Bos taurus Gene: HGD
Summary
InnateDB Gene IDBG-632879.2
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol HGD
Gene Name homogentisate 1,2-dioxygenase
Synonyms
Species Bos taurus
Ensembl Gene ENSBTAG00000015895
Encoded Proteins
homogentisate 1,2-dioxygenase
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 ENSG00000113924:
This gene encodes the enzyme homogentisate 1,2 dioxygenase. This enzyme is involved in the catabolism of the amino acids tyrosine and phenylalanine. Mutations in this gene are the cause of the autosomal recessive metabolism disorder alkaptonuria.[provided by RefSeq, May 2010]
Gene Information
Type Protein coding
Genomic Location Chromosome 1:65942080-65984708
Strand Reverse strand
Band
Transcripts
ENSBTAT00000061425 ENSBTAP00000053295
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 8 interaction(s) predicted by orthology.
Predicted by orthology
Total 8 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0004411 homogentisate 1,2-dioxygenase activity
GO:0051213 dioxygenase activity
Biological Process
GO:0006520 cellular amino acid metabolic process
GO:0006559 L-phenylalanine catabolic process
GO:0006570 tyrosine metabolic process
GO:0055114 oxidation-reduction process
Cellular Component
GO:0070062 extracellular vesicular exosome
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
Tyrosine metabolism pathway
Tyrosine metabolism pathway
INOH
Tyrosine metabolism pathway
PID NCI
Cross-References
SwissProt
TrEMBL B8YB76 F1MLF8
UniProt Splice Variant
Entrez Gene 507496
UniGene Bt.19899
RefSeq NM_001144852
HUGO
OMIM
CCDS
HPRD
IMGT
EMBL DAAA02001564 FJ515744
GenPept ACL37011
RNA Seq Atlas 507496