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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 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. |
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. |
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. |
abnormal copulatory plug deposition Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal copulatory plug deposition phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 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. |
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. |
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-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. |
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. |
abnormal mitochondria in muscle tissue Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal mitochondria in muscle tissue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Abnormal Mitochondria In Muscle Tissue Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abnormal Mitochondria In Muscle Tissue in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
decreased circulating c4 and predominant mesangial c4 deposition Gene SetFrom GAD Gene-Disease Associations genes associated with the disease decreased circulating c4 and predominant mesangial c4 deposition in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
deposition Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term deposition in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
generalized amyloid deposition Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the generalized amyloid deposition phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
iga deposition in the glomerulus Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the iga deposition in the glomerulus phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
amyloid deposition in the vitreous humor Gene SetFrom HPO Gene-Disease Associations genes associated with the amyloid deposition in the vitreous humor phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
generalized amyloid deposition Gene SetFrom HPO Gene-Disease Associations genes associated with the generalized amyloid deposition phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
increased collagen deposition in the muscles Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased collagen deposition in the muscles phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
vitreous body deposition Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the vitreous body deposition phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
Deposition of new CENPA-containing nucleosomes at the centromere Gene Setproteins participating in the Deposition of new CENPA-containing nucleosomes at the centromere pathway from the Reactome Pathways dataset. |
Calcium Pyrophosphate Deposition Disease Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Calcium Pyrophosphate Deposition Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Eggshell Calcium Deposition Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Eggshell Calcium Deposition in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Heavy Chain Deposition Disease Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Heavy Chain Deposition Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Calcium Pyrophosphate Dihydrate Deposition Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Calcium Pyrophosphate Dihydrate Deposition in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Generalized Amyloid Deposition Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Amyloid Deposition in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Pigment Deposition In The Trabecular Meshwork Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Pigment Deposition In The Trabecular Meshwork in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Iga Deposition In The Glomerulus Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Iga Deposition In The Glomerulus in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Amyloid Deposition In The Vitreous Humor Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Amyloid Deposition In The Vitreous Humor in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
failure of copulatory plug deposition Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the failure of copulatory plug deposition phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased collagen deposition in the muscles Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased collagen deposition in the muscles phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
vitreous body deposition Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the vitreous body deposition phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased copulatory plug deposition Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased copulatory plug deposition phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Deposition of new CENPA-containing nucleosomes at the centromere Gene Setproteins participating in the Deposition of new CENPA-containing nucleosomes at the centromere pathway from the Reactome Pathways 2024 dataset. |
Cerebral amyloid deposition (PET imaging) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cerebral amyloid deposition (PET imaging) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Cerebral amyloid deposition in APOEe4 non-carriers (PET imaging) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cerebral amyloid deposition in APOEe4 non-carriers (PET imaging) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Cerebral amyloid deposition positivity (PET imaging) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cerebral amyloid deposition positivity (PET imaging) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
role of mitochondria in apoptotic signaling Gene SetFrom Biocarta Pathways proteins participating in the role of mitochondria in apoptotic signaling pathway from the Biocarta Pathways dataset. |
mitochondria Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term mitochondria in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
negative regulation of release of cytochrome c from mitochondria Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of release of cytochrome c from mitochondria biological process from the curated GO Biological Process Annotations 2015 dataset. |
release of cytochrome c from mitochondria Gene SetFrom GO Biological Process Annotations 2015 genes participating in the release of cytochrome c from mitochondria biological process from the curated GO Biological Process Annotations 2015 dataset. |
mitochondria-nucleus signaling pathway Gene SetFrom GO Biological Process Annotations 2015 genes participating in the mitochondria-nucleus signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of release of cytochrome c from mitochondria Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of release of cytochrome c from mitochondria biological process from the curated GO Biological Process Annotations 2015 dataset. |
intracellular distribution of mitochondria Gene SetFrom GO Biological Process Annotations 2015 genes participating in the intracellular distribution of mitochondria biological process from the curated GO Biological Process Annotations 2015 dataset. |
release of matrix enzymes from mitochondria Gene SetFrom GO Biological Process Annotations 2015 genes participating in the release of matrix enzymes from mitochondria biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of release of cytochrome c from mitochondria Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of release of cytochrome c from mitochondria biological process from the curated GO Biological Process Annotations 2015 dataset. |
subsarcolemmal accumulations of abnormally shaped mitochondria Gene SetFrom HPO Gene-Disease Associations genes associated with the subsarcolemmal accumulations of abnormally shaped mitochondria phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Clustered mitochondria protein, N-terminal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Clustered mitochondria protein, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
DNA-directed DNA-polymerase, family A, mitochondria Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the DNA-directed DNA-polymerase, family A, mitochondria protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Protohaem IX farnesyltransferase, mitochondria Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Protohaem IX farnesyltransferase, mitochondria protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Mitochondria-eating protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Mitochondria-eating protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Carbonic anhydrase VB, mitochondria Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Carbonic anhydrase VB, mitochondria protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Clustered mitochondria protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Clustered mitochondria protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
ATPase inhibitor, IATP, mitochondria Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the ATPase inhibitor, IATP, mitochondria protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Mitochondria fission 1 protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Mitochondria fission 1 protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ribosomal protein S2, bacteria/mitochondria/plastid Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ribosomal protein S2, bacteria/mitochondria/plastid protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Uncharacterised protein family UPF0317, mitochondria Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Uncharacterised protein family UPF0317, mitochondria protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ribosomal protein L50, mitochondria Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ribosomal protein L50, mitochondria protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Domain of unknown function DUF1713, mitochondria Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Domain of unknown function DUF1713, mitochondria protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
fatty acid elongation in mitochondria Gene SetFrom KEGG Pathways proteins participating in the fatty acid elongation in mitochondria pathway from the KEGG Pathways dataset. |
increased mitochondria number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased mitochondria number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased mitochondria size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased mitochondria size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased mitochondria number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased mitochondria number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased mitochondria size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased mitochondria size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
dilated mitochondria Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the dilated mitochondria phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
Activation of NOXA and translocation to mitochondria Gene Setproteins participating in the Activation of NOXA and translocation to mitochondria pathway from the Reactome Pathways dataset. |
Activation of BAD and translocation to mitochondria Gene Setproteins participating in the Activation of BAD and translocation to mitochondria pathway from the Reactome Pathways dataset. |
Activation of BIM and translocation to mitochondria Gene Setproteins participating in the Activation of BIM and translocation to mitochondria pathway from the Reactome Pathways dataset. |
