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MIR1263 microRNA 1263 [ Homo sapiens (human) ]

Gene ID: 100302148, updated on 10-Oct-2023

Summary

Official Symbol
MIR1263provided by HGNC
Official Full Name
microRNA 1263provided by HGNC
Primary source
HGNC:HGNC:35329
See related
Ensembl:ENSG00000221251 miRBase:MI0006398; AllianceGenome:HGNC:35329
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
MIRN1263; hsa-mir-1263
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:
3q26.1
Exon count:
1
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 3 NC_000003.12 (164171471..164171556, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 3 NC_060927.1 (166954195..166954280, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 3 NC_000003.11 (163889259..163889344, complement)

Chromosome 3 - NC_000003.12Genomic Context describing neighboring genes Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_66489 Neighboring gene RNA, U7 small nuclear 82 pseudogene Neighboring gene H3K27ac hESC enhancer GRCh37_chr3:163470926-163471426 Neighboring gene NANOG hESC enhancer GRCh37_chr3:163497107-163497624 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr3:163625147-163625703 Neighboring gene uncharacterized LOC102724419 Neighboring gene NGRN pseudogene 1 Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr3:163897108-163898307 Neighboring gene H3K27ac hESC enhancer GRCh37_chr3:164038591-164039092 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr3:164049948-164050849 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr3:164050850-164051750 Neighboring gene uncharacterized LOC105374189 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr3:164059961-164060513 Neighboring gene uncharacterized LOC105374190

Genomic regions, transcripts, and products

Bibliography

GeneRIFs: Gene References Into Functions

What's a GeneRIF?

Phenotypes

EBI GWAS Catalog

Description
Gene-age interactions in blood pressure regulation: a large-scale investigation with the CHARGE, Global BPgen, and ICBP Consortia.
EBI GWAS Catalog

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_031665.1 RNA Sequence

    Status: PROVISIONAL

    Source sequence(s)
    AC018457
    Related
    ENST00000408324.1

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_000003.12 Reference GRCh38.p14 Primary Assembly

    Range
    164171471..164171556 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060927.1 Alternate T2T-CHM13v2.0

    Range
    166954195..166954280 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)