Across TCGA pan-cancer cohorts, DYNC1LI2 Mutation is linked to patient survival in 2 of 34 cancer types, making it a survival-associated DYNC1LI2 data layer compared with 20 for mass-spec protein and 5 for mass-spec protein.
The strongest signal is observed in prostate adenocarcinoma (PRAD), where higher DYNC1LI2 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated DYNC1LI2 expression acts as an unfavorable survival marker.
PRAD and SKCM are the cancer types where DYNC1LI2 Mutation most reproducibly stratifies survival.