Across TCGA patient cohorts, RASSF9 mutation is significantly associated with the RNA expression of many other genes, with 1,242 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible RASSF9-associated genes across cancer lineages are NOL12, SPINT5P, and DHFRP5. Each is linked with RASSF9 in more than 1 cancer types. Because this analysis shows association rather than direction, both RASSF9-to-partner and partner-to-RASSF9 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 (RASSF9→partner) and Y-score (partner→RASSF9) 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
UCEC	NOL12 →	+0.284	+2.518	.004	.001	3	2
BLCA	SPINT5P →	+0.170	+4.685	.003	.007	3	2
LIHC	DHFRP5 →	+0.052	+5.317	<.001	.002	3	2
LIHC	KRTAP20-1 →	+0.113	+4.293	<.001	.009	3	2
SKCM	RNU6-197P →	+0.155	+2.053	<.001	.009	3	2
LIHC	LINC02727 →	+0.055	+4.894	<.001	.004	3	2

Each partner links to its Q-omics profile. Showing the 6 strongest of 1,242 associations by consensus.

Exploration

RASSF9 survival (RNA) · tumor vs normal (RNA) · all RASSF9 data types