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MIR4697 microRNA 4697 [ Homo sapiens (human) ]

Gene ID: 100616119, updated on 12-Oct-2019

Summary

Official Symbol
MIR4697provided by HGNC
Official Full Name
microRNA 4697provided by HGNC
Primary source
HGNC:HGNC:41570
See related
Ensembl:ENSG00000284020 miRBase:MI0017330
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]

Genomic context

See MIR4697 in Genome Data Viewer
Location:
11q25
Exon count:
1
Annotation release Status Assembly Chr Location
109.20190905 current GRCh38.p13 (GCF_000001405.39) 11 NC_000011.10 (133898504..133898581, complement)
105 previous assembly GRCh37.p13 (GCF_000001405.25) 11 NC_000011.9 (133768399..133768476, complement)

Chromosome 11 - NC_000011.10Genomic Context describing neighboring genes Neighboring gene spermatogenesis associated 19 Neighboring gene calponin 2 pseudogene Neighboring gene MIR4697 host gene Neighboring gene immunoglobulin superfamily member 9B Neighboring gene long intergenic non-protein coding RNA 2730

Genomic regions, transcripts, and products

Bibliography

Phenotypes

NHGRI GWAS Catalog

Description
Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease.
NHGRI GWA Catalog

NCBI Reference Sequences (RefSeq)

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_039846.1 RNA Sequence

    Status: PROVISIONAL

    Source sequence(s)
    AP001979
    Related
    ENST00000582977.1

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 109.20190905

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000011.10 Reference GRCh38.p13 Primary Assembly

    Range
    133898504..133898581 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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