Coc
Gene Detail

Symbol Name ID

Coc coralliform cataract MGI:88442

Feature Type

heritable phenotypic marker

Genetic Map

Chromosome 16
Syntenic

Mapping data(1)

Alleles and phenotypes

All alleles(1) : Radiation induced(1)
 

Heterozygous and homozygous mutants exhibit small spherical opacities in the central part of the lens.

 
Human Diseases Modeled Using Mouse Coc (1)    Alleles Annotated to Human Diseases(1)   

Other database links

Entrez Gene

109792

References

(Earliest) J:9528 Kratochvilova J, et al., Phenotypic characterization and genetic analysis of twenty dominant cataract mutations detected in offspring of irradiated male mice. Genet Res. 1988 Oct;52(2):125-34
(Latest) J:44211 Sidjanin DJ, et al., Mapping of the autosomal dominant cataract mutation (Coc) on mouse chromosome 16. Invest Ophthalmol Vis Sci. 1997 Nov;38(12):2502-7
All references(3)

Other accession IDs

MGD-MRK-2046