long intergenic non-protein coding RNA 492Genealiases: []
Q-omics provides the consensus-scored LINC00492 profile across patient tissues and cancer cell-line models. LINC00492 expression is associated with patient survival in 16 of 34 cancer types, with the highest sampling consensus in KICH. Among the 18 cancer types available for tumor–normal comparison, LINC00492 is differentially expressed in 5, with the highest sampling consensus in KIRC. Additionally, LINC00492 RNA expression shows 8,502 significant gene co-expression associations, with the highest sampling consensus in THYM. Together, these results highlight KICH, KIRC, and THYM as cancer lineages where LINC00492 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 LINC00492 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes LINC00492 survival associations across molecular data types. LINC00492 RNA expression shows survival associations in the most cancer types (16). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible LINC00492 RNA expression–survival associations across cancer types. High LINC00492 expression shows unfavorable associations in KICH, DLBC, COAD, UCS and UCEC, but favorable associations in ESCA. The KICH 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 KICH as the clearest survival context for LINC00492 RNA expression.
This table summarizes LINC00492 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 KIRC for RNA.
This table ranks reproducible tumor–normal expression differences for LINC00492. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. LINC00492 shows lower tumor expression in KIRC, HNSC, KICH and KIRP and higher tumor expression in LUSC. The KIRC box plot shows higher LINC00492 RNA expression in normal versus tumor tissue (log2 FC = −0.154, t-test p < 0.001).
This table shows molecular features associated with LINC00492 in patient tissues and cancer cell lines. In patient samples, LINC00492 shows the broadest associations at the RNA and protein expression levels, with THYM recurring as the lineage with the largest associated feature set.
