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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 .
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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 .
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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 .