Across TCGA pan-cancer cohorts, CRYGS Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated CRYGS data layer compared with 23 for mass-spec protein and 1 for mass-spec protein.
The strongest signal is observed in sarcoma (SARC), where higher CRYGS Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated CRYGS expression acts as an unfavorable survival marker.
SARC, UCEC, and PRAD are the cancer types where CRYGS Mutation most reproducibly stratifies survival.