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MIR876 microRNA 876 [ Homo sapiens (human) ]

Gene ID: 100126310, updated on 10-Oct-2023

Summary

Official Symbol
MIR876provided by HGNC
Official Full Name
microRNA 876provided by HGNC
Primary source
HGNC:HGNC:33653
See related
Ensembl:ENSG00000215966 miRBase:MI0005542; AllianceGenome:HGNC:33653
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
MIRN876; mir-876; hsa-mir-876
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:
9p21.1
Exon count:
1
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 9 NC_000009.12 (28863626..28863706, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 9 NC_060933.1 (28876891..28876971, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 9 NC_000009.11 (28863624..28863704, complement)

Chromosome 9 - NC_000009.12Genomic Context describing neighboring genes Neighboring gene leucine rich repeat and Ig domain containing 2 Neighboring gene uncharacterized LOC124902136 Neighboring gene uncharacterized LOC105376003 Neighboring gene potassium channel tetramerization domain containing 10 pseudogene 1 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr9:28688087-28688762 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_107568 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr9:28775137-28775636 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr9:28820708-28821279 Neighboring gene NANOG hESC enhancer GRCh37_chr9:28929045-28929614 Neighboring gene NANOG hESC enhancer GRCh37_chr9:28938893-28939474 Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:28970143-28971066 Neighboring gene microRNA 873 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_107603 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_107631 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 19824 Neighboring gene NANOG hESC enhancer GRCh37_chr9:29251246-29251747 Neighboring gene pyruvate dehydrogenase kinase 1 pseudogene 1

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_030597.1 RNA Sequence

    Status: PROVISIONAL

    Source sequence(s)
    AL158072
    Related
    ENST00000401147.1

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_000009.12 Reference GRCh38.p14 Primary Assembly

    Range
    28863626..28863706 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060933.1 Alternate T2T-CHM13v2.0

    Range
    28876891..28876971 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)