MIR2392
gene geneOn this page
Also known as hsa-mir-2392
Summary
MIR2392 (microRNA 2392, HGNC:41843) is a microRNA gene on chromosome 14q32.2.
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 100616495 — 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:41843 |
| Approved symbol | MIR2392 |
| Name | microRNA 2392 |
| Location | 14q32.2 |
| Locus type | RNA, micro |
| Status | Approved |
| Aliases | hsa-mir-2392 |
| Ensembl gene | ENSG00000266461 |
| Ensembl biotype | miRNA |
| Entrez | 100616495 |
| RNAcentral | URS0000759E16 — miRNA, 84 nt, 2 organism(s) |
Gene structure
Transcript identifiers
Ensembl transcripts: 1 — 1 miRNA
ENST00000584881
RefSeq mRNA: 0 — MANE Select: None
Canonical transcript exons
ENST00000584881 — 1 exons
| Exon | Start | End |
|---|---|---|
| ENSE00002719980 | 100814491 | 100814574 |
Expression profiles
Bgee: expression breadth tissue_specific, 9 present calls, max score 73.61.
Top tissues by expression
9 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| monocyte | CL:0000576 | 73.61 | gold quality |
| blood | UBERON:0000178 | 72.11 | gold quality |
| muscle layer of sigmoid colon | UBERON:0035805 | 69.07 | gold quality |
| skin of abdomen | UBERON:0001416 | 66.87 | gold quality |
| intestine | UBERON:0000160 | 65.89 | gold quality |
| lower esophagus muscularis layer | UBERON:0035833 | 65.19 | gold quality |
| colon | UBERON:0001155 | 64.04 | gold quality |
| small intestine Peyer’s patch | UBERON:0003454 | 60.74 | gold quality |
| left testis | UBERON:0004533 | 45.55 | gold quality |
Single-cell (SCXA)
Detected in 1 experiment(s), a significant marker in 0.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-ANND-3 | no | 0.29 |
Regulation
Is transcription factor: no
Literature-anchored findings (GeneRIF, showing 6)
- These findings indicate that the miR-2392-MAML3/WHSC1-Slug/Twist1 regulatory axis plays a critical role in GC metastasis. (PMID:28512191)
- CACNA1G-AS1 promotes hepatocellular carcinoma progression through regulating the miR-2392/C1orf61 pathway. (PMID:30908634)
- BTXA regulates the epithelial-mesenchymal transition and autophagy of keloid fibroblasts via modulating miR-1587/miR-2392 targeted ZEB2. (PMID:31652445)
- Role of miR-2392 in driving SARS-CoV-2 infection. (PMID:34624208)
- miR-2392 functions as tumour suppressor and inhibits malignant progression of hepatocellular carcinoma via directly targeting JAG2. (PMID:35485355)
- Positive effect of miR-2392 on fibroblast to cardiomyocyte-like cell fate transition: An in silico and in vitro study. (PMID:37393060)
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.