SLC25A16, solute carrier family 25 member 16

SLC25A16, solute carrier family 25 member 16

• This gene encodes a protein that contains three tandemly repeated mitochondrial carrier protein domains. The encoded protein is localized in the inner membrane and facilitates the rapid transport and exchange of molecules between the cytosol and the mitochondrial matrix space. This gene has a possible role in Graves' disease. [provided by RefSeq, Jul 2008]

• Gene Synonyms (graves disease carrier protein, mitochondrial solute carrier protein homolog, solute carrier family 25 (mitochondrial carrier; Graves disease autoantigen), member 16, D10S105E, GDA, GDC, HGT.1, ML7, hML7,)
• NCBI Gene ID: 8034
• Species: Homo sapiens (Human)
• UNIPROT ID#>>B4DHV9
  UNIPROT ID#>>P16260
  UNIPROT ID#>>B4DPV4
• 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 25 member 16 interacts with:

• carnosine dipeptidase 1
  dickkopf WNT signaling pathway inhibitor 3
  dystrobrevin binding protein 1
  ER degradation enhancing alpha-mannosidase like protein 2
  family with sequence similarity 131 member B
  Fas associated factor family member 2
  protein phosphatase 6 regulatory subunit 2
  ring finger protein 123
  ring finger protein 126
  stromal cell derived factor 4
  thioredoxin domain containing 15
  torsin 1A interacting protein 2

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.