HNRNPR

Across TCGA patient cohorts, HNRNPR mutation is significantly associated with the RNA expression of many other genes, with 2,057 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible HNRNPR-associated genes across cancer lineages are ETF1P3, MIR4797, and SNORD114-18. Each is linked with HNRNPR in more than 2 cancer types. Because this analysis shows association rather than direction, both HNRNPR-to-partner and partner-to-HNRNPR results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, ETF1P3 grouped by HNRNPR-low versus HNRNPR-high in BLCA.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (HNRNPR→partner) and Y-score (partner→HNRNPR) 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	ETF1P3 →	+0.073	+4.396	<.001	.006	3	3
LUAD	MIR4797 →	+0.525	+4.510	.005	.005	3	3
BLCA	SNORD114-18 →	+0.655	+5.444	<.001	.002	3	3
UCEC	SNRPEP7 →	+0.179	+2.236	.001	.002	3	3
HNSC	MIR572 →	+0.231	+4.327	<.001	.009	3	2
BLCA	RNU6-938P →	+0.299	+5.018	<.001	.004	3	2

Each partner links to its Q-omics profile. Showing the 6 strongest of 2,057 associations by consensus.

ETF1P3 by HNRNPR expression — BLCA

Explore this box plot interactively →