Across TCGA pan-cancer cohorts, SPRYD3 Mutation is linked to patient survival in 4 of 34 cancer types, making it a survival-associated SPRYD3 data layer compared with 28 for mass-spec protein and 5 for mass-spec protein.
The strongest signal is observed in colon adenocarcinoma (COAD), where higher SPRYD3 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated SPRYD3 expression acts as an unfavorable survival marker, although some lineages such as SKCM show a favorable association.
COAD, ACC, and UCEC are the cancer types where SPRYD3 Mutation most reproducibly stratifies survival.