PRAME

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

Across TCGA patient cohorts, PRAME mutation is significantly associated with the total protein of many other genes, with 23 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible PRAME-associated genes across cancer lineages are ACC1, 4E-BP1, and eEF2. Each is linked with PRAME in more than 2 cancer types. Because this analysis shows association rather than direction, both PRAME-to-partner and partner-to-PRAME 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 (PRAME→partner) and Y-score (partner→PRAME) 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
UCECACC1 →+0.433+3.183.001.00933
UCEC4E-BP1 →+0.337+2.584.001.00133
LUSCeEF2 →+0.181+2.179.035.03532
SKCMMEK1_p_S217_S221 →+0.227+2.182.043.03332
UCECCyclin-B1 →+0.490+3.459.022.00532
UCECeIF4E →+0.181+3.247.025<.00132
Each partner links to its Q-omics profile. Showing the 6 strongest of 23 associations by consensus.

Exploration