Your search for "slc19a2" returned 98 TaqMan® SNP Genotyping Assays
solute carrier family 19 member 2
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]
AV276020, AW322295, DDA1, SLC19A2, TC1, THMD1, THT1, THTR1, TRMA
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