Release of apoptotic factors from the mitochondria Gene Setproteins participating in the Release of apoptotic factors from the mitochondria pathway from the Reactome Pathways dataset. |
Activation, myristolyation of BID and translocation to mitochondria Gene Setproteins participating in the Activation, myristolyation of BID and translocation to mitochondria pathway from the Reactome Pathways dataset. |
Activation of BMF and translocation to mitochondria Gene Setproteins participating in the Activation of BMF and translocation to mitochondria pathway from the Reactome Pathways dataset. |
Activation of PUMA and translocation to mitochondria Gene Setproteins participating in the Activation of PUMA and translocation to mitochondria pathway from the Reactome Pathways dataset. |
Proximal Myopathy With Focal Depletion Of Mitochondria Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Proximal Myopathy With Focal Depletion Of Mitochondria in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Subsarcolemmal Accumulations Of Abnormally Shaped Mitochondria Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Subsarcolemmal Accumulations Of Abnormally Shaped Mitochondria in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
release of cytochrome c from mitochondria Gene SetFrom GO Biological Process Annotations 2023 genes participating in the release of cytochrome c from mitochondria biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of release of cytochrome c from mitochondria Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of release of cytochrome c from mitochondria biological process from the curated GO Biological Process Annotations 2023 dataset. |
intracellular distribution of mitochondria Gene SetFrom GO Biological Process Annotations 2023 genes participating in the intracellular distribution of mitochondria biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of release of cytochrome c from mitochondria Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of release of cytochrome c from mitochondria biological process from the curated GO Biological Process Annotations 2023 dataset. |
release of matrix enzymes from mitochondria Gene SetFrom GO Biological Process Annotations 2023 genes participating in the release of matrix enzymes from mitochondria biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of release of cytochrome c from mitochondria Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of release of cytochrome c from mitochondria biological process from the curated GO Biological Process Annotations 2023 dataset. |
Electron transport chain OXPHOS system in mitochondria Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Electron transport chain OXPHOS system in mitochondria pathway from the WikiPathways Pathways 2024 dataset. |
Activation of BAD and translocation to mitochondria Gene Setproteins participating in the Activation of BAD and translocation to mitochondria pathway from the Reactome Pathways 2024 dataset. |
Activation of BIM and translocation to mitochondria Gene Setproteins participating in the Activation of BIM and translocation to mitochondria pathway from the Reactome Pathways 2024 dataset. |
Activation of BMF and translocation to mitochondria Gene Setproteins participating in the Activation of BMF and translocation to mitochondria pathway from the Reactome Pathways 2024 dataset. |
Activation of NOXA and translocation to mitochondria Gene Setproteins participating in the Activation of NOXA and translocation to mitochondria pathway from the Reactome Pathways 2024 dataset. |
Activation of PUMA and translocation to mitochondria Gene Setproteins participating in the Activation of PUMA and translocation to mitochondria pathway from the Reactome Pathways 2024 dataset. |
Activation, myristolyation of BID and translocation to mitochondria Gene Setproteins participating in the Activation, myristolyation of BID and translocation to mitochondria pathway from the Reactome Pathways 2024 dataset. |
Release of apoptotic factors from the mitochondria Gene Setproteins participating in the Release of apoptotic factors from the mitochondria pathway from the Reactome Pathways 2024 dataset. |
release of cytochrome c from mitochondria Gene SetFrom GO Biological Process Annotations 2025 genes participating in the release of cytochrome c from mitochondria biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of release of cytochrome c from mitochondria Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of release of cytochrome c from mitochondria biological process from the curated GO Biological Process Annotations 2025 dataset. |
intracellular distribution of mitochondria Gene SetFrom GO Biological Process Annotations 2025 genes participating in the intracellular distribution of mitochondria biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of release of cytochrome c from mitochondria Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of release of cytochrome c from mitochondria biological process from the curated GO Biological Process Annotations 2025 dataset. |
release of matrix enzymes from mitochondria Gene SetFrom GO Biological Process Annotations 2025 genes participating in the release of matrix enzymes from mitochondria biological process from the curated GO Biological Process Annotations 2025 dataset. |
mitochondria-nucleus signaling pathway Gene SetFrom GO Biological Process Annotations 2025 genes participating in the mitochondria-nucleus signaling pathway biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of release of cytochrome c from mitochondria Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of release of cytochrome c from mitochondria biological process from the curated GO Biological Process Annotations 2025 dataset. |
mitochondria-associated endoplasmic reticulum membrane Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the mitochondria-associated endoplasmic reticulum membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
mitochondria-associated endoplasmic reticulum membrane Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the mitochondria-associated endoplasmic reticulum membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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 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. |
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 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 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 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 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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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 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 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 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 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 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. |
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. |
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. |
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. |
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 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. |
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. |
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. |
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. |
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. |
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. |
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 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. |
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. |
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. |
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 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. |
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. |
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. |
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. |
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. |
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 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 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 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. |
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. |
IRON CARBONYL Gene Setinteracting proteins for the IRON CARBONYL drug from theDGIdb Drug Targets 2026 dataset. |
Thyroid hormone metabolism, abnormal Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Thyroid hormone metabolism, abnormal phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
X-linked mental retardation with short stature, hypogonadism and abnormal gait Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the X-linked mental retardation with short stature, hypogonadism and abnormal gait phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Reflex, Abnormal Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Reflex, Abnormal from the curated CTD Gene-Disease Associations dataset. |
Neutrophil Chemotactic Response, Abnormal Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neutrophil Chemotactic Response, Abnormal from the curated CTD Gene-Disease Associations dataset. |
Thyroid Hormone Metabolism, Abnormal Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Thyroid Hormone Metabolism, Abnormal from the curated CTD Gene-Disease Associations dataset. |
abnormal retinal correspondence Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease abnormal retinal correspondence in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
abnormal splicing Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abnormal splicing in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
ekg, abnormal Gene SetFrom GAD Gene-Disease Associations genes associated with the disease ekg, abnormal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
ekg, abnormal; brugada syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease ekg, abnormal; brugada syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abnormal urogenital development Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abnormal urogenital development in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abnormal fibrin polymerization and thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abnormal fibrin polymerization and thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abnormal Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term abnormal in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
abnormal cannabidiol Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the abnormal cannabidiol ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
