Homo sapiens solute carrier family 17 member 8 (SLC17A8), transcript v - Nucleotide

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Sequential genome-wide CRISPR-Cas9 screens identify genes regulating cell-surface expression of tetraspanins. [Cell Rep. 2023]
Sequential genome-wide CRISPR-Cas9 screens identify genes regulating cell-surface expression of tetraspanins.
Yang J, Guo F, Chin HS, Chen GB, Ang CH, Lin Q, Hong W, Fu NY. Cell Rep. 2023 Feb 28; 42(2):112065. Epub 2023 Jan 31.
The c.824C>A and c.616dupA mutations in the SLC17a8 gene are associated with auditory neuropathy and lead to defective expression of VGluT3. [Neuroreport. 2021]
The c.824C>A and c.616dupA mutations in the SLC17a8 gene are associated with auditory neuropathy and lead to defective expression of VGluT3.
Qi Y, Gong S, Liu K, Song Y. Neuroreport. 2021 Aug 4; 32(11):949-956.
Dual proteome-scale networks reveal cell-specific remodeling of the human interactome. [Cell. 2021]
Dual proteome-scale networks reveal cell-specific remodeling of the human interactome.
Huttlin EL, Bruckner RJ, Navarrete-Perea J, Cannon JR, Baltier K, Gebreab F, Gygi MP, Thornock A, Zarraga G, Tam S, et al. Cell. 2021 May 27; 184(11):3022-3040.e28. Epub 2021 May 6.

RefSeq alternative splicing
See the other reference mRNA sequence splice variant for the SLC17A8 gene (NM_139319.3).
RefSeq protein product
See the reference protein sequence for vesicular glutamate transporter 3 isoform 2 (NP_001138760.1).

Protein
Protein sequence from Nucleotide coding region
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Nucleotide