Across TCGA cell cohorts, CES1P1 protein abundance is significantly associated with the go_rna of many other GO terms, with 241 significant associations in total. BLOOD_Leukemia shows the largest number of these associations.

The most reproducible CES1P1-associated GO terms across cancer lineages are Negative regulation of RNA export from nucleus, Mitochondrial transport, and Regulation of delayed rectifier potassium channel activity. Each is linked with CES1P1 in more than 1 cancer types. Because this analysis shows association rather than direction, both CES1P1-to-partner and partner-to-CES1P1 results are reported.

Each partner links to its own Q-omics profile.

protein abundance associated GO terms by consensus

Ranked by combined sampling and lineage consensus. X-score (CES1P1→partner) and Y-score (partner→CES1P1) 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_NSCLC_LUAD	Negative regulation of RNA export from nucleus →	-0.158	-5.025	.007	.001	3	2
LUNG_NSCLC_LUAD	Mitochondrial transport →	+0.146	+4.865	.004	.002	3	2
BLOOD_Leukemia	Regulation of delayed rectifier potassium channel activity →	+0.249	+2.247	.004	.002	3	2
BLOOD_Leukemia	Negative regulation of primary miRNA processing →	+0.330	+2.247	<.001	.002	3	2
BLOOD_Leukemia	Regulation of autophagosome assembly →	+0.068	+3.072	.004	<.001	3	2
BLOOD_Leukemia	Ectodermal placode development →	+0.159	+2.855	.004	<.001	3	2

Each partner links to its Q-omics profile. Showing the 6 strongest of 241 associations by consensus.

Exploration

CES1P1 survival (RNA) · tumor vs normal (RNA) · all CES1P1 data types