| Human Disease |
Glycogen Storage Disease of Heart, Lethal Congenital OMIM ID: 261740 |
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| Synonyms | Glycogen Storage Disease of Heart; Phosphorylase Kinase Deficiency of Heart | |||||||||||||||||||||
| 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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Transgenes and other genome features |
Transgenes and other genome features developed in mice to model this disease.
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| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Tg(Myh6-PRKAG2*T400N)1Feah/0 |
involves: FVB/N | J:162180 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Tg(Myh6-tTA)55Rbns/0 Tg(Myh6/tetO-PRKAG2*N488I)1Chib/0 |
Not Specified | J:145090 | 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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