SCMD Saccharomyces Cerevisiae Morphological Database
My Gene List My Parameter List
Keywords: (ex. rad52, polarisome)

Sortable ORF Parameter Sheet

Parameter Name:D126_A1B
Stain Type:Nucleus
Nucleus Status:A1B
Parameter Type:Average
click the datasheet labels in order to sort the table

page: [ top ] [ prev ] ... 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 ... [ next ] [ last ]
Download the whole table as an [XML ] or [Tab-separated sheet ] format.
ORF Std. Name D126_A1B
YAL022c FUN26 21.5
Nucleoside transporter with broad nucleoside selectivity; localized to intracellular membranes
YNL220w ADE12 21.5
adenylosuccinate synthetase
YOR012w 21.5
Hypothetical ORF
YGL222c EDC1 21.5
RNA-binding protein, activates mRNA decapping directly by binding to the mRNA substrate and enhancing the activity of the decapping proteins Dcp1p and Dcp2p
YLR343w GAS2 21.5
YGL210w YPT32 21.5
GTPase|YPT31 homolog|ras homolog
YCR014c POL4 21.5
DNA polymerase IV
YBL031w SHE1 21.5
Cytoskeletal protein of unknown function; overexpression causes growth arrest
YPL162c 21.5
Hypothetical ORF
YKL208w CBT1 21.5
Subunit of complex involved in processing of the 3' end of cytochrome b pre-mRNA
YBR013c 21.5
Hypothetical ORF
YDR178w SDH4 21.5
succinate dehydrogenase membrane anchor subunit
YKL092c BUD2 21.5
GTPase activating factor for Rsr1p/Bud1p required for both axial and bipolar budding patterns: mutants exhibit random budding in all cell types
YOL147c PEX11 21.5
peroxisomal membrane protein
YCL057w PRD1 21.5
Zinc metalloendopeptidase, found in the cytoplasm and intermembrane space of mitochondria
YGR222w PET54 21.5
Protein required for splicing of the COX1 intron AI5 beta; also specifically required, together with Pet122p and Pet494p, for translation of the COX3 mRNA; located in the mitochondrial inner membrane
YLR225c 21.5
Hypothetical ORF
YNL035c 21.6
Hypothetical ORF
YIR013c GAT4 21.6
Protein containing GATA family zinc finger motifs
YKR019c IRS4 21.6
Protein involved in rDNA silencing, contains a C-terminal Eps15 homology (EH) domain and a DNA polymerase B signature motif; mutation in IRS4 confers an increase in rDNA silencing
YAL004w 21.6
Hypothetical ORF
YFR024c-A LSB3 21.6
Protein containing a C-terminal SH3 domain: binds Las17p, which is a homolog of human Wiskott-Aldrich Syndrome protein involved in actin patch assembly and actin polymerization
YLR402w 21.6
Hypothetical ORF
YJL216c 21.6
Protein of unknown function, transcriptionally activated by Yrm1p along with genes involved in multidrug resistance
YMR101c SRT1 21.6
YNL193w 21.6
Hypothetical ORF
YMR164c MSS11 21.6
758 amino acid polypeptide with poly-glutamine and poly-asparagine domains
YDR511w ACN9 21.6
Protein of the mitochondrial intermembrane space, required for acetate utilization and gluconeogenesis; has orthologs in higher eukaryotes
YOR354c MSC6 21.6
Protein of unknown function, green fluorescent protein (GFP)-fusion protein localizes to mitochondria; msc6 mutants are defective in directing meiotic recombination events to homologous chromatids
YIL158w 21.6
Hypothetical ORF
YIL050w PCL7 21.6
YCR010c ADY2 21.6
Accumulation of DYads: member of the TC 9.B.33 YaaH family of putative transporters: Protein involved in Accumulation of DYads
YKL137w 21.6
Hypothetical ORF
YNR065c 21.6
Sortilin homolog, interacts with proteins of the endocytic machinery
YLR326w 21.6
Hypothetical ORF
YGL057c 21.6
Hypothetical ORF
YMR257c PET111 21.6
translational activator of cytochrome C oxidase subunit II
YFL010w-A AUA1 21.6
Protein required for the negative regulation by ammonia of Gap1p, which is a general amino acid permease
YKR085c MRPL20 21.6
Mitochondrial ribosomal protein of the large subunit
YGR289c MAL11 21.6
alpha-glucoside transporter|hexose transporter|maltose permease
YGL237c HAP2 21.6
transcriptional activator protein of CYC1 (component of HAP2/HAP3 heteromer)
YPR156c TPO3 21.6
Polyamine transport protein
YMR278w 21.6
Hypothetical ORF
YOR019w 21.6
Hypothetical ORF
YKR034w DAL80 21.6
Negative regulator of genes in multiple nitrogen degradation pathways: expression is regulated by nitrogen levels and by Gln3p: member of the GATA-binding family, forms homodimers and heterodimers with Deh1p
YKR041w 21.6
Hypothetical ORF
YML022w APT1 21.6
adenine phosphoribosyltransferase
YNL196c 21.6
Sporulation-specific protein with a leucine zipper motif
YDR399w HPT1 21.6
Dimeric hypoxanthine-guanine phosphoribosyltransferase, catalyzes the formation of both inosine monophosphate and guanosine monophosphate: mutations in the human homolog HPRT1 can cause Lesch-Nyhan syndrome and Kelley-Seegmiller syndrome
YGR167w CLC1 21.6
clathrin light chain
page: [ top ] [ prev ] ... 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 ... [ next ] [ last ]