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Functional homolog of human NPC2/He1, which is a cholesterol-binding protein whose deficiency causes Niemann-Pick type C2 disease involving retention of cholesterol in lysosomes
Localization:
Intensity:
Fold change:
Significance:
-
C’ GFP library in SD
vacuole22.96 -
N' NOP1pr-GFP in SD
ER,vacuole112.377 -
N' TEF2pr-mCherry in SD
vacuole54.0111 -
N' NATIVEpr-GFP in SD
vacuole32.8799 -
N' TEF2pr-VC and Cyto-VN in SD
#N/A0 -
C’ GFP library in SD+DTT
vacuole16.360.71Yes -
C’ GFP library in SD+H2O2
vacuole19.310.84No -
C’ GFP library in Starvation Media
vacuole45.051.96Yes -
C’ GFP library on the background of Pup2-DaMP
N/A -
C’ GFP library on the background of CCT mutant
N/A0N/AYes