| Human Disease |
Cardiomyopathy, Familial Hypertrophic, 2; CMH2 OMIM ID: 115195 |
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| View all models | View ALL (5) 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 |
| Tg(Myh6-Tnnt2)117Lnwd/0 |
involves: C57BL/6 | J:48301 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Tg(Myh6-Tnnt2)191Lnwd/0 |
involves: C57BL/6 | J:48301 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Tg(Myh6-TNNT2*R92Q)#Ajm/0 |
involves: C3H * C57BL/6 * ICR | J:162685, J:161899 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Tg(Tnnt2-TNNT2*R92Q)#Ajm/0 |
involves: C3H * C57BL/6 * ICR | J:117554 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Tg(Tnnt2-TNNT2*R92Q)M-2Ajm/0 |
involves: C3H * C57BL/6 * ICR | J:117554 | View |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 05/22/2013 MGI 5.13 |
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