Homo sapiens potassium voltage-gated channel subfamily Q member 1 (KCN - Nucleotide

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Genetic characterization of KCNQ1 variants improves risk stratification in type 1 long QT syndrome patients. [Europace. 2024]
Genetic characterization of KCNQ1 variants improves risk stratification in type 1 long QT syndrome patients.
Morgat C, Fressart V, Porretta AP, Neyroud N, Messali A, Temmar Y, Algalarrondo V, Surget E, Bloch A, Leenhardt A, et al. Europace. 2024 Jun 3; 26(6).
A mutation in the cardiac KV7.1 channel possibly disrupts interaction with Yotiao protein. [Biochem Biophys Res Commun. 2024]
A mutation in the cardiac KV7.1 channel possibly disrupts interaction with Yotiao protein.
Li B, Karlova M, Zhang H, Pustovit OB, Mai L, Novoseletsky V, Podolyak D, Zaklyazminskaya EV, Abramochkin DV, Sokolova OS. Biochem Biophys Res Commun. 2024 Jun 25; 714:149947. Epub 2024 Apr 16.
Clinical characterization of type 1 long QT syndrome caused by C-terminus Kv7.1 variants. [Heart Rhythm. 2024]
Clinical characterization of type 1 long QT syndrome caused by C-terminus Kv7.1 variants.
Kashiwa A, Itoh H, Makiyama T, Wada Y, Ozawa J, Kato K, Fukuyama M, Nakajima T, Ohno S, Horie M. Heart Rhythm. 2024 Jul; 21(7):1113-1120. Epub 2024 Feb 15.

RefSeq protein product
See the reference protein sequence for potassium voltage-gated channel subfamily KQT member 1 isoform 1 (NP_000209.2).

Protein
Protein sequence from Nucleotide coding region
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Kv7.1 [Guide to Pharmacology]
Kv7.1
Guide to Pharmacology
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Nucleotide