abnormal eye physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal eye physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal renal physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal renal physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal gallbladder morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal gallbladder morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal gallbladder physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal gallbladder physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal intraocular pressure Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal intraocular pressure phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal eating behavior Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal eating behavior phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal thrombosis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal thrombosis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal leukocyte count Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal leukocyte count phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal iris pigmentation Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal iris pigmentation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal bone structure Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal bone structure phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal emotion/affect behavior Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal emotion/affect behavior phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal bleeding Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal bleeding phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal atrioventricular conduction Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal atrioventricular conduction phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal hair quantity Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal hair quantity phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal nervous system electrophysiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal nervous system electrophysiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal male reproductive system physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal male reproductive system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal external genitalia Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal external genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal ekg Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal ekg phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal axial skeleton morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal axial skeleton morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal immunoglobulin level Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal immunoglobulin level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal monocyte count Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal monocyte count phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal neutrophil cell number Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal neutrophil cell number phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal facial shape Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal facial shape phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal platelet count Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal platelet count phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal aggressive, impulsive or violent behavior Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal aggressive, impulsive or violent behavior phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
acquired abnormal hair pattern Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the acquired abnormal hair pattern phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal glomerular filtration rate Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal glomerular filtration rate phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal eye morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal eye morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal testosterone level Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal testosterone level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal joint morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal joint morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal motor neuron morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal motor neuron morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal biliary tract morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal biliary tract morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal neuron morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal neuron morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal genital system morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal genital system morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal appendicular skeleton morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal appendicular skeleton morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal cortical bone morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal cortical bone morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal electrophysiology of sinoatrial node origin Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal electrophysiology of sinoatrial node origin phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal respiratory system morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal respiratory system morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal number of teeth Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal number of teeth phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal hair pattern Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal hair pattern phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal circulating creatinine level Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal circulating creatinine level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal peripheral nervous system morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal peripheral nervous system morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal autonomic nervous system physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal autonomic nervous system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal platelet function Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal platelet function phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal muscle tone Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal muscle tone phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal diaphysis morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal diaphysis morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal spermatogenesis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal spermatogenesis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal hemoglobin Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal hemoglobin phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal internal genitalia Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal internal genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal glucose homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal glucose homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal renal morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal renal morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal dermatoglyphics Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal dermatoglyphics phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal gallbladder morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal gallbladder morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal ossification of hand bones Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal ossification of hand bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal bone structure Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal bone structure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal branching pattern of the aortic arch Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal branching pattern of the aortic arch phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal motor nerve conduction velocity Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal motor nerve conduction velocity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal maternal serum screening Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal maternal serum screening phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal rod and cone electroretinograms Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal rod and cone electroretinograms phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal albumin level Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal albumin level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal enchondral ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal enchondral ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal number of vertebrae Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal number of vertebrae phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal platelet membrane protein expression Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal platelet membrane protein expression phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal male reproductive system physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal male reproductive system physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal placental size Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal placental size phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal central microtubular pair morphology of respiratory motile cilia Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal central microtubular pair morphology of respiratory motile cilia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal platelet granules Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal platelet granules phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal subcutaneous fat tissue distribution Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal subcutaneous fat tissue distribution phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal electroretinogram Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal electroretinogram phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal lung lobation Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal lung lobation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal flash visual evoked potentials Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal flash visual evoked potentials phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal peripheral nervous system synaptic transmission Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal peripheral nervous system synaptic transmission phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal urine phosphate concentration Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal urine phosphate concentration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal drinking behavior Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal drinking behavior phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal sperm motility Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal sperm motility phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal fear/anxiety-related behavior Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal fear/anxiety-related behavior phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal renal corticomedullary differentiation Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal renal corticomedullary differentiation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal humeral ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal humeral ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal delayed hypersensitivity skin test Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal delayed hypersensitivity skin test phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal upper motor neuron morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal upper motor neuron morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal protein n-linked glycosylation Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal protein n-linked glycosylation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal echocardiogram Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal echocardiogram phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal serum ferritin Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal