SLC18A2

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

Across TCGA patient cohorts, SLC18A2 mutation is significantly associated with the RNA expression of many other genes, with 2,905 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SLC18A2-associated genes across cancer lineages are RN7SKP245, STARD4, and DDIT4. Each is linked with SLC18A2 in more than 2 cancer types. Because this analysis shows association rather than direction, both SLC18A2-to-partner and partner-to-SLC18A2 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, RN7SKP245 grouped by SLC18A2-low versus SLC18A2-high in CESC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SLC18A2→partner) and Y-score (partner→SLC18A2) 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
CESCRN7SKP245 →+0.106+4.812<.001<.00133
SKCMSTARD4 →+0.856+2.603.004.00533
UCECDDIT4 →+1.036+2.459<.001<.00133
UCECTRABD →+0.377+4.119.009<.00133
UCECTYMS →+0.759+3.095.001<.00133
UCECRCC1 →+0.391+2.595.009.00533
Each partner links to its Q-omics profile. Showing the 6 strongest of 2,905 associations by consensus.

RN7SKP245 by SLC18A2 expression — CESC

Box plot of RN7SKP245 in SLC18A2-low vs SLC18A2-high samples in CESC.

Explore this box plot interactively →

Exploration