Enc
Gene Detail

Symbol Name ID

Enc embryonic nucleus cataract MGI:95391

Feature Type

heritable phenotypic marker

Genetic Map

Chromosome Unknown

Alleles and phenotypes

All alleles(1) : Radiation induced(1)
 

Mice homozygous for a radiation-induced mutation die prior to birth. Heterozygous mutants are fully viable and fertile but exhibit a small bilateral opacity limited to the central part of the lens, with incomplete penetrance; opacities of the embryonic nucleus and the posterior suture are observed.

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

Gene Ontology (GO) classifications

All GO classifications: (1 annotations)

Process

camera-type eye development

Other database links

Entrez Gene

104374

References

(Earliest) J:13942 Kratochvilova J, New cataract mutants. Mouse News Lett. 1983;68:86
(Latest) 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
All references(3)

Other accession IDs

MGD-MRK-9501