Homo sapiens potassium voltage-gated channel subfamily H member 5 (KCN - Nucleotide

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Mechanism underlying delayed rectifying in human voltage-mediated activation Eag2 channel. [Nat Commun. 2023]
Mechanism underlying delayed rectifying in human voltage-mediated activation Eag2 channel.
Zhang M, Shan Y, Pei D. Nat Commun. 2023 Mar 16; 14(1):1470. Epub 2023 Mar 16.
Neurodevelopmental and Epilepsy Phenotypes in Individuals With Missense Variants in the Voltage-Sensing and Pore Domains of KCNH5. [Neurology. 2023]
Neurodevelopmental and Epilepsy Phenotypes in Individuals With Missense Variants in the Voltage-Sensing and Pore Domains of KCNH5.
Happ HC, Sadleir LG, Zemel M, de Valles-Ibáñez G, Hildebrand MS, McConkie-Rosell A, McDonald M, May H, Sands T, Aggarwal V, et al. Neurology. 2023 Feb 7; 100(6):e603-e615. Epub 2022 Oct 28.
A novel loss-of-function mutation of the voltage-gated potassium channel Kv10.2 involved in epilepsy and autism. [Orphanet J Rare Dis. 2022]
A novel loss-of-function mutation of the voltage-gated potassium channel Kv10.2 involved in epilepsy and autism.
Galán-Vidal J, Socuéllamos PG, Baena-Nuevo M, Contreras L, González T, Pérez-Poyato MS, Valenzuela C, González-Lamuño D, Gandarillas A. Orphanet J Rare Dis. 2022 Sep 6; 17(1):345. Epub 2022 Sep 6.

RefSeq alternative splicing
See 4 reference mRNA sequence splice variants for the KCNH5 gene.

Protein
Protein sequence from Nucleotide coding region
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RNA
RNA sequence records that are annotated on the current genomic nucleotide sequences. The RNA records represent aligned or predicted transcripts of the current records.

Order Kcnh5 cDNA clone/Protein/Antibody/RNAi [OriGene]
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Nucleotide