SLC39A11

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

Across TCGA patient cohorts, SLC39A11 mutation is significantly associated with the RNA expression of many other genes, with 2,397 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SLC39A11-associated genes across cancer lineages are RNU5E-9P, PDE4DIPP3, and OR5H5P. Each is linked with SLC39A11 in more than 1 cancer types. Because this analysis shows association rather than direction, both SLC39A11-to-partner and partner-to-SLC39A11 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, RNU5E-9P grouped by SLC39A11-low versus SLC39A11-high in COAD.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SLC39A11→partner) and Y-score (partner→SLC39A11) 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
COADRNU5E-9P →+0.251+5.087<.001.00232
COADPDE4DIPP3 →+0.033+3.271.008.00932
STADOR5H5P →+0.155+5.070<.001.00432
CESCMIR7-3 →+0.370+6.342<.001.00132
CESCDNMT3AP1 →+0.030+5.418<.001.00532
UCECHIRA →+0.479+3.732<.001<.00132
Each partner links to its Q-omics profile. Showing the 6 strongest of 2,397 associations by consensus.

RNU5E-9P by SLC39A11 expression — COAD

Box plot of RNU5E-9P in SLC39A11-low vs SLC39A11-high samples in COAD.

Explore this box plot interactively →

Exploration