Across TCGA pan-cancer cohorts, SLC66A1L Mutation is linked to patient survival in 4 of 34 cancer types, making it a survival-associated SLC66A1L data layer compared with 26 for mass-spec protein.
The strongest signal is observed in cervical squamous cell carcinoma and endocervical adenocarcinoma (CESC), where higher SLC66A1L Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated SLC66A1L expression acts as an unfavorable survival marker.
CESC, SARC, and SKCM are the cancer types where SLC66A1L Mutation most reproducibly stratifies survival.