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MIR1538 microRNA 1538 [ Homo sapiens (human) ]

Gene ID: 100302119, updated on 10-Oct-2023

Summary

Official Symbol
MIR1538provided by HGNC
Official Full Name
microRNA 1538provided by HGNC
Primary source
HGNC:HGNC:35382
See related
Ensembl:ENSG00000223109 miRBase:MI0007259; AllianceGenome:HGNC:35382
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
MIRN1538; hsa-mir-1538
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:
16q22.1
Exon count:
1
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 16 NC_000016.10 (69565808..69565868, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 16 NC_060940.1 (75368012..75368072, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 16 NC_000016.9 (69599711..69599771, complement)

Chromosome 16 - NC_000016.10Genomic Context describing neighboring genes Neighboring gene transmembrane protein 111 pseudogene Neighboring gene ReSE screen-validated silencer GRCh37_chr16:69477408-69477690 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 11038 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 11039 Neighboring gene cytochrome b5 type B Neighboring gene ReSE screen-validated silencer GRCh37_chr16:69488879-69489096 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 11040 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 11041 Neighboring gene uncharacterized LOC105371325 Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr16:69556814-69558013 Neighboring gene Sharpr-MPRA regulatory region 4304 Neighboring gene P300/CBP strongly-dependent group 1 enhancer GRCh37_chr16:69563811-69565010 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:69597937-69598833 Neighboring gene ReSE screen-validated silencer GRCh37_chr16:69599594-69599770 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 7663 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 7664 Neighboring gene nuclear factor of activated T cells 5 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 11043 Neighboring gene MPRA-validated peak2631 silencer Neighboring gene small nucleolar RNA, C/D box 13H

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_031719.1 RNA Sequence

    Status: PROVISIONAL

    Source sequence(s)
    AC009032
    Related
    ENST00000411177.1

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_000016.10 Reference GRCh38.p14 Primary Assembly

    Range
    69565808..69565868 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060940.1 Alternate T2T-CHM13v2.0

    Range
    75368012..75368072 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)