Name

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.

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.

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.

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.

leigh syndrome, due to cox deficiency Gene Set

From OMIM Gene-Disease Associations

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

leigh syndrome due to cytochrome c oxidase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the leigh syndrome due to cytochrome c oxidase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

leigh syndrome and cytochrome c oxidase deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leigh syndrome and cytochrome c oxidase deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cox4 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term cox4 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations 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.

antithrombin iii deficiency; gastrointestinal hemorrhage; protein c deficiency; protein s deficiency; splenomegaly; thrombophilia; turner syndrome; venous thrombosis; xo syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease antithrombin iii deficiency; gastrointestinal hemorrhage; protein c deficiency; protein s deficiency; splenomegaly; thrombophilia; turner syndrome; venous thrombosis; xo syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cytochrome-c oxidase deficiency; leigh disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cytochrome-c oxidase deficiency; leigh disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

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.

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.

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.

leigh syndrome Gene Set

From OMIM Gene-Disease Associations

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

3-methylglutaconic aciduria with deafness, encephalopathy, and leigh-like syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the 3-methylglutaconic aciduria with deafness, encephalopathy, and leigh-like syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

THROMBOPHILIA, FAMILIAL, DUE TO DECREASED RELEASE OF TISSUE PLASMINOGEN ACTIVATOR;THPH9 HYPERFIBRINOLYSIS, FAMILIAL, DUE TO INCREASED RELEASE OF TISSUE PLASMINOGEN Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease THROMBOPHILIA, FAMILIAL, DUE TO DECREASED RELEASE OF TISSUE PLASMINOGEN ACTIVATOR;THPH9 HYPERFIBRINOLYSIS, FAMILIAL, DUE TO INCREASED RELEASE OF TISSUE PLASMINOGEN from the curated CTD Gene-Disease Associations dataset.

Ehlers-Danlos-like syndrome due to tenascin-X deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ehlers-Danlos-like syndrome due to tenascin-X deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

ehlers-danlos syndrome, autosomal recessive, due to tenascin x deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the ehlers-danlos syndrome, autosomal recessive, due to tenascin x deficiency 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.

encephalopahty, lethal, due to defective mitochondrial peroxisomal fission Gene Set

From OMIM Gene-Disease Associations

genes associated with the encephalopahty, lethal, due to defective mitochondrial peroxisomal fission phenotype from the curated OMIM Gene-Disease Associations dataset.

Leigh Disease Gene Set

From CTD Gene-Disease Associations

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

leigh disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease leigh disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

leigh disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

leigh Gene Set

From GeneRIF Biological Term Annotations

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

Leigh Disease Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Leigh Disease phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

factor v deficiency; hypoprothrombinemias; protein c deficiency; protein s deficiency; pulmonary embolism; thrombophilia; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease factor v deficiency; hypoprothrombinemias; protein c deficiency; protein s deficiency; pulmonary embolism; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

activated protein c resistance; antithrombin iii deficiency; pregnancy complications, hematologic; protein c deficiency; protein s deficiency; puerperal disorders; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease activated protein c resistance; antithrombin iii deficiency; pregnancy complications, hematologic; protein c deficiency; protein s deficiency; puerperal disorders; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Carbonic anhydrase va deficiency, hyperammonemia due to Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Carbonic anhydrase va deficiency, hyperammonemia due to phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

SCID due to ADA deficiency, delayed onset Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the SCID due to ADA deficiency, delayed onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Thrombophilia due to protein S deficiency, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Thrombophilia due to protein S deficiency, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glutathione synthetase deficiency of erythrocytes, hemolytic anemia due to Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glutathione synthetase deficiency of erythrocytes, hemolytic anemia due to phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Severe combined immunodeficiency due to ADA deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Severe combined immunodeficiency due to ADA deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Gamma-glutamylcysteine synthetase deficiency, hemolytic anemia due to Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Gamma-glutamylcysteine synthetase deficiency, hemolytic anemia due to phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

HNSHA due to aldolase A deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the HNSHA due to aldolase A deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Thrombophilia, hereditary, due to protein C deficiency, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Thrombophilia, hereditary, due to protein C deficiency, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Gaucher disease, atypical, due to saposin C deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Gaucher disease, atypical, due to saposin C deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Disordered steroidogenesis due to cytochrome p450 oxidoreductase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Disordered steroidogenesis due to cytochrome p450 oxidoreductase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hemolytic anemia due to hexokinase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hemolytic anemia due to hexokinase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Homocysteinemia due to MTHFR deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Homocysteinemia due to MTHFR deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Immunodeficiency due to ficolin 3 deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Immunodeficiency due to ficolin 3 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypermethioninemia due to adenosine kinase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypermethioninemia due to adenosine kinase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Uridine 5-prime monophosphate hydrolase deficiency, hemolytic anemia due to Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Uridine 5-prime monophosphate hydrolase deficiency, hemolytic anemia due to phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Muscular dystrophy, congenital, due to ITGA7 deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Muscular dystrophy, congenital, due to ITGA7 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Homocystinuria due to MTHFR deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Homocystinuria due to MTHFR deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Complement component 4, partial deficiency of, due to dysfunctional c1 inhibitor Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Complement component 4, partial deficiency of, due to dysfunctional c1 inhibitor phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy due to partial LAMA2 deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy due to partial LAMA2 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Megaloblastic anemia due to dihydrofolate reductase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Megaloblastic anemia due to dihydrofolate reductase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Obesity, severe, due to leptin deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Obesity, severe, due to leptin deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Adenylate kinase deficiency, hemolytic anemia due to Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Adenylate kinase deficiency, hemolytic anemia due to phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Thrombophilia, hereditary, due to protein C deficiency, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Thrombophilia, hereditary, due to protein C deficiency, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hyperphenylalaninemia, bh4-deficient, a, due to partial pts deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hyperphenylalaninemia, bh4-deficient, a, due to partial pts deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital adrenal hyperplasia due to 21 hydroxylase deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital adrenal hyperplasia due to 21 hydroxylase deficiency from the curated CTD Gene-Disease Associations dataset.

HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO GLUCOSE PHOSPHATE ISOMERASE DEFICIENCY Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO GLUCOSE PHOSPHATE ISOMERASE DEFICIENCY from the curated CTD Gene-Disease Associations dataset.

Cardioencephalomyopathy, Fatal Infantile, due to Cytochrome C Oxidase Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardioencephalomyopathy, Fatal Infantile, due to Cytochrome C Oxidase Deficiency from the curated CTD Gene-Disease Associations dataset.

Glutathione Synthetase Deficiency of Erythrocytes, Hemolytic Anemia due to Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glutathione Synthetase Deficiency of Erythrocytes, Hemolytic Anemia due to from the curated CTD Gene-Disease Associations dataset.

Congenital thrombotic disease, due to Protein C deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital thrombotic disease, due to Protein C deficiency from the curated CTD Gene-Disease Associations dataset.

ORNITHINE TRANSCARBAMYLASE DEFICIENCY, HYPERAMMONEMIA DUE TO Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ORNITHINE TRANSCARBAMYLASE DEFICIENCY, HYPERAMMONEMIA DUE TO from the curated CTD Gene-Disease Associations dataset.

Adenylate Kinase Deficiency, Hemolytic Anemia Due To Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Adenylate Kinase Deficiency, Hemolytic Anemia Due To from the curated CTD Gene-Disease Associations dataset.

Neurodegeneration Due To Cerebral Folate Transport Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neurodegeneration Due To Cerebral Folate Transport Deficiency from the curated CTD Gene-Disease Associations dataset.

THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL DOMINANT Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL DOMINANT from the curated CTD Gene-Disease Associations dataset.

Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency from the curated CTD Gene-Disease Associations dataset.

Severe combined immunodeficiency due to adenosine deaminase deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Severe combined immunodeficiency due to adenosine deaminase deficiency from the curated CTD Gene-Disease Associations dataset.

Methylmalonic Aciduria due to Methylmalonyl-CoA Mutase Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Methylmalonic Aciduria due to Methylmalonyl-CoA Mutase Deficiency from the curated CTD Gene-Disease Associations dataset.

Uridine 5-Prime Monophosphate Hydrolase Deficiency, Hemolytic Anemia due to Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Uridine 5-Prime Monophosphate Hydrolase Deficiency, Hemolytic Anemia due to from the curated CTD Gene-Disease Associations dataset.

Krabbe Disease, Atypical, due to Saposin A Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Krabbe Disease, Atypical, due to Saposin A Deficiency from the curated CTD Gene-Disease Associations dataset.

Dystonia, Dopa-Responsive, due to Sepiapterin Reductase Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Dystonia, Dopa-Responsive, due to Sepiapterin Reductase Deficiency from the curated CTD Gene-Disease Associations dataset.

