Across TCGA patient cohorts, NBPF22P mutation is significantly associated with the RNA expression of many other genes, with 3,461 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible NBPF22P-associated genes across cancer lineages are SSRP1, MRPL39, and MRPS18C. Each is linked with NBPF22P in more than 2 cancer types. Because this analysis shows association rather than direction, both NBPF22P-to-partner and partner-to-NBPF22P 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 (NBPF22P→partner) and Y-score (partner→NBPF22P) 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
UCEC	SSRP1 →	+0.490	+3.754	.001	<.001	3	3
UCEC	MRPL39 →	+0.502	+2.637	<.001	<.001	3	3
UCEC	MRPS18C →	+0.404	+3.627	<.001	.001	3	3
UCEC	HARS1 →	+0.326	+2.273	<.001	<.001	3	3
UCEC	KNSTRN →	+0.570	+2.491	<.001	.001	3	3
UCEC	MTHFD1 →	+0.578	+2.235	<.001	.001	3	3

Each partner links to its Q-omics profile. Showing the 6 strongest of 3,461 associations by consensus.

Exploration

NBPF22P survival (RNA) · tumor vs normal (RNA) · all NBPF22P data types