| Human Disease |
Cardiomyopathy, Familial Hypertrophic, 14; CMH14 OMIM ID: 613251 |
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| View all models | View ALL (6) 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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Transgenes and other genome features |
Transgenes and other genome features developed in mice to model this disease.
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| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Myh6tm3.1Jse/Myh6+ |
involves: 129X1/SvJ | J:165269 | View |
| Myh6tm2Jse/Myh6+ |
involves: 129S1/Sv | J:95600 | View |
| Myh6tm1Jse/Myh6+ |
129S.129X1-Myh6tm1Jse | J:104363 | View |
| Myh6tm1Jse/Myh6+ |
involves: 129X1/SvJ | J:32960, J:95600 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Tg(Myh6*)131Lnwd/0 |
involves: C57BL/6 * CBA | J:31537 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Tg(Myh6*)140Lnwd/0 |
involves: C57BL/6 * CBA | J:31537, J:36522 | 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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