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    MIR147A microRNA 147a [ Homo sapiens (human) ]

    Gene ID: 406939, updated on 2-Nov-2024

    Summary

    Official Symbol
    MIR147Aprovided by HGNC
    Official Full Name
    microRNA 147aprovided by HGNC
    Primary source
    HGNC:HGNC:31534
    See related
    Ensembl:ENSG00000207814 miRBase:MI0000262; AllianceGenome:HGNC:31534
    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
    MIR147; MIRN147; hsa-mir-147a
    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 MIR147A in Genome Data Viewer
    Location:
    9q33.2
    Exon count:
    1
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 9 NC_000009.12 (120244979..120245050, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 9 NC_060933.1 (132438809..132438880, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 9 NC_000009.11 (123007257..123007328, complement)

    Chromosome 9 - NC_000009.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC124902259 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:122817148-122817743 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:122817744-122818338 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr9:122879131-122879760 Neighboring gene Sharpr-MPRA regulatory region 9522 Neighboring gene uncharacterized LOC124902260 Neighboring gene uncharacterized LOC105376253 Neighboring gene MPRA-validated peak7326 silencer Neighboring gene ReSE screen-validated silencer GRCh37_chr9:123142787-123142995 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:123152383-123152883 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:123164680-123165648 Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chr9:123174184-123174980 Neighboring gene CDK5 regulatory subunit associated protein 2 Neighboring gene H3K27ac hESC enhancer GRCh37_chr9:123251855-123252356 Neighboring gene H3K27ac hESC enhancer GRCh37_chr9:123252357-123252856 Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:123342117-123342679

    Genomic regions, transcripts, and products

    Bibliography

    GeneRIFs: Gene References Into Functions

    What's a GeneRIF?

    Phenotypes

    EBI GWAS Catalog

    Description
    Genome-wide association of lipid-lowering response to statins in combined study populations.
    EBI GWAS Catalog
    Genome-wide association studies and heritability estimates of body mass index related phenotypes in bangladeshi adults.
    EBI GWAS Catalog

    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_029604.1 RNA Sequence

      Status: PROVISIONAL

      Source sequence(s)
      AL592549
      Related
      ENST00000385079.1

    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_000009.12 Reference GRCh38.p14 Primary Assembly

      Range
      120244979..120245050 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060933.1 Alternate T2T-CHM13v2.0

      Range
      132438809..132438880 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)