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abnormal brain copper level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal brain copper level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased brain copper level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased brain copper level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased brain copper level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased brain copper level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased brain copper level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased brain copper level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased brain copper level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased brain copper level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal liver copper level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal liver copper level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating copper level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating copper level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal intestine copper level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal intestine copper level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal copper level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal copper level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal kidney copper level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal kidney copper level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal liver copper level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal liver copper level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal copper level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal copper level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
brain concussion; brain injuries; brain ischemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain concussion; brain injuries; brain ischemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
decreased circulating copper level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating copper level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased liver copper level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased liver copper level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased intestine copper level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased intestine copper level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased liver copper level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased liver copper level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased kidney copper level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased kidney copper level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating copper level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating copper level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased liver copper level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased liver copper level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased liver copper level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased liver copper level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating copper level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating copper level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating copper level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating copper level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased kidney copper level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased kidney copper level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased intestine copper level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased intestine copper level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased brainstem copper level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased brainstem copper level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 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 brain zinc level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal brain zinc level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal brain cholesterol level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal brain cholesterol level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
Abnormal Brain Lactate Level By Mrs Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Brain Lactate Level By Mrs in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormal Brain Choline Level By Mrs Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Brain Choline Level By Mrs in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations 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 brain cholesterol level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal brain cholesterol level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal copper homeostasis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal copper homeostasis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal copper homeostasis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal copper homeostasis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
brain infarction; brain ischemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain infarction; brain ischemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arterial occlusive diseases; brain infarction; brain ischemia; coronary artery disease; stroke; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arterial occlusive diseases; brain infarction; brain ischemia; coronary artery disease; stroke; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain edema; brain injuries; cerebral hemorrhage, traumatic; skull fractures; traumatic cerebral hemorrhage Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain edema; brain injuries; cerebral hemorrhage, traumatic; skull fractures; traumatic cerebral hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain damage, chronic; brain injuries Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain damage, chronic; brain injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain edema; brain injuries Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain edema; brain injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain infarction; brain ischemia; cerebrovascular disorders; hypertension; leukoaraiosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain infarction; brain ischemia; cerebrovascular disorders; hypertension; leukoaraiosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain concussion; brain injuries; unconsciousness Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain concussion; brain injuries; unconsciousness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain edema; brain hemorrhage, traumatic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain edema; brain hemorrhage, traumatic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
asphyxia neonatorum; brain ischemia; hypoxia-ischemia, brain Gene SetFrom GAD Gene-Disease Associations genes associated with the disease asphyxia neonatorum; brain ischemia; hypoxia-ischemia, brain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; brain infarction; brain ischemia; intracranial arteriosclerosis; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; brain infarction; brain ischemia; intracranial arteriosclerosis; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain damage, chronic; hypoxia-ischemia, brain; infant, newborn, diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain damage, chronic; hypoxia-ischemia, brain; infant, newborn, diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain hypoxia; burns; hypoxia, brain; spinal cord injuries Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain hypoxia; burns; hypoxia, brain; spinal cord injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Brain volume in infants (intracranial brain volume) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Brain volume in infants (intracranial brain volume) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
increased brain sterol level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased brain sterol level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased brain cholesterol level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased brain cholesterol level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased brain sterol level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased brain sterol level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased brain zinc level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased brain zinc level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased brain cholesterol level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased brain cholesterol level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
Reduced Brain N-Acetyl Aspartate Level By Mrs Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Brain N-Acetyl Aspartate Level By Mrs in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Elevated Brain Lactate Level By Mrs Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Elevated Brain Lactate Level By Mrs in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Elevated Brain Choline Level By Mrs Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Elevated Brain Choline Level By Mrs in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Reduced Brain Creatine Level By Mrs Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Brain Creatine Level By Mrs in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Reduced Brain Choline Level By Mrs Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Brain Choline Level By Mrs in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Reduced Brain Glutamine Level By Mrs Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Brain Glutamine Level By Mrs in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Elevated Brain N-Acetyl Aspartate Level By Mrs Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Elevated Brain N-Acetyl Aspartate Level By Mrs in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
decreased brain cholesterol level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased brain cholesterol level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased brain cholesterol level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased brain cholesterol level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased brain zinc level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased brain zinc level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased brain glycogen level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased brain glycogen 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. |
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. |
increased brain manganese level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased brain manganese level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased brain plasmalogen level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased brain plasmalogen level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
copper sulfate-500 Gene SetFrom CMAP Signatures of Differentially Expressed Genes for Small Molecules genes differentially expressed following the copper sulfate-500 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset. |
copper sulfate-438 Gene SetFrom CMAP Signatures of Differentially Expressed Genes for Small Molecules genes differentially expressed following the copper sulfate-438 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset. |
copper sulfate-459 Gene SetFrom CMAP Signatures of Differentially Expressed Genes for Small Molecules genes differentially expressed following the copper sulfate-459 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset. |
copper sulfate-575 Gene SetFrom CMAP Signatures of Differentially Expressed Genes for Small Molecules genes differentially expressed following the copper sulfate-575 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset. |
copper bis(3,5-diisopropylsalicylate) Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical copper bis(3,5-diisopropylsalicylate) from the curated CTD Gene-Chemical Interactions dataset. |
copper protoporphyrin IX Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical copper protoporphyrin IX from the curated CTD Gene-Chemical Interactions dataset. |
Copper Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Copper from the curated CTD Gene-Chemical Interactions dataset. |
bis((2-oxindol-3-ylimino)-2-(2-aminoethyl)pyridine-N,N')copper(II) Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical bis((2-oxindol-3-ylimino)-2-(2-aminoethyl)pyridine-N,N')copper(II) from the curated CTD Gene-Chemical Interactions dataset. |
copper pyruvaldehyde bis(N(4)-methylthiosemicarbazone) complex Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical copper pyruvaldehyde bis(N(4)-methylthiosemicarbazone) complex from the curated CTD Gene-Chemical Interactions dataset. |
(4,4-dimethyl-2,2-bipyridine)(acetylacetonate)copper(II) Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical (4,4-dimethyl-2,2-bipyridine)(acetylacetonate)copper(II) from the curated CTD Gene-Chemical Interactions dataset. |
(4-amino-1,4-dihydro-3-(2-pyridyl)-5-thioxo-1,2,4-triazole)copper(II) Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical (4-amino-1,4-dihydro-3-(2-pyridyl)-5-thioxo-1,2,4-triazole)copper(II) from the curated CTD Gene-Chemical Interactions dataset. |
Copper Sulfate Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Copper Sulfate from the curated CTD Gene-Chemical Interactions dataset. |
copper (N-2-hydroxyacetophenone)glycinate Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical copper (N-2-hydroxyacetophenone)glycinate from the curated CTD Gene-Chemical Interactions dataset. |
copper histidine Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical copper histidine from the curated CTD Gene-Chemical Interactions dataset. |
copper (II) diacetyl-di(N(4)-methylthiosemicarbazone) Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical copper (II) diacetyl-di(N(4)-methylthiosemicarbazone) from the curated CTD Gene-Chemical Interactions dataset. |
copper Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term copper in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
cellular copper ion homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cellular copper ion homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of copper ion transmembrane transport Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of copper ion transmembrane transport biological process from the curated GO Biological Process Annotations 2015 dataset. |
copper ion transport Gene SetFrom GO Biological Process Annotations 2015 genes participating in the copper ion transport biological process from the curated GO Biological Process Annotations 2015 dataset. |
copper ion import Gene SetFrom GO Biological Process Annotations 2015 genes participating in the copper ion import biological process from the curated GO Biological Process Annotations 2015 dataset. |
copper ion homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the copper ion homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
detoxification of copper ion Gene SetFrom GO Biological Process Annotations 2015 genes participating in the detoxification of copper ion biological process from the curated GO Biological Process Annotations 2015 dataset. |
copper ion export Gene SetFrom GO Biological Process Annotations 2015 genes participating in the copper ion export biological process from the curated GO Biological Process Annotations 2015 dataset. |
response to copper ion Gene SetFrom GO Biological Process Annotations 2015 genes participating in the response to copper ion biological process from the curated GO Biological Process Annotations 2015 dataset. |
copper ion import into cell Gene SetFrom GO Biological Process Annotations 2015 genes participating in the copper ion import into cell biological process from the curated GO Biological Process Annotations 2015 dataset. |
cellular response to copper ion Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cellular response to copper ion biological process from the curated GO Biological Process Annotations 2015 dataset. |
cellular response to copper ion starvation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cellular response to copper ion starvation biological process from the curated GO Biological Process Annotations 2015 dataset. |
intracellular copper ion transport Gene SetFrom GO Biological Process Annotations 2015 genes participating in the intracellular copper ion transport biological process from the curated GO Biological Process Annotations 2015 dataset. |
plasma membrane copper ion transport Gene SetFrom GO Biological Process Annotations 2015 genes participating in the plasma membrane copper ion transport biological process from the curated GO Biological Process Annotations 2015 dataset. |
copper ion transmembrane transport Gene SetFrom GO Biological Process Annotations 2015 genes participating in the copper ion transmembrane transport biological process from the curated GO Biological Process Annotations 2015 dataset. |
copper ion transmembrane transporter activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the copper ion transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
copper ion binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the copper ion binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
copper uptake transmembrane transporter activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the copper uptake transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
heme-copper terminal oxidase activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the heme-copper terminal oxidase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
copper chaperone activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the copper chaperone activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
copper-transporting atpase activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the copper-transporting atpase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
copper-dependent protein binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the copper-dependent protein binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
superoxide dismutase copper chaperone activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the superoxide dismutase copper chaperone activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
copper-exporting atpase activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the copper-exporting atpase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
abnormality of copper homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of copper homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
Copper Gene SetFrom HMDB Metabolites of Enzymes interacting proteins for the Copper metabolite from the curated HMDB Metabolites of Enzymes dataset. |
abnormality of copper homeostasis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of copper homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
high nonceruloplasmin-bound serum copper Gene SetFrom HPO Gene-Disease Associations genes associated with the high nonceruloplasmin-bound serum copper phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Copper amine oxidase, N2/N3-terminal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Copper amine oxidase, N2/N3-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Cytochrome c oxidase copper chaperone Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Cytochrome c oxidase copper chaperone protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Copper centre Cu(A) Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Copper centre Cu(A) protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Copper type II, ascorbate-dependent monooxygenase, histidine-cluster-2 conserved site Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Copper type II, ascorbate-dependent monooxygenase, histidine-cluster-2 conserved site 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. |
