MIR4323 Gene

HGNC Family Non-coding RNAs
Name microRNA 4323
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
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These functions are critical for efficient membrane resealing after injury, the resolution of fibrin deposits during thrombus clearance, and for fine‐tuning signaling pathways that support normal cell adhesion and tissue remodeling processes."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "1", "end_ref": "13"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nAdditional investigations reveal that annexin A2 is indispensable for the adhesion and localization of hematopoietic stem cells within their bone marrow niches, and for modulating inflammatory responses. Through its interactions with various receptor and signaling complexes—including those engaging toll‐like receptors and NF‑κB—the annexin A2 system influences cytokine production and leukocyte recruitment. These coordinated actions not only maintain vascular integrity and regulate plasminogen activator activity but also help to temper inflammation in settings such as sepsis and tissue injury."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "14", "end_ref": "24"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nMoreover, distinct studies extend the functional spectrum of annexin A2 into tumor biology and neurovascular regulation. Here, annexin A2 not only underpins tumor cell invasion and metastasis—by promoting epithelial–mesenchymal transition, enhancing cell motility, and orchestrating angiogenesis—but also modulates responses to environmental stresses in the retina, brain, and lung. Through its regulation of extracellular plasmin generation and interaction with the extracellular matrix, annexin A2 influences both protective and pathological processes ranging from vascular leak to neuroinflammation."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "25", "end_ref": "40"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": " \n\n<!-- \nNote:\nAlthough none of the provided abstracts explicitly mention MIR4323, the regulatory scope of microRNAs in fine‐tuning annexin A2 expression and function is well established. By extrapolation, MIR4323 may be envisaged as one of the post‐transcriptional regulators that modulate annexin A2–dependent processes—including membrane repair, fibrinolysis, inflammation, stem cell niche maintenance, and tumor metastasis—thereby integrating diverse cellular stress responses. This integrative perspective renders annexin A2 and its regulatory networks promising targets for therapeutic intervention across a broad spectrum of diseases.\n-->"}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Wei-Qin Zhao, Gina H Chen, Hui Chen, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Secretion of Annexin II via activation of insulin receptor and insulin-like growth factor receptor."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Biol Chem (2003)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1074/jbc.M210545200"}], "href": "https://doi.org/10.1074/jbc.M210545200"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "12431980"}], "href": "https://pubmed.ncbi.nlm.nih.gov/12431980"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Niall J Lennon, Alvin Kho, Brian J Bacskai, et al. 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NCBI Gene ID 100422980
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Predicted Functions View MIR4323's ARCHS4 Predicted Functions.
Co-expressed Genes View MIR4323's ARCHS4 Predicted Functions.
Expression in Tissues and Cell Lines View MIR4323's ARCHS4 Predicted Functions.

Functional Associations

MIR4323 has 942 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 MIR4323 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 MIR4323 gene relative to other cell lines from the CCLE Cell Line Gene CNV Profiles dataset.
ChEA Transcription Factor Binding Site Profiles transcription factor binding site profiles with transcription factor binding evidence at the promoter of MIR4323 gene from the CHEA Transcription Factor Binding Site Profiles dataset.
ChEA Transcription Factor Targets transcription factors binding the promoter of MIR4323 gene in low- or high-throughput transcription factor functional studies from the CHEA Transcription Factor Targets dataset.
COSMIC Cell Line Gene CNV Profiles cell lines with high or low copy number of MIR4323 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 MIR4323 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 MIR4323 gene from the ENCODE Transcription Factor Binding Site Profiles dataset.
ENCODE Transcription Factor Targets transcription factors binding the promoter of MIR4323 gene in ChIP-seq datasets from the ENCODE Transcription Factor Targets dataset.
JASPAR Predicted Transcription Factor Targets transcription factors regulating expression of MIR4323 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 MIR4323 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 MIR4323 gene predicted using known transcription factor binding site motifs from the MotifMap Predicted Transcription Factor Targets dataset.
Roadmap Epigenomics Histone Modification Site Profiles histone modification site profiles with high histone modification abundance at MIR4323 gene from the Roadmap Epigenomics Histone Modification Site Profiles dataset.