HSDL2

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

Across TCGA patient cohorts, HSDL2 mutation is significantly associated with the total protein of many other genes, with 8 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible HSDL2-associated genes across cancer lineages are SCD, Shc_pY317, and CD49b. Each is linked with HSDL2 in more than 1 cancer types. Because this analysis shows association rather than direction, both HSDL2-to-partner and partner-to-HSDL2 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, SCD grouped by HSDL2-low versus HSDL2-high in UCEC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (HSDL2→partner) and Y-score (partner→HSDL2) 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
UCECSCD →-0.168-2.990.003.03631
UCECShc_pY317 →-0.193-3.321.015.01031
UCECCD49b →-0.475-3.150.001.01931
UCECGab2 →+0.380+3.321.042.01021
UCECAxl →+0.286+2.818.016.03521
UCECVHL →-1.097-3.000.002.03621
Each partner links to its Q-omics profile. Showing the 6 strongest of 8 associations by consensus.

SCD by HSDL2 expression — UCEC

Box plot of SCD in HSDL2-low vs HSDL2-high samples in UCEC.

Explore this box plot interactively →

Exploration