MIR1204

gene
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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

FieldValue
HGNC IDHGNC:37059
Approved symbolMIR1204
NamemicroRNA 1204
Location8q24.21
Locus typeRNA, micro
StatusApproved
Aliaseshsa-mir-1204
Ensembl geneENSG00000283710
Ensembl biotypemiRNA
Entrez100302185
RNAcentralURS000075D2B1 — 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

ExonStartEnd
ENSE00001565023127795962127796028

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):

TissueAnatomy IDExpression scoreQuality
esophagogastric junction muscularis propriaUBERON:003584167.24gold quality
subcutaneous adipose tissueUBERON:000219064.77gold quality
esophagus mucosaUBERON:000246962.33gold quality
bloodUBERON:000017861.87gold quality
skin of legUBERON:000151159.67gold quality
omental fat padUBERON:001041454.29gold quality
gastrocnemiusUBERON:000138852.26gold quality
tibial nerveUBERON:000132350.70gold quality
right testisUBERON:000453441.75gold quality

Single-cell (SCXA)

Detected in 1 experiment(s), a significant marker in 0.

ExperimentMarker?Max mean expression
E-ANND-3no0.00

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.

No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.