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Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia
Neuronal pentraxin-2 is a protein that in humans is encoded by the NPTX2 gene.[5][6]
NPTX2 | |||||||||||||||||||||||||||||||||||||||||||||||||||
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Aliases | NPTX2, NARP, NP-II, NP2, neuronal pentraxin 2 | ||||||||||||||||||||||||||||||||||||||||||||||||||
External IDs | OMIM: 600750; MGI: 1858209; HomoloGene: 1892; GeneCards: NPTX2; OMA:NPTX2 - orthologs | ||||||||||||||||||||||||||||||||||||||||||||||||||
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This gene encodes a member of the family of neuronal pentraxins, synaptic proteins that are related to C-reactive protein. This protein is involved in excitatory synapse formation. It also plays a role in clustering of alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA)-type glutamate receptors at established synapses, resulting in non-apoptotic cell death of dopaminergic nerve cells.[6]
Up-regulation of this gene in Parkinson disease (PD) tissues suggests that the protein may be involved in the pathology of PD
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