Across TCGA patient cohorts, MIR891B mutation is significantly associated with the RNA expression of many other genes, with 17 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible MIR891B-associated genes across cancer lineages are RNU4-13P, RNA5SP30, and HMGB1P9. Each is linked with MIR891B in more than 1 cancer types. Because this analysis shows association rather than direction, both MIR891B-to-partner and partner-to-MIR891B 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 (MIR891B→partner) and Y-score (partner→MIR891B) 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
UCEC	RNU4-13P →	+0.220	+4.727	<.001	.003	3	1
UCEC	RNA5SP30 →	+0.644	+3.608	<.001	.002	3	1
UCEC	HMGB1P9 →	+0.223	+4.005	.001	.002	3	1
UCEC	DPP10-AS2 →	+0.065	+4.400	.003	.006	3	1
UCEC	NRXN2-AS1 →	+0.335	+3.867	.009	.002	3	1
UCEC	RNU6-927P →	+0.465	+3.827	<.001	.003	3	1

Each partner links to its Q-omics profile. Showing the 6 strongest of 17 associations by consensus.

Exploration

MIR891B survival (RNA) · tumor vs normal (RNA) · all MIR891B data types