PREDICTED: Homo sapiens solute carrier family 52 member 3 (SLC52A3), t - Nucleotide

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A dual-activity topoisomerase complex regulates mRNA translation and turnover. [Nucleic Acids Res. 2022]
A dual-activity topoisomerase complex regulates mRNA translation and turnover.
Su S, Xue Y, Sharov A, Zhang Y, Lee SK, Martindale JL, Li W, Ku WL, Zhao K, De S, et al. Nucleic Acids Res. 2022 Jul 8; 50(12):7013-7033.
Three cases of adult-onset Brown-Vialetto-Van Laere syndrome: Novel variants in SLC52A3 gene and MRI abnormalities. [Neuromuscul Disord. 2021]
Three cases of adult-onset Brown-Vialetto-Van Laere syndrome: Novel variants in SLC52A3 gene and MRI abnormalities.
Carey G, Kuchcinski G, Gauvrit F, Defebvre L, Nguyen S, Dhaenens CM, Dessein AF, Vianey-Saban C, Acquaviva C, Tard C. Neuromuscul Disord. 2021 Aug; 31(8):752-755. Epub 2021 Jun 26.
Promotion of rs3746804 (p. L267P) polymorphism to intracellular SLC52A3a trafficking and riboflavin transportation in esophageal cancer cells. [Amino Acids. 2021]
Promotion of rs3746804 (p. L267P) polymorphism to intracellular SLC52A3a trafficking and riboflavin transportation in esophageal cancer cells.
Long L, Pang XX, Zeng FM, Zhan XH, Xie YH, Pan F, Wang W, Liao LD, Xu XE, Li B, et al. Amino Acids. 2021 Aug; 53(8):1197-1209. Epub 2021 Jul 5.

RefSeq alternative splicing
See 9 reference mRNA sequence splice variants for the SLC52A3 gene.
RefSeq protein product
See the reference protein sequence for solute carrier family 52, riboflavin transporter, member 3 isoform X1 (XP_054178896.1).

PREDICTED: Homo sapiens solute carrier family 52 member 3 (SLC52A3), transcript ...
PREDICTED: Homo sapiens solute carrier family 52 member 3 (SLC52A3), transcript variant X3, mRNA
gi|2462579289|ref|XM_054322921.1|

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Nucleotide