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MIR1206 microRNA 1206 [ Homo sapiens (human) ]

Gene ID: 100302170, updated on 10-Oct-2023

Summary

Official Symbol
MIR1206provided by HGNC
Official Full Name
microRNA 1206provided by HGNC
Primary source
HGNC:HGNC:35272
See related
Ensembl:ENSG00000283200 miRBase:MI0006339; AllianceGenome:HGNC:35272
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
MIRN1206; hsa-mir-1206
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:
8q24.21
Exon count:
1
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 8 NC_000008.11 (128008898..128008956)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 8 NC_060932.1 (129136749..129136807)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 8 NC_000008.10 (129021144..129021202)

Chromosome 8 - NC_000008.11Genomic Context describing neighboring genes Neighboring gene Pvt1 oncogene Neighboring gene CRISPRi-validated MYC e2 enhancer Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr8:128976545-128977156 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 19535 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 27954 Neighboring gene microRNA 1205 Neighboring gene H3K27ac hESC enhancer GRCh37_chr8:129004541-129005042 Neighboring gene H3K27ac hESC enhancer GRCh37_chr8:129005043-129005542 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 27956 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 27957 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr8:129013561-129014142 Neighboring gene RNA, variant U1 small nuclear 32 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 27958 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr8:129037427-129037927 Neighboring gene RNA, U4 small nuclear 25, pseudogene Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr8:129050073-129050724 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr8:129050725-129051374 Neighboring gene CRISPRi-validated MYC e3 enhancer Neighboring gene CRISPRi-validated MYC e4 enhancer Neighboring gene microRNA 1207

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_031611.1 RNA Sequence

    Status: PROVISIONAL

    Source sequence(s)
    AC103705
    Related
    ENST00000637127.1

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_000008.11 Reference GRCh38.p14 Primary Assembly

    Range
    128008898..128008956
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060932.1 Alternate T2T-CHM13v2.0

    Range
    129136749..129136807
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)