| Name | VSTM2A overlapping transcript 1 |
| Summary |
{"type": "root", "children": [{"type": "p", "children": [{"type": "t", "text": "\nThe study (PMID:"}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": "investigates the developmental expression and intracellular distribution of a gene product in the myotonic dystrophy (DM1) putative gene cluster. Although the abstract centers on the DMWD gene, which shows stable mRNA levels but gradually increasing protein levels in the developing mouse brain—with notable enrichment in neurons, particularly in regions dense with synaptic connections—it does not provide direct functional insights into VSTM2A-OT1. This indirect context leaves open the possibility that, if VSTM2A-OT1 is associated with the DM1 region, its role might similarly influence aspects of neuronal function or disease manifestation, but its specific function remains to be determined.\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nThe findings underscore the importance of analyzing spatial and temporal expression patterns to understand gene contributions within critical genomic clusters. While the current abstract (PMID:"}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": "does not explicitly address VSTM2A-OT1, the observed developmental regulation and subcellular localization of the DMWD gene product suggest that further investigation into related transcripts—such as VSTM2A-OT1—could reveal novel insights into their roles in neuronal signaling and the pathophysiology of myotonic dystrophy.\n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Jolanda H A M Westerlaken, Catharina E E M Van der Zee, Wilma Peters, et al. "}, {"type": "b", "children": [{"type": "t", "text": "The DMWD protein from the myotonic dystrophy (DM1) gene region is developmentally regulated and is present most prominently in synapse-dense brain areas."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Brain Res (2003)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/s0006-8993(03)02430-2"}], "href": "https://doi.org/10.1016/s0006-8993(03"}, {"type": "t", "text": "02430-2) PMID: "}, {"type": "a", "children": [{"type": "t", "text": "12691844"}], "href": "https://pubmed.ncbi.nlm.nih.gov/12691844"}]}]}]}
|
| Synonyms | GS1-18A18.1 |
| NCBI Gene ID | 285878 |
| API | |
| Download Associations | |
| Predicted Functions |
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| Co-expressed Genes |
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| Expression in Tissues and Cell Lines |
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VSTM2A-OT1 has 143 functional associations with biological entities spanning 2 categories (cell line, cell type or tissue, gene, protein or microRNA) extracted from 5 datasets.
Click the + buttons to view associations for VSTM2A-OT1 from the datasets below.
If available, associations are ranked by standardized value
| Dataset | Summary | |
|---|---|---|
| CCLE Cell Line Gene CNV Profiles | cell lines with high or low copy number of VSTM2A-OT1 gene relative to other cell lines from the CCLE Cell Line Gene CNV Profiles dataset. | |
| GEO Signatures of Differentially Expressed Genes for Gene Perturbations | gene perturbations changing expression of VSTM2A-OT1 gene from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset. | |
| GEO Signatures of Differentially Expressed Genes for Kinase Perturbations | kinase perturbations changing expression of VSTM2A-OT1 gene from the GEO Signatures of Differentially Expressed Genes for Kinase Perturbations dataset. | |
| GTEx Tissue Gene Expression Profiles | tissues with high or low expression of VSTM2A-OT1 gene relative to other tissues from the GTEx Tissue Gene Expression Profiles dataset. | |
| Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles | cell lines with high or low copy number of VSTM2A-OT1 gene relative to other cell lines from the Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles dataset. | |