PRLH

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

Across TCGA patient cohorts, PRLH mutation is significantly associated with the RNA expression of many other genes, with 96 significant associations in total. SKCM shows the largest number of these associations.

The most reproducible PRLH-associated genes across cancer lineages are UBE2V1P6, RN7SL470P, and MIR132. Each is linked with PRLH in more than 1 cancer types. Because this analysis shows association rather than direction, both PRLH-to-partner and partner-to-PRLH results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, UBE2V1P6 grouped by PRLH-low versus PRLH-high in LUAD.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (PRLH→partner) and Y-score (partner→PRLH) 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
LUADUBE2V1P6 →+0.108+5.099<.001.00832
UCECRN7SL470P →+0.448+4.279<.001.00831
UCECMIR132 →+0.850+4.771<.001.00631
UCECLINC01897 →+0.277+4.326.002.00731
UCECDUXAP3 →+0.425+4.525<.001.00531
SKCMNOX3 →+0.224+4.096<.001<.00131
Each partner links to its Q-omics profile. Showing the 6 strongest of 96 associations by consensus.

UBE2V1P6 by PRLH expression — LUAD

Box plot of UBE2V1P6 in PRLH-low vs PRLH-high samples in LUAD.

Explore this box plot interactively →

Exploration