SEMA3C

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, SEMA3C Mutation is linked to patient survival in 10 of 34 cancer types, making it a survival-associated SEMA3C data layer compared with 23 for mass-spec protein and 3 for mass-spec protein.

The strongest signal is observed in ovarian serous cystadenocarcinoma (OV), where higher SEMA3C Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated SEMA3C expression acts as an unfavorable survival marker, although some lineages such as UCEC and BLCA show a favorable association.

OV, UCEC, and LUAD are the cancer types where SEMA3C 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
OVOSMedianII,III,IV0.0760.844<.00148view →
UCECDFSMedianAll1.0000.618.00136view →
LUADOSMedianIII,IV0.2710.670.01221view →
LIHCOSMedianIII,IV0.1180.615.00314view →
DLBCOSMedianAll0.6240.928.00513view →
SARCOSMedianAll0.0220.861<.00112view →
BLCAOSMedianII,III,IV1.0000.412.02512view →
COADOSMedianIII,IV0.2080.791.00811view →
SKCMDFSMedianAll0.0870.757<.0019view →
PRADDFSMedianAll0.0850.774<.0016view →
Pink = unfavorable, green = favorable. Showing the 10 strongest of 10 lineages.

SEMA3C–OV (OS)

Kaplan–Meier survival curve for SEMA3C mutant vs wild-type samples in OV.

Open the OV breakdown →

Exploration