LEXM

Across TCGA pan-cancer cohorts, LEXM Mutation is linked to patient survival in 4 of 34 cancer types, making it a survival-associated LEXM data layer compared with 23 for mass-spec protein.

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

SARC, LIHC, and BLCA are the cancer types where LEXM 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
SARC	DFS	Median	All	0.101	0.632	.011	6	view →
LIHC	DFS	Median	All	0.100	0.543	.038	6	view →
BLCA	DFS	Median	IV	1.000	0.195	.040	2	view →
SKCM	OS	Median	All	0.574	0.876	.017	1	view →

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

LEXM–SARC (DFS)

Open the SARC breakdown →