Across TCGA cell cohorts, CNR2 mutation is significantly associated with the RNA expression of many other genes, with 6 significant associations in total. LARGE_INTESTINE shows the largest number of these associations.

The most reproducible CNR2-associated genes across cancer lineages are MYF5, FABP12, and KRTAP22-2. Each is linked with CNR2 in more than 1 cancer types. Because this analysis shows association rather than direction, both CNR2-to-partner and partner-to-CNR2 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 (CNR2→partner) and Y-score (partner→CNR2) 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
BLOOD_Myeloma	MYF5 →	+0.016	+4.807	<.001	.006	3	1
BLOOD_Myeloma	FABP12 →	+0.060	+4.807	<.001	.006	3	1
BLOOD_Myeloma	KRTAP22-2 →	+0.229	+4.807	<.001	.006	3	1
LARGE_INTESTINE	MAGEB4 →	+0.022	+5.415	<.001	.004	3	1
LARGE_INTESTINE	RBMY1B →	+0.006	+5.415	<.001	.004	3	1
LARGE_INTESTINE	RBMY1D →	+0.006	+5.415	<.001	.004	3	1

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

Exploration

CNR2 survival (RNA) · tumor vs normal (RNA) · all CNR2 data types