| Human Disease |
Muscular Dystrophy, Limb-Girdle, Type 2A; LGMD2A OMIM ID: 253600 |
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| Synonyms | Leyden-Moebius Muscular Dystrophy; Muscular Dystrophy, Limb-Girdle, Type 2; LGMD2; Muscular Dystrophy, Pelvofemoral | |||||||||||||||||||||
| View all models | View ALL (2) 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 |
| Capn3tm1Jsb/Capn3tm1Jsb |
either: 129/Sv-Capn3tm1Jsb or (involves: 129/Sv * C57BL/6) | J:66862 | View |
| Capn3tm1.1Hiso/Capn3tm1.1Hiso |
B6.129P2-Capn3tm1.1Hiso | J:163711 | 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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