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.
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JCGG-STR024580
GlyTouCan:
G65996GC
GlyCosmos Glycans:
G65996GC
|
JCGG-STR026178
GlyTouCan:
G53394BX
GlyCosmos Glycans:
G53394BX
|
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JCGG-STR026178
GlyTouCan:
G53394BX
GlyCosmos Glycans:
G53394BX
|
JCGG-STR026209
GlyTouCan:
G43547MI
GlyCosmos Glycans:
G43547MI
|
ALG2 Alias | |
Designation | GDP-Mannose:ManGlcNAc2-PP-dolichol alpha-1,3-mannosyltransferase, GDP-Mannose:Man2GlcNAc2-PP-dolichol alpha-1,6-mannosyltransferase |
Organism | Homo sapiens |
GeneID | 85365 |
HGNC | ALG2 (23159) |
mRNA | NM_033087 |
map | 9q22-31 |
Protein | NP_149078 |
EC# | 2.4.1.132 |
CAZy | GT4 |
GlyCosmos Glycogenes | ALG2 |
OMIM | 607905 |
CDG Ii , Congenital Disorder of Glycosylation type Ii | |
GDGDB | CON00351 |
Human Protein Atlas | ENSG00000119523 |
data available from v22.proteinatlas.org