LMBR1L

Across TCGA pan-cancer cohorts, LMBR1L Mutation is linked to patient survival in 4 of 34 cancer types, making it a survival-associated LMBR1L data layer compared with 25 for mass-spec protein.

The strongest signal is observed in rectum adenocarcinoma (READ), where higher LMBR1L Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated LMBR1L expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.

READ, LIHC, and UCEC are the cancer types where LMBR1L 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
READ	DFS	Median	All	0.112	0.845	.001	12	view →
LIHC	DFS	Median	All	0.150	0.557	.006	10	view →
UCEC	DFS	Median	All	0.964	0.829	.033	4	view →
ACC	DFS	Median	All	0.195	0.748	.003	3	view →

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

LMBR1L–READ (DFS)

Open the READ breakdown →