Name

Mitochondrial DNA depletion syndrome 4B, MNGIE type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mitochondrial DNA depletion syndrome 4B, MNGIE type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

MITOCHONDRIAL DNA DEPLETION SYNDROME 4B (MNGIE TYPE) Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MITOCHONDRIAL DNA DEPLETION SYNDROME 4B (MNGIE TYPE) from the curated CTD Gene-Disease Associations dataset.

MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE TYPE) Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE TYPE) from the curated CTD Gene-Disease Associations dataset.

mitochondrial dna depletion syndrome 4b (mngie type) Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial dna depletion syndrome 4b (mngie type) phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial dna depletion syndrome 1 (mngie type) Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial dna depletion syndrome 1 (mngie type) phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial dna depletion syndrome 8b (mngie type) Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial dna depletion syndrome 8b (mngie type) phenotype from the curated OMIM Gene-Disease Associations dataset.

Mitochondrial DNA depletion syndrome 12 (cardiomyopathic type) Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mitochondrial DNA depletion syndrome 12 (cardiomyopathic type) phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type) Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type) phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mitochondrial DNA depletion syndrome 7 (hepatocerebral type) Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mitochondrial DNA depletion syndrome 7 (hepatocerebral type) phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

MITOCHONDRIAL DNA DEPLETION SYNDROME 4A (ALPERS TYPE) Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MITOCHONDRIAL DNA DEPLETION SYNDROME 4A (ALPERS TYPE) from the curated CTD Gene-Disease Associations dataset.

MITOCHONDRIAL DNA DEPLETION SYNDROME 8A (ENCEPHALOMYOPATHIC TYPE WITH RENAL TUBULOPATHY) Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MITOCHONDRIAL DNA DEPLETION SYNDROME 8A (ENCEPHALOMYOPATHIC TYPE WITH RENAL TUBULOPATHY) from the curated CTD Gene-Disease Associations dataset.

MITOCHONDRIAL DNA DEPLETION SYNDROME 9 (ENCEPHALOMYOPATHIC TYPE WITH METHYLMALONIC ACIDURIA) Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MITOCHONDRIAL DNA DEPLETION SYNDROME 9 (ENCEPHALOMYOPATHIC TYPE WITH METHYLMALONIC ACIDURIA) from the curated CTD Gene-Disease Associations dataset.

MITOCHONDRIAL DNA DEPLETION SYNDROME 6 (HEPATOCEREBRAL TYPE) Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MITOCHONDRIAL DNA DEPLETION SYNDROME 6 (HEPATOCEREBRAL TYPE) from the curated CTD Gene-Disease Associations dataset.

MITOCHONDRIAL DNA DEPLETION SYNDROME 7 (HEPATOCEREBRAL TYPE) Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MITOCHONDRIAL DNA DEPLETION SYNDROME 7 (HEPATOCEREBRAL TYPE) from the curated CTD Gene-Disease Associations dataset.

MITOCHONDRIAL DNA DEPLETION SYNDROME 3 (HEPATOCEREBRAL TYPE) Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MITOCHONDRIAL DNA DEPLETION SYNDROME 3 (HEPATOCEREBRAL TYPE) from the curated CTD Gene-Disease Associations dataset.

MITOCHONDRIAL DNA DEPLETION SYNDROME 2 (MYOPATHIC TYPE) Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MITOCHONDRIAL DNA DEPLETION SYNDROME 2 (MYOPATHIC TYPE) from the curated CTD Gene-Disease Associations dataset.

mitochondrial dna depletion syndrome 4a (alpers type) Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial dna depletion syndrome 4a (alpers type) phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial dna depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria) Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial dna depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria) phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial dna depletion syndrome 6 (hepatocerebral type) Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial dna depletion syndrome 6 (hepatocerebral type) phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial dna depletion syndrome 12 (cardiomyopathic type) Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial dna depletion syndrome 12 (cardiomyopathic type) phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial dna depletion syndrome 2 (myopathic type) Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial dna depletion syndrome 2 (myopathic type) phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial dna depletion syndrome 13 (encephalomyopathic type) Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial dna depletion syndrome 13 (encephalomyopathic type) phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial dna depletion syndrome 3 (hepatocerebral type) Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial dna depletion syndrome 3 (hepatocerebral type) phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial dna depletion syndrome 7 (hepatocerebral type) Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial dna depletion syndrome 7 (hepatocerebral type) phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial dna depletion syndrome 8a (encephalomyopathic type with renal tubulopathy) Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial dna depletion syndrome 8a (encephalomyopathic type with renal tubulopathy) phenotype from the curated OMIM Gene-Disease Associations dataset.

Mitochondrial DNA depletion syndrome 9 (encephalomyopathic with methylmalonic aciduria) Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mitochondrial DNA depletion syndrome 9 (encephalomyopathic with methylmalonic aciduria) phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mitochondrial DNA depletion syndrome 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mitochondrial DNA depletion syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria) Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria) phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mitochondrial DNA depletion syndrome 11 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mitochondrial DNA depletion syndrome 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mitochondrial DNA-depletion syndrome 3, hepatocerebral Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mitochondrial DNA-depletion syndrome 3, hepatocerebral phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

MITOCHONDRIAL DNA DEPLETION SYNDROME 5 (ENCEPHALOMYOPATHIC WITH OR WITHOUT METHYLMALONIC ACIDURIA) Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MITOCHONDRIAL DNA DEPLETION SYNDROME 5 (ENCEPHALOMYOPATHIC WITH OR WITHOUT METHYLMALONIC ACIDURIA) from the curated CTD Gene-Disease Associations dataset.

mitochondrial dna depletion syndrome 11 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial dna depletion syndrome 11 phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial dna depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria) Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial dna depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria) phenotype from the curated OMIM Gene-Disease Associations dataset.

depletion of mitochondrial dna in muscle tissue Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the depletion of mitochondrial dna in muscle tissue phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

depletion of mitochondrial dna in liver Gene Set

From HPO Gene-Disease Associations

genes associated with the depletion of mitochondrial dna in liver phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

depletion of mitochondrial dna in muscle tissue Gene Set

From HPO Gene-Disease Associations

genes associated with the depletion of mitochondrial dna in muscle tissue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1;MC5DN1 MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, ATPAF2 TYPE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1;MC5DN1 MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, ATPAF2 TYPE from the curated CTD Gene-Disease Associations dataset.

DNA nucleotidylexotransferase (TdT) / DNA-directed DNA/RNA polymerase mu Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA nucleotidylexotransferase (TdT) / DNA-directed DNA/RNA polymerase mu protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DNA topoisomerase I, DNA binding, eukaryotic-type Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA topoisomerase I, DNA binding, eukaryotic-type protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DNA topoisomerase, type IA, DNA-binding domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA topoisomerase, type IA, DNA-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DNA helicase (DNA repair), Rad3 type Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA helicase (DNA repair), Rad3 type protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DNA topoisomerase I, DNA binding, mixed alpha/beta motif, eukaryotic-type Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA topoisomerase I, DNA binding, mixed alpha/beta motif, eukaryotic-type protein domain from the InterPro Predicted Protein Domain Annotations dataset.

deafness; diabetes mellitus, type 1; diabetes mellitus, type 2; mitochondrial diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease deafness; diabetes mellitus, type 1; diabetes mellitus, type 2; mitochondrial diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hodgkin's lymphoma, lymphocytic depletion Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease hodgkin's lymphoma, lymphocytic depletion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

behavioral traits; tryptophan depletion sensitivity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease behavioral traits; tryptophan depletion sensitivity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

depletion Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term depletion in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

response to sterol depletion Gene Set

From GO Biological Process Annotations

genes participating in the response to sterol depletion biological process from the curated GO Biological Process Annotations dataset.

cellular response to sterol depletion Gene Set

From GO Biological Process Annotations

genes participating in the cellular response to sterol depletion biological process from the curated GO Biological Process Annotations dataset.

depletion of components of the alternative complement pathway Gene Set

From HPO Gene-Disease Associations

genes associated with the depletion of components of the alternative complement pathway phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

digeorge syndrome; pharyngeal pouch; syndrome; velo-cardio-facial syndrome; 22q11 deletion syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease digeorge syndrome; pharyngeal pouch; syndrome; velo-cardio-facial syndrome; 22q11 deletion syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.

Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 3 from the curated CTD Gene-Disease Associations dataset.

Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 4 from the curated CTD Gene-Disease Associations dataset.

Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 2 from the curated CTD Gene-Disease Associations dataset.

Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 1 from the curated CTD Gene-Disease Associations dataset.

Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 5 from the curated CTD Gene-Disease Associations dataset.

dna damage; glaucoma, open-angle; mitochondrial diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dna damage; glaucoma, open-angle; mitochondrial diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

regulation of mitochondrial dna metabolic process Gene Set

From GO Biological Process Annotations

genes participating in the regulation of mitochondrial dna metabolic process biological process from the curated GO Biological Process Annotations dataset.

positive regulation of mitochondrial dna replication Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of mitochondrial dna replication biological process from the curated GO Biological Process Annotations dataset.

negative regulation of mitochondrial dna replication Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of mitochondrial dna replication biological process from the curated GO Biological Process Annotations dataset.

mitochondrial dna replication Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial dna replication biological process from the curated GO Biological Process Annotations dataset.

regulation of mitochondrial dna replication Gene Set

From GO Biological Process Annotations

genes participating in the regulation of mitochondrial dna replication biological process from the curated GO Biological Process Annotations dataset.

negative regulation of mitochondrial dna metabolic process Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of mitochondrial dna metabolic process biological process from the curated GO Biological Process Annotations dataset.

mitochondrial dna repair Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial dna repair biological process from the curated GO Biological Process Annotations dataset.

positive regulation of mitochondrial dna metabolic process Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of mitochondrial dna metabolic process biological process from the curated GO Biological Process Annotations dataset.

mitochondrial dna metabolic process Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial dna metabolic process biological process from the curated GO Biological Process Annotations dataset.

multiple mitochondrial dna deletions Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the multiple mitochondrial dna deletions phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

multiple mitochondrial dna deletions Gene Set

From HPO Gene-Disease Associations

genes associated with the multiple mitochondrial dna deletions phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

decreased mitochondrial dna content Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased mitochondrial dna content phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

progressive external ophthalmoplegia with mitochondrial dna deletions 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the progressive external ophthalmoplegia with mitochondrial dna deletions 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

dna-dependent protein kinase-dna ligase 4 complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the dna-dependent protein kinase-dna ligase 4 complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

DNA ligase IV-Xrcc4-DNA-protein kinase complex Gene Set

From CORUM Protein Complexes

proteins in the DNA ligase IV-Xrcc4-DNA-protein kinase complex protein complex from the CORUM Protein Complexes dataset.

DNA ligase III-XRCC1-PNK-DNA-pol III multiprotein complex Gene Set

From CORUM Protein Complexes

proteins in the DNA ligase III-XRCC1-PNK-DNA-pol III multiprotein complex protein complex from the CORUM Protein Complexes dataset.

dna synthesis involved in dna repair Gene Set

From GO Biological Process Annotations

genes participating in the dna synthesis involved in dna repair biological process from the curated GO Biological Process Annotations dataset.

dna-dependent dna replication Gene Set

From GO Biological Process Annotations

genes participating in the dna-dependent dna replication biological process from the curated GO Biological Process Annotations dataset.

dna damage response, detection of dna damage Gene Set

From GO Biological Process Annotations

genes participating in the dna damage response, detection of dna damage biological process from the curated GO Biological Process Annotations dataset.

positive regulation of dna-dependent dna replication initiation Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of dna-dependent dna replication initiation biological process from the curated GO Biological Process Annotations dataset.

dna dealkylation involved in dna repair Gene Set

From GO Biological Process Annotations

genes participating in the dna dealkylation involved in dna repair biological process from the curated GO Biological Process Annotations dataset.

dna strand elongation involved in dna replication Gene Set

From GO Biological Process Annotations

genes participating in the dna strand elongation involved in dna replication biological process from the curated GO Biological Process Annotations dataset.

regulation of dna-dependent dna replication initiation Gene Set

From GO Biological Process Annotations

genes participating in the regulation of dna-dependent dna replication initiation biological process from the curated GO Biological Process Annotations dataset.

regulation of dna-dependent dna replication Gene Set

From GO Biological Process Annotations

genes participating in the regulation of dna-dependent dna replication biological process from the curated GO Biological Process Annotations dataset.

dna ligation involved in dna recombination Gene Set

From GO Biological Process Annotations

genes participating in the dna ligation involved in dna recombination biological process from the curated GO Biological Process Annotations dataset.

positive regulation of dna-dependent dna replication Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of dna-dependent dna replication biological process from the curated GO Biological Process Annotations dataset.

negative regulation of dna-dependent dna replication Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of dna-dependent dna replication biological process from the curated GO Biological Process Annotations dataset.

dna ligation involved in dna repair Gene Set

From GO Biological Process Annotations

genes participating in the dna ligation involved in dna repair biological process from the curated GO Biological Process Annotations dataset.

dna-dependent dna replication maintenance of fidelity Gene Set

From GO Biological Process Annotations

genes participating in the dna-dependent dna replication maintenance of fidelity biological process from the curated GO Biological Process Annotations dataset.

dna unwinding involved in dna replication Gene Set

From GO Biological Process Annotations

genes participating in the dna unwinding involved in dna replication biological process from the curated GO Biological Process Annotations dataset.

dna-dependent protein kinase-dna ligase 4 complex Gene Set

From GO Cellular Component Annotations

proteins localized to the dna-dependent protein kinase-dna ligase 4 complex cellular component from the curated GO Cellular Component Annotations dataset.

single-stranded dna-dependent atp-dependent dna helicase activity Gene Set

From GO Molecular Function Annotations

genes performing the single-stranded dna-dependent atp-dependent dna helicase activity molecular function from the curated GO Molecular Function Annotations dataset.

dna-directed dna polymerase activity Gene Set

From GO Molecular Function Annotations

genes performing the dna-directed dna polymerase activity molecular function from the curated GO Molecular Function Annotations dataset.

