KRTAP4-17P

Across TCGA patient cohorts, KRTAP4-17P RNA expression is significantly associated with the go_rna of many other GO terms, with 4,033 significant associations in total. BLCA shows the largest number of these associations.

The most reproducible KRTAP4-17P-associated GO terms across cancer lineages are Regulation of intracellular estrogen receptor signaling pathway, Telomere maintenance via recombination, and Regulation of cyclin-dependent protein kinase activity. Each is linked with KRTAP4-17P in more than 7 cancer types. Because this analysis shows association rather than direction, both KRTAP4-17P-to-partner and partner-to-KRTAP4-17P results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, Regulation of intracellular estrogen receptor signaling pathway grouped by KRTAP4-17P-low versus KRTAP4-17P-high in STAD.

RNA expression associated GO terms by consensus

Ranked by combined sampling and lineage consensus. X-score (KRTAP4-17P→partner) and Y-score (partner→KRTAP4-17P) are standardized regression coefficients; both directions are reported because the association is undirected. p-values are from the association test.

Lineage	Partner GO term	X-score	Y-score	p(X)	p(Y)	Sampling consensus	Lineage consensus
STAD	Regulation of intracellular estrogen receptor signaling pathway →	+0.038	+0.191	<.001	<.001	3	7
ESCA	Telomere maintenance via recombination →	+0.040	+0.423	<.001	<.001	3	7
LIHC	Regulation of cyclin-dependent protein kinase activity →	+0.050	+0.069	<.001	.003	2	8
ESCA	Vesicle tethering to Golgi →	+0.040	+0.394	<.001	<.001	2	7
STAD	DNA strand elongation →	+0.045	+0.182	<.001	<.001	3	6
LIHC	Negative regulation of post-translational protein modification →	+0.048	+0.066	<.001	.003	2	7

Each partner links to its Q-omics profile. Showing the 6 strongest of 4,033 associations by consensus.

Regulation of intracellular estrogen receptor signaling pathway by KRTAP4-17P expression — STAD

Explore this box plot interactively →