Statements (23)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:gene
|
| gptkbp:alternativeSplicing |
yes
|
| gptkbp:associatedWith |
gptkb:Angelman_syndrome
gptkb:Prader-Willi_syndrome |
| gptkbp:encodes |
ATPase phospholipid transporting 10A
|
| gptkbp:Entrez_Gene_ID |
57194
ENSG00000184009 |
| gptkbp:expressedIn |
gptkb:placenta
brain |
| gptkbp:function |
phospholipid translocation
|
| gptkbp:HGNC_ID |
HGNC:19154
|
| https://www.w3.org/2000/01/rdf-schema#label |
ATP10A
|
| gptkbp:imprint |
yes
|
| gptkbp:locatedOnChromosome |
gptkb:chromosome_15
|
| gptkbp:location |
gptkb:15q11-q13
|
| gptkbp:OMIM |
601225
|
| gptkbp:organism |
gptkb:Homo_sapiens
|
| gptkbp:orthologInMouse |
Atp10a
|
| gptkbp:proteinFamily |
P-type ATPase
|
| gptkbp:UniProtID |
Q9Y2Q0
|
| gptkbp:bfsParent |
gptkb:Angelman_syndrome_critical_region
gptkb:chromosome_15_(human) |
| gptkbp:bfsLayer |
8
|