MIR302F

gene
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Also known as hsa-mir-302f

Summary

MIR302F (microRNA 302f, HGNC:35349) is a microRNA gene on chromosome 18q12.1.

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 100302131 — 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:35349
Approved symbolMIR302F
NamemicroRNA 302f
Location18q12.1
Locus typeRNA, micro
StatusApproved
Aliaseshsa-mir-302f
Ensembl geneENSG00000283218
Ensembl biotypemiRNA
Entrez100302131
RNAcentralURS000075C007 — miRNA, 51 nt, 2 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 miRNA

ENST00000635955

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000635955 — 1 exons

ExonStartEnd
ENSE000037958243029891030298960

Expression profiles

Bgee: expression breadth broad, 13 present calls, max score 75.43.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
bloodUBERON:000017875.43gold quality
esophagus mucosaUBERON:000246970.31gold quality
lower esophagus muscularis layerUBERON:003583369.78gold quality
transverse colonUBERON:000115768.56gold quality
subcutaneous adipose tissueUBERON:000219068.55gold quality
right frontal lobeUBERON:000281067.99gold quality
skin of legUBERON:000151167.04gold quality
spleenUBERON:000210665.98gold quality
prostate glandUBERON:000236765.31gold quality
vaginaUBERON:000099664.44gold quality
endocervixUBERON:000045862.92gold quality
left ovaryUBERON:000211962.26gold quality
left testisUBERON:000453350.32gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no0.33

Regulation

Is transcription factor: no

Literature-anchored findings (GeneRIF, showing 2)

  • FGF12, RBFOX1, and MIR302F could be important in human heterotaxy, because they were noted in multiple cases. Further investigation into genes involved in the NODAL, BMP, and WNT body patterning pathways and into the dosage effects of FGF12, RBFOX1, and MIR302F is warranted. (PMID:27637763)
  • The present study revealed three gout specific loci, CNTN5, MIR302F, ZNF724, to be clearly associated with mechanisms of gout development, which distinctly differ from the known gout risk loci that basically elevate serum uric acid level. This meta-analysis is the first to reveal the loci associated with crystal-induced inflammation, the last step in gout development that aggravates asymptomatic hyperuricaemia into gout. (PMID:31289104)

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.