MIR3922

gene
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Also known as hsa-mir-3922

Summary

MIR3922 (microRNA 3922, HGNC:38895) is a microRNA gene on chromosome 12q23.3.

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 100500843 — 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:38895
Approved symbolMIR3922
NamemicroRNA 3922
Location12q23.3
Locus typeRNA, micro
StatusApproved
Aliaseshsa-mir-3922
Ensembl geneENSG00000264295
Ensembl biotypemiRNA
Entrez100500843
RNAcentralURS000075D152 — miRNA, 84 nt, 1 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 miRNA

ENST00000585192

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000585192 — 1 exons

ExonStartEnd
ENSE00002702260104591633104591716

Expression profiles

Bgee: expression breadth broad, 21 present calls, max score 78.46.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
bloodUBERON:000017878.46gold quality
heart left ventricleUBERON:000208477.64gold quality
monocyteCL:000057674.82gold quality
gastrocnemiusUBERON:000138873.26gold quality
muscle layer of sigmoid colonUBERON:003580569.07gold quality
liverUBERON:000210768.65gold quality
minor salivary glandUBERON:000183068.33gold quality
stomachUBERON:000094567.81gold quality
left adrenal glandUBERON:000123467.78gold quality
intestineUBERON:000016067.49gold quality
lower esophagus muscularis layerUBERON:003583366.02gold quality
transverse colonUBERON:000115765.53gold quality
body of stomachUBERON:000116163.09gold quality
omental fat padUBERON:001041462.25gold quality
small intestine Peyer’s patchUBERON:000345458.56gold quality
pituitary glandUBERON:000000758.11gold quality
esophagus mucosaUBERON:000246954.89gold quality
right frontal lobeUBERON:000281054.88gold quality
cerebellar hemisphereUBERON:000224553.95gold quality
corpus callosumUBERON:000233652.34gold quality
hypothalamusUBERON:000189849.30gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no0.44

Regulation

Is transcription factor: no

Literature-anchored findings (GeneRIF, showing 1)

  • HOXC-AS3 is aberrantly overexpressed in breast cancers especially the HER2+ type. High expression of HOXC-AS3 has a relationship with poor clinical outcomes of breast cancer. HOXC-AS3 regulates cell invasion and migration both in vitro and in vivo. Results demonstrated that miR-3922-5p was a direct target of HOXC-AS3, and PPP1R1A was a target of miR-3922-5p in breast cancer. (PMID:31797701)

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.