Across TCGA pan-cancer cohorts, ADAM22 Mutation is linked to patient survival in 4 of 34 cancer types, making it a survival-associated ADAM22 data layer compared with 24 for mass-spec protein and 2 for mass-spec protein.
The strongest signal is observed in ovarian serous cystadenocarcinoma (OV), where higher ADAM22 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated ADAM22 expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.
OV, UCEC, and LUSC are the cancer types where ADAM22 Mutation most reproducibly stratifies survival.