solute carrier family 13 member 1 isoform X7 [Homo sapiens]

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Rare variant analyses in large-scale cohorts identified SLC13A1 associated with chronic pain. [Pain. 2023]
Rare variant analyses in large-scale cohorts identified SLC13A1 associated with chronic pain.
Ao X, Parisien M, Zidan M, Grant AV, Martinsen AE, Winsvold BS, Diatchenko L. Pain. 2023 Aug 1; 164(8):1841-1851. Epub 2023 Mar 22.
Serum sulfate level and Slc13a1 mRNA expression remain unaltered in a mouse model of moderate vitamin D deficiency. [Mol Cell Biochem. 2023]
Serum sulfate level and Slc13a1 mRNA expression remain unaltered in a mouse model of moderate vitamin D deficiency.
Atcheson RJ, Burne THJ, Dawson PA. Mol Cell Biochem. 2023 Aug; 478(8):1771-1777. Epub 2022 Dec 25.
Biallelic variants in the SLC13A1 sulfate transporter gene cause hyposulfatemia with a mild spondylo-epi-metaphyseal dysplasia. [Clin Genet. 2023]
Biallelic variants in the SLC13A1 sulfate transporter gene cause hyposulfatemia with a mild spondylo-epi-metaphyseal dysplasia.
van de Kamp JM, Bökenkamp A, Smith DEC, Wamelink MMC, Jansen EEW, Struys EA, Waisfisz Q, Verkleij M, Hartmann MF, Wang R, et al. Clin Genet. 2023 Jan; 103(1):45-52. Epub 2022 Oct 3.

RefSeq genomic sequence
See the genomic reference sequence for the SLC13A1 gene (NG_050641.2).
RefSeq mRNA
See reference mRNA sequence for the SLC13A1 gene (XM_011516519.4).
RefSeq protein isoforms
See 19 reference sequence protein isoforms for the SLC13A1 gene.

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Protein