MIR505
gene geneOn this page
Also known as hsa-mir-505
Summary
MIR505 (microRNA 505, HGNC:32140) is a microRNA gene on chromosome Xq27.1.
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 574508 — 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:32140 |
| Approved symbol | MIR505 |
| Name | microRNA 505 |
| Location | Xq27.1 |
| Locus type | RNA, micro |
| Status | Approved |
| Aliases | hsa-mir-505 |
| Ensembl gene | ENSG00000207633 |
| Ensembl biotype | miRNA |
| OMIM | 301053 |
| Entrez | 574508 |
| RNAcentral | URS000072D134 — miRNA, 84 nt, 19 organism(s) |
Gene structure
Transcript identifiers
Ensembl transcripts: 1 — 1 miRNA
ENST00000384901
RefSeq mRNA: 0 — MANE Select: None
Canonical transcript exons
ENST00000384901 — 1 exons
| Exon | Start | End |
|---|---|---|
| ENSE00001499908 | 139924148 | 139924231 |
Expression profiles
Bgee: expression breadth broad, 52 present calls, max score 82.31.
Top tissues by expression
52 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| liver | UBERON:0002107 | 82.31 | gold quality |
| blood | UBERON:0000178 | 80.65 | gold quality |
| kidney | UBERON:0002113 | 78.67 | gold quality |
| lung | UBERON:0002048 | 78.18 | gold quality |
| gastrocnemius | UBERON:0001388 | 76.87 | gold quality |
| stomach | UBERON:0000945 | 76.32 | gold quality |
| calcaneal tendon | UBERON:0003701 | 75.78 | gold quality |
| heart | UBERON:0000948 | 75.48 | gold quality |
| monocyte | CL:0000576 | 74.28 | gold quality |
| intestine | UBERON:0000160 | 73.70 | gold quality |
| right atrium auricular region | UBERON:0006631 | 72.93 | gold quality |
| minor salivary gland | UBERON:0001830 | 72.87 | gold quality |
| adult mammalian kidney | UBERON:0000082 | 71.73 | gold quality |
| endometrium | UBERON:0001295 | 71.18 | gold quality |
| body of stomach | UBERON:0001161 | 70.56 | gold quality |
| multicellular organism | UBERON:0000468 | 70.39 | gold quality |
| nucleus accumbens | UBERON:0001882 | 69.14 | gold quality |
| colon | UBERON:0001155 | 68.69 | gold quality |
| muscle layer of sigmoid colon | UBERON:0035805 | 68.31 | gold quality |
| esophagus mucosa | UBERON:0002469 | 68.24 | gold quality |
| body of pancreas | UBERON:0001150 | 68.03 | gold quality |
| tibial artery | UBERON:0007610 | 67.97 | gold quality |
| popliteal artery | UBERON:0002250 | 67.79 | gold quality |
| urinary bladder | UBERON:0001255 | 67.33 | gold quality |
| subcutaneous adipose tissue | UBERON:0002190 | 66.91 | gold quality |
| left lobe of thyroid gland | UBERON:0001120 | 66.73 | gold quality |
| esophagogastric junction muscularis propria | UBERON:0035841 | 66.48 | gold quality |
| right coronary artery | UBERON:0001625 | 66.03 | gold quality |
| right hemisphere of cerebellum | UBERON:0014890 | 66.02 | gold quality |
| cerebellum | UBERON:0002037 | 66.01 | gold quality |
Single-cell (SCXA)
Detected in 1 experiment(s), a significant marker in 0.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-ANND-3 | no | 0.95 |
Regulation
Is transcription factor: no
Literature-anchored findings (GeneRIF, showing 32)
- miR-505 is a novel tumor suppressive miRNA and inhibits cell proliferation by inducing apoptosis (PMID:22051041)
- MicroRNA-505 was found to be a novel circulating signature of hypertension. (PMID:25449503)
- Results identified rs111638916 SNP in the PSMD10 3’-UTR as a risk factor for gastric cancer (GC) and acted as a tumor promoting factor. SNP rs111638916 was also regulated by miR-505, resulting in its up-regulation in patients with GA and AA genotypes. (PMID:26394032)
- miR-505 acts as tumor suppressor in endometrial cancer by regulating TGF-alpha. (PMID:26832151)
- Notably, High-Mobility Group Box 1 knockdown apparently promoted cell proliferation and invasion in MHCC97. SIGNIFICANCE: We investigated that MiR-505 regulates proliferation and invasion in MHCC97 cells via targeting High-Mobility Group Box 1 (PMID:27259809)
- miR-505-5p and miR-193b-3p have the potential to serve as a biomarker for the assessment of imatinib therapy response in newly diagnosed CML patients. (PMID:28093001)
- Low cervical tumor expression of miR-505 was associated with patients’ advanced tumor stage and short survival. (PMID:28577497)
