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HGD Genehomogentisate 1,2-dioxygenase 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] |
Homogentisate 1,2-dioxygenase Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Homogentisate 1,2-dioxygenase protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
homogentisate catabolic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the homogentisate catabolic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
homogentisate metabolic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the homogentisate metabolic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
homogentisate catabolic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the homogentisate catabolic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
homogentisate metabolic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the homogentisate metabolic process biological process from the curated GO Biological Process Annotations 2025 dataset. |