long intergenic non-protein coding RNA 1709Genealiases: []
Q-omics provides the consensus-scored LINC01709 profile across patient tissues and cancer cell-line models. LINC01709 expression is associated with patient survival in 16 of 34 cancer types, with the highest sampling consensus in LIHC. Among the 18 cancer types available for tumor–normal comparison, LINC01709 is differentially expressed in 1, with the highest sampling consensus in COAD. Additionally, LINC01709 RNA expression shows 5,893 significant pathway-activity associations, with the highest sampling consensus in STAD. Together, these results highlight LIHC, COAD, and STAD as cancer lineages where LINC01709 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 LINC01709 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes LINC01709 survival associations across molecular data types. LINC01709 RNA expression shows survival associations in the most cancer types (16). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible LINC01709 RNA expression–survival associations across cancer types. High LINC01709 expression shows unfavorable associations in LIHC, KICH, STAD, DLBC and KIRC, but favorable associations in HNSC. The LIHC Kaplan–Meier curve shows clear separation, with the high-expression group declining faster, consistent with the unfavorable association (log-rank p < 0.001). Together, the overview and detailed table identify LIHC as the clearest survival context for LINC01709 RNA expression.
This table summarizes LINC01709 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 1. The strongest signals are observed in COAD for RNA.
This table ranks reproducible tumor–normal expression differences for LINC01709. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. LINC01709 shows higher tumor expression in COAD. The COAD box plot shows higher LINC01709 RNA expression in tumor versus normal tissue (log2 FC = +0.122, t-test p = .007).
This table shows molecular features associated with LINC01709 in patient tissues and cancer cell lines. In patient samples, LINC01709 shows the broadest associations at the RNA and protein expression levels, with STAD recurring as the lineage with the largest associated feature set.
