Across TCGA pan-cancer cohorts, STYX Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated STYX data layer compared with 25 for mass-spec protein and 6 for mass-spec protein.
The strongest signal is observed in colon adenocarcinoma (COAD), where higher STYX Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated STYX expression acts as an unfavorable survival marker.
COAD, CESC, and UCEC are the cancer types where STYX Mutation most reproducibly stratifies survival.