PDE1C

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

Across TCGA patient cohorts, PDE1C mutation is significantly associated with the total protein of many other genes, with 51 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible PDE1C-associated genes across cancer lineages are FASN, INPP4B, and 4E-BP1. Each is linked with PDE1C in more than 3 cancer types. Because this analysis shows association rather than direction, both PDE1C-to-partner and partner-to-PDE1C results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, FASN grouped by PDE1C-low versus PDE1C-high in STAD.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (PDE1C→partner) and Y-score (partner→PDE1C) 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
STADFASN →+0.664+2.823.003.03434
COADINPP4B →-0.327-3.169.036.01833
UCEC4E-BP1 →+0.264+2.584<.001<.00133
UCEC14-3-3_beta →-0.065-1.738.020.01132
UCECeEF2 →+0.249+1.106.013.02032
COADEGFR_pY1068 →-0.405-2.309.003.03332
Each partner links to its Q-omics profile. Showing the 6 strongest of 51 associations by consensus.

FASN by PDE1C expression — STAD

Box plot of FASN in PDE1C-low vs PDE1C-high samples in STAD.

Explore this box plot interactively →

Exploration