PILRA

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

The strongest signal is observed in kidney renal papillary cell carcinoma (KIRP), where higher PILRA Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated PILRA expression acts as an unfavorable survival marker.

KIRP, KIRC, and PRAD are the cancer types where PILRA 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
KIRP	DFS	Median	All	0.038	0.920	<.001	22	view →
KIRC	OS	Median	All	0.167	0.655	.038	12	view →
PRAD	DFS	Median	All	0.085	0.774	<.001	6	view →
LIHC	OS	Median	All	0.167	0.688	.035	6	view →

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

PILRA–KIRP (DFS)

Open the KIRP breakdown →