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Cgct Gene Detail
Summary
  • Symbol
    Cgct
  • Name
    congenital cataract
  • Synonyms
    Cad
  • Feature Type
    heritable phenotypic marker
  • IDs
    MGI:88242
    NCBI Gene: 104146
  • Alliance
    gene page
Location &
Maps
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  • Sequence Map
    Genome coordinates not available from the current reference assembly.
  • Genetic Map
    Chromosome 4, Syntenic
Mutations,
Alleles, and
Phenotypes
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  • Phenotype Summary
    6 phenotypes 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.
Mutations in this gene result in cataracts.
Expression
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  • Other Mouse Links
    GEO
Sequences &
Gene Models
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Other
Accession IDs
less
MGD-MRK-1722
References
more
  • Summaries
    All 5
    Phenotypes 2
  • Earliest
    J:347620 Davidorf F, et al., A study of a hereditary cataract in the mouse. J Morphol. 1966 May;119(1):89-100
  • Latest
    J:5298 Tissot RG, et al., A new congenital cataract in the mouse. J Hered. 1972 Jul-Aug;63(4):197-201
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources
Funding Information
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Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory