NELFCD

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

Across TCGA patient cohorts, NELFCD mutation is significantly associated with the total protein of many other genes, with 36 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible NELFCD-associated genes across cancer lineages are GAPDH, PCNA, and Shc_pY317. Each is linked with NELFCD in more than 1 cancer types. Because this analysis shows association rather than direction, both NELFCD-to-partner and partner-to-NELFCD results are reported.

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

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (NELFCD→partner) and Y-score (partner→NELFCD) 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
UCECGAPDH →+0.518+2.700.008.00532
UCECPCNA →+0.228+1.847.003.00832
UCECShc_pY317 →-0.123-1.807.027.02532
UCECSTAT3_pY705 →-0.259-1.896.007.01532
UCECASNS →+0.465+1.807<.001.02532
UCECATM →-0.384-1.847.021.00832
Each partner links to its Q-omics profile. Showing the 6 strongest of 36 associations by consensus.

GAPDH by NELFCD expression — UCEC

Box plot of GAPDH in NELFCD-low vs NELFCD-high samples in UCEC.

Explore this box plot interactively →

Exploration