Copper homeostasis protein CutC Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Copper homeostasis protein CutC protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Uncharacterised domain, di-copper centre Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Uncharacterised domain, di-copper centre protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Copper chaperone SCO1/SenC Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Copper chaperone SCO1/SenC protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Copper type II, ascorbate-dependent monooxygenase-like, C-terminal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Copper type II, ascorbate-dependent monooxygenase-like, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Copper amine oxidase, N-terminal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Copper amine oxidase, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Copper type II, ascorbate-dependent monooxygenase, histidine-cluster-1 conserved site Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Copper type II, ascorbate-dependent monooxygenase, histidine-cluster-1 conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Tyrosinase copper-binding domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Tyrosinase copper-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ctr copper transporter Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ctr copper transporter protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Superoxide dismutase, copper/zinc, binding site Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Superoxide dismutase, copper/zinc, binding site protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Superoxide dismutase, copper/zinc binding domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Superoxide dismutase, copper/zinc binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Heavy metal-associated domain, copper ion-binding Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Heavy metal-associated domain, copper ion-binding protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Amyloidogenic glycoprotein, copper-binding Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Amyloidogenic glycoprotein, copper-binding protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Copper amine oxidase Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Copper amine oxidase protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Periplasmic copper-binding protein NosD, beta helix domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Periplasmic copper-binding protein NosD, beta helix domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Copper amine oxidase, N2-terminal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Copper amine oxidase, N2-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Copper type II, ascorbate-dependent monooxygenase, N-terminal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Copper type II, ascorbate-dependent monooxygenase, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Copper amine oxidase, C-terminal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Copper amine oxidase, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Copper amine oxidase, N3-terminal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Copper amine oxidase, N3-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Multicopper oxidase, copper-binding site Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Multicopper oxidase, copper-binding site protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Multi-copper polyphenol oxidoreductase, laccase Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Multi-copper polyphenol oxidoreductase, laccase protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Copper homeostasis CutC domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Copper homeostasis CutC domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Cytochrome c oxidase, subunit I, copper-binding site Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Cytochrome c oxidase, subunit I, copper-binding site protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Copper-Overload Cirrhosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Copper-Overload Cirrhosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Copper Toxicosis, Idiopathic Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Copper Toxicosis, Idiopathic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abnormality Of Copper Homeostasis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Copper Homeostasis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
High Nonceruloplasmin-Bound Serum Copper Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype High Nonceruloplasmin-Bound Serum Copper in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Copper Accumulation In Liver Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Copper Accumulation In Liver in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Decreased Urinary Copper Concentration Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Decreased Urinary Copper Concentration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
copper ion transport Gene SetFrom GO Biological Process Annotations 2023 genes participating in the copper ion transport biological process from the curated GO Biological Process Annotations 2023 dataset. |
protein maturation by copper ion transfer Gene SetFrom GO Biological Process Annotations 2023 genes participating in the protein maturation by copper ion transfer biological process from the curated GO Biological Process Annotations 2023 dataset. |
copper ion import Gene SetFrom GO Biological Process Annotations 2023 genes participating in the copper ion import biological process from the curated GO Biological Process Annotations 2023 dataset. |
plasma membrane copper ion transport Gene SetFrom GO Biological Process Annotations 2023 genes participating in the plasma membrane copper ion transport biological process from the curated GO Biological Process Annotations 2023 dataset. |
intracellular copper ion homeostasis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the intracellular copper ion homeostasis biological process from the curated GO Biological Process Annotations 2023 dataset. |
response to copper ion Gene SetFrom GO Biological Process Annotations 2023 genes participating in the response to copper ion biological process from the curated GO Biological Process Annotations 2023 dataset. |
cellular response to copper ion Gene SetFrom GO Biological Process Annotations 2023 genes participating in the cellular response to copper ion biological process from the curated GO Biological Process Annotations 2023 dataset. |
cellular response to copper ion starvation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the cellular response to copper ion starvation biological process from the curated GO Biological Process Annotations 2023 dataset. |
copper ion homeostasis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the copper ion homeostasis biological process from the curated GO Biological Process Annotations 2023 dataset. |
copper ion export Gene SetFrom GO Biological Process Annotations 2023 genes participating in the copper ion export biological process from the curated GO Biological Process Annotations 2023 dataset. |
copper ion transmembrane transport Gene SetFrom GO Biological Process Annotations 2023 genes participating in the copper ion transmembrane transport biological process from the curated GO Biological Process Annotations 2023 dataset. |
response to copper ion starvation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the response to copper ion starvation biological process from the curated GO Biological Process Annotations 2023 dataset. |
copper ion binding Gene SetFrom GO Molecular Function Annotations 2023 genes performing the copper ion binding molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
copper ion transmembrane transporter activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the copper ion transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
P-type divalent copper transporter activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the P-type divalent copper transporter activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
superoxide dismutase copper chaperone activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the superoxide dismutase copper chaperone activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
P-type monovalent copper transporter activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the P-type monovalent copper transporter activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
Copper homeostasis Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Copper homeostasis pathway from the WikiPathways Pathways 2024 dataset. |
Copper metabolism Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Copper metabolism pathway from the WikiPathways Pathways 2024 dataset. |
copper ion transport Gene SetFrom GO Biological Process Annotations 2025 genes participating in the copper ion transport biological process from the curated GO Biological Process Annotations 2025 dataset. |
copper ion import Gene SetFrom GO Biological Process Annotations 2025 genes participating in the copper ion import biological process from the curated GO Biological Process Annotations 2025 dataset. |
plasma membrane copper ion transport Gene SetFrom GO Biological Process Annotations 2025 genes participating in the plasma membrane copper ion transport biological process from the curated GO Biological Process Annotations 2025 dataset. |
intracellular copper ion homeostasis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the intracellular copper ion homeostasis biological process from the curated GO Biological Process Annotations 2025 dataset. |
response to copper ion Gene SetFrom GO Biological Process Annotations 2025 genes participating in the response to copper ion biological process from the curated GO Biological Process Annotations 2025 dataset. |
cellular response to copper ion Gene SetFrom GO Biological Process Annotations 2025 genes participating in the cellular response to copper ion biological process from the curated GO Biological Process Annotations 2025 dataset. |
copper ion homeostasis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the copper ion homeostasis biological process from the curated GO Biological Process Annotations 2025 dataset. |
copper ion export Gene SetFrom GO Biological Process Annotations 2025 genes participating in the copper ion export biological process from the curated GO Biological Process Annotations 2025 dataset. |
copper ion transmembrane transport Gene SetFrom GO Biological Process Annotations 2025 genes participating in the copper ion transmembrane transport biological process from the curated GO Biological Process Annotations 2025 dataset. |
copper ion binding Gene SetFrom GO Molecular Function Annotations 2025 genes performing the copper ion binding molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
copper ion transmembrane transporter activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the copper ion transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
P-type divalent copper transporter activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the P-type divalent copper transporter activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
superoxide dismutase copper chaperone activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the superoxide dismutase copper chaperone activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
P-type monovalent copper transporter activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the P-type monovalent copper transporter activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
Copper deficiency myelopathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Copper deficiency myelopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Copper ion transmembrane transporter complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Copper ion transmembrane transporter complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Superoxide dismutase copper chaperone complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Superoxide dismutase copper chaperone complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Copper levels Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Copper levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 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 brain white matter morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal brain white matter morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal brain meninges morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal brain meninges morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal brain wave pattern Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal brain wave pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal brain ventricular system morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal brain ventricular system morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal brain ventricle size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal brain ventricle size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal blood-brain barrier function Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal blood-brain barrier function phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal brain weight Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal brain weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal brain ependyma motile cilium morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal brain ependyma motile cilium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal brain ependyma morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal brain ependyma morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal brain vasculature morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal brain vasculature morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal brain size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal brain size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal brain pia mater morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal brain pia mater morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal brain ventricle morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal brain ventricle morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal brain ependyma motile cilium physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal brain ependyma motile cilium physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal brain commissure morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal brain commissure morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal brain morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal brain morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal brain interneuron morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal brain interneuron morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal brain internal capsule morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal brain internal capsule morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal brain dura mater morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal brain dura mater morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
Abnormal Brain Fdg Positron Emission Tomography Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abnormal Brain Fdg Positron Emission Tomography in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abnormal Metabolic Brain Imaging By Mrs Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Metabolic Brain Imaging By Mrs in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
abnormal brain development Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal brain development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal brain morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal brain morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal brain commissure morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal brain commissure morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal brain ventricular system morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal brain ventricular system morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal brain ependyma morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal brain ependyma morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal brain vasculature morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal brain vasculature morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal brain ventricle morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal brain ventricle morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal brain interneuron morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal brain interneuron morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal brain wave pattern Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal brain wave pattern phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal brain white matter morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal brain white matter morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal brain internal capsule morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal brain internal capsule morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal brain meninges morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal brain meninges morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal brain thrombosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal brain thrombosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal brain dura mater morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal brain dura mater morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal blood-brain barrier function Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal blood-brain barrier function phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal brain size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal brain size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal brain ependyma motile cilium morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal brain ependyma motile cilium morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal brain ependyma motile cilium physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal brain ependyma motile cilium physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal brain pia mater morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal brain pia mater morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal brain ependyma motile cilium location or orientation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal brain ependyma motile cilium location or orientation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal brain artery topology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal brain artery topology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal brain weight Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal brain weight phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal brain morphology Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the abnormal brain morphology phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
Abnormal brain morphology Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Abnormal brain morphology phenotype from the curated ClinVar Gene-Phenotype Associations 2025 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 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 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 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 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 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. |
