MIR17HG

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

Across TCGA patient cohorts, MIR17HG mutation is significantly associated with the RNA expression of many other genes, with 2,005 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible MIR17HG-associated genes across cancer lineages are HSPE1P21, USP9YP2, and LINC02079. Each is linked with MIR17HG in more than 1 cancer types. Because this analysis shows association rather than direction, both MIR17HG-to-partner and partner-to-MIR17HG 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 (MIR17HG→partner) and Y-score (partner→MIR17HG) 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
UCECHSPE1P21 →+0.227+2.126<.001.00732
UCECUSP9YP2 →+0.020+5.258<.001<.00132
LUSCLINC02079 →+0.113+5.733<.001.00132
UCECIGKV3OR2-5 →+0.538+1.911.003.00732
UCECSNRPGP17 →+0.310+1.879<.001.00931
UCECRPL23AP90 →+0.338+2.004.001.00631
Each partner links to its Q-omics profile. Showing the 6 strongest of 2,005 associations by consensus.

Exploration