Across TCGA patient cohorts, HNRNPAB mutation is significantly associated with the RNA expression of many other genes, with 1,821 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible HNRNPAB-associated genes across cancer lineages are MAPK11, RN7SL808P, and CCL5. Each is linked with HNRNPAB in more than 1 cancer types. Because this analysis shows association rather than direction, both HNRNPAB-to-partner and partner-to-HNRNPAB 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 (HNRNPAB→partner) and Y-score (partner→HNRNPAB) 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	MAPK11 →	+0.718	+3.700	<.001	.001	3	2
UCEC	RN7SL808P →	+0.033	+3.002	.003	.006	3	2
UCEC	CCL5 →	+1.354	+2.413	<.001	<.001	3	1
UCEC	MAP3K4-AS1 →	+0.630	+2.436	<.001	.001	3	1
UCEC	ZNHIT3 →	+0.364	+2.413	.006	<.001	3	1
UCEC	MIR6075 →	+0.229	+2.550	.001	<.001	3	1

Each partner links to its Q-omics profile. Showing the 6 strongest of 1,821 associations by consensus.

Exploration

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