CTIF

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

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

KICH, COAD, and CHOL are the cancer types where CTIF 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
KICH	DFS	Median	All	0.102	0.848	.004	13	view →
COAD	OS	Median	All	0.111	0.871	<.001	12	view →
CHOL	OS	Median	All	0.155	0.725	.029	3	view →
LGG	OS	Median	All	0.306	0.799	.009	3	view →
UCEC	DFS	Median	II,III,IV	0.915	0.441	.047	2	view →

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

CTIF–KICH (DFS)

Open the KICH breakdown →