- Authors showed that Mir505-3p was capable of inhibiting tumor proliferation driven by SRSF1 in two neural tumor cell lines, Neuro-2a (N2a) and U251, exclusively in serum-reduced condition. Authors observed that the protein level of SRSF1 was gradually promoted by increasing concentration of serum. (PMID:29120871)
- MACs from Familial hypercholesterolemia (FH)-MACs have an inflammatory phenotype that is characterized by the up-regulation of CCR3, CCR4, and CXCR1 under the control of miR-505-3p. These results suggest a chronic inflammatory condition in FH innate immunity cells that is not reverted by standard lipid-lowering treatment (PMID:29457550)
- MiR-505 mediated MTX resistance, propagation, cell cycle and metastasis by targeting RASSF8 in colorectal cancer (PMID:29726011)
- HMGB1 knockdown and miR-505 overexpression promoted ADM-induced DNA damage in HCC cells. (PMID:29803174)
- miR-505, by inversely regulating NPDC1 may have a functional role in regulating human Parkinson’s disease (PMID:30025813)
- Results showed that miR505 is downregulated in bone metastatic prostate cancer (PCa) tissues. miR505 negatively regulated TGF-beta signaling by directly targeting downstream effectors of TGFbeta signaling, SMAD2 and SMAD3, further inhibiting the invasion and migration abilities of PCa cells. (PMID:30365141)
- In donation after circulatory death (DCD) grafts, high levels of miR-505-3p in preservation fluid are associated with increased risk of delayed graft function after kidney transplantation. (PMID:30444806)
- the data revealed the novel role and target of miR505 in NSCLC cells, which may provide novel insights regarding its role in the carcinogenesis of NSCLC and its potential values for clinical applications. (PMID:30628663)
- Study find that miR505 was significantly increased in lung adenocarcinoma (LA). miR505 functions as an oncogene, promoting lung cancer cell proliferation and inhibiting cancer cell apoptosis via the targeting of TP53AIP1. Finally, it was confirmed that miR505 in plasma extracellular vesicles (EVs) could be delivered to lung cancer cells, inhibiting cell apoptosis and promoting cell proliferation by targeting TP53AIP1. (PMID:30864684)
- MiR-505 suppressed the growth of hepatocellular carcinoma cells via targeting IGF-1R. (PMID:31160483)
- Low miR505 expression is associated with prostate cancer progression. (PMID:31322225)
- Data showed that miR-505 was correlated with cervical carcinoma (CC) histology grade, tumor size, FIGO stage, and lymph node metastasis. miR-505 inhibits TGF-beta1-induced migration, invasion, and EMT. LncRNA-CTS is a molecular sponge for miR-505 in CC. (PMID:31499118)
- LEF-AS1 participates in occurrence of colorectal cancer through adsorbing miR-505 and promoting KIF3B expression. (PMID:31773695)
- The long noncoding RNA CRAL reverses cisplatin resistance via the miR-505/CYLD/AKT axis in human gastric cancer cells. (PMID:31885317)
- miR-505 inhibits proliferation of osteosarcoma via HMGB1. (PMID:32348630)
- LncRNA ZEB1-AS1 promotes pancreatic cancer progression by regulating miR-505-3p/TRIB2 axis. (PMID:32513531)
- microR-505/heterogeneous nuclear ribonucleoprotein M inhibits hepatocellular carcinoma cell proliferation and induces cell apoptosis through the Wnt/beta-catenin signaling pathway. (PMID:32940078)
- MiR-505 inhibits prostate cancer cell invasion, metastasis and epithelial-to-mesenchymal transition through targeting HMGB-1. (PMID:33099950)
- Ultrasound Microbubble-Mediated microRNA-505 Regulates Cervical Cancer Cell Growth via AKT2. (PMID:33123457)
- lncRNA KTN1AS1 promotes glioma cell proliferation and invasion by negatively regulating miR5053p. (PMID:33125151)
- The long noncoding RNA DLGAP1-AS2 facilitates cholangiocarcinoma progression via miR-505 and GALNT10. (PMID:33301605)
- miR-505 inhibits replication of Borna disease virus 1 via inhibition of HMGB1-mediated autophagy. (PMID:35060474)
- Long Non-coding RNA KTN1-AS1 Targets miR-505 to Promote Glioblastoma Progression. (PMID:36762036)
- Upregulation of lncRNA PTOV1-AS1 in hepatocellular carcinoma contributes to disease progression and sorafenib resistance through regulating miR-505. (PMID:37352125)
- HuR-induced circ_0082319 contributes to hepatocellular carcinoma by elevating PTK2 through miR-505-3p. (PMID:37878047)
Cross-species orthologs
1 orthologs
| Organism | Symbol | Gene ID |
|---|---|---|
| mus_musculus | Mir505 | ENSMUSG00000070081 |
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.