DNA-directed DNA polymerase, family B, exonuclease domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA-directed DNA polymerase, family B, exonuclease domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DNA-directed DNA polymerase, family B, multifunctional domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA-directed DNA polymerase, family B, multifunctional domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Methylated-DNA-[protein]-cysteine S-methyltransferase, DNA binding Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Methylated-DNA-[protein]-cysteine S-methyltransferase, DNA binding protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DNA glycosylase/AP lyase, H2TH DNA-binding Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA glycosylase/AP lyase, H2TH DNA-binding protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DNA-directed DNA polymerase, family B, conserved site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA-directed DNA polymerase, family B, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DNA-directed DNA-polymerase, family A, mitochondria Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA-directed DNA-polymerase, family A, mitochondria protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Zinc finger, DNA-directed DNA polymerase, family B, alpha Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Zinc finger, DNA-directed DNA polymerase, family B, alpha protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DNA-directed DNA polymerase X Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA-directed DNA polymerase X protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DNA-directed DNA/RNA polymerase mu Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA-directed DNA/RNA polymerase mu protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DNA-directed DNA polymerase, family A, conserved site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA-directed DNA polymerase, family A, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DNA-directed DNA polymerase, family A, palm domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA-directed DNA polymerase, family A, palm domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DNA-directed DNA polymerase, family B Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA-directed DNA polymerase, family B protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DNA glycosylase/AP lyase, zinc finger domain, DNA-binding site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA glycosylase/AP lyase, zinc finger domain, DNA-binding site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Translesion synthesis by DNA polymerases bypassing lesion on DNA template Gene Set

From Reactome Pathways

proteins participating in the Translesion synthesis by DNA polymerases bypassing lesion on DNA template pathway from the Reactome Pathways dataset.

Integration of viral DNA into host genomic DNA Gene Set

From Reactome Pathways

proteins participating in the Integration of viral DNA into host genomic DNA pathway from the Reactome Pathways dataset.

albuminuria; chronic renal failure; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; glycosuria; kidney failure, chronic; proteinuria Gene Set

From GAD Gene-Disease Associations

genes associated with the disease albuminuria; chronic renal failure; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; glycosuria; kidney failure, chronic; proteinuria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 1; diabetes mellitus, type 2; hypoglycemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 1; diabetes mellitus, type 2; hypoglycemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; hypertension Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atherosclerosis; coronary artery disease; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies; fam hyperbetalipoproteinaemia; hyperlipoproteinemia type ii; hypertriglyceridemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atherosclerosis; coronary artery disease; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies; fam hyperbetalipoproteinaemia; hyperlipoproteinemia type ii; hypertriglyceridemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; disease susceptibility; polyendocrinopathies, autoimmune Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; disease susceptibility; polyendocrinopathies, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic retinopathy; genetic predisposition to disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic retinopathy; genetic predisposition to disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, rheumatoid; coronary artery disease; crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; hypertension; rheumatoid arthritis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, rheumatoid; coronary artery disease; crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; hypertension; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic angiopathies; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic angiopathies; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; wolfram syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; wolfram syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance; metabolic syndrome x; obesity; overweight Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance; metabolic syndrome x; obesity; overweight in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; metabolic syndrome x Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; metabolic syndrome x in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; hypertension; insulin resistance; metabolic syndrome x; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; hypertension; insulin resistance; metabolic syndrome x; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; metabolic syndrome x; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; metabolic syndrome x; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance; metabolic syndrome x Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance; metabolic syndrome x in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; metabolic syndrome x; myocardial ischemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; metabolic syndrome x; myocardial ischemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; diabetes mellitus type ii; diabetes mellitus, type 2; metabolic syndrome x Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; diabetes mellitus type ii; diabetes mellitus, type 2; metabolic syndrome x in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance; metabolic syndrome x Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance; metabolic syndrome x in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Mitochondrial complex III deficiency, nuclear type 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mitochondrial complex III deficiency, nuclear type 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mitochondrial complex III deficiency, nuclear type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mitochondrial complex III deficiency, nuclear type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 7 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 8 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Aspartate-tRNA ligase, class IIb, bacterial/mitochondrial-type Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Aspartate-tRNA ligase, class IIb, bacterial/mitochondrial-type protein domain from the InterPro Predicted Protein Domain Annotations dataset.

?mitochondrial complex (atp synthase) deficiency, nuclear type 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?mitochondrial complex (atp synthase) deficiency, nuclear type 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial complex v (atp synthase) deficiency, nuclear type 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial complex v (atp synthase) deficiency, nuclear type 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial complex v (atp synthase) deficiency, nuclear type 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial complex v (atp synthase) deficiency, nuclear type 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

?mitochondrial complex iii deficiency, nuclear type 9 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?mitochondrial complex iii deficiency, nuclear type 9 phenotype from the curated OMIM Gene-Disease Associations dataset.

?mitochondrial complex iii deficiency, nuclear type 8 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?mitochondrial complex iii deficiency, nuclear type 8 phenotype from the curated OMIM Gene-Disease Associations dataset.

?mitochondrial complex iii deficiency, nuclear type 7 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?mitochondrial complex iii deficiency, nuclear type 7 phenotype from the curated OMIM Gene-Disease Associations dataset.

?mitochondrial complex iii deficiency, nuclear type 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?mitochondrial complex iii deficiency, nuclear type 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

?mitochondrial complex v (atp synthase) deficiency, nuclear type 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?mitochondrial complex v (atp synthase) deficiency, nuclear type 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial complex iii deficiency, nuclear type 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial complex iii deficiency, nuclear type 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial complex iii deficiency, nuclear type 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial complex iii deficiency, nuclear type 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial complex iii deficiency, nuclear type 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial complex iii deficiency, nuclear type 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial complex iii deficiency, nuclear type 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial complex iii deficiency, nuclear type 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial complex iii deficiency, nuclear type 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial complex iii deficiency, nuclear type 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

stuve-wiedemann syndrome/schwartz-jampel type 2 syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the stuve-wiedemann syndrome/schwartz-jampel type 2 syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

Leigh syndrome due to mitochondrial complex I deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Leigh syndrome due to mitochondrial complex I deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Leigh syndrome due to mitochondrial complex II deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Leigh syndrome due to mitochondrial complex II deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple mitochondrial dysfunctions syndrome 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple mitochondrial dysfunctions syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple mitochondrial dysfunctions syndrome 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple mitochondrial dysfunctions syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mitochondrial neurogastrointestinal encephalopathy syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mitochondrial neurogastrointestinal encephalopathy syndrome from the curated CTD Gene-Disease Associations dataset.

MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 1 from the curated CTD Gene-Disease Associations dataset.

hearing loss, sensorineural; learning disorders; melas syndrome; migraine disorders; mitochondrial diseases; sensorineural hearing loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing loss, sensorineural; learning disorders; melas syndrome; migraine disorders; mitochondrial diseases; sensorineural hearing loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leigh syndrome due to mitochondrial complex i deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the leigh syndrome due to mitochondrial complex i deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

multiple mitochondrial dysfunctions syndrome 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the multiple mitochondrial dysfunctions syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

multiple mitochondrial dysfunctions syndrome 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the multiple mitochondrial dysfunctions syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

leigh syndrome due to mitochondrial cox4 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the leigh syndrome due to mitochondrial cox4 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial recessive ataxia syndrome (includes sando and scae) Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial recessive ataxia syndrome (includes sando and scae) phenotype from the curated OMIM Gene-Disease Associations dataset.

leigh syndrome due to mitochondrial complex 1 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the leigh syndrome due to mitochondrial complex 1 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

?multiple mitochondrial dysfunctions syndrome 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?multiple mitochondrial dysfunctions syndrome 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

Lynch syndrome:Lynch syndrome:Lynch syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Lynch syndrome:Lynch syndrome:Lynch syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

fatigue syndrome, chronic; fatigue syndrome; postviral; persian gulf syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fatigue syndrome, chronic; fatigue syndrome; postviral; persian gulf syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

nocturnal myoclonus syndrome; restless legs syndrome; tourette syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease nocturnal myoclonus syndrome; restless legs syndrome; tourette syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

meconium aspiration syndrome; resp distress syndrome neonatal; respiratory distress syndrome, newborn; sleep disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease meconium aspiration syndrome; resp distress syndrome neonatal; respiratory distress syndrome, newborn; sleep disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adult respiratory distress syndrome; respiratory distress syndrome, adult; severe acute respiratory syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adult respiratory distress syndrome; respiratory distress syndrome, adult; severe acute respiratory syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

insulin resistance; metabolic syndrome x; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease insulin resistance; metabolic syndrome x; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; diabetes mellitus; diabetes mellitus, type 2; diabetic angiopathies; dna damage Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; diabetes mellitus; diabetes mellitus, type 2; diabetic angiopathies; dna damage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

rna polymerase iii type 3 promoter dna binding Gene Set

From GO Molecular Function Annotations

genes performing the rna polymerase iii type 3 promoter dna binding molecular function from the curated GO Molecular Function Annotations dataset.

dna topoisomerase type ii (atp-hydrolyzing) activity Gene Set

From GO Molecular Function Annotations

genes performing the dna topoisomerase type ii (atp-hydrolyzing) activity molecular function from the curated GO Molecular Function Annotations dataset.

rna polymerase iii type 1 promoter dna binding Gene Set

From GO Molecular Function Annotations

genes performing the rna polymerase iii type 1 promoter dna binding molecular function from the curated GO Molecular Function Annotations dataset.

dna topoisomerase type i activity Gene Set

From GO Molecular Function Annotations

genes performing the dna topoisomerase type i activity molecular function from the curated GO Molecular Function Annotations dataset.

rna polymerase iii type 2 promoter dna binding Gene Set

From GO Molecular Function Annotations

genes performing the rna polymerase iii type 2 promoter dna binding molecular function from the curated GO Molecular Function Annotations dataset.

DNA-directed RNA polymerase, RpoA/D/Rpb3-type Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA-directed RNA polymerase, RpoA/D/Rpb3-type protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DNA topoisomerase, type IA, central region, subdomain 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA topoisomerase, type IA, central region, subdomain 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DNA topoisomerase, type IA, central region, subdomain 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA topoisomerase, type IA, central region, subdomain 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DNA topoisomerase, type IIA, subunit A/C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA topoisomerase, type IIA, subunit A/C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DNA topoisomerase I, catalytic core, eukaryotic-type Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA topoisomerase I, catalytic core, eukaryotic-type protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DNA topoisomerase I, catalytic core, alpha-helical subdomain, eukaryotic-type Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA topoisomerase I, catalytic core, alpha-helical subdomain, eukaryotic-type protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DNA-directed RNA polymerase, phage-type Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA-directed RNA polymerase, phage-type protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DNA topoisomerase, type IIA, central domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA topoisomerase, type IIA, central domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DNA topoisomerase, type IIA-like domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA topoisomerase, type IIA-like domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DNA binding HTH domain, Psq-type Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA binding HTH domain, Psq-type protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DNA-binding RFX-type winged-helix domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA-binding RFX-type winged-helix domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DNA/RNA helicase, ATP-dependent, DEAH-box type, conserved site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA/RNA helicase, ATP-dependent, DEAH-box type, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DNA topoisomerase, type IA, central Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA topoisomerase, type IA, central protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DNA topoisomerase, type IIA, subunit B, domain 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA topoisomerase, type IIA, subunit B, domain 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DNA topoisomerase, type IA Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA topoisomerase, type IA protein domain from the InterPro Predicted Protein Domain Annotations dataset.

HTH CenpB-type DNA-binding domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the HTH CenpB-type DNA-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Zinc finger, DNA glycosylase/AP lyase-type Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Zinc finger, DNA glycosylase/AP lyase-type protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DNA topoisomerase, type IA, active site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA topoisomerase, type IA, active site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Heat shock factor (HSF)-type, DNA-binding Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Heat shock factor (HSF)-type, DNA-binding protein domain from the InterPro Predicted Protein Domain Annotations dataset.

