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MIR606 microRNA 606 [ Homo sapiens (human) ]

Gene ID: 693191, updated on 4-Dec-2023

Summary

Official Symbol
MIR606provided by HGNC
Official Full Name
microRNA 606provided by HGNC
Primary source
HGNC:HGNC:32862
See related
Ensembl:ENSG00000207583 miRBase:MI0003619; AllianceGenome:HGNC:32862
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
MIRN606; hsa-mir-606
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:
10q22.2
Exon count:
1
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 10 NC_000010.11 (75552458..75552553)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 10 NC_060934.1 (76426529..76426624)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 10 NC_000010.10 (77312216..77312311)

Chromosome 10 - NC_000010.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC101929234 Neighboring gene uncharacterized LOC107984293 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr10:77191190-77191690 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr10:77191691-77192191 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr10:77210325-77211210 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr10:77234571-77235319 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr10:77235320-77236067 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr10:77297811-77298425 Neighboring gene leucine rich melanocyte differentiation associated Neighboring gene NANOG-H3K4me1 hESC enhancer GRCh37_chr10:77356902-77357728 Neighboring gene NANOG hESC enhancer GRCh37_chr10:77359991-77360570 Neighboring gene uncharacterized LOC105378367 Neighboring gene ReSE screen-validated silencer GRCh37_chr10:77488076-77488220 Neighboring gene NANOG hESC enhancer GRCh37_chr10:77509344-77509845 Neighboring gene Sharpr-MPRA regulatory region 10683 Neighboring gene uncharacterized LOC124902463

Genomic regions, transcripts, and products

Bibliography

Related articles in PubMed

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_030337.1 RNA Sequence

    Status: PROVISIONAL

    Source sequence(s)
    AL589863
    Related
    ENST00000384851.1

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_000010.11 Reference GRCh38.p14 Primary Assembly

    Range
    75552458..75552553
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060934.1 Alternate T2T-CHM13v2.0

    Range
    76426529..76426624
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)