ACVR2A

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

Across TCGA patient cohorts, ACVR2A mutation is significantly associated with the total protein of many other genes, with 73 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible ACVR2A-associated genes across cancer lineages are ASNS, ATM, and eIF4G. Each is linked with ACVR2A in more than 2 cancer types. Because this analysis shows association rather than direction, both ACVR2A-to-partner and partner-to-ACVR2A results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, ASNS grouped by ACVR2A-low versus ACVR2A-high in COAD.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (ACVR2A→partner) and Y-score (partner→ACVR2A) 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
COADASNS →+0.757+2.593<.001.00633
UCECATM →-0.724-2.321<.001<.00133
UCECeIF4G →+0.262+1.184.004.02232
COADFASN →+0.418+1.882.010.03132
UCECFoxM1 →+0.201+1.584.009.00232
UCECFOXO3a_pS318_S321 →-0.097-1.642.008.00532
Each partner links to its Q-omics profile. Showing the 6 strongest of 73 associations by consensus.

ASNS by ACVR2A expression — COAD

Box plot of ASNS in ACVR2A-low vs ACVR2A-high samples in COAD.

Explore this box plot interactively →

Exploration