long intergenic non-protein coding RNA 1940Genealiases: []
Q-omics provides the consensus-scored LINC01940 profile across patient tissues and cancer cell-line models. LINC01940 expression is associated with patient survival in 21 of 34 cancer types, with the highest sampling consensus in ACC. Among the 18 cancer types available for tumor–normal comparison, LINC01940 is differentially expressed in 7, with the highest sampling consensus in UCEC. Additionally, LINC01940 RNA expression shows 7,935 significant gene co-expression associations, with the highest sampling consensus in TGCT. Together, these results highlight ACC, UCEC, and TGCT as cancer lineages where LINC01940 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 LINC01940 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes LINC01940 survival associations across molecular data types. LINC01940 RNA expression shows survival associations in the most cancer types (21). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible LINC01940 RNA expression–survival associations across cancer types. High LINC01940 expression shows unfavorable associations in ACC, PAAD and KIRC, but favorable associations in DLBC, ESCA and UCS. 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 LINC01940 RNA expression.
This table summarizes LINC01940 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 7. The strongest signals are observed in UCEC for RNA.
This table ranks reproducible tumor–normal expression differences for LINC01940. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. LINC01940 shows lower tumor expression in UCEC, BRCA, BLCA and KICH and higher tumor expression in PAAD and LUSC. The UCEC box plot shows higher LINC01940 RNA expression in normal versus tumor tissue (log2 FC = −0.072, t-test p < 0.001).
This table shows molecular features associated with LINC01940 in patient tissues and cancer cell lines. In patient samples, LINC01940 shows the broadest associations at the RNA and protein expression levels, with TGCT recurring as the lineage with the largest associated feature set.
