"sequence_id","alias","species","description","type"
"AFR93870","No alias","Cryptococcus neoformans","bloom syndrome protein;Helicase conserved C-terminal domain;HRDC domain;RecQ zinc-binding;RQC domain;DEAD/DEAH box helicase","protein_coding"
"AOA66834","No alias","Komagataella phaffii","HRDC domain","protein_coding"
"CAG78930","No alias","Yarrowia lipolytica","DEAD/DEAH box helicase domain","protein_coding"
"CBF86151","No alias","Aspergillus nidulans","Putative uncharacterized proteinRecQ helicase MUSN","protein_coding"
"EAA34794","No alias","Neurospora crassa","RQC domain","protein_coding"
"EAL87589","No alias","Aspergillus fumigatus","RecQ family helicase MusN","protein_coding"
"EAU89723","No alias","Coprinopsis cinerea","DNA helicase","protein_coding"
"EED56246","No alias","Aspergillus flavus","RecQ family helicase MusN","protein_coding"
"EFI26818","No alias","Coprinopsis cinerea","ATP-dependent DNA helicase","protein_coding"
"EGR52672","No alias","Trichoderma reesei","HRDC domain","protein_coding"
"ESU05747","No alias","Fusarium graminearum","ATP-dependent DNA helicase RecQ, zinc-binding domain","protein_coding"
"KHC82077","No alias","Candida albicans","RecQ family ATP-dependent DNA helicase;RecQ zinc-binding;Helicase conserved C-terminal domain;DEAD/DEAH box helicase;HRDC domain;RQC domain","protein_coding"
"MGG_05700T0","No alias","Pyricularia oryzae","RecQ helicase MUSN [Source:UniProtKB/TrEMBL;Acc:G4MP38]","protein_coding"
"SPAC2G11.12.1","No alias","Schizosaccharomyces pombe","RecQ type DNA helicase Rqh1 [Source:PomBase;Acc:SPAC2G11.12]","protein_coding"
"YMR190C","No alias","Saccharomyces cerevisiae","RecQ family nucleolar DNA helicase; role in genome integrity maintenance, chromosome synapsis, meiotic joint molecule/crossover formation; stimulates activity of Top3p; rapidly lost in response to rapamycin in Rrd1p-dependent manner; forms nuclear foci upon DNA replication stress; yeast SGS1 complements mutations in human homolog BLM implicated in Bloom syndrome; also similar to human WRN implicated in Werner syndrome; human BLM and WRN can each complement yeast null mutant [Source:SGD;Acc:S000004802]","protein_coding"