Q-omics provides the consensus-scored GXYLT1P4 profile across patient tissues and cancer cell-line models. GXYLT1P4 expression is associated with patient survival in 21 of 34 cancer types, with the highest sampling consensus in UCEC. Among the 18 cancer types available for tumor–normal comparison, GXYLT1P4 is differentially expressed in 8, with the highest sampling consensus in COAD. Additionally, GXYLT1P4 RNA expression shows 13,819 significant gene co-expression associations, with the highest sampling consensus in TGCT. Together, these results highlight UCEC, COAD, and TGCT as cancer lineages where GXYLT1P4 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 GXYLT1P4 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes GXYLT1P4 survival associations across molecular data types. GXYLT1P4 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 GXYLT1P4 RNA expression–survival associations across cancer types. High GXYLT1P4 expression shows unfavorable associations in UCEC, UCS, KICH, MESO and THCA, but favorable associations in BRCA. The UCEC Kaplan–Meier curve shows clear separation, with the high-expression group declining faster, consistent with the unfavorable association (log-rank p = .018). Together, the overview and detailed table identify UCEC as the clearest survival context for GXYLT1P4 RNA expression.
This table summarizes GXYLT1P4 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 COAD for RNA.
This table ranks reproducible tumor–normal expression differences for GXYLT1P4. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. GXYLT1P4 shows lower tumor expression in COAD, THCA, BRCA, LUAD, PAAD and READ. The COAD box plot shows higher GXYLT1P4 RNA expression in normal versus tumor tissue (log2 FC = −0.023, t-test p < 0.001).
This table shows molecular features associated with GXYLT1P4 in patient tissues and cancer cell lines. In patient samples, GXYLT1P4 shows the broadest associations at the RNA and protein expression levels, with TGCT recurring as the lineage with the largest associated feature set.