C4-type zinc-finger of DNA polymerase delta Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the C4-type zinc-finger of DNA polymerase delta protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DNA primase, UL52/UL70 type, Herpesviridae Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA primase, UL52/UL70 type, Herpesviridae protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DNA topoisomerase, type IIA, conserved site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA topoisomerase, type IIA, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DNA polymerase type-Y, HhH motif Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA polymerase type-Y, HhH motif protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DNA topoisomerase, type IA, zn finger Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA topoisomerase, type IA, zn finger protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DNA helicase, ATP-dependent, RecQ type Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA helicase, ATP-dependent, RecQ type protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DNA topoisomerase, type IA, domain 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA topoisomerase, type IA, domain 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Zinc finger C2H2-type/integrase DNA-binding domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Zinc finger C2H2-type/integrase DNA-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DNA/RNA-binding domain, Est1-type Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA/RNA-binding domain, Est1-type protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DNA helicase, UvrD/REP type Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA helicase, UvrD/REP type protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DNA topoisomerase, type IA, core domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA topoisomerase, type IA, core domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DNA topoisomerase, type IIA, subunit A/ C-terminal, alpha-beta Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA topoisomerase, type IIA, subunit A/ C-terminal, alpha-beta protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DNA topoisomerase, type IIA Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA topoisomerase, type IIA protein domain from the InterPro Predicted Protein Domain Annotations dataset.

p53/RUNT-type transcription factor, DNA-binding domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the p53/RUNT-type transcription factor, DNA-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DNA repair nuclease, XPF-type/Helicase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA repair nuclease, XPF-type/Helicase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Type IIA DNA topoisomerase subunit A, alpha-helical domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Type IIA DNA topoisomerase subunit A, alpha-helical domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DNA topoisomerase I, eukaryotic-type Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA topoisomerase I, eukaryotic-type protein domain from the InterPro Predicted Protein Domain Annotations dataset.

dna damage; ehlers-danlos syndrome; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dna damage; ehlers-danlos syndrome; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cockayne syndrome; dna damage Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cockayne syndrome; dna damage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; hyperinsulinism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; hyperinsulinism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; hypertriglyceridemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; hypertriglyceridemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral infarction; diabetes mellitus type ii; diabetes mellitus, type 2 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral infarction; diabetes mellitus type ii; diabetes mellitus, type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic nephropathies; hypertension; kidney failure, chronic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic nephropathies; hypertension; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; hypertrophy, left ventricular; left ventricular hypertrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; hypertrophy, left ventricular; left ventricular hypertrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; glucose metabolism disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; glucose metabolism disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; hyperinsulinism; insulin resistance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; hyperinsulinism; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; familial type 3 hyperlipoproteinaemia; hyperinsulinism; hyperlipoproteinemia type iii; peripheral vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; familial type 3 hyperlipoproteinaemia; hyperinsulinism; hyperlipoproteinemia type iii; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; hypertrophy; insulin resistance; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; hypertrophy; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; edema Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; edema in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic nephropathies Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic nephropathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus, type 2; hyperlipoproteinemia type i; hypertriglyceridemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, type 2; hyperlipoproteinemia type i; hypertriglyceridemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic renal failure; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; kidney failure, chronic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic renal failure; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic renal failure; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; kidney failure, chronic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic renal failure; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; hyperhomocysteinemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; hyperhomocysteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; diabetic retinopathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; diabetic retinopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; diabetes mellitus type ii; diabetes mellitus, type 2 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; diabetes mellitus type ii; diabetes mellitus, type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; hemochromatosis; insulin resistance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; hemochromatosis; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes, type 2; diabetes, type 1 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes, type 2; diabetes, type 1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; body weight; diabetes mellitus type ii; diabetes mellitus, type 2 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; body weight; diabetes mellitus type ii; diabetes mellitus, type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; diabetic neuropathies; insulin resistance; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; diabetic neuropathies; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

albuminuria; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease albuminuria; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic renal failure; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic neuropathies; kidney failure, chronic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic renal failure; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic neuropathies; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

familial type 3 hyperlipoproteinaemia; hyperlipoproteinemia type iii Gene Set

From GAD Gene-Disease Associations

genes associated with the disease familial type 3 hyperlipoproteinaemia; hyperlipoproteinemia type iii in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus; diabetes mellitus type ii; diabetes mellitus, type 2 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus; diabetes mellitus type ii; diabetes mellitus, type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; hyperlipidemias; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; hyperlipidemias; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; weight gain Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; weight gain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; hypertension; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; hypertension; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; diabetic neuropathies; disease susceptibility Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; diabetic neuropathies; disease susceptibility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; hearing disorders; hearing problem Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; hearing disorders; hearing problem in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; chronic renal failure; diabetes complications; diabetes mellitus type ii; diabetes mellitus, type 2; kidney failure, chronic; myocardial infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; chronic renal failure; diabetes complications; diabetes mellitus type ii; diabetes mellitus, type 2; kidney failure, chronic; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes, type 2 ; diabetes, type 1 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes, type 2 ; diabetes, type 1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary artery disease; diabetes mellitus type ii; diabetes mellitus, type 2; dyslipidemias Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary artery disease; diabetes mellitus type ii; diabetes mellitus, type 2; dyslipidemias in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic retinopathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic retinopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

calcinosis; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies Gene Set

From GAD Gene-Disease Associations

genes associated with the disease calcinosis; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; hypertension Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

colorectal neoplasms; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; iron overload Gene Set

From GAD Gene-Disease Associations

genes associated with the disease colorectal neoplasms; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; iron overload in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; endometrial neoplasms; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; endometrial neoplasms; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acute-phase reaction; diabetes mellitus type ii; diabetes mellitus, type 2 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acute-phase reaction; diabetes mellitus type ii; diabetes mellitus, type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atherosclerosis; diabetes complications; diabetes mellitus type ii; diabetes mellitus, type 2; myocardial infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atherosclerosis; diabetes complications; diabetes mellitus type ii; diabetes mellitus, type 2; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; diabetes mellitus type ii; diabetes mellitus, type 2; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; diabetes mellitus type ii; diabetes mellitus, type 2; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; diabetes, gestational; gestational diabetes mellitus Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; diabetes, gestational; gestational diabetes mellitus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic retinopathy; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic retinopathy; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

albuminuria; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease albuminuria; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, rheumatoid; atrial fibrillation; crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, type 2; multiple sclerosis; rheumatoid arthritis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, rheumatoid; atrial fibrillation; crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, type 2; multiple sclerosis; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adenoma; adrenal gland neoplasms; adrenal neoplasm; diabetes mellitus type ii; diabetes mellitus, type 2 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenoma; adrenal gland neoplasms; adrenal neoplasm; diabetes mellitus type ii; diabetes mellitus, type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic renal failure; diabetes mellitus type ii; diabetes mellitus, type 2; glomerulonephritis; kidney failure, chronic; polycystic kidney, autosomal dominant Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic renal failure; diabetes mellitus type ii; diabetes mellitus, type 2; glomerulonephritis; kidney failure, chronic; polycystic kidney, autosomal dominant in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; memory disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arteriosclerosis; diabetes mellitus type ii; diabetes mellitus, type 2 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arteriosclerosis; diabetes mellitus type ii; diabetes mellitus, type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; diabetes mellitus type ii; diabetes mellitus, type 2; thinness Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; diabetes mellitus type ii; diabetes mellitus, type 2; thinness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; diabetes mellitus type ii; diabetes mellitus, type 2 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; diabetes mellitus type ii; diabetes mellitus, type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus, type 1; diabetes mellitus, type 2 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, type 1; diabetes mellitus, type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alcoholism; diabetes mellitus type ii; diabetes mellitus, type 2; pancreatic neoplasm; pancreatic neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alcoholism; diabetes mellitus type ii; diabetes mellitus, type 2; pancreatic neoplasm; pancreatic neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance; obesity; weight loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance; obesity; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies; hypertension; insulin resistance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies; hypertension; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebrovascular disorders; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies; peripheral vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebrovascular disorders; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance; overweight Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance; overweight in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; pancreatic neoplasm; pancreatic neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; pancreatic neoplasm; pancreatic neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus, type 1; diabetes mellitus, type 2; insulin resistance; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, type 1; diabetes mellitus, type 2; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; kidney failure; kidney; failure Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; kidney failure; kidney; failure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes, type 2; hypertension; diabetes, type 1 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes, type 2; hypertension; diabetes, type 1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary stenosis; diabetes mellitus type ii; diabetes mellitus, type 2 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary stenosis; diabetes mellitus type ii; diabetes mellitus, type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; hypercholesterolemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; hypercholesterolemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

angina pectoris; coronary artery disease; coronary restenosis; diabetes mellitus type ii; diabetes mellitus, type 2 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease angina pectoris; coronary artery disease; coronary restenosis; diabetes mellitus type ii; diabetes mellitus, type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; diabetes mellitus type ii; diabetes mellitus, type 2; inflammation; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; diabetes mellitus type ii; diabetes mellitus, type 2; inflammation; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic renal failure; diabetes mellitus type ii; diabetes mellitus, type 2; kidney failure, chronic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic renal failure; diabetes mellitus type ii; diabetes mellitus, type 2; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; pancreatitis, alcoholic; pancreatitis, chronic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; pancreatitis, alcoholic; pancreatitis, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carotid artery diseases; diabetes mellitus type ii; diabetes mellitus, type 2; disease models, animal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carotid artery diseases; diabetes mellitus type ii; diabetes mellitus, type 2; disease models, animal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, type 2; psoriasis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, type 2; psoriasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; dementia; diabetes mellitus type ii; diabetes mellitus, type 2; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; dementia; diabetes mellitus type ii; diabetes mellitus, type 2; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; vitamin d deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; vitamin d deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; obesity; overweight Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; obesity; overweight in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; diabetic retinopathy; myocardial infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; diabetic retinopathy; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; diabetes mellitus type ii; diabetes mellitus, type 2; inflammation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; diabetes mellitus type ii; diabetes mellitus, type 2; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; lipid metabolism, inborn errors Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; lipid metabolism, inborn errors in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cataract; diabetes mellitus type ii; diabetes mellitus, type 2; myopia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cataract; diabetes mellitus type ii; diabetes mellitus, type 2; myopia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; hyperlipidemias Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; hyperlipidemias in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes complications; diabetes mellitus type ii; diabetes mellitus, type 2 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes complications; diabetes mellitus type ii; diabetes mellitus, type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; dyslipidemias Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; dyslipidemias in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; hyperglycemia; insulin resistance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; hyperglycemia; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; diabetes, gestational; gestational diabetes mellitus (disorder) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; diabetes, gestational; gestational diabetes mellitus (disorder) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; inflammation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes, type 2; hypertension; diabetes, type 1; albuminuria Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes, type 2; hypertension; diabetes, type 1; albuminuria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; hypercholesterolemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; hypercholesterolemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; diabetes, gestational; gestational diabetes mellitus ; iron overload Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; diabetes, gestational; gestational diabetes mellitus ; iron overload in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

albuminuria; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease albuminuria; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blindness; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic retinopathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blindness; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic retinopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies; intermittent claudication Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies; intermittent claudication in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; diabetic neuropathies Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; diabetic neuropathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary artery disease; diabetes mellitus type ii; diabetes mellitus, type 2 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary artery disease; diabetes mellitus type ii; diabetes mellitus, type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; diseases in twins Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; diseases in twins in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; death, sudden; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; death, sudden; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; myocardial infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic kidney insufficiency; diabetes mellitus type ii; diabetes mellitus, type 2; renal insufficiency, chronic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic kidney insufficiency; diabetes mellitus type ii; diabetes mellitus, type 2; renal insufficiency, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; diabetic retinopathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; diabetic retinopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies; diabetic nephropathies; diabetic nephropathy; diabetic neuropathies Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies; diabetic nephropathies; diabetic nephropathy; diabetic neuropathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic angiopathies Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic angiopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

type 1 and type 2 muscle fiber minicore regions Gene Set

From HPO Gene-Disease Associations

genes associated with the type 1 and type 2 muscle fiber minicore regions phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

type 1 fibers relatively smaller than type 2 fibers Gene Set

From HPO Gene-Disease Associations

genes associated with the type 1 fibers relatively smaller than type 2 fibers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

P-type ATPase, subfamily IIA, PMR1-type Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the P-type ATPase, subfamily IIA, PMR1-type protein domain from the InterPro Predicted Protein Domain Annotations dataset.

P-type ATPase, subfamily IIA, SERCA-type Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the P-type ATPase, subfamily IIA, SERCA-type protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Protein-tyrosine phosphatase, receptor type R/non-receptor type 5 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Protein-tyrosine phosphatase, receptor type R/non-receptor type 5 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ephrin receptor type-A /type-B Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ephrin receptor type-A /type-B protein domain from the InterPro Predicted Protein Domain Annotations dataset.

K/Cl co-transporter, type 1/type 3 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the K/Cl co-transporter, type 1/type 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ocular albinism, type i, nettleship-falls type Gene Set

From OMIM Gene-Disease Associations

genes associated with the ocular albinism, type i, nettleship-falls type phenotype from the curated OMIM Gene-Disease Associations dataset.

