Name

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

Pyridoxamine 5-Prime-Phosphate Oxidase Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pyridoxamine 5-Prime-Phosphate Oxidase Deficiency from the curated CTD Gene-Disease Associations dataset.

Uridine-5'-Monophosphate Gene Set

From DrugBank Drug Targets

interacting proteins for the Uridine-5'-Monophosphate drug from the curated DrugBank Drug Targets dataset.

Uridine-5'-Monophosphate Glucopyranosyl-Monophosphateester Gene Set

From DrugBank Drug Targets

interacting proteins for the Uridine-5'-Monophosphate Glucopyranosyl-Monophosphateester drug from the curated DrugBank Drug Targets dataset.

2-amino-uridine-5'-monophosphate Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the 2-amino-uridine-5'-monophosphate ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

Uridine 5'-monophosphate Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the Uridine 5'-monophosphate metabolite from the curated HMDB Metabolites of Enzymes dataset.

anemia; anemia, sickle cell; hemoglobin c disease; hemoglobin sc disease; heterozygous haemoglobin s; malaria, falciparum; parasitemia; sickle cell anemia; sickle cell trait Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia; anemia, sickle cell; hemoglobin c disease; hemoglobin sc disease; heterozygous haemoglobin s; malaria, falciparum; parasitemia; sickle cell anemia; sickle cell trait in GWAS and other genetic association datasets from the GAD Gene-Disease 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.

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.

anemia, iron deficiency; anemia of chronic disease Gene Set

From GAD Gene-Disease Associations

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

alpha thalassemia; alpha-thalassemia; anemia, sickle cell; glucosephosphate dehydrogenase deficiency; hemolysis; sickle cell anemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha thalassemia; alpha-thalassemia; anemia, sickle cell; glucosephosphate dehydrogenase deficiency; hemolysis; sickle cell anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, sickle cell; glucosephosphate dehydrogenase deficiency; sickle cell anemia Gene Set

From GAD Gene-Disease Associations

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

dna 5'-adenosine monophosphate hydrolase activity Gene Set

From GO Molecular Function Annotations

genes performing the dna 5'-adenosine monophosphate hydrolase activity molecular function from the curated GO Molecular Function Annotations dataset.

Prime and Bond NT Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical Prime and Bond NT from the curated CTD Gene-Chemical Interactions dataset.

prime Gene Set

From GeneRIF Biological Term Annotations

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

reduced orotidine 5-prime phosphate decarboxylase activity Gene Set

From HPO Gene-Disease Associations

genes associated with the reduced orotidine 5-prime phosphate decarboxylase activity phenotype by mapping known disease genes to disease phenotypes from the HPO 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.

Hemolytic anemia Gene Set

From ClinVar Gene-Phenotype Associations

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

Renal tubular acidosis, distal, with hemolytic anemia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Renal tubular acidosis, distal, with hemolytic anemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Anemia, Hemolytic, Congenital Nonspherocytic Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Anemia, Hemolytic, Congenital Nonspherocytic from the curated CTD Gene-Disease Associations dataset.

Renal Tubular Acidosis, Distal, With Hemolytic Anemia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Renal Tubular Acidosis, Distal, With Hemolytic Anemia from the curated CTD Gene-Disease Associations dataset.

Anemia, Hemolytic Gene Set

From CTD Gene-Disease Associations

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

Anemia, Hemolytic, Congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Anemia, Hemolytic, Congenital from the curated CTD Gene-Disease Associations dataset.

SYSTEMIC LUPUS ERYTHEMATOSUS WITH HEMOLYTIC ANEMIA, SUSCEPTIBILITY TO, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease SYSTEMIC LUPUS ERYTHEMATOSUS WITH HEMOLYTIC ANEMIA, SUSCEPTIBILITY TO, 1 from the curated CTD Gene-Disease Associations dataset.

Anemia, Hemolytic, Autoimmune Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Anemia, Hemolytic, Autoimmune from the curated CTD Gene-Disease Associations dataset.

hemolytic anemia Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

congenital hemolytic anemia Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

hemolytic anemia Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

genes associated with the disease hemolytic anemia in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

autoimmune hemolytic anemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

congenital nonspherocytic hemolytic anemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

hemolytic anemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

congenital hemolytic anemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

hereditary nonspherocytic hemolytic anemia (hnsha). Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hereditary nonspherocytic hemolytic anemia (hnsha). in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hereditary hemolytic anemia. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hereditary hemolytic anemia. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, hemolytic Gene Set

From GAD Gene-Disease Associations

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

anemia, hemolytic; hepatitis c, chronic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, hemolytic; hepatitis c, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hereditary hemolytic anemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hereditary hemolytic anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic hemolytic anemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic hemolytic anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hemolytic anemia Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease hemolytic anemia in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

congenital hemolytic anemia Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease congenital hemolytic anemia in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

hemolytic anemia Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the hemolytic anemia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

nonspherocytic hemolytic anemia Gene Set

From HPO Gene-Disease Associations

genes associated with the nonspherocytic hemolytic anemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

fava bean-induced hemolytic anemia Gene Set

From HPO Gene-Disease Associations

genes associated with the fava bean-induced hemolytic anemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

compensated hemolytic anemia Gene Set

From HPO Gene-Disease Associations

genes associated with the compensated hemolytic anemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

coombs-positive hemolytic anemia Gene Set

From HPO Gene-Disease Associations

genes associated with the coombs-positive hemolytic anemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

autoimmune hemolytic anemia Gene Set

From HPO Gene-Disease Associations

genes associated with the autoimmune hemolytic anemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hemolytic anemia Gene Set

From HPO Gene-Disease Associations

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

congenital hemolytic anemia Gene Set

From HPO Gene-Disease Associations

genes associated with the congenital hemolytic anemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

microangiopathic hemolytic anemia Gene Set

From HPO Gene-Disease Associations

genes associated with the microangiopathic hemolytic anemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

chronic hemolytic anemia Gene Set

From HPO Gene-Disease Associations

genes associated with the chronic hemolytic anemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

episodic hemolytic anemia Gene Set

From HPO Gene-Disease Associations

genes associated with the episodic hemolytic anemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Anemia, Hemolytic, Congenital Nonspherocytic Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Anemia, Hemolytic, Congenital Nonspherocytic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Anemia, Hemolytic Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Anemia, Hemolytic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Anemia, Hemolytic, Congenital Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Anemia, Hemolytic, Congenital phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Anemia, Hemolytic, Autoimmune Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Anemia, Hemolytic, Autoimmune phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

decreased susceptibility to autoimmune hemolytic anemia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to autoimmune hemolytic anemia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

hemolytic anemia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the hemolytic anemia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to autoimmune hemolytic anemia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to autoimmune hemolytic anemia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

hemolytic anemia, cd59-mediated, with or without immune-mediated polyneuropathy Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemolytic anemia, cd59-mediated, with or without immune-mediated polyneuropathy phenotype from the curated OMIM Gene-Disease Associations dataset.

anemia, neonatal hemolytic, fatal and near-fatal Gene Set

From OMIM Gene-Disease Associations

genes associated with the anemia, neonatal hemolytic, fatal and near-fatal phenotype from the curated OMIM Gene-Disease Associations dataset.

{systemic lupus erythematosus with hemolytic anemia} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {systemic lupus erythematosus with hemolytic anemia} phenotype from the curated OMIM Gene-Disease Associations dataset.

anemia, hemolytic, rh-null, regulator type Gene Set

From OMIM Gene-Disease Associations

genes associated with the anemia, hemolytic, rh-null, regulator type phenotype from the curated OMIM 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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

Adenosine monophosphate deaminase deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Adenosine monophosphate deaminase deficiency from the curated CTD Gene-Disease 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.

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.

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.

anemia, sickle cell; bacterial infections; enterobacteriaceae infections; osteomyelitis; sepsis; sickle cell anemia; staphylococcal infections; systemic infection; unspecified osteomyelitis nos Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell; bacterial infections; enterobacteriaceae infections; osteomyelitis; sepsis; sickle cell anemia; staphylococcal infections; systemic infection; unspecified osteomyelitis nos in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, sickle cell; infarction; ischemia; sickle cell anemia; vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell; infarction; ischemia; sickle cell anemia; vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, sickle cell; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; sickle cell anemia Gene Set

From GAD Gene-Disease Associations

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

anemia, aplastic; aplastic anemia; myelodysplastic syndromes; preleukemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, aplastic; aplastic anemia; myelodysplastic syndromes; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, sickle cell; apoplexy; sickle cell anemia; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell; apoplexy; sickle cell anemia; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, sickle cell; beta thalassemia; beta-thalassemia; sickle cell anemia Gene Set

From GAD Gene-Disease Associations

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

anemia, sickle cell; pain; sickle cell anemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell; pain; sickle cell anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, sickle cell; sickle cell anemia; thalassemia Gene Set

From GAD Gene-Disease Associations

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

anemia, sickle cell; beta thalassemia; beta-thalassemia; sickle cell anemia; thrombophilia Gene Set

From GAD Gene-Disease Associations

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

anemia, aplastic; aplastic anemia; leukemia, myeloid; myelodysplastic syndromes; myeloid leukemia; preleukemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, aplastic; aplastic anemia; leukemia, myeloid; myelodysplastic syndromes; myeloid leukemia; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, sickle cell; bone diseases; sickle cell anemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell; bone diseases; sickle cell anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, sickle cell; inflammation; sickle cell anemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell; inflammation; sickle cell anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, sickle cell; glycogen storage disease type i; sickle cell anemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell; glycogen storage disease type i; sickle cell anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fanconi anemia; fanconi's anemia; kidney neoplasms; nephroblastoma; wilms tumor Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fanconi anemia; fanconi's anemia; kidney neoplasms; nephroblastoma; wilms tumor in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, aplastic; aplastic anemia; genetic diseases, inborn; graft vs host disease; hematologic neoplasms; recurrence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, aplastic; aplastic anemia; genetic diseases, inborn; graft vs host disease; hematologic neoplasms; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, sickle cell; bacterial infections; sickle cell anemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell; bacterial infections; sickle cell anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, sickle cell; sickle cell anemia Gene Set

From GAD Gene-Disease Associations

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

fanconi anemia; fanconi's anemia; hematologic diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fanconi anemia; fanconi's anemia; hematologic diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, sickle cell; sickle cell anemia; trachoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell; sickle cell anemia; trachoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, refractory; anemia, sideroblastic; myelodysplastic syndromes; thrombocytosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, refractory; anemia, sideroblastic; myelodysplastic syndromes; thrombocytosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, sickle cell; heterozygous haemoglobin s; malaria; sickle cell anemia; sickle cell trait Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell; heterozygous haemoglobin s; malaria; sickle cell anemia; sickle cell trait in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, sickle cell; hemochromatosis; iron overload; sickle cell anemia Gene Set

From GAD Gene-Disease Associations

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

albuminuria; alpha thalassemia; alpha-thalassemia; anemia, sickle cell; sickle cell anemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease albuminuria; alpha thalassemia; alpha-thalassemia; anemia, sickle cell; sickle cell anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, diamond-blackfan; diamond-blackfan anemia Gene Set

From GAD Gene-Disease Associations

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

anemia, aplastic; aplastic anemia; disease susceptibility Gene Set

From GAD Gene-Disease Associations

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

anemia, sideroblastic; hemochromatosis; myelodysplastic syndromes; preleukemia; sideroblastic anemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sideroblastic; hemochromatosis; myelodysplastic syndromes; preleukemia; sideroblastic anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, sickle cell; beta thalassemia; beta-thalassemia; blood coagulation disorders, inherited; sickle cell anemia; vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell; beta thalassemia; beta-thalassemia; blood coagulation disorders, inherited; sickle cell anemia; vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, aplastic; aplastic anemia; hemoglobinuria, paroxysmal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, aplastic; aplastic anemia; hemoglobinuria, paroxysmal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, aplastic; aplastic anemia Gene Set

From GAD Gene-Disease Associations

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

alpha thalassemia; alpha-thalassemia; anemia, sickle cell; bone necrosis; osteonecrosis; sickle cell anemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha thalassemia; alpha-thalassemia; anemia, sickle cell; bone necrosis; osteonecrosis; sickle cell anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alpha thalassemia; alpha-thalassemia; anemia, sickle cell; sickle cell anemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha thalassemia; alpha-thalassemia; anemia, sickle cell; sickle cell anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, sickle cell; peripheral vascular diseases; sickle cell anemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell; peripheral vascular diseases; sickle cell anemia 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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

{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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

{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.

