| Human Disease |
Gitelman Syndrome OMIM ID: 263800 |
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| Synonyms | Hypomagnesemia-Hypokalemia, Primary Renotubular, with Hypocalciuria; Potassium and Magnesium Depletion | ||||||||||||||||||||||||||||||||
| View all models | View ALL (3) 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 |
| Slc12a3tm1Ges/Slc12a3tm1Ges |
Not Specified | J:50596 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Stk39tm1.2Slin/Stk39tm1.2Slin |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | J:165706 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Wnk4tm1Pfi/Wnk4tm1Pfi |
involves: 129S6/SvEvTac * C57BL/6J | J:184790 | View |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 05/08/2013 MGI 5.13 |
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