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SLC27A3

Official Full Name
solute carrier family 27 member 3
Organism
Homo sapiens
GeneID
11000
Background
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]
Synonyms
FATP3; ACSVL3; VLCS-3;

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