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.

Hypermethioninemia with s-adenosylhomocysteine hydrolase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypermethioninemia with s-adenosylhomocysteine hydrolase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

3-hydroxyisobutryl-coa hydrolase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the 3-hydroxyisobutryl-coa hydrolase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hypermethioninemia with deficiency of s-adenosylhomocysteine hydrolase Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypermethioninemia with deficiency of s-adenosylhomocysteine hydrolase phenotype from the curated OMIM Gene-Disease Associations dataset.

Defective AHCY causes Hypermethioninemia with S-adenosylhomocysteine hydrolase deficiency (HMAHCHD) Gene Set

From Reactome Pathways

proteins participating in the Defective AHCY causes Hypermethioninemia with S-adenosylhomocysteine hydrolase deficiency (HMAHCHD) pathway from the Reactome Pathways dataset.

toxoplasmosis, cerebral; toxoplasmosis, congenital; toxoplasmosis, ocular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease toxoplasmosis, cerebral; toxoplasmosis, congenital; toxoplasmosis, ocular in GWAS and other genetic association datasets from the GAD 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.

Uridine Diphosphate Glucuronic Acid Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical Uridine Diphosphate Glucuronic Acid from the curated CTD Gene-Chemical Interactions dataset.

Uridine Diphosphate N-Acetylgalactosamine Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical Uridine Diphosphate N-Acetylgalactosamine from the curated CTD Gene-Chemical Interactions dataset.

Uridine Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical Uridine from the curated CTD Gene-Chemical Interactions dataset.

Uridine Diphosphate Galactose Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical Uridine Diphosphate Galactose from the curated CTD Gene-Chemical Interactions dataset.

Uridine Diphosphate Glucose Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical Uridine Diphosphate Glucose from the curated CTD Gene-Chemical Interactions dataset.

Uridine Triphosphate Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical Uridine Triphosphate from the curated CTD Gene-Chemical Interactions dataset.

Uridine Diphosphate Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical Uridine Diphosphate from the curated CTD Gene-Chemical Interactions dataset.

Uridine-5'-Diphosphate Gene Set

From DrugBank Drug Targets

interacting proteins for the Uridine-5'-Diphosphate drug from the curated DrugBank Drug Targets dataset.

P1-(Adenosine-5'-P5-(Uridine-5')Pentaphosphate Gene Set

From DrugBank Drug Targets

interacting proteins for the P1-(Adenosine-5'-P5-(Uridine-5')Pentaphosphate drug from the curated DrugBank Drug Targets dataset.

Uridine-2',3'-Vanadate Gene Set

From DrugBank Drug Targets

interacting proteins for the Uridine-2',3'-Vanadate drug from the curated DrugBank Drug Targets dataset.

Uridine 5'-Triphosphate Gene Set

From DrugBank Drug Targets

interacting proteins for the Uridine 5'-Triphosphate drug from the curated DrugBank Drug Targets dataset.

Uridine-Diphosphate-N-Acetylglucosamine Gene Set

From DrugBank Drug Targets

interacting proteins for the Uridine-Diphosphate-N-Acetylglucosamine drug from the curated DrugBank Drug Targets dataset.

Glucose-Uridine-C1,5'-Diphosphate Gene Set

From DrugBank Drug Targets

interacting proteins for the Glucose-Uridine-C1,5'-Diphosphate drug from the curated DrugBank Drug Targets dataset.

Phosphoric Acid-2'-[2'-Deoxy-Uridine]Ester-5'-Guanosine Ester Gene Set

From DrugBank Drug Targets

interacting proteins for the Phosphoric Acid-2'-[2'-Deoxy-Uridine]Ester-5'-Guanosine Ester drug from the curated DrugBank Drug Targets dataset.

Uridine-Diphosphate-N-Acetylgalactosamine Gene Set

From DrugBank Drug Targets

interacting proteins for the Uridine-Diphosphate-N-Acetylgalactosamine drug from the curated DrugBank Drug Targets dataset.

Uridine Diphosphate Galactose Gene Set

From DrugBank Drug Targets

interacting proteins for the Uridine Diphosphate Galactose drug from the curated DrugBank Drug Targets dataset.

Uridine Gene Set

From DrugBank Drug Targets

interacting proteins for the Uridine drug from the curated DrugBank Drug Targets dataset.

6-Aminohexyl-Uridine-C1,5'-Diphosphate Gene Set

From DrugBank Drug Targets

interacting proteins for the 6-Aminohexyl-Uridine-C1,5'-Diphosphate drug from the curated DrugBank Drug Targets dataset.

uridine Gene Set

From GeneRIF Biological Term Annotations

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

trna wobble position uridine thiolation Gene Set

From GO Biological Process Annotations

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

cytidine to uridine editing Gene Set

From GO Biological Process Annotations

genes participating in the cytidine to uridine editing biological process from the curated GO Biological Process Annotations dataset.

uridine transport Gene Set

From GO Biological Process Annotations

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

trna wobble uridine modification Gene Set

From GO Biological Process Annotations

genes participating in the trna wobble uridine modification 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.

uridine metabolic process Gene Set

From GO Biological Process Annotations

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

uridine kinase activity Gene Set

From GO Molecular Function Annotations

genes performing the uridine kinase activity molecular function from the curated GO Molecular Function Annotations dataset.

uridine-diphosphatase activity Gene Set

From GO Molecular Function Annotations

genes performing the uridine-diphosphatase activity molecular function from the curated GO Molecular Function Annotations dataset.

rrna (uridine-2'-o-)-methyltransferase activity Gene Set

From GO Molecular Function Annotations

genes performing the rrna (uridine-2'-o-)-methyltransferase activity molecular function from the curated GO Molecular Function Annotations dataset.

uridine phosphorylase activity Gene Set

From GO Molecular Function Annotations

genes performing the uridine phosphorylase activity molecular function from the curated GO Molecular Function Annotations dataset.

rrna (uridine) methyltransferase activity Gene Set

From GO Molecular Function Annotations

genes performing the rrna (uridine) methyltransferase activity molecular function from the curated GO Molecular Function Annotations dataset.

uridine nucleotide receptor activity Gene Set

From GO Molecular Function Annotations

genes performing the uridine nucleotide receptor activity molecular function from the curated GO Molecular Function Annotations dataset.

Uridine Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the Uridine metabolite from the curated HMDB Metabolites of Enzymes dataset.

Uridine diphosphategalactose Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the Uridine diphosphategalactose metabolite from the curated HMDB Metabolites of Enzymes dataset.

Uridine diphosphate glucuronic acid Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the Uridine diphosphate glucuronic acid metabolite from the curated HMDB Metabolites of Enzymes dataset.

Uridine diphosphate glucose Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the Uridine diphosphate glucose metabolite from the curated HMDB Metabolites of Enzymes dataset.

Uridine diphosphate-N-acetylglucosamine Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the Uridine diphosphate-N-acetylglucosamine metabolite from the curated HMDB Metabolites of Enzymes dataset.

Uridine 2',3'-cyclic phosphate Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the Uridine 2',3'-cyclic phosphate metabolite from the curated HMDB Metabolites of Enzymes dataset.

Uridine 2'-phosphate Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the Uridine 2'-phosphate metabolite from the curated HMDB Metabolites of Enzymes dataset.

Uridine diphosphate-N-acetylgalactosamine Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the Uridine diphosphate-N-acetylgalactosamine metabolite from the curated HMDB Metabolites of Enzymes dataset.

Uridine 5'-diphosphate Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the Uridine 5'-diphosphate metabolite from the curated HMDB Metabolites of Enzymes dataset.

Uridine triphosphate Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the Uridine triphosphate metabolite from the curated HMDB Metabolites of Enzymes dataset.

Uridine-cytidine kinase 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Uridine-cytidine kinase 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Uridine-cytidine kinase 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Uridine-cytidine kinase 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Uridine kinase like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Uridine kinase like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Uridine phosphorylase, eukaryotic Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Uridine phosphorylase, eukaryotic protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Uridine-cytidine kinase-like 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Uridine-cytidine kinase-like 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Phosphoribulokinase/uridine kinase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Phosphoribulokinase/uridine kinase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Anemia, Iron-Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Anemia, Iron-Deficiency from the curated CTD Gene-Disease Associations dataset.

Iron-Refractory Iron Deficiency Anemia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Iron-Refractory Iron Deficiency Anemia from the curated CTD Gene-Disease Associations dataset.

iron deficiency anemia Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

genes associated with the disease iron deficiency anemia in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

folic acid deficiency anemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

deficiency anemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

iron deficiency anemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

pyridoxine deficiency anemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

protein-deficiency anemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

alpha-thalassemia; anemia; glucosephosphate dehydrogenase deficiency; malaria, falciparum; sickle cell trait Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha-thalassemia; anemia; glucosephosphate dehydrogenase deficiency; malaria, falciparum; sickle cell trait in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alpha-thalassemia; anemia, sickle cell; glucosephosphate dehydrogenase deficiency; hemolysis; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha-thalassemia; anemia, sickle cell; glucosephosphate dehydrogenase deficiency; hemolysis; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, iron deficiency Gene Set

From GAD Gene-Disease Associations

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

sickle cell anemia; g6pd deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease sickle cell anemia; g6pd deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia; gastritis, atrophic; nervous system diseases; vitamin b 12 deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia; gastritis, atrophic; nervous system diseases; vitamin b 12 deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, iron-deficiency; kidney failure, chronic Gene Set

From GAD Gene-Disease Associations

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

anemia, iron-deficiency; hemochromatosis; inflammation Gene Set

From GAD Gene-Disease Associations

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

anemia, iron-deficiency; hemochromatosis Gene Set

From GAD Gene-Disease Associations

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

anemia, iron-deficiency; malaria Gene Set

From GAD Gene-Disease Associations

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

anemia, iron-deficiency; polycythemia vera Gene Set

From GAD Gene-Disease Associations

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

anemia, iron-deficiency Gene Set

From GAD Gene-Disease Associations

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

anemia, iron-deficiency; avitaminosis Gene Set

From GAD Gene-Disease Associations

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

iron deficiency anemia Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease iron deficiency anemia in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

iron deficiency anemia Gene Set

From HPO Gene-Disease Associations

genes associated with the iron deficiency anemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Anemia, Iron-Deficiency Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Anemia, Iron-Deficiency phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

iron-refractory iron deficiency anemia Gene Set

From OMIM Gene-Disease Associations

genes associated with the iron-refractory iron deficiency anemia phenotype from the curated OMIM Gene-Disease Associations dataset.

anemia; drug toxicity; lymphoma, non-hodgkin; precursor cell lymphoblastic leukemia-lymphoma; thrombocytopenia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia; drug toxicity; lymphoma, non-hodgkin; precursor cell lymphoblastic leukemia-lymphoma; thrombocytopenia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Atypical hemolytic-uremic syndrome 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Atypical hemolytic-uremic syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Atypical hemolytic-uremic syndrome 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Atypical hemolytic-uremic syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

atypical hemolytic-uremic syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the atypical hemolytic-uremic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Atypical Hemolytic Uremic Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Atypical Hemolytic Uremic Syndrome from the curated CTD Gene-Disease Associations dataset.

