INHBC

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

Across TCGA cell cohorts, INHBC mutation is significantly associated with the RNA expression of many other genes, with 2 significant associations in total. BLOOD_Myeloma shows the largest number of these associations.

The most reproducible INHBC-associated genes across cancer lineages are SERPINA7 and C1orf158. Each is linked with INHBC in more than 1 cancer types. Because this analysis shows association rather than direction, both INHBC-to-partner and partner-to-INHBC results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, SERPINA7 grouped by INHBC-low versus INHBC-high in BLOOD_Myeloma.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (INHBC→partner) and Y-score (partner→INHBC) 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
BLOOD_MyelomaSERPINA7 →+0.459+4.807<.001.00631
BLOOD_MyelomaC1orf158 →+0.053+4.807<.001.00631
Each partner links to its Q-omics profile. Showing the 2 strongest of 2 associations by consensus.

SERPINA7 by INHBC expression — BLOOD_Myeloma

Box plot of SERPINA7 in INHBC-low vs INHBC-high samples in BLOOD_Myeloma.

Explore this box plot interactively →

Exploration