Across TCGA pan-cancer cohorts, SCYL2 Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated SCYL2 data layer compared with 25 for mass-spec protein and 8 for mass-spec protein.
The strongest signal is observed in lung squamous cell carcinoma (LUSC), where higher SCYL2 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated SCYL2 expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.
LUSC, PRAD, and UCEC are the cancer types where SCYL2 Mutation most reproducibly stratifies survival.