CSRNP2

Across TCGA cell cohorts, CSRNP2 mutation is significantly associated with the mutation status of many other genes, with 1,159 significant associations in total. LARGE_INTESTINE shows the largest number of these associations.

The most reproducible CSRNP2-associated genes across cancer lineages are NUCB2, ELF1, and RNF113A. Each is linked with CSRNP2 in more than 2 cancer types. Because this analysis shows association rather than direction, both CSRNP2-to-partner and partner-to-CSRNP2 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, NUCB2 grouped by CSRNP2-low versus CSRNP2-high in BLOOD_Leukemia.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (CSRNP2→partner) and Y-score (partner→CSRNP2) 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
BLOOD_Leukemia	NUCB2 →	+4.894	+4.894	.004	.004	1	3
BLOOD_Leukemia	ELF1 →	+4.309	+4.560	.007	.007	1	3
BLOOD_Leukemia	RNF113A →	+4.309	+4.560	.007	.007	1	3
BLOOD_Leukemia	RBM42 →	+5.894	+5.321	.002	.002	1	3
BLOOD_Leukemia	STAB2 →	+2.779	+4.326	.006	.006	1	3
BLOOD_Leukemia	AHCTF1 →	+2.779	+4.326	.006	.006	1	3

Each partner links to its Q-omics profile. Showing the 6 strongest of 1,159 associations by consensus.

NUCB2 by CSRNP2 expression — BLOOD_Leukemia

Explore this box plot interactively →