INTS3

Across TCGA pan-cancer cohorts, INTS3 Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated INTS3 data layer compared with 27 for mass-spec protein and 5 for mass-spec protein.

The strongest signal is observed in lymphoid neoplasm diffuse large b-cell lymphoma (DLBC), where higher INTS3 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated INTS3 expression acts as an unfavorable survival marker, although some lineages such as STAD show a favorable association.

DLBC, PRAD, and STAD are the cancer types where INTS3 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
DLBC	OS	Median	II,III,IV	0.118	0.802	.025	12	view →
PRAD	DFS	Median	All	0.085	0.774	<.001	6	view →
STAD	OS	Median	III,IV	1.000	0.362	.040	3	view →

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

INTS3–DLBC (OS)

Open the DLBC breakdown →