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GPR12

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

GPR12
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Probable G-protein coupled receptor 12 is a protein that in humans is encoded by the GPR12 gene.[5][6][7]

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The gene product of GPR12 is an orphan receptor, meaning that its endogenous ligand is currently unknown. Gene disruption of GPR12 in mice results in dyslipidemia and obesity.[8]

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Ligands

Inverse agonists

Evolution

Paralogues

Source:[10]

References

Further reading

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