MIR323A

gene
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Also known as hsa-mir-323

Summary

MIR323A (microRNA 323a, HGNC:31766) is a microRNA gene on chromosome 14q32.31.

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 442897 — 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:31766
Approved symbolMIR323A
NamemicroRNA 323a
Location14q32.31
Locus typeRNA, micro
StatusApproved
Aliaseshsa-mir-323
Ensembl geneENSG00000199069
Ensembl biotypemiRNA
Entrez442897
RNAcentralURS000075AB81 — miRNA, 86 nt, 45 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 miRNA

ENST00000362199

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000362199 — 1 exons

ExonStartEnd
ENSE00001436962101025732101025817

Expression profiles

Bgee: expression breadth broad, 37 present calls, max score 93.17.

Top tissues by expression

37 total, by Bgee expression score (0-100, higher = more expressed):

TissueAnatomy IDExpression scoreQuality
colonUBERON:000115593.17gold quality
adrenal tissueUBERON:001830391.16gold quality
intestineUBERON:000016085.68gold quality
stomachUBERON:000094579.72gold quality
heartUBERON:000094872.77gold quality
islet of LangerhansUBERON:000000672.63gold quality
lungUBERON:000204872.20gold quality
bloodUBERON:000017870.70gold quality
body of pancreasUBERON:000115069.68gold quality
ascending aortaUBERON:000149668.80gold quality
body of stomachUBERON:000116168.43gold quality
left adrenal glandUBERON:000123467.38gold quality
thoracic aortaUBERON:000151567.14gold quality
liverUBERON:000210766.97gold quality
skin of abdomenUBERON:000141666.70gold quality
putamenUBERON:000187466.65gold quality
omental fat padUBERON:001041465.90gold quality
tibial arteryUBERON:000761065.68gold quality
right hemisphere of cerebellumUBERON:001489065.50gold quality
nucleus accumbensUBERON:000188265.39gold quality
left ovaryUBERON:000211964.78gold quality
anterior cingulate cortexUBERON:000983564.77gold quality
dorsolateral prefrontal cortexUBERON:000983464.41gold quality
Ammon’s hornUBERON:000195464.40gold quality
cerebellar hemisphereUBERON:000224564.36gold quality
subcutaneous adipose tissueUBERON:000219063.97gold quality
skin of legUBERON:000151163.41gold quality
urinary bladderUBERON:000125563.05gold quality
hypothalamusUBERON:000189862.75gold quality
caudate nucleusUBERON:000187361.70gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no0.16

Regulation

Is transcription factor: no

Literature-anchored findings (GeneRIF, showing 27)

