NCOA2

Across TCGA pan-cancer cohorts, NCOA2 Mutation is linked to patient survival in 5 of 34 cancer types, making it a survival-associated NCOA2 data layer compared with 25 for mass-spec protein and 5 for mass-spec protein.

The strongest signal is observed in liver hepatocellular carcinoma (LIHC), where higher NCOA2 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated NCOA2 expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.

LIHC, UCEC, and PRAD are the cancer types where NCOA2 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	0.127	0.559	<.001	18	view →
UCEC	DFS	Median	II,III,IV	0.895	0.301	.008	18	view →
PRAD	DFS	Median	All	0.085	0.774	<.001	6	view →
SKCM	DFS	Median	All	0.058	0.757	<.001	6	view →
ACC	DFS	Median	All	0.195	0.748	.003	3	view →

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

NCOA2–LIHC (DFS)

Open the LIHC breakdown →