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SLC19A2 / TC1

solute carrier family 19 (thiamine transporter), member 2

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

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The data on this page has been compiled from LifeSpan internal sources, the National Center for Biotechnology Information (NCBI), and The Universal Protein Resource (UniProt).

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