Across TCGA pan-cancer cohorts, FICD Mutation is linked to patient survival in 2 of 34 cancer types, making it a survival-associated FICD data layer compared with 24 for mass-spec protein and 3 for mass-spec protein.
The strongest signal is observed in rectum adenocarcinoma (READ), where higher FICD Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated FICD expression acts as an unfavorable survival marker.
READ and UCEC are the cancer types where FICD Mutation most reproducibly stratifies survival.