Hemolytic-Uremic Syndrome Gene Set

From CTD Gene-Disease Associations

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

hemolytic-uremic syndrome Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

hemolytic-uremic syndrome Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

hemolytic disease of the newborn Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hemolytic disease of the newborn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

haemolytic-uraemic syndrome; hemolytic-uremic syndrome; recurrence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease haemolytic-uraemic syndrome; hemolytic-uremic syndrome; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hemolytic-uremic syndrome; kidney failure, acute Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hemolytic-uremic syndrome; kidney failure, acute in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

escherichia coli infections; haemolytic-uraemic syndrome; hemolytic-uremic syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease escherichia coli infections; haemolytic-uraemic syndrome; hemolytic-uremic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic renal failure; haemolytic-uraemic syndrome; hemolytic-uremic syndrome; kidney failure, chronic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic renal failure; haemolytic-uraemic syndrome; hemolytic-uremic syndrome; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

haemolytic-uraemic syndrome; hemolytic-uremic syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease haemolytic-uraemic syndrome; hemolytic-uremic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hemolytic-uremic syndrome Gene Set

From GAD Gene-Disease Associations

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

hemolytic uremic syndrome Gene Set

From GAD Gene-Disease Associations

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

hemolytic disease Gene Set

From GAD Gene-Disease Associations

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

hemolytic-uremic syndrome; purpura, thrombotic thrombocytopenic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hemolytic-uremic syndrome; purpura, thrombotic thrombocytopenic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atypical hemolytic uremic syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atypical hemolytic uremic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

haemolytic-uraemic syndrome; hematologic diseases; hemolytic-uremic syndrome; purpura, thrombocytopenic; thrombocytopenic purpura Gene Set

From GAD Gene-Disease Associations

genes associated with the disease haemolytic-uraemic syndrome; hematologic diseases; hemolytic-uremic syndrome; purpura, thrombocytopenic; thrombocytopenic purpura in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hemolytic Gene Set

From GeneRIF Biological Term Annotations

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

hemolytic-uremic syndrome Gene Set

From HPO Gene-Disease Associations

genes associated with the hemolytic-uremic syndrome phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

macrocytic hemolytic disease Gene Set

From HPO Gene-Disease Associations

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

spontaneous hemolytic crises Gene Set

From HPO Gene-Disease Associations

genes associated with the spontaneous hemolytic crises phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Hemolytic-Uremic Syndrome Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Hemolytic-Uremic Syndrome phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

{hemolytic uremic syndrome, atypical, susceptibility to, 3} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {hemolytic uremic syndrome, atypical, susceptibility to, 3} phenotype from the curated OMIM Gene-Disease Associations dataset.

{hemolytic uremic syndrome, atypical, susceptibility to, 1} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {hemolytic uremic syndrome, atypical, susceptibility to, 1} phenotype from the curated OMIM Gene-Disease Associations dataset.

{hemolytic uremic syndrome, atypical, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {hemolytic uremic syndrome, atypical, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{hemolytic uremic syndrome, atypical, susceptibility to, 4} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {hemolytic uremic syndrome, atypical, susceptibility to, 4} phenotype from the curated OMIM Gene-Disease Associations dataset.

{hemolytic uremic syndrome, atypical, susceptibility to, 6} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {hemolytic uremic syndrome, atypical, susceptibility to, 6} phenotype from the curated OMIM Gene-Disease Associations dataset.

{hemolytic uremic syndrome, atypical, susceptibility to, 2} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {hemolytic uremic syndrome, atypical, susceptibility to, 2} phenotype from the curated OMIM Gene-Disease Associations dataset.

{hemolytic uremic syndrome, atypical, susceptibility to, 5} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {hemolytic uremic syndrome, atypical, susceptibility to, 5} phenotype from the curated OMIM Gene-Disease Associations dataset.

cyclic adenosine monophosphate-5108 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the cyclic adenosine monophosphate-5108 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

cyclic adenosine monophosphate-2969 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the cyclic adenosine monophosphate-2969 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

cyclic adenosine monophosphate-3531 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the cyclic adenosine monophosphate-3531 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

cyclic adenosine monophosphate-5533 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the cyclic adenosine monophosphate-5533 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

8-Bromo Cyclic Adenosine Monophosphate Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical 8-Bromo Cyclic Adenosine Monophosphate from the curated CTD Gene-Chemical Interactions dataset.

Guanosine Monophosphate Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical Guanosine Monophosphate from the curated CTD Gene-Chemical Interactions dataset.

Cytidine Monophosphate Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical Cytidine Monophosphate from the curated CTD Gene-Chemical Interactions dataset.

phenolphthalein monophosphate Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical phenolphthalein monophosphate from the curated CTD Gene-Chemical Interactions dataset.

N(6)-benzyl-cyclic adenosine 5'-monophosphate Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical N(6)-benzyl-cyclic adenosine 5'-monophosphate from the curated CTD Gene-Chemical Interactions dataset.

diethylstilbestrol monophosphate Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical diethylstilbestrol monophosphate from the curated CTD Gene-Chemical Interactions dataset.

cladribine monophosphate Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical cladribine monophosphate from the curated CTD Gene-Chemical Interactions dataset.

6-iodouridine 5'-monophosphate Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical 6-iodouridine 5'-monophosphate from the curated CTD Gene-Chemical Interactions dataset.

cisplatin-deoxy(guanosine monophosphate guanosine) adduct Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical cisplatin-deoxy(guanosine monophosphate guanosine) adduct from the curated CTD Gene-Chemical Interactions dataset.

Adenosine Monophosphate Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical Adenosine Monophosphate from the curated CTD Gene-Chemical Interactions dataset.

8-(4-chloro-phenylthio)-2'-O-methyladenosine-3'-5'-cyclic monophosphate Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical 8-(4-chloro-phenylthio)-2'-O-methyladenosine-3'-5'-cyclic monophosphate from the curated CTD Gene-Chemical Interactions dataset.

Purine Riboside-5'-Monophosphate Gene Set

From DrugBank Drug Targets

interacting proteins for the Purine Riboside-5'-Monophosphate drug from the curated DrugBank Drug Targets dataset.

N7-Methyl-Guanosine-5'-Monophosphate Gene Set

From DrugBank Drug Targets

interacting proteins for the N7-Methyl-Guanosine-5'-Monophosphate drug from the curated DrugBank Drug Targets dataset.

N-Pyridoxyl-Glycine-5-Monophosphate Gene Set

From DrugBank Drug Targets

interacting proteins for the N-Pyridoxyl-Glycine-5-Monophosphate drug from the curated DrugBank Drug Targets dataset.

Riboflavin Monophosphate Gene Set

From DrugBank Drug Targets

interacting proteins for the Riboflavin Monophosphate drug from the curated DrugBank Drug Targets dataset.

6-Chloropurine Riboside, 5'-Monophosphate Gene Set

From DrugBank Drug Targets

interacting proteins for the 6-Chloropurine Riboside, 5'-Monophosphate drug from the curated DrugBank Drug Targets dataset.

Cytidine-3'-Monophosphate Gene Set

From DrugBank Drug Targets

interacting proteins for the Cytidine-3'-Monophosphate drug from the curated DrugBank Drug Targets dataset.

8-Bromo-Adenosine-5'-Monophosphate Gene Set

From DrugBank Drug Targets

interacting proteins for the 8-Bromo-Adenosine-5'-Monophosphate drug from the curated DrugBank Drug Targets dataset.

Adenosine monophosphate Gene Set

From DrugBank Drug Targets

interacting proteins for the Adenosine monophosphate drug from the curated DrugBank Drug Targets dataset.

Cytidine-5'-Monophosphate Gene Set

From DrugBank Drug Targets

interacting proteins for the Cytidine-5'-Monophosphate drug from the curated DrugBank Drug Targets dataset.

N6-ISOPENTENYL-ADENOSINE-5'-MONOPHOSPHATE Gene Set

From DrugBank Drug Targets

interacting proteins for the N6-ISOPENTENYL-ADENOSINE-5'-MONOPHOSPHATE drug from the curated DrugBank Drug Targets dataset.

Guanosine-3'-Monophosphate-5'-Diphosphate Gene Set

From DrugBank Drug Targets

interacting proteins for the Guanosine-3'-Monophosphate-5'-Diphosphate drug from the curated DrugBank Drug Targets dataset.

Cyclic Adenosine Monophosphate Gene Set

From DrugBank Drug Targets

interacting proteins for the Cyclic Adenosine Monophosphate drug from the curated DrugBank Drug Targets dataset.

2'-Deoxycytidine-2'-Deoxyadenosine-3',5'-Monophosphate Gene Set

From DrugBank Drug Targets

interacting proteins for the 2'-Deoxycytidine-2'-Deoxyadenosine-3',5'-Monophosphate drug from the curated DrugBank Drug Targets dataset.

Ribavirin Monophosphate Gene Set

From DrugBank Drug Targets

interacting proteins for the Ribavirin Monophosphate drug from the curated DrugBank Drug Targets dataset.

cyclic 3',5'-thymidine monophosphate Gene Set

From DrugBank Drug Targets

interacting proteins for the cyclic 3',5'-thymidine monophosphate drug from the curated DrugBank Drug Targets dataset.

Guanosine-5'-Monophosphate Gene Set

From DrugBank Drug Targets

interacting proteins for the Guanosine-5'-Monophosphate drug from the curated DrugBank Drug Targets dataset.

5--Monophosphate-9-Beta-D-Ribofuranosyl Xanthine Gene Set

From DrugBank Drug Targets

interacting proteins for the 5--Monophosphate-9-Beta-D-Ribofuranosyl Xanthine drug from the curated DrugBank Drug Targets dataset.

3'-Azido-3'-Deoxythymidine-5'-Monophosphate Gene Set

From DrugBank Drug Targets

interacting proteins for the 3'-Azido-3'-Deoxythymidine-5'-Monophosphate drug from the curated DrugBank Drug Targets dataset.

1-[2-DEOXYRIBOFURANOSYL]-2,4-DIFLUORO-5-METHYL-BENZENE-5'MONOPHOSPHATE Gene Set

From DrugBank Drug Targets

interacting proteins for the 1-[2-DEOXYRIBOFURANOSYL]-2,4-DIFLUORO-5-METHYL-BENZENE-5'MONOPHOSPHATE drug from the curated DrugBank Drug Targets dataset.

2',3'-Dideoxythymidine-5'-Monophosphate Gene Set

From DrugBank Drug Targets

interacting proteins for the 2',3'-Dideoxythymidine-5'-Monophosphate drug from the curated DrugBank Drug Targets dataset.

Cyclic Guanosine Monophosphate Gene Set

From DrugBank Drug Targets

interacting proteins for the Cyclic Guanosine Monophosphate drug from the curated DrugBank Drug Targets dataset.

PUROMYCIN AMINONUCLEOSIDE-5'-MONOPHOSPHATE Gene Set

From DrugBank Drug Targets

interacting proteins for the PUROMYCIN AMINONUCLEOSIDE-5'-MONOPHOSPHATE drug from the curated DrugBank Drug Targets dataset.

2',5'-DIDEOXY-ADENOSINE 3'-MONOPHOSPHATE Gene Set

From DrugBank Drug Targets

interacting proteins for the 2',5'-DIDEOXY-ADENOSINE 3'-MONOPHOSPHATE drug from the curated DrugBank Drug Targets dataset.

