Alg9
View description
Mannosyltransferase, involved in N-linked glycosylation; catalyzes the transfer of mannose from Dol-P-Man to lipid-linked oligosaccharides; mutation of the human ortholog causes type 1 congenital disorders of glycosylation
Localization:
Intensity:
Fold change:
Significance:
  • C’ GFP library in SD
    YNL219C
    ER
    42.09
  • N' NOP1pr-GFP in SD
    YNL219C
    ER
    72.7619
  • N' TEF2pr-mCherry in SD
    YNL219C
    ER
    10.0929
  • N' NATIVEpr-GFP in SD
    YNL219C
    ER
    35.9033
  • N' TEF2pr-VC and Cyto-VN in SD
    noimage.png
    #N/A
    0
  • C’ GFP library in SD+DTT 
    YNL219C
    ER
    20.58
    0.48
    Yes
  • C’ GFP library in SD+H2O2
    YNL219C
    ER
    36.26
    0.86
    No
  • C’ GFP library in Starvation Media
    YNL219C
    ER
    46.57
    1.1
    No
  • C’ GFP library on the background of Pup2-DaMP
    noimage.png
    ER
  • C’ GFP library on the background of CCT mutant
    noimage.png
    ER
    38.0406
    0.903434
    No
Tel: +972-8-934-6460 | Fax: +972-8-943-6373 | Email: michal.breker@weizmann.ac.il |Last Updated: Thursday, November 22, 2018 - 15:53