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Other Specified Iron Deficiency Anemias Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Other Specified Iron Deficiency Anemias in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
anemia, iron-deficiency; hemochromatosis; iron deficiency anaemia; iron overload Gene SetFrom 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; iron deficiency anaemia; iron overload Gene SetFrom 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; iron deficiency anaemia; tuberculosis, pulmonary Gene SetFrom 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; beta thalassemia; beta-thalassemia; iron deficiency anaemia Gene SetFrom 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 SetFrom 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; hemochromatosis; iron deficiency anaemia Gene SetFrom 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. |
Other Specified Peritonitis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Other Specified Peritonitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Other Specified Forms Of Pleural Effusion, Except Tuberculous Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Other Specified Forms Of Pleural Effusion, Except Tuberculous in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Other Specified Congenital Malformations Of Respiratory System Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Other Specified Congenital Malformations Of Respiratory System in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Other Specified Senile Psychotic Conditions Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Other Specified Senile Psychotic Conditions in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Other Specified Congenital Malformation Syndromes, Not Elsewhere Classified In Icd10Cm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Other Specified Congenital Malformation Syndromes, Not Elsewhere Classified In Icd10Cm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Other Specified Schistosomiasis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Other Specified Schistosomiasis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Other Specified Diabetes Mellitus With Unspecified Complications Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Other Specified Diabetes Mellitus With Unspecified Complications in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Other Specified Congenital Malformations Of Brain Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Other Specified Congenital Malformations Of Brain in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Other Specified Immunodeficiencies Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Other Specified Immunodeficiencies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Other Specified Extrapyramidal And Movement Disorders Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Other Specified Extrapyramidal And Movement Disorders in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Other Specified Nonscarring Hair Loss Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Other Specified Nonscarring Hair Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Other Specified Disorders Of Adrenal Gland Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Other Specified Disorders Of Adrenal Gland in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Other Specified Coagulation Defects Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Other Specified Coagulation Defects in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Other Specified Congenital Malformations Of Skin Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Other Specified Congenital Malformations Of Skin in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Other Specified Cardiac Arrhythmias Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Other Specified Cardiac Arrhythmias in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Other Specified Conduction Disorders Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Other Specified Conduction Disorders in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Other Specified Hemorrhagic Conditions Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Other Specified Hemorrhagic Conditions in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Iron-Refractory Iron Deficiency Anemia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Iron-Refractory Iron Deficiency Anemia from the curated CTD Gene-Disease Associations dataset. |
iron-refractory iron deficiency anemia Gene SetFrom OMIM Gene-Disease Associations genes associated with the iron-refractory iron deficiency anemia phenotype from the curated OMIM Gene-Disease Associations dataset. |
Iron-Refractory Iron Deficiency Anemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Iron-Refractory Iron Deficiency Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Iron-refractory iron deficiency anemia Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Iron-refractory iron deficiency anemia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Heinz Body Anemias Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Heinz Body Anemias from the curated CTD Gene-Disease Associations dataset. |
anemias Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term anemias in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
heinz body anemias, alpha- Gene SetFrom OMIM Gene-Disease Associations genes associated with the heinz body anemias, alpha- phenotype from the curated OMIM Gene-Disease Associations dataset. |
heinz body anemias, beta- Gene SetFrom OMIM Gene-Disease Associations genes associated with the heinz body anemias, beta- phenotype from the curated OMIM Gene-Disease Associations dataset. |
Refractory Anemias Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Refractory Anemias in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Heinz Body Anemias Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Heinz Body Anemias in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
entry of organism into cell of other organism by promotion of phagocytosis in other organism involved in symbiotic interaction Gene SetFrom GO Biological Process Annotations 2015 genes participating in the entry of organism into cell of other organism by promotion of phagocytosis in other organism involved in symbiotic interaction biological process from the curated GO Biological Process Annotations 2015 dataset. |
Other Congenital Malformation Syndromes With Other Skeletal Changes Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Other Congenital Malformation Syndromes With Other Skeletal Changes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
hemochromatosis; iron metabolism disorders; iron overload Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hemochromatosis; iron metabolism disorders; iron overload in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
iron metabolism disorders; iron overload Gene SetFrom GAD Gene-Disease Associations genes associated with the disease iron metabolism disorders; iron overload in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Iron status biomarkers (total iron binding capacity) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Iron status biomarkers (total iron binding capacity) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Iron status biomarkers (iron levels) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Iron status biomarkers (iron levels) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
apolipoprotein c3 haplotype specified by the ssti polymorphism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apolipoprotein c3 haplotype specified by the ssti polymorphism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
specified Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term specified in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
EWSR1_KD_GDS4962_467_human_not specified Gene SetFrom GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the EWSR1_KD_GDS4962_467_human_not specified gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset. |
Supratentorial Embryonal Tumor, Not Otherwise Specified Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Supratentorial Embryonal Tumor, Not Otherwise Specified in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
High Grade B-Cell Lymphoma, Not Otherwise Specified Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease High Grade B-Cell Lymphoma, Not Otherwise Specified in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Central Nervous System Embryonal Tumor, Not Otherwise Specified Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Central Nervous System Embryonal Tumor, Not Otherwise Specified in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Metastatic Cervical Squamous Cell Carcinoma, Not Otherwise Specified Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Metastatic Cervical Squamous Cell Carcinoma, Not Otherwise Specified in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
factor v deficiency; hypoprothrombinemias; protein c deficiency; protein s deficiency; pulmonary embolism; thrombophilia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease factor v deficiency; hypoprothrombinemias; protein c deficiency; protein s deficiency; pulmonary embolism; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
antithrombin iii deficiency; gastrointestinal hemorrhage; protein c deficiency; protein s deficiency; splenomegaly; thrombophilia; turner syndrome; venous thrombosis; xo syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease antithrombin iii deficiency; gastrointestinal hemorrhage; protein c deficiency; protein s deficiency; splenomegaly; thrombophilia; turner syndrome; venous thrombosis; xo syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
activated protein c resistance; antithrombin iii deficiency; pregnancy complications, hematologic; protein c deficiency; protein s deficiency; puerperal disorders; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; antithrombin iii deficiency; pregnancy complications, hematologic; protein c deficiency; protein s deficiency; puerperal disorders; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Anemia, Iron-Deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Anemia, Iron-Deficiency from the curated CTD Gene-Disease Associations dataset. |
iron deficiency anemia Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease iron deficiency anemia in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
iron deficiency anemia Gene SetFrom DISEASES Text-mining Gene-Disease Association 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. |
alpha 1-antitrypsin deficiency; fibrosis; iron overload Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alpha 1-antitrypsin deficiency; fibrosis; iron overload in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anemia, iron deficiency Gene SetFrom 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; anemia of chronic disease Gene SetFrom 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. |
anemia, iron-deficiency; kidney failure, chronic Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
iron deficiency, inherited Gene SetFrom GAD Gene-Disease Associations genes associated with the disease iron deficiency, inherited in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anemia, iron-deficiency; polycythemia vera Gene SetFrom 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 SetFrom 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 SetFrom 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 Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Iron deficiency phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
iron deficiency anemia Gene SetFrom 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 SetFrom 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 SetFrom 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 Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Iron Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Chronic Iron Deficiency Anaemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Chronic Iron Deficiency Anaemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Iron deficiency anemia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Iron deficiency anemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Iron deficiency anemia Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Iron deficiency anemia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Cortical dysplasia, complex, with other brain malformations 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cortical dysplasia, complex, with other brain malformations 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cortical dysplasia, complex, with other brain malformations 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cortical dysplasia, complex, with other brain malformations 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cortical dysplasia, complex, with other brain malformations 6 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cortical dysplasia, complex, with other brain malformations 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cortical dysplasia, complex, with other brain malformations 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cortical dysplasia, complex, with other brain malformations 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cortical dysplasia, complex, with other brain malformations 5 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cortical dysplasia, complex, with other brain malformations 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Aplasia cutis congenita, reticulolinear, with microcephaly, facial dysmorphism, and other congenital anomalies Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Aplasia cutis congenita, reticulolinear, with microcephaly, facial dysmorphism, and other congenital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
other organism cell Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the other organism cell cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
other organism part Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the other organism part cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
other organism Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the other organism cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
other organism cell membrane Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the other organism cell membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
other organism presynaptic membrane Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the other organism presynaptic membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
other organism membrane Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the other organism membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
other organism cell Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the other organism cell cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
other organism part Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the other organism part cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
other organism Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the other organism cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
other organism cell membrane Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the other organism cell membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
other organism presynaptic membrane Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the other organism presynaptic membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
other organism membrane Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the other organism membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
other organism postsynaptic membrane Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the other organism postsynaptic membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
atherosclerosis, coronary; diabetes, type 1; nephropathy in other diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atherosclerosis, coronary; diabetes, type 1; nephropathy in other diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
nephropathy in other diseases; cerebrovascular disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease nephropathy in other diseases; cerebrovascular disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
genetically deficient metabolism of debrisoquine and other drugs Gene SetFrom GAD Gene-Disease Associations genes associated with the disease genetically deficient metabolism of debrisoquine and other drugs in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
nephropathy in other diseases; peripheral vascular disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease nephropathy in other diseases; peripheral vascular disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
subclinical atherosclerosis traits (other) Gene SetFrom GAD Gene-Disease Associations genes associated with the disease subclinical atherosclerosis traits (other) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
retinopathy, diabetic; nephropathy in other diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease retinopathy, diabetic; nephropathy in other diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
dementia in other conditions Gene SetFrom GAD Gene-Disease Associations genes associated with the disease dementia in other conditions in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes, type 2; nephropathy in other diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes, type 2; nephropathy in other diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
other metabolic traits Gene SetFrom GAD Gene-Disease Associations genes associated with the disease other metabolic traits in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lymph node involvement and other histopathological indicators of high metastatic potential Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lymph node involvement and other histopathological indicators of high metastatic potential in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
nephropathy in other diseases; diabetes Gene SetFrom GAD Gene-Disease Associations genes associated with the disease nephropathy in other diseases; diabetes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
nephropathy in other diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease nephropathy in other diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
type 2 diabetes and other traits Gene SetFrom GAD Gene-Disease Associations genes associated with the disease type 2 diabetes and other traits in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
tumor proliferation and other prognostic indicators Gene SetFrom GAD Gene-Disease Associations genes associated with the disease tumor proliferation and other prognostic indicators in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
nephropathy in other diseases; retinopathy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease nephropathy in other diseases; retinopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pulmonary function traits (other) Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pulmonary function traits (other) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes, type 1; nephropathy in other diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes, type 1; nephropathy in other diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes, type 1; blood pressure, arterial; nephropathy in other diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes, type 1; blood pressure, arterial; nephropathy in other diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lupus erythematosus; nephropathy in other diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lupus erythematosus; nephropathy in other diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
other erythrocyte phenotypes Gene SetFrom GAD Gene-Disease Associations genes associated with the disease other erythrocyte phenotypes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
other Gene SetFrom GAD High Level Gene-Disease Associations genes associated with the disease other in GWAS and other genetic association datasets from the GAD High Level Gene-Disease Associations dataset. |
other Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term other in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
membrane disruption in other organism Gene SetFrom GO Biological Process Annotations 2015 genes participating in the membrane disruption in other organism biological process from the curated GO Biological Process Annotations 2015 dataset. |
modulation by organism of apoptotic process in other organism involved in symbiotic interaction Gene SetFrom GO Biological Process Annotations 2015 genes participating in the modulation by organism of apoptotic process in other organism involved in symbiotic interaction biological process from the curated GO Biological Process Annotations 2015 dataset. |
response to defense-related nitric oxide production by other organism involved in symbiotic interaction Gene SetFrom GO Biological Process Annotations 2015 genes participating in the response to defense-related nitric oxide production by other organism involved in symbiotic interaction biological process from the curated GO Biological Process Annotations 2015 dataset. |
modulation of molecular function in other organism Gene SetFrom GO Biological Process Annotations 2015 genes participating in the modulation of molecular function in other organism biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation by organism of defense response of other organism involved in symbiotic interaction Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation by organism of defense response of other organism involved in symbiotic interaction biological process from the curated GO Biological Process Annotations 2015 dataset. |
entry into cell of other organism involved in symbiotic interaction Gene SetFrom GO Biological Process Annotations 2015 genes participating in the entry into cell of other organism involved in symbiotic interaction biological process from the curated GO Biological Process Annotations 2015 dataset. |
modulation of phagocytosis in other organism involved in symbiotic interaction Gene SetFrom GO Biological Process Annotations 2015 genes participating in the modulation of phagocytosis in other organism involved in symbiotic interaction biological process from the curated GO Biological Process Annotations 2015 dataset. |
killing of cells of other organism Gene SetFrom GO Biological Process Annotations 2015 genes participating in the killing of cells of other organism biological process from the curated GO Biological Process Annotations 2015 dataset. |
modification of morphology or physiology of other organism involved in symbiotic interaction Gene SetFrom GO Biological Process Annotations 2015 genes participating in the modification of morphology or physiology of other organism involved in symbiotic interaction biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation by organism of defense-related nitric oxide production in other organism involved in symbiotic interaction Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation by organism of defense-related nitric oxide production in other organism involved in symbiotic interaction biological process from the curated GO Biological Process Annotations 2015 dataset. |
movement in environment of other organism involved in symbiotic interaction Gene SetFrom GO Biological Process Annotations 2015 genes participating in the movement in environment of other organism involved in symbiotic interaction biological process from the curated GO Biological Process Annotations 2015 dataset. |
