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Gene Symbol |
UCP2 |
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Aliases |
BMIQ4, SLC25A8, UCPH |
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Entrez Gene ID |
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Gene Name |
Uncoupling protein 2 |
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Chromosomal Location |
11q13.4 |
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HGNC ID |
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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]
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RefSeq DNA |
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RefSeq mRNA |
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e!Ensembl
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Protein Information |
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Protein Name |
Mitochondrial uncoupling protein 2, solute carrier family 25 member 8, uncoupling protein 2 (mitochondrial, proton carrier) |
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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 |
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UniProt |
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Pfam |
Pfam Accession |
Pfam ID |
PF00153 |
Mito_carr |
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Interactions |
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STRING |
MINT |
IntAct |
ENSP00000465356 |
P02654 |
P02654 |
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View interactions
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Associated Diseases
Disease group | Disease Name | References |
Cardiovascular Diseases |
Hypertensive disease |
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Digestive System Diseases |
Fatty Liver |
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Endocrine System Diseases |
Diabetes Mellitus |
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PCOS |
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Neoplasms |
Carcinoma |
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Anaplastic Carcinoma |
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Nervous System Diseases |
Cerebral Ischemia |
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Stroke |
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Nutritional and Metabolic Diseases |
Obesity |
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Gluocose Intolerance |
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Psychiatric/Brain disorders |
Bipolar Disorder |
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Schizophrenia |
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Eating Disorders |
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References |
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PubMed ID |
Associated gene/s |
Associated condition |
Genetic Mutation |
Diagnostic Criteria |
Association with PCOS |
Ethnicity |
Conclusion |
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CYP11A1 |
Hyperandrogenaemia |
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Related
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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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