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 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 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 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 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 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 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 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 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 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 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 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 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 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 blood gas level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal blood gas level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal catecholamine level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal catecholamine level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating estradiol level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating estradiol level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating glucagon level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating glucagon level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating pyruvate kinase level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating pyruvate kinase level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal thromboxane level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal thromboxane level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating prothrombin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating prothrombin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating sodium level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating sodium level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating magnesium level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating magnesium level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating transferrin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating transferrin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal acute phase protein level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal acute phase protein level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating interleukin-17 level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating interleukin-17 level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal urine bicarbonate level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal urine bicarbonate level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal liver zinc level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal liver zinc level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating atrial natriuretic factor level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating atrial natriuretic factor level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal transforming growth factor beta level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal transforming growth factor beta level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating interleukin-1 level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating interleukin-1 level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating corticosterone level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating corticosterone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal urine amino acid level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal urine amino acid level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating unsaturated transferrin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating unsaturated transferrin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating pituitary hormone level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating pituitary hormone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal urine protein level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal urine protein level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating aldosterone level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating aldosterone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal triglyceride level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal triglyceride level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal creatine level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal creatine level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating complement protein level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating complement protein level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating hormone level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating hormone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal vitamin b12 level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal vitamin b12 level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal igd level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal igd level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating triiodothyronine level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating triiodothyronine level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal testosterone level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal testosterone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal liver cholesterol level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal liver cholesterol level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal urine nucleotide level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal urine nucleotide level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal adiponectin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal adiponectin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating apolipoprotein e level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating apolipoprotein e level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating interleukin-18 level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating interleukin-18 level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal neopterin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal neopterin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal plant sterol level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal plant sterol level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal vitamin d level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal vitamin d level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating dihydrotestosterone level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating dihydrotestosterone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal leukotriene level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal leukotriene level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal immunoglobulin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal immunoglobulin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal erythrocyte potassium level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal erythrocyte potassium level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal urine insulin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal urine insulin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating interleukin-4 level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating interleukin-4 level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal level of surface class ii molecules Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal level of surface class ii molecules phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal insulin-like growth factor i level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal insulin-like growth factor i 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 iga level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal iga level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating antithrombin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating antithrombin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal igg2b level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal igg2b 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 circulating gonadotropin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating gonadotropin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating c-reactive protein level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating c-reactive protein level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal igg level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal igg level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal glycogen level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal glycogen level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating insulin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating insulin 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 circulating ketone body level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating ketone body level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating alkaline phosphatase level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating alkaline phosphatase level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal urine progesterone level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal urine progesterone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal free fatty acids level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal free fatty acids level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal urine deoxycorticosterone level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal urine deoxycorticosterone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal erythrocyte magnesium level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal erythrocyte magnesium level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal urine corticosterone level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal urine corticosterone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal igg2c level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal igg2c level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pituitary hormone level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pituitary hormone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating apolipoprotein level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating apolipoprotein level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal vitamin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal vitamin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal thyroid-stimulating hormone level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal thyroid-stimulating hormone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating interleukin-16 level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating interleukin-16 level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal carbon dioxide level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal carbon dioxide level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal alpha-fetoprotein level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal alpha-fetoprotein level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal urine catecholamine level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal urine catecholamine level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating ghrelin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating ghrelin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal phospholipid level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal phospholipid level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal sphingomyelin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal sphingomyelin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating lipoprotein level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating lipoprotein level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal urine hormone level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal urine hormone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating estrogen level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating estrogen level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal retinol level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal retinol level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating potassium level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating potassium level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating adrenaline level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating adrenaline level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating amylase level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating amylase level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal urine prostaglandin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal urine prostaglandin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating interleukin-2 level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating interleukin-2 level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating serum amyloid protein level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating serum amyloid protein level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating protein level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating protein level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating free fatty acids level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating free fatty acids level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal liver triglyceride level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal liver triglyceride level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating erythropoietin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating erythropoietin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cytokine level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cytokine level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal fatty acid level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal fatty acid level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal follicle stimulating hormone level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal follicle stimulating hormone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal urine nucleoside level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal urine nucleoside level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating phospholipid level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating phospholipid level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal level of surface class i molecules Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal level of surface class i molecules phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating gastrin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating gastrin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal vitamin c level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal vitamin c level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal igg1 level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal igg1 level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating interleukin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating interleukin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal collagen level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal collagen level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal urine nitrite level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal urine nitrite level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal urine calcium level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal urine calcium level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal platelet serotonin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal platelet serotonin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal glycosaminoglycan level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal glycosaminoglycan level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating parathyroid hormone level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating parathyroid hormone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal urine potassium level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal urine potassium 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 igg2a level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal igg2a level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating mineral level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating mineral level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal platelet adp level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal platelet adp level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal fat-soluble vitamin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal fat-soluble vitamin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal haptoglobin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal haptoglobin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating vldl cholesterol level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating vldl cholesterol level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal thiamin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal thiamin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating androgen level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating androgen level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal mineral level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal mineral level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating ferritin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating ferritin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating fibrinogen level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating fibrinogen level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating interferon-beta level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating interferon-beta level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal erythropoietin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal erythropoietin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal blood urea nitrogen level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal blood urea nitrogen level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal urine creatinine level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal urine creatinine level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating cytokine level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating cytokine level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal thyroxine level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal thyroxine level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal lactate dehydrogenase level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal lactate dehydrogenase level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating glucocorticoid level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating glucocorticoid level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating ldl cholesterol level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating ldl cholesterol level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal urine uric acid level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal urine uric acid level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating interleukin-3 level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating interleukin-3 level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal vitamin a level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal vitamin a level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cholesterol level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cholesterol level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal neurotransmitter