VTI1B

Across TCGA pan-cancer cohorts, VTI1B Mutation is linked to patient survival in 4 of 34 cancer types, making it a survival-associated VTI1B data layer compared with 22 for mass-spec protein and 5 for mass-spec protein.

The strongest signal is observed in stomach adenocarcinoma (STAD), where higher VTI1B Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated VTI1B expression acts as an unfavorable survival marker.

STAD, COAD, and BLCA are the cancer types where VTI1B 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	All	0.095	0.539	.006	18	view →
COAD	DFS	Median	All	0.140	0.783	<.001	18	view →
BLCA	DFS	Median	IV	0.087	0.480	<.001	6	view →
UCEC	OS	Median	IV	0.231	0.592	.036	6	view →

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

VTI1B–STAD (OS)

Open the STAD breakdown →