"sequence_id","alias","species","description","type"
"AFR96200","No alias","Cryptococcus neoformans","alpha-1,2-mannosyltransferase;Alg9-like mannosyltransferase family","protein_coding"
"AOA67775","No alias","Komagataella phaffii","GPI mannosyltransferase","protein_coding"
"CAG80132","No alias","Yarrowia lipolytica","GPI mannosyltransferase","protein_coding"
"CAK39949","No alias","Aspergillus niger","Alg9-like mannosyltransferase family","protein_coding"
"CBF88896","No alias","Aspergillus nidulans","alpha-1,2-mannosyltransferase","protein_coding"
"EAA26676","No alias","Neurospora crassa","GPI mannosyltransferase","protein_coding"
"EAL90719","No alias","Aspergillus fumigatus","alpha-1,2-mannosyltransferase (Alg9), putative","protein_coding"
"EAU92828","No alias","Coprinopsis cinerea","asparagine-linked glycosylation 9 protein isoform a","protein_coding"
"EDN96446","No alias","Sclerotinia sclerotiorum","GPI mannosyltransferase","protein_coding"
"EED54504","No alias","Aspergillus flavus","alpha-1,2-mannosyltransferase (Alg9), putative","protein_coding"
"EGR51150","No alias","Trichoderma reesei","GPI mannosyltransferase","protein_coding"
"ESU11178","No alias","Fusarium graminearum","GPI mannosyltransferase","protein_coding"
"KHC83486","No alias","Candida albicans","alpha-1,2-mannosyltransferase;Alg9-like mannosyltransferase family","protein_coding"
"MGG_14835T0","No alias","Pyricularia oryzae","Mannosyl transferase [Source:UniProtKB/TrEMBL;Acc:G4N8S7]","protein_coding"
"POW13341","No alias","Puccinia striiformis","GPI mannosyltransferase","protein_coding"
"SPAC1834.05.1","No alias","Schizosaccharomyces pombe","mannosyltransferase complex subunit Alg9 (predicted) [Source:PomBase;Acc:SPAC1834.05]","protein_coding"
"YNL219C","No alias","Saccharomyces cerevisiae","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]","protein_coding"