FNIP2

Across TCGA patient cohorts, FNIP2 mutation is significantly associated with the RNA expression of many other genes, with 3,960 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible FNIP2-associated genes across cancer lineages are SNRPGP8, RNU6-693P, and RNY1P1. Each is linked with FNIP2 in more than 2 cancer types. Because this analysis shows association rather than direction, both FNIP2-to-partner and partner-to-FNIP2 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, SNRPGP8 grouped by FNIP2-low versus FNIP2-high in COAD.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (FNIP2→partner) and Y-score (partner→FNIP2) 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	SNRPGP8 →	+0.213	+4.399	<.001	.006	3	3
COAD	RNU6-693P →	+0.470	+4.399	<.001	.006	3	3
BLCA	RNY1P1 →	+0.210	+3.996	<.001	.002	3	3
BLCA	RN7SL478P →	+0.233	+3.098	<.001	.007	3	3
UCEC	HIRA →	+0.353	+2.939	.001	<.001	3	2
UCEC	FBXO7 →	+0.466	+2.786	<.001	<.001	3	2

Each partner links to its Q-omics profile. Showing the 6 strongest of 3,960 associations by consensus.

SNRPGP8 by FNIP2 expression — COAD

Explore this box plot interactively →