2'-Deoxyuridine 3'-Monophosphate Gene Set

From DrugBank Drug Targets

interacting proteins for the 2'-Deoxyuridine 3'-Monophosphate drug from the curated DrugBank Drug Targets dataset.

N'-Pyridoxyl-Lysine-5'-Monophosphate Gene Set

From DrugBank Drug Targets

interacting proteins for the N'-Pyridoxyl-Lysine-5'-Monophosphate drug from the curated DrugBank Drug Targets dataset.

Cytidine-5'-Monophosphate-5-N-Acetylneuraminic Acid Gene Set

From DrugBank Drug Targets

interacting proteins for the Cytidine-5'-Monophosphate-5-N-Acetylneuraminic Acid drug from the curated DrugBank Drug Targets dataset.

6-O-Phosphoryl Inosine Monophosphate Gene Set

From DrugBank Drug Targets

interacting proteins for the 6-O-Phosphoryl Inosine Monophosphate drug from the curated DrugBank Drug Targets dataset.

Cytidine-2'-Monophosphate Gene Set

From DrugBank Drug Targets

interacting proteins for the Cytidine-2'-Monophosphate drug from the curated DrugBank Drug Targets dataset.

monophosphate Gene Set

From GeneRIF Biological Term Annotations

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

purine deoxyribonucleoside monophosphate metabolic process Gene Set

From GO Biological Process Annotations

genes participating in the purine deoxyribonucleoside monophosphate metabolic process biological process from the curated GO Biological Process Annotations dataset.

nucleoside monophosphate biosynthetic process Gene Set

From GO Biological Process Annotations

genes participating in the nucleoside monophosphate biosynthetic process biological process from the curated GO Biological Process Annotations dataset.

purine nucleoside monophosphate biosynthetic process Gene Set

From GO Biological Process Annotations

genes participating in the purine nucleoside monophosphate biosynthetic process biological process from the curated GO Biological Process Annotations dataset.

deoxyribonucleoside monophosphate biosynthetic process Gene Set

From GO Biological Process Annotations

genes participating in the deoxyribonucleoside monophosphate biosynthetic process biological process from the curated GO Biological Process Annotations dataset.

pyrimidine deoxyribonucleoside monophosphate catabolic process Gene Set

From GO Biological Process Annotations

genes participating in the pyrimidine deoxyribonucleoside monophosphate catabolic process biological process from the curated GO Biological Process Annotations dataset.

nucleoside monophosphate catabolic process Gene Set

From GO Biological Process Annotations

genes participating in the nucleoside monophosphate catabolic process biological process from the curated GO Biological Process Annotations dataset.

purine ribonucleoside monophosphate catabolic process Gene Set

From GO Biological Process Annotations

genes participating in the purine ribonucleoside monophosphate catabolic process biological process from the curated GO Biological Process Annotations dataset.

ribonucleoside monophosphate catabolic process Gene Set

From GO Biological Process Annotations

genes participating in the ribonucleoside monophosphate catabolic process biological process from the curated GO Biological Process Annotations dataset.

ribonucleoside monophosphate metabolic process Gene Set

From GO Biological Process Annotations

genes participating in the ribonucleoside monophosphate metabolic process biological process from the curated GO Biological Process Annotations dataset.

purine ribonucleoside monophosphate biosynthetic process Gene Set

From GO Biological Process Annotations

genes participating in the purine ribonucleoside monophosphate biosynthetic process biological process from the curated GO Biological Process Annotations dataset.

ribonucleoside monophosphate biosynthetic process Gene Set

From GO Biological Process Annotations

genes participating in the ribonucleoside monophosphate biosynthetic process biological process from the curated GO Biological Process Annotations dataset.

pyrimidine nucleoside monophosphate catabolic process Gene Set

From GO Biological Process Annotations

genes participating in the pyrimidine nucleoside monophosphate catabolic process biological process from the curated GO Biological Process Annotations dataset.

pyrimidine ribonucleoside monophosphate biosynthetic process Gene Set

From GO Biological Process Annotations

genes participating in the pyrimidine ribonucleoside monophosphate biosynthetic process biological process from the curated GO Biological Process Annotations dataset.

pyrimidine nucleoside monophosphate metabolic process Gene Set

From GO Biological Process Annotations

genes participating in the pyrimidine nucleoside monophosphate metabolic process biological process from the curated GO Biological Process Annotations dataset.

pyrimidine deoxyribonucleoside monophosphate metabolic process Gene Set

From GO Biological Process Annotations

genes participating in the pyrimidine deoxyribonucleoside monophosphate metabolic process biological process from the curated GO Biological Process Annotations dataset.

nucleoside monophosphate metabolic process Gene Set

From GO Biological Process Annotations

genes participating in the nucleoside monophosphate metabolic process biological process from the curated GO Biological Process Annotations dataset.

pyrimidine ribonucleoside monophosphate metabolic process Gene Set

From GO Biological Process Annotations

genes participating in the pyrimidine ribonucleoside monophosphate metabolic process biological process from the curated GO Biological Process Annotations dataset.

nucleoside monophosphate phosphorylation Gene Set

From GO Biological Process Annotations

genes participating in the nucleoside monophosphate phosphorylation biological process from the curated GO Biological Process Annotations dataset.

pyrimidine deoxyribonucleoside monophosphate biosynthetic process Gene Set

From GO Biological Process Annotations

genes participating in the pyrimidine deoxyribonucleoside monophosphate biosynthetic process biological process from the curated GO Biological Process Annotations dataset.

purine nucleoside monophosphate metabolic process Gene Set

From GO Biological Process Annotations

genes participating in the purine nucleoside monophosphate metabolic process biological process from the curated GO Biological Process Annotations dataset.

purine nucleoside monophosphate catabolic process Gene Set

From GO Biological Process Annotations

genes participating in the purine nucleoside monophosphate catabolic process biological process from the curated GO Biological Process Annotations dataset.

deoxyribonucleoside monophosphate catabolic process Gene Set

From GO Biological Process Annotations

genes participating in the deoxyribonucleoside monophosphate catabolic process biological process from the curated GO Biological Process Annotations dataset.

dolichyl monophosphate biosynthetic process Gene Set

From GO Biological Process Annotations

genes participating in the dolichyl monophosphate biosynthetic process biological process from the curated GO Biological Process Annotations dataset.

purine ribonucleoside monophosphate metabolic process Gene Set

From GO Biological Process Annotations

genes participating in the purine ribonucleoside monophosphate metabolic process biological process from the curated GO Biological Process Annotations dataset.

deoxyribonucleoside monophosphate metabolic process Gene Set

From GO Biological Process Annotations

genes participating in the deoxyribonucleoside monophosphate metabolic process biological process from the curated GO Biological Process Annotations dataset.

pyrimidine nucleoside monophosphate biosynthetic process Gene Set

From GO Biological Process Annotations

genes participating in the pyrimidine nucleoside monophosphate biosynthetic process biological process from the curated GO Biological Process Annotations dataset.

inositol monophosphate 1-phosphatase activity Gene Set

From GO Molecular Function Annotations

genes performing the inositol monophosphate 1-phosphatase activity molecular function from the curated GO Molecular Function Annotations dataset.

deoxyribonucleoside 5'-monophosphate n-glycosidase activity Gene Set

From GO Molecular Function Annotations

genes performing the deoxyribonucleoside 5'-monophosphate n-glycosidase activity molecular function from the curated GO Molecular Function Annotations dataset.

inositol monophosphate phosphatase activity Gene Set

From GO Molecular Function Annotations

genes performing the inositol monophosphate phosphatase activity molecular function from the curated GO Molecular Function Annotations dataset.

cyclic pyranopterin monophosphate synthase activity Gene Set

From GO Molecular Function Annotations

genes performing the cyclic pyranopterin monophosphate synthase activity molecular function from the curated GO Molecular Function Annotations dataset.

phosphatidylinositol monophosphate phosphatase activity Gene Set

From GO Molecular Function Annotations

genes performing the phosphatidylinositol monophosphate phosphatase activity molecular function from the curated GO Molecular Function Annotations dataset.

inositol monophosphate 4-phosphatase activity Gene Set

From GO Molecular Function Annotations

genes performing the inositol monophosphate 4-phosphatase activity molecular function from the curated GO Molecular Function Annotations dataset.

inositol monophosphate 3-phosphatase activity Gene Set

From GO Molecular Function Annotations

genes performing the inositol monophosphate 3-phosphatase activity molecular function from the curated GO Molecular Function Annotations dataset.

farnesyl monophosphate Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the farnesyl monophosphate ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

Cytidine monophosphate N-acetylneuraminic acid Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the Cytidine monophosphate N-acetylneuraminic acid metabolite from the curated HMDB Metabolites of Enzymes dataset.

Cyclic pyranopterin monophosphate Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the Cyclic pyranopterin monophosphate metabolite from the curated HMDB Metabolites of Enzymes dataset.

5-Fluorodeoxyuridine monophosphate Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the 5-Fluorodeoxyuridine monophosphate metabolite from the curated HMDB Metabolites of Enzymes dataset.

6-Thioxanthine 5'-monophosphate Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the 6-Thioxanthine 5'-monophosphate metabolite from the curated HMDB Metabolites of Enzymes dataset.

Thiamine monophosphate Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the Thiamine monophosphate metabolite from the curated HMDB Metabolites of Enzymes dataset.

6-Methylthiopurine 5'-monophosphate ribonucleotide Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the 6-Methylthiopurine 5'-monophosphate ribonucleotide metabolite from the curated HMDB Metabolites of Enzymes dataset.

5-Fluorouridine monophosphate Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the 5-Fluorouridine monophosphate metabolite from the curated HMDB Metabolites of Enzymes dataset.

2'-Deoxyguanosine 5'-monophosphate Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the 2'-Deoxyguanosine 5'-monophosphate metabolite from the curated HMDB Metabolites of Enzymes dataset.

Cytidine monophosphate Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the Cytidine monophosphate metabolite from the curated HMDB Metabolites of Enzymes dataset.

6-Methylthioguanosine monophosphate Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the 6-Methylthioguanosine monophosphate metabolite from the curated HMDB Metabolites of Enzymes dataset.

6-Thioguanosine monophosphate Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the 6-Thioguanosine monophosphate metabolite from the curated HMDB Metabolites of Enzymes dataset.

Deoxyadenosine monophosphate Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the Deoxyadenosine monophosphate metabolite from the curated HMDB Metabolites of Enzymes dataset.

Adenosine monophosphate Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the Adenosine monophosphate metabolite from the curated HMDB Metabolites of Enzymes dataset.

6-Thioinosine-5'-monophosphate Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the 6-Thioinosine-5'-monophosphate metabolite from the curated HMDB Metabolites of Enzymes dataset.

Deoxyribose 5-monophosphate Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the Deoxyribose 5-monophosphate metabolite from the curated HMDB Metabolites of Enzymes dataset.

Thymidine 3',5'-cyclic monophosphate Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the Thymidine 3',5'-cyclic monophosphate metabolite from the curated HMDB Metabolites of Enzymes dataset.

Guanosine monophosphate Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the Guanosine monophosphate metabolite from the curated HMDB Metabolites of Enzymes dataset.

Guanosine monophosphate reductase 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Guanosine monophosphate reductase 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Inosine-5'-monophosphate dehydrogenase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Inosine-5'-monophosphate dehydrogenase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

BRD-K85767870_Adenosine 5'-monophosphate monohydrate_MCF7_6.0_h_10.0_um Gene Set

From LINCS L1000 CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the BRD-K85767870_Adenosine 5'-monophosphate monohydrate_MCF7_6.0_h_10.0_um small molecule perturbation from the LINCS L1000 CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

Purine ribonucleoside monophosphate biosynthesis Gene Set

From Reactome Pathways

proteins participating in the Purine ribonucleoside monophosphate biosynthesis pathway from the Reactome Pathways dataset.

