Overview
| Alternate Names: | ATPase, Cu(2+)- transporting, beta polypeptide; ATPase, Cu++ transporting, beta polypeptide (Wilson disease); OTTHUMP00000040880; Wilson disease-associated protein; copper pump 2; copper-transporting ATPase 2 |
|---|---|
| Alternate Symbols: | PWD; WC1; WD; WND |
| PharmGKB Accession Id: | PA73 |
Details
| Cytogenetic Location: | chr13 : q14.3 |
|---|---|
| GP mRNA Boundary†: | chr13 : 51404806 - 51483631 |
| GP Gene Boundary†: | chr13 : 51401806 - 51493631 |
| Strand: | minus |
| Product Name: | ATPase, Cu(2+)- transporting, beta polypeptide, ATPase, Cu++ transporting, beta polypeptide, ATPase, Cu++ transporting, beta polypeptide (Wilson disease), ATPase, Cu++ transporting, beta polypeptide isoform a, ATPase, Cu++ transporting, beta polypeptide isoform b, OTTHUMP00000040880, WD protein, Wilson disease-associated protein, copper pump 2, copper-transporting ATPase 2 |
†
The mRNA boundaries are calculated using the gene's default feature set from NCBI, mapped
onto the UCSC Golden Path. PharmGKB sets gene boundaries by expanding the mRNA boundaries
by no less than 10,000 bases upstream (5') and 3,000 bases downstream (3') to allow for
potential regulatory regions.
PharmGKB Curated Pathways
Curated Information
The following drugs are in curated knowledge about this gene.
| Drug | Relationship | Evidence | |
|---|---|---|---|
|
cisplatin |
|
Publications |
|
docetaxel |
|
Publications |
|
|
gemcitabine |
|
Publications |
|
|
platinum |
|
Publications |
Curated Information
The following diseases are in curated knowledge about this gene.
| Disease | Relationship | Evidence | |
|---|---|---|---|
|
|
Carcinoma, Non-Small-Cell Lung |
|
Publications |
|
|
Neoplasms |
|
Publications |
Downloads
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LinkOuts
- Entrez Gene ID:
- 540
- OMIM Accession:
- 277900
- 606882
- UCSC Genome Browser ID:
- NM_000053
- Ref Seq NM Accession:
- NM_000053
- NM_001005918
- Ref Seq NP Accession:
- AAA16173
- AAA79211
- AAA79212
- AAA92667
- AAB34086
- AAB34087
- AAB52902
- AAD01998
- AAD14987
- AAF67661
- AAG27536
- AAG27537
- AAI17201
- AAI43974
- AAI43976
- AAI43977
- AAY41166
- BAD92698
- BAG63463
- BAG63775
- CAI12888
- CAI13428
- EAX08892
- EAX08893
- EAX08894
- EAX08895
- EAX08896
- NP_000044
- NP_001005918
- P35670
- Q17RT3
- Q9GZP5
- Q9NZ25
- Ref Seq NT Accession:
- AC_000056
- AC_000145
- NC_000013
- NG_008806
- NT_024524
- NW_001838074
- NW_925473
- UniProtKB Accesssion:
- ATP7B_HUMAN (P35670)
- Ensembl ID:
- ENSG00000123191
- GenAtlas ID:
- ATP7B
- GeneCard ID:
- ATP7B
- SOURCE ID:
- ATP7B
- MutDB ID:
- ATP7B
- PromoLign ID:
- ortho_5453
- ALFRED ID:
- LO009949F
- HuGE ID:
- ATP7B
- Comparative Toxicogenomics Acc ID:
- 540
- ModBase:
- P35670