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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Cdh23v-Alb
Albany waltzer
MGI:1857310
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Cdh23v-Alb/Cdh23v-Alb involves: C3H/HeJ * C57BL/6 MGI:2654804
hm2
Cdh23v-Alb/Cdh23v-Alb involves: C3H/HeJ * C57BL/6 * CBA/Ca MGI:3714990


Genotype
MGI:2654804
hm1
Allelic
Composition
Cdh23v-Alb/Cdh23v-Alb
Genetic
Background
involves: C3H/HeJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cdh23v-Alb mutation (2 available); any Cdh23 mutation (283 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
hearing/vestibular/ear
• at E18.5, stereocilia of the inner hair cells (IHCs) are positioned correctly, but are in a disorganized line instead of a crescent shape
• at P4, IHCs remain disorganized
• at E18.5, the outer hair cells (OHCs) appear immature
• at P4, all OHCs project stereocilia, but they are present in random clumps instead of a V-shaped pattern
• at E18.5, the kinocilium is often misplaced from the lateral pole of each cell; the stereocilia, when present, are positioned correctly
• in some cases at E18.5, outer hair cells (OHCs) projected no recognizable stereocilia
• in some cases at E18.5, outer hair cells (OHCs) projected fewer stereocilia
• at P4, stereocilia appear thick and are often fused and disorganized

reproductive system
• litter sizes tend to be smaller than controls

behavior/neurological
• Background Sensitivity: 74% of deaf homozygous mice exhibited cirling; however, when mice are backcrossed to M. m. castaneus, this frequency drops to 21%

nervous system
• at E18.5, stereocilia of the inner hair cells (IHCs) are positioned correctly, but are in a disorganized line instead of a crescent shape
• at P4, IHCs remain disorganized
• at E18.5, the outer hair cells (OHCs) appear immature
• at P4, all OHCs project stereocilia, but they are present in random clumps instead of a V-shaped pattern
• at E18.5, the kinocilium is often misplaced from the lateral pole of each cell; the stereocilia, when present, are positioned correctly
• in some cases at E18.5, outer hair cells (OHCs) projected no recognizable stereocilia
• in some cases at E18.5, outer hair cells (OHCs) projected fewer stereocilia
• at P4, stereocilia appear thick and are often fused and disorganized

cellular
• at E18.5, the kinocilium is often misplaced from the lateral pole of each cell; the stereocilia, when present, are positioned correctly

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
Usher syndrome type 1D DOID:0110831 OMIM:601067
J:66698




Genotype
MGI:3714990
hm2
Allelic
Composition
Cdh23v-Alb/Cdh23v-Alb
Genetic
Background
involves: C3H/HeJ * C57BL/6 * CBA/Ca
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cdh23v-Alb mutation (2 available); any Cdh23 mutation (283 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
vision/eye
N
• mice do not exhibit signs of retinal degeneration up to 12 months of age and the melanosomes of the retinal pigment epithelium (RPE) are properly localized
• electroretinography analysis indicates that a- and b-waves are slightly attenuated and the implicit times are slightly faster than controls, but these changes are not statistically significant





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last database update
09/03/2024
MGI 6.24
The Jackson Laboratory