CDK-mediated phosphorylation and removal of Cdc6

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Results for "CDK-mediated phosphorylation and removal of Cdc6": 1002 gene sets

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CDK-mediated phosphorylation and removal of Cdc6 Gene Set From Reactome Pathways 2014 proteins participating in the CDK-mediated phosphorylation and removal of Cdc6 pathway from the Reactome Pathways dataset.
CDK-mediated phosphorylation and removal of Cdc6 Gene Set From Reactome Pathways 2024 proteins participating in the CDK-mediated phosphorylation and removal of Cdc6 pathway from the Reactome Pathways 2024 dataset.
H19 Rb E2F1 and CDK beta catenin in colorectal cancer Gene Set From WikiPathways Pathways 2024 proteins participating in the H19 Rb E2F1 and CDK beta catenin in colorectal cancer pathway from the WikiPathways Pathways 2024 dataset.
MCM8-ORC2-CDC6 complex Gene Set From CORUM Protein Complexes proteins in the MCM8-ORC2-CDC6 complex protein complex from the CORUM Protein Complexes dataset.
cdc6 Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term cdc6 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
CDC6, C-terminal domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the CDC6, C-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Cell division protein Cdc6/18 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cell division protein Cdc6/18 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
BL9062 (CDC6) Gene Set From NURSA Protein Complexes proteins in the BL9062 (CDC6) protein complex recovered by IP-MS from the NURSA Protein Complexes dataset.
CDC6 Gene Set From Pathway Commons Protein-Protein Interactions interacting proteins for CDC6 from the Pathway Commons Protein-Protein Interactions dataset.
CDC6 association with the ORC:origin complex Gene Set From Reactome Pathways 2014 proteins participating in the CDC6 association with the ORC:origin complex pathway from the Reactome Pathways dataset.
CDT1 association with the CDC6:ORC:origin complex Gene Set From Reactome Pathways 2014 proteins participating in the CDT1 association with the CDC6:ORC:origin complex pathway from the Reactome Pathways dataset.
CDC6 Gene Set From LINCS L1000 CMAP CRISPR Knockout Consensus Signatures genes differentially expressed following the CDC6 gene perturbation from the LINCS L1000 CMAP CRISPR Knockout Consensus Signatures dataset.
CDC6 association with the ORC:origin complex Gene Set From Reactome Pathways 2024 proteins participating in the CDC6 association with the ORC:origin complex pathway from the Reactome Pathways 2024 dataset.
CDC6 Gene Set From CM4AI KOLF21J CRISPRi Gene Perturbation Atlas genes differentially expressed following the CDC6 gene perturbation from the CM4AI KOLF21J CRISPRi Gene Perturbation Atlas.
cdk regulation of dna replication Gene Set From Biocarta Pathways proteins participating in the cdk regulation of dna replication pathway from the Biocarta Pathways dataset.
CAK complex (Cdk-activating kinase complex) Gene Set From CORUM Protein Complexes proteins in the CAK complex (Cdk-activating kinase complex) protein complex from the CORUM Protein Complexes dataset.
CAK core complex (Cdk-activating kinase core complex) Gene Set From CORUM Protein Complexes proteins in the CAK core complex (Cdk-activating kinase core complex) protein complex from the CORUM Protein Complexes dataset.
cdk Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term cdk in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Inhibitor of CDK interacting with cyclin A1 Gene Set From 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.
Cdk-activating kinase assembly factor MAT1, centre Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cdk-activating kinase assembly factor MAT1, centre protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Cdk-activating kinase assembly factor MAT1/Tfb3 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cdk-activating kinase assembly factor MAT1/Tfb3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
cdk Gene Set From Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term cdk in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.
cyclin/CDK positive transcription elongation factor complex Gene Set From GO Cellular Component Annotations 2023 proteins localized to the cyclin/CDK positive transcription elongation factor complex cellular component from the curated GO Cellular Component Annotations 2023 dataset.
cdk/crk-inhibitor Gene Set From LINCS L1000 CMAP Chemical Perturbation Consensus Signatures genes differentially expressed following the cdk/crk-inhibitor small molecule perturbation from the LINCS L1000 CMAP Chemical Perturbation Consensus Signatures dataset.
cyclin/CDK positive transcription elongation factor complex Gene Set From GO Cellular Component Annotations 2025 proteins localized to the cyclin/CDK positive transcription elongation factor complex cellular component from the curated GO Cellular Component Annotations 2025 dataset.
cyclin/CDK positive transcription elongation factor complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the cyclin/CDK positive transcription elongation factor complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
cyclin/CDK positive transcription elongation factor complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the cyclin/CDK positive transcription elongation factor complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Pho85-Pho80 CDK-cyclin complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Pho85-Pho80 CDK-cyclin complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
CDK INHIBITOR SNS-032 Gene Set From DGIdb Drug Targets 2026 interacting proteins for the CDK INHIBITOR SNS-032 drug from theDGIdb Drug Targets 2026 dataset.
CDK INHIBITOR 4.35 Gene Set From DGIdb Drug Targets 2026 interacting proteins for the CDK INHIBITOR 4.35 drug from theDGIdb Drug Targets 2026 dataset.
CDK INHIBITOR AT7519 Gene Set From DGIdb Drug Targets 2026 interacting proteins for the CDK INHIBITOR AT7519 drug from theDGIdb Drug Targets 2026 dataset.
CDK/CRK INHIBITOR Gene Set From DGIdb Drug Targets 2026 interacting proteins for the CDK/CRK INHIBITOR drug from theDGIdb Drug Targets 2026 dataset.
removal Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term removal in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
removal of rna primer involved in mitotic dna replication Gene Set From GO Biological Process Annotations 2015 genes participating in the removal of rna primer involved in mitotic dna replication biological process from the curated GO Biological Process Annotations 2015 dataset.
trna 5'-leader removal Gene Set From GO Biological Process Annotations 2015 genes participating in the trna 5'-leader removal biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of removal of superoxide radicals Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of removal of superoxide radicals biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of protein modification by small protein conjugation or removal Gene Set From 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.
dna replication, removal of rna primer Gene Set From GO Biological Process Annotations 2015 genes participating in the dna replication, removal of rna primer biological process from the curated GO Biological Process Annotations 2015 dataset.
removal of superoxide radicals Gene Set From GO Biological Process Annotations 2015 genes participating in the removal of superoxide radicals biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of protein modification by small protein conjugation or removal Gene Set From 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.
regulation of protein modification by small protein conjugation or removal Gene Set From 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 modification by small protein removal Gene Set From 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 initiator methionine removal Gene Set From GO Biological Process Annotations 2015 genes participating in the protein initiator methionine removal biological process from the curated GO Biological Process Annotations 2015 dataset.
nucleotide-excision repair, dna damage removal Gene Set From GO Biological Process Annotations 2015 genes participating in the nucleotide-excision repair, dna damage removal biological process from the curated GO Biological Process Annotations 2015 dataset.
protein modification by small protein conjugation or removal Gene Set From 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.
glutamate removal from folates Gene Set From HumanCyc Pathways proteins participating in the glutamate removal from folates pathway from the HumanCyc Pathways dataset.
Removal of licensing factors from origins Gene Set From Reactome Pathways 2014 proteins participating in the Removal of licensing factors from origins pathway from the Reactome Pathways dataset.
Orc1 removal from chromatin Gene Set From Reactome Pathways 2014 proteins participating in the Orc1 removal from chromatin pathway from the Reactome Pathways dataset.
Base-free sugar-phosphate removal via the single-nucleotide replacement pathway Gene Set From Reactome Pathways 2014 proteins participating in the Base-free sugar-phosphate removal via the single-nucleotide replacement pathway pathway from the Reactome Pathways dataset.
Removal of aminoterminal propeptides from gamma-carboxylated proteins Gene Set From Reactome Pathways 2014 proteins participating in the Removal of aminoterminal propeptides from gamma-carboxylated proteins pathway from the Reactome Pathways dataset.
Removal of the Flap Intermediate Gene Set From Reactome Pathways 2014 proteins participating in the Removal of the Flap Intermediate pathway from the Reactome Pathways dataset.
Removal of the Flap Intermediate from the C-strand Gene Set From Reactome Pathways 2014 proteins participating in the Removal of the Flap Intermediate from the C-strand pathway from the Reactome Pathways dataset.
Removal of DNA patch containing abasic residue Gene Set From Reactome Pathways 2014 proteins participating in the Removal of DNA patch containing abasic residue pathway from the Reactome Pathways dataset.
tRNA 5'-leader removal Gene Set From GO Biological Process Annotations 2023 genes participating in the tRNA 5'-leader removal biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of removal of superoxide radicals Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of removal of superoxide radicals biological process from the curated GO Biological Process Annotations 2023 dataset.
removal of superoxide radicals Gene Set From GO Biological Process Annotations 2023 genes participating in the removal of superoxide radicals biological process from the curated GO Biological Process Annotations 2023 dataset.
base-excision repair, AP site formation via deaminated base removal Gene Set From GO Biological Process Annotations 2023 genes participating in the base-excision repair, AP site formation via deaminated base removal biological process from the curated GO Biological Process Annotations 2023 dataset.
DNA replication, removal of RNA primer Gene Set From GO Biological Process Annotations 2023 genes participating in the DNA replication, removal of RNA primer biological process from the curated GO Biological Process Annotations 2023 dataset.
protein initiator methionine removal involved in protein maturation Gene Set From 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 deglycation, methylglyoxal removal Gene Set From GO Biological Process Annotations 2023 genes participating in the protein deglycation, methylglyoxal removal biological process from the curated GO Biological Process Annotations 2023 dataset.
protein deglycation, glyoxal removal Gene Set From GO Biological Process Annotations 2023 genes participating in the protein deglycation, glyoxal removal biological process from the curated GO Biological Process Annotations 2023 dataset.
guanine deglycation, methylglyoxal removal Gene Set From GO Biological Process Annotations 2023 genes participating in the guanine deglycation, methylglyoxal removal biological process from the curated GO Biological Process Annotations 2023 dataset.
guanine deglycation, glyoxal removal Gene Set From GO Biological Process Annotations 2023 genes participating in the guanine deglycation, glyoxal removal biological process from the curated GO Biological Process Annotations 2023 dataset.
protein modification by small protein removal Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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.
protein initiator methionine removal Gene Set From GO Biological Process Annotations 2023 genes participating in the protein initiator methionine removal biological process from the curated GO Biological Process Annotations 2023 dataset.
Abasic sugar-phosphate removal via the single-nucleotide replacement pathway Gene Set From Reactome Pathways 2024 proteins participating in the Abasic sugar-phosphate removal via the single-nucleotide replacement pathway pathway from the Reactome Pathways 2024 dataset.
Orc1 removal from chromatin Gene Set From Reactome Pathways 2024 proteins participating in the Orc1 removal from chromatin pathway from the Reactome Pathways 2024 dataset.
Removal of aminoterminal propeptides from gamma-carboxylated proteins Gene Set From Reactome Pathways 2024 proteins participating in the Removal of aminoterminal propeptides from gamma-carboxylated proteins pathway from the Reactome Pathways 2024 dataset.
Removal of the Flap Intermediate Gene Set From Reactome Pathways 2024 proteins participating in the Removal of the Flap Intermediate pathway from the Reactome Pathways 2024 dataset.
Removal of the Flap Intermediate from the C-strand Gene Set From Reactome Pathways 2024 proteins participating in the Removal of the Flap Intermediate from the C-strand pathway from the Reactome Pathways 2024 dataset.