modulation by organism of defense response of other organism involved in symbiotic interaction Gene SetFrom GO Biological Process Annotations 2015 genes participating in the modulation by organism of defense response of other organism involved in symbiotic interaction biological process from the curated GO Biological Process Annotations 2015 dataset. |
modulation of signal transduction in other organism Gene SetFrom GO Biological Process Annotations 2015 genes participating in the modulation of signal transduction in other organism biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation by organism of programmed cell death in other organism involved in symbiotic interaction Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation by organism of programmed cell death in other organism involved in symbiotic interaction biological process from the curated GO Biological Process Annotations 2015 dataset. |
modulation of programmed cell death in other organism Gene SetFrom GO Biological Process Annotations 2015 genes participating in the modulation of programmed cell death in other organism biological process from the curated GO Biological Process Annotations 2015 dataset. |
modulation of signal transduction in other organism involved in symbiotic interaction Gene SetFrom GO Biological Process Annotations 2015 genes participating in the modulation of signal transduction in other organism involved in symbiotic interaction biological process from the curated GO Biological Process Annotations 2015 dataset. |
defense response to other organism Gene SetFrom GO Biological Process Annotations 2015 genes participating in the defense response to other organism biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of killing of cells of other organism Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of killing of cells of other organism biological process from the curated GO Biological Process Annotations 2015 dataset. |
modulation by organism of immune response of other organism involved in symbiotic interaction Gene SetFrom GO Biological Process Annotations 2015 genes participating in the modulation by organism of immune response of other organism involved in symbiotic interaction biological process from the curated GO Biological Process Annotations 2015 dataset. |
hemolysis in other organism Gene SetFrom GO Biological Process Annotations 2015 genes participating in the hemolysis in other organism biological process from the curated GO Biological Process Annotations 2015 dataset. |
induction by organism of defense response of other organism involved in symbiotic interaction Gene SetFrom GO Biological Process Annotations 2015 genes participating in the induction by organism of defense response of other organism involved in symbiotic interaction biological process from the curated GO Biological Process Annotations 2015 dataset. |
modulation of transcription in other organism involved in symbiotic interaction Gene SetFrom GO Biological Process Annotations 2015 genes participating in the modulation of transcription in other organism involved in symbiotic interaction biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation by organism of apoptotic process in other organism involved in symbiotic interaction Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation by organism of apoptotic process in other organism involved in symbiotic interaction biological process from the curated GO Biological Process Annotations 2015 dataset. |
response to defenses of other organism involved in symbiotic interaction Gene SetFrom GO Biological Process Annotations 2015 genes participating in the response to defenses of other organism involved in symbiotic interaction biological process from the curated GO Biological Process Annotations 2015 dataset. |
modulation of apoptotic process in other organism Gene SetFrom GO Biological Process Annotations 2015 genes participating in the modulation of apoptotic process in other organism biological process from the curated GO Biological Process Annotations 2015 dataset. |
modification of morphology or physiology of other organism Gene SetFrom GO Biological Process Annotations 2015 genes participating in the modification of morphology or physiology of other organism biological process from the curated GO Biological Process Annotations 2015 dataset. |
response to other organism Gene SetFrom GO Biological Process Annotations 2015 genes participating in the response to other organism biological process from the curated GO Biological Process Annotations 2015 dataset. |
induction by organism of immune response of other organism involved in symbiotic interaction Gene SetFrom GO Biological Process Annotations 2015 genes participating in the induction by organism of immune response of other organism involved in symbiotic interaction biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation by organism of immune response of other organism involved in symbiotic interaction Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation by organism of immune response of other organism involved in symbiotic interaction biological process from the curated GO Biological Process Annotations 2015 dataset. |
translocation of molecules into other organism involved in symbiotic interaction Gene SetFrom GO Biological Process Annotations 2015 genes participating in the translocation of molecules into other organism involved in symbiotic interaction biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of killing of cells of other organism Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of killing of cells of other organism biological process from the curated GO Biological Process Annotations 2015 dataset. |
evasion or tolerance of defense response of other organism involved in symbiotic interaction Gene SetFrom GO Biological Process Annotations 2015 genes participating in the evasion or tolerance of defense response of other organism involved in symbiotic interaction biological process from the curated GO Biological Process Annotations 2015 dataset. |
cytolysis in other organism involved in symbiotic interaction Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cytolysis in other organism involved in symbiotic interaction biological process from the curated GO Biological Process Annotations 2015 dataset. |
cytolysis in other organism Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cytolysis in other organism biological process from the curated GO Biological Process Annotations 2015 dataset. |
hemolysis in other organism involved in symbiotic interaction Gene SetFrom GO Biological Process Annotations 2015 genes participating in the hemolysis in other organism involved in symbiotic interaction biological process from the curated GO Biological Process Annotations 2015 dataset. |
response to defense-related reactive oxygen species production by other organism involved in symbiotic interaction Gene SetFrom GO Biological Process Annotations 2015 genes participating in the response to defense-related reactive oxygen species production by other organism involved in symbiotic interaction biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation by organism of programmed cell death in other organism involved in symbiotic interaction Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation by organism of programmed cell death in other organism involved in symbiotic interaction biological process from the curated GO Biological Process Annotations 2015 dataset. |
disruption of cells of other organism Gene SetFrom GO Biological Process Annotations 2015 genes participating in the disruption of cells of other organism biological process from the curated GO Biological Process Annotations 2015 dataset. |
modulation of molecular function in other organism involved in symbiotic interaction Gene SetFrom GO Biological Process Annotations 2015 genes participating in the modulation of molecular function in other organism involved in symbiotic interaction biological process from the curated GO Biological Process Annotations 2015 dataset. |
entry into other organism involved in symbiotic interaction Gene SetFrom GO Biological Process Annotations 2015 genes participating in the entry into other organism involved in symbiotic interaction biological process from the curated GO Biological Process Annotations 2015 dataset. |
response to immune response of other organism involved in symbiotic interaction Gene SetFrom GO Biological Process Annotations 2015 genes participating in the response to immune response of other organism involved in symbiotic interaction biological process from the curated GO Biological Process Annotations 2015 dataset. |
detection of other organism Gene SetFrom GO Biological Process Annotations 2015 genes participating in the detection of other organism biological process from the curated GO Biological Process Annotations 2015 dataset. |
induction by organism of defense-related nitric oxide production in other organism involved in symbiotic interaction Gene SetFrom GO Biological Process Annotations 2015 genes participating in the induction by organism of defense-related nitric oxide production in other organism involved in symbiotic interaction biological process from the curated GO Biological Process Annotations 2015 dataset. |
dissemination or transmission of organism from other organism involved in symbiotic interaction Gene SetFrom GO Biological Process Annotations 2015 genes participating in the dissemination or transmission of organism from other organism involved in symbiotic interaction biological process from the curated GO Biological Process Annotations 2015 dataset. |
modulation by organism of defense-related nitric oxide production in other organism involved in symbiotic interaction Gene SetFrom GO Biological Process Annotations 2015 genes participating in the modulation by organism of defense-related nitric oxide production in other organism involved in symbiotic interaction biological process from the curated GO Biological Process Annotations 2015 dataset. |
modulation of catalytic activity in other organism involved in symbiotic interaction Gene SetFrom GO Biological Process Annotations 2015 genes participating in the modulation of catalytic activity in other organism involved in symbiotic interaction biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation by organism of phagocytosis in other organism involved in symbiotic interaction Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation by organism of phagocytosis in other organism involved in symbiotic interaction biological process from the curated GO Biological Process Annotations 2015 dataset. |
intracellular protein transport in other organism involved in symbiotic interaction Gene SetFrom GO Biological Process Annotations 2015 genes participating in the intracellular protein transport in other organism involved in symbiotic interaction biological process from the curated GO Biological Process Annotations 2015 dataset. |
translocation of peptides or proteins into other organism involved in symbiotic interaction Gene SetFrom GO Biological Process Annotations 2015 genes participating in the translocation of peptides or proteins into other organism involved in symbiotic interaction biological process from the curated GO Biological Process Annotations 2015 dataset. |
modulation of programmed cell death in other organism involved in symbiotic interaction Gene SetFrom GO Biological Process Annotations 2015 genes participating in the modulation of programmed cell death in other organism involved in symbiotic interaction biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of catalytic activity in other organism involved in symbiotic interaction Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of catalytic activity in other organism involved in symbiotic interaction biological process from the curated GO Biological Process Annotations 2015 dataset. |
disruption of cells of other organism involved in symbiotic interaction Gene SetFrom GO Biological Process Annotations 2015 genes participating in the disruption of cells of other organism involved in symbiotic interaction biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of molecular function in other organism involved in symbiotic interaction Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of molecular function in other organism involved in symbiotic interaction biological process from the curated GO Biological Process Annotations 2015 dataset. |
killing of cells in other organism involved in symbiotic interaction Gene SetFrom GO Biological Process Annotations 2015 genes participating in the killing of cells in other organism involved in symbiotic interaction biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of apoptotic process in other organism Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of apoptotic process in other organism biological process from the curated GO Biological Process Annotations 2015 dataset. |
avoidance of defenses of other organism involved in symbiotic interaction Gene SetFrom GO Biological Process Annotations 2015 genes participating in the avoidance of defenses of other organism involved in symbiotic interaction biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of molecular function in other organism Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of molecular function in other organism biological process from the curated GO Biological Process Annotations 2015 dataset. |
evasion or tolerance of defenses of other organism involved in symbiotic interaction Gene SetFrom GO Biological Process Annotations 2015 genes participating in the evasion or tolerance of defenses of other organism involved in symbiotic interaction biological process from the curated GO Biological Process Annotations 2015 dataset. |
evasion or tolerance of immune response of other organism involved in symbiotic interaction Gene SetFrom GO Biological Process Annotations 2015 genes participating in the evasion or tolerance of immune response of other organism involved in symbiotic interaction biological process from the curated GO Biological Process Annotations 2015 dataset. |
other organism cell Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the other organism cell cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
other organism part Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the other organism part cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
other organism cell membrane Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the other organism cell membrane cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
other organism presynaptic membrane Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the other organism presynaptic membrane cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
other organism membrane Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the other organism membrane cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
oxidoreductase activity, acting on other nitrogenous compounds as donors Gene SetFrom GO Molecular Function Annotations 2015 genes performing the oxidoreductase activity, acting on other nitrogenous compounds as donors molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
transferase activity, transferring acyl groups other than amino-acyl groups Gene SetFrom GO Molecular Function Annotations 2015 genes performing the transferase activity, transferring acyl groups other than amino-acyl groups molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, with nad(p)h as one donor, and the other dehydrogenated Gene SetFrom GO Molecular Function Annotations 2015 genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, with nad(p)h as one donor, and the other dehydrogenated molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
transferase activity, transferring alkyl or aryl (other than methyl) groups Gene SetFrom GO Molecular Function Annotations 2015 genes performing the transferase activity, transferring alkyl or aryl (other than methyl) groups molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
phosphotransferase activity, for other substituted phosphate groups Gene SetFrom GO Molecular Function Annotations 2015 genes performing the phosphotransferase activity, for other substituted phosphate groups molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
Non-alcoholic fatty liver disease histology (other) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Non-alcoholic fatty liver disease histology (other) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Subclinical atherosclerosis traits (other) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Subclinical atherosclerosis traits (other) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Common traits (Other) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Common traits (Other) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Other erythrocyte phenotypes Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Other erythrocyte phenotypes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Type 2 diabetes and other traits Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Type 2 diabetes and other traits phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Aspartate/other aminotransferase Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Aspartate/other aminotransferase protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
other aberrant phenotype Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the other aberrant phenotype phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
other phenotype Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the other phenotype phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
corneal opacification and other ocular anomalies Gene SetFrom OMIM Gene-Disease Associations genes associated with the corneal opacification and other ocular anomalies phenotype from the curated OMIM Gene-Disease Associations dataset. |
aplasia cutis congenita, reticulolinear, with mmicrocephaly, facial dysmorphism and other congenital anomalies Gene SetFrom OMIM Gene-Disease Associations genes associated with the aplasia cutis congenita, reticulolinear, with mmicrocephaly, facial dysmorphism and other congenital anomalies phenotype from the curated OMIM Gene-Disease Associations dataset. |
cortical dysplasia, complex, with other brain malformations 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the cortical dysplasia, complex, with other brain malformations 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
cortical dysplasia, complex, with other brain malformations 3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the cortical dysplasia, complex, with other brain malformations 3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
cortical dysplasia, complex, with other brain malformations 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the cortical dysplasia, complex, with other brain malformations 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
cortical dysplasia, complex, with other brain malformations 6 Gene SetFrom OMIM Gene-Disease Associations genes associated with the cortical dysplasia, complex, with other brain malformations 6 phenotype from the curated OMIM Gene-Disease Associations dataset. |
cortical dysplasia, complex, with other brain malformations 4 Gene SetFrom OMIM Gene-Disease Associations genes associated with the cortical dysplasia, complex, with other brain malformations 4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
cortical dysplasia, complex, with other brain malformations 5 Gene SetFrom OMIM Gene-Disease Associations genes associated with the cortical dysplasia, complex, with other brain malformations 5 phenotype from the curated OMIM Gene-Disease Associations dataset. |
craniosynostosis with radiohumeral fusions and other skeletal and craniofacial anomalies Gene SetFrom OMIM Gene-Disease Associations genes associated with the craniosynostosis with radiohumeral fusions and other skeletal and craniofacial anomalies phenotype from the curated OMIM Gene-Disease Associations dataset. |
RXR and RAR heterodimerization with other nuclear receptor Gene SetFrom PID Pathways proteins participating in the RXR and RAR heterodimerization with other nuclear receptor pathway from the PID Pathways dataset. |
Defective CYP26B1 causes Radiohumeral fusions with other skeletal and craniofacial anomalies (RHFCA) Gene Setproteins participating in the Defective CYP26B1 causes Radiohumeral fusions with other skeletal and craniofacial anomalies (RHFCA) pathway from the Reactome Pathways dataset. |
Formyl peptide receptors bind formyl peptides and many other ligands Gene Setproteins participating in the Formyl peptide receptors bind formyl peptides and many other ligands pathway from the Reactome Pathways dataset. |
Other semaphorin interactions Gene Setproteins participating in the Other semaphorin interactions pathway from the Reactome Pathways dataset. |
Assembly of collagen fibrils and other multimeric structures Gene Setproteins participating in the Assembly of collagen fibrils and other multimeric structures pathway from the Reactome Pathways dataset. |
APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins in late mitosis/early G1 Gene Setproteins participating in the APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins in late mitosis/early G1 pathway from the Reactome Pathways dataset. |
Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds Gene Setproteins participating in the Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds pathway from the Reactome Pathways dataset. |
other source Gene SetFrom TISSUES Experimental Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue other source in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset. |
other source Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue other source in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
GPCRs, Other(Homo sapiens) Gene SetFrom WikiPathways Pathways 2014 proteins participating in the GPCRs, Other(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset. |
GPCRs, Other(Mus musculus) Gene SetFrom WikiPathways Pathways 2014 proteins participating in the GPCRs, Other(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset. |
