PDGFRL

RNA expression — cross-omics
Cross-omicsRNA → FUNCTION-RNACell-linePairwise association · TCGA cohorts

Across TCGA cell cohorts, PDGFRL RNA expression is significantly associated with the go_rna of many other GO terms, with 2,798 significant associations in total. BLOOD_Lymphoma shows the largest number of these associations.

The most reproducible PDGFRL-associated GO terms across cancer lineages are Negative regulation of amyloid fibril formation, Positive regulation of protein exit from endoplasmic reticulum, and Positive regulation of B cell activation. Each is linked with PDGFRL in more than 8 cancer types. Because this analysis shows association rather than direction, both PDGFRL-to-partner and partner-to-PDGFRL results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, Negative regulation of amyloid fibril formation grouped by PDGFRL-low versus PDGFRL-high in LUNG_NSCLC_LUSC.

RNA expression associated GO terms by consensus

Ranked by combined sampling and lineage consensus. X-score (PDGFRL→partner) and Y-score (partner→PDGFRL) are standardized regression coefficients; both directions are reported because the association is undirected. p-values are from the association test.
LineagePartner GO termX-scoreY-scorep(X)p(Y)Sampling consensusLineage consensus
LUNG_NSCLC_LUSCNegative regulation of amyloid fibril formation →+0.253+1.368<.001.00139
SOFT_TISSUEPositive regulation of protein exit from endoplasmic reticulum →+0.093+1.330<.001.00438
BLOOD_LymphomaPositive regulation of B cell activation →-0.079-0.682<.001.00437
BONEEnergy derivation by oxidation of organic compounds →+0.052+1.409.001<.00137
BLOOD_LymphomaRegulation of protein exit from endoplasmic reticulum →+0.067+0.625.006.00937
KIDNEYGolgi vesicle transport →+0.040+0.995<.001<.00137
Each partner links to its Q-omics profile. Showing the 6 strongest of 2,798 associations by consensus.

Negative regulation of amyloid fibril formation by PDGFRL expression — LUNG_NSCLC_LUSC

Box plot of Negative regulation of amyloid fibril formation in PDGFRL-low vs PDGFRL-high samples in LUNG_NSCLC_LUSC.

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Exploration