Q-omics provides the consensus-scored LINC01230 profile across patient tissues and cancer cell-line models. LINC01230 expression is associated with patient survival in 20 of 34 cancer types, with the highest sampling consensus in ACC. Among the 18 cancer types available for tumor–normal comparison, LINC01230 is differentially expressed in 10, with the highest sampling consensus in KIRC. Additionally, LINC01230 RNA expression shows 6,958 significant pathway-activity associations, with the highest sampling consensus in STAD. Together, these results highlight ACC, KIRC, and STAD as cancer lineages where LINC01230 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 LINC01230 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes LINC01230 survival associations across molecular data types. LINC01230 RNA expression shows survival associations in the most cancer types (20). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible LINC01230 RNA expression–survival associations across cancer types. High LINC01230 expression shows unfavorable associations in ACC, KIRC, KIRP and LGG, but favorable associations in BRCA and UVM. The ACC 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 ACC as the clearest survival context for LINC01230 RNA expression.
This table summarizes LINC01230 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 LINC01230. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. LINC01230 shows lower tumor expression in KIRC, KIRP, BRCA, COAD and READ and higher tumor expression in KICH. The KIRC box plot shows higher LINC01230 RNA expression in normal versus tumor tissue (log2 FC = −2.696, t-test p < 0.001).
This table shows molecular features associated with LINC01230 in patient tissues and cancer cell lines. In patient samples, LINC01230 shows the broadest associations at the RNA and protein expression levels, with STAD recurring as the lineage with the largest associated feature set.
