Across TCGA pan-cancer cohorts, NOBOX Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated NOBOX data layer compared with 14 for mass-spec protein and 1 for mass-spec protein.
The strongest signal is observed in colon adenocarcinoma (COAD), where higher NOBOX Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated NOBOX expression acts as an unfavorable survival marker.
COAD, KIRC, and LUSC are the cancer types where NOBOX Mutation most reproducibly stratifies survival.