Statements (15)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:gene
|
| gptkbp:associatedWith |
gptkb:Angelman_syndrome
gptkb:Prader-Willi_syndrome |
| gptkbp:encodes |
NIPA2 protein
|
| gptkbp:Entrez_Gene_ID |
374900
|
| gptkbp:fullName |
non imprinted in Prader-Willi/Angelman syndrome 2
|
| gptkbp:function |
magnesium transporter
|
| gptkbp:geneType |
protein-coding
|
| gptkbp:HGNC_ID |
HGNC:21298
|
| https://www.w3.org/2000/01/rdf-schema#label |
NIPA2
|
| gptkbp:locatedOnChromosome |
15q11.2
|
| gptkbp:organism |
gptkb:Homo_sapiens
|
| gptkbp:UniProtID |
Q8NFW8
|
| gptkbp:bfsParent |
gptkb:15q11.2_microdeletion_syndrome
|
| gptkbp:bfsLayer |
8
|