Across TCGA pan-cancer cohorts, SYNRG Mutation is linked to patient survival in 5 of 34 cancer types, making it a survival-associated SYNRG data layer compared with 27 for mass-spec protein and 7 for mass-spec protein.
The strongest signal is observed in uterine corpus endometrial carcinoma (UCEC), where higher SYNRG Mutation is associated with better disease-free survival. In most high-consensus cancer types, elevated SYNRG expression acts as an unfavorable survival marker, although some lineages such as UCEC and MESO show a favorable association.
UCEC, LUAD, and MESO are the cancer types where SYNRG Mutation most reproducibly stratifies survival.