level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal neurotransmitter level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal somatostatin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal somatostatin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating triglyceride level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating triglyceride level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal apolipoprotein level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal apolipoprotein level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating interleukin-13 level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating interleukin-13 level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating hdl cholesterol level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating hdl cholesterol level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal serotonin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal serotonin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal thyroid hormone level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal thyroid hormone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal urine sulfate level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal urine sulfate level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating ammonia level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating ammonia level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal blood uric acid level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal blood uric acid level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal aldosterone level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal aldosterone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating non-hdl cholesterol level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating non-hdl cholesterol level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating factor ix level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating factor ix level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating bicarbonate level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating bicarbonate level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal luteinizing hormone level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal luteinizing hormone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal liver glycogen level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal liver glycogen level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating lactate level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating lactate level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating creatine kinase level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating creatine kinase level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating creatinine level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating creatinine level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal chloride level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal chloride level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating interleukin-6 level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating interleukin-6 level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating interleukin-10 level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating interleukin-10 level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal urine phosphate level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal urine phosphate level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal corticosterone level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal corticosterone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating bilirubin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating bilirubin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating phosphate level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating phosphate level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal noradrenaline level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal noradrenaline level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal urine chloride ion level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal urine chloride ion 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 igg3 level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal igg3 level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal chemokine level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal chemokine 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 circulating interferon level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating interferon level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating glucose level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating glucose level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating calcium level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating calcium level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal urine urea nitrogen level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal urine urea nitrogen level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating total protein level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating total protein level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal urine glucose level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal urine glucose level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal urine organic anion level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal urine organic anion level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal adrenaline level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal adrenaline level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating serum albumin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating serum albumin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating creatine level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating creatine level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal porphyrin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal porphyrin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal platelet calcium level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal platelet calcium level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating testosterone level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating testosterone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating carnitine level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating carnitine level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal enzyme/ coenzyme level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal enzyme/ coenzyme level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal lipoprotein level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal lipoprotein level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal urine sodium level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal urine sodium level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal tumor necrosis factor level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal tumor necrosis factor level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal glycosylated hemoglobin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal glycosylated hemoglobin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating homocysteine level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating homocysteine level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating lipase level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating lipase level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal prolactin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal prolactin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal lipid level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal lipid level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating mineralocorticoid level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating mineralocorticoid level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating interferon-gamma level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating interferon-gamma level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal glycerol level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal glycerol level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal interferon level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal interferon level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating fructosamine level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating fructosamine level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal urine ammonia level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal urine ammonia level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal prostaglandin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal prostaglandin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal growth hormone level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal growth hormone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hormone level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hormone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal creatine kinase level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal creatine kinase level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating renin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating renin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pancreas iron level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pancreas iron level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal folic acid level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal folic acid level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating amino acid level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating amino acid level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating interleukin-1 beta level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating interleukin-1 beta level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating glutamate dehydrogenase level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating glutamate dehydrogenase level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating interleukin-12 level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating interleukin-12 level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal selenium level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal selenium level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating aspartate transaminase level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating aspartate transaminase level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal dopamine level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal dopamine level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal intercellular signaling peptide or protein level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal intercellular signaling peptide or protein level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating interferon-alpha level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating interferon-alpha level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating osteocalcin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating osteocalcin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal biopterin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal biopterin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal glutathione level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal glutathione level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal urine glycosaminoglycan level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal urine glycosaminoglycan level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal sterol level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal sterol level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal igm level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal igm level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal protein level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal protein level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating interleukin-5 level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating interleukin-5 level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal urine magnesium level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal urine magnesium level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating alanine transaminase level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating alanine transaminase level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal adrenocorticotropin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal adrenocorticotropin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating enzyme level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating enzyme level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal amino acid level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal amino acid level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating interleukin-12b level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating interleukin-12b level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating interleukin-9 level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating interleukin-9 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 fasted circulating glucose level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal fasted circulating glucose level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating tumor necrosis factor level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating tumor necrosis factor level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating noradrenaline level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating noradrenaline level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal ige level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal ige level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal urine enzyme level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal urine enzyme level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal progesterone level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal progesterone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal vitamin e level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal vitamin e level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating progesterone level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating progesterone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating chloride level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating chloride level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating factor viii level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating factor viii level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal complement protein level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal complement protein level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal sphingolipid level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal sphingolipid level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal ceramide level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal ceramide level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating lipid level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating lipid level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal bile salt level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal bile salt level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal interleukin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal interleukin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating cholesterol level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating cholesterol level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating plant sterol level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating plant sterol level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating glycerol level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating glycerol level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal platelet atp level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal platelet atp level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating thyroxine level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating thyroxine level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating leptin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating leptin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating antidiuretic hormone level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating antidiuretic hormone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating insulin-like growth factor i level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating insulin-like growth factor i level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal oxygen level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal oxygen level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
Abnormal C-Peptide Level Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal C-Peptide Level in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormal Circulating Insulin Level Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Circulating Insulin Level in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormal Apolipoprotein Level Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Apolipoprotein Level in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormal Aldolase Level Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Aldolase Level in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormal Serum Interleukin Level Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Serum Interleukin Level in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormal Vitamin B12 Level Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Vitamin B12 Level in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormal Immunoglobulin Level Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Immunoglobulin Level in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormal Circulating Follicle-Stimulating Hormone Level Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Circulating Follicle-Stimulating Hormone Level in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormal Prolactin Level Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Prolactin Level in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Serum Testosterone Level Abnormal Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Serum Testosterone Level Abnormal in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormal B-Type Natriuretic Peptide Level Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal B-Type Natriuretic Peptide Level in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormal Serum Interferon-Gamma Level Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Serum Interferon-Gamma Level in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormal Albumin Level Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Albumin Level in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormal Serum Dehydroepiandrosterone Level Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Serum Dehydroepiandrosterone Level in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormal Thyroid Hormone Level Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Thyroid Hormone Level in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
abnormal noradrenaline level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal noradrenaline level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hormone level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hormone level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal lipid level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal lipid level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating HDL cholesterol level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating HDL cholesterol level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal cholesterol level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cholesterol level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating cholesterol level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating cholesterol level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal iron level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal iron level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal protein level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal protein level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal vitamin E level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal vitamin E level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal fat-soluble vitamin level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal fat-soluble vitamin level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal vitamin D level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal vitamin D level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating amino acid level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating amino acid level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating LDL cholesterol level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating LDL cholesterol level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating free fatty acids level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating free fatty acids level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal enzyme/coenzyme level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal enzyme/coenzyme level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal thromboxane level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal thromboxane level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating glucose level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating glucose level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal bile salt level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal bile salt level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal amino acid level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal amino acid level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal immunoglobulin level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal immunoglobulin level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal tumor necrosis factor level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal tumor necrosis factor level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal thyroid hormone level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal thyroid hormone level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating enzyme level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating enzyme level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal phospholipid level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal phospholipid level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal level of surface class II molecules Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal level of surface class II molecules phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal corticosterone level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal corticosterone level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating pyruvate kinase level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating pyruvate kinase level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal chemokine level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal chemokine level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal interleukin level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal interleukin level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal cytokine level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cytokine level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal interferon level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal interferon level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal acute phase protein level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal acute phase protein level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating renin level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating renin level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating mineral level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating mineral level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating phospholipid level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating phospholipid level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal vitamin A level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal vitamin A level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal urine nucleoside level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal urine nucleoside level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating protein level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating protein level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal urine catecholamine level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal urine catecholamine level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal blood urea nitrogen level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal blood urea nitrogen level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating bilirubin level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating bilirubin level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating alanine transaminase level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating alanine transaminase level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating alkaline phosphatase level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating alkaline phosphatase level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating aspartate transaminase level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating aspartate transaminase level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal retinol level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal retinol level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal thyroid-stimulating hormone level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal thyroid-stimulating hormone level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal aldosterone level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal aldosterone level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal urine enzyme level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal urine enzyme level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating estrogen level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating estrogen level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal selenium level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal selenium level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating sodium level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating sodium level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating potassium level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating potassium level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating progesterone level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating progesterone level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal dopamine level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal dopamine level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating serum albumin level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating serum albumin level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal biopterin level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal biopterin level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal neopterin level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal neopterin level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal fatty acids level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal fatty acids level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal vitamin C level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal vitamin C level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating tumor necrosis factor level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating tumor necrosis factor level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal serotonin level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal serotonin level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal urine calcium level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal urine calcium level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal urine amino acid level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal urine amino acid level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating cytokine level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating cytokine level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal adrenaline level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal adrenaline level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal complement protein level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal complement protein level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal testosterone level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal testosterone level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal sphingolipid level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal sphingolipid level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating insulin-like growth factor I level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating insulin-like growth factor I level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal urine organic anion level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal urine organic anion level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating insulin level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating insulin level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal milk zinc level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal milk zinc level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal mineral level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal mineral level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating ketone body level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating ketone body level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal synaptic neurotransmitter level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal synaptic neurotransmitter level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal skeletal muscle triglyceride level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal skeletal muscle triglyceride level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating corticosterone level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating corticosterone level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating estradiol level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating estradiol level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal adrenocorticotropin level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal adrenocorticotropin level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal growth hormone level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal growth hormone level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal thyroxine level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal thyroxine level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal triiodothyronine level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal triiodothyronine level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating lipid level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating lipid level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal prostaglandin level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal prostaglandin 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 circulating amylase level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating amylase level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating lipase level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating lipase level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal blood gas level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal blood gas level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal urine protein level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal urine protein level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating calcium level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating calcium level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating magnesium level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating magnesium level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating creatinine level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating creatinine level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating hormone level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating hormone level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal folic acid level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal folic acid level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating interferon level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating interferon level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal sphingomyelin level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal sphingomyelin level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal triglyceride level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal triglyceride level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal urine albumin level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal urine albumin level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating lipoprotein level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating lipoprotein level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal leukotriene level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal leukotriene level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating interleukin-6 level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating interleukin-6 level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating serum amyloid protein level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating serum amyloid protein level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating phosphate level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating phosphate level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal pituitary hormone level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal pituitary hormone level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating leptin level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating leptin level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating chemokine level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating chemokine level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating adrenaline level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating adrenaline level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating noradrenaline level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating noradrenaline level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating homocysteine level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating homocysteine level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal oxygen level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal oxygen level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal urine nucleotide level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal urine nucleotide level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal vitamin level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal vitamin level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal glycogen level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal glycogen level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal level of surface class I molecules Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal level of surface class I molecules phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal bradykinin level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal bradykinin level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating hyaluronic acid level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating hyaluronic acid level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating apolipoprotein level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating apolipoprotein level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating triiodothyronine level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating triiodothyronine level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating interferon-gamma level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating interferon-gamma level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating pancreatic peptide level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating pancreatic peptide level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal glycerol level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal glycerol level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal carbon dioxide level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal carbon dioxide level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating testosterone level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating testosterone level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating antidiuretic hormone level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating antidiuretic hormone level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating interleukin level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating interleukin 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 complement protein level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating complement protein level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating triglyceride level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating triglyceride level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal ceramide level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal ceramide level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal galactolipid level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal galactolipid level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating ghrelin level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating ghrelin level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal insulin-like growth factor I level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal insulin-like growth factor I level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating pituitary hormone level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating pituitary hormone level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating interferon-beta level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating interferon-beta level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating interleukin-1 beta level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating interleukin-1 beta level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating interleukin-10 level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating interleukin-10 level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating interleukin-4 level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating