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Glycan Structure Repository
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Glycoconjugate Repository
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Glycomics MS raw data Repository
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Glycomics MS Repository for glycan annotations from GlycoWorkbench
LM-GlycoRepo
Repository for lectin-assisted multimodality data
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Guidelines
MIRAGE
glutamate ionotropic receptor AMPA type subunit 1
Summary
- Gene Symbol
-
- GRIA1
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Alternative splicing
- Cell membrane
- Cell projection
- Disease variant
- Disulfide bond
- Endoplasmic reticulum
- Endosome
- Glycoprotein
- Intellectual disability
- Ligand-gated ion channel
- Palmitate
- Phosphoprotein
- Postsynaptic cell membrane
- Proteomics identification
- Receptor
- Reference proteome
- Signal
- Transmembrane helix
- Proteins
| UniProt | Protein Name |
|---|---|
| P42261 |
|
| A0A9L9PXG3 |
|
| Q59GL5 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| cellular response to L-glutamate | ||
| cellular response to brain-derived neurotrophic factor stimulus | ||
| conditioned place preference | ||
| response to psychosocial stress | ||
| positive regulation of excitatory postsynaptic potential |
GO Hierarchy
biological process
cellular process [inference]
response to stimulus [inference]
biological regulation [inference]
| GO Term | Evidence Code | PMID |
|---|---|---|
| recycling endosome | ||
| recycling endosome membrane | ||
| excitatory synapse | ||
| synaptic membrane | ||
| presynapse |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| amyloid-beta binding | ||
| G-protein alpha-subunit binding | ||
| AMPA glutamate receptor activity | ||
| AMPA glutamate receptor activity | ||
| AMPA glutamate receptor activity |
GO Hierarchy
molecular function
transporter activity [inference]
binding [inference]
molecular transducer activity [inference]
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- GLUTAMATE RECEPTOR
- Functional Category
-
- E: Amino acid transport and metabolism
- P: Inorganic ion transport and metabolism
- T: Signal transduction mechanisms
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0060307 | autosomal dominant intellectual developmental disorder | |
| DOID:0081235 | autosomal recessive intellectual developmental disorder 76 | |
| DOID:1826 | epilepsy |
