MIR1204
gene geneOn this page
Also known as hsa-mir-1204
Summary
MIR1204 (microRNA 1204, HGNC:37059) is a microRNA gene on chromosome 8q24.21.
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 100302185 — 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:37059 |
| Approved symbol | MIR1204 |
| Name | microRNA 1204 |
| Location | 8q24.21 |
| Locus type | RNA, micro |
| Status | Approved |
| Aliases | hsa-mir-1204 |
| Ensembl gene | ENSG00000283710 |
| Ensembl biotype | miRNA |
| Entrez | 100302185 |
| RNAcentral | URS000075D2B1 — miRNA, 67 nt, 19 organism(s) |
Gene structure
Transcript identifiers
Ensembl transcripts: 1 — 1 miRNA
ENST00000408388
RefSeq mRNA: 0 — MANE Select: None
Canonical transcript exons
ENST00000408388 — 1 exons
| Exon | Start | End |
|---|---|---|
| ENSE00001565023 | 127795962 | 127796028 |
Expression profiles
Bgee: expression breadth tissue_specific, 9 present calls, max score 67.24.
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 | 67.24 | gold quality |
| subcutaneous adipose tissue | UBERON:0002190 | 64.77 | gold quality |
| esophagus mucosa | UBERON:0002469 | 62.33 | gold quality |
| blood | UBERON:0000178 | 61.87 | gold quality |
| skin of leg | UBERON:0001511 | 59.67 | gold quality |
| omental fat pad | UBERON:0010414 | 54.29 | gold quality |
| gastrocnemius | UBERON:0001388 | 52.26 | gold quality |
| tibial nerve | UBERON:0001323 | 50.70 | gold quality |
| right testis | UBERON:0004534 | 41.75 | 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 7)
- p53-Dependent induction of PVT1 and miR-1204. (PMID:22110125)
- MiR-1204 sensitizes nasopharyngeal carcinoma cells to paclitaxel both in vitro and in vivo (PMID:25756509)
- High miR1204 expression is associated with epithelial-mesenchymal transition and metastasis in breast cancer. (PMID:29555976)
- MiR-1204 promotes ovarian squamous cell carcinoma growth by increasing glucose uptake. (PMID:30304996)
- upregulated miR-1204 in non-small-cell lung cancer (NSCLC) is associated with NSCLC progression and promotes NSCLC cell proliferation by downregulating PITX1. (PMID:30549141)
- MiR-1204 induces apoptosis of non-small cell lung cancer cells by inhibiting the expression of DEK. The mechanism of apoptosis involves down-regulation of Bcl-2 and up-regulation of Bax expression. (PMID:31246264)
- miR-1204 Positioning in 8q24.21 Involved in the Tumorigenesis of Colorectal Cancer by Targeting MASPIN. (PMID:39082173)
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.