Across TCGA patient cohorts, SAPCD2 mutation is significantly associated with the RNA expression of many other genes, with 73 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SAPCD2-associated genes across cancer lineages are RNVU1-17, UBL5P3, and PLSCR5-AS1. Each is linked with SAPCD2 in more than 1 cancer types. Because this analysis shows association rather than direction, both SAPCD2-to-partner and partner-to-SAPCD2 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 (SAPCD2→partner) and Y-score (partner→SAPCD2) 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	RNVU1-17 →	+0.455	+6.003	.005	.002	3	2
UCEC	UBL5P3 →	+0.201	+3.396	.002	.006	3	2
UCEC	PLSCR5-AS1 →	+0.089	+4.137	.004	.008	3	2
HNSC	OR8B4 →	+0.039	+7.954	<.001	.008	3	1
UCEC	AQP7P5 →	+0.069	+3.957	<.001	.002	3	1
UCEC	MIR6892 →	+0.539	+2.863	<.001	.009	3	1

Each partner links to its Q-omics profile. Showing the 6 strongest of 73 associations by consensus.

Exploration

SAPCD2 survival (RNA) · tumor vs normal (RNA) · all SAPCD2 data types