Homo sapiens K-Cl cotransporter KCC3a-S1 isoform (SLC12A6) mRNA, compl - 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.
Expanding the phenotype of SLC12A6-associated sensorimotor neuropathy. [BMJ Case Rep. 2021]
Expanding the phenotype of SLC12A6-associated sensorimotor neuropathy.
Bogdanova-Mihaylova P, McNamara P, Burton-Jones S, Murphy SM. BMJ Case Rep. 2021 Oct 27; 14(10). Epub 2021 Oct 27.

RefSeq alternative splicing
See 13 reference mRNA sequence splice variants for the SLC12A6 gene.

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Nucleotide