CPRiL

Got2

glutamic-oxaloacetic transaminase 2

Enables several functions, including L-aspartate:2-oxoglutarate aminotransferase activity; anion binding activity; and identical protein binding activity. Involved in several processes, including dicarboxylic acid metabolic process; lactation; and response to morphine. Located in several cellular components, including T-tubule; mitochondrial inner membrane; and perikaryon. Part of protein-containing complex. Biomarker of acute kidney failure; neurodegenerative disease; obesity; and schizophrenia. Human ortholog(s) of this gene implicated in developmental and epileptic encephalopathy 82. Orthologous to human GOT2 (glutamic-oxaloacetic transaminase 2). [provided by Alliance of Genome Resources, Apr 2022]

• aspartate aminotransferase, mitochondrial
• FABP-1
• FABPpm
Glutamate oxaloacetate transaminase 2, mitochondrial (aspartate aminotransferase 2)
fatty acid-binding protein
glutamic-oxaloacetic transaminase 2, mitochondrial (aspartate aminotransferase 2)
kynurenine aminotransferase 4
kynurenine aminotransferase IV
kynurenine--oxoglutarate transaminase 4
kynurenine--oxoglutarate transaminase IV
mAspAT
plasma membrane-associated fatty acid-binding protein
transaminase A
ASPATA
mAAT