MIR1283-1
gene geneOn this page
Also known as hsa-mir-1283-1
Summary
MIR1283-1 (microRNA 1283-1, HGNC:35255) is a microRNA gene on chromosome 19q13.42.
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 100302265 — 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:35255 |
| Approved symbol | MIR1283-1 |
| Name | microRNA 1283-1 |
| Location | 19q13.42 |
| Locus type | RNA, micro |
| Status | Approved |
| Aliases | hsa-mir-1283-1 |
| Ensembl gene | ENSG00000221421 |
| Ensembl biotype | miRNA |
| OMIM | 620644 |
| Entrez | 100302265 |
| RNAcentral | URS000075C919 — miRNA, 87 nt, 1 organism(s) |
Gene structure
Transcript identifiers
Ensembl transcripts: 1 — 1 miRNA
ENST00000408494
RefSeq mRNA: 0 — MANE Select: None
Canonical transcript exons
ENST00000408494 — 1 exons
| Exon | Start | End |
|---|---|---|
| ENSE00001807918 | 53688481 | 53688567 |
Expression profiles
Bgee: expression breadth tissue_specific, 8 present calls, max score 65.33.
Top tissues by expression
8 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| fundus of stomach | UBERON:0001160 | 65.33 | gold quality |
| ascending aorta | UBERON:0001496 | 64.75 | gold quality |
| skin of abdomen | UBERON:0001416 | 64.16 | gold quality |
| myometrium | UBERON:0001296 | 63.89 | gold quality |
| vagina | UBERON:0000996 | 63.84 | gold quality |
| urinary bladder | UBERON:0001255 | 63.25 | gold quality |
| dorsolateral prefrontal cortex | UBERON:0009834 | 62.96 | gold quality |
| left testis | UBERON:0004533 | 45.26 | gold quality |
Single-cell (SCXA)
Detected in 1 experiment(s), a significant marker in 0.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-ANND-3 | no | 0.65 |
Regulation
Is transcription factor: no
Literature-anchored findings (GeneRIF, showing 6)
- genetic association studies in a population in China: Data suggest that an SNP in ATF1 (rs11169571) is associated with essential hypertension in the population studied; altered binding of microRNA-1283 appears to be involved. (PMID:26149214)
- regulates the PERK/ATF4 pathway in vascular injury by targeting ATF4 (PMID:27537404)
- Dysregulation in the expression of (lncRNA-TSIX, TP53INP2 mRNA, miRNA-1283) in spinal cord injury. (PMID:32535070)
- MicroRNA 1283 alleviates cardiomyocyte damage caused by hypoxia /reoxygenation via targeting GADD45A and inactivating the JNK and p38 MAPK signaling pathways. (PMID:33293495)
- miR-1283 Contributes to Endoplasmic Reticulum Stress in the Development of Hypertension Through the Activating Transcription Factor-4 (ATF4)/C/EBP-Homologous Protein (CHOP) Signaling Pathway. (PMID:33911065)
- KLF14/miR-1283/TFAP2C axis inhibits HER2-positive breast cancer progression via declining tumor cell proliferation. (PMID:36752341)
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.