BRMS1L

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, BRMS1L Mutation is linked to patient survival in 2 of 34 cancer types, making it a survival-associated BRMS1L data layer compared with 24 for mass-spec protein and 5 for mass-spec protein.

The strongest signal is observed in skin cutaneous melanoma (SKCM), where higher BRMS1L Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated BRMS1L expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.

SKCM and UCEC are the cancer types where BRMS1L Mutation most reproducibly stratifies survival.

Mutation survival associations by lineage

Ranked by sampling consensus. AUC1 and AUC2 indicate survival in the high- and low-expression groups, respectively; the lower AUC marks the poorer-surviving group. p-values are from the log-rank test.
LineageMeasureSplitStageAUC1
high
AUC2
low
pSampling consensus
SKCMDFSMedianAll0.1210.739<.00133view →
UCECDFSMedianAll0.9430.623.0362view →
Pink = unfavorable, green = favorable. Showing the 2 strongest of 2 lineages.

BRMS1L–SKCM (DFS)

Kaplan–Meier survival curve for BRMS1L mutant vs wild-type samples in SKCM.

Open the SKCM breakdown →

Exploration