Alcohol Or Other Drugs Use Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Alcohol Or Other Drugs Use in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Other Acute Reactions To Stress Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Other Acute Reactions To Stress in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Other Cataract Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Other Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Other Creutzfeldt-Jakob Disease Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Other Creutzfeldt-Jakob Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Other Hypoparathyroidism Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Other Hypoparathyroidism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cancer Other Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cancer Other in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Primary Malignant Neoplasm Of Ovary And Other Uterine Adnexa Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Primary Malignant Neoplasm Of Ovary And Other Uterine Adnexa in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Other Headache Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Other Headache Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Other Disorders Of Branched-Chain Amino-Acid Metabolism Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Other Disorders Of Branched-Chain Amino-Acid Metabolism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Other Congenital Malformations Of Anterior Segment Of Eye Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Other Congenital Malformations Of Anterior Segment Of Eye in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Other Hyperaldosteronism Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Other Hyperaldosteronism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Ankylosing Spondylitis And Other Inflammatory Spondylopathies Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Ankylosing Spondylitis And Other Inflammatory Spondylopathies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Other Malformations Of Cerebral Vessels Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Other Malformations Of Cerebral Vessels in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Other And Unspecified Reactive Psychosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Other And Unspecified Reactive Psychosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Radiohumeral Fusions With Other Skeletal And Craniofacial Anomalies Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Radiohumeral Fusions With Other Skeletal And Craniofacial Anomalies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Other Cardiomyopathies Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Other Cardiomyopathies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Other Stomatitis And Mucositis (Ulcerative) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Other Stomatitis And Mucositis (Ulcerative) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Other Sphingolipidosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Other Sphingolipidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Other Congenital Anomalies Of Nervous System Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Other Congenital Anomalies Of Nervous System in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Tympanosclerosis Involving Other Combination Of Structures Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Tympanosclerosis Involving Other Combination Of Structures in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Other Chronic Tubulo-Interstitial Nephritis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Other Chronic Tubulo-Interstitial Nephritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Other Congenital Malformations Of Spine, Not Associated With Scoliosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Other Congenital Malformations Of Spine, Not Associated With Scoliosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Other Restrictive Cardiomyopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Other Restrictive Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Other Alcohol-Induced Mental Disorders Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Other Alcohol-Induced Mental Disorders in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Other Deletions Of Part Of A Chromosome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Other Deletions Of Part Of A Chromosome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Other Dermatoses Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Other Dermatoses in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Other Chondrocalcinosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Other Chondrocalcinosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Heart Defects, Congenital, And Other Congenital Anomalies Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Heart Defects, Congenital, And Other Congenital Anomalies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Other Congenital Ichthyosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Other Congenital Ichthyosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Other Doubling Of Uterus Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Other Doubling Of Uterus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Disseminated Due To Other Mycobacteria Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Disseminated Due To Other Mycobacteria in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Other Epidermolysis Bullosa Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Other Epidermolysis Bullosa in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Other Congenital Corneal Malformations Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Other Congenital Corneal Malformations in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Acute Myeloid Leukemia/Other Myeloid Malignancies Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Acute Myeloid Leukemia/Other Myeloid Malignancies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cluster Headaches And Other Trigeminal Autonomic Cephalgias Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cluster Headaches And Other Trigeminal Autonomic Cephalgias in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Other Combined Immunodeficiencies Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Other Combined Immunodeficiencies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Other Disorders Of Lipoid Metabolism Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Other Disorders Of Lipoid Metabolism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Other Reduction Deformities Of Brain Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Other Reduction Deformities Of Brain in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Other Ureteric Obstruction Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Other Ureteric Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Hangover From Any Alcohol Or Other Drugs Substance Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hangover From Any Alcohol Or Other Drugs Substance in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Other Alopecia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Other Alopecia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Other Emphysema Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Other Emphysema in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Other Lesions Of Median Nerve Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Other Lesions Of Median Nerve in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Other License Status Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Other License Status in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Other Dystonia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Other Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Other Heart Block Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Other Heart Block in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
phosphotransferase activity, for other substituted phosphate groups Gene SetFrom GO Molecular Function Annotations 2023 genes performing the phosphotransferase activity, for other substituted phosphate groups molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
acyltransferase activity, transferring groups other than amino-acyl groups Gene SetFrom GO Molecular Function Annotations 2023 genes performing the acyltransferase activity, transferring groups other than amino-acyl groups molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
oxidoreductase activity, acting on other nitrogenous compounds as donors, cytochrome as acceptor Gene SetFrom GO Molecular Function Annotations 2023 genes performing the oxidoreductase activity, acting on other nitrogenous compounds as donors, cytochrome as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
oxidoreductase activity, acting on other nitrogenous compounds as donors, oxygen as acceptor Gene SetFrom GO Molecular Function Annotations 2023 genes performing the oxidoreductase activity, acting on other nitrogenous compounds as donors, oxygen as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
oxidoreductase activity, acting on other nitrogenous compounds as donors, with NAD or NADP as acceptor Gene SetFrom GO Molecular Function Annotations 2023 genes performing the oxidoreductase activity, acting on other nitrogenous compounds as donors, with NAD or NADP as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
Human - PBMC - L1 - other T cell Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - PBMC - L1 - other T cell cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Bone Marrow - L1 - Other T Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Bone Marrow - L1 - Other T cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
GPCRs other Gene SetFrom WikiPathways Pathways 2024 proteins participating in the GPCRs other pathway from the WikiPathways Pathways 2024 dataset. |
APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins in late mitosis/early G1 Gene Setproteins participating in the APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins in late mitosis/early G1 pathway from the Reactome Pathways 2024 dataset. |
Assembly of collagen fibrils and other multimeric structures Gene Setproteins participating in the Assembly of collagen fibrils and other multimeric structures pathway from the Reactome Pathways 2024 dataset. |
Formyl peptide receptors bind formyl peptides and many other ligands Gene Setproteins participating in the Formyl peptide receptors bind formyl peptides and many other ligands pathway from the Reactome Pathways 2024 dataset. |
Latent infection - Other responses of Mtb to phagocytosis Gene Setproteins participating in the Latent infection - Other responses of Mtb to phagocytosis pathway from the Reactome Pathways 2024 dataset. |
Other interleukin signaling Gene Setproteins participating in the Other interleukin signaling pathway from the Reactome Pathways 2024 dataset. |
Other semaphorin interactions Gene Setproteins participating in the Other semaphorin interactions pathway from the Reactome Pathways 2024 dataset. |
TFAP2 (AP-2) family regulates transcription of other transcription factors Gene Setproteins participating in the TFAP2 (AP-2) family regulates transcription of other transcription factors pathway from the Reactome Pathways 2024 dataset. |
phosphotransferase activity, for other substituted phosphate groups Gene SetFrom GO Molecular Function Annotations 2025 genes performing the phosphotransferase activity, for other substituted phosphate groups molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
acyltransferase activity, transferring groups other than amino-acyl groups Gene SetFrom GO Molecular Function Annotations 2025 genes performing the acyltransferase activity, transferring groups other than amino-acyl groups molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
oxidoreductase activity, acting on other nitrogenous compounds as donors, cytochrome as acceptor Gene SetFrom GO Molecular Function Annotations 2025 genes performing the oxidoreductase activity, acting on other nitrogenous compounds as donors, cytochrome as acceptor molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
oxidoreductase activity, acting on other nitrogenous compounds as donors, with NAD or NADP as acceptor Gene SetFrom GO Molecular Function Annotations 2025 genes performing the oxidoreductase activity, acting on other nitrogenous compounds as donors, with NAD or NADP as acceptor molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
Complex cortical dysplasia with other brain malformations 2 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Complex cortical dysplasia with other brain malformations 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Complex cortical dysplasia with other brain malformations Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Complex cortical dysplasia with other brain malformations in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Complex cortical dysplasia with other brain malformations 7 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Complex cortical dysplasia with other brain malformations 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Complex cortical dysplasia with other brain malformations 6 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Complex cortical dysplasia with other brain malformations 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Complex cortical dysplasia with other brain malformations 3 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Complex cortical dysplasia with other brain malformations 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Complex cortical dysplasia with other brain malformations 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Complex cortical dysplasia with other brain malformations 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Other source Gene SetFrom TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Other source in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 dataset. |
Other source Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Other source in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Other organism part Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Other organism part cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Other organism part Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Other organism part cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Other organism cell membrane Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Other organism cell membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Fluorouracil response - Other Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Fluorouracil response - Other phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Plasma free amino acid levels (adjusted for one other PFAA) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Plasma free amino acid levels (adjusted for one other PFAA) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Plasma free amino acid levels (adjusted for twenty other PFAAs) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Plasma free amino acid levels (adjusted for twenty other PFAAs) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Non-alcoholic fatty liver disease histology (other) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Non-alcoholic fatty liver disease histology (other) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Other erythrocyte phenotypes Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Other erythrocyte phenotypes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Common traits (Other) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Common traits (Other) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Subclinical atherosclerosis traits (other) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Subclinical atherosclerosis traits (other) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Strenuous sports or other exercises Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Strenuous sports or other exercises phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Other types of O-glycan biosynthesis Gene SetFrom KEGG Pathways 2026 proteins participating in the Other types of O-glycan biosynthesis pathway from the KEGG Pathways 2026 dataset. |
Other glycan degradation Gene SetFrom KEGG Pathways 2026 proteins participating in the Other glycan degradation pathway from the KEGG Pathways 2026 dataset. |
Ubiquinone and other terpenoid-quinone biosynthesis Gene SetFrom KEGG Pathways 2026 proteins participating in the Ubiquinone and other terpenoid-quinone biosynthesis pathway from the KEGG Pathways 2026 dataset. |
Drug metabolism - other enzymes Gene SetFrom KEGG Pathways 2026 proteins participating in the Drug metabolism - other enzymes pathway from the KEGG Pathways 2026 dataset. |
Autophagy - other Gene SetFrom KEGG Pathways 2026 proteins participating in the Autophagy - other pathway from the KEGG Pathways 2026 dataset. |
Endocrine and other factor-regulated calcium reabsorption Gene SetFrom KEGG Pathways 2026 proteins participating in the Endocrine and other factor-regulated calcium reabsorption pathway from the KEGG Pathways 2026 dataset. |
Neuraminidase deficiency with beta-galactosidase deficiency Gene SetFrom 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 SetFrom 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 SetFrom GAD Gene-Disease Associations genes associated with the disease eclampsia; pre-eclampsia; protein c deficiency; protein s deficiency; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
blood coagulation disorders, inherited; protein c deficiency; protein s deficiency; thrombophilia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease blood coagulation disorders, inherited; protein c deficiency; protein s deficiency; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
blood coagulation disorders; protein c deficiency; protein s deficiency; pulmonary embolism; pulmonary embolisms; thrombosis; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease blood coagulation disorders; protein c deficiency; protein s deficiency; pulmonary embolism; pulmonary embolisms; thrombosis; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
folic acid deficiency; fractures, bone; osteoporosis, postmenopausal; riboflavin deficiency Gene SetFrom 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 SetFrom GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; blood coagulation disorders; liver diseases; protein c deficiency; protein s deficiency; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
choline deficiency; dna damage; folic acid deficiency Gene SetFrom 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 SetFrom 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 SetFrom GAD Gene-Disease Associations genes associated with the disease protein c deficiency; protein s deficiency; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
folic acid deficiency; hyperhomocysteinemia; thromboembolism; venous insufficiency; vitamin b 12 deficiency Gene SetFrom 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 SetFrom GAD Gene-Disease Associations genes associated with the disease neoplasms; protein c deficiency; protein s deficiency; venous thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; folic acid deficiency; hyperhomocysteinemia; kidney failure, chronic; vitamin b 12 deficiency Gene SetFrom 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 Setproteins 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 Setproteins 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 Setproteins participating in the Defective TPMT causes Thiopurine S-methyltransferase deficiency (TPMT deficiency) pathway from the Reactome Pathways dataset. |
Defective HK1 causes hexokinase deficiency (HK deficiency) Gene Setproteins participating in the Defective HK1 causes hexokinase deficiency (HK deficiency) pathway from the Reactome Pathways 2024 dataset. |
Sulfite oxidase deficiency due to molybdenum cofactor deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Sulfite oxidase deficiency due to molybdenum cofactor deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Iron accumulation in brain Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Iron accumulation in brain phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Neurodegeneration with brain iron accumulation 2b Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Neurodegeneration with brain iron accumulation 2b phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hypochromic microcytic anemia with iron overload Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypochromic microcytic anemia with iron overload phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Neurodegeneration with brain iron accumulation 5 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Neurodegeneration with brain iron accumulation 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Neurodegeneration with brain iron accumulation 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Neurodegeneration with brain iron accumulation 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Neurodegeneration with brain iron accumulation 6 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Neurodegeneration with brain iron accumulation 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
high-affinity iron permease complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the high-affinity iron permease complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
Iron Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Iron from the curated CTD Gene-Chemical Interactions dataset. |
Iron, Dietary Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Iron, Dietary from the curated CTD Gene-Chemical Interactions dataset. |
iron(III)-ascorbic acid complex Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical iron(III)-ascorbic acid complex from the curated CTD Gene-Chemical Interactions dataset. |
5,10,15,20-tetrakis(4-sulfonatophenyl)porphyrinato iron(III) chloride Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical 5,10,15,20-tetrakis(4-sulfonatophenyl)porphyrinato iron(III) chloride from the curated CTD Gene-Chemical Interactions dataset. |
Iron Chelating Agents Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Iron Chelating Agents from the curated CTD Gene-Chemical Interactions dataset. |
Iron-Dextran Complex Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Iron-Dextran Complex from the curated CTD Gene-Chemical Interactions dataset. |
iron protoporphyrin IX Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical iron protoporphyrin IX from the curated CTD Gene-Chemical Interactions dataset. |
iron(II)-ascorbic acid complex Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical iron(II)-ascorbic acid complex from the curated CTD Gene-Chemical Interactions dataset. |
5,10,15,20-tetrakis(N-methyl-4'-pyridyl)porphyrinato-iron(III) Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical 5,10,15,20-tetrakis(N-methyl-4'-pyridyl)porphyrinato-iron(III) from the curated CTD Gene-Chemical Interactions dataset. |
Iron Metabolism Disorders Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Iron Metabolism Disorders from the curated CTD Gene-Disease Associations dataset. |
NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2A Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2A from the curated CTD Gene-Disease Associations dataset. |
Iron Overload Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Iron Overload from the curated CTD Gene-Disease Associations dataset. |
NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2B Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2B from the curated CTD Gene-Disease Associations dataset. |
Anemia, Hypochromic Microcytic, With Iron Overload Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Anemia, Hypochromic Microcytic, With Iron Overload from the curated CTD Gene-Disease Associations dataset. |
Neurodegeneration with brain iron accumulation (NBIA) Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neurodegeneration with brain iron accumulation (NBIA) from the curated CTD Gene-Disease Associations dataset. |
Iron-Regulatory Proteins Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Iron-Regulatory Proteins in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
Iron Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Iron in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
iron metabolism disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease iron metabolism disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
iron metabolism disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease iron metabolism disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
