HARS1

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

Across TCGA patient cohorts, HARS1 mutation is significantly associated with the RNA expression of many other genes, with 3,011 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible HARS1-associated genes across cancer lineages are LINC02713, SPANXN2, and RPPH1-2P. Each is linked with HARS1 in more than 1 cancer types. Because this analysis shows association rather than direction, both HARS1-to-partner and partner-to-HARS1 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, LINC02713 grouped by HARS1-low versus HARS1-high in CESC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (HARS1→partner) and Y-score (partner→HARS1) 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
CESCLINC02713 →+0.050+5.306<.001.00632
CESCSPANXN2 →+0.088+6.569<.001.00132
BRCARPPH1-2P →+0.103+7.731<.001.00932
UCECXPC →+0.566+3.491.003.00232
UCECSLC4A1AP →+0.476+3.470.004.00232
UCECMYH9 →+0.518+3.223.005.00932
Each partner links to its Q-omics profile. Showing the 6 strongest of 3,011 associations by consensus.

LINC02713 by HARS1 expression — CESC

Box plot of LINC02713 in HARS1-low vs HARS1-high samples in CESC.

Explore this box plot interactively →

Exploration