long intergenic non-protein coding RNA 1989Genealiases: []
Q-omics provides the consensus-scored LINC01989 profile across patient tissues and cancer cell-line models. LINC01989 expression is associated with patient survival in 23 of 34 cancer types, with the highest sampling consensus in DLBC. Among the 18 cancer types available for tumor–normal comparison, LINC01989 is differentially expressed in 4, with the highest sampling consensus in COAD. Additionally, LINC01989 RNA expression shows 7,169 significant gene co-expression associations, with the highest sampling consensus in THYM. Together, these results highlight DLBC, COAD, and THYM as cancer lineages where LINC01989 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 LINC01989 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes LINC01989 survival associations across molecular data types. LINC01989 RNA expression shows survival associations in the most cancer types (23). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible LINC01989 RNA expression–survival associations across cancer types. High LINC01989 expression shows unfavorable associations in DLBC, BLCA, UVM, KIRC, COAD and ACC. The DLBC Kaplan–Meier curve shows clear separation, with the high-expression group declining faster, consistent with the unfavorable association (log-rank p = .002). Together, the overview and detailed table identify DLBC as the clearest survival context for LINC01989 RNA expression.
This table summarizes LINC01989 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 4. The strongest signals are observed in COAD for RNA.
This table ranks reproducible tumor–normal expression differences for LINC01989. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. LINC01989 shows lower tumor expression in COAD and KICH and higher tumor expression in HNSC and THCA. The COAD box plot shows higher LINC01989 RNA expression in normal versus tumor tissue (log2 FC = −0.190, t-test p < 0.001).
This table shows molecular features associated with LINC01989 in patient tissues and cancer cell lines. In patient samples, LINC01989 shows the broadest associations at the RNA and protein expression levels, with THYM recurring as the lineage with the largest associated feature set.