iron metabolism disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease iron metabolism disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
Iron Dextran Gene Setinteracting proteins for the Iron Dextran drug from the curated DrugBank Drug Targets dataset. |
carcinoma, hepatocellular; hepatitis c; iron overload; lcc - liver cell carcinoma; liver cirrhosis; liver neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, hepatocellular; hepatitis c; iron overload; lcc - liver cell carcinoma; liver cirrhosis; liver neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hepatitis c, chronic; iron overload Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hepatitis c, chronic; iron overload in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
amyotrophic lateral sclerosis; iron metabolism disorders; nerve degeneration Gene SetFrom GAD Gene-Disease Associations genes associated with the disease amyotrophic lateral sclerosis; iron metabolism disorders; nerve degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fibrosis; iron overload Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fibrosis; iron overload in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hemochromatosis; iron overload; joint diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hemochromatosis; iron overload; joint diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
iron levels; soluble transferrin receptor; transferrin Gene SetFrom GAD Gene-Disease Associations genes associated with the disease iron levels; soluble transferrin receptor; transferrin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hepatitis c, chronic; iron overload; porphyria cutanea tarda Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hepatitis c, chronic; iron overload; porphyria cutanea tarda in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
beta thalassemia; beta-thalassemia; hemochromatosis; iron overload; metal metabolism, inborn errors Gene SetFrom GAD Gene-Disease Associations genes associated with the disease beta thalassemia; beta-thalassemia; hemochromatosis; iron overload; metal metabolism, inborn errors in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
increased serum iron transferrin saturation and hemoglobin Gene SetFrom GAD Gene-Disease Associations genes associated with the disease increased serum iron transferrin saturation and hemoglobin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, hepatocellular; hepatitis c; iron overload; lcc - liver cell carcinoma; liver cirrhosis, alcoholic; liver neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, hepatocellular; hepatitis c; iron overload; lcc - liver cell carcinoma; liver cirrhosis, alcoholic; liver neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
beta-thalassemia; iron overload Gene SetFrom GAD Gene-Disease Associations genes associated with the disease beta-thalassemia; iron overload in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcoholic liver diseases; fatty liver; iron overload; liver cirrhosis; liver diseases, alcoholic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcoholic liver diseases; fatty liver; iron overload; liver cirrhosis; liver diseases, alcoholic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
leukemia; hemochromatosis; iron metabolism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease leukemia; hemochromatosis; iron metabolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hepatic iron and fibrosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hepatic iron and fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fatty liver; iron overload; liver cirrhosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fatty liver; iron overload; liver cirrhosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fatty liver; insulin resistance; iron overload Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fatty liver; insulin resistance; iron overload in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hemochromatosis; hepatitis c, chronic; iron overload; liver diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hemochromatosis; hepatitis c, chronic; iron overload; liver diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
serum markers of iron status Gene SetFrom GAD Gene-Disease Associations genes associated with the disease serum markers of iron status in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
beta thalassemia; beta-thalassemia; cardiomyopathies; iron overload Gene SetFrom GAD Gene-Disease Associations genes associated with the disease beta thalassemia; beta-thalassemia; cardiomyopathies; iron overload in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
iron overload; varicose ulcer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease iron overload; varicose ulcer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
iron metabolism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease iron metabolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
iron-regulatory proteins Gene SetFrom GAD Gene-Disease Associations genes associated with the disease iron-regulatory proteins in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
colorectal neoplasms; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; iron overload Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colorectal neoplasms; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; iron overload in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hemochromatosis; iron overload Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hemochromatosis; iron overload in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fatty liver; iron overload Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fatty liver; iron overload in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
liver function; iron levels; ferritin; transferrin saturation Gene SetFrom GAD Gene-Disease Associations genes associated with the disease liver function; iron levels; ferritin; transferrin saturation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcoholism; iron overload; liver diseases, alcoholic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcoholism; iron overload; liver diseases, alcoholic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
iron levels Gene SetFrom GAD Gene-Disease Associations genes associated with the disease iron levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hemochromatosis; iron overload; liver diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hemochromatosis; iron overload; liver diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
iron overload; myeloproliferative disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease iron overload; myeloproliferative disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
serum iron concentration Gene SetFrom GAD Gene-Disease Associations genes associated with the disease serum iron concentration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes mellitus; hemochromatosis; iron overload Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes mellitus; hemochromatosis; iron overload in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arthralgia; diabetes mellitus, type 2; fatigue; hemochromatosis; iron overload Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arthralgia; diabetes mellitus, type 2; fatigue; hemochromatosis; iron overload in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anemia, sickle cell; hemochromatosis; iron overload; sickle cell anemia Gene SetFrom 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. |
chromosome inversion; hemochromatosis; inversion, chromosome; iron overload; thalassemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome inversion; hemochromatosis; inversion, chromosome; iron overload; thalassemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
beta thalassemia; beta-thalassemia; iron overload Gene SetFrom GAD Gene-Disease Associations genes associated with the disease beta thalassemia; beta-thalassemia; iron overload in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
iron overload; thalassemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease iron overload; thalassemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
iron Gene SetFrom GAD Gene-Disease Associations genes associated with the disease iron in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
iron load Gene SetFrom GAD Gene-Disease Associations genes associated with the disease iron load in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
iron status and erythrocyte volume Gene SetFrom GAD Gene-Disease Associations genes associated with the disease iron status and erythrocyte volume in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
c-reactive protein; ferritin; iron Gene SetFrom GAD Gene-Disease Associations genes associated with the disease c-reactive protein; ferritin; iron in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hemochromatosis; hepatitis c, chronic; iron overload; liver cirrhosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hemochromatosis; hepatitis c, chronic; iron overload; liver cirrhosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
gaucher disease; iron overload; splenomegaly Gene SetFrom GAD Gene-Disease Associations genes associated with the disease gaucher disease; iron overload; splenomegaly in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
gastrointestinal hemorrhage; hemorrhoids; iron overload Gene SetFrom GAD Gene-Disease Associations genes associated with the disease gastrointestinal hemorrhage; hemorrhoids; iron overload in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
iron burden Gene SetFrom GAD Gene-Disease Associations genes associated with the disease iron burden in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
iron overload Gene SetFrom GAD Gene-Disease Associations genes associated with the disease iron overload in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hemochromatosis; iron overload; pigmentation disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hemochromatosis; iron overload; pigmentation disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
disease models, animal; hemochromatosis; iron overload; liver cirrhosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease disease models, animal; hemochromatosis; iron overload; liver cirrhosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
iron stores Gene SetFrom GAD Gene-Disease Associations genes associated with the disease iron stores in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hepatitis c; iron overload; porphyria cutanea tarda Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hepatitis c; iron overload; porphyria cutanea tarda in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
genetic polymorphism of cytochrome p450 2a6 and the body status of iron stores Gene SetFrom GAD Gene-Disease Associations genes associated with the disease genetic polymorphism of cytochrome p450 2a6 and the body status of iron stores in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes mellitus type ii; diabetes mellitus, type 2; diabetes, gestational; gestational diabetes mellitus ; iron overload Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; diabetes, gestational; gestational diabetes mellitus ; iron overload in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anemia; hemoglobinopathies; iron overload; thalassemia Gene SetFrom 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. |
activated protein c resistance; hemochromatosis; iron overload; thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; hemochromatosis; iron overload; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arthritis; diabetes complications; heart diseases; hemochromatosis; iron overload; liver diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arthritis; diabetes complications; heart diseases; hemochromatosis; iron overload; liver diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hepatitis c, chronic; iron overload; liver cirrhosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hepatitis c, chronic; iron overload; liver cirrhosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
iron overload; liver diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease iron overload; liver diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
iron Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term iron in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
ferrous iron import Gene SetFrom GO Biological Process Annotations 2015 genes participating in the ferrous iron import biological process from the curated GO Biological Process Annotations 2015 dataset. |
sequestering of iron ion Gene SetFrom GO Biological Process Annotations 2015 genes participating in the sequestering of iron ion biological process from the curated GO Biological Process Annotations 2015 dataset. |
ferrous iron transport Gene SetFrom GO Biological Process Annotations 2015 genes participating in the ferrous iron transport biological process from the curated GO Biological Process Annotations 2015 dataset. |
cellular response to iron ion starvation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cellular response to iron ion starvation biological process from the curated GO Biological Process Annotations 2015 dataset. |
iron ion import Gene SetFrom GO Biological Process Annotations 2015 genes participating in the iron ion import biological process from the curated GO Biological Process Annotations 2015 dataset. |
iron chelate transport Gene SetFrom GO Biological Process Annotations 2015 genes participating in the iron chelate transport biological process from the curated GO Biological Process Annotations 2015 dataset. |
iron incorporation into metallo-sulfur cluster Gene SetFrom GO Biological Process Annotations 2015 genes participating in the iron incorporation into metallo-sulfur cluster biological process from the curated GO Biological Process Annotations 2015 dataset. |
cellular iron ion homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cellular iron ion homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
mitochondrial iron ion transport Gene SetFrom GO Biological Process Annotations 2015 genes participating in the mitochondrial iron ion transport biological process from the curated GO Biological Process Annotations 2015 dataset. |
intracellular sequestering of iron ion Gene SetFrom GO Biological Process Annotations 2015 genes participating in the intracellular sequestering of iron ion biological process from the curated GO Biological Process Annotations 2015 dataset. |
iron ion import into cell Gene SetFrom GO Biological Process Annotations 2015 genes participating in the iron ion import into cell biological process from the curated GO Biological Process Annotations 2015 dataset. |
iron assimilation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the iron assimilation biological process from the curated GO Biological Process Annotations 2015 dataset. |
iron ion homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the iron ion homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of translational initiation by iron Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of translational initiation by iron biological process from the curated GO Biological Process Annotations 2015 dataset. |
ferric iron import into cell Gene SetFrom GO Biological Process Annotations 2015 genes participating in the ferric iron import into cell biological process from the curated GO Biological Process Annotations 2015 dataset. |
iron ion transmembrane transport Gene SetFrom GO Biological Process Annotations 2015 genes participating in the iron ion transmembrane transport biological process from the curated GO Biological Process Annotations 2015 dataset. |
ferric iron transport Gene SetFrom GO Biological Process Annotations 2015 genes participating in the ferric iron transport biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of translational initiation by iron Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of translational initiation by iron biological process from the curated GO Biological Process Annotations 2015 dataset. |
iron-sulfur cluster assembly Gene SetFrom GO Biological Process Annotations 2015 genes participating in the iron-sulfur cluster assembly biological process from the curated GO Biological Process Annotations 2015 dataset. |
response to iron(ii) ion Gene SetFrom GO Biological Process Annotations 2015 genes participating in the response to iron(ii) ion biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of transcription from rna polymerase ii promoter in response to iron Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of transcription from rna polymerase ii promoter in response to iron biological process from the curated GO Biological Process Annotations 2015 dataset. |
iron assimilation by chelation and transport Gene SetFrom GO Biological Process Annotations 2015 genes participating in the iron assimilation by chelation and transport biological process from the curated GO Biological Process Annotations 2015 dataset. |
multicellular organismal iron ion homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the multicellular organismal iron ion homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
response to iron ion Gene SetFrom GO Biological Process Annotations 2015 genes participating in the response to iron ion biological process from the curated GO Biological Process Annotations 2015 dataset. |
cellular response to iron ion Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cellular response to iron ion biological process from the curated GO Biological Process Annotations 2015 dataset. |
response to iron(iii) ion Gene SetFrom GO Biological Process Annotations 2015 genes participating in the response to iron(iii) ion biological process from the curated GO Biological Process Annotations 2015 dataset. |
cellular response to iron(iii) ion Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cellular response to iron(iii) ion biological process from the curated GO Biological Process Annotations 2015 dataset. |
ferric iron import Gene SetFrom GO Biological Process Annotations 2015 genes participating in the ferric iron import biological process from the curated GO Biological Process Annotations 2015 dataset. |
iron ion transport Gene SetFrom GO Biological Process Annotations 2015 genes participating in the iron ion transport biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of translational initiation by iron Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of translational initiation by iron biological process from the curated GO Biological Process Annotations 2015 dataset. |
iron coordination entity transport Gene SetFrom GO Biological Process Annotations 2015 genes participating in the iron coordination entity transport biological process from the curated GO Biological Process Annotations 2015 dataset. |
oxidoreductase activity, acting on iron-sulfur proteins as donors Gene SetFrom GO Molecular Function Annotations 2015 genes performing the oxidoreductase activity, acting on iron-sulfur proteins as donors molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
ferrous iron uptake transmembrane transporter activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the ferrous iron uptake transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced iron-sulfur protein as one donor, and incorporation of one atom of oxygen Gene SetFrom GO Molecular Function Annotations 2015 genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced iron-sulfur protein as one donor, and incorporation of one atom of oxygen molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
iron-cytochrome-c reductase activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the iron-cytochrome-c reductase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
3 iron, 4 sulfur cluster binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the 3 iron, 4 sulfur cluster binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
2 iron, 2 sulfur cluster binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the 2 iron, 2 sulfur cluster binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
4 iron, 4 sulfur cluster binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the 4 iron, 4 sulfur cluster binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
iron ion transmembrane transporter activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the iron ion transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
dinitrosyl-iron complex binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the dinitrosyl-iron complex binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
oxidoreductase activity, acting on iron-sulfur proteins as donors, nad or nadp as acceptor Gene SetFrom GO Molecular Function Annotations 2015 genes performing the oxidoreductase activity, acting on iron-sulfur proteins as donors, nad or nadp as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
acireductone dioxygenase [iron(ii)-requiring] activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the acireductone dioxygenase [iron(ii)-requiring] activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
iron ion binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the iron ion binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
iron-responsive element binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the iron-responsive element binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
iron-sulfur cluster binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the iron-sulfur cluster binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
ferrous iron transmembrane transporter activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the ferrous iron transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
ferric iron binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the ferric iron binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
iron chaperone activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the iron chaperone activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
ferrous iron binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the ferrous iron binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
Iron status biomarkers Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Iron status biomarkers phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Iron levels Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Iron levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Type 2 diabetes (dietary heme iron intake interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Type 2 diabetes (dietary heme iron intake interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
iron metabolism disease Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease iron metabolism disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
abnormal serum iron Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal serum iron phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of iron homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of iron homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
increased serum iron Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the increased serum iron phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of iron homeostasis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of iron homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
