Homo sapiens neuronal delayed-rectifier voltage-gated potassium channe - Nucleotide

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Clinical and genetic analysis of 18 patients with KCNQ2 mutations from South China. [Turk J Pediatr. 2024]
Clinical and genetic analysis of 18 patients with KCNQ2 mutations from South China.
Cao B, Peng B, Tian Y, Wang X, Li X, Zhu H, Shen H, Chen W. Turk J Pediatr. 2024 May 23; 66(2):191-204. Epub 2024 May 23.
KCNQ2 mutations cause unique neonatal behavior arrests without motor seizures: Functional characterization. [Epilepsy Behav. 2024]
KCNQ2 mutations cause unique neonatal behavior arrests without motor seizures: Functional characterization.
Wong SH, Liou YM, Yang JJ, Lee IC. Epilepsy Behav. 2024 Jul; 156:109798. Epub 2024 May 23.
Effect of a sensing charge mutation on the deactivation of KV7.2 channels. [J Gen Physiol. 2024]
Effect of a sensing charge mutation on the deactivation of KV7.2 channels.
Mehrdel B, Villalba-Galea CA. J Gen Physiol. 2024 Mar 4; 156(3). Epub 2024 Jan 18.

RefSeq alternative splicing
See 22 reference mRNA sequence splice variants for the KCNQ2 gene.

Human DNA sequence from clone RP1-63M2 on chromosome 20, complete sequence
Human DNA sequence from clone RP1-63M2 on chromosome 20, complete sequence
gi|8574371|emb|AL121906.18|

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Nucleotide