ZNF646

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, ZNF646 Mutation is linked to patient survival in 11 of 34 cancer types, making it a survival-associated ZNF646 data layer compared with 25 for mass-spec protein and 3 for mass-spec protein.

The strongest signal is observed in lung squamous cell carcinoma (LUSC), where higher ZNF646 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated ZNF646 expression acts as an unfavorable survival marker, although some lineages such as UCEC and STAD show a favorable association.

LUSC, KICH, and ESCA are the cancer types where ZNF646 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
LUSCDFSMedianAll0.0450.798<.00118view →
KICHDFSMedianAll0.1020.848.00413view →
ESCADFSMedianII,III,IV0.1890.528.00612view →
UCECDFSMedianAll0.7880.630.00612view →
SCLCOSMedianAll0.3010.711.0189view →
LGGOSMedianAll0.1630.889<.0016view →
ACCDFSMedianAll0.0890.666.0176view →
SKCMOSMedianIII,IV0.2230.729<.0016view →
KIRPOSMedianAll0.1110.702.0323view →
LUADOSMedianAll0.1760.670.0393view →
STADOSMedianIV1.0000.299.0472view →
Pink = unfavorable, green = favorable. Showing the 11 strongest of 11 lineages.

ZNF646–LUSC (DFS)

Kaplan–Meier survival curve for ZNF646 mutant vs wild-type samples in LUSC.

Open the LUSC breakdown →

Exploration