Search results for Locus Summary pages at SGD
Your query, F2, returned 82 hits to the following gene names:
| Match | Gene Name | Systematic Name | Alias(es) | Position Info | Description | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| ABF2 | ABF2 | YMR072W | Mitochondrial DNA-binding protein; involved in mitochondrial DNA replication and recombination, member of HMG1 DNA-binding protein family; activity may be regulated by protein kinase A phosphorylation; ABF2 has a paralog, IXR1, that arose from the whole genome duplication | ||||||||||||||
| ACF2 | ACF2 | YLR144C | ENG2, PCA1 | Intracellular beta-1,3-endoglucanase; expression is induced during sporulation; may have a role in cortical actin cytoskeleton assembly; protein abundance increases in response to DNA replication stress | |||||||||||||
| ARF2 | ARF2 | YDL137W |
ChrIV:216529 to 217074 | ORF Map | GBrowse
Genetic position: -64 cM | ADP-ribosylation factor; GTPase of the Ras superfamily involved in regulation of coated formation vesicles in intracellular trafficking within the Golgi; ARF2 has a paralog, ARF1, that arose from the whole genome duplication | |||||||||||||
| ASF2 | ASF2 | YDL197C | Anti-silencing protein that causes derepression of silent loci when overexpressed | ||||||||||||||
| ATF2 | ATF2 | YGR177C | Alcohol acetyltransferase, may play a role in steroid detoxification; forms volatile esters during fermentation, which is important for brewing and winemaking | ||||||||||||||
| BDF2 | BDF2 | YDL070W | Protein involved in transcription initiation; acts at TATA-containing promoters; associates with the basal transcription factor TFIID; contains two bromodomains; corresponds to the C-terminal region of mammalian TAF1; redundant with Bdf1p; protein abundance increases in response to DNA replication stress; BDF2 has a paralog, BDF1, that arose from the whole genome duplication | ||||||||||||||
| BUF2 | RFA1 | YAR007C | BUF2, FUN3, RPA1, RPA70 | Subunit of heterotrimeric Replication Protein A (RPA), which is a highly conserved single-stranded DNA binding protein involved in DNA replication, repair, and recombination | |||||||||||||
| CAF20 | CAF20 | YOR276W | CAF2, CAP20, p20 | Phosphoprotein of the mRNA cap-binding complex involved in translational control, repressor of cap-dependent translation initiation, competes with eIF4G for binding to eIF4E | |||||||||||||
| CBF2 | CBF2 | YGR140W | CBF3A, CEP2, CTF14, NDC10, CSL5 | Essential kinetochore protein; component of the CBF3 multisubunit complex that binds to the CDEIII region of the centromere; Cbf2p also binds to the CDEII region possibly forming a different multimeric complex, ubiquitinated in vivo; relative distribution to the spindle pole body decreases upon DNA replication stress | |||||||||||||
| CHF2 | DMA2 | YNL116W | CHF2, ubiquitin-conjugating protein DMA2 | Ubiquitin-protein ligase (E3); controls septin dynamics and spindle position checkpoint (SPOC) with ligase Dma1p by regulating recruitment of Elm1p to bud neck; regulates levels of eIF2 subunit Gcd11p, as well as abundance, localization, and ubiquitination of Cdk inhibitory kinase Swe1p; ortholog of human RNF8, similar to human Chfr; contains FHA and RING finger domains; DMA2 has a paralog, DMA1, that arose from the whole genome duplication | |||||||||||||
| DAF2 | STE3 | YKL178C | DAF2 | Receptor for a factor pheromone, couples to MAP kinase cascade to mediate pheromone response; transcribed in alpha cells and required for mating by alpha cells, ligand bound receptors endocytosed and recycled to the plasma membrane; GPCR | |||||||||||||
| DBF2 | DBF2 | YGR092W | Ser/Thr kinase involved in transcription and stress response; functions as part of a network of genes in exit from mitosis; localization is cell cycle regulated; activated by Cdc15p during the exit from mitosis; also plays a role in regulating the stability of SWI5 and CLB2 mRNAs; phosphorylates Chs2p to regulate primary septum formation and Hof1p to regulate cytokinesis; DBF2 has a paralog, DBF20, that arose from the whole genome duplication | ||||||||||||||
