SLC44A2

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

Across TCGA patient cohorts, SLC44A2 mutation is significantly associated with the RNA expression of many other genes, with 3,492 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SLC44A2-associated genes across cancer lineages are RNU4-14P, PYGB, and CENPT. Each is linked with SLC44A2 in more than 2 cancer types. Because this analysis shows association rather than direction, both SLC44A2-to-partner and partner-to-SLC44A2 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, RNU4-14P grouped by SLC44A2-low versus SLC44A2-high in HNSC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SLC44A2→partner) and Y-score (partner→SLC44A2) 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
HNSCRNU4-14P →+0.469+4.084<.001.00533
UCECPYGB →+0.418+1.805.001.00732
UCECCENPT →+0.282+2.055.007.00532
UCECCORO2B →-0.506-2.662.004<.00132
UCECBLOC1S6 →+0.399+1.923.004.00932
UCECGPI →+0.537+1.847<.001<.00132
Each partner links to its Q-omics profile. Showing the 6 strongest of 3,492 associations by consensus.

RNU4-14P by SLC44A2 expression — HNSC

Box plot of RNU4-14P in SLC44A2-low vs SLC44A2-high samples in HNSC.

Explore this box plot interactively →

Exploration