| Human Disease |
Arrhythmogenic Right Ventricular Dysplasia, Familial, 12; ARVD12 OMIM ID: 611528 |
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| Synonyms | Arrhythmogenic Right Ventricular Cardiomyopathy 12; ARVC12 | |||||||||||||||||||||
| 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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| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Juptm1.1Shou/Juptm1.1Shou Tg(Myh6-cre)2182Mds/0 |
involves: 129 * C57BL/6J | J:177567 | View |
| Juptm1.1Glr/Juptm1.1Glr Tg(Myh6-cre/Esr1*)1Jmk/0 |
involves: 129S6/SvEvTac * C57BL/6 * FVB * SJL | J:170618 | 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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