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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
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 | ||
| mitochondrial fragmentation involved in apoptotic process | ||
| postsynaptic density assembly | ||
| central nervous system development | ||
| axonogenesis involved in innervation |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| synaptic cleft | ||
| endoplasmic reticulum | ||
| transport vesicle | ||
| glutamatergic synapse |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| metal ion binding |
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- Uncharacterized protein
- Functional Category
-
- E: Amino acid transport and metabolism
- O: Posttranslational modification, protein turnover, chaperones
- 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 | OrthoDB | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|---|
| 112920878 | VULVU13544 | |||
| 113437235 | PSETE08347 | |||
| 113571453 | ELEEL08177 | |||
| 113877694 | BOBOX14233 | |||
| 114034393 | VOMUR20928 | |||
| 114588943 | PODMU13754 | |||
| 115047581 | ECHNA48998 | |||
| 115171397 | SALTR92101 | |||
| 115202082 | SALTR26268 | |||
| 115387288 | SALFA22161 |