Gaucher Disease, Atypical, Due To Saposin C Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Gaucher Disease, Atypical, Due To Saposin C Deficiency from the curated CTD Gene-Disease Associations dataset.

Gamma-Glutamylcysteine Synthetase Deficiency, Hemolytic Anemia due to Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Gamma-Glutamylcysteine Synthetase Deficiency, Hemolytic Anemia due to from the curated CTD Gene-Disease Associations dataset.

THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL RECESSIVE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL RECESSIVE from the curated CTD Gene-Disease Associations dataset.

Congenital adrenal hyperplasia due to 11-Beta-hydroxylase deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital adrenal hyperplasia due to 11-Beta-hydroxylase deficiency from the curated CTD Gene-Disease Associations dataset.

Metachromatic Leukodystrophy due to Saposin B Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Metachromatic Leukodystrophy due to Saposin B Deficiency from the curated CTD Gene-Disease Associations dataset.

HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO HEXOKINASE DEFICIENCY Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO HEXOKINASE DEFICIENCY from the curated CTD Gene-Disease Associations dataset.

{chronic infections, due to mbl deficiency} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {chronic infections, due to mbl deficiency} phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombophilia due to hrg deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombophilia due to hrg deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

severe combined immunodeficiency due to il2 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the severe combined immunodeficiency due to il2 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombophilia due to protein s deficiency, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombophilia due to protein s deficiency, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

hemolytic anemia due to phosphofructokinase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemolytic anemia due to phosphofructokinase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

nephropathy due to cfhr5 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the nephropathy due to cfhr5 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

megaloblastic anemia due to dihydrofolate reductase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the megaloblastic anemia due to dihydrofolate reductase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombophilia due to protein s deficiency, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombophilia due to protein s deficiency, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

chronic granulomatous disease, autosomal, due to deficiency of cyba Gene Set

From OMIM Gene-Disease Associations

genes associated with the chronic granulomatous disease, autosomal, due to deficiency of cyba phenotype from the curated OMIM Gene-Disease Associations dataset.

?isolated growth hormone deficiency due to defect in ghrf Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?isolated growth hormone deficiency due to defect in ghrf phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombophilia due to heparin cofactor ii deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombophilia due to heparin cofactor ii deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

obesity, morbid, due to leptin receptor deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the obesity, morbid, due to leptin receptor deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

glucocorticoid deficiency, due to acth unresponsiveness Gene Set

From OMIM Gene-Disease Associations

genes associated with the glucocorticoid deficiency, due to acth unresponsiveness phenotype from the curated OMIM Gene-Disease Associations dataset.

hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, congenital, due to partial lama2 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, congenital, due to partial lama2 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

immunodeficiency due to purine nucleoside phosphorylase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the immunodeficiency due to purine nucleoside phosphorylase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hemolytic anemia due to glutathione peroxidase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemolytic anemia due to glutathione peroxidase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombophilia due to protein c deficiency, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombophilia due to protein c deficiency, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

lacticacidemia due to pdx1 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the lacticacidemia due to pdx1 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, congenital, due to itga7 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, congenital, due to itga7 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

anemia, hemolytic, due to umph1 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the anemia, hemolytic, due to umph1 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

homocystinuria due to mthfr deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the homocystinuria due to mthfr deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

severe combined immunodeficiency due to ada deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the severe combined immunodeficiency due to ada deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombophilia due to protein c deficiency, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombophilia due to protein c deficiency, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

adrenal hyperplasia, congenital, due to 11-beta-hydroxylase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the adrenal hyperplasia, congenital, due to 11-beta-hydroxylase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

cirrhosis due to liver phosphorylase kinase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the cirrhosis due to liver phosphorylase kinase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hemolytic anemia due to gamma-glutamylcysteine synthetase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemolytic anemia due to gamma-glutamylcysteine synthetase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

metachromatic leukodystrophy due to sap-b deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the metachromatic leukodystrophy due to sap-b deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

obesity, morbid, due to leptin deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the obesity, morbid, due to leptin deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

growth retardation with deafness and mental retardation due to igf1 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the growth retardation with deafness and mental retardation due to igf1 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hyperammonemia due to carbonic anhydrase va deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hyperammonemia due to carbonic anhydrase va deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hemolytic anemia due to g6pd deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemolytic anemia due to g6pd deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hemolytic anemia due to glutathione synthetase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemolytic anemia due to glutathione synthetase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hypermethioninemia, persistent, autosomal dominant, due to methionine adenosyltransferase i/iii deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypermethioninemia, persistent, autosomal dominant, due to methionine adenosyltransferase i/iii deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hemolytic anemia due to adenylate kinase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemolytic anemia due to adenylate kinase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hemolytic anemia due to glutathione reductase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemolytic anemia due to glutathione reductase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

emphysema due to aat deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the emphysema due to aat deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

obesity, adrenal insufficiency, and red hair due to pomc deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the obesity, adrenal insufficiency, and red hair due to pomc deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombophilia due to antithrombin iii deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombophilia due to antithrombin iii deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

erythrocytosis due to bisphosphoglycerate mutase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the erythrocytosis due to bisphosphoglycerate mutase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hyperandrogenism, nonclassic type, due to 21-hydroxylase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hyperandrogenism, nonclassic type, due to 21-hydroxylase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

aica-ribosiduria due to atic deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the aica-ribosiduria due to atic deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hypoaldosteronism, congenital, due to cmo i deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypoaldosteronism, congenital, due to cmo i deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

chronic granulomatous disease due to deficiency of ncf-2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the chronic granulomatous disease due to deficiency of ncf-2 phenotype from the curated OMIM Gene-Disease Associations dataset.

chronic granulomatous disease due to deficiency of ncf-1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the chronic granulomatous disease due to deficiency of ncf-1 phenotype from the curated OMIM Gene-Disease Associations dataset.

cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

hypermethioninemia due to adenosine kinase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypermethioninemia due to adenosine kinase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

dystonia, dopa-responsive, due to sepiapterin reductase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the dystonia, dopa-responsive, due to sepiapterin reductase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

pyogenic bacterial infections, recurrent, due to myd88 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the pyogenic bacterial infections, recurrent, due to myd88 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

neurodegeneration due to cerebral folate transport deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the neurodegeneration due to cerebral folate transport deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

immunodeficiency due to ficolin 3 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the immunodeficiency due to ficolin 3 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hemolytic anemia due to triosephosphate isomerase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemolytic anemia due to triosephosphate isomerase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

{resistance to malaria due to g6pd deficiency} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {resistance to malaria due to g6pd deficiency} phenotype from the curated OMIM Gene-Disease Associations dataset.

hemolytic anemia due to hexokinase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemolytic anemia due to hexokinase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

myopathy due to cpt ii deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the myopathy due to cpt ii deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

emphysema-cirrhosis, due to aat deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the emphysema-cirrhosis, due to aat deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hypoaldosteronism, congenital, due to cmo ii deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypoaldosteronism, congenital, due to cmo ii deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

?male infertility due to acrosin deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?male infertility due to acrosin deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

myopathy due to myoadenylate deaminase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the myopathy due to myoadenylate deaminase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

Defective GCLC causes Hemolytic anemia due to gamma-glutamylcysteine synthetase deficiency (HAGGSD) Gene Set

From Reactome Pathways

proteins participating in the Defective GCLC causes Hemolytic anemia due to gamma-glutamylcysteine synthetase deficiency (HAGGSD) pathway from the Reactome Pathways 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.

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.

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.

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 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 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 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.

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 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 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 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 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 iv deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial complex iv deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

complex i, mitochondrial respiratory chain, deficiency of Gene Set

From OMIM Gene-Disease Associations

genes associated with the complex i, mitochondrial respiratory chain, deficiency of phenotype from the curated OMIM Gene-Disease Associations dataset.

