CNTNAP3P2

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, CNTNAP3P2 Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated CNTNAP3P2 data layer compared with 19 for mass-spec protein.

The strongest signal is observed in colon adenocarcinoma (COAD), where higher CNTNAP3P2 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated CNTNAP3P2 expression acts as an unfavorable survival marker.

COAD, PRAD, and BLCA are the cancer types where CNTNAP3P2 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
COADDFSMedianAll0.1400.783<.00118view →
PRADDFSMedianAll0.0850.774<.0016view →
BLCADFSMedianIII,IV0.1390.572.0266view →
Pink = unfavorable, green = favorable. Showing the 3 strongest of 3 lineages.

CNTNAP3P2–COAD (DFS)

Kaplan–Meier survival curve for CNTNAP3P2 mutant vs wild-type samples in COAD.

Open the COAD breakdown →

Exploration