Module number 893




Database revision : gnsdb28.10
Date : Tue Feb 25 17:17:23 2003
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Cond101:mrpl33\n Cond292:Glucosamine\n Cond102:mrt4\n Cond541:fus3D+50nMaF,30min/wtlog10(intensity)\n mYPL251W:Unknown ,, Unknown\n Cond248:ymr030w\n mABP1:Actin binding protein,actin binding protein,Null mutant is v\niable\n mYLR179C:Unknown ,, Unknown\n mYER152C:Unknown ,, Unknown\n mHCR1:High Copy suppressor of RPG1,,viable\n Meiosis.Series0:The core meiotic transcriptome in budding yeasts.  Nat Genet\n. 2000 Dec;26(4):415-23.\n Cond183:ubp8\n Cond130:rml2(**13)\n Cond266:ynd1\n Cond121:qcr2(haploid)\n mPDC1:pyruvate decarboxylase,pyruvate decarboxylase,undetectable p\nyruvate decarboxylase activity in pdc1pdc5 double mutants\n Cond93:kre1\n mESS1:Mitotic regulator; structurally and functionally homologous \nto human PIN1,peptidyl-prolyl cis-trans isomerase (PPIase),N\null mutant is inviable; arrest phenotype of mitotic arrest a\nnd nuclear fragmentation\n Cond280:FKS1(tetpromoter)\n Cond185:ubr2\n Cond190:vps8\n Cond140:rps24a(**9)\n mSCS2:Likely to be involved in regulating INO1 expression, suppres\nsor of a dominant nuclear mutation that is inositol-dependen\nt in the presence of choline,,Null mutant is viable but is a\nn inositol auxotroph above 34 deg.\n Cond105:nrf1\n Cond106:nta1\n mSIM1:(putative) invovled in control of DNA replication,,Null muta\nnt is viable; mutant allows an extra round of DNA replicatio\nn without mitosis\n Cond28:cla4(haploid)\n mRNH35:RNase H(35), a 35 kDa ribonuclease H,,Null mutant is viable \nbut shows 75% reduction of RNase H activity in cell extracts\n Cond81:hog1(haploid)\n GCN4.gcn4:Transcriptional profiling shows that Gcn4p is a master regul\nator of gene expression during amino acid starvation in yeas\nt.  Mol Cell Biol. 2001 Jul;21(13):4347-68.\n Cond808:Na15'\n Cond940:6h\n mTHR1:homoserine kinase,homoserine kinase,Null mutant is viable, t\nhreonine auxotroph\n COMP.:Functional classification via a compendium of knockouts. Hug\nes et.al., cell 2000.\n Mating.Mating:Signaling and circuitry of multiple MAPK pathways revealed b\ny a matrix of global gene expression profiles.  Science. 200\n0 Feb 4;287(5454):873-80\n Cond210:yer002w\n Cond200:yel001c\n Cond245:ymr014w\n mCCW12:Hypothetical ORF,cell wall mannoprotein,Null mutant is viabl\ne and shows decrease in mating efficiency and defect in aggl\nutination\n mDPH5:diphthamide biosynthesis,,Null mutant is viable\n mGSP1:maintenance of nuclear organization; homologous to mammalian\n Ran, a small nuclear GTPase of the ras superfamily,GTP-bind\ning protein,Null mutant is inviable\n Cond285:RHO1(tetpromoter)\n COMP.CH:Functional classification via a compendium of knockouts. Hug\nes et.al., cell 2000.\n Cond61:fks1(haploid)\n mERV46:ER vesicle protein of 46 kDa,ER-Golgi transport vesicle prot\nein,Null mutant is viable but cold sensitive.\n Cond86:imp2'(**12)\n mRET2:coatomer (COPI) complex delta subunit,,ret2-1 mutant is ther\nmosensitive and shows defects in retrieval of dilysine-tagge\nd proteins from the Golgi back to the ER and, at the non-per\nmissive temperature, in forward ER-to-Golgi transport\n mDSK2:Required with RAD23 for duplication of the spindle pole body\n,ubiquitin-like protein,Null mutant is viable\n mCAF120:Hypothetical ORF,,Null mutant is viable\n mSOD2:Manganese-containing superoxide dismutase,Mn-containing supe\nroxide dismutase,Null mutant is viable; growth is impaired b\ny oxygen; SOD2 is required for sporulation\n Cond238:yml005w\n Cond273:yor078w\n Cond287:2-deoxy-D-glucose\n mPTC2:Protein phosphatase type 2C,protein phosphatase type 2C,\n mCYC8:General repressor of transcription (with Tup1p); mediates gl\nucose repression,,Null mutant is viable; high level constitu\ntivity for invertase, clumpiness, temperature-sensitive grow\nth, alpha-specific mating defects and failure of homozygous \ndiploids to sporulate\n mCAM1:Calcium and phospholipid binding protein homologous to trans\nlation elongation factor 1-gamma (EF-1gamma),calcium and pho\nspholipid binding protein homologous to translation elongati\non factor 1-gamma (EF-1gamma),Null mutant is viable under no\nrmal growth conditions\n mMSL5:branchpoint bridging protein -- component of the splicing co\nmmitment complex,,\n Cond145:rts1\n Cond127:ras2(haploid)\n mYGR210C:Unknown ,, Unknown\n Cond139:rpl8a\n Cond43:dot4\n COMP.KO:Functional classification via a compendium of knockouts. Hug\nes et.al., cell 2000.