Matches in DBpedia 2014 for { <http://dbpedia.org/resource/ALG3> ?p ?o. }
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- ALG3 abstract "Dolichyl-P-Man:Man(5)GlcNAc(2)-PP-dolichyl mannosyltransferase is an enzyme that in humans is encoded by the ALG3 gene.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.".
- ALG3 entrezgene "10195".
- ALG3 wikiPageExternalLink NBK1332.
- ALG3 wikiPageID "15227748".
- ALG3 wikiPageRevisionID "590541978".
- ALG3 hasPhotoCollection ALG3.
- ALG3 requireManualInspection "no".
- ALG3 summaryText "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 characterized by abnormal N-glycosylation.".
- ALG3 updateCitations "yes".
- ALG3 updatePage "yes".
- ALG3 updateProteinBox "yes".
- ALG3 updateSummary "yes".
- ALG3 type Biomolecule.
- ALG3 type Protein.
- ALG3 type BiologicalObject.
- ALG3 comment "Dolichyl-P-Man:Man(5)GlcNAc(2)-PP-dolichyl mannosyltransferase is an enzyme that in humans is encoded by the ALG3 gene.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.".
- ALG3 label "ALG3".
- ALG3 sameAs m.03hmldz.
- ALG3 sameAs Q4652348.
- ALG3 sameAs Q4652348.
- ALG3 sameAs ALG3.
- ALG3 wasDerivedFrom ALG3?oldid=590541978.
- ALG3 isPrimaryTopicOf ALG3.