  • the authors identified miR-221/222 and miR-323-3p as novel dysregulated miR in rheumatoid arthritis synovial fibroblasts (PMID:22562984)
  • results demonstrates that miR-326, miR-130a, miR-155, miR-210 and the 4 miRNA-interactions could serve as prognostic and predictive markers for survival of GBM patients (PMID:23302469)
  • Circulating miR-323-3p was markedly elevated in acute coronary syndrome patients for at least one year. (PMID:25124998)
  • Over-expression of miR-323-5p could promote apoptosis of U251 cells and inhibit the proliferation and migration of the glioma cells. miR-323-5p directly targets IGF1R. (PMID:25556445)
  • miR-323 may increase VEGF-A-mediated cancer vascularization in PC cells through AdipoR1 suppression. (PMID:26160610)
  • MiRNA-323-5p inhibited human cerebral glioma U373 cell proliferation and promoted its apoptosis by reducing IGF-1R (PMID:26656446)
  • Low miR323 expression is associated with invasion and metastasis in pancreatic ductal adenocarcinoma. (PMID:26908446)
  • Our data suggest that miR-323-3p acts in a negative feedback loop to control the production of IL-22 in IL-22/IL-17-producing T cells and might thus impact the T-cell responses in asthma. (PMID:27059796)
  • This study demonstrated that overexpression of miR-323a-3p and miR-369-3p in glioblastoma cells inhibited their proliferation and migration in vitro. Mice implanted with glioblastoma cells overexpressing miR323a-3p. (PMID:27573219)
  • The expression of miR-323a-5p was significantly elevated in the cortex and plasma of FCD patients. These results suggest that abnormal expression of miR-323a-5p could be used for improving the current diagnosis of FCD. (PMID:27824513)
  • High miR323 expression is associated with cardiomyopathy in Friedreich’s ataxia. (PMID:28701783)
  • Study demonstrates a novel regulatory mechanism of the miR-323a-3p/MET/SMAD3/SNAIL circuit that is involved in the EMT regulation of BCa. (PMID:28837140)
  • T-C haplotype, increasing miR-323b expression, could down-regulated Pax8 expression. (PMID:29271476)
  • miR-323a-3p suppresses growth of osteosarcoma cells via targeting lactate dehydrogenase A and inhibits the glycolysis of osteosarcoma. (PMID:30088225)
  • Results show that the level of miR-323 in human cumulus cells (CCs) of women with polycystic ovary syndrome (PCOS) was down-regulated, compared with that of the control group. Further findings suggest that miR-323 targeting IGF-1 regulates the steroidogenesis and the activity of CCs, which plays an important role in the occurrence and development of PCOS. (PMID:30300681)
  • miR323 suppresses nerve cell apoptosis in cerebral infarction via the TGFbeta1/SMAD3 signaling pathway. (PMID:30535466)
  • miR-323a-5p and miR-342-5p are new tumor-suppressive microRNAs for neuroblastoma. (PMID:30770954)
  • miR-323a expression in bladder cancer (BC) contributed to enhanced BC cell proliferation and migration mainly by targeting c-Met. (PMID:31180621)
  • miR-323-3p promotes proliferation and inhibits apoptosis of cumulus cells in polycystic ovary syndrome (PMID:31549864)
  • MiR-323-3p Targeting Transmembrane Protein with EGF-Like and 2 Follistatin Domain (TMEFF2) Inhibits Human Lung Cancer A549 Cell Apoptosis by Regulation of AKT and ERK Signaling Pathways. (PMID:32009129)
  • Long non-coding RNA SNHG7 promotes neuroblastoma progression through sponging miR-323a-5p and miR-342-5p. (PMID:32534305)
  • miR-323a regulates ERBB4 and is involved in depression. (PMID:33219358)
  • Suppression of microRNA-323-3p restrains vascular endothelial cell apoptosis via promoting sirtuin-1 expression in coronary heart disease. (PMID:33460661)
  • Identification of serum exosomal miR-98-5p, miR-183-5p, miR-323-3p and miR-19b-3p as potential biomarkers for glioblastoma patients and investigation of their mechanisms. (PMID:34837760)
  • MiR-323a regulates ErbB3/EGFR and blocks gefitinib resistance acquisition in colorectal cancer. (PMID:35319011)
  • miRNA-323a-3p promoted intracranial, aneurysm-induced inflammation via AMPK/NF-kappaB signaling pathway by AdipoR1. (PMID:36047894)
  • Tumor-suppressive miR-323a inhibits pancreatic cancer cell proliferation and glycolysis through targeting HK-2. (PMID:36416387)

Cross-species orthologs

2 orthologs

OrganismSymbolGene ID
mus_musculusMir323ENSMUSG00000065617
rattus_norvegicusMir323ENSRNOG00000035454

Paralogs (16): MIR494 (ENSG00000194717), MIR377 (ENSG00000199015), MIR381 (ENSG00000199020), MIR369 (ENSG00000199025), MIR410 (ENSG00000199092), MIR409 (ENSG00000199107), MIR539 (ENSG00000202560), MIR487A (ENSG00000207742), MIR487B (ENSG00000207754), MIR656 (ENSG00000207959), MIR496 (ENSG00000207961), MIR154 (ENSG00000207978), MIR323B (ENSG00000208004), MIR1185-1 (ENSG00000221525), MIR1185-2 (ENSG00000221614), MIR382 (ENSG00000283170)

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.