Across TCGA patient cohorts, BNIP3P1 mutation is significantly associated with the RNA expression of many other genes, with 1,532 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible BNIP3P1-associated genes across cancer lineages are AGGF1P7, LINC00092, and CPLX3. Each is linked with BNIP3P1 in more than 2 cancer types. Because this analysis shows association rather than direction, both BNIP3P1-to-partner and partner-to-BNIP3P1 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 (BNIP3P1→partner) and Y-score (partner→BNIP3P1) 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
HNSC	AGGF1P7 →	+0.060	+4.636	<.001	.006	3	3
SKCM	LINC00092 →	-0.487	-3.662	.006	.001	3	3
CESC	CPLX3 →	+0.016	+5.342	<.001	.002	3	2
HNSC	NECAP1P1 →	+0.087	+4.495	.002	.002	3	2
UCEC	EIF1AD →	+0.446	+3.470	<.001	.002	3	2
BRCA	RNA5SP430 →	+0.447	+7.731	<.001	.009	3	2

Each partner links to its Q-omics profile. Showing the 6 strongest of 1,532 associations by consensus.

Exploration

BNIP3P1 survival (RNA) · tumor vs normal (RNA) · all BNIP3P1 data types