Statements (18)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:gene
|
| gptkbp:alternativeName |
gptkb:B(0)AT1
solute carrier family 7 member 19 |
| gptkbp:associatedWith |
gptkb:Hartnup_disease
|
| gptkbp:encodes |
gptkb:Sodium-dependent_neutral_amino_acid_transporter_B(0)AT1
|
| gptkbp:Entrez_Gene_ID |
130624
|
| gptkbp:expressedIn |
gptkb:kidney
intestine |
| gptkbp:function |
amino acid transport
|
| gptkbp:HGNC_ID |
HGNC:18116
|
| https://www.w3.org/2000/01/rdf-schema#label |
SLC7A19
|
| gptkbp:locatedOnChromosome |
gptkb:chromosome_19
|
| gptkbp:memberOf |
gptkb:solute_carrier_family
|
| gptkbp:mutationAssociatedWith |
gptkb:Hartnup_disorder
|
| gptkbp:OMIM |
608893
|
| gptkbp:UniProtID |
gptkb:Q695T7
|
| gptkbp:bfsParent |
gptkb:solute_carrier_family
|
| gptkbp:bfsLayer |
6
|