Homo sapiens solute carrier family 52 member 1 (SLC52A1), transcript v - Nucleotide

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Riboflavin 1 Transporter Deficiency: Novel SLC52A1 Variants and Expansion of the Phenotypic Spectrum. [Genes (Basel). 2023]
Riboflavin 1 Transporter Deficiency: Novel SLC52A1 Variants and Expansion of the Phenotypic Spectrum.
Grünert SC, Ziagaki A, Heinen A, Schumann A, Tucci S, Spiekerkoetter U, Schmidts M. Genes (Basel). 2023 Jul 7; 14(7). Epub 2023 Jul 7.
Riboflavin transporter SLC52A1, a target of p53, suppresses cellular senescence by activating mitochondrial complex II. [Mol Biol Cell. 2021]
Riboflavin transporter SLC52A1, a target of p53, suppresses cellular senescence by activating mitochondrial complex II.
Nagano T, Awai Y, Kuwaba S, Osumi T, Mio K, Iwasaki T, Kamada S. Mol Biol Cell. 2021 Nov 1; 32(21):br10. Epub 2021 Sep 15.
Whole-exome Sequencing Identifies SLC52A1 and ZNF106 Variants as Novel Genetic Risk Factors for (Early) Multiple-organ Failure in Acute Pancreatitis. [Ann Surg. 2022]
Whole-exome Sequencing Identifies SLC52A1 and ZNF106 Variants as Novel Genetic Risk Factors for (Early) Multiple-organ Failure in Acute Pancreatitis.
van den Berg FF, Issa Y, Vreijling JP, Lerch MM, Weiss FU, Besselink MG, Baas F, Boermeester MA, van Santvoort HC, Dutch Pancreatitis Study Group. Ann Surg. 2022 Jun 1; 275(6):e781-e788. Epub 2021 Jan 8.

RefSeq alternative splicing
See 8 reference mRNA sequence splice variants for the SLC52A1 gene.
RefSeq protein product
See the reference protein sequence for solute carrier family 52, riboflavin transporter, member 1 precursor (NP_060456.3).

Protein
Protein sequence from Nucleotide coding region
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solute carrier family 52 member 1 / SLC52A1 [Guide to Pharmacology]
solute carrier family 52 member 1 / SLC52A1
Guide to Pharmacology
GenScript latest version of gene cDNA ORF Clone [GenScript latest version of g...]
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Nucleotide