NME8

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

Across TCGA patient cohorts, NME8 mutation is significantly associated with the RNA expression of many other genes, with 4,402 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible NME8-associated genes across cancer lineages are SNHG30, SNHG21, and GPR3. Each is linked with NME8 in more than 3 cancer types. Because this analysis shows association rather than direction, both NME8-to-partner and partner-to-NME8 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, SNHG30 grouped by NME8-low versus NME8-high in UCEC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (NME8→partner) and Y-score (partner→NME8) 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
UCECSNHG30 →+0.614+1.857<.001<.00134
UCECSNHG21 →+0.591+2.443<.001<.00134
SKCMGPR3 →+0.510+1.813.002<.00134
READRNU6-705P →+0.505+4.202.002.00833
STADRNA5SP198 →+0.385+4.951<.001<.00133
UCECPOLE2 →+0.651+3.269<.001<.00133
Each partner links to its Q-omics profile. Showing the 6 strongest of 4,402 associations by consensus.

SNHG30 by NME8 expression — UCEC

Box plot of SNHG30 in NME8-low vs NME8-high samples in UCEC.

Explore this box plot interactively →

Exploration