| HGNC Family | Non-coding RNAs |
| Name | microRNA 6884 |
| 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": "\nIn a recent study on hypertrophic scarring (HS), integrated RNA sequencing analysis revealed that among the many differentially expressed RNAs involved in the pathology of HS, hsa‐miR‑6884‑5p (MIR6884) emerged as a key component of a competing endogenous RNA (ceRNA) regulatory network. Specifically, MIR6884 was found to interact with the long noncoding RNA MEG3 and target the mRNA for ADAMTS14, a gene implicated in extracellular matrix remodeling. This interaction suggests that MIR6884 may play an important role in modulating the expression of genes involved in collagen deposition and extracellular matrix organization—two processes that are central to the formation of hypertrophic scars."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": "\n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Xiaodong Li, Zeliang He, Julei Zhang, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Identification of crucial noncoding RNAs and mRNAs in hypertrophic scars via RNA sequencing."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "FEBS Open Bio (2021)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1002/2211-5463.13167"}], "href": "https://doi.org/10.1002/2211-5463.13167"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "33932142"}], "href": "https://pubmed.ncbi.nlm.nih.gov/33932142"}]}]}]}
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| Synonyms | HSA-MIR-6884 |
| NCBI Gene ID | 102466757 |
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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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MIR6884 has 0 functional associations with biological entities spanning 0 categories () extracted from 0 datasets.
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If available, associations are ranked by standardized value
| Dataset | Summary |
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