MIR517B
gene geneOn this page
Also known as hsa-mir-517b
Summary
MIR517B (microRNA 517b, HGNC:32115) 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 574483 — 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:32115 |
| Approved symbol | MIR517B |
| Name | microRNA 517b |
| Location | 19q13.42 |
| Locus type | RNA, micro |
| Status | Approved |
| Aliases | hsa-mir-517b |
| Ensembl gene | ENSG00000207837 |
| Ensembl biotype | miRNA |
| OMIM | 620613 |
| Entrez | 574483 |
| RNAcentral | URS000075C4A5 — miRNA, 67 nt, 4 organism(s) |
Gene structure
Transcript identifiers
Ensembl transcripts: 1 — 1 miRNA
ENST00000385102
RefSeq mRNA: 0 — MANE Select: None
Canonical transcript exons
ENST00000385102 — 1 exons
| Exon | Start | End |
|---|---|---|
| ENSE00001500108 | 53721076 | 53721142 |
Expression profiles
Bgee: expression breadth tissue_specific, 4 present calls, max score 78.95.
Top tissues by expression
4 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| blood | UBERON:0000178 | 78.95 | gold quality |
| placenta | UBERON:0001987 | 77.81 | gold quality |
| lower esophagus muscularis layer | UBERON:0035833 | 66.18 | gold quality |
| right ovary | UBERON:0002118 | 65.03 | 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)
- underexpressed in complete hydatidiform mole (PMID:22672989)
- MiR-517b overexpression increased expression of the anti-angiogenic protein, sFLT1. (PMID:25799546)
- MiR-517-5p is highly expressed in placental samples of preeclampsia pregnancies, which could promote proliferative and invasive abilities of cells by inhibiting ERK/MMP-2 pathway. (PMID:30402831)
- miR-517b-3p promotes the progression of portal vein tumor thrombus via activating Wnt/beta-catenin signaling pathway in hepatocellular carcinoma. (PMID:35666423)
Cross-species orthologs
0 orthologs
Paralogs (24): MIR520E (ENSG00000207599), MIR515-2 (ENSG00000207615), MIR515-1 (ENSG00000207616), MIR516A2 (ENSG00000207620), MIR526A1 (ENSG00000207629), MIR521-1 (ENSG00000207634), MIR518F (ENSG00000207706), MIR525 (ENSG00000207711), MIR520B (ENSG00000207722), MIR517A (ENSG00000207734), MIR520C (ENSG00000207738), MIR516A1 (ENSG00000207767), MIR519C (ENSG00000207788), MIR519B (ENSG00000207825), MIR518B (ENSG00000207862), MIR516B1 (ENSG00000207946), MIR518E (ENSG00000207987), MIR524 (ENSG00000283289), MIR518D (ENSG00000283330), MIR523 (ENSG00000283455), MIR518C (ENSG00000283490), MIR520F (ENSG00000283540), MIR522 (ENSG00000283685), MIR519A2 (ENSG00000284362)
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.