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.