Across TCGA pan-cancer cohorts, SH3BGRL Mutation is linked to patient survival in 6 of 34 cancer types, making it a survival-associated SH3BGRL data layer compared with 24 for mass-spec protein and 7 for mass-spec protein.
The strongest signal is observed in uterine corpus endometrial carcinoma (UCEC), where higher SH3BGRL Mutation is associated with better disease-free survival. In most high-consensus cancer types, elevated SH3BGRL expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.
UCEC, SCLC, and BLCA are the cancer types where SH3BGRL Mutation most reproducibly stratifies survival.