| Name | long intergenic non-protein coding RNA 1412 |
| Summary |
{"type": "root", "children": [{"type": "p", "children": [{"type": "t", "text": "\n LINC01412 is a long intergenic noncoding RNA that has been implicated in several age‐related conditions and complex disease processes through its potential regulatory roles. In one study of age‐related nuclear cataract – the most common form of cataract causing blindness – genetic signals suggest that LINC01412 may be involved in the inherited risk of lens opacification, possibly by modulating the expression of genes important for lens transparency and homeostasis."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": "\n "}]}, {"type": "t", "text": "\n "}, {"type": "p", "children": [{"type": "t", "text": "\n In a separate large-scale genome-wide association study investigating aortic valve stenosis, a newly identified locus on chromosome 1p21 near PALMD was reported. The findings raise the possibility that LINC01412, located in the vicinity of this locus, could contribute to valve pathology through transcriptional or posttranscriptional regulation of nearby gene networks, thereby influencing the structural and functional integrity of the aortic valve."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "2"}]}, {"type": "t", "text": "\n "}]}, {"type": "t", "text": "\n "}, {"type": "p", "children": [{"type": "t", "text": "\n Moreover, an analysis examining the variable response to selective serotonin reuptake inhibitors in patients with major depressive disorder – particularly in the context of co-occurring conditions such as coronary artery disease and obesity – has implicated gene regulatory mechanisms potentially involving LINC01412. This suggests that LINC01412 might be contributing to metabolic and cardiovascular pathways that affect SSRI treatment outcomes by modulating gene networks across different organ systems."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "3"}]}, {"type": "t", "text": "\n "}]}, {"type": "t", "text": "\n "}, {"type": "p", "children": [{"type": "t", "text": "\n Collectively, these findings point toward a multifaceted role for LINC01412 in regulating gene expression networks essential for maintaining ocular clarity, valve structure, and metabolic balance in conditions that affect both cardiovascular and neuropsychiatric health.\n "}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Ekaterina Yonova-Doing, Wanting Zhao, Robert P Igo, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Common variants in SOX-2 and congenital cataract genes contribute to age-related nuclear cataract."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Commun Biol (2020)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/s42003-020-01421-2"}], "href": "https://doi.org/10.1038/s42003-020-01421-2"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "33311586"}], "href": "https://pubmed.ncbi.nlm.nih.gov/33311586"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Anna Helgadottir, Gudmar Thorleifsson, Solveig Gretarsdottir, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Genome-wide analysis yields new loci associating with aortic valve stenosis."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Nat Commun (2018)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/s41467-018-03252-6"}], "href": "https://doi.org/10.1038/s41467-018-03252-6"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "29511194"}], "href": "https://pubmed.ncbi.nlm.nih.gov/29511194"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "Azmeraw T Amare, Klaus Oliver Schubert, Fasil Tekola-Ayele, et al. "}, {"type": "b", "children": [{"type": "t", "text": "The association of obesity and coronary artery disease genes with response to SSRIs treatment in major depression."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Neural Transm (Vienna) (2019)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1007/s00702-018-01966-x"}], "href": "https://doi.org/10.1007/s00702-018-01966-x"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "30610379"}], "href": "https://pubmed.ncbi.nlm.nih.gov/30610379"}]}]}]}
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| NCBI Gene ID | 101928455 |
| API | |
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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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LINC01412 has 0 functional associations with biological entities spanning 0 categories () extracted from 0 datasets.
Click the + buttons to view associations for LINC01412 from the datasets below.
If available, associations are ranked by standardized value
| Dataset | Summary |
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