MIR3144

gene
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Also known as hsa-mir-3144

Summary

MIR3144 (microRNA 3144, HGNC:38331) is a microRNA gene on chromosome 6q22.31.

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 100422951 — 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:38331
Approved symbolMIR3144
NamemicroRNA 3144
Location6q22.31
Locus typeRNA, micro
StatusApproved
Aliaseshsa-mir-3144
Ensembl geneENSG00000265725
Ensembl biotypemiRNA
Entrez100422951
RNAcentralURS000075EF28 — miRNA, 79 nt, 1 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 miRNA

ENST00000579460

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000579460 — 1 exons

ExonStartEnd
ENSE00002707230120015179120015257

Expression profiles

Bgee: expression breadth broad, 21 present calls, max score 83.07.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
heartUBERON:000094883.07gold quality
bloodUBERON:000017878.38gold quality
lungUBERON:000204875.57gold quality
monocyteCL:000057672.28gold quality
stomachUBERON:000094570.21gold quality
intestineUBERON:000016065.55gold quality
body of stomachUBERON:000116164.94gold quality
esophagus mucosaUBERON:000246964.63gold quality
tibial arteryUBERON:000761064.14gold quality
subcutaneous adipose tissueUBERON:000219063.09gold quality
nucleus accumbensUBERON:000188262.62gold quality
thyroid glandUBERON:000204662.49gold quality
dorsolateral prefrontal cortexUBERON:000983462.37gold quality
vaginaUBERON:000099661.94gold quality
right frontal lobeUBERON:000281059.45gold quality
liverUBERON:000210758.60gold quality
muscle layer of sigmoid colonUBERON:003580557.45gold quality
thoracic mammary glandUBERON:000520057.42gold quality
colonUBERON:000115555.59gold quality
hypothalamusUBERON:000189854.74gold quality
left testisUBERON:000453335.67silver quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no0.82

Regulation

Is transcription factor: no

Literature-anchored findings (GeneRIF, showing 2)

  • Data show that the site targeted by two microRNAs, miR-875 and miR-3144 is located in HPV16 E6 oncogene open reading frame (ORF). (PMID:25913515)
  • In silico analysis suggested that rs1972820 located in the 3’UTR of ERBB4 gene affects the binding affinity of miR-3144-3p a potential oncomiRNA. Statistical analysis showed a significant association between SNP rs1972820 G allele and reduced breast cancer risk, odds ratio = 0.443 (95% CI: 0.196-0.998). (PMID:28508829)

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.