- GJA9
Gap junction protein, alpha 9, 36kDa, also known as GJA9, is a human
gene .cite web | title = Entrez Gene: GJA9 gap junction protein, alpha 9, 36kDa| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=57369| accessdate = ]PBB_Summary
section_title =
summary_text = GJA9, also called connexin-36 (CX36), is a member of the connexin gene family that is expressed predominantly in mammalian neurons. Connexins associate in groups of 6 and are organized radially around a central pore to form connexons. Each gap junction intercellular channel is formed by the conjunction of 2 connexons. See GJB2 (MIM 121011) for additional background information on connexins. [supplied by OMIM] cite web | title = Entrez Gene: GJA9 gap junction protein, alpha 9, 36kDa| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=57369| accessdate = ]References
Further reading
PBB_Further_reading
citations =
*cite journal | author=Belluardo N, Trovato-Salinaro A, Mudò G, "et al." |title=Structure, chromosomal localization, and brain expression of human Cx36 gene. |journal=J. Neurosci. Res. |volume=57 |issue= 5 |pages= 740–52 |year= 1999 |pmid= 10462698 |doi=
*cite journal | author=Strausberg RL, Feingold EA, Grouse LH, "et al." |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899–903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899
*cite journal | author=de Brouwer AP, Pennings RJ, Roeters M, "et al." |title=Mutations in the calcium-binding motifs of CDH23 and the 35delG mutation in GJB2 cause hearing loss in one family. |journal=Hum. Genet. |volume=112 |issue= 2 |pages= 156–63 |year= 2003 |pmid= 12522556 |doi= 10.1007/s00439-002-0833-0
*cite journal | author=Martin D, Tawadros T, Meylan L, "et al." |title=Critical role of the transcriptional repressor neuron-restrictive silencer factor in the specific control of connexin36 in insulin-producing cell lines. |journal=J. Biol. Chem. |volume=278 |issue= 52 |pages= 53082–9 |year= 2004 |pmid= 14565956 |doi= 10.1074/jbc.M306861200
*cite journal | author=Bathelier C, François M, Lucotte G |title=Neonatal detection of the 35delG mutation of the GJB2 gene in families at risk for deafness. |journal=Genet. Couns. |volume=15 |issue= 1 |pages= 61–6 |year= 2004 |pmid= 15083701 |doi=
*cite journal | author=Degen J, Meier C, Van Der Giessen RS, "et al." |title=Expression pattern of lacZ reporter gene representing connexin36 in transgenic mice. |journal=J. Comp. Neurol. |volume=473 |issue= 4 |pages= 511–25 |year= 2004 |pmid= 15116387 |doi= 10.1002/cne.20085
*cite journal | author=Mas C, Taske N, Deutsch S, "et al." |title=Association of the connexin36 gene with juvenile myoclonic epilepsy. |journal=J. Med. Genet. |volume=41 |issue= 7 |pages= e93 |year= 2004 |pmid= 15235036 |doi=
*cite journal | author=Gerhard DS, Wagner L, Feingold EA, "et al." |title=The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). |journal=Genome Res. |volume=14 |issue= 10B |pages= 2121–7 |year= 2004 |pmid= 15489334 |doi= 10.1101/gr.2596504
*cite journal | author=Dobrenis K, Chang HY, Pina-Benabou MH, "et al." |title=Human and mouse microglia express connexin36, and functional gap junctions are formed between rodent microglia and neurons. |journal=J. Neurosci. Res. |volume=82 |issue= 3 |pages= 306–15 |year= 2006 |pmid= 16211561 |doi= 10.1002/jnr.20650
*cite journal | author=Hempelmann A, Heils A, Sander T |title=Confirmatory evidence for an association of the connexin-36 gene with juvenile myoclonic epilepsy. |journal=Epilepsy Res. |volume=71 |issue= 2-3 |pages= 223–8 |year= 2006 |pmid= 16876983 |doi= 10.1016/j.eplepsyres.2006.06.021
*cite journal | author=Aleksic B, Ishihara R, Takahashi N, "et al." |title=Gap junction coding genes and schizophrenia: a genetic association study. |journal=J. Hum. Genet. |volume=52 |issue= 6 |pages= 498–501 |year= 2007 |pmid= 17427027 |doi= 10.1007/s10038-007-0142-5PBB_Controls
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