Q-omics provides the consensus-scored LDLRAD4-AS1 profile across patient tissues and cancer cell-line models. LDLRAD4-AS1 expression is associated with patient survival in 19 of 34 cancer types, with the highest sampling consensus in KICH. Among the 18 cancer types available for tumor–normal comparison, LDLRAD4-AS1 is differentially expressed in 14, with the highest sampling consensus in LUSC. Additionally, LDLRAD4-AS1 RNA expression shows 13,862 significant gene co-expression associations, with the highest sampling consensus in ESCA. Together, these results highlight KICH, LUSC, and ESCA as cancer lineages where LDLRAD4-AS1 shows reproducible signals across survival, tumor–normal expression, and patient cross-omics analyses.
Every result is evaluated using two consensus scores. Sampling consensus measures how consistently a finding is reproduced within a cancer lineage across different conditions. Lineage consensus measures how broadly the result is shared across cancer types, distinguishing pan-cancer signals from lineage-specific patterns.
Premium analyses for LDLRAD4-AS1 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes LDLRAD4-AS1 survival associations across molecular data types. LDLRAD4-AS1 RNA expression shows survival associations in the most cancer types (19). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible LDLRAD4-AS1 RNA expression–survival associations across cancer types. High LDLRAD4-AS1 expression shows unfavorable associations in KICH and UVM, but favorable associations in LUAD, KIRC, LIHC and ACC. The KICH Kaplan–Meier curve shows clear separation, with the high-expression group declining faster, consistent with the unfavorable association (log-rank p = .001). Together, the overview and detailed table identify KICH as the clearest survival context for LDLRAD4-AS1 RNA expression.
This table summarizes LDLRAD4-AS1 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 14. The strongest signals are observed in LUSC for RNA.
This table ranks reproducible tumor–normal expression differences for LDLRAD4-AS1. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. LDLRAD4-AS1 shows lower tumor expression in LUSC, THCA, KIRP, HNSC, COAD and UCEC. The LUSC box plot shows higher LDLRAD4-AS1 RNA expression in normal versus tumor tissue (log2 FC = −0.483, t-test p < 0.001).
This table shows molecular features associated with LDLRAD4-AS1 in patient tissues and cancer cell lines. In patient samples, LDLRAD4-AS1 shows the broadest associations at the RNA and protein expression levels, with ESCA recurring as the lineage with the largest associated feature set.