Bartter syndrome, type 3, with hypocalciuria Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bartter syndrome, type 3, with hypocalciuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Short rib-polydactyly syndrome, Majewski type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Short rib-polydactyly syndrome, Majewski type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Nephrotic syndrome, type 9 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Nephrotic syndrome, type 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Nephrotic syndrome, type 8 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Nephrotic syndrome, type 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bare Lymphocyte Syndrome, Type II, Complementation Group D Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bare Lymphocyte Syndrome, Type II, Complementation Group D phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Usher syndrome, type 1C Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Usher syndrome, type 1C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Usher syndrome, type 1F Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Usher syndrome, type 1F phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Usher syndrome, type 1D Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Usher syndrome, type 1D phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Usher syndrome, type 1J Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Usher syndrome, type 1J phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Duane syndrome type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Duane syndrome type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Usher syndrome, type 2C Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Usher syndrome, type 2C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Usher syndrome, type 2D Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Usher syndrome, type 2D phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bernard-Soulier syndrome, type A2, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bernard-Soulier syndrome, type A2, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Waardenburg syndrome type 2A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Waardenburg syndrome type 2A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Usher syndrome, type 2A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Usher syndrome, type 2A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bartter syndrome antenatal type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bartter syndrome antenatal type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bartter syndrome antenatal type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bartter syndrome antenatal type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bartter syndrome, type 4b Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bartter syndrome, type 4b phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Waardenburg syndrome type 4B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Waardenburg syndrome type 4B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Usher syndrome, type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Usher syndrome, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autoimmune lymphoproliferative syndrome, type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autoimmune lymphoproliferative syndrome, type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bartter syndrome type 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bartter syndrome type 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bartter syndrome type 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bartter syndrome type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Stickler syndrome, type 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Stickler syndrome, type 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Stickler syndrome, type 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Stickler syndrome, type 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Stickler syndrome, type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Stickler syndrome, type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Usher syndrome, type 1B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Usher syndrome, type 1B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Usher syndrome, type 1G Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Usher syndrome, type 1G phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ehlers-Danlos syndrome progeroid type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ehlers-Danlos syndrome progeroid type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Larsen syndrome, dominant type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Larsen syndrome, dominant type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ehlers-Danlos syndrome, musculocontractural type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ehlers-Danlos syndrome, musculocontractural type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Meckel syndrome type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Meckel syndrome type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Meckel syndrome type 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Meckel syndrome type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Meckel syndrome type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Meckel syndrome type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Meckel syndrome type 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Meckel syndrome type 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Meckel syndrome type 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Meckel syndrome type 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Nephrotic syndrome, type 10 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Nephrotic syndrome, type 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Popliteal pterygium syndrome lethal type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Popliteal pterygium syndrome lethal type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple pterygium syndrome Escobar type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple pterygium syndrome Escobar type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Schwartz Jampel syndrome type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Schwartz Jampel syndrome type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE V Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE V phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Acrocallosal syndrome, Schinzel type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Acrocallosal syndrome, Schinzel type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Meckel syndrome, type 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Meckel syndrome, type 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ehlers-Danlos syndrome, type 7B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ehlers-Danlos syndrome, type 7B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ehlers-Danlos syndrome, musculocontractural type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ehlers-Danlos syndrome, musculocontractural type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Carbohydrate-deficient glycoprotein syndrome type I Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Carbohydrate-deficient glycoprotein syndrome type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autoimmune polyglandular syndrome type 1, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autoimmune polyglandular syndrome type 1, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Nephrotic syndrome, type 5, with or without ocular abnormalities Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Nephrotic syndrome, type 5, with or without ocular abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Loeys-Dietz syndrome, type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Loeys-Dietz syndrome, type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Stickler syndrome type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Stickler syndrome type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Polyglandular autoimmune syndrome, type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Polyglandular autoimmune syndrome, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bernard-Soulier syndrome, type A1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bernard-Soulier syndrome, type A1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

AUTOIMMUNE POLYENDOCRINOPATHY SYNDROME, TYPE I Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the AUTOIMMUNE POLYENDOCRINOPATHY SYNDROME, TYPE I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Griscelli syndrome type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Griscelli syndrome type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Griscelli syndrome type 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Griscelli syndrome type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cockayne syndrome type A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cockayne syndrome type A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Leigh syndrome, French Canadian type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Leigh syndrome, French Canadian type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

XERODERMA PIGMENTOSUM, TYPE F/COCKAYNE SYNDROME Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the XERODERMA PIGMENTOSUM, TYPE F/COCKAYNE SYNDROME phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Loeys-Dietz syndrome type 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Loeys-Dietz syndrome type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Oto-palato-digital syndrome, type I Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Oto-palato-digital syndrome, type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cockayne syndrome, type B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cockayne syndrome, type B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

STICKLER SYNDROME, TYPE I, NONSYNDROMIC OCULAR Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the STICKLER SYNDROME, TYPE I, NONSYNDROMIC OCULAR phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autoimmune polyglandular syndrome type 1, with reversible metaphyseal dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autoimmune polyglandular syndrome type 1, with reversible metaphyseal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Stickler syndrome, type 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Stickler syndrome, type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Axenfeld-Rieger syndrome type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Axenfeld-Rieger syndrome type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Axenfeld-Rieger syndrome type 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Axenfeld-Rieger syndrome type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Trichorhinophalangeal syndrome type 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Trichorhinophalangeal syndrome type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glucose transporter type 1 deficiency syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glucose transporter type 1 deficiency syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ehlers-Danlos syndrome, type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ehlers-Danlos syndrome, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ehlers-Danlos syndrome, type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ehlers-Danlos syndrome, type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ehlers-Danlos syndrome, type 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ehlers-Danlos syndrome, type 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

THIAMINE METABOLISM DYSFUNCTION SYNDROME 5 (EPISODIC ENCEPHALOPATHY TYPE) Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the THIAMINE METABOLISM DYSFUNCTION SYNDROME 5 (EPISODIC ENCEPHALOPATHY TYPE) phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Nephrotic syndrome, type 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Nephrotic syndrome, type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bare lymphocyte syndrome type 2, complementation group E Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bare lymphocyte syndrome type 2, complementation group E phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bare lymphocyte syndrome type 2, complementation group A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bare lymphocyte syndrome type 2, complementation group A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Meckel syndrome, type 11 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Meckel syndrome, type 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Oto-palato-digital syndrome, type II Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Oto-palato-digital syndrome, type II phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Loeys-Dietz syndrome, type 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Loeys-Dietz syndrome, type 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Usher syndrome, type 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Usher syndrome, type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

BARE LYMPHOCYTE SYNDROME, TYPE II, COMPLEMENTATION GROUP B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the BARE LYMPHOCYTE SYNDROME, TYPE II, COMPLEMENTATION GROUP B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autoimmune lymphoproliferative syndrome, type 1a Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autoimmune lymphoproliferative syndrome, type 1a phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bernard-Soulier syndrome type C Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bernard-Soulier syndrome type C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ehlers-Danlos syndrome, type 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ehlers-Danlos syndrome, type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Peeling skin syndrome, acral type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Peeling skin syndrome, acral type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pena-Shokeir syndrome type I Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pena-Shokeir syndrome type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

USHER SYNDROME, TYPE IJ Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease USHER SYNDROME, TYPE IJ from the curated CTD Gene-Disease Associations dataset.

Bartter syndrome, antenatal type 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bartter syndrome, antenatal type 1 from the curated CTD Gene-Disease Associations dataset.

Waardenburg syndrome, type 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Waardenburg syndrome, type 4 from the curated CTD Gene-Disease Associations dataset.

Usher syndrome, type 1C Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Usher syndrome, type 1C from the curated CTD Gene-Disease Associations dataset.

Usher syndrome, type 1F Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Usher syndrome, type 1F from the curated CTD Gene-Disease Associations dataset.

Griscelli syndrome type 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Griscelli syndrome type 2 from the curated CTD Gene-Disease Associations dataset.

Griscelli syndrome type 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Griscelli syndrome type 3 from the curated CTD Gene-Disease Associations dataset.

Griscelli syndrome type 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Griscelli syndrome type 1 from the curated CTD Gene-Disease Associations dataset.

Usher Syndrome, Type IG Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Usher Syndrome, Type IG from the curated CTD Gene-Disease Associations dataset.

USHER SYNDROME, TYPE IIIA Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease USHER SYNDROME, TYPE IIIA from the curated CTD Gene-Disease Associations dataset.

Usher syndrome, type 2A Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Usher syndrome, type 2A from the curated CTD Gene-Disease Associations dataset.

USHER SYNDROME, TYPE IID Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease USHER SYNDROME, TYPE IID from the curated CTD Gene-Disease Associations dataset.

Waardenburg Syndrome, Type 2C Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Waardenburg Syndrome, Type 2C from the curated CTD Gene-Disease Associations dataset.

Heart-hand syndrome, Slovenian type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Heart-hand syndrome, Slovenian type from the curated CTD Gene-Disease Associations dataset.

Blepharophimosis syndrome type 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Blepharophimosis syndrome type 1 from the curated CTD Gene-Disease Associations dataset.

AXENFELD-RIEGER SYNDROME, TYPE 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease AXENFELD-RIEGER SYNDROME, TYPE 1 from the curated CTD Gene-Disease Associations dataset.

AXENFELD-RIEGER SYNDROME, TYPE 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease AXENFELD-RIEGER SYNDROME, TYPE 3 from the curated CTD Gene-Disease Associations dataset.

AXENFELD-RIEGER SYNDROME, TYPE 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease AXENFELD-RIEGER SYNDROME, TYPE 2 from the curated CTD Gene-Disease Associations dataset.

Usher Syndrome, Type IH Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Usher Syndrome, Type IH from the curated CTD Gene-Disease Associations dataset.

MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE from the curated CTD Gene-Disease Associations dataset.

Waardenburg Syndrome, Type 4b Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Waardenburg Syndrome, Type 4b from the curated CTD Gene-Disease Associations dataset.

Waardenburg Syndrome, Type 4c Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Waardenburg Syndrome, Type 4c from the curated CTD Gene-Disease Associations dataset.

Bartter syndrome, type 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bartter syndrome, type 3 from the curated CTD Gene-Disease Associations dataset.

Bare Lymphocyte Syndrome, Type I Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bare Lymphocyte Syndrome, Type I from the curated CTD Gene-Disease Associations dataset.

Meckel syndrome type 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Meckel syndrome type 2 from the curated CTD Gene-Disease Associations dataset.

Ehlers-Danlos Syndrome, Type VIII Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ehlers-Danlos Syndrome, Type VIII from the curated CTD Gene-Disease Associations dataset.

Simpson-Golabi-Behmel Syndrome, Type 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Simpson-Golabi-Behmel Syndrome, Type 2 from the curated CTD Gene-Disease Associations dataset.

Ehlers-Danlos syndrome type 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ehlers-Danlos syndrome type 3 from the curated CTD Gene-Disease Associations dataset.

Ehlers-Danlos syndrome type 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ehlers-Danlos syndrome type 2 from the curated CTD Gene-Disease Associations dataset.

Ehlers-Danlos syndrome type 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ehlers-Danlos syndrome type 1 from the curated CTD Gene-Disease Associations dataset.

Ehlers-Danlos syndrome type 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ehlers-Danlos syndrome type 6 from the curated CTD Gene-Disease Associations dataset.

Usher syndrome, type 1B Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Usher syndrome, type 1B from the curated CTD Gene-Disease Associations dataset.

Usher syndrome, type 1D Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Usher syndrome, type 1D from the curated CTD Gene-Disease Associations dataset.

Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.

Kenny-Caffey syndrome, Type 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Kenny-Caffey syndrome, Type 1 from the curated CTD Gene-Disease Associations dataset.

Meckel syndrome type 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Meckel syndrome type 3 from the curated CTD Gene-Disease Associations dataset.

Meckel syndrome type 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Meckel syndrome type 1 from the curated CTD Gene-Disease Associations dataset.

Alpha-Thalassemia Mental Retardation Syndrome, Deletion-Type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alpha-Thalassemia Mental Retardation Syndrome, Deletion-Type from the curated CTD Gene-Disease Associations dataset.

Laron syndrome type 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Laron syndrome type 2 from the curated CTD Gene-Disease Associations dataset.

Pena Shokeir syndrome, type 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pena Shokeir syndrome, type 1 from the curated CTD Gene-Disease Associations dataset.

Crigler Najjar syndrome, type 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Crigler Najjar syndrome, type 2 from the curated CTD Gene-Disease Associations dataset.

Long QT syndrome type 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Long QT syndrome type 3 from the curated CTD Gene-Disease Associations dataset.

Alport syndrome, recessive type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alport syndrome, recessive type from the curated CTD Gene-Disease Associations dataset.

Meckel Syndrome, Type 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Meckel Syndrome, Type 4 from the curated CTD Gene-Disease Associations dataset.

Usher syndrome, type 1E Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Usher syndrome, type 1E from the curated CTD Gene-Disease Associations dataset.

WAARDENBURG SYNDROME, TYPE 4A Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease WAARDENBURG SYNDROME, TYPE 4A from the curated CTD Gene-Disease Associations dataset.

Bartter Syndrome, Type 4A Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bartter Syndrome, Type 4A from the curated CTD Gene-Disease Associations dataset.

Bartter Syndrome, Type 4b Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bartter Syndrome, Type 4b from the curated CTD Gene-Disease Associations dataset.

BERNARD-SOULIER SYNDROME, TYPE A2, AUTOSOMAL DOMINANT Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease BERNARD-SOULIER SYNDROME, TYPE A2, AUTOSOMAL DOMINANT from the curated CTD Gene-Disease Associations dataset.

Hyper-IgM Immunodeficiency Syndrome, Type 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hyper-IgM Immunodeficiency Syndrome, Type 1 from the curated CTD Gene-Disease Associations dataset.

Bartter syndrome, antenatal , type 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bartter syndrome, antenatal , type 2 from the curated CTD Gene-Disease Associations dataset.

Meckel Syndrome, Type 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Meckel Syndrome, Type 6 from the curated CTD Gene-Disease Associations dataset.

Meckel Syndrome, Type 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Meckel Syndrome, Type 5 from the curated CTD Gene-Disease Associations dataset.

