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Symbol Name ID |
Cdhr1
cadherin-related family member 1 MGI:2157782 |
| Darker colors indicate more annotations |
| Human Phenotypes | Attenuation of retinal blood vessels |
Retinal pigment epithelial atrophy |
Rod-cone dystrophy |
Color vision defect |
Nyctalopia |
Photophobia |
Constriction of peripheral visual field |
Progressive visual loss |
| Disease(s) Associated with CDHR1 | ||||||||
| cone-rod dystrophy 15 |
| Mouse Phenotypes | abnormal retina morphology |
increased susceptibility to age-related retinal degeneration |
abnormal eye electrophysiology |
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| Availability | Mouse Genotype | |||
| Cdhr1tm1Nat/Cdhr1tm1Nat | ||||
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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