tRNA 5'-leader removal Gene Set From GO Biological Process Annotations 2025 genes participating in the tRNA 5'-leader removal biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of removal of superoxide radicals Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of removal of superoxide radicals biological process from the curated GO Biological Process Annotations 2025 dataset.
removal of superoxide radicals Gene Set From GO Biological Process Annotations 2025 genes participating in the removal of superoxide radicals biological process from the curated GO Biological Process Annotations 2025 dataset.
base-excision repair, AP site formation via deaminated base removal Gene Set From GO Biological Process Annotations 2025 genes participating in the base-excision repair, AP site formation via deaminated base removal biological process from the curated GO Biological Process Annotations 2025 dataset.
DNA replication, removal of RNA primer Gene Set From GO Biological Process Annotations 2025 genes participating in the DNA replication, removal of RNA primer biological process from the curated GO Biological Process Annotations 2025 dataset.
guanine deglycation, methylglyoxal removal Gene Set From GO Biological Process Annotations 2025 genes participating in the guanine deglycation, methylglyoxal removal biological process from the curated GO Biological Process Annotations 2025 dataset.
guanine deglycation, glyoxal removal Gene Set From GO Biological Process Annotations 2025 genes participating in the guanine deglycation, glyoxal removal biological process from the curated GO Biological Process Annotations 2025 dataset.
protein modification by small protein removal Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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.
atp-binding and phosphorylation-dependent chloride channel activity Gene Set From GO Molecular Function Annotations 2015 genes performing the atp-binding and phosphorylation-dependent chloride channel activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
NAD phosphorylation and dephosphorylation Gene Set From HumanCyc Pathways proteins participating in the NAD phosphorylation and dephosphorylation pathway from the HumanCyc Pathways dataset.
RNA Pol II CTD phosphorylation and interaction with CE Gene Set From Reactome Pathways 2014 proteins participating in the RNA Pol II CTD phosphorylation and interaction with CE pathway from the Reactome Pathways dataset.
Phosphorylation of CD3 and TCR zeta chains Gene Set From Reactome Pathways 2014 proteins participating in the Phosphorylation of CD3 and TCR zeta chains pathway from the Reactome Pathways dataset.
TAK1 activates NFkB by phosphorylation and activation of IKKs complex Gene Set From Reactome Pathways 2014 proteins participating in the TAK1 activates NFkB by phosphorylation and activation of IKKs complex pathway from the Reactome Pathways dataset.
Phosphorylation of CD3 and TCR zeta chains Gene Set From Reactome Pathways 2024 proteins participating in the Phosphorylation of CD3 and TCR zeta chains pathway from the Reactome Pathways 2024 dataset.
RNA Pol II CTD phosphorylation and interaction with CE Gene Set From Reactome Pathways 2024 proteins participating in the RNA Pol II CTD phosphorylation and interaction with CE pathway from the Reactome Pathways 2024 dataset.
RNA Pol II CTD phosphorylation and interaction with CE during HIV infection Gene Set From Reactome Pathways 2024 proteins participating in the RNA Pol II CTD phosphorylation and interaction with CE during HIV infection pathway from the Reactome Pathways 2024 dataset.
Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds Gene Set From Reactome Pathways 2014 proteins 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 Set From 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 Set From 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.
regulation of bad phosphorylation Gene Set From Biocarta Pathways proteins participating in the regulation of bad phosphorylation pathway from the Biocarta Pathways dataset.
pkc-catalyzed phosphorylation of inhibitory phosphoprotein of myosin phosphatase Gene Set From Biocarta Pathways proteins participating in the pkc-catalyzed phosphorylation of inhibitory phosphoprotein of myosin phosphatase pathway from the Biocarta Pathways dataset.
regulation of p27 phosphorylation during cell cycle progression Gene Set From Biocarta Pathways proteins participating in the regulation of p27 phosphorylation during cell cycle progression pathway from the Biocarta Pathways dataset.
multiple antiapoptotic pathways from igf-1r signaling lead to bad phosphorylation Gene Set From Biocarta Pathways proteins participating in the multiple antiapoptotic pathways from igf-1r signaling lead to bad phosphorylation pathway from the Biocarta Pathways dataset.
phosphorylation of mek1 by cdk5/p35 down regulates the map kinase pathway Gene Set From Biocarta Pathways proteins participating in the phosphorylation of mek1 by cdk5/p35 down regulates the map kinase pathway pathway from the Biocarta Pathways dataset.
Combined oxidative phosphorylation deficiency 9 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Combined oxidative phosphorylation deficiency 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Combined oxidative phosphorylation deficiency 8 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Combined oxidative phosphorylation deficiency 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Combined oxidative phosphorylation deficiency 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Combined oxidative phosphorylation deficiency 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Combined oxidative phosphorylation deficiency 7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Combined oxidative phosphorylation deficiency 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Combined oxidative phosphorylation deficiency 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Combined oxidative phosphorylation deficiency 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Combined oxidative phosphorylation deficiency 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Combined oxidative phosphorylation deficiency 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Combined oxidative phosphorylation deficiency 18 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Combined oxidative phosphorylation deficiency 18 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Combined oxidative phosphorylation deficiency 17 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Combined oxidative phosphorylation deficiency 17 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Combined oxidative phosphorylation deficiency 16 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Combined oxidative phosphorylation deficiency 16 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Combined oxidative phosphorylation deficiency 14 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Combined oxidative phosphorylation deficiency 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Combined oxidative phosphorylation deficiency 13 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Combined oxidative phosphorylation deficiency 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Combined oxidative phosphorylation deficiency 12 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Combined oxidative phosphorylation deficiency 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Combined oxidative phosphorylation deficiency 11 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Combined oxidative phosphorylation deficiency 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Combined oxidative phosphorylation deficiency 10 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Combined oxidative phosphorylation deficiency 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Combined oxidative phosphorylation deficiency 22 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Combined oxidative phosphorylation deficiency 22 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Combined oxidative phosphorylation deficiency 20 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Combined oxidative phosphorylation deficiency 20 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Combined oxidative phosphorylation deficiency 21 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Combined oxidative phosphorylation deficiency 21 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Combined oxidative phosphorylation deficiency 15 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Combined oxidative phosphorylation deficiency 15 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Combined Oxidative Phosphorylation Deficiency 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Combined Oxidative Phosphorylation Deficiency 3 from the curated CTD Gene-Disease Associations dataset.
Combined Oxidative Phosphorylation Deficiency 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Combined Oxidative Phosphorylation Deficiency 2 from the curated CTD Gene-Disease Associations dataset.
COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 7 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 7 from the curated CTD Gene-Disease Associations dataset.
COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 6 from the curated CTD Gene-Disease Associations dataset.
Combined Oxidative Phosphorylation Deficiency 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Combined Oxidative Phosphorylation Deficiency 1 from the curated CTD Gene-Disease Associations dataset.
Combined Oxidative Phosphorylation Deficiency 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Combined Oxidative Phosphorylation Deficiency 5 from the curated CTD Gene-Disease Associations dataset.
Combined Oxidative Phosphorylation Deficiency 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Combined Oxidative Phosphorylation Deficiency 4 from the curated CTD Gene-Disease Associations dataset.
phosphorylation Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term phosphorylation in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
i-kappab phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the i-kappab phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of tyrosine phosphorylation of stat1 protein Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of tyrosine phosphorylation of stat1 protein biological process from the curated GO Biological Process Annotations 2015 dataset.
pathway-restricted smad protein phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the pathway-restricted smad protein phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
histone h3-t6 phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the histone h3-t6 phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
histone-tyrosine phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the histone-tyrosine phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of oxidative phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of oxidative phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
histone-threonine phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the histone-threonine phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of tyrosine phosphorylation of stat protein Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of tyrosine phosphorylation of stat protein biological process from the curated GO Biological Process Annotations 2015 dataset.
peptidyl-serine phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the peptidyl-serine phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of tyrosine phosphorylation of stat5 protein Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of tyrosine phosphorylation of stat5 protein biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of tyrosine phosphorylation of stat protein Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of tyrosine phosphorylation of stat protein biological process from the curated GO Biological Process Annotations 2015 dataset.
nucleoside diphosphate phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the nucleoside diphosphate phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
peptidyl-threonine phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the peptidyl-threonine phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of translational initiation by eif2 alpha phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of translational initiation by eif2 alpha phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of i-kappab phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of i-kappab phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of peptidyl-serine phosphorylation of stat protein Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of peptidyl-serine phosphorylation of stat protein biological process from the curated GO Biological Process Annotations 2015 dataset.
jun phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the jun phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of histone phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of histone phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of pathway-restricted smad protein phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of pathway-restricted smad protein phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of protein phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of protein phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of tyrosine phosphorylation of stat3 protein Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of tyrosine phosphorylation of stat3 protein biological process from the curated GO Biological Process Annotations 2015 dataset.
