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MIRAGE
cholinergic receptor nicotinic alpha 2 subunit
Summary
- Gene Symbol
-
- CHRNA2
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Alternative splicing
- Cell membrane
- Disease variant
- Disulfide bond
- Epilepsy
- Glycoprotein
- Ligand-gated ion channel
- Postsynaptic cell membrane
- Receptor
- Reference proteome
- Signal
- Transmembrane helix
- Proteins
| UniProt | Protein Name |
|---|---|
| Q15822 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| monoatomic ion transport | ||
| ion transport | ||
| signal transduction | ||
| synaptic transmission, cholinergic | ||
| neuromuscular synaptic transmission |
| GO Term | Evidence Code | PMID |
|---|---|---|
| nucleoplasm | ||
| plasma membrane | ||
| plasma membrane | ||
| plasma membrane | ||
| acetylcholine-gated channel complex |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| acetylcholine receptor activity | ||
| acetylcholine-gated monoatomic cation-selective channel activity | ||
| acetylcholine-gated monoatomic cation-selective channel activity | ||
| quaternary ammonium group binding | ||
| heterocyclic compound binding |
GO Hierarchy
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- acetylcholine receptor subunit
- Functional Category
-
- E: Amino acid transport and metabolism
- T: Signal transduction mechanisms
- X: Mobilome: prophages, transposons
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0060685 | autosomal dominant nocturnal frontal lobe epilepsy 4 | |
| DOID:0081119 | benign familial infantile seizures 6 |
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 1134 | FB:FBgn0266347 | ||
| 1135 | Xenbase:XB-GENE-1013893 | ||
| 1136 | FB:FBgn0266347 | ||
| 1137 | FB:FBgn0266347 | ||
| 1138 | FB:FBgn0266347 | ||
| 1140 | FB:FBgn0266347 | ||
| 1141 | FB:FBgn0266347 | ||
| 1142 | FB:FBgn0266347 | ||
| 1144 | FB:FBgn0266347 | ||
| 1145 | FB:FBgn0266347 |
