NPTX2

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

NPTX2

Neuronal pentraxin-2 is a protein that in humans is encoded by the NPTX2 gene.[5][6]

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NPTX2
Identifiers
AliasesNPTX2, NARP, NP-II, NP2, neuronal pentraxin 2
External IDsOMIM: 600750; MGI: 1858209; HomoloGene: 1892; GeneCards: NPTX2; OMA:NPTX2 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_002523

NM_016789

RefSeq (protein)

NP_002514

NP_058069

Location (UCSC)Chr 7: 98.62 – 98.63 MbChr 5: 144.48 – 144.49 Mb
PubMed search[3][4]
Wikidata
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Function

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]

Clinical significance

Up-regulation of this gene in Parkinson disease (PD) tissues suggests that the protein may be involved in the pathology of PD

References

Further reading

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