long intergenic non-protein coding RNA 1831Genealiases: []
Q-omics provides the consensus-scored LINC01831 profile across patient tissues and cancer cell-line models. LINC01831 expression is associated with patient survival in 11 of 34 cancer types, with the highest sampling consensus in KIRC. Among the 18 cancer types available for tumor–normal comparison, LINC01831 is differentially expressed in 5, with the highest sampling consensus in KIRC. Additionally, LINC01831 RNA expression shows 5,871 significant pathway-activity associations, with the highest sampling consensus in STAD. Together, these results highlight KIRC, and STAD as cancer lineages where LINC01831 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 LINC01831 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes LINC01831 survival associations across molecular data types. LINC01831 RNA expression shows survival associations in the most cancer types (11). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible LINC01831 RNA expression–survival associations across cancer types. High LINC01831 expression shows unfavorable associations in KIRC, LGG, COAD, KICH, BRCA and LUAD. The KIRC 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 KIRC as the clearest survival context for LINC01831 RNA expression.
This table summarizes LINC01831 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 LINC01831. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. LINC01831 shows lower tumor expression in KIRC, KICH, LIHC, KIRP and CHOL. The KIRC box plot shows higher LINC01831 RNA expression in normal versus tumor tissue (log2 FC = −0.752, t-test p < 0.001).
This table shows molecular features associated with LINC01831 in patient tissues and cancer cell lines. In patient samples, LINC01831 shows the broadest associations at the RNA and protein expression levels, with STAD recurring as the lineage with the largest associated feature set.
