MIR4767

gene
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Also known as hsa-mir-4767

Summary

MIR4767 (microRNA 4767, HGNC:41548) is a microRNA gene on chromosome Xp22.31.

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 100616467 — 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:41548
Approved symbolMIR4767
NamemicroRNA 4767
LocationXp22.31
Locus typeRNA, micro
StatusApproved
Aliaseshsa-mir-4767
Ensembl geneENSG00000264268
Ensembl biotypemiRNA
Entrez100616467
RNAcentralURS000075C952 — miRNA, 78 nt, 1 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 miRNA

ENST00000582827

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000582827 — 1 exons

ExonStartEnd
ENSE0000272203871478607147937

Expression profiles

Bgee: expression breadth broad, 16 present calls, max score 71.27.

FANTOM5 (CAGE): breadth ubiquitous, TPM avg 2.8464 / max 55.0547, expressed in 1094 samples.

FANTOM5 promoters (1 alternative TSS)

Promoter IDTPM avgSamples expressed
1954182.84641094

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
gastrocnemiusUBERON:000138871.27gold quality
minor salivary glandUBERON:000183068.05gold quality
caudate nucleusUBERON:000187367.98gold quality
colonUBERON:000115565.65gold quality
stomachUBERON:000094564.50gold quality
muscle layer of sigmoid colonUBERON:003580562.55gold quality
body of stomachUBERON:000116160.50gold quality
multicellular organismUBERON:000046856.93gold quality
omental fat padUBERON:001041456.85gold quality
lower esophagus muscularis layerUBERON:003583356.15gold quality
left lobe of thyroid glandUBERON:000112052.32gold quality
tibial nerveUBERON:000132350.26gold quality
liverUBERON:000210748.64gold quality
spleenUBERON:000210643.04silver quality
left testisUBERON:000453335.92gold quality
skin of abdomenUBERON:000141634.48silver quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no1.17

Regulation

Is transcription factor: no

Literature-anchored findings (GeneRIF, showing 3)

  • Study provides evidence that Long Noncoding RNA LOC100129973 suppresses apoptosis by targeting miR-4707-5p and miR-4767 in vascular endothelial cells. (PMID:26887505)
  • our study provides evidence that miR-4756 accelerates the process of diabetic kidney disease (DKD) through Sestrin2, suggesting that targeting miR-4756 may be a novel strategy for DKD treatment. (PMID:30145827)
  • LINC00858 promotes colorectal cancer by sponging miR-4766-5p to regulate PAK2. (PMID:31902050)

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.

  • Disease cohort memberships (association, not causation — diseases whose associated-gene cohort lists this gene; a subset are also under Associated diseases): recessive X-linked ichthyosis