increased serum iron Gene SetFrom HPO Gene-Disease Associations genes associated with the increased serum iron phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal iron deposition in mitochondria Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal iron deposition in mitochondria phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal serum iron Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal serum iron phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Iron Metabolism Disorders Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Iron Metabolism Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Iron Overload Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Iron Overload phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
iron-sulfur cluster biosynthesis Gene SetFrom HumanCyc Pathways proteins participating in the iron-sulfur cluster biosynthesis pathway from the HumanCyc Pathways dataset. |
Adrenodoxin, iron-sulphur binding site Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Adrenodoxin, iron-sulphur binding site protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Rieske iron-sulphur protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Rieske iron-sulphur protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
NADH:ubiquinone oxidoreductase, iron-sulphur subunit 5 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the NADH:ubiquinone oxidoreductase, iron-sulphur subunit 5 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Tricarboxylate/iron carrier Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Tricarboxylate/iron carrier protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Alcohol dehydrogenase, iron-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Alcohol dehydrogenase, iron-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
NADH dehydrogenase [ubiquinone] (complex I), iron-sulphur protein 6, mitochondria Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the NADH dehydrogenase [ubiquinone] (complex I), iron-sulphur protein 6, mitochondria protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
4Fe-4S ferredoxin, iron-sulphur binding, conserved site Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the 4Fe-4S ferredoxin, iron-sulphur binding, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Rieske [2Fe-2S] iron-sulphur domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Rieske [2Fe-2S] iron-sulphur domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Aromatic amino acid hydroxylase, iron/copper binding site Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Aromatic amino acid hydroxylase, iron/copper binding site protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Manganese/iron superoxide dismutase Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Manganese/iron superoxide dismutase protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Iron sulphur-containing domain, CDGSH-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Iron sulphur-containing domain, CDGSH-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Iron regulatory protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Iron regulatory protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
2Fe-2S ferredoxin, iron-sulphur binding site Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the 2Fe-2S ferredoxin, iron-sulphur binding site protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
NADH-ubiquinone oxidoreductase 51 kDa subunit, iron-sulphur binding domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the NADH-ubiquinone oxidoreductase 51 kDa subunit, iron-sulphur binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Manganese/iron superoxide dismutase, binding site Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Manganese/iron superoxide dismutase, binding site protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
MoaA/nifB/pqqE, iron-sulphur binding, conserved site Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the MoaA/nifB/pqqE, iron-sulphur binding, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Iron/zinc purple acid phosphatase-like C-terminal domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Iron/zinc purple acid phosphatase-like C-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
NADH:ubiquinone oxidoreductase, subunit G, iron-sulphur binding Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the NADH:ubiquinone oxidoreductase, subunit G, iron-sulphur binding protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Endonuclease III, iron-sulphur binding site Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Endonuclease III, iron-sulphur binding site protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Transferrin family, iron binding site Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Transferrin family, iron binding site protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Oxoglutarate/iron-dependent dioxygenase Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Oxoglutarate/iron-dependent dioxygenase protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Rieske iron-sulphur protein, C-terminal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Rieske iron-sulphur protein, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ubiquinol-cytochrome c reductase, iron-sulphur subunit Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ubiquinol-cytochrome c reductase, iron-sulphur subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc/iron permease Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc/iron permease protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Iron hydrogenase, small subunit-like Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Iron hydrogenase, small subunit-like protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Succinate dehydrogenase/fumarate reductase iron-sulphur protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Succinate dehydrogenase/fumarate reductase iron-sulphur protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Manganese/iron superoxide dismutase, C-terminal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Manganese/iron superoxide dismutase, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Iron hydrogenase, large subunit, C-terminal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Iron hydrogenase, large subunit, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Probable cytosolic iron-sulfur protein assembly protein, CIAO1/Cia1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Probable cytosolic iron-sulfur protein assembly protein, CIAO1/Cia1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Iron regulatory protein 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Iron regulatory protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Iron sulphur domain-containing, mitoNEET, N-terminal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Iron sulphur domain-containing, mitoNEET, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Aconitate/iron regulatory protein 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Aconitate/iron regulatory protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Manganese/iron superoxide dismutase, N-terminal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Manganese/iron superoxide dismutase, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Oxoglutarate/iron-dependent oxygenase, C-terminal degradation domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Oxoglutarate/iron-dependent oxygenase, C-terminal degradation domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Lipoxygenase, iron binding site Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Lipoxygenase, iron binding site protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Endonuclease III-like, iron-sulphur cluster loop motif Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Endonuclease III-like, iron-sulphur cluster loop motif protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Iron sulphur-containing domain, CDGSH-type, subfamily Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Iron sulphur-containing domain, CDGSH-type, subfamily protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
NFU1 iron-sulfur cluster scaffold homologue Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the NFU1 iron-sulfur cluster scaffold homologue protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
4Fe-4S ferredoxin-type, iron-sulphur binding domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the 4Fe-4S ferredoxin-type, iron-sulphur binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Iron hydrogenase Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Iron hydrogenase protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
abnormal brain iron level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal brain iron level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating iron level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating iron level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal spleen iron level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal spleen iron level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal iron level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal iron level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased spleen iron level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased spleen iron level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal liver iron level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal liver iron level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased pancreas iron level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased pancreas iron level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased circulating iron level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating iron level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal heart iron level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal heart iron level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal intestinal iron level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal intestinal iron level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal iron homeostasis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal iron homeostasis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating iron level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating iron level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased spleen iron level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased spleen iron level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pancreas iron level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pancreas iron level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal kidney iron level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal kidney iron level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased liver iron level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased liver iron level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased liver iron level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased liver iron level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased kidney iron level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased kidney iron level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
neurodegeneration with brain iron accumulation 4 Gene SetFrom OMIM Gene-Disease Associations genes associated with the neurodegeneration with brain iron accumulation 4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
neurodegeneration with brain iron accumulation 6 Gene SetFrom OMIM Gene-Disease Associations genes associated with the neurodegeneration with brain iron accumulation 6 phenotype from the curated OMIM Gene-Disease Associations dataset. |
neurodegeneration with brain iron accumulation 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the neurodegeneration with brain iron accumulation 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
neurodegeneration with brain iron accumulation 3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the neurodegeneration with brain iron accumulation 3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
neurodegeneration with brain iron accumulation 2b Gene SetFrom OMIM Gene-Disease Associations genes associated with the neurodegeneration with brain iron accumulation 2b phenotype from the curated OMIM Gene-Disease Associations dataset. |
?anemia, hypochromic microcytic, with iron overload 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the ?anemia, hypochromic microcytic, with iron overload 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
neurodegeneration with brain iron accululation 5 Gene SetFrom OMIM Gene-Disease Associations genes associated with the neurodegeneration with brain iron accululation 5 phenotype from the curated OMIM Gene-Disease Associations dataset. |
Mtb iron assimilation by chelation Gene Setproteins participating in the Mtb iron assimilation by chelation pathway from the Reactome Pathways dataset. |
Iron uptake and transport Gene Setproteins participating in the Iron uptake and transport pathway from the Reactome Pathways dataset. |
Mitochondrial iron-sulfur cluster biogenesis Gene Setproteins participating in the Mitochondrial iron-sulfur cluster biogenesis pathway from the Reactome Pathways dataset. |
Cytosolic iron-sulfur cluster assembly Gene Setproteins participating in the Cytosolic iron-sulfur cluster assembly pathway from the Reactome Pathways dataset. |
Iron uptake and transport(Homo sapiens) Gene SetFrom WikiPathways Pathways 2014 proteins participating in the Iron uptake and transport(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset. |
Iron metabolism in placenta(Homo sapiens) Gene SetFrom WikiPathways Pathways 2014 proteins participating in the Iron metabolism in placenta(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset. |
Iron Homeostasis(Mus musculus) Gene SetFrom WikiPathways Pathways 2014 proteins participating in the Iron Homeostasis(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset. |
Iron Overload Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Iron Overload in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Chronic Iron Overload Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Chronic Iron Overload in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Iron Overload, Autosomal Dominant Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Iron Overload, Autosomal Dominant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cardiac Iron Overload Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cardiac Iron Overload in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Iron Loading Anemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Iron Loading Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Anemia, Hypochromic Microcytic, With Iron Overload 1 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Anemia, Hypochromic Microcytic, With Iron Overload 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Anemia, Hypochromic Microcytic, With Iron Overload 2 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Anemia, Hypochromic Microcytic, With Iron Overload 2 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Iron Level Result Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Iron Level Result in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Iron Measurement Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Iron Measurement in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of Iron Homeostasis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Iron Homeostasis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Elevated Hepatic Iron Concentration Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Elevated Hepatic Iron Concentration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Serum Iron Raised Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Serum Iron Raised in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Serum Iron Low (Finding) Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Serum Iron Low (Finding) in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Iron Binding Capacity Total Measurement Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Iron Binding Capacity Total Measurement in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Serum Iron Measurement Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Serum Iron Measurement in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Total Iron Binding Capacity Function Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Total Iron Binding Capacity Function in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Iron Accumulation Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Iron Accumulation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Genetic Hyperferritinemia Without Iron Overload Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Genetic Hyperferritinemia Without Iron Overload in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormal Iron Deposition In Mitochondria Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Iron Deposition In Mitochondria in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Increased Total Iron Binding Capacity Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Increased Total Iron Binding Capacity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
iron-sulfur cluster assembly Gene SetFrom GO Biological Process Annotations 2023 genes participating in the iron-sulfur cluster assembly biological process from the curated GO Biological Process Annotations 2023 dataset. |
intracellular iron ion homeostasis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the intracellular iron ion homeostasis biological process from the curated GO Biological Process Annotations 2023 dataset. |
iron ion transmembrane transport Gene SetFrom GO Biological Process Annotations 2023 genes participating in the iron ion transmembrane transport biological process from the curated GO Biological Process Annotations 2023 dataset. |
iron-sulfur cluster export from the mitochondrion Gene SetFrom GO Biological Process Annotations 2023 genes participating in the iron-sulfur cluster export from the mitochondrion biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of iron-sulfur cluster assembly Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of iron-sulfur cluster assembly biological process from the curated GO Biological Process Annotations 2023 dataset. |
protein maturation by iron-sulfur cluster transfer Gene SetFrom GO Biological Process Annotations 2023 genes participating in the protein maturation by iron-sulfur cluster transfer biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of iron ion import across plasma membrane Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of iron ion import across plasma membrane biological process from the curated GO Biological Process Annotations 2023 dataset. |
iron ion transport Gene SetFrom GO Biological Process Annotations 2023 genes participating in the iron ion transport biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of iron ion transport Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of iron ion transport biological process from the curated GO Biological Process Annotations 2023 dataset. |
cellular response to iron ion Gene SetFrom GO Biological Process Annotations 2023 genes participating in the cellular response to iron ion biological process from the curated GO Biological Process Annotations 2023 dataset. |
multicellular organismal-level iron ion homeostasis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the multicellular organismal-level iron ion homeostasis biological process from the curated GO Biological Process Annotations 2023 dataset. |
response to iron ion Gene SetFrom GO Biological Process Annotations 2023 genes participating in the response to iron ion biological process from the curated GO Biological Process Annotations 2023 dataset. |
response to iron(II) ion Gene SetFrom GO Biological Process Annotations 2023 genes participating in the response to iron(II) ion biological process from the curated GO Biological Process Annotations 2023 dataset. |
intracellular sequestering of iron ion Gene SetFrom GO Biological Process Annotations 2023 genes participating in the intracellular sequestering of iron ion biological process from the curated GO Biological Process Annotations 2023 dataset. |
iron import into cell Gene SetFrom GO Biological Process Annotations 2023 genes participating in the iron import into cell biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of ferrous iron binding Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of ferrous iron binding biological process from the curated GO Biological Process Annotations 2023 dataset. |
iron incorporation into metallo-sulfur cluster Gene SetFrom GO Biological Process Annotations 2023 genes participating in the iron incorporation into metallo-sulfur cluster biological process from the curated GO Biological Process Annotations 2023 dataset. |
reductive iron assimilation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the reductive iron assimilation biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of translational initiation by iron Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of translational initiation by iron biological process from the curated GO Biological Process Annotations 2023 dataset. |
response to iron ion starvation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the response to iron ion starvation biological process from the curated GO Biological Process Annotations 2023 dataset. |
iron ion import across plasma membrane Gene SetFrom GO Biological Process Annotations 2023 genes participating in the iron ion import across plasma membrane biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of iron ion import across plasma membrane Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of iron ion import across plasma membrane biological process from the curated GO Biological Process Annotations 2023 dataset. |
iron ion export across plasma membrane Gene SetFrom GO Biological Process Annotations 2023 genes participating in the iron ion export across plasma membrane biological process from the curated GO Biological Process Annotations 2023 dataset. |
iron import into the mitochondrion Gene SetFrom GO Biological Process Annotations 2023 genes participating in the iron import into the mitochondrion biological process from the curated GO Biological Process Annotations 2023 dataset. |
endocytic iron import into cell Gene SetFrom GO Biological Process Annotations 2023 genes participating in the endocytic iron import into cell biological process from the curated GO Biological Process Annotations 2023 dataset. |
iron-sulfur cluster transmembrane transport Gene SetFrom GO Biological Process Annotations 2023 genes participating in the iron-sulfur cluster transmembrane transport biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of iron-sulfur cluster assembly Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of iron-sulfur cluster assembly biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of iron ion transmembrane transport Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of iron ion transmembrane transport biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of iron ion import across plasma membrane Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of iron ion import across plasma membrane biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of ferrous iron binding Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of ferrous iron binding biological process from the curated GO Biological Process Annotations 2023 dataset. |
