OR9A2

Across TCGA cell cohorts, OR9A2 RNA expression is significantly associated with the go_rna of many other GO terms, with 1,072 significant associations in total. BLOOD_Leukemia shows the largest number of these associations.

The most reproducible OR9A2-associated GO terms across cancer lineages are Cellular response to nutrient levels, Regulation of RNA polymerase II transcription preinitiation complex assembly, and Error-free translesion synthesis. Each is linked with OR9A2 in more than 4 cancer types. Because this analysis shows association rather than direction, both OR9A2-to-partner and partner-to-OR9A2 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, Cellular response to nutrient levels grouped by OR9A2-low versus OR9A2-high in LUNG_SCLC.

RNA expression associated GO terms by consensus

Ranked by combined sampling and lineage consensus. X-score (OR9A2→partner) and Y-score (partner→OR9A2) 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
LUNG_SCLC	Cellular response to nutrient levels →	+0.054	+0.046	<.001	.001	3	5
BLOOD_Leukemia	Regulation of RNA polymerase II transcription preinitiation complex assembly →	+0.082	+0.015	.003	.002	3	5
BLOOD_Leukemia	Error-free translesion synthesis →	+0.100	+0.014	<.001	<.001	3	5
LUNG_SCLC	Positive regulation of intracellular steroid hormone receptor signaling pathway →	+0.129	+0.041	<.001	.005	2	5
LARGE_INTESTINE	Positive regulation of intracellular estrogen receptor signaling pathway →	+0.121	+0.010	<.001	.003	3	4
OVARY	Negative regulation of cytoplasmic pattern recognition receptor signaling pathway →	+0.072	+0.008	.003	.004	3	4

Each partner links to its Q-omics profile. Showing the 6 strongest of 1,072 associations by consensus.

Cellular response to nutrient levels by OR9A2 expression — LUNG_SCLC

Explore this box plot interactively →