| Name | long intergenic non-protein coding RNA 351 |
| Summary |
{"type": "root", "children": [{"type": "p", "children": [{"type": "t", "text": "\n In a meta-analysis of genome‐wide association studies addressing the genetic basis of Gilles de la Tourette Syndrome (TS) and Attention Deficit/Hyperactivity Disorder (ADHD), the authors primarily highlighted variants in genes such as TBC1D7, GUCY1A3, RAP1GDS1, and CHST11 (1). Notably, this abstract does not provide any information regarding LINC00351, and thus no functional insights on LINC00351 can be derived from it. Further investigations would be necessary to elucidate any potential role of LINC00351 in the context of TS, ADHD, or related neurodevelopmental processes."}]}, {"type": "t", "text": "\n "}, {"type": "p", "children": [{"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": ""}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Fotis Tsetsos, Shanmukha S Padmanabhuni, John Alexander, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Meta-Analysis of Tourette Syndrome and Attention Deficit Hyperactivity Disorder Provides Support for a Shared Genetic Basis."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Front Neurosci (2016)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.3389/fnins.2016.00340"}], "href": "https://doi.org/10.3389/fnins.2016.00340"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "27499730"}], "href": "https://pubmed.ncbi.nlm.nih.gov/27499730"}]}]}]}
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| NCBI Gene ID | 100874137 |
| 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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LINC00351 has 157 functional associations with biological entities spanning 2 categories (disease, phenotype or trait, cell line, cell type or tissue) extracted from 4 datasets.
Click the + buttons to view associations for LINC00351 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 LINC00351 gene relative to other cell lines from the CCLE Cell Line Gene CNV Profiles dataset. | |
| COSMIC Cell Line Gene CNV Profiles | cell lines with high or low copy number of LINC00351 gene relative to other cell lines from the COSMIC Cell Line Gene CNV Profiles dataset. | |
| GWAS Catalog SNP-Phenotype Associations | phenotypes associated with LINC00351 gene in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. | |
| Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles | cell lines with high or low copy number of LINC00351 gene relative to other cell lines from the Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles dataset. | |