Across TCGA pan-cancer cohorts, IMPG2 Mutation is linked to patient survival in 6 of 34 cancer types, making it a survival-associated IMPG2 data layer compared with 22 for mass-spec protein and 1 for mass-spec protein.
The strongest signal is observed in cervical squamous cell carcinoma and endocervical adenocarcinoma (CESC), where higher IMPG2 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated IMPG2 expression acts as an unfavorable survival marker, although some lineages such as UCEC and ESCA show a favorable association.
CESC, SKCM, and UCEC are the cancer types where IMPG2 Mutation most reproducibly stratifies survival.