SFTPB

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

Across TCGA patient cohorts, SFTPB mutation is significantly associated with the RNA expression of many other genes, with 489 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SFTPB-associated genes across cancer lineages are DNM1P24, RN7SL185P, and PKN3. Each is linked with SFTPB in more than 1 cancer types. Because this analysis shows association rather than direction, both SFTPB-to-partner and partner-to-SFTPB results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, DNM1P24 grouped by SFTPB-low versus SFTPB-high in HNSC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SFTPB→partner) and Y-score (partner→SFTPB) 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
HNSCDNM1P24 →+0.094+7.954<.001.00832
HNSCRN7SL185P →+0.134+7.954<.001.00832
UCECPKN3 →+0.633+2.818.004.00132
UCECACOT7 →+0.658+3.337.009.00532
UCECMYO9B →+0.434+2.828.006.00132
UCECTTC24 →+0.233+3.392.005.00632
Each partner links to its Q-omics profile. Showing the 6 strongest of 489 associations by consensus.

DNM1P24 by SFTPB expression — HNSC

Box plot of DNM1P24 in SFTPB-low vs SFTPB-high samples in HNSC.

Explore this box plot interactively →

Exploration