RANBP1

Across TCGA patient cohorts, RANBP1 mutation is significantly associated with the RNA expression of many other genes, with 111 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible RANBP1-associated genes across cancer lineages are UBE2V1P10, LINC02497, and SLC20A1P3. Each is linked with RANBP1 in more than 1 cancer types. Because this analysis shows association rather than direction, both RANBP1-to-partner and partner-to-RANBP1 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, UBE2V1P10 grouped by RANBP1-low versus RANBP1-high in BLCA.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (RANBP1→partner) and Y-score (partner→RANBP1) 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
BLCA	UBE2V1P10 →	+0.169	+7.640	<.001	.009	3	2
COAD	LINC02497 →	+0.168	+5.003	<.001	.004	3	2
COAD	SLC20A1P3 →	+0.095	+5.917	<.001	.001	3	2
UCEC	VDAC1P10 →	+0.159	+3.092	<.001	.003	3	2
BRCA	RN7SKP221 →	+0.099	+8.471	<.001	.005	3	1
BRCA	TRDD1 →	+1.367	+9.057	<.001	.003	3	1

Each partner links to its Q-omics profile. Showing the 6 strongest of 111 associations by consensus.

UBE2V1P10 by RANBP1 expression — BLCA

Explore this box plot interactively →