MIRLET7A2
gene geneOn this page
Also known as hsa-let-7a-2
Summary
MIRLET7A2 (microRNA let-7a-2, HGNC:31477) is a microRNA gene on chromosome 11q24.1.
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 406882 — 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:31477 |
| Approved symbol | MIRLET7A2 |
| Name | microRNA let-7a-2 |
| Location | 11q24.1 |
| Locus type | RNA, micro |
| Status | Approved |
| Aliases | hsa-let-7a-2 |
| Ensembl gene | ENSG00000198975 |
| Ensembl biotype | miRNA |
| OMIM | 612142 |
| Entrez | 406882 |
| RNAcentral | URS00003F0B88 — miRNA, 72 nt, 23 organism(s) |
Gene structure
Transcript identifiers
Ensembl transcripts: 1 — 1 miRNA
ENST00000362105
RefSeq mRNA: 0 — MANE Select: None
Canonical transcript exons
ENST00000362105 — 1 exons
| Exon | Start | End |
|---|---|---|
| ENSE00001436868 | 122146522 | 122146593 |
Expression profiles
Bgee: expression breadth broad, 62 present calls, max score 80.19.
Top tissues by expression
62 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| calcaneal tendon | UBERON:0003701 | 80.19 | gold quality |
| kidney | UBERON:0002113 | 79.19 | gold quality |
| adrenal tissue | UBERON:0018303 | 77.33 | gold quality |
| endometrium | UBERON:0001295 | 77.04 | gold quality |
| blood | UBERON:0000178 | 76.24 | gold quality |
| stomach | UBERON:0000945 | 75.50 | gold quality |
| liver | UBERON:0002107 | 74.06 | gold quality |
| left uterine tube | UBERON:0001303 | 73.32 | gold quality |
| body of stomach | UBERON:0001161 | 71.90 | gold quality |
| monocyte | CL:0000576 | 71.20 | gold quality |
| intestine | UBERON:0000160 | 71.02 | gold quality |
| corpus callosum | UBERON:0002336 | 70.72 | gold quality |
| esophagogastric junction muscularis propria | UBERON:0035841 | 70.15 | gold quality |
| heart | UBERON:0000948 | 69.97 | gold quality |
| substantia nigra | UBERON:0002038 | 69.87 | gold quality |
| gastrocnemius | UBERON:0001388 | 69.83 | gold quality |
| lung | UBERON:0002048 | 69.29 | gold quality |
| hypothalamus | UBERON:0001898 | 69.01 | gold quality |
| thoracic aorta | UBERON:0001515 | 68.38 | gold quality |
| tibial artery | UBERON:0007610 | 68.35 | gold quality |
| ascending aorta | UBERON:0001496 | 68.31 | gold quality |
| colon | UBERON:0001155 | 68.04 | gold quality |
| descending thoracic aorta | UBERON:0002345 | 67.99 | gold quality |
| adipose tissue | UBERON:0001013 | 67.79 | gold quality |
| omental fat pad | UBERON:0010414 | 67.78 | gold quality |
| transverse colon | UBERON:0001157 | 67.48 | gold quality |
| right atrium auricular region | UBERON:0006631 | 66.78 | gold quality |
| muscle layer of sigmoid colon | UBERON:0035805 | 66.68 | gold quality |
| brain | UBERON:0000955 | 66.38 | gold quality |
| Ammon’s horn | UBERON:0001954 | 66.38 | gold quality |
Single-cell (SCXA)
Detected in 1 experiment(s), a significant marker in 0.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-ANND-3 | no | 1.20 |
Regulation
Is transcription factor: no
Upstream regulators (CollecTRI, top): CEBPA, VDR
Literature-anchored findings (GeneRIF, showing 22)
- The characterization and functional analysis of the promoter of the human miRNA let-7a2 in A549 cell lines, is reported. (PMID:21365266)
- data indicated that 1,25-(OH)2VD3 could upregulate the transcription of hsa-let-7a-2 in lung cancer cells and the up-regulation of hsa-let-7a-2 expression induced by 1,25-(OH)2VD3 might mediate the anti-proliferation effects of 1,25-(OH)2VD3 in lung cancer cells (PMID:23566834)
- esults indicate that both Sp1 and PARP1 contribute to FBN1 gene expression. These observations add to our understanding of the transcriptional regulation of FBN1 gene expression (PMID:23860321)
- Results show that microRNAs Let-7a and miR-335 expression levels were significantly downregulated in the tumors of patients with a BRCA mutation and correlated with tumor prognosis. (PMID:24942235)
