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SLC35A1

Official Full Name
solute carrier family 35 member A1
Organism
Homo sapiens
GeneID
10559
Background
The protein encoded by this gene is found in the membrane of the Golgi apparatus, where it transports nucleotide sugars into the Golgi. One such nucleotide sugar is CMP-sialic acid, which is imported into the Golgi by the encoded protein and subsequently glycosylated. Defects in this gene are a cause of congenital disorder of glycosylation type 2F (CDG2F). Two transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Dec 2009]
Synonyms
CST; hCST; CDG2F; CMPST;

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