MIR5581

gene
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Also known as hsa-mir-5581

Summary

MIR5581 (microRNA 5581, HGNC:43527) is a microRNA gene on chromosome 1p34.3.

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 100847010 — 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:43527
Approved symbolMIR5581
NamemicroRNA 5581
Location1p34.3
Locus typeRNA, micro
StatusApproved
Aliaseshsa-mir-5581
Ensembl geneENSG00000263675
Ensembl biotypemiRNA
Entrez100847010
RNAcentralURS000075EF33 — ncRNA, 60 nt, 2 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 miRNA

ENST00000580821

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000580821 — 1 exons

ExonStartEnd
ENSE000027168493750093537500994

Expression profiles

Bgee: expression breadth ubiquitous, 114 present calls, max score 91.01.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
skeletal muscle tissueUBERON:000113491.01gold quality
right uterine tubeUBERON:000130289.20gold quality
duodenumUBERON:000211488.82gold quality
endometriumUBERON:000129587.57gold quality
vermiform appendixUBERON:000115486.68gold quality
adrenal tissueUBERON:001830386.62gold quality
rectumUBERON:000105284.88gold quality
tonsilUBERON:000237284.53gold quality
apex of heartUBERON:000209884.10gold quality
lymph nodeUBERON:000002982.87gold quality
placentaUBERON:000198782.56gold quality
fundus of stomachUBERON:000116081.76gold quality
bone marrowUBERON:000237181.67gold quality
muscle of legUBERON:000138380.94gold quality
stomachUBERON:000094580.79gold quality
bloodUBERON:000017880.76gold quality
right coronary arteryUBERON:000162580.73gold quality
prefrontal cortexUBERON:000045180.61gold quality
body of pancreasUBERON:000115080.39gold quality
body of stomachUBERON:000116180.31gold quality
monocyteCL:000057680.19gold quality
gastrocnemiusUBERON:000138880.00gold quality
tibial nerveUBERON:000132379.62gold quality
pancreasUBERON:000126479.50gold quality
pituitary glandUBERON:000000779.36gold quality
small intestineUBERON:000210879.34gold quality
adenohypophysisUBERON:000219679.34gold quality
small intestine Peyer’s patchUBERON:000345478.88gold quality
right lobe of thyroid glandUBERON:000111978.78gold quality
heart left ventricleUBERON:000208478.25gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no1.00

Regulation

Is transcription factor: no

Literature-anchored findings (GeneRIF, showing 1)

  • Functionally, LINC00961 overexpression obviously inhibited cell proliferation, migration, and invasion in hepatocellular carcinoma cells. Mechanistically, LINC00961 regulated cardiolipin synthase 1 expression via sponging miR-5581-3p. (PMID:30825207)

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.