LINC02449

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

Across TCGA patient cohorts, LINC02449 mutation is significantly associated with the RNA expression of many other genes, with 50 significant associations in total. STAD shows the largest number of these associations.

The most reproducible LINC02449-associated genes across cancer lineages are LINC02462, PRAMEF32P, and TSPY18P. Each is linked with LINC02449 in more than 1 cancer types. Because this analysis shows association rather than direction, both LINC02449-to-partner and partner-to-LINC02449 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 (LINC02449→partner) and Y-score (partner→LINC02449) 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
LUADLINC02462 →+0.323+5.554<.001.00432
HNSCPRAMEF32P →+0.034+7.954<.001.00831
HNSCTSPY18P →+0.069+7.954<.001.00831
HNSCMIR4693 →+0.388+7.954<.001.00831
HNSCMIR6795 →+0.418+7.954<.001.00831
STADRNA5SP326 →+0.609+5.026<.001.00931
Each partner links to its Q-omics profile. Showing the 6 strongest of 50 associations by consensus.

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