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Symbol Name ID |
Cc2d2a
coiled-coil and C2 domain containing 2A MGI:1924487 |
| Darker colors indicate more annotations |
| Human Phenotypes | Aplasia of the bladder |
Horseshoe kidney |
Renal cyst |
Stage 5 chronic kidney disease |
| Disease(s) Associated with CC2D2A | ||||
| Joubert syndrome 9 | ||||
| Meckel syndrome 6 |
| Mouse Phenotypes | abnormal renal tubule epithelial cell primary cilium morphology |
kidney cyst |
polycystic kidney |
duplex kidney |
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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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