long intergenic non-protein coding RNA 2772Genealiases: []
Q-omics provides the consensus-scored LINC02772 profile across patient tissues and cancer cell-line models. LINC02772 expression is associated with patient survival in 18 of 34 cancer types, with the highest sampling consensus in LUSC. Among the 18 cancer types available for tumor–normal comparison, LINC02772 is differentially expressed in 10, with the highest sampling consensus in LUAD. Additionally, LINC02772 RNA expression shows 9,940 significant gene co-expression associations, with the highest sampling consensus in TGCT. Together, these results highlight LUSC, LUAD, and TGCT as cancer lineages where LINC02772 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 LINC02772 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes LINC02772 survival associations across molecular data types. LINC02772 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 LINC02772 RNA expression–survival associations across cancer types. High LINC02772 expression shows unfavorable associations in LUSC, KIRC, HNSC, KIRP, LGG and BRCA. The LUSC 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 LUSC as the clearest survival context for LINC02772 RNA expression.
This table summarizes LINC02772 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 10. The strongest signals are observed in KIRC for RNA.
This table ranks reproducible tumor–normal expression differences for LINC02772. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. LINC02772 shows lower tumor expression in LUAD, KIRC, KIRP and LUSC and higher tumor expression in KICH and COAD. The LUAD box plot shows higher LINC02772 RNA expression in normal versus tumor tissue (log2 FC = −2.188, t-test p < 0.001).
This table shows molecular features associated with LINC02772 in patient tissues and cancer cell lines. In patient samples, LINC02772 shows the broadest associations at the RNA and protein expression levels, with TGCT recurring as the lineage with the largest associated feature set.
