PLEK2

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

Across TCGA patient cohorts, PLEK2 mutation is significantly associated with the total protein of many other genes, with 7 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible PLEK2-associated genes across cancer lineages are MEK1, Notch1, and Paxillin. Each is linked with PLEK2 in more than 1 cancer types. Because this analysis shows association rather than direction, both PLEK2-to-partner and partner-to-PLEK2 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, MEK1 grouped by PLEK2-low versus PLEK2-high in UCEC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (PLEK2→partner) and Y-score (partner→PLEK2) 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
UCECMEK1 →+0.495+3.169.013.01931
UCECNotch1 →+0.223+2.820.003.03531
UCECPaxillin →+0.328+3.009.021.01931
UCECEGFR_pY1068 →-0.304-3.169.027.02021
UCECTuberin →+0.387+3.169.008.02021
UCECVEGFR2 →+0.381+2.817.019.03621
Each partner links to its Q-omics profile. Showing the 6 strongest of 7 associations by consensus.

MEK1 by PLEK2 expression — UCEC

Box plot of MEK1 in PLEK2-low vs PLEK2-high samples in UCEC.

Explore this box plot interactively →

Exploration