GPRC6A

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, GPRC6A Mutation is linked to patient survival in 10 of 34 cancer types, making it a survival-associated GPRC6A data layer compared with 24 for mass-spec protein.

The strongest signal is observed in ovarian serous cystadenocarcinoma (OV), where higher GPRC6A Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated GPRC6A expression acts as an unfavorable survival marker, although some lineages such as UCEC and SKCM show a favorable association.

OV, UCEC, and COAD are the cancer types where GPRC6A 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
OVDFSMedianAll0.2490.542.00536view →
UCECDFSMedianII,III,IV1.0000.297<.00134view →
COADOSMedianII,III,IV0.2240.792.00118view →
SKCMOSMedianII,III,IV0.9650.818<.00115view →
BRCAOSMedianIII,IV0.5140.906.00110view →
SARCDFSMedianAll0.1730.612.0206view →
SCLCDFSMedianIII,IV0.2630.586.0236view →
BLCAOSMedianII,III,IV1.0000.423.0374view →
LUADOSMedianIII,IV0.2050.687.0153view →
LGGOSMedianAll0.6590.908.0262view →
Pink = unfavorable, green = favorable. Showing the 10 strongest of 10 lineages.

GPRC6A–OV (DFS)

Kaplan–Meier survival curve for GPRC6A mutant vs wild-type samples in OV.

Open the OV breakdown →

Exploration