Q-omics provides the consensus-scored FAM83C-AS1 profile across patient tissues and cancer cell-line models. FAM83C-AS1 expression is associated with patient survival in 24 of 34 cancer types, with the highest sampling consensus in COAD. Among the 18 cancer types available for tumor–normal comparison, FAM83C-AS1 is differentially expressed in 9, with the highest sampling consensus in LUSC. Additionally, FAM83C-AS1 RNA expression shows 12,047 significant gene co-expression associations, with the highest sampling consensus in THYM. Together, these results highlight COAD, LUSC, and THYM as cancer lineages where FAM83C-AS1 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 FAM83C-AS1 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes FAM83C-AS1 survival associations across molecular data types. FAM83C-AS1 RNA expression shows survival associations in the most cancer types (24). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible FAM83C-AS1 RNA expression–survival associations across cancer types. High FAM83C-AS1 expression shows unfavorable associations in COAD, ACC, KIRC and LAML, but favorable associations in UVM and PAAD. The COAD 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 COAD as the clearest survival context for FAM83C-AS1 RNA expression.
This table summarizes FAM83C-AS1 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 LUSC for RNA.
This table ranks reproducible tumor–normal expression differences for FAM83C-AS1. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. FAM83C-AS1 shows lower tumor expression in KICH and higher tumor expression in LUSC, LUAD, COAD, LIHC and BRCA. The LUSC box plot shows higher FAM83C-AS1 RNA expression in tumor versus normal tissue (log2 FC = +0.986, t-test p < 0.001).
This table shows molecular features associated with FAM83C-AS1 in patient tissues and cancer cell lines. In patient samples, FAM83C-AS1 shows the broadest associations at the RNA and protein expression levels, with THYM recurring as the lineage with the largest associated feature set.
