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Cdh23v-df
Spontaneous Allele Detail
Summary
Symbol: Cdh23v-df
Name: cadherin related 23 (otocadherin); deaf
MGI ID: MGI:1856229
Gene: Cdh23  Location: Chr10:60138527-60532269 bp, - strand  Genetic Position: Chr10, 30.11 cM
Alliance: Cdh23v-df page
Mutation
origin
Strain of Origin:  Neurological stock
Mutation
description
Allele Type:    Spontaneous
Inheritance:    Recessive
Phenotypes
Key:
hm homozygous ht heterozygous tg involves transgenes phenotype observed
cn conditional genotype  cx complex: > 1 genome feature ot other: hemizygous, indeterminate,... N normal phenotype
Genotype/
Background:
Allelic Composition
Genetic Background
Cell Line(s)
Not Specified
 
Phenotypes:
Affected Systems
show or hide all annotated terms
 
behavior/neurological
abnormal motor capabilities/coordination/movement
absent pinna reflex
craniofacial
abnormal ear position
growth/size/body
abnormal ear position
hearing/vestibular/ear
abnormal ear position
organ of Corti degeneration
abnormal stria vascularis morphology
deafness
nervous system
abnormal cochlear ganglion morphology
View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 4 anatomical structure(s)
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 0 strains available      Cell Lines: 0 lines available
Carrying any Cdh23 Mutation:  281 strains or lines available
References
Original:  J:12997 Deol MS, A gene for uncomplicated deafness in the mouse. J Embryol Exp Morphol. 1956;4(2):190-195
All:  2 reference(s)

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)
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last database update
03/25/2025
MGI 6.24
The Jackson Laboratory