MIR1224
gene geneOn this page
Also known as hsa-mir-1224
Summary
MIR1224 (microRNA 1224, HGNC:33923) is a microRNA gene on chromosome 3q27.1.
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 100187716 — 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:33923 |
| Approved symbol | MIR1224 |
| Name | microRNA 1224 |
| Location | 3q27.1 |
| Locus type | RNA, micro |
| Status | Approved |
| Aliases | hsa-mir-1224 |
| Ensembl gene | ENSG00000221120 |
| Ensembl biotype | miRNA |
| OMIM | 611620 |
| Entrez | 100187716 |
| RNAcentral | URS00006378D3 — miRNA, 85 nt, 4 organism(s) |
Gene structure
Transcript identifiers
Ensembl transcripts: 1 — 1 miRNA
ENST00000408193
RefSeq mRNA: 0 — MANE Select: None
Canonical transcript exons
ENST00000408193 — 1 exons
| Exon | Start | End |
|---|---|---|
| ENSE00001564828 | 184241405 | 184241489 |
Expression profiles
Bgee: expression breadth broad, 67 present calls, max score 94.83.
Top tissues by expression
67 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| primordial germ cell in gonad | CL:0000670 ∩ UBERON:0000991 | 94.83 | gold quality |
| gastrocnemius | UBERON:0001388 | 73.68 | gold quality |
| right adrenal gland | UBERON:0001233 | 73.55 | gold quality |
| adrenal gland | UBERON:0002369 | 72.53 | gold quality |
| heart left ventricle | UBERON:0002084 | 72.31 | gold quality |
| body of pancreas | UBERON:0001150 | 71.65 | gold quality |
| left adrenal gland | UBERON:0001234 | 71.55 | gold quality |
| blood | UBERON:0000178 | 71.32 | gold quality |
| liver | UBERON:0002107 | 70.98 | gold quality |
| right adrenal gland cortex | UBERON:0035827 | 70.91 | gold quality |
| right hemisphere of cerebellum | UBERON:0014890 | 70.89 | gold quality |
| heart | UBERON:0000948 | 69.92 | gold quality |
| right lobe of liver | UBERON:0001114 | 69.66 | gold quality |
| cerebellar hemisphere | UBERON:0002245 | 69.57 | gold quality |
| left adrenal gland cortex | UBERON:0035825 | 69.54 | gold quality |
| body of stomach | UBERON:0001161 | 68.95 | gold quality |
| right atrium auricular region | UBERON:0006631 | 68.93 | gold quality |
| amygdala | UBERON:0001876 | 68.16 | gold quality |
| right frontal lobe | UBERON:0002810 | 68.13 | gold quality |
| frontal cortex | UBERON:0001870 | 68.09 | gold quality |
| stomach | UBERON:0000945 | 67.74 | gold quality |
| esophagogastric junction muscularis propria | UBERON:0035841 | 67.71 | gold quality |
| tibial artery | UBERON:0007610 | 67.27 | gold quality |
| endometrium | UBERON:0001295 | 66.94 | gold quality |
| ascending aorta | UBERON:0001496 | 66.85 | gold quality |
| lung | UBERON:0002048 | 66.85 | gold quality |
| brain | UBERON:0000955 | 66.65 | gold quality |
| dorsolateral prefrontal cortex | UBERON:0009834 | 66.30 | gold quality |
| anterior cingulate cortex | UBERON:0009835 | 66.22 | gold quality |
| C1 segment of cervical spinal cord | UBERON:0006469 | 66.16 | 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 21)
- These data indicate that miR-1224-5p may inhibit tumor-associated activity in malignant gliomas by targeting CREB1. (PMID:25648114)
- miR-1224 is a previously unrecognised regulator of proliferation after Acute Liver Failure in hepatocytes and represents a novel and specific biomarker of liver injury with prognostic value in Acute Liver Failure. (PMID:28645739)
- MiR-1224 is a specific modulator of angiogenesis. EPN2 mRNA is a direct target of miR-1224 (PMID:28717225)
- Overexpression of miR-1224-5p led to inhibition of keloid fibroblast proliferation, promotion of apoptosis and decrease of migration and invasion. Our results suggest that downregulation of miR-1224-5p may be one of the mechanisms involved in the occurrence and development of keloids. (PMID:29050938)
- Findings indicate that miR-1224-5p promotes hepatic lipogenesis by suppressing AMPKalpha1 expression. (PMID:29474539)
- infection with Bacillus Calmette-Guerin resulted in an increase in miR-1224 expression in monocyte-derived macrophages (PMID:29908542)
- that upregulation in miR-1224-5p expression may decrease proliferation, induce apoptosis, inhibit migration and invasion, and suppress tube formation in TECs of human HCC. MiR-1224-5p may serve as a potential tumor suppressor in HCC. (PMID:30964106)
- Low expression of miR1224 is associated with osteosarcoma progression. (PMID:31419446)
- LncRNA NEAT1/miR-1224/KLF3 contributes to cell proliferation, apoptosis and invasion in lung cancer. (PMID:31646570)
- Low miR1224 expression is associated with papillomavirus-infected laryngeal papillomas. (PMID:32002629)
- LncRNA MIR4435-2HG potentiates the proliferation and invasion of glioblastoma cells via modulating miR-1224-5p/TGFBR2 axis. (PMID:32319715)
- LncRNA linc00460 sponges miR-1224-5p to promote esophageal cancer metastatic potential and epithelial-mesenchymal transition. (PMID:32534700)
- MiR-1224-5p acts as a tumor suppressor via inhibiting the malignancy of rectal cancer through targeting SLC29A3. (PMID:32738187)
- Circular RNA EGLN3 silencing represses renal cell carcinoma progression through the miR-1224-3p/HMGXB3 axis. (PMID:34274607)
- Exosomal-mediated transfer of APCDD1L-AS1 induces 5-fluorouracil resistance in oral squamous cell carcinoma via miR-1224-5p/nuclear receptor binding SET domain protein 2 (NSD2) axis. (PMID:34546854)
- MiR-1224-5p attenuates polycystic ovary syndrome through inhibiting NOD-like receptor protein 3 inflammasome activation via targeting Forkhead box O 1. (PMID:34637688)
- Microrna-1224-5p Is a Potential Prognostic and Therapeutic Biomarker in Glioblastoma: Integrating Bioinformatics and Clinical Analyses. (PMID:35678909)
- MicroRNA-1224-5p Aggravates Sepsis-Related Acute Lung Injury in Mice. (PMID:35799888)
- Long Non-coding RNA SPAG5-AS1 Attenuates Diabetic Retinal Vascular Dysfunction by Inhibiting Human Retinal Microvascular Endothelial Cell Proliferation, Migration, and Tube Formation by Regulating the MicroRNA-1224-5p/IRS-1 Axis. (PMID:36346578)
- Circ_0008450 regulates keloid-derived fibroblast proliferation, migration, invasion and apoptosis with increased IGFBP5 through sponging miR-1224-5p. (PMID:36918335)
- CircRSU1 alleviates LPS-induced human pulmonary microvascular endothelial cell injury by targeting miR-1224-5p/ITGA5 axis. (PMID:38312030)
Cross-species orthologs
1 orthologs
| Organism | Symbol | Gene ID |
|---|---|---|
| mus_musculus | Mir1224 | ENSMUSG00000080669 |
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.