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MIR548M microRNA 548m [ Homo sapiens (human) ]

Gene ID: 100313772, updated on 10-Oct-2023

Summary

Official Symbol
MIR548Mprovided by HGNC
Official Full Name
microRNA 548mprovided by HGNC
Primary source
HGNC:HGNC:35331
See related
Ensembl:ENSG00000221187 miRBase:MI0006400; AllianceGenome:HGNC:35331
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
MIRN548M
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

Location:
Xq21.33
Exon count:
1
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) X NC_000023.11 (95063141..95063226, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) X NC_060947.1 (93508429..93508514, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (94318140..94318225, complement)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene cyclin B1 interacting protein 1 pseudogene 3 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chrX:94100291-94100831 Neighboring gene uncharacterized LOC107985710 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chrX:94117653-94118233 Neighboring gene H3K27ac hESC enhancer GRCh37_chrX:94142296-94142796 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chrX:94162743-94163280 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chrX:94163281-94163816 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chrX:94347448-94348142 Neighboring gene CDK7 strongly-dependent group 2 enhancer GRCh37_chrX:94544817-94546016 Neighboring gene uncharacterized LOC124905288 Neighboring gene calmodulin 1 pseudogene 1

Genomic regions, transcripts, and products

Bibliography

General gene information

Other Names

  • hsa-mir-548m

Gene Ontology Provided by GOA

Process Evidence Code Pubs
involved_in miRNA-mediated post-transcriptional gene silencing IEA
Inferred from Electronic Annotation
more info
 
Component Evidence Code Pubs
part_of RISC complex IEA
Inferred from Electronic Annotation
more info
 

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_031667.1 RNA Sequence

    Status: PROVISIONAL

    Source sequence(s)
    AL390966
    Related
    ENST00000408260.1

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_10

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000023.11 Reference GRCh38.p14 Primary Assembly

    Range
    95063141..95063226 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060947.1 Alternate T2T-CHM13v2.0

    Range
    93508429..93508514 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)