and anterior segment dysgenesis syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Craniofacial anomalies and anterior segment dysgenesis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Deafness with labyrinthine aplasia microtia and microdontia (LAMM) Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Deafness with labyrinthine aplasia microtia and microdontia (LAMM) phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Multiple Cutaneous and Mucosal Venous Malformations Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Multiple Cutaneous and Mucosal Venous Malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Neuropathy hereditary sensory and autonomic type 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Neuropathy hereditary sensory and autonomic type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microcephaly with mental retardation and digital anomalies Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microcephaly with mental retardation and digital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Peripheral neuropathy, myopathy, hoarseness, and hearing loss Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Peripheral neuropathy, myopathy, hoarseness, and hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Immunodeficiency, X-Linked, with magnesium defect, Epstein-Barr virus infection, and neoplasia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Immunodeficiency, X-Linked, with magnesium defect, Epstein-Barr virus infection, and neoplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Growth retardation, developmental delay, coarse facies, and early death Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Growth retardation, developmental delay, coarse facies, and early death phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Inflammatory skin and bowel disease, neonatal, 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Inflammatory skin and bowel disease, neonatal, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Anemia sideroblastic and spinocerebellar ataxia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Anemia sideroblastic and spinocerebellar ataxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Facial dysmorphism, immunodeficiency, livedo, and short stature Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Facial dysmorphism, immunodeficiency, livedo, and short stature phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Deafness, congenital heart defects, and posterior embryotoxon Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Deafness, congenital heart defects, and posterior embryotoxon phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Infertility associated with multi-tailed spermatozoa and excessive DNA Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Infertility associated with multi-tailed spermatozoa and excessive DNA phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Iris coloboma with ptosis, hypertelorism, and mental retardation Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Iris coloboma with ptosis, hypertelorism, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Rigidity and multifocal seizure syndrome, lethal neonatal Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Rigidity and multifocal seizure syndrome, lethal neonatal phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Alopecia, neurologic defects, and endocrinopathy syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Alopecia, neurologic defects, and endocrinopathy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mullerian aplasia and hyperandrogenism Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mullerian aplasia and hyperandrogenism phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Knuckle pads, deafness AND leukonychia syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Knuckle pads, deafness AND leukonychia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblJ TYPE Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblJ TYPE phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Inclusion body myopathy with early-onset paget disease and frontotemporal dementia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Inclusion body myopathy with early-onset paget disease and frontotemporal dementia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Multicentric osteolysis, nodulosis and arthropathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Multicentric osteolysis, nodulosis and arthropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Stapes ankylosis with broad thumb and toes Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Stapes ankylosis with broad thumb and toes phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Corneal dystrophy and perceptive deafness Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Corneal dystrophy and perceptive deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma and woolly hair Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma and woolly hair phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Proteinuria, low molecular weight, with hypercalciuria and nephrocalcinosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Proteinuria, low molecular weight, with hypercalciuria and nephrocalcinosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Noonan syndrome and Noonan-related syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Noonan syndrome and Noonan-related syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopathy, lactic acidosis, and sideroblastic anemia 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myopathy, lactic acidosis, and sideroblastic anemia 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Neuropathy, hereditary motor and sensory, Okinawa type Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Neuropathy, hereditary motor and sensory, Okinawa type phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microcephaly, short stature, and impaired glucose metabolism Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, short stature, and impaired glucose metabolism phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hemorrhagic destruction of the brain, subependymal calcification, and cataracts Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hemorrhagic destruction of the brain, subependymal calcification, and cataracts phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Jervell and Lange-Nielsen syndrome 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Jervell and Lange-Nielsen syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Macrocephaly, alopecia, cutis laxa, and scoliosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Macrocephaly, alopecia, cutis laxa, and scoliosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hypomyelination and Congenital Cataract Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypomyelination and Congenital Cataract phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hirschsprung disease, cardiac defects, and autonomic dysfunction Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hirschsprung disease, cardiac defects, and autonomic dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cardiomyopathy dilated with woolly hair and keratoderma Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cardiomyopathy dilated with woolly hair and keratoderma phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Arthrogryposis, renal dysfunction, and cholestasis 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Arthrogryposis, renal dysfunction, and cholestasis 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cataract and cardiomyopathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cataract and cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Inflammatory skin and bowel disease, neonatal Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Inflammatory skin and bowel disease, neonatal phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mental retardation X-linked with cerebellar hypoplasia and distinctive facial appearance Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mental retardation X-linked with cerebellar hypoplasia and distinctive facial appearance phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cataract, microphthalmia and nystagmus Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cataract, microphthalmia and nystagmus phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Foveal hypoplasia and anterior segment dysgenesis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Foveal hypoplasia and anterior segment dysgenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A7 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A6 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A8 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Bone fragility with contractures, arterial rupture, and deafness Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Bone fragility with contractures, arterial rupture, and deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Gyrate atrophy of choroid and retina with pyridoxine-responsive ornithinemia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Gyrate atrophy of choroid and retina with pyridoxine-responsive ornithinemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ulna and fibula absence of with severe limb deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ulna and fibula absence of with severe limb deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Dendritic cell, monocyte, B lymphocyte, and natural killer lymphocyte deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Dendritic cell, monocyte, B lymphocyte, and natural killer lymphocyte deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Factor v and factor viii, combined deficiency of, 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Factor v and factor viii, combined deficiency of, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopathy, areflexia, respiratory distress, and dysphagia, early-onset Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myopathy, areflexia, respiratory distress, and dysphagia, early-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Alpha/beta T-cell lymphopenia with gamma/delta T-cell expansion, severe cytomegalovirus infection, and autoimmunity Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Alpha/beta T-cell lymphopenia with gamma/delta T-cell expansion, severe cytomegalovirus infection, and autoimmunity phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary Paragangliomas and Pheochromocytomas Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary Paragangliomas and Pheochromocytomas phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
