ScRAPdb    Saccharomyces cerevisiae Reference Assembly Panel Database (ScRAPdb)



A searchable table of the S. cerevisiae pangenome ORFs defined in Peter et al. (2018) Nature (LINK) is provided below. The listed core/accessory classification and origin assignment are based on the original study. Click on the PanORF ID to find out the detailed presence/absence pattern of the corresponding pangenome ORF in both ScRAPdb and the 1002ScGP strain collections (which were recalculated by ScRAPdb).



PanORF ID                                               SGD systematic Name SGD standard name Alias Description                                               Type Origin assignment Mostly likely origin species NCBI megablast hit
6323-YMR254C YMR254C NA NA Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data Core NA NA NA
6324-YMR255W YMR255W GFD1 NA Coiled-coiled protein of unknown function; identified as a high-copy suppressor of a dbp5 mutation; protein abundance increases in response to DNA replication stress Core NA NA NA
6325-YMR256C YMR256C COX7 cytochrome c oxidase subunit VII Subunit VII of cytochrome c oxidase (Complex IV); Complex IV is the terminal member of the mitochondrial inner membrane electron transport chain Core NA NA NA
6326-YMR257C YMR257C PET111 NA Mitochondrial translational activator specific for the COX2 mRNA; located in the mitochondrial inner membrane Core NA NA NA
6327-YMR258C YMR258C ROY1 NA GTPase inhibitor with similarity to F-box proteins; inhibits Ypt52p GTPase activity by preventing Ypt52p from binding GTP; involved in regulating intracellular trafficking; physically interacts with Skp1p Core NA NA NA
6328-YMR259C YMR259C TRM732 tRNA methylation protein TRM732 Protein involved in 2'-O-methylation of C32 of substrate tRNAs; interacts with 2'-O-ribose methyltransferase Trm7p; green fluorescent protein (GFP)-fusion protein localizes to the cytoplasm; non-essential gene; yeast null mutant can be functionally complemented by human THADA, mutations in which have been implicated in epithelial thyroid adenomas, type 2 diabetes, and polycystic ovary syndrome (PCOS) Core NA NA NA
6329-YMR260C YMR260C TIF11 NA Translation initiation factor eIF1A; essential protein that forms a complex with Sui1p (eIF1) and the 40S ribosomal subunit and scans for the start codon; C-terminus associates with Fun12p (eIF5B); N terminus interacts with eIF2 and eIF3 Core NA NA NA
6330-YMR261C YMR261C TPS3 trehalose 6-phosphate synthase/phosphatase complex subunit Regulatory subunit of trehalose-6-phosphate synthase/phosphatase; involved in synthesis of storage carbohydrate trehalose; expression is induced by stress conditions and repressed by the Ras-cAMP pathway; TPS3 has a paralog, TSL1, that arose from the whole genome duplication Core NA NA NA
6331-YMR262W YMR262W NA putative endodeoxyribonuclease Protein of unknown function; interacts weakly with Knr4p; YMR262W is not an essential gene Core NA NA NA
6332-YMR263W YMR263W SAP30 NA Component of Rpd3L histone deacetylase complex; involved in silencing at telomeres, rDNA, and silent mating-type loci; involved in telomere maintenance Core NA NA NA
6333-YMR264W YMR264W CUE1 KIS4 Ubiquitin-binding protein; ER membrane protein that recruits and integrates the ubiquitin-conjugating enzyme Ubc7p into ER membrane-bound ubiquitin ligase complexes that function in the ER-associated degradation (ERAD) pathway for misfolded proteins; contains a CUE domain that binds ubiquitin to facilitate intramolecular monoubiquitination and to promote diubiquitin elongation, facilitating polyubiquitin chain formation Core NA NA NA
6334-YMR265C YMR265C NA NA Putative protein of unknown function Core NA NA NA
6335-YMR266W YMR266W RSN1 NA Membrane protein of unknown function; overexpression suppresses NaCl sensitivity of sro7 mutant cells by restoring sodium pump (Ena1p) localization to the plasma membrane Accessory Ancestral NA NA
6336-YMR267W YMR267W PPA2 inorganic diphosphatase PPA2|IPP2 Mitochondrial inorganic pyrophosphatase; required for mitochondrial function and possibly involved in energy generation from inorganic pyrophosphate; human ortholog, PPA2, functionally complements the null mutant; mutations in human PPA2 cause a mitochondrial disease resulting in sudden unexpected cardiac arrest in infants Core NA NA NA
6337-YMR268C YMR268C PRP24 U6 snRNP complex subunit PRP24 Splicing factor that reanneals snRNPs during spliceosome recycling; reanneals U4 and U6 snRNPs Core NA NA NA

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