SLC9A8

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

Across TCGA cell cohorts, SLC9A8 mutation is significantly associated with the RNA expression of many other genes, with 31 significant associations in total. LARGE_INTESTINE shows the largest number of these associations.

The most reproducible SLC9A8-associated genes across cancer lineages are LGI1, C1QL2, and TAAR6. Each is linked with SLC9A8 in more than 1 cancer types. Because this analysis shows association rather than direction, both SLC9A8-to-partner and partner-to-SLC9A8 results are reported.

Each partner links to its own Q-omics profile.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SLC9A8→partner) and Y-score (partner→SLC9A8) 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_LeukemiaLGI1 →+0.129+5.539<.001.00331
BLOOD_LeukemiaC1QL2 →+0.019+4.922<.001.00931
BLOOD_LeukemiaTAAR6 →+0.012+4.922.001.00931
BLOOD_LeukemiaBPIFB6 →+0.063+5.969<.001.00131
BLOOD_LeukemiaOR4F15 →+0.006+5.201<.001.00631
BLOOD_LeukemiaSPPL2C →+0.012+4.922<.001.00931
Each partner links to its Q-omics profile. Showing the 6 strongest of 31 associations by consensus.

Exploration