Pub. Date : 2007 Jan
PMID : 16996289
10 Functional Relationships(s)Download |
Sentence | Compound Name | Protein Name | Organism |
| 1 | Sjogren-Larsson syndrome (SLS) is an inherited neurocutaneous disorder caused by mutations in the ALDH3A2 gene that encodes fatty aldehyde dehydrogenase (FALDH), an enzyme that catalyzes the oxidation of fatty aldehyde to fatty acid. | fatty aldehyde | aldehyde dehydrogenase 3 family member A2 | Homo sapiens |
| 2 | Sjogren-Larsson syndrome (SLS) is an inherited neurocutaneous disorder caused by mutations in the ALDH3A2 gene that encodes fatty aldehyde dehydrogenase (FALDH), an enzyme that catalyzes the oxidation of fatty aldehyde to fatty acid. | fatty aldehyde | aldehyde dehydrogenase 3 family member A2 | Homo sapiens |
| 3 | Sjogren-Larsson syndrome (SLS) is an inherited neurocutaneous disorder caused by mutations in the ALDH3A2 gene that encodes fatty aldehyde dehydrogenase (FALDH), an enzyme that catalyzes the oxidation of fatty aldehyde to fatty acid. | Fatty Acids | aldehyde dehydrogenase 3 family member A2 | Homo sapiens |
| 4 | Sjogren-Larsson syndrome (SLS) is an inherited neurocutaneous disorder caused by mutations in the ALDH3A2 gene that encodes fatty aldehyde dehydrogenase (FALDH), an enzyme that catalyzes the oxidation of fatty aldehyde to fatty acid. | Fatty Acids | aldehyde dehydrogenase 3 family member A2 | Homo sapiens |
| 5 | Sjogren-Larsson syndrome (SLS) is an inherited neurocutaneous disorder caused by mutations in the ALDH3A2 gene that encodes fatty aldehyde dehydrogenase (FALDH), an enzyme that catalyzes the oxidation of fatty aldehyde to fatty acid. | Fatty Acids | aldehyde dehydrogenase 3 family member A2 | Homo sapiens |
| 6 | FALDH oxidizes fatty aldehyde substrates arising from metabolism of fatty alcohols, leukotriene B4, ether glycerolipids and other potential sources such as sphingolipids. | fatty aldehyde | aldehyde dehydrogenase 3 family member A2 | Homo sapiens |
| 7 | FALDH oxidizes fatty aldehyde substrates arising from metabolism of fatty alcohols, leukotriene B4, ether glycerolipids and other potential sources such as sphingolipids. | Fatty Alcohols | aldehyde dehydrogenase 3 family member A2 | Homo sapiens |
| 8 | FALDH oxidizes fatty aldehyde substrates arising from metabolism of fatty alcohols, leukotriene B4, ