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Symbol
Name
ID
Gjb2
gap junction protein, beta 2
MGI:95720
Phenotype annotations related to homeostasis/metabolism
Darker colors indicate more annotations
Human Phenotypes
Scarring alopecia of scalp
Corneal scarring
Postexertional symptom exacerbation
Disease(s) Associated with GJB2
autosomal dominant keratitis-ichthyosis-deafness syndrome
Vohwinkel syndrome

Mouse Phenotypes
lymphedema
impaired skin barrier function
Availability Mouse Genotype
Gjb2tm2.2Kwi/Gjb2+
Tg(Pgk1-cre)1Lni/0  (conditional)
Gjb2tm3.1(Gjb1)Kwi/Gjb2+
Tg(KRT5-cre)5132Jlj/0  (conditional)

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
04/16/2024
MGI 6.23
The Jackson Laboratory