RNASEH2A

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

Across TCGA patient cohorts, RNASEH2A mutation is significantly associated with the total protein of many other genes, with 12 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible RNASEH2A-associated genes across cancer lineages are PCNA, ERK2, and VHL. Each is linked with RNASEH2A in more than 1 cancer types. Because this analysis shows association rather than direction, both RNASEH2A-to-partner and partner-to-RNASEH2A results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, PCNA grouped by RNASEH2A-low versus RNASEH2A-high in UCEC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (RNASEH2A→partner) and Y-score (partner→RNASEH2A) 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
UCECPCNA →+0.282+2.999.006.03532
UCECERK2 →+0.216+3.000.020.03631
UCECVHL →-1.479-3.169<.001.01831
UCECBak →+0.303+3.321.012.01031
UCECbeta-Catenin →+0.506+2.459.038.02031
UCECCyclin-B1 →+0.759+3.169.005.01931
Each partner links to its Q-omics profile. Showing the 6 strongest of 12 associations by consensus.

PCNA by RNASEH2A expression — UCEC

Box plot of PCNA in RNASEH2A-low vs RNASEH2A-high samples in UCEC.

Explore this box plot interactively →

Exploration