MINK1

Across TCGA pan-cancer cohorts, MINK1 Mutation is linked to patient survival in 4 of 34 cancer types, making it a survival-associated MINK1 data layer compared with 27 for mass-spec protein and 4 for mass-spec protein.

The strongest signal is observed in uterine corpus endometrial carcinoma (UCEC), where higher MINK1 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated MINK1 expression acts as an unfavorable survival marker.

UCEC, HNSC, and PRAD are the cancer types where MINK1 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
UCEC	OS	Median	IV	0.225	0.772	<.001	12	view →
HNSC	OS	Median	All	0.268	0.713	.011	6	view →
PRAD	DFS	Median	All	0.617	0.886	.011	6	view →
BLCA	DFS	Median	IV	0.124	0.475	.034	3	view →

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

MINK1–UCEC (OS)

Open the UCEC breakdown →