QuickView for SLC19A2 (gene)

Gene Symbol:

SLC19A2 Homo sapiens

Full name:

solute carrier family 19 member 2

Synonyms:

TC1, THMD1, THT1, THTR1, TRMA, thiamine transporter 1, high affinity thiamine transporter, reduced folate carrier protein (RFC) like, solute carrier family 19 (thiamine transporter), member 2, thTr-1

Genomic Location:

Chr 1: 167699791-167721865

Description:

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.

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.

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Orthologs:

Mus musculus ,  Rattus norvegicus ,  D. melanogaster ,  C. elegans ,  Macaca mulatta ,  Gallus gallus ,  Pan troglodytes ,  Canis lupus familiaris ,  Bos taurus ,  Danio rerio

External Links:

Entrez Gene

Transcription Factor
Binding Sites:

GGGACCA_MIR133A_MIR133B ,  GTACTGT_MIR101 ,  ACCAAAG_MIR9 ,  TTGTTT_FOXO4_01 ,  CTGAGCC_MIR24

miRNA binding sites
(Source: TargetScan):

Predicted Gene Targets for miR-101 ,  Predicted Gene Targets for miR-133 ,  Predicted Gene Targets for miR-24 ,  Predicted Gene Targets for miR-9

Cytogenetic Map:

1q24.2

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