Across TCGA pan-cancer cohorts, MED23 Mutation is linked to patient survival in 5 of 34 cancer types, making it a survival-associated MED23 data layer compared with 27 for mass-spec protein and 6 for mass-spec protein.
The strongest signal is observed in bladder urothelial carcinoma (BLCA), where higher MED23 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated MED23 expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.
BLCA, UCEC, and LUSC are the cancer types where MED23 Mutation most reproducibly stratifies survival.