| Human Disease |
Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or without Atrial Dysfunction and/or Dilated Cardiomyopathy; CPVT1 OMIM ID: 604772 |
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| Synonyms | Ventricular Tachycardia, Stress-Induced Polymorphic; VTSIP | ||||||||||||||||||||||||||||||||
| View all models | View ALL (4) 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 |
| Ryr2tm1Sgp/Ryr2+ |
involves: 129/Sv * C57BL/6 | J:109683 | View |
| Ryr2tm1.1Maya/Ryr2+ |
C57BL/6J-Ryr2tm1.1Maya | J:159451 | View |
| Ryr2tm1.1Clhh/Ryr2tm1.1Clhh |
129S/SvEv-Ryr2tm1.1Clhh | J:186379 | View |
| 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 05/22/2013 MGI 5.13 |
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