LINC00158

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

Across TCGA patient cohorts, LINC00158 mutation is significantly associated with the RNA expression of many other genes, with 60 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible LINC00158-associated genes across cancer lineages are NUTF2P8, RN7SL248P, and RPS29P32. Each is linked with LINC00158 in more than 1 cancer types. Because this analysis shows association rather than direction, both LINC00158-to-partner and partner-to-LINC00158 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 (LINC00158→partner) and Y-score (partner→LINC00158) 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
UCECNUTF2P8 →+0.192+3.982<.001.00331
UCECRN7SL248P →+0.139+4.722<.001.00431
UCECRPS29P32 →+0.871+3.599<.001.00731
UCECMIR8053 →+0.527+4.582<.001.00531
UCECRN7SL478P →+0.389+3.354<.001.00731
UCECSSTR5 →+1.657+3.608<.001.00931
Each partner links to its Q-omics profile. Showing the 6 strongest of 60 associations by consensus.

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