KCNV2: Difference between revisions

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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  |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 |display-authors=etal}}
*{{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 |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=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=  }}
*{{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=  }}

Revision as of 13:03, 4 November 2018

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Identifiers
Aliases
External IDsGeneCards: [1]
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

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RefSeq (protein)

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Location (UCSC)n/an/a
PubMed searchn/an/a
Wikidata
View/Edit Human

Potassium voltage-gated channel subfamily V member 2 is a protein that in humans is encoded by the KCNV2 gene.[1][2] The protein encoded by this gene is a voltage-gated potassium channel subunit.[1][2]{

References

  1. 1.0 1.1 Ottschytsch N, Raes A, Van Hoorick D, Snyders DJ (Jun 2002). "Obligatory heterotetramerization of three previously uncharacterized Kv channel alpha-subunits identified in the human genome". Proc Natl Acad Sci U S A. 99 (12): 7986–91. doi:10.1073/pnas.122617999. PMC 123007. PMID 12060745.
  2. 2.0 2.1 Gutman GA, Chandy KG, Grissmer S, Lazdunski M, McKinnon D, Pardo LA, Robertson GA, Rudy B, Sanguinetti MC, Stuhmer W, Wang X (Dec 2005). "International Union of Pharmacology. LIII. Nomenclature and molecular relationships of voltage-gated potassium channels". Pharmacol Rev. 57 (4): 473–508. doi:10.1124/pr.57.4.10. PMID 16382104.

Further reading

External links