Tissue expression
Cell line expression
Protein structure

SLC19A2

Solute carrier family 19 member 2
THTR1, TRMA 
This gene encodes the thiamin transporter protein. Mutations in this gene cause thiamin-responsive megaloblastic anemia syndrome (TRMA), which is an autosomal recessive disorder characterized by diabetes mellitus, megaloblastic anemia and sensorineural deafness. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2016]
More gene data

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107 antibodies from 20 providers.

Antibody properties

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AntibodyRefsTypeWBELICCIPIHCFC
Biorbyt
15 antibodies
Invitrogen Antibodies
7 antibodies
antibodies-online
27 antibodies
Novus Biologicals
4 antibodies
Abnova Corporation
4 antibodies
Atlas Antibodies
2 antibodies
Cusabio Biotech Co., Ltd
5 antibodies
Abgent
1 antibody
GeneTex
1 antibody
NovoPro Bioscience Inc.
1 antibody
Aviva Systems Biology
1 antibody
OriGene
1 antibody
Bioss
3 antibodies
Creative Diagnostics
3 antibodies
Abbexa
5 antibodies
MyBioSource
2 antibodies
Creative Biolabs
4 antibodies
MilliporeSigma / Merck KGaA
3 antibodies
Leading Biology
1 antibody