X-linked rolandic epilepsy with mental retardation and speech dyspraxia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the X-linked rolandic epilepsy with mental retardation and speech dyspraxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Band-like calcification with simplified gyration and polymicrogyria Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Band-like calcification with simplified gyration and polymicrogyria phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hypercarotenemia and vitamin a deficiency, autosomal dominant Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypercarotenemia and vitamin a deficiency, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A14 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microcephaly, epilepsy, and diabetes syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, epilepsy, and diabetes syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cerebellar ataxia and hypogonadotropic hypogonadism Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia and hypogonadotropic hypogonadism phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Epilepsy, X-linked, with variable learning disabilities and behavior disorders Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Epilepsy, X-linked, with variable learning disabilities and behavior disorders phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Optic atrophy and cataract, autosomal dominant Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Optic atrophy and cataract, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cataract, juvenile, with microcornea and glucosuria Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cataract, juvenile, with microcornea and glucosuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VII Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VII phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cerebellar ataxia, deafness, and narcolepsy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, deafness, and narcolepsy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cutis laxa with severe pulmonary, gastrointestinal, and urinary abnormalities Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cutis laxa with severe pulmonary, gastrointestinal, and urinary abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Juvenile macular degeneration and hypotrichosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Juvenile macular degeneration and hypotrichosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary motor and sensory neuropathy with optic atrophy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary motor and sensory neuropathy with optic atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE I, SEVERE Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE I, SEVERE phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary leiomyomatosis and renal cell cancer Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary leiomyomatosis and renal cell cancer phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Monocyte and dendritic cell deficiency, autosomal recessive Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Monocyte and dendritic cell deficiency, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microcephaly, hiatal hernia and nephrotic syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, hiatal hernia and nephrotic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
T-cell immunodeficiency, congenital alopecia and nail dystrophy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the T-cell immunodeficiency, congenital alopecia and nail dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pancreatic agenesis and congenital heart disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pancreatic agenesis and congenital heart disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microcornea, rod-cone dystrophy, cataract, and posterior staphyloma Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microcornea, rod-cone dystrophy, cataract, and posterior staphyloma phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Jervell and Lange-Nielsen syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Jervell and Lange-Nielsen syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Combined malonic and methylmalonic aciduria Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Combined malonic and methylmalonic aciduria phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microcornea, myopic chorioretinal atrophy, and telecanthus Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microcornea, myopic chorioretinal atrophy, and telecanthus phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glomerulocystic kidney disease with hyperuricemia and isosthenuria Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glomerulocystic kidney disease with hyperuricemia and isosthenuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Thrombocytopenia, platelet dysfunction, hemolysis, and imbalanced globin synthesis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Thrombocytopenia, platelet dysfunction, hemolysis, and imbalanced globin synthesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cutis Gyrata syndrome of Beare and Stevenson Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cutis Gyrata syndrome of Beare and Stevenson phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microcephaly and chorioretinopathy, autosomal recessive, 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microcephaly and chorioretinopathy, autosomal recessive, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Corneal intraepithelial dyskeratosis and ectodermal dysplasia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Corneal intraepithelial dyskeratosis and ectodermal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Aniridia, cerebellar ataxia, and mental retardation Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Aniridia, cerebellar ataxia, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
X-linked hereditary motor and sensory neuropathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the X-linked hereditary motor and sensory neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Renal tubular acidosis, proximal, with ocular abnormalities and mental retardation Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Renal tubular acidosis, proximal, with ocular abnormalities and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Craniosynostosis and dental anomalies Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Craniosynostosis and dental anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mycobacterial and viral infections, susceptibility to, autosomal recessive Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mycobacterial and viral infections, susceptibility to, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Obesity, hyperphagia, and developmental delay Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Obesity, hyperphagia, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cerebroretinal microangiopathy with calcifications and cysts Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cerebroretinal microangiopathy with calcifications and cysts phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Generalized epilepsy and paroxysmal dyskinesia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Generalized epilepsy and paroxysmal dyskinesia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Alacrima, achalasia, and mental retardation syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Alacrima, achalasia, and mental retardation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microcephaly, normal intelligence and immunodeficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, normal intelligence and immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Calcification of joints and arteries Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Calcification of joints and arteries phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hypotrichosis and recurrent skin vesicles Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypotrichosis and recurrent skin vesicles phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Epidermolysa bullosa simplex and limb girdle muscular dystrophy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Epidermolysa bullosa simplex and limb girdle muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Psychomotor retardation, epilepsy, and craniofacial dysmorphism Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Psychomotor retardation, epilepsy, and craniofacial dysmorphism phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Epiphyseal dysplasia, multiple, with myopia and conductive deafness Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Epiphyseal dysplasia, multiple, with myopia and conductive deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Frontotemporal dementia and/or amyotrophic lateral sclerosis 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Frontotemporal dementia and/or amyotrophic lateral sclerosis 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cutaneous telangiectasia and cancer syndrome, familial Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cutaneous telangiectasia and cancer syndrome, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC, SEVERE Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC, SEVERE phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pineal hyperplasia AND diabetes mellitus syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pineal hyperplasia AND diabetes mellitus syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Morbid obesity and spermatogenic failure Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Morbid obesity and spermatogenic failure phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Skeletal defects, genital hypoplasia, and mental retardation Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Skeletal defects, genital hypoplasia, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Sideroblastic anemia with b-cell immunodeficiency, periodic fevers, and developmental delay Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Sideroblastic anemia with b-cell immunodeficiency, periodic fevers, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Striatal necrosis, bilateral, and progressive polyneuropathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Striatal necrosis, bilateral, and progressive polyneuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary sensory and autonomic neuropathy type IIA Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary sensory and autonomic neuropathy type IIA phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopia, high, with cataract and vitreoretinal degeneration Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myopia, high, with cataract and vitreoretinal degeneration phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Combined deficiency of factor V and factor VIII, 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Combined deficiency of factor V and factor VIII, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Camptodactyly, tall stature, and hearing loss syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Camptodactyly, tall stature, and hearing loss syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Corneal fragility keratoglobus, blue sclerae AND joint hypermobility Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Corneal fragility keratoglobus, blue sclerae AND joint hypermobility phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pyogenic arthritis, pyoderma gangrenosum and acne Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pyogenic arthritis, pyoderma gangrenosum and acne phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopathy, areflexia, respiratory distress, and dysphagia, early-onset, mild variant Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myopathy, areflexia, respiratory distress, and dysphagia, early-onset, mild variant phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Growth deficiency and mental retardation with facial dysmorphism Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Growth deficiency and mental retardation with facial dysmorphism phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital Cataracts, Facial Dysmorphism, and Neuropathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital Cataracts, Facial Dysmorphism, and Neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Deafness, cochlear, with myopia and intellectual impairment Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Deafness, cochlear, with myopia and intellectual impairment phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Combined deficiency of sialidase AND beta galactosidase Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Combined deficiency of sialidase AND beta galactosidase phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
X-linked mental retardation with short stature, hypogonadism and abnormal gait Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the X-linked mental retardation with short stature, hypogonadism and abnormal gait phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microcephaly, postnatal progressive, with seizures and brain atrophy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, postnatal progressive, with seizures and brain atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cardiomyopathy, dilated, with woolly hair, keratoderma, and tooth agenesis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cardiomyopathy, dilated, with woolly hair, keratoderma, and tooth agenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Retinal dystrophy, iris coloboma, and comedogenic acne syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Retinal dystrophy, iris coloboma, and comedogenic acne syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Aplasia cutis congenita, reticulolinear, with microcephaly, facial dysmorphism, and other congenital anomalies Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Aplasia cutis congenita, reticulolinear, with microcephaly, facial dysmorphism, and other congenital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ichthyosis, follicular atrophoderma, hypotrichosis, and hypohidrosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ichthyosis, follicular atrophoderma, hypotrichosis, and hypohidrosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
mrna cleavage and polyadenylation specificity factor complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the mrna cleavage and polyadenylation specificity factor complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
mitochondrial sorting and assembly machinery complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the mitochondrial sorting and assembly machinery complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
cortical layer of collagen and cuticulin-based cuticle extracellular matrix Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the cortical layer of collagen and cuticulin-based cuticle extracellular matrix cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
collagen and cuticulin-based cuticle extracellular matrix Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the collagen and cuticulin-based cuticle extracellular matrix cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
mrna cleavage and polyadenylation specificity factor complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the mrna cleavage and polyadenylation specificity factor complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
collagen and cuticulin-based cuticle extracellular matrix part Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the collagen and cuticulin-based cuticle extracellular matrix part cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
mitochondrial sorting and assembly machinery complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the mitochondrial sorting and assembly machinery complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
TRBP containing complex (DICER, RPL7A, EIF6, MOV10 and subunits of the 60S ribosomal particle) Gene Setproteins in the TRBP containing complex (DICER, RPL7A, EIF6, MOV10 and subunits of the 60S ribosomal particle) protein complex from the CORUM Protein Complexes dataset. |
NRD complex (Nucleosome remodeling and deacetylation complex) Gene Setproteins in the NRD complex (Nucleosome remodeling and deacetylation complex) protein complex from the CORUM Protein Complexes dataset. |
6S methyltransferase and RG-containing Sm proteins complex Gene Setproteins in the 6S methyltransferase and RG-containing Sm proteins complex protein complex from the CORUM Protein Complexes dataset. |
Remodeling and spacing factor (RSF) complex Gene Setproteins in the Remodeling and spacing factor (RSF) complex protein complex from the CORUM Protein Complexes dataset. |
PBAF complex (Polybromo- and BAF containing complex) Gene Setproteins in the PBAF complex (Polybromo- and BAF containing complex) protein complex from the CORUM Protein Complexes dataset. |
Cleavage and polyadenylation factor (CPSF) Gene Setproteins in the Cleavage and polyadenylation factor (CPSF) protein complex from the CORUM Protein Complexes dataset. |
Respiratory chain complex I (intermediate I/200kD and III/250kD), mitochondrial Gene Setproteins in the Respiratory chain complex I (intermediate I/200kD and III/250kD), mitochondrial protein complex from the CORUM Protein Complexes dataset. |
Nucleic and chromatin Fanconi complex Gene Setproteins in the Nucleic and chromatin Fanconi complex protein complex from the CORUM Protein Complexes dataset. |
Respiratory chain complex I (intermediate V/380kD and VI/480kD), mitochondrial Gene Setproteins in the Respiratory chain complex I (intermediate V/380kD and VI/480kD), mitochondrial protein complex from the CORUM Protein Complexes dataset. |
ATP-utilizing chromatin assembly and remodeling factor (hACF) complex Gene Setproteins in the ATP-utilizing chromatin assembly and remodeling factor (hACF) complex protein complex from the CORUM Protein Complexes dataset. |
Amino Acids, Peptides, and Proteins Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Amino Acids, Peptides, and Proteins from the curated CTD Gene-Chemical Interactions dataset. |
Bile Acids and Salts Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Bile Acids and Salts from the curated CTD Gene-Chemical Interactions dataset. |
Prime and Bond NT Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Prime and Bond NT from the curated CTD Gene-Chemical Interactions dataset. |
