gptkbp:instanceOf
|
gptkb:protein
|
gptkbp:alternativeName
|
gptkb:Citrin
gptkb:Solute_carrier_family_25_member_13
|
gptkbp:associatedWith
|
gptkb:Citrullinemia_type_II
Neonatal intrahepatic cholestasis caused by citrin deficiency
|
gptkbp:EC_number
|
2.A.29.22
|
gptkbp:Entrez_Gene_ID
|
10165
ENSP00000361624
|
gptkbp:family
|
gptkb:mitochondrial_carrier_family
|
gptkbp:function
|
catalyzes the exchange of cytoplasmic glutamate with mitochondrial aspartate
|
gptkbp:gene
|
gptkb:SLC25A13
|
https://www.w3.org/2000/01/rdf-schema#label
|
O95477
|
gptkbp:length
|
675 amino acids
|
gptkbp:locatedOnChromosome
|
7q21.3
|
gptkbp:molecularWeight
|
74 kDa
|
gptkbp:organism
|
gptkb:Homo_sapiens
|
gptkbp:protein_name
|
gptkb:Calcium-binding_mitochondrial_carrier_protein_Aralar2
|
gptkbp:RefSeq
|
NP_004857.2
|
gptkbp:reviewedBy
|
yes
|
gptkbp:sequenceStatus
|
complete
|
gptkbp:subcellularLocation
|
mitochondrial inner membrane
|
gptkbp:tissue_specificity
|
gptkb:kidney
heart
liver
pancreas
|
gptkbp:transmembraneDomains
|
6
|
gptkbp:UniProt_entry_name
|
gptkb:ARAL2_HUMAN
|
gptkbp:UniProtID
|
gptkb:O95477
|
gptkbp:bfsParent
|
gptkb:ABCA1
gptkb:ABCG1
|
gptkbp:bfsLayer
|
7
|