Across TCGA pan-cancer cohorts, PRR22 Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated PRR22 data layer compared with 22 for mass-spec protein.
The strongest signal is observed in colon adenocarcinoma (COAD), where higher PRR22 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated PRR22 expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.
COAD, PRAD, and UCEC are the cancer types where PRR22 Mutation most reproducibly stratifies survival.