NPTX1

NPTX1
Identifiers
Aliases	NPTX1, NP1, neuronal pentraxin 1
External IDs	OMIM: 602367; MGI: 107811; HomoloGene: 1891; GeneCards: NPTX1; OMA:NPTX1 - orthologs
Gene location (Human)
Chr.	Chromosome 17 (human)
End	80,477,843 bp
Gene location (Mouse)
Chr.	Chromosome 11 (mouse)
End	119,438,579 bp
RNA expression pattern
	Top expressed in
	cerebellar vermis; ; paraflocculus of cerebellum; ; middle temporal gyrus; ; frontal pole; ; right hemisphere of cerebellum; ; parietal lobe; ; postcentral gyrus; ; superior frontal gyrus; ; Brodmann area 10; ; orbitofrontal cortex;
	Top expressed in
	lobe of cerebellum; ; cerebellar vermis; ; dentate gyrus of hippocampal formation granule cell; ; primary motor cortex; ; subiculum; ; habenula; ; prefrontal cortex; ; ventromedial nucleus; ; anterior amygdaloid area; ; hippocampus proper;
	More reference expression data
	n/a
Gene ontology
Molecular function	metal ion binding;
Cellular component	transport vesicle; cytoplasmic vesicle; plasma membrane; neuron projection; glutamatergic synapse;
Biological process	central nervous system development; axonogenesis involved in innervation; chemical synaptic transmission; regulation of postsynaptic neurotransmitter receptor activity;
	Sources:Amigo / QuickGO
Orthologs
	4884
	18164
	ENSG00000171246
	ENSMUSG00000025582
	Q15818
	Q62443
	NM_002522
	NM_008730
	NP_002513
	NP_032756
	Wikidata
View/Edit Human	View/Edit Mouse

Neuronal pentraxin-1 (NP1) is a protein that in humans is encoded by the NPTX1 gene.