PHLDB2

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

Across TCGA patient cohorts, PHLDB2 mutation is significantly associated with the total protein of many other genes, with 63 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible PHLDB2-associated genes across cancer lineages are GAPDH, eIF4E, and CD49b. Each is linked with PHLDB2 in more than 2 cancer types. Because this analysis shows association rather than direction, both PHLDB2-to-partner and partner-to-PHLDB2 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, GAPDH grouped by PHLDB2-low versus PHLDB2-high in STAD.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (PHLDB2→partner) and Y-score (partner→PHLDB2) 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
STADGAPDH →+0.678+3.169<.001.01933
UCECeIF4E →+0.175+1.784.003<.00133
SKCMCD49b →+0.192+1.765.003.01033
UCEC4E-BP1 →+0.333+2.662<.001<.00133
UCECSrc_pY416 →-0.156-1.738.022.01133
UCECVHL →-0.619-1.125.001.02933
Each partner links to its Q-omics profile. Showing the 6 strongest of 63 associations by consensus.

GAPDH by PHLDB2 expression — STAD

Box plot of GAPDH in PHLDB2-low vs PHLDB2-high samples in STAD.

Explore this box plot interactively →

Exploration