RSPH14

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

Across TCGA patient cohorts, RSPH14 mutation is significantly associated with the RNA expression of many other genes, with 1,745 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible RSPH14-associated genes across cancer lineages are RNU6-391P, TRAJ9, and RNA5SP411. Each is linked with RSPH14 in more than 2 cancer types. Because this analysis shows association rather than direction, both RSPH14-to-partner and partner-to-RSPH14 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, RNU6-391P grouped by RSPH14-low versus RSPH14-high in UCEC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (RSPH14→partner) and Y-score (partner→RSPH14) 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
UCECRNU6-391P →+0.201+3.027<.001.00133
UCECTRAJ9 →+0.657+2.006<.001.00233
UCECRNA5SP411 →+0.867+1.808.001.00732
BRCAKRT18P12 →+0.095+4.220<.001.00932
BRCARNA5SP113 →+0.308+5.711<.001.00132
BRCARPL38P1 →+0.303+5.396<.001.00132
Each partner links to its Q-omics profile. Showing the 6 strongest of 1,745 associations by consensus.

RNU6-391P by RSPH14 expression — UCEC

Box plot of RNU6-391P in RSPH14-low vs RSPH14-high samples in UCEC.

Explore this box plot interactively →

Exploration