RSPH9

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

Across TCGA patient cohorts, RSPH9 mutation is significantly associated with the RNA expression of many other genes, with 1,194 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible RSPH9-associated genes across cancer lineages are SNORD116-15, PGBD4P2, and TMEM225. Each is linked with RSPH9 in more than 1 cancer types. Because this analysis shows association rather than direction, both RSPH9-to-partner and partner-to-RSPH9 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, SNORD116-15 grouped by RSPH9-low versus RSPH9-high in UCEC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (RSPH9→partner) and Y-score (partner→RSPH9) 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
UCECSNORD116-15 →+0.312+2.384.003.00232
READPGBD4P2 →+0.162+6.257<.001.00131
READTMEM225 →+0.114+5.039<.001.00831
READRNU6-1274P →+0.547+5.925<.001.00231
READFOXO1B →+0.146+5.039<.001.00831
READOR6K5P →+0.057+6.257<.001.00131
Each partner links to its Q-omics profile. Showing the 6 strongest of 1,194 associations by consensus.

SNORD116-15 by RSPH9 expression — UCEC

Box plot of SNORD116-15 in RSPH9-low vs RSPH9-high samples in UCEC.

Explore this box plot interactively →

Exploration