SLC19A2

gene product
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. [provided by RefSeq, Jul 2008]
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31 antibodies from 8 providers.

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AntibodyRefsTypeWBELICCIPIHCFC
Novus Biologicals
6 antibodies
Abnova Corporation
3 antibodies
antibodies-online
9 antibodies
Atlas Antibodies
2 antibodies
LifeSpan BioSciences, Inc.
2 antibodies
Creative Biomart
5 antibodies
Sigma-Aldrich
3 antibodies
Aviva Systems Biology
1 antibody