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Symbol
Name
ID
Gjb2
gap junction protein, beta 2
MGI:95720
Phenotype annotations related to cardiovascular system
*Aspects of the system are reported to show a normal phenotype.
Darker colors indicate more annotations
Human Phenotypes
Keratoconjunctivitis sicca
Erythema
Urticaria
Disease(s) Associated with GJB2
autosomal dominant keratitis-ichthyosis-deafness syndrome

Mouse Phenotypes
cardiovascular system phenotype
abnormal placental labyrinth vasculature morphology
Availability Mouse Genotype
Gjb2tm1Kwi/Gjb2tm1Kwi
Gjb2tm3.2(Gjb1)Kwi/Gjb2+ *

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
11/12/2019
MGI 6.14
The Jackson Laboratory