Pentose phosphate pathway (hexose monophosphate shunt) Gene Set

From Reactome Pathways

proteins participating in the Pentose phosphate pathway (hexose monophosphate shunt) pathway from the Reactome Pathways 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.

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.

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.

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.

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.

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.

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.

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.

Kininogen deficiency, total Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Kininogen deficiency, total phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

toll-like receptor 2-toll-like receptor 6 protein complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the toll-like receptor 2-toll-like receptor 6 protein complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

toll-like receptor 1-toll-like receptor 2 protein complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the toll-like receptor 1-toll-like receptor 2 protein complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

acrylonitrile metabolism/toxicity; ethylene oxide metabolism/toxicity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acrylonitrile metabolism/toxicity; ethylene oxide metabolism/toxicity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chorioretinitis; ocular toxoplasmosis; toxoplasmosis, ocular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chorioretinitis; ocular toxoplasmosis; toxoplasmosis, ocular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

conjunctivitis; epidermal necrolysis, toxic; stevens-johnson syndrome; toxic epidermal necrolysis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease conjunctivitis; epidermal necrolysis, toxic; stevens-johnson syndrome; toxic epidermal necrolysis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

drug toxicity; epidermal necrolysis, toxic; stevens-johnson syndrome; toxic epidermal necrolysis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease drug toxicity; epidermal necrolysis, toxic; stevens-johnson syndrome; toxic epidermal necrolysis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ocular toxoplasmosis; toxoplasmosis, ocular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ocular toxoplasmosis; toxoplasmosis, ocular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

efavirenz toxicity; nevirapine toxicity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease efavirenz toxicity; nevirapine toxicity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

epidermal necrolysis, toxic; stevens-johnson syndrome; toxic epidermal necrolysis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease epidermal necrolysis, toxic; stevens-johnson syndrome; toxic epidermal necrolysis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

toll-like receptor 2-toll-like receptor 6 protein complex Gene Set

From GO Cellular Component Annotations

proteins localized to the toll-like receptor 2-toll-like receptor 6 protein complex cellular component from the curated GO Cellular Component Annotations dataset.

toll-like receptor 1-toll-like receptor 2 protein complex Gene Set

From GO Cellular Component Annotations

proteins localized to the toll-like receptor 1-toll-like receptor 2 protein complex cellular component from the curated GO Cellular Component Annotations dataset.

Primary tooth development (time to first tooth eruption) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Primary tooth development (time to first tooth eruption) phenotype in GWAS datasets from the GWAS Catalog SNP-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.

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.

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.

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.

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.

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.

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.

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.

{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.

GALNS-lysosomal hydrolase 1.27 MDa complex Gene Set

From CORUM Protein Complexes

proteins in the GALNS-lysosomal hydrolase 1.27 MDa complex protein complex from the CORUM Protein Complexes dataset.

htl hydrolase Gene Set

From GAD Gene-Disease Associations

genes associated with the disease htl hydrolase in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

microsomal epoxide hydrolase Gene Set

From GAD Gene-Disease Associations

genes associated with the disease microsomal epoxide hydrolase in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hydrolase Gene Set

From GeneRIF Biological Term Annotations

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

positive regulation of hydrolase activity Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of hydrolase activity biological process from the curated GO Biological Process Annotations dataset.

negative regulation of hydrolase activity Gene Set

From GO Biological Process Annotations

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

regulation of hydrolase activity Gene Set

From GO Biological Process Annotations

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

ubiquitinyl hydrolase activity Gene Set

From GO Molecular Function Annotations

genes performing the ubiquitinyl hydrolase activity molecular function from the curated GO Molecular Function Annotations dataset.

serine hydrolase activity Gene Set

From GO Molecular Function Annotations

genes performing the serine hydrolase activity molecular function from the curated GO Molecular Function Annotations dataset.

hydroxyacylglutathione hydrolase activity Gene Set

From GO Molecular Function Annotations

genes performing the hydroxyacylglutathione hydrolase activity molecular function from the curated GO Molecular Function Annotations dataset.

hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in linear amidines Gene Set

From GO Molecular Function Annotations

genes performing the hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in linear amidines molecular function from the curated GO Molecular Function Annotations dataset.

acyl-[acyl-carrier-protein] hydrolase activity Gene Set

From GO Molecular Function Annotations

genes performing the acyl-[acyl-carrier-protein] hydrolase activity molecular function from the curated GO Molecular Function Annotations dataset.

hydrolase activity, acting on acid anhydrides, catalyzing transmembrane movement of substances Gene Set

From GO Molecular Function Annotations

genes performing the hydrolase activity, acting on acid anhydrides, catalyzing transmembrane movement of substances molecular function from the curated GO Molecular Function Annotations dataset.

choloyl-coa hydrolase activity Gene Set

From GO Molecular Function Annotations

genes performing the choloyl-coa hydrolase activity molecular function from the curated GO Molecular Function Annotations dataset.

hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in linear amides Gene Set

From GO Molecular Function Annotations

genes performing the hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in linear amides molecular function from the curated GO Molecular Function Annotations dataset.

triphosphoric monoester hydrolase activity Gene Set

From GO Molecular Function Annotations

genes performing the triphosphoric monoester hydrolase activity molecular function from the curated GO Molecular Function Annotations dataset.

hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds Gene Set

From GO Molecular Function Annotations

genes performing the hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds molecular function from the curated GO Molecular Function Annotations dataset.

hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in cyclic amidines Gene Set

From GO Molecular Function Annotations

genes performing the hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in cyclic amidines molecular function from the curated GO Molecular Function Annotations dataset.

ufm1 hydrolase activity Gene Set

From GO Molecular Function Annotations

genes performing the ufm1 hydrolase activity molecular function from the curated GO Molecular Function Annotations dataset.

alkenylglycerophosphoethanolamine hydrolase activity Gene Set

From GO Molecular Function Annotations

genes performing the alkenylglycerophosphoethanolamine hydrolase activity molecular function from the curated GO Molecular Function Annotations dataset.

diphosphoric monoester hydrolase activity Gene Set

From GO Molecular Function Annotations

genes performing the diphosphoric monoester hydrolase activity molecular function from the curated GO Molecular Function Annotations dataset.

carboxylic ester hydrolase activity Gene Set

From GO Molecular Function Annotations

genes performing the carboxylic ester hydrolase activity molecular function from the curated GO Molecular Function Annotations dataset.

all-trans-retinyl-palmitate hydrolase, 11-cis retinol forming activity Gene Set

From GO Molecular Function Annotations

genes performing the all-trans-retinyl-palmitate hydrolase, 11-cis retinol forming activity molecular function from the curated GO Molecular Function Annotations dataset.

long-chain acyl-coa hydrolase activity Gene Set

From GO Molecular Function Annotations

genes performing the long-chain acyl-coa hydrolase activity molecular function from the curated GO Molecular Function Annotations dataset.

phosphoric ester hydrolase activity Gene Set

From GO Molecular Function Annotations

genes performing the phosphoric ester hydrolase activity molecular function from the curated GO Molecular Function Annotations dataset.

alkenylglycerophosphocholine hydrolase activity Gene Set

From GO Molecular Function Annotations

genes performing the alkenylglycerophosphocholine hydrolase activity molecular function from the curated GO Molecular Function Annotations dataset.

cardiolipin hydrolase activity Gene Set

From GO Molecular Function Annotations

genes performing the cardiolipin hydrolase activity molecular function from the curated GO Molecular Function Annotations dataset.

palmitoyl-(protein) hydrolase activity Gene Set

From GO Molecular Function Annotations

genes performing the palmitoyl-(protein) hydrolase activity molecular function from the curated GO Molecular Function Annotations dataset.

fatty acid amide hydrolase activity Gene Set

From GO Molecular Function Annotations

genes performing the fatty acid amide hydrolase activity molecular function from the curated GO Molecular Function Annotations dataset.

acetyl-coa hydrolase activity Gene Set

From GO Molecular Function Annotations

genes performing the acetyl-coa hydrolase activity molecular function from the curated GO Molecular Function Annotations dataset.

phenanthrene-9,10-epoxide hydrolase activity Gene Set

From GO Molecular Function Annotations

genes performing the phenanthrene-9,10-epoxide hydrolase activity molecular function from the curated GO Molecular Function Annotations dataset.

succinyl-coa hydrolase activity Gene Set

From GO Molecular Function Annotations

genes performing the succinyl-coa hydrolase activity molecular function from the curated GO Molecular Function Annotations dataset.

myristoyl-[acyl-carrier-protein] hydrolase activity Gene Set

From GO Molecular Function Annotations

genes performing the myristoyl-[acyl-carrier-protein] hydrolase activity molecular function from the curated GO Molecular Function Annotations dataset.

ether hydrolase activity Gene Set

From GO Molecular Function Annotations

genes performing the ether hydrolase activity molecular function from the curated GO Molecular Function Annotations dataset.

dihydrocoumarin hydrolase activity Gene Set

From GO Molecular Function Annotations

genes performing the dihydrocoumarin hydrolase activity molecular function from the curated GO Molecular Function Annotations dataset.

hydrolase activity, acting on ether bonds Gene Set

From GO Molecular Function Annotations

genes performing the hydrolase activity, acting on ether bonds molecular function from the curated GO Molecular Function Annotations dataset.

pantetheine hydrolase activity Gene Set

From GO Molecular Function Annotations

genes performing the pantetheine hydrolase activity molecular function from the curated GO Molecular Function Annotations dataset.

palmitoyl hydrolase activity Gene Set

From GO Molecular Function Annotations

genes performing the palmitoyl hydrolase activity molecular function from the curated GO Molecular Function Annotations dataset.

palmitoyl-coa hydrolase activity Gene Set

From GO Molecular Function Annotations

genes performing the palmitoyl-coa hydrolase activity molecular function from the curated GO Molecular Function Annotations dataset.

hydrolase activity, acting on acid carbon-carbon bonds, in ketonic substances Gene Set

From GO Molecular Function Annotations

genes performing the hydrolase activity, acting on acid carbon-carbon bonds, in ketonic substances molecular function from the curated GO Molecular Function Annotations dataset.

hydrolase activity, acting on ester bonds Gene Set

From GO Molecular Function Annotations

genes performing the hydrolase activity, acting on ester bonds molecular function from the curated GO Molecular Function Annotations dataset.

very long chain acyl-coa hydrolase activity Gene Set

From GO Molecular Function Annotations

genes performing the very long chain acyl-coa hydrolase activity molecular function from the curated GO Molecular Function Annotations dataset.

thiolester hydrolase activity Gene Set

From GO Molecular Function Annotations

genes performing the thiolester hydrolase activity molecular function from the curated GO Molecular Function Annotations dataset.

acylpyruvate hydrolase activity Gene Set

From GO Molecular Function Annotations

genes performing the acylpyruvate hydrolase activity molecular function from the curated GO Molecular Function Annotations dataset.

hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides Gene Set

From GO Molecular Function Annotations

genes performing the hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides molecular function from the curated GO Molecular Function Annotations dataset.

phosphoric diester hydrolase activity Gene Set

From GO Molecular Function Annotations

genes performing the phosphoric diester hydrolase activity molecular function from the curated GO Molecular Function Annotations dataset.

hepoxilin-epoxide hydrolase activity Gene Set

From GO Molecular Function Annotations

genes performing the hepoxilin-epoxide hydrolase activity molecular function from the curated GO Molecular Function Annotations dataset.

adp-ribosylarginine hydrolase activity Gene Set

From GO Molecular Function Annotations

genes performing the adp-ribosylarginine hydrolase activity molecular function from the curated GO Molecular Function Annotations dataset.

acyl-coa hydrolase activity Gene Set

From GO Molecular Function Annotations

genes performing the acyl-coa hydrolase activity molecular function from the curated GO Molecular Function Annotations dataset.