Waardenburg Syndrome, Type 2D Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Waardenburg Syndrome, Type 2D from the curated CTD Gene-Disease Associations dataset.

Autoimmune polyendocrinopathy syndrome, type 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Autoimmune polyendocrinopathy syndrome, type 1 from the curated CTD Gene-Disease Associations dataset.

Trichorhinophalangeal Syndrome, Type III Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Trichorhinophalangeal Syndrome, Type III from the curated CTD Gene-Disease Associations dataset.

EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE 1 from the curated CTD Gene-Disease Associations dataset.

Oto-palato-digital syndrome, type 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Oto-palato-digital syndrome, type 2 from the curated CTD Gene-Disease Associations dataset.

Leigh syndrome , French Canadian type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Leigh syndrome , French Canadian type from the curated CTD Gene-Disease Associations dataset.

Stickler syndrome, type 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Stickler syndrome, type 3 from the curated CTD Gene-Disease Associations dataset.

Stickler syndrome, type 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Stickler syndrome, type 2 from the curated CTD Gene-Disease Associations dataset.

Orofaciodigital syndrome type1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Orofaciodigital syndrome type1 from the curated CTD Gene-Disease Associations dataset.

Klippel Feil syndrome dominant type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Klippel Feil syndrome dominant type from the curated CTD Gene-Disease Associations dataset.

Waardenburg syndrome type 2B Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Waardenburg syndrome type 2B from the curated CTD Gene-Disease Associations dataset.

Waardenburg syndrome type 2A Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Waardenburg syndrome type 2A from the curated CTD Gene-Disease Associations dataset.

Waardenburg syndrome type 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Waardenburg syndrome type 2 from the curated CTD Gene-Disease Associations dataset.

Scapuloperoneal Syndrome, Neurogenic, Kaeser Type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Scapuloperoneal Syndrome, Neurogenic, Kaeser Type from the curated CTD Gene-Disease Associations dataset.

NEPHROTIC SYNDROME, TYPE 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NEPHROTIC SYNDROME, TYPE 3 from the curated CTD Gene-Disease Associations dataset.

NEPHROTIC SYNDROME, TYPE 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NEPHROTIC SYNDROME, TYPE 4 from the curated CTD Gene-Disease Associations dataset.

Autoimmune Lymphoproliferative Syndrome, Type IIA Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Autoimmune Lymphoproliferative Syndrome, Type IIA from the curated CTD Gene-Disease Associations dataset.

Larsen syndrome, dominant type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Larsen syndrome, dominant type from the curated CTD Gene-Disease Associations dataset.

Stickler Syndrome, Type I, Nonsyndromic Ocular Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Stickler Syndrome, Type I, Nonsyndromic Ocular from the curated CTD Gene-Disease Associations dataset.

Ehlers-Danlos Syndrome, Type VII, Autosomal Recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ehlers-Danlos Syndrome, Type VII, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.

Stickler syndrome, type 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Stickler syndrome, type 1 from the curated CTD Gene-Disease Associations dataset.

Oto-Palato-digital syndrome type 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Oto-Palato-digital syndrome type 1 from the curated CTD Gene-Disease Associations dataset.

TRICHORHINOPHALANGEAL SYNDROME, TYPE I Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease TRICHORHINOPHALANGEAL SYNDROME, TYPE I from the curated CTD Gene-Disease Associations dataset.

Orofaciodigital syndrome, Shashi type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Orofaciodigital syndrome, Shashi type from the curated CTD Gene-Disease Associations dataset.

Peeling skin syndrome, acral type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Peeling skin syndrome, acral type from the curated CTD Gene-Disease Associations dataset.

trichorhinophalangeal syndrome type ii Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease trichorhinophalangeal syndrome type ii from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

autoimmune polyendocrine syndrome type 2 Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease autoimmune polyendocrine syndrome type 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

autoimmune polyendocrine syndrome type 1 Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease autoimmune polyendocrine syndrome type 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

trichorhinophalangeal syndrome type ii Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease trichorhinophalangeal syndrome type ii in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

type i ehlers-danlos syndrome Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease type i ehlers-danlos syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

type vi ehlers-danlos syndrome Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease type vi ehlers-danlos syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

trichorhinophalangeal syndrome type i Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease trichorhinophalangeal syndrome type i in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

retinitis pigmentosa; leber congenital amaurosis; usher syndrome type i Gene Set

From GAD Gene-Disease Associations

genes associated with the disease retinitis pigmentosa; leber congenital amaurosis; usher syndrome type i in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus, type 2; long qt syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, type 2; long qt syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus, type 2; inflammation; insulin resistance; metabolic syndrome x; myocardial infarction; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, type 2; inflammation; insulin resistance; metabolic syndrome x; myocardial infarction; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus, type 2; diabetic angiopathies; long qt syndrome; myocardial infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, type 2; diabetic angiopathies; long qt syndrome; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lupus erythematosus; rheumatoid arthritis; sjogren's syndrome; diabetes, type 1 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lupus erythematosus; rheumatoid arthritis; sjogren's syndrome; diabetes, type 1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes, type 2; metabolic syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes, type 2; metabolic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ehlers-danlos syndrome type iv Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ehlers-danlos syndrome type iv in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus, type 2; fatty liver; metabolic syndrome x Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, type 2; fatty liver; metabolic syndrome x in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes, type 2; polycystic ovarian syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes, type 2; polycystic ovarian syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus, type 2; obesity; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, type 2; obesity; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus, type 2; metabolic syndrome x; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, type 2; metabolic syndrome x; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic ketoacidosis; disease susceptibility; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic ketoacidosis; disease susceptibility; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes, type 2 ; metabolic syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes, type 2 ; metabolic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, rheumatoid; autoimmune diseases; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; lupus erythematosus, systemic; rheumatoid arthritis; sjogren's syndrome; systemic lupus erythematosus Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, rheumatoid; autoimmune diseases; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; lupus erythematosus, systemic; rheumatoid arthritis; sjogren's syndrome; systemic lupus erythematosus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus, type 2; metabolic syndrome x Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, type 2; metabolic syndrome x in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

mild ehlers-danlos syndrome type iv Gene Set

From GAD Gene-Disease Associations

genes associated with the disease mild ehlers-danlos syndrome type iv in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes, type 2; hypertension; metabolic syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes, type 2; hypertension; metabolic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes, type 2; glucose tolerance; metabolic syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes, type 2; glucose tolerance; metabolic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus, type 2; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, type 2; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus; diabetes mellitus, type 2; insulin resistance; metabolic syndrome x Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus; diabetes mellitus, type 2; insulin resistance; metabolic syndrome x in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes, type 2; polymetabolic syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes, type 2; polymetabolic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus, type 2; insulin resistance; metabolic syndrome x Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, type 2; insulin resistance; metabolic syndrome x in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Usher syndrome type-1C protein-binding protein 1, PDZ domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Usher syndrome type-1C protein-binding protein 1, PDZ domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

{retinal disease in usher syndrome type iia, modifier of} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {retinal disease in usher syndrome type iia, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset.

scapuloperoneal syndrome, neurogenic, kaeser type Gene Set

From OMIM Gene-Disease Associations

genes associated with the scapuloperoneal syndrome, neurogenic, kaeser type phenotype from the curated OMIM Gene-Disease Associations dataset.

ehlers-danlos syndrome, progeroid type, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ehlers-danlos syndrome, progeroid type, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

ehlers-danlos syndrome, progeroid type, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ehlers-danlos syndrome, progeroid type, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

autoimmune lymphoproliferative syndrome, type ib Gene Set

From OMIM Gene-Disease Associations

genes associated with the autoimmune lymphoproliferative syndrome, type ib phenotype from the curated OMIM Gene-Disease Associations dataset.

autoimmune lymphoproliferative syndrome, type ia Gene Set

From OMIM Gene-Disease Associations

genes associated with the autoimmune lymphoproliferative syndrome, type ia phenotype from the curated OMIM Gene-Disease Associations dataset.

autoimmune lymphoproliferative syndrome, type ii Gene Set

From OMIM Gene-Disease Associations

genes associated with the autoimmune lymphoproliferative syndrome, type ii phenotype from the curated OMIM Gene-Disease Associations dataset.

opitz gbbb syndrome, type i Gene Set

From OMIM Gene-Disease Associations

genes associated with the opitz gbbb syndrome, type i phenotype from the curated OMIM Gene-Disease Associations dataset.

ehlers-danlos syndrome, musculocontractural type 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ehlers-danlos syndrome, musculocontractural type 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation syndrome, x-linked, siderius type Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation syndrome, x-linked, siderius type phenotype from the curated OMIM Gene-Disease Associations dataset.

waardenburg syndrome, type 2e, with or without neurologic involvement Gene Set

From OMIM Gene-Disease Associations

genes associated with the waardenburg syndrome, type 2e, with or without neurologic involvement phenotype from the curated OMIM Gene-Disease Associations dataset.

popliteal pterygium syndrome 2, lethal type Gene Set

From OMIM Gene-Disease Associations

genes associated with the popliteal pterygium syndrome 2, lethal type phenotype from the curated OMIM Gene-Disease Associations dataset.

ehlers-danlos syndrome, type i Gene Set

From OMIM Gene-Disease Associations

genes associated with the ehlers-danlos syndrome, type i phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation syndrome, x-linked, armfield type Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation syndrome, x-linked, armfield type phenotype from the curated OMIM Gene-Disease Associations dataset.

multiple pterygium syndrome, lethal type Gene Set

From OMIM Gene-Disease Associations

genes associated with the multiple pterygium syndrome, lethal type phenotype from the curated OMIM Gene-Disease Associations dataset.

usher syndrome, type 1f Gene Set

From OMIM Gene-Disease Associations

genes associated with the usher syndrome, type 1f phenotype from the curated OMIM Gene-Disease Associations dataset.

usher syndrome, type 1g Gene Set

From OMIM Gene-Disease Associations

genes associated with the usher syndrome, type 1g phenotype from the curated OMIM Gene-Disease Associations dataset.

usher syndrome, type 1d Gene Set

From OMIM Gene-Disease Associations

genes associated with the usher syndrome, type 1d phenotype from the curated OMIM Gene-Disease Associations dataset.

crigler-najjar syndrome, type i Gene Set

From OMIM Gene-Disease Associations

genes associated with the crigler-najjar syndrome, type i phenotype from the curated OMIM Gene-Disease Associations dataset.

stickler syndrome, type iii Gene Set

From OMIM Gene-Disease Associations

genes associated with the stickler syndrome, type iii phenotype from the curated OMIM Gene-Disease Associations dataset.

usher syndrome, type ij Gene Set

From OMIM Gene-Disease Associations

genes associated with the usher syndrome, type ij phenotype from the curated OMIM Gene-Disease Associations dataset.

usher syndrome, type ik Gene Set

From OMIM Gene-Disease Associations

genes associated with the usher syndrome, type ik phenotype from the curated OMIM Gene-Disease Associations dataset.

leigh syndrome, french-canadian type Gene Set

From OMIM Gene-Disease Associations

genes associated with the leigh syndrome, french-canadian type phenotype from the curated OMIM Gene-Disease Associations dataset.

ehlers-danlos syndrome, type vi Gene Set

From OMIM Gene-Disease Associations

genes associated with the ehlers-danlos syndrome, type vi phenotype from the curated OMIM Gene-Disease Associations dataset.

ehlers-danlos syndrome, type viii Gene Set

From OMIM Gene-Disease Associations

genes associated with the ehlers-danlos syndrome, type viii phenotype from the curated OMIM Gene-Disease Associations dataset.

ehlers-danlos syndrome, type viic Gene Set

From OMIM Gene-Disease Associations

genes associated with the ehlers-danlos syndrome, type viic phenotype from the curated OMIM Gene-Disease Associations dataset.

ehlers-danlos syndrome, type viib Gene Set

From OMIM Gene-Disease Associations

genes associated with the ehlers-danlos syndrome, type viib phenotype from the curated OMIM Gene-Disease Associations dataset.

ehlers-danlos syndrome, type viia Gene Set

From OMIM Gene-Disease Associations

genes associated with the ehlers-danlos syndrome, type viia phenotype from the curated OMIM Gene-Disease Associations dataset.

autoimmune lymphoproliferative syndrome, type iii Gene Set

From OMIM Gene-Disease Associations

genes associated with the autoimmune lymphoproliferative syndrome, type iii phenotype from the curated OMIM Gene-Disease Associations dataset.

stickler syndrome, type i Gene Set

From OMIM Gene-Disease Associations

genes associated with the stickler syndrome, type i phenotype from the curated OMIM Gene-Disease Associations dataset.

?ehlers-danlos syndrome, musculocontractural type 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?ehlers-danlos syndrome, musculocontractural type 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

waardenburg syndrome, type 4b Gene Set

From OMIM Gene-Disease Associations

genes associated with the waardenburg syndrome, type 4b phenotype from the curated OMIM Gene-Disease Associations dataset.

waardenburg syndrome, type 4c Gene Set

From OMIM Gene-Disease Associations

genes associated with the waardenburg syndrome, type 4c phenotype from the curated OMIM Gene-Disease Associations dataset.

waardenburg syndrome, type 4a Gene Set

From OMIM Gene-Disease Associations

genes associated with the waardenburg syndrome, type 4a phenotype from the curated OMIM Gene-Disease Associations dataset.

ehlers-danlos syndrome, autosomal dominant, hypermobility type Gene Set

From OMIM Gene-Disease Associations

genes associated with the ehlers-danlos syndrome, autosomal dominant, hypermobility type phenotype from the curated OMIM Gene-Disease Associations dataset.

thiamine metabolism dysfunction syndrome 4 (progressive polyneuropathy type) Gene Set

From OMIM Gene-Disease Associations

genes associated with the thiamine metabolism dysfunction syndrome 4 (progressive polyneuropathy type) phenotype from the curated OMIM Gene-Disease Associations dataset.

usher syndrome, type 1d/f digenic Gene Set

From OMIM Gene-Disease Associations

genes associated with the usher syndrome, type 1d/f digenic phenotype from the curated OMIM Gene-Disease Associations dataset.

griscelli syndrome, type 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the griscelli syndrome, type 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

griscelli syndrome, type 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the griscelli syndrome, type 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

griscelli syndrome, type 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the griscelli syndrome, type 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

bare lymphocyte syndrome, type i Gene Set

From OMIM Gene-Disease Associations

genes associated with the bare lymphocyte syndrome, type i phenotype from the curated OMIM Gene-Disease Associations dataset.

autoimmune polyendocrinopathy syndrome , type i, with or without reversible metaphyseal dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the autoimmune polyendocrinopathy syndrome , type i, with or without reversible metaphyseal dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

knobloch syndrome, type 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the knobloch syndrome, type 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

heart-hand syndrome, slovenian type Gene Set

From OMIM Gene-Disease Associations

genes associated with the heart-hand syndrome, slovenian type phenotype from the curated OMIM Gene-Disease Associations dataset.

xeroderma pigmentosum, type f/cockayne syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the xeroderma pigmentosum, type f/cockayne syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

nephrotic syndrome, type 10 Gene Set

From OMIM Gene-Disease Associations

genes associated with the nephrotic syndrome, type 10 phenotype from the curated OMIM Gene-Disease Associations dataset.

trichorhinophalangeal syndrome, type iii Gene Set

From OMIM Gene-Disease Associations

genes associated with the trichorhinophalangeal syndrome, type iii phenotype from the curated OMIM Gene-Disease Associations dataset.

waardenburg syndrome, type 2a Gene Set

From OMIM Gene-Disease Associations

genes associated with the waardenburg syndrome, type 2a phenotype from the curated OMIM Gene-Disease Associations dataset.

waardenburg syndrome, type 2b Gene Set

From OMIM Gene-Disease Associations

genes associated with the waardenburg syndrome, type 2b phenotype from the curated OMIM Gene-Disease Associations dataset.

waardenburg syndrome, type 2c Gene Set

From OMIM Gene-Disease Associations

genes associated with the waardenburg syndrome, type 2c phenotype from the curated OMIM Gene-Disease Associations dataset.

waardenburg syndrome, type 2d Gene Set

From OMIM Gene-Disease Associations

genes associated with the waardenburg syndrome, type 2d phenotype from the curated OMIM Gene-Disease Associations dataset.

ehlers-danlos syndrome, type iii Gene Set

From OMIM Gene-Disease Associations

genes associated with the ehlers-danlos syndrome, type iii phenotype from the curated OMIM Gene-Disease Associations dataset.

bartter syndrome, type 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the bartter syndrome, type 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

amelogenesis imperfecta, type ig (enamel-renal syndrome) Gene Set

From OMIM Gene-Disease Associations

genes associated with the amelogenesis imperfecta, type ig (enamel-renal syndrome) phenotype from the curated OMIM Gene-Disease Associations dataset.

axenfeld-rieger syndrome, type 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the axenfeld-rieger syndrome, type 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

axenfeld-rieger syndrome, type 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the axenfeld-rieger syndrome, type 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

bernard-soulier syndrome, type a2 (dominant) Gene Set

From OMIM Gene-Disease Associations

genes associated with the bernard-soulier syndrome, type a2 (dominant) phenotype from the curated OMIM Gene-Disease Associations dataset.

bare lymphocyte syndrome, type ii, complementation group c Gene Set

From OMIM Gene-Disease Associations

genes associated with the bare lymphocyte syndrome, type ii, complementation group c phenotype from the curated OMIM Gene-Disease Associations dataset.

bare lymphocyte syndrome, type ii, complementation group a Gene Set

From OMIM Gene-Disease Associations

genes associated with the bare lymphocyte syndrome, type ii, complementation group a phenotype from the curated OMIM Gene-Disease Associations dataset.

bare lymphocyte syndrome, type ii, complementation group d Gene Set

From OMIM Gene-Disease Associations

genes associated with the bare lymphocyte syndrome, type ii, complementation group d phenotype from the curated OMIM Gene-Disease Associations dataset.

simpson-golabi-behmel syndrome, type 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the simpson-golabi-behmel syndrome, type 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

simpson-golabi-behmel syndrome, type 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the simpson-golabi-behmel syndrome, type 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

ehlers-danlos syndrome, type ii Gene Set

From OMIM Gene-Disease Associations

genes associated with the ehlers-danlos syndrome, type ii phenotype from the curated OMIM Gene-Disease Associations dataset.

ehlers-danlos syndrome, type iv Gene Set

From OMIM Gene-Disease Associations

genes associated with the ehlers-danlos syndrome, type iv phenotype from the curated OMIM Gene-Disease Associations dataset.

usher syndrome, type 3a Gene Set

From OMIM Gene-Disease Associations

genes associated with the usher syndrome, type 3a phenotype from the curated OMIM Gene-Disease Associations dataset.

usher syndrome, type 1b Gene Set

From OMIM Gene-Disease Associations

genes associated with the usher syndrome, type 1b phenotype from the curated OMIM Gene-Disease Associations dataset.

usher syndrome, type 1c Gene Set

From OMIM Gene-Disease Associations

genes associated with the usher syndrome, type 1c phenotype from the curated OMIM Gene-Disease Associations dataset.

usher syndrome, type 1e Gene Set

From OMIM Gene-Disease Associations

genes associated with the usher syndrome, type 1e phenotype from the curated OMIM Gene-Disease Associations dataset.

usher syndrome, type 1h Gene Set

From OMIM Gene-Disease Associations

genes associated with the usher syndrome, type 1h phenotype from the curated OMIM Gene-Disease Associations dataset.

meckel syndrome, type 11 Gene Set

From OMIM Gene-Disease Associations

genes associated with the meckel syndrome, type 11 phenotype from the curated OMIM Gene-Disease Associations dataset.

stickler syndrome, type iv Gene Set

From OMIM Gene-Disease Associations

genes associated with the stickler syndrome, type iv phenotype from the curated OMIM Gene-Disease Associations dataset.

bare lymphocyte syndrome, type i, due to tap2 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the bare lymphocyte syndrome, type i, due to tap2 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

?stickler syndrome, type v Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?stickler syndrome, type v phenotype from the curated OMIM Gene-Disease Associations dataset.

bernard-soulier syndrome, type a1 (recessive) Gene Set

From OMIM Gene-Disease Associations

genes associated with the bernard-soulier syndrome, type a1 (recessive) phenotype from the curated OMIM Gene-Disease Associations dataset.

?autoimmune lymphoproliferative syndrome, type iib Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?autoimmune lymphoproliferative syndrome, type iib phenotype from the curated OMIM Gene-Disease Associations dataset.

bernard-soulier syndrome, type c Gene Set

From OMIM Gene-Disease Associations

genes associated with the bernard-soulier syndrome, type c phenotype from the curated OMIM Gene-Disease Associations dataset.

bernard-soulier syndrome, type b Gene Set

From OMIM Gene-Disease Associations

genes associated with the bernard-soulier syndrome, type b phenotype from the curated OMIM Gene-Disease Associations dataset.

loeys-dietz syndrome, type 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the loeys-dietz syndrome, type 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

loeys-dietz syndrome, type 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the loeys-dietz syndrome, type 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

loeys-dietz syndrome, type 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the loeys-dietz syndrome, type 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

bartter syndrome, type 4a Gene Set

From OMIM Gene-Disease Associations

genes associated with the bartter syndrome, type 4a phenotype from the curated OMIM Gene-Disease Associations dataset.

persistent mullerian duct syndrome, type i Gene Set

From OMIM Gene-Disease Associations

genes associated with the persistent mullerian duct syndrome, type i phenotype from the curated OMIM Gene-Disease Associations dataset.

autoimmune lymphoproliferative syndrome, type v Gene Set

From OMIM Gene-Disease Associations

genes associated with the autoimmune lymphoproliferative syndrome, type v phenotype from the curated OMIM Gene-Disease Associations dataset.

schwartz-jampel syndrome, type 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the schwartz-jampel syndrome, type 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

loeys-dietz syndrome, type 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the loeys-dietz syndrome, type 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

otopalatodigital syndrome, type i Gene Set

From OMIM Gene-Disease Associations

genes associated with the otopalatodigital syndrome, type i phenotype from the curated OMIM Gene-Disease Associations dataset.

nephrotic syndrome, type 8 Gene Set

From OMIM Gene-Disease Associations

genes associated with the nephrotic syndrome, type 8 phenotype from the curated OMIM Gene-Disease Associations dataset.

usher syndrome, type 2c, gpr98/pdzd7 digenic Gene Set

From OMIM Gene-Disease Associations

genes associated with the usher syndrome, type 2c, gpr98/pdzd7 digenic phenotype from the curated OMIM Gene-Disease Associations dataset.

scapuloperoneal syndrome, myopathic type Gene Set

From OMIM Gene-Disease Associations

genes associated with the scapuloperoneal syndrome, myopathic type phenotype from the curated OMIM Gene-Disease Associations dataset.

opitz gbbb syndrome, type ii Gene Set

From OMIM Gene-Disease Associations

genes associated with the opitz gbbb syndrome, type ii phenotype from the curated OMIM Gene-Disease Associations dataset.

waardenburg syndrome, type 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the waardenburg syndrome, type 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

waardenburg syndrome, type 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the waardenburg syndrome, type 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

persistent mullerian duct syndrome, type ii Gene Set

From OMIM Gene-Disease Associations

genes associated with the persistent mullerian duct syndrome, type ii phenotype from the curated OMIM Gene-Disease Associations dataset.

autoimmune lymphoproliferative syndrome type iv Gene Set

From OMIM Gene-Disease Associations

genes associated with the autoimmune lymphoproliferative syndrome type iv phenotype from the curated OMIM Gene-Disease Associations dataset.

stickler syndrome, type ii Gene Set

From OMIM Gene-Disease Associations

genes associated with the stickler syndrome, type ii phenotype from the curated OMIM Gene-Disease Associations dataset.

usher syndrome type 3b Gene Set

From OMIM Gene-Disease Associations

genes associated with the usher syndrome type 3b phenotype from the curated OMIM Gene-Disease Associations dataset.

otopalatodigital syndrome, type ii Gene Set

From OMIM Gene-Disease Associations

genes associated with the otopalatodigital syndrome, type ii phenotype from the curated OMIM Gene-Disease Associations dataset.

alpha-thalassemia/mental retardation syndrome, type 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the alpha-thalassemia/mental retardation syndrome, type 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type) Gene Set

From OMIM Gene-Disease Associations

genes associated with the thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type) phenotype from the curated OMIM Gene-Disease Associations dataset.

nephrotic syndrome, type 9 Gene Set

From OMIM Gene-Disease Associations

genes associated with the nephrotic syndrome, type 9 phenotype from the curated OMIM Gene-Disease Associations dataset.

nephrotic syndrome, type 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the nephrotic syndrome, type 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

nephrotic syndrome, type 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the nephrotic syndrome, type 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

nephrotic syndrome, type 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the nephrotic syndrome, type 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

nephrotic syndrome, type 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the nephrotic syndrome, type 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

nephrotic syndrome, type 7 Gene Set

From OMIM Gene-Disease Associations

genes associated with the nephrotic syndrome, type 7 phenotype from the curated OMIM Gene-Disease Associations dataset.

nephrotic syndrome, type 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the nephrotic syndrome, type 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

bartter syndrome, type 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the bartter syndrome, type 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

bartter syndrome, type 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the bartter syndrome, type 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

bartter syndrome, type 4b, digenic Gene Set

From OMIM Gene-Disease Associations

genes associated with the bartter syndrome, type 4b, digenic phenotype from the curated OMIM Gene-Disease Associations dataset.

kenny-caffey syndrome, type 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the kenny-caffey syndrome, type 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

cockayne syndrome, type b Gene Set

From OMIM Gene-Disease Associations

genes associated with the cockayne syndrome, type b phenotype from the curated OMIM Gene-Disease Associations dataset.

cockayne syndrome, type a Gene Set

From OMIM Gene-Disease Associations

genes associated with the cockayne syndrome, type a phenotype from the curated OMIM Gene-Disease Associations dataset.

rieger syndrome, type 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the rieger syndrome, type 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

usher syndrome, type 2a Gene Set

From OMIM Gene-Disease Associations

genes associated with the usher syndrome, type 2a phenotype from the curated OMIM Gene-Disease Associations dataset.

thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2) Gene Set

From OMIM Gene-Disease Associations

genes associated with the thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2) phenotype from the curated OMIM Gene-Disease Associations dataset.

bare lymphocyte syndrome, type ii, complementation group e Gene Set

From OMIM Gene-Disease Associations

genes associated with the bare lymphocyte syndrome, type ii, complementation group e phenotype from the curated OMIM Gene-Disease Associations dataset.

usher syndrome, type iic, gpr98/pdzd7 digenic Gene Set

From OMIM Gene-Disease Associations

genes associated with the usher syndrome, type iic, gpr98/pdzd7 digenic phenotype from the curated OMIM Gene-Disease Associations dataset.

trichorhinophalangeal syndrome, type i Gene Set

From OMIM Gene-Disease Associations

genes associated with the trichorhinophalangeal syndrome, type i phenotype from the curated OMIM Gene-Disease Associations dataset.

nephrotic syndrome, type 5, with or without ocular abnormalities Gene Set

From OMIM Gene-Disease Associations

genes associated with the nephrotic syndrome, type 5, with or without ocular abnormalities phenotype from the curated OMIM Gene-Disease Associations dataset.

usher syndrome, type 2c Gene Set

From OMIM Gene-Disease Associations

genes associated with the usher syndrome, type 2c phenotype from the curated OMIM Gene-Disease Associations dataset.

usher syndrome, type 2d Gene Set

From OMIM Gene-Disease Associations

genes associated with the usher syndrome, type 2d phenotype from the curated OMIM Gene-Disease Associations dataset.

crigler-najjar syndrome, type ii Gene Set

From OMIM Gene-Disease Associations

genes associated with the crigler-najjar syndrome, type ii phenotype from the curated OMIM Gene-Disease Associations dataset.