- Results show that LOX-1 is a target of let- 7a and let-7b, and they inhibit the expression of LOX-1 by targeting its 3’-UTR. (PMID:25247304)
- overexpression of Lin28 can suppress the biological behavior of gastric cancer in vitro, and let-7 miRNA may play an important role in the process (PMID:25515921)
- High let-7a-2-3p and low miR-188-5p expression could be potentially used as favorably prognostic biomarkers. (PMID:25646775)
- Results show evidence that let-7a expression in osteosarcoma (OS) cells is significantly reduced and inversely correlated with E2F2 expression levels and that let-7a plays an important role in OS cell proliferation and tumorigenesis by targeting E2F2. (PMID:25647078)
- Plasma miR-20a and let-7a levels are significantly altered in patients with ESCC and can be used as potential biomarkers in the diagnosis of esophageal squamous cell carcinoma. (PMID:25914476)
- Our current findings identify a regulatory network of miR let-7a-USP35-ABIN-2 pathway, which may serve as potential therapeutic targets to help us control the human cancer progression (PMID:26348204)
- let-7 is a tumor suppressor that negatively regulates RAS, also in Ewing Sarcoma, and HIF-1alpha may contribute to the aggressive metastatic behavior of Ewing Sarcoma (PMID:26393682)
- These findings uncover a miR-372/let-7 axis regulating human primordial germ cell (PGC) specification. (PMID:27066911)
- Let-7a inhibition by HBV mRNAs resulted in enhanced HCC cell colony formation and tumor growth, providing evidence of the oncogenic potential of HBV mRNAs. (PMID:27693636)
- TGF-beta induces MIR100HG lncRNA, encoding miR-100, let-7a and miR-125b that control pancreatic ductal adenocarcinoma tumorigenesis. Pro-tumorigenic miR-100 and miR-125b increase and anti-tumorigenic let-7a is unchanged, as TGF-beta also induces LIN28B. The induction of LIN28B results in the up-regulation of miR-100 and miR-125b, with let-7a unchanged despite being part of the same MIR100HG primary transcript. (PMID:29748571)
- Expression of let-7a-5p in pneumoconiosis is downregulated, while reduced let-7a-5p corresponds to high expression of BCL2L1 and poor survival of lung adenocarcinoma patients. (PMID:30497474)
- Inhibition effect of exosomes-mediated Let-7a on the development and metastasis of triple negative breast cancer by down-regulating the expression of c-Myc. (PMID:31298382)
- Study provides evidence that let-7a miRNA positively regulates translational readthrough of AGO1. (PMID:31330067)
- Salivary miR-let-7a-5p and miR-3928 were significantly down regulated in saliva of head and neck squamous cell carcinoma patients, and have the potential to be novel non-invasive biomarkers for early detection and prognosis head and neck squamous cell carcinoma. (PMID:32208417)
- Let-7a-5p represses proliferation, migration, invasion and epithelial-mesenchymal transition by targeting Smad2 in TGF-b2-induced human lens epithelial cells. (PMID:32345785)
- Predictive Value of let-7a for Cancer Cell Repopulation between Chemotherapy and Long-Term Survival: A Prospective Study. (PMID:34686505)
- Pre-miRNA Hsa-Let-7a-2: a Novel Intracellular Partner of Angiotensin II Type 2 Receptor Negatively Regulating its Signals. (PMID:35637969)
- LncRNA SNHG4 promotes prostate cancer cell survival and resistance to enzalutamide through a let-7a/RREB1 positive feedback loop and a ceRNA network. (PMID:37596700)
Cross-species orthologs
0 orthologs
Paralogs (10): MIRLET7E (ENSG00000198972), MIRLET7C (ENSG00000199030), MIRLET7F1 (ENSG00000199072), MIRLET7D (ENSG00000199133), MIRLET7G (ENSG00000199150), MIRLET7A1 (ENSG00000199165), MIRLET7I (ENSG00000199179), MIRLET7F2 (ENSG00000208012), MIR98 (ENSG00000271886), MIRLET7A3 (ENSG00000283990)
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.