|
Symbol Name ID |
Myocd
myocardin MGI:2137495 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Atrial septal defect |
Ventricular septal defect |
Bicuspid aortic valve |
Left ventricular noncompaction cardiomyopathy |
Patent ductus arteriosus |
| Disease(s) Associated with MYOCD | |||||
| congenital megabladder |
| Mouse Phenotypes | cardiovascular system phenotype |
abnormal blood vessel morphology |
abnormal dorsal aorta morphology |
abnormal angiogenesis |
patent ductus arteriosus |
absent vitelline blood vessels |
abnormal vascular smooth muscle morphology |
abnormal myocardial fiber morphology |
abnormal intercalated disk morphology |
myocardial fiber degeneration |
myocardial fiber disarray |
increased heart atrium size |
enlarged heart |
increased heart ventricle size |
pericardial effusion |
cardiac fibrosis |
dilated cardiomyopathy |
decreased cardiac muscle contractility |
abnormal heart echocardiography feature |
increased cardiomyocyte apoptosis |
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| Availability | Mouse Genotype | ||||||||||||||||||||
| Myocdtm1Eno/Myocdtm1Eno | * | ||||||||||||||||||||
| Myocdem1Blk/Myocdtm1.1Msp | * | ||||||||||||||||||||
| Myocdtm1Msp/Myocdtm1Msp H2az2Tg(Wnt1-cre)11Rth/H2az2+ (conditional) |
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| Myocdtm1Msp/Myocdtm1Msp Tg(Pax3-cre)1Joe/0 (conditional) |
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| Myocdtm1Msp/Myocdtm1Msp Tg(Myh6-cre)2182Mds/0 (conditional) |
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| Myocdtm1Msp/Myocdtm1Msp A1cfTg(Myh6-cre/Esr1*)1Jmk/A1cf+ (conditional) |
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| Myocdtm1Msp/Myocdtm1Msp (conditional) | |||||||||||||||||||||
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 04/23/2024 MGI 6.23 |
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