SAMD1

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

Across TCGA patient cohorts, SAMD1 mutation is significantly associated with the RNA expression of many other genes, with 99 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SAMD1-associated genes across cancer lineages are NEK6, NRG2, and PRCD. Each is linked with SAMD1 in more than 1 cancer types. Because this analysis shows association rather than direction, both SAMD1-to-partner and partner-to-SAMD1 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, NEK6 grouped by SAMD1-low versus SAMD1-high in SCLC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SAMD1→partner) and Y-score (partner→SAMD1) 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
SCLCNEK6 →+2.674+3.921.001.00131
SCLCNRG2 →+1.134+3.009<.001.00331
SCLCPRCD →+0.306+3.921.006.00131
CESCRN7SL415P →+0.143+5.812<.001.00331
CESCRPS27P12 →+0.211+5.969<.001.00231
CESCRN7SL314P →+0.174+6.569<.001.00131
Each partner links to its Q-omics profile. Showing the 6 strongest of 99 associations by consensus.

NEK6 by SAMD1 expression — SCLC

Box plot of NEK6 in SAMD1-low vs SAMD1-high samples in SCLC.

Explore this box plot interactively →

Exploration