dolichyl-P-Man:Man(7)GlcNAc(2)-PP-dolichyl-alpha-1,6-mannosyltransferase (mannosyltransferase ALG12 homolog, hALG12, membrane protein SB87, ALG12)
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Function
- required for protein glycosylation
- adds the 8th mannose residue in an alpha-1,6 linkage onto the dolichol-PP-oligosaccharide precursor (dolichol-PP-Man(7)GlcNAc(2))
Structure
- belongs to the glycosyltransferase 22 family
Compartment
Expression
- expressed in fibroblasts
Pathology
- defects in ALG12 are the cause of congenital disorder of glycosylation type Ig
More general terms
Additional terms
References
- ↑ UniProt http://www.uniprot.org/uniprot/Q9BV10.html
- ↑ GeneReviews https://www.genecards.org/cgi-bin/carddisp.pl?gene=ALG12
GGDB, GlycoGene database http://ggdb.muse.aist.go.jp/GGDB/index.jsp