Homo sapiens potassium voltage-gated channel subfamily Q member 2 (KCN - 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 protein product
See the reference protein sequence for potassium voltage-gated channel subfamily KQT member 2 isoform b (NP_742104.1).

Protein
Protein sequence from Nucleotide coding region
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F-box protein SKIP24 isoform X2 [Oryza sativa Japonica Group]
F-box protein SKIP24 isoform X2 [Oryza sativa Japonica Group]
gi|1002235569|ref|XP_015621983.1|

Protein

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Nucleotide