Across TCGA pan-cancer cohorts, ZBTB32 Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated ZBTB32 data layer compared with 29 for mass-spec protein.
The strongest signal is observed in stomach adenocarcinoma (STAD), where higher ZBTB32 Mutation is associated with better disease-free survival. In most high-consensus cancer types, elevated ZBTB32 expression acts as an unfavorable survival marker, although some lineages such as STAD show a favorable association.
STAD, UCEC, and LIHC are the cancer types where ZBTB32 Mutation most reproducibly stratifies survival.