Module number 901




Database revision : gnsdb28.10
Date : Tue Feb 25 17:06:49 2003
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Cond717:t2-SSD1\n mREX3:RNA EXonuclease; member of 3'->5' exonuclease family. See Mo\nser et al. 1997 Nucleic acids Res. 25:5110-5118,,Mutants exh\nibit RNase MRP RNA processing defect; functions redundantly \nwith REX1 and REX2 in U5 snRNA and RNase P RNA processing\n mMCM16:Involved in a nonessential role that governs the kinetochore\n-microtubule mediated process of chromosome segregation,,Nul\nl mutant is viable, exhibits increased sensitivity to the an\nitmitotic drugs benomyl and thiabenzadole; exhibits a high r\nate of chromosome III loss without a significant increase in\n recombination frequency, may exhibit altered kinetochore as\nsembly\n Cond720:t0+SSD1,H44\n Cond716:t2+SSD1wt\n Cond708:t0+SSD1\n Cond725:t4-SSD1,M31\n COMP.KO:Functional classification via a compendium of knockouts. Hug\nes et.al., cell 2000.\n mPOP5:Processing Of Precursors - refer to a group of proteins that\n appear to be components of both RNase P and RNase MRP,RNase\n MRP subunit (putative) , RNase P integral subunit,Null muta\nnt is inviable; transient depletion of Pop5p causes loss of \nRNase P and RNase MRP function\n mTHI22:THI for thiamine metabolism. Transcribed in the presence of \nlow level of thiamine (10-8M) and turned off in the presence\n of high level (10-6M) of thiamine. Under the positive contr\nol of THI2 and THI3.,,null mutant is viable\n mGFD2:Unknown ,, Unknown\n mYGR093W:Unknown ,, Unknown\n mSWD1:YAR003W,,\n mYHL039W:Unknown ,, Unknown\n mSNF12:73 kDa subunit of the SWI/SNF transcription activation compl\nex, homolog of Rsc6p subunit of the RSC chromatin remodeling\n complex,RSC chromatin remodeling complex Rsc6p subunit homo\nlog , SWI/SNF transcription activation complex 73 kDa subuni\nt,Null mutant is viable but is temperature-sensitive, fails \nto transcribe SWI/SNF-dependent genes such as SUC2 and INO1,\n sucrose non-fermenting, defective in transcriptional activa\ntion by the glucocorticoid receptor; snf12 mutants are insen\nsitive to expression of Adenovirus E1A protein\n mYGL085W:Unknown ,, Unknown\n SGD.GO:Functional classification via a compendium of knockouts. Hug\nes et.al., cell 2000.\n mGTR1:Involved in the function of the Pho84 phosphate transporter,\nsmall GTPase (putative),Null mutant is viable but grows slow\nly, is cold-sensitive, and has defects in phosphate uptake\n Cond205:yel033w\n mMNN5:mannan synthesis,golgi alpha-1,2-mannosyltransferase (putati\nve),Null mutant is viable but defective in addition of the a\nlpha-1,3-linked mannose branch to the mannan structure found\n on N-linked glycans.\n mARO9:aromatic amino acid aminotransferase II,aromatic amino acid \naminotransferase II,Null mutant is viable\n Cond723:t2-SSD1,M31\n mYOR154W:Unknown ,, Unknown\n Cond724:t4+SSD1,H44\n Cond714:t0+SSD1wt\n Cond715:t0-SSD1\n mRAD57:Required for X-ray damage repair, meiotic recombination, wil\nd-type levels of sporulation and viable spores,RecA homolog \n, interacts with Rad 55p by two-hybrid analysis , similar to\n DMC1, RAD51, and RAD55,Null mutant is viable, radiation sen\nsitive\n Cond713:t4+Vec\n mYDR003W:Unknown ,, Unknown\n COMP.:Functional classification via a compendium of knockouts. Hug\nes et.al., cell 2000.\n mMOD5:transfer RNA isopentenyl transferase,transfer RNA isopenteny\nl transferase,Null mutant is viable but temperature sensitiv\ne and cannot grow on nonfermentable carbon sources.\n mRIB7:Protein involved in the biosynthesis of riboflavin, second s\ntep in the riboflavin biosynthesis pathway,,\n mYOR004W:Unknown ,, Unknown\n mESA1:contains amino-terminal chromodomains; Essential SAS family \nAcetyltransferase sharing homology with acetyltransferases f\nrom many different organisms,acetyltransferase in the SAS ge\nne family,Null mutant is inviable\n mAAT1:aspartate aminotransferase, mitochondrial,aspartate aminotra\nnsferase,Null mutant is viable; aat1 leu2 double mutant is i\nnviable.\n mYOR013W:Unknown ,, Unknown\n mYPT32:probably involved in intra-Golgi transport or in the formati\non of transport vesicles at the most distal Golgi compartmen\nt,GTPase , YPT31 homolog , ras homolog,Null mutant is viable\n; ypt31 ypt32 double deletion mutants are inviable\n mYCR060W:Unknown ,, Unknown\n mDST1:Meiotic DNA recombination factor,RNA polymerase II elongatio\nn factor , transcription elongation factor,Null mutant is vi\nable; reduced induction of DNA strand transfer; sensitivity \nto 6-azauracil\n Cond718:t4+SSD1wt\n Cond721:t0-SSD1,M31\n mCSN12:Unknown ,, Unknown\n mHLJ1:Homologous to E coli dnaJ protein,,\n mHRB1:an ORF of unknown function located in a centromeric region d\nuplicated between chromosomes III and XIV,hypothetical RNA-b\ninding protein,\n Cond709:t0+Vec\n mCYC1:iso-1-cytochrome c,iso-1-cytochrome c,Cytochrome c deficienc\ny\n Cond710:t2+SSD1\n mCDC36:Required for Start B in mitosis and for meiosis I spindle po\nle body separation,basal transcription inhibitor , transcrip\ntional regulator , basal transcription inhibitor , transcrip\ntional regulator,Null mutant is viable, cdc36 mutant arrests\n in G(sub)1; forms shmoo morphology at restrictive temperatu\nre, arrests at pachytene at the mononucleate stage with dupl\nicated spindle pole bodies and no spindles\n
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Computational Genomics Lab, Tel-Aviv uniresity