Across TCGA patient cohorts, INPP5F mutation is significantly associated with the RNA expression of many other genes, with 2,244 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible INPP5F-associated genes across cancer lineages are ATRIP, SNORD3C, and RBM17P1. Each is linked with INPP5F in more than 2 cancer types. Because this analysis shows association rather than direction, both INPP5F-to-partner and partner-to-INPP5F 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 (INPP5F→partner) and Y-score (partner→INPP5F) 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	ATRIP →	+0.130	+2.759	.001	.004	3	3
CESC	SNORD3C →	+0.049	+4.812	<.001	.006	3	3
SKCM	RBM17P1 →	+0.016	+3.291	.002	.006	3	3
COAD	RNU6-260P →	+0.556	+3.113	<.001	.002	3	3
CESC	RNU1-62P →	+0.174	+4.539	<.001	.008	3	2
UCEC	SUMO2P15 →	+0.174	+1.200	.001	.008	3	2

Each partner links to its Q-omics profile. Showing the 6 strongest of 2,244 associations by consensus.

Exploration

INPP5F survival (RNA) · tumor vs normal (RNA) · all INPP5F data types