Q-omics provides the consensus-scored LINC01323 profile across patient tissues and cancer cell-line models. LINC01323 expression is associated with patient survival in 13 of 34 cancer types, with the highest sampling consensus in LIHC. Among the 18 cancer types available for tumor–normal comparison, LINC01323 is differentially expressed in 2, with the highest sampling consensus in THCA. Additionally, LINC01323 RNA expression shows 9,421 significant gene co-expression associations, with the highest sampling consensus in SARC. Together, these results highlight LIHC, THCA, and SARC as cancer lineages where LINC01323 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 LINC01323 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes LINC01323 survival associations across molecular data types. LINC01323 RNA expression shows survival associations in the most cancer types (13). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible LINC01323 RNA expression–survival associations across cancer types. High LINC01323 expression shows unfavorable associations in LIHC, KIRC, KIRP, BRCA, READ and DLBC. The LIHC Kaplan–Meier curve shows clear separation, with the high-expression group declining faster, consistent with the unfavorable association (log-rank p = .005). Together, the overview and detailed table identify LIHC as the clearest survival context for LINC01323 RNA expression.
This table summarizes LINC01323 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 2. The strongest signals are observed in THCA for RNA.
This table ranks reproducible tumor–normal expression differences for LINC01323. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. LINC01323 shows lower tumor expression in THCA and KIRC. The THCA box plot shows higher LINC01323 RNA expression in normal versus tumor tissue (log2 FC = −0.211, t-test p < 0.001).
This table shows molecular features associated with LINC01323 in patient tissues and cancer cell lines. In patient samples, LINC01323 shows the broadest associations at the RNA and protein expression levels, with SARC recurring as the lineage with the largest associated feature set.
