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Gene Information

Gene symbol: SLC19A1

Gene name: solute carrier family 19 (folate transporter), member 1

HGNC ID: 10937

Synonyms: FOLT

Related Genes

#	Gene Symbol	Number of hits
1	SLC19A2	1 hits

Related Sentences

#	PMID	Sentence
1	10391221	Mutations in a new gene, SLC19A2, encoding a putative transmembrane protein homologous to the reduced folate carrier proteins, were found in all affected individuals in six TRMA families, suggesting that a defective thiamine transporter protein (THTR-1) may underlie the TRMA syndrome.
2	10391223	Thiamine-responsive megaloblastic anaemia syndrome (TRMA; MIM 249270) is an autosomal recessive disorder with features that include megaloblastic anaemia, mild thrombocytopenia and leucopenia, sensorineural deafness and diabetes mellitus.
3	10391223	Here we report the cloning of a new gene, SLC19A2, identified from high-through-put genomic sequences due to homology with SLC19A1, encoding reduced folate carrier 1 (refs 8-10).
4	14622275	The gene associated with this disease encodes for thiamine transporter 1 (THTR1), a member of the SLC19 solute carrier family including THTR2 and the reduced folate carrier (RFC).