MIR629 microRNA 629 [hom*o sapiens (human)] - Gene (2024)

Summary

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Official Symbol
MIR629provided by HGNC
Official Full Name
microRNA 629provided by HGNC
Primary source
HGNC:HGNC:32885
See related
Ensembl:ENSG00000207965 miRBase:MI0003643; AllianceGenome:HGNC:32885
Gene type
ncRNA
RefSeq status
PROVISIONAL
Organism
hom*o sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; hom*o
Also known as
MIRN629; mir-629; hsa-mir-629
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

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See MIR629 in Genome Data Viewer

Location:
15q23
Exon count:
1
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 15 NC_000015.10 (70079372..70079468, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 15 NC_060939.1 (67901600..67901696, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 15 NC_000015.9 (70371711..70371807, complement)

Chromosome 15 - NC_000015.10MIR629 microRNA 629 [hom*o sapiens (human)] - Gene (1)Neighboring gene uncharacterized LOC101929129Neighboring gene ATAC-STARR-seq lymphoblastoid active region 9665Neighboring gene ATAC-STARR-seq lymphoblastoid active region 9666Neighboring gene NANOG-H3K4me1 hESC enhancer GRCh37_chr15:70282987-70283875Neighboring gene H3K4me1 hESC enhancer GRCh37_chr15:70292527-70293028Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr15:70307241-70307744Neighboring gene ATAC-STARR-seq lymphoblastoid active region 9667Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_40838Neighboring gene uncharacterized LOC124903518Neighboring gene H3K4me1 hESC enhancer GRCh37_chr15:70324572-70325184Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr15:70325185-70325795Neighboring gene ATAC-STARR-seq lymphoblastoid active region 9669Neighboring gene ATAC-STARR-seq lymphoblastoid active region 9668Neighboring gene ATAC-STARR-seq lymphoblastoid active region 9670Neighboring gene H3K4me1 hESC enhancer GRCh37_chr15:70349697-70350197Neighboring gene H3K4me1 hESC enhancer GRCh37_chr15:70359676-70360176Neighboring gene H3K4me1 hESC enhancer GRCh37_chr15:70360177-70360677Neighboring gene H3K4me1 hESC enhancer GRCh37_chr15:70363742-70364242Neighboring gene TLE family member 3, transcriptional corepressorNeighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr15:70370658-70371264Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr15:70371265-70371871Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr15:70374946-70375494Neighboring gene H3K4me1 hESC enhancer GRCh37_chr15:70380981-70381568Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 6602Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 6603Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 6604Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chr15:70390514-70391488Neighboring gene VISTA enhancer hs359Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 6607Neighboring gene H3K4me1 hESC enhancer GRCh37_chr15:70402651-70403162Neighboring gene NANOG-H3K4me1 hESC enhancer GRCh37_chr15:70403675-70404186Neighboring gene H3K4me1 hESC enhancer GRCh37_chr15:70404187-70404696Neighboring gene Sharpr-MPRA regulatory region 6929Neighboring gene ATAC-STARR-seq lymphoblastoid active region 9671Neighboring gene ATAC-STARR-seq lymphoblastoid active region 9672Neighboring gene uncharacterized LOC107984734Neighboring gene H3K27ac hESC enhancer GRCh37_chr15:70432131-70432636Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr15:70433141-70433644Neighboring gene H3K4me1 hESC enhancer GRCh37_chr15:70472929-70473512Neighboring gene H3K4me1 hESC enhancer GRCh37_chr15:70473513-70474096Neighboring gene H3K4me1 hESC enhancer GRCh37_chr15:70479256-70479756Neighboring gene H3K4me1 hESC enhancer GRCh37_chr15:70482961-70483463Neighboring gene RNA, U6 small nuclear 745, pseudogene

Genomic regions, transcripts, and products

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Go to reference sequence details

Go to nucleotide: Graphics FASTA GenBank

Bibliography

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Related articles in PubMed

  1. MicroRNA-629-5p promotes osteosarcoma proliferation and migration by targeting caveolin 1. Gao C, et al. Braz J Med Biol Res, 2021. PMID 33886809, Free PMC Article
  2. Upregulation of Serum miR-629 Predicts Poor Prognosis for Non-Small-Cell Lung Cancer. Liu F, et al. Dis Markers, 2021. PMID 33763157, Free PMC Article
  3. Circular RNA circNRIP1 promotes migration and invasion in cervical cancer by sponging miR-629-3p and regulating the PTP4A1/ERK1/2 pathway. Li X, et al. Cell Death Dis, 2020 May 26. PMID 32457332, Free PMC Article
  4. MiR-629-5p promotes the invasion of lung adenocarcinoma via increasing both tumor cell invasion and endothelial cell permeability. Li Y, et al. Oncogene, 2020 Apr. PMID 32108166
  5. Serum miR-629 is a novel molecular marker for diagnosis and the prognosis of pancreatic cancer. Shi W, et al. Eur Rev Med Pharmacol Sci, 2018 Aug. PMID 30178840

See all (24) citations in PubMed

GeneRIFs: Gene References Into Functions

What's a GeneRIF?

