ALG2

Last Update:2016-08-10

ALG2 encodes alpha-mannosyltransferase that is involved in the synthesis of lipid-linked oligosaccharides in the endoplasmic reticulum. GDP-mannose is used for the donor substrate. ALG2 appears to be involved in transfer of both alpha-1,3- and alpha-1,6-linked mannose. ALG2 complements the defect of the yeast alg2 mutant. Mutation of ALG2 is associated with congenital disorder of glycosylation type 1I.

Keyword: congenital disorders of glycosylation ,  lipid-linked oligosaccharide
JCGG-STR024580
GlyTouCan: G65996GC
GlyCosmos Glycans: G65996GC
JCGG-STR026178
GlyTouCan: G53394BX
GlyCosmos Glycans: G53394BX
JCGG-STR026178
GlyTouCan: G53394BX
GlyCosmos Glycans: G53394BX
JCGG-STR026209
GlyTouCan: G43547MI
GlyCosmos Glycans: G43547MI

Mannosyltransferases


GGDB Symbol ALG2    Alias
DesignationGDP-Mannose:ManGlcNAc2-PP-dolichol alpha-1,3-mannosyltransferase, GDP-Mannose:Man2GlcNAc2-PP-dolichol alpha-1,6-mannosyltransferase
OrganismHomo sapiens
GeneID 85365
HGNC ALG2 (23159)
mRNA NM_033087
map9q22-31
Protein NP_149078
EC# 2.4.1.132   
CAZy GT4   
GlyCosmos Glycogenes ALG2
OMIM 607905
Disease name CDG Ii ,  Congenital Disorder of Glycosylation type Ii
GDGDB CON00351   
Human Protein Atlas ENSG00000119523
Open ALL Close ALL

Orthologous Gene

Acceptor Substrates (Reference)

Acceptor Substrates (KEM-C)

Expression

RNA Expression from Human Protein Atlas
This RNA expression data uses "HPA data" from the Human Protein Atlas. Tissue RNA Expression

data available from v22.proteinatlas.org

Expression (Reference)

Gene Ontology

This page does not indicate all of the enzymatic reaction, and expression of "ALG2".