MIR3167

gene
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Also known as hsa-mir-3167

Summary

MIR3167 (microRNA 3167, HGNC:38242) is a microRNA gene on chromosome 11q24.2.

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 100422918 — 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:38242
Approved symbolMIR3167
NamemicroRNA 3167
Location11q24.2
Locus typeRNA, micro
StatusApproved
Aliaseshsa-mir-3167
Ensembl geneENSG00000266215
Ensembl biotypemiRNA
Entrez100422918
RNAcentralURS000075A4F3 — miRNA, 85 nt, 1 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 miRNA

ENST00000579623

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000579623 — 1 exons

ExonStartEnd
ENSE00002700762126988458126988542

Expression profiles

Bgee: expression breadth broad, 39 present calls, max score 89.68.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
corpus callosumUBERON:000233689.68gold quality
kidneyUBERON:000211384.13gold quality
monocyteCL:000057683.65gold quality
omental fat padUBERON:001041476.52gold quality
calcaneal tendonUBERON:000370172.13gold quality
skin of legUBERON:000151170.61gold quality
islet of LangerhansUBERON:000000668.86gold quality
right atrium auricular regionUBERON:000663168.41gold quality
heartUBERON:000094867.49gold quality
liverUBERON:000210767.47gold quality
lower esophagus muscularis layerUBERON:003583366.94gold quality
Brodmann (1909) area 9UBERON:001354065.94gold quality
stomachUBERON:000094565.66gold quality
transverse colonUBERON:000115765.62gold quality
minor salivary glandUBERON:000183065.17gold quality
Ammon’s hornUBERON:000195465.15gold quality
brainUBERON:000095565.11gold quality
dorsolateral prefrontal cortexUBERON:000983464.90gold quality
anterior cingulate cortexUBERON:000983564.73gold quality
esophagogastric junction muscularis propriaUBERON:003584164.46gold quality
subcutaneous adipose tissueUBERON:000219064.45gold quality
muscle layer of sigmoid colonUBERON:003580564.41gold quality
left coronary arteryUBERON:000162664.28gold quality
colonUBERON:000115564.02gold quality
nucleus accumbensUBERON:000188263.79gold quality
amygdalaUBERON:000187663.23gold quality
right ovaryUBERON:000211862.86gold quality
caudate nucleusUBERON:000187362.82gold quality
right frontal lobeUBERON:000281062.44gold quality
right hemisphere of cerebellumUBERON:001489061.34gold 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 1)

  • FOXD1-AS1 promotes malignant behaviours of prostate cancer cells via the miR-3167/YWHAZ axis. (PMID:34674391)

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.