Across TCGA patient cohorts, OXLD1 mutation is significantly associated with the RNA expression of many other genes, with 57 significant associations in total. LUSC shows the largest number of these associations.

The most reproducible OXLD1-associated genes across cancer lineages are RNA5SP356, GLRXP1, and EIF2AP4. Each is linked with OXLD1 in more than 1 cancer types. Because this analysis shows association rather than direction, both OXLD1-to-partner and partner-to-OXLD1 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 (OXLD1→partner) and Y-score (partner→OXLD1) 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
BRCA	RNA5SP356 →	+0.272	+8.055	<.001	.007	3	2
LUSC	GLRXP1 →	+0.164	+5.548	.003	.004	3	2
CESC	EIF2AP4 →	+0.031	+5.201	<.001	.007	3	1
CESC	OR7E111P →	+0.047	+5.669	<.001	.003	3	1
CESC	BRWD1P3 →	+0.114	+5.010	<.001	.009	3	1
COAD	SDCBP2P1 →	+0.114	+6.917	<.001	<.001	3	1

Each partner links to its Q-omics profile. Showing the 6 strongest of 57 associations by consensus.

Exploration

OXLD1 survival (RNA) · tumor vs normal (RNA) · all OXLD1 data types