FPR2

Across TCGA pan-cancer cohorts, FPR2 Mutation is linked to patient survival in 4 of 34 cancer types, making it a survival-associated FPR2 data layer compared with 22 for mass-spec protein and 2 for mass-spec protein.

The strongest signal is observed in liver hepatocellular carcinoma (LIHC), where higher FPR2 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated FPR2 expression acts as an unfavorable survival marker.

LIHC, ESCA, and LUSC are the cancer types where FPR2 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.

Lineage	Measure	Split	Stage	AUC1 high	AUC2 low	p	Sampling consensus
LIHC	DFS	Median	All	0.038	0.553	<.001	9	view →
ESCA	OS	Median	II,III,IV	0.206	0.686	.004	6	view →
LUSC	OS	Median	II,III,IV	0.235	0.618	.014	6	view →
UCEC	OS	Median	IV	0.231	0.592	.036	6	view →

Pink = unfavorable, green = favorable. Showing the 4 strongest of 4 lineages.

FPR2–LIHC (DFS)

Open the LIHC breakdown →