Sequence of this protein is as follows: LFRGYHGPLD LYPEFYRIAT DPTIHTVPEG RPVNVCVGKE WYRFPSSFLL PDNWQLQFIP SEFRGQLPKP FAEGPLATRI VPTDMNDQNL EEPSRYIDIS KCHYLVDLDT MRETPREPKY SSNKEEWISL AYRPFLDASR SSKLLRAFYV PFLSDQYTVY VNYTILKPRK AKQIRKKSGG
This gene encodes an alpha-1,2-mannosyltransferase enzyme that functions in lipid-linked oligosaccharide assembly. Mutations in this gene result in congenital disorder of glycosylation type Il. Multiple transcript variants encoding different isoforms have been found for this gene.
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Protein Aliases: Alpha-1,2-mannosyltransferase ALG9; asparagine-linked glycosylation 9 alpha-12-mannosyltransferase-like protein; asparagine-linked glycosylation 9 homolog (S. cerevisiae, alpha- 1,2-mannosyltransferase); asparagine-linked glycosylation 9 homolog (yeast, alpha- 1,2-mannosyltransferase); asparagine-linked glycosylation 9, alpha-1,2-mannosyltransferase homolog; Asparagine-linked glycosylation protein 9 homolog; disrupted in bipolar affective disorder 1; Disrupted in bipolar disorder protein 1; dol-P-Man dependent alpha-1,2-mannosyltransferase; Dol-P-Man:Man(6)GlcNAc(2)-PP-Dol alpha-1,2-mannosyltransferase; Dol-P-Man:Man(8)GlcNAc(2)-PP-Dol alpha-1,2-mannosyltransferase; dolichyl-P-Man:Man(6)GlcNAc(2)-PP-dolichol alpha-1,2-mannosyltransferase; dolichyl-P-Man:Man(8)GlcNAc(2)-PP-dolichol alpha-1,2-mannosyltransferase; loss of heterozygosity, 11, chromosomal region 1 gene J product
Gene Aliases: ALG9; CDG1L; DIBD1; GIKANIS; LOH11CR1J
UniProt ID: (Human) Q9H6U8
Entrez Gene ID: (Human) 79796