RINL

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

Across TCGA patient cohorts, RINL mutation is significantly associated with the RNA expression of many other genes, with 1,615 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible RINL-associated genes across cancer lineages are RNA5SP412, RNU6-886P, and RNA5SP453. Each is linked with RINL in more than 1 cancer types. Because this analysis shows association rather than direction, both RINL-to-partner and partner-to-RINL 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 (RINL→partner) and Y-score (partner→RINL) 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
UCECRNA5SP412 →+0.698+2.092<.001.00732
COADRNU6-886P →+0.285+3.374<.001.00832
CESCRNA5SP453 →+0.333+5.306<.001.00632
SKCMEGLN3-AS1 →+0.216+3.894.002.00832
LUSCMIR4686 →+0.436+3.678<.001.00432
UCECRNA5SP418 →+1.028+2.348<.001.00132
Each partner links to its Q-omics profile. Showing the 6 strongest of 1,615 associations by consensus.

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