Across TCGA pan-cancer cohorts, PRR36 Mutation is linked to patient survival in 2 of 34 cancer types, making it a survival-associated PRR36 data layer compared with 25 for mass-spec protein and 7 for mass-spec protein.
The strongest signal is observed in mesothelioma (MESO), where higher PRR36 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated PRR36 expression acts as an unfavorable survival marker.
MESO and UCEC are the cancer types where PRR36 Mutation most reproducibly stratifies survival.