PALLD

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

Across TCGA patient cohorts, PALLD mutation is significantly associated with the RNA expression of many other genes, with 5,743 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible PALLD-associated genes across cancer lineages are HASPIN, CTNS, and RFC2. Each is linked with PALLD in more than 2 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, HASPIN grouped by PALLD-low versus PALLD-high in UCEC.

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
UCECHASPIN →+0.791+2.925<.001<.00133
UCECCTNS →+0.374+1.743<.001<.00133
UCECRFC2 →+0.381+1.960<.001<.00133
UCECMTHFD2 →+0.520+1.890.001.00133
HNSCRN7SL306P →+0.209+4.245<.001.00833
UCECRPL23AP82 →+0.481+2.936<.001<.00133
Each partner links to its Q-omics profile. Showing the 6 strongest of 5,743 associations by consensus.

HASPIN by PALLD expression — UCEC

Box plot of HASPIN in PALLD-low vs PALLD-high samples in UCEC.

Explore this box plot interactively →

Exploration