UNC13A

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, UNC13A Mutation is linked to patient survival in 8 of 34 cancer types, making it a survival-associated UNC13A data layer compared with 21 for mass-spec protein and 1 for mass-spec protein.

The strongest signal is observed in thymoma (THYM), where higher UNC13A Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated UNC13A expression acts as an unfavorable survival marker, although some lineages such as SCLC and UCEC show a favorable association.

THYM, HNSC, and SCLC are the cancer types where UNC13A 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
THYMOSMedianIII,IV0.1030.944<.00142view →
HNSCOSMedianII,III,IV0.0510.712<.00136view →
SCLCDFSMedianAll0.6220.224.00634view →
THCADFSMedianAll0.0700.896<.00118view →
LIHCOSMedianII,III,IV0.3270.777.01318view →
UCECDFSMedianIII,IV0.9220.523.01816view →
LGGOSMedianAll0.6630.897.0035view →
READOSMedianAll0.6520.828.0483view →
Pink = unfavorable, green = favorable. Showing the 8 strongest of 8 lineages.

UNC13A–THYM (OS)

Kaplan–Meier survival curve for UNC13A mutant vs wild-type samples in THYM.

Open the THYM breakdown →

Exploration