iron coordination entity transport Gene SetFrom GO Biological Process Annotations 2023 genes participating in the iron coordination entity transport biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of translational initiation by iron Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of translational initiation by iron biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of iron ion transmembrane transport Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of iron ion transmembrane transport biological process from the curated GO Biological Process Annotations 2023 dataset. |
iron ion binding Gene SetFrom GO Molecular Function Annotations 2023 genes performing the iron ion binding molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
ferrous iron binding Gene SetFrom GO Molecular Function Annotations 2023 genes performing the ferrous iron binding molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
ABC-type iron-sulfur cluster transporter activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the ABC-type iron-sulfur cluster transporter activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
2 iron, 2 sulfur cluster binding Gene SetFrom GO Molecular Function Annotations 2023 genes performing the 2 iron, 2 sulfur cluster binding molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
iron-responsive element binding Gene SetFrom GO Molecular Function Annotations 2023 genes performing the iron-responsive element binding molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
3 iron, 4 sulfur cluster binding Gene SetFrom GO Molecular Function Annotations 2023 genes performing the 3 iron, 4 sulfur cluster binding molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
4 iron, 4 sulfur cluster binding Gene SetFrom GO Molecular Function Annotations 2023 genes performing the 4 iron, 4 sulfur cluster binding molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
iron ion transmembrane transporter activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the iron ion transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
ferrous iron transmembrane transporter activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the ferrous iron transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
oxidoreductase activity, acting on iron-sulfur proteins as donors, NAD or NADP as acceptor Gene SetFrom GO Molecular Function Annotations 2023 genes performing the oxidoreductase activity, acting on iron-sulfur proteins as donors, NAD or NADP as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
acireductone dioxygenase [iron(II)-requiring] activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the acireductone dioxygenase [iron(II)-requiring] activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced iron-sulfur protein as one donor, and incorporation of one atom of oxygen Gene SetFrom GO Molecular Function Annotations 2023 genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced iron-sulfur protein as one donor, and incorporation of one atom of oxygen molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
abnormal iron level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal iron level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal iron homeostasis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal iron homeostasis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased liver iron level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased liver iron level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased spleen iron level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased spleen iron level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating iron level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating iron level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased liver iron level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased liver iron level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased kidney iron level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased kidney iron level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased spleen iron level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased spleen iron level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating iron level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating iron level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased intestinal iron level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased intestinal iron level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal brain iron level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal brain iron level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating iron level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating iron level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased brain iron level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased brain iron level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased pancreas iron level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased pancreas iron level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased heart iron level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased heart iron level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal liver iron level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal liver iron level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal kidney iron level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal kidney iron level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased pancreas iron level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased pancreas iron level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased heart iron level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased heart iron level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased intestinal iron level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased intestinal iron level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased brain iron level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased brain iron level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating iron level Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the decreased circulating iron level phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
increased circulating iron level Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the increased circulating iron level phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
abnormal circulating iron level Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the abnormal circulating iron level phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
Iron metabolism in placenta Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Iron metabolism in placenta pathway from the WikiPathways Pathways 2024 dataset. |
Neurodegeneration with brain iron accumulation NBIA subtypes pathway Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Neurodegeneration with brain iron accumulation NBIA subtypes pathway pathway from the WikiPathways Pathways 2024 dataset. |
Iron sulfur cluster biogenesis Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Iron sulfur cluster biogenesis pathway from the WikiPathways Pathways 2024 dataset. |
Iron metabolism disorders Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Iron metabolism disorders pathway from the WikiPathways Pathways 2024 dataset. |
Cytosolic iron-sulfur cluster assembly Gene Setproteins participating in the Cytosolic iron-sulfur cluster assembly pathway from the Reactome Pathways 2024 dataset. |
Defective SLC11A2 causes hypochromic microcytic anemia, with iron overload 1 (AHMIO1) Gene Setproteins participating in the Defective SLC11A2 causes hypochromic microcytic anemia, with iron overload 1 (AHMIO1) pathway from the Reactome Pathways 2024 dataset. |
Iron uptake and transport Gene Setproteins participating in the Iron uptake and transport pathway from the Reactome Pathways 2024 dataset. |
Mitochondrial iron-sulfur cluster biogenesis Gene Setproteins participating in the Mitochondrial iron-sulfur cluster biogenesis pathway from the Reactome Pathways 2024 dataset. |
Mtb iron assimilation by chelation Gene Setproteins participating in the Mtb iron assimilation by chelation pathway from the Reactome Pathways 2024 dataset. |
iron-sulfur cluster assembly Gene SetFrom GO Biological Process Annotations 2025 genes participating in the iron-sulfur cluster assembly biological process from the curated GO Biological Process Annotations 2025 dataset. |
intracellular iron ion homeostasis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the intracellular iron ion homeostasis biological process from the curated GO Biological Process Annotations 2025 dataset. |
iron ion transmembrane transport Gene SetFrom GO Biological Process Annotations 2025 genes participating in the iron ion transmembrane transport biological process from the curated GO Biological Process Annotations 2025 dataset. |
iron-sulfur cluster export from the mitochondrion Gene SetFrom GO Biological Process Annotations 2025 genes participating in the iron-sulfur cluster export from the mitochondrion biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of iron-sulfur cluster assembly Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of iron-sulfur cluster assembly biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of iron ion import across plasma membrane Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of iron ion import across plasma membrane biological process from the curated GO Biological Process Annotations 2025 dataset. |
iron ion transport Gene SetFrom GO Biological Process Annotations 2025 genes participating in the iron ion transport biological process from the curated GO Biological Process Annotations 2025 dataset. |
multicellular organismal-level iron ion homeostasis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the multicellular organismal-level iron ion homeostasis biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of iron ion transport Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of iron ion transport biological process from the curated GO Biological Process Annotations 2025 dataset. |
cellular response to iron ion Gene SetFrom GO Biological Process Annotations 2025 genes participating in the cellular response to iron ion biological process from the curated GO Biological Process Annotations 2025 dataset. |
response to iron ion Gene SetFrom GO Biological Process Annotations 2025 genes participating in the response to iron ion biological process from the curated GO Biological Process Annotations 2025 dataset. |
response to iron(II) ion Gene SetFrom GO Biological Process Annotations 2025 genes participating in the response to iron(II) ion biological process from the curated GO Biological Process Annotations 2025 dataset. |
iron import into cell Gene SetFrom GO Biological Process Annotations 2025 genes participating in the iron import into cell biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of ferrous iron binding Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of ferrous iron binding biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of iron export across plasma membrane Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of iron export across plasma membrane biological process from the curated GO Biological Process Annotations 2025 dataset. |
response to iron ion starvation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the response to iron ion starvation biological process from the curated GO Biological Process Annotations 2025 dataset. |
iron incorporation into metallo-sulfur cluster Gene SetFrom GO Biological Process Annotations 2025 genes participating in the iron incorporation into metallo-sulfur cluster biological process from the curated GO Biological Process Annotations 2025 dataset. |
reductive iron assimilation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the reductive iron assimilation biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of translational initiation by iron Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of translational initiation by iron biological process from the curated GO Biological Process Annotations 2025 dataset. |
intestinal iron absorption Gene SetFrom GO Biological Process Annotations 2025 genes participating in the intestinal iron absorption biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of iron export across plasma membrane Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of iron export across plasma membrane biological process from the curated GO Biological Process Annotations 2025 dataset. |
iron ion import across plasma membrane Gene SetFrom GO Biological Process Annotations 2025 genes participating in the iron ion import across plasma membrane biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of iron ion import across plasma membrane Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of iron ion import across plasma membrane biological process from the curated GO Biological Process Annotations 2025 dataset. |
iron ion export across plasma membrane Gene SetFrom GO Biological Process Annotations 2025 genes participating in the iron ion export across plasma membrane biological process from the curated GO Biological Process Annotations 2025 dataset. |
iron import into the mitochondrion Gene SetFrom GO Biological Process Annotations 2025 genes participating in the iron import into the mitochondrion biological process from the curated GO Biological Process Annotations 2025 dataset. |
endocytic iron import into cell Gene SetFrom GO Biological Process Annotations 2025 genes participating in the endocytic iron import into cell biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of iron ion transmembrane transport Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of iron ion transmembrane transport biological process from the curated GO Biological Process Annotations 2025 dataset. |
iron-sulfur cluster transmembrane transport Gene SetFrom GO Biological Process Annotations 2025 genes participating in the iron-sulfur cluster transmembrane transport biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of iron-sulfur cluster assembly Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of iron-sulfur cluster assembly biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of iron ion transmembrane transport Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of iron ion transmembrane transport biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of iron ion import across plasma membrane Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of iron ion import across plasma membrane biological process from the curated GO Biological Process Annotations 2025 dataset. |
iron coordination entity transport Gene SetFrom GO Biological Process Annotations 2025 genes participating in the iron coordination entity transport biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of iron export across plasma membrane Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of iron export across plasma membrane biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of translational initiation by iron Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of translational initiation by iron biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of iron ion transport Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of iron ion transport biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of iron ion transmembrane transport Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of iron ion transmembrane transport biological process from the curated GO Biological Process Annotations 2025 dataset. |
iron ion binding Gene SetFrom GO Molecular Function Annotations 2025 genes performing the iron ion binding molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
ferrous iron binding Gene SetFrom GO Molecular Function Annotations 2025 genes performing the ferrous iron binding molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
ABC-type iron-sulfur cluster transporter activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the ABC-type iron-sulfur cluster transporter activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
dinitrosyl-iron complex binding Gene SetFrom GO Molecular Function Annotations 2025 genes performing the dinitrosyl-iron complex binding molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
2 iron, 2 sulfur cluster binding Gene SetFrom GO Molecular Function Annotations 2025 genes performing the 2 iron, 2 sulfur cluster binding molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
ferric iron binding Gene SetFrom GO Molecular Function Annotations 2025 genes performing the ferric iron binding molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
iron-responsive element binding Gene SetFrom GO Molecular Function Annotations 2025 genes performing the iron-responsive element binding molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
iron-sulfur cluster binding Gene SetFrom GO Molecular Function Annotations 2025 genes performing the iron-sulfur cluster binding molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
3 iron, 4 sulfur cluster binding Gene SetFrom GO Molecular Function Annotations 2025 genes performing the 3 iron, 4 sulfur cluster binding molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
4 iron, 4 sulfur cluster binding Gene SetFrom GO Molecular Function Annotations 2025 genes performing the 4 iron, 4 sulfur cluster binding molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
iron ion transmembrane transporter activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the iron ion transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
ferrous iron transmembrane transporter activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the ferrous iron transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
iron ion transmembrane transporter inhibitor activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the iron ion transmembrane transporter inhibitor activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
oxidoreductase activity, acting on iron-sulfur proteins as donors, NAD or NADP as acceptor Gene SetFrom GO Molecular Function Annotations 2025 genes performing the oxidoreductase activity, acting on iron-sulfur proteins as donors, NAD or NADP as acceptor molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
acireductone dioxygenase [iron(II)-requiring] activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the acireductone dioxygenase [iron(II)-requiring] activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced iron-sulfur protein as one donor, and incorporation of one atom of oxygen Gene SetFrom GO Molecular Function Annotations 2025 genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced iron-sulfur protein as one donor, and incorporation of one atom of oxygen molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
Neurodegeneration with brain iron accumulation 4 Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Neurodegeneration with brain iron accumulation 4 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Neurodegeneration with brain iron accumulation Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Neurodegeneration with brain iron accumulation from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Neurodegeneration with brain iron accumulation 2b Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Neurodegeneration with brain iron accumulation 2b from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Neurodegeneration with brain iron accumulation 5 Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Neurodegeneration with brain iron accumulation 5 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
African iron overload Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease African iron overload from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Neurodegeneration with brain iron accumulation 3 Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Neurodegeneration with brain iron accumulation 3 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Iron metabolism disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Iron metabolism disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Iron metabolism disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Iron metabolism disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Neurodegeneration with brain iron accumulation 4 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neurodegeneration with brain iron accumulation 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Neurodegeneration with brain iron accumulation 5 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neurodegeneration with brain iron accumulation 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Neurodegeneration with brain iron accumulation Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neurodegeneration with brain iron accumulation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Neurodegeneration with brain iron accumulation 2a Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neurodegeneration with brain iron accumulation 2a in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Neurodegeneration with brain iron accumulation 3 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neurodegeneration with brain iron accumulation 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Neurodegeneration with brain iron accumulation 2b Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neurodegeneration with brain iron accumulation 2b in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
African iron overload Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease African iron overload in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Neurodegeneration with brain iron accumulation 6 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neurodegeneration with brain iron accumulation 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Mitochondrial iron-sulfur cluster assembly complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Mitochondrial iron-sulfur cluster assembly complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
iron-sulfur cluster assembly complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the iron-sulfur cluster assembly complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
iron-sulfur cluster assembly complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the iron-sulfur cluster assembly complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
iron-sulfur cluster transfer complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the iron-sulfur cluster transfer complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Mitochondrial iron-sulfur cluster assembly complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Mitochondrial iron-sulfur cluster assembly complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
vanadium-iron nitrogenase complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the vanadium-iron nitrogenase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
high-affinity iron permease complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the high-affinity iron permease complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Iron accumulation in brain Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Iron accumulation in brain phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Iron Overload Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Iron Overload phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Neurotransmitter Regulation and Iron Homeostasis Gene SetFrom CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Neurotransmitter Regulation and Iron Homeostasis assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset. |
