Across TCGA pan-cancer cohorts, ANKRD62 Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated ANKRD62 data layer compared with 21 for mass-spec protein and 2 for mass-spec protein.
The strongest signal is observed in cholangiocarcinoma (CHOL), where higher ANKRD62 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated ANKRD62 expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.
CHOL, UCEC, and LIHC are the cancer types where ANKRD62 Mutation most reproducibly stratifies survival.