The GJB4 gene (GJB4 is the acronym for gap junction protein beta 4) is a protein-coding gene located on chromosome 1p34.3.
The gene encodes a transmembrane connexin protein that is an essential component of gap junctions.
Mutations in this gene are associated with erythrokeratoderma variabilis
Non-syndromic hearing loss (Adadey SM et al. 2020).
An important paralog of this gene is GJB5.
In animal experiments, overexpression of GJB4 in primary pancreatic islet cells resulted in inhibition of islet cell proliferation and a decrease in insulin secretion.