MIR133A2

gene
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Also known as hsa-mir-133a-2

Summary

MIR133A2 (microRNA 133a-2, HGNC:31518) is a microRNA gene on chromosome 20q13.33.

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.

Source: NCBI Gene 406923 — RefSeq curated summary.

At a glance

  • Gene type: non-coding (miRNA) — no protein product; not a drug target. Variant/disease associations are omitted (they would be positional, from an overlapping protein-coding gene).

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:31518
Approved symbolMIR133A2
NamemicroRNA 133a-2
Location20q13.33
Locus typeRNA, micro
StatusApproved
Aliaseshsa-mir-133a-2
Ensembl geneENSG00000284508
Ensembl biotypemiRNA
OMIM610255
Entrez406923
RNAcentralURS000075E14C — miRNA, 102 nt, 16 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 miRNA

ENST00000347538

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000347538 — 1 exons

ExonStartEnd
ENSE000013936846256491262565013

Expression profiles

Bgee: expression breadth broad, 28 present calls, max score 87.98.

Top tissues by expression

28 total, by Bgee expression score (0-100, higher = more expressed):

TissueAnatomy IDExpression scoreQuality
skeletal muscle tissueUBERON:000113487.98gold quality
muscle of legUBERON:000138382.28gold quality
gastrocnemiusUBERON:000138879.90gold quality
urinary bladderUBERON:000125576.32gold quality
heart left ventricleUBERON:000208475.97gold quality
heartUBERON:000094875.61gold quality
right atrium auricular regionUBERON:000663175.28gold quality
monocyteCL:000057674.63gold quality
minor salivary glandUBERON:000183071.55gold quality
stomachUBERON:000094571.21gold quality
body of stomachUBERON:000116170.79gold quality
tibial arteryUBERON:000761070.22gold quality
transverse colonUBERON:000115769.86gold quality
esophagogastric junction muscularis propriaUBERON:003584169.60gold quality
colonUBERON:000115569.44gold quality
thoracic aortaUBERON:000151568.90gold quality
lower esophagus muscularis layerUBERON:003583368.89gold quality
muscle layer of sigmoid colonUBERON:003580568.83gold quality
myometriumUBERON:000129668.80gold quality
thoracic mammary glandUBERON:000520068.60gold quality
left coronary arteryUBERON:000162668.58gold quality
ascending aortaUBERON:000149667.79gold quality
esophagus mucosaUBERON:000246967.76gold quality
omental fat padUBERON:001041467.74gold quality
vaginaUBERON:000099665.62gold quality
skin of legUBERON:000151154.68gold quality
left testisUBERON:000453350.58gold quality
right frontal lobeUBERON:000281050.50gold quality

Single-cell (SCXA)

Detected in 1 experiment(s), a significant marker in 0.

ExperimentMarker?Max mean expression
E-ANND-3no0.00

Regulation

Is transcription factor: no

Literature-anchored findings (GeneRIF, showing 36)

