MIR1207
gene geneOn this page
Also known as hsa-mir-1207
Summary
MIR1207 (microRNA 1207, HGNC:35273) 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 100302175 — 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:35273 |
| Approved symbol | MIR1207 |
| Name | microRNA 1207 |
| Location | 8q24.21 |
| Locus type | RNA, micro |
| Status | Approved |
| Aliases | hsa-mir-1207 |
| Ensembl gene | ENSG00000221176 |
| Ensembl biotype | miRNA |
| Entrez | 100302175 |
| RNAcentral | URS000063AB20 — miRNA, 87 nt, 2 organism(s) |
Gene structure
Transcript identifiers
Ensembl transcripts: 1 — 1 miRNA
ENST00000408249
RefSeq mRNA: 0 — MANE Select: None
Canonical transcript exons
ENST00000408249 — 1 exons
| Exon | Start | End |
|---|---|---|
| ENSE00001564884 | 128049152 | 128049238 |
Expression profiles
Bgee: expression breadth broad, 31 present calls, max score 80.19.
Top tissues by expression
31 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| blood | UBERON:0000178 | 80.19 | gold quality |
| gastrocnemius | UBERON:0001388 | 76.50 | gold quality |
| adrenal tissue | UBERON:0018303 | 75.51 | gold quality |
| kidney | UBERON:0002113 | 74.53 | gold quality |
| liver | UBERON:0002107 | 70.06 | gold quality |
| colon | UBERON:0001155 | 69.87 | gold quality |
| ascending aorta | UBERON:0001496 | 68.93 | gold quality |
| left lobe of thyroid gland | UBERON:0001120 | 68.73 | gold quality |
| body of stomach | UBERON:0001161 | 67.74 | gold quality |
| right adrenal gland | UBERON:0001233 | 67.72 | gold quality |
| right atrium auricular region | UBERON:0006631 | 67.72 | gold quality |
| left adrenal gland | UBERON:0001234 | 67.56 | gold quality |
| transverse colon | UBERON:0001157 | 67.33 | gold quality |
| omental fat pad | UBERON:0010414 | 65.75 | gold quality |
| body of uterus | UBERON:0009853 | 64.32 | gold quality |
| stomach | UBERON:0000945 | 64.19 | gold quality |
| skin of leg | UBERON:0001511 | 63.52 | gold quality |
| subcutaneous adipose tissue | UBERON:0002190 | 63.49 | gold quality |
| right ovary | UBERON:0002118 | 62.94 | gold quality |
| right lobe of thyroid gland | UBERON:0001119 | 62.13 | gold quality |
| esophagus mucosa | UBERON:0002469 | 61.62 | gold quality |
| prostate gland | UBERON:0002367 | 61.37 | gold quality |
| esophagogastric junction muscularis propria | UBERON:0035841 | 60.78 | gold quality |
| ectocervix | UBERON:0012249 | 60.57 | gold quality |
| small intestine Peyer’s patch | UBERON:0003454 | 60.42 | gold quality |
| skin of abdomen | UBERON:0001416 | 57.51 | gold quality |
| minor salivary gland | UBERON:0001830 | 56.23 | gold quality |
| upper lobe of left lung | UBERON:0008952 | 55.62 | gold quality |
| left ovary | UBERON:0002119 | 54.02 | gold quality |
| tibial nerve | UBERON:0001323 | 53.30 | 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 27)
- variant 1936T prevents hsa-miR-1207-5p from down-regulating HBEGF in podocytes (PMID:22319602)
- miR-1207-5p, a PVT1-derived microRNA, is abundantly expressed in kidney cells, and is upregulated by glucose and TGF-beta1. (PMID:24204837)
- MiR-1207-5p and miR-1266 suppress gastric cancer growth and invasion by targeting TERT. (PMID:24481448)
- miR-1207 plays a vital role in promoting the cancer stem cell-like phenotype in ovarian cancer by activating the Wnt/beta-catenin signaling pathway. (PMID:26337084)
