Across TCGA pan-cancer cohorts, ICAM5 Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated ICAM5 data layer compared with 23 for mass-spec protein and 5 for mass-spec protein.
The strongest signal is observed in rectum adenocarcinoma (READ), where higher ICAM5 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated ICAM5 expression acts as an unfavorable survival marker.
READ, GBM, and SCLC are the cancer types where ICAM5 Mutation most reproducibly stratifies survival.