long intergenic non-protein coding RNA 2122Genealiases: []
Q-omics provides the consensus-scored LINC02122 profile across patient tissues and cancer cell-line models. LINC02122 expression is associated with patient survival in 17 of 34 cancer types, with the highest sampling consensus in UCS. Among the 18 cancer types available for tumor–normal comparison, LINC02122 is differentially expressed in 6, with the highest sampling consensus in LUAD. Additionally, LINC02122 RNA expression shows 6,733 significant gene co-expression associations, with the highest sampling consensus in LIHC. Together, these results highlight UCS, LUAD, and LIHC as cancer lineages where LINC02122 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 LINC02122 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes LINC02122 survival associations across molecular data types. LINC02122 RNA expression shows survival associations in the most cancer types (17). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible LINC02122 RNA expression–survival associations across cancer types. High LINC02122 expression shows unfavorable associations in UCS, LGG, UCEC, LAML, READ and KIRC. The UCS Kaplan–Meier curve shows clear separation, with the high-expression group declining faster, consistent with the unfavorable association (log-rank p = .002). Together, the overview and detailed table identify UCS as the clearest survival context for LINC02122 RNA expression.
This table summarizes LINC02122 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 6. The strongest signals are observed in LUAD for RNA.
This table ranks reproducible tumor–normal expression differences for LINC02122. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. LINC02122 shows lower tumor expression in HNSC and KIRC and higher tumor expression in LUAD, BLCA, BRCA and KICH. The LUAD box plot shows higher LINC02122 RNA expression in tumor versus normal tissue (log2 FC = +0.994, t-test p < 0.001).
This table shows molecular features associated with LINC02122 in patient tissues and cancer cell lines. In patient samples, LINC02122 shows the broadest associations at the RNA and protein expression levels, with LIHC recurring as the lineage with the largest associated feature set.
