Statements (13)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:protein
|
| gptkbp:associatedWith |
gptkb:hereditary_spastic_paraplegia
|
| gptkbp:encodedBy |
NIPA1 gene
|
| gptkbp:foundIn |
gptkb:Homo_sapiens
|
| gptkbp:function |
magnesium transporter
|
| gptkbp:gene |
NIPA1 gene
|
| gptkbp:locatedOnChromosome |
gptkb:15q11-q13
|
| gptkbp:mutationAssociatedWith |
spastic paraplegia type 6
|
| gptkbp:OMIM |
608145
|
| gptkbp:UniProtID |
Q7RTP0
|
| gptkbp:bfsParent |
gptkb:15q11.2_microdeletion_syndrome
|
| gptkbp:bfsLayer |
8
|
| http://www.w3.org/2000/01/rdf-schema#label |
NIPA1
|