| Gene Symbol | ATP7A |
| Full Name | ATP7A - Copper-transporting ATPase 1 |
| Chromosome | Xq21.1 |
| Protein Type | Protein |
| Function | is an important component in the neurobiology of neurodegenerative diseases. |
| Primary Expression | most tissues except the liver, making it the primary copper transporter for extrahepatic copper metabolism |
| Molecular Weight | 163 kDa |
| Amino Acids | 1500 aa |
| UniProt ID | [Q9Y5K9](https://www.uniprot.org/uniprot/Q9Y5K9) |
| Ensembl ID | ENSG00000136939 |
| OMIM | 300011 |
| GeneCards | ATP7A |
| Human Protein Atlas | ATP7A |
| Associated Diseases | Menkes disease, developmental delay, neurodegeneration |
| Interactions | VCP, P53, Aβ, FDX1, AND, CP |
| KG Connections | 51 knowledge graph edges |
| Databases | GeneCardsNCBI GeneHPASTRING |