PNLIPRP2

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

Across TCGA patient cohorts, PNLIPRP2 mutation is significantly associated with the total protein of many other genes, with 30 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible PNLIPRP2-associated genes across cancer lineages are p38-MAPK, VEGFR2, and 4E-BP1. Each is linked with PNLIPRP2 in more than 2 cancer types. Because this analysis shows association rather than direction, both PNLIPRP2-to-partner and partner-to-PNLIPRP2 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, p38-MAPK grouped by PNLIPRP2-low versus PNLIPRP2-high in LUAD.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (PNLIPRP2→partner) and Y-score (partner→PNLIPRP2) 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
LUADp38-MAPK →-0.225-2.917.010.03432
UCECVEGFR2 →+0.314+1.920.008.00932
UCEC4E-BP1 →+0.320+3.199.003.00923
UCECCyclin-B1 →+0.628+1.906.005.01632
LUADCyclin-E2 →+0.261+3.016<.001.01931
UCEC14-3-3_beta →-0.096-1.847.017.04931
Each partner links to its Q-omics profile. Showing the 6 strongest of 30 associations by consensus.

p38-MAPK by PNLIPRP2 expression — LUAD

Box plot of p38-MAPK in PNLIPRP2-low vs PNLIPRP2-high samples in LUAD.

Explore this box plot interactively →

Exploration