SLC19A2
solute carrier family 19 (thiamine transporter), member 2
Synonyms:
TC1, THMD1, THT1, THTR1, TRMA
Species:
Human SLC19A2 (10560), Mouse Slc19a2 (116914), Rat Slc19a2 (289175), cow SLC19A2 (532860), domestic cat SLC19A2 (664737), Horse SLC19A2 (100058457), dog SLC19A2 (490353), chicken SLC19A2 (427957), Zebrafish slc19a2 (569085), domestic guinea pig Slc19a2 (100717365) ...More
UniProtKB ID:
Gene ID:
- Human(10560) Summary: 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]
- Mouse(116914) solute carrier family 19 (thiamine transporter), member 2
- Rat(289175) solute carrier family 19 (thiamine transporter), member 2
- cow(532860) solute carrier family 19 (thiamine transporter), member 2
- domestic cat(664737) solute carrier family 19 (thiamine transporter), member 2
- Horse(100058457) solute carrier family 19 (thiamine transporter), member 2
- dog(490353) solute carrier family 19 (thiamine transporter), member 2
- chicken(427957) solute carrier family 19 (thiamine transporter), member 2
- Zebrafish(569085) solute carrier family 19 (thiamine transporter), member 2
- domestic guinea pig(100717365) solute carrier family 19 (thiamine transporter), member 2
- naked mole-rat(101702163) solute carrier family 19 (thiamine transporter), member 2
- sheep(101123393) solute carrier family 19 (thiamine transporter), member 2
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