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    MIR597 microRNA 597 [ Homo sapiens (human) ]

    Gene ID: 693182, updated on 10-Dec-2024

    Summary

    Official Symbol
    MIR597provided by HGNC
    Official Full Name
    microRNA 597provided by HGNC
    Primary source
    HGNC:HGNC:32853
    See related
    Ensembl:ENSG00000207701 miRBase:MI0003609; AllianceGenome:HGNC:32853
    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
    MIRN597; mir-597; hsa-mir-597
    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 MIR597 in Genome Data Viewer
    Location:
    8p23.1
    Exon count:
    1
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 8 NC_000008.11 (9741672..9741768)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 8 NC_060932.1 (10002196..10002292, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 8 NC_000008.10 (9599182..9599278)

    Chromosome 8 - NC_000008.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105379231 Neighboring gene uncharacterized LOC124901884 Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr8:9240606-9241805 Neighboring gene DENN domain containing 4A pseudogene Neighboring gene ATAC-STARR-seq lymphoblastoid active region 26983 Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr8:9413105-9413766 Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr8:9413767-9414426 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 26984 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 26985 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 26986 Neighboring gene tankyrase Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 18908 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 26987 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 26988 Neighboring gene small nucleolar RNA U13 Neighboring gene uncharacterized LOC124902056

    Genomic regions, transcripts, and products

    Bibliography

    GeneRIFs: Gene References Into Functions

    What's a GeneRIF?

    Phenotypes

    EBI GWAS Catalog

    Description
    Genome-wide association study identifies three novel susceptibility loci for severe Acne vulgaris.
    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_030327.1 RNA Sequence

      Status: PROVISIONAL

      Source sequence(s)
      AC103834
      Related
      ENST00000384968.1

    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_000008.11 Reference GRCh38.p14 Primary Assembly

      Range
      9741672..9741768
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Reference GRCh38.p14 PATCHES

    Genomic

    1. NW_018654717.1 Reference GRCh38.p14 PATCHES

      Range
      3609806..3609902 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060932.1 Alternate T2T-CHM13v2.0

      Range
      10002196..10002292 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)