IPO13

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, IPO13 Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated IPO13 data layer compared with 21 for mass-spec protein and 6 for mass-spec protein.

The strongest signal is observed in lung squamous cell carcinoma (LUSC), where higher IPO13 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated IPO13 expression acts as an unfavorable survival marker.

LUSC, LIHC, and LGG are the cancer types where IPO13 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
LUSCDFSMedianAll0.0790.792<.00124view →
LIHCDFSMedianAll0.0810.527.01212view →
LGGOSMedianAll0.2380.799<.0016view →
Pink = unfavorable, green = favorable. Showing the 3 strongest of 3 lineages.

IPO13–LUSC (DFS)

Kaplan–Meier survival curve for IPO13 mutant vs wild-type samples in LUSC.

Open the LUSC breakdown →

Exploration