Across TCGA patient cohorts, EBF2 mutation is significantly associated with the RNA expression of many other genes, with 3,502 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible EBF2-associated genes across cancer lineages are RN7SL712P, SULT6B1, and DNAJA1P1. Each is linked with EBF2 in more than 3 cancer types. Because this analysis shows association rather than direction, both EBF2-to-partner and partner-to-EBF2 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 (EBF2→partner) and Y-score (partner→EBF2) 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	RN7SL712P →	+0.529	+3.900	<.001	.001	3	4
READ	SULT6B1 →	+0.065	+4.827	<.001	.002	3	3
CESC	DNAJA1P1 →	+0.047	+4.891	<.001	<.001	3	3
UCEC	UBTFL11 →	+0.066	+1.397	<.001	.004	3	3
COAD	HSBP1 →	+0.492	+3.240	.002	.008	3	3
COAD	RN7SL472P →	+0.901	+2.769	<.001	.003	3	3

Each partner links to its Q-omics profile. Showing the 6 strongest of 3,502 associations by consensus.

Exploration

EBF2 survival (RNA) · tumor vs normal (RNA) · all EBF2 data types