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STT3B

Official Full Name
STT3 oligosaccharyltransferase complex catalytic subunit B
Organism
Homo sapiens
GeneID
201595
Background
The protein encoded by this gene is a catalytic subunit of a protein complex that transfers oligosaccharides onto asparagine residues. Defects in this gene are a cause of congenital disorder of glycosylation Ix (CDG1X). [provided by RefSeq, Jun 2014]
Synonyms
SIMP; CDG1X; STT3-B;

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