?mitochondrial complex i deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?mitochondrial complex i deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial complex i deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial complex i deficiency 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 pyruvate carrier deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial pyruvate carrier deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial respiratory chain complex ii deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial respiratory chain complex ii deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial phosphate carrier deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial phosphate carrier deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial complex ii deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial complex ii deficiency 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 iv deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?mitochondrial complex iv deficiency 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.

pepck deficiency, mitochondrial Gene Set

From OMIM Gene-Disease Associations

genes associated with the pepck deficiency, mitochondrial 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.

mitochondrial complex 1 deficiency Gene Set

From OMIM Gene-Disease Associations

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

Neuraminidase deficiency with beta-galactosidase deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neuraminidase deficiency with beta-galactosidase deficiency from the curated CTD Gene-Disease Associations dataset.

eclampsia; pre-eclampsia; protein c deficiency; protein s deficiency; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease eclampsia; pre-eclampsia; protein c deficiency; protein s deficiency; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood coagulation disorders, inherited; protein c deficiency; protein s deficiency; thrombophilia; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood coagulation disorders, inherited; protein c deficiency; protein s deficiency; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood coagulation disorders; protein c deficiency; protein s deficiency; pulmonary embolism; pulmonary embolisms; thrombosis; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood coagulation disorders; protein c deficiency; protein s deficiency; pulmonary embolism; pulmonary embolisms; thrombosis; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, iron-deficiency; iron deficiency anaemia; tuberculosis, pulmonary Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, iron-deficiency; iron deficiency anaemia; tuberculosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

folic acid deficiency; fractures, bone; osteoporosis, postmenopausal; riboflavin deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease folic acid deficiency; fractures, bone; osteoporosis, postmenopausal; riboflavin deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

activated protein c resistance; blood coagulation disorders; liver diseases; protein c deficiency; protein s deficiency; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease activated protein c resistance; blood coagulation disorders; liver diseases; protein c deficiency; protein s deficiency; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, iron-deficiency; hemochromatosis; iron deficiency anaemia; iron overload Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, iron-deficiency; hemochromatosis; iron deficiency anaemia; iron overload in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

choline deficiency; dna damage; folic acid deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease choline deficiency; dna damage; folic acid deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

folic acid deficiency; pregnancy complications; prenatal exposure delayed effects; psychomotor disorders; vitamin b 12 deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease folic acid deficiency; pregnancy complications; prenatal exposure delayed effects; psychomotor disorders; vitamin b 12 deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, iron-deficiency; beta thalassemia; beta-thalassemia; iron deficiency anaemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, iron-deficiency; beta thalassemia; beta-thalassemia; iron deficiency anaemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, iron-deficiency; iron deficiency anaemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, iron-deficiency; iron deficiency anaemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

protein c deficiency; protein s deficiency; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease protein c deficiency; protein s deficiency; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

folic acid deficiency; hyperhomocysteinemia; thromboembolism; venous insufficiency; vitamin b 12 deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease folic acid deficiency; hyperhomocysteinemia; thromboembolism; venous insufficiency; vitamin b 12 deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, iron-deficiency; iron deficiency anaemia; iron overload Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, iron-deficiency; iron deficiency anaemia; iron overload in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

neoplasms; protein c deficiency; protein s deficiency; venous thromboembolism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neoplasms; protein c deficiency; protein s deficiency; venous thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, iron-deficiency; hemochromatosis; iron deficiency anaemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, iron-deficiency; hemochromatosis; iron deficiency anaemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic renal failure; folic acid deficiency; hyperhomocysteinemia; kidney failure, chronic; vitamin b 12 deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic renal failure; folic acid deficiency; hyperhomocysteinemia; kidney failure, chronic; vitamin b 12 deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Defective GSS causes Glutathione synthetase deficiency (GSS deficiency) Gene Set

From Reactome Pathways

proteins participating in the Defective GSS causes Glutathione synthetase deficiency (GSS deficiency) pathway from the Reactome Pathways dataset.

Defective CYP11B2 causes Corticosterone methyloxidase 1 deficiency (CMO-1 deficiency) Gene Set

From Reactome Pathways

proteins participating in the Defective CYP11B2 causes Corticosterone methyloxidase 1 deficiency (CMO-1 deficiency) pathway from the Reactome Pathways dataset.

Defective TPMT causes Thiopurine S-methyltransferase deficiency (TPMT deficiency) Gene Set

From Reactome Pathways

proteins participating in the Defective TPMT causes Thiopurine S-methyltransferase deficiency (TPMT deficiency) pathway from the Reactome Pathways 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 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 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 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 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 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.

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 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 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 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.

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 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 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.

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.

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 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.

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.

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 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.

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.

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 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 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 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 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.

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.

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 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.

?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.

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.

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.

Megaloblastic anemia due to inborn errors of metabolism Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Megaloblastic anemia due to inborn errors of metabolism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Thrombophilia due to activated protein C resistance Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Thrombophilia due to activated protein C resistance phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pseudohermaphroditism, female, with hypokalemia, due to glucocorticoid resistance Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pseudohermaphroditism, female, with hypokalemia, due to glucocorticoid resistance phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Thrombophilia due to thrombomodulin defect Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Thrombophilia due to thrombomodulin defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Immunodeficiency due to defect in cd3-zeta Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Immunodeficiency due to defect in cd3-zeta phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Homocystinuria-Megaloblastic anemia due to defect in cobalamin metabolism, cblE complementation type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Homocystinuria-Megaloblastic anemia due to defect in cobalamin metabolism, cblE complementation type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Immune dysfunction with T-cell inactivation due to calcium entry defect 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Immune dysfunction with T-cell inactivation due to calcium entry defect 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Immune dysfunction with T-cell inactivation due to calcium entry defect 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Immune dysfunction with T-cell inactivation due to calcium entry defect 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Thrombophilia, X-Linked, Due To Factor Ix Defect Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Thrombophilia, X-Linked, Due To Factor Ix Defect from the curated CTD Gene-Disease Associations dataset.

Homocystinuria-Megaloblastic Anemia due to Defect in Cobalamin Metabolism, CblE Complementation Type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Homocystinuria-Megaloblastic Anemia due to Defect in Cobalamin Metabolism, CblE Complementation Type from the curated CTD Gene-Disease Associations dataset.

METHYLMALONIC ACIDURIA DUE TO TRANSCOBALAMIN RECEPTOR DEFECT Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease METHYLMALONIC ACIDURIA DUE TO TRANSCOBALAMIN RECEPTOR DEFECT from the curated CTD Gene-Disease Associations dataset.

Pseudohyperkalemia, Familial, 2, due to Red Cell Leak Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pseudohyperkalemia, Familial, 2, due to Red Cell Leak from the curated CTD Gene-Disease Associations dataset.

HEPATIC FIBROSIS, SEVERE, SUSCEPTIBILITY TO, DUE TO SCHISTOSOMA MANSONI INFECTION Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease HEPATIC FIBROSIS, SEVERE, SUSCEPTIBILITY TO, DUE TO SCHISTOSOMA MANSONI INFECTION from the curated CTD Gene-Disease Associations dataset.

Encephalopathy, Neonatal Severe, Due To Mecp2 Mutations Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Encephalopathy, Neonatal Severe, Due To Mecp2 Mutations from the curated CTD Gene-Disease Associations dataset.

Thrombophilia Due To Elevated Histidine-Rich Glycoprotein Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Thrombophilia Due To Elevated Histidine-Rich Glycoprotein from the curated CTD Gene-Disease Associations dataset.

Thrombophilia due to Activated Protein C Resistance Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Thrombophilia due to Activated Protein C Resistance from the curated CTD Gene-Disease Associations dataset.

Immunodeficiency due to Defect in CD3-Zeta Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Immunodeficiency due to Defect in CD3-Zeta from the curated CTD Gene-Disease Associations dataset.

Immunodeficiency due to Defect in MAPBP-Interacting Protein Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Immunodeficiency due to Defect in MAPBP-Interacting Protein from the curated CTD Gene-Disease Associations dataset.

Immune dysfunction with T-cell inactivation due to calcium entry defect 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Immune dysfunction with T-cell inactivation due to calcium entry defect 1 from the curated CTD Gene-Disease Associations dataset.

Immune dysfunction with T-cell inactivation due to calcium entry defect 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Immune dysfunction with T-cell inactivation due to calcium entry defect 2 from the curated CTD Gene-Disease Associations dataset.

thrombocytopenia due to platelet alloimmunization Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease thrombocytopenia due to platelet alloimmunization in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

pneumoconiosis due to talc Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease pneumoconiosis due to talc in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

hereditary spastic paraparesis due to a frame shift mutat Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hereditary spastic paraparesis due to a frame shift mutat in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

depressed suicide; suicide due to depression Gene Set

From GAD Gene-Disease Associations

genes associated with the disease depressed suicide; suicide due to depression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

due Gene Set

From GeneRIF Biological Term Annotations

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

anemia due to reduced life span of red cells Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the anemia due to reduced life span of red cells phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

decreased cervical spine flexion due to contractures of posterior cervical muscles Gene Set