3-hydroxyisobutyryl-coa hydrolase activity Gene Set

From GO Molecular Function Annotations

genes performing the 3-hydroxyisobutyryl-coa hydrolase activity molecular function from the curated GO Molecular Function Annotations dataset.

hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in cyclic amides Gene Set

From GO Molecular Function Annotations

genes performing the hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in cyclic amides molecular function from the curated GO Molecular Function Annotations dataset.

sulfuric ester hydrolase activity Gene Set

From GO Molecular Function Annotations

genes performing the sulfuric ester hydrolase activity molecular function from the curated GO Molecular Function Annotations dataset.

acyloxyacyl hydrolase activity Gene Set

From GO Molecular Function Annotations

genes performing the acyloxyacyl hydrolase activity molecular function from the curated GO Molecular Function Annotations dataset.

hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in nitriles Gene Set

From GO Molecular Function Annotations

genes performing the hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in nitriles molecular function from the curated GO Molecular Function Annotations dataset.

aminoacyl-trna hydrolase activity Gene Set

From GO Molecular Function Annotations

genes performing the aminoacyl-trna hydrolase activity molecular function from the curated GO Molecular Function Annotations dataset.

fumarylpyruvate hydrolase activity Gene Set

From GO Molecular Function Annotations

genes performing the fumarylpyruvate hydrolase activity molecular function from the curated GO Molecular Function Annotations dataset.

glutathione hydrolase activity Gene Set

From GO Molecular Function Annotations

genes performing the glutathione hydrolase activity molecular function from the curated GO Molecular Function Annotations dataset.

hydrolase activity, hydrolyzing o-glycosyl compounds Gene Set

From GO Molecular Function Annotations

genes performing the hydrolase activity, hydrolyzing o-glycosyl compounds molecular function from the curated GO Molecular Function Annotations dataset.

cis-stilbene-oxide hydrolase activity Gene Set

From GO Molecular Function Annotations

genes performing the cis-stilbene-oxide hydrolase activity molecular function from the curated GO Molecular Function Annotations dataset.

hydrolase activity, acting on acid anhydrides Gene Set

From GO Molecular Function Annotations

genes performing the hydrolase activity, acting on acid anhydrides molecular function from the curated GO Molecular Function Annotations dataset.

medium-chain acyl-coa hydrolase activity Gene Set

From GO Molecular Function Annotations

genes performing the medium-chain acyl-coa hydrolase activity molecular function from the curated GO Molecular Function Annotations dataset.

oleoyl-[acyl-carrier-protein] hydrolase activity Gene Set

From GO Molecular Function Annotations

genes performing the oleoyl-[acyl-carrier-protein] hydrolase activity molecular function from the curated GO Molecular Function Annotations dataset.

trialkylsulfonium hydrolase activity Gene Set

From GO Molecular Function Annotations

genes performing the trialkylsulfonium hydrolase activity molecular function from the curated GO Molecular Function Annotations dataset.

hydrolase activity, acting on acid carbon-carbon bonds Gene Set

From GO Molecular Function Annotations

genes performing the hydrolase activity, acting on acid carbon-carbon bonds molecular function from the curated GO Molecular Function Annotations dataset.

hydrolase activity, acting on acid sulfur-nitrogen bonds Gene Set

From GO Molecular Function Annotations

genes performing the hydrolase activity, acting on acid sulfur-nitrogen bonds molecular function from the curated GO Molecular Function Annotations dataset.

all-trans-retinyl-ester hydrolase, 11-cis retinol forming activity Gene Set

From GO Molecular Function Annotations

genes performing the all-trans-retinyl-ester hydrolase, 11-cis retinol forming activity molecular function from the curated GO Molecular Function Annotations dataset.

hydrolase activity Gene Set

From GO Molecular Function Annotations

genes performing the hydrolase activity molecular function from the curated GO Molecular Function Annotations dataset.

epoxide hydrolase activity Gene Set

From GO Molecular Function Annotations

genes performing the epoxide hydrolase activity molecular function from the curated GO Molecular Function Annotations dataset.

leukotriene-a4 hydrolase activity Gene Set

From GO Molecular Function Annotations

genes performing the leukotriene-a4 hydrolase activity molecular function from the curated GO Molecular Function Annotations dataset.

hydrolase activity, hydrolyzing n-glycosyl compounds Gene Set

From GO Molecular Function Annotations

genes performing the hydrolase activity, hydrolyzing n-glycosyl compounds molecular function from the curated GO Molecular Function Annotations dataset.

3,4-dihydrocoumarin hydrolase activity Gene Set

From GO Molecular Function Annotations

genes performing the 3,4-dihydrocoumarin hydrolase activity molecular function from the curated GO Molecular Function Annotations dataset.

acetylpyruvate hydrolase activity Gene Set

From GO Molecular Function Annotations

genes performing the acetylpyruvate hydrolase activity molecular function from the curated GO Molecular Function Annotations dataset.

hydrolase activity, acting on glycosyl bonds Gene Set

From GO Molecular Function Annotations

genes performing the hydrolase activity, acting on glycosyl bonds molecular function from the curated GO Molecular Function Annotations dataset.

coa hydrolase activity Gene Set

From GO Molecular Function Annotations

genes performing the coa hydrolase activity molecular function from the curated GO Molecular Function Annotations dataset.

s-formylglutathione hydrolase activity Gene Set

From GO Molecular Function Annotations

genes performing the s-formylglutathione hydrolase activity molecular function from the curated GO Molecular Function Annotations dataset.

palmitoyl-[acyl-carrier-protein] hydrolase activity Gene Set

From GO Molecular Function Annotations

genes performing the palmitoyl-[acyl-carrier-protein] hydrolase activity molecular function from the curated GO Molecular Function Annotations dataset.

phenanthrene-epoxide hydrolase activity Gene Set

From GO Molecular Function Annotations

genes performing the phenanthrene-epoxide hydrolase activity molecular function from the curated GO Molecular Function Annotations dataset.

Glycoside hydrolase, family 13, N-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glycoside hydrolase, family 13, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glycoside hydrolase, family 37, conserved site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glycoside hydrolase, family 37, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Serine hydrolase FSH Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Serine hydrolase FSH protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glycoside hydrolase 38/57, N-terminal domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glycoside hydrolase 38/57, N-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glycoside hydrolase, family 22, conserved site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glycoside hydrolase, family 22, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ubiquitinyl hydrolase, UCH37 type Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ubiquitinyl hydrolase, UCH37 type protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Acyl transferase/acyl hydrolase/lysophospholipase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Acyl transferase/acyl hydrolase/lysophospholipase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Peptidase C12, ubiquitin carboxyl-terminal hydrolase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Peptidase C12, ubiquitin carboxyl-terminal hydrolase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glycoside hydrolase family 20, catalytic core Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glycoside hydrolase family 20, catalytic core protein domain from the InterPro Predicted Protein Domain Annotations dataset.

NUDIX hydrolase domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the NUDIX hydrolase domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

HAD-superfamily hydrolase, subfamily IA, REG-2-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the HAD-superfamily hydrolase, subfamily IA, REG-2-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glycoside hydrolase, family 29, conserved site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glycoside hydrolase, family 29, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ubiquitin carboxyl-terminal hydrolase USP Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ubiquitin carboxyl-terminal hydrolase USP protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Carbon-nitrogen hydrolase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Carbon-nitrogen hydrolase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glycoside hydrolase, family 2/20, immunoglobulin-like beta-sandwich domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glycoside hydrolase, family 2/20, immunoglobulin-like beta-sandwich domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

HAD-superfamily hydrolase, subfamily IIA, CECR5 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the HAD-superfamily hydrolase, subfamily IIA, CECR5 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glycosyl hydrolase family 38, C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glycosyl hydrolase family 38, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Nudix hydrolase 6-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Nudix hydrolase 6-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Alpha/Beta hydrolase fold Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Alpha/Beta hydrolase fold protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Putative hydrolase RBBP9/YdeN Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Putative hydrolase RBBP9/YdeN protein domain from the InterPro Predicted Protein Domain Annotations dataset.

HAD-superfamily hydrolase, subfamily IIB Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the HAD-superfamily hydrolase, subfamily IIB protein domain from the InterPro Predicted Protein Domain Annotations dataset.

HAD-superfamily hydrolase, subfamily IIA Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the HAD-superfamily hydrolase, subfamily IIA protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glycoside hydrolase, family 63 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glycoside hydrolase, family 63 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ubiquitin carboxyl-terminal hydrolase L1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ubiquitin carboxyl-terminal hydrolase L1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Alpha/beta hydrolase fold-3 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Alpha/beta hydrolase fold-3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Alpha/beta hydrolase fold-1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Alpha/beta hydrolase fold-1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Alpha/beta hydrolase fold-5 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Alpha/beta hydrolase fold-5 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Peptidase C19, ubiquitin carboxyl-terminal hydrolase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Peptidase C19, ubiquitin carboxyl-terminal hydrolase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Hydroxyacylglutathione hydrolase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Hydroxyacylglutathione hydrolase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glycoside hydrolase, family 47 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glycoside hydrolase, family 47 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

S-formylglutathione hydrolase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the S-formylglutathione hydrolase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

2-deoxynucleoside 5-phosphate N-hydrolase 1, DNPH1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the 2-deoxynucleoside 5-phosphate N-hydrolase 1, DNPH1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

BAAT/Acyl-CoA thioester hydrolase C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the BAAT/Acyl-CoA thioester hydrolase C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Epoxide hydrolase, N-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Epoxide hydrolase, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glycoside hydrolase/deacetylase, beta/alpha-barrel Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glycoside hydrolase/deacetylase, beta/alpha-barrel protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glycoside hydrolase, family 22 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glycoside hydrolase, family 22 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glycoside hydrolase, family 23 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glycoside hydrolase, family 23 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glycoside hydrolase, family 27 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glycoside hydrolase, family 27 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glycoside hydrolase, family 29 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glycoside hydrolase, family 29 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Epoxide hydrolase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Epoxide hydrolase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

HAD-superfamily hydrolase,subfamily IIIA Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the HAD-superfamily hydrolase,subfamily IIIA protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glycoside hydrolase, catalytic domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glycoside hydrolase, catalytic domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glycoside hydrolase family 31, N-terminal domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glycoside hydrolase family 31, N-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glycoside hydrolase, family 18, catalytic domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glycoside hydrolase, family 18, catalytic domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Dienelactone hydrolase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Dienelactone hydrolase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

HAD-superfamily hydrolase, subfamily IB, PSPase-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the HAD-superfamily hydrolase, subfamily IB, PSPase-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glycoside hydrolase-type carbohydrate-binding, subgroup Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glycoside hydrolase-type carbohydrate-binding, subgroup protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glycosyl hydrolase family 99 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glycosyl hydrolase family 99 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Peptidyl-tRNA hydrolase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Peptidyl-tRNA hydrolase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Choloylglycine hydrolase/Peptidase C59 family Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Choloylglycine hydrolase/Peptidase C59 family protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Lactate dehydrogenase/glycoside hydrolase, family 4, C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Lactate dehydrogenase/glycoside hydrolase, family 4, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glycoside hydrolase, family 22, lysozyme Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glycoside hydrolase, family 22, lysozyme protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glycoside hydrolase, family 1, active site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glycoside hydrolase, family 1, active site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Acyl-CoA thioester hydrolase/bile acid-CoA amino acid N-acetyltransferase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Acyl-CoA thioester hydrolase/bile acid-CoA amino acid N-acetyltransferase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Alpha/beta hydrolase domain-containing protein 14B Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Alpha/beta hydrolase domain-containing protein 14B protein domain from the InterPro Predicted Protein Domain Annotations dataset.

