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Gjb6tm1Kwi
Targeted Allele Detail
Nomenclature
Symbol: Gjb6tm1Kwi
Name: gap junction protein, beta 6; targeted mutation 1, Klaus Willecke
MGI ID: MGI:2447863
Synonyms: connexin30-, Cx30-, Cx30lacZ
Gene: Gjb6  Location: Chr14:57123303-57133611 bp, - strand  Genetic Position: Chr14, 30.1 cM
Transmission electron microscopy analysis of stria vascularis capillaries in Gjb6tm1Kwi/Gjb6tm1Kwi mice

Show the 1 phenotype image(s) involving this allele.

Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:80917
Parent Cell Line:  HM-1 (ES Cell)
Strain of Origin:  129P2/OlaHsd-Hprtb-m3
Mutation
description
Allele Type:    Targeted (Null/knockout, Reporter)
Mutations:    Insertion, Intragenic deletion
 
Mutation details
Phenotypes
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View phenotypes for all genotypes (concatenated display).
Disease models
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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 Gjb6 Mutation:  3 strains or lines available
References
Original:  J:80917 Teubner B, et al., Connexin30 (Gjb6)-deficiency causes severe hearing impairment and lack of endocochlear potential. Hum Mol Genet. 2003 Jan 1;12(1):13-21
All:  34 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
07/15/2014
MGI 5.18
The Jackson Laboratory