RNASEH2C

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

Across TCGA patient cohorts, RNASEH2C mutation is significantly associated with the RNA expression of many other genes, with 47 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible RNASEH2C-associated genes across cancer lineages are RNU6-1213P, RN7SL478P, and MIR557. Each is linked with RNASEH2C in more than 1 cancer types. Because this analysis shows association rather than direction, both RNASEH2C-to-partner and partner-to-RNASEH2C results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, RNU6-1213P grouped by RNASEH2C-low versus RNASEH2C-high in UCEC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (RNASEH2C→partner) and Y-score (partner→RNASEH2C) 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
UCECRNU6-1213P →+0.258+4.069<.001.00832
UCECRN7SL478P →+0.402+2.676<.001.00731
CESCMIR557 →+0.341+5.342<.001.00231
CESCOR7E93P →+0.052+4.812<.001.00631
BLCARNU6-756P →+0.333+7.640<.001.00931
CESCRN7SL73P →+0.389+4.276<.001.00831
Each partner links to its Q-omics profile. Showing the 6 strongest of 47 associations by consensus.

RNU6-1213P by RNASEH2C expression — UCEC

Box plot of RNU6-1213P in RNASEH2C-low vs RNASEH2C-high samples in UCEC.

Explore this box plot interactively →

Exploration