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    SLC13A3 solute carrier family 13 member 3 [ Homo sapiens (human) ]

    Gene ID: 64849, updated on 4-Jan-2025

    GeneRIFs: Gene References Into Functions

    GeneRIFPubMed TitleDate
    SLC13A3 is a major effector downstream of activated beta-catenin in liver cancer pathogenesis.

    SLC13A3 is a major effector downstream of activated β-catenin in liver cancer pathogenesis.
    Zhao W, Wang X, Han L, Zhang C, Wang C, Kong D, Zhang M, Xu T, Li G, Hu G, Luo J, Yee SW, Yang J, Stahl A, Chen X, Zhang Y., Free PMC Article

    09/4/2024
    Structural and functional implications of SLC13A3 and SLC9A6 mutations: an in silico approach to understanding intellectual disability.

    Structural and functional implications of SLC13A3 and SLC9A6 mutations: an in silico approach to understanding intellectual disability.
    Hussain SI, Muhammad N, Shah SUD, Fardous F, Khan SA, Khan N, Rehman AU, Siddique M, Wasan SA, Niaz R, Ullah H, Khan N, Muhammad N, Mirza MU, Wasif N, Khan S., Free PMC Article

    11/1/2023
    Association of Single Nucleotide Polymorphisms in KCNA10 and SLC13A3 Genes with the Susceptibility to Chronic Kidney Disease of Unknown Etiology in Central Indian Patients.

    Association of Single Nucleotide Polymorphisms in KCNA10 and SLC13A3 Genes with the Susceptibility to Chronic Kidney Disease of Unknown Etiology in Central Indian Patients.
    Kumari R, Tiwari S, Atlani M, Anirudhan A, Goel SK, Kumar A.

    07/27/2023
    NaDC3-related immunostaining was detected in the basolateral membrane of proximal tubules and in the basolateral membrane and/or luminal membrane of principal cells in connecting segments and collecting ducts

    Distribution of organic anion transporters NaDC3 and OAT1-3 along the human nephron.
    Breljak D, Ljubojević M, Hagos Y, Micek V, Balen Eror D, Vrhovac Madunić I, Brzica H, Karaica D, Radović N, Kraus O, Anzai N, Koepsell H, Burckhardt G, Burckhardt BC, Sabolić I.

    07/22/2017
    OAT1 and NaDC3 in the basolateral membrane and OAT4 in the luminal membrane of proximal tubule cells are responsible for the avid renal secretion of N-carbamoylglutamate.

    Transporters involved in renal excretion of N-carbamoylglutamate, an orphan drug to treat inborn n-acetylglutamate synthase deficiency.
    Schwob E, Hagos Y, Burckhardt G, Burckhardt BC.

    02/14/2015
    In a study addressing genetic, social, and environmental contributors of chronic kidney disease with tubulointerstitial damages in Sri Lanka, SNP rs6066043 of SLC13A3 was found attributable risk of 50%.

    An integrative study of the genetic, social and environmental determinants of chronic kidney disease characterized by tubulointerstitial damages in the North Central Region of Sri Lanka.
    Nanayakkara S, Senevirathna ST, Abeysekera T, Chandrajith R, Ratnatunga N, Gunarathne ED, Yan J, Hitomi T, Muso E, Komiya T, Harada KH, Liu W, Kobayashi H, Okuda H, Sawatari H, Matsuda F, Yamada R, Watanabe T, Miyataka H, Himeno S, Koizumi A.

    12/27/2014
    study concludes NaDC3 present at the basolateral membrane of proximal tubule cells mediates sodium-dependent glutathione (GSH) uptake; the kinetic data show that NaDC3 is a low-affinity GSH transporter

    Glutathione is a low-affinity substrate of the human sodium-dependent dicarboxylate transporter.
    Schorbach L, Krick W, Burckhardt G, Burckhardt BC.

    07/5/2014
    The data 1) reveal alpha-ketoglutarate as a common high-affinity substrate of NaDC3, OAT1, and OAT3

    Differential interaction of dicarboxylates with human sodium-dicarboxylate cotransporter 3 and organic anion transporters 1 and 3.
    Kaufhold M, Schulz K, Breljak D, Gupta S, Henjakovic M, Krick W, Hagos Y, Sabolic I, Burckhardt BC, Burckhardt G.

    12/17/2011
    The results indicate that SLC13A3 is a direct downstream target of PITX2 transcriptional regulation and that levels of PITX2 and SLC13A3 modulate responses to oxidative stress in ocular cells.

    PITX2 is involved in stress response in cultured human trabecular meshwork cells through regulation of SLC13A3.
    Strungaru MH, Footz T, Liu Y, Berry FB, Belleau P, Semina EV, Raymond V, Walter MA., Free PMC Article

    12/17/2011
    NaDC3 promotes cellular senescence probably by inhibiting NAD(+)-dependent SIRT1.

    High-affinity Na(+)-dependent dicarboxylate cotransporter promotes cellular senescence by inhibiting SIRT1.
    Liu W, Hong Q, Bai XY, Fu B, Xie Y, Zhang X, Li J, Shi S, Lv Y, Sun X, Chen X., Free PMC Article

    01/29/2011
    Observational study of gene-disease association. (HuGE Navigator)

    Heterogeneity in gene loci associated with type 2 diabetes on human chromosome 20q13.1.
    Bento JL, Palmer ND, Zhong M, Roh B, Lewis JP, Wing MR, Pandya H, Freedman BI, Langefeld CD, Rich SS, Bowden DW, Mychaleckyj JC., Free PMC Article

    07/16/2008
    The narrow substrate specificity prevents interaction of drugs with dicarboxylate-like structure with hNaDC-3 and ensures sufficient support of the proximal tubule cells with alpha-ketoglutarate for anion secretion via organic anion transporter 1 or 3.

    Substrate specificity of the human renal sodium dicarboxylate cotransporter, hNaDC-3, under voltage-clamp conditions.
    Burckhardt BC, Lorenz J, Kobbe C, Burckhardt G.

    01/21/2010
    We provide direct evidence of the localization of NaDC3 at the basolateral membrane of human renal proximal tubule cells and identify a di-hydrophobic amino acid motif VW as basolateral localization signal in the N-terminal cytoplasmic domain of NaDC3.

    Identification of basolateral membrane targeting signal of human sodium-dependent dicarboxylate transporter 3.
    Bai X, Chen X, Feng Z, Hou K, Zhang P, Fu B, Shi S.

    01/21/2010
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