RANBP9

Across TCGA patient cohorts, RANBP9 mutation is significantly associated with the RNA expression of many other genes, with 2,158 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible RANBP9-associated genes across cancer lineages are CSGALNACT2P2, RNA5SP453, and CLRN1. Each is linked with RANBP9 in more than 1 cancer types. Because this analysis shows association rather than direction, both RANBP9-to-partner and partner-to-RANBP9 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, CSGALNACT2P2 grouped by RANBP9-low versus RANBP9-high in PRAD.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (RANBP9→partner) and Y-score (partner→RANBP9) 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
PRAD	CSGALNACT2P2 →	+0.164	+5.288	<.001	.006	3	2
SKCM	RNA5SP453 →	+0.207	+4.385	<.001	.008	3	2
SCLC	CLRN1 →	+0.995	+4.502	.002	.004	3	1
BLCA	OTOL1 →	+0.317	+3.883	<.001	.006	3	1
BLCA	OR5G5P →	+0.082	+4.213	<.001	.003	3	1
BLCA	RNU6-1181P →	+0.228	+4.562	<.001	.006	3	1

Each partner links to its Q-omics profile. Showing the 6 strongest of 2,158 associations by consensus.

CSGALNACT2P2 by RANBP9 expression — PRAD

Explore this box plot interactively →