MIR4319

gene
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Also known as hsa-mir-4319

Summary

MIR4319 (microRNA 4319, HGNC:38212) is a microRNA gene on chromosome 18q12.3.

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 100422829 — 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:38212
Approved symbolMIR4319
NamemicroRNA 4319
Location18q12.3
Locus typeRNA, micro
StatusApproved
Aliaseshsa-mir-4319
Ensembl geneENSG00000265957
Ensembl biotypemiRNA
Entrez100422829
RNAcentralURS000075A53A — ncRNA, 85 nt, 3 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 miRNA

ENST00000577285

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000577285 — 1 exons

ExonStartEnd
ENSE000027281694497008244970166

Expression profiles

Bgee: expression breadth broad, 79 present calls, max score 80.12.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
kidneyUBERON:000211380.12gold quality
bloodUBERON:000017879.68gold quality
bone marrowUBERON:000237178.83gold quality
liverUBERON:000210777.82gold quality
calcaneal tendonUBERON:000370176.36gold quality
monocyteCL:000057676.31gold quality
muscle of legUBERON:000138375.73gold quality
placentaUBERON:000198775.72gold quality
stomachUBERON:000094575.49gold quality
gastrocnemiusUBERON:000138874.90gold quality
adult mammalian kidneyUBERON:000008274.77gold quality
adrenal tissueUBERON:001830373.76gold quality
heartUBERON:000094873.35gold quality
corpus callosumUBERON:000233673.10gold quality
islet of LangerhansUBERON:000000672.62gold quality
thoracic mammary glandUBERON:000520071.16gold quality
right atrium auricular regionUBERON:000663171.14gold quality
prefrontal cortexUBERON:000045170.40gold quality
heart left ventricleUBERON:000208469.78gold quality
intestineUBERON:000016068.92gold quality
body of pancreasUBERON:000115068.74gold quality
colonUBERON:000115568.74gold quality
body of stomachUBERON:000116168.62gold quality
tibial arteryUBERON:000761068.30gold quality
lungUBERON:000204868.16gold quality
esophagogastric junction muscularis propriaUBERON:003584167.49gold quality
thoracic aortaUBERON:000151567.48gold quality
left ovaryUBERON:000211967.20gold quality
ascending aortaUBERON:000149667.07gold quality
transverse colonUBERON:000115766.94gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no0.31

Regulation

Is transcription factor: no

Literature-anchored findings (GeneRIF, showing 12)

  • The growth and chemo-resistance of prostate cancer cells may be suppressed via re-expression of miR-4319 that inhibits Her-2 signaling. (PMID:29633185)
  • MiR-4319 as a tumor suppressor gene in the maintenance of cancer stem cells stemness and confirmed that miR-4319 could inhibit the tumor initiation and metastasis of cancer stem cells mainly through downregulation of E2F2, which afforded the database to help understand the aggressive phenotype of triple-negative breast cancer. (PMID:30021199)
  • Study demonstrates that miR-4319 is expressed at a low level in colorectal cancer (CRC) tissues, which predicts the poor clinical outcome of CRC. MiR-4319 regulates the proliferation, cell cycle, invasion and migration of CRC cells. Mechanically, miR-4319 is found to be transcriptionally regulated by PLZF, and acts as a tumour suppressor in CRC by targeting ABTB1. (PMID:31065369)
  • MiR-4319 was proved to elicit tumor-suppressive role in tumorigenesis of NSCLC through hampering cell proliferation and migration as well as inducing apoptosis. (PMID:31096145)
  • miR-4319 inhibited the development of thyroid cancer by modulating FUS-stabilized SMURF1. (PMID:31148243)
  • GNAS-AS1/miR-4319/NECAB3 axis promotes tumor progression of non-small cell lung cancer by altering macrophage polarization. (PMID:31267263)
  • miR-4319 Suppresses the Growth of Esophageal Squamous Cell Carcinoma Via Targeting NLRC5. (PMID:31746301)
  • Long non-coding RNA LINC00426 contributes to doxorubicin resistance by sponging miR-4319 in osteosarcoma. (PMID:32620145)
  • lncRNA DANCR Promotes Proliferation and Metastasis of Breast Cancer Cells Through Sponging miR-4319 and Upregulating VAPB. (PMID:32818383)
  • Long non-coding RNA HOXA-AS3 facilitates the malignancy in colorectal cancer by miR-4319/SPNS2 axis. (PMID:34671931)
  • MiR-4319 targets tuftelin 1 to reduce malignancy of cervical cancer cells. (PMID:38650156)
  • CircATXN7 regulates the proliferation and invasion of esophageal cancer cells through miR-4319/NLRC5. (PMID:39121974)

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.

No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.