MIR3151
gene geneOn this page
Also known as hsa-mir-3151
Summary
MIR3151 (microRNA 3151, HGNC:38266) is a microRNA gene on chromosome 8q22.3.
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 100422992 — 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:38266 |
| Approved symbol | MIR3151 |
| Name | microRNA 3151 |
| Location | 8q22.3 |
| Locus type | RNA, micro |
| Status | Approved |
| Aliases | hsa-mir-3151 |
| Ensembl gene | ENSG00000265657 |
| Ensembl biotype | miRNA |
| Entrez | 100422992 |
| RNAcentral | URS000075C6C0 — miRNA, 76 nt, 2 organism(s) |
Gene structure
Transcript identifiers
Ensembl transcripts: 1 — 1 miRNA
ENST00000583423
RefSeq mRNA: 0 — MANE Select: None
Canonical transcript exons
ENST00000583423 — 1 exons
| Exon | Start | End |
|---|---|---|
| ENSE00002719005 | 103154614 | 103154689 |
Expression profiles
Bgee: expression breadth tissue_specific, 9 present calls, max score 68.55.
Top tissues by expression
9 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| esophagogastric junction muscularis propria | UBERON:0035841 | 68.55 | gold quality |
| dorsolateral prefrontal cortex | UBERON:0009834 | 68.37 | gold quality |
| tibial artery | UBERON:0007610 | 67.42 | gold quality |
| skin of abdomen | UBERON:0001416 | 64.72 | gold quality |
| subcutaneous adipose tissue | UBERON:0002190 | 60.47 | gold quality |
| skin of leg | UBERON:0001511 | 60.34 | gold quality |
| cerebellar hemisphere | UBERON:0002245 | 60.33 | gold quality |
| putamen | UBERON:0001874 | 59.39 | gold quality |
| left lobe of thyroid gland | UBERON:0001120 | 54.58 | gold quality |
Single-cell (SCXA)
Detected in 1 experiment(s), a significant marker in 0.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-ANND-3 | no | 0.30 |
Regulation
Is transcription factor: no
Literature-anchored findings (GeneRIF, showing 5)
- high expression of miR-3151 is an independent prognosticator for poor outcome in cytogenetically normal-AML and affects different outcome end points than its host gene, BAALC (PMID:22529287)
- miR-3151 introns within BAALC have roles in driving leukemogenesis by deregulating the TP53 pathway (PMID:24736457)
- miR-3151 emerged as independent prognostic marker in younger patients with acute myeloid leukemia (PMID:26430723)
- miR-3151 silencing by DNA methylation protected chronic lymphocytic leukemia cells from apoptosis by over-expression of its direct targets MADD and PIK3R2, constitutive activation of MEK/ERK and PI3K/AKT signaling , and over-expression of MCL1. (PMID:26517243)
- Characterization of TP53 as a downstream effector of miR-3151 provides evidence for a causal link between BRAF mutations and TP53 inactivation (PMID:26582795)
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.