interleukin-4 level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal luteinizing hormone level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal luteinizing hormone level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal urine organic cation level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal urine organic cation level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal urine sodium level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal urine sodium level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal urine urea nitrogen level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal urine urea nitrogen level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal follicle stimulating hormone level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal follicle stimulating hormone level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal glycosaminoglycan level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal glycosaminoglycan level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal free fatty acids level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal free fatty acids level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal thiamin level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal thiamin level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal liver zinc level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal liver zinc level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal milk calcium level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal milk calcium level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal milk phosphate level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal milk phosphate level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal progesterone level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal progesterone level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating interleukin-5 level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating interleukin-5 level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal somatostatin level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal somatostatin level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal ganglioside level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal ganglioside level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating histamine level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating histamine level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating angiotensinogen level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating angiotensinogen level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating interleukin-12b level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating interleukin-12b level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal urine potassium level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal urine potassium level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating apolipoprotein E level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating apolipoprotein E level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating adiponectin level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating adiponectin level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal vitamin B12 level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal vitamin B12 level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating gonadotropin level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating gonadotropin level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal apolipoprotein level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal apolipoprotein level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal IgG level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal IgG level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal IgG1 level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal IgG1 level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal IgG2 level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal IgG2 level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal lipoprotein level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal lipoprotein level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal glycosphingolipid level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal glycosphingolipid level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal muscle glycogen level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal muscle glycogen level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal fasting circulating glucose level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal fasting circulating glucose level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating unsaturated transferrin level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating unsaturated transferrin level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal collagen level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal collagen level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal catecholamine level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal catecholamine level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal manganese level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal manganese level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal chloride level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal chloride level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal liver triglyceride level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal liver triglyceride level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal IgM level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal IgM level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal zinc level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal zinc level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal glutamic acid level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal glutamic acid level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating non-HDL cholesterol level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating non-HDL cholesterol level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal nervous system dopamine level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal nervous system dopamine level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal ether lipid level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal ether lipid level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating androgen level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating androgen level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal calcium level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal calcium level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal sulfate level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal sulfate level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal blood uric acid level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal blood uric acid level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating creatine kinase level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating creatine kinase level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating glucose level Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the abnormal circulating glucose level phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
abnormal blood urea nitrogen level Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the abnormal blood urea nitrogen level phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
abnormal circulating phosphate level Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the abnormal circulating phosphate level phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
abnormal circulating iron level Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the abnormal circulating iron level phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
abnormal blood uric acid level Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the abnormal blood uric acid level phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
abnormal circulating alkaline phosphatase level Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the abnormal circulating alkaline phosphatase level phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
abnormal circulating calcium level Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the abnormal circulating calcium level phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
abnormal circulating LDL cholesterol level Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the abnormal circulating LDL cholesterol level phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
Brain stem Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Brain stem relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles 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. |
Brain small vessel disease with hemorrhage Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Brain small vessel disease with hemorrhage phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hemorrhagic destruction of the brain, subependymal calcification, and cataracts Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hemorrhagic destruction of the brain, subependymal calcification, and cataracts phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A7 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A6 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A8 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A8 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. |
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A14 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Muscle eye brain disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Muscle eye brain disease 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. |
Cortical dysplasia, complex, with other brain malformations 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cortical dysplasia, complex, with other brain malformations 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cortical dysplasia, complex, with other brain malformations 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cortical dysplasia, complex, with other brain malformations 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cortical dysplasia, complex, with other brain malformations 6 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cortical dysplasia, complex, with other brain malformations 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cortical dysplasia, complex, with other brain malformations 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cortical dysplasia, complex, with other brain malformations 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cortical dysplasia, complex, with other brain malformations 5 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cortical dysplasia, complex, with other brain malformations 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microcephaly, postnatal progressive, with seizures and brain atrophy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, postnatal progressive, with seizures and brain atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Kir4.1-alpha-1-syntrophin complex, whole brain lysate Gene Setproteins in the Kir4.1-alpha-1-syntrophin complex, whole brain lysate protein complex from the CORUM Protein Complexes dataset. |
Kir4.1-dystrophin complex, whole brain lysate Gene Setproteins in the Kir4.1-dystrophin complex, whole brain lysate protein complex from the CORUM Protein Complexes dataset. |
PS1-E-cadherin-catenin complex, brain Gene Setproteins in the PS1-E-cadherin-catenin complex, brain protein complex from the CORUM Protein Complexes dataset. |
Brain-derived dystrobrevin-syntrophin complex Gene Setproteins in the Brain-derived dystrobrevin-syntrophin complex protein complex from the CORUM Protein Complexes dataset. |
Kir4.1-beta-dystroglycan complex, whole brain lysate Gene Setproteins in the Kir4.1-beta-dystroglycan complex, whole brain lysate protein complex from the CORUM Protein Complexes dataset. |
Pick Disease of the Brain Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Pick Disease of the Brain from the curated CTD Gene-Disease Associations dataset. |
Hypoxia, Brain Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hypoxia, Brain from the curated CTD Gene-Disease Associations dataset. |
Hypoxia-Ischemia, Brain Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hypoxia-Ischemia, Brain from the curated CTD Gene-Disease Associations dataset. |
Brain Stem Infarctions Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Brain Stem Infarctions from the curated CTD Gene-Disease Associations dataset. |
Brain Edema Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Brain Edema from the curated CTD Gene-Disease Associations dataset. |
MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY from the curated CTD Gene-Disease Associations dataset. |
Brain Infarction Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Brain Infarction from the curated CTD Gene-Disease Associations dataset. |
PROSTATE CANCER/BRAIN CANCER SUSCEPTIBILITY Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease PROSTATE CANCER/BRAIN CANCER SUSCEPTIBILITY from the curated CTD Gene-Disease Associations dataset. |
Brain Stem Neoplasms Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Brain Stem Neoplasms from the curated CTD Gene-Disease Associations dataset. |
Brain Neoplasms Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Brain Neoplasms 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. |
Brain Small Vessel Disease with Hemorrhage Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Brain Small Vessel Disease with Hemorrhage from the curated CTD Gene-Disease Associations dataset. |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 2 from the curated CTD Gene-Disease Associations dataset. |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 6 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 6 from the curated CTD Gene-Disease Associations dataset. |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5 from the curated CTD Gene-Disease Associations dataset. |
Brain Damage, Chronic Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Brain Damage, Chronic from the curated CTD Gene-Disease Associations dataset. |
Brain Ischemia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Brain Ischemia from the curated CTD Gene-Disease Associations dataset. |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4 from the curated CTD Gene-Disease Associations dataset. |
Brain Diseases Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Brain Diseases from the curated CTD Gene-Disease Associations dataset. |
Brain Injuries Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Brain Injuries from the curated CTD Gene-Disease Associations dataset. |
Brain Diseases, Metabolic Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Brain Diseases, Metabolic from the curated CTD Gene-Disease Associations dataset. |
Brain Abscess Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Brain Abscess from the curated CTD Gene-Disease Associations dataset. |
HEMORRHAGIC DESTRUCTION OF THE BRAIN, SUBEPENDYMAL CALCIFICATION, AND CATARACTS Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease HEMORRHAGIC DESTRUCTION OF THE BRAIN, SUBEPENDYMAL CALCIFICATION, AND CATARACTS 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. |
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. |
Brain Diseases, Metabolic, Inborn Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Brain Diseases, Metabolic, Inborn from the curated CTD Gene-Disease Associations dataset. |
Brain Mapping Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Brain Mapping in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
Natriuretic Peptide, Brain Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Natriuretic Peptide, Brain in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
Brain Waves Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Brain Waves in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
Brain Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Brain in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
brain disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease brain disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
brain infarction Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease brain infarction in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
brain cancer Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease brain cancer in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
brain disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease brain disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
brain stem infarction Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease brain stem infarction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
brain stem astrocytic neoplasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease brain stem astrocytic neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
brain ischemia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease brain ischemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
brain glioblastoma multiforme Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease brain glioblastoma multiforme in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
brain glioma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease brain glioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
brain germinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease brain germinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
brain stem cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease brain stem cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
brain stem glioma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease brain stem glioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
brain ependymoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease brain ependymoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
brain compression Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease brain compression in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
brain edema Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease brain edema in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
brain oligodendroglioma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease brain oligodendroglioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
brain disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease brain disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
brain angioma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease brain angioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
brain infarction Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease brain infarction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
brain meningioma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease brain meningioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
brain cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease brain cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
brain sarcoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease brain sarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
brain injuries; dementia, vascular; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain injuries; dementia, vascular; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain neoplasms; chromosome aberrations; chromosome abnormality; glioma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain neoplasms; chromosome aberrations; chromosome abnormality; glioma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain morphology Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain morphology in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain neoplasms; meningioma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain neoplasms; meningioma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
