MLXIP

Across TCGA pan-cancer cohorts, MLXIP Mutation is linked to patient survival in 5 of 34 cancer types, making it a survival-associated MLXIP data layer compared with 24 for mass-spec protein and 6 for mass-spec protein.

The strongest signal is observed in uterine corpus endometrial carcinoma (UCEC), where higher MLXIP Mutation is associated with better disease-free survival. In most high-consensus cancer types, elevated MLXIP expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.

UCEC, COAD, and HNSC are the cancer types where MLXIP 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	DFS	Median	II,III,IV	0.931	0.303	.009	22	view →
COAD	OS	Median	All	0.001	0.871	<.001	12	view →
HNSC	OS	Median	IV	0.176	0.639	.040	6	view →
LUAD	OS	Median	All	0.276	0.697	.040	3	view →
SKCM	OS	Median	III,IV	0.179	0.721	<.001	3	view →

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

MLXIP–UCEC (DFS)

Open the UCEC breakdown →