|
gptkbp:instanceOf
|
gptkb:protein
|
|
gptkbp:alternativeName
|
gptkb:Citrin
gptkb:Solute_carrier_family_25_member_13
|
|
gptkbp:associatedWith
|
gptkb:Citrin_deficiency
Adult-onset type II citrullinemia
Neonatal intrahepatic cholestasis caused by citrin deficiency
|
|
gptkbp:biologicalProcess
|
gptkb:malate-aspartate_shuttle
transmembrane transporter activity
calcium ion binding
aspartate transport
|
|
gptkbp:enzymeCommissionNumber
|
--
|
|
gptkbp:gene
|
gptkb:SLC25A13
|
|
gptkbp:gene_ID_(Ensembl)
|
ENSG00000104228
|
|
gptkbp:gene_ID_(Entrez)
|
10165
|
|
gptkbp:gene_ID_(HGNC)
|
HGNC:10987
|
|
gptkbp:hasIsoform
|
2
|
|
https://www.w3.org/2000/01/rdf-schema#label
|
Q9ULV3
|
|
gptkbp:last_modified
|
2021-02-10
|
|
gptkbp:last_sequence_update
|
2001-06-01
|
|
gptkbp:length
|
675
|
|
gptkbp:locatedOnChromosome
|
7q21.3
|
|
gptkbp:mass_(Da)
|
74,000
|
|
gptkbp:organism
|
gptkb:Homo_sapiens
|
|
gptkbp:protein_name
|
gptkb:Calcium-binding_mitochondrial_carrier_protein_Aralar2
|
|
gptkbp:proteinFamily
|
gptkb:mitochondrial_carrier_family
|
|
gptkbp:reviewedBy
|
yes
|
|
gptkbp:sequenceStatus
|
complete
|
|
gptkbp:sequenceVersion
|
2
|
|
gptkbp:subcellularLocation
|
mitochondrion inner membrane
|
|
gptkbp:UniProtID
|
gptkb:Q9ULV3
|
|
gptkbp:bfsParent
|
gptkb:CIZ1
|
|
gptkbp:bfsLayer
|
7
|