SLC26A2, solute carrier family 26 member 2

SLC26A2, solute carrier family 26 member 2

• The diastrophic dysplasia sulfate transporter is a transmembrane glycoprotein implicated in the pathogenesis of several human chondrodysplasias. It apparently is critical in cartilage for sulfation of proteoglycans and matrix organization. [provided by RefSeq, Jul 2008]

• Gene Synonyms (D5S1708, DTD, DTDST, EDM4, MST153, MSTP157, sulfate transporter, diastrophic dysplasia protein, solute carrier family 26 (anion exchanger), member 2, solute carrier family 26 (sulfate transporter), member 2, sulfate anion transporter 1,)
• NCBI Gene ID: 1836
• Species: Homo sapiens (Human)
• UNIPROT ID#>>P50443
• 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 26 member 2 interacts with:

• alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase B
  ERGIC and golgi 3
  family with sequence similarity 189 member A2
  galectin 3
  galectin 8
  HRas proto-oncogene, GTPase
  KRAS proto-oncogene, GTPase
  lectin, galactoside-binding, soluble, 3 binding protein
  nicotinamide nucleotide transhydrogenase
  premelanosome protein
  solute carrier family 22 member 16
  solute carrier family 22 member 6
  solute carrier family 22 member 9
  TNF alpha induced protein 3
  transmembrane protein 52B
  VAMP associated protein B and C

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.