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Gja1tm8.1Kwi
Targeted Allele Detail
Summary
Symbol: Gja1tm8.1Kwi
Name: gap junction protein, alpha 1; targeted mutation 8.1, Klaus Willecke
MGI ID: MGI:3776014
Synonyms: Cx43G138R
Gene: Gja1  Location: Chr10:56253297-56266519 bp, + strand  Genetic Position: Chr10, 28.64 cM
Alliance: Gja1tm8.1Kwi page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:132032
Parent Cell Line:  HM-1 (ES Cell)
Strain of Origin:  129P2/OlaHsd-Hprt1b-m3
Mutation
description
Allele Type:    Targeted
Mutations:    Insertion, Intragenic deletion, Nucleotide substitutions
 
Mutation detailsGerm-line, cre-mediated recombantion was used to remove the wild-type locus and the neo cassette that resulted in the expression of the modified locus and IRES-eGFP cassette. (J:132032)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
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 Gja1 Mutation:  60 strains or lines available
References
Original:  J:132032 Dobrowolski R, et al., The conditional connexin43G138R mouse mutant represents a new model of hereditary oculodentodigital dysplasia in humans. Hum Mol Genet. 2008 Feb 15;17(4):539-54
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