Waardenburg syndrome type 2 Gene Set

From PhosphoSitePlus Phosphosite-Disease Associations

proteins associated with the disease Waardenburg syndrome type 2 from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.

Mitochondrial diseases Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mitochondrial diseases phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mitochondrial complex I deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mitochondrial complex I deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

RRM2B-related mitochondrial disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the RRM2B-related mitochondrial disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Nuclearly-encoded mitochondrial complex V (ATP synthase) deficiency 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Nuclearly-encoded mitochondrial complex V (ATP synthase) deficiency 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Nuclearly-encoded mitochondrial complex V (ATP synthase) deficiency 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Nuclearly-encoded mitochondrial complex V (ATP synthase) deficiency 2 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.

Mitochondrial complex III deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mitochondrial complex III deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mitochondrial phosphate carrier deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mitochondrial phosphate carrier deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mitochondrial pyruvate carrier deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mitochondrial pyruvate carrier deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mitochondrial trifunctional protein deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mitochondrial trifunctional protein deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mitochondrial complex II deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mitochondrial complex II deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

mitochondrial envelope Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial envelope cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial respiratory chain complex ii Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial respiratory chain complex ii cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial respiratory chain complex iv Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial respiratory chain complex iv cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial outer membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial outer membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial proton-transporting atp synthase complex, catalytic core f(1) Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial proton-transporting atp synthase complex, catalytic core f(1) cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial alpha-ketoglutarate dehydrogenase complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial alpha-ketoglutarate dehydrogenase complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial respiratory chain complex i Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial respiratory chain complex i cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

integral component of mitochondrial membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the integral component of mitochondrial membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial inner membrane peptidase complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial inner membrane peptidase complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial endopeptidase clp complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial endopeptidase clp complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial fatty acid beta-oxidation multienzyme complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial fatty acid beta-oxidation multienzyme complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial small ribosomal subunit Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial small ribosomal subunit cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

intrinsic component of mitochondrial outer membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the intrinsic component of mitochondrial outer membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

extrinsic component of mitochondrial outer membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the extrinsic component of mitochondrial outer membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial part Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial part cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

sperm mitochondrial sheath Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the sperm mitochondrial sheath cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

integral component of mitochondrial outer membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the integral component of mitochondrial outer membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial large ribosomal subunit Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial large ribosomal subunit cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial proton-transporting atp synthase complex, coupling factor f(o) Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial proton-transporting atp synthase complex, coupling factor f(o) cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial membrane part Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial membrane part cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial nucleoid Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial nucleoid cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial inner membrane presequence translocase complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial inner membrane presequence translocase complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial ribosome Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial ribosome cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

intrinsic component of mitochondrial inner membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the intrinsic component of mitochondrial inner membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial outer membrane translocase complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial outer membrane translocase complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial crista Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial crista cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

integral component of mitochondrial inner membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the integral component of mitochondrial inner membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

intrinsic component of mitochondrial membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the intrinsic component of mitochondrial membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

extrinsic component of mitochondrial inner membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the extrinsic component of mitochondrial inner membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial respiratory chain Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial respiratory chain cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial degradosome Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial degradosome cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial proton-transporting atp synthase complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial proton-transporting atp synthase complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial inner membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial inner membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial chromosome Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial chromosome cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial permeability transition pore complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial permeability transition pore complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial intermembrane space protein transporter complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial intermembrane space protein transporter complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial intermembrane space Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial intermembrane space 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.

mitochondrial respiratory chain complex iii Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial respiratory chain complex iii cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial pyruvate dehydrogenase complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial pyruvate dehydrogenase complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial proton-transporting atp synthase, catalytic core Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial proton-transporting atp synthase, catalytic core cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial tricarboxylic acid cycle enzyme complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial tricarboxylic acid cycle enzyme complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial matrix Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial matrix cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

cytoplasmic side of mitochondrial outer membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the cytoplasmic side of mitochondrial outer membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial envelope Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial envelope cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial respiratory chain complex iv Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial respiratory chain complex iv cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial outer membrane Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial outer membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial prohibitin complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial prohibitin complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial alpha-ketoglutarate dehydrogenase complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial alpha-ketoglutarate dehydrogenase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial respiratory chain complex i Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial respiratory chain complex i cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

integral component of mitochondrial membrane Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the integral component of mitochondrial membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial inner membrane peptidase complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial inner membrane peptidase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial fatty acid beta-oxidation multienzyme complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial fatty acid beta-oxidation multienzyme complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial small ribosomal subunit Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial small ribosomal subunit cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

3-methylcrotonyl-coa carboxylase complex, mitochondrial Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the 3-methylcrotonyl-coa carboxylase complex, mitochondrial cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial part Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial part cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

sperm mitochondrial sheath Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the sperm mitochondrial sheath cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial intermembrane space protein transporter complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial intermembrane space protein transporter complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial large ribosomal subunit Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial large ribosomal subunit cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial membrane part Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial membrane part cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial ribonuclease p complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial ribonuclease p complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial nucleoid Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial nucleoid cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial inner membrane presequence translocase complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial inner membrane presequence translocase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial ribosome Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial ribosome cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial respiratory chain supercomplex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial respiratory chain supercomplex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

intrinsic component of mitochondrial inner membrane Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the intrinsic component of mitochondrial inner membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial outer membrane translocase complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial outer membrane translocase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial crista Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial crista cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

integral component of mitochondrial inner membrane Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the integral component of mitochondrial inner membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

intrinsic component of mitochondrial membrane Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the intrinsic component of mitochondrial membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial respiratory chain Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial respiratory chain cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial derivative Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial derivative cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial degradosome Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial degradosome cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial cloud Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial cloud cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial proton-transporting atp synthase complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial proton-transporting atp synthase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial membrane Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial inner membrane Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial inner membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial creatine kinase complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial creatine kinase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial chromosome Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial chromosome cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial permeability transition pore complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial permeability transition pore complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial intermembrane space Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial intermembrane space cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial crista junction Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial crista junction cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial electron transfer flavoprotein complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial electron transfer flavoprotein complex 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.

mitochondrial respiratory chain complex ii Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial respiratory chain complex ii cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial processing peptidase complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial processing peptidase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial inner membrane protein insertion complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial inner membrane protein insertion complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial respiratory chain complex iii Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial respiratory chain complex iii cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial pyruvate dehydrogenase complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial pyruvate dehydrogenase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial tricarboxylic acid cycle enzyme complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial tricarboxylic acid cycle enzyme complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial matrix Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial matrix cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

Respiratory chain complex I, mitochondrial Gene Set

From CORUM Protein Complexes

proteins in the Respiratory chain complex I, mitochondrial protein complex from the CORUM Protein Complexes dataset.

Respiratory chain complex I (incomplete NDUFAF1 assembly), mitochondrial Gene Set

From CORUM Protein Complexes

proteins in the Respiratory chain complex I (incomplete NDUFAF1 assembly), mitochondrial protein complex from the CORUM Protein Complexes dataset.

Respiratory chain complex I (intermediate VII/650kD), mitochondrial Gene Set

From CORUM Protein Complexes

proteins in the Respiratory chain complex I (intermediate VII/650kD), mitochondrial protein complex from the CORUM Protein Complexes dataset.

Respiratory chain complex I (lambda subunit) mitochondrial Gene Set

From CORUM Protein Complexes

proteins in the Respiratory chain complex I (lambda subunit) mitochondrial protein complex from the CORUM Protein Complexes dataset.

Cytochrome bc1-complex (EC 1.10.2.2), mitochondrial Gene Set

From CORUM Protein Complexes

proteins in the Cytochrome bc1-complex (EC 1.10.2.2), mitochondrial protein complex from the CORUM Protein Complexes dataset.

Respiratory chain complex I (gamma subunit) mitochondrial Gene Set

From CORUM Protein Complexes

proteins in the Respiratory chain complex I (gamma subunit) mitochondrial protein complex from the CORUM Protein Complexes dataset.

Respiratory chain complex I (beta subunit) mitochondrial Gene Set

From CORUM Protein Complexes

proteins in the Respiratory chain complex I (beta subunit) mitochondrial protein complex from the CORUM Protein Complexes dataset.

Respiratory chain complex I (intermediate IV/310kD), mitochondrial Gene Set

From CORUM Protein Complexes

proteins in the Respiratory chain complex I (intermediate IV/310kD), mitochondrial protein complex from the CORUM Protein Complexes dataset.

Succinate dehydrogenase complex II (EC 1.3.5.1), mitochondrial Gene Set

From CORUM Protein Complexes

proteins in the Succinate dehydrogenase complex II (EC 1.3.5.1), mitochondrial protein complex from the CORUM Protein Complexes dataset.

55S ribosome, mitochondrial Gene Set

From CORUM Protein Complexes

proteins in the 55S ribosome, mitochondrial protein complex from the CORUM Protein Complexes dataset.

TIM (TIMM23, TIMM50) complex, mitochondrial Gene Set

From CORUM Protein Complexes

proteins in the TIM (TIMM23, TIMM50) complex, mitochondrial protein complex from the CORUM Protein Complexes dataset.

F1F0-ATP synthase (EC 3.6.3.14), mitochondrial Gene Set

From CORUM Protein Complexes

proteins in the F1F0-ATP synthase (EC 3.6.3.14), mitochondrial protein complex from the CORUM Protein Complexes dataset.

Cytochrome c oxidase (EC 1.9.3.1), mitochondrial Gene Set

From CORUM Protein Complexes

proteins in the Cytochrome c oxidase (EC 1.9.3.1), mitochondrial protein complex from the CORUM Protein Complexes dataset.

Respiratory chain complex I (incomplete intermediate), mitochondrial Gene Set

From CORUM Protein Complexes

proteins in the Respiratory chain complex I (incomplete intermediate), mitochondrial protein complex from the CORUM Protein Complexes dataset.

28S ribosomal subunit, mitochondrial Gene Set

From CORUM Protein Complexes

proteins in the 28S ribosomal subunit, mitochondrial protein complex from the CORUM Protein Complexes dataset.

TIM (TIMM17ab, TIMM23, TIMM44) complex, mitochondrial Gene Set

From CORUM Protein Complexes

proteins in the TIM (TIMM17ab, TIMM23, TIMM44) complex, mitochondrial protein complex from the CORUM Protein Complexes dataset.

Respiratory chain complex I (incomplete intermediate ND1, ND2, ND3, CIA30 assembly), mitochondrial Gene Set

From CORUM Protein Complexes

proteins in the Respiratory chain complex I (incomplete intermediate ND1, ND2, ND3, CIA30 assembly), mitochondrial protein complex from the CORUM Protein Complexes dataset.

Respiratory chain complex I (holoenzyme), mitochondrial Gene Set

From CORUM Protein Complexes

proteins in the Respiratory chain complex I (holoenzyme), mitochondrial protein complex from the CORUM Protein Complexes dataset.

39S ribosomal subunit, mitochondrial Gene Set

From CORUM Protein Complexes

proteins in the 39S ribosomal subunit, mitochondrial protein complex from the CORUM Protein Complexes dataset.

Respiratory chain complex I (intermediate II/230kD), mitochondrial Gene Set

From CORUM Protein Complexes

proteins in the Respiratory chain complex I (intermediate II/230kD), mitochondrial 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.

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.

Respiratory chain complex I (early intermediate NDUFAF1 assembly), mitochondrial Gene Set

From CORUM Protein Complexes

proteins in the Respiratory chain complex I (early intermediate NDUFAF1 assembly), mitochondrial protein complex from the CORUM Protein Complexes dataset.

TIM (TIMM9, TIMM10) complex, mitochondrial Gene Set

From CORUM Protein Complexes

proteins in the TIM (TIMM9, TIMM10) complex, mitochondrial protein complex from the CORUM Protein Complexes dataset.

Mitochondrial Phosphate Carrier Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mitochondrial Phosphate Carrier Deficiency from the curated CTD Gene-Disease Associations dataset.

