Across TCGA patient cohorts, RSBN1L mutation is significantly associated with the RNA expression of many other genes, with 2,359 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible RSBN1L-associated genes across cancer lineages are RNU6-940P, MRPS15P1, and ANKRD20A6P. Each is linked with RSBN1L in more than 2 cancer types. Because this analysis shows association rather than direction, both RSBN1L-to-partner and partner-to-RSBN1L results are reported.

Each partner links to its own Q-omics profile.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (RSBN1L→partner) and Y-score (partner→RSBN1L) are standardized regression coefficients; both directions are reported because the association is undirected. p-values are from the association test.

Lineage	Partner gene	X-score	Y-score	p(X)	p(Y)	Sampling consensus	Lineage consensus
READ	RNU6-940P →	+0.280	+5.096	<.001	.002	3	3
READ	MRPS15P1 →	+0.082	+3.827	.001	.006	3	2
READ	ANKRD20A6P →	+0.152	+4.341	<.001	.007	3	2
CESC	AIDAP3 →	+0.050	+5.812	<.001	.003	3	2
COAD	RPL9P6 →	+0.385	+5.435	<.001	.005	3	2
COAD	RPL23AP56 →	+0.193	+6.392	<.001	.001	3	2

Each partner links to its Q-omics profile. Showing the 6 strongest of 2,359 associations by consensus.

Exploration

RSBN1L survival (RNA) · tumor vs normal (RNA) · all RSBN1L data types