"sequence_id","alias","species","description","type"
"AFR94407","No alias","Cryptococcus neoformans","dolichyl-P-Man:Man(5)GlcNAc(2)-PP-dolichyl mannosyltransferase;ALG3 protein","protein_coding"
"AOA69559","No alias","Komagataella phaffii","Glycosyltransferase, ALG3","protein_coding"
"CAG79067","No alias","Yarrowia lipolytica","Glycosyltransferase, ALG3","protein_coding"
"CAK43166","No alias","Aspergillus niger","ALG3 protein","protein_coding"
"CBF90192","No alias","Aspergillus nidulans","Man","protein_coding"
"EAA33023","No alias","Neurospora crassa","Glycosyltransferase, ALG3","protein_coding"
"EAL91414","No alias","Aspergillus fumigatus","alpha-1,3-mannosyltransferase (Alg3), putative","protein_coding"
"EDN99170","No alias","Sclerotinia sclerotiorum","Glycosyltransferase, ALG3","protein_coding"
"EED49221","No alias","Aspergillus flavus","alpha-1,3-mannosyltransferase (Alg3), putative","protein_coding"
"EFI28445","No alias","Coprinopsis cinerea","No description available","protein_coding"
"EGR51059","No alias","Trichoderma reesei","Glycosyltransferase, ALG3","protein_coding"
"ESU16263","No alias","Fusarium graminearum","Glycosyltransferase, ALG3","protein_coding"
"KHC72916","No alias","Candida albicans","alpha-1,3-mannosyltransferase;ALG3 protein","protein_coding"
"KHC73570","No alias","Candida albicans","alpha-1,3-mannosyltransferase;ALG3 protein","protein_coding"
"MGG_08010T0","No alias","Pyricularia oryzae","Dolichyl-P-Man:Man(5)GlcNAc(2)-PP-dolichyl mannosyltransferase [Source:UniProtKB/TrEMBL;Acc:G4MX55]","protein_coding"
"SPAC7D4.06c.1","No alias","Schizosaccharomyces pombe","dolichol-P-Man dependent alpha(1-3) mannosyltransferase Alg3 (predicted) [Source:PomBase;Acc:SPAC7D4.06c]","protein_coding"
"YBL082C","No alias","Saccharomyces cerevisiae","Dolichol-P-Man dependent alpha(1-3) mannosyltransferase; involved in synthesis of dolichol-linked oligosaccharide donor for N-linked glycosylation of proteins; G353A missense mutation in human ortholog ALG3 implicated in carbohydrate deficient glycoprotein syndrome type IV, which is characterized by microcephaly, severe epilepsy, minimal psychomotor development, partial deficiency of sialic acids in serum glycoproteins; wild-type human ALG3 can complement yeast alg3 mutant [Source:SGD;Acc:S000000178]","protein_coding"