Across TCGA patient cohorts, C1QTNF12 mutation is significantly associated with the RNA expression of many other genes, with 15 significant associations in total. SKCM shows the largest number of these associations.

The most reproducible C1QTNF12-associated genes across cancer lineages are OR1F2P, MIR33A, and BMS1P17. Each is linked with C1QTNF12 in more than 1 cancer types. Because this analysis shows association rather than direction, both C1QTNF12-to-partner and partner-to-C1QTNF12 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 (C1QTNF12→partner) and Y-score (partner→C1QTNF12) 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	OR1F2P →	+0.185	+4.237	<.001	.008	3	1
COAD	MIR33A →	+0.577	+4.693	<.001	.007	3	1
COAD	BMS1P17 →	+0.086	+5.037	<.001	.002	3	1
COAD	RN7SL861P →	+0.253	+4.831	<.001	.003	3	1
COAD	GLTPP1 →	+0.074	+4.790	.005	.006	3	1
COAD	IGHV1OR15-4 →	+0.301	+4.354	.001	.007	3	1

Each partner links to its Q-omics profile. Showing the 6 strongest of 15 associations by consensus.

Exploration

C1QTNF12 survival (RNA) · tumor vs normal (RNA) · all C1QTNF12 data types