| DBF20 | DBF20 | YPR111W | Ser/Thr kinase involved in late nuclear division; one of the mitotic exit network (MEN) proteins; necessary for the execution of cytokinesis; also plays a role in regulating the stability of SWI5 and CLB2 mRNAs; DBF20 has a paralog, DBF2, that arose from the whole genome duplication | ||||||||||||||
| DNF2 | DNF2 | YDR093W | aminophospholipid-translocating P4-type ATPase DNF2 | Aminophospholipid translocase (flippase) that localizes primarily to the plasma membrane; contributes to endocytosis, protein transport and cell polarity; type 4 P-type ATPase; DNF2 has a paralog, DNF1, that arose from the whole genome duplication | |||||||||||||
| DSF2 | DSF2 | YBR007C | Deletion suppressor of mpt5 mutation; relocalizes from bud neck to cytoplasm upon DNA replication stress | ||||||||||||||
| EAF2 | SWC4 | YGR002C | EAF2, GOD1 | Component of the Swr1p complex that incorporates Htz1p into chromatin; component of the NuA4 histone acetyltransferase complex | |||||||||||||
| ERF2 | ERF2 | YLR246W | Subunit of a palmitoyltransferase, composed of Erf2p and Shr5p, that adds a palmitoyl lipid moiety to heterolipidated substrates such as Ras1p and Ras2p through a thioester linkage; mutants partially mislocalize Ras2p to the vacuole | ||||||||||||||
| ESF2 | ESF2 | YNR054C | ABT1 | Essential nucleolar protein involved in pre-18S rRNA processing; binds to RNA and stimulates ATPase activity of Dbp8; involved in assembly of the small subunit (SSU) processome | |||||||||||||
| FCF2 | FCF2 | YLR051C | Essential nucleolar protein involved in the early steps of 35S rRNA processing; interacts with Faf1p; member of a transcriptionally co-regulated set of genes called the RRB regulon | ||||||||||||||
| GEF2 | VMA3 | YEL027W | CLS7, GEF2, CUP5 | Proteolipid subunit of the vacuolar H(+)-ATPase V0 sector (subunit c; dicyclohexylcarbodiimide binding subunit); required for vacuolar acidification and important for copper and iron metal ion homeostasis | |||||||||||||
| GRF2 | REB1 | YBR049C | GRF2 | RNA polymerase I enhancer binding protein; DNA binding protein that binds to genes transcribed by both RNA polymerase I and RNA polymerase II; required for termination of RNA polymerase I transcription; REB1 has a paralog, NSI1, that arose from the whole genome duplication | |||||||||||||
| GSF2 | GSF2 | YML048W | ECM6 | ER localized integral membrane protein that may promote secretion of certain hexose transporters, including Gal2p; involved in glucose-dependent repression | |||||||||||||
| HDF2 | YKU80 | YMR106C | HDF2 | Subunit of the telomeric Ku complex (Yku70p-Yku80p), involved in telomere length maintenance, structure and telomere position effect; relocates to sites of double-strand cleavage to promote nonhomologous end joining during DSB repair | |||||||||||||
| HHF2 | HHF2 | YNL030W | Histone H4, core histone protein required for chromatin assembly and chromosome function; one of two identical histone proteins (see also HHF1); contributes to telomeric silencing; N-terminal domain involved in maintaining genomic integrity | ||||||||||||||
| HPF2 | PST1 | YDR055W | HPF2 | Cell wall protein that contains a putative GPI-attachment site; secreted by regenerating protoplasts; up-regulated by activation of the cell integrity pathway, as mediated by Rlm1p; upregulated by cell wall damage via disruption of FKS1; PST1 has a paralog, ECM33, that arose from the whole genome duplication | |||||||||||||
| HUF2 | FLC2 | YAL053W | HUF2 | Putative FAD transporter; required for uptake of FAD into endoplasmic reticulum; involved in cell wall maintenance; FLC2 has a paralog, YOR365C, that arose from the whole genome duplication | |||||||||||||
