MIR302E
gene geneOn this page
Also known as hsa-mir-302e
Summary
MIR302E (microRNA 302e, HGNC:35348) is a microRNA gene on chromosome 11p15.4.
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 100313774 — 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:35348 |
| Approved symbol | MIR302E |
| Name | microRNA 302e |
| Location | 11p15.4 |
| Locus type | RNA, micro |
| Status | Approved |
| Aliases | hsa-mir-302e |
| Ensembl gene | ENSG00000221703 |
| Ensembl biotype | miRNA |
| Entrez | 100313774 |
| RNAcentral | URS000075B201 — miRNA, 72 nt, 3 organism(s) |
Gene structure
Transcript identifiers
Ensembl transcripts: 1 — 1 miRNA
ENST00000408776
RefSeq mRNA: 0 — MANE Select: None
Canonical transcript exons
ENST00000408776 — 1 exons
| Exon | Start | End |
|---|---|---|
| ENSE00001565411 | 7234766 | 7234837 |
Expression profiles
Bgee: expression breadth tissue_specific, 7 present calls, max score 78.04.
Top tissues by expression
7 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| heart | UBERON:0000948 | 78.04 | gold quality |
| kidney | UBERON:0002113 | 75.37 | gold quality |
| intestine | UBERON:0000160 | 70.26 | gold quality |
| transverse colon | UBERON:0001157 | 65.04 | gold quality |
| C1 segment of cervical spinal cord | UBERON:0006469 | 63.82 | gold quality |
| minor salivary gland | UBERON:0001830 | 59.13 | gold quality |
| left testis | UBERON:0004533 | 44.00 | gold quality |
Single-cell (SCXA)
Detected in 1 experiment(s), a significant marker in 0.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-ANND-3 | no | 0.33 |
Regulation
Is transcription factor: no
Literature-anchored findings (GeneRIF, showing 4)
- Ectopic miR-302e remarkably suppressed the luciferase activity and expression of RelA, whereas down-regulation of miR-302e increased RelA luciferase activity and expression (PMID:29748238)
- The results of the present study indicated that sevoflurane exerts its neurotoxic effect by regulating the hsamiR302e/OXR1 axis. Therefore, the manipulation of the hsamiR302e/OXR1 pathway will be useful for preventing sevofluraneinduced neurotoxicity. (PMID:30221705)
- The inhibiting effects of FGD5-AS1 knockdown on colorectal cancer (CRC) cell proliferation, migration, and invasion, and the promoting effects on CRC cell apoptosis could be revived by miR-302e suppression or CDCA7 upregulation. (PMID:31332696)
- CircRhoC promotes tumorigenicity and progression in ovarian cancer by functioning as a miR-302e sponge to positively regulate VEGFA. (PMID:31639291)
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.