Across TCGA pan-cancer cohorts, IRAK4 Mutation is linked to patient survival in 2 of 34 cancer types, making it a survival-associated IRAK4 data layer compared with 25 for mass-spec protein and 5 for mass-spec protein.
The strongest signal is observed in uterine carcinosarcoma (UCS), where higher IRAK4 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated IRAK4 expression acts as an unfavorable survival marker.
UCS and ESCA are the cancer types where IRAK4 Mutation most reproducibly stratifies survival.