long intergenic non-protein coding RNA 1808Genealiases: []
Q-omics provides the consensus-scored LINC01808 profile across patient tissues and cancer cell-line models. LINC01808 expression is associated with patient survival in 9 of 34 cancer types, with the highest sampling consensus in KICH. Among the 18 cancer types available for tumor–normal comparison, LINC01808 is differentially expressed in 2, with the highest sampling consensus in BLCA. Additionally, LINC01808 RNA expression shows 5,317 significant pathway-activity associations, with the highest sampling consensus in STAD. Together, these results highlight KICH, BLCA, and STAD as cancer lineages where LINC01808 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 LINC01808 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes LINC01808 survival associations across molecular data types. LINC01808 RNA expression shows survival associations in the most cancer types (9). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible LINC01808 RNA expression–survival associations across cancer types. High LINC01808 expression shows unfavorable associations in KICH, READ, ACC, UVM and PCPG, but favorable associations in BRCA. The KICH 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 KICH as the clearest survival context for LINC01808 RNA expression.
This table summarizes LINC01808 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 2. The strongest signals are observed in BLCA for RNA.
This table ranks reproducible tumor–normal expression differences for LINC01808. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. LINC01808 shows higher tumor expression in BLCA and LUSC. The BLCA box plot shows higher LINC01808 RNA expression in tumor versus normal tissue (log2 FC = +0.104, t-test p = .045).
This table shows molecular features associated with LINC01808 in patient tissues and cancer cell lines. In patient samples, LINC01808 shows the broadest associations at the RNA and protein expression levels, with STAD recurring as the lineage with the largest associated feature set.