From HPO Gene-Disease Associations

genes associated with the decreased cervical spine flexion due to contractures of posterior cervical muscles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

anemia due to reduced life span of red cells Gene Set

From HPO Gene-Disease Associations

genes associated with the anemia due to reduced life span of red cells phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

restricted neck movement due to contractures Gene Set

From HPO Gene-Disease Associations

genes associated with the restricted neck movement due to contractures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

chronic rhinitis due to narrow nasal airway Gene Set

From HPO Gene-Disease Associations

genes associated with the chronic rhinitis due to narrow nasal airway phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

osteomyelitis due to immunodeficiency Gene Set

From HPO Gene-Disease Associations

genes associated with the osteomyelitis due to immunodeficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

osteomyelitis or necrosis, distal, due to sensory neuropathy (feet) Gene Set

From HPO Gene-Disease Associations

genes associated with the osteomyelitis or necrosis, distal, due to sensory neuropathy (feet) phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

bowing of limbs due to multiple fractures Gene Set

From HPO Gene-Disease Associations

genes associated with the bowing of limbs due to multiple fractures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

respiratory insufficiency due to muscle weakness Gene Set

From HPO Gene-Disease Associations

genes associated with the respiratory insufficiency due to muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

osteomyelitis leading to amputation due to slow healing fractures Gene Set

From HPO Gene-Disease Associations

genes associated with the osteomyelitis leading to amputation due to slow healing fractures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

weakness due to upper motor neuron dysfunction Gene Set

From HPO Gene-Disease Associations

genes associated with the weakness due to upper motor neuron dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

self-mutilation of tongue and lips due to involuntary movements Gene Set

From HPO Gene-Disease Associations

genes associated with the self-mutilation of tongue and lips due to involuntary movements phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

respiratory insufficiency due to defective ciliary clearance Gene Set

From HPO Gene-Disease Associations

genes associated with the respiratory insufficiency due to defective ciliary clearance phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

recurrent infections due to aspiration Gene Set

From HPO Gene-Disease Associations

genes associated with the recurrent infections due to aspiration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

generalized hypotonia due to defect at the neuromuscular junction Gene Set

From HPO Gene-Disease Associations

genes associated with the generalized hypotonia due to defect at the neuromuscular junction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

chronic hepatitis due to cryptospridium infection Gene Set

From HPO Gene-Disease Associations

genes associated with the chronic hepatitis due to cryptospridium infection phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

subperiosteal erosions due to secondary hyperparathyroidism Gene Set

From HPO Gene-Disease Associations

genes associated with the subperiosteal erosions due to secondary hyperparathyroidism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

painless fractures due to injury Gene Set

From HPO Gene-Disease Associations

genes associated with the painless fractures due to injury phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hepatic abscesses due to immunodeficiency Gene Set

From HPO Gene-Disease Associations

genes associated with the hepatic abscesses due to immunodeficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cellulitis due to immunodeficiency Gene Set

From HPO Gene-Disease Associations

genes associated with the cellulitis due to immunodeficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

decreased sweating due to autonomic dysfunction Gene Set

From HPO Gene-Disease Associations

genes associated with the decreased sweating due to autonomic dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

intermittent episodes of respiratory insufficiency due to muscle weakness Gene Set

From HPO Gene-Disease Associations

genes associated with the intermittent episodes of respiratory insufficiency due to muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

orthostatic hypotension due to autonomic dysfunction Gene Set

From HPO Gene-Disease Associations

genes associated with the orthostatic hypotension due to autonomic dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

{hepatic fibrosis susceptibility due to schistosoma mansoni infection} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {hepatic fibrosis susceptibility due to schistosoma mansoni infection} phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombophilia due to thrombomodulin defect Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombophilia due to thrombomodulin defect phenotype from the curated OMIM Gene-Disease Associations dataset.

bleeding disorder due to p2rx1 defect Gene Set

From OMIM Gene-Disease Associations

genes associated with the bleeding disorder due to p2rx1 defect phenotype from the curated OMIM Gene-Disease Associations dataset.

hypercholesterolemia, due to ligand-defective apo b Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypercholesterolemia, due to ligand-defective apo b phenotype from the curated OMIM Gene-Disease Associations dataset.

disordered steroidogenesis due to cytochrome p450 oxidoreductase Gene Set

From OMIM Gene-Disease Associations

genes associated with the disordered steroidogenesis due to cytochrome p450 oxidoreductase phenotype from the curated OMIM Gene-Disease Associations dataset.

hemorrhagic diathesis due to 'antithrombin' pittsburgh Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemorrhagic diathesis due to 'antithrombin' pittsburgh phenotype from the curated OMIM Gene-Disease Associations dataset.

hypothyroidism, congenital, due to thyroid dysgenesis or hypoplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypothyroidism, congenital, due to thyroid dysgenesis or hypoplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

omphalocele due to duplication of 1p31.3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the omphalocele due to duplication of 1p31.3 phenotype from the curated OMIM Gene-Disease Associations dataset.

gigantism due to ghrf hypersecretion Gene Set

From OMIM Gene-Disease Associations

genes associated with the gigantism due to ghrf hypersecretion phenotype from the curated OMIM Gene-Disease Associations dataset.

pseudohyperkalemia, familial, 2, due to red cell leak Gene Set

From OMIM Gene-Disease Associations

genes associated with the pseudohyperkalemia, familial, 2, due to red cell leak phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombophilia, familial, due to decreased release of plat Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombophilia, familial, due to decreased release of plat phenotype from the curated OMIM Gene-Disease Associations dataset.

macrocytic anemia, refractory, due to 5q deletion, somatic Gene Set

From OMIM Gene-Disease Associations

genes associated with the macrocytic anemia, refractory, due to 5q deletion, somatic phenotype from the curated OMIM Gene-Disease Associations dataset.

{hypercholesterolemia, familial, due to ldlr defect, modifier of} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {hypercholesterolemia, familial, due to ldlr defect, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset.

{drug-induced liver injury due to flucloxacillin} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {drug-induced liver injury due to flucloxacillin} phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombophilia due to activated protein c resistance Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombophilia due to activated protein c resistance phenotype from the curated OMIM Gene-Disease Associations dataset.

?male pseudohermaphroditism due to defective lh Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?male pseudohermaphroditism due to defective lh phenotype from the curated OMIM Gene-Disease Associations dataset.

hydrocephalus due to aqueductal stenosis Gene Set

From OMIM Gene-Disease Associations

genes associated with the hydrocephalus due to aqueductal stenosis phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombophilia due to elevated hrg Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombophilia due to elevated hrg phenotype from the curated OMIM Gene-Disease Associations dataset.

thalassemia due to hb lepore Gene Set

From OMIM Gene-Disease Associations

genes associated with the thalassemia due to hb lepore phenotype from the curated OMIM Gene-Disease Associations dataset.

rickets due to defect in vitamin d 25-hydroxylation Gene Set

From OMIM Gene-Disease Associations

genes associated with the rickets due to defect in vitamin d 25-hydroxylation phenotype from the curated OMIM Gene-Disease Associations dataset.

methylmalonic aciduria due to transcobalamin receptor defect Gene Set

From OMIM Gene-Disease Associations

genes associated with the methylmalonic aciduria due to transcobalamin receptor defect phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombophilia, x-linked, due to factor ix defect Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombophilia, x-linked, due to factor ix defect phenotype from the curated OMIM Gene-Disease Associations dataset.

{thrombophilia, susceptibility to, due to factor v leiden} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {thrombophilia, susceptibility to, due to factor v leiden} phenotype from the curated OMIM Gene-Disease Associations dataset.

immunodeficiency due to defect in mapbp-interacting protein Gene Set

From OMIM Gene-Disease Associations

genes associated with the immunodeficiency due to defect in mapbp-interacting protein phenotype from the curated OMIM Gene-Disease Associations dataset.

goiter, familial, due to ttf-1 defect Gene Set

From OMIM Gene-Disease Associations

genes associated with the goiter, familial, due to ttf-1 defect phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombophilia due to thrombin defect Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombophilia due to thrombin defect phenotype from the curated OMIM Gene-Disease Associations dataset.

hyperfibrinolysis, familial, due to increased release of plat Gene Set

From OMIM Gene-Disease Associations

genes associated with the hyperfibrinolysis, familial, due to increased release of plat phenotype from the curated OMIM Gene-Disease Associations dataset.

hemosiderosis, systemic, due to aceruloplasminemia Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemosiderosis, systemic, due to aceruloplasminemia phenotype from the curated OMIM Gene-Disease Associations dataset.

methylmalonic aciduria, vitamin b12-responsive, due to defect in synthesis of adenosylcobalamin, cblb complementation type Gene Set

From OMIM Gene-Disease Associations

genes associated with the methylmalonic aciduria, vitamin b12-responsive, due to defect in synthesis of adenosylcobalamin, cblb complementation type phenotype from the curated OMIM Gene-Disease Associations dataset.

Apoptosis-related network due to altered Notch3 in ovarian cancer(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Apoptosis-related network due to altered Notch3 in ovarian cancer(Homo sapiens) pathway from the Wikipathways Pathways dataset.

Glut1 deficiency syndrome 1, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glut1 deficiency syndrome 1, autosomal recessive 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.

Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ehlers-Danlos syndrome caused by tenascin-X deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ehlers-Danlos syndrome caused by tenascin-X deficiency from the curated CTD Gene-Disease Associations dataset.

Growth mental deficiency syndrome of Myhre Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Growth mental deficiency syndrome of Myhre from the curated CTD Gene-Disease Associations dataset.

GLUT1 DEFICIENCY SYNDROME 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease GLUT1 DEFICIENCY SYNDROME 2 from the curated CTD Gene-Disease Associations dataset.

Leukocyte-Adhesion Deficiency Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Leukocyte-Adhesion Deficiency Syndrome from the curated CTD Gene-Disease Associations dataset.

MYASTHENIC SYNDROME, CONGENITAL, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MYASTHENIC SYNDROME, CONGENITAL, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY from the curated CTD Gene-Disease Associations dataset.

cerebral creatine deficiency syndrome Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease cerebral creatine deficiency syndrome from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

leukocyte-adhesion deficiency syndrome Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

cerebral creatine deficiency syndrome Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

rh deficiency syndrome Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

alpha 1-antitrypsin deficiency; aortic stenosis, supravalvular; dislocations; scoliosis; williams syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha 1-antitrypsin deficiency; aortic stenosis, supravalvular; dislocations; scoliosis; williams syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

magnesium deficiency; wasting syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease magnesium deficiency; wasting syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucosephosphate dehydrogenase deficiency; hemoglobinuria; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucosephosphate dehydrogenase deficiency; hemoglobinuria; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

myasthenic syndrome, congenital, associated with facial dysmorphism and acetylcholine receptor deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the myasthenic syndrome, congenital, associated with facial dysmorphism and acetylcholine receptor deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

cerebral creatine deficiency syndrome 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cerebral creatine deficiency syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

glut1 deficiency syndrome 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the glut1 deficiency syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

glut1 deficiency syndrome 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the glut1 deficiency syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

autoinflammation, antibody deficiency, and immune dysregulation syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the autoinflammation, antibody deficiency, and immune dysregulation syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

cerebral creatine deficiency syndrome 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cerebral creatine deficiency syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

cerebral creatine deficiency syndrome 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cerebral creatine deficiency syndrome 3 phenotype from the curated OMIM Gene-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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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 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.

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 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.

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.

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 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.

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.

termination of mitochondrial transcription Gene Set

From GO Biological Process Annotations

genes participating in the termination of mitochondrial transcription biological process from the curated GO Biological Process Annotations dataset.

mitochondrial genome maintenance Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial genome maintenance biological process from the curated GO Biological Process Annotations dataset.

mitochondrial alanyl-trna aminoacylation Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial alanyl-trna aminoacylation biological process from the curated GO Biological Process Annotations dataset.

mitochondrial fragmentation involved in apoptotic process Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial fragmentation involved in apoptotic process biological process from the curated GO Biological Process Annotations dataset.

mitochondrial respiratory chain complex ii assembly Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial respiratory chain complex ii assembly 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.

regulation of mitochondrial electron transport, nadh to ubiquinone Gene Set

From GO Biological Process Annotations

genes participating in the regulation of mitochondrial electron transport, nadh to ubiquinone biological process from the curated GO Biological Process Annotations dataset.

mitochondrial depolarization Gene Set

From GO Biological Process Annotations

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

inner mitochondrial membrane organization Gene Set

From GO Biological Process Annotations

genes participating in the inner mitochondrial membrane organization biological process from the curated GO Biological Process Annotations dataset.

mitochondrial rna 5'-end processing Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial rna 5'-end processing biological process from the curated GO Biological Process Annotations dataset.

mitochondrial asparaginyl-trna aminoacylation Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial asparaginyl-trna aminoacylation 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.

mitochondrial ribosome assembly Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial ribosome assembly biological process from the curated GO Biological Process Annotations dataset.

mitochondrial proton-transporting atp synthase complex assembly Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial proton-transporting atp synthase complex assembly biological process from the curated GO Biological Process Annotations dataset.

mitochondrial trna wobble uridine modification Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial trna wobble uridine modification biological process from the curated GO Biological Process Annotations dataset.

mitochondrial translation Gene Set

From GO Biological Process Annotations

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

mitochondrial atp synthesis coupled electron transport Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial atp synthesis coupled electron transport biological process from the curated GO Biological Process Annotations dataset.

mitochondrial respiratory chain complex iii assembly Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial respiratory chain complex iii assembly biological process from the curated GO Biological Process Annotations dataset.

mitochondrial protein processing Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial protein processing biological process from the curated GO Biological Process Annotations dataset.

regulation of mitochondrial outer membrane permeabilization involved in apoptotic signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the regulation of mitochondrial outer membrane permeabilization involved in apoptotic signaling pathway biological process from the curated GO Biological Process Annotations dataset.

positive regulation of mitochondrial translation Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of mitochondrial translation 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.

negative regulation of mitochondrial fusion Gene Set

From GO Biological Process Annotations

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

negative regulation of mitochondrial calcium ion concentration Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of mitochondrial calcium ion concentration biological process from the curated GO Biological Process Annotations dataset.

trna aminoacylation for mitochondrial protein translation Gene Set

From GO Biological Process Annotations

genes participating in the trna aminoacylation for mitochondrial protein translation biological process from the curated GO Biological Process Annotations dataset.

mitochondrial ornithine transport Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial ornithine transport biological process from the curated GO Biological Process Annotations dataset.

regulation of mitochondrial membrane permeability involved in programmed necrotic cell death Gene Set

From GO Biological Process Annotations

genes participating in the regulation of mitochondrial membrane permeability involved in programmed necrotic cell death biological process from the curated GO Biological Process Annotations dataset.

mitochondrial transport Gene Set

From GO Biological Process Annotations

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

mitochondrial tyrosyl-trna aminoacylation Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial tyrosyl-trna aminoacylation biological process from the curated GO Biological Process Annotations dataset.

regulation of mitochondrial fission Gene Set

From GO Biological Process Annotations

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

mitochondrial electron transport, cytochrome c to oxygen Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial electron transport, cytochrome c to oxygen biological process from the curated GO Biological Process Annotations dataset.

protein import into mitochondrial outer membrane Gene Set

From GO Biological Process Annotations

genes participating in the protein import into mitochondrial outer membrane biological process from the curated GO Biological Process Annotations dataset.

mitochondrial respiratory chain complex iii biogenesis Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial respiratory chain complex iii biogenesis biological process from the curated GO Biological Process Annotations dataset.

positive regulation of mitochondrial outer membrane permeabilization involved in apoptotic signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of mitochondrial outer membrane permeabilization involved in apoptotic signaling pathway biological process from the curated GO Biological Process Annotations dataset.

mitochondrial atp synthesis coupled proton transport Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial atp synthesis coupled proton transport biological process from the curated GO Biological Process Annotations dataset.

mitochondrial fusion Gene Set

From GO Biological Process Annotations

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

transcription from mitochondrial promoter Gene Set

From GO Biological Process Annotations

genes participating in the transcription from mitochondrial promoter biological process from the curated GO Biological Process Annotations dataset.

mitochondrial rna processing Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial rna processing biological process from the curated GO Biological Process Annotations dataset.

mitochondrial respiratory chain complex i biogenesis Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial respiratory chain complex i biogenesis 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.

mitochondrial envelope Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial envelope cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial respiratory chain complex iv Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial respiratory chain complex iv cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial outer membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial outer membrane cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial proton-transporting atp synthase complex, catalytic core f(1) Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial proton-transporting atp synthase complex, catalytic core f(1) cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial alpha-ketoglutarate dehydrogenase complex Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial alpha-ketoglutarate dehydrogenase complex cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial respiratory chain complex i Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial respiratory chain complex i cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial inner membrane peptidase complex Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial inner membrane peptidase complex cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial endopeptidase clp complex Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial endopeptidase clp complex cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial fatty acid beta-oxidation multienzyme complex Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial fatty acid beta-oxidation multienzyme complex cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial respiratory chain complex ii Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial respiratory chain complex ii cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial small ribosomal subunit Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial small ribosomal subunit cellular component from the curated GO Cellular Component Annotations dataset.

intrinsic component of mitochondrial outer membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the intrinsic component of mitochondrial outer membrane cellular component from the curated GO Cellular Component Annotations dataset.

extrinsic component of mitochondrial outer membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the extrinsic component of mitochondrial outer membrane cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial part Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial part cellular component from the curated GO Cellular Component Annotations dataset.

sperm mitochondrial sheath Gene Set

From GO Cellular Component Annotations

proteins localized to the sperm mitochondrial sheath cellular component from the curated GO Cellular Component Annotations dataset.

