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MIR1471 microRNA 1471 [ Homo sapiens (human) ]

Gene ID: 100302126, updated on 17-Sep-2024

Summary

Official Symbol
MIR1471provided by HGNC
Official Full Name
microRNA 1471provided by HGNC
Primary source
HGNC:HGNC:35380
See related
Ensembl:ENSG00000222246 miRBase:MI0007076; AllianceGenome:HGNC:35380
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
MIRN1471; hsa-mir-1471
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 MIR1471 in Genome Data Viewer
Location:
2q37.1
Exon count:
1
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 2 NC_000002.12 (231892242..231892298, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 2 NC_060926.1 (232378868..232378924, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 2 NC_000002.11 (232756952..232757008, complement)

Chromosome 2 - NC_000002.12Genomic Context describing neighboring genes Neighboring gene ribosomal protein L28 pseudogene 2 Neighboring gene COP9 signalosome subunit 7B Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 12450 Neighboring gene guanidinoacetate N-methyltransferase pseudogene 1 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:232769840-232770458 Neighboring gene H3K27ac hESC enhancer GRCh37_chr2:232770459-232771076 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 12453 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 12452 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 12451 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr2:232791796-232792450 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 17318 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 12454 Neighboring gene natriuretic peptide C Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr2:232854631-232855252 Neighboring gene DIS3 like 3'-5' exoribonuclease 2 Neighboring gene MPRA-validated peak4085 silencer Neighboring gene ReSE screen-validated silencer GRCh37_chr2:232986245-232986439 Neighboring gene Sharpr-MPRA regulatory region 7061 Neighboring gene microRNA 562

Genomic regions, transcripts, and products

Bibliography

Related articles in PubMed

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_031717.1 RNA Sequence

    Status: PROVISIONAL

    Source sequence(s)
    AC013435
    Related
    ENST00000410314.1

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
    231892242..231892298 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060926.1 Alternate T2T-CHM13v2.0

    Range
    232378868..232378924 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)