SAMD8

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

Across TCGA cell cohorts, SAMD8 mutation is significantly associated with the RNA expression of many other genes, with 3 significant associations in total. BLOOD_Leukemia shows the largest number of these associations.

The most reproducible SAMD8-associated genes across cancer lineages are PPP1R2C, OR9K2, and REC114. Each is linked with SAMD8 in more than 1 cancer types. Because this analysis shows association rather than direction, both SAMD8-to-partner and partner-to-SAMD8 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, PPP1R2C grouped by SAMD8-low versus SAMD8-high in BLOOD_Leukemia.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SAMD8→partner) and Y-score (partner→SAMD8) 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_LeukemiaPPP1R2C →+0.240+4.539<.001.00731
BLOOD_LeukemiaOR9K2 →+0.021+4.539<.001.00731
BLOOD_LeukemiaREC114 →+0.179+4.409<.001.00531
Each partner links to its Q-omics profile. Showing the 3 strongest of 3 associations by consensus.

PPP1R2C by SAMD8 expression — BLOOD_Leukemia

Box plot of PPP1R2C in SAMD8-low vs SAMD8-high samples in BLOOD_Leukemia.

Explore this box plot interactively →

Exploration