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Symbol Name ID |
Cc2d2a
coiled-coil and C2 domain containing 2A MGI:1924487 |
| Darker colors indicate more annotations |
| Human Phenotypes | Conductive hearing impairment |
Sensorineural hearing impairment |
| Disease(s) Associated with CC2D2A | ||
| retinitis pigmentosa |
| Mouse Phenotypes | abnormal kinocilium morphology |
abnormal cochlear hair cell stereociliary bundle morphology |
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| Availability | Mouse Genotype | ||
| 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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