phosphatidylinositol phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the phosphatidylinositol phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of phosphorylation of rna polymerase ii c-terminal domain serine 2 residues Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of phosphorylation of rna polymerase ii c-terminal domain serine 2 residues biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of oxidative phosphorylation uncoupler activity Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of oxidative phosphorylation uncoupler activity biological process from the curated GO Biological Process Annotations 2015 dataset.
dna damage induced protein phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the dna damage induced protein phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
histone-serine phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the histone-serine phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
cdp phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the cdp phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of peptidyl-serine phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of peptidyl-serine phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
dgdp phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the dgdp phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of tyrosine phosphorylation of stat6 protein Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of tyrosine phosphorylation of stat6 protein biological process from the curated GO Biological Process Annotations 2015 dataset.
serine phosphorylation of stat protein Gene Set From GO Biological Process Annotations 2015 genes participating in the serine phosphorylation of stat protein biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of eif2 alpha phosphorylation by heme Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of eif2 alpha phosphorylation by heme biological process from the curated GO Biological Process Annotations 2015 dataset.
carbohydrate phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the carbohydrate phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of tyrosine phosphorylation of stat6 protein Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of tyrosine phosphorylation of stat6 protein biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
nucleotide phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the nucleotide phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of pathway-restricted smad protein phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of pathway-restricted smad protein phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
serine phosphorylation of stat3 protein Gene Set From GO Biological Process Annotations 2015 genes participating in the serine phosphorylation of stat3 protein biological process from the curated GO Biological Process Annotations 2015 dataset.
histone h2a-t120 phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the histone h2a-t120 phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
histone h2a-s1 phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the histone h2a-s1 phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of tyrosine phosphorylation of stat4 protein Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of tyrosine phosphorylation of stat4 protein biological process from the curated GO Biological Process Annotations 2015 dataset.
histone phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the histone phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
tyrosine phosphorylation of stat2 protein Gene Set From GO Biological Process Annotations 2015 genes participating in the tyrosine phosphorylation of stat2 protein biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of histone phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of histone phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of protein kinase activity by regulation of protein phosphorylation Gene Set From 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 peptidyl-threonine phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of peptidyl-threonine phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of oxidative phosphorylation uncoupler activity Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of oxidative phosphorylation uncoupler activity biological process from the curated GO Biological Process Annotations 2015 dataset.
inositol phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the inositol phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
histone h2a-s139 phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the histone h2a-s139 phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
histone h3-t11 phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the histone h3-t11 phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of tyrosine phosphorylation of stat1 protein Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of tyrosine phosphorylation of stat1 protein biological process from the curated GO Biological Process Annotations 2015 dataset.
tyrosine phosphorylation of stat5 protein Gene Set From GO Biological Process Annotations 2015 genes participating in the tyrosine phosphorylation of stat5 protein biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of tyrosine phosphorylation of stat1 protein Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of tyrosine phosphorylation of stat1 protein biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of thioredoxin peroxidase activity by peptidyl-threonine phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of thioredoxin peroxidase activity by peptidyl-threonine phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of peptidyl-serine phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of peptidyl-serine phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
histone h3-s10 phosphorylation involved in chromosome condensation Gene Set From GO Biological Process Annotations 2015 genes participating in the histone h3-s10 phosphorylation involved in chromosome condensation biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of protein phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of protein phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
histone h3-s28 phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the histone h3-s28 phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
cmp phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the cmp phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
histone h2a phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the histone h2a phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
oxidative phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the oxidative phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
damp phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the damp phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
histone h3-t3 phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the histone h3-t3 phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of phosphorylation of rna polymerase ii c-terminal domain Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of phosphorylation of rna polymerase ii c-terminal domain biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of peptidyl-serine phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of peptidyl-serine phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
signal transduction by phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the signal transduction by phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of tyrosine phosphorylation of stat4 protein Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of tyrosine phosphorylation of stat4 protein biological process from the curated GO Biological Process Annotations 2015 dataset.
common-partner smad protein phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the common-partner smad protein phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
amp phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the amp phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of tyrosine phosphorylation of stat protein Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of tyrosine phosphorylation of stat protein biological process from the curated GO Biological Process Annotations 2015 dataset.
histone h3-y41 phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the histone h3-y41 phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
histone h3-s10 phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the histone h3-s10 phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
inhibitory g-protein coupled receptor phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the inhibitory g-protein coupled receptor phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
tyrosine phosphorylation of stat1 protein Gene Set From GO Biological Process Annotations 2015 genes participating in the tyrosine phosphorylation of stat1 protein biological process from the curated GO Biological Process Annotations 2015 dataset.
dcmp phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the dcmp phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of eif2 alpha phosphorylation by dsrna Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of eif2 alpha phosphorylation by dsrna biological process from the curated GO Biological Process Annotations 2015 dataset.
tdp phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the tdp phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
tyrosine phosphorylation of stat3 protein Gene Set From GO Biological Process Annotations 2015 genes participating in the tyrosine phosphorylation of stat3 protein biological process from the curated GO Biological Process Annotations 2015 dataset.
tyrosine phosphorylation of stat protein Gene Set From GO Biological Process Annotations 2015 genes participating in the tyrosine phosphorylation of stat protein biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of peptidyl-tyrosine phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of peptidyl-tyrosine phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
nucleoside monophosphate phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the nucleoside monophosphate phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
lipid phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the lipid phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of peptidyl-tyrosine phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of peptidyl-tyrosine phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of tyrosine phosphorylation of stat3 protein Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of tyrosine phosphorylation of stat3 protein biological process from the curated GO Biological Process Annotations 2015 dataset.
dadp phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the dadp phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
udp phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the udp phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of actin phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of actin phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
gdp phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the gdp phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of phosphorylation of rna polymerase ii c-terminal domain serine 2 residues Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of phosphorylation of rna polymerase ii c-terminal domain serine 2 residues biological process from the curated GO Biological Process Annotations 2015 dataset.
phosphorylation of rna polymerase ii c-terminal domain Gene Set From GO Biological Process Annotations 2015 genes participating in the phosphorylation of rna polymerase ii c-terminal domain biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
protein phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the protein phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of tyrosine phosphorylation of stat6 protein Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of tyrosine phosphorylation of stat6 protein biological process from the curated GO Biological Process Annotations 2015 dataset.
histone h3-t3 phosphorylation involved in chromosome passenger complex localization to kinetochore Gene Set From GO Biological Process Annotations 2015 genes participating in the histone h3-t3 phosphorylation involved in chromosome passenger complex localization to kinetochore biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of oxidative phosphorylation uncoupler activity Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of oxidative phosphorylation uncoupler activity biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of peptidyl-threonine phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of peptidyl-threonine phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of tyrosine phosphorylation of stat5 protein Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of tyrosine phosphorylation of stat5 protein biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of oxidative phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of oxidative phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of phosphorylation of rna polymerase ii c-terminal domain Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of phosphorylation of rna polymerase ii c-terminal domain biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of histone phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of histone phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of pathway-restricted smad protein phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of pathway-restricted smad protein phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of i-kappab phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of i-kappab phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of peptidyl-tyrosine phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of peptidyl-tyrosine phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of tyrosine phosphorylation of stat5 protein Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of tyrosine phosphorylation of stat5 protein biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of peptidyl-threonine phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of peptidyl-threonine phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of peptidyl-serine phosphorylation of stat protein Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of peptidyl-serine phosphorylation of stat protein biological process from the curated GO Biological Process Annotations 2015 dataset.
