Across TCGA cell cohorts, QRICH1 mutation is significantly associated with the RNA expression of many other genes, with 10 significant associations in total. BLOOD_Lymphoma shows the largest number of these associations.

The most reproducible QRICH1-associated genes across cancer lineages are CLEC4F, FAM205A, and REG3G. Each is linked with QRICH1 in more than 1 cancer types. Because this analysis shows association rather than direction, both QRICH1-to-partner and partner-to-QRICH1 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 (QRICH1→partner) and Y-score (partner→QRICH1) 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
LARGE_INTESTINE	CLEC4F →	+0.196	+2.974	.006	.006	3	1
LARGE_INTESTINE	FAM205A →	+0.018	+3.614	<.001	.006	3	1
BLOOD_Lymphoma	REG3G →	+0.044	+4.867	<.001	.009	3	1
BLOOD_Lymphoma	IFNL3 →	+0.142	+5.209	<.001	.005	3	1
BLOOD_Lymphoma	KRTAP4-1 →	+0.207	+4.867	<.001	.009	3	1
BLOOD_Lymphoma	TEX51 →	+0.026	+5.643	<.001	.002	3	1

Each partner links to its Q-omics profile. Showing the 6 strongest of 10 associations by consensus.

Exploration

QRICH1 survival (RNA) · tumor vs normal (RNA) · all QRICH1 data types