  • miR-133a showed dysregulation in myocardial infarction or fetal hearts when compared to healthy adults. (PMID:20075508)
  • The functional significance of miR-133a in cancer cell lines derived from lung squamous cell carcinoma (SCC) and the identification of miR-133a-regulated novel cancer networks in lung-SCC, are reported. (PMID:22089643)
  • DNA methylation regulates the expression of the miR-1-1 and miR-133a-2 cluster in colorectal cancer cell lines (PMID:22766685)
  • the tumor suppressor role of miR-133a in lung cancer (PMID:24816813)
  • This review identified and summarized the results of studies of miR-133 with emphasis on its function in human diseases in muscle and cancer. [Review] (PMID:24975488)
  • Suggest circulating miR-1, miR-133a, and miR-206 as potential biomarkers of muscle damage or adaptation to exercise. (PMID:25146754)
  • The downregulation of miR-133a may play an important role in the progression of colorectal cancer and can be used as an independent factor to determine CRC prognosis. (PMID:25170220)
  • Suggest that miR-133a is downregulated in gastric cancer and functions as a tumor suppressor in vitro and in vivo partly by repressing IGF1R. (PMID:25780292)
  • Aged patients with sinus rhythm exhibited significantly higher expression levels of HCN2 and HCN4 channel mRNA and protein (P<0.05), but significantly lower expression levels of miR1 and 133, compared with those of adult patients with sinus rhythm. (PMID:26005035)
  • miR-133b/a-3p acts as a tumor suppressor in gastric cancer by directly targeting Mcl-1 and Bcl-xL. (PMID:26276722)
  • miRNA-208b and miRNA-133a show distinct profiling in peripheral blood cells isolated from untreated patients with recently diagnosed essential hypertension. Their gene expression levels reveal a strong correlation with urinary albumin excretion levels. (PMID:26984682)
  • Study found that miR-150-5p and miR-133a expression was significantly downregulated in glioma tissues compared with normal tissues, and that MT1-MMP expression was inversely upregulated in glioma tissues. Knockdown of MT1-MMP by specific siRNAs in U87 and U251 glioma cells induced suppression of cell proliferation and invasion/migration. (PMID:27154818)
  • Serum miR-133 is a new very useful marker for diagnosing of lymphoma associated hemophagocytic syndrome (PMID:28869447)
  • MiR-133a prevents the bone formation by inhibiting the RUNX2/BMP2 signaling pathway, negatively regulating the fracture healing. (PMID:29771401)
  • results indicate that miR-133a-3p is a target of smoking-induced changes in HPV(+) oropharyngeal squamous cell carcinoma patients and alters the expression of EGFR and HuR which may promote HPV associated oropharyngeal cancer (PMID:30289952)
  • the IGF1R oncogene which is an important regulator of MEK/ERK signaling pathway, was positively regulated by AFAP1-AS1 through ameliorating miR-133a-mediated IGF1R repression in pancreatic cancer tissues. (PMID:30300116)
  • Study indicated that miR-133a might act as a tumor suppressor and be a valuable independent prognostic and diagnostic biomarker for non-small cell lung cancer (NSCLC), and NSCLC patients with high expression of miR-133 might have a better prognosis.[meta-analysis] (PMID:30458455)
  • The Impact of MicroRNA-133a on Prognosis and Clinicopathological Parameters for Digestive System Cancers: a Comprehensive Study Based on Meta-Analysis and TCGA Database. (PMID:30810894)
  • circP4HB enhances epithelial-mesenchymal transition and metastatic disease through miR-133a-5p sequestration (PMID:31005252)
  • Wnt signalling mediates miR-133a nuclear re-localization for the transcriptional control of Dnmt3b in cardiac cells. (PMID:31249372)
  • homeostasis and physiological function of AQP1 in endothelial health are maintained by the MEF2C and miR-133a-3p.1 regulatory circuit (PMID:31254364)
  • miR-576, miR-616 and miR-133a-2 are three newly discovered biomarkers of renal cell carcinoma in this study. (PMID:31350524)
  • reveals that upregulated miR-133a and downregulated connective tissue growth factor suppress cell proliferation, migration, and invasion in human glioma (PMID:31381269)
  • The study identified TGF-beta1-induced miR-133a as an anti-fibrotic factor. It functions as a feed-back negative regulator of TGF-beta1 profibrogenic pathways. (PMID:31511493)
  • High miR-133a levels in the circulation anticipates presentation of clinical events in familial hypercholesterolaemia patients. (PMID:32061123)
  • Overexpression of miR-133a-3p inhibits fibrosis and proliferation of keloid fibroblasts by regulating IRF5 to inhibit the TGF-beta/Smad2 pathway. (PMID:32205184)
  • The Diagnostic Value of Mir-133a in ST Elevation and Non-ST Elevation Myocardial Infarction: A Meta-Analysis. (PMID:32218383)
  • MiR-133 Targets YES1 and Inhibits the Growth of Triple-Negative Breast Cancer Cells. (PMID:32462982)
  • Hypoxia induced exosomal circRNA promotes metastasis of Colorectal Cancer via targeting GEF-H1/RhoA axis. (PMID:32724467)
  • Regulator of G-protein signalling 3 and its regulator microRNA-133a mediate cell proliferation in gastric cancer. (PMID:32928707)
  • MiR-133a Promoted cerebral ischemia/reperfusion injury by targeting brain-derived neurotrophic factor. (PMID:33222435)
  • The Expression and Role of microRNA-133a in Plasma of Patients with Kawasaki Disease. (PMID:33501869)
  • MiR-133a-3p attenuates resistance of non-small cell lung cancer cells to gefitinib by targeting SPAG5. (PMID:34057242)
  • Aberrant expression of miR-133a in endothelial cells inhibits angiogenesis by reducing pro-angiogenic but increasing anti-angiogenic gene expression. (PMID:36042288)
  • hsa-mir-133a-2 promotes the proliferation and invasion of cervical cancer cells by targeting the LAMB3-mediated PI3K/ATK pathway. (PMID:36305754)
  • Investigation of miR-133a, miR-637 and miR-944 genes expression and their relationship with PI3K/AKT signaling in women with breast cancer. (PMID:36656380)

Cross-species orthologs

3 orthologs

OrganismSymbolGene ID
danio_reriomir133a-1ENSDARG00000104548
mus_musculusMir133a-1ENSMUSG00000065399
rattus_norvegicusMir3582ENSRNOG00000035651

Paralogs (2): MIR133B (ENSG00000199080), MIR133A1 (ENSG00000283927)

Protein

Non-coding RNA — no protein product; not a drug target.

Function

No curated pathway, Gene-Ontology, or interaction data.

Disease & clinical

No curated disease, variant, or cancer-driver associations.

Drugs & pharmacology

No drug or pharmacology data — not an established drug target.

No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.