Q-omics provides the consensus-scored SIGLEC24P profile across patient tissues and cancer cell-line models. SIGLEC24P expression is associated with patient survival in 11 of 34 cancer types, with the highest sampling consensus in KIRC. Additionally, SIGLEC24P RNA expression shows 6,140 significant pathway-activity associations, with the highest sampling consensus in STAD. Together, these results highlight KIRC, and STAD as cancer lineages where SIGLEC24P 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.