MIR4293
gene geneOn this page
Also known as hsa-mir-4293
Summary
MIR4293 (microRNA 4293, HGNC:38270) is a microRNA gene on chromosome 10p13.
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 100422843 — 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:38270 |
| Approved symbol | MIR4293 |
| Name | microRNA 4293 |
| Location | 10p13 |
| Locus type | RNA, micro |
| Status | Approved |
| Aliases | hsa-mir-4293 |
| Ensembl gene | ENSG00000266321 |
| Ensembl biotype | miRNA |
| Entrez | 100422843 |
| RNAcentral | URS000075C2F1 — miRNA, 78 nt, 1 organism(s) |
Gene structure
Transcript identifiers
Ensembl transcripts: 1 — 1 miRNA
ENST00000584305
RefSeq mRNA: 0 — MANE Select: None
Canonical transcript exons
ENST00000584305 — 1 exons
| Exon | Start | End |
|---|---|---|
| ENSE00002728862 | 14383200 | 14383277 |
Expression profiles
Bgee: expression breadth tissue_specific, 10 present calls, max score 77.45.
Top tissues by expression
10 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| blood | UBERON:0000178 | 77.45 | gold quality |
| monocyte | CL:0000576 | 73.68 | gold quality |
| Brodmann (1909) area 9 | UBERON:0013540 | 71.36 | gold quality |
| substantia nigra | UBERON:0002038 | 64.76 | gold quality |
| skin of abdomen | UBERON:0001416 | 63.50 | gold quality |
| right frontal lobe | UBERON:0002810 | 61.72 | gold quality |
| lung | UBERON:0002048 | 59.41 | gold quality |
| left lobe of thyroid gland | UBERON:0001120 | 58.24 | gold quality |
| corpus callosum | UBERON:0002336 | 56.39 | gold quality |
| colon | UBERON:0001155 | 47.53 | gold quality |
Single-cell (SCXA)
Detected in 1 experiment(s), a significant marker in 0.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-ANND-3 | no | 0.49 |
Regulation
Is transcription factor: no
Literature-anchored findings (GeneRIF, showing 6)
- This study provides the first evidence that miR-449b rs10061133 and miR-4293 rs12220909 are associated with esophageal squamous cell carcinoma risk in Chinese population. (PMID:26055141)
- The GC/CC genotypes of miR-4293 rs12220909 were associated significantly with decreased non-small cell lung cancer susceptibility, which indicates that the mutant allele C of rs12220909 can influence the function of miR-4293. (PMID:28410417)
- Whether miR-4293 rs12220909 variant affects cancer susceptibility: evidence from 11255 subjects. (PMID:32496828)
- Association of miR-4293 rs12220909 polymorphism with cancer risk: A meta-analysis of 8394 subjects. (PMID:32769868)
- miR-4293 upregulates lncRNA WFDC21P by suppressing mRNA-decapping enzyme 2 to promote lung carcinoma proliferation. (PMID:34301920)
- Novel susceptibility loci for steroid-associated osteonecrosis of the femoral head in systemic lupus erythematosus. (PMID:34850884)
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.