PALLD

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

Across TCGA cell cohorts, PALLD mutation is significantly associated with the mutation status of many other genes, with 2,767 significant associations in total. LARGE_INTESTINE shows the largest number of these associations.

The most reproducible PALLD-associated genes across cancer lineages are SLC4A4, ESPL1, and APEH. Each is linked with PALLD in more than 4 cancer types. Because this analysis shows association rather than direction, both PALLD-to-partner and partner-to-PALLD results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, SLC4A4 grouped by PALLD-low versus PALLD-high in BLOOD_Leukemia.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (PALLD→partner) and Y-score (partner→PALLD) 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_LeukemiaSLC4A4 →+4.894+5.870<.001<.00115
STOMACHESPL1 →+4.025+2.942.009.00914
LARGE_INTESTINEAPEH →+4.372+2.611<.001<.00114
SKINDNHD1 →+3.357+3.532.005.00514
BLOOD_LeukemiaMGRN1 →+4.894+4.894.004.00414
BLOOD_LeukemiaOAS2 →+4.894+4.894.004.00414
Each partner links to its Q-omics profile. Showing the 6 strongest of 2,767 associations by consensus.

SLC4A4 by PALLD expression — BLOOD_Leukemia

Box plot of SLC4A4 in PALLD-low vs PALLD-high samples in BLOOD_Leukemia.

Explore this box plot interactively →

Exploration