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    MIR5000 microRNA 5000 [ Homo sapiens (human) ]

    Gene ID: 100846995, updated on 17-Sep-2024

    Summary

    Official Symbol
    MIR5000provided by HGNC
    Official Full Name
    microRNA 5000provided by HGNC
    Primary source
    HGNC:HGNC:43464
    See related
    Ensembl:ENSG00000263909 miRBase:MI0017866; AllianceGenome:HGNC:43464
    Gene type
    ncRNA
    RefSeq status
    PROVISIONAL
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    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 MIR5000 in Genome Data Viewer
    Location:
    2p12
    Exon count:
    1
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 2 NC_000002.12 (75090812..75090914)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 2 NC_060926.1 (75099650..75099752)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 2 NC_000002.11 (75317939..75318041)

    Chromosome 2 - NC_000002.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105374809 Neighboring gene H3K27ac hESC enhancer GRCh37_chr2:75185356-75185856 Neighboring gene H3K27ac hESC enhancer GRCh37_chr2:75185857-75186357 Neighboring gene NANOG hESC enhancer GRCh37_chr2:75211079-75211580 Neighboring gene DNA polymerase epsilon 4, accessory subunit Neighboring gene uncharacterized LOC124907850 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 11678 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 11679 Neighboring gene tachykinin receptor 1 Neighboring gene ReSE screen-validated silencer GRCh37_chr2:75319672-75319876 Neighboring gene uncharacterized LOC105374811 Neighboring gene NANOG hESC enhancer GRCh37_chr2:75440885-75441885 Neighboring gene H3K27ac hESC enhancer GRCh37_chr2:75444277-75444776 Neighboring gene ReSE screen-validated silencer GRCh37_chr2:75444809-75444984 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr2:75446173-75446920 Neighboring gene uncharacterized LOC107985900 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 16084 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 16085 Neighboring gene uncharacterized LOC105374810

    Genomic regions, transcripts, and products

    Bibliography

    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_049796.1 RNA Sequence

      Status: PROVISIONAL

      Source sequence(s)
      AC007400
      Related
      ENST00000577717.1

    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_000002.12 Reference GRCh38.p14 Primary Assembly

      Range
      75090812..75090914
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060926.1 Alternate T2T-CHM13v2.0

      Range
      75099650..75099752
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)