PRR35

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, PRR35 Mutation is linked to patient survival in 5 of 34 cancer types, making it a survival-associated PRR35 data layer compared with 27 for mass-spec protein.

The strongest signal is observed in pancreatic adenocarcinoma (PAAD), where higher PRR35 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated PRR35 expression acts as an unfavorable survival marker.

PAAD, STAD, and COAD are the cancer types where PRR35 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
PAADOSMedianAll0.0600.641<.00124view →
STADDFSMedianAll0.1490.710<.00118view →
COADDFSMedianAll0.2200.793<.0016view →
PRADDFSMedianAll0.0850.774<.0016view →
UCECOSMedianIV0.2310.592.0366view →
Pink = unfavorable, green = favorable. Showing the 5 strongest of 5 lineages.

PRR35–PAAD (OS)

Kaplan–Meier survival curve for PRR35 mutant vs wild-type samples in PAAD.

Open the PAAD breakdown →

Exploration