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CrygcLop20
Spontaneous Allele Detail
Summary
Symbol: CrygcLop20
Name: crystallin, gamma C; lens opacity 20
MGI ID: MGI:6356332
Gene: Crygc  Location: Chr1:65110684-65112691 bp, - strand  Genetic Position: Chr1, 32.81 cM
Alliance: CrygcLop20 page
Mutation
origin
Strain of Origin:  (BALB/cJ x A/J)F1
Mutation
description
Allele Type:    Spontaneous (Hypomorph)
Mutation:    Insertion
 
Mutation detailsThis spontaneous 2 base pair insertion (GC) in exon 3 causes a frameshift after codon 124 and premature stop at codon 147. (J:277888)
Inheritance:    Semidominant
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: 1 strain available      Cell Lines: 0 lines available
Carrying any Crygc Mutation:  13 strains or lines available
References
Original:  J:277888 Chang Bo, The lens opacity 20 spontaneous mutation in Crygc. MGI Direct Data Submission. 2019;
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