GJB3 Gene

gap junction protein, beta 3, 31kDa

This gene is a member of the connexin gene family. The encoded protein is a component of gap junctions, which are composed of arrays of intercellular channels that provide a route for the diffusion of low molecular weight materials from cell to cell. Mutations in this gene can cause non-syndromic deafness or erythrokeratodermia variabilis, a skin disorder. Alternative splicing results in multiple transcript variants encoding the same protein. [provided by RefSeq, Jul 2008]

gjb3 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term gjb3 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

GJB3 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for GJB3 from the Pathway Commons Protein-Protein Interactions dataset.

Deafness, digenic, GJB2/GJB3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, digenic, GJB2/GJB3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

deafness, digenic, gjb2/gjb3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, digenic, gjb2/gjb3 phenotype from the curated OMIM Gene-Disease Associations dataset.