Module number 2615




Database revision : gnsdb28.10
Date : Tue Feb 25 17:23:05 2003
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mMEP1:ammonia permease,ammonia permease,\n mMRPL4:essential for mitochondrial function and for proper cell gro\nwth under non-respiratory conditions,ribosomal protein 60S L\n4,Null mutant is viable, fails to grow on nonfermentable car\nbon sources, has growth defects on fermentable carbon source\ns\n UME6.ume6:The Ume6 regulon coordinates metabolic and meiotic gene expr\nession in yeast. Proc Natl Acad Sci U S A. 2002 Oct 15;99(2\n1):13431-6.\n mVPS75:Unknown ,, Unknown\n mAPQ12:Unknown ,, Unknown\n mYJR001W:Unknown ,, Unknown\n mPDR15:similar to Pdr5p and Pdr10p,multidrug resistance transporter\n (putative),\n Cond947:W303_YPA\n mMKK1:Mitogen-activated kinase-kinase involved in protein kinase C\n pathway,MAP kinase kinase (MEK),Null mutant is viable but c\nannot grow on glycerol, is sensitive to nitrogen starvation,\n and cannot grow at elevated temperatures unless supplemente\nd with sorbitol.\n Meiosis.Series0:The core meiotic transcriptome in budding yeasts. Nat Genet\n. 2000 Dec;26(4):415-23.\n mSMM1:Suppressor of Mitochondrial Mutation in the tRNAasp gene; Di\nhydrouridine synthase 2,tRNA dihydrouridine synthase,Overexp\nression weakly suppresses a mutation affecting the maturatio\nn of mitochondrial tRNA-Asp.\n mLGE1:Unknown ,, Unknown\n mSPI1:Stationary Phase Induced; strongly expressed during stationa\nry phase, and trancription is dependent on MSN2/MSN4.,,\n mYML108W:Unknown ,, Unknown\n Cond754: COMP.KO:Functional classification via a compendium of knockouts. Hug\nes et.al., cell 2000.\n mACS1:one of 2 acetyl-coA synthetases in yeast,acetyl CoA syntheta\nse,Null mutant is viable and grows on ethanol or glucose (bu\nt not acetate) as sole carbon source (but with long lag-phas\ne); acs1 acs2 double null mutant is inviable\n mASK1:Hypothetical ORF,,Null mutant is inviable\n Cond937:t=0\n mCUP9:homeobox domain similar human proto-oncogene PBX1,DNA bindin\ng protein (putative),Null mutant is viable, associated with \nloss of copper resistance\n mZRG8:Zinc regulated gene,,\n mMST1:mitochondrial threonine-tRNA synthetase,,Null mutant is viab\nle\n mGSP2:maintenance of nuclear organization; homologous to mammalian\n Ran, a small nuclear GTPase of the ras superfamily,GTP-bind\ning protein , Gsp1p homolog,Null mutant is viable\n mSEC61:membrane component of ER protein translocation apparatus,,Nu\nll mutant is inviable. Conditional alleles are defective for\n protein translocation and the export of misfolded proteins \nfrom the endoplasmic reticulum at the restrictive temperatur\ne.\n mHOF1:SH3 domain containing-protein required for cytokinesis,,Null\n mutant is defective in cytokinesis\n mYHR034C:Unknown ,, Unknown\n mPBI2:Proteinase inhibitor that inhibits protease Prb1p (yscB),pro\nteinase inhibitor I2B (PBI2),Null mutant is viable but shows\n 50% elevation of protein degradation rate when cells are su\nbject to nutritional stress\n mYJR115W:Unknown ,, Unknown\n mGPG1:Unknown ,, Unknown\n mIMP2':Protein involved in nucleo-mitochondrial control of maltose,\n galactose and raffinose utilization,transcription factor,Nu\nll mutant is viable, Inability to grow on maltose, galactose\n and raffinose in respiratory-deficient conditions or in the\n presence of ethidium bromide and erythromycin; leaky phenot\nype on oxidizable carbon sources: sensitivity to heat shock \nand sporulation deficiency\n SGD.GO:Functional classification via a compendium of knockouts. Hug\nes et.al., cell 2000.\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 mBUD13:Hypothetical ORF,,Null mutant is viable; diploid null mutant\ns exhibit unipolar budding and elongate phenotype.\n Cond59:erp4\n mNBP1:Nap1p Binding Protein ,,Null mutant is inviable\n mGAP1:general amino acid permease,general amino acid permease,abol\nished activity of the general amino acid transport system\n mPUP1:putative proteasome subunit,proteasome subunit (putative),\n mCNE1:Functions in endoplasmic reticulum protein quality control,c\nalnexin and calreticulin homolog,Null mutant is viable, incr\nease of cell-surface expression of ste2-3p, increase in secr\netion of heterologously expressed mammalian alpha 1-antitryp\nsin\n fkh1,2sf.Series0:Two yeast forkhead genes regulate the cell cycle and pseudoh\nyphal growth. Nature. 2000 Jul 6;406(6791):90-4.\n mYNL108C:Unknown ,, Unknown\n mHST1:Homolog of SIR2,,Overexpression restores transcriptional sil\nencing in a sir2 mutant\n
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Computational Genomics Lab, Tel-Aviv uniresity