| Human Disease |
Muscular Dystrophy-Dystroglycanopathy (congenital with Mental Retardation), Type B, 6; MDDGB6 OMIM ID: 608840 |
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| Synonyms | Muscular Dystrophy, Congenital, Large-Related; Muscular Dystrophy, Congenital, Type 1D; MDC1D | |||||||||||||||||||||
| 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 |
| Largemyd-3J/Largemyd-3J |
STOCK Largemyd-3J/GrsrJ | J:160357 | 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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