integral component of mitochondrial membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the integral component of mitochondrial membrane cellular component from the curated GO Cellular Component Annotations dataset.

integral component of mitochondrial outer membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the integral component of mitochondrial outer membrane cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial large ribosomal subunit Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial large ribosomal subunit cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial proton-transporting atp synthase complex, coupling factor f(o) Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial proton-transporting atp synthase complex, coupling factor f(o) cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial membrane part Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial membrane part cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial ribonuclease p complex Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial ribonuclease p complex cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial nucleoid Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial nucleoid cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial ribosome Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial ribosome cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial outer membrane translocase complex Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial outer membrane translocase complex cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial crista Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial crista cellular component from the curated GO Cellular Component Annotations dataset.

integral component of mitochondrial inner membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the integral component of mitochondrial inner membrane cellular component from the curated GO Cellular Component Annotations dataset.

intrinsic component of mitochondrial membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the intrinsic component of mitochondrial membrane cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial inner membrane presequence translocase complex Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial inner membrane presequence translocase complex cellular component from the curated GO Cellular Component Annotations dataset.

extrinsic component of mitochondrial inner membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the extrinsic component of mitochondrial inner membrane cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial respiratory chain Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial respiratory chain cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial proton-transporting atp synthase complex Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial proton-transporting atp synthase complex cellular component from the curated GO Cellular Component Annotations dataset.

intrinsic component of mitochondrial inner membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the intrinsic component of mitochondrial inner membrane cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial membrane cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial inner membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial inner membrane cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial chromosome Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial chromosome cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial permeability transition pore complex Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial permeability transition pore complex cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial degradosome Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial degradosome cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial intermembrane space protein transporter complex Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial intermembrane space protein transporter complex cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial intermembrane space Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial intermembrane space cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial sorting and assembly machinery complex Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial sorting and assembly machinery complex cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial respiratory chain complex iii Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial respiratory chain complex iii cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial pyruvate dehydrogenase complex Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial pyruvate dehydrogenase complex cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial proton-transporting atp synthase, catalytic core Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial proton-transporting atp synthase, catalytic core cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial tricarboxylic acid cycle enzyme complex Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial tricarboxylic acid cycle enzyme complex cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial matrix Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial matrix cellular component from the curated GO Cellular Component Annotations dataset.

cytoplasmic side of mitochondrial outer membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the cytoplasmic side of mitochondrial outer membrane cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial heavy strand promoter anti-sense binding Gene Set

From GO Molecular Function Annotations

genes performing the mitochondrial heavy strand promoter anti-sense binding molecular function from the curated GO Molecular Function Annotations dataset.

mitochondrial light strand promoter anti-sense binding Gene Set

From GO Molecular Function Annotations

genes performing the mitochondrial light strand promoter anti-sense binding molecular function from the curated GO Molecular Function Annotations dataset.

mitochondrial light strand promoter sense binding Gene Set

From GO Molecular Function Annotations

genes performing the mitochondrial light strand promoter sense binding molecular function from the curated GO Molecular Function Annotations dataset.

mitochondrial ribosome binding Gene Set

From GO Molecular Function Annotations

genes performing the mitochondrial ribosome binding molecular function from the curated GO Molecular Function Annotations dataset.

mitochondrial heavy strand promoter sense binding Gene Set

From GO Molecular Function Annotations

genes performing the mitochondrial heavy strand promoter sense binding molecular function from the curated GO Molecular Function 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.

muscle abnormality related to mitochondrial dysfunction Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the muscle abnormality related to mitochondrial dysfunction phenotype in GWAS datasets from the GWASdb SNP-Phenotype 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.

mitochondrial myopathy Gene Set

From HPO Gene-Disease Associations

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

decreased activity of mitochondrial complex ii Gene Set

From HPO Gene-Disease Associations

genes associated with the decreased activity of mitochondrial complex ii phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

decreased activity of mitochondrial complex iv Gene Set

From HPO Gene-Disease Associations

genes associated with the decreased activity of mitochondrial complex iv phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

mitochondrial malic enzyme reduced Gene Set

From HPO Gene-Disease Associations

genes associated with the mitochondrial malic enzyme reduced phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

muscle abnormality related to mitochondrial dysfunction Gene Set

From HPO Gene-Disease Associations

genes associated with the muscle abnormality related to mitochondrial dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

decreased mitochondrial complex iii activity in liver tissue Gene Set

From HPO Gene-Disease Associations

genes associated with the decreased mitochondrial complex iii activity in liver tissue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

mitochondrial respiratory chain defects Gene Set

From HPO Gene-Disease Associations

genes associated with the mitochondrial respiratory chain defects phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of mitochondrial metabolism Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of mitochondrial metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

mitochondrial inheritance Gene Set

From HPO Gene-Disease Associations

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

decreased activity of mitochondrial respiratory chain Gene Set

From HPO Gene-Disease Associations

genes associated with the decreased activity of mitochondrial respiratory chain phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

decreased activity of mitochondrial complex iii Gene Set

From HPO Gene-Disease Associations

genes associated with the decreased activity of mitochondrial complex iii phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal mitochondrial morphology Gene Set

From HPO Gene-Disease Associations

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

decreased activity of mitochondrial atp synthase complex Gene Set

From HPO Gene-Disease Associations

genes associated with the decreased activity of mitochondrial atp synthase complex phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal mitochondrial shape Gene Set

From HPO Gene-Disease Associations

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

abnormal activity of mitochondrial respiratory chain Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal activity of mitochondrial respiratory chain phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease 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.

decreased activity of mitochondrial complex i Gene Set

From HPO Gene-Disease Associations

genes associated with the decreased activity of mitochondrial complex i phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

mitochondrial encephalopathy Gene Set

From HPO Gene-Disease Associations

genes associated with the mitochondrial encephalopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease 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.

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 Diseases Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Mitochondrial Diseases phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Mitochondrial Myopathies Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Mitochondrial Myopathies phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Mitochondrial Encephalomyopathies Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Mitochondrial Encephalomyopathies phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

mitochondrial L-carnitine shuttle Gene Set

From HumanCyc Pathways

proteins participating in the mitochondrial L-carnitine shuttle pathway from the HumanCyc Pathways dataset.

dTMP de novo biosynthesis (mitochondrial) Gene Set

From HumanCyc Pathways

proteins participating in the dTMP de novo biosynthesis (mitochondrial) pathway from the HumanCyc Pathways dataset.

Mitochondrial import inner membrane translocase subunit Tim21 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial import inner membrane translocase subunit Tim21 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Aconitase, mitochondrial-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Aconitase, mitochondrial-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial chaperone BCS1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial chaperone BCS1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial ATP synthase subunit g, animal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial ATP synthase subunit g, animal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial import inner membrane translocase subunit Tim44 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial import inner membrane translocase subunit Tim44 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial outer membrane transport complex, Sam37/metaxin Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial outer membrane transport complex, Sam37/metaxin protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial carrier protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial carrier protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ribosomal protein L27/L41, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ribosomal protein L27/L41, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial degradasome RNA helicase subunit, C-terminal domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial degradasome RNA helicase subunit, C-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial genome maintenance exonuclease 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial genome maintenance exonuclease 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial brown fat uncoupling protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial brown fat uncoupling protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial 28S ribosomal protein S31 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial 28S ribosomal protein S31 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ribosomal protein S24/S35, mitochondrial, conserved domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ribosomal protein S24/S35, mitochondrial, conserved domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ribosomal protein S27, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ribosomal protein S27, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial import inner membrane translocase subunit Tim10/Tim12 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial import inner membrane translocase subunit Tim10/Tim12 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial carrier domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial carrier domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ribosomal protein S23/Rsm25, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ribosomal protein S23/Rsm25, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Small GTPase superfamily, mitochondrial Rho Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Small GTPase superfamily, mitochondrial Rho protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial fission regulator 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial fission regulator 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

