| Name | microRNA 5698 |
| 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": "\nThe studies provided offer important insights into cellular responses in distinct biological contexts. In the first study, the authors describe a novel p53 target gene, Ptprv, which plays a key role in mediating G1 cell cycle arrest after DNA damage. Ptprv is transcriptionally activated by p53 and is essential for proper checkpoint control, as its loss disrupts G1 arrest without compromising p53‐dependent apoptosis."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": "\n \nDis primis duis mauris potenti non at sociosqu ultricies massa. In the second study, the focus is on the osteotesticular protein tyrosine phosphatase (OST), a molecule expressed during early skeletogenesis that appears to be involved in the commitment of mesenchymal cells to bone formation. The spatiotemporal expression of OST mRNA suggests a role in regulating the delicate balance of bone development processes independent of Runx2/Cbfa1."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "2"}]}, {"type": "t", "text": "\n\nFusce class lectus fringilla commodo sit blandit pellentesque. Although these abstracts provide detailed views on cell cycle regulation and bone development through protein-coding genes like Ptprv and OST, neither study addresses the function of MIR5698. As such, based on the information provided, there is no evidence linking MIR5698 to these pathways, leaving its role in these or other processes to be determined in future research."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": "\n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Gilles Doumont, Alain Martoriati, Chantal Beekman, et al. "}, {"type": "b", "children": [{"type": "t", "text": "G1 checkpoint failure and increased tumor susceptibility in mice lacking the novel p53 target Ptprv."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "EMBO J (2005)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/sj.emboj.7600769"}], "href": "https://doi.org/10.1038/sj.emboj.7600769"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "16107883"}], "href": "https://pubmed.ncbi.nlm.nih.gov/16107883"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Laurie A Yunker, Anne Undersander, Jane B Lian, et al. "}, {"type": "b", "children": [{"type": "t", "text": "The tyrosine phosphatase, OST-PTP, is expressed in mesenchymal progenitor cells early during skeletogenesis in the mouse."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Cell Biochem (2004)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1002/jcb.20183"}], "href": "https://doi.org/10.1002/jcb.20183"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "15660420"}], "href": "https://pubmed.ncbi.nlm.nih.gov/15660420"}]}]}]}
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| NCBI Gene ID | 100847024 |
| 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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MIR5698 has 159 functional associations with biological entities spanning 2 categories (cell line, cell type or tissue, gene, protein or microRNA) extracted from 4 datasets.
Click the + buttons to view associations for MIR5698 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 MIR5698 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 MIR5698 gene relative to other cell lines from the COSMIC Cell Line Gene CNV Profiles dataset. | |
| Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles | cell lines with high or low copy number of MIR5698 gene relative to other cell lines from the Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles dataset. | |
| MotifMap Predicted Transcription Factor Targets | transcription factors regulating expression of MIR5698 gene predicted using known transcription factor binding site motifs from the MotifMap Predicted Transcription Factor Targets dataset. | |