Across TCGA pan-cancer cohorts, SMOC1 Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated SMOC1 data layer compared with 21 for mass-spec protein and 5 for mass-spec protein.
The strongest signal is observed in uterine carcinosarcoma (UCS), where higher SMOC1 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated SMOC1 expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.
UCS, PRAD, and UCEC are the cancer types where SMOC1 Mutation most reproducibly stratifies survival.