PARL

Across TCGA pan-cancer cohorts, PARL Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated PARL data layer compared with 22 for mass-spec protein and 4 for mass-spec protein.

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

STAD, UCEC, and SKCM are the cancer types where PARL 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
STAD	OS	Median	III,IV	0.126	0.632	.001	12	view →
UCEC	OS	Median	IV	0.231	0.592	.036	6	view →
SKCM	DFS	Median	II,III,IV	0.037	0.683	<.001	6	view →

Pink = unfavorable, green = favorable. Showing the 3 strongest of 3 lineages.

PARL–STAD (OS)

Open the STAD breakdown →