| Human Disease |
Glucocorticoid-Remediable Aldosteronism; GRA OMIM ID: 103900 |
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| Synonyms | ACTH-Dependent Hyperaldosteronism Syndrome; Aldosteronism, Sensitive to Dexamethasone; FH I; Glucocorticoid-Suppressible Hyperaldosteronism; GSH; Hyperaldosteronism, Familial, Type I | ||||||||||||||||||||||||||||
| View all models | View ALL (2) mouse models for this human disease. | ||||||||||||||||||||||||||||
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Genes and mouse models |
Mutations in human and/or mouse homologs are associated with this disease
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| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Kcnk3tm1Sgb/Kcnk3tm1Sgb |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | J:188335 | View |
| Dkk3tm1Cni/Dkk3tm1Cni Kcnk3tm1Sgb/Kcnk3tm1Sgb |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | J:188335 | View |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 06/05/2013 MGI 5.13 |
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