| Name | EML2 antisense RNA 1 |
| Summary |
{"type": "root", "children": [{"type": "p", "children": [{"type": "t", "text": "This study employs a population-scale biobank with extensive genomic and phenotypic data to perform a comprehensive analysis of genetic associations across more than 2,000 traits using truncated singular value decomposition. The approach successfully identified latent components of genetic variation—thereby shedding light on how specific variants and genes, such as GPR151 and PDE3B, contribute to obesity‐related traits and adipocyte biology (1). Notably, the abstract does not mention the noncoding RNA EML2‑AS1, and thus its function remains uncharacterized in the context of this analysis (1)."}]}, {"type": "t", "text": "\n "}, {"type": "p", "children": [{"type": "t", "text": "Citation:."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": ""}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Yosuke Tanigawa, Jiehan Li, Johanne M Justesen, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Components of genetic associations across 2,138 phenotypes in the UK Biobank highlight adipocyte biology."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Nat Commun (2019)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/s41467-019-11953-9"}], "href": "https://doi.org/10.1038/s41467-019-11953-9"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "31492854"}], "href": "https://pubmed.ncbi.nlm.nih.gov/31492854"}]}]}]}
|
| Synonyms | C19ORF83 |
| Proteins | CS083_HUMAN |
| NCBI Gene ID | 100287177 |
| 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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EML2-AS1 has 315 functional associations with biological entities spanning 2 categories (cell line, cell type or tissue, gene, protein or microRNA) extracted from 9 datasets.
Click the + buttons to view associations for EML2-AS1 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 EML2-AS1 gene relative to other cell lines from the CCLE Cell Line Gene CNV Profiles dataset. | |
| HPA Cell Line Gene Expression Profiles | cell lines with high or low expression of EML2-AS1 gene relative to other cell lines from the HPA Cell Line Gene Expression Profiles dataset. | |
| HPA Tissue Gene Expression Profiles | tissues with high or low expression of EML2-AS1 gene relative to other tissues from the HPA Tissue Gene Expression Profiles dataset. | |
| HPA Tissue Sample Gene Expression Profiles | tissue samples with high or low expression of EML2-AS1 gene relative to other tissue samples from the HPA Tissue Sample Gene Expression Profiles dataset. | |
| Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles | cell lines with high or low copy number of EML2-AS1 gene relative to other cell lines from the Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles dataset. | |
| Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles | cell lines with high or low expression of EML2-AS1 gene relative to other cell lines from the Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles dataset. | |
| Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Mutation Profiles | cell lines with EML2-AS1 gene mutations from the Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Mutation Profiles dataset. | |
| TargetScan Predicted Conserved microRNA Targets | microRNAs regulating expression of EML2-AS1 gene predicted using conserved miRNA seed sequences from the TargetScan Predicted Conserved microRNA Targets dataset. | |
| TargetScan Predicted Nonconserved microRNA Targets | microRNAs regulating expression of EML2-AS1 gene predicted using nonconserved miRNA seed sequences from the TargetScan Predicted Nonconserved microRNA Targets dataset. | |