Across TCGA pan-cancer cohorts, ATP2A2 Mutation is linked to patient survival in 5 of 34 cancer types, making it a survival-associated ATP2A2 data layer compared with 24 for mass-spec protein and 6 for mass-spec protein.
The strongest signal is observed in uterine corpus endometrial carcinoma (UCEC), where higher ATP2A2 Mutation is associated with better disease-free survival. In most high-consensus cancer types, elevated ATP2A2 expression acts as an unfavorable survival marker, although some lineages such as UCEC and LUSC show a favorable association.
UCEC, COAD, and ESCA are the cancer types where ATP2A2 Mutation most reproducibly stratifies survival.