C18orf32

Across TCGA patient cohorts, C18orf32 mutation is significantly associated with the RNA expression of many other genes, with 816 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible C18orf32-associated genes across cancer lineages are RN7SL134P, MIR190A, and RNU6-558P. Each is linked with C18orf32 in more than 1 cancer types. Because this analysis shows association rather than direction, both C18orf32-to-partner and partner-to-C18orf32 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, RN7SL134P grouped by C18orf32-low versus C18orf32-high in BLCA.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (C18orf32→partner) and Y-score (partner→C18orf32) 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
BLCA	RN7SL134P →	+0.233	+4.926	<.001	.002	3	2
BLCA	MIR190A →	+0.487	+5.444	<.001	.002	3	2
UCEC	RNU6-558P →	+0.495	+1.645	.002	.009	3	2
HNSC	RNU6-1169P →	+0.365	+5.182	<.001	.007	3	1
HNSC	CFTRP3 →	+0.235	+5.912	<.001	.002	3	1
HNSC	MIR518E →	+0.548	+5.241	<.001	.007	3	1

Each partner links to its Q-omics profile. Showing the 6 strongest of 816 associations by consensus.

RN7SL134P by C18orf32 expression — BLCA

Explore this box plot interactively →