| LIF2 | NEJ1 | YLR265C | LIF2 | Protein involved in regulation of nonhomologous end joining; interacts with DNA ligase IV components Dnl4p and Lif1p; repressed by MAT heterozygosity; regulates cellular distribution of Lif1p | |||||||||||||
| LPF2 | BRO1 | YPL084W | LPF2, VPS31, ASI6, NPI3 | Cytoplasmic class E vacuolar protein sorting (VPS) factor that coordinates deubiquitination in the multivesicular body (MVB) pathway by recruiting Doa4p to endosomes | |||||||||||||
| MEF2 | MEF2 | YJL102W | Mitochondrial elongation factor involved in translational elongation | ||||||||||||||
| MHF2 | MHF2 | YDL160C-A | Component of the heterotetrameric MHF histone-fold complex; in humans the MMF complex interacts with both DNA and Mph1p ortholog FANCM to stabilize and remodel blocked replication forks and repair damaged DNA; mhf2 srs2 double mutants are MMS hypersensitive; orthologous to human centromere constitutive-associated network (CCAN) subunit CENP-X, also known as MHF2 | ||||||||||||||
| MIF2 | MAS2 | YHR024C | MIF2, mitochondrial processing protease alpha subunit | Larger subunit of the mitochondrial processing protease (MPP), essential processing enzyme that cleaves the N-terminal targeting sequences from mitochondrially imported proteins | |||||||||||||
| MIF2 | MIF2 | YKL089W | Protein required for structural integrity of elongating spindles; localizes to the kinetochore; interacts with histones H2A, H2B, and H4; phosphorylated by Ipl1p; orthologous to human centromere constitutive-associated network (CCAN) subunit CENP-C and fission yeast cnp3 | ||||||||||||||
| MOF2 | SUI1 | YNL244C | MOF2, RFR1 | Translation initiation factor eIF1; component of a complex involved in recognition of the initiator codon; modulates translation accuracy at the initiation phase | |||||||||||||
| MTF2 | MTF2 | YDL044C | NAM1 | Mitochondrial matrix protein that interacts with an N-terminal region of mitochondrial RNA polymerase (Rpo41p) and couples RNA processing and translation to transcription | |||||||||||||
| NNF2 | NNF2 | YGR089W | Protein that exhibits physical and genetic interactions with Rpb8p, which is a subunit of RNA polymerases I, II, and III; computational analysis of large-scale protein-protein interaction data suggests a role in chromosome segregation | ||||||||||||||
| NTF2 | NTF2 | YER009W | Nuclear envelope protein, interacts with GDP-bound Gsp1p and with proteins of the nuclear pore to transport Gsp1p into the nucleus where it is an essential player in nucleocytoplasmic transport | ||||||||||||||
| NUF2 | NUF2 | YOL069W | Component of the evolutionarily conserved kinetochore-associated Ndc80 complex (Ndc80p-Nuf2p-Spc24p-Spc25p); involved in chromosome segregation, spindle checkpoint activity and kinetochore clustering | ||||||||||||||
| OAF2 | PIP2 | YOR363C | OAF2 | Autoregulatory oleate-specific transcriptional activator of peroxisome proliferation, contains Zn(2)-Cys(6) cluster domain, forms heterodimer with Oaf1p, binds oleate response elements (OREs), activates beta-oxidation genes; PIP2 has a paralog, OAF1, that arose from the whole genome duplication | |||||||||||||
| PBF2 | DOT6 | YER088C | PBF2 | Protein involved in rRNA and ribosome biogenesis; binds polymerase A and C motif; subunit of the RPD3L histone deacetylase complex; has chromatin specific SANT domain; involved in telomeric gene silencing and filamentation; DOT6 has a paralog, TOD6, that arose from the whole genome duplication; relative distribution to the nucleus increases upon DNA replication stress | |||||||||||||
| PPF2 | PEA2 | YER149C | DFG9, PPF2 | Coiled-coil polarisome protein required for polarized morphogenesis, cell fusion, and low affinity Ca2+ influx; forms polarisome complex with Bni1p, Bud6p, and Spa2p; localizes to sites of polarized growth | |||||||||||||
| PSF2 | PSF2 | YJL072C | CDC102 | Subunit of the GINS complex (Sld5p, Psf1p, Psf2p, Psf3p), which is localized to DNA replication origins and implicated in assembly of the DNA replication machinery | |||||||||||||
