| HGNC Family | Non-coding RNAs |
| Name | microRNA 6770-1 |
| 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 none of the provided abstracts describe MIR6770-1 directly, the detailed functional studies of the STAM protein family—which MIR6770-1 is suggested to be linked with in this context—offer insights into potential processes it may influence. The abstracts document that STAM proteins (STAM1 and STAM2) assemble with key endocytic regulators such as Hrs and Eps15 to form multiprotein complexes that sort ubiquitinated membrane receptors into the multivesicular body pathway. These interactions facilitate the recruitment of signaling complexes to clathrin-enriched endosomal microdomains and play vital roles in receptor internalization and subsequent degradation."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "1", "end_ref": "3"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nIn addition to their endocytic sorting functions, STAM proteins are critical for proper T-cell development. Conditional knockout experiments demonstrate that loss of both STAM1 and STAM2 leads to impaired thymocyte proliferation and survival—a defect linked to enhanced apoptotic programs despite largely intact proximal T-cell–receptor and cytokine receptor signaling. This underscores the importance of STAM-mediated regulatory checkpoints in lymphocyte development."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "4"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nMoreover, in vivo expression analyses reveal that STAM2 exhibits widespread temporal and spatial expression during embryogenesis—in organs such as the developing neural tube, heart, brain regions, and various peripheral tissues—indicating its involvement in multiple developmental pathways. Consequently, any regulatory element associated with the STAM gene locus, including MIR6770-1, could be hypothesized to modulate these diverse processes by fine-tuning the expression or activity of STAM proteins."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "5"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nThus, while the abstracts do not directly address MIR6770-1, its genomic association with STAM2 suggests that MIR6770-1 may have a regulatory role—possibly at the post‐transcriptional level—that impacts receptor trafficking, signal transduction, and developmental programs governed by the STAM proteins.\n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Kristi G Bache, Camilla Raiborg, Anja Mehlum, et al. "}, {"type": "b", "children": [{"type": "t", "text": "STAM and Hrs are subunits of a multivalent ubiquitin-binding complex on early endosomes."}]}, {"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.M210843200"}], "href": "https://doi.org/10.1074/jbc.M210843200"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "12551915"}], "href": "https://pubmed.ncbi.nlm.nih.gov/12551915"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Tomonori Kaneko, Takashi Kumasaka, Tadashi Ganbe, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Structural insight into modest binding of a non-PXXP ligand to the signal transducing adaptor molecule-2 Src homology 3 domain."}]}, {"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.M306677200"}], "href": "https://doi.org/10.1074/jbc.M306677200"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "13129930"}], "href": "https://pubmed.ncbi.nlm.nih.gov/13129930"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "Chikako Kanazawa, Eiji Morita, Mitsuhiro Yamada, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Effects of deficiencies of STAMs and Hrs, mammalian class E Vps proteins, on receptor downregulation."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Biochem Biophys Res Commun (2003)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.bbrc.2003.08.078"}], "href": "https://doi.org/10.1016/j.bbrc.2003.08.078"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "13679051"}], "href": "https://pubmed.ncbi.nlm.nih.gov/13679051"}]}, {"type": "r", "ref": 4, "children": [{"type": "t", "text": "Mitsuhiro Yamada, Naoto Ishii, Hironobu Asao, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Signal-transducing adaptor molecules STAM1 and STAM2 are required for T-cell development and survival."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Mol Cell Biol (2002)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1128/MCB.22.24.8648-8658.2002"}], "href": "https://doi.org/10.1128/MCB.22.24.8648-8658.2002"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "12446783"}], "href": "https://pubmed.ncbi.nlm.nih.gov/12446783"}]}, {"type": "r", "ref": 5, "children": [{"type": "t", "text": "Marija Curlin, Katarina Kapuralin, Andres F Muro, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Stam2 expression pattern during embryo development."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Gene Expr Patterns (2012)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.gep.2011.11.005"}], "href": "https://doi.org/10.1016/j.gep.2011.11.005"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "22143071"}], "href": "https://pubmed.ncbi.nlm.nih.gov/22143071"}]}]}]}
|
| Synonyms | HSA-MIR-6770-1 |
| NCBI Gene ID | 102465461 |
| API | |
| Download Associations | |
| Predicted Functions |
![]() |
| Co-expressed Genes |
![]() |
| Expression in Tissues and Cell Lines |
![]() |
MIR6770-1 has 0 functional associations with biological entities spanning 0 categories () extracted from 0 datasets.
Click the + buttons to view associations for MIR6770-1 from the datasets below.
If available, associations are ranked by standardized value
| Dataset | Summary |
|---|