P-loop containing nucleoside triphosphate hydrolase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the P-loop containing nucleoside triphosphate hydrolase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glycoside hydrolase, family 2, active site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glycoside hydrolase, family 2, active site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glycoside hydrolase, family 65, central catalytic Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glycoside hydrolase, family 65, central catalytic protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glycoside hydrolase family 31 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glycoside hydrolase family 31 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Epoxide hydrolase-like Gene Set

From InterPro Predicted Protein Domain Annotations

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

Glycoside hydrolase, family 85 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glycoside hydrolase, family 85 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ubiquitin carboxyl-terminal hydrolase, C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ubiquitin carboxyl-terminal hydrolase, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

S-adenosyl-L-homocysteine hydrolase, conserved site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the S-adenosyl-L-homocysteine hydrolase, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glycoside hydrolase family 15 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glycoside hydrolase family 15 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

S-adenosyl-L-homocysteine hydrolase, NAD binding domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the S-adenosyl-L-homocysteine hydrolase, NAD binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Peptidyl-tRNA hydrolase, conserved site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Peptidyl-tRNA hydrolase, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Uncharacterised protein family UPF0017, hydrolase-like, conserved site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Uncharacterised protein family UPF0017, hydrolase-like, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glycoside hydrolase, family 35, conserved site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glycoside hydrolase, family 35, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glycosyl hydrolase, family 13, catalytic domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glycosyl hydrolase, family 13, catalytic domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DBC1/CARP1 catalytically inactive NUDIX hydrolase domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DBC1/CARP1 catalytically inactive NUDIX hydrolase domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Peptidase C1B, bleomycin hydrolase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Peptidase C1B, bleomycin hydrolase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glycoside hydrolase, family 38, central domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glycoside hydrolase, family 38, central domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glycoside hydrolase, family 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glycoside hydrolase, family 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glycoside hydrolase, family 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glycoside hydrolase, family 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glycoside hydrolase, clan GH-D Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glycoside hydrolase, clan GH-D protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Leukotriene A4 hydrolase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Leukotriene A4 hydrolase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

HAD-superfamily hydrolase, subfamily IIA, hypothetical 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the HAD-superfamily hydrolase, subfamily IIA, hypothetical 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glycoside hydrolase, chitinase active site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glycoside hydrolase, chitinase active site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Metal-dependent hydrolase, composite domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Metal-dependent hydrolase, composite domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

NUDIX hydrolase domain-like Gene Set

From InterPro Predicted Protein Domain Annotations

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

Predicted HAD-superfamily phosphatase, subfamily IA/Epoxide hydrolase, N-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Predicted HAD-superfamily phosphatase, subfamily IA/Epoxide hydrolase, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Peptidyl-tRNA hydrolase, PTH2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Peptidyl-tRNA hydrolase, PTH2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

NUDIX hydrolase, conserved site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the NUDIX hydrolase, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Partial AB-hydrolase lipase domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Partial AB-hydrolase lipase domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Peptidase M1, leukotriene A4 hydrolase, aminopeptidase C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Peptidase M1, leukotriene A4 hydrolase, aminopeptidase C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Peptidase M1, alanine aminopeptidase/leukotriene A4 hydrolase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Peptidase M1, alanine aminopeptidase/leukotriene A4 hydrolase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glycoside hydrolase, family 2, TIM barrel Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glycoside hydrolase, family 2, TIM barrel protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Peptidase C26, gamma-glutamyl hydrolase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Peptidase C26, gamma-glutamyl hydrolase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glycosyl hydrolase, family 13, all-beta Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glycosyl hydrolase, family 13, all-beta protein domain from the InterPro Predicted Protein Domain Annotations dataset.

NUDIX hydrolase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the NUDIX hydrolase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

HAD-superfamily hydrolase, subfamily IA, CTE7 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the HAD-superfamily hydrolase, subfamily IA, CTE7 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glycoside hydrolase superfamily Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glycoside hydrolase superfamily protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glycoside hydrolase, family 79 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glycoside hydrolase, family 79 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Choloylglycine hydrolase/NAAA C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Choloylglycine hydrolase/NAAA C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ADP-ribosylarginine hydrolase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ADP-ribosylarginine hydrolase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ubiquitinyl hydrolase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ubiquitinyl hydrolase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Peptidyl-tRNA hydrolase II domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Peptidyl-tRNA hydrolase II domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glycoside hydrolase, family 59 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glycoside hydrolase, family 59 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glycoside hydrolase, families 57/38, central domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glycoside hydrolase, families 57/38, central domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glycoside hydrolase, family 2, conserved site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glycoside hydrolase, family 2, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Adenine nucleotide alpha hydrolase-like domains Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Adenine nucleotide alpha hydrolase-like domains protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glycoside hydrolase, family 30 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glycoside hydrolase, family 30 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glycoside hydrolase, family 35 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glycoside hydrolase, family 35 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glycoside hydrolase, family 37 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glycoside hydrolase, family 37 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glycoside hydrolase, family 39 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glycoside hydrolase, family 39 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

AB-hydrolase YheT, putative Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the AB-hydrolase YheT, putative protein domain from the InterPro Predicted Protein Domain Annotations dataset.

HAD-superfamily hydrolase, subfamily IG, 5'-nucleotidase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the HAD-superfamily hydrolase, subfamily IG, 5'-nucleotidase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

NUDIX hydrolase, NudL, conserved site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the NUDIX hydrolase, NudL, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glycosyl hydrolase, family 13, subfamily, catalytic domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glycosyl hydrolase, family 13, subfamily, catalytic domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Transthyretin/hydroxyisourate hydrolase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Transthyretin/hydroxyisourate hydrolase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Transthyretin/hydroxyisourate hydrolase, superfamily Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Transthyretin/hydroxyisourate hydrolase, superfamily protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glycoside hydrolase family 38, N-terminal domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glycoside hydrolase family 38, N-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

HAD-superfamily hydrolase, subfamily IIID Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the HAD-superfamily hydrolase, subfamily IIID protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glycoside hydrolase, family 13 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glycoside hydrolase, family 13 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

HAD hydrolase, subfamily IA Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the HAD hydrolase, subfamily IA protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glycoside hydrolase, family 2, immunoglobulin-like beta-sandwich Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glycoside hydrolase, family 2, immunoglobulin-like beta-sandwich protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ubiquitin carboxyl-terminal hydrolase 10 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ubiquitin carboxyl-terminal hydrolase 10 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Arachidonate Epoxygenase Epoxide Hydrolase(Mus musculus) Gene Set

From Wikipathways Pathways

proteins participating in the Arachidonate Epoxygenase Epoxide Hydrolase(Mus musculus) pathway from the Wikipathways Pathways dataset.

Arachidonate Epoxygenase / Epoxide Hydrolase(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Arachidonate Epoxygenase / Epoxide Hydrolase(Homo sapiens) pathway from the Wikipathways Pathways dataset.

Fanconi anemia, complementation group O Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fanconi anemia, complementation group O phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fanconi anemia, complementation group A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fanconi anemia, complementation group A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcytic anemia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcytic anemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopathy, lactic acidosis, and sideroblastic anemia 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopathy, lactic acidosis, and sideroblastic anemia 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Diamond-Blackfan anemia 11 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Diamond-Blackfan anemia 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Diamond-Blackfan anemia 10 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Diamond-Blackfan anemia 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hereditary sideroblastic anemia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary sideroblastic anemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Anemia sideroblastic and spinocerebellar ataxia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Anemia sideroblastic and spinocerebellar ataxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Diamond-Blackfan anemia 8 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Diamond-Blackfan anemia 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Diamond-Blackfan anemia 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Diamond-Blackfan anemia 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Diamond-Blackfan anemia 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Diamond-Blackfan anemia 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Diamond-Blackfan anemia 7 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Diamond-Blackfan anemia 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fanconi anemia, complementation group Q Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fanconi anemia, complementation group Q phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fanconi anemia, complementation group M Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fanconi anemia, complementation group M phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fanconi anemia, complementation group N Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fanconi anemia, complementation group N phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fanconi anemia, complementation group E Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fanconi anemia, complementation group E phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fanconi anemia, complementation group F Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fanconi anemia, complementation group F phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fanconi anemia, complementation group G Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fanconi anemia, complementation group G phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopathy, lactic acidosis, and sideroblastic anemia 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopathy, lactic acidosis, and sideroblastic anemia 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital dyserythropoietic anemia, type I Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital dyserythropoietic anemia, type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fanconi anemia, complementation group I Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fanconi anemia, complementation group I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fanconi anemia, complementation group C Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fanconi anemia, complementation group C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypochromic microcytic anemia with iron overload Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypochromic microcytic anemia with iron overload phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Aplastic anemia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Aplastic anemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital dyserythropoietic anemia, type II Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital dyserythropoietic anemia, type II phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

ANEMIA, DYSERYTHROPOIETIC CONGENITAL, TYPE IV Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the ANEMIA, DYSERYTHROPOIETIC CONGENITAL, TYPE IV phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fanconi anemia, complementation group D2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fanconi anemia, complementation group D2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Sideroblastic anemia with b-cell immunodeficiency, periodic fevers, and developmental delay Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Sideroblastic anemia with b-cell immunodeficiency, periodic fevers, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ib Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ib phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Anemia, sideroblastic, pyridoxine-refractory, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Anemia, sideroblastic, pyridoxine-refractory, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

FA core complex (Fanconi anemia core complex) Gene Set

From CORUM Protein Complexes

proteins in the FA core complex (Fanconi anemia core complex) protein complex from the CORUM Protein Complexes dataset.

FA core complex 1 (Fanconi anemia core complex 1) Gene Set

From CORUM Protein Complexes

proteins in the FA core complex 1 (Fanconi anemia core complex 1) protein complex from the CORUM Protein Complexes dataset.

FA complex (Fanconi anemia complex), cytoplasmic Gene Set

From CORUM Protein Complexes

proteins in the FA complex (Fanconi anemia complex), cytoplasmic protein complex from the CORUM Protein Complexes dataset.

FA complex (Fanconi anemia complex) Gene Set

From CORUM Protein Complexes

proteins in the FA complex (Fanconi anemia complex) protein complex from the CORUM Protein Complexes dataset.

Anemia, Aplastic Gene Set

From CTD Gene-Disease Associations

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

Exocrine Pancreatic Insufficiency, Dyserythropoietic Anemia, and Calvarial Hyperostosis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Exocrine Pancreatic Insufficiency, Dyserythropoietic Anemia, and Calvarial Hyperostosis from the curated CTD Gene-Disease Associations dataset.

FANCONI ANEMIA, COMPLEMENTATION GROUP C Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease FANCONI ANEMIA, COMPLEMENTATION GROUP C from the curated CTD Gene-Disease Associations dataset.

Diamond-Blackfan Anemia 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Diamond-Blackfan Anemia 4 from the curated CTD Gene-Disease Associations dataset.

FANCONI ANEMIA, COMPLEMENTATION GROUP E Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease FANCONI ANEMIA, COMPLEMENTATION GROUP E from the curated CTD Gene-Disease Associations dataset.

