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Gjb2tm1Ugds
Targeted Allele Detail
Summary
Symbol: Gjb2tm1Ugds
Name: gap junction protein, beta 2; targeted mutation 1, Unite de Genetique des Deficits Sensoriels
MGI ID: MGI:2183509
Synonyms: Cx26fl, Cx26fl, Cx26loxP, Gjb2tm1Ptt
Gene: Gjb2  Location: Chr14:57336059-57342159 bp, - strand  Genetic Position: Chr14, 30.1 cM, cytoband D1-E1
Alliance: Gjb2tm1Ugds page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:77823
Parent Cell Line:  HM-1 (ES Cell)
Strain of Origin:  129P2/OlaHsd-Hprt1b-m3
Mutation
description
Allele Type:    Targeted (Conditional ready, No functional change)
Mutation:    Insertion
 
Mutation detailsThe coding region in exon 2 was flanked by a loxP site in intron 1 and a floxed neo cassette inserted into exon 2. Immunohistofluorescence analysis showed that the expression pattern of this floxed allele did not differ from that of wild-type. (J:77823)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Disease models
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Expression
In Structures Affected by this Mutation: 4 anatomical structure(s)
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 3 strains available      Cell Lines: 0 lines available
Carrying any Gjb2 Mutation:  22 strains or lines available
References
Original:  J:77823 Cohen-Salmon M, et al., Targeted ablation of connexin26 in the inner ear epithelial gap junction network causes hearing impairment and cell death. Curr Biol. 2002 Jul 9;12(13):1106-11
All:  41 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