UNC13B

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, UNC13B Mutation is linked to patient survival in 7 of 34 cancer types, making it a survival-associated UNC13B data layer compared with 23 for mass-spec protein and 8 for mass-spec protein.

The strongest signal is observed in rectum adenocarcinoma (READ), where higher UNC13B Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated UNC13B expression acts as an unfavorable survival marker.

READ, UCEC, and ESCA are the cancer types where UNC13B 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
READOSMedianIII,IV0.2770.901<.00115view →
UCECOSMedianIV0.2250.772<.00112view →
ESCADFSMedianII,III,IV0.2060.528.01512view →
ACCDFSMedianAll0.0570.623.0019view →
LUSCOSMedianIII,IV0.1120.664.0036view →
PRADDFSMedianAll0.1380.888<.0016view →
LIHCOSMedianAll0.4720.787.0272view →
Pink = unfavorable, green = favorable. Showing the 7 strongest of 7 lineages.

Exploration