Across TCGA pan-cancer cohorts, KCNIP1 Mutation is linked to patient survival in 4 of 34 cancer types, making it a survival-associated KCNIP1 data layer compared with 27 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 KCNIP1 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated KCNIP1 expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.
CESC, SKCM, and KICH are the cancer types where KCNIP1 Mutation most reproducibly stratifies survival.