drospirenone and ethinyl estradiol combination Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical drospirenone and ethinyl estradiol combination from the curated CTD Gene-Chemical Interactions dataset. |
Hypophosphatemic Rickets And Hyperparathyroidism Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hypophosphatemic Rickets And Hyperparathyroidism from the curated CTD Gene-Disease Associations dataset. |
Severe Combined Immunodeficiency with Microcephaly, Growth Retardation, and Sensitivity to Ionizing Radiation Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Severe Combined Immunodeficiency with Microcephaly, Growth Retardation, and Sensitivity to Ionizing Radiation from the curated CTD Gene-Disease Associations dataset. |
Fibular hypoplasia and complex brachydactyly Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Fibular hypoplasia and complex brachydactyly from the curated CTD Gene-Disease Associations dataset. |
Synovitis granulomatous with uveitis and cranial neuropathies Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Synovitis granulomatous with uveitis and cranial neuropathies from the curated CTD Gene-Disease Associations dataset. |
MENTAL RETARDATION, ANTERIOR MAXILLARY PROTRUSION, AND STRABISMUS Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MENTAL RETARDATION, ANTERIOR MAXILLARY PROTRUSION, AND STRABISMUS from the curated CTD Gene-Disease Associations dataset. |
Hereditary Sensory and Motor Neuropathy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary Sensory and Motor Neuropathy from the curated CTD Gene-Disease Associations dataset. |
Preaxial deficiency, postaxial polydactyly and hypospadias Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Preaxial deficiency, postaxial polydactyly and hypospadias from the curated CTD Gene-Disease Associations dataset. |
Combined Cellular And Humoral Immune Defects With Granulomas Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Combined Cellular And Humoral Immune Defects With Granulomas from the curated CTD Gene-Disease Associations dataset. |
OSTEOMYELITIS, STERILE MULTIFOCAL, WITH PERIOSTITIS AND PUSTULOSIS Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease OSTEOMYELITIS, STERILE MULTIFOCAL, WITH PERIOSTITIS AND PUSTULOSIS from the curated CTD Gene-Disease Associations dataset. |
Corpus Callosum, Agenesis of, with Mental Retardation, Ocular Coloboma, and Micrognathia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Corpus Callosum, Agenesis of, with Mental Retardation, Ocular Coloboma, and Micrognathia from the curated CTD Gene-Disease Associations dataset. |
Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia from the curated CTD Gene-Disease Associations dataset. |
Epilepsy, rolandic with paroxysmal exercise-induced dystonia and writer's cramp Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, rolandic with paroxysmal exercise-induced dystonia and writer's cramp from the curated CTD Gene-Disease Associations dataset. |
Low Molecular Weight Proteinuria with Hypercalciuria and Nephrocalcinosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Low Molecular Weight Proteinuria with Hypercalciuria and Nephrocalcinosis from the curated CTD Gene-Disease Associations dataset. |
Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma from the curated CTD Gene-Disease Associations dataset. |
Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema from the curated CTD Gene-Disease Associations dataset. |
Microtia, Hearing Impairment, And Cleft Palate Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Microtia, Hearing Impairment, And Cleft Palate from the curated CTD Gene-Disease Associations dataset. |
OSTEOCHONDRITIS DISSECANS, SHORT STATURE, AND EARLY-ONSET OSTEOARTHRITIS Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease OSTEOCHONDRITIS DISSECANS, SHORT STATURE, AND EARLY-ONSET OSTEOARTHRITIS from the curated CTD Gene-Disease Associations dataset. |
Neuropathy, Hereditary Sensory And Autonomic, Type IIB Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, Hereditary Sensory And Autonomic, Type IIB from the curated CTD Gene-Disease Associations dataset. |
Acromegaloid features, overgrowth, cleft palate, and hernia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Acromegaloid features, overgrowth, cleft palate, and hernia from the curated CTD Gene-Disease Associations dataset. |
Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome from the curated CTD Gene-Disease Associations dataset. |
46,XX SEX REVERSAL WITH DYSGENESIS OF KIDNEYS, ADRENALS, AND LUNGS Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease 46,XX SEX REVERSAL WITH DYSGENESIS OF KIDNEYS, ADRENALS, AND LUNGS from the curated CTD Gene-Disease Associations dataset. |
Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease from the curated CTD Gene-Disease Associations dataset. |
Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress from the curated CTD Gene-Disease Associations dataset. |
Exocrine Pancreatic Insufficiency, Dyserythropoietic Anemia, and Calvarial Hyperostosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Exocrine Pancreatic Insufficiency, Dyserythropoietic Anemia, and Calvarial Hyperostosis from the curated CTD Gene-Disease Associations dataset. |
Craniosynostosis, anal anomalies, and porokeratosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Craniosynostosis, anal anomalies, and porokeratosis from the curated CTD Gene-Disease Associations dataset. |
Sacral defect and anterior sacral meningocele Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Sacral defect and anterior sacral meningocele from the curated CTD Gene-Disease Associations dataset. |
Classical Lissencephalies and Subcortical Band Heterotopias Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Classical Lissencephalies and Subcortical Band Heterotopias from the curated CTD Gene-Disease Associations dataset. |
Epiphyseal Dysplasia, Multiple, with Myopia and Conductive Deafness Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Epiphyseal Dysplasia, Multiple, with Myopia and Conductive Deafness from the curated CTD Gene-Disease Associations dataset. |
Optic atrophy 1 and deafness Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Optic atrophy 1 and deafness from the curated CTD Gene-Disease Associations dataset. |
Neuropathy, hereditary motor and sensory, Russe type Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, hereditary motor and sensory, Russe type from the curated CTD Gene-Disease Associations dataset. |
Blepharophimosis, Ptosis, and Epicanthus Inversus Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Blepharophimosis, Ptosis, and Epicanthus Inversus from the curated CTD Gene-Disease Associations dataset. |
Hypotrichosis And Recurrent Skin Vesicles Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hypotrichosis And Recurrent Skin Vesicles from the curated CTD Gene-Disease Associations dataset. |
Signs and Symptoms, Digestive Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Signs and Symptoms, Digestive from the curated CTD Gene-Disease Associations dataset. |
Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia from the curated CTD Gene-Disease Associations dataset. |
Methylmalonic Aciduria and Homocystinuria, CblD Type Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Methylmalonic Aciduria and Homocystinuria, CblD Type from the curated CTD Gene-Disease Associations dataset. |
Head and Neck Neoplasms Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Head and Neck Neoplasms from the curated CTD Gene-Disease Associations dataset. |
MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES from the curated CTD Gene-Disease Associations dataset. |
Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects from the curated CTD Gene-Disease Associations dataset. |
Cataract, Juvenile, With Microcornea And Glucosuria Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, Juvenile, With Microcornea And Glucosuria from the curated CTD Gene-Disease Associations dataset. |
HEREDITARY LEIOMYOMATOSIS AND RENAL CELL CANCER Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease HEREDITARY LEIOMYOMATOSIS AND RENAL CELL CANCER from the curated CTD Gene-Disease Associations dataset. |
Venous Malformations, Multiple Cutaneous and Mucosal Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Venous Malformations, Multiple Cutaneous and Mucosal from the curated CTD Gene-Disease Associations dataset. |
BAND-LIKE CALCIFICATION WITH SIMPLIFIED GYRATION AND POLYMICROGYRIA Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease BAND-LIKE CALCIFICATION WITH SIMPLIFIED GYRATION AND POLYMICROGYRIA from the curated CTD Gene-Disease Associations dataset. |
Postoperative Nausea and Vomiting Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Postoperative Nausea and Vomiting from the curated CTD Gene-Disease Associations dataset. |
Myopathy with lactic acidosis and sideroblastic anemia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy with lactic acidosis and sideroblastic anemia from the curated CTD Gene-Disease Associations dataset. |
Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells from the curated CTD Gene-Disease Associations dataset. |
MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY from the curated CTD Gene-Disease Associations dataset. |
Keratitis, Ichthyosis, and Deafness (KID) Syndrome Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Keratitis, Ichthyosis, and Deafness (KID) Syndrome from the curated CTD Gene-Disease Associations dataset. |
Bifid Nose With Or Without Anorectal And Renal Anomalies Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Bifid Nose With Or Without Anorectal And Renal Anomalies from the curated CTD Gene-Disease Associations dataset. |
