SLC6A7

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

Across TCGA patient cohorts, SLC6A7 mutation is significantly associated with the RNA expression of many other genes, with 1,041 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SLC6A7-associated genes across cancer lineages are NOP2, KRT8P49, and RNU6-548P. Each is linked with SLC6A7 in more than 2 cancer types. Because this analysis shows association rather than direction, both SLC6A7-to-partner and partner-to-SLC6A7 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, NOP2 grouped by SLC6A7-low versus SLC6A7-high in SKCM.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SLC6A7→partner) and Y-score (partner→SLC6A7) 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
SKCMNOP2 →+0.333+3.604.009.00133
UCECKRT8P49 →+0.240+2.669<.001.00432
SKCMRNU6-548P →+0.604+2.402.001.00532
CESCNMD3P2 →+0.047+5.010.001.00932
SKCMATP5MD →+0.367+3.208.004.00932
SKCMFCER1A →-0.675-3.559.006.00232
Each partner links to its Q-omics profile. Showing the 6 strongest of 1,041 associations by consensus.

NOP2 by SLC6A7 expression — SKCM

Box plot of NOP2 in SLC6A7-low vs SLC6A7-high samples in SKCM.

Explore this box plot interactively →

Exploration