Symbol Name ID |
Cdh23
cadherin related 23 (otocadherin) MGI:1890219 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Rod-cone dystrophy |
Disease(s) Associated with CDH23 | |
autosomal recessive nonsyndromic deafness 12 | |
Usher syndrome type 1D |
Mouse Phenotypes | vision/eye phenotype |
decreased a-wave implicit time |
decreased b-wave implicit time |
abnormal eye electrophysiology |
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Availability | Mouse Genotype | ||||
Cdh23v-2J/Cdh23v-2J | * | ||||
Cdh23v-11J/Cdh23v-11J | * | ||||
Cdh23v-Alb/Cdh23v-Alb | * | ||||
Cdh23v/Cdh23v | * |
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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