Congenital Cataracts, Facial Dysmorphism, And Neuropathy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Congenital Cataracts, Facial Dysmorphism, And Neuropathy from the curated CTD Gene-Disease Associations dataset. |
Corneal dystrophy and perceptive deafness Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Corneal dystrophy and perceptive deafness from the curated CTD Gene-Disease Associations dataset. |
VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY from the curated CTD Gene-Disease Associations dataset. |
Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 3 from the curated CTD Gene-Disease Associations dataset. |
Mental Retardation, Skeletal Dysplasia, and Abducens Palsy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, Skeletal Dysplasia, and Abducens Palsy from the curated CTD Gene-Disease Associations dataset. |
Hypopituitarism and septooptic 'dysplasia' Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hypopituitarism and septooptic 'dysplasia' from the curated CTD Gene-Disease Associations dataset. |
PALMOPLANTAR HYPERKERATOSIS WITH SQUAMOUS CELL CARCINOMA OF SKIN AND 46,XX SEX REVERSAL Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease PALMOPLANTAR HYPERKERATOSIS WITH SQUAMOUS CELL CARCINOMA OF SKIN AND 46,XX SEX REVERSAL from the curated CTD Gene-Disease Associations dataset. |
Angiopathy, Hereditary, With Nephropathy, Aneurysms, And Muscle Cramps Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Angiopathy, Hereditary, With Nephropathy, Aneurysms, And Muscle Cramps from the curated CTD Gene-Disease Associations dataset. |
Aplasia of Lacrimal and Salivary Glands Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Aplasia of Lacrimal and Salivary Glands from the curated CTD Gene-Disease Associations dataset. |
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IA Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IA from the curated CTD Gene-Disease Associations dataset. |
Deafness, Cataract, Retinitis Pigmentosa, And Sperm Abnormalities Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Deafness, Cataract, Retinitis Pigmentosa, And Sperm Abnormalities from the curated CTD Gene-Disease Associations dataset. |
MICROCEPHALY, SEIZURES, AND DEVELOPMENTAL DELAY Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MICROCEPHALY, SEIZURES, AND DEVELOPMENTAL DELAY from the curated CTD Gene-Disease Associations dataset. |
Glomerulocystic Kidney Disease with Hyperuricemia and Isosthenuria Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Glomerulocystic Kidney Disease with Hyperuricemia and Isosthenuria from the curated CTD Gene-Disease Associations dataset. |
Calcification of Joints and Arteries Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Calcification of Joints and Arteries from the curated CTD Gene-Disease Associations dataset. |
CHOANAL ATRESIA AND LYMPHEDEMA Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease CHOANAL ATRESIA AND LYMPHEDEMA from the curated CTD Gene-Disease Associations dataset. |
Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis from the curated CTD Gene-Disease Associations dataset. |
Hereditary Motor And Sensory Neuropathy, Type IIC Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary Motor And Sensory Neuropathy, Type IIC from the curated CTD Gene-Disease Associations dataset. |
Asthma, Nasal Polyps, And Aspirin Intolerance Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Asthma, Nasal Polyps, And Aspirin Intolerance from the curated CTD Gene-Disease Associations dataset. |
Neoplasms, Germ Cell and Embryonal Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neoplasms, Germ Cell and Embryonal from the curated CTD Gene-Disease Associations dataset. |
Hereditary Motor And Sensory Neuropathy VI Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary Motor And Sensory Neuropathy VI from the curated CTD Gene-Disease Associations dataset. |
Cutis Gyrata Syndrome of Beare And Stevenson Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cutis Gyrata Syndrome of Beare And Stevenson from the curated CTD Gene-Disease Associations dataset. |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 2 from the curated CTD Gene-Disease Associations dataset. |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 6 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 6 from the curated CTD Gene-Disease Associations dataset. |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5 from the curated CTD Gene-Disease Associations dataset. |
Wounds and Injuries Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Wounds and Injuries from the curated CTD Gene-Disease Associations dataset. |
Schizophrenia and Disorders with Psychotic Features Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Schizophrenia and Disorders with Psychotic Features from the curated CTD Gene-Disease Associations dataset. |
Hypoprebetalipoproteinemia, Acanthocytosis, Retinitis Pigmentosa, And Pallidal Degeneration Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hypoprebetalipoproteinemia, Acanthocytosis, Retinitis Pigmentosa, And Pallidal Degeneration from the curated CTD Gene-Disease Associations dataset. |
Sleep Initiation and Maintenance Disorders Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Sleep Initiation and Maintenance Disorders from the curated CTD Gene-Disease Associations dataset. |
Methylmalonic Aciduria and Homocystinuria, CblF Type Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Methylmalonic Aciduria and Homocystinuria, CblF Type from the curated CTD Gene-Disease Associations dataset. |
Scaphocephaly, Maxillary Retrusion, And Mental Retardation Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Scaphocephaly, Maxillary Retrusion, And Mental Retardation from the curated CTD Gene-Disease Associations dataset. |
Cataract and cardiomyopathy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cataract and cardiomyopathy from the curated CTD Gene-Disease Associations dataset. |
Ectrodactyly, Ectodermal Dysplasia, And Cleft Lip/Palate Syndrome 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Ectrodactyly, Ectodermal Dysplasia, And Cleft Lip/Palate Syndrome 1 from the curated CTD Gene-Disease Associations dataset. |
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IIA Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IIA from the curated CTD Gene-Disease Associations dataset. |
FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF, 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF, 1 from the curated CTD Gene-Disease Associations dataset. |
Neuropathy, hereditary motor and sensory, Okinawa type Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, hereditary motor and sensory, Okinawa type from the curated CTD Gene-Disease Associations dataset. |
Spastic Paraplegia, Optic Atrophy, and Neuropathy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Spastic Paraplegia, Optic Atrophy, and Neuropathy from the curated CTD Gene-Disease Associations dataset. |
Generalized Epilepsy and Paroxysmal Dyskinesia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Generalized Epilepsy and Paroxysmal Dyskinesia from the curated CTD Gene-Disease Associations dataset. |
Hereditary Breast and Ovarian Cancer Syndrome Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary Breast and Ovarian Cancer Syndrome from the curated CTD Gene-Disease Associations dataset. |
Keratosis palmoplantaris with periodontopathia and onychogryposis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Keratosis palmoplantaris with periodontopathia and onychogryposis from the curated CTD Gene-Disease Associations dataset. |
Intracranial Embolism and Thrombosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Intracranial Embolism and Thrombosis from the curated CTD Gene-Disease Associations dataset. |
LEUKOENCEPHALOPATHY WITH DYSTONIA AND MOTOR NEUROPATHY Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease LEUKOENCEPHALOPATHY WITH DYSTONIA AND MOTOR NEUROPATHY from the curated CTD Gene-Disease Associations dataset. |
Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, And Cataract Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, And Cataract from the curated CTD Gene-Disease Associations dataset. |
FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF, 2 from the curated CTD Gene-Disease Associations dataset. |
Microtia With Nasolacrimal Duct Imperforation And Eye Coloboma Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Microtia With Nasolacrimal Duct Imperforation And Eye Coloboma from the curated CTD Gene-Disease Associations dataset. |
Nevi and Melanomas Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Nevi and Melanomas from the curated CTD Gene-Disease Associations dataset. |
Epilepsy, X-Linked, with Variable Learning Disabilities and Behavior Disorders Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, X-Linked, with Variable Learning Disabilities and Behavior Disorders from the curated CTD Gene-Disease Associations dataset. |
Attention Deficit and Disruptive Behavior Disorders Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Attention Deficit and Disruptive Behavior Disorders from the curated CTD Gene-Disease Associations dataset. |
Cardiomyopathy dilated with Woolly hair and keratoderma Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy dilated with Woolly hair and keratoderma from the curated CTD Gene-Disease Associations dataset. |
Microcephaly, microphthalmia, ectrodactyly of lower limbs, and prognathism Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Microcephaly, microphthalmia, ectrodactyly of lower limbs, and prognathism from the curated CTD Gene-Disease Associations dataset. |
