Across TCGA pan-cancer cohorts, SORD Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated SORD data layer compared with 23 for mass-spec protein and 3 for mass-spec protein.
The strongest signal is observed in rectum adenocarcinoma (READ), where higher SORD Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated SORD expression acts as an unfavorable survival marker.
READ, LIHC, and LGG are the cancer types where SORD Mutation most reproducibly stratifies survival.