Across TCGA patient cohorts, NEURL1B mutation is significantly associated with the RNA expression of many other genes, with 51 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible NEURL1B-associated genes across cancer lineages are RN7SL810P, RN7SL307P, and FAM8A2P. Each is linked with NEURL1B in more than 1 cancer types. Because this analysis shows association rather than direction, both NEURL1B-to-partner and partner-to-NEURL1B 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 (NEURL1B→partner) and Y-score (partner→NEURL1B) 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
CESC	RN7SL810P →	+0.169	+4.874	.004	.002	3	1
CESC	RN7SL307P →	+0.085	+4.669	.001	.007	3	1
CESC	FAM8A2P →	+0.031	+4.539	<.001	.008	3	1
CESC	MIR1273H →	+0.227	+4.539	<.001	.008	3	1
CESC	HSBP1P2 →	+0.215	+4.276	<.001	.008	3	1
CESC	MIR7-3 →	+0.275	+5.342	<.001	.002	3	1

Each partner links to its Q-omics profile. Showing the 6 strongest of 51 associations by consensus.

Exploration

NEURL1B survival (RNA) · tumor vs normal (RNA) · all NEURL1B data types