Iron status biomarkers (transferrin saturation) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Iron status biomarkers (transferrin saturation) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Iron status biomarkers (ferritin levels) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Iron status biomarkers (ferritin levels) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Iron status biomarkers Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Iron status biomarkers phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Iron status biomarkers (transferrin levels) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Iron status biomarkers (transferrin levels) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Iron levels Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Iron levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Type 2 diabetes (dietary heme iron intake interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Type 2 diabetes (dietary heme iron intake interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Liver iron content Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Liver iron content phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Trifunctional protein deficiency with myopathy and neuropathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Trifunctional protein deficiency with myopathy and neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Bifunctional peroxisomal enzyme deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Bifunctional peroxisomal enzyme deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
X-linked ichthyosis with steryl-sulfatase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the X-linked ichthyosis with steryl-sulfatase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Phosphoglycerate dehydrogenase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Phosphoglycerate dehydrogenase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Galactosylceramide beta-galactosidase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Galactosylceramide beta-galactosidase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Isolated 17,20-lyase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Isolated 17,20-lyase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Endplate acetylcholinesterase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Endplate acetylcholinesterase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Sepiapterin reductase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Sepiapterin reductase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Methionine adenosyltransferase deficiency, autosomal recessive Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Methionine adenosyltransferase deficiency, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pyruvate dehydrogenase E2 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pyruvate dehydrogenase E2 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Carbonic anhydrase va deficiency, hyperammonemia due to Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Carbonic anhydrase va deficiency, hyperammonemia due to phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LATE-ONSET Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LATE-ONSET phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Coenzyme Q10 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Coenzyme Q10 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Deficiency of ribose-5-phosphate isomerase Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Deficiency of ribose-5-phosphate isomerase phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Kininogen deficiency, total Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Kininogen deficiency, total phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
6-pyruvoyl-tetrahydropterin synthase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the 6-pyruvoyl-tetrahydropterin synthase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Combined oxidative phosphorylation deficiency 9 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Combined oxidative phosphorylation deficiency 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Combined oxidative phosphorylation deficiency 8 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Combined oxidative phosphorylation deficiency 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
N-terminal acetyltransferase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the N-terminal acetyltransferase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Combined oxidative phosphorylation deficiency 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Combined oxidative phosphorylation deficiency 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Combined oxidative phosphorylation deficiency 7 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Combined oxidative phosphorylation deficiency 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Combined oxidative phosphorylation deficiency 6 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Combined oxidative phosphorylation deficiency 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Combined oxidative phosphorylation deficiency 5 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Combined oxidative phosphorylation deficiency 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Complement component 7 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Complement component 7 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Creatine deficiency, X-linked Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Creatine deficiency, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Birbeck granule deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Birbeck granule deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glucocorticoid deficiency 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glucocorticoid deficiency 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glucocorticoid deficiency 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glucocorticoid deficiency 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
SCID due to ADA deficiency, delayed onset Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the SCID due to ADA deficiency, delayed onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Properdin deficiency, X-linked Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Properdin deficiency, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
PROPERDIN DEFICIENCY, TYPE II Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the PROPERDIN DEFICIENCY, TYPE II phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Complement factor d deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Complement factor d deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Thrombophilia due to protein S deficiency, autosomal recessive Gene SetFrom 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. |
Hypermethioninemia with s-adenosylhomocysteine hydrolase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypermethioninemia with s-adenosylhomocysteine hydrolase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Methylmalonyl-CoA epimerase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Methylmalonyl-CoA epimerase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Complement component 8 deficiency type 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Complement component 8 deficiency type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Testosterone 17-beta-dehydrogenase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Testosterone 17-beta-dehydrogenase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Acyl-CoA dehydrogenase family, member 9, deficiency of Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Acyl-CoA dehydrogenase family, member 9, deficiency of phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Deficiency of 2-methylbutyryl-CoA dehydrogenase Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Deficiency of 2-methylbutyryl-CoA dehydrogenase phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Deficiency of isobutyryl-CoA dehydrogenase Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Deficiency of isobutyryl-CoA dehydrogenase phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glutathione synthetase deficiency of erythrocytes, hemolytic anemia due to Gene SetFrom 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. |
Autoinflammation, antibody deficiency, and immune dysregulation, plcg2-associated Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Autoinflammation, antibody deficiency, and immune dysregulation, plcg2-associated phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cerebral folate deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cerebral folate deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Phosphoserine aminotransferase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Phosphoserine aminotransferase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Severe combined immunodeficiency due to ADA deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Severe combined immunodeficiency due to ADA deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Carnitine acylcarnitine translocase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Carnitine acylcarnitine translocase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Partial hypoxanthine-guanine phosphoribosyltransferase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Partial hypoxanthine-guanine phosphoribosyltransferase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Succinyl-CoA acetoacetate transferase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Succinyl-CoA acetoacetate transferase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Carnitine palmitoyltransferase I deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Carnitine palmitoyltransferase I deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mitochondrial complex I deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mitochondrial complex I deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Gamma-glutamylcysteine synthetase deficiency, hemolytic anemia due to Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Gamma-glutamylcysteine synthetase deficiency, hemolytic anemia due to phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
HNSHA due to aldolase A deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the HNSHA due to aldolase A deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Platelet-activating factor acetylhydrolase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Platelet-activating factor acetylhydrolase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary C1 esterase inhibitor deficiency - dysfunctional factor Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary C1 esterase inhibitor deficiency - dysfunctional factor phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Lipase deficiency combined Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Lipase deficiency combined phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
5-Oxoprolinase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the 5-Oxoprolinase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glucocorticoid deficiency with achalasia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glucocorticoid deficiency with achalasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Proopiomelanocortin deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Proopiomelanocortin deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pituitary hormone deficiency, combined Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pituitary hormone deficiency, combined phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Intrinsic factor deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Intrinsic factor deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
21-hydroxylase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the 21-hydroxylase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glutaryl-CoA oxidase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glutaryl-CoA oxidase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Nuclearly-encoded mitochondrial complex V (ATP synthase) deficiency 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Nuclearly-encoded mitochondrial complex V (ATP synthase) deficiency 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Nuclearly-encoded mitochondrial complex V (ATP synthase) deficiency 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Nuclearly-encoded mitochondrial complex V (ATP synthase) deficiency 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Corticosterone methyloxidase type 1 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Corticosterone methyloxidase type 1 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Thiopurine methyltransferase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Thiopurine methyltransferase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
METHYLCOBALAMIN DEFICIENCY, cblG TYPE Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the METHYLCOBALAMIN DEFICIENCY, cblG TYPE phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Carnitine palmitoyltransferase II deficiency, infantile Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Carnitine palmitoyltransferase II deficiency, infantile phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Lactate dehydrogenase b deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Lactate dehydrogenase b deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Combined oxidative phosphorylation deficiency 18 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Combined oxidative phosphorylation deficiency 18 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Combined oxidative phosphorylation deficiency 17 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Combined oxidative phosphorylation deficiency 17 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Combined oxidative phosphorylation deficiency 16 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Combined oxidative phosphorylation deficiency 16 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Combined oxidative phosphorylation deficiency 14 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Combined oxidative phosphorylation deficiency 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Combined oxidative phosphorylation deficiency 13 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Combined oxidative phosphorylation deficiency 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Combined oxidative phosphorylation deficiency 12 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Combined oxidative phosphorylation deficiency 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Combined oxidative phosphorylation deficiency 11 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Combined oxidative phosphorylation deficiency 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Combined oxidative phosphorylation deficiency 10 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Combined oxidative phosphorylation deficiency 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Deficiency of 3-hydroxyacyl-CoA dehydrogenase Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Deficiency of 3-hydroxyacyl-CoA dehydrogenase phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Plasminogen deficiency, type I Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Plasminogen deficiency, type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Molybdenum cofactor deficiency, complementation group C Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Molybdenum cofactor deficiency, complementation group C phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Molybdenum cofactor deficiency, complementation group B Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Molybdenum cofactor deficiency, complementation group B phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Molybdenum cofactor deficiency, complementation group A Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Molybdenum cofactor deficiency, complementation group A phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Biotinidase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Biotinidase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Autosomal dominant isolated somatotropin deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Autosomal dominant isolated somatotropin deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hypohidrotic ectodermal dysplasia with immune deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypohidrotic ectodermal dysplasia with immune deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Deficiency of phosphoserine phosphatase Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Deficiency of phosphoserine phosphatase phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Isolated growth hormone deficiency type 1B Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Isolated growth hormone deficiency type 1B phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Deficiency of butyryl-CoA dehydrogenase Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Deficiency of butyryl-CoA dehydrogenase phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Anhidrotic ectodermal dysplasia with immune deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Anhidrotic ectodermal dysplasia with immune deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Complete combined 17-alpha-hydroxylase/17,20-lyase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Complete combined 17-alpha-hydroxylase/17,20-lyase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
3 Methylcrotonyl-CoA carboxylase 1 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the 3 Methylcrotonyl-CoA carboxylase 1 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Deficiency of hyaluronoglucosaminidase Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Deficiency of hyaluronoglucosaminidase phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Sulfite oxidase deficiency, isolated Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Sulfite oxidase deficiency, isolated phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Plasminogen activator inhibitor type 1 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Plasminogen activator inhibitor type 1 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pyruvate dehydrogenase phosphatase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pyruvate dehydrogenase phosphatase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Combined oxidative phosphorylation deficiency 22 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Combined oxidative phosphorylation deficiency 22 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Combined oxidative phosphorylation deficiency 20 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Combined oxidative phosphorylation deficiency 20 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Combined oxidative phosphorylation deficiency 21 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Combined oxidative phosphorylation deficiency 21 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Monoamine oxidase A deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Monoamine oxidase A deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Factor V deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Factor V deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Thrombophilia, hereditary, due to protein C deficiency, autosomal dominant Gene SetFrom 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. |
Adenine phosphoribosyltransferase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Adenine phosphoribosyltransferase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ehlers-Danlos-like syndrome due to tenascin-X deficiency Gene SetFrom 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. |
Glutamate formiminotransferase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glutamate formiminotransferase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hypoglycemia with deficiency of glycogen synthetase in the liver Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypoglycemia with deficiency of glycogen synthetase in the liver phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
LEUKOCYTE ADHESION DEFICIENCY, TYPE III Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the LEUKOCYTE ADHESION DEFICIENCY, TYPE III phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Follicle-stimulating hormone deficiency, isolated Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Follicle-stimulating hormone deficiency, isolated phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ganglioside sialidase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ganglioside sialidase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
C1q deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the C1q deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Interferon gamma receptor deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Interferon gamma receptor deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Platelet glycoprotein IV deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Platelet glycoprotein IV deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
N-acetylaspartate deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the N-acetylaspartate deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Adenylosuccinate lyase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Adenylosuccinate lyase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Triosephosphate isomerase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Triosephosphate isomerase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Gaucher disease, atypical, due to saposin C deficiency Gene SetFrom 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 SetFrom 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. |
Aromatase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Aromatase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary factor II deficiency disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary factor II deficiency disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mitochondrial complex III deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mitochondrial complex III deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Factor xiii, a subunit, deficiency of Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Factor xiii, a subunit, deficiency of phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mitochondrial complex III deficiency, nuclear type 5 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mitochondrial complex III deficiency, nuclear type 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mitochondrial complex III deficiency, nuclear type 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mitochondrial complex III deficiency, nuclear type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
3-methylcrotonyl CoA carboxylase 2 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the 3-methylcrotonyl CoA carboxylase 2 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hemolytic anemia due to hexokinase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hemolytic anemia due to hexokinase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Leigh syndrome due to mitochondrial complex I deficiency Gene SetFrom 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. |
