NOSIP

Across TCGA pan-cancer cohorts, NOSIP Mutation is linked to patient survival in 5 of 34 cancer types, making it a survival-associated NOSIP data layer compared with 26 for mass-spec protein and 6 for mass-spec protein.

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

LIHC, PRAD, and ESCA are the cancer types where NOSIP 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	0.046	0.553	<.001	18	view →
PRAD	DFS	Median	All	0.085	0.774	<.001	6	view →
ESCA	OS	Median	II,III,IV	0.216	0.702	.014	6	view →
COAD	DFS	Median	All	0.469	0.785	.032	2	view →
UCEC	DFS	Median	All	1.000	0.635	.040	2	view →

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

NOSIP–LIHC (DFS)

Open the LIHC breakdown →