adp phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the adp phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
dcdp phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the dcdp phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of tyrosine phosphorylation of stat3 protein Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of tyrosine phosphorylation of stat3 protein biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of protein phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of protein phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
peptidyl-tyrosine phosphorylation Gene Set From GO Biological Process Annotations 2015 genes participating in the peptidyl-tyrosine phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset.
oxidative phosphorylation uncoupler activity Gene Set From GO Molecular Function Annotations 2015 genes performing the oxidative phosphorylation uncoupler activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
pyrimidine deoxyribonucleotide phosphorylation Gene Set From HumanCyc Pathways proteins participating in the pyrimidine deoxyribonucleotide phosphorylation pathway from the HumanCyc Pathways dataset.
CMP phosphorylation Gene Set From HumanCyc Pathways proteins participating in the CMP phosphorylation pathway from the HumanCyc Pathways dataset.
Dual specificity tyrosine-phosphorylation-regulated kinase 1A Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Dual specificity tyrosine-phosphorylation-regulated kinase 1A protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Neuromodulin, palmitoylation/phosphorylation site Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Neuromodulin, palmitoylation/phosphorylation site protein domain from the InterPro Predicted Protein Domain Annotations dataset.
P-type ATPase, phosphorylation site Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the P-type ATPase, phosphorylation site protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Kinase phosphorylation domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Kinase phosphorylation domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Synapsin, phosphorylation site Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Synapsin, phosphorylation site protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Rapamycin-insensitive companion of mTOR, phosphorylation-site Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Rapamycin-insensitive companion of mTOR, phosphorylation-site protein domain from the InterPro Predicted Protein Domain Annotations dataset.
oxidative phosphorylation Gene Set From KEGG Pathways proteins participating in the oxidative phosphorylation pathway from the KEGG Pathways dataset.
abnormal oxidative phosphorylation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal oxidative phosphorylation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
combined oxidative phosphorylation deficiency 20 Gene Set From OMIM Gene-Disease Associations genes associated with the combined oxidative phosphorylation deficiency 20 phenotype from the curated OMIM Gene-Disease Associations dataset.
?combined oxidative phosphorylation deficiency 19 Gene Set From OMIM Gene-Disease Associations genes associated with the ?combined oxidative phosphorylation deficiency 19 phenotype from the curated OMIM Gene-Disease Associations dataset.
?combined oxidative phosphorylation deficiency 16 Gene Set From OMIM Gene-Disease Associations genes associated with the ?combined oxidative phosphorylation deficiency 16 phenotype from the curated OMIM Gene-Disease Associations dataset.
combined oxidative phosphorylation deficiency 18 Gene Set From OMIM Gene-Disease Associations genes associated with the combined oxidative phosphorylation deficiency 18 phenotype from the curated OMIM Gene-Disease Associations dataset.
combined oxidative phosphorylation deficiency 17 Gene Set From OMIM Gene-Disease Associations genes associated with the combined oxidative phosphorylation deficiency 17 phenotype from the curated OMIM Gene-Disease Associations dataset.
combined oxidative phosphorylation deficiency 15 Gene Set From OMIM Gene-Disease Associations genes associated with the combined oxidative phosphorylation deficiency 15 phenotype from the curated OMIM Gene-Disease Associations dataset.
combined oxidative phosphorylation deficiency 14 Gene Set From OMIM Gene-Disease Associations genes associated with the combined oxidative phosphorylation deficiency 14 phenotype from the curated OMIM Gene-Disease Associations dataset.
combined oxidative phosphorylation deficiency 13 Gene Set From OMIM Gene-Disease Associations genes associated with the combined oxidative phosphorylation deficiency 13 phenotype from the curated OMIM Gene-Disease Associations dataset.
combined oxidative phosphorylation deficiency 12 Gene Set From OMIM Gene-Disease Associations genes associated with the combined oxidative phosphorylation deficiency 12 phenotype from the curated OMIM Gene-Disease Associations dataset.
combined oxidative phosphorylation deficiency 11 Gene Set From OMIM Gene-Disease Associations genes associated with the combined oxidative phosphorylation deficiency 11 phenotype from the curated OMIM Gene-Disease Associations dataset.
combined oxidative phosphorylation deficiency 10 Gene Set From OMIM Gene-Disease Associations genes associated with the combined oxidative phosphorylation deficiency 10 phenotype from the curated OMIM Gene-Disease Associations dataset.
combined oxidative phosphorylation deficiency 9 Gene Set From OMIM Gene-Disease Associations genes associated with the combined oxidative phosphorylation deficiency 9 phenotype from the curated OMIM Gene-Disease Associations dataset.
combined oxidative phosphorylation deficiency 8 Gene Set From OMIM Gene-Disease Associations genes associated with the combined oxidative phosphorylation deficiency 8 phenotype from the curated OMIM Gene-Disease Associations dataset.
combined oxidative phosphorylation deficiency 3 Gene Set From OMIM Gene-Disease Associations genes associated with the combined oxidative phosphorylation deficiency 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
combined oxidative phosphorylation deficiency 2 Gene Set From OMIM Gene-Disease Associations genes associated with the combined oxidative phosphorylation deficiency 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
combined oxidative phosphorylation deficiency 1 Gene Set From OMIM Gene-Disease Associations genes associated with the combined oxidative phosphorylation deficiency 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
combined oxidative phosphorylation deficiency 7 Gene Set From OMIM Gene-Disease Associations genes associated with the combined oxidative phosphorylation deficiency 7 phenotype from the curated OMIM Gene-Disease Associations dataset.
combined oxidative phosphorylation deficiency 6 Gene Set From OMIM Gene-Disease Associations genes associated with the combined oxidative phosphorylation deficiency 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
combined oxidative phosphorylation deficiency 5 Gene Set From OMIM Gene-Disease Associations genes associated with the combined oxidative phosphorylation deficiency 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
combined oxidative phosphorylation deficiency 4 Gene Set From OMIM Gene-Disease Associations genes associated with the combined oxidative phosphorylation deficiency 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
?combined oxidative phosphorylation deficiency 21 Gene Set From OMIM Gene-Disease Associations genes associated with the ?combined oxidative phosphorylation deficiency 21 phenotype from the curated OMIM Gene-Disease Associations dataset.
?combined oxidative phosphorylation deficiency 22 Gene Set From OMIM Gene-Disease Associations genes associated with the ?combined oxidative phosphorylation deficiency 22 phenotype from the curated OMIM Gene-Disease Associations dataset.
SMAD2/3 Phosphorylation Motif Mutants in Cancer Gene Set From Reactome Pathways 2014 proteins participating in the SMAD2/3 Phosphorylation Motif Mutants in Cancer pathway from the Reactome Pathways dataset.
CREB phosphorylation through the activation of CaMKII Gene Set From Reactome Pathways 2014 proteins participating in the CREB phosphorylation through the activation of CaMKII pathway from the Reactome Pathways dataset.
CREB phosphorylation Gene Set From Reactome Pathways 2014 proteins participating in the CREB phosphorylation pathway from the Reactome Pathways dataset.
Phosphorylation of the APC/C Gene Set From Reactome Pathways 2014 proteins participating in the Phosphorylation of the APC/C pathway from the Reactome Pathways dataset.
Phosphorylation of proteins involved in the G2/M transition by Cyclin A:Cdc2 complexes Gene Set From Reactome Pathways 2014 proteins participating in the Phosphorylation of proteins involved in the G2/M transition by Cyclin A:Cdc2 complexes pathway from the Reactome Pathways dataset.
Activation of PPARGC1A (PGC-1alpha) by phosphorylation Gene Set From Reactome Pathways 2014 proteins participating in the Activation of PPARGC1A (PGC-1alpha) by phosphorylation pathway from the Reactome Pathways dataset.
Beta-catenin phosphorylation cascade Gene Set From Reactome Pathways 2014 proteins participating in the Beta-catenin phosphorylation cascade pathway from the Reactome Pathways dataset.
CREB phosphorylation through the activation of Adenylate Cyclase Gene Set From Reactome Pathways 2014 proteins participating in the CREB phosphorylation through the activation of Adenylate Cyclase pathway from the Reactome Pathways dataset.
Phosphorylation of proteins involved in G1/S transition by active Cyclin E:Cdk2 complexes Gene Set From Reactome Pathways 2014 proteins participating in the Phosphorylation of proteins involved in G1/S transition by active Cyclin E:Cdk2 complexes pathway from the Reactome Pathways dataset.
Phosphorylation of Emi1 Gene Set From Reactome Pathways 2014 proteins participating in the Phosphorylation of Emi1 pathway from the Reactome Pathways dataset.
CREB phosphorylation through the activation of CaMKK Gene Set From Reactome Pathways 2014 proteins participating in the CREB phosphorylation through the activation of CaMKK pathway from the Reactome Pathways dataset.
phosphorylation site mutants of CTNNB1 are not targeted to the proteasome by the destruction complex Gene Set From Reactome Pathways 2014 proteins participating in the phosphorylation site mutants of CTNNB1 are not targeted to the proteasome by the destruction complex pathway from the Reactome Pathways dataset.
CREB phosphorylation through the activation of Ras Gene Set From Reactome Pathways 2014 proteins participating in the CREB phosphorylation through the activation of Ras pathway from the Reactome Pathways dataset.
Oxidative phosphorylation(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Oxidative phosphorylation(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Oxidative phosphorylation(Homo sapiens) Gene Set From WikiPathways Pathways 2014 proteins participating in the Oxidative phosphorylation(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset.
Combined Oxidative Phosphorylation Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Combined Oxidative Phosphorylation Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Oxidative Phosphorylation Deficiencies Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Oxidative Phosphorylation Deficiencies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Combined Oxidative Phosphorylation Deficiency Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Combined Oxidative Phosphorylation Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
positive regulation of protein phosphorylation Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of protein phosphorylation biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of peptidyl-threonine phosphorylation Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of peptidyl-threonine phosphorylation biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of peptidyl-serine phosphorylation Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of peptidyl-serine phosphorylation biological process from the curated GO Biological Process Annotations 2023 dataset.
tyrosine phosphorylation of STAT protein Gene Set From GO Biological Process Annotations 2023 genes participating in the tyrosine phosphorylation of STAT protein biological process from the curated GO Biological Process Annotations 2023 dataset.
protein phosphorylation Gene Set From GO Biological Process Annotations 2023 genes participating in the protein phosphorylation biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of peptidyl-tyrosine phosphorylation Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of peptidyl-tyrosine phosphorylation biological process from the curated GO Biological Process Annotations 2023 dataset.
I-kappaB phosphorylation Gene Set From GO Biological Process Annotations 2023 genes participating in the I-kappaB phosphorylation biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of protein phosphorylation Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of protein phosphorylation biological process from the curated GO Biological Process Annotations 2023 dataset.
phosphorylation Gene Set From GO Biological Process Annotations 2023 genes participating in the phosphorylation biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of pathway-restricted SMAD protein phosphorylation Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of pathway-restricted SMAD protein phosphorylation biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of phosphorylation Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of phosphorylation biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of tyrosine phosphorylation of STAT protein Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of tyrosine phosphorylation of STAT protein biological process from the curated GO Biological Process Annotations 2023 dataset.
