Homo sapiens solute carrier family 5 member 7 (SLC5A7), transcript var - Nucleotide

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Genetic analysis of a family affected by congenital myasthenic syndrome due to a Novel mutation in the SLC5A7 gene. [BMC Neurol. 2024]
Genetic analysis of a family affected by congenital myasthenic syndrome due to a Novel mutation in the SLC5A7 gene.
Tian S, Sun H, Gao FF, Zhang K, Nan J, Niu M, Jia X, Xu G, Ge W. BMC Neurol. 2024 Jun 17; 24(1):206. Epub 2024 Jun 17.
CircFBXW4 Suppresses Colorectal Cancer Progression by Regulating the MiR-338-5p/SLC5A7 Axis. [Adv Sci (Weinh). 2024]
CircFBXW4 Suppresses Colorectal Cancer Progression by Regulating the MiR-338-5p/SLC5A7 Axis.
Song W, Fu J, Wu J, Ren J, Xiang R, Kong C, Fu T. Adv Sci (Weinh). 2024 May; 11(18):e2300129. Epub 2024 Mar 10.
Targeted demethylation of the SLC5A7 promotor inhibits colorectal cancer progression. [Clin Epigenetics. 2022]
Targeted demethylation of the SLC5A7 promotor inhibits colorectal cancer progression.
Li Y, Liu B, Yin X, Jiang Z, Fang C, Chen N, Zhang B, Dai L, Yin Y. Clin Epigenetics. 2022 Jul 20; 14(1):92. Epub 2022 Jul 20.

RefSeq alternative splicing
See 12 reference mRNA sequence splice variants for the SLC5A7 gene.
RefSeq protein product
See the reference protein sequence for high affinity choline transporter 1 isoform a (NP_068587.1).

Protein
Protein sequence from Nucleotide coding region
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Nucleotide