Q-omics provides the consensus-scored FNDC1-IT1 profile across patient tissues and cancer cell-line models. FNDC1-IT1 expression is associated with patient survival in 20 of 34 cancer types, with the highest sampling consensus in ACC. Among the 18 cancer types available for tumor–normal comparison, FNDC1-IT1 is differentially expressed in 8, with the highest sampling consensus in HNSC. Additionally, FNDC1-IT1 RNA expression shows 11,520 significant protein co-abundance associations, with the highest sampling consensus in PDAC. Together, these results highlight ACC, HNSC, and PDAC as cancer lineages where FNDC1-IT1 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 FNDC1-IT1 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes FNDC1-IT1 survival associations across molecular data types. FNDC1-IT1 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 FNDC1-IT1 RNA expression–survival associations across cancer types. High FNDC1-IT1 expression shows unfavorable associations in ACC, KIRP, MESO, THYM and KICH, but favorable associations in DLBC. 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 FNDC1-IT1 RNA expression.
This table summarizes FNDC1-IT1 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 8. The strongest signals are observed in HNSC for RNA.
This table ranks reproducible tumor–normal expression differences for FNDC1-IT1. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. FNDC1-IT1 shows higher tumor expression in HNSC, LUAD, BRCA, BLCA, LUSC and COAD. The HNSC box plot shows higher FNDC1-IT1 RNA expression in tumor versus normal tissue (log2 FC = +0.220, t-test p < 0.001).
This table shows molecular features associated with FNDC1-IT1 in patient tissues and cancer cell lines. In patient samples, FNDC1-IT1 shows the broadest associations at the RNA and protein expression levels, with PDAC recurring as the lineage with the largest associated feature set.
