Species: Hu, Mu, Rt, RM
Applications: WB, ICC/IF
Host: Rabbit Polyclonal
Species: Hu
Applications: WB, ELISA
Host: Mouse Monoclonal
Species: Hu, Mu
Applications: IHC
Host: Rabbit Polyclonal
Species: Hu
Applications: WB
Species: Hu
Applications: WB, ELISA, MA, AP
Species: Hu
Applications: AC
Description
SLC19A2 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.
Bioinformatics
| Entrez |
Human
|
| Uniprot |
Human
Human
Human
|
| Product By Gene ID |
10560 |
| Alternate Names |
- high affinity thiamine transporter
- reduced folate carrier protein (RFC) like
- solute carrier family 19 (thiamine transporter), member 2
- Solute carrier family 19 member 2
- TC1
- Thiamine carrier 1
- thiamine transporter 1
- THT1
- ThTr1
- ThTr-1
- THTR1thTr-1
- TRMA
|
