MIR6796 Gene

HGNC Family Non-coding RNAs
Name microRNA 6796
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 studies have underscored the pivotal role of the endoplasmic reticulum (ER) in immune cell function, particularly during phagocytosis, where ER-localized SNARE proteins such as syntaxin 18 facilitate direct membrane fusion events at the plasma or phagosomal membranes. Although these studies (e.g."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": "do not explicitly mention MIR6796, they describe mechanisms and regulatory protein complexes that could be modulated by noncoding RNAs, including microRNAs like MIR6796, to fine-tune phagocytic activities.\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nA complementary investigation focused on the SNARE protein Sec22b revealed that its overexpression impairs phagocytosis, acting as a negative regulator in ER-mediated phagosome formation."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "2"}]}, {"type": "t", "text": " The functional balance between positive mediators (syntaxin 18 and D12) and inhibitory factors (Sec22b) is critical for phagocytosis efficiency. Although MIR6796 is not directly referenced in these experiments, the existence of such tightly controlled molecular networks suggests that MIR6796 could participate in regulating these pathways by modulating the expression or activity of key SNARE proteins.\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nIn a different context, a study screening circular RNAs (circRNAs) for their potential roles within competing endogenous RNA (ceRNA) networks revealed molecules influencing the expression of matrix metalloproteinase 9 (MMP9), a key player in acute ischemic stroke."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "3"}]}, {"type": "t", "text": " Although MIR6796 is not explicitly described, its categorization as a microRNA hints at the possibility that it may intersect with such ceRNA networks. In this scenario, MIR6796 could indirectly influence MMP9 levels and thereby impact extracellular matrix remodeling and stroke outcomes.\n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Kiyotaka Hatsuzawa, Taku Tamura, Hitoshi Hashimoto, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Involvement of syntaxin 18, an endoplasmic reticulum (ER)-localized SNARE protein, in ER-mediated phagocytosis."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Mol Biol Cell (2006)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1091/mbc.e05-12-1174"}], "href": "https://doi.org/10.1091/mbc.e05-12-1174"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "16790498"}], "href": "https://pubmed.ncbi.nlm.nih.gov/16790498"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Kiyotaka Hatsuzawa, Hitoshi Hashimoto, Hiromi Hashimoto, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Sec22b is a negative regulator of phagocytosis in macrophages."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Mol Biol Cell (2009)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1091/mbc.e09-03-0241"}], "href": "https://doi.org/10.1091/mbc.e09-03-0241"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "19710423"}], "href": "https://pubmed.ncbi.nlm.nih.gov/19710423"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "Tian Xu, Yuqing Li, Ning Zhu, et al. "}, {"type": "b", "children": [{"type": "t", "text": "circSKA3 acts as a sponge of miR-6796-5p to be associated with outcomes of ischemic stroke by regulating matrix metalloproteinase 9 expression."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Eur J Neurol (2022)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1111/ene.15164"}], "href": "https://doi.org/10.1111/ene.15164"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "34725884"}], "href": "https://pubmed.ncbi.nlm.nih.gov/34725884"}]}]}]}
Synonyms HSA-MIR-6796
NCBI Gene ID 102465477
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Predicted Functions View MIR6796's ARCHS4 Predicted Functions.
Co-expressed Genes View MIR6796's ARCHS4 Predicted Functions.
Expression in Tissues and Cell Lines View MIR6796's ARCHS4 Predicted Functions.

Functional Associations

MIR6796 has 0 functional associations with biological entities spanning 0 categories () extracted from 0 datasets.

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Dataset Summary