Optic atrophy and cataract, autosomal dominant Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Optic atrophy and cataract, autosomal dominant from the curated CTD Gene-Disease Associations dataset. |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4 from the curated CTD Gene-Disease Associations dataset. |
Skeletal Defects, Genital Hypoplasia, And Mental Retardation Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Skeletal Defects, Genital Hypoplasia, And Mental Retardation from the curated CTD Gene-Disease Associations dataset. |
Hypermanganesemia with Dystonia Polycythemia and Cirrhosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hypermanganesemia with Dystonia Polycythemia and Cirrhosis from the curated CTD Gene-Disease Associations dataset. |
Juvenile macular degeneration and hypotrichosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Juvenile macular degeneration and hypotrichosis from the curated CTD Gene-Disease Associations dataset. |
ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS from the curated CTD Gene-Disease Associations dataset. |
Mullerian Aplasia and Hyperandrogenism Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Mullerian Aplasia and Hyperandrogenism from the curated CTD Gene-Disease Associations dataset. |
Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay from the curated CTD Gene-Disease Associations dataset. |
Esophageal and Gastric Varices Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Esophageal and Gastric Varices from the curated CTD Gene-Disease Associations dataset. |
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC from the curated CTD Gene-Disease Associations dataset. |
Hypogammaglobulinemia and Isolated growth hormone deficiency, X-linked Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hypogammaglobulinemia and Isolated growth hormone deficiency, X-linked from the curated CTD Gene-Disease Associations dataset. |
Carcinoma, squamous cell of head and neck Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Carcinoma, squamous cell of head and neck from the curated CTD Gene-Disease Associations dataset. |
Polycythemia, primary familial and congenital Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Polycythemia, primary familial and congenital from the curated CTD Gene-Disease Associations dataset. |
Extravasation of Diagnostic and Therapeutic Materials Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Extravasation of Diagnostic and Therapeutic Materials from the curated CTD Gene-Disease Associations dataset. |
Ichthyosis, Leukocyte Vacuoles, Alopecia, And Sclerosing Cholangitis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Ichthyosis, Leukocyte Vacuoles, Alopecia, And Sclerosing Cholangitis from the curated CTD Gene-Disease Associations dataset. |
Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 2 from the curated CTD Gene-Disease Associations dataset. |
Knuckle pads, leuconychia and sensorineural deafness Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Knuckle pads, leuconychia and sensorineural deafness from the curated CTD Gene-Disease Associations dataset. |
Renal Tubular Acidosis, Proximal, With Ocular Abnormalities And Mental Retardation Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Renal Tubular Acidosis, Proximal, With Ocular Abnormalities And Mental Retardation from the curated CTD Gene-Disease Associations dataset. |
Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked from the curated CTD Gene-Disease Associations dataset. |
Hyperekplexia and Epilepsy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hyperekplexia and Epilepsy from the curated CTD Gene-Disease Associations dataset. |
Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia from the curated CTD Gene-Disease Associations dataset. |
Epidermolysis Bullosa With Congenital Localized Absence Of Skin And Deformity Of Nails Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Epidermolysis Bullosa With Congenital Localized Absence Of Skin And Deformity Of Nails from the curated CTD Gene-Disease Associations dataset. |
Iris hypoplasia and glaucoma Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Iris hypoplasia and glaucoma from the curated CTD Gene-Disease Associations dataset. |
NATURAL KILLER CELL AND GLUCOCORTICOID DEFICIENCY WITH DNA REPAIR DEFECT Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease NATURAL KILLER CELL AND GLUCOCORTICOID DEFICIENCY WITH DNA REPAIR DEFECT from the curated CTD Gene-Disease Associations dataset. |
Sarcoma family syndrome of Li and Fraumeni Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Sarcoma family syndrome of Li and Fraumeni from the curated CTD Gene-Disease Associations dataset. |
PACHYGYRIA WITH MENTAL RETARDATION, SEIZURES, AND ARACHNOID CYSTS Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease PACHYGYRIA WITH MENTAL RETARDATION, SEIZURES, AND ARACHNOID CYSTS from the curated CTD Gene-Disease Associations dataset. |
Nephropathy with Pretibial Epidermolysis Bullosa and Deafness Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Nephropathy with Pretibial Epidermolysis Bullosa and Deafness from the curated CTD Gene-Disease Associations dataset. |
Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome from the curated CTD Gene-Disease Associations dataset. |
Lipoid Proteinosis of Urbach and Wiethe Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Lipoid Proteinosis of Urbach and Wiethe from the curated CTD Gene-Disease Associations dataset. |
Hypertelorism with esophageal abnormality and hypospadias Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hypertelorism with esophageal abnormality and hypospadias from the curated CTD Gene-Disease Associations dataset. |
Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis from the curated CTD Gene-Disease Associations dataset. |
Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 from the curated CTD Gene-Disease Associations dataset. |
Bone Fragility with Contractures, Arterial Rupture, and Deafness Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Bone Fragility with Contractures, Arterial Rupture, and Deafness from the curated CTD Gene-Disease Associations dataset. |
Thrombocytopenia, Platelet Dysfunction, Hemolysis, and Imbalanced Globin Synthesis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Thrombocytopenia, Platelet Dysfunction, Hemolysis, and Imbalanced Globin Synthesis from the curated CTD Gene-Disease Associations dataset. |
Jervell And Lange-Nielsen Syndrome 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Jervell And Lange-Nielsen Syndrome 2 from the curated CTD Gene-Disease Associations dataset. |
Neoplasms, Glandular and Epithelial Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neoplasms, Glandular and Epithelial from the curated CTD Gene-Disease Associations dataset. |
Ectodermal dysplasia, ectrodactyly, and macular dystrophy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Ectodermal dysplasia, ectrodactyly, and macular dystrophy from the curated CTD Gene-Disease Associations dataset. |
Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Alopecia, Neurologic Defects, and Endocrinopathy Syndrome from the curated CTD Gene-Disease Associations dataset. |
Retinitis Pigmentosa, X-Linked, And Sinorespiratory Infections, With Or Without Deafness Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Retinitis Pigmentosa, X-Linked, And Sinorespiratory Infections, With Or Without Deafness from the curated CTD Gene-Disease Associations dataset. |
Early-onset ataxia with oculomotor apraxia and hypoalbuminemia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Early-onset ataxia with oculomotor apraxia and hypoalbuminemia from the curated CTD Gene-Disease Associations dataset. |
Pyogenic arthritis, pyoderma gangrenosum, and acne Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Pyogenic arthritis, pyoderma gangrenosum, and acne from the curated CTD Gene-Disease Associations dataset. |
Epidermolysa bullosa simplex and limb girdle muscular dystrophy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Epidermolysa bullosa simplex and limb girdle muscular dystrophy from the curated CTD Gene-Disease Associations dataset. |
Cleft Palate, Isolated, And Mental Retardation Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cleft Palate, Isolated, And Mental Retardation from the curated CTD Gene-Disease Associations dataset. |
Absent radii and thrombocytopenia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Absent radii and thrombocytopenia from the curated CTD Gene-Disease Associations dataset. |
Hypercarotenemia And Vitamin A Deficiency, Autosomal Dominant Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hypercarotenemia And Vitamin A Deficiency, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset. |
HEMORRHAGIC DESTRUCTION OF THE BRAIN, SUBEPENDYMAL CALCIFICATION, AND CATARACTS Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease HEMORRHAGIC DESTRUCTION OF THE BRAIN, SUBEPENDYMAL CALCIFICATION, AND CATARACTS from the curated CTD Gene-Disease Associations dataset. |
Microcephaly with Mental Retardation and Digital Anomalies Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Microcephaly with Mental Retardation and Digital Anomalies from the curated CTD Gene-Disease Associations dataset. |
Macrocephaly with Multiple Epiphyseal Dysplasia and Distinctive Facies Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Macrocephaly with Multiple Epiphyseal Dysplasia and Distinctive Facies from the curated CTD Gene-Disease Associations dataset. |
STAPES ANKYLOSIS WITH BROAD THUMB AND TOES Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease STAPES ANKYLOSIS WITH BROAD THUMB AND TOES from the curated CTD Gene-Disease Associations dataset. |
