| Core Data | Database Links |
|---|
| Approved Symbol + |
ATP7B |
RefSeq IDs + |
| Approved Name + |
ATPase, Cu++ transporting, beta polypeptide |
NM_000053 |
GenBank |
EMBL |
DDBJ |
UCSC |
| HGNC ID + |
HGNC:870 |
Accession Numbers + |
| Status + |
Approved |
U11700 |
GenBank |
EMBL |
DDBJ |
UCSC |
| Chromosome + |
13q14.3 |
Mouse Genome Database ID + |
| Previous Symbols + |
WND |
MGI:103297 |
MGD ID |
| Previous Names + |
"ATPase, Cu++ transporting, beta polypeptide (Wilson disease)" |
Rat Genome Database ID (mapped data supplied by RGD) + |
| Aliases + |
|
RGD:2180 |
RGD ID |
| Name Aliases + |
"Wilson disease" |
Entrez Gene ID + |
| Locus Type + |
gene with protein product |
540 |
Gene |
Map Viewer |
| |
CCDS IDs + |
| Gene Symbol Links |
CCDS41892.1 |
CCDS ID |
|
|
Pubmed IDs + |
| 8298641, 8298639 |
PMID |
CiteXplore |
| VEGA IDs + |
| OTTHUMG00000017406 |
VEGA GeneView |
| Specialist Database Links |
Ensembl ID (mapped data supplied by Ensembl) + |
|
|
ENSG00000123191 |
Ensembl GeneView |
UCSC |
| OMIM ID (mapped data supplied by NCBI) + |
| Locus Specific Database Links |
606882 |
OMIM |
Wilson Disease Mutation Database,
UMD Locus Specific Databases |
UCSC ID (mapped data supplied by UCSC) + |
| uc001vfw.2 |
UCSC Index |
| UniProt ID (mapped data supplied by UniProt) + |
| |
P35670 |
UniProt |
UCSC |
|
