| Human Disease |
Muscular Dystrophy, Limb-Girdle, Type 2H; LGMD2H OMIM ID: 254110 |
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| Synonyms | Muscular Dystrophy, Hutterite Type; Sarcotubular Myopathy | |||||||||||||||||||||
| 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 |
| Trim32tm1Spc/Trim32tm1Spc |
involves: 129S/SvEvBrd * BALB/cJ * C57BL/6J | J:175798 | View |
| Trim32Gt(BGA355)Byg/Trim32Gt(BGA355)Byg |
involves: 129P2/OlaHsd * C57BL/6 | J:146155 | 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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