BCS1L

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, BCS1L Mutation is linked to patient survival in 4 of 34 cancer types, making it a survival-associated BCS1L data layer compared with 27 for mass-spec protein and 4 for mass-spec protein.

The strongest signal is observed in lung squamous cell carcinoma (LUSC), where higher BCS1L Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated BCS1L expression acts as an unfavorable survival marker, although some lineages such as SKCM show a favorable association.

LUSC, UCEC, and PRAD are the cancer types where BCS1L 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
LUSCOSMedianAll0.1380.776<.00112view →
UCECOSMedianIV0.2310.592.0366view →
PRADDFSMedianAll0.0850.774<.0016view →
SKCMOSMedianAll1.0000.331.0441view →
Pink = unfavorable, green = favorable. Showing the 4 strongest of 4 lineages.

BCS1L–LUSC (OS)

Kaplan–Meier survival curve for BCS1L mutant vs wild-type samples in LUSC.

Open the LUSC breakdown →

Exploration