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MIR1266 microRNA 1266 [ Homo sapiens (human) ]

Gene ID: 100302202, updated on 17-Sep-2024

Summary

Official Symbol
MIR1266provided by HGNC
Official Full Name
microRNA 1266provided by HGNC
Primary source
HGNC:HGNC:35334
See related
Ensembl:ENSG00000221052 miRBase:MI0006403; AllianceGenome:HGNC:35334
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
MIRN1266; mir-1266; hsa-mir-1266
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 MIR1266 in Genome Data Viewer
Location:
15q21.2
Exon count:
1
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 15 NC_000015.10 (52277117..52277200, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 15 NC_060939.1 (50085399..50085482, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 15 NC_000015.9 (52569314..52569397, complement)

Chromosome 15 - NC_000015.10Genomic Context describing neighboring genes Neighboring gene G protein subunit beta 5 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 6445 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr15:52472339-52472840 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_39732 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr15:52483687-52484186 Neighboring gene competing endogenous lncRNA 1 for miR-4707-5p and miR-4767 Neighboring gene uncharacterized LOC105370820 Neighboring gene ReSE screen-validated silencer GRCh37_chr15:52521219-52521393 Neighboring gene myosin VC Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr15:52549514-52550090 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr15:52552397-52552972 Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chr15:52578302-52579058 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 9425 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_39766 Neighboring gene uncharacterized LOC105370819 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 6446 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 9426 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr15:52630438-52631014 Neighboring gene myosin VA Neighboring gene ATAC-STARR-seq lymphoblastoid active region 9427 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 9428 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 9429 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr15:52684277-52684953 Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chr15:52751737-52752632 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr15:52757960-52758715 Neighboring gene NANOG-H3K4me1 hESC enhancer GRCh37_chr15:52769819-52770320 Neighboring gene NANOG-H3K4me1 hESC enhancer GRCh37_chr15:52770321-52770820 Neighboring gene negCOR silencer S8 Neighboring gene eukaryotic translation elongation factor 1 beta 2 pseudogene 1

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_031670.1 RNA Sequence

    Status: PROVISIONAL

    Source sequence(s)
    AC010674
    Related
    ENST00000408125.3

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000015.10 Reference GRCh38.p14 Primary Assembly

    Range
    52277117..52277200 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060939.1 Alternate T2T-CHM13v2.0

    Range
    50085399..50085482 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)