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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
Localization:
Intensity:
Fold change:
Significance:
  • C’ GFP library in SD
    YDR399W
    cytosol
    227.15
  • N' NOP1pr-GFP in SD
    YDR399W
    cytosol
    140.994
  • N' TEF2pr-mCherry in SD
    YDR399W
    cytosol
    0
  • N' NATIVEpr-GFP in SD
    noimage.png
    missing
    0
  • N' TEF2pr-VC and Cyto-VN in SD
    noimage.png
    missing
    0
  • C’ GFP library in SD+DTT 
    YDR399W
    cytosol
    116.21
    0.51
    Yes
  • C’ GFP library in SD+H2O2
    YDR399W
    cytosol
    172.13
    0.75
    No
  • C’ GFP library in Starvation Media
    YDR399W
    nucleus
    N/A
    N/A
    Yes
  • C’ GFP library on the background of Pup2-DaMP
    noimage.png
    cytosol
  • C’ GFP library on the background of CCT mutant
    noimage.png
    cytosol
    186.812
    0.822373
    No