ZNF333

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, ZNF333 Mutation is linked to patient survival in 7 of 34 cancer types, making it a survival-associated ZNF333 data layer compared with 23 for mass-spec protein.

The strongest signal is observed in uterine carcinosarcoma (UCS), where higher ZNF333 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated ZNF333 expression acts as an unfavorable survival marker, although some lineages such as UCEC and STAD show a favorable association.

UCS, LGG, and LIHC are the cancer types where ZNF333 Mutation most reproducibly stratifies survival.

Mutation survival associations by lineage

Ranked by sampling consensus. AUC1 and AUC2 indicate survival in the high- and low-expression groups, respectively; the lower AUC marks the poorer-surviving group. p-values are from the log-rank test.
LineageMeasureSplitStageAUC1
high
AUC2
low
pSampling consensus
UCSDFSMedianAll0.0680.524<.00148view →
LGGOSMedianAll0.1330.811<.00112view →
LIHCDFSMedianAll0.0440.553<.00112view →
UCECDFSMedianAll0.9720.828.0198view →
SCLCOSMedianAll0.1780.660.0026view →
STADOSMedianIV0.8050.283.0316view →
LUSCDFSMedianII,III,IV0.1850.709.0183view →
Pink = unfavorable, green = favorable. Showing the 7 strongest of 7 lineages.

ZNF333–UCS (DFS)

Kaplan–Meier survival curve for ZNF333 mutant vs wild-type samples in UCS.

Open the UCS breakdown →

Exploration