HSBP1L1

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

Across TCGA patient cohorts, HSBP1L1 mutation is significantly associated with the RNA expression of many other genes, with 17 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible HSBP1L1-associated genes across cancer lineages are MIR4727, LSP1P3, and RNU6-151P. Each is linked with HSBP1L1 in more than 1 cancer types. Because this analysis shows association rather than direction, both HSBP1L1-to-partner and partner-to-HSBP1L1 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 (HSBP1L1→partner) and Y-score (partner→HSBP1L1) 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
UCECMIR4727 →+0.793+4.551<.001.00931
UCECLSP1P3 →+0.704+4.233<.001.00931
UCECRNU6-151P →+0.932+4.326<.001.00731
UCECMIR188 →+0.488+5.582<.001.00231
UCECIGLJ5 →+1.046+4.937<.001.00531
UCECTRAJ58 →+1.214+5.073<.001.00131
Each partner links to its Q-omics profile. Showing the 6 strongest of 17 associations by consensus.

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