Across TCGA patient cohorts, GNB1L mutation is significantly associated with the RNA expression of many other genes, with 1,287 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible GNB1L-associated genes across cancer lineages are RN7SL555P, MIR6131, and RNA5SP394. Each is linked with GNB1L in more than 2 cancer types. Because this analysis shows association rather than direction, both GNB1L-to-partner and partner-to-GNB1L 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 (GNB1L→partner) and Y-score (partner→GNB1L) 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
COAD	RN7SL555P →	+0.442	+3.496	.008	.008	3	3
SKCM	MIR6131 →	+0.118	+4.906	<.001	.001	3	2
CESC	RNA5SP394 →	+0.246	+4.345	<.001	.002	3	2
COAD	MTND1P33 →	+0.123	+4.251	<.001	.008	3	2
COAD	RN7SL151P →	+1.078	+4.239	<.001	.001	3	2
COAD	OR56A7P →	+0.033	+4.547	<.001	.005	3	2

Each partner links to its Q-omics profile. Showing the 6 strongest of 1,287 associations by consensus.

Exploration

GNB1L survival (RNA) · tumor vs normal (RNA) · all GNB1L data types