CD109

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

Across TCGA patient cohorts, CD109 mutation is significantly associated with the total protein of many other genes, with 81 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible CD109-associated genes across cancer lineages are PKC-b-II_pS660, c-Met_pY1235, and N-Ras. Each is linked with CD109 in more than 2 cancer types. Because this analysis shows association rather than direction, both CD109-to-partner and partner-to-CD109 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, PKC-b-II_pS660 grouped by CD109-low versus CD109-high in COAD.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (CD109→partner) and Y-score (partner→CD109) 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
COADPKC-b-II_pS660 →-0.423-2.898.001.00133
COADc-Met_pY1235 →+0.105+2.459.006.01833
UCECN-Ras →-0.115-3.143.006.01833
UCECCaspase-8 →-0.248-2.558.005<.00133
UCECCyclin-E2 →+0.147+1.817.013.01533
LUADMSH2 →+0.318+2.186.020.03432
Each partner links to its Q-omics profile. Showing the 6 strongest of 81 associations by consensus.

PKC-b-II_pS660 by CD109 expression — COAD

Box plot of PKC-b-II_pS660 in CD109-low vs CD109-high samples in COAD.

Explore this box plot interactively →

Exploration