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MIRAGE
glutamate ionotropic receptor NMDA type subunit 1
Summary
- Gene Symbol
-
- GRIN1
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Alternative splicing
- Calcium
- Cell membrane
- Disease variant
- Disulfide bond
- Epilepsy
- Glycoprotein
- Intellectual disability
- Ligand-gated ion channel
- Magnesium
- Metal-binding
- Phosphoprotein
- Postsynaptic cell membrane
- Proteomics identification
- Receptor
- Reference proteome
- Signal
- Transmembrane helix
- Zinc
- Proteins
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| monoatomic ion transport |
|
|
| ion transport |
|
|
| monoatomic cation transport |
|
|
| chemical synaptic transmission |
|
|
| brain development |
|
GO Hierarchy
biological process
cellular process [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]
regulation of metabolic process [inference]
regulation of transmembrane transport [inference]
positive regulation of cellular process [inference]
| GO Term | Evidence Code | PMID |
|---|---|---|
| plasma membrane |
|
|
| plasma membrane |
|
|
| plasma membrane |
|
|
| plasma membrane |
|
|
| synaptic vesicle |
|
| GO Term | Evidence Code | PMID |
|---|---|---|
| amyloid-beta binding |
|
|
| NMDA glutamate receptor activity |
|
|
| NMDA glutamate receptor activity |
|
|
| NMDA glutamate receptor activity |
|
|
| NMDA glutamate receptor activity |
|
GO Hierarchy
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
| Gene Ontology |
|---|
| NMDA glutamate receptor activity |
| ligand-gated monoatomic ion channel activity |
| monoatomic ion channel activity |
| monoatomic ion transport |
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:3526 | cerebral infarction | |
| DOID:0070387 | developmental and epileptic encephalopathy 101 | |
| DOID:1574 | alcohol use disorder | |
| DOID:0070038 | autosomal dominant intellectual developmental disorder 8 |
Ortholog
| Species | Gene ID | Alliance of Genome Resources |
|---|---|---|
| 14810 | MGI:95819 | |
| 24408 | RGD:2736 | |
| 40665 | FB:FBgn0010399 | |
| 397953 | Xenbase:XB-GENE-866327 |