serum ferritin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal female reproductive system physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal female reproductive system physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal hypothalamus morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal hypothalamus morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal axial skeleton morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal axial skeleton morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal calcification of the carpal bones Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal calcification of the carpal bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal testosterone level Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal testosterone level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal peripheral myelination Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal peripheral myelination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal speech discrimination Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal speech discrimination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal genital system morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal genital system morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal morphology of bones of the lower limbs Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal morphology of bones of the lower limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal liver function tests during pregnancy Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal liver function tests during pregnancy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal cortical bone morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal cortical bone morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal hypothalamus physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal hypothalamus physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal trabecular bone morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal trabecular bone morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal electrophysiology of sinoatrial node origin Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal electrophysiology of sinoatrial node origin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal metacarpal morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal metacarpal morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal t3/t4 ratio Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal t3/t4 ratio phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal glycosylation Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal glycosylation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal iris vasculature Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal iris vasculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal pupillary function Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal pupillary function phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal posturing Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal posturing phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal natural killer cell physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal natural killer cell physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal external genitalia Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal external genitalia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal immunoglobulin level Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal immunoglobulin level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
congenital abnormal hair pattern Gene SetFrom HPO Gene-Disease Associations genes associated with the congenital abnormal hair pattern phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal nervous system electrophysiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal nervous system electrophysiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal autonomic nervous system physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal autonomic nervous system physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal monocyte count Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal monocyte count phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal atrial arrangement Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal atrial arrangement phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal morphology of ulna Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal morphology of ulna phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal circulating renin Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal circulating renin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal retinal folds Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal retinal folds phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal pancreas size Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal pancreas size phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal urine sodium concentration Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal urine sodium concentration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal vestibulo-ocular reflex Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal vestibulo-ocular reflex phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal vertebral pedicle morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal vertebral pedicle morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal tendon morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal tendon morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal glucose homeostasis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal glucose homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal leukocyte count Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal leukocyte count phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal tarsal ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal tarsal ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal spermatogenesis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal spermatogenesis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal size of pituitary gland Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal size of pituitary gland phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal urine potassium concentration Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal urine potassium concentration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal synaptic transmission at the neuromuscular junction Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal synaptic transmission at the neuromuscular junction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal peripheral nervous system morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal peripheral nervous system morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal pupillary light reflex Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal pupillary light reflex phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal pyramidal signs Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal pyramidal signs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal biliary tract morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal biliary tract morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal pigmentation of the oral mucosa Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal pigmentation of the oral mucosa phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal hair pattern Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal hair pattern phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal number of incisors Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal number of incisors phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal localization of kidney Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal localization of kidney phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal elasticity of skin Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal elasticity of skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal platelet volume Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal platelet volume phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal vas deferens morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal vas deferens morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal muscle tone Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal muscle tone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal lower motor neuron morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal lower motor neuron morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal ciliary motility Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal ciliary motility phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal atrioventricular conduction Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal atrioventricular conduction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal metatarsal ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal metatarsal ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal st segment Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal st segment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal sweat homeostasis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal sweat homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal nasal base Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal nasal base phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal pelvis bone ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal pelvis bone ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal sperm morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal sperm morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal ossification of the pubic bone Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal ossification of the pubic bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal isoelectric focusing of serum transferrin Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal isoelectric focusing of serum transferrin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal hemoglobin Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal hemoglobin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal morphology of bones of the upper limbs Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal morphology of bones of the upper limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal nasal morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal nasal morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal ossification involving the femoral head and neck Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal ossification involving the femoral head and neck phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal concentration of calcium in blood Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal concentration of calcium in blood phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal emotion/affect behavior Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal emotion/affect behavior phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal epiphyseal ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal epiphyseal ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal urine cytology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal urine cytology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal palmar dermatoglyphics Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal palmar dermatoglyphics phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal neuron morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal neuron morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal