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SLC19A2


Official Full Name
solute carrier family 19 member 2
Organism
Homo sapiens
Gene ID
10560
Background
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]
Synonyms
TC1; THT1; TRMA; THMD1; THTR1

Cat.No. Product Name Price
SHG225557 shRNA set against Mouse Slc19a2(NM_054087.2) Inquiry
SHH408872 shRNA set against Human SLC19A2 (NM_006996.2) Inquiry
SHH408876 shRNA set against Mouse SLC19A2 (NM_054087.2) Inquiry
SHH408880 shRNA set against Rat SLC19A2 (NM_001030024.1) Inquiry
SHL000228 shRNA set against Rat Slc19a2(NM_001030024.1) Inquiry
Cat.No. Product Name Price
CDFR004148 Rat Slc19a2 cDNA Clone(NM_001030024.1) Inquiry
MiUTR1M-10776 SLC19A2 miRNA 3'UTR clone Inquiry
MiUTR1R-07395 SLC19A2 miRNA 3'UTR clone Inquiry
MiUTR3H-06402 SLC19A2 miRNA 3'UTR clone Inquiry
CDCB189263 Rabbit SLC19A2 ORF clone (XM_002715273.2) Inquiry
CDCR054162 Mouse Slc19a2 ORF clone (NM_054087.2) Inquiry
CDCR371177 Rat Slc19a2 ORF Clone(NM_001030024.1) Inquiry
CDCS413015 Human SLC19A2 ORF Clone (BC018514) Inquiry
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