MIR770
gene geneOn this page
Also known as hsa-mir-770
Summary
MIR770 (microRNA 770, HGNC:33143) 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 768222 — 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:33143 |
| Approved symbol | MIR770 |
| Name | microRNA 770 |
| Location | 14q32.2 |
| Locus type | RNA, micro |
| Status | Approved |
| Aliases | hsa-mir-770 |
| Ensembl gene | ENSG00000211574 |
| Ensembl biotype | miRNA |
| Entrez | 768222 |
| RNAcentral | URS000075BA84 — miRNA, 98 nt, 16 organism(s) |
Gene structure
Transcript identifiers
Ensembl transcripts: 1 — 1 miRNA
ENST00000390219
RefSeq mRNA: 0 — MANE Select: None
Canonical transcript exons
ENST00000390219 — 1 exons
| Exon | Start | End |
|---|---|---|
| ENSE00001507646 | 100852390 | 100852487 |
Expression profiles
Bgee: expression breadth broad, 36 present calls, max score 95.92.
Top tissues by expression
36 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| anterior cingulate cortex | UBERON:0009835 | 95.92 | gold quality |
| C1 segment of cervical spinal cord | UBERON:0006469 | 86.50 | gold quality |
| gastrocnemius | UBERON:0001388 | 71.40 | gold quality |
| blood | UBERON:0000178 | 70.96 | gold quality |
| heart left ventricle | UBERON:0002084 | 69.49 | gold quality |
| right atrium auricular region | UBERON:0006631 | 69.12 | gold quality |
| right lobe of liver | UBERON:0001114 | 68.47 | gold quality |
| left lobe of thyroid gland | UBERON:0001120 | 67.47 | gold quality |
| thoracic aorta | UBERON:0001515 | 65.07 | gold quality |
| lower esophagus muscularis layer | UBERON:0035833 | 65.06 | gold quality |
| right lobe of thyroid gland | UBERON:0001119 | 65.03 | gold quality |
| esophagogastric junction muscularis propria | UBERON:0035841 | 64.96 | gold quality |
| skin of abdomen | UBERON:0001416 | 63.11 | gold quality |
| thyroid gland | UBERON:0002046 | 62.95 | gold quality |
| tibial artery | UBERON:0007610 | 62.94 | gold quality |
| esophagus mucosa | UBERON:0002469 | 62.82 | gold quality |
| body of stomach | UBERON:0001161 | 62.28 | gold quality |
| small intestine Peyer’s patch | UBERON:0003454 | 62.12 | gold quality |
| ascending aorta | UBERON:0001496 | 62.00 | gold quality |
| minor salivary gland | UBERON:0001830 | 61.90 | gold quality |
| vagina | UBERON:0000996 | 61.75 | gold quality |
| body of pancreas | UBERON:0001150 | 61.01 | gold quality |
| skin of leg | UBERON:0001511 | 60.82 | gold quality |
| transverse colon | UBERON:0001157 | 60.58 | gold quality |
| subcutaneous adipose tissue | UBERON:0002190 | 60.52 | gold quality |
| upper lobe of left lung | UBERON:0008952 | 59.55 | gold quality |
| muscle layer of sigmoid colon | UBERON:0035805 | 58.07 | gold quality |
| omental fat pad | UBERON:0010414 | 57.56 | gold quality |
| tibial nerve | UBERON:0001323 | 56.40 | gold quality |
| urinary bladder | UBERON:0001255 | 53.53 | gold quality |
Single-cell (SCXA)
Detected in 1 experiment(s), a significant marker in 0.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-ANND-3 | no | 0.00 |
Regulation
Is transcription factor: no
Literature-anchored findings (GeneRIF, showing 19)
- overexpression of PCGEM1 in synoviocytes suppressed miR-770 by direct binding (PMID:26340084)
- microRNA-770 was identified as an important downstream target of Wnt/beta-catenin signaling, to inhibit FBXW7 expression through targeting its 3’-untranslated region. Thus, our results suggest a previously unknown Wnt/beta catenin-miR-770-FBXW7 molecular network in the HCC development. (PMID:26602384)
- Five miRNAs were significantly upregulated in type 2 diabetes mellitus patients (p < 0.05) including miR-661, miR-571, miR-770-5p, miR-892b and miR-1303. Moreover, the levels of the five miRNAs were higher in patients with complications than in those without complications. (PMID:26831044)
- Results indicate that ERCC excision repair 2 (ERCC2) is a potential target of miR-770-5p. (PMID:27449101)
- MiR-770-5p and PBK levels were inversely correlated in xenograft model mice. (PMID:28333152)
- MEG3 and miR-770 was significantly downregulated in gastric cardia adenocarcinoma patients and cell lines, and their expression was associated with TNM stage and lymph node metastasis. Overexpression of MEG3 and miR-770 inhibited gastric cancer cell proliferation and invasion in vitro. (PMID:28345805)
- study indicates that miR-770 functions as a tumor suppressor and it might be a potential biomarker and therapeutic target in non-small cell lung cancer. (PMID:28882645)
- The miR-770 could suppress the doxorubicin-resistance and metastasis of triple negative breast cancer cells, which broaden our insights into the underlying mechanisms in chemo-resistance and metastasis and the tumor suppression effect of miR-770 was mediated by targeting of STMN1. (PMID:29323124)
- Circulating mir-770-5p was negatively correlated with HbA1c in Type 1 diabetics. (PMID:29453204)
- Overexpression of miR-770 indicates a favorable prognosis and suppresses tumorigenesis by modulating PI3K-AKT pathway in glioma. (PMID:31002138)
- miR-770-5p regulates cancer cell proliferation by targeting several genes involved in the HER2 signaling pathway. (PMID:31009516)
- Long noncoding RNA TPT1-AS1 downregulates the microRNA-770-5p expression to inhibit glioma cell autophagy and promote proliferation through STMN1 upregulation. (PMID:31637705)
- Dysregulation of microRNA-770-5p influences pancreatic-beta-cell function by targeting TP53 regulated inhibitor of apoptosis 1 in gestational diabetes mellitus. (PMID:32016984)
- MiR-770-5p facilitates podocyte apoptosis and inflammation in diabetic nephropathy by targeting TIMP3. (PMID:32309847)
- MiR-770 promotes oral squamous cell carcinoma migration and invasion by regulating the Sirt7/Smad4 pathway. (PMID:33326690)
- miR-770-5p regulates EMT and invasion in TNBC cells by targeting DNMT3A. (PMID:33798630)
- CircABCC3 knockdown inhibits glioblastoma cell malignancy by regulating miR-770-5p/SOX2 axis through PI3K/AKT signaling pathway. (PMID:33811842)
- MiR-770-5p, miR-661 and miR-571 expression level in serum and tissue samples of foot ulcer caused by diabetes mellitus type II in Iranian population. (PMID:34643918)
- The important role of miR-770 as a novel potential diagnostic and therapeutic target for human cancer and other diseases. (PMID:37267769)
Cross-species orthologs
2 orthologs
| Organism | Symbol | Gene ID |
|---|---|---|
| mus_musculus | Mir770 | ENSMUSG00000076451 |
| rattus_norvegicus | Mir770 | ENSRNOG00000040384 |
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.