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Heritable Phenotypic Marker : Coc coralliform cataract

Primary Identifier	MGI:88442	Organism	mouse, laboratory
Chromosome	16	Mgi Type	heritable phenotypic marker

description

FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0)

Used to study cataract.
PHENOTYPE: Heterozygous and homozygous mutants exhibit small spherical opacities in the central part of the lens. [provided by MGI curators]

synonyms:
Coc,
MGD-MRK-2046,
coralliform cataract

earliestPublication:
Kratochvilova J, et al. (1988) Phenotypic characterization and genetic analysis of twenty dominant cataract mutations detected in offspring of irradiated male mice. Genet Res 52(2):125-34

Features --> Cross References

Genome

Sequence Feature Displayer

JG Browse Displayer

0 Involved In Mutations

0 Transgenic Expressors

Canonical gene --> CDSs in specific strains.

Canonical gene --> Exons in specific strains

Canonical gene --> Strain-specific IDs, biotypes, and locations

Canonical gene --> Transcripts in specific strains.

Features --> Overlapping features

Proteins

Gene --> Proteins

Function

Mouse features --> Functions (GO terms)

Homology

Genes --> Homologs

Interactions

Gene --> Protein-Protein Interactions

Expression

Gene --> Expression annotations

Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

Mouse features --> Human diseases

Literature

Mouse features --> Publications

Other

0 Driver For

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