Bos taurus Gene: BT.68753
Summary
InnateDB Gene IDBG-634802.3
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol BT.68753
Gene Name tyrosine aminotransferase
Synonyms
Species Bos taurus
Ensembl Gene ENSBTAG00000002214
Encoded Proteins
tyrosine aminotransferase
tyrosine aminotransferase
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 ENSG00000198650:
This nuclear gene encodes a mitochondrial protein tyrosine aminotransferase which is present in the liver and catalyzes the conversion of L-tyrosine into p-hydroxyphenylpyruvate. Mutations in this gene cause tyrosinemia (type II, Richner-Hanhart syndrome), a disorder accompanied by major skin and corneal lesions, with possible mental retardation. A regulator gene for tyrosine aminotransferase is X-linked. [provided by RefSeq, Jul 2008]
Gene Information
Type Protein coding
Genomic Location Chromosome 18:39571695-39629597
Strand Forward strand
Band
Transcripts
ENSBTAT00000046462 ENSBTAP00000043762
ENSBTAT00000002866 ENSBTAP00000002866
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
They are also associated with 3 interaction(s) predicted by orthology.
Predicted by orthology
Total 3 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0003824 catalytic activity
GO:0004838 L-tyrosine:2-oxoglutarate aminotransferase activity
GO:0008483 transaminase activity
GO:0016829 lyase activity
GO:0030170 pyridoxal phosphate binding
Biological Process
GO:0006103 2-oxoglutarate metabolic process
GO:0006520 cellular amino acid metabolic process
GO:0006536 glutamate metabolic process
GO:0006572 tyrosine catabolic process
GO:0008152 metabolic process
GO:0009058 biosynthetic process
GO:0009072 aromatic amino acid family metabolic process
GO:0009074 aromatic amino acid family catabolic process
Cellular Component
GO:0005739 mitochondrion
Orthologs
Species
Homo sapiens
Mus musculus
Gene ID
Gene Order
Pathway Predictions based on Human Orthology Data
NETPATH
REACTOME
Phenylalanine and tyrosine catabolism pathway
Metabolism of amino acids and derivatives pathway
Metabolism pathway
Phenylalanine and tyrosine catabolism pathway
Metabolism pathway
Metabolism of amino acids and derivatives pathway
KEGG
Phenylalanine metabolism pathway
Phenylalanine, tyrosine and tryptophan biosynthesis pathway
Ubiquinone and other terpenoid-quinone biosynthesis pathway
Tyrosine metabolism pathway
Cysteine and methionine metabolism pathway
Tyrosine metabolism pathway
Ubiquinone and other terpenoid-quinone biosynthesis pathway
Phenylalanine metabolism pathway
Phenylalanine, tyrosine and tryptophan biosynthesis pathway
Cysteine and methionine metabolism pathway
INOH
Phenylalanine degradation pathway
Tyrosine metabolism pathway
PID NCI
FOXA2 and FOXA3 transcription factor networks
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene
UniGene Bt.23731 Bt.68753
RefSeq NM_001034590 XM_005218652 XM_005218653 XM_005218654 XM_005218655 XM_005218656
HUGO
OMIM
CCDS
HPRD
IMGT
EMBL
GenPept
RNA Seq Atlas