peptidyl-threonine phosphorylation Gene Set From GO Biological Process Annotations 2023 genes participating in the peptidyl-threonine phosphorylation biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of peptidyl-threonine phosphorylation Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of peptidyl-threonine phosphorylation biological process from the curated GO Biological Process Annotations 2023 dataset.
peptidyl-serine phosphorylation Gene Set From GO Biological Process Annotations 2023 genes participating in the peptidyl-serine phosphorylation biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of phosphorylation Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of phosphorylation biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of protein phosphorylation Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of protein phosphorylation biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of peptidyl-serine phosphorylation Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of peptidyl-serine phosphorylation biological process from the curated GO Biological Process Annotations 2023 dataset.
pathway-restricted SMAD protein phosphorylation Gene Set From GO Biological Process Annotations 2023 genes participating in the pathway-restricted SMAD protein phosphorylation biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of pathway-restricted SMAD protein phosphorylation Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of pathway-restricted SMAD protein phosphorylation biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of endoplasmic reticulum stress-induced eIF2 alpha phosphorylation Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of endoplasmic reticulum stress-induced eIF2 alpha phosphorylation biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of oxidative phosphorylation Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of oxidative phosphorylation biological process from the curated GO Biological Process Annotations 2023 dataset.
peptidyl-tyrosine phosphorylation Gene Set From GO Biological Process Annotations 2023 genes participating in the peptidyl-tyrosine phosphorylation biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of tyrosine phosphorylation of STAT protein Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of tyrosine phosphorylation of STAT protein biological process from the curated GO Biological Process Annotations 2023 dataset.
oxidative phosphorylation Gene Set From GO Biological Process Annotations 2023 genes participating in the oxidative phosphorylation biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of oxidative phosphorylation Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of oxidative phosphorylation biological process from the curated GO Biological Process Annotations 2023 dataset.
lipid phosphorylation Gene Set From GO Biological Process Annotations 2023 genes participating in the lipid phosphorylation biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of peptidyl-tyrosine phosphorylation Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of peptidyl-tyrosine phosphorylation biological process from the curated GO Biological Process Annotations 2023 dataset.
common-partner SMAD protein phosphorylation Gene Set From GO Biological Process Annotations 2023 genes participating in the common-partner SMAD protein phosphorylation biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of I-kappaB phosphorylation Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of I-kappaB phosphorylation biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of peptidyl-serine phosphorylation of STAT protein Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of peptidyl-serine phosphorylation of STAT protein biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of phosphorylation Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of phosphorylation biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of protein kinase activity by regulation of protein phosphorylation Gene Set From 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.
regulation of eIF2 alpha phosphorylation by dsRNA Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of eIF2 alpha phosphorylation by dsRNA biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of pathway-restricted SMAD protein phosphorylation Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of pathway-restricted SMAD protein phosphorylation biological process from the curated GO Biological Process Annotations 2023 dataset.
carbohydrate phosphorylation Gene Set From GO Biological Process Annotations 2023 genes participating in the carbohydrate phosphorylation biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of peptidyl-tyrosine phosphorylation Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of peptidyl-tyrosine phosphorylation biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of peptidyl-serine phosphorylation Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of peptidyl-serine phosphorylation biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of peptidyl-serine phosphorylation of STAT protein Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of peptidyl-serine phosphorylation of STAT protein biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of tyrosine phosphorylation of STAT protein Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of tyrosine phosphorylation of STAT protein biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of oxidative phosphorylation Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of oxidative phosphorylation biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of oxidative phosphorylation uncoupler activity Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of oxidative phosphorylation uncoupler activity biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of inhibitory G protein-coupled receptor phosphorylation Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of inhibitory G protein-coupled receptor phosphorylation biological process from the curated GO Biological Process Annotations 2023 dataset.
JUN phosphorylation Gene Set From GO Biological Process Annotations 2023 genes participating in the JUN phosphorylation biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of I-kappaB phosphorylation Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of I-kappaB phosphorylation biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of oxidative phosphorylation uncoupler activity Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of oxidative phosphorylation uncoupler activity biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of actin phosphorylation Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of actin phosphorylation biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of thioredoxin peroxidase activity by peptidyl-threonine phosphorylation Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of thioredoxin peroxidase activity by peptidyl-threonine phosphorylation biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of translational initiation by eIF2 alpha phosphorylation Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of translational initiation by eIF2 alpha phosphorylation biological process from the curated GO Biological Process Annotations 2023 dataset.
eiF2alpha phosphorylation in response to endoplasmic reticulum stress Gene Set From GO Biological Process Annotations 2023 genes participating in the eiF2alpha phosphorylation in response to endoplasmic reticulum stress biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of endoplasmic reticulum stress-induced eIF2 alpha phosphorylation Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of endoplasmic reticulum stress-induced eIF2 alpha phosphorylation biological process from the curated GO Biological Process Annotations 2023 dataset.
serine phosphorylation of STAT protein Gene Set From GO Biological Process Annotations 2023 genes participating in the serine phosphorylation of STAT protein biological process from the curated GO Biological Process Annotations 2023 dataset.
AMP phosphorylation Gene Set From GO Biological Process Annotations 2023 genes participating in the AMP phosphorylation biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of peptidyl-threonine phosphorylation Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of peptidyl-threonine phosphorylation biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of I-kappaB phosphorylation Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of I-kappaB phosphorylation biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of peptidyl-serine phosphorylation of STAT protein Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of peptidyl-serine phosphorylation of STAT protein biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of oxidative phosphorylation uncoupler activity Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of oxidative phosphorylation uncoupler activity biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of inhibitory G protein-coupled receptor phosphorylation Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of inhibitory G protein-coupled receptor phosphorylation biological process from the curated GO Biological Process Annotations 2023 dataset.
peptidyl-aspartic acid phosphorylation Gene Set From GO Biological Process Annotations 2023 genes participating in the peptidyl-aspartic acid phosphorylation biological process from the curated GO Biological Process Annotations 2023 dataset.
nucleoside monophosphate phosphorylation Gene Set From GO Biological Process Annotations 2023 genes participating in the nucleoside monophosphate phosphorylation biological process from the curated GO Biological Process Annotations 2023 dataset.
phosphorylation-dependent protein binding Gene Set From GO Molecular Function Annotations 2023 genes performing the phosphorylation-dependent protein binding molecular function from the curated GO Molecular Function Annotations 2023 dataset.
abnormal oxidative phosphorylation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal oxidative phosphorylation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Oxidative phosphorylation Gene Set From WikiPathways Pathways 2024 proteins participating in the Oxidative phosphorylation pathway from the WikiPathways Pathways 2024 dataset.
Activation of PPARGC1A (PGC-1alpha) by phosphorylation Gene Set From Reactome Pathways 2024 proteins participating in the Activation of PPARGC1A (PGC-1alpha) by phosphorylation pathway from the Reactome Pathways 2024 dataset.
Beta-catenin phosphorylation cascade Gene Set From Reactome Pathways 2024 proteins participating in the Beta-catenin phosphorylation cascade pathway from the Reactome Pathways 2024 dataset.
CREB phosphorylation Gene Set From Reactome Pathways 2024 proteins participating in the CREB phosphorylation pathway from the Reactome Pathways 2024 dataset.
CREB1 phosphorylation through the activation of Adenylate Cyclase Gene Set From Reactome Pathways 2024 proteins participating in the CREB1 phosphorylation through the activation of Adenylate Cyclase pathway from the Reactome Pathways 2024 dataset.
CREB1 phosphorylation through the activation of CaMKII/CaMKK/CaMKIV cascasde Gene Set From Reactome Pathways 2024 proteins participating in the CREB1 phosphorylation through the activation of CaMKII/CaMKK/CaMKIV cascasde pathway from the Reactome Pathways 2024 dataset.
Loss of phosphorylation of MECP2 at T308 Gene Set From Reactome Pathways 2024 proteins participating in the Loss of phosphorylation of MECP2 at T308 pathway from the Reactome Pathways 2024 dataset.
Phosphorylation of Emi1 Gene Set From Reactome Pathways 2024 proteins participating in the Phosphorylation of Emi1 pathway from the Reactome Pathways 2024 dataset.
Phosphorylation of proteins involved in G1/S transition by active Cyclin E:Cdk2 complexes Gene Set From Reactome Pathways 2024 proteins participating in the Phosphorylation of proteins involved in G1/S transition by active Cyclin E:Cdk2 complexes pathway from the Reactome Pathways 2024 dataset.
Phosphorylation of proteins involved in the G2/M transition by Cyclin A:Cdc2 complexes Gene Set From Reactome Pathways 2024 proteins participating in the Phosphorylation of proteins involved in the G2/M transition by Cyclin A:Cdc2 complexes pathway from the Reactome Pathways 2024 dataset.
Phosphorylation of the APC/C Gene Set From Reactome Pathways 2024 proteins participating in the Phosphorylation of the APC/C pathway from the Reactome Pathways 2024 dataset.
Post-translational protein phosphorylation Gene Set From Reactome Pathways 2024 proteins participating in the Post-translational protein phosphorylation pathway from the Reactome Pathways 2024 dataset.
Regulation of TP53 Activity through Phosphorylation Gene Set From Reactome Pathways 2024 proteins participating in the Regulation of TP53 Activity through Phosphorylation pathway from the Reactome Pathways 2024 dataset.
SMAD2/3 Phosphorylation Motif Mutants in Cancer Gene Set From Reactome Pathways 2024 proteins participating in the SMAD2/3 Phosphorylation Motif Mutants in Cancer pathway from the Reactome Pathways 2024 dataset.
positive regulation of protein phosphorylation Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of protein phosphorylation biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of peptidyl-threonine phosphorylation Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of peptidyl-threonine phosphorylation biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of peptidyl-serine phosphorylation Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of peptidyl-serine phosphorylation biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of oxidative phosphorylation Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of oxidative phosphorylation biological process from the curated GO Biological Process Annotations 2025 dataset.
