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CrygeZ2
Spontaneous Allele Detail
Summary
Symbol: CrygeZ2
Name: crystallin, gamma E; Z2
MGI ID: MGI:3578340
Gene: Cryge  Location: Chr1:65087713-65090308 bp, - strand  Genetic Position: Chr1, 32.8 cM
Alliance: CrygeZ2 page
Mutation
origin
Strain of Origin:  Not Specified
Mutation
description
Allele Type:    Spontaneous
Mutation:    Intragenic deletion
    A deletion of nt 12-21 causes the addition of 119 new amino acids at Ile4. (J:90087)
Inheritance:    Not Specified
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 2 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 Cryge Mutation:  23 strains or lines available
Notes
The strain of origin is either (102/ElxC3H/El)F1 or DBA/2
References
Original:  J:90087 Graw J, et al., Genetic and allelic heterogeneity of Cryg mutations in eight distinct forms of dominant cataract in the mouse. Invest Ophthalmol Vis Sci. 2004 Apr;45(4):1202-13
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