Orders Processing,
Shipping & Receiving,
Warehouse
2 Shaker Rd Suites
B001/B101
Shirley, MA 01464
Production Lab
Floor 6, Suite 620
20700 44th Avenue W
Lynnwood, WA 98036
SLC19A2 / TC1 is 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.
Gene Name: | solute carrier family 19 (thiamine transporter), member 2 |
Family/Subfamily: | Transporter , Reduced folate carrier |
Synonyms: | SLC19A2, HTHTR1, Thiamine carrier 1, THTR1, ThTr-1, Thiamine transporter 1, THMD1, TRMA, TC1, THT1 |
Target Sequences: | AF160812 AAF15129.1 O60779 |
If you do not find the reagent or information you require, please contact Customer.Support@LSBio.com to inquire about additional products in development.