About Help FAQ

Symbol
Name
ID

Cdh23
cadherin related 23 (otocadherin)
MGI:1890219

Phenotype annotations related to vision/eye

*	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	Rod-cone dystrophy
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
Availability	Mouse Genotype	vision/eye phenotype	decreased a-wave implicit time	decreased b-wave implicit time	abnormal eye electrophysiology
	Cdh23^v-2J/Cdh23^v-2J	*
	Cdh23^v-11J/Cdh23^v-11J	*
	Cdh23^v-Alb/Cdh23^v-Alb	*
	Cdh23^v/Cdh23^v	*

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 04/30/2024 MGI 6.23