Homo sapiens solute carrier family 12 member 6 (SLC12A6), transcript v - Nucleotide

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Late-onset sensory-motor axonal neuropathy, a novel SLC12A6-related phenotype. [Brain. 2023]
Late-onset sensory-motor axonal neuropathy, a novel SLC12A6-related phenotype.
Løseth S, Høyer H, Le KM, Delpire E, Kinge E, Lande A, Hilmarsen HT, Fagerheim T, Nilssen Ø, Braathen GJ. Brain. 2023 Mar 1; 146(3):912-922.
Novel heterozygous variants of SLC12A6 in Japanese families with Charcot-Marie-Tooth disease. [Ann Clin Transl Neurol. 2022]
Novel heterozygous variants of SLC12A6 in Japanese families with Charcot-Marie-Tooth disease.
Ando M, Higuchi Y, Yuan J, Yoshimura A, Taniguchi T, Takei J, Takeuchi M, Hiramatsu Y, Shimizu F, Kubota M, et al. Ann Clin Transl Neurol. 2022 Jul; 9(7):902-911. Epub 2022 Jun 22.
In-Depth In Vivo Crosslinking in Minutes by a Compact, Membrane-Permeable, and Alkynyl-Enrichable Crosslinker. [Anal Chem. 2022]
In-Depth In Vivo Crosslinking in Minutes by a Compact, Membrane-Permeable, and Alkynyl-Enrichable Crosslinker.
Gao H, Zhao L, Zhong B, Zhang B, Gong Z, Zhao B, Liu Y, Zhao Q, Zhang L, Zhang Y. Anal Chem. 2022 May 31; 94(21):7551-7558. Epub 2022 May 16.

RefSeq alternative splicing
See 13 reference mRNA sequence splice variants for the SLC12A6 gene.
RefSeq protein product
See the reference protein sequence for solute carrier family 12 member 6 isoform c (NP_001035960.1).

Protein
Protein sequence from Nucleotide coding region
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Nucleotide