LPL

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

Across TCGA patient cohorts, LPL mutation is significantly associated with the total protein of many other genes, with 26 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible LPL-associated genes across cancer lineages are A-Raf_pS299, MEK1, and AMPK_pT172. Each is linked with LPL in more than 1 cancer types. Because this analysis shows association rather than direction, both LPL-to-partner and partner-to-LPL results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, A-Raf_pS299 grouped by LPL-low versus LPL-high in UCEC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (LPL→partner) and Y-score (partner→LPL) 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
UCECA-Raf_pS299 →-0.092-1.700.030.04232
UCECMEK1 →+0.307+2.321.017.00532
UCECAMPK_pT172 →+0.325+2.013.025.00132
UCECINPP4B →-0.343-2.379.002<.00131
UCECNotch1 →+0.194+2.916<.001<.00131
UCECp27_pT198 →+0.093+2.321.014.03431
Each partner links to its Q-omics profile. Showing the 6 strongest of 26 associations by consensus.

A-Raf_pS299 by LPL expression — UCEC

Box plot of A-Raf_pS299 in LPL-low vs LPL-high samples in UCEC.

Explore this box plot interactively →

Exploration