| Human Disease |
Glycogen Storage Disease V OMIM ID: 232600 |
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| Synonyms | Gsd V; GSD5; Mcardle Disease; Muscle Glycogen Phosphorylase Deficiency; Myophosphorylase Deficiency; PYGM Deficiency | ||||||||||||||||||||||||||||
| 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 |
| Hif1atm3Rsjo/Hif1atm3Rsjo Tg(Ckmm-cre)5Khn/? |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * FVB | J:97761 | 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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