astrocytoma; brain neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease astrocytoma; brain neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain neoplasms; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain neoplasms; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain tumors Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain tumors in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anoxia; brain injuries; hypotension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anoxia; brain injuries; hypotension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
astrocytoma; brain neoplasms; neoplasm invasiveness Gene SetFrom GAD Gene-Disease Associations genes associated with the disease astrocytoma; brain neoplasms; neoplasm invasiveness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain neoplasms; cerebellar neoplasms; ganglioglioma; glioma; medulloblastoma; neuroectodermal tumor, primitive; neuroectodermal tumors, primitive Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain neoplasms; cerebellar neoplasms; ganglioglioma; glioma; medulloblastoma; neuroectodermal tumor, primitive; neuroectodermal tumors, primitive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
astrocytoma; brain neoplasms; glioblastoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease astrocytoma; brain neoplasms; glioblastoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain ischemia; foramen ovale, patent; stroke; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain ischemia; foramen ovale, patent; stroke; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain injuries Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; brain ischemia; sinus thrombosis, intracranial; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; sinus thrombosis, intracranial; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain ischemia; recurrence; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain ischemia; recurrence; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain neoplasms; breast neoplasms; laryngeal neoplasm; laryngeal neoplasms; mammary neoplasms; neoplasms; thyroid neoplasm; thyroid neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain neoplasms; breast neoplasms; laryngeal neoplasm; laryngeal neoplasms; mammary neoplasms; neoplasms; thyroid neoplasm; thyroid neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain ischemia; heart diseases; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain ischemia; heart diseases; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; stroke, lacunar; atherothrombotic brain infarction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; stroke, lacunar; atherothrombotic brain infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
traumatic brain imjury Gene SetFrom GAD Gene-Disease Associations genes associated with the disease traumatic brain imjury in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain lesion load Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain lesion load in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain neoplasms; glioma; oligodendroglioma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain neoplasms; glioma; oligodendroglioma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain ischemia; intracranial arteriosclerosis; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain ischemia; intracranial arteriosclerosis; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arteriosclerosis; brain ischemia; carotid artery diseases; cerebrovascular disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arteriosclerosis; brain ischemia; carotid artery diseases; cerebrovascular disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atherosclerosis; brain infarction; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atherosclerosis; brain infarction; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain ischemia; hypertension; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain ischemia; hypertension; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
astrocytoma; brain neoplasms; oligodendroglioma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease astrocytoma; brain neoplasms; oligodendroglioma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain ischemia; inflammation Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain ischemia; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain ischemia; cerebrovascular disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain ischemia; cerebrovascular disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
astrocytoma; brain neoplasms; meningeal neoplasms; meningioma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease astrocytoma; brain neoplasms; meningeal neoplasms; meningioma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
traumatic brain injury. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease traumatic brain injury. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain ischemia; hyperhomocysteinemia; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain ischemia; hyperhomocysteinemia; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; atherosclerosis; brain ischemia; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; atherosclerosis; brain ischemia; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; brain infarction; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; brain infarction; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; brain ischemia; coronary disease; coronary heart disease; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; coronary disease; coronary heart disease; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; brain ischemia; carotid artery stenosis; carotid stenosis; infarction, middle cerebral artery; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; carotid artery stenosis; carotid stenosis; infarction, middle cerebral artery; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; brain ischemia; cerebral hemorrhage; cerebral hemorrhages; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; cerebral hemorrhage; cerebral hemorrhages; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain activity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain activity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain damage, chronic; hypertension; myocardial ischemia; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain damage, chronic; hypertension; myocardial ischemia; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain ischemia; inflammation; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain ischemia; inflammation; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; brain ischemia; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
myocardial infarct; brain infarction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease myocardial infarct; brain infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain ischemia; carotid stenosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain ischemia; carotid stenosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain atrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; brain ischemia; stroke; thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; stroke; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain ischemia; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain ischemia; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain receptor-binding characteristics Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain receptor-binding characteristics in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain aging Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain aging in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrial fibrillation; brain ischemia; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrial fibrillation; brain ischemia; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain ischemia; intracranial arteriosclerosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain ischemia; intracranial arteriosclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain neoplasms; kidney diseases; leukemia; neurotoxicity syndromes Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain neoplasms; kidney diseases; leukemia; neurotoxicity syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; brain ischemia; carotid artery diseases; hemochromatosis; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; carotid artery diseases; hemochromatosis; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; brain ischemia; diabetes complications; hypertension; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; diabetes complications; hypertension; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain ischemia; intracranial thrombosis; ischemic attack, transient; migraine disorders; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain ischemia; intracranial thrombosis; ischemic attack, transient; migraine disorders; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain infarction; hyperhomocysteinemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain infarction; hyperhomocysteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain ischemia; diabetes mellitus; hemiplegia; hypercholesterolemia; hypertension; obesity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain ischemia; diabetes mellitus; hemiplegia; hypercholesterolemia; hypertension; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain ischemia; stroke; vascular diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain ischemia; stroke; vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain tumor Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain tumor in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain ischemia; hypertension; osteoporosis; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain ischemia; hypertension; osteoporosis; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain ischemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain ischemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
amphetamine-related disorders; brain diseases, metabolic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease amphetamine-related disorders; brain diseases, metabolic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fetal diseases; hypoxia-ischemia, brain; infant, newborn, diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fetal diseases; hypoxia-ischemia, brain; infant, newborn, diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain neoplasms; hemangioma, cavernous, central nervous system Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain neoplasms; hemangioma, cavernous, central nervous system in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain injuries; hypopituitarism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain injuries; hypopituitarism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; brain infarction; recurrence; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; brain infarction; recurrence; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anemia; brain death Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anemia; brain death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
myocardial infarction; brain infarction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease myocardial infarction; brain infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain lesions or calcifications Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain lesions or calcifications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain ischemia; intracranial arterial diseases; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain ischemia; intracranial arterial diseases; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; atrial septal defects; brain ischemia; diabetes mellitus; heart septal defects, atrial; hypertension; intracranial thrombosis; ischemic attack, transient; stroke; transient ischemic attack Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; atrial septal defects; brain ischemia; diabetes mellitus; heart septal defects, atrial; hypertension; intracranial thrombosis; ischemic attack, transient; stroke; transient ischemic attack in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypoxia-ischemia, brain; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypoxia-ischemia, brain; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain injuries; nerve degeneration Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain injuries; nerve degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain ischemia; carotid artery diseases; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain ischemia; carotid artery diseases; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer's disease; abeta load in brain Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer's disease; abeta load in brain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain hemorrhage Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain injuries; fatigue; sleep disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain injuries; fatigue; sleep disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain ischemia; subarachnoid hemorrhage Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain ischemia; subarachnoid hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrial fibrillation; brain ischemia; coronary thrombosis; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrial fibrillation; brain ischemia; coronary thrombosis; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
astrocytoma; brain neoplasms; ependymoma; glioma; neoplasm metastasis; oligodendroglioma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease astrocytoma; brain neoplasms; ependymoma; glioma; neoplasm metastasis; oligodendroglioma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain ischemia; stroke; thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain ischemia; stroke; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; arterial occlusive diseases; atherosclerosis; brain ischemia; carotid artery diseases; embolism; ischemic attack, transient; stroke; transient ischemic attack Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; arterial occlusive diseases; atherosclerosis; brain ischemia; carotid artery diseases; embolism; ischemic attack, transient; stroke; transient ischemic attack in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain injuries; wounds, penetrating Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain injuries; wounds, penetrating in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; brain ischemia; cardiovascular diseases; coronary disease; coronary heart disease; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; cardiovascular diseases; coronary disease; coronary heart disease; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain ischemia; carotid artery diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain ischemia; carotid artery diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aphasia; brain ischemia; cardiovascular diseases; cerebral hemorrhage; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aphasia; brain ischemia; cardiovascular diseases; cerebral hemorrhage; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain ischemia; myocardial infarction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain ischemia; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain imaging Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain imaging in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain ischemia; coronary disease; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain ischemia; coronary disease; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain aneurysm Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain aneurysm in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
asthma; brain neoplasms; eczema; glioma; hay fever; hypersensitivity; rhinitis, allergic, seasonal Gene SetFrom GAD Gene-Disease Associations genes associated with the disease asthma; brain neoplasms; eczema; glioma; hay fever; hypersensitivity; rhinitis, allergic, seasonal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain infarction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain ischemia; diabetes mellitus; intracranial arteriosclerosis; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain ischemia; diabetes mellitus; intracranial arteriosclerosis; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain infarction; cerebral arterial diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain infarction; cerebral arterial diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain ischemia; hyperlipidemias; hypertension; intracranial arteriosclerosis; obesity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain ischemia; hyperlipidemias; hypertension; intracranial arteriosclerosis; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain function Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain function in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain ischemia; myocardial ischemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain ischemia; myocardial ischemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain ischemia; hyperhomocysteinemia; intracranial arterial diseases; sinus thrombosis, intracranial; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain ischemia; hyperhomocysteinemia; intracranial arterial diseases; sinus thrombosis, intracranial; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; brain ischemia; cardiovascular diseases; myocardial infarction; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; cardiovascular diseases; myocardial infarction; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain ischemia; cerebral infarction; intracranial aneurysm; subarachnoid hemorrhage Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain ischemia; cerebral infarction; intracranial aneurysm; subarachnoid hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrophy; brain diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrophy; brain diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain ischemia; cerebral hemorrhage; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain ischemia; cerebral hemorrhage; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain neoplasms; glioblastoma; oligodendroglioma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain neoplasms; glioblastoma; oligodendroglioma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain ischemia; diabetes mellitus; hyperlipidemias; myocardial infarction; stroke; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain ischemia; diabetes mellitus; hyperlipidemias; myocardial infarction; stroke; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain mapping Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain mapping in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain injury, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain injury, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain infarction; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain infarction; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain injuries; intracranial hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain injuries; intracranial hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain ischemia; intracranial hemorrhages; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain ischemia; intracranial hemorrhages; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anoxia; asphyxia; brain ischemia; disease models, animal; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anoxia; asphyxia; brain ischemia; disease models, animal; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; hypoxia-ischemia, brain; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; hypoxia-ischemia, brain; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain hemorrhage; stroke, ischemic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain hemorrhage; stroke, ischemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain injuries; epilepsy, post-traumatic; seizures Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain injuries; epilepsy, post-traumatic; seizures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
