solute carrier family 11 member 1Genealiases: LSH · NRAMP · NRAMP1
Q-omics provides the consensus-scored SLC11A1 profile across patient tissues and cancer cell-line models. SLC11A1 expression is associated with patient survival in 24 of 34 cancer types, with the highest sampling consensus in KIRC. Among the 18 cancer types available for tumor–normal comparison, SLC11A1 is differentially expressed in 17, with the highest sampling consensus in HNSC. Additionally, SLC11A1 RNA expression shows 21,998 significant protein co-abundance associations, with the highest sampling consensus in GBM. Together, these results highlight KIRC, HNSC, and GBM as cancer lineages where SLC11A1 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 SLC11A1 — synthetic lethality, tumor antigen, and pembrolizumab response.
This table summarizes SLC11A1 survival associations across molecular data types. SLC11A1 RNA expression shows survival associations in the most cancer types (24), followed by mutation status (5) and mass-spec protein abundance (3). The rightmost column indicates the cancer type with the highest sampling consensus for each molecular layer.
This table ranks reproducible SLC11A1 RNA expression–survival associations across cancer types. High SLC11A1 expression shows unfavorable associations in KIRC, ACC, LGG, LIHC, THCA and COAD. The KIRC 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 KIRC as the clearest survival context for SLC11A1 RNA expression.
This table summarizes SLC11A1 tumor–normal expression differences by data type. RNA shows broader differences across cancer types, with a lineage consensus of 17, while mass-spec protein shows differences in 2. The strongest signals are observed in KIRC for RNA and LUAD for protein.
This table ranks reproducible tumor–normal expression differences for SLC11A1. A negative fold-change indicates higher expression in normal tissue than in tumor tissue. SLC11A1 shows lower tumor expression in LUAD and higher tumor expression in HNSC, KIRC, COAD, KIRP and BLCA. The HNSC box plot shows higher SLC11A1 RNA expression in tumor versus normal tissue (log2 FC = +1.527, t-test p < 0.001).
This table shows molecular features associated with SLC11A1 in patient tissues and cancer cell lines. In patient samples, SLC11A1 shows the broadest associations at the RNA and protein expression levels, with GBM recurring as the lineage with the largest associated feature set. In cancer cell lines, SLC11A1 RNA and mutation anchors are most strongly linked to RNA-expression features, especially in KIDNEY, while CRISPR and shRNA rows add functional-dependency signals in PANCREAS and BLOOD_Leukemia.
