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MIR4668 microRNA 4668 [ Homo sapiens (human) ]

Gene ID: 100616114, updated on 10-Oct-2023

Summary

Official Symbol
MIR4668provided by HGNC
Official Full Name
microRNA 4668provided by HGNC
Primary source
HGNC:HGNC:41545
See related
Ensembl:ENSG00000266315 miRBase:MI0017298; AllianceGenome:HGNC:41545
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
mir-4668
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 MIR4668 in Genome Data Viewer
Location:
9q31.3
Exon count:
1
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 9 NC_000009.12 (111932100..111932169)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 9 NC_060933.1 (124103447..124103516)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 9 NC_000009.11 (114694380..114694449)

Chromosome 9 - NC_000009.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC124902249 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_106030 Neighboring gene RNA, U6 small nuclear 1013, pseudogene Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr9:114630592-114631111 Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:114637095-114637945 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:114648577-114649405 Neighboring gene H3K27ac hESC enhancer GRCh37_chr9:114658545-114659128 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 20185 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 28799 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 28800 Neighboring gene UDP-glucose ceramide glucosyltransferase Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 20186 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 28801 Neighboring gene uncharacterized LOC124902250 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 28802 Neighboring gene ReSE screen-validated silencer GRCh37_chr9:114736633-114736863 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 28803 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 28804 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 28805 Neighboring gene RNA, U6 small nuclear 710, pseudogene

Genomic regions, transcripts, and products

Bibliography

Interactions

Products Interactant Other Gene Complex Source Pubs Description

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_039814.1 RNA Sequence

    Status: PROVISIONAL

    Source sequence(s)
    AL442066
    Related
    ENST00000582284.1

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
    111932100..111932169
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060933.1 Alternate T2T-CHM13v2.0

    Range
    124103447..124103516
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)