tyrosine phosphorylation of STAT protein Gene Set From GO Biological Process Annotations 2025 genes participating in the tyrosine phosphorylation of STAT protein biological process from the curated GO Biological Process Annotations 2025 dataset.
protein phosphorylation Gene Set From GO Biological Process Annotations 2025 genes participating in the protein phosphorylation biological process from the curated GO Biological Process Annotations 2025 dataset.
I-kappaB phosphorylation Gene Set From GO Biological Process Annotations 2025 genes participating in the I-kappaB phosphorylation biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of protein phosphorylation Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of protein phosphorylation biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of phosphorylation Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of phosphorylation biological process from the curated GO Biological Process Annotations 2025 dataset.
peptidyl-threonine phosphorylation Gene Set From GO Biological Process Annotations 2025 genes participating in the peptidyl-threonine phosphorylation biological process from the curated GO Biological Process Annotations 2025 dataset.
peptidyl-serine phosphorylation Gene Set From GO Biological Process Annotations 2025 genes participating in the peptidyl-serine phosphorylation biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of phosphorylation Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of phosphorylation biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of protein phosphorylation Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of protein phosphorylation biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of peptidyl-tyrosine phosphorylation Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of peptidyl-tyrosine phosphorylation biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of tyrosine phosphorylation of STAT protein Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of tyrosine phosphorylation of STAT protein biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of oxidative phosphorylation Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of oxidative phosphorylation biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of tyrosine phosphorylation of STAT protein Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of tyrosine phosphorylation of STAT protein biological process from the curated GO Biological Process Annotations 2025 dataset.
oxidative phosphorylation Gene Set From GO Biological Process Annotations 2025 genes participating in the oxidative phosphorylation biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of oxidative phosphorylation Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of oxidative phosphorylation biological process from the curated GO Biological Process Annotations 2025 dataset.
lipid phosphorylation Gene Set From GO Biological Process Annotations 2025 genes participating in the lipid phosphorylation biological process from the curated GO Biological Process Annotations 2025 dataset.
phosphorylation Gene Set From GO Biological Process Annotations 2025 genes participating in the phosphorylation biological process from the curated GO Biological Process Annotations 2025 dataset.
peptidyl-tyrosine phosphorylation Gene Set From GO Biological Process Annotations 2025 genes participating in the peptidyl-tyrosine phosphorylation biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of peptidyl-tyrosine phosphorylation Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of peptidyl-tyrosine phosphorylation biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of peptidyl-serine phosphorylation of STAT protein Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of peptidyl-serine phosphorylation of STAT protein biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of phosphorylation Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of phosphorylation biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of protein kinase activity by regulation of protein phosphorylation Gene Set From 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.
regulation of eIF2 alpha phosphorylation by dsRNA Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of eIF2 alpha phosphorylation by dsRNA biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of peptidyl-serine phosphorylation Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of peptidyl-serine phosphorylation biological process from the curated GO Biological Process Annotations 2025 dataset.
carbohydrate phosphorylation Gene Set From GO Biological Process Annotations 2025 genes participating in the carbohydrate phosphorylation biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of peptidyl-serine phosphorylation of STAT protein Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of peptidyl-serine phosphorylation of STAT protein biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of oxidative phosphorylation uncoupler activity Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of oxidative phosphorylation uncoupler activity biological process from the curated GO Biological Process Annotations 2025 dataset.
JUN phosphorylation Gene Set From GO Biological Process Annotations 2025 genes participating in the JUN phosphorylation biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of peptidyl-threonine phosphorylation Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of peptidyl-threonine phosphorylation biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of peptidyl-tyrosine phosphorylation Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of peptidyl-tyrosine phosphorylation biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of endoplasmic reticulum stress-induced eIF2 alpha phosphorylation Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of endoplasmic reticulum stress-induced eIF2 alpha phosphorylation biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of thioredoxin peroxidase activity by peptidyl-threonine phosphorylation Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of thioredoxin peroxidase activity by peptidyl-threonine phosphorylation biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of tyrosine phosphorylation of STAT protein Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of tyrosine phosphorylation of STAT protein biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of I-kappaB phosphorylation Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of I-kappaB phosphorylation biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of peptidyl-serine phosphorylation Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of peptidyl-serine phosphorylation biological process from the curated GO Biological Process Annotations 2025 dataset.
eiF2alpha phosphorylation in response to endoplasmic reticulum stress Gene Set From GO Biological Process Annotations 2025 genes participating in the eiF2alpha phosphorylation in response to endoplasmic reticulum stress biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of endoplasmic reticulum stress-induced eIF2 alpha phosphorylation Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of endoplasmic reticulum stress-induced eIF2 alpha phosphorylation biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of translational initiation by eIF2 alpha phosphorylation Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of translational initiation by eIF2 alpha phosphorylation biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of peptidyl-threonine phosphorylation Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of peptidyl-threonine phosphorylation biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of peptidyl-serine phosphorylation of STAT protein Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of peptidyl-serine phosphorylation of STAT protein biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of I-kappaB phosphorylation Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of I-kappaB phosphorylation biological process from the curated GO Biological Process Annotations 2025 dataset.
phosphorylation-dependent protein binding Gene Set From GO Molecular Function Annotations 2025 genes performing the phosphorylation-dependent protein binding molecular function from the curated GO Molecular Function Annotations 2025 dataset.
Combined oxidative phosphorylation deficiency 12 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Combined oxidative phosphorylation deficiency 12 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Combined oxidative phosphorylation deficiency Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Combined oxidative phosphorylation deficiency from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Combined oxidative phosphorylation deficiency 1 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Combined oxidative phosphorylation deficiency 1 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Combined oxidative phosphorylation deficiency 12 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Combined oxidative phosphorylation deficiency 12 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Combined oxidative phosphorylation deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Combined oxidative phosphorylation deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Combined oxidative phosphorylation deficiency 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Combined oxidative phosphorylation deficiency 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Combined oxidative phosphorylation deficiency 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Combined oxidative phosphorylation deficiency 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Combined oxidative phosphorylation deficiency 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Combined oxidative phosphorylation deficiency 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Combined oxidative phosphorylation deficiency 52 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Combined oxidative phosphorylation deficiency 52 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Combined oxidative phosphorylation deficiency 39 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Combined oxidative phosphorylation deficiency 39 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Combined oxidative phosphorylation deficiency 6 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Combined oxidative phosphorylation deficiency 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Combined oxidative phosphorylation deficiency 32 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Combined oxidative phosphorylation deficiency 32 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Combined oxidative phosphorylation deficiency 21 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Combined oxidative phosphorylation deficiency 21 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Combined oxidative phosphorylation deficiency 54 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Combined oxidative phosphorylation deficiency 54 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Combined oxidative phosphorylation deficiency 30 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Combined oxidative phosphorylation deficiency 30 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Combined oxidative phosphorylation deficiency 10 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Combined oxidative phosphorylation deficiency 10 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Combined oxidative phosphorylation deficiency 24 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Combined oxidative phosphorylation deficiency 24 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Combined oxidative phosphorylation deficiency 31 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Combined oxidative phosphorylation deficiency 31 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Combined oxidative phosphorylation deficiency 29 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Combined oxidative phosphorylation deficiency 29 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Combined oxidative phosphorylation deficiency 34 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Combined oxidative phosphorylation deficiency 34 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Combined oxidative phosphorylation deficiency 49 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Combined oxidative phosphorylation deficiency 49 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Combined oxidative phosphorylation deficiency 43 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Combined oxidative phosphorylation deficiency 43 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Combined oxidative phosphorylation deficiency 19 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Combined oxidative phosphorylation deficiency 19 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Combined oxidative phosphorylation deficiency 9 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Combined oxidative phosphorylation deficiency 9 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Combined oxidative phosphorylation deficiency 7 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Combined oxidative phosphorylation deficiency 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Combined oxidative phosphorylation deficiency 20 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Combined oxidative phosphorylation deficiency 20 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Combined oxidative phosphorylation deficiency 18 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Combined oxidative phosphorylation deficiency 18 