| Human Disease |
Arrhythmogenic Right Ventricular Dysplasia, Familial, 2; ARVD2 OMIM ID: 600996 |
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| Synonyms | Arrhythmogenic Right Ventricular Cardiomyopathy 2; ARVC2 | |||||||||||||||||||||
| 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 |
| Ryr2tm1Slh/Ryr2+ |
involves: 129S7/SvEvBrd * C57BL/6 | J:111780 | 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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