csf lactate level Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal csf lactate level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal facial shape Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal facial shape phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal joint morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal joint morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal vertebral segmentation and fusion Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal vertebral segmentation and fusion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal internal genitalia Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal internal genitalia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal oral glucose tolerance Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal oral glucose tolerance phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal bone collagen fibril morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal bone collagen fibril morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal delivery Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal delivery phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal middle ear reflexes Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal middle ear reflexes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal mitochondrial morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal mitochondrial morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal cervical curvature Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal cervical curvature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal bleeding Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal bleeding phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal myelination Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal myelination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal mitochondrial shape Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal mitochondrial shape phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal auditory evoked potentials Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal auditory evoked potentials phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal activity of mitochondrial respiratory chain Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal activity of mitochondrial respiratory chain phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal location of ears Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal location of ears phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal cns myelination Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal cns myelination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal eye physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal eye physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal renal physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal renal physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal synaptic transmission Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal synaptic transmission phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal eating behavior Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal eating behavior phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal atrioventricular connection Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal atrioventricular connection phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal ventriculo-arterial connection Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal ventriculo-arterial connection phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal anterior horn cell morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal anterior horn cell morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal germ cell morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal germ cell morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal upper to lower segment ratio Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal upper to lower segment ratio phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal form of the vertebral bodies Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal form of the vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal biliary tract physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal biliary tract physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal urine output Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal urine output phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal blistering of the skin Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal blistering of the skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal diaphysis morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal diaphysis morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal cholesterol homeostasis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal cholesterol homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal urine citrate concentration Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal urine citrate concentration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal size of the palpebral fissures Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal size of the palpebral fissures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal hand morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal hand morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal hair quantity Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal hair quantity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal anatomic location of the heart Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal anatomic location of the heart phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal morphology of forearm bone Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal morphology of forearm bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal circulating aldosterone Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal circulating aldosterone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal male germ cell morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal male germ cell morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal platelet morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal platelet morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal circulating creatinine level Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal circulating creatinine level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal platelet function Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal platelet function phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal large intestine physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal large intestine physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal facial expression Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal facial expression phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal urine chloride concentration Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal urine chloride concentration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal vascular physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal vascular physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal vertebral ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal vertebral ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal renal morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal renal morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal heart morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal heart morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal hair laboratory examination Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal hair laboratory examination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal retinal pigmentation Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal retinal pigmentation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal shape of the palpebral fissure Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal shape of the palpebral fissure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal lymphocyte count Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal lymphocyte count phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal conjugate eye movement Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal conjugate eye movement phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal autonomic nervous system morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal autonomic nervous system morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal pulmonary lymphatics Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal pulmonary lymphatics phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal bone ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal bone ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal pattern of respiration Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal pattern of respiration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal protein glycosylation Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal protein glycosylation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal hair whorl Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal hair whorl phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal connection of the cardiac segments Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal connection of the cardiac segments phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal cartilage collagen Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal cartilage collagen phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal umbilical stump bleeding Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal umbilical stump bleeding phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal social behavior Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal social behavior phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal cortical gyration Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal cortical gyration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal number of permanent teeth Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal number of permanent teeth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal sex determination Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal sex determination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal prolactin level Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal prolactin level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal respiratory system morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal respiratory system morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal number of teeth Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal number of teeth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal respiratory epithelium morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal respiratory epithelium morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal axonemal organization of respiratory motile cilia Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal axonemal organization of respiratory motile cilia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal foot bone ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal foot bone ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal shape of the radius Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal shape of the radius phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal neutrophil cell number Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal neutrophil cell number phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal platelet count Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal platelet count phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal eye morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal eye morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal cone-mediated electroretinogram Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal cone-mediated electroretinogram phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal basal ganglia mri signal intensity Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal basal ganglia mri signal intensity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal respiratory motile cilium morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal respiratory motile cilium morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal sensory nerve conduction velocity Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal sensory nerve conduction velocity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal muscle glycogen content Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal muscle glycogen content phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal appendicular skeleton morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal appendicular skeleton morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal hand bone ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal hand bone ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal number of erythroid precursors Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal number of erythroid precursors phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal respiratory motile cilium physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal respiratory motile cilium physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal urine magnesium concentration Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal urine magnesium concentration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal rapid eye movement (rem) sleep Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal rapid eye movement (rem) sleep phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal nerve conduction velocity Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal nerve conduction velocity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal thrombosis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal thrombosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal glucose tolerance Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal glucose tolerance phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal ekg Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal ekg phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal levels of creatine kinase in blood Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal levels of creatine kinase in blood phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal ejaculation Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal ejaculation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal aggressive, impulsive or violent behavior Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal aggressive, impulsive or violent behavior phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal motor neuron morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal motor neuron morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal urinary electrolyte concentration Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal urinary electrolyte concentration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal finger flexion creases Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal finger flexion creases phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal metaphyseal trabeculation Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal metaphyseal trabeculation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal umbilical cord blood vessels Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal umbilical cord blood vessels phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal head movements Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal head movements phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
acquired abnormal hair pattern Gene SetFrom HPO Gene-Disease Associations genes associated with the acquired abnormal hair pattern phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal facility in opposing the shoulders Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal facility in opposing the shoulders phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal migration of corneal endothelium Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal migration of corneal endothelium phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal gallbladder physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal gallbladder physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal intraocular pressure Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal intraocular pressure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal shape of the frontal region Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal shape of the frontal region phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal iris pigmentation Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal iris pigmentation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal urinary sulfate concentration Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal urinary sulfate concentration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal spatial orientation of the cardiac segments Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal spatial orientation of the cardiac segments phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal morphology of the radius Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal morphology of the radius phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal rib ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal rib ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal glomerular filtration rate Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal glomerular filtration rate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal sternal ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal sternal ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal shape of the occiput Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal shape of the occiput phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal involuntary eye movements Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal involuntary eye movements phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal metaphyseal vascular invasion Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal metaphyseal vascular invasion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal enzyme/coenzyme activity Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal enzyme/coenzyme activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal cartilage morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal cartilage morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal peripheral action potential amplitude Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal peripheral action potential amplitude phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Reflex, Abnormal Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Reflex, Abnormal phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Spindle assembly abnormal protein 6 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Spindle assembly abnormal protein 6 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
DMRT/protein doublesex/protein male abnormal 3 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the DMRT/protein doublesex/protein male abnormal 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Protein male abnormal 21-related Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Protein male abnormal 21-related protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Abnormal spindle-like microcephaly-associated protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Abnormal spindle-like microcephaly-associated protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
abnormal clitoris morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal clitoris morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal male genitalia morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal male genitalia morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal lung volume Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal lung volume phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal basilar membrane morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal basilar membrane morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal neural fold elevation formation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal neural fold elevation formation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal sensory capabilities/reflexes/nociception Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal sensory capabilities/reflexes/nociception phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal behavioral response to anesthetic Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal behavioral response to anesthetic phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal trigeminal ganglion morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal trigeminal ganglion morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal auditory brainstem response waveform shape Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal auditory brainstem response waveform shape phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal retinal photoreceptor layer morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal photoreceptor layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal bradykinin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal bradykinin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal fetal derived definitive erythrocyte cell number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal fetal derived definitive erythrocyte cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal paravertebral ganglion morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal paravertebral ganglion morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal nasal cavity morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal nasal cavity morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal primary sex determination Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal primary sex determination phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hippocampus stratum lacunosum morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hippocampus stratum lacunosum morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal gallbladder morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal gallbladder morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal ectomesenchyme morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal ectomesenchyme morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal male urethra morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal male urethra morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal bone marrow cell number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal bone marrow cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal zona glomerulosa morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal zona glomerulosa morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal ear development Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal ear development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal surfactant secretion Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal surfactant