MIR329-2
gene geneOn this page
Also known as hsa-mir-329-2
Summary
MIR329-2 (microRNA 329-2, HGNC:32051) is a microRNA gene on chromosome 14q32.31.
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 574409 — 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:32051 |
| Approved symbol | MIR329-2 |
| Name | microRNA 329-2 |
| Location | 14q32.31 |
| Locus type | RNA, micro |
| Status | Approved |
| Aliases | hsa-mir-329-2 |
| Ensembl gene | ENSG00000207762 |
| Ensembl biotype | miRNA |
| Entrez | 574409 |
| RNAcentral | URS000075D4D9 — miRNA, 84 nt, 1 organism(s) |
Gene structure
Transcript identifiers
Ensembl transcripts: 1 — 1 miRNA
ENST00000385029
RefSeq mRNA: 0 — MANE Select: None
Canonical transcript exons
ENST00000385029 — 1 exons
| Exon | Start | End |
|---|---|---|
| ENSE00001500036 | 101027100 | 101027183 |
Expression profiles
Bgee: expression breadth broad, 47 present calls, max score 96.82.
Top tissues by expression
47 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| adrenal tissue | UBERON:0018303 | 96.82 | gold quality |
| stomach | UBERON:0000945 | 85.12 | gold quality |
| lung | UBERON:0002048 | 84.03 | gold quality |
| kidney | UBERON:0002113 | 82.77 | gold quality |
| Brodmann (1909) area 9 | UBERON:0013540 | 79.57 | gold quality |
| calcaneal tendon | UBERON:0003701 | 77.67 | gold quality |
| intestine | UBERON:0000160 | 77.48 | gold quality |
| monocyte | CL:0000576 | 76.75 | gold quality |
| heart | UBERON:0000948 | 75.64 | gold quality |
| fundus of stomach | UBERON:0001160 | 75.38 | gold quality |
| gastrocnemius | UBERON:0001388 | 75.06 | gold quality |
| blood | UBERON:0000178 | 72.51 | gold quality |
| Ammon’s horn | UBERON:0001954 | 70.69 | gold quality |
| colon | UBERON:0001155 | 70.43 | gold quality |
| body of stomach | UBERON:0001161 | 69.49 | gold quality |
| dorsolateral prefrontal cortex | UBERON:0009834 | 69.22 | gold quality |
| prefrontal cortex | UBERON:0000451 | 67.99 | gold quality |
| lower esophagus muscularis layer | UBERON:0035833 | 67.53 | gold quality |
| left adrenal gland cortex | UBERON:0035825 | 67.44 | gold quality |
| omental fat pad | UBERON:0010414 | 66.92 | gold quality |
| right frontal lobe | UBERON:0002810 | 66.67 | gold quality |
| putamen | UBERON:0001874 | 66.45 | gold quality |
| transverse colon | UBERON:0001157 | 66.07 | gold quality |
| subcutaneous adipose tissue | UBERON:0002190 | 65.57 | gold quality |
| tibial nerve | UBERON:0001323 | 65.39 | gold quality |
| right atrium auricular region | UBERON:0006631 | 65.32 | gold quality |
| esophagus mucosa | UBERON:0002469 | 65.27 | gold quality |
| hypothalamus | UBERON:0001898 | 65.21 | gold quality |
| right adrenal gland | UBERON:0001233 | 65.05 | gold quality |
| right hemisphere of cerebellum | UBERON:0014890 | 64.86 | 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 9)
- Report feedback loop between PTTG1 targeting miRNAs,including mir329, PTTG1 and p53 that promotes pituitary tumorigenesis. (PMID:26320179)
- Evidence for a novel role for miR-362-3p and miR-329 as tumor suppressors. (PMID:26337669)
- Data show that knockdown of bromodomain containing 4 (BRD4) reversed the effect of microRNA miR-329 inhibition. (PMID:26456956)
- Data indicate GRB2 as a direct target of miR-329 in pancreatic cancer cells, and expression of GRB2 was inversely correlated with miR-329 expression in pancreatic cancer patients. (PMID:26885689)
- Results indicate that miR-329 played a pivotal role in lung cancer through inhibiting cell proliferation, migration, invasion, and promoting apoptosis by targeting oncogenic MET. (PMID:26909600)
- Results show that miRNA-329 was down-regulated in the gastric cancer (GC) cells and tissues. The up-regulation of miRNA-329 might inhibit the proliferation and promote the apoptosis of GC cells via targeting KDM1A. (PMID:29130516)
- ZFAS1 could serve as an oncogene in the tumorigenesis of bladder cancer, and discovered the functional regulatory network of ZFAS1 sponging miR-329. (PMID:29653362)
- The tumor suppressor role played by miR-329 in melanoma might be achieved through inhibiting the oncogenic beta-catenin pathway activation by downregulating HMGB2 expression. (PMID:31219186)
- Exosomal lncRNA PCAT1 Promotes Tumor Circulating Cell-Mediated Colorectal Cancer Liver Metastasis by Regulating the Activity of the miR-329-3p/Netrin-1-CD146 Complex. (PMID:36093435)
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.