|
Symbol Name ID |
Mypn
myopalladin MGI:1916052 |
| Darker colors indicate more annotations |
| Human Phenotypes | Ventricular septal hypertrophy |
Left ventricular hypertrophy |
Cardiomyopathy |
Dilated cardiomyopathy |
Hypertrophic cardiomyopathy |
Increased left ventricular end-diastolic volume |
Mitral regurgitation |
Atrial fibrillation |
First degree atrioventricular block |
Congestive heart failure |
| Disease(s) Associated with MYPN | ||||||||||
| dilated cardiomyopathy 1KK | ||||||||||
| nemaline myopathy 11 |
| Mouse Phenotypes | abnormal myocardial fiber morphology |
abnormal intercalated disk morphology |
abnormal heart atrium morphology |
abnormal heart left ventricle morphology |
cardiac interstitial fibrosis |
abnormal cardiac muscle relaxation |
abnormal heart echocardiography feature |
irregular heartbeat |
atrioventricular block |
abnormal T wave |
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| Availability | Mouse Genotype | ||||||||||
| Mypntm1.1Epu/Mypn+ | |||||||||||
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 04/30/2024 MGI 6.23 |
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