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MIRAGE
syntaxin binding protein 1
Summary
- Gene Symbol
-
- STXBP1
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Alternative splicing
- Cytoplasm
- Disease variant
- Epilepsy
- Intellectual disability
- Membrane
- Phosphoprotein
- Protein transport
- Proteomics identification
- Reference proteome
- Proteins
| UniProt | Protein Name |
|---|---|
| P61764 |
|
| A0A1B0GWF2 |
|
| A0A1B0GVQ5 |
|
| A0A1B0GTP9 |
|
| A0A0D9SG72 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| platelet degranulation |
|
|
| developmental process involved in reproduction |
|
|
| intracellular protein transport |
|
|
| vesicle docking involved in exocytosis |
|
|
| vesicle docking involved in exocytosis |
|
GO Hierarchy
biological process
cellular process [inference]
localization [inference]
biological regulation [inference]
regulation of biological process [inference]
regulation of signaling [inference]
regulation of localization [inference]
positive regulation of biological process [inference]
regulation of cellular process [inference]
regulation of cell communication [inference]
positive regulation of cellular process [inference]
regulation of cellular component organization [inference]
regulation of vesicle-mediated transport [inference]
regulation of secretion by cell [inference]
| GO Term | Evidence Code | PMID |
|---|---|---|
| nucleoplasm |
|
|
| cytoplasm |
|
|
| cytoplasm |
|
|
| mitochondrion |
|
|
| cytosol |
|
| GO Term | Evidence Code | PMID |
|---|---|---|
| SNARE binding |
|
|
| SNARE binding |
|
|
| RNA binding |
|
|
| protein binding |
|
|
| syntaxin-1 binding |
|
GO Hierarchy
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- syntaxin binding
- Functional Category
-
- E: Amino acid transport and metabolism
- G: Carbohydrate transport and metabolism
- T: Signal transduction mechanisms
| Gene Ontology |
|---|
| syntaxin-1 binding |
| vesicle docking involved in exocytosis |
| InterPro |
|---|
| Sec1-like protein |
| Sec1-like superfamily |
| Sec1-like, domain 1 |
| Sec1-like, domain 2 |
| Sec1-like, domain 3a |
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0080436 | developmental and epileptic encephalopathy 4 | |
| DOID:0050562 | West syndrome |
Ortholog
| Species | Gene ID | Alliance of Genome Resources |
|---|---|---|
| 20910 | MGI:107363 |