\n mSOL2:multicopy suppressor of los1-1,,Null mutant is viable\n mRNQ1:Rich in asparagine (N) and glutamine (Q),transferable epigen\netic modifier,\n Cond134:rpl12a\n Cond58:erp2\n Cond170:ste20(**11)\n Cond256:ymr141c\n Cond52:erd1\n Cond26:cka2\n Cond62:fpr1\n Stress.Menadione:Genomic expression programs in the response of yeast cells t\no environmental changes.  Mol Biol Cell. 2000 Dec;11(12):424\n1-57\n mILV6:acetolactate synthase regulatory subunit,,\n mADE3:Required for the biosynthesis of purines, thymidylate, methi\nonine, histidine, pantothenic acid and formylmethionyl-tRNA,\nC1-tetrahydrofolate synthase,Null mutant is viable, adenine \nauxotroph, histidine auxotroph\n SGD.GO:Functional classification via a compendium of knockouts. Hug\nes et.al., cell 2000.\n mAHP1:alkyl hydroperoxide reductase,alkyl hydroperoxide reductase,\nhypersensitive to tert-butyl hydroperoxide\n mPAN1:Involved in actin organization and endocytosis,,Null mutant \nis inviable; conditional mutants show arrest of translation \ninitiation, alterations in mRNA poly(A) tail lengths, and al\ntered cellular location of Mod5p\n Cond205:yel033w\n Cond284:PMA1(tetpromoter)\n Cond91:kim4\n mPIB2:Phosphatidylinositol 3-phosphate binding,,\n mFAS2:Trifunctional enzyme,fatty acid synthase alpha subunit,Fatty\n acid synthetase deficient\n Cond283:KAR2(tetpromoter)\n mCSR1:chs5 spa2 rescue; isolated as a multicopy suppressor of the \nlethality of chs5 spa2 double mutant at 37 degrees.,,Null mu\ntant is viable\n mPRY3:Pathogen Related in Sc, contains homology to the plant PR-1 \nclass of pathogen related proteins. The protein sequence is \nover 60% identical with the Pry2p & Pry3p over 145 resid. PR\nY1 is >35% identical (50% similar) to tobacco PR-1c protein.\n,,\n Cond474:gcn4D+/-100mM3AT(KNY124)\n mPAC10:Polypeptide 3 of a Yeast Non-native Actin Binding Complex, h\nomolog of a component of the bovine NABC complex,bovine NABC\n complex component homolog , non-native actin binding comple\nx polypeptide 3 , bovine NABC complex component homolog , no\nn-native actin binding complex polypeptide 3 , bovine NABC c\nomplex component homolog , non-native actin binding complex \npolypeptide 3,Null mutant is viable, benomyl sensitive, cold\n sensitive, microtubules disassemble at 14 degrees celsius, \npac10 mutants exhibit synthetic lethality with tub4-1, cin8,\n cin1, pac2 and rbl2 mutants\n Cond103:msu1\n mLGE1:Unknown ,, Unknown\n mYCR051W:Unknown ,, Unknown\n mTUP1:general repressor of transcription (with Cyc8p); mediates gl\nucose repression,glucose repression regulatory protein, exhi\nbits similarity to beta subunits of G proteins,Null mutant i\ns viable; exhibits flocculent colony morphology\n Calcin.Na:Genome-wide analysis of gene expression regulated by the cal\ncineurin/Crz1p signaling pathway in Saccharomyces cerevisiae\n.  J Biol Chem. 2002 Aug 23;277(34):31079-88\n mCAR2:ornithine aminotransferase,ornithine aminotransferase,Catabo\nlism of arginine defective\n mSTP22:Ste pseudorevertant; required for vacuolar targeting of temp\nerature-sensitive plasma membrane proteins; homologous to th\ne mouse and human Tsg101 tumor susceptibility gene; mutants \nexhibit a Class E Vps phenotype.,,\n Cond161:sod1(haploid)\n mYRF1-6:Y'-helicase protein 1,Y'-helicase protein 1,\n mRPP0:Homology to rat P0, human P0, and E. coli L10e,ribosomal pro\ntein P0 (A0) (L10E),Null mutant is inviable\n COMP.TE:Functional classification via a compendium of knockouts. Hug\nes et.al., cell 2000.\n Cond347:1_mM_Menadione_(30_min)_redo\n mDAT1:datin, an oligo(dA).oligo(dT)-binding protein,datin , oligo(\ndA).oligo(dT)-binding protein,Null mutant is viable, but phe\nnotypically distinguishable\n mLCB1:Involved in sphingolipid biosynthesis; may catalyze the firs\nt step in biosynthesis of long-chain sphingolipids,serine pa\nlmitoyltransferase component (putative),Null mutant is viabl\ne; auxotrophic for long-chain component of sphingolipids; ho\nmozygous lcb1 diploids fail to sporulate\n Cond641:DES459_(mec1-)_+_0.02%_MMS_-_15_min\n Cond40:dig1,dig2\n mCYC8 mTUP1 mABP1 mESS1 mCAR2 mAHP1 mRPP0

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Computational Genomics Lab, Tel-Aviv uniresity