FNBP1L

Across TCGA patient cohorts, FNBP1L mutation is significantly associated with the RNA expression of many other genes, with 2,744 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible FNBP1L-associated genes across cancer lineages are HMGN2P32, SLC20A1P3, and MIR3135A. Each is linked with FNBP1L in more than 1 cancer types. Because this analysis shows association rather than direction, both FNBP1L-to-partner and partner-to-FNBP1L results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, HMGN2P32 grouped by FNBP1L-low versus FNBP1L-high in COAD.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (FNBP1L→partner) and Y-score (partner→FNBP1L) 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	HMGN2P32 →	+0.977	+3.589	<.001	.009	3	2
COAD	SLC20A1P3 →	+0.060	+4.917	.004	.003	3	2
UCEC	MIR3135A →	+0.252	+1.753	.001	.004	3	2
UCEC	RNA5SP412 →	+0.389	+1.493	<.001	.009	3	2
UCEC	RNVU1-28 →	+0.568	+1.635	<.001	<.001	3	2
SKCM	MIR8082 →	+0.409	+3.490	<.001	.008	3	2

Each partner links to its Q-omics profile. Showing the 6 strongest of 2,744 associations by consensus.

HMGN2P32 by FNBP1L expression — COAD

Explore this box plot interactively →