Symbol Name ID |
Gjb2
gap junction protein, beta 2 MGI:95720 |
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 |
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Availability | Mouse Genotype | ||
Gjb2tm2.2Kwi/Gjb2+ Tg(Pgk1-cre)1Lni/0 (conditional) |
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Gjb2tm3.1(Gjb1)Kwi/Gjb2+ Tg(KRT5-cre)5132Jlj/0 (conditional) |
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 |
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