Mannosyltransferase, involved in N-linked glycosylation; catalyzes the transfer of both the seventh mannose residue on B-arm and ninth mannose residue on the C-arm from Dol-P-Man to lipid-linked oligosaccharides; human homolog ALG9 can complement yeast null mutant; mutation of human homolog causes type 1 congenital disorders of glycosylation [Source:SGD;Acc:S000005163]
Chromosome XIV: 235,996-237,663 reverse strand.
R64-1-1:BK006947.3
This gene has 1 transcript (splice variant), 317 orthologues and 3 paralogues.
Name | Transcript ID | bp | Protein | Translation ID | Biotype | UniProt | RefSeq | Flags |
---|---|---|---|---|---|---|---|---|
ALG9 | YNL219C_mRNA | 1668 | 555aa | YNL219C | Protein coding | P53868 | - | Ensembl Canonical, |