TRAPPC9

Across TCGA pan-cancer cohorts, TRAPPC9 Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated TRAPPC9 data layer compared with 20 for mass-spec protein and 6 for mass-spec protein.

The strongest signal is observed in stomach adenocarcinoma (STAD), where higher TRAPPC9 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated TRAPPC9 expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.

STAD, UCEC, and CHOL are the cancer types where TRAPPC9 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	0.184	0.730	.002	18	view →
UCEC	DFS	Median	II,III,IV	0.915	0.436	.027	10	view →
CHOL	OS	Median	All	0.155	0.725	.029	3	view →

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

TRAPPC9–STAD (OS)

Open the STAD breakdown →