STARD8

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

Across TCGA patient cohorts, STARD8 mutation is significantly associated with the RNA expression of many other genes, with 6,081 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible STARD8-associated genes across cancer lineages are NOL7, LDHAP7, and KRTAP5-9. Each is linked with STARD8 in more than 2 cancer types. Because this analysis shows association rather than direction, both STARD8-to-partner and partner-to-STARD8 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, NOL7 grouped by STARD8-low versus STARD8-high in SKCM.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (STARD8→partner) and Y-score (partner→STARD8) 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
SKCMNOL7 →+0.414+2.353.005.00333
UCECLDHAP7 →+0.606+2.113<.001<.00133
UCECKRTAP5-9 →-0.403-1.754<.001<.00133
UCECMMP12 →+1.078+2.091<.001<.00133
UCECBAG1 →+0.539+2.169<.001<.00133
UCECSLC25A11 →+0.354+2.002<.001<.00133
Each partner links to its Q-omics profile. Showing the 6 strongest of 6,081 associations by consensus.

NOL7 by STARD8 expression — SKCM

Box plot of NOL7 in STARD8-low vs STARD8-high samples in SKCM.

Explore this box plot interactively →

Exploration