SUPT20HL1

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

Across TCGA patient cohorts, SUPT20HL1 mutation is significantly associated with the RNA expression of many other genes, with 1,302 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SUPT20HL1-associated genes across cancer lineages are RPL12P5, RNU6-986P, and EZH2P1. Each is linked with SUPT20HL1 in more than 2 cancer types. Because this analysis shows association rather than direction, both SUPT20HL1-to-partner and partner-to-SUPT20HL1 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 (SUPT20HL1→partner) and Y-score (partner→SUPT20HL1) 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
SKCMRPL12P5 →+0.065+4.282<.001.00933
BLCARNU6-986P →+0.471+4.840<.001.00233
SKCMEZH2P1 →+0.108+3.730.007.00833
BRCASNRPGP19 →+0.141+4.630<.001.00632
HNSCOR51T1 →+0.033+4.505<.001.00132
HNSCSNORD90 →+0.339+3.681<.001.00532
Each partner links to its Q-omics profile. Showing the 6 strongest of 1,302 associations by consensus.

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