Homo sapiens voltage-gated channel subfamily H member 2 (KCNH2) gene, - Nucleotide

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Dissecting the associations of KCNH2 genetic polymorphisms with various types of cardiac arrhythmias. [Gene. 2024]
Dissecting the associations of KCNH2 genetic polymorphisms with various types of cardiac arrhythmias.
Li S, Zhang Z, Ding Y, Yu T, Qin Z, Guo S. Gene. 2024 Mar 20; 899:148132. Epub 2024 Jan 3.
Identification and characterization of two novel KCNH2 mutations contributing to long QT syndrome. [PLoS One. 2024]
Identification and characterization of two novel KCNH2 mutations contributing to long QT syndrome.
Owusu-Mensah A, Treat J, Bernardi J, Pfeiffer R, Goodrow R, Tsevi B, Lam V, Audette M, Cordeiro JM, Deo M. PLoS One. 2024; 19(1):e0287206. Epub 2024 Jan 5.
Functional and clinical characterization of a novel homozygous KCNH2 missense variant in the pore region of Kv11.1 leading to a viable but severe long-QT syndrome. [Gene. 2024]
Functional and clinical characterization of a novel homozygous KCNH2 missense variant in the pore region of Kv11.1 leading to a viable but severe long-QT syndrome.
Delinière A, Jaupart L, Janin A, Millat G, Boulin T, Andrini O, Chevalier P. Gene. 2024 Mar 1; 897:148076. Epub 2023 Dec 10.

RefSeq alternative splicing
See 18 reference mRNA sequence splice variants for the KCNH2 gene.

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Order Kcnh2 cDNA clone/Protein/Antibody/RNAi [OriGene]
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Nucleotide