OPRL1

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, OPRL1 Mutation is linked to patient survival in 8 of 34 cancer types, making it a survival-associated OPRL1 data layer compared with 22 for mass-spec protein and 3 for mass-spec protein.

The strongest signal is observed in ovarian serous cystadenocarcinoma (OV), where higher OPRL1 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated OPRL1 expression acts as an unfavorable survival marker, although some lineages such as UCEC and SKCM show a favorable association.

OV, ESCA, and STAD are the cancer types where OPRL1 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
OVDFSMedianII,III,IV0.2220.541.03818view →
ESCAOSMedianII,III,IV0.1300.703<.00118view →
STADDFSMedianAll0.2790.713.00915view →
UCECDFSMedianAll1.0000.632.01610view →
LIHCDFSMedianAll0.1210.555.0079view →
SKCMDFSMedianIII,IV0.8910.459.0158view →
PRADDFSMedianAll0.6170.886.0136view →
GBMOSMedianAll0.0750.416.0113view →
Pink = unfavorable, green = favorable. Showing the 8 strongest of 8 lineages.

OPRL1–OV (DFS)

Kaplan–Meier survival curve for OPRL1 mutant vs wild-type samples in OV.

Open the OV breakdown →

Exploration