MIR526B

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

Across TCGA patient cohorts, MIR526B mutation is significantly associated with the RNA expression of many other genes, with 18 significant associations in total. SKCM shows the largest number of these associations.

The most reproducible MIR526B-associated genes across cancer lineages are IFNA12P, NICN2P, and KRT18P43. Each is linked with MIR526B in more than 1 cancer types. Because this analysis shows association rather than direction, both MIR526B-to-partner and partner-to-MIR526B 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 (MIR526B→partner) and Y-score (partner→MIR526B) 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
SKCMIFNA12P →+0.115+4.867<.001.00531
SKCMNICN2P →+0.092+4.440<.001.00631
SKCMKRT18P43 →+0.035+4.594<.001.00831
SKCMLINC01333 →+0.063+6.219<.001<.00131
SKCMOR51A7 →+0.050+5.199<.001.00331
SKCMRNU6-502P →+0.311+4.771<.001.00631
Each partner links to its Q-omics profile. Showing the 6 strongest of 18 associations by consensus.

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