TTC22

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

Across TCGA patient cohorts, TTC22 mutation is significantly associated with the RNA expression of many other genes, with 2,236 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible TTC22-associated genes across cancer lineages are RN7SL601P, INTS10, and ANAPC15. Each is linked with TTC22 in more than 1 cancer types. Because this analysis shows association rather than direction, both TTC22-to-partner and partner-to-TTC22 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, RN7SL601P grouped by TTC22-low versus TTC22-high in BRCA.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (TTC22→partner) and Y-score (partner→TTC22) 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
BRCARN7SL601P →+0.133+7.731<.001.00932
SKCMINTS10 →+0.758+3.366.004.00532
SKCMANAPC15 →+0.711+3.328<.001.00532
SKCMSOD1 →+0.564+3.328.001.00532
SKCMDBIP2 →+0.126+2.393.004.00932
UCECTRIM35 →+0.589+3.386<.001.00432
Each partner links to its Q-omics profile. Showing the 6 strongest of 2,236 associations by consensus.

RN7SL601P by TTC22 expression — BRCA

Box plot of RN7SL601P in TTC22-low vs TTC22-high samples in BRCA.

Explore this box plot interactively →

Exploration