HSPA1B

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

Across TCGA cell cohorts, HSPA1B mutation is significantly associated with the RNA expression of many other genes, with 3 significant associations in total. SKIN shows the largest number of these associations.

The most reproducible HSPA1B-associated genes across cancer lineages are OR10H5, C16orf82, and DCD. Each is linked with HSPA1B in more than 1 cancer types. Because this analysis shows association rather than direction, both HSPA1B-to-partner and partner-to-HSPA1B results are reported.

Each partner links to its own Q-omics profile.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (HSPA1B→partner) and Y-score (partner→HSPA1B) 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
SKINOR10H5 →+0.012+4.977<.001.00731
SKINC16orf82 →+0.016+4.977<.001.00731
LUNG_NSCLC_LUADDCD →+0.045+5.266<.001.00131
Each partner links to its Q-omics profile. Showing the 3 strongest of 3 associations by consensus.

Exploration