| Name | BMS1 pseudogene 1 |
| Summary |
{"type": "root", "children": [{"type": "p", "children": [{"type": "t", "text": "\nStudies in these abstracts have converged on the importance of divalent cation transport and inflammatory regulation as mediated by the natural‐resistance–associated macrophage protein 1 (commonly known as NRAMP1 and encoded by SLC11A1). NRAMP1 localizes to late endosomes and lysosomes in phagocytes, where it restricts intracellular pathogens—notably Salmonella, Mycobacterium, Leishmania, and Brucella—by modulating iron, magnesium, and other metal availabilities essential for microbial growth. In addition, NRAMP1 function is closely linked to macrophage activation, cytokine production, and the triggering of antimicrobial effector mechanisms (for example, nitric oxide synthesis) as well as influencing antigen presentation and inflammation‐related gene expression. Collectively, these reports indicate that NRAMP1 plays a bifunctional role in both directly limiting pathogen access to essential nutrients and in orchestrating the ensuing host immune response."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "1", "end_ref": "34"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nA second set of studies has elucidated the role of chromatin‐remodeling factors—especially Lsh (also known as HELLS)—in the regulation of de novo DNA methylation and genome organization. Lsh facilitates the methylation of both repetitive and unique sequences by enabling DNA methyltransferases (such as Dnmt3a/3b) to access nucleosomal DNA, thereby contributing not only to the maintenance of genomic integrity but also to the regulation of gene expression during cellular differentiation and immune responses. In addition, Lsh influences the silencing of critical stem cell–associated genes and participates in the response to DNA damage, underscoring its multifaceted role in cell biology."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "35", "end_ref": "40"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nNone of the provided abstracts directly address the gene BMS1P1. However, by analogy to the roles of NRAMP1 in modulating metal ion trafficking and immune activation, and Lsh in directing epigenetic reprogramming and chromatin accessibility, one may speculate that BMS1P1—if functionally active—could be involved in fundamental cellular processes such as ribosome biogenesis or RNA processing that in turn influence cell growth and possibly immune regulation. Further focused investigation will be needed to define the precise functions of BMS1P1 and to determine whether it, like its functional counterparts, acts as a modulator of critical cellular responses.\n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Victoriano Mulero, Susan Searle, Jenefer M Blackwell, et al. 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| NCBI Gene ID | 399761 |
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| Predicted Functions |
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| Co-expressed Genes |
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| Expression in Tissues and Cell Lines |
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BMS1P1 has 1 functional associations with biological entities spanning 1 categories (cell line, cell type or tissue) extracted from 1 datasets.
Click the + buttons to view associations for BMS1P1 from the datasets below.
If available, associations are ranked by standardized value
| Dataset | Summary | |
|---|---|---|
| CellMarker Gene-Cell Type Associations | cell types associated with BMS1P1 gene from the CellMarker Gene-Cell Type Associations dataset. | |