Multiple sulfatase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Multiple sulfatase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Corticosteroid-binding globulin deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Corticosteroid-binding globulin deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Combined oxidative phosphorylation deficiency 15 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Combined oxidative phosphorylation deficiency 15 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Corticosterone methyloxidase type 2 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Corticosterone methyloxidase type 2 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Complement component 9 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Complement component 9 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Holocarboxylase synthetase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Holocarboxylase synthetase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
2,4-Dienoyl-CoA reductase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the 2,4-Dienoyl-CoA reductase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
LIPOPROTEIN(a) DEFICIENCY, CONGENITAL Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the LIPOPROTEIN(a) DEFICIENCY, CONGENITAL phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Deficiency of glycerate kinase Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Deficiency of glycerate kinase phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ataxia with vitamin E deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ataxia with vitamin E deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 7 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 6 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 8 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Deficiency of galactokinase Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Deficiency of galactokinase phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
ACTH deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the ACTH deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
PROPERDIN DEFICIENCY, TYPE III Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the PROPERDIN DEFICIENCY, TYPE III phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Carboxylesterase 1 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Carboxylesterase 1 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Purine-nucleoside phosphorylase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Purine-nucleoside phosphorylase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Neonatal intrahepatic cholestasis caused by citrin deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Neonatal intrahepatic cholestasis caused by citrin deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Complement component 6 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Complement component 6 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Antithrombin III deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Antithrombin III deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Inosine triphosphatase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Inosine triphosphatase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Growth hormone deficiency with pituitary anomalies Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Growth hormone deficiency with pituitary anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pyruvate dehydrogenase lipoic acid synthetase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pyruvate dehydrogenase lipoic acid synthetase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ulna and fibula absence of with severe limb deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ulna and fibula absence of with severe limb deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Dendritic cell, monocyte, B lymphocyte, and natural killer lymphocyte deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Dendritic cell, monocyte, B lymphocyte, and natural killer lymphocyte deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Homocysteinemia due to MTHFR deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Homocysteinemia due to MTHFR deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Deficiency of pyrroline-5-carboxylate reductase Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Deficiency of pyrroline-5-carboxylate reductase phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Immunodeficiency due to ficolin 3 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Immunodeficiency due to ficolin 3 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Sarcosine dehydrogenase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Sarcosine dehydrogenase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Factor v and factor viii, combined deficiency of, 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Factor v and factor viii, combined deficiency of, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Branched-chain ketoacid dehydrogenase kinase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Branched-chain ketoacid dehydrogenase kinase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
L-ferritin deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the L-ferritin deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Medium-chain acyl-coenzyme A dehydrogenase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Medium-chain acyl-coenzyme A dehydrogenase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Arginase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Arginase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hepatic lipase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hepatic lipase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Factor X deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Factor X deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hypercarotenemia and vitamin a deficiency, autosomal dominant Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypercarotenemia and vitamin a deficiency, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pyruvate dehydrogenase E3-binding protein deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pyruvate dehydrogenase E3-binding protein deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary factor IX deficiency disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary factor IX deficiency disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Alpha-fetoprotein deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Alpha-fetoprotein deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hypermethioninemia due to adenosine kinase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypermethioninemia due to adenosine kinase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Vitamin k-dependent clotting factors, combined deficiency of, 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Vitamin k-dependent clotting factors, combined deficiency of, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Deficiency of iodide peroxidase Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Deficiency of iodide peroxidase phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glycosylphosphatidylinositol deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glycosylphosphatidylinositol deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Vitamin k-dependent clotting factors, combined deficiency of, 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Vitamin k-dependent clotting factors, combined deficiency of, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Leukocyte adhesion deficiency type 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Leukocyte adhesion deficiency type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital lactase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital lactase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Caspase-8 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Caspase-8 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Uridine 5-prime monophosphate hydrolase deficiency, hemolytic anemia due to Gene SetFrom 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. |
Phosphoglycerate kinase 1 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Phosphoglycerate kinase 1 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Anaphylotoxin inactivator deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Anaphylotoxin inactivator deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
3-Oxo-5 alpha-steroid delta 4-dehydrogenase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the 3-Oxo-5 alpha-steroid delta 4-dehydrogenase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cytochrome-c oxidase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cytochrome-c oxidase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Enterokinase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Enterokinase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Coenzyme Q10 deficiency, primary, 6 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Coenzyme Q10 deficiency, primary, 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Coenzyme Q10 deficiency, primary, 5 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Coenzyme Q10 deficiency, primary, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Coenzyme Q10 deficiency, primary, 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Coenzyme Q10 deficiency, primary, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Coenzyme Q10 deficiency, primary, 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Coenzyme Q10 deficiency, primary, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Erythrocyte amp deaminase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Erythrocyte amp deaminase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Factor VII deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Factor VII deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Autosomal dominant CD11C+/CD1C+ dendritic cell deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Autosomal dominant CD11C+/CD1C+ dendritic cell deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Apolipoprotein a-i deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Apolipoprotein a-i deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glut1 deficiency syndrome 1, autosomal recessive Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glut1 deficiency syndrome 1, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Gamma-aminobutyric acid transaminase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Gamma-aminobutyric acid transaminase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myeloperoxidase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myeloperoxidase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mitochondrial phosphate carrier deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mitochondrial phosphate carrier deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary factor XI deficiency disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary factor XI deficiency disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Porphobilinogen synthase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Porphobilinogen synthase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Very long chain acyl-CoA dehydrogenase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Very long chain acyl-CoA dehydrogenase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
IRAK4 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the IRAK4 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Leukocyte adhesion deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Leukocyte adhesion deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Muscular dystrophy, congenital, due to ITGA7 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Muscular dystrophy, congenital, due to ITGA7 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cortisone reductase deficiency 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cortisone reductase deficiency 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Arginine:glycine amidinotransferase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Arginine:glycine amidinotransferase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pyruvate kinase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pyruvate kinase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Methionine adenosyltransferase deficiency, autosomal dominant Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Methionine adenosyltransferase deficiency, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Muscle AMP deaminase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Muscle AMP deaminase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Dihydropyrimidinase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Dihydropyrimidinase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Dimethylglycine dehydrogenase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Dimethylglycine dehydrogenase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Deficiency of hydroxymethylglutaryl-CoA lyase Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Deficiency of hydroxymethylglutaryl-CoA lyase phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Monocyte and dendritic cell deficiency, autosomal recessive Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Monocyte and dendritic cell deficiency, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pyruvate dehydrogenase E1-alpha deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pyruvate dehydrogenase E1-alpha deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Isovaleryl-CoA dehydrogenase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Isovaleryl-CoA dehydrogenase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cd59 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cd59 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ornithine aminotransferase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ornithine aminotransferase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Sphingolipid activator protein 1 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Sphingolipid activator protein 1 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Deficiency of ferroxidase Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Deficiency of ferroxidase phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Combined partial 17-alpha-hydroxylase/17,20-lyase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Combined partial 17-alpha-hydroxylase/17,20-lyase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Deficiency of steroid 11-beta-monooxygenase Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Deficiency of steroid 11-beta-monooxygenase phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Lysosomal acid lipase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Lysosomal acid lipase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Dopamine beta hydroxylase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Dopamine beta hydroxylase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Butyrylcholinesterase deficiency, fluoride-resistant, japanese type Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Butyrylcholinesterase deficiency, fluoride-resistant, japanese type phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
UDPglucose-4-epimerase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the UDPglucose-4-epimerase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Homocystinuria due to MTHFR deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Homocystinuria due to MTHFR deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Deficiency of alpha-mannosidase Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Deficiency of alpha-mannosidase phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency Gene SetFrom 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. |
Insulin-like growth factor I deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Insulin-like growth factor I deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Leigh syndrome due to mitochondrial complex II deficiency Gene SetFrom 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. |
Pituitary hormone deficiency, combined 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pituitary hormone deficiency, combined 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pituitary hormone deficiency, combined 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pituitary hormone deficiency, combined 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pituitary hormone deficiency, combined 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pituitary hormone deficiency, combined 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pituitary hormone deficiency, combined 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pituitary hormone deficiency, combined 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Complement component 4, partial deficiency of, due to dysfunctional c1 inhibitor Gene SetFrom 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. |
Pyruvate carboxylase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pyruvate carboxylase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Gluthathione synthetase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Gluthathione synthetase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Fumarase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Fumarase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Deficiency of transaldolase Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Deficiency of transaldolase phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mitochondrial pyruvate carrier deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mitochondrial pyruvate carrier deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pyruvate dehydrogenase E1-beta deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pyruvate dehydrogenase E1-beta deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
MASP2 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the MASP2 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Argininosuccinate lyase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Argininosuccinate lyase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Prekallikrein deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Prekallikrein deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Chitotriosidase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Chitotriosidase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the 4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Anti-plasmin deficiency, congenital Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Anti-plasmin deficiency, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Prothrombin deficiency, congenital Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Prothrombin deficiency, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mitochondrial trifunctional protein deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mitochondrial trifunctional protein deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
GTP cyclohydrolase I deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the GTP cyclohydrolase I deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Deficiency of malonyl-CoA decarboxylase Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Deficiency of malonyl-CoA decarboxylase phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
3 beta-Hydroxysteroid dehydrogenase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the 3 beta-Hydroxysteroid dehydrogenase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Succinate-semialdehyde dehydrogenase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Succinate-semialdehyde dehydrogenase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
X-linked agammaglobulinemia with growth hormone deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the X-linked agammaglobulinemia with growth hormone deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Okt4 epitope deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Okt4 epitope deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Deficiency of acetyl-CoA acetyltransferase Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Deficiency of acetyl-CoA acetyltransferase phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mitochondrial complex II deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mitochondrial complex II deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mineralocorticoid deficiency, isolated Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mineralocorticoid deficiency, isolated phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Complement 1s deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Complement 1s deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Dihydropteridine reductase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Dihydropteridine reductase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mannose-binding protein deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mannose-binding protein deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glucose transporter type 1 deficiency syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glucose transporter type 1 deficiency syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myd88 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myd88 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cd8 deficiency, familial Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cd8 deficiency, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital muscular dystrophy due to partial LAMA2 deficiency Gene SetFrom 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. |
Acid-labile subunit deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Acid-labile subunit deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Fructose-biphosphatase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Fructose-biphosphatase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Megaloblastic anemia due to dihydrofolate reductase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Megaloblastic anemia due to dihydrofolate reductase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Complement factor B deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Complement factor B deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Obesity, severe, due to leptin deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Obesity, severe, due to leptin deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Beta-hydroxyisobutyryl-CoA deacylase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Beta-hydroxyisobutyryl-CoA deacylase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary factor VIII deficiency disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary factor VIII deficiency disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Proline dehydrogenase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Proline dehydrogenase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Factor H deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Factor H deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glutamine deficiency, congenital Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glutamine deficiency, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Deficiency of aromatic-L-amino-acid decarboxylase Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Deficiency of aromatic-L-amino-acid decarboxylase phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glycine N-methyltransferase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glycine N-methyltransferase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ornithine carbamoyltransferase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ornithine carbamoyltransferase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Sucrase-isomaltase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Sucrase-isomaltase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |