TRAF3IP2

Across TCGA pan-cancer cohorts, TRAF3IP2 Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated TRAF3IP2 data layer compared with 24 for mass-spec protein and 5 for mass-spec protein.

The strongest signal is observed in rectum adenocarcinoma (READ), where higher TRAF3IP2 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated TRAF3IP2 expression acts as an unfavorable survival marker.

READ, KIRC, and PRAD are the cancer types where TRAF3IP2 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
READ	OS	Median	III,IV	0.328	0.751	.003	9	view →
KIRC	OS	Median	All	0.178	0.655	.042	6	view →
PRAD	DFS	Median	All	0.740	0.935	.008	6	view →

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

TRAF3IP2–READ (OS)

Open the READ breakdown →