ZNF587B

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, ZNF587B Mutation is linked to patient survival in 5 of 34 cancer types, making it a survival-associated ZNF587B data layer compared with 24 for mass-spec protein.

The strongest signal is observed in stomach adenocarcinoma (STAD), where higher ZNF587B Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated ZNF587B expression acts as an unfavorable survival marker, although some lineages such as BLCA show a favorable association.

STAD, ESCA, and LGG are the cancer types where ZNF587B 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
STADOSMedianAll0.2160.689<.00130view →
ESCAOSMedianII,III,IV0.1170.687<.00118view →
LGGDFSMedianAll0.0830.833<.00112view →
SKCMOSMedianIII,IV0.2330.705.0343view →
BLCADFSMedianIII,IV1.0000.269.0402view →
Pink = unfavorable, green = favorable. Showing the 5 strongest of 5 lineages.

ZNF587B–STAD (OS)

Kaplan–Meier survival curve for ZNF587B mutant vs wild-type samples in STAD.

Open the STAD breakdown →

Exploration