| Human Disease |
Muscular Dystrophy, Limb-Girdle, Type 1A; LGMD1A OMIM ID: 159000 |
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| Synonyms | LGMD1; Muscular Dystrophy, Proximal, Type 1A | |||||||||||||||||||||
| 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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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 |
| Myottm1.1Moza/Myottm1.1Moza |
involves: 129S1/Sv * 129X1/SvJ * ICR | J:117709 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Tg(ACTA1-MYOT*T57I)71Mah/? |
involves: C57BL/6 * SJL | J:110377 | 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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