HMGB1

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

Across TCGA patient cohorts, HMGB1 mutation is significantly associated with the RNA expression of many other genes, with 2,463 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible HMGB1-associated genes across cancer lineages are FANCB, CDCA2, and CENPP. Each is linked with HMGB1 in more than 1 cancer types. Because this analysis shows association rather than direction, both HMGB1-to-partner and partner-to-HMGB1 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 (HMGB1→partner) and Y-score (partner→HMGB1) 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
UCECFANCB →+0.411+2.247<.001.00132
UCECCDCA2 →+0.779+2.752<.001<.00132
UCECCENPP →+0.371+3.126<.001<.00132
CESCRN7SL97P →+0.149+4.559<.001.00632
UCECIARS1 →+0.582+1.703<.001.00632
UCECKIF9-AS1 →+0.375+2.063<.001.00432
Each partner links to its Q-omics profile. Showing the 6 strongest of 2,463 associations by consensus.

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