| HGNC Family | Non-coding RNAs |
| Name | microRNA 3680-1 |
| 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": "\nRecent studies have implicated members of the MIR3680 gene family in the regulation of skeletal homeostasis. In patients with chronic kidney disease–mineral and bone disorder (CKD-MBD), miR-3680-5p expression was found to be significantly associated with parathyroid hormone levels through modulation of the ubiquitin proteolysis pathway, suggesting a potential role in the degradation of parathyroid hormone and its related proteins. Similarly, emerging evidence in osteoarthritis (OA) research points to a role for miR-3680-3p in the regulation of joint tissue homeostasis and disease progression."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nIn the context of CKD-MBD, patients undergoing peritoneal dialysis were observed to exhibit differential expression of miR-3680-5p when stratified by parathyroid hormone levels. Bioinformatic predictions identified several ubiquitin-specific proteases—USP6, USP32, USP46—and DLT as targets, suggesting that miR-3680-5p may influence the ubiquitin proteolysis pathway, thereby modulating the degradation of parathyroid hormone and contributing to skeletal alterations seen in CKD-MBD."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nIn osteoarthritis, the focus has shifted toward miR-3680-3p, where preliminary investigations seek to elucidate its role in knee joint degeneration and cartilage metabolism. Although the precise molecular mechanisms remain under exploration, this miRNA is emerging as a promising candidate in understanding and potentially modulating OA progression."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "2"}]}, {"type": "t", "text": "\n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Sohyun Jeong, Jung Mi Oh, Kook-Hwan Oh, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Differentially expressed miR-3680-5p is associated with parathyroid hormone regulation in peritoneal dialysis patients."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "PLoS One (2017)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1371/journal.pone.0170535"}], "href": "https://doi.org/10.1371/journal.pone.0170535"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "28152049"}], "href": "https://pubmed.ncbi.nlm.nih.gov/28152049"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Yanping Xie, Jianwei Li, Yanhui Suo, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Downregulation of miR-3680-3p inhibits the progression of osteoarthritis via targeting OGG1."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Arch Gerontol Geriatr (2022)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.archger.2022.104626"}], "href": "https://doi.org/10.1016/j.archger.2022.104626"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "35092863"}], "href": "https://pubmed.ncbi.nlm.nih.gov/35092863"}]}]}]}
|
| Synonyms | MIR3680, HSA-MIR-3680-1 |
| NCBI Gene ID | 100500917 |
| API | |
| Download Associations | |
| Predicted Functions |
![]() |
| Co-expressed Genes |
![]() |
| Expression in Tissues and Cell Lines |
![]() |
MIR3680-1 has 351 functional associations with biological entities spanning 3 categories (molecular profile, cell line, cell type or tissue, gene, protein or microRNA) extracted from 7 datasets.
Click the + buttons to view associations for MIR3680-1 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 MIR3680-1 gene relative to other cell lines from the CCLE Cell Line Gene CNV Profiles dataset. | |
| ENCODE Histone Modification Site Profiles | histone modification site profiles with high histone modification abundance at MIR3680-1 gene from the ENCODE Histone Modification Site Profiles dataset. | |
| ENCODE Transcription Factor Binding Site Profiles | transcription factor binding site profiles with transcription factor binding evidence at the promoter of MIR3680-1 gene from the ENCODE Transcription Factor Binding Site Profiles dataset. | |
| ENCODE Transcription Factor Targets | transcription factors binding the promoter of MIR3680-1 gene in ChIP-seq datasets from the ENCODE Transcription Factor Targets dataset. | |
| GTEx Tissue Gene Expression Profiles | tissues with high or low expression of MIR3680-1 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 MIR3680-1 gene relative to other cell lines from the Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles dataset. | |
| Roadmap Epigenomics Histone Modification Site Profiles | histone modification site profiles with high histone modification abundance at MIR3680-1 gene from the Roadmap Epigenomics Histone Modification Site Profiles dataset. | |