ATP6V1E2

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, ATP6V1E2 Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated ATP6V1E2 data layer compared with 23 for mass-spec protein.

The strongest signal is observed in colon adenocarcinoma (COAD), where higher ATP6V1E2 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated ATP6V1E2 expression acts as an unfavorable survival marker.

COAD, SKCM, and ACC are the cancer types where ATP6V1E2 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
COADOSMedianAll0.0260.871<.0016view →
SKCMOSMedianAll0.3810.786.0026view →
ACCDFSMedianAll0.1950.748.0033view →
Pink = unfavorable, green = favorable. Showing the 3 strongest of 3 lineages.

ATP6V1E2–COAD (OS)

Kaplan–Meier survival curve for ATP6V1E2 mutant vs wild-type samples in COAD.

Open the COAD breakdown →

Exploration