Across TCGA pan-cancer cohorts, AAGAB Mutation is linked to patient survival in 5 of 34 cancer types, making it a survival-associated AAGAB data layer compared with 23 for mass-spec protein and 7 for mass-spec protein.
The strongest signal is observed in lung squamous cell carcinoma (LUSC), where higher AAGAB Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated AAGAB expression acts as an unfavorable survival marker, although some lineages such as BLCA and SCLC show a favorable association.
LUSC, BLCA, and KIRC are the cancer types where AAGAB Mutation most reproducibly stratifies survival.