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Coc Gene Detail
Summary
  • Symbol
    Coc
  • Name
    coralliform cataract
  • Feature Type
    heritable phenotypic marker
  • IDs
    MGI:88442
    NCBI Gene: 109792
Location & Maps
more
  • Sequence Map
    Genome coordinates not available
  • Genetic Map
    Chromosome 16, Syntenic
  • Mapping Data
    1 experiment
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    1 phenotype from 1 allele in 1 genetic background
    2 phenotype references
Phenotype Overview

adipose tissue
behavior/neurological
cardiovascular system
cellular
craniofacial
digestive/alimentary system
embryo
endocrine/exocrine glands
growth/size/body
hearing/vestibular/ear
hematopoietic system
homeostasis/metabolism
integument
immune system
limbs/digits/tail
liver/biliary system
mortality/aging
muscle
nervous system
pigmentation
renal/urinary system
reproductive system
respiratory system
skeleton
taste/olfaction
neoplasm
vision/eye

Click cells to view annotations.
  • All Mutations and Alleles
    1
  • Radiation induced
    1
Heterozygous and homozygous mutants exhibit small spherical opacities in the central part of the lens.
Sequences &
Gene Models
less
Other
Accession IDs
less
MGD-MRK-2046
References
more
  • Summaries
    All 3
    Phenotypes 2
  • 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

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
09/27/2016
MGI 6.05
The Jackson Laboratory