Across TCGA pan-cancer cohorts, STYXL1 Mutation is linked to patient survival in 4 of 34 cancer types, making it a survival-associated STYXL1 data layer compared with 29 for mass-spec protein.
The strongest signal is observed in colon adenocarcinoma (COAD), where higher STYXL1 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated STYXL1 expression acts as an unfavorable survival marker, although some lineages such as UCEC and SKCM show a favorable association.
COAD, UCEC, and SKCM are the cancer types where STYXL1 Mutation most reproducibly stratifies survival.