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Identification
HMDB Protein ID HMDBP10780
Secondary Accession Numbers
  • 17049
Name Solute carrier family 19 thiamine transporter member 2
Synonyms Not Available
Gene Name SLC19A2
Protein Type Unknown
Biological Properties
General Function Not Available
Specific Function Not Available
Pathways Not Available
Reactions Not Available
GO Classification Not Available
Cellular Location Not Available
Gene Properties
Chromosome Location Chromosome:1
Locus 1q23.3
SNPs SLC19A2
Gene Sequence
>47 bp
ATGGATGTGCCCGGCCCGGTGTCTCGGCGGGCGGCGGCGGCGGCGGC
Protein Properties
Number of Residues 16
Molecular Weight 1539.7
Theoretical pI 10.45
Pfam Domain Function Not Available
Signals
  • None
Transmembrane Regions
  • None
Protein Sequence
>Solute carrier family 19 thiamine transporter member 2
MDVPGPVSRRAAAAAA
GenBank ID Protein 164370706
UniProtKB/Swiss-Prot ID B0FBR7
UniProtKB/Swiss-Prot Entry Name B0FBR7_HUMAN
PDB IDs Not Available
GenBank Gene ID EU302825
GeneCard ID SLC19A2
GenAtlas ID Not Available
HGNC ID Not Available
References
General References
  1. Fleming JC, Tartaglini E, Steinkamp MP, Schorderet DF, Cohen N, Neufeld EJ: The gene mutated in thiamine-responsive anaemia with diabetes and deafness (TRMA) encodes a functional thiamine transporter. Nat Genet. 1999 Jul;22(3):305-8. [PubMed:10391222 ]