PRTFDC1

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

Across TCGA patient cohorts, PRTFDC1 mutation is significantly associated with the RNA expression of many other genes, with 471 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible PRTFDC1-associated genes across cancer lineages are RNU6-939P, RN7SKP286, and RNA5SP519. Each is linked with PRTFDC1 in more than 1 cancer types. Because this analysis shows association rather than direction, both PRTFDC1-to-partner and partner-to-PRTFDC1 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, RNU6-939P grouped by PRTFDC1-low versus PRTFDC1-high in SKCM.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (PRTFDC1→partner) and Y-score (partner→PRTFDC1) 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
SKCMRNU6-939P →+0.587+5.508<.001<.00132
UCECRN7SKP286 →+0.040+3.890<.001.00732
UCECRNA5SP519 →+0.448+2.398<.001.00432
UCECCCDC163 →+0.560+3.600<.001.00131
UCECDNAJB5-DT →+0.403+2.840<.001.00231
CESCBNIP3P2 →+0.056+5.252<.001.00231
Each partner links to its Q-omics profile. Showing the 6 strongest of 471 associations by consensus.

RNU6-939P by PRTFDC1 expression — SKCM

Box plot of RNU6-939P in PRTFDC1-low vs PRTFDC1-high samples in SKCM.

Explore this box plot interactively →

Exploration