ACVR1C

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

Across TCGA patient cohorts, ACVR1C mutation is significantly associated with the RNA expression of many other genes, with 4,701 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible ACVR1C-associated genes across cancer lineages are RNU6-728P, HAUS1, and DCTN3. Each is linked with ACVR1C in more than 2 cancer types. Because this analysis shows association rather than direction, both ACVR1C-to-partner and partner-to-ACVR1C results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, RNU6-728P grouped by ACVR1C-low versus ACVR1C-high in HNSC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (ACVR1C→partner) and Y-score (partner→ACVR1C) 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
HNSCRNU6-728P →+0.175+4.936<.001.00333
UCECHAUS1 →+0.678+3.091<.001<.00133
SKCMDCTN3 →+0.343+2.913.008.00133
SKCMGSTO1 →+0.872+3.597<.001.00133
HNSCRNY4P3 →+0.314+3.517<.001.00832
HNSCRN7SKP161 →+0.172+3.685.001.00332
Each partner links to its Q-omics profile. Showing the 6 strongest of 4,701 associations by consensus.

RNU6-728P by ACVR1C expression — HNSC

Box plot of RNU6-728P in ACVR1C-low vs ACVR1C-high samples in HNSC.

Explore this box plot interactively →

Exploration