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Malignant cells showed weak cytoplasmic positivity or were negative. Moderately stained cases were observed in for example prostate, pancreatic and renal cancers.
GENE INFORMATION
Gene name
SLC19A2 (HGNC Symbol)
Synonyms
THTR1, TRMA
Description
Solute carrier family 19 (thiamine transporter), member 2 (HGNC Symbol)
Entrez gene 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]