- Data show that long noncoding RNA BC032469 could directly bind to miR-1207-5p and modulate the derepression of hTERT. (PMID:26549025)
- downregulation of miR-1207-5p and miR-4695-3p expression may lead to increased TRIM21 levels in the minor salivary glands, which contributes to the development of Sjogren’s syndrome (PMID:26888739)
- miR-1207-5p and CSF1 expression levels and their relationship with lung cancer survival and metastasis status were assayed by means of a lung cancer tissue microarray. (PMID:27107415)
- our study suggests that miR12075p/FASN plays an important role in hepatocellular carcinoma (PMID:27461404)
- these studies have revealed a novel microRNA-1207-3p/FNDC1/FN1/AR regulatory pathway in prostate cancer. (PMID:27693493)
- A novel target of miR-1207-5p is identified heme oxygenase-1 mRNA by western blotting and Ago2 immunoprecipitation. knockdown of mir-1207-5p by miR-1207-5p mimic down-regulated heme oxygenase-1 gene expression. (PMID:28228215)
- PVT1-derived miR-1207-5p promotes the proliferation of breast cancer cells by targeting STAT6. (PMID:28235236)
- Downregulation of hsa-miR-208a-3p and hsa-miR-1207-5p may be involved in the occurrence of medulloblastoma (PMID:28481393)
- The Tyr113His T/C variant of rs1051740 and very slow phenotype alters EPHX1, miR-26b-5p and miR-1207-5p expression, and contributes towards low blood iron levels and low birthweights. (PMID:28789952)
- lower expression correlated with advanced stage and lymph node metastasis and shorter patient overall survival in colorectal cancer (PMID:29226644)
- Low expression of MIR1207 is associated with Nasopharyngeal Cancer. (PMID:30141114)
- Data found that miR-1207 expression was decreased in nasopharyngeal carcinoma (NPC) tissues, and LINC00319 facilitated cell proliferation in vitro via sponging miR-1207-5p in NPC cells. (PMID:30243935)
- Correlation between miR-1207-5p expression with steroid-induced necrosis of femoral head and VEGF expression. (PMID:31002120)
- CircHIPK3 promotes colorectal cancer cells proliferation and metastasis via modulating of miR-1207-5p/FMNL2 signal. (PMID:32046858)
- Characterization of antiapoptotic microRNAs in primary Sjogren’s syndrome. (PMID:32575162)
- MiR-1207-5p/CX3CR1 axis regulates the progression of osteoarthritis via the modulation of the activity of NF-kappaB pathway. (PMID:32597559)
- Plasma microRNA-1207-5p as a Potential Biomarker for Diagnosis and Prognosis of Colorectal Cancer. (PMID:32902212)
- miR-1207-5p Can Contribute to Dysregulation of Inflammatory Response in COVID-19 via Targeting SARS-CoV-2 RNA. (PMID:33194826)
- MiR-1207-5p targets PYCR1 to inhibit the progression of prostate cancer. (PMID:34461437)
- Long non-coding RNA LUADT1 promotes nasopharyngeal carcinoma cell proliferation and invasion by downregulating miR-1207-5p. (PMID:34738862)
- Down-regulation of lncRNA LUADT1 suppresses cervical cancer cell growth by sequestering microRNA-1207-5p. (PMID:35538030)
- LncRNA PVT1 Regulates miR-1207-5p to Affect Colon Cancer Proliferation and Migration via the Wnt6/beta-catenin2 Pathway. (PMID:35763386)
- Knockdown of LINC01138 protects human chondrocytes against IL-1beta-induced damage by regulating the hsa-miR-1207-5p/KIAA0101 axis. (PMID:36705420)
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
- Disease cohort memberships (association, not causation — diseases whose associated-gene cohort lists this gene; a subset are also under Associated diseases): Bell’s palsy