Protein Domain : Mannosyltransferase ALG2 IPR027054

Type  Family
Description  ALG2 mannosylates Man2GlcNAc(2)-dolichol diphosphate and Man1GlcNAc(2)-dolichol diphosphate to form Man3GlcNAc(2)-dolichol diphosphate [].Defects in ALG2 are the cause of congenital disorder of glycosylation type 1I (CDG1I). CDGs are a family of severe inherited diseases caused by a defect in protein N-glycosylation. They are characterised by under-glycosylated serum proteins [ ].
Short Name  ALG2

0 Child Features

1 Gene Families

120 Genes

2 Ontology Annotations

0 Parent Features

14 Publications

USDA
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