KCNV2
{{Short description|Protein-coding gene in the species Homo sapiens}}
{{Infobox_gene}}
Potassium voltage-gated channel subfamily V member 2 is a protein that in humans is encoded by the KCNV2 gene.{{cite journal |vauthors=Ottschytsch N, Raes A, Van Hoorick D, Snyders DJ | title = Obligatory heterotetramerization of three previously uncharacterized Kv channel alpha-subunits identified in the human genome | journal = Proc Natl Acad Sci U S A | volume = 99 | issue = 12 | pages = 7986–91 |date=Jun 2002 | pmid = 12060745 | pmc = 123007 | doi = 10.1073/pnas.122617999 | bibcode = 2002PNAS...99.7986O | doi-access = free }}{{cite journal |vauthors=Gutman GA, Chandy KG, Grissmer S, Lazdunski M, McKinnon D, Pardo LA, Robertson GA, Rudy B, Sanguinetti MC, Stuhmer W, Wang X | title = International Union of Pharmacology. LIII. Nomenclature and molecular relationships of voltage-gated potassium channels | journal = Pharmacol Rev | volume = 57 | issue = 4 | pages = 473–508 |date=Dec 2005 | pmid = 16382104 | doi = 10.1124/pr.57.4.10 | s2cid = 219195192 }} The protein encoded by this gene is a voltage-gated potassium channel subunit.
References
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Further reading
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- {{cite journal |vauthors=Wu H, Cowing JA, Michaelides M, etal |title=Mutations in the gene KCNV2 encoding a voltage-gated potassium channel subunit cause "cone dystrophy with supernormal rod electroretinogram" in humans. |journal=Am. J. Hum. Genet. |volume=79 |issue= 3 |pages= 574–9 |year= 2006 |pmid= 16909397 |doi= 10.1086/507568 |pmc=1559534 }}
- {{cite journal |author1=Ben Salah S |author2=Kamei S |author3=Sénéćhal A |title=Novel KCNV2 mutations in cone dystrophy with supernormal rod electroretinogram. |journal=Am. J. Ophthalmol. |volume=145 |issue= 6 |pages= 1099–106 |year= 2008 |pmid= 18400204 |doi= 10.1016/j.ajo.2008.02.004 |s2cid=8716306 |display-authors=etal|url=http://www.hal.inserm.fr/inserm-00259328/document }}
- {{cite journal |vauthors=Gerhard DS, Wagner L, Feingold EA, etal |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 |pmc=528928 }}
- {{cite journal |vauthors=Balijepalli RC, Delisle BP, Balijepalli SY, etal |title=Kv11.1 (ERG1) K+ channels localize in cholesterol and sphingolipid enriched membranes and are modulated by membrane cholesterol. |journal=Channels (Austin) |volume=1 |issue= 4 |pages= 263–72 |year= 2007|pmid= 18708743 |doi= 10.4161/chan.4946|doi-access=free }}
- {{cite journal |vauthors=Wistow G, Bernstein SL, Wyatt MK, etal |title=Expressed sequence tag analysis of human retina for the NEIBank Project: retbindin, an abundant, novel retinal cDNA and alternative splicing of other retina-preferred gene transcripts. |journal=Mol. Vis. |volume=8 |pages= 196–204 |year= 2002 |pmid= 12107411 }}
- {{cite journal |vauthors=Strausberg RL, Feingold EA, Grouse LH, etal |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= 2002 |pmid= 12477932 |doi= 10.1073/pnas.242603899 |pmc=139241 |bibcode=2002PNAS...9916899M |doi-access=free }}
- {{cite journal |vauthors=Thiagalingam S, McGee TL, Weleber RG, etal |title=Novel mutations in the KCNV2 gene in patients with cone dystrophy and a supernormal rod electroretinogram. |journal=Ophthalmic Genet. |volume=28 |issue= 3 |pages= 135–42 |year= 2007 |pmid= 17896311 |doi= 10.1080/13816810701503681 |s2cid=6288000 }}
- {{cite journal |vauthors=Humphray SJ, Oliver K, Hunt AR, etal |title=DNA sequence and analysis of human chromosome 9. |journal=Nature |volume=429 |issue= 6990 |pages= 369–74 |year= 2004 |pmid= 15164053 |doi= 10.1038/nature02465 |pmc=2734081 |bibcode=2004Natur.429..369H }}
- {{cite journal |vauthors=Wissinger B, Dangel S, Jägle H, etal |title=Cone dystrophy with supernormal rod response is strictly associated with mutations in KCNV2. |journal=Invest. Ophthalmol. Vis. Sci. |volume=49 |issue= 2 |pages= 751–7 |year= 2008 |pmid= 18235024 |doi= 10.1167/iovs.07-0471 |doi-access= free }}
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External links
- {{MeshName|Kv8.2+Potassium+Channel}}
- {{MeshName|KCNV2+protein,+human}}
{{Ion channels|g3}}
{{membrane-protein-stub}}