Across TCGA pan-cancer cohorts, ARHGAP42 Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated ARHGAP42 data layer compared with 22 for mass-spec protein and 5 for mass-spec protein.
The strongest signal is observed in rectum adenocarcinoma (READ), where higher ARHGAP42 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated ARHGAP42 expression acts as an unfavorable survival marker.
READ, UCEC, and LIHC are the cancer types where ARHGAP42 Mutation most reproducibly stratifies survival.