TMPRSS13

Across TCGA pan-cancer cohorts, TMPRSS13 Mutation is linked to patient survival in 5 of 34 cancer types, making it a survival-associated TMPRSS13 data layer compared with 26 for mass-spec protein and 1 for mass-spec protein.

The strongest signal is observed in acute myeloid leukemia (LAML), where higher TMPRSS13 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated TMPRSS13 expression acts as an unfavorable survival marker, although some lineages such as UCEC and STAD show a favorable association.

LAML, UCEC, and GBM are the cancer types where TMPRSS13 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
LAML	DFS	Median	All	0.028	0.572	<.001	12	view →
UCEC	DFS	Median	All	0.954	0.627	.016	10	view →
GBM	OS	Median	All	0.086	0.415	.010	6	view →
STAD	DFS	Median	II,III,IV	1.000	0.378	.046	6	view →
LIHC	DFS	Median	All	0.150	0.557	.004	6	view →

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

TMPRSS13–LAML (DFS)

Open the LAML breakdown →