SLC39A4

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

Across TCGA cell cohorts, SLC39A4 mutation is significantly associated with the RNA expression of many other genes, with 22 significant associations in total. BLOOD_Leukemia shows the largest number of these associations.

The most reproducible SLC39A4-associated genes across cancer lineages are METTL21C, FAM205A, and AVP. Each is linked with SLC39A4 in more than 1 cancer types. Because this analysis shows association rather than direction, both SLC39A4-to-partner and partner-to-SLC39A4 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, METTL21C grouped by SLC39A4-low versus SLC39A4-high in BLOOD_Myeloma.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SLC39A4→partner) and Y-score (partner→SLC39A4) 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
BLOOD_MyelomaMETTL21C →+0.041+3.716.008.00531
BLOOD_MyelomaFAM205A →+0.027+3.977<.001.00631
CNSAVP →+0.083+4.981<.001.00831
LUNG_SCLCATP6V1G3 →+0.287+4.269.006.00531
LUNG_SCLCRBMY1F →+0.782+4.643<.001.00431
LARGE_INTESTINEPTH →+0.033+3.099.001.00231
Each partner links to its Q-omics profile. Showing the 6 strongest of 22 associations by consensus.

METTL21C by SLC39A4 expression — BLOOD_Myeloma

Box plot of METTL21C in SLC39A4-low vs SLC39A4-high samples in BLOOD_Myeloma.

Explore this box plot interactively →

Exploration