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neuronal pentraxin 1
Summary
- Gene Symbol
-
- NPTX1
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Calcium
- Cytoplasmic vesicle
- Disease variant
- Disulfide bond
- Endoplasmic reticulum
- Glycoprotein
- Metal-binding
- Reference proteome
- Secreted
- Signal
- Spinocerebellar ataxia
- Proteins
| UniProt | Protein Name |
|---|---|
| Q15818 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| mitochondrial transport | ||
| chemical synaptic transmission | ||
| central nervous system development | ||
| cellular response to potassium ion | ||
| mitochondrial fragmentation involved in apoptotic process |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| endoplasmic reticulum | ||
| transport vesicle | ||
| synaptic cleft | ||
| glutamatergic synapse | ||
| glutamatergic synapse |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| metal ion binding |
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- neuronal pentraxin-1
- Functional Category
-
- E: Amino acid transport and metabolism
- Q: Secondary metabolites biosynthesis, transport and catabolism
- T: Signal transduction mechanisms
| Gene Ontology |
|---|
| axonogenesis involved in innervation |
| InterPro |
|---|
| Concanavalin A-like lectin/glucanase domain superfamily |
| Pentaxin, conserved site |
| Pentraxin-related |
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:1441 | autosomal dominant cerebellar ataxia |
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 101119737 | SHEEP03312 | ||
| 101162683 | ORYLA16898 | ||
| 101575872 | OCTDE18031 | ||
| 101608871 | JACJA06687 | ||
| 101723897 | HETGA06733 | ||
| 101944237 | CHRPI03714 | ||
| 101955313 | ICTTR01842 | ||
| 102018309 | CHILA20924 | ||
| 102115692 | MACFA14999 | ||
| 102184943 | CAPHI11268 |
