Across TCGA pan-cancer cohorts, PLA2G5 Mutation is linked to patient survival in 5 of 34 cancer types, making it a survival-associated PLA2G5 data layer compared with 25 for mass-spec protein and 2 for mass-spec protein.
The strongest signal is observed in colon adenocarcinoma (COAD), where higher PLA2G5 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated PLA2G5 expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.
COAD, READ, and LUSC are the cancer types where PLA2G5 Mutation most reproducibly stratifies survival.