Across TCGA pan-cancer cohorts, CIDEB Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated CIDEB data layer compared with 26 for mass-spec protein and 1 for mass-spec protein.
The strongest signal is observed in skin cutaneous melanoma (SKCM), where higher CIDEB Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated CIDEB expression acts as an unfavorable survival marker.
SKCM, COAD, and CHOL are the cancer types where CIDEB Mutation most reproducibly stratifies survival.