PRPS2

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

Across TCGA patient cohorts, PRPS2 mutation is significantly associated with the RNA expression of many other genes, with 1,628 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible PRPS2-associated genes across cancer lineages are CDH12P1, LINC02349, and MTATP6P21. Each is linked with PRPS2 in more than 1 cancer types. Because this analysis shows association rather than direction, both PRPS2-to-partner and partner-to-PRPS2 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, CDH12P1 grouped by PRPS2-low versus PRPS2-high in SKCM.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (PRPS2→partner) and Y-score (partner→PRPS2) 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
SKCMCDH12P1 →+0.092+4.614<.001.00632
SKCMLINC02349 →+0.082+4.385<.001.00832
UCECMTATP6P21 →+0.216+1.645<.001.00832
UCECPRPS1P1 →+0.068+1.868.001.00532
UCECRN7SL354P →+0.153+1.526.002.00732
UCECRNA5SP413 →+1.040+1.649<.001.00332
Each partner links to its Q-omics profile. Showing the 6 strongest of 1,628 associations by consensus.

CDH12P1 by PRPS2 expression — SKCM

Box plot of CDH12P1 in PRPS2-low vs PRPS2-high samples in SKCM.

Explore this box plot interactively →

Exploration