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    MIR1266 microRNA 1266 [ Homo sapiens (human) ]

    Gene ID: 100302202, updated on 10-Dec-2024

    Summary

    Official Symbol
    MIR1266provided by HGNC
    Official Full Name
    microRNA 1266provided by HGNC
    Primary source
    HGNC:HGNC:35334
    See related
    Ensembl:ENSG00000221052 miRBase:MI0006403; AllianceGenome:HGNC:35334
    Gene type
    ncRNA
    RefSeq status
    PROVISIONAL
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    MIRN1266; mir-1266; hsa-mir-1266
    Summary
    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]
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    Genomic context

    See MIR1266 in Genome Data Viewer
    Location:
    15q21.2
    Exon count:
    1
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 15 NC_000015.10 (52277117..52277200, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 15 NC_060939.1 (50085399..50085482, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 15 NC_000015.9 (52569314..52569397, complement)

    Chromosome 15 - NC_000015.10Genomic Context describing neighboring genes Neighboring gene G protein subunit beta 5 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 6445 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr15:52472339-52472840 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_39732 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr15:52483687-52484186 Neighboring gene competing endogenous lncRNA 1 for miR-4707-5p and miR-4767 Neighboring gene uncharacterized LOC105370820 Neighboring gene ReSE screen-validated silencer GRCh37_chr15:52521219-52521393 Neighboring gene myosin VC Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr15:52549514-52550090 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr15:52552397-52552972 Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chr15:52578302-52579058 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 9425 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_39766 Neighboring gene uncharacterized LOC105370819 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 6446 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 9426 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr15:52630438-52631014 Neighboring gene myosin VA Neighboring gene ATAC-STARR-seq lymphoblastoid active region 9427 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 9428 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 9429 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr15:52684277-52684953 Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chr15:52751737-52752632 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr15:52757960-52758715 Neighboring gene NANOG-H3K4me1 hESC enhancer GRCh37_chr15:52769819-52770320 Neighboring gene NANOG-H3K4me1 hESC enhancer GRCh37_chr15:52770321-52770820 Neighboring gene negCOR silencer S8 Neighboring gene eukaryotic translation elongation factor 1 beta 2 pseudogene 1

    Genomic regions, transcripts, and products

    Bibliography

    GeneRIFs: Gene References Into Functions

    What's a GeneRIF?

    NCBI Reference Sequences (RefSeq)

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    RefSeqs maintained independently of Annotated Genomes

    These reference sequences exist independently of genome builds. Explain

    These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

    RNA

    1. NR_031670.1 RNA Sequence

      Status: PROVISIONAL

      Source sequence(s)
      AC010674
      Related
      ENST00000408125.3

    RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

    The following sections contain reference sequences that belong to a specific genome build. Explain

    Reference GRCh38.p14 Primary Assembly

    Genomic

    1. NC_000015.10 Reference GRCh38.p14 Primary Assembly

      Range
      52277117..52277200 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060939.1 Alternate T2T-CHM13v2.0

      Range
      50085399..50085482 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)