Across TCGA pan-cancer cohorts, WASHC5 Mutation is linked to patient survival in 5 of 34 cancer types, making it a survival-associated WASHC5 data layer compared with 26 for mass-spec protein and 5 for mass-spec protein.
The strongest signal is observed in prostate adenocarcinoma (PRAD), where higher WASHC5 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated WASHC5 expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.
PRAD, UCEC, and KIRP are the cancer types where WASHC5 Mutation most reproducibly stratifies survival.