MIR302F
gene geneOn this page
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
| Field | Value |
|---|---|
| HGNC ID | HGNC:35349 |
| Approved symbol | MIR302F |
| Name | microRNA 302f |
| Location | 18q12.1 |
| Locus type | RNA, micro |
| Status | Approved |
| Aliases | hsa-mir-302f |
| Ensembl gene | ENSG00000283218 |
| Ensembl biotype | miRNA |
| Entrez | 100302131 |
| RNAcentral | URS000075C007 — 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
| Exon | Start | End |
|---|---|---|
| ENSE00003795824 | 30298910 | 30298960 |
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):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| blood | UBERON:0000178 | 75.43 | gold quality |
| esophagus mucosa | UBERON:0002469 | 70.31 | gold quality |
| lower esophagus muscularis layer | UBERON:0035833 | 69.78 | gold quality |
| transverse colon | UBERON:0001157 | 68.56 | gold quality |
| subcutaneous adipose tissue | UBERON:0002190 | 68.55 | gold quality |
| right frontal lobe | UBERON:0002810 | 67.99 | gold quality |
| skin of leg | UBERON:0001511 | 67.04 | gold quality |
| spleen | UBERON:0002106 | 65.98 | gold quality |
| prostate gland | UBERON:0002367 | 65.31 | gold quality |
| vagina | UBERON:0000996 | 64.44 | gold quality |
| endocervix | UBERON:0000458 | 62.92 | gold quality |
| left ovary | UBERON:0002119 | 62.26 | gold quality |
| left testis | UBERON:0004533 | 50.32 | gold quality |
Single-cell (SCXA)
Detected in 1 experiment(s), a significant marker in 0.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-ANND-3 | no | 0.33 |
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.
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.