Across TCGA pan-cancer cohorts, SH3GL1 Mutation is linked to patient survival in 4 of 34 cancer types, making it a survival-associated SH3GL1 data layer compared with 26 for mass-spec protein and 1 for mass-spec protein.
The strongest signal is observed in stomach adenocarcinoma (STAD), where higher SH3GL1 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated SH3GL1 expression acts as an unfavorable survival marker, although some lineages such as SKCM show a favorable association.
STAD, HNSC, and UCEC are the cancer types where SH3GL1 Mutation most reproducibly stratifies survival.