MIR219A2
gene geneOn this page
Also known as hsa-mir-219-2
Summary
MIR219A2 (microRNA 219a-2, HGNC:31598) is a microRNA gene on chromosome 9q34.11.
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 407003 — 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:31598 |
| Approved symbol | MIR219A2 |
| Name | microRNA 219a-2 |
| Location | 9q34.11 |
| Locus type | RNA, micro |
| Status | Approved |
| Aliases | hsa-mir-219-2 |
| Ensembl gene | ENSG00000284185 |
| Ensembl biotype | miRNA |
| Entrez | 407003 |
| RNAcentral | URS000075B0B0 — miRNA, 97 nt, 30 organism(s) |
Gene structure
Transcript identifiers
Ensembl transcripts: 1 — 1 miRNA
ENST00000385220
RefSeq mRNA: 0 — MANE Select: None
Canonical transcript exons
ENST00000385220 — 1 exons
| Exon | Start | End |
|---|---|---|
| ENSE00001500226 | 128392618 | 128392714 |
Expression profiles
Bgee: expression breadth tissue_specific, 9 present calls, max score 79.34.
Top tissues by expression
9 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| muscle of leg | UBERON:0001383 | 79.34 | gold quality |
| skeletal muscle tissue | UBERON:0001134 | 78.81 | gold quality |
| heart left ventricle | UBERON:0002084 | 75.25 | gold quality |
| blood | UBERON:0000178 | 74.79 | gold quality |
| esophagogastric junction muscularis propria | UBERON:0035841 | 69.17 | gold quality |
| vagina | UBERON:0000996 | 64.26 | gold quality |
| left lobe of thyroid gland | UBERON:0001120 | 62.80 | gold quality |
| esophagus mucosa | UBERON:0002469 | 62.46 | gold quality |
| cerebellar hemisphere | UBERON:0002245 | 47.97 | silver quality |
Single-cell (SCXA)
Detected in 1 experiment(s), a significant marker in 0.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-ANND-3 | no | 0.00 |
Regulation
Is transcription factor: no
Literature-anchored findings (GeneRIF, showing 16)
- although miR-219-2 and 199b can be hemizygously lost in a significant proportion of CML cases with der(9q) deletion, they are unlikely to play a dominant role in this disease pathogenesis (PMID:18548097)
- In inflammatory exudates miR-219-2 is a key regulator of lipid mediators of inflammation and a component of the active resolution programs that may be relevant in the pathogenesis of inflammatory diseases. (PMID:22957142)
- TLX and miR-219 have an important role in both normal neurodevelopment and in schizophrenia patient iPSC-derived NSCs. TLX has a role in regulating microRNA processing, independent of its well-characterized role in transcriptional regulation. (PMID:26965827)
- Suppression of miR-219-5p may benefit the liver regeneration and prevent cirrhosis through increasing KGF. (PMID:27855391)
- study suggests that miR-219-5p may have potential applications in the diagnosis and treatment of epithelial ovarian cancer (PMID:28890378)
- Overexpression of miR-219a-5p in MDA-MB-231 cells could inhibit the expression of MRTF-A as revealed by real-time PCR and western blot analysis (PMID:29077787)
- We have been able to identify and validate absence of miR-219 detection in CSF of multiple sclerosis patients compared to controls (PMID:29202778)
- miR-219-5p could inhibit wound healing by targeting TMEM98 in keratinocytes. (PMID:30338788)
- miR-219-5p might function as a tumor suppressor in esophageal squamous cell carcinoma by directly targeting CCNA2 expression. (PMID:30766610)
- miR-219a-5p is a potentially valuable indicator of the diagnosis, prognosis of traumatic brain injury and appears to regulate neuronal apoptosis and death. (PMID:31077370)
- lncRNA MEG3 modified epithelial-mesenchymal transition of ovarian cancer cells by sponging miR-219a-5p and regulating EGFR. (PMID:31161607)
- Results found that miR-219a expression is downregulated in triple-negative breast cancer (TNBC) cells, and its overexpression could inhibit both HCP5 and BIRC3 mRNA level. (PMID:31215169)
- LBX2-AS1/miR-219a-2-3p/FUS/LBX2 positive feedback loop contributes to the proliferation of gastric cancer. (PMID:31673844)
- Modulation of NMDA receptor by miR-219 in the amygdala and hippocampus of patients with mesial temporal lobe epilepsy. (PMID:32111564)
- miR-219a-5p enhances the radiosensitivity of non-small cell lung cancer cells through targeting CD164. (PMID:32364222)
- IgGs from Human Milk Hydrolyze microRNAs. (PMID:32443717)
Cross-species orthologs
3 orthologs
| Organism | Symbol | Gene ID |
|---|---|---|
| danio_rerio | mir219-3 | ENSDARG00000102905 |
| mus_musculus | Mir219a-2 | ENSMUSG00000065485 |
| drosophila_melanogaster | mir-219 | FBGN0262376 |
Paralogs (1): MIR219B (ENSG00000283335)
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.