PHYKPL

Across TCGA pan-cancer cohorts, PHYKPL Mutation is linked to patient survival in 5 of 34 cancer types, making it a survival-associated PHYKPL data layer compared with 24 for mass-spec protein and 5 for mass-spec protein.

The strongest signal is observed in uterine corpus endometrial carcinoma (UCEC), where higher PHYKPL Mutation is associated with better disease-free survival. In most high-consensus cancer types, elevated PHYKPL expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.

UCEC, BLCA, and LUAD are the cancer types where PHYKPL 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
UCEC	DFS	Median	II,III,IV	1.000	0.441	.022	12	view →
BLCA	OS	Median	III,IV	0.153	0.684	.010	6	view →
LUAD	OS	Median	All	0.323	0.685	.019	6	view →
ACC	DFS	Median	All	0.195	0.748	.003	3	view →
SKCM	OS	Median	All	0.431	0.784	.022	3	view →

Pink = unfavorable, green = favorable. Showing the 5 strongest of 5 lineages.

PHYKPL–UCEC (DFS)

Open the UCEC breakdown →