| Core Data | Database Links |
|---|
| Approved Symbol + |
ATP7A |
RefSeq IDs + |
| Approved Name + |
ATPase, Cu++ transporting, alpha polypeptide |
NM_000052 |
GenBank |
EMBL |
DDBJ |
UCSC |
| HGNC ID + |
HGNC:869 |
Accession Numbers + |
| Status + |
Approved |
L06133 |
GenBank |
EMBL |
DDBJ |
UCSC |
| Chromosome + |
Xq13.2-q13.3 |
Mouse Genome Database ID + |
| Previous Symbols + |
MNK |
MGI:99400 |
MGD ID |
| Previous Names + |
"Menkes syndrome" |
Rat Genome Database ID (mapped data supplied by RGD) + |
| Aliases + |
|
RGD:2179 |
RGD ID |
| Name Aliases + |
|
Entrez Gene ID + |
| Locus Type + |
gene with protein product |
538 |
Gene |
Map Viewer |
| |
CCDS IDs + |
| Gene Symbol Links |
CCDS35339.1 |
CCDS ID |
|
|
Pubmed IDs + |
| 10079817 |
PMID |
CiteXplore |
| VEGA IDs + |
| OTTHUMG00000021885 |
VEGA GeneView |
| Specialist Database Links |
Ensembl ID (mapped data supplied by Ensembl) + |
|
|
ENSG00000165240 |
Ensembl GeneView |
UCSC |
| OMIM ID (mapped data supplied by NCBI) + |
| Locus Specific Database Links |
300011 |
OMIM |
| Mental Retardation database |
UCSC ID (mapped data supplied by UCSC) + |
| uc004ecx.3 |
UCSC Index |
| UniProt ID (mapped data supplied by UniProt) + |
| |
Q04656 |
UniProt |
UCSC |
|
