Across TCGA pan-cancer cohorts, PEX10 Mutation is linked to patient survival in 2 of 34 cancer types, making it a survival-associated PEX10 data layer compared with 23 for mass-spec protein and 5 for mass-spec protein.
The strongest signal is observed in prostate adenocarcinoma (PRAD), where higher PEX10 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated PEX10 expression acts as an unfavorable survival marker.
PRAD and ACC are the cancer types where PEX10 Mutation most reproducibly stratifies survival.