FANCONI ANEMIA, COMPLEMENTATION GROUP F Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease FANCONI ANEMIA, COMPLEMENTATION GROUP F from the curated CTD Gene-Disease Associations dataset.

Anemia, Diamond-Blackfan, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Anemia, Diamond-Blackfan, 2 from the curated CTD Gene-Disease Associations dataset.

Fanconi Anemia, Complementation Group J Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Fanconi Anemia, Complementation Group J from the curated CTD Gene-Disease Associations dataset.

Anemia, sideroblastic spinocerebellar ataxia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Anemia, sideroblastic spinocerebellar ataxia from the curated CTD Gene-Disease Associations dataset.

Fanconi Anemia, Complementation Group B Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Fanconi Anemia, Complementation Group B from the curated CTD Gene-Disease Associations dataset.

Fanconi Anemia, Complementation Group N Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Fanconi Anemia, Complementation Group N from the curated CTD Gene-Disease Associations dataset.

MEGALOBLASTIC ANEMIA 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MEGALOBLASTIC ANEMIA 1 from the curated CTD Gene-Disease Associations dataset.

Myopathy with lactic acidosis and sideroblastic anemia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Myopathy with lactic acidosis and sideroblastic anemia from the curated CTD Gene-Disease Associations dataset.

Fanconi Anemia Gene Set

From CTD Gene-Disease Associations

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

Anemia, Hypoplastic, Congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Anemia, Hypoplastic, Congenital from the curated CTD Gene-Disease Associations dataset.

Anemia, Diamond-Blackfan Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Anemia, Diamond-Blackfan from the curated CTD Gene-Disease Associations dataset.

Anemia, Megaloblastic Gene Set

From CTD Gene-Disease Associations

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

Anemia, Sideroblastic Gene Set

From CTD Gene-Disease Associations

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

Anemia, Sickle Cell Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Anemia, Sickle Cell from the curated CTD Gene-Disease Associations dataset.

FANCONI ANEMIA, COMPLEMENTATION GROUP D2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease FANCONI ANEMIA, COMPLEMENTATION GROUP D2 from the curated CTD Gene-Disease Associations dataset.

Thiamine responsive megaloblastic anemia syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Thiamine responsive megaloblastic anemia syndrome from the curated CTD Gene-Disease Associations dataset.

Anemia, Macrocytic Gene Set

From CTD Gene-Disease Associations

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

X-linked sideroblastic anemia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease X-linked sideroblastic anemia from the curated CTD Gene-Disease Associations dataset.

Fanconi Anemia, Complementation Group I Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Fanconi Anemia, Complementation Group I from the curated CTD Gene-Disease Associations dataset.

FANCONI ANEMIA, COMPLEMENTATION GROUP O Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease FANCONI ANEMIA, COMPLEMENTATION GROUP O from the curated CTD Gene-Disease Associations dataset.

Anemia, Sideroblastic, Pyridoxine-Refractory, Autosomal Recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Anemia, Sideroblastic, Pyridoxine-Refractory, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.

Anemia Gene Set

From CTD Gene-Disease Associations

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

Fanconi Anemia, Complementation Group D1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Fanconi Anemia, Complementation Group D1 from the curated CTD Gene-Disease Associations dataset.

DIAMOND-BLACKFAN ANEMIA 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease DIAMOND-BLACKFAN ANEMIA 6 from the curated CTD Gene-Disease Associations dataset.

Anemia, Diamond-Blackfan, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Anemia, Diamond-Blackfan, 3 from the curated CTD Gene-Disease Associations dataset.

Diamond-Blackfan Anemia 9 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Diamond-Blackfan Anemia 9 from the curated CTD Gene-Disease Associations dataset.

Diamond-Blackfan Anemia 8 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Diamond-Blackfan Anemia 8 from the curated CTD Gene-Disease Associations dataset.

Diamond-Blackfan Anemia 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Diamond-Blackfan Anemia 5 from the curated CTD Gene-Disease Associations dataset.

Diamond-Blackfan Anemia 7 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Diamond-Blackfan Anemia 7 from the curated CTD Gene-Disease Associations dataset.

THROMBOCYTOPENIA, X-LINKED, WITH OR WITHOUT DYSERYTHROPOIETIC ANEMIA Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease THROMBOCYTOPENIA, X-LINKED, WITH OR WITHOUT DYSERYTHROPOIETIC ANEMIA from the curated CTD Gene-Disease Associations dataset.

Anemia, Refractory Gene Set

From CTD Gene-Disease Associations

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

Anemia, Hypochromic Microcytic, With Iron Overload Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Anemia, Hypochromic Microcytic, With Iron Overload from the curated CTD Gene-Disease Associations dataset.

Anemia, Neonatal Gene Set

From CTD Gene-Disease Associations

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

Diamond-Blackfan Anemia 10 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Diamond-Blackfan Anemia 10 from the curated CTD Gene-Disease Associations dataset.

Anemia, hypochromic microcytic Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Anemia, hypochromic microcytic from the curated CTD Gene-Disease Associations dataset.

Anemia, Dyserythropoietic, Congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Anemia, Dyserythropoietic, Congenital from the curated CTD Gene-Disease Associations dataset.

Anemia Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Anemia in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

Anemia, Sickle Cell Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Anemia, Sickle Cell in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

anemia Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

fanconi's anemia Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease fanconi's anemia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

diamond-blackfan anemia Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

sideroblastic anemia Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

normocytic anemia Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

x-linked sideroblastic anemia with ataxia Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease x-linked sideroblastic anemia with ataxia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

congenital dyserythropoietic anemia Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

aplastic anemia Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

congenital hypoplastic anemia Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

x-linked sideroblastic anemia Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease x-linked sideroblastic anemia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

anemia Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

genes associated with the disease anemia in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

microcytic anemia Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

genes associated with the disease microcytic anemia in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

normocytic anemia Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

genes associated with the disease normocytic anemia in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

anemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

fanconi's anemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

sickle cell anemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

pernicious anemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

anemia of prematurity Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

neonatal anemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

sideroblastic anemia with spinocerebellar ataxia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

microcytic anemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

myelophthisic anemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

x-linked sideroblastic anemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

pyridoxine-responsive sideroblastic anemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

congenital hypoplastic anemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

hypochromic microcytic anemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

macrocytic anemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

normocytic anemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

diamond-blackfan anemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

x-linked sideroblastic anemia with ataxia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease x-linked sideroblastic anemia with ataxia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

congenital dyserythropoietic anemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

sideroblastic anemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

hypochromic anemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

megaloblastic anemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

aplastic anemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

anemia; hepatitis c Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia; hepatitis c in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia; malaria, falciparum; parasitemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia; malaria, falciparum; parasitemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia; malaria, cerebral; malaria, falciparum; parasitemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia; malaria, cerebral; malaria, falciparum; parasitemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia; thrombocytopenic purpura, idiopathic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia; thrombocytopenic purpura, idiopathic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, sickle cell; beta-thalassemia; sickle cell trait; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell; beta-thalassemia; sickle cell trait; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alpha thalassemia; alpha-thalassemia; anemia; malaria, cerebral; malaria, falciparum Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha thalassemia; alpha-thalassemia; anemia; malaria, cerebral; malaria, falciparum in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, aplastic; fanconi syndrome; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, aplastic; fanconi syndrome; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

sickle cell anemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease sickle cell anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, malaria related; malaria, cerebral Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, malaria related; malaria, cerebral in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia; malaria; parasitemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia; malaria; parasitemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, sickle cell; pain Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell; pain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bloom syndrome; fanconi's anemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bloom syndrome; fanconi's anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia in pregnancy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia in pregnancy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, aplastic; Gene Set

From GAD Gene-Disease Associations

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

anemia, sickle cell; ischemia; recurrence; respiratory tract infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell; ischemia; recurrence; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, aplastic Gene Set

From GAD Gene-Disease Associations

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

cholelithiasis; sickle cell anemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholelithiasis; sickle cell anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, sickle cell; kidney diseases; lung diseases; nervous system diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell; kidney diseases; lung diseases; nervous system diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, sickle cell; lung diseases; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell; lung diseases; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia; brain death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia; brain death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia; kidney diseases; red-cell aplasia, pure Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia; kidney diseases; red-cell aplasia, pure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, sickle cell; osteomyelitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell; osteomyelitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

amyloidosis; anemia; chronic disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease amyloidosis; anemia; chronic disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diamond-blackfan anemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diamond-blackfan anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, sickle cell; gallbladder diseases; hyperbilirubinemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell; gallbladder diseases; hyperbilirubinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, refractory; myelodysplastic syndromes; preleukemia; refractory anaemia -retired- Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, refractory; myelodysplastic syndromes; preleukemia; refractory anaemia -retired- in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

stroke; sickle cell anemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease stroke; sickle cell anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia; malaria Gene Set

From GAD Gene-Disease Associations

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

fanconi anemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fanconi anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aplastic anemia, acquired Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aplastic anemia, acquired in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alpha-thalassemia; anemia; malaria Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha-thalassemia; anemia; malaria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebrovascular disease; sickle cell anemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebrovascular disease; sickle cell anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia; malaria, falciparum Gene Set

From GAD Gene-Disease Associations

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

alpha-thalassemia; anemia, sickle cell; cholelithiasis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha-thalassemia; anemia, sickle cell; cholelithiasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

malarial anemia and cerebral malaria Gene Set

From GAD Gene-Disease Associations

genes associated with the disease malarial anemia and cerebral malaria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, sickle cell; hepatitis c Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell; hepatitis c in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, sickle cell; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

malarial anemia in ghanaian children Gene Set

From GAD Gene-Disease Associations

genes associated with the disease malarial anemia in ghanaian children in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, sickle cell Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, sickle cell; beta-thalassemia; hemoglobinopathies Gene Set

From GAD Gene-Disease Associations

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

alpha-thalassemia; anemia; beta-thalassemia; hiv infections; pregnancy complications, hematologic; pregnancy complications, infectious Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha-thalassemia; anemia; beta-thalassemia; hiv infections; pregnancy complications, hematologic; pregnancy complications, infectious in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia; hepatitis c, chronic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia; hepatitis c, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia; malaria; malaria, falciparum; parasitemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia; malaria; malaria, falciparum; parasitemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic nonspherocytic anemia. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic nonspherocytic anemia. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aplastic anemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aplastic anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia; inflammation; kidney failure, chronic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia; inflammation; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alpha-thalassemia; anemia, hypochromic Gene Set

From GAD Gene-Disease Associations

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

anemia Gene Set

From GAD Gene-Disease Associations

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

anemia, sickle cell; arterial occlusive diseases; constriction, pathologic; ischemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell; arterial occlusive diseases; constriction, pathologic; ischemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alpha thalassemia; alpha-thalassemia; anemia, hypochromic Gene Set

From GAD Gene-Disease Associations

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

macrothrombocytopenia and anemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease macrothrombocytopenia and anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia; chronic renal failure; kidney failure, chronic Gene Set

From GAD Gene-Disease Associations

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

anemia; hemoglobinopathies; iron overload; thalassemia Gene Set

From GAD Gene-Disease Associations

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

anemia, sickle cell; bacteremia; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell; bacteremia; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

sickle cell anemia; thalassemia; gilbert syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease sickle cell anemia; thalassemia; gilbert syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia Gene Set

From GeneRIF Biological Term Annotations

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

Systolic blood pressure in sickle cell anemia Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Systolic blood pressure in sickle cell anemia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Sickle cell anemia (haemolysis) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Sickle cell anemia (haemolysis) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Ribavirin-induced anemia Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Ribavirin-induced anemia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

anemia