  1. Long Noncoding RNA MAGI2-AS3 Represses Cell Progression in Clear Cell Renal Cell Carcinoma by Modulating the miR-629-5p/PRDM16 Axis.

    Title: Long Noncoding RNA MAGI2-AS3 Represses Cell Progression in Clear Cell Renal Cell Carcinoma by Modulating the miR-629-5p/PRDM16 Axis.

  2. Mir-629 Repressed LATS2 Expression and Promoted the Proliferation of Prostate Cancer Cells.

    Title: Mir-629 Repressed LATS2 Expression and Promoted the Proliferation of Prostate Cancer Cells.

  3. RNA-sequencing of human aortic valves identifies that miR-629-3p and TAGLN miRNA-mRNA pair involving in calcified aortic valve disease.

    Title: RNA-sequencing of human aortic valves identifies that miR-629-3pand TAGLNmiRNA-mRNA pair involving incalcified aortic valve disease.

  4. Overexpression of Long Non-Coding RNA MIR22HG Represses Proliferation and Enhances Apoptosis via miR-629-5p/TET3 Axis in Osteosarcoma Cells.

    Title: Overexpression of Long Non-Coding RNA MIR22HG Represses Proliferation and Enhances Apoptosis via miR-629-5p/TET3 Axis in Osteosarcoma Cells.

  5. Upregulation of Serum miR-629 Predicts Poor Prognosis for Non-Small-Cell Lung Cancer.

    Title: Upregulation of Serum miR-629 Predicts Poor Prognosis for Non-Small-Cell Lung Cancer.

  6. MicroRNA-629 promotes the tumorigenesis of non-small-cell lung cancer by targeting FOXO1 and activating PI3K/AKT pathway.

    Title: MicroRNA-629 promotes the tumorigenesis of non-small-cell lung cancer by targeting FOXO1 and activating PI3K/AKT pathway.

  7. MicroRNA-629-5p promotes osteosarcoma proliferation and migration by targeting caveolin 1.

    Title: MicroRNA-629-5p promotes osteosarcoma proliferation and migration by targeting caveolin 1.

  8. Circular RNA circNRIP1 promotes migration and invasion in cervical cancer by sponging miR-629-3p and regulating the PTP4A1/ERK1/2 pathway.

    Title: Circular RNA circNRIP1 promotes migration and invasion in cervical cancer by sponging miR-629-3p and regulating the PTP4A1/ERK1/2 pathway.

  9. MiR-629-5p promotes the invasion of lung adenocarcinoma via increasing both tumor cell invasion and endothelial cell permeability.

    Title: MiR-629-5p promotes the invasion of lung adenocarcinoma via increasing both tumor cell invasion and endothelial cell permeability.

  10. MiR-629 regulates hypoxic pulmonary vascular remodelling by targeting FOXO3 and PERP.

    Title: MiR-629 regulates hypoxic pulmonary vascular remodelling by targeting FOXO3 and PERP.

Submit: New GeneRIF Correction See all GeneRIFs (22)

Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

Variation

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See variants in ClinVar

See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

See Variation Viewer (GRCh38)

Genotypes

  • See SNP Geneview Report
  • See 1000 Genomes Browser (GRCh37.p13)

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_030714.1 RNA Sequence

    Status: PROVISIONAL

    Source sequence(s)
    AC026583, AC068327
    Related
    ENST00000385230.1

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_000015.10Reference GRCh38.p14 Primary Assembly

    Range
    70079372..70079468 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060939.1Alternate T2T-CHM13v2.0

    Range
    67901600..67901696 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

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Nucleotide Protein
Heading Accession and Version

Additional links

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Gene LinkOut

The following LinkOut resources are supplied by external providers. These providers are responsible for maintaining the links.

Molecular Biology Databases

Research Materials

MIR629 microRNA 629 [hom*o sapiens (human)] - Gene (2024)

FAQs

What is the miRNA in humans? ›

Genes for microRNA are as much a part of the human genome as genes that code for proteins. Cells make microRNA using a process that resembles the early steps of protein synthesis. The microRNA gene is activated, the DNA strand opens up and the gene is copied, or transcribed, in the form of RNA.

How many miRNA genes are in the human body? ›

The human genome may encode over 1900 miRNAs, However, only about 500 human miRNAs represent bona fide miRNAs in the manually curated miRNA gene database MirGeneDB. miRNAs are abundant in many mammalian cell types miRNAs appear to target about 60% of the genes of humans and other mammals.

