MIR4520-1

gene
On this page

Also known as hsa-mir-4520a

Summary

MIR4520-1 (microRNA 4520-1, HGNC:41775) is a microRNA gene on chromosome 17p13.1.

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 100616401 — 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:41775
Approved symbolMIR4520-1
NamemicroRNA 4520-1
Location17p13.1
Locus typeRNA, micro
StatusApproved
Aliaseshsa-mir-4520a
Ensembl geneENSG00000264468
Ensembl biotypemiRNA
Entrez100616401
RNAcentralURS000075F124 — miRNA, 70 nt, 10 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 miRNA

ENST00000582609

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000582609 — 1 exons

ExonStartEnd
ENSE0000271667666554406655509

Expression profiles

Bgee: expression breadth broad, 92 present calls, max score 90.25.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
vermiform appendixUBERON:000115490.25gold quality
duodenumUBERON:000211484.81gold quality
sural nerveUBERON:001548883.75gold quality
lower esophagus mucosaUBERON:003583483.47gold quality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099182.25gold quality
monocyteCL:000057678.88gold quality
bloodUBERON:000017878.07gold quality
lymph nodeUBERON:000002977.67gold quality
tonsilUBERON:000237276.11gold quality
skin of abdomenUBERON:000141676.03gold quality
esophagus mucosaUBERON:000246975.56gold quality
zone of skinUBERON:000001475.49gold quality
skin of legUBERON:000151174.85gold quality
esophagusUBERON:000104374.66gold quality
pituitary glandUBERON:000000774.29gold quality
muscle of legUBERON:000138373.85gold quality
islet of LangerhansUBERON:000000673.43gold quality
putamenUBERON:000187473.26gold quality
adenohypophysisUBERON:000219673.21gold quality
gastrocnemiusUBERON:000138872.57gold quality
small intestineUBERON:000210872.53gold quality
right lobe of liverUBERON:000111472.50gold quality
endometriumUBERON:000129572.38gold quality
metanephros cortexUBERON:001053372.08gold quality
pancreasUBERON:000126472.03gold quality
caudate nucleusUBERON:000187371.72gold quality
liverUBERON:000210771.71gold quality
small intestine Peyer’s patchUBERON:000345471.68gold quality
prefrontal cortexUBERON:000045171.32gold quality
saliva-secreting glandUBERON:000104471.27gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no0.35

Regulation

Is transcription factor: no

Literature-anchored findings (GeneRIF, showing 1)

  • RHEB, the main activator of mTOR signaling, is a valid target of miR-4520a with the relative expression levels of the latter being significantly deregulated in FMF patients and highly dependent on the presence of pyrin mutations. (PMID:27636101)

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.