long intergenic non-protein coding RNA 2108Genealiases: []
Q-omics provides the consensus-scored LINC02108 profile across patient tissues and cancer cell-line models. LINC02108 expression is associated with patient survival in 11 of 34 cancer types, with the highest sampling consensus in COAD. Among the 18 cancer types available for tumor–normal comparison, LINC02108 is differentially expressed in 5, with the highest sampling consensus in STAD. Additionally, LINC02108 RNA expression shows 5,886 significant pathway-activity associations, with the highest sampling consensus in STAD. Together, these results highlight COAD, and STAD as cancer lineages where LINC02108 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 LINC02108 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes LINC02108 survival associations across molecular data types. LINC02108 RNA expression shows survival associations in the most cancer types (11). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible LINC02108 RNA expression–survival associations across cancer types. High LINC02108 expression shows unfavorable associations in COAD, OV, READ, LIHC, KIRP and UVM. The COAD 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 COAD as the clearest survival context for LINC02108 RNA expression.
This table summarizes LINC02108 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 5. The strongest signals are observed in STAD for RNA.
This table ranks reproducible tumor–normal expression differences for LINC02108. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. LINC02108 shows higher tumor expression in STAD, HNSC, LUSC, BLCA and COAD. The STAD box plot shows higher LINC02108 RNA expression in tumor versus normal tissue (log2 FC = +0.107, t-test p = .005).
This table shows molecular features associated with LINC02108 in patient tissues and cancer cell lines. In patient samples, LINC02108 shows the broadest associations at the RNA and protein expression levels, with STAD recurring as the lineage with the largest associated feature set.
