MIR513A1
gene geneOn this page
Also known as hsa-mir-513-1hsa-mir-513a-1
Summary
MIR513A1 (microRNA 513a-1, HGNC:32141) is a microRNA gene on chromosome Xq27.3.
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 574509 — 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:32141 |
| Approved symbol | MIR513A1 |
| Name | microRNA 513a-1 |
| Location | Xq27.3 |
| Locus type | RNA, micro |
| Status | Approved |
| Aliases | hsa-mir-513-1, hsa-mir-513a-1 |
| Ensembl gene | ENSG00000207873 |
| Ensembl biotype | miRNA |
| Entrez | 574509 |
| RNAcentral | URS000075E43A — miRNA, 129 nt, 1 organism(s) |
Gene structure
Transcript identifiers
Ensembl transcripts: 1 — 1 miRNA
ENST00000385138
RefSeq mRNA: 0 — MANE Select: None
Canonical transcript exons
ENST00000385138 — 1 exons
| Exon | Start | End |
|---|---|---|
| ENSE00001500144 | 147213463 | 147213591 |
Expression profiles
Bgee: expression breadth broad, 42 present calls, max score 89.64.
Top tissues by expression
42 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| blood | UBERON:0000178 | 89.64 | gold quality |
| adult mammalian kidney | UBERON:0000082 | 76.63 | gold quality |
| cortex of kidney | UBERON:0001225 | 70.33 | gold quality |
| right lobe of liver | UBERON:0001114 | 70.19 | gold quality |
| liver | UBERON:0002107 | 70.00 | gold quality |
| stomach | UBERON:0000945 | 69.95 | gold quality |
| body of pancreas | UBERON:0001150 | 69.13 | gold quality |
| skin of leg | UBERON:0001511 | 68.77 | gold quality |
| subcutaneous adipose tissue | UBERON:0002190 | 68.36 | gold quality |
| ascending aorta | UBERON:0001496 | 68.20 | gold quality |
| gastrocnemius | UBERON:0001388 | 67.90 | gold quality |
| lower esophagus muscularis layer | UBERON:0035833 | 67.40 | gold quality |
| omental fat pad | UBERON:0010414 | 66.66 | gold quality |
| left ovary | UBERON:0002119 | 66.44 | gold quality |
| colon | UBERON:0001155 | 66.27 | gold quality |
| esophagus mucosa | UBERON:0002469 | 66.20 | gold quality |
| tibial artery | UBERON:0007610 | 65.91 | gold quality |
| transverse colon | UBERON:0001157 | 65.33 | gold quality |
| intestine | UBERON:0000160 | 65.19 | gold quality |
| tibial nerve | UBERON:0001323 | 64.90 | gold quality |
| spleen | UBERON:0002106 | 64.53 | gold quality |
| caudate nucleus | UBERON:0001873 | 64.00 | gold quality |
| corpus callosum | UBERON:0002336 | 63.97 | gold quality |
| body of uterus | UBERON:0009853 | 63.39 | gold quality |
| ectocervix | UBERON:0012249 | 63.38 | gold quality |
| nucleus accumbens | UBERON:0001882 | 63.23 | gold quality |
| gall bladder | UBERON:0002110 | 63.14 | gold quality |
| metanephros cortex | UBERON:0010533 | 62.86 | gold quality |
| Ammon’s horn | UBERON:0001954 | 62.68 | gold quality |
| left adrenal gland | UBERON:0001234 | 62.63 | gold quality |
Single-cell (SCXA)
Detected in 1 experiment(s), a significant marker in 0.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-ANND-3 | no | 1.22 |
Regulation
Is transcription factor: no
Literature-anchored findings (GeneRIF, showing 13)
- miR-513a-3p is involved in the control of the LHCGR expression by an inversely regulated mechanism at the post-transcriptional level. (PMID:24747085)
- Low expression of miR-513b is associated with lymph node metastases in gastric cancer. (PMID:25095979)
- MiR-513a-5p promotes dichlorvos induced apoptosis by targeting Bcl-2. (PMID:30372899)
- Circular RNA MYLK promotes tumour growth and metastasis via modulating miR-513a-5p/VEGFC signalling in renal cell carcinoma. (PMID:32342645)
- LncRNA PCAT6 aggravates the progression of bladder cancer cells by targeting miR-513a-5p. (PMID:33090394)
- [Deleted in lymphocytic leukemia 1 promoted proliferation and apoptosis of nephroblastoma cells through regulating miR-513a-5p and RANBP2 pathway]. (PMID:33113626)
- MiR-513a-3p inhibits EMT mediated by HOXB7 and promotes sensitivity to cisplatin in ovarian cancer cells. (PMID:33155195)
- lncRNA MIR4435-2HG promoted clear cell renal cell carcinoma malignant progression via miR-513a-5p/KLF6 axis. (PMID:33460239)
- Knockdown of circBFAR inhibits proliferation and glycolysis in gastric cancer by sponging miR-513a-3p/hexokinase 2 axis. (PMID:33979737)
- Long non-coding RNA titin-antisense RNA1 contributes to growth and metastasis of cholangiocarcinoma by suppressing microRNA-513a-5p to upregulate stratifin. (PMID:34903127)
- MiR-513a-3p promotes radiation-induced apoptosis of human lung cells by inhibiting glutathione S-transferase P1. (PMID:35459441)
- CircRNA.0007127 triggers apoptosis through the miR-513a-5p/CASP8 axis in K-562 cells. (PMID:36111570)
- Circ_0003998 upregulates ARK5 expression to elevate 5-Fluorouracil resistance in hepatocellular carcinoma through binding to miR-513a-5p. (PMID:36255069)
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.