Across TCGA pan-cancer cohorts, CCDC24 Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated CCDC24 data layer compared with 23 for mass-spec protein.
The strongest signal is observed in stomach adenocarcinoma (STAD), where higher CCDC24 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated CCDC24 expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.
STAD, PRAD, and UCEC are the cancer types where CCDC24 Mutation most reproducibly stratifies survival.