NADH dehydrogenase ubiquinone Fe-S protein 4, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the NADH dehydrogenase ubiquinone Fe-S protein 4, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial inner membrane translocase complex, subunit Tim23 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial inner membrane translocase complex, subunit Tim23 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Fatty acid oxidation complex, alpha subunit, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Fatty acid oxidation complex, alpha subunit, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ribosomal protein L55, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ribosomal protein L55, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial substrate/solute carrier Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial substrate/solute carrier protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Phenylalanyl-tRNA synthetase, class IIc, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Phenylalanyl-tRNA synthetase, class IIc, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial outer membrane translocase complex, subunit Tom20 domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial outer membrane translocase complex, subunit Tom20 domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ribosomal protein 63, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ribosomal protein 63, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ribosomal protein S32, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ribosomal protein S32, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ATPase, F0 complex, subunit 8, mitochondrial, Metazoan Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ATPase, F0 complex, subunit 8, mitochondrial, Metazoan protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial Rho-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial Rho-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial inner membrane protease subunit 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial inner membrane protease subunit 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ribosomal protein L35, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ribosomal protein L35, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial outer membrane transport complex protein, metaxin Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial outer membrane transport complex protein, metaxin protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial inner membrane protein Mitofilin Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial inner membrane protein Mitofilin protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ribosomal protein S28, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ribosomal protein S28, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ATPase, F0 complex, subunit F6, mitochondrial subgroup Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ATPase, F0 complex, subunit F6, mitochondrial subgroup protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ribosomal protein L53, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ribosomal protein L53, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial import inner membrane translocase subunit Tim16 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial import inner membrane translocase subunit Tim16 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial Na(+)/H(+) exchanger NHA2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial Na(+)/H(+) exchanger NHA2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Adenylate kinase 4, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Adenylate kinase 4, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial F1-F0 ATP synthase subunit F, predicted Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial F1-F0 ATP synthase subunit F, predicted protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ribosomal protein L1, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ribosomal protein L1, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ATP synthase subunit s, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ATP synthase subunit s, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

T-cell activation inhibitor, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the T-cell activation inhibitor, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial glycoprotein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial glycoprotein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial apoptosis-inducing factor, C-terminal domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial apoptosis-inducing factor, C-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ATPase, F0 complex, subunit E, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ATPase, F0 complex, subunit E, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial pyruvate carrier Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial pyruvate carrier protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ATPase, F0 complex, subunit G, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ATPase, F0 complex, subunit G, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Hydroxymethylglutaryl-CoA lyase, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Hydroxymethylglutaryl-CoA lyase, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ribosomal protein S23/S29, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ribosomal protein S23/S29, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial import inner membrane translocase subunit Tim50 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial import inner membrane translocase subunit Tim50 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ribosomal protein S29, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ribosomal protein S29, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ribosomal protein L51, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ribosomal protein L51, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial ribonuclease P, tRNA methyltransferase protein 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial ribonuclease P, tRNA methyltransferase protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ribosomal protein L28/L40, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ribosomal protein L28/L40, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial proteolipid Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial proteolipid protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial import protein TIM15 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial import protein TIM15 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial import receptor subunit TOM7 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial import receptor subunit TOM7 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ribosomal protein S23/S25, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ribosomal protein S23/S25, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ribosomal protein L47, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ribosomal protein L47, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial transcription factor TFB2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial transcription factor TFB2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cytochrome P450, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cytochrome P450, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ATPase, F1 complex, epsilon subunit, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ATPase, F1 complex, epsilon subunit, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Spermatogenesis-associated protein 19, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Spermatogenesis-associated protein 19, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Adenylate kinase 3/4, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Adenylate kinase 3/4, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial matrix Mmp37 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial matrix Mmp37 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

NAD(P) transhydrogenase, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the NAD(P) transhydrogenase, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial import receptor subunit TOM6 homologue Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial import receptor subunit TOM6 homologue protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial inner membrane translocase complex, subunit Tim17 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial inner membrane translocase complex, subunit Tim17 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ribosomal protein S27/S33, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ribosomal protein S27/S33, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial ubiquitin ligase activator of NFKB 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial ubiquitin ligase activator of NFKB 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial 18kDa protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial 18kDa protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Succinate dehydrogenase assembly factor 2, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Succinate dehydrogenase assembly factor 2, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial inner membrane translocase subunit Tim17/Tim22/Tim23/peroxisomal protein PMP24 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial inner membrane translocase subunit Tim17/Tim22/Tim23/peroxisomal protein PMP24 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ATPase, F0 complex, subunit F6, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ATPase, F0 complex, subunit F6, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Lon protease homolog, chloroplastic/mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Lon protease homolog, chloroplastic/mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial antiviral-signalling protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial antiviral-signalling protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial import receptor subunit TOM5 homologue Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial import receptor subunit TOM5 homologue protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Calcium-binding mitochondrial carrier protein Aralar2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Calcium-binding mitochondrial carrier protein Aralar2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glutamate-tRNA ligase, bacterial/mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glutamate-tRNA ligase, bacterial/mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations 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.

Cytochrome c oxidase subunit VIIa-related, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cytochrome c oxidase subunit VIIa-related, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial outer membrane translocase complex, subunit Tom22 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial outer membrane translocase complex, subunit Tom22 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial Rho GTPase 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial Rho GTPase 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial distribution/morphology family 35/apoptosis Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial distribution/morphology family 35/apoptosis protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ribosomal protein S22, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ribosomal protein S22, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ribosomal protein L37, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ribosomal protein L37, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial ribosomal protein L48 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial ribosomal protein L48 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ATPase, F0 complex, subunit D, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ATPase, F0 complex, subunit D, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

mitochondrial part Gene Set

From LOCATE Curated Protein Localization Annotations

proteins localized to the mitochondrial part cellular component in low- or high-throughput protein localization assays from the LOCATE Curated Protein Localization Annotations dataset.

mitochondrial outer membrane Gene Set

From LOCATE Curated Protein Localization Annotations

proteins localized to the mitochondrial outer membrane cellular component in low- or high-throughput protein localization assays from the LOCATE Curated Protein Localization Annotations dataset.

mitochondrial inner membrane Gene Set

From LOCATE Curated Protein Localization Annotations

proteins localized to the mitochondrial inner membrane cellular component in low- or high-throughput protein localization assays from the LOCATE Curated Protein Localization Annotations dataset.

mitochondrial membrane Gene Set

From LOCATE Curated Protein Localization Annotations

proteins localized to the mitochondrial membrane cellular component in low- or high-throughput protein localization assays from the LOCATE Curated Protein Localization Annotations dataset.

abnormal mitochondrial proliferation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal mitochondrial proliferation phenotype in transgenic mice from the MPO Gene-Phenotype 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.

abnormal mitochondrial chromosome morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal mitochondrial chromosome morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent sperm mitochondrial sheath Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent sperm mitochondrial sheath phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal sperm mitochondrial sheath morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal sperm mitochondrial sheath morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

disorganized mitochondrial cristae Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the disorganized mitochondrial cristae phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal mitochondrial inner membrane morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal mitochondrial inner membrane morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal mitochondrial shape Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal mitochondrial shape phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal mitochondrial physiology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal mitochondrial physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal mitochondrial crista morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal mitochondrial crista morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased mitochondrial proliferation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased mitochondrial proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal mitochondrial atp synthesis coupled electron transport Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal mitochondrial atp synthesis coupled electron transport phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal mitochondrial matrix morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal mitochondrial matrix morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased mitochondrial proliferation Gene Set

From MPO Gene-Phenotype Associations

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

myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay Gene Set

From OMIM Gene-Disease Associations

genes associated with the myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay phenotype from the curated OMIM Gene-Disease Associations dataset.

{deafness, mitochondrial, modifier of} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {deafness, mitochondrial, modifier of} phenotype from the curated OMIM Gene-Disease 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.

mitochondrial myopathy and sideroblastic anemia 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial myopathy and sideroblastic anemia 1 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.

mitochondrial Gene Set

From Phosphosite Textmining Biological Term Annotations

proteins co-occuring with the biological term mitochondrial in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.

Mitochondrial biogenesis Gene Set

From Reactome Pathways

proteins participating in the Mitochondrial biogenesis pathway from the Reactome Pathways dataset.

Import of palmitoyl-CoA into the mitochondrial matrix Gene Set

From Reactome Pathways

proteins participating in the Import of palmitoyl-CoA into the mitochondrial matrix pathway from the Reactome Pathways dataset.

Transcription from mitochondrial promoters Gene Set

From Reactome Pathways

proteins participating in the Transcription from mitochondrial promoters pathway from the Reactome Pathways dataset.

Vpr-mediated induction of apoptosis by mitochondrial outer membrane permeabilization Gene Set

From Reactome Pathways

proteins participating in the Vpr-mediated induction of apoptosis by mitochondrial outer membrane permeabilization pathway from the Reactome Pathways dataset.

Mitochondrial Fatty Acid Beta-Oxidation Gene Set

From Reactome Pathways

proteins participating in the Mitochondrial Fatty Acid Beta-Oxidation pathway from the Reactome Pathways dataset.

