Across TCGA pan-cancer cohorts, LRRC37A2 Mutation is linked to patient survival in 2 of 34 cancer types, making it a survival-associated LRRC37A2 data layer compared with 31 for mass-spec protein.
The strongest signal is observed in prostate adenocarcinoma (PRAD), where higher LRRC37A2 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated LRRC37A2 expression acts as an unfavorable survival marker.
PRAD and LIHC are the cancer types where LRRC37A2 Mutation most reproducibly stratifies survival.