MIR7848 Gene

HGNC Family Non-coding RNAs
Name microRNA 7848
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": "\nAlthough the provided collection of abstracts offers a wide-ranging view of transient receptor potential (TRP) channel functions—most notably those of TRPV1 in nociception, thermoregulation, neurogenic inflammation, metabolic homeostasis, and cellular signaling"}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "1", "end_ref": "4"}]}, {"type": "t", "text": ", there is no discussion or experimental data concerning MIR7848 in any of these reports. Instead, these studies concentrate on elucidating the multifaceted roles of TRPV1 and other TRP channels—for example, demonstrating that TRPV1 contributes to rapid sensitization of nociceptive neurons"}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "5", "end_ref": "10"}]}, {"type": "t", "text": ", and that its activation and modulation are critically involved in sensory perception, inflammatory hyperalgesia, and even metabolic regulation.\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nAdditional reports detail TRPV1 contributions to complex phenomena such as pruritus"}, {"type": "fg", "children": [{"type": "fg_f", "ref": "11"}]}, {"type": "t", "text": ", neuro-immune interactions"}, {"type": "fg", "children": [{"type": "fg_f", "ref": "13"}]}, {"type": "t", "text": ", and the regulation of pancreatic, adipose, and skeletal muscle functions."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "14", "end_ref": "20"}]}, {"type": "t", "text": " These findings extend to central nervous system roles—such as the modulation of fear‐related behavior and synaptic plasticity—as well as to peripheral mechanisms including vascular and bladder sensory functions."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "21", "end_ref": "29"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nMoreover, other studies in this set have expanded the panorama of TRPV1-related biology to include roles in phagocytosis and cell membrane trafficking, as well as its therapeutic exploitation in strategies for obesity, atherosclerosis, and neuropathies."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "30", "end_ref": "36"}]}, {"type": "t", "text": " Similarly, investigations addressing novel modalities of TRPV1 modulation—for instance, via endogenous ligands such as oxidized linoleic acid metabolites or ATP, as well as via engineered nanoparticle systems—further underline the channel’s extensive physiological and therapeutic relevance."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "37", "end_ref": "41"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nIn sum, while these numerous studies"}, {"type": "fg", "children": [{"type": "fg_f", "ref": "24"}, {"type": "fg_f", "ref": "3"}, {"type": "fg_f", "ref": "42"}, {"type": "fg_f", "ref": "11"}, {"type": "fg_f", "ref": "4"}, {"type": "fg_f", "ref": "43"}, {"type": "fg_f", "ref": "20"}]}, {"type": "t", "text": "collectively advance our understanding of TRPV1 and its associated cellular pathways in sensory neuron function, inflammation, metabolism, and beyond, not one of them addresses or mentions MIR7848. Consequently, the function of MIR7848 is not elucidated in these abstracts; its potential roles, interactions, or regulatory effects remain undetermined and represent an open area for future research.\n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "L A Birder, Y Nakamura, S Kiss, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Altered urinary bladder function in mice lacking the vanilloid receptor TRPV1."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Nat Neurosci (2002)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/nn902"}], "href": "https://doi.org/10.1038/nn902"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "12161756"}], "href": "https://pubmed.ncbi.nlm.nih.gov/12161756"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Vijay Lyall, Gerard L Heck, Anna K Vinnikova, et al. 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Synonyms HSA-MIR-7848
NCBI Gene ID 102466865
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Predicted Functions View MIR7848's ARCHS4 Predicted Functions.
Co-expressed Genes View MIR7848's ARCHS4 Predicted Functions.
Expression in Tissues and Cell Lines View MIR7848's ARCHS4 Predicted Functions.

Functional Associations

MIR7848 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