MIR4725

gene
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Also known as hsa-mir-4725

Summary

MIR4725 (microRNA 4725, HGNC:41608) is a microRNA gene on chromosome 17q11.2.

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 100616449 — 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:41608
Approved symbolMIR4725
NamemicroRNA 4725
Location17q11.2
Locus typeRNA, micro
StatusApproved
Aliaseshsa-mir-4725
Ensembl geneENSG00000265976
Ensembl biotypemiRNA
Entrez100616449
RNAcentralURS000075A8E3 — miRNA, 90 nt, 1 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 miRNA

ENST00000581700

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000581700 — 1 exons

ExonStartEnd
ENSE000027322203157526931575358

Expression profiles

Bgee: expression breadth broad, 61 present calls, max score 78.56.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
monocyteCL:000057678.56gold quality
liverUBERON:000210773.75gold quality
adrenal tissueUBERON:001830373.39gold quality
heartUBERON:000094872.39gold quality
stomachUBERON:000094572.18gold quality
heart left ventricleUBERON:000208472.14gold quality
calcaneal tendonUBERON:000370171.73gold quality
gastrocnemiusUBERON:000138871.65gold quality
left coronary arteryUBERON:000162671.36gold quality
bloodUBERON:000017870.92gold quality
olfactory segment of nasal mucosaUBERON:000538670.80gold quality
body of stomachUBERON:000116170.16gold quality
esophagogastric junction muscularis propriaUBERON:003584168.64gold quality
endometriumUBERON:000129568.63gold quality
body of pancreasUBERON:000115068.44gold quality
right lobe of liverUBERON:000111467.84gold quality
ascending aortaUBERON:000149667.79gold quality
putamenUBERON:000187467.75gold quality
thoracic aortaUBERON:000151567.67gold quality
omental fat padUBERON:001041467.57gold quality
adipose tissueUBERON:000101367.02gold quality
tibial arteryUBERON:000761066.84gold quality
lower esophagus muscularis layerUBERON:003583366.82gold quality
skin of abdomenUBERON:000141666.38gold quality
subcutaneous adipose tissueUBERON:000219066.21gold quality
colonUBERON:000115565.99gold quality
esophagus mucosaUBERON:000246965.94gold quality
muscle layer of sigmoid colonUBERON:003580565.91gold quality
zone of skinUBERON:000001465.89gold quality
thoracic mammary glandUBERON:000520065.68gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no0.41

Regulation

Is transcription factor: no

Literature-anchored findings (GeneRIF, showing 1)

  • this study showed that the mir-4725-3p targeting stromal interacting molecule 1 signaling is involved in xanthohumol inhibition of glioma cell invasion. (PMID:29747239)

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.