OTX1

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, OTX1 Mutation is linked to patient survival in 6 of 34 cancer types, making it a survival-associated OTX1 data layer compared with 30 for mass-spec protein.

The strongest signal is observed in kidney renal clear cell carcinoma (KIRC), where higher OTX1 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated OTX1 expression acts as an unfavorable survival marker.

KIRC, LIHC, and SARC are the cancer types where OTX1 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
KIRCOSMedianII,III,IV0.0620.789<.00132view →
LIHCDFSMedianAll0.0890.544<.00121view →
SARCOSMedianAll0.1330.860<.00112view →
STADOSMedianIV0.0010.544<.00112view →
UCECOSMedianIV0.2310.592.0366view →
ESCADFSMedianAll0.1920.535.0373view →
Pink = unfavorable, green = favorable. Showing the 6 strongest of 6 lineages.

OTX1–KIRC (OS)

Kaplan–Meier survival curve for OTX1 mutant vs wild-type samples in KIRC.

Open the KIRC breakdown →

Exploration