| Human Disease |
Muscular Dystrophy-Dystroglycanopathy (limb-Girdle), Type C, 5; MDDGC5 OMIM ID: 607155 |
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| Synonyms | Muscular Dystrophy, Limb-Girdle, Type 2I; LGMD2I; Muscular Dystrophy-Dystroglycanopathy, Limb-Girdle, Frkp-Related | |||||||||||||||||||||
| 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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| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Fkrptm1Itl/Fkrptm1Itl |
involves: 129S6/SvEvTac * C57BL/6N | J:164448 | 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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