MIR3183 Gene

HGNC Family Non-coding RNAs
Name microRNA 3183
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 first study (PMID:"}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": "focused on Acylglycerol kinase (AGK) and its overexpression in multiple cancers, including breast cancer. Although that report primarily evaluated the clinical significance and biological role of AGK in tumorigenesis, it did not provide any direct evidence regarding the function of MIR3183. Consequently, no functional association between MIR3183 and AGK‐dependent oncogenic processes was described in this work.\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nThe second study (PMID:"}, {"type": "fg", "children": [{"type": "fg_f", "ref": "2"}]}, {"type": "t", "text": "examined the role of AGK in hematopoiesis, demonstrating that megakaryocyte/platelet-specific deletion of AGK leads to thrombocytopenia and splenomegaly through disrupted thrombocytopoiesis and altered JAK2/Stat3 signaling. Intriguingly, this study revealed that AGK’s impact on megakaryocyte differentiation and platelet biogenesis occurred independently of its kinase activity, and modifications in JAK2 binding further modulated this process. However, similar to the previous study, no insights into the function or regulatory contribution of MIR3183 were provided.\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nIn summary, while both abstracts underscore critical roles for AGK in cancer biology and platelet production, neither study addressed or implicated MIR3183 in these pathways. As such, the functional involvement of MIR3183 remains uncharacterized in the context of these investigations, warranting future studies to explore whether and how MIR3183 might interact with AGK regulatory networks or contribute to similar cellular processes.\n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Xi Wang, Chuyong Lin, Xiaohui Zhao, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Acylglycerol kinase promotes cell proliferation and tumorigenicity in breast cancer via suppression of the FOXO1 transcription factor."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Mol Cancer (2014)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1186/1476-4598-13-106"}], "href": "https://doi.org/10.1186/1476-4598-13-106"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "24886245"}], "href": "https://pubmed.ncbi.nlm.nih.gov/24886245"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Haojie Jiang, Zhuo Yu, Nan Ding, et al. "}, {"type": "b", "children": [{"type": "t", "text": "The role of AGK in thrombocytopoiesis and possible therapeutic strategies."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Blood (2020)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1182/blood.2019003851"}], "href": "https://doi.org/10.1182/blood.2019003851"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "32202634"}], "href": "https://pubmed.ncbi.nlm.nih.gov/32202634"}]}]}]}
Synonyms MIR-3183
NCBI Gene ID 100422835
API
Download Associations
Predicted Functions View MIR3183's ARCHS4 Predicted Functions.
Co-expressed Genes View MIR3183's ARCHS4 Predicted Functions.
Expression in Tissues and Cell Lines View MIR3183's ARCHS4 Predicted Functions.

Functional Associations

MIR3183 has 208 functional associations with biological entities spanning 3 categories (molecular profile, cell line, cell type or tissue, gene, protein or microRNA) extracted from 11 datasets.

Click the + buttons to view associations for MIR3183 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 MIR3183 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 MIR3183 gene relative to other cell lines from the COSMIC Cell Line Gene CNV Profiles dataset.
ENCODE Histone Modification Site Profiles histone modification site profiles with high histone modification abundance at MIR3183 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 MIR3183 gene from the ENCODE Transcription Factor Binding Site Profiles dataset.
ENCODE Transcription Factor Targets transcription factors binding the promoter of MIR3183 gene in ChIP-seq datasets from the ENCODE Transcription Factor Targets dataset.
GTEx Tissue Gene Expression Profiles tissues with high or low expression of MIR3183 gene relative to other tissues from the GTEx Tissue Gene Expression Profiles dataset.
JASPAR Predicted Transcription Factor Targets transcription factors regulating expression of MIR3183 gene predicted using known transcription factor binding site motifs from the JASPAR Predicted Transcription Factor Targets dataset.
Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles cell lines with high or low copy number of MIR3183 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 MIR3183 gene predicted using known transcription factor binding site motifs from the MotifMap Predicted Transcription Factor Targets dataset.
Roadmap Epigenomics Cell and Tissue DNA Methylation Profiles cell types and tissues with high or low DNA methylation of MIR3183 gene relative to other cell types and tissues from the Roadmap Epigenomics Cell and Tissue DNA Methylation Profiles dataset.
Roadmap Epigenomics Histone Modification Site Profiles histone modification site profiles with high histone modification abundance at MIR3183 gene from the Roadmap Epigenomics Histone Modification Site Profiles dataset.