Across TCGA pan-cancer cohorts, FXYD7 Mutation is linked to patient survival in 2 of 34 cancer types, making it a survival-associated FXYD7 data layer compared with 20 for mass-spec protein and 1 for mass-spec protein.
The strongest signal is observed in rectum adenocarcinoma (READ), where higher FXYD7 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated FXYD7 expression acts as an unfavorable survival marker.
READ and CHOL are the cancer types where FXYD7 Mutation most reproducibly stratifies survival.