HMGN1

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

Across TCGA patient cohorts, HMGN1 mutation is significantly associated with the RNA expression of many other genes, with 261 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible HMGN1-associated genes across cancer lineages are NUTF2, TBC1D13, and GRPEL1. Each is linked with HMGN1 in more than 1 cancer types. Because this analysis shows association rather than direction, both HMGN1-to-partner and partner-to-HMGN1 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 (HMGN1→partner) and Y-score (partner→HMGN1) 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
UCECNUTF2 →+0.570+3.201<.001.00931
UCECTBC1D13 →+0.528+3.459.001.00531
UCECGRPEL1 →+0.502+3.202.003.00931
UCECCYP27B1 →+0.730+3.491<.001.00231
UCECDAP →+0.596+3.491.003.00231
UCECABCB6 →+0.656+3.470.001.00331
Each partner links to its Q-omics profile. Showing the 6 strongest of 261 associations by consensus.

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