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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
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 |
|---|---|---|---|
| 1491 | CTH | cystathionine gamma-lyase | |
| 1892 | ECHS1 | enoyl-CoA hydratase, short chain 1 | |
| 2653 | GCSH | glycine cleavage system protein H | |
| 2752 | GLUL | glutamate-ammonia ligase | |
| 3155 | HMGCL | 3-hydroxy-3-methylglutaryl-CoA lyase | |
| 4144 | MAT2A | methionine adenosyltransferase 2A | |
| 5095 | PCCA | propionyl-CoA carboxylase subunit alpha | |
| 5096 | PCCB | propionyl-CoA carboxylase subunit beta | |
| 5832 | ALDH18A1 | aldehyde dehydrogenase 18 family member A1 | |
| 6470 | SHMT1 | serine hydroxymethyltransferase 1 |
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 12036 | Bcat2 | branched chain aminotransferase 2, mitochondrial | |
| 14645 | Glul | glutamate-ammonia ligase | |
| 15356 | Hmgcl | 3-hydroxy-3-methylglutaryl-Coenzyme A lyase | |
| 20425 | Shmt1 | serine hydroxymethyltransferase 1 (soluble) | |
| 56454 | Aldh18a1 | aldehyde dehydrogenase 18 family, member A1 | |
| 58875 | Hibadh | 3-hydroxyisobutyrate dehydrogenase | |
| 66904 | Pccb | propionyl Coenzyme A carboxylase, beta polypeptide | |
| 76282 | Gpt | glutamic pyruvic transaminase, soluble | |
| 107869 | Cth | cystathionine gamma lyase | |
| 108037 | Shmt2 | serine hydroxymethyltransferase 2 (mitochondrial) |
