| HGNC Family | Non-coding RNAs |
| Name | microRNA 6729 |
| Description | microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009] |
| Summary |
{"type": "root", "children": [{"type": "p", "children": [{"type": "t", "text": "\nAlthough the query inquires about MIR6729, neither abstract explicitly discusses this microRNA. Instead, the provided studies focus on PSD3 (also known as EFA6D), a gene with diverse roles in metabolic and neuronal processes. In one study, a coding variant in PSD3 (L186T) was identified that is associated with a reduced risk of fatty liver disease, with PSD3 downregulation leading to decreased intracellular lipid accumulation in both human hepatocytes and animal models."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": "\n \nDis primis, further characterization of PSD3 reveals that it exists in multiple splice variants with distinct expression profiles in the brain. The study demonstrates that specific isoforms, such as EFA6D1b/c and EFA6D1s, have unique subcellular distributions in neurons, suggesting that PSD3 contributes to neuronal signaling and structural organization in different cellular compartments."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "2"}]}, {"type": "t", "text": "\n\nFusce class lectus fringilla commodo sit blandit pellentesque. Although the abstracts do not address MIR6729 directly, deciphering the function of PSD3 provides a framework to potentially explore regulatory mechanisms involving microRNAs in the future. Additional research will be necessary to establish whether and how MIR6729 might interact with PSD3 or influence the pathways modulated by this gene.\n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Rosellina M Mancina, Kavitha Sasidharan, Anna Lindblom, et al. "}, {"type": "b", "children": [{"type": "t", "text": "PSD3 downregulation confers protection against fatty liver disease."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Nat Metab (2022)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/s42255-021-00518-0"}], "href": "https://doi.org/10.1038/s42255-021-00518-0"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "35102341"}], "href": "https://pubmed.ncbi.nlm.nih.gov/35102341"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Masahiro Fukaya, Shingo Ohta, Yoshinobu Hara, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Distinct subcellular localization of alternative splicing variants of EFA6D, a guanine nucleotide exchange factor for Arf6, in the mouse brain."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Comp Neurol (2016)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1002/cne.24048"}], "href": "https://doi.org/10.1002/cne.24048"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "27241101"}], "href": "https://pubmed.ncbi.nlm.nih.gov/27241101"}]}]}]}
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| Synonyms | HSA-MIR-6729 |
| NCBI Gene ID | 102466982 |
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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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MIR6729 has 0 functional associations with biological entities spanning 0 categories () extracted from 0 datasets.
Click the + buttons to view associations for MIR6729 from the datasets below.
If available, associations are ranked by standardized value
| Dataset | Summary |
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