Statements (28)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:gene
|
| gptkbp:alternativeName |
gptkb:Na+/K+_ATPase_alpha-2_subunit
gptkb:sodium/potassium-transporting_ATPase_alpha-2_chain |
| gptkbp:associatedWith |
gptkb:alternating_hemiplegia_of_childhood
gptkb:familial_hemiplegic_migraine_type_2 |
| gptkbp:discoveredIn |
1992
|
| gptkbp:encodes |
gptkb:Sodium/potassium-transporting_ATPase_subunit_alpha-2
|
| gptkbp:Entrez_Gene_ID |
gptkb:ENSG00000163399
477 GC01M160073 |
| gptkbp:expressedIn |
gptkb:skeletal_muscle
brain heart |
| gptkbp:function |
ion transport
maintenance of electrochemical gradients |
| gptkbp:HGNC_ID |
gptkb:HGNC:797
|
| https://www.w3.org/2000/01/rdf-schema#label |
ATP1A2
|
| gptkbp:locatedOnChromosome |
chromosome 1
1q23.2 |
| gptkbp:mutationAssociatedWith |
neurological disorders
|
| gptkbp:OMIM |
182340
|
| gptkbp:organism |
gptkb:Homo_sapiens
|
| gptkbp:orthologInMouse |
gptkb:Atp1a2
|
| gptkbp:proteinFamily |
gptkb:P-type_cation_transport_ATPase
|
| gptkbp:UniProtID |
gptkb:P50993
|
| gptkbp:bfsParent |
gptkb:Hemiplegic_migraine
gptkb:A2S2 |
| gptkbp:bfsLayer |
7
|