Cutis Laxa With Severe Pulmonary, Gastrointestinal, And Urinary Abnormalities Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cutis Laxa With Severe Pulmonary, Gastrointestinal, And Urinary Abnormalities from the curated CTD Gene-Disease Associations dataset. |
Polyhydramnios, Megalencephaly, And Symptomatic Epilepsy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Polyhydramnios, Megalencephaly, And Symptomatic Epilepsy from the curated CTD Gene-Disease Associations dataset. |
Mental retardation, X-linked, with cerebellar hypoplasia and distinctive facial appearance Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Mental retardation, X-linked, with cerebellar hypoplasia and distinctive facial appearance from the curated CTD Gene-Disease Associations dataset. |
Alpha/Beta T-Cell Lymphopenia with Gamma/Delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Alpha/Beta T-Cell Lymphopenia with Gamma/Delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity from the curated CTD Gene-Disease Associations dataset. |
Dehydrated Hereditary Stomatocytosis, Pseudohyperkalemia, and Perinatal Edema Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Dehydrated Hereditary Stomatocytosis, Pseudohyperkalemia, and Perinatal Edema from the curated CTD Gene-Disease Associations dataset. |
Mental Retardation, Severe, With Spasticity And Pigmentary Tapetoretinal Degeneration Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, Severe, With Spasticity And Pigmentary Tapetoretinal Degeneration from the curated CTD Gene-Disease Associations dataset. |
Signs and Symptoms, Respiratory Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Signs and Symptoms, Respiratory from the curated CTD Gene-Disease Associations dataset. |
Renal cysts and diabetes syndrome Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Renal cysts and diabetes syndrome from the curated CTD Gene-Disease Associations dataset. |
Neuropathy, hereditary motor and sensory, LOM type Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, hereditary motor and sensory, LOM type from the curated CTD Gene-Disease Associations dataset. |
Nephroblastomatosis, fetal ascites, macrosomia and Wilms tumor Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Nephroblastomatosis, fetal ascites, macrosomia and Wilms tumor from the curated CTD Gene-Disease Associations dataset. |
Hereditary Angioedema Types I and II Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary Angioedema Types I and II from the curated CTD Gene-Disease Associations dataset. |
Drug-Related Side Effects and Adverse Reactions Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Drug-Related Side Effects and Adverse Reactions from the curated CTD Gene-Disease Associations dataset. |
Insect Bites and Stings Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Insect Bites and Stings from the curated CTD Gene-Disease Associations dataset. |
T-cell immunodeficiency, congenital alopecia and nail dystrophy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease T-cell immunodeficiency, congenital alopecia and nail dystrophy from the curated CTD Gene-Disease Associations dataset. |
Foveal Hypoplasia and Anterior Segment Dysgenesis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Foveal Hypoplasia and Anterior Segment Dysgenesis from the curated CTD Gene-Disease Associations dataset. |
Cubitus Valgus with Mental Retardation and Unusual Facies Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cubitus Valgus with Mental Retardation and Unusual Facies from the curated CTD Gene-Disease Associations dataset. |
Ophthalmoplegia, External, and Myopia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Ophthalmoplegia, External, and Myopia from the curated CTD Gene-Disease Associations dataset. |
Deafness, Sensorineural, And Male Infertility Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Deafness, Sensorineural, And Male Infertility from the curated CTD Gene-Disease Associations dataset. |
Hereditary Sensory and Autonomic Neuropathies Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary Sensory and Autonomic Neuropathies from the curated CTD Gene-Disease Associations dataset. |
Histiocytosis with joint contractures and sensorineural deafness Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Histiocytosis with joint contractures and sensorineural deafness from the curated CTD Gene-Disease Associations dataset. |
Rolandic Epilepsy, Mental Retardation, and Speech Dyspraxia, X-Linked Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Rolandic Epilepsy, Mental Retardation, and Speech Dyspraxia, X-Linked from the curated CTD Gene-Disease Associations dataset. |
Leiomyomatosis, esophageal and vulval, with nephropathy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Leiomyomatosis, esophageal and vulval, with nephropathy from the curated CTD Gene-Disease Associations dataset. |
Growth Retardation, Developmental Delay, Coarse Facies, And Early Death Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Growth Retardation, Developmental Delay, Coarse Facies, And Early Death from the curated CTD Gene-Disease Associations dataset. |
Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis from the curated CTD Gene-Disease Associations dataset. |
Embolism and Thrombosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Embolism and Thrombosis from the curated CTD Gene-Disease Associations dataset. |
Religion and Psychology Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Religion and Psychology in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
Attention Deficit and Disruptive Behavior Disorders Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Attention Deficit and Disruptive Behavior Disorders in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
Body Weights and Measures Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Body Weights and Measures in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
Nevi and Melanomas Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Nevi and Melanomas in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
Head and Neck Neoplasms Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Head and Neck Neoplasms in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
blepharophimosis, ptosis, and epicanthus inversus syndrome Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease blepharophimosis, ptosis, and epicanthus inversus syndrome from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
degeneration of macula and posterior pole Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease degeneration of macula and posterior pole from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
eye and adnexa disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease eye and adnexa disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
combined t cell and b cell immunodeficiency Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease combined t cell and b cell immunodeficiency from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
eye and adnexa disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease eye and adnexa disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
inflammatory and toxic neuropathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease inflammatory and toxic neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
mucinous tubular and spindle renal cell carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease mucinous tubular and spindle renal cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
pustulosis of palm and sole Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease pustulosis of palm and sole in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
hand, foot and mouth disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hand, foot and mouth disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
tooth and nail syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease tooth and nail syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
extrapyramidal and movement disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease extrapyramidal and movement disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
mononeuritis of upper limb and mononeuritis multiplex Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease mononeuritis of upper limb and mononeuritis multiplex in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
lung mixed small cell and squamous cell carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease lung mixed small cell and squamous cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
autoimmune disease of skin and connective tissue Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease autoimmune disease of skin and connective tissue in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
histiocytic and dendritic cell cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease histiocytic and dendritic cell cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
methylmalonic aciduria and homocystinuria type cblc Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease methylmalonic aciduria and homocystinuria type cblc in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
blepharophimosis, ptosis, and epicanthus inversus syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease blepharophimosis, ptosis, and epicanthus inversus syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
germ cell and embryonal cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease germ cell and embryonal cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
mixed endometrial stromal and smooth muscle tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease mixed endometrial stromal and smooth muscle tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
