MIR548AT

gene
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Also known as hsa-mir-548at

Summary

MIR548AT (microRNA 548at, HGNC:43517) is a microRNA gene on chromosome 17q21.2.

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 100847030 — 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:43517
Approved symbolMIR548AT
NamemicroRNA 548at
Location17q21.2
Locus typeRNA, micro
StatusApproved
Aliaseshsa-mir-548at
Ensembl geneENSG00000264314
Ensembl biotypemiRNA
Entrez100847030
RNAcentralURS000075E451 — miRNA, 58 nt, 1 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 miRNA

ENST00000578714

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000578714 — 1 exons

ExonStartEnd
ENSE000027055424249477342494830

Expression profiles

Bgee: expression breadth broad, 83 present calls, max score 81.84.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
adrenal tissueUBERON:001830381.84gold quality
bloodUBERON:000017877.82gold quality
muscle of legUBERON:000138375.80gold quality
monocyteCL:000057674.81gold quality
gastrocnemiusUBERON:000138874.44gold quality
liverUBERON:000210774.37gold quality
endometriumUBERON:000129573.79gold quality
rectumUBERON:000105273.29gold quality
heart left ventricleUBERON:000208473.18gold quality
islet of LangerhansUBERON:000000672.23gold quality
ectocervixUBERON:001224971.83gold quality
heartUBERON:000094871.67gold quality
right frontal lobeUBERON:000281071.09gold quality
left adrenal gland cortexUBERON:003582570.44gold quality
body of pancreasUBERON:000115070.41gold quality
right atrium auricular regionUBERON:000663170.36gold quality
stomachUBERON:000094570.18gold quality
urinary bladderUBERON:000125569.76gold quality
tibial arteryUBERON:000761069.73gold quality
esophagogastric junction muscularis propriaUBERON:003584169.34gold quality
body of stomachUBERON:000116169.18gold quality
kidneyUBERON:000211368.69gold quality
left adrenal glandUBERON:000123468.59gold quality
intestineUBERON:000016068.52gold quality
right lobe of liverUBERON:000111468.48gold quality
right coronary arteryUBERON:000162568.48gold quality
ascending aortaUBERON:000149668.30gold quality
esophagus mucosaUBERON:000246968.27gold quality
transverse colonUBERON:000115768.20gold quality
lower esophagusUBERON:001347368.20gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no1.22

Regulation

Is transcription factor: no

Literature-anchored findings (GeneRIF, showing 1)

  • This study demonstrated that miR-548at-5p were not associated to PD, which suggest they may not contribute to the gene susceptibility of PD at least in Chinese Han population. (PMID:29209904)

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.