MIR4274

gene
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Also known as hsa-mir-4274

Summary

MIR4274 (microRNA 4274, HGNC:38194) is a microRNA gene on chromosome 4p16.1.

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 100422826 — 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:38194
Approved symbolMIR4274
NamemicroRNA 4274
Location4p16.1
Locus typeRNA, micro
StatusApproved
Aliaseshsa-mir-4274
Ensembl geneENSG00000266690
Ensembl biotypemiRNA
Entrez100422826
RNAcentralURS000075A146 — miRNA, 91 nt, 1 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 miRNA

ENST00000579577

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000579577 — 1 exons

ExonStartEnd
ENSE0000269737274600287460118

Expression profiles

Bgee: expression breadth broad, 31 present calls, max score 77.68.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
liverUBERON:000210777.68gold quality
body of stomachUBERON:000116175.93gold quality
monocyteCL:000057675.67gold quality
adult mammalian kidneyUBERON:000008274.05gold quality
anterior cingulate cortexUBERON:000983572.11gold quality
stomachUBERON:000094571.11gold quality
Brodmann (1909) area 9UBERON:001354070.22gold quality
omental fat padUBERON:001041469.90gold quality
dorsolateral prefrontal cortexUBERON:000983468.56gold quality
substantia nigraUBERON:000203866.70gold quality
thyroid glandUBERON:000204665.83gold quality
right frontal lobeUBERON:000281065.46gold quality
skin of legUBERON:000151164.92gold quality
lower esophagus muscularis layerUBERON:003583364.29gold quality
esophagus mucosaUBERON:000246963.52gold quality
hypothalamusUBERON:000189863.08gold quality
skin of abdomenUBERON:000141662.76gold quality
tibial nerveUBERON:000132362.13gold quality
minor salivary glandUBERON:000183061.81gold quality
left ovaryUBERON:000211960.80gold quality
nucleus accumbensUBERON:000188260.47gold quality
Ammon’s hornUBERON:000195460.36gold quality
putamenUBERON:000187460.34gold quality
caudate nucleusUBERON:000187359.81gold quality
small intestine Peyer’s patchUBERON:000345459.28gold quality
vaginaUBERON:000099658.11gold quality
pituitary glandUBERON:000000754.28gold quality
colonUBERON:000115548.32gold quality
testisUBERON:000047347.09gold quality
right testisUBERON:000453446.11gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no0.32

Regulation

Is transcription factor: no

Literature-anchored findings (GeneRIF, showing 1)

  • This study demonstrated that the levels of CSF hsa-miR-4274 can differentiate parkinsonian spectrum from patients with Normal Pressure Hydrocephalus , Alzheimer disease, and normal control. (PMID:27911315)

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.