spinal canal and spinal cord meningioma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease spinal canal and spinal cord meningioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
ovarian germ cell monodermal and highly specialized teratoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease ovarian germ cell monodermal and highly specialized teratoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
degeneration of macula and posterior pole Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease degeneration of macula and posterior pole in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
combined t cell and b cell immunodeficiency Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease combined t cell and b cell immunodeficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
mature t-cell and nk-cell lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease mature t-cell and nk-cell lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
eye and adnexa disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease eye and adnexa disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
breast and lung cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease breast and lung cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
increased chromosome aberrations and higher lung cancer risk Gene SetFrom GAD Gene-Disease Associations genes associated with the disease increased chromosome aberrations and higher lung cancer risk in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hyper-ige syndrome and severe eczema. atopy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hyper-ige syndrome and severe eczema. atopy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
factor viii and factor ix genes Gene SetFrom GAD Gene-Disease Associations genes associated with the disease factor viii and factor ix genes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
flecainide and paroxetine Gene SetFrom GAD Gene-Disease Associations genes associated with the disease flecainide and paroxetine in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pre-term delivery infant mortality and malaria morbidity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pre-term delivery infant mortality and malaria morbidity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alopecia and lumbar herniated disk Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alopecia and lumbar herniated disk in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
baroreflex and blood pressure regulation Gene SetFrom GAD Gene-Disease Associations genes associated with the disease baroreflex and blood pressure regulation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
neuropathy, hereditary motor and sensory Gene SetFrom GAD Gene-Disease Associations genes associated with the disease neuropathy, hereditary motor and sensory in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
psoriasis, psoriatic arthritis, and sapho syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease psoriasis, psoriatic arthritis, and sapho syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
platelet reactivity and clopidogrel resistance Gene SetFrom GAD Gene-Disease Associations genes associated with the disease platelet reactivity and clopidogrel resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; neoplasms, germ cell and embryonal; neoplasms, testis; testicular neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; neoplasms, germ cell and embryonal; neoplasms, testis; testicular neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
low mpa exposure and acute rejection in mmf/tacrolimus-treated kidney transplant patients Gene SetFrom GAD Gene-Disease Associations genes associated with the disease low mpa exposure and acute rejection in mmf/tacrolimus-treated kidney transplant patients in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multisystem atrophy, progressive supranuclear palsy and corticobasal degeneration Gene SetFrom GAD Gene-Disease Associations genes associated with the disease multisystem atrophy, progressive supranuclear palsy and corticobasal degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
jervell and lange-nielsen syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease jervell and lange-nielsen syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anovulation and fecundity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anovulation and fecundity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
proteinuria and cardiovascular disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease proteinuria and cardiovascular disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
thyroid and neurological abnormalities Gene SetFrom GAD Gene-Disease Associations genes associated with the disease thyroid and neurological abnormalities in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
homocysteine, folate and vitamin b12 levels Gene SetFrom GAD Gene-Disease Associations genes associated with the disease homocysteine, folate and vitamin b12 levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension and obesity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension and obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
child hyperactivity-impulsivity and oppositional behaviors Gene SetFrom GAD Gene-Disease Associations genes associated with the disease child hyperactivity-impulsivity and oppositional behaviors in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
head and neck squamous cell carcinoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease head and neck squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
asthma and atopy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease asthma and atopy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hiv-rna and cellular hiv-dna levels Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hiv-rna and cellular hiv-dna levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
insulin release and insulin sensitivity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease insulin release and insulin sensitivity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hip bone loss and fracture Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hip bone loss and fracture in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
risperidone and perospirone Gene SetFrom GAD Gene-Disease Associations genes associated with the disease risperidone and perospirone in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
infectious risk and outcome in surgical intensive care patients Gene SetFrom GAD Gene-Disease Associations genes associated with the disease infectious risk and outcome in surgical intensive care patients in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cleft lip and palate Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cleft lip and palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
reduced muscle mrna levels and insulin resistance Gene SetFrom GAD Gene-Disease Associations genes associated with the disease reduced muscle mrna levels and insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hemostatic factors and hematological phenotypes Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hemostatic factors and hematological phenotypes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
reduced gene expression and lower plasma levels of beta2-glycoprotein i Gene SetFrom GAD Gene-Disease Associations genes associated with the disease reduced gene expression and lower plasma levels of beta2-glycoprotein i in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
menarche and menopause (age at onset) Gene SetFrom GAD Gene-Disease Associations genes associated with the disease menarche and menopause (age at onset) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multiple organ failure; sepsis; shock, septic; wounds and injuries Gene SetFrom GAD Gene-Disease Associations genes associated with the disease multiple organ failure; sepsis; shock, septic; wounds and injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
dna damage; head and neck neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease dna damage; head and neck neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, squamous cell; head and neck neoplasms; neoplasms, second primary; squamous cell carcinoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; head and neck neoplasms; neoplasms, second primary; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adult respiratory distress syndrome; respiratory distress syndrome, adult; sepsis; systemic infection; wounds and injuries Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adult respiratory distress syndrome; respiratory distress syndrome, adult; sepsis; systemic infection; wounds and injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adiposity and abdominal obesity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adiposity and abdominal obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
breast and carcinoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease breast and carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
tropical pancreatitis and type ii diabetes mellitus Gene SetFrom GAD Gene-Disease Associations genes associated with the disease tropical pancreatitis and type ii diabetes mellitus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
polymyositis and dermatomyositis. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease polymyositis and dermatomyositis. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
head and neck neoplasms; neoplasms, squamous cell Gene SetFrom GAD Gene-Disease Associations genes associated with the disease head and neck neoplasms; neoplasms, squamous cell in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |