| Human Disease |
Cardiomyopathy, Familial Hypertrophic, 4; CMH4 OMIM ID: 115197 |
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| View all models | View ALL (4) 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 |
| Mybpc3tm1Rmos/Mybpc3tm1Rmos |
either: (involves: 129) or (involves: 129 * C57BL/6) | J:95725 | View |
| Mybpc3tm1Jse/Mybpc3tm1Jse |
Not Specified | J:58295 | View |
| Mybpc3tm1Lcrr/Mybpc3+ |
involves: 129S4/SvJae * Black Swiss | J:101903 | View |
| Mybpc3tm1.1Jse/Mybpc3tm1.1Jse |
Not Specified | J:58295 | 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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