Across TCGA patient cohorts, FSCN2 mutation is significantly associated with the RNA expression of many other genes, with 91 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible FSCN2-associated genes across cancer lineages are OR8D2, MTCO3P16, and H2AP. Each is linked with FSCN2 in more than 1 cancer types. Because this analysis shows association rather than direction, both FSCN2-to-partner and partner-to-FSCN2 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 (FSCN2→partner) and Y-score (partner→FSCN2) 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
BLCA	OR8D2 →	+0.065	+6.618	<.001	.001	3	2
COAD	MTCO3P16 →	+0.117	+4.308	<.001	.009	3	2
KIRP	H2AP →	+0.077	+5.301	<.001	.003	3	2
UCEC	SNORD116-16 →	+0.808	+4.188	.001	.009	3	2
UCEC	IGLVI-38 →	+0.248	+5.146	<.001	.001	3	2
UCEC	MRPS22P1 →	+0.077	+4.937	.009	.005	3	1

Each partner links to its Q-omics profile. Showing the 6 strongest of 91 associations by consensus.

Exploration

FSCN2 survival (RNA) · tumor vs normal (RNA) · all FSCN2 data types