secretion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cerebellum fastigial nucleus morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebellum fastigial nucleus morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal social/conspecific interaction Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal social/conspecific interaction phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hippocampus size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hippocampus size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal tooth morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal tooth morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal neutrophil differentiation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal neutrophil differentiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal vomer bone morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal vomer bone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal endplate potential Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal endplate potential phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal sagittal suture morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal sagittal suture morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal semicircular canal morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal semicircular canal morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal estrous cycle Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal estrous cycle phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cd4-positive t cell differentiation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cd4-positive t cell differentiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal neuron differentiation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal neuron differentiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal long bone metaphysis morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal long bone metaphysis morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal testis size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal testis size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal vascular endothelial cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal vascular endothelial cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal sympathetic neuron innervation pattern Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal sympathetic neuron innervation pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal melanosome transport Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal melanosome transport phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal inferior colliculus morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal inferior colliculus morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal tongue muscle morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal tongue muscle morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal retinal inner nuclear layer morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal inner nuclear layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal keratinocyte physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal keratinocyte physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal behavioral response to methamphetamine Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal behavioral response to methamphetamine phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal auditory brainstem response Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal auditory brainstem response phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal macrophage derived foam cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal macrophage derived foam cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal heart left atrium weight Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal heart left atrium weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal malleus morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal malleus morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal scala vestibuli morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal scala vestibuli morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pupillary reflex Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pupillary reflex phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal interdigital cell death Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal interdigital cell death phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal schwann cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal schwann cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal posterior definitive endoderm morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal posterior definitive endoderm morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal keratinocyte morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal keratinocyte morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal renal protein reabsorption Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal renal protein reabsorption phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal habenula morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal habenula morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal urine antidiuretic hormone level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal urine antidiuretic hormone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal embryonic tissue morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal embryonic tissue morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal laryngeal mucosa morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal laryngeal mucosa morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal plasma membrane morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal plasma membrane morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating angiotensinogen level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating angiotensinogen level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal b cell apoptosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal b cell apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal corneocyte envelope morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal corneocyte envelope morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal primordial ovarian follicle number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal primordial ovarian follicle number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal prostate gland dorsolateral lobe morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal prostate gland dorsolateral lobe morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal vestibular nerve morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal vestibular nerve morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal retinal melanocyte morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal melanocyte morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cochlear inner hair cell number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cochlear inner hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal parametrial fat pad morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal parametrial fat pad morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal effector t cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal effector t cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal urine aldosterone level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal urine aldosterone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal roof plate morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal roof plate morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal bone healing Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal bone healing phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal rhombomere 4 morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal rhombomere 4 morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal heart right ventricle size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal heart right ventricle size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal snout morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal snout morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal optic disc morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal optic disc morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal parasympathetic ganglion morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal parasympathetic ganglion morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal blinking Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal blinking phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cerebellar molecular layer Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebellar molecular layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating interleukin-1 alpha level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating interleukin-1 alpha level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal thyroid gland development Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal thyroid gland development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal efferent ductules of testis morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal efferent ductules of testis morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal periocular mesenchyme morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal periocular mesenchyme morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal purkinje cell number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal purkinje cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating pancreatic peptide level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating pancreatic peptide level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal frontonasal prominence morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal frontonasal prominence morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal gas homeostasis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal gas homeostasis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal intestinal mucosa morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal intestinal mucosa morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal dermis papillary layer morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal dermis papillary layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hair shaft morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hair shaft morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cellular replicative senescence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cellular replicative senescence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal throat morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal throat morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal nasolacrimal duct morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal nasolacrimal duct morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal first pharyngeal arch morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal first pharyngeal arch morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal loop of henle descending limb morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal loop of henle descending limb morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal triiodothyronine level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal triiodothyronine level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal visual acuity Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal visual acuity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating