SMARCD1

Across TCGA pan-cancer cohorts, SMARCD1 Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated SMARCD1 data layer compared with 27 for mass-spec protein and 6 for mass-spec protein.

The strongest signal is observed in prostate adenocarcinoma (PRAD), where higher SMARCD1 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated SMARCD1 expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.

PRAD, COAD, and UCEC are the cancer types where SMARCD1 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
PRAD	DFS	Median	All	0.085	0.774	<.001	6	view →
COAD	DFS	Median	II,III,IV	0.232	0.746	.002	3	view →
UCEC	DFS	Median	All	0.959	0.628	.037	2	view →

Pink = unfavorable, green = favorable. Showing the 3 strongest of 3 lineages.

SMARCD1–PRAD (DFS)

Open the PRAD breakdown →