Homo sapiens mRNA for solute carrier family 19, member 2 variant prote - Nucleotide

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Identification of the amino acid residues involved in the species-dependent differences in the pyridoxine transport function of SLC19A3. [J Biol Chem. 2022]
Identification of the amino acid residues involved in the species-dependent differences in the pyridoxine transport function of SLC19A3.
Miyake K, Yasujima T, Takahashi S, Yamashiro T, Yuasa H. J Biol Chem. 2022 Aug; 298(8):102161. Epub 2022 Jun 17.
Whole-Exome Sequencing Revealed a Pathogenic Nonsense Variant in the SLC19A2 Gene in an Iranian Family with Thiamine-Responsive Megaloblastic Anemia. [Lab Med. 2022]
Whole-Exome Sequencing Revealed a Pathogenic Nonsense Variant in the SLC19A2 Gene in an Iranian Family with Thiamine-Responsive Megaloblastic Anemia.
Mohsen-Pour N, Naderi N, Ghasemi S, Hesami M, Maleki M, Kalayinia S. Lab Med. 2022 Nov 3; 53(6):640-650.
Animal species differences in the pyridoxine transport function of SLC19A3: Absence of Slc19a3-mediated pyridoxine uptake in the rat small intestine. [Drug Metab Pharmacokinet. 2022]
Animal species differences in the pyridoxine transport function of SLC19A3: Absence of Slc19a3-mediated pyridoxine uptake in the rat small intestine.
Yamashiro T, Yasujima T, Yuasa H. Drug Metab Pharmacokinet. 2022 Jun; 44:100456. Epub 2022 Mar 9.

RefSeq alternative splicing
See 2 reference mRNA sequence splice variants for the SLC19A2 gene.

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Nucleotide