Symbol Name ID |
Gjb2
gap junction protein, beta 2 MGI:95720 |
Darker colors indicate more annotations |
Human Phenotypes | Failure to thrive |
Postnatal growth retardation |
Disease(s) Associated with GJB2 | ||
autosomal dominant keratitis-ichthyosis-deafness syndrome |
Mouse Phenotypes | embryonic growth retardation |
decreased embryo size |
decreased body size |
decreased fetal size |
fetal growth retardation |
|
Availability | Mouse Genotype | |||||
Gjb2tm1Kwi/Gjb2tm1Kwi | ||||||
Gjb2tm1Mony/Gjb2tm1Mony | ||||||
Gjb2tm2.2Kwi/Gjb2+ Tg(Pgk1-cre)1Lni/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) |
||
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support. |
last database update 04/16/2024 MGI 6.23 |
|
|