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Combined oxidative phosphorylation deficiency 22 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Combined oxidative phosphorylation deficiency 22 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Combined oxidative phosphorylation deficiency 23 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Combined oxidative phosphorylation deficiency 23 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Combined oxidative phosphorylation deficiency 35 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Combined oxidative phosphorylation deficiency 35 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Combined oxidative phosphorylation deficiency 13 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Combined oxidative phosphorylation deficiency 13 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Combined oxidative phosphorylation deficiency 27 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Combined oxidative phosphorylation deficiency 27 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Combined oxidative phosphorylation deficiency 26 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Combined oxidative phosphorylation deficiency 26 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Combined oxidative phosphorylation deficiency 15 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Combined oxidative phosphorylation deficiency 15 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Combined oxidative phosphorylation deficiency 40 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Combined oxidative phosphorylation deficiency 40 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Combined oxidative phosphorylation deficiency 14 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Combined oxidative phosphorylation deficiency 14 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Combined oxidative phosphorylation deficiency 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Combined oxidative phosphorylation deficiency 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Combined oxidative phosphorylation deficiency 33 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Combined oxidative phosphorylation deficiency 33 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Combined oxidative phosphorylation deficiency 11 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Combined oxidative phosphorylation deficiency 11 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Combined oxidative phosphorylation deficiency 16 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Combined oxidative phosphorylation deficiency 16 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Combined oxidative phosphorylation deficiency 8 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Combined oxidative phosphorylation deficiency 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Combined oxidative phosphorylation deficiency 51 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Combined oxidative phosphorylation deficiency 51 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Combined oxidative phosphorylation deficiency 44 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Combined oxidative phosphorylation deficiency 44 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Combined oxidative phosphorylation deficiency 25 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Combined oxidative phosphorylation deficiency 25 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Combined oxidative phosphorylation deficiency 53 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Combined oxidative phosphorylation deficiency 53 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Combined oxidative phosphorylation deficiency 17 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Combined oxidative phosphorylation deficiency 17 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Combined oxidative phosphorylation deficiency 28 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Combined oxidative phosphorylation deficiency 28 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Combined oxidative phosphorylation deficiency 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Combined oxidative phosphorylation deficiency 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Combined oxidative phosphorylation defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Combined oxidative phosphorylation defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hepatoencephalopathy due to combined oxidative phosphorylation defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hepatoencephalopathy due to combined oxidative phosphorylation defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Fatal mitochondrial disease due to combined oxidative phosphorylation defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Fatal mitochondrial disease due to combined oxidative phosphorylation defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Combined oxidative phosphorylation deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Combined oxidative phosphorylation deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Mitochondrial oxidative phosphorylation disorder Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Mitochondrial oxidative phosphorylation disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Oxidative phosphorylation Gene Set From KEGG Pathways 2026 proteins participating in the Oxidative phosphorylation pathway from the KEGG Pathways 2026 dataset.
basic mechanism of action of ppara pparb(d) and pparg and effects on gene expression Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From Reactome Pathways 2014 proteins 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 Set From Reactome Pathways 2014 proteins 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 Set From Reactome Pathways 2014 proteins 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 Set From Reactome Pathways 2014 proteins 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 Set From Reactome Pathways 2014 proteins 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 Set From Reactome Pathways 2014 proteins 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 Set From Reactome Pathways 2014 proteins 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 Set From Reactome Pathways 2014 proteins 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From WikiPathways Pathways 2024 proteins participating in the SREBF and miR33 in cholesterol and lipid homeostasis pathway from the WikiPathways Pathways 2024 dataset.
ApoE and miR 146 in inflammation and atherosclerosis Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From Reactome Pathways 2024 proteins 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 Set From Reactome Pathways 2024 proteins 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 Set From Reactome Pathways 2024 proteins 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 Set From Reactome Pathways 2024 proteins 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 Set From Reactome Pathways 2024 proteins 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 Set From Reactome Pathways 2024 proteins 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 Set From Reactome Pathways 2024 proteins 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 Set From Reactome Pathways 2024 proteins participating in the PTK6 Regulates RTKs and Their Effectors AKT1 and DOK1 pathway from the Reactome Pathways 2024 dataset.
Synthesis and processing of ENV and VPU Gene Set From Reactome Pathways 2024 proteins 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 Set From Reactome Pathways 2024 proteins 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 Set From Reactome Pathways 2024 proteins 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 Set From Reactome Pathways 2024 proteins 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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.
Basic cell groups and regions Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From Biocarta Pathways proteins participating in the role of erbb2 in signal transduction and oncology pathway from the Biocarta Pathways dataset.
corticosteroids and cardioprotection Gene Set From Biocarta Pathways proteins participating in the corticosteroids and cardioprotection pathway from the Biocarta Pathways dataset.
cyclins and cell cycle regulation Gene Set From Biocarta Pathways proteins participating in the cyclins and cell cycle regulation pathway from the Biocarta Pathways dataset.
mechanism of acetaminophen activity and toxicity Gene Set From 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 Set From 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 Set From 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 Set From Biocarta Pathways proteins participating in the thrombin signaling and protease-activated receptors pathway from the Biocarta Pathways dataset.
antigen processing and presentation Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From Biocarta Pathways proteins participating in the regulation of eif-4e and p70s6 kinase pathway from the Biocarta Pathways dataset.
estrogen responsive protein efp controls cell cycle and breast tumors growth Gene Set From Biocarta Pathways proteins participating in the estrogen responsive protein efp controls cell cycle and breast tumors growth pathway from the Biocarta Pathways dataset.
vegf hypoxia and angiogenesis Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From Biocarta Pathways proteins participating in the phosphoinositides and their downstream targets pathway from the Biocarta Pathways dataset.
melanocyte development and pigmentation pathway Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From Biocarta Pathways proteins participating in the ion channels and their functional role in vascular endothelium pathway from the Biocarta Pathways dataset.
fosb gene expression and drug abuse Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From ClinVar Gene-Phenotype Associations genes associated with the Hypothyroidism, central, and testicular enlargement phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Trifunctional protein deficiency with myopathy and neuropathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Trifunctional protein deficiency with myopathy and neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Retinal dystrophy, juvenile cataracts, and short stature syndrome Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From ClinVar Gene-Phenotype Associations genes associated with the Ichthyosis, follicular atrophoderma, hypotrichosis, and hypohidrosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
calcium- and calmodulin-dependent protein kinase complex Gene Set From 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.
mrna cleavage and polyadenylation specificity factor complex Gene Set From 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 Set From 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.
calcium- and calmodulin-dependent protein kinase complex Gene Set From 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.
cortical layer of collagen and cuticulin-based cuticle extracellular matrix Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From CORUM Protein Complexes proteins 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 Set From CORUM Protein Complexes proteins 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 Set From CORUM Protein Complexes proteins 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 Set From CORUM Protein Complexes proteins in the Remodeling and spacing factor (RSF) complex protein complex from the CORUM Protein Complexes dataset.
PBAF complex (Polybromo- and BAF containing complex) Gene Set From CORUM Protein Complexes proteins in the PBAF complex (Polybromo- and BAF containing complex) protein complex from the CORUM Protein Complexes dataset.
Cleavage and polyadenylation factor (CPSF) Gene Set From CORUM Protein Complexes proteins in the Cleavage and polyadenylation factor (CPSF) protein complex from the CORUM Protein Complexes dataset.
Apoptosis- and splicing-associated protein complex (ASAP-L), SAP18-RNPS1-Acinus-L Gene Set From CORUM Protein Complexes proteins in the Apoptosis- and splicing-associated protein complex (ASAP-L), SAP18-RNPS1-Acinus-L protein complex from the CORUM Protein Complexes dataset.
Respiratory chain complex I (intermediate I/200kD and III/250kD), mitochondrial Gene Set From CORUM Protein Complexes proteins 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 Set From CORUM Protein Complexes proteins 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 Set From CORUM Protein Complexes proteins in the Respiratory chain complex I (intermediate V/380kD and VI/480kD), mitochondrial protein complex from the CORUM Protein Complexes dataset.
Apoptosis- and splicing-associated protein complex (ASAP-S), SAP18-RNPS1-Acinus-S Gene Set From CORUM Protein Complexes proteins in the Apoptosis- and splicing-associated protein complex (ASAP-S), SAP18-RNPS1-Acinus-S protein complex from the CORUM Protein Complexes dataset.
ATP-utilizing chromatin assembly and remodeling factor (hACF) complex Gene Set From CORUM Protein Complexes proteins in the ATP-utilizing chromatin assembly and remodeling factor (hACF) complex protein complex from the CORUM Protein Complexes dataset.
20S methylosome and RG-containing Sm protein complex Gene Set From CORUM Protein Complexes proteins in the 20S methylosome and RG-containing Sm protein complex protein complex from the CORUM Protein Complexes dataset.
Amino Acids, Peptides, and Proteins Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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.
Trifunctional Protein Deficiency With Myopathy And Neuropathy Gene Set From 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.
MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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.

