Mus musculus Gene: Got2
Summary
InnateDB Gene IDBG-184632.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol Got2
Gene Name glutamate oxaloacetate transaminase 2, mitochondrial
Synonyms AL022787; FABP-pm; Got-2; mAspAT
Species Mus musculus
Ensembl Gene ENSMUSG00000031672
Encoded Proteins
glutamate oxaloacetate transaminase 2, mitochondrial
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene does not have any Entrez summary - the following is the summary from its human ortholog ENSG00000125166:
Glutamic-oxaloacetic transaminase is a pyridoxal phosphate-dependent enzyme which exists in cytoplasmic and inner-membrane mitochondrial forms, GOT1 and GOT2, respectively. GOT plays a role in amino acid metabolism and the urea and tricarboxylic acid cycles. The two enzymes are homodimeric and show close homology. [provided by RefSeq, Jul 2008]
Glutamic-oxaloacetic transaminase is a pyridoxal phosphate-dependent enzyme which exists in cytoplasmic and inner-membrane mitochondrial forms, GOT1 and GOT2, respectively. GOT plays a role in amino acid metabolism and the urea and tricarboxylic acid cycles. The two enzymes are homodimeric and show close homology. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2013]
Gene Information
Type Protein coding
Genomic Location Chromosome 8:95864134-95888547
Strand Reverse strand
Band D1
Transcripts
ENSMUST00000034097 ENSMUSP00000034097
ENSMUST00000147040
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 15 experimentally validated interaction(s) in this database.
They are also associated with 27 interaction(s) predicted by orthology.
Experimentally validated
Total 15 [view]
Protein-Protein 15 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 27 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0004069 L-aspartate:2-oxoglutarate aminotransferase activity
GO:0016212 kynurenine-oxoglutarate transaminase activity
GO:0030170 pyridoxal phosphate binding
GO:0044822 poly(A) RNA binding
GO:0080130 L-phenylalanine:2-oxoglutarate aminotransferase activity
Biological Process
GO:0006103 2-oxoglutarate metabolic process
GO:0006107 oxaloacetate metabolic process
GO:0006531 aspartate metabolic process
GO:0006532 aspartate biosynthetic process
GO:0006533 aspartate catabolic process
GO:0006536 glutamate metabolic process
GO:0009058 biosynthetic process
GO:0015908 fatty acid transport
GO:0019550 glutamate catabolic process to aspartate
GO:0019551 glutamate catabolic process to 2-oxoglutarate
GO:0045471 response to ethanol
GO:0097052 L-kynurenine metabolic process
Cellular Component
GO:0005739 mitochondrion
GO:0005743 mitochondrial inner membrane
GO:0005759 mitochondrial matrix
GO:0005886 plasma membrane
GO:0070062 extracellular vesicular exosome
Orthologs
Species
Homo sapiens
Bos taurus
Gene ID
Gene Order
Not yet available
Pathways
NETPATH
REACTOME
Disease pathway
Glucose metabolism pathway
Metabolism pathway
Metabolism of amino acids and derivatives pathway
Gluconeogenesis pathway
Glycogen storage diseases pathway
Amino acid synthesis and interconversion (transamination) pathway
Myoclonic epilepsy of Lafora pathway
Metabolism of carbohydrates pathway
KEGG
Tyrosine metabolism pathway
Arginine and proline metabolism pathway
Phenylalanine metabolism pathway
Phenylalanine, tyrosine and tryptophan biosynthesis pathway
Alanine, aspartate and glutamate metabolism pathway
Cysteine and methionine metabolism pathway
Fat digestion and absorption pathway
INOH
PID NCI
Pathway Predictions based on Human Orthology Data
NETPATH
REACTOME
Gluconeogenesis pathway
Amino acid synthesis and interconversion (transamination) pathway
Myoclonic epilepsy of Lafora pathway
Metabolism of carbohydrates pathway
Metabolism of amino acids and derivatives pathway
Metabolism pathway
Disease pathway
Glucose metabolism pathway
Glycogen storage diseases pathway
Metabolism of carbohydrates pathway
Metabolism of amino acids and derivatives pathway
Myoclonic epilepsy of Lafora pathway
Gluconeogenesis pathway
Glycogen storage diseases pathway
Glucose metabolism pathway
Metabolism pathway
Amino acid synthesis and interconversion (transamination) pathway
Disease pathway
KEGG
Phenylalanine metabolism pathway
Arginine and proline metabolism pathway
Phenylalanine, tyrosine and tryptophan biosynthesis pathway
Tyrosine metabolism pathway
Cysteine and methionine metabolism pathway
Alanine, aspartate and glutamate metabolism pathway
Fat digestion and absorption pathway
INOH
Phenylalanine degradation pathway
Arginine Proline metabolism pathway
Methionine Cysteine metabolism pathway
Alanine Aspartate Asparagine metabolism pathway
Glycine Serine metabolism pathway
PID NCI
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene
UniGene Mm.230169
RefSeq NM_010325
OMIM
CCDS CCDS22568
HPRD
IMGT
MGI ID
MGI Symbol
EMBL
GenPept
RNA Seq Atlas