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Symbol Name ID |
Cc2d2a
coiled-coil and C2 domain containing 2A MGI:1924487 |
| Darker colors indicate more annotations |
| Human Phenotypes | Abnormal retinal vascular morphology |
Attenuation of retinal blood vessels |
| Disease(s) Associated with CC2D2A | ||
| retinitis pigmentosa |
| Mouse Phenotypes | persistent truncus arteriosus |
double outlet right ventricle |
double outlet right ventricle with atrioventricular septal defect |
tricuspid valve atresia |
biventricular, discordant atrioventricular connection |
common atrium |
dextrocardia |
superior-inferior ventricles |
atrioventricular septal defect |
complete atrioventricular septal defect |
muscular ventricular septal defect |
ventricular septal defect |
pulmonary valve atresia |
hemorrhage |
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| Availability | Mouse Genotype | ||||||||||||||
| Cc2d2ab2b1035Clo/Cc2d2ab2b1035Clo | |||||||||||||||
| Cc2d2atm1Asw/Cc2d2atm1Asw | |||||||||||||||
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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