|Gap junction protein, beta 2, 26kDa|
Rendering based on PDB .
|Symbols||; CX26; DFNA3; DFNA3A; DFNB1; DFNB1A; HID; KID; NSRD1; PPK|
|External IDs||IUPHAR: GeneCards:|
Gap junction beta-2 protein (GJB2), also known as connexin 26 (Cx26) — is a protein that in humans is encoded by the GJB2 gene. Defects in this gene lead to the most common form of congenital deafness in developed countries, called DFNB1 (also known as connexin 26 deafness or GJB2-related deafness).
Gap junctions were first characterized by electron microscopy as regionally specialized structures on plasma membranes of contacting adherent cells. These structures were shown to consist of cell-to-cell channels. Proteins, called connexins, purified from fractions of enriched gap junctions from different tissues differ. The connexins are designated by their molecular mass. Another system of nomenclature divides gap junction proteins into two categories, alpha and beta, according to sequence similarities at the nucleotide and amino acid levels. For example, CX43 (MIM 121014) is designated alpha-1 gap junction protein, whereas CX32 (GJB1; MIM 304040) and CX26 (this protein) are called beta-1 and beta-2 gap junction proteins, respectively. This nomenclature emphasizes that CX32 and CX26 are more homologous to each other than either of them is to CX43.
- "Entrez Gene: GJB2 gap junction protein, beta 2, 26kDa".
- Kenneson A, Van Naarden Braun K, Boyle C (2002). "GJB2 (connexin 26) variants and nonsyndromic sensorineural hearing loss: a HuGE review.". Genet. Med. 4 (4): 258–74.
- Thalmann R, Henzl MT, Killick R, et al. (2003). "Toward an understanding of cochlear homeostasis: the impact of location and the role of OCP1 and OCP2.". Acta Otolaryngol. 123 (2): 203–8.
- Yotsumoto S, Hashiguchi T, Chen X, et al. (2003). "Novel mutations in GJB2 encoding connexin-26 in Japanese patients with keratitis-ichthyosis-deafness syndrome.". Br. J. Dermatol. 148 (4): 649–53.
- Apps SA, Rankin WA, Kurmis AP (2007). "Connexin 26 mutations in autosomal recessive deafness disorders: a review.". International journal of audiology 46 (2): 75–81.
- Welch KO, Marin RS, Pandya A, Arnos KS (2007). "Compound heterozygosity for dominant and recessive GJB2 mutations: effect on phenotype and review of the literature.". Am. J. Med. Genet. A 143 (14): 1567–73.
- Harris, A. and Locke, D. (2009). Connexins, A Guide. New York: Springer. p. 574.
- Smith, Richard JH; Shearer, A Eliot; Hildebrand, Michael S; Van Camp, Guy (2014-01-09). Deafness and Hereditary Hearing Loss Overview. NBK1434. In Pagon RA, Bird TD, Dolan CR, et al., ed. (1993–). GeneReviews™ [Internet]. Seattle WA: University of Washington, Seattle.
- Smith, Richard JH; Sheffield, Abraham M; Van Camp, Guy (2012-04-19). Nonsyndromic Hearing Loss and Deafness, DFNA3. NBK1536. In GeneReviews
- Smith, Richard JH; Van Camp, Guy (2014-01-02). Nonsyndromic Hearing Loss and Deafness, DFNB1. NBK1272. In GeneReviews