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MIR4458 microRNA 4458 [ Homo sapiens (human) ]

Gene ID: 100616142, updated on 2-Nov-2024

Summary

Official Symbol
MIR4458provided by HGNC
Official Full Name
microRNA 4458provided by HGNC
Primary source
HGNC:HGNC:41674
See related
Ensembl:ENSG00000284000 miRBase:MI0016804; AllianceGenome:HGNC:41674
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
mir-4458
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 MIR4458 in Genome Data Viewer
Location:
5p15.31
Exon count:
1
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 5 NC_000005.10 (8460925..8460999)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 5 NC_060929.1 (8400787..8400861)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 5 NC_000005.9 (8461038..8461112)

Chromosome 5 - NC_000005.10Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC102723339 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr5:8060973-8061591 Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr5:8090277-8091476 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr5:8165851-8166352 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr5:8166353-8166852 Neighboring gene long intergenic non-protein coding RNA 2226 Neighboring gene FAST kinase domains 3 pseudogene Neighboring gene ATAC-STARR-seq lymphoblastoid active region 22347 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 15907 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 15908 Neighboring gene NANOG hESC enhancer GRCh37_chr5:8473920-8474541 Neighboring gene MIR4458 host gene Neighboring gene uncharacterized LOC105374647 Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr5:8549695-8550894 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr5:8606154-8606898 Neighboring gene MT-ND6 pseudogene 2

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_039663.1 RNA Sequence

    Status: PROVISIONAL

    Source sequence(s)
    AC091965
    Related
    ENST00000578872.1

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_000005.10 Reference GRCh38.p14 Primary Assembly

    Range
    8460925..8460999
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060929.1 Alternate T2T-CHM13v2.0

    Range
    8400787..8400861
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)