solute carrier family 25 member 24
GPTKB entity
Statements (18)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:protein
|
| gptkbp:associatedWith |
gptkb:Kenny-Caffey_syndrome_type_2
Gracile bone dysplasia |
| gptkbp:biologicalProcess |
ATP-Mg/Pi carrier activity
|
| gptkbp:cellularComponent |
mitochondrial inner membrane
|
| gptkbp:encodedBy |
SLC25A24 gene
|
| gptkbp:Entrez_Gene_ID |
79751
|
| gptkbp:foundIn |
gptkb:Homo_sapiens
|
| gptkbp:function |
mitochondrial solute carrier
|
| gptkbp:gene |
gptkb:SLC25A24
|
| gptkbp:HGNC_ID |
HGNC:18141
|
| https://www.w3.org/2000/01/rdf-schema#label |
solute carrier family 25 member 24
|
| gptkbp:locatedOnChromosome |
1q22
|
| gptkbp:OMIM |
610010
|
| gptkbp:UniProtID |
Q6NUK1
|
| gptkbp:bfsParent |
gptkb:ENSG00000180008
gptkb:SLC25A24 |
| gptkbp:bfsLayer |
8
|