Across TCGA patient cohorts, AP1G2 mutation is significantly associated with the RNA expression of many other genes, with 4,186 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible AP1G2-associated genes across cancer lineages are ENO2, LINC01692, and MIR1911. Each is linked with AP1G2 in more than 3 cancer types. Because this analysis shows association rather than direction, both AP1G2-to-partner and partner-to-AP1G2 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 (AP1G2→partner) and Y-score (partner→AP1G2) 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	ENO2 →	+0.658	+2.258	<.001	<.001	3	4
LIHC	LINC01692 →	+0.123	+4.690	<.001	.003	3	3
STAD	MIR1911 →	+0.357	+3.951	<.001	.002	3	3
UCEC	ZNF543 →	+0.456	+2.470	<.001	<.001	3	3
CESC	RN7SL810P →	+0.152	+3.289	<.001	.003	3	3
SKCM	MTND5P30 →	+0.024	+2.809	.002	.004	3	3

Each partner links to its Q-omics profile. Showing the 6 strongest of 4,186 associations by consensus.

Exploration

AP1G2 survival (RNA) · tumor vs normal (RNA) · all AP1G2 data types