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    MIR181A1 microRNA 181a-1 [ Homo sapiens (human) ]

    Gene ID: 406995, updated on 10-Dec-2024

    Summary

    Official Symbol
    MIR181A1provided by HGNC
    Official Full Name
    microRNA 181a-1provided by HGNC
    Primary source
    HGNC:HGNC:31590
    See related
    Ensembl:ENSG00000207759 MIM:612742; miRBase:MI0000289; AllianceGenome:HGNC:31590
    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
    MIR213; MIRN213; mir-213; MIRN181A1; mir-181a-1; hsa-mir-181a-1
    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 MIR181A1 in Genome Data Viewer
    Location:
    1q32.1
    Exon count:
    1
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 1 NC_000001.11 (198859044..198859153, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 1 NC_060925.1 (198117684..198117793, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 1 NC_000001.10 (198828173..198828282, complement)

    Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene protein tyrosine phosphatase receptor type C Neighboring gene PTPRC intron CAGE-defined mid-level expression enhancer Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr1:198670715-198671264 Neighboring gene phosphatidylethanolamine binding protein 1 pseudogene 3 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 1667 Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr1:198776880-198778079 Neighboring gene MIR181A1 host gene Neighboring gene microRNA 181b-1 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 2285 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 2286 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 2287 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 2288 Neighboring gene ribosomal protein S2 pseudogene 9 Neighboring gene long intergenic non-protein coding RNA 1222 Neighboring gene long intergenic non-protein coding RNA 1221

    Genomic regions, transcripts, and products

    Bibliography

    GeneRIFs: Gene References Into Functions

    What's a GeneRIF?

    Phenotypes

    EBI GWAS Catalog

    Description
    Seventy-five genetic loci influencing the human red blood cell.
    EBI GWAS Catalog

    Pathways from PubChem

    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_029626.1 RNA Sequence

      Status: PROVISIONAL

      Source sequence(s)
      AL136321
      Related
      ENST00000385026.1

    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_000001.11 Reference GRCh38.p14 Primary Assembly

      Range
      198859044..198859153 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060925.1 Alternate T2T-CHM13v2.0

      Range
      198117684..198117793 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)