NOB1

Across TCGA pan-cancer cohorts, NOB1 Mutation is linked to patient survival in 4 of 34 cancer types, making it a survival-associated NOB1 data layer compared with 24 for mass-spec protein and 7 for mass-spec protein.

The strongest signal is observed in stomach adenocarcinoma (STAD), where higher NOB1 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated NOB1 expression acts as an unfavorable survival marker, although some lineages such as SKCM show a favorable association.

STAD, PRAD, and UCEC are the cancer types where NOB1 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	0.001	0.630	<.001	18	view →
PRAD	DFS	Median	All	0.085	0.774	<.001	6	view →
UCEC	OS	Median	IV	0.231	0.592	.036	6	view →
SKCM	DFS	Median	III,IV	1.000	0.466	.025	4	view →

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

NOB1–STAD (OS)

Open the STAD breakdown →