UCP2

Gene Information
 
Gene Symbol
UCP2
 
Aliases
BMIQ4, SLC25A8, UCPH
 
Entrez Gene ID
 
Gene Name
Uncoupling protein 2
 
Chromosomal Location
11q13.4
 
HGNC ID
 
Summary
Mitochondrial uncoupling proteins (UCP) are members of the larger family of mitochondrial anion carrier proteins (MACP). UCPs separate oxidative phosphorylation from ATP synthesis with energy dissipated as heat, also referred to as the mitochondrial proton leak. UCPs facilitate the transfer of anions from the inner to the outer mitochondrial membrane and the return transfer of protons from the outer to the inner mitochondrial membrane. They also reduce the mitochondrial membrane potential in mammalian cells. Tissue specificity occurs for the different UCPs and the exact methods of how UCPs transfer H+/OH- are not known. UCPs contain the three homologous protein domains of MACPs. This gene is expressed in many tissues, with the greatest expression in skeletal muscle. It is thought to play a role in nonshivering thermogenesis, obesity and diabetes. Chromosomal order is 5'-UCP3-UCP2-3'. [provided by RefSeq, Jul 2008]
 
RefSeq DNA
 
RefSeq mRNA
  e!Ensembl
Gene
Transcript  
Protein

Gene Ontology (GO)

GO ID Ontology Function Evidence Reference
GO:0001666 Biological process Response to hypoxia IDA 22292025
GO:0009409 Biological process Response to cold IBA 21873635
GO:0120162 Biological process Positive regulation of cold-induced thermogenesis ISS 28130074
GO:1990542 Biological process Mitochondrial transmembrane transport IBA 21873635
GO:1990845 Biological process Adaptive thermogenesis IBA 21873635
Protein Information
 
Protein Name
Mitochondrial uncoupling protein 2, solute carrier family 25 member 8, uncoupling protein 2 (mitochondrial, proton carrier)
 
Function
UCP are mitochondrial transporter proteins that create proton leaks across the inner mitochondrial membrane, thus uncoupling oxidative phosphorylation from ATP synthesis. As a result, energy is dissipated in the form of heat
 
Refseq Proteins
 
UniProt
 
Pfam
Pfam Accession Pfam ID
PF00153 Mito_carr
Pathways
 
Reactome
 

 

The fatty acid cycling model
The proton buffering model

Interactions
 
STRING MINT IntAct
ENSP00000465356 P02654 P02654
    View interactions
     

Associated Diseases

Disease groupDisease NameReferences
Cardiovascular Diseases
Hypertensive disease
Digestive System Diseases
Fatty Liver
Endocrine System Diseases
Diabetes Mellitus
PCOS
Neoplasms
Carcinoma
References
 
 
PubMed ID Associated gene/s Associated condition Genetic Mutation Diagnostic Criteria Association with PCOS Ethnicity Conclusion
CYP11A1 
Hyperandrogenaemia 
 
 
Related 
 
In conclusion, in PCOS patients, there was a correlation between UCP-2 and CYP11A1 expression, which was significantly higher than in the control group. These changes in UCP-2 and CYP11A1 expression may mediate follicle development in PCOS. 

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