| PUF2 | PUF2 | YPR042C | mRNA-binding protein; member of the PUF protein family, which is defined by the presence of Pumilio homology domains that confer RNA binding activity; preferentially binds mRNAs encoding membrane-associated proteins; PUF2 has a paralog, JSN1, that arose from the whole genome duplication | ||||||||||||||
| PZF240 | REG1 | YDR028C | HEX2, PZF240, SPP43, SRN1 | Regulatory subunit of type 1 protein phosphatase Glc7p; involved in negative regulation of glucose-repressible genes; involved in regulation of the nucleocytoplasmic shuttling of Hxk2p; REG1 has a paralog, REG2, that arose from the whole genome duplication | |||||||||||||
| RBF20 | TMA20 | YER007C-A | RBF20 | Protein of unknown function that associates with ribosomes; has a putative RNA binding domain; interacts with Tma22p; null mutant exhibits translation defects; has homology to human oncogene MCT-1; protein abundance increases in response to DNA replication stress | |||||||||||||
| RBF22 | TMA22 | YJR014W | RBF22 | Protein of unknown function; associates with ribosomes and has a putative RNA binding domain; interacts with Tma20p; similar to human GRAP and human DRP1, which interacts with human Tma20p homolog MCT-1; protein abundance increases in response to DNA replication stress | |||||||||||||
| RCF2 | RCF2 | YNR018W | AIM38 | Cytochrome c oxidase subunit; has a role in assembly of respiratory supercomplexes; similar to Rcf1p, and either Rcf1p or Rcf2p is required for late-stage assembly of the Cox12p and Cox13p subunits and for cytochrome c oxidase activity; associates with the cytochrome c oxidase - cytochrome bc1 supercomplex; null mutant accumulates reactive oxygen species; member of the conserved hypoxia induced gene family; C. elegans homolog is functional in yeast | |||||||||||||
| REF2 | REF2 | YDR195W | RNA-binding protein involved in the cleavage step of mRNA 3'-end formation prior to polyadenylation, and in snoRNA maturation; part of holo-CPF subcomplex APT, which associates with 3'-ends of snoRNA- and mRNA-encoding genes | ||||||||||||||
| RF2 | RF2 | RF2 |
ChrMito | ||||||||||||||
| RIF2 | RIF2 | YLR453C | Protein that binds to the Rap1p C-terminus; acts synergistically with Rif1p to help control telomere length and establish telomeric silencing; deletion results in telomere elongation; RIF2 has a paralog, ORC4, that arose from the whole genome duplication | ||||||||||||||
| RLF2 | RLF2 | YPR018W | CAC1 | Largest subunit (p90) of the Chromatin Assembly Complex (CAF-1); chromatin assembly by CAF-1 is important for multiple processes including silencing at telomeres, mating type loci, and rDNA; maintenance of kinetochore structure; deactivation of the DNA damage checkpoint after DNA repair; and chromatin dynamics during transcription | |||||||||||||
| RPF2 | RPF2 | YKR081C | Essential protein involved in the processing of pre-rRNA and the assembly of the 60S ribosomal subunit; interacts with ribosomal protein L11; localizes predominantly to the nucleolus; constituent of 66S pre-ribosomal particles | ||||||||||||||
| RSF2 | RSF2 | YJR127C | ZMS1 | Zinc-finger protein; involved in transcriptional control of both nuclear and mitochondrial genes, many of which specify products required for glycerol-based growth, respiration, and other functions; RSF2 has a paralog, TDA9, that arose from the whole genome duplication; relocalizes from nucleus to cytoplasm upon DNA replication stress | |||||||||||||
| RUF2 | SNR82 | snR82 | RUF2 |
ChrVII:316788 to 317055 | ORF Map | GBrowse
| H/ACA box small nucleolar RNA (snoRNA); guides pseudouridylation of large subunit (LSU) rRNA at positions U1110, U2349, and U2351 | ||||||||||||
| RUF20 | RUF20 | RUF20 |
ChrVI:131503 to 131061 | ORF Map | GBrowse Note: this feature is encoded on the Crick strand.
