Across TCGA pan-cancer cohorts, MYO15B Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated MYO15B data layer compared with 23 for mass-spec protein and 1 for mass-spec protein.
The strongest signal is observed in ovarian serous cystadenocarcinoma (OV), where higher MYO15B Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated MYO15B expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.
OV, UCEC, and SARC are the cancer types where MYO15B Mutation most reproducibly stratifies survival.