Across TCGA patient cohorts, KLRC2 mutation is significantly associated with the RNA expression of many other genes, with 699 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible KLRC2-associated genes across cancer lineages are MYEOV, ANKHD1, and H3P38. Each is linked with KLRC2 in more than 1 cancer types. Because this analysis shows association rather than direction, both KLRC2-to-partner and partner-to-KLRC2 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 (KLRC2→partner) and Y-score (partner→KLRC2) 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	MYEOV →	+1.727	+3.459	<.001	.005	3	2
UCEC	ANKHD1 →	+0.419	+3.507	<.001	.002	3	2
LIHC	H3P38 →	+0.138	+5.268	<.001	.006	3	1
SKCM	CASKP1 →	+0.041	+3.487	.003	.005	3	1
SKCM	LINC02559 →	+0.094	+4.039	<.001	.009	3	1
SKCM	MTND2P6 →	+0.024	+3.776	<.001	.003	3	1

Each partner links to its Q-omics profile. Showing the 6 strongest of 699 associations by consensus.

Exploration

KLRC2 survival (RNA) · tumor vs normal (RNA) · all KLRC2 data types