GLIPR1L1

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, GLIPR1L1 Mutation is linked to patient survival in 7 of 34 cancer types, making it a survival-associated GLIPR1L1 data layer compared with 19 for mass-spec protein.

The strongest signal is observed in lung adenocarcinoma (LUAD), where higher GLIPR1L1 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated GLIPR1L1 expression acts as an unfavorable survival marker.

LUAD, KIRC, and LUSC are the cancer types where GLIPR1L1 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
LUADOSMedianAll0.1580.835<.00136view →
KIRCOSMedianAll0.0570.881<.00112view →
LUSCOSMedianAll0.1720.762.00212view →
LIHCDFSMedianAll0.0440.553<.00112view →
SARCOSMedianAll0.0160.861<.0016view →
PRADDFSMedianAll0.0850.774<.0016view →
BLCAOSMedianIII,IV0.2280.684.0236view →
Pink = unfavorable, green = favorable. Showing the 7 strongest of 7 lineages.

GLIPR1L1–LUAD (OS)

Kaplan–Meier survival curve for GLIPR1L1 mutant vs wild-type samples in LUAD.

Open the LUAD breakdown →

Exploration