SLC27A3, solute carrier family 27 member 3

SLC27A3, solute carrier family 27 member 3

• This gene belongs to a family of integral membrane proteins and encodes a protein that is involved in lipid metabolism. The increased expression of this gene in human neural stem cells derived from induced pluripotent stem cells suggests that it plays an important role in early brain development. Naturally occurring mutations in this gene are associated with autism spectrum disorders. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2017]

• Gene Synonyms (ACSVL3, FATP3, VLCS-3, solute carrier family 27 member 3, arachidonate--CoA ligase, long-chain fatty acid transport protein 3, solute carrier family 27 (fatty acid transporter), member 3, very long-chain acyl-CoA synthetase homolog 3,)
• NCBI Gene ID: 11000
• Species: Homo sapiens (Human)
• UNIPROT ID#>>X6R3N0
  UNIPROT ID#>>Q5K4L6
• 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 27 member 3 interacts with:

• ADAM metallopeptidase domain 33
  endoplasmic reticulum lectin 1
  killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 2
  leucine rich repeat and fibronectin type III domain containing 4
  limb development membrane protein 1 like
  mucolipin 3
  pleckstrin homology domain containing A4
  RCC1 domain containing 1
  transmembrane serine protease 3
  zinc and ring finger 4

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.