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Gja8Aey69
Chemically induced Allele Detail
Summary
Symbol: Gja8Aey69
Name: gap junction protein, alpha 8; abnormal eyes 69
MGI ID: MGI:6342052
Gene: Gja8  Location: Chr3:96820882-96833336 bp, - strand  
Alliance: Gja8Aey69 page
Mutation
origin
Strain of Origin:  C3HeB/FeJ
Mutation
description
Allele Type:    Chemically induced (ENU) (Not Specified)
Mutation:    Single point mutation
 
Mutation detailsENU treatment caused an T>C mutation in the coding region (c.71T>C) that leads to to the change of valine codon 24 to alanine (p.Val24Ala). This mutation is linked to H3c14 and the two mutations are found in mice with a dominant small-eye phenotype (microphthalmia without a lens but with retinal hyperproliferation). (J:277247)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
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 Gja8 Mutation:  33 strains or lines available
References
Original:  J:277247 Vetrivel S, et al., Mutation in the mouse histone gene Hist2h3c1 leads to degeneration of the lens vesicle and severe microphthalmia. Exp Eye Res. 2019 Apr 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
12/10/2024
MGI 6.24
The Jackson Laboratory