SELENON

Across TCGA pan-cancer cohorts, SELENON Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated SELENON data layer compared with 18 for mass-spec protein and 4 for mass-spec protein.

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

UCEC, ACC, and PRAD are the cancer types where SELENON 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	All	1.000	0.618	.005	20	view →
ACC	DFS	Median	All	0.089	0.666	.017	6	view →
PRAD	DFS	Median	All	0.098	0.776	<.001	6	view →

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

SELENON–UCEC (DFS)

Open the UCEC breakdown →