MIR610

gene
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Also known as hsa-mir-610

Summary

MIR610 (microRNA 610, HGNC:32866) is a microRNA gene on chromosome 11p14.1.

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 693195 — 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:32866
Approved symbolMIR610
NamemicroRNA 610
Location11p14.1
Locus typeRNA, micro
StatusApproved
Aliaseshsa-mir-610
Ensembl geneENSG00000207874
Ensembl biotypemiRNA
OMIM612330
Entrez693195
RNAcentralURS000075D59C — miRNA, 96 nt, 3 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 miRNA

ENST00000385139

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000385139 — 1 exons

ExonStartEnd
ENSE000015001452805681528056910

Expression profiles

Bgee: expression breadth broad, 20 present calls, max score 87.62.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
adrenal tissueUBERON:001830387.62gold quality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099183.38gold quality
heartUBERON:000094881.94gold quality
kidneyUBERON:000211376.94gold quality
endometriumUBERON:000129576.03gold quality
right lobe of liverUBERON:000111472.35gold quality
esophagogastric junction muscularis propriaUBERON:003584170.45gold quality
skin of legUBERON:000151170.22gold quality
body of stomachUBERON:000116170.13gold quality
lungUBERON:000204869.63gold quality
transverse colonUBERON:000115768.79gold quality
bloodUBERON:000017868.47gold quality
lower esophagus muscularis layerUBERON:003583366.12gold quality
ascending aortaUBERON:000149665.78gold quality
left lobe of thyroid glandUBERON:000112064.54gold quality
esophagus mucosaUBERON:000246963.34gold quality
small intestine Peyer’s patchUBERON:000345462.75gold quality
left adrenal glandUBERON:000123460.68gold quality
right frontal lobeUBERON:000281051.03gold quality
left testisUBERON:000453343.10gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no1.31

Regulation

Is transcription factor: no

Literature-anchored findings (GeneRIF, showing 7)

  • we demonstrated that miR610-mediated inhibition of VASP expression resulted in a significant reduction in the migration and invasion properties of gastric cancer cells. (PMID:22189055)
  • Inhibition of miR-610 promoted, but overexpression of miR-610 reduced, HCC cell proliferation. (PMID:25491321)
  • Bioinformatics analysis further revealed cyclin D2 (CCND2) and AKT3, putative tumor promoters, as potential targets of miR610. Data from reporter assays showed that miR610 directly binds to the 3’untranslated (PMID:26782072)
  • the present study is the first to provide evidence suggesting that miR610 directly targets MDM2 proto-oncogene E3 ubiquitin protein ligase to function as a tumor suppressor in glioma. (PMID:27485527)
  • FEZF1-AS1 promoted multiple myeloma cells proliferation through regulating miR-610/Akt3 axis. (PMID:29864963)
  • miR-610 expression was significantly downregulated in both oral squamous cell carcinoma (OSCC) tissues and cell lines. Low miR-610 expression was associated with advanced T classification, TNM stage and poorer prognosis. Overexpression of miR-610 significantly suppressed OSCC cells proliferation, migration, invasion and EMT process. Mechanistically, AGK was confirmed to be the downstream target of miR-610 in OSCC cells. (PMID:30657560)
  • Circular RNA hsa_circ_0000144 aggravates ovarian Cancer progression by regulating ELK3 via sponging miR-610. (PMID:36243865)

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.