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MIRAGE
AP-2 complex subunit mu
Summary
- UniProt ID
- Q96CW1
- Gene Symbol
-
- AP2M1
- CLAPM1
- KIAA0109
- Gene ID
- 1173
- Organism
- Homo sapiens (human)
External Links
- GlyGen
- Q96CW1
- PubChem
- Q96CW1
- The Human Metabolome Database
- HMDBP14128
- RaftProt
- Q96CW1
- Re-Glyco
- Q96CW1
Annotation
- Keyword
-
- 3D-structure
- Alternative splicing
- Cell membrane
- Coated pit
- Disease variant
- Endocytosis
- Epilepsy
- Intellectual disability
- Lipid-binding
- Phosphoprotein
- Protein transport
- Reference proteome
- Gene Ontology (GO)
| GO Term |
|---|
| plasma membrane |
| cytosol |
| lysosomal membrane |
| clathrin-coated pit |
| synaptic vesicle |
| cytoplasmic side of plasma membrane |
| AP-2 adaptor complex |
| endocytic vesicle membrane |
| clathrin-coated endocytic vesicle |
| extracellular exosome |
Sequence
MIGGLFIYNHKGEVLISRVYRDDIGRNAVDAFRVNVIHARQQVRSPVTNIARTSFFHVKRSNIWLAAVTKQNVNAAMVFEFLYKMCDVMAAYFGKISEENIKNNFVLIYELLDEILDFGYPQNSETGALKTFITQQGIKSQHQTKEEQSQITSQVTGQIGWRREGIKYRRNELFLDVLESVNLLMSPQGQVLSAHVSGRVVMKSYLSGMPECKFGMNDKIVIEKQGKGTADETSKSGKQSIAIDDCTFHQCVRLSKFDSERSISFIPPDGEFELMRYRTTKDIILPFRVIPLVREVGRTKLEVKVVIKSNFKPSLLAQKIEVRIPTPLNTSGVQVICMKGKAKYKASENAIVWKIKRMAGMKESQISAEIELLPTNDKKKWARPPISMNFEVPFAPSGLKVRYLKVFEPKLNYSDHDVIKWVRYIGRSGIYETRC
Glycosylation Sites
G80920RR
Feature
: Glycosylation Site from GlyGen
: Glycosylation Site from UniProt
Pathway
| Pathway Name | Organism |
|---|---|
| Cargo recognition for clathrin-mediated endocytosis | Homo sapiens |
| Clathrin-mediated endocytosis | Homo sapiens |
| EPH-ephrin mediated repulsion of cells | Homo sapiens |
| Formation of annular gap junctions | Homo sapiens |
| Gap junction degradation | Homo sapiens |
| LDL clearance | Homo sapiens |
| MHC class II antigen presentation | Homo sapiens |
| Nef Mediated CD4 Down-regulation | Homo sapiens |
| Nef Mediated CD8 Down-regulation | Homo sapiens |
| Nef mediated downregulation of CD28 cell surface expression | Homo sapiens |
Disease
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0060307 | autosomal dominant intellectual developmental disorder |