Harmonizome 3.0

CDK-mediated phosphorylation and removal of Cdc6 Gene Set

CDK-mediated phosphorylation and removal of Cdc6 Gene Set

H19 Rb E2F1 and CDK beta catenin in colorectal cancer Gene Set

MCM8-ORC2-CDC6 complex Gene Set

cdc6 Gene Set

CDC6, C-terminal domain Gene Set

Cell division protein Cdc6/18 Gene Set

BL9062 (CDC6) Gene Set

CDC6 Gene Set

CDC6 association with the ORC:origin complex Gene Set

CDT1 association with the CDC6:ORC:origin complex Gene Set

CDC6 Gene Set

CDC6 association with the ORC:origin complex Gene Set

CDC6 Gene Set

cdk regulation of dna replication Gene Set

CAK complex (Cdk-activating kinase complex) Gene Set

CAK core complex (Cdk-activating kinase core complex) Gene Set

cdk Gene Set

Inhibitor of CDK interacting with cyclin A1 Gene Set

Cdk-activating kinase assembly factor MAT1, centre Gene Set

Cdk-activating kinase assembly factor MAT1/Tfb3 Gene Set

cdk Gene Set

cyclin/CDK positive transcription elongation factor complex Gene Set

cdk/crk-inhibitor Gene Set

cyclin/CDK positive transcription elongation factor complex Gene Set

cyclin/CDK positive transcription elongation factor complex Gene Set

cyclin/CDK positive transcription elongation factor complex Gene Set

Pho85-Pho80 CDK-cyclin complex Gene Set

CDK INHIBITOR SNS-032 Gene Set

CDK INHIBITOR 4.35 Gene Set

CDK INHIBITOR AT7519 Gene Set

CDK/CRK INHIBITOR Gene Set

removal Gene Set

removal of rna primer involved in mitotic dna replication Gene Set

trna 5'-leader removal Gene Set

regulation of removal of superoxide radicals Gene Set

negative regulation of protein modification by small protein conjugation or removal Gene Set

dna replication, removal of rna primer Gene Set

removal of superoxide radicals Gene Set

positive regulation of protein modification by small protein conjugation or removal Gene Set

regulation of protein modification by small protein conjugation or removal Gene Set

protein modification by small protein removal Gene Set

protein initiator methionine removal Gene Set

nucleotide-excision repair, dna damage removal Gene Set

protein modification by small protein conjugation or removal Gene Set

glutamate removal from folates Gene Set

Removal of licensing factors from origins Gene Set

Orc1 removal from chromatin Gene Set

Base-free sugar-phosphate removal via the single-nucleotide replacement pathway Gene Set

Removal of aminoterminal propeptides from gamma-carboxylated proteins Gene Set

Removal of the Flap Intermediate Gene Set

Removal of the Flap Intermediate from the C-strand Gene Set

Removal of DNA patch containing abasic residue Gene Set

tRNA 5'-leader removal Gene Set

regulation of removal of superoxide radicals Gene Set

removal of superoxide radicals Gene Set

base-excision repair, AP site formation via deaminated base removal Gene Set

DNA replication, removal of RNA primer Gene Set

protein initiator methionine removal involved in protein maturation Gene Set

protein deglycation, methylglyoxal removal Gene Set

protein deglycation, glyoxal removal Gene Set

guanine deglycation, methylglyoxal removal Gene Set

guanine deglycation, glyoxal removal Gene Set

protein modification by small protein removal Gene Set

regulation of protein modification by small protein conjugation or removal Gene Set

positive regulation of protein modification by small protein conjugation or removal Gene Set

negative regulation of protein modification by small protein conjugation or removal Gene Set

protein modification by small protein conjugation or removal Gene Set

protein initiator methionine removal Gene Set

Abasic sugar-phosphate removal via the single-nucleotide replacement pathway Gene Set

Orc1 removal from chromatin Gene Set

Removal of aminoterminal propeptides from gamma-carboxylated proteins Gene Set

Removal of the Flap Intermediate Gene Set

Removal of the Flap Intermediate from the C-strand Gene Set

tRNA 5'-leader removal Gene Set

regulation of removal of superoxide radicals Gene Set

removal of superoxide radicals Gene Set

base-excision repair, AP site formation via deaminated base removal Gene Set

DNA replication, removal of RNA primer Gene Set