PABPC1L2A

mutation — cross-omics
Cross-omicsMUTATION → PROTEIN-RPPAPatientPairwise association · TCGA cohorts

Across TCGA patient cohorts, PABPC1L2A mutation is significantly associated with the total protein of many other genes, with 13 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible PABPC1L2A-associated genes across cancer lineages are GAPDH, NF2, and p27_pT157. Each is linked with PABPC1L2A in more than 1 cancer types. Because this analysis shows association rather than direction, both PABPC1L2A-to-partner and partner-to-PABPC1L2A results are reported.

Each partner links to its own Q-omics profile.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (PABPC1L2A→partner) and Y-score (partner→PABPC1L2A) are standardized regression coefficients; both directions are reported because the association is undirected. p-values are from the association test.
LineagePartner geneX-scoreY-scorep(X)p(Y)Sampling consensusLineage consensus
UCECGAPDH →+0.599+3.169.042.02031
UCECNF2 →+0.269+3.169.023.02031
UCECp27_pT157 →-0.081-3.169.010.02031
UCECTuberin →+0.409+2.817.005.03631
UCECCyclin-D1 →-0.182-3.169.040.02031
UCECKu80 →+0.380+3.183.003.01021
Each partner links to its Q-omics profile. Showing the 6 strongest of 13 associations by consensus.

Exploration