Across TCGA pan-cancer cohorts, SNX31 Mutation is linked to patient survival in 4 of 34 cancer types, making it a survival-associated SNX31 data layer compared with 24 for mass-spec protein.
The strongest signal is observed in uterine corpus endometrial carcinoma (UCEC), where higher SNX31 Mutation is associated with better disease-free survival. In most high-consensus cancer types, elevated SNX31 expression acts as an unfavorable survival marker, although some lineages such as UCEC and SKCM show a favorable association.
UCEC, LUAD, and PRAD are the cancer types where SNX31 Mutation most reproducibly stratifies survival.