|
gptkbp:instanceOf
|
gptkb:gene
|
|
gptkbp:alsoKnownAs
|
aspartate aminotransferase, mitochondrial
|
|
gptkbp:associatedWith
|
mitochondrial aspartate aminotransferase deficiency
|
|
gptkbp:discoveredIn
|
1960s
|
|
gptkbp:encodes
|
mitochondrial aspartate aminotransferase
|
|
gptkbp:Entrez_Gene_ID
|
2806
ENSG00000120053
|
|
gptkbp:enzymeCommissionNumber
|
2.6.1.1
|
|
gptkbp:expressedIn
|
gptkb:kidney
brain
heart
liver
|
|
gptkbp:fullName
|
glutamic-oxaloacetic transaminase 2
|
|
gptkbp:function
|
catalyzes the reversible transfer of an amino group between aspartate and glutamate
|
|
gptkbp:geneType
|
protein-coding
|
|
gptkbp:HGNC_ID
|
4437
|
|
https://www.w3.org/2000/01/rdf-schema#label
|
GOT2
|
|
gptkbp:length
|
430 amino acids
|
|
gptkbp:locatedOnChromosome
|
16q21
|
|
gptkbp:location
|
mitochondrion
|
|
gptkbp:molecularWeight
|
48 kDa
|
|
gptkbp:mutationAssociatedWith
|
metabolic disorders
|
|
gptkbp:OMIM
|
138150
|
|
gptkbp:organism
|
gptkb:Homo_sapiens
|
|
gptkbp:orthologInMouse
|
Got2
|
|
gptkbp:relatedToMetabolicPathway
|
gptkb:malate-aspartate_shuttle
amino acid metabolism
|
|
gptkbp:UniProtID
|
P00505
|
|
gptkbp:bfsParent
|
gptkb:aspartate_aminotransferase
gptkb:oxaloacetate_transaminase
|
|
gptkbp:bfsLayer
|
7
|