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Protein-coding gene in the species Homo sapiens
Potassium voltage-gated channel subfamily V member 2 is a protein that in humans is encoded by the KCNV2 gene .[ 5] [ 6] The protein encoded by this gene is a voltage-gated potassium channel subunit.[ 5] [ 6]
^ a b c GRCh38: Ensembl release 89: ENSG00000168263 – Ensembl , May 2017
^ a b c GRCm38: Ensembl release 89: ENSMUSG00000047298 – Ensembl , May 2017
^ "Human PubMed Reference:" . National Center for Biotechnology Information, U.S. National Library of Medicine .
^ "Mouse PubMed Reference:" . National Center for Biotechnology Information, U.S. National Library of Medicine .
^ a b 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. Bibcode :2002PNAS...99.7986O . doi :10.1073/pnas.122617999 . PMC 123007 . PMID 12060745 .
^ a b 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 . S2CID 219195192 .
Wu H, Cowing JA, Michaelides M, et al. (2006). "Mutations in the gene KCNV2 encoding a voltage-gated potassium channel subunit cause "cone dystrophy with supernormal rod electroretinogram" in humans" . Am. J. Hum. Genet . 79 (3): 574– 9. doi :10.1086/507568 . PMC 1559534 . PMID 16909397 .
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Thiagalingam S, McGee TL, Weleber RG, et al. (2007). "Novel mutations in the KCNV2 gene in patients with cone dystrophy and a supernormal rod electroretinogram". Ophthalmic Genet . 28 (3): 135– 42. doi :10.1080/13816810701503681 . PMID 17896311 . S2CID 6288000 .
Humphray SJ, Oliver K, Hunt AR, et al. (2004). "DNA sequence and analysis of human chromosome 9" . Nature . 429 (6990): 369– 74. Bibcode :2004Natur.429..369H . doi :10.1038/nature02465 . PMC 2734081 . PMID 15164053 .
Wissinger B, Dangel S, Jägle H, et al. (2008). "Cone dystrophy with supernormal rod response is strictly associated with mutations in KCNV2" . Invest. Ophthalmol. Vis. Sci . 49 (2): 751– 7. doi :10.1167/iovs.07-0471 . PMID 18235024 .