SEC22C

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, SEC22C Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated SEC22C data layer compared with 25 for mass-spec protein.

The strongest signal is observed in kidney renal papillary cell carcinoma (KIRP), where higher SEC22C Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated SEC22C expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.

KIRP, COAD, and UCEC are the cancer types where SEC22C 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
KIRPOSMedianAll0.2700.904<.00112view →
COADOSMedianAll0.0010.871<.00112view →
UCECOSMedianAll1.0000.660.0318view →
Pink = unfavorable, green = favorable. Showing the 3 strongest of 3 lineages.

SEC22C–KIRP (OS)

Kaplan–Meier survival curve for SEC22C mutant vs wild-type samples in KIRP.

Open the KIRP breakdown →

Exploration