Regulator Go Based Analysis
mTEC1	147	transcription f..	DNA repair(0,11)	mitotic cell cycle(0,17)	cell cycle(0,32)	transcription factor of the TEA/ATTS DNA-binding domain family, regulator of Ty1 expression#TEA/ATTS DNA-binding domain family, regulator of Ty1 expression | transcription factor#Null mutant is viable
mKIN82	199	Putative serine..	hydrogen transport(0,11)	main pathways of carbohydrate metabolism(2.7e-05,12)	transport(3.6e-05,25)	Putative serine/threonine protein kinase most similar to cyclic nucleotide-dependent protein kinase subfamily and the protein kinase C subfamily#serine/threonine kinase (putative) | similar to cyclic nucleotide-dependent protein kinase subfamily and the protein kinase C subfamily#Null mutant is viable
mUGA3	71	Transcriptional..	urea cycle intermediate metabolism(0,9)	methionine and threonine metabolism(0,6)	sulfate assimilation(0,6)	Transcriptional activator necessary for gamma-aminobutyrate (GABA)-dependent induction of GABA genes (such as UGA1, UGA2, UGA4)#zinc finger transcription factor of the Zn(2)-Cys(6) binuclear cluster domain type#Null mutant is viable but exhibits defects in activation of UGA1 and UGA4.
mYAP6	261	bZIP protein#	catabolism(0,24)	proteolysis and peptidolysis(0,17)	protein folding(2.9e-05,12)	bZIP protein##
mHMS2	532	High-copy mep2 ..	protein biosynthesis(0,148)	RNA metabolism(0,42)	cytoplasm organization and biogenesis(0,70)	High-copy mep2 suppressor#heat shock transcription factor homolog#Null mutant is viable; multicopy expression suppresses the pseudohyphal defect of mep2/mep2 strains
mIKS1	197	ira1* kinase su..	stress response(0,25)	carbohydrate metabolism(0.00021,13)	catabolism(0.000266,15)	ira1* kinase suppressor#serine/threonine kinase (putative)#Null mutant is heat shock sensitive
mHSL1	34	Negative regula..	mitotic cell cycle(0,10)	axial budding(0,5)	DNA replication and chromosome cycle(3e-06,7)	Negative regulator of swe1 kinase (which regulates cdc28)#protein kinase  (putative) | similar to S. pombe cdr1/nim1#Null mutant is viable; synthetically lethal with histone H3 mutations; G2 delay
mCDC5	55	CDC5 is dispens..	cell cycle(0,19)	M phase(0,12)	mitotic cell cycle(1e-06,10)	CDC5 is dispensable for premeiotic DNA synthesis and recombination, but required for tripartite synaptonemal complexes, haploidization, and spores#protein kinase#Null mutant is inviable. cdc5(ts) mutants form synaptonemal complexes lacking central elements and arrest either at meiosis I with broken spindles or at meiosis II with short spindles. Late shifts to a restrictive temperature result in reductional dyads; each spore contains an entire meiosis II short spindle with unseparated chromatids. In some strains at semi-permissive temperature, chromosomes segregate reductionally or equationally depending upon the centromere.
mGIC1	54	Gtpase-interact..	cytoskeleton organization and biogenesis(0.000289,7)	cell wall organization and biogenesis(0.001334,4)	cell organization and biogenesis(0.001776,11)	Gtpase-interacting component 1##Null mutant is viable; gic1 gic2 double null is temperature sensitive at 33 degrees C
mSST2	318	Protein involve..	mRNA catabolism(0.000337,5)	mating (sensu Fungi)(0.001458,14)	protein targeting(0.001964,11)	Protein involved in desensitization to alpha-factor pheromone#GTPase activating protein (GAP) | RGS (regulator of G-protein signalling) family#Null mutants are viable and exhibit increased sensitivity to mating factors
mBAS1	414	Transcription f..	microtubule-based process(0.000823,13)	pre-replicative complex formation and maintenance(0.001554,6)	transcription regulation(0.004943,8)	Transcription factor regulating basal and induced activity of histidine and adenine biosynthesis genes#transcription factor#
mRGM1	445	Putative transc..	fatty acid beta-oxidation(0.001511,5)	vitamin B1 metabolism(0.002226,6)	fat-soluble vitamin metabolism(0.003946,6)	Putative transcriptional repressor with proline-rich zinc fingers#transcriptional repressor with proline-rich zinc fingers (putative)#Null mutant is viable; overexpression of RGM1 greatly impairs cell growth.