SPTBN1

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

Across TCGA cell cohorts, SPTBN1 mutation is significantly associated with the mutation status of many other genes, with 5,869 significant associations in total. LARGE_INTESTINE shows the largest number of these associations.

The most reproducible SPTBN1-associated genes across cancer lineages are KDM5A, SPEN, and UBE4B. Each is linked with SPTBN1 in more than 6 cancer types. Because this analysis shows association rather than direction, both SPTBN1-to-partner and partner-to-SPTBN1 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, KDM5A grouped by SPTBN1-low versus SPTBN1-high in BLOOD_Lymphoma.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SPTBN1→partner) and Y-score (partner→SPTBN1) 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_LymphomaKDM5A →+3.554+3.731.003.00317
PANCREASSPEN →+3.321+3.614.006.00616
BLOOD_LymphomaUBE4B →+2.969+3.337.009.00916
OVARYTLN1 →+4.196+2.632.002.00216
BREASTSACS →+4.807+3.857.002.00216
BLOOD_LymphomaTNXB →+2.269+3.287.007.00716
Each partner links to its Q-omics profile. Showing the 6 strongest of 5,869 associations by consensus.

KDM5A by SPTBN1 expression — BLOOD_Lymphoma

Box plot of KDM5A in SPTBN1-low vs SPTBN1-high samples in BLOOD_Lymphoma.

Explore this box plot interactively →

Exploration