sulfate level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating sulfate level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal parturition Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal parturition phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal scala tympani morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal scala tympani morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal external urethral orifice morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal external urethral orifice morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal male reproductive gland physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal male reproductive gland physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal chorioallantoic fusion Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal chorioallantoic fusion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal purkinje cell dendrite morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal purkinje cell dendrite morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal lens development Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal lens development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pituitary diverticulum morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pituitary diverticulum morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal arteriole morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal arteriole morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal outer hair cell stereociliary bundle morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal outer hair cell stereociliary bundle morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pancreatic endocrine progenitor cell proliferation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pancreatic endocrine progenitor cell proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cd4-positive, cd25-positive, alpha-beta regulatory t cell number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cd4-positive, cd25-positive, alpha-beta regulatory t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal rosenthal canal morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal rosenthal canal morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pr interval Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pr interval phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal enterocyte apoptosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal enterocyte apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal renal glomerulus basement membrane thickness Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal renal glomerulus basement membrane thickness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal superior vagus ganglion morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal superior vagus ganglion morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal melanoblast morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal melanoblast morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal urinary bladder weight Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal urinary bladder weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal single cell response threshold Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal single cell response threshold phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal dermis reticular layer morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal dermis reticular layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal body height Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal body height phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal kidney epithelial cell primary cilium physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal kidney epithelial cell primary cilium physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal optic stalk morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal optic stalk morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal neural tube mantle layer morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal neural tube mantle layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal posterior cardinal vein morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal posterior cardinal vein morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal renal tubule epithelial cell primary cilium morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal renal tubule epithelial cell primary cilium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal intramembranous bone ossification Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal intramembranous bone ossification phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal ear distance/ position Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal ear distance/ position phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal mitochondrion morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal mitochondrion morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal maxillary sinus morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal maxillary sinus morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal otic vesicle development Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal otic vesicle development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal brown adipose tissue physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal brown adipose tissue physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal lymph node b cell domain morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal lymph node b cell domain morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating lactate dehydrogenase level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating lactate dehydrogenase level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal plasmacytoid dendritic cell number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal plasmacytoid dendritic cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal urinary bladder morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal urinary bladder morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal retinal rod cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal rod cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal digestive system development Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal digestive system development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal auditory summating potential Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal auditory summating potential phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal paired-pulse inhibition Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal paired-pulse inhibition phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal aortic arch and aortic arch branch attachment Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal aortic arch and aortic arch branch attachment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal retinal ganglion cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal ganglion cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal postnatal growth Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal postnatal growth phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal brain development Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal brain development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal memory t cell number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal memory t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal miniature inhibitory postsynaptic currents Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal miniature inhibitory postsynaptic currents phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal osteocyte morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal osteocyte morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal axillary lymph node morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal axillary lymph node morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal costal cartilage morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal costal cartilage morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal splenocyte morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal splenocyte morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating chemokine level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating chemokine level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cerebellum posterior vermis morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebellum posterior vermis morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal thalamus morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal thalamus morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hair medulla air spaces Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hair medulla air spaces phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal zigzag hair morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal zigzag hair morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal xenobiotic induced morbidity/mortality Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal xenobiotic induced morbidity/mortality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal kidney epithelium morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal kidney epithelium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pons morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pons morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal b cell anergy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal b cell anergy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal rr interval Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal rr interval phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal somite size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal somite size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pancreatic acinar cell zymogen granule morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pancreatic acinar cell zymogen granule morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal meibomian gland development Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal meibomian gland development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal basophil physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal basophil physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cerebellum vermis lobule ii morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebellum vermis lobule ii morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal tubuloglomerular feedback response Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal tubuloglomerular feedback response phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal b wave amplitude Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal b wave amplitude phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal urine organic cation level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal urine organic cation level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal embryo attachment Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal embryo attachment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal myogenesis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal myogenesis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal eye morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal eye morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal kidney collecting duct morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal kidney collecting duct morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |