SPTY2D1

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

Across TCGA patient cohorts, SPTY2D1 mutation is significantly associated with the RNA expression of many other genes, with 3,110 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SPTY2D1-associated genes across cancer lineages are ANKRD20A6P, SNORD127, and ADAD1. Each is linked with SPTY2D1 in more than 2 cancer types. Because this analysis shows association rather than direction, both SPTY2D1-to-partner and partner-to-SPTY2D1 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, ANKRD20A6P grouped by SPTY2D1-low versus SPTY2D1-high in READ.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SPTY2D1→partner) and Y-score (partner→SPTY2D1) 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
READANKRD20A6P →+0.224+4.341<.001.00733
COADSNORD127 →+0.918+3.015<.001.00533
BRCAADAD1 →+0.163+3.264<.001.00933
UCECTHAP3 →+0.252+1.839.001.00233
UCECPSMB6 →+0.349+1.941<.001<.00133
BLCAOR7E31P →+0.073+3.423<.001.00632
Each partner links to its Q-omics profile. Showing the 6 strongest of 3,110 associations by consensus.

ANKRD20A6P by SPTY2D1 expression — READ

Box plot of ANKRD20A6P in SPTY2D1-low vs SPTY2D1-high samples in READ.

Explore this box plot interactively →

Exploration