MIR596

gene
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Also known as hsa-mir-596

Summary

MIR596 (microRNA 596, HGNC:32852) is a microRNA gene on chromosome 8p23.3.

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 693181 — 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:32852
Approved symbolMIR596
NamemicroRNA 596
Location8p23.3
Locus typeRNA, micro
StatusApproved
Aliaseshsa-mir-596
Ensembl geneENSG00000207826
Ensembl biotypemiRNA
Entrez693181
RNAcentralURS000075AC80 — miRNA, 77 nt, 1 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 miRNA

ENST00000385091

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000385091 — 1 exons

ExonStartEnd
ENSE0000150009718172311817307

Expression profiles

Bgee: expression breadth broad, 64 present calls, max score 96.14.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
sural nerveUBERON:001548896.14gold quality
lymph nodeUBERON:000002980.77gold quality
kidneyUBERON:000211377.00gold quality
monocyteCL:000057675.19gold quality
gastrocnemiusUBERON:000138872.53gold quality
bloodUBERON:000017871.35gold quality
heart left ventricleUBERON:000208471.00gold quality
stomachUBERON:000094570.88gold quality
heartUBERON:000094870.21gold quality
ascending aortaUBERON:000149670.01gold quality
body of stomachUBERON:000116169.82gold quality
right atrium auricular regionUBERON:000663168.33gold quality
right lungUBERON:000216768.22gold quality
body of pancreasUBERON:000115067.93gold quality
endometriumUBERON:000129567.76gold quality
tibial arteryUBERON:000761067.44gold quality
transverse colonUBERON:000115766.62gold quality
rectumUBERON:000105266.54gold quality
minor salivary glandUBERON:000183066.25gold quality
substantia nigraUBERON:000203865.95gold quality
C1 segment of cervical spinal cordUBERON:000646965.90gold quality
nucleus accumbensUBERON:000188265.88gold quality
anterior cingulate cortexUBERON:000983565.29gold quality
putamenUBERON:000187465.15gold quality
Ammon’s hornUBERON:000195465.15gold quality
thoracic mammary glandUBERON:000520065.01gold quality
lower esophagus muscularis layerUBERON:003583364.86gold quality
myometriumUBERON:000129664.81gold quality
vaginaUBERON:000099664.74gold quality
cerebral cortexUBERON:000095664.66gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no0.46

Regulation

Is transcription factor: no

Literature-anchored findings (GeneRIF, showing 12)

  • MIR596 is frequently observed in oral squamous cell carcinoma and regulates expression of LGAL3BP. (PMID:23233740)
  • findings may help clarify the molecular mechanism of the tumor-suppressive effect through down-regulation of LGALS3BP by miR-596 in Oral Squamous Cell Carcinoma (PMID:26502662)
  • Among the hits, miR-596 was identified as a regulator of p53. The overexpression of miR-596 significantly increased p53 at the protein level, thereby inducing apoptosis. (PMID:28732184)
  • miR-596 overexpression effectively inhibited MAPK/ERK signaling, cell proliferation, migration, and invasion and increased the cell apoptosis of melanoma cells. In addition, we found that miR-596 directly targets MEK1 and two apoptotic proteins, MCL1, and BCL2L1, in melanoma cells (PMID:29183729)
  • MiR-596 has a tumor suppressive role in gastric cancer and is downregulated partly due to promoter hypermethylation. Furthermore, PRDX1 is one of the putative target genes of miR-596. (PMID:30886505)
  • these results demonstrate that CREPT exerts an oncogenic role in glioma and its expression is regulated by miR-596. (PMID:30995540)
  • RHPN1-AS1 Drives the Progression of Hepatocellular Carcinoma via Regulating miR-596/IGF2BP2 Axis. (PMID:31692433)
  • MiR-596 inhibits osteoblastic differentiation and cell proliferation by targeting Smad3 in steroid-induced osteonecrosis of femoral head. (PMID:32410637)
  • MicroRNA-596 is epigenetically inactivated and suppresses prostatic cancer cell growth and migration via regulating Wnt/beta-catenin signaling. (PMID:33387246)
  • Plasma exosomal miR-596: a novel biomarker predicts survival in patients with idiopathic pulmonary artery hypertension. (PMID:33788649)
  • Exosomal circPRRX1 functions as a ceRNA for miR-596 to promote the proliferation, migration, invasion, and reduce radiation sensitivity of gastric cancer cells via the upregulation of NF-kappaB activating protein. (PMID:36206097)
  • [LncRNA LINC00342 regulates gastric cancer cell proliferation, migration and invasion by targeting miR-596]. (PMID:37933652)

Cross-species orthologs

0 orthologs

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.