MIR137HG

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

Across TCGA patient cohorts, MIR137HG mutation is significantly associated with the RNA expression of many other genes, with 1,372 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible MIR137HG-associated genes across cancer lineages are RNVU1-28, RNA5SP413, and LYZL1. Each is linked with MIR137HG in more than 1 cancer types. Because this analysis shows association rather than direction, both MIR137HG-to-partner and partner-to-MIR137HG 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 (MIR137HG→partner) and Y-score (partner→MIR137HG) 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
UCECRNVU1-28 →+0.909+2.957<.001<.00132
UCECRNA5SP413 →+1.116+2.277<.001.00432
CESCLYZL1 →+0.056+5.418<.001.00531
CESCKRTAP4-9 →+0.538+5.103<.001.00831
CESCDNAJA1P1 →+0.053+5.306<.001.00631
CESCLINC00351 →+0.172+5.201<.001.00731
Each partner links to its Q-omics profile. Showing the 6 strongest of 1,372 associations by consensus.

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