Mitochondrial Diseases Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mitochondrial Diseases from the curated CTD Gene-Disease Associations dataset.

Mitochondrial Complex III Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mitochondrial Complex III Deficiency from the curated CTD Gene-Disease Associations dataset.

Mitochondrial Myopathies Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mitochondrial Myopathies from the curated CTD Gene-Disease Associations dataset.

Mitochondrial Encephalomyopathies Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mitochondrial Encephalomyopathies 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.

Mitochondrial Complex II Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mitochondrial Complex II Deficiency from the curated CTD Gene-Disease Associations dataset.

Mitochondrial complex I deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mitochondrial complex I deficiency from the curated CTD Gene-Disease Associations dataset.

mitochondrial myopathy Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease mitochondrial myopathy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

mitochondrial metabolism disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease mitochondrial metabolism disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

mitochondrial encephalomyopathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease mitochondrial encephalomyopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

mitochondrial metabolism disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease mitochondrial metabolism disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

mitochondrial myopathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease mitochondrial myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

intestinal pseudo-obstruction; mitochondrial diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease intestinal pseudo-obstruction; mitochondrial diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

mitochondrial diseases; nerve degeneration; presbycusis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease mitochondrial diseases; nerve degeneration; presbycusis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

mitochondrial myopathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease mitochondrial myopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

mitochondrial diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease mitochondrial diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus; hearing disorders; hearing problem; mitochondrial diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus; hearing disorders; hearing problem; mitochondrial diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

mitochondrial Gene Set

From GAD High Level Gene-Disease Associations

genes associated with the disease mitochondrial in GWAS and other genetic association datasets from the GAD High Level Gene-Disease Associations dataset.

mitochondrial Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term mitochondrial in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

MELAS - Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes_Muscle - Striated (Skeletal) (MMHCC)_GSE1462 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during MELAS - Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes_Muscle - Striated (Skeletal) (MMHCC)_GSE1462 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

mitochondrial respiratory chain complex ii biogenesis Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial respiratory chain complex ii biogenesis biological process from the curated GO Biological Process Annotations dataset.

positive regulation of mitochondrial calcium ion concentration Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of mitochondrial calcium ion concentration biological process from the curated GO Biological Process Annotations dataset.

regulation of mitochondrial depolarization Gene Set

From GO Biological Process Annotations

genes participating in the regulation of mitochondrial depolarization biological process from the curated GO Biological Process Annotations dataset.

negative regulation of mitochondrial depolarization Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of mitochondrial depolarization biological process from the curated GO Biological Process Annotations dataset.

protein insertion into mitochondrial membrane Gene Set

From GO Biological Process Annotations

genes participating in the protein insertion into mitochondrial membrane biological process from the curated GO Biological Process Annotations dataset.

positive regulation of mitochondrial fission Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of mitochondrial fission biological process from the curated GO Biological Process Annotations dataset.

negative regulation of mitochondrial outer membrane permeabilization involved in apoptotic signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of mitochondrial outer membrane permeabilization involved in apoptotic signaling pathway biological process from the curated GO Biological Process Annotations dataset.

positive regulation of protein import into mitochondrial outer membrane Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of protein import into mitochondrial outer membrane biological process from the curated GO Biological Process Annotations dataset.

positive regulation of protein insertion into mitochondrial membrane involved in apoptotic signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of protein insertion into mitochondrial membrane involved in apoptotic signaling pathway biological process from the curated GO Biological Process Annotations dataset.

regulation of protein insertion into mitochondrial membrane involved in apoptotic signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the regulation of protein insertion into mitochondrial membrane involved in apoptotic signaling pathway biological process from the curated GO Biological Process Annotations dataset.

mitochondrial rna 3'-end processing Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial rna 3'-end processing biological process from the curated GO Biological Process Annotations dataset.

regulation of protein import into mitochondrial outer membrane Gene Set

From GO Biological Process Annotations

genes participating in the regulation of protein import into mitochondrial outer membrane biological process from the curated GO Biological Process Annotations dataset.

mitochondrial outer membrane permeabilization involved in programmed cell death Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial outer membrane permeabilization involved in programmed cell death biological process from the curated GO Biological Process Annotations dataset.

mitochondrial fission Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial fission biological process from the curated GO Biological Process Annotations dataset.

outer mitochondrial membrane organization Gene Set

From GO Biological Process Annotations

genes participating in the outer mitochondrial membrane organization biological process from the curated GO Biological Process Annotations dataset.

protein import into mitochondrial intermembrane space Gene Set

From GO Biological Process Annotations

genes participating in the protein import into mitochondrial intermembrane space biological process from the curated GO Biological Process Annotations dataset.

positive regulation of mitochondrial membrane permeability Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of mitochondrial membrane permeability biological process from the curated GO Biological Process Annotations dataset.

mitochondrial threonyl-trna aminoacylation Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial threonyl-trna aminoacylation biological process from the curated GO Biological Process Annotations dataset.

mitochondrial respiratory chain complex iv biogenesis Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial respiratory chain complex iv biogenesis biological process from the curated GO Biological Process Annotations dataset.

mitochondrial electron transport, ubiquinol to cytochrome c Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial electron transport, ubiquinol to cytochrome c biological process from the curated GO Biological Process Annotations dataset.

positive regulation of mitochondrial depolarization Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of mitochondrial depolarization biological process from the curated GO Biological Process Annotations dataset.

mitochondrial membrane organization Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial membrane organization biological process from the curated GO Biological Process Annotations dataset.

mitochondrial trna 3'-end processing Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial trna 3'-end processing biological process from the curated GO Biological Process Annotations dataset.

mitochondrial rna surveillance Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial rna surveillance biological process from the curated GO Biological Process Annotations dataset.

mitochondrial rna catabolic process Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial rna catabolic process biological process from the curated GO Biological Process Annotations dataset.

mitochondrial mrna surveillance Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial mrna surveillance biological process from the curated GO Biological Process Annotations dataset.

mitochondrial electron transport, nadh to ubiquinone Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial electron transport, nadh to ubiquinone biological process from the curated GO Biological Process Annotations dataset.

positive regulation of mitochondrial membrane potential Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of mitochondrial membrane potential biological process from the curated GO Biological Process Annotations dataset.

negative regulation of mitochondrial fission Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of mitochondrial fission biological process from the curated GO Biological Process Annotations dataset.

mitochondrial trna 3'-trailer cleavage, endonucleolytic Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial trna 3'-trailer cleavage, endonucleolytic biological process from the curated GO Biological Process Annotations dataset.

mitochondrial rna modification Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial rna modification biological process from the curated GO Biological Process Annotations dataset.

mitochondrial membrane fission Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial membrane fission biological process from the curated GO Biological Process Annotations dataset.

mitochondrial trna modification Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial trna modification biological process from the curated GO Biological Process Annotations dataset.

mitochondrial respiratory chain complex i assembly Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial respiratory chain complex i assembly biological process from the curated GO Biological Process Annotations dataset.

mitochondrial respiratory chain complex assembly Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial respiratory chain complex assembly biological process from the curated GO Biological Process Annotations dataset.

mitochondrial mrna catabolic process Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial mrna catabolic process biological process from the curated GO Biological Process Annotations dataset.

apoptotic mitochondrial changes Gene Set

From GO Biological Process Annotations

genes participating in the apoptotic mitochondrial changes biological process from the curated GO Biological Process Annotations dataset.

protein import into mitochondrial matrix Gene Set

From GO Biological Process Annotations

genes participating in the protein import into mitochondrial matrix biological process from the curated GO Biological Process Annotations dataset.

mitochondrial electron transport, succinate to ubiquinone Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial electron transport, succinate to ubiquinone biological process from the curated GO Biological Process Annotations dataset.

mitochondrial respiratory chain complex iv assembly Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial respiratory chain complex iv assembly biological process from the curated GO Biological Process Annotations dataset.

mitochondrial pyrimidine nucleotide import Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial pyrimidine nucleotide import biological process from the curated GO Biological Process Annotations dataset.

mitochondrial outer membrane permeabilization Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial outer membrane permeabilization biological process from the curated GO Biological Process Annotations dataset.

negative regulation of mitochondrial membrane permeability involved in apoptotic process Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of mitochondrial membrane permeability involved in apoptotic process biological process from the curated GO Biological Process Annotations dataset.

mitochondrial iron ion transport Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial iron ion transport biological process from the curated GO Biological Process Annotations dataset.

transcription initiation from mitochondrial promoter Gene Set

From GO Biological Process Annotations

genes participating in the transcription initiation from mitochondrial promoter biological process from the curated GO Biological Process Annotations dataset.

mitochondrial translational elongation Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial translational elongation biological process from the curated GO Biological Process Annotations dataset.

mitochondrial mrna polyadenylation Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial mrna polyadenylation biological process from the curated GO Biological Process Annotations dataset.

regulation of mitochondrial membrane permeability Gene Set

From GO Biological Process Annotations

genes participating in the regulation of mitochondrial membrane permeability biological process from the curated GO Biological Process Annotations dataset.

negative regulation of mitochondrial translation Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of mitochondrial translation biological process from the curated GO Biological Process Annotations dataset.

protein insertion into mitochondrial membrane involved in apoptotic signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the protein insertion into mitochondrial membrane involved in apoptotic signaling pathway biological process from the curated GO Biological Process Annotations dataset.

positive regulation of mitochondrial rna catabolic process Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of mitochondrial rna catabolic process biological process from the curated GO Biological Process Annotations dataset.

mitochondrial calcium ion homeostasis Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial calcium ion homeostasis biological process from the curated GO Biological Process Annotations dataset.

negative regulation of mitochondrial membrane potential Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of mitochondrial membrane potential biological process from the curated GO Biological Process Annotations dataset.

mitochondrial calcium ion transport Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial calcium ion transport biological process from the curated GO Biological Process Annotations dataset.

mitochondrial rna metabolic process Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial rna metabolic process biological process from the curated GO Biological Process Annotations dataset.

mitochondrial pyruvate transport Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial pyruvate transport biological process from the curated GO Biological Process Annotations dataset.

mitochondrial protein catabolic process Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial protein catabolic process biological process from the curated GO Biological Process Annotations dataset.

mitochondrial translational initiation Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial translational initiation biological process from the curated GO Biological Process Annotations dataset.

mitochondrial translational termination Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial translational termination biological process from the curated GO Biological Process Annotations dataset.

positive regulation of mitochondrial electron transport, nadh to ubiquinone Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of mitochondrial electron transport, nadh to ubiquinone biological process from the curated GO Biological Process Annotations dataset.

positive regulation of mitochondrial membrane permeability involved in apoptotic process Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of mitochondrial membrane permeability involved in apoptotic process biological process from the curated GO Biological Process Annotations dataset.

stress-induced mitochondrial fusion Gene Set

From GO Biological Process Annotations

genes participating in the stress-induced mitochondrial fusion biological process from the curated GO Biological Process Annotations dataset.

regulation of mitochondrial translation Gene Set

From GO Biological Process Annotations

genes participating in the regulation of mitochondrial translation biological process from the curated GO Biological Process Annotations dataset.

protein import into mitochondrial inner membrane Gene Set

From GO Biological Process Annotations

genes participating in the protein import into mitochondrial inner membrane biological process from the curated GO Biological Process Annotations dataset.

negative regulation of mitochondrial membrane permeability Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of mitochondrial membrane permeability biological process from the curated GO Biological Process Annotations dataset.

negative regulation of mitochondrial electron transport, nadh to ubiquinone Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of mitochondrial electron transport, nadh to ubiquinone biological process from the curated GO Biological Process Annotations dataset.

regulation of mitochondrial rna catabolic process Gene Set

From GO Biological Process Annotations

genes participating in the regulation of mitochondrial rna catabolic process biological process from the curated GO Biological Process Annotations dataset.

regulation of mitochondrial fusion Gene Set

From GO Biological Process Annotations

genes participating in the regulation of mitochondrial fusion biological process from the curated GO Biological Process Annotations dataset.

mitochondrial ncrna surveillance Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial ncrna surveillance biological process from the curated GO Biological Process Annotations dataset.

mitochondrial transmembrane transport Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial transmembrane transport biological process from the curated GO Biological Process Annotations dataset.

negative regulation of mitochondrial rna catabolic process Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of mitochondrial rna catabolic process biological process from the curated GO Biological Process Annotations dataset.

establishment of protein localization to mitochondrial membrane Gene Set

From GO Biological Process Annotations

genes participating in the establishment of protein localization to mitochondrial membrane biological process from the curated GO Biological Process Annotations dataset.

positive regulation of mitochondrial fusion Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of mitochondrial fusion biological process from the curated GO Biological Process Annotations dataset.

regulation of mitochondrial membrane permeability involved in apoptotic process Gene Set

From GO Biological Process Annotations

genes participating in the regulation of mitochondrial membrane permeability involved in apoptotic process biological process from the curated GO Biological Process Annotations dataset.

dynamin polymerization involved in mitochondrial fission Gene Set

From GO Biological Process Annotations

genes participating in the dynamin polymerization involved in mitochondrial fission biological process from the curated GO Biological Process Annotations dataset.

regulation of mitochondrial membrane potential Gene Set

From GO Biological Process Annotations

genes participating in the regulation of mitochondrial membrane potential biological process from the curated GO Biological Process Annotations dataset.

mitochondrial trna methylation Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial trna methylation biological process from the curated GO Biological Process Annotations dataset.