SLC39A2

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

Across TCGA cell cohorts, SLC39A2 mutation is significantly associated with the RNA expression of many other genes, with 4 significant associations in total. BLOOD_Leukemia shows the largest number of these associations.

The most reproducible SLC39A2-associated genes across cancer lineages are SLC15A5, OR10H5, and SYCN. Each is linked with SLC39A2 in more than 1 cancer types. Because this analysis shows association rather than direction, both SLC39A2-to-partner and partner-to-SLC39A2 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, SLC15A5 grouped by SLC39A2-low versus SLC39A2-high in LARGE_INTESTINE.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SLC39A2→partner) and Y-score (partner→SLC39A2) 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
LARGE_INTESTINESLC15A5 →+0.017+4.415<.001.00731
BLOOD_LeukemiaOR10H5 →+0.070+4.922<.001.00931
BLOOD_LeukemiaSYCN →+0.047+5.539<.001.00331
BLOOD_LeukemiaUSP17L3 →+0.012+4.922.009.00931
Each partner links to its Q-omics profile. Showing the 4 strongest of 4 associations by consensus.

SLC15A5 by SLC39A2 expression — LARGE_INTESTINE

Box plot of SLC15A5 in SLC39A2-low vs SLC39A2-high samples in LARGE_INTESTINE.

Explore this box plot interactively →

Exploration