PLPPR1

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

Across TCGA patient cohorts, PLPPR1 mutation is significantly associated with the RNA expression of many other genes, with 2,923 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible PLPPR1-associated genes across cancer lineages are RN7SL393P, RNA5SP410, and RNA5SP414. Each is linked with PLPPR1 in more than 2 cancer types. Because this analysis shows association rather than direction, both PLPPR1-to-partner and partner-to-PLPPR1 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, RN7SL393P grouped by PLPPR1-low versus PLPPR1-high in SKCM.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (PLPPR1→partner) and Y-score (partner→PLPPR1) 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
SKCMRN7SL393P →+0.073+2.684<.001.00433
UCECRNA5SP410 →+0.463+1.724<.001.00133
UCECRNA5SP414 →+0.341+1.554.001.00932
BRCARNA5SP416 →+0.482+7.471<.001.00832
UCECVTI1B →+0.400+1.700<.001.00232
UCECSEC23A →+0.402+1.522.007.00932
Each partner links to its Q-omics profile. Showing the 6 strongest of 2,923 associations by consensus.

RN7SL393P by PLPPR1 expression — SKCM

Box plot of RN7SL393P in PLPPR1-low vs PLPPR1-high samples in SKCM.

Explore this box plot interactively →

Exploration