long intergenic non-protein coding RNA 1391Genealiases: []
Q-omics provides the consensus-scored LINC01391 profile across patient tissues and cancer cell-line models. LINC01391 expression is associated with patient survival in 20 of 34 cancer types, with the highest sampling consensus in UVM. Among the 18 cancer types available for tumor–normal comparison, LINC01391 is differentially expressed in 9, with the highest sampling consensus in HNSC. Additionally, LINC01391 RNA expression shows 9,940 significant gene co-expression associations, with the highest sampling consensus in TGCT. Together, these results highlight UVM, HNSC, and TGCT as cancer lineages where LINC01391 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 LINC01391 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes LINC01391 survival associations across molecular data types. LINC01391 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 LINC01391 RNA expression–survival associations across cancer types. High LINC01391 expression shows unfavorable associations in UVM, MESO, ACC and BLCA, but favorable associations in UCS and UCEC. The UVM 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 UVM as the clearest survival context for LINC01391 RNA expression.
This table summarizes LINC01391 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 9. The strongest signals are observed in HNSC for RNA.
This table ranks reproducible tumor–normal expression differences for LINC01391. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. LINC01391 shows lower tumor expression in UCEC and higher tumor expression in HNSC, LUSC, BLCA, PRAD and LUAD. The HNSC box plot shows higher LINC01391 RNA expression in tumor versus normal tissue (log2 FC = +0.109, t-test p < 0.001).
This table shows molecular features associated with LINC01391 in patient tissues and cancer cell lines. In patient samples, LINC01391 shows the broadest associations at the RNA and protein expression levels, with TGCT recurring as the lineage with the largest associated feature set.
