INHBB

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

Across TCGA patient cohorts, INHBB mutation is significantly associated with the RNA expression of many other genes, with 3,648 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible INHBB-associated genes across cancer lineages are MIR6803, RN7SL346P, and ZFYVE19. Each is linked with INHBB in more than 2 cancer types. Because this analysis shows association rather than direction, both INHBB-to-partner and partner-to-INHBB results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, MIR6803 grouped by INHBB-low versus INHBB-high in UCEC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (INHBB→partner) and Y-score (partner→INHBB) 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
UCECMIR6803 →+0.137+4.308<.001.00333
BLCARN7SL346P →+0.187+4.533.001.00533
UCECZFYVE19 →+0.431+3.831.001<.00132
UCECSF1 →+0.428+3.480<.001.00232
UCECLETM1 →+0.502+3.716<.001<.00132
UCECEDC4 →+0.718+2.914.001.00132
Each partner links to its Q-omics profile. Showing the 6 strongest of 3,648 associations by consensus.

MIR6803 by INHBB expression — UCEC

Box plot of MIR6803 in INHBB-low vs INHBB-high samples in UCEC.

Explore this box plot interactively →

Exploration