| Human Disease |
Cardiomyopathy, Familial Hypertrophic, 12; CMH12 OMIM ID: 612124 |
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| View all models | View ALL (1) 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 |
| Csrp3tm1.1Rkn/Csrp3tm1.1Rkn |
either: (involves: Black Swiss) or (involves: C57BL/6N) | J:170878 | 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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