Across TCGA pan-cancer cohorts, ANKDD1B Mutation is linked to patient survival in 2 of 34 cancer types, making it a survival-associated ANKDD1B data layer compared with 21 for mass-spec protein.
The strongest signal is observed in mesothelioma (MESO), where higher ANKDD1B Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated ANKDD1B expression acts as an unfavorable survival marker.
MESO and UCEC are the cancer types where ANKDD1B Mutation most reproducibly stratifies survival.