SBF1

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, SBF1 Mutation is linked to patient survival in 10 of 34 cancer types, making it a survival-associated SBF1 data layer compared with 27 for mass-spec protein and 6 for mass-spec protein.

The strongest signal is observed in bladder urothelial carcinoma (BLCA), where higher SBF1 Mutation is associated with better overall survival. In most high-consensus cancer types, elevated SBF1 expression acts as an unfavorable survival marker, although some lineages such as BLCA and UCEC show a favorable association.

BLCA, LIHC, and MESO are the cancer types where SBF1 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
BLCAOSMedianII,III,IV1.0000.698.00824view →
LIHCOSMedianAll0.0510.775<.00124view →
MESODFSMedianIII,IV0.0780.376.0129view →
UCECDFSMedianAll0.9370.624.0168view →
ACCOSMedianAll0.1770.632.0217view →
KIRCDFSMedianAll0.1270.865<.0016view →
ESCAOSMedianII,III,IV0.3290.707.0146view →
PRADDFSMedianAll0.0850.774.0036view →
HNSCOSMedianAll0.3030.608.0396view →
COADDFSMedianIII,IV0.1460.616.0266view →
Pink = unfavorable, green = favorable. Showing the 10 strongest of 10 lineages.

SBF1–BLCA (OS)

Kaplan–Meier survival curve for SBF1 mutant vs wild-type samples in BLCA.

Open the BLCA breakdown →

Exploration