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MIR656 microRNA 656 [ Homo sapiens (human) ]

Gene ID: 724026, updated on 15-Oct-2023

Summary

Official Symbol
MIR656provided by HGNC
Official Full Name
microRNA 656provided by HGNC
Primary source
HGNC:HGNC:32912
See related
Ensembl:ENSG00000207959 MIM:616376; miRBase:MI0003678; AllianceGenome:HGNC:32912
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
MIRN656; mir-656; hsa-mir-656
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:
14q32.31
Exon count:
1
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 14 NC_000014.9 (101066724..101066801)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 14 NC_060938.1 (95302111..95302188)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 14 NC_000014.8 (101533061..101533138)

Chromosome 14 - NC_000014.9Genomic Context describing neighboring genes Neighboring gene microRNA 369 Neighboring gene microRNA 410 Neighboring gene uncharacterized LOC105370670 Neighboring gene maternally expressed 9 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr14:101542889-101543546 Neighboring gene ReSE screen-validated silencer GRCh37_chr14:101544070-101544290 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr14:101550379-101550879 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr14:101581665-101582556 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr14:101582557-101583446 Neighboring gene uncharacterized LOC124903386 Neighboring gene long intergenic non-protein coding RNA 2285

Genomic regions, transcripts, and products

Bibliography

GeneRIFs: Gene References Into Functions

What's a GeneRIF?

Phenotypes

EBI GWAS Catalog

Description
A genome-wide search for loci interacting with known prostate cancer risk-associated genetic variants.
EBI GWAS Catalog

General gene information

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_030392.1 RNA Sequence

    Status: PROVISIONAL

    Source sequence(s)
    AL132709
    Related
    ENST00000385224.1

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_000014.9 Reference GRCh38.p14 Primary Assembly

    Range
    101066724..101066801
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060938.1 Alternate T2T-CHM13v2.0

    Range
    95302111..95302188
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)