SAMD14

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

Across TCGA cell cohorts, SAMD14 mutation is significantly associated with the RNA expression of many other genes, with 15 significant associations in total. SKIN shows the largest number of these associations.

The most reproducible SAMD14-associated genes across cancer lineages are NPVF, GLYATL3, and KLF18. Each is linked with SAMD14 in more than 1 cancer types. Because this analysis shows association rather than direction, both SAMD14-to-partner and partner-to-SAMD14 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, NPVF grouped by SAMD14-low versus SAMD14-high in KIDNEY.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SAMD14→partner) and Y-score (partner→SAMD14) 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
KIDNEYNPVF →+0.020+5.000<.001.00531
KIDNEYGLYATL3 →+0.043+5.000<.001.00531
KIDNEYKLF18 →+0.006+5.000<.001.00531
LARGE_INTESTINEOR10Q1 →+0.101+3.920.003.00531
LARGE_INTESTINEOR52B6 →+0.081+3.920<.001.00531
BLOOD_LeukemiaMAGEB4 →+0.046+4.705<.001.00331
Each partner links to its Q-omics profile. Showing the 6 strongest of 15 associations by consensus.

NPVF by SAMD14 expression — KIDNEY

Box plot of NPVF in SAMD14-low vs SAMD14-high samples in KIDNEY.

Explore this box plot interactively →

Exploration