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MIR548AM microRNA 548am [ Homo sapiens (human) ]

Gene ID: 100616428, updated on 17-Sep-2024

Summary

Official Symbol
MIR548AMprovided by HGNC
Official Full Name
microRNA 548amprovided by HGNC
Primary source
HGNC:HGNC:41637
See related
Ensembl:ENSG00000265144 miRBase:MI0016904; AllianceGenome:HGNC:41637
Gene type
ncRNA
RefSeq status
PROVISIONAL
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
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 MIR548AM in Genome Data Viewer
Location:
Xp22.2
Exon count:
1
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) X NC_000023.11 (16627012..16627085, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) X NC_060947.1 (16209478..16209551, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (16645135..16645208, complement)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene heat shock protein 90 alpha family class B member 1 pseudogene Neighboring gene RNA, 7SL, cytoplasmic 658, pseudogene Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chrX:16593879-16594382 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chrX:16595896-16596399 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chrX:16596400-16596904 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chrX:16596905-16597407 Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chrX:16597568-16598414 Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chrX:16598415-16599261 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chrX:16604766-16605549 Neighboring gene H3K4me1 hESC enhancer GRCh37_chrX:16625033-16625533 Neighboring gene CTP synthase 2 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chrX:16647850-16648497 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chrX:16648498-16649144 Neighboring gene S100 calcium binding protein G Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 20678 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 20679 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 29454 Neighboring gene Sharpr-MPRA regulatory region 4999 Neighboring gene synapse associated protein 1

Genomic regions, transcripts, and products

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_039762.1 RNA Sequence

    Status: PROVISIONAL

    Source sequence(s)
    AL445467
    Related
    ENST00000584298.1

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_000023.11 Reference GRCh38.p14 Primary Assembly

    Range
    16627012..16627085 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060947.1 Alternate T2T-CHM13v2.0

    Range
    16209478..16209551 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)