MIR568
gene geneOn this page
Also known as hsa-mir-568
Summary
MIR568 (microRNA 568, HGNC:32824) is a microRNA gene on chromosome 3q13.31.
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 693153 — 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:32824 |
| Approved symbol | MIR568 |
| Name | microRNA 568 |
| Location | 3q13.31 |
| Locus type | RNA, micro |
| Status | Approved |
| Aliases | hsa-mir-568 |
| Ensembl gene | ENSG00000284134 |
| Ensembl biotype | miRNA |
| Entrez | 693153 |
| RNAcentral | URS000075AF78 — miRNA, 95 nt, 4 organism(s) |
Gene structure
Transcript identifiers
Ensembl transcripts: 1 — 1 miRNA
ENST00000385036
RefSeq mRNA: 0 — MANE Select: None
Canonical transcript exons
ENST00000385036 — 1 exons
| Exon | Start | End |
|---|---|---|
| ENSE00001500043 | 114316475 | 114316569 |
Expression profiles
Bgee: expression breadth broad, 11 present calls, max score 83.86.
Top tissues by expression
11 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| primordial germ cell in gonad | CL:0000670 ∩ UBERON:0000991 | 83.86 | gold quality |
| hypothalamus | UBERON:0001898 | 78.62 | gold quality |
| subcutaneous adipose tissue | UBERON:0002190 | 71.58 | gold quality |
| blood | UBERON:0000178 | 70.38 | gold quality |
| anterior cingulate cortex | UBERON:0009835 | 68.07 | gold quality |
| heart left ventricle | UBERON:0002084 | 63.80 | gold quality |
| skin of leg | UBERON:0001511 | 58.88 | gold quality |
| body of stomach | UBERON:0001161 | 58.61 | gold quality |
| esophagus mucosa | UBERON:0002469 | 54.86 | gold quality |
| tibial artery | UBERON:0007610 | 54.75 | gold quality |
| skin of abdomen | UBERON:0001416 | 48.53 | 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 4)
- increased PBEF/NAMPT expression induced by bioactive agonists involves epigenetic regulation with hsa-miR-374a and hsa-miR-568 (PMID:24053186)
- Data indicate that nuclear factor of activated T cells 5 (NFAT5) is a direct target of miR-568. (PMID:24355664)
- Our results demonstrated a significant association between sporadic KC and hsa-mir-568 rs149509568 polymorphism, suggesting a potential role of the has-mir-568 in KC pathogenesis. (PMID:26845316)
- Hsa_circ_0097009 regulates proliferation, apoptosis, migration and invasion of hepatocellular carcinoma cells via miR-568/RNF38 axis. (PMID:36598315)
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.