long intergenic non-protein coding RNA 2328Genealiases: []
Q-omics provides the consensus-scored LINC02328 profile across patient tissues and cancer cell-line models. LINC02328 expression is associated with patient survival in 25 of 34 cancer types, with the highest sampling consensus in SKCM. Among the 18 cancer types available for tumor–normal comparison, LINC02328 is differentially expressed in 14, with the highest sampling consensus in HNSC. Additionally, LINC02328 RNA expression shows 17,476 significant gene co-expression associations, with the highest sampling consensus in UVM. Together, these results highlight SKCM, HNSC, and UVM as cancer lineages where LINC02328 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 LINC02328 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes LINC02328 survival associations across molecular data types. LINC02328 RNA expression shows survival associations in the most cancer types (25). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible LINC02328 RNA expression–survival associations across cancer types. High LINC02328 expression shows unfavorable associations in KIRP, KIRC, UVM and HNSC, but favorable associations in SKCM and UCS. The SKCM Kaplan–Meier curve shows clear separation, with the low-expression group declining faster, consistent with the favorable association (log-rank p < 0.001). Together, the overview and detailed table identify SKCM as the clearest survival context for LINC02328 RNA expression.
This table summarizes LINC02328 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 HNSC for RNA.
This table ranks reproducible tumor–normal expression differences for LINC02328. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. LINC02328 shows lower tumor expression in LUAD, KICH, COAD and BRCA and higher tumor expression in HNSC and KIRC. The HNSC box plot shows higher LINC02328 RNA expression in tumor versus normal tissue (log2 FC = +1.258, t-test p < 0.001).
This table shows molecular features associated with LINC02328 in patient tissues and cancer cell lines. In patient samples, LINC02328 shows the broadest associations at the RNA and protein expression levels, with UVM recurring as the lineage with the largest associated feature set.
