Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
LM-GlycoRepo
Repository for lectin-assisted multimodality data
All Resources
Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / OrganismsTools
SugarDrawer
GlycanBuilder
Glycan Converters
GlycoMaple
GlycomeAtlas
LM-GlycomeAtlas
GALAXY
MCAW
GlycoSim
GRable
Guidelines
MIRAGE
synaptosome associated protein 25
Summary
- Gene Symbol
-
- SNAP25
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Alternative splicing
- Cell membrane
- Coiled coil
- Congenital myasthenic syndrome
- Cytoplasm
- Disease variant
- Intellectual disability
- Palmitate
- Phosphoprotein
- Reference proteome
- Repeat
- Synaptosome
- Proteins
| UniProt | Protein Name |
|---|---|
| P60880 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| SNARE complex assembly | ||
| regulation of synapse assembly | ||
| presynaptic dense core vesicle exocytosis | ||
| endosomal transport | ||
| exocytosis |
GO Hierarchy
biological process
cellular process [inference]
localization [inference]
biological regulation [inference]
| GO Term | Evidence Code | PMID |
|---|---|---|
| filopodium | ||
| lamellipodium | ||
| extrinsic component of presynaptic membrane | ||
| specific granule membrane | ||
| glutamatergic synapse |
| GO Term | Evidence Code | PMID |
|---|---|---|
| syntaxin-1 binding | ||
| myosin binding | ||
| protein domain specific binding | ||
| transmembrane transporter binding | ||
| voltage-gated potassium channel activity |
GO Hierarchy
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- SNARE
- Functional Category
-
- C: Energy production and conversion
- E: Amino acid transport and metabolism
- T: Signal transduction mechanisms
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0110683 | congenital myasthenic syndrome 18 | |
| DOID:1094 | attention deficit hyperactivity disorder | |
| DOID:14250 | Down syndrome | |
| DOID:5419 | schizophrenia | |
| DOID:9352 | type 2 diabetes mellitus | |
| DOID:9970 | obesity |
Ortholog
| Species | Gene ID | OrthoDB | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|---|
| 20614 | MGI:98331 | MOUSE35496 | ||
| 25012 | RGD:3728 | RATNO27226 | ||
| 30711 | ZFIN:ZDB-GENE-980526-392 | DANRE12264 | ||
| 30712 | ZFIN:ZDB-GENE-980526-468 | DANRE19151 | ||
| 41193 | FB:FBgn0266720 | |||
| 179427 | WB:WBGene00004364 | |||
| 380202 | Xenbase:XB-GENE-948776 | |||
| 399171 | Xenbase:XB-GENE-17338634 | |||
| 458096 | 9598_0:005104 | PANTR24359 | ||
| 477158 | CANLF09299 |
