long intergenic non-protein coding RNA 2828Genealiases: []
Q-omics provides the consensus-scored LINC02828 profile across patient tissues and cancer cell-line models. LINC02828 expression is associated with patient survival in 18 of 34 cancer types, with the highest sampling consensus in LGG. Among the 18 cancer types available for tumor–normal comparison, LINC02828 is differentially expressed in 9, with the highest sampling consensus in KIRC. Additionally, LINC02828 RNA expression shows 11,059 significant gene co-expression associations, with the highest sampling consensus in SARC. Together, these results highlight LGG, KIRC, and SARC as cancer lineages where LINC02828 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 LINC02828 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes LINC02828 survival associations across molecular data types. LINC02828 RNA expression shows survival associations in the most cancer types (18). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible LINC02828 RNA expression–survival associations across cancer types. High LINC02828 expression shows unfavorable associations in LGG, OV, STAD, KIRC and GBM, but favorable associations in SKCM. The LGG 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 LGG as the clearest survival context for LINC02828 RNA expression.
This table summarizes LINC02828 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 9. The strongest signals are observed in KIRC for RNA.
This table ranks reproducible tumor–normal expression differences for LINC02828. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. LINC02828 shows lower tumor expression in LUSC and LUAD and higher tumor expression in KIRC, KIRP, THCA and HNSC. The KIRC box plot shows higher LINC02828 RNA expression in tumor versus normal tissue (log2 FC = +0.567, t-test p < 0.001).
This table shows molecular features associated with LINC02828 in patient tissues and cancer cell lines. In patient samples, LINC02828 shows the broadest associations at the RNA and protein expression levels, with SARC recurring as the lineage with the largest associated feature set.
