SLC25A47

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

Across TCGA patient cohorts, SLC25A47 mutation is significantly associated with the RNA expression of many other genes, with 236 significant associations in total. SKCM shows the largest number of these associations.

The most reproducible SLC25A47-associated genes across cancer lineages are IFNA10, RNU6-165P, and MARK2P12. Each is linked with SLC25A47 in more than 2 cancer types. Because this analysis shows association rather than direction, both SLC25A47-to-partner and partner-to-SLC25A47 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, IFNA10 grouped by SLC25A47-low versus SLC25A47-high in SCLC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SLC25A47→partner) and Y-score (partner→SLC25A47) 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
SCLCIFNA10 →+0.101+4.847<.001.00933
HNSCRNU6-165P →+0.345+5.936<.001.00133
LUADMARK2P12 →+0.147+4.575<.001.00132
SKCMRPSAP37 →+0.018+3.282<.001.00532
CESCNF1P3 →+0.473+4.669<.001.00732
HNSCMIR520C →+0.387+4.655<.001.00732
Each partner links to its Q-omics profile. Showing the 6 strongest of 236 associations by consensus.

IFNA10 by SLC25A47 expression — SCLC

Box plot of IFNA10 in SLC25A47-low vs SLC25A47-high samples in SCLC.

Explore this box plot interactively →

Exploration