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Cgct
Spontaneous Allele Detail
Summary
Symbol: Cgct
Name: congenital cataract
MGI ID: MGI:1856700
Gene: Cgct  Location: unknown  Genetic Position: Chr4, Syntenic
Alliance: Cgct page
Mutation
origin
Strain of Origin:  random-bred Swiss
Mutation
description
Allele Type:    Spontaneous
Inheritance:    Semidominant
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 1 anatomical structure(s)
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 0 strains available      Cell Lines: 0 lines available
Carrying any Cgct Mutation:  0 strains or lines available
References
Original:  J:5298 Tissot RG, et al., A new congenital cataract in the mouse. J Hered. 1972 Jul-Aug;63(4):197-201
All:  1 reference(s)

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)
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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory