Homo sapiens solute carrier family 34 member 3 (SLC34A3), transcript v - Nucleotide

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Rare variants in the sodium-dependent phosphate transporter gene SLC34A3 explain missing heritability of urinary stone disease. [Kidney Int. 2023]
Rare variants in the sodium-dependent phosphate transporter gene SLC34A3 explain missing heritability of urinary stone disease.
Sadeghi-Alavijeh O, Chan MMY, Moochhala SH, Genomics England Research Consortium, Howles S, Gale DP, Böckenhauer D. Kidney Int. 2023 Nov; 104(5):975-984. Epub 2023 Jul 4.
Relationship between clinical phenotype and in vitro analysis of 13 NPT2c/SCL34A3 mutants. [Sci Rep. 2023]
Relationship between clinical phenotype and in vitro analysis of 13 NPT2c/SCL34A3 mutants.
Brazier F, Courbebaisse M, David A, Bergerat D, Leroy C, Lindner M, Maruani G, Saint Jacques C, Letavernier E, Hureaux M, et al. Sci Rep. 2023 Jan 3; 13(1):85. Epub 2023 Jan 3.
The genetic polymorphisms of XPR1 and SCL34A3 are associated with Fanconi syndrome in Chinese patients of tumor-induced osteomalacia. [J Endocrinol Invest. 2021]
The genetic polymorphisms of XPR1 and SCL34A3 are associated with Fanconi syndrome in Chinese patients of tumor-induced osteomalacia.
Jiang Y, Li X, Feng J, Li M, Wang O, Xing XP, Xia WB. J Endocrinol Invest. 2021 Apr; 44(4):773-780. Epub 2020 Jul 28.

RefSeq protein product
See the reference protein sequence for sodium-dependent phosphate transport protein 2C (NP_543153.2).

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Homo sapiens solute carrier family 34 member 3 (SLC34A3), transcript variant 3, ...
Homo sapiens solute carrier family 34 member 3 (SLC34A3), transcript variant 3, mRNA
gi|2199215562|ref|NM_080877.3|

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