EPS8L2

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, EPS8L2 Mutation is linked to patient survival in 4 of 34 cancer types, making it a survival-associated EPS8L2 data layer compared with 24 for mass-spec protein and 5 for mass-spec protein.

The strongest signal is observed in adrenocortical carcinoma (ACC), where higher EPS8L2 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated EPS8L2 expression acts as an unfavorable survival marker.

ACC, UCEC, and HNSC are the cancer types where EPS8L2 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
ACCOSMedianAll0.1880.820<.00112view →
UCECOSMedianIV0.2310.592.0366view →
HNSCOSMedianII,III,IV0.2220.710.0313view →
BLCADFSMedianIII,IV0.1210.488.0203view →
Pink = unfavorable, green = favorable. Showing the 4 strongest of 4 lineages.

EPS8L2–ACC (OS)

Kaplan–Meier survival curve for EPS8L2 mutant vs wild-type samples in ACC.

Open the ACC breakdown →

Exploration