| HGNC Family | Non-coding RNAs |
| Name | microRNA 6836 |
| 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 investigations into cellular differentiation have revealed the importance of finely tuned gene regulation in various biological processes. For instance, one study detailed the role of Deltex4 (DTX4) in adipogenic differentiation using 3T3-L1 preadipocytes, showing that DTX4 protein expression increases as differentiation proceeds. Stable knockdown of DTX4 led to decreased lipid droplet formation, reduced expression of key adipogenic transcription factors (C/EBPα and PPARγ), and impaired mitotic clonal expansion. These findings underscore the complex regulatory networks required for proper cell differentiation."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nIn a related line of inquiry, another study focused on the role of micro ribonucleic acid (miR)-6836-3p in the context of hypertrophic scar formation. Although the comprehensive mechanism remains under investigation, this work is aimed at elucidating how miR-6836-3p may modulate gene expression and associated signaling pathways during the process of scar formation. The exploration of miR-6836-3p’s function is anticipated to provide insights into pathways that could be therapeutically targeted to ameliorate pathological scarring."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "2"}]}, {"type": "t", "text": "\n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Zonggui Wang, Zhong Dai, Yaqiong Pan, et al. "}, {"type": "b", "children": [{"type": "t", "text": "E3 ubiquitin ligase DTX4 is required for adipogenic differentiation in 3T3-L1 preadipocytes cell line."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Biochem Biophys Res Commun (2017)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.bbrc.2017.08.083"}], "href": "https://doi.org/10.1016/j.bbrc.2017.08.083"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "28842252"}], "href": "https://pubmed.ncbi.nlm.nih.gov/28842252"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "F Liu, W-W Chen, Y Li, et al. "}, {"type": "b", "children": [{"type": "t", "text": "MiR-6836-3p promotes proliferation of hypertrophic scar fibroblasts by targeting CTGF."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Eur Rev Med Pharmacol Sci (2018)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.26355/eurrev_201807_15396"}], "href": "https://doi.org/10.26355/eurrev_201807_15396"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "30024593"}], "href": "https://pubmed.ncbi.nlm.nih.gov/30024593"}]}]}]}
|
| Synonyms | HSA-MIR-6836 |
| NCBI Gene ID | 102465503 |
| API | |
| Download Associations | |
| Predicted Functions |
![]() |
| Co-expressed Genes |
![]() |
| Expression in Tissues and Cell Lines |
![]() |
MIR6836 has 0 functional associations with biological entities spanning 0 categories () extracted from 0 datasets.
Click the + buttons to view associations for MIR6836 from the datasets below.
If available, associations are ranked by standardized value
| Dataset | Summary |
|---|