MIR4537

gene
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Also known as hsa-mir-4537

Summary

MIR4537 (microRNA 4537, HGNC:41682) is a microRNA gene on chromosome 14q32.33.

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 100616422 — 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:41682
Approved symbolMIR4537
NamemicroRNA 4537
Location14q32.33
Locus typeRNA, micro
StatusApproved
Aliaseshsa-mir-4537
Ensembl geneENSG00000264781
Ensembl biotypemiRNA
Entrez100616422
RNAcentralURS00007E3603 — ncRNA, 70 nt, 2 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 miRNA

ENST00000581717

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000581717 — 1 exons

ExonStartEnd
ENSE00002689254105859484105859553

Expression profiles

Bgee: expression breadth ubiquitous, 101 present calls, max score 99.53.

FANTOM5 (CAGE): breadth tissue_specific, TPM avg 0.0063 / max 3.0917, expressed in 2 samples.

FANTOM5 promoters (1 alternative TSS)

Promoter IDTPM avgSamples expressed
1452890.00632

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
vermiform appendixUBERON:000115499.53gold quality
duodenumUBERON:000211499.48gold quality
granulocyteCL:000009499.38gold quality
spleenUBERON:000210699.23gold quality
lymph nodeUBERON:000002999.20gold quality
tonsilUBERON:000237298.25gold quality
bone marrowUBERON:000237197.04gold quality
small intestineUBERON:000210896.68gold quality
small intestine Peyer’s patchUBERON:000345496.33gold quality
mucosa of transverse colonUBERON:000499195.33gold quality
bloodUBERON:000017894.18gold quality
saliva-secreting glandUBERON:000104494.11gold quality
transverse colonUBERON:000115793.98gold quality
minor salivary glandUBERON:000183093.81gold quality
fundus of stomachUBERON:000116093.03gold quality
rectumUBERON:000105292.60gold quality
intestineUBERON:000016092.46gold quality
colonUBERON:000115590.16gold quality
body of stomachUBERON:000116189.91gold quality
stomachUBERON:000094589.53gold quality
gall bladderUBERON:000211087.57gold quality
urinary bladderUBERON:000125586.36gold quality
leukocyteCL:000073883.31gold quality
left uterine tubeUBERON:000130383.26gold quality
monocyteCL:000057682.89gold quality
endocervixUBERON:000045882.20gold quality
lungUBERON:000204881.61gold quality
thoracic mammary glandUBERON:000520081.23gold quality
upper lobe of left lungUBERON:000895279.94gold quality
liverUBERON:000210779.36gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no0.00

Regulation

Is transcription factor: no

Literature-anchored findings (GeneRIF, showing 1)

  • MiRNA-4537 functions as a tumor suppressor in gastric cancer and increases the radiosensitivity of gastric cancer cells. (PMID:34670480)

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.