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SLC19A3

  • Official Full Name

    solute carrier family 19, member 3

  • Overview

    This gene encodes a ubiquitously expressed transmembrane thiamine transporter that lacks folate transport activity. Mutations in this gene cause biotin-responsive basal ganglia disease (BBGD); a recessive disorder manifested in childhood that progresses to chronic encephalopathy, dystonia, quadriparesis, and death if untreated. Patients with BBGD have bilateral necrosis in the head of the caudate nucleus and in the putamen. Administration of high doses of biotin in the early progression of the disorder eliminates pathological symptoms while delayed treatment results in residual paraparesis, mild mental retardation, or dystonia. Administration of thiamine is ineffective in the treatment of this disorder. Experiments have failed to show that this protein can transport biotin. Mutations in this gene also cause a Wernickes-like encephalopathy.
  • Synonyms

    SLC19A3; solute carrier family 19, member 3; thiamine transporter 2; THTR2; thTr 2; thTr-2;

  • Cell & Tissue Lysates
  • Recombinant Proteins
  • Protein Pre-coupled Magnetic Beads
  • Human
  • Mouse
  • Rhesus Macaque
  • HEK293
  • HEK293T
  • Insect Cell
  • Mammalian Cell
  • 8His
  • MBP,Flag
  • Strep,Flag
  • C
  • Myc
  • DDK
  • His
  • His (Fc)
  • Avi
  • N/A
Species Cat.# Product name Source (Host) Tag Protein Length Price
Human SLC19A3-599HCL Recombinant Human SLC19A3 lysate HEK293 N/A
Human SLC19A3-0664H Recombinant Human SLC19A3 Protein (D2-L496), 8×His-Strep, Flag tagged Insect Cell 8His-Strep,Flag D2-L496
Human SLC19A3-177H Recombinant Human SLC19A3 Protein, MYC/DDK-tagged, C13 and N15-labeled HEK293 C-Myc/DDK
Human SLC19A3-0663H Recombinant Human SLC19A3 Protein (D2-L496), 8×His-MBP, Flag tagged Insect Cell 8His-MBP,Flag D2-L496
Mouse SLC19A3-15251M Recombinant Mouse SLC19A3 Protein Mammalian Cell His
Mouse Slc19a3-5908M Recombinant Mouse Slc19a3 Protein, Myc/DDK-tagged HEK293T Myc/DDK
Mouse SLC19A3-8247M-B Recombinant Mouse SLC19A3 Protein Pre-coupled Magnetic Beads HEK293
Mouse SLC19A3-8247M Recombinant Mouse SLC19A3 Protein, His (Fc)-Avi-tagged HEK293 His (Fc)-Avi
Rhesus Macaque SLC19A3-4228R Recombinant Rhesus monkey SLC19A3 Protein, His-tagged Mammalian Cell His
Rhesus Macaque SLC19A3-4044R Recombinant Rhesus Macaque SLC19A3 Protein, His (Fc)-Avi-tagged HEK293 His (Fc)-Avi
Rhesus Macaque SLC19A3-4044R-B Recombinant Rhesus Macaque SLC19A3 Protein Pre-coupled Magnetic Beads HEK293
  • Involved Pathway
  • Protein Function
  • Interacting Protein
  • SLC19A3 Related Articles

SLC19A3 involved in several pathways and played different roles in them. We selected most pathways SLC19A3 participated on our site, such as Vitamin digestion and absorption, which may be useful for your reference. Also, other proteins which involved in the same pathway with SLC19A3 were listed below. Creative BioMart supplied nearly all the proteins listed, you can search them on our site.

Pathway Name Pathway Related Protein
Vitamin digestion and absorptionSLC46A1;SLC52A3;TCN2;SCARB1;SLC23A1;BTD;ABCC1;APOB;APOA1

SLC19A3 has several biochemical functions, for example, thiamine uptake transmembrane transporter activity. Some of the functions are cooperated with other proteins, some of the functions could acted by SLC19A3 itself. We selected most functions SLC19A3 had, and list some proteins which have the same functions with SLC19A3. You can find most of the proteins on our site.

Function Related Protein
thiamine uptake transmembrane transporter activitySLC19A3;SLC19A3B;SLC19A2;C2orf83

SLC19A3 has direct interactions with proteins and molecules. Those interactions were detected by several methods such as yeast two hybrid, co-IP, pull-down and so on. We selected proteins and molecules interacted with SLC19A3 here. Most of them are supplied by our site. Hope this information will be useful for your research of SLC19A3.

CREB3; C3orf38; CREB3L4; TAB2

Laverdiere, I; Guillemette, C; et al. Cyclosporine and methotrexate-related pharmacogenomic predictors of acute graft-versus-host disease. HAEMATOLOGICA 100:275-283(2015).
Dahlin, A; Wittwer, M; et al. A pharmacogenetic candidate gene study of tenofovir-associated Fanconi syndrome. PHARMACOGENETICS AND GENOMICS 25:82-92(2015).
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