RNA Polymerase I, RNA Polymerase III, and Mitochondrial Transcription Gene Set

From Reactome Pathways

proteins participating in the RNA Polymerase I, RNA Polymerase III, and Mitochondrial Transcription pathway from the Reactome Pathways dataset.

Mitochondrial Uncoupling Proteins Gene Set

From Reactome Pathways

proteins participating in the Mitochondrial Uncoupling Proteins pathway from the Reactome Pathways dataset.

Mitochondrial transcription initiation Gene Set

From Reactome Pathways

proteins participating in the Mitochondrial transcription initiation pathway from the Reactome Pathways dataset.

Mitochondrial ABC transporters Gene Set

From Reactome Pathways

proteins participating in the Mitochondrial ABC transporters pathway from the Reactome Pathways dataset.

mitochondrial fatty acid beta-oxidation of unsaturated fatty acids Gene Set

From Reactome Pathways

proteins participating in the mitochondrial fatty acid beta-oxidation of unsaturated fatty acids pathway from the Reactome Pathways dataset.

Mitochondrial translation initiation Gene Set

From Reactome Pathways

proteins participating in the Mitochondrial translation initiation pathway from the Reactome Pathways dataset.

Mitochondrial tRNA aminoacylation Gene Set

From Reactome Pathways

proteins participating in the Mitochondrial tRNA aminoacylation pathway from the Reactome Pathways dataset.

Transcriptional activation of mitochondrial biogenesis Gene Set

From Reactome Pathways

proteins participating in the Transcriptional activation of mitochondrial biogenesis pathway from the Reactome Pathways dataset.

Mitochondrial transcription termination Gene Set

From Reactome Pathways

proteins participating in the Mitochondrial transcription termination pathway from the Reactome Pathways dataset.

Mitochondrial translation termination Gene Set

From Reactome Pathways

proteins participating in the Mitochondrial translation termination pathway from the Reactome Pathways dataset.

Mitochondrial protein import Gene Set

From Reactome Pathways

proteins participating in the Mitochondrial protein import pathway from the Reactome Pathways dataset.

Mitochondrial translation elongation Gene Set

From Reactome Pathways

proteins participating in the Mitochondrial translation elongation pathway from the Reactome Pathways dataset.

Mitochondrial translation Gene Set

From Reactome Pathways

proteins participating in the Mitochondrial translation pathway from the Reactome Pathways dataset.

mitochondrial fatty acid beta-oxidation of saturated fatty acids Gene Set

From Reactome Pathways

proteins participating in the mitochondrial fatty acid beta-oxidation of saturated fatty acids pathway from the Reactome Pathways dataset.

Mitochondrial iron-sulfur cluster biogenesis Gene Set

From Reactome Pathways

proteins participating in the Mitochondrial iron-sulfur cluster biogenesis pathway from the Reactome Pathways dataset.

Mitochondrial Gene Expression(Mus musculus) Gene Set

From Wikipathways Pathways

proteins participating in the Mitochondrial Gene Expression(Mus musculus) pathway from the Wikipathways Pathways dataset.

Mitochondrial LC-Fatty Acid Beta-Oxidation(Mus musculus) Gene Set

From Wikipathways Pathways

proteins participating in the Mitochondrial LC-Fatty Acid Beta-Oxidation(Mus musculus) pathway from the Wikipathways Pathways dataset.

Mitochondrial LC-Fatty Acid Beta-Oxidation(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Mitochondrial LC-Fatty Acid Beta-Oxidation(Homo sapiens) pathway from the Wikipathways Pathways dataset.

Mitochondrial Gene Expression(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Mitochondrial Gene Expression(Homo sapiens) pathway from the Wikipathways Pathways dataset.

Lynch syndrome:Turcot syndrome Gene Set

From ClinVar Gene-Phenotype Associations

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

Hereditary cancer-predisposing syndrome:Lynch syndrome Gene Set

From ClinVar Gene-Phenotype Associations

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

Zunich neuroectodermal syndrome:Zunich neuroectodermal syndrome Gene Set

From ClinVar Gene-Phenotype Associations

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

Von Hippel-Lindau syndrome:Hereditary cancer-predisposing syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Von Hippel-Lindau syndrome:Hereditary cancer-predisposing syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Noonan syndrome and Noonan-related syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Noonan syndrome and Noonan-related syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Lynch syndrome:Hereditary cancer-predisposing syndrome Gene Set

From ClinVar Gene-Phenotype Associations

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

Lynch syndrome:Lynch syndrome Gene Set

From ClinVar Gene-Phenotype Associations

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

Marfan's syndrome:Marfan's syndrome Gene Set

From ClinVar Gene-Phenotype Associations

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

Hereditary cancer-predisposing syndrome:Peutz-Jeghers syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary cancer-predisposing syndrome:Peutz-Jeghers syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

IFAP syndrome with or without BRESHECK syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the IFAP syndrome with or without BRESHECK syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Lynch syndrome I:Lynch syndrome Gene Set

From ClinVar Gene-Phenotype Associations

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

Hereditary cancer-predisposing syndrome:Hereditary cancer-predisposing syndrome Gene Set

From ClinVar Gene-Phenotype Associations

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

Miller-McKusick-Malvaux-Syndrome (3M Syndrome) Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Miller-McKusick-Malvaux-Syndrome (3M Syndrome) from the curated CTD Gene-Disease Associations dataset.

Digeorge Syndrome/Velocardiofacial Syndrome Complex 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Digeorge Syndrome/Velocardiofacial Syndrome Complex 2 from the curated CTD Gene-Disease Associations dataset.

menarch; natural menopause; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious Gene Set

From GAD Gene-Disease Associations

genes associated with the disease menarch; natural menopause; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

amyloidosis; behcet syndrome; familial mediterranean fever; irritable bowel syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease amyloidosis; behcet syndrome; familial mediterranean fever; irritable bowel syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; cystic fibrosis; klinefelter syndrome; klinefelter's syndrome; oligospermia; sex chromosome aberrations; translocation, genetic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; cystic fibrosis; klinefelter syndrome; klinefelter's syndrome; oligospermia; sex chromosome aberrations; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adult respiratory distress syndrome; respiratory distress syndrome, adult; sepsis; systemic infection; wounds and injuries Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adult respiratory distress syndrome; respiratory distress syndrome, adult; sepsis; systemic infection; wounds and injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hyperhomocysteinemia; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

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

adult respiratory distress syndrome; multiple organ failure; respiratory distress syndrome, adult; wounds and injuries Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adult respiratory distress syndrome; multiple organ failure; respiratory distress syndrome, adult; wounds and injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cornelia de lange syndrome; de lange syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cornelia de lange syndrome; de lange syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fatigue syndrome, chronic; fatigue syndrome; postviral Gene Set

From GAD Gene-Disease Associations

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

pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormalities, multiple; aortic aneurysm, thoracic; marfan syndrome; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; aortic aneurysm, thoracic; marfan syndrome; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

resp distress syndrome neonatal; respiratory distress syndrome, newborn Gene Set

From GAD Gene-Disease Associations

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

obstetric labor, premature; resp distress syndrome neonatal; respiratory distress syndrome, newborn; tachycardia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease obstetric labor, premature; resp distress syndrome neonatal; respiratory distress syndrome, newborn; tachycardia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hyperandrogenism; polycystic ovarian syndrome; polycystic ovary syndrome; puberty, precocious Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hyperandrogenism; polycystic ovarian syndrome; polycystic ovary syndrome; puberty, precocious in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bronchopulmonary dysplasia; resp distress syndrome neonatal; respiratory distress syndrome, newborn; respiratory tract infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bronchopulmonary dysplasia; resp distress syndrome neonatal; respiratory distress syndrome, newborn; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lung diseases; resp distress syndrome neonatal; respiratory distress syndrome, newborn Gene Set

From GAD Gene-Disease Associations

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

hyperandrogenism; insulin resistance; obesity; polycystic ovarian syndrome; polycystic ovary syndrome; thinness Gene Set

From GAD Gene-Disease Associations

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

restless legs syndrome; tourette syndrome Gene Set

From GAD Gene-Disease Associations

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

endometriosis; infertility, female; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease endometriosis; infertility, female; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

polycystic ovarian syndrome; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

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

obesity; natural menopause; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious; thrombophilia; tobacco use disorder Gene Set

From GAD Gene-Disease Associations

genes associated with the disease obesity; natural menopause; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious; thrombophilia; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fetal alcohol syndrome; syndrome; fetal, alcohol (dysmorphic) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fetal alcohol syndrome; syndrome; fetal, alcohol (dysmorphic) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

behcet syndrome; uveomeningoencephalitic syndrome Gene Set

From GAD Gene-Disease Associations

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

hyperandrogenism; hyperinsulinism; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

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