amnesia; brain injuries Gene SetFrom GAD Gene-Disease Associations genes associated with the disease amnesia; brain injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
childhood brain tumors ; residential insecticide exposure Gene SetFrom GAD Gene-Disease Associations genes associated with the disease childhood brain tumors ; residential insecticide exposure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain ischemia; myocardial infarction; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain ischemia; myocardial infarction; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; brain ischemia; ischemic attack, transient; stroke; thrombosis; transient ischemic attack Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; ischemic attack, transient; stroke; thrombosis; transient ischemic attack in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain neoplasms; glioblastoma; neoplasm recurrence, local Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain neoplasms; glioblastoma; neoplasm recurrence, local in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain hemorrhage; cerebrovascular disease; thrombosis, deep vein Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain hemorrhage; cerebrovascular disease; thrombosis, deep vein in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain neoplasms; occupational diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain neoplasms; occupational diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain diseases; mental retardation, x-linked Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain diseases; mental retardation, x-linked in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adult brain tumors Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adult brain tumors in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain ischemia; cerebral arterial diseases; intracranial embolism; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain ischemia; cerebral arterial diseases; intracranial embolism; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain ischemia; dementia; myocardial infarction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain ischemia; dementia; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain infarction; inflammation Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain infarction; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain injuries; memory disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain injuries; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain ischemia; cerebral infarction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain ischemia; cerebral infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; brain ischemia; encephalitis; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; encephalitis; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; atrial fibrillation; brain ischemia; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; atrial fibrillation; brain ischemia; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
normalized brain volume, multiple sclerosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease normalized brain volume, multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aphasia; aphasia, nos; apoplexy; brain ischemia; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aphasia; aphasia, nos; apoplexy; brain ischemia; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain injuries; inflammation; postoperative complications Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain injuries; inflammation; postoperative complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain neoplasms; meningioma; nervous system neoplasms; neurilemmoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain neoplasms; meningioma; nervous system neoplasms; neurilemmoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; brain ischemia; inflammation; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; inflammation; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain neoplasms; oligodendroglioma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain neoplasms; oligodendroglioma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain ischemia; coronary disease; myocardial infarction; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain ischemia; coronary disease; myocardial infarction; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain ischemia; genetic predisposition to disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain ischemia; genetic predisposition to disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain ischemia; diabetes mellitus; genetic diseases, inborn; hypertension; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain ischemia; diabetes mellitus; genetic diseases, inborn; hypertension; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; brain ischemia; intracranial embolism and thrombosis; sinus thrombosis, intracranial; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; intracranial embolism and thrombosis; sinus thrombosis, intracranial; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; brain ischemia; carotid artery, internal, dissection; hyperhomocysteinemia; stroke; vertebral artery dissection Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; carotid artery, internal, dissection; hyperhomocysteinemia; stroke; vertebral artery dissection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain neoplasms; glioma; meningioma; neuroma, acoustic; neuromas, acoustic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain neoplasms; glioma; meningioma; neuroma, acoustic; neuromas, acoustic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain ischemia; dementia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain ischemia; dementia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain ischemia; cardiovascular diseases; carotid artery diseases; myocardial infarction; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain ischemia; cardiovascular diseases; carotid artery diseases; myocardial infarction; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain ischemia; intracranial hemorrhages; myocardial infarction; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain ischemia; intracranial hemorrhages; myocardial infarction; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
childhood brain tumor Gene SetFrom GAD Gene-Disease Associations genes associated with the disease childhood brain tumor in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain neoplasms; glioblastoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain neoplasms; glioblastoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; brain ischemia; cerebral infarction; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; cerebral infarction; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain neoplasms; glioma; neoplasm recurrence, local Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain neoplasms; glioma; neoplasm recurrence, local in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain ischemia; intracranial hemorrhages; myocardial infarction; stroke; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain ischemia; intracranial hemorrhages; myocardial infarction; stroke; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain ischemia; hemorrhage Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain ischemia; hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain ischemia; subarachnoid hemorrhage; vasospasm, intracranial Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain ischemia; subarachnoid hemorrhage; vasospasm, intracranial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain injuries; closed head injuries; head injuries, closed Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain injuries; closed head injuries; head injuries, closed in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain ischemia; ischemic attack, transient; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain ischemia; ischemic attack, transient; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain diseases; neurodegenerative diseases; supranuclear palsy, progressive Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain diseases; neurodegenerative diseases; supranuclear palsy, progressive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; brain ischemia; hypertension; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; hypertension; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
natriuretic peptide, brain Gene SetFrom GAD Gene-Disease Associations genes associated with the disease natriuretic peptide, brain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain ischemia; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain ischemia; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain neoplasms; glioma; meningeal neoplasms; meningioma; neuroma, acoustic; neuromas, acoustic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain neoplasms; glioma; meningeal neoplasms; meningioma; neuroma, acoustic; neuromas, acoustic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain neoplasms; glioma; meningeal neoplasms; meningioma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain neoplasms; glioma; meningeal neoplasms; meningioma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain infarction; cadasil; cerebral hemorrhage; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain infarction; cadasil; cerebral hemorrhage; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; brain ischemia; dementia, vascular; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; dementia, vascular; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain ischemia; giant cell arteritis; optic neuritis; temporal arteritis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain ischemia; giant cell arteritis; optic neuritis; temporal arteritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain electrical response Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain electrical response in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; brain infarction; cerebrovascular disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; brain infarction; cerebrovascular disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; brain ischemia; cerebral hemorrhage; cerebral hemorrhages; hypertension; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; cerebral hemorrhage; cerebral hemorrhages; hypertension; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain ischemia; cardiovascular diseases; coronary disease; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain ischemia; cardiovascular diseases; coronary disease; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain ischemia; thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain ischemia; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain ischemia; coronary artery disease; intracranial arteriosclerosis; myocardial infarction; stroke; vasculitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain ischemia; coronary artery disease; intracranial arteriosclerosis; myocardial infarction; stroke; vasculitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; brain ischemia; cerebrovascular accident; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; cerebrovascular accident; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; dementia; dementia, vascular; lewy body disease; pick disease of the brain Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; dementia; dementia, vascular; lewy body disease; pick disease of the brain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; brain ischemia; intracranial hemorrhages; stroke; subarachnoid hemorrhage Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; intracranial hemorrhages; stroke; subarachnoid hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain edema; infarction, middle cerebral artery Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain edema; infarction, middle cerebral artery in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain neoplasms; meningioma; neurilemmoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain neoplasms; meningioma; neurilemmoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atherosclerosis; brain ischemia; carotid stenosis; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atherosclerosis; brain ischemia; carotid stenosis; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain neoplasms; leukemia, myeloid, acute; neoplasms, second primary; precursor cell lymphoblastic leukemia-lymphoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain neoplasms; leukemia, myeloid, acute; neoplasms, second primary; precursor cell lymphoblastic leukemia-lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain neoplasms; lung neoplasms; melanoma; neoplasm metastasis; neoplasm of lung ; skin neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain neoplasms; lung neoplasms; melanoma; neoplasm metastasis; neoplasm of lung ; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcoholism; atrophy; brain diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcoholism; atrophy; brain diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain edema; cerebral hemorrhage; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain edema; cerebral hemorrhage; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain injuries; seizures Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain injuries; seizures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
altered brain levels of apolipoprotein e Gene SetFrom GAD Gene-Disease Associations genes associated with the disease altered brain levels of apolipoprotein e in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain ischemia; cardiovascular diseases; coronary disease; peripheral vascular diseases; stroke; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain ischemia; cardiovascular diseases; coronary disease; peripheral vascular diseases; stroke; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain ischemia; hyperlipidemias; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain ischemia; hyperlipidemias; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
astrocytoma; brain neoplasms; glioma; oligodendroglioma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease astrocytoma; brain neoplasms; glioma; oligodendroglioma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
athletic injuries; brain concussion; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease athletic injuries; brain concussion; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain structure Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain structure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
volumetric brain mri Gene SetFrom GAD Gene-Disease Associations genes associated with the disease volumetric brain mri in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain hemorrhage; stroke; stroke, lacunar Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain hemorrhage; stroke; stroke, lacunar in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arterial occlusive diseases; brain ischemia; coronary disease; hyperhomocysteinemia; peripheral vascular diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arterial occlusive diseases; brain ischemia; coronary disease; hyperhomocysteinemia; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain concussion Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain concussion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain infarction; carotid artery diseases; intracranial thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain infarction; carotid artery diseases; intracranial thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain infarction; cerebral amyloid angiopathy; dementia; diabetes mellitus; hyperinsulinism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain infarction; cerebral amyloid angiopathy; dementia; diabetes mellitus; hyperinsulinism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain neoplasms; glioma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain neoplasms; glioma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; brain ischemia; hyperhomocysteinemia; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; hyperhomocysteinemia; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain diseases; muscular dystrophies Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain diseases; muscular dystrophies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain injuries; cerebrovascular disorders; migraine disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain injuries; cerebrovascular disorders; migraine disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; brain ischemia; diabetic angiopathies; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; diabetic angiopathies; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; brain ischemia; infarction, middle cerebral artery; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; infarction, middle cerebral artery; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
schizophrenia; brain atrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease schizophrenia; brain atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cerebral infarction; hypoxia-ischemia, brain Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cerebral infarction; hypoxia-ischemia, brain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
frontal brain electrical asymmetry Gene SetFrom GAD Gene-Disease Associations genes associated with the disease frontal brain electrical asymmetry in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain infarction; intracranial arteriosclerosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain infarction; intracranial arteriosclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain ischemia; coronary artery disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain ischemia; coronary artery disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; brain ischemia; intracranial hemorrhages; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; intracranial hemorrhages; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain ischemia; diabetes mellitus; hyperlipidemias; hypertension; intracranial embolism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain ischemia; diabetes mellitus; hyperlipidemias; hypertension; intracranial embolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arteriosclerosis; brain ischemia; recurrence Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arteriosclerosis; brain ischemia; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
athletic injuries; brain concussion Gene SetFrom GAD Gene-Disease Associations genes associated with the disease athletic injuries; brain concussion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apnea; apoplexy; blood coagulation disorders; brain ischemia; cerebrovascular disorders; hypotony, muscle; muscle hypotonia; protein c deficiency; seizures; stroke; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apnea; apoplexy; blood coagulation disorders; brain ischemia; cerebrovascular disorders; hypotony, muscle; muscle hypotonia; protein c deficiency; seizures; stroke; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain imaging in schizophrenia (interaction) Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain imaging in schizophrenia (interaction) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain injuries; dementia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain injuries; dementia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term brain in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
Huntington's Disease_CNS - Brain - Striatum (MMHCC)_GSE9857 Gene SetFrom GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Huntington's Disease_CNS - Brain - Striatum (MMHCC)_GSE9857 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset. |