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    MIR28 microRNA 28 [ Homo sapiens (human) ]

    Gene ID: 407020, updated on 2-Nov-2024

    Summary

    Official Symbol
    MIR28provided by HGNC
    Official Full Name
    microRNA 28provided by HGNC
    Primary source
    HGNC:HGNC:31615
    See related
    Ensembl:ENSG00000207651 MIM:612154; miRBase:MI0000086; AllianceGenome:HGNC:31615
    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
    MIRN28; miR-28; hsa-mir-28
    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 MIR28 in Genome Data Viewer
    Location:
    3q28
    Exon count:
    1
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 3 NC_000003.12 (188688781..188688866)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 3 NC_060927.1 (191506060..191506145)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 3 NC_000003.11 (188406569..188406654)

    Chromosome 3 - NC_000003.12Genomic Context describing neighboring genes Neighboring gene LIM domain containing preferred translocation partner in lipoma Neighboring gene uncharacterized LOC124906316 Neighboring gene LPP antisense RNA 1 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr3:188353620-188354172 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr3:188354173-188354724 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 14996 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr3:188600655-188601154 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr3:188600153-188600654 Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr3:188618060-188619259 Neighboring gene Sharpr-MPRA regulatory region 14211 Neighboring gene NANOG hESC enhancer GRCh37_chr3:188655166-188655667 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr3:188655787-188656288 Neighboring gene Sharpr-MPRA regulatory region 11355 Neighboring gene NANOG hESC enhancer GRCh37_chr3:188674939-188675473 Neighboring gene TPRG1 antisense RNA 1 Neighboring gene ENOPH1 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_029502.1 RNA Sequence

      Status: PROVISIONAL

      Source sequence(s)
      AC063932
      Related
      ENST00000384918.1

    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_000003.12 Reference GRCh38.p14 Primary Assembly

      Range
      188688781..188688866
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060927.1 Alternate T2T-CHM13v2.0

      Range
      191506060..191506145
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)