| Human Disease |
Bartter Syndrome, Type 4a OMIM ID: 602522 |
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| 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 |
| Bsndtm1Tjj/Bsndtm1Tjj Tg(Sox10-cre)1Wdr/0 |
involves: 129/Sv * 129X1/SvJ * C57BL/6 | J:143314 | View |
| Bsndtm1.1Suc/Bsndtm1.1Suc |
involves: 129S4/SvJae * C57BL/6 | J:175265 | 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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