SLC19A2, solute carrier family 19 member 2

SLC19A2, solute carrier family 19 member 2

• 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. [provided by RefSeq, Feb 2016]

• Gene 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,)
• NCBI Gene ID: 10560
• Species: Homo sapiens (Human)
• UNIPROT ID#>>A0A024R8Y5
  UNIPROT ID#>>A0A024R928
  UNIPROT ID#>>O60779
• View the NCBI Database for this Gene »

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

solute carrier family 19 member 2 interacts with:

• adhesion G protein-coupled receptor G5
  ceramide synthase 2
  complement component 5a receptor 2
  C-type lectin domain family 2 member D
  limb development membrane protein 1 like
  protein O-mannose kinase
  signal peptide peptidase like 2B
  solute carrier family 2 member 12
  solute carrier family 22 member 9
  Yip1 domain family member 3
  zinc finger FYVE-type containing 27

Paste a protein or nucleic acid sequence in the box below to confirm that it matches this gene’s reference sequence(s). Click on a link under RELATED ORF CLONES to see how a sequence matches to an experimentally-validated ORF clone.