Symbol Name ID |
Cc2d2a
coiled-coil and C2 domain containing 2A MGI:1924487 |
Darker colors indicate more annotations |
Human Phenotypes | Obesity |
Disease(s) Associated with CC2D2A | |
retinitis pigmentosa |
Mouse Phenotypes | cleft palate |
decreased embryo size |
decreased body weight |
kidney cyst |
polycystic kidney |
postnatal growth retardation |
prenatal growth retardation |
heterotaxia |
situs inversus |
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Availability | Mouse Genotype | |||||||||
Cc2d2ab2b1035Clo/Cc2d2ab2b1035Clo | ||||||||||
Cc2d2atm1Asw/Cc2d2atm1Asw | ||||||||||
Cc2d2atm1a(EUCOMM)Wtsi/Cc2d2a+ |
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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