What is the clinical significance of microRNA? ›

MicroRNAs are critical to cell physiology and development. They are also implicated in pathological processes such as autoimmune diseases, viral infections and carcinogenesis.

What is the largest human gene in the human genome? ›

The largest known gene is the human dystrophin gene, which has 79 exons spanning at least 2,300 kilobases (kb).

What disease is caused by miRNA? ›

Cardiac Failure

Cardiac hypertrophy in humans is a major determinant of mortality and morbidity in cardiovascular diseases. Because miRNAs are important regulators for the differentiation and growth of cardiac cells, they are hypothesized to have an important role in cardiac hypertrophy and heart failure (82).

What is MicroRNA in health and disease? ›

Since then, thousands have been identified in humans. MicroRNAs play roles in many diseases including cancer, where they can act as oncogenes or tumor suppressors. They have also been linked to other diseases like cardiovascular disease and neurodegenerative disorders.

What is the purpose of MicroRNAs? ›

MiRNAs play a vital role in regulating numerous metabolic and cellular pathways, notably those controlling cell proliferation, differentiation and survival [13-18, 238-240]. Dysregulation of miRNA expression profiles has been demonstrated in most tumors examined [24, 241].

What does miRNA mean? ›

Derived from the Slavic element mir, Mirna means "peaceful." It is often confused with the name "Myrna"(/myrrhna/), which is not Slavic in origin, but Celtic and means "beloved" and also "tender." In Circassian culture, Mirna means "This Eye": "Mir" stands for "this" and "Na" stands for "Eye". Mirna. Pronunciation.

How do you identify miRNA for a gene? ›

With bioinformatic methods, putative miRNAs are first predicted in genome sequences based on the structural features of miRNA. These algorithms essentially identify hairpin structures in non-coding and non-repetitive regions of the genome that are characteristic of miRNA precursor sequences.

What disease is microRNA biomarkers? ›

Researchers have mainly focused on finding miRNA signatures that are representative of diseases, including cancer, viral infections, nervous system disorders, cardiovascular disorders, muscular disorders, diabetes, and other diseases, and several studies have been specifically designed to validate miRNAs as biomarkers ...

What is microRNA in the brain? ›

In addition to controlling the morphology of neurons and synaptic sites, microRNAs can also regulate neural migration in the hippocampus. Neuronal migration is key to the brain development. In this process, cells move from their place of origin to their site of integration (Faini et al., 2021).

What are the benefits of miRNA? ›

Furthermore, miR-159, abundant in broccoli, has been shown to suppress breast tumor development in in vitro and in vivo models. An analysis of miRNAs from rice revealed their binding affinity for various human genes involved in neurological diseases, cancer, and cardiovascular disease.

What is the most abundant gene in human? ›

Transposable genetic elements, DNA sequences that can replicate and insert copies of themselves at other locations within a host genome, are an abundant component in the human genome. The most abundant transposon lineage, Alu, has about 50,000 active copies, and can be inserted into intragenic and intergenic regions.

How many possible human DNA combinations are there? ›

The total possible combination of alleles for those genes in humans is approximately 70,368,744,177,664. This is trillions of times more combinations than the number of people who have ever lived.

How many genes does it take to make a human? ›

About a half-century ago the estimated number of human genes was in the millions. Today we're down to about 20,000. We now know, for example, that bananas, with their 30,000 genes, have 50 percent more genes than we do.

What is miRNA in the brain? ›

microRNAs Are Powerful Post-Transcriptional Regulators of Gene Expression in the Brain. microRNAs (miRNAs) are a class of short non-coding RNAs of ~22 nucleotides in length that constitute an important component of the regulatory circuitry determining expression patterns.

What is the function of miRNA in the immune system? ›

miRNAs regulate both innate and adaptive immune responses. miRNA expression levels are dysregulated in diseases of immunological origin, such as cancer and autoimmunity. Altered miRNA expression can subsequently exacerbate disease severity.

What is miRNA in obesity? ›

MiRNAs control adipogenesis, the process by which pre-adipocytes differentiate into mature adipocytes, and also influence adipocyte metabolism, insulin sensitivity, and lipid storage [11]. The dysregulation of miRNAs in adipose tissue has been associated with obesity and related metabolic disorders.

What is an example of miRNA? ›

Non-canonical miRNA Biogenesis Pathways

Pre-miRNAs produced by the Drosha/DGCR8-independent pathway resemble Dicer substrates. An example of such pre-miRNAs is mirtrons, which are produced from the introns of mRNA during splicing (35, 36). Another example is the 7-methylguanosine (m7G)-capped pre-miRNA.

References

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