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This gene encodes a transmembrane connexin protein that is a component of gap junctions. Mutations in this gene have been associated with erythrokeratodermia variabilis, progressive symmetric erythrokeratoderma and hearing impairment.
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Protein Aliases: Connexin-30.3; Cx30.3; Gap junction beta-4 protein; gap junction membrane channel protein beta 4
Gene Aliases: Cnx30.3; Cx30.3; Cxn-30.3; Gjb-4; Gjb4
UniProt ID: (Mouse) Q02738
Entrez Gene ID: (Mouse) 14621
Molecular Function: gap junction
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