MIR4306
gene geneOn this page
Also known as hsa-mir-4306
Summary
MIR4306 (microRNA 4306, HGNC:38350) is a microRNA gene on chromosome 13q32.3.
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 100422861 — 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:38350 |
| Approved symbol | MIR4306 |
| Name | microRNA 4306 |
| Location | 13q32.3 |
| Locus type | RNA, micro |
| Status | Approved |
| Aliases | hsa-mir-4306 |
| Ensembl gene | ENSG00000263615 |
| Ensembl biotype | miRNA |
| Entrez | 100422861 |
| RNAcentral | URS000075A81F — miRNA, 91 nt, 1 organism(s) |
Gene structure
Transcript identifiers
Ensembl transcripts: 1 — 1 miRNA
ENST00000583390
RefSeq mRNA: 0 — MANE Select: None
Canonical transcript exons
ENST00000583390 — 1 exons
| Exon | Start | End |
|---|---|---|
| ENSE00002686034 | 99643059 | 99643149 |
Expression profiles
Bgee: expression breadth broad, 58 present calls, max score 91.73.
Top tissues by expression
58 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| adult mammalian kidney | UBERON:0000082 | 91.73 | gold quality |
| primordial germ cell in gonad | CL:0000670 ∩ UBERON:0000991 | 88.65 | gold quality |
| kidney | UBERON:0002113 | 82.36 | gold quality |
| blood | UBERON:0000178 | 82.10 | gold quality |
| liver | UBERON:0002107 | 78.81 | gold quality |
| anterior cingulate cortex | UBERON:0009835 | 76.37 | gold quality |
| adrenal tissue | UBERON:0018303 | 75.37 | gold quality |
| stomach | UBERON:0000945 | 75.35 | gold quality |
| monocyte | CL:0000576 | 73.86 | gold quality |
| body of uterus | UBERON:0009853 | 73.37 | gold quality |
| left adrenal gland cortex | UBERON:0035825 | 72.11 | gold quality |
| calcaneal tendon | UBERON:0003701 | 72.06 | gold quality |
| right lobe of liver | UBERON:0001114 | 71.25 | gold quality |
| tibial artery | UBERON:0007610 | 71.10 | gold quality |
| putamen | UBERON:0001874 | 70.43 | gold quality |
| intestine | UBERON:0000160 | 68.70 | gold quality |
| ascending aorta | UBERON:0001496 | 68.53 | gold quality |
| tonsil | UBERON:0002372 | 68.06 | gold quality |
| subcutaneous adipose tissue | UBERON:0002190 | 67.69 | gold quality |
| transverse colon | UBERON:0001157 | 67.68 | gold quality |
| body of pancreas | UBERON:0001150 | 67.46 | gold quality |
| colon | UBERON:0001155 | 67.30 | gold quality |
| lung | UBERON:0002048 | 67.09 | gold quality |
| lower esophagus muscularis layer | UBERON:0035833 | 67.09 | gold quality |
| esophagogastric junction muscularis propria | UBERON:0035841 | 66.91 | gold quality |
| Ammon’s horn | UBERON:0001954 | 65.87 | gold quality |
| muscle layer of sigmoid colon | UBERON:0035805 | 65.73 | gold quality |
| vagina | UBERON:0000996 | 65.42 | gold quality |
| minor salivary gland | UBERON:0001830 | 65.09 | gold quality |
| skin of abdomen | UBERON:0001416 | 65.06 | gold quality |
Single-cell (SCXA)
Detected in 1 experiment(s), a significant marker in 0.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-ANND-3 | no | 0.57 |
Regulation
Is transcription factor: no
Literature-anchored findings (GeneRIF, showing 10)
- The level of miR-4306 was significantly increased in Arteriosclerosis Obliterans. (PMID:26370316)
- ATP13A2 inhibition by hsa-miR-4306 efficiently restored manganese-induced cytotoxicity in cultured neurons. (PMID:28302480)
- In conclusion, our study suggested that intercellular transfer of miR-4306 by platelet microparticles inhibited the HMDMs migration through VEGFA/ERK1/2/ NF-kappaB signaling pathways. (PMID:30183452)
- Regulation of capillary tubules and lipid formation in vascular endothelial cells and macrophages via extracellular vesicle-mediated microRNA-4306 transfer has been reported. (PMID:30477383)
- These findings suggest that miR-4306 acts as a tumor suppressor in triple-negative breast cancer and is a potential therapeutic target for triple-negative breast cancer treatment. (PMID:30867840)
- LncRNA LINC00958 promotes tumor progression through miR-4306/CEMIP axis in osteosarcoma. (PMID:33928604)
- miR-4306 Suppresses Proliferation of Esophageal Squamous Cell Carcinoma Cell by Targeting SIX3. (PMID:34021861)
- The regulation of long non-coding RNA 00958 (LINC00958) for oral squamous cell carcinoma (OSCC) cells death through absent in melanoma 2 (AIM2) depending on microRNA-4306 and Sirtuin1 (SIRT1) in vitro. (PMID:34384029)
- CircAGFG1 acts as a sponge of miR-4306 to stimulate esophageal cancer progression by modulating MAPRE2 expression. (PMID:34461454)
- The role of the miR-4306/PAK6 axis in degenerative nucleus pulposus cells in human intervertebral disc degeneration. (PMID:36423859)
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.