Across TCGA pan-cancer cohorts, MED22 Mutation is linked to patient survival in 2 of 34 cancer types, making it a survival-associated MED22 data layer compared with 25 for mass-spec protein and 5 for mass-spec protein.
The strongest signal is observed in mesothelioma (MESO), where higher MED22 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated MED22 expression acts as an unfavorable survival marker.
MESO and SKCM are the cancer types where MED22 Mutation most reproducibly stratifies survival.