sodium channel protein type 9 subunit alpha isoform X4 [Homo sapiens]

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Identification and In-Silico study of non-synonymous functional SNPs in the human SCN9A gene. [PLoS One. 2024]
Identification and In-Silico study of non-synonymous functional SNPs in the human SCN9A gene.
Waheed S, Ramzan K, Ahmad S, Khan MS, Wajid M, Ullah H, Umar A, Iqbal R, Ullah R, Bari A. PLoS One. 2024; 19(2):e0297367. Epub 2024 Feb 23.
Structural basis for severe pain caused by mutations in the voltage sensors of sodium channel NaV1.7. [J Gen Physiol. 2023]
Structural basis for severe pain caused by mutations in the voltage sensors of sodium channel NaV1.7.
Wisedchaisri G, Gamal El-Din TM, Powell NM, Zheng N, Catterall WA. J Gen Physiol. 2023 Dec 4; 155(12). Epub 2023 Oct 30.
Erythromelalgia caused by the missense mutation p.Arg220Pro in an alternatively spliced exon of SCN9A (NaV1.7). [Hum Mol Genet. 2024]
Erythromelalgia caused by the missense mutation p.Arg220Pro in an alternatively spliced exon of SCN9A (NaV1.7).
Deuis JR, Kumble S, Keramidas A, Ragnarsson L, Simons C, Pais L, White SM, Vetter I. Hum Mol Genet. 2024 Jan 7; 33(2):103-109.

RefSeq genomic sequence
See the genomic reference sequence for the SCN9A gene (NG_012798.1).
RefSeq mRNA
See reference mRNA sequence for the SCN9A gene (XM_017004669.2).
RefSeq protein isoforms
See 14 reference sequence protein isoforms for the SCN9A gene.

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Protein