SLC9A3, solute carrier family 9 member A3

SLC9A3, solute carrier family 9 member A3

• The protein encoded by this gene is an epithelial brush border Na/H exchanger that uses an inward sodium ion gradient to expel acids from the cell. Defects in this gene are a cause of congenital secretory sodium diarrhea. Pseudogenes of this gene exist on chromosomes 10 and 22. [provided by RefSeq, Mar 2016]

• Gene Synonyms (sodium/hydrogen exchanger 3, Na(+)/H(+) exchanger 3, solute carrier family 9 (sodium/hydrogen exchanger), solute carrier family 9 (sodium/hydrogen exchanger), member 3, solute carrier family 9, subfamily A (NHE3, cation proton antiporter 3), member 3, DIAR8, NHE-3, NHE3,)
• NCBI Gene ID: 6550
• Species: Homo sapiens (Human)
• UNIPROT ID#>>P48764
• 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 9 member A3 interacts with:

• calcineurin like EF-hand protein 1
  calcineurin like EF-hand protein 2
  microtubule associated serine/threonine kinase 2
  NEDD4 like E3 ubiquitin protein ligase
  SH3 and multiple ankyrin repeat domains 2
  SLC9A3 regulator 1
  SLC9A3 regulator 2
  solute carrier family 9 (sodium/hydrogen exchanger), member 3 regulator 1
  solute carrier family 9 member A3
  ubiquitin specific peptidase 48

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.