| RNA of Unknown Function | |||||||||||||
| RUF21 | RUF21 | RUF21 |
ChrVI:58521 to 57815 | ORF Map | GBrowse Note: this feature is encoded on the Crick strand.
| RNA of Unknown Function | |||||||||||||
| RUF22 | RUF22 | RUF22 |
ChrVI:199813 to 199299 | ORF Map | GBrowse Note: this feature is encoded on the Crick strand.
| RNA of Unknown Function; precise location of 3' end uncertain; RUF22 may be longer than currently annotated | |||||||||||||
| RUF23 | RUF23 | RUF23 |
ChrVI:221714 to 221967 | ORF Map | GBrowse
| RNA of Unknown Function; precise location of 3' end uncertain; RUF23 may be longer than currently annotated | |||||||||||||
| SGF29 | SGF29 | YCL010C | Component of the HAT/Core module of the SAGA, SLIK, and ADA complexes; HAT/Core module also contains Gcn5p, Ngg1p, and Ada2p; binds methylated histone H3K4; involved in transcriptional regulation through SAGA and TBP recruitment to target promoters and H3 acetylation | ||||||||||||||
| SIF2 | SIF2 | YBR103W | EMB1 | WD40 repeat-containing subunit of the Set3C histone deacetylase complex, which represses early/middle sporulation genes; antagonizes telomeric silencing; binds specifically to the Sir4p N-terminus | |||||||||||||
| SMF2 | SMF2 | YHR050W | divalent metal ion transporter SMF2 | Divalent metal ion transporter involved in manganese homeostasis; has broad specificity for di-valent and tri-valent metals; post-translationally regulated by levels of metal ions; member of the Nramp family of metal transport proteins | |||||||||||||
| SNF2 | SNF2 | YOR290C | GAM1, HAF1, SWI2, TYE3 | Catalytic subunit of the SWI/SNF chromatin remodeling complex involved in transcriptional regulation; contains DNA-stimulated ATPase activity; functions interdependently in transcriptional activation with Snf5p and Snf6p | |||||||||||||
| SRF2 | YJR114W | SRF2 | Dubious open reading frame unlikely to encode a protein, based on available experimental and comparative sequence data; partially overlaps the verified ORF RSM7/YJR113C | ||||||||||||||
| SSF2 | SSF2 | YDR312W | Protein required for ribosomal large subunit maturation; functionally redundant with Ssf1p; member of the Brix family; SSF2 has a paralog, SSF1, that arose from the whole genome duplication | ||||||||||||||
| STF2 | STF2 | YGR008C | Protein involved in resistance to dessication stress; Stf2p exhibits antioxidant properties, and its overexpression prevents ROS accumulation and apoptosis; binds to F0 sector of mitochondrial F1F0 ATPase in vitro and may modulate the inhibitory action of Inh1p and Stf1p; protein abundance increases in response to DNA replication stress; STF2 has a paralog, TMA10, that arose from the whole genome duplication | ||||||||||||||
| SUF2 | SUF2 | tP(AGG)C |
ChrIII:123648 to 123577 | ORF Map | GBrowse Note: this feature is encoded on the Crick strand.
Genetic position: 2 cM | Proline tRNA (tRNA-Pro), predicted by tRNAscan-SE analysis; can mutate to suppress +1 frameshift mutations in proline codons | |||||||||||||
| SUF20 | SUF20 | tG(GCC)F1 |
ChrVI:162228 to 162298 | ORF Map | GBrowse
Genetic position: 6 cM | Glycine tRNA (tRNA-Gly), predicted by tRNAscan-SE analysis; can mutate to suppress +1 frameshift mutations in glycine codons | |||||||||||||
| SUF21 | SUF21 | SUF21 |
ChrXVI Genetic position: 3 cM | ||||||||||||||
| SUF22 | SUF22 | SUF22 |
ChrXIII Genetic position: -31 cM | ||||||||||||||
| SUF23 | SUF23 | SUF23 |
ChrX Genetic position: 35 cM | ||||||||||||||
| SUF24 | SUF24 | SUF24 |
ChrIV Genetic position: 160 cM | ||||||||||||||
| SUF25 | SUF25 | SUF25 |
ChrIV Genetic position: -115 cM | ||||||||||||||
| SYF2 | SYF2 | YGR129W | NTC31 | Member of the NineTeen Complex (NTC) that contains Prp19p and stabilizes U6 snRNA in catalytic forms of the spliceosome containing U2, U5, and U6 snRNAs; isy1 syf2 cells have defective spindles activiating cell cycle arrest | |||||||||||||
| TAF2 | TAF2 | YCR042C | TAF150, TSM1, TafII150 | TFIID subunit (150 kDa), involved in RNA polymerase II transcription initiation | |||||||||||||
| TAF23 TAF25 |
TAF10 | YDR167W | TAF23, TAF25, TafII25 | Subunit (145 kDa) of TFIID and SAGA complexes, involved in RNA polymerase II transcription initiation and in chromatin modification | |||||||||||||
| TEF2 | TEF2 | YBR118W | EF-1 alpha, eEF1A | Translational elongation factor EF-1 alpha; also encoded by TEF1; functions in the binding reaction of aminoacyl-tRNA (AA-tRNA) to ribosomes; may also have a role in tRNA re-export from the nucleus; TEF2 has a paralog, TEF1, that arose from the whole genome duplication | |||||||||||||
| tG(GCC)F2 | tG(GCC)F2 |
ChrVI:181044 to 180974 | ORF Map | GBrowse Note: this feature is encoded on the Crick strand.
| Glycine tRNA (tRNA-Gly), predicted by tRNAscan-SE analysis | ||||||||||||||
| TIF2 | TIF2 | YJL138C | eIF4A | Translation initiation factor eIF4A; DEA(D/H)-box RNA helicase that couples ATPase activity to RNA binding and unwinding; forms a dumbbell structure of two compact domains connected by a linker; interacts with eIF4G; protein abundance increases in response to DNA replication stress; TIF2 has a paralog, TIF1, that arose from the whole genome duplication | |||||||||||||
| TOF2 | TOF2 | YKR010C | Protein required for rDNA silencing and mitotic rDNA condensation; stimulates Cdc14p phosphatase activity and biphasic release to promote rDNA repeat segregation; required for condensin recruitment to the replication fork barrier site; TOF2 has a paralog, NET1, that arose from the whole genome duplication | ||||||||||||||
| tY(GUA)F2 | SUP6 | tY(GUA)F2 |
ChrVI:210707 to 210619 | ORF Map | GBrowse Note: this feature is encoded on the Crick strand.
Genetic position: 38 cM | Tyrosine tRNA (tRNA-Tyr), predicted by tRNAscan-SE analysis; can mutate to suppress ochre nonsense mutations | |||||||||||||
| UPF2 | NMD2 | YHR077C | IFS1, SUA1, UPF2, SUP111 | Protein involved in the nonsense-mediated mRNA decay (NMD) pathway; interacts with Nam7p and Upf3p; involved in telomere maintenance | |||||||||||||
| yIF2 | FUN12 | YAL035W | yIF2, eIF5B | GTPase required for general translation initiation; promotes Met-tRNAiMet binding to ribosomes and ribosomal subunit joining; promotes GTP-dependent maturation of 18S rRNA by Nob1p; protein abundance increases in response to DNA replication stress; homolog of bacterial IF2 | |||||||||||||
| YLF2 | YLF2 | YHL014C | YLF1 | Protein of unknown function, has weak similarity to E. coli GTP-binding protein gtp1; the authentic, non-tagged protein is detected in highly purified mitochondria in high-throughput studies |


