Across TCGA patient cohorts, RBMXL1 mutation is significantly associated with the RNA expression of many other genes, with 3,180 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible RBMXL1-associated genes across cancer lineages are SNORA10B, TRAJ12, and CASP1P1. Each is linked with RBMXL1 in more than 2 cancer types. Because this analysis shows association rather than direction, both RBMXL1-to-partner and partner-to-RBMXL1 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 (RBMXL1→partner) and Y-score (partner→RBMXL1) 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	SNORA10B →	+0.475	+3.472	<.001	.003	3	3
UCEC	TRAJ12 →	+0.436	+1.655	.001	.004	3	3
CESC	CASP1P1 →	+0.108	+4.144	<.001	.009	3	2
CESC	MTCO1P1 →	+0.023	+4.144	<.001	.009	3	2
STAD	RPL7AP56 →	+0.141	+4.219	<.001	.009	3	2
STAD	MIR4749 →	+0.371	+6.417	<.001	<.001	3	2

Each partner links to its Q-omics profile. Showing the 6 strongest of 3,180 associations by consensus.

Exploration

RBMXL1 survival (RNA) · tumor vs normal (RNA) · all RBMXL1 data types