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amino acid metabolic disorder
Summary
- Synonym
-
- inborn errors of amino acid metabolism
- Definition
- An inherited metabolic disorder that is characterized by impaired synthesis and degradation of amino acids.
- Super Class
- inherited metabolic disorder
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 2653 | GCSH | glycine cleavage system protein H | |
| 2752 | GLUL | glutamate-ammonia ligase | |
| 3155 | HMGCL | 3-hydroxy-3-methylglutaryl-CoA lyase | |
| 4329 | ALDH6A1 | aldehyde dehydrogenase 6 family member A1 | |
| 5095 | PCCA | propionyl-CoA carboxylase subunit alpha | |
| 5096 | PCCB | propionyl-CoA carboxylase subunit beta |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| P15104 | Glutamine synthetase | |
| Q02252 | Methylmalonate-semialdehyde/malonate-semialdehyde dehydrogenase [acylating], mitochondrial |
