FNBP1L

Across TCGA cell cohorts, FNBP1L mutation is significantly associated with the mutation status of many other genes, with 1,367 significant associations in total. LARGE_INTESTINE shows the largest number of these associations.

The most reproducible FNBP1L-associated genes across cancer lineages are GOLGA2, CLCN7, and ABCC8. Each is linked with FNBP1L in more than 3 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, GOLGA2 grouped by FNBP1L-low versus FNBP1L-high in OVARY.

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
OVARY	GOLGA2 →	+3.345	+3.345	.007	.007	1	4
BLOOD_Leukemia	CLCN7 →	+4.894	+4.894	.004	.004	1	3
BLOOD_Lymphoma	ABCC8 →	+3.510	+4.108	.003	.003	1	3
BLOOD_Leukemia	ANKRD44 →	+3.672	+5.083	.001	.001	1	3
BLOOD_Lymphoma	SSH2 →	+5.247	+4.429	.005	.005	1	3
BLOOD_Lymphoma	SCYL1 →	+5.247	+4.429	.005	.005	1	3

Each partner links to its Q-omics profile. Showing the 6 strongest of 1,367 associations by consensus.

GOLGA2 by FNBP1L expression — OVARY

Explore this box plot interactively →