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ALG3

Official Full Name
ALG3 alpha-1,3- mannosyltransferase
Organism
Homo sapiens
GeneID
10195
Background
This gene encodes a member of the ALG3 family. The encoded protein catalyses the addition of the first dol-P-Man derived mannose in an alpha 1,3 linkage to Man5GlcNAc2-PP-Dol. Defects in this gene have been associated with congenital disorder of glycosylation type Id (CDG-Id) characterized by abnormal N-glycosylation. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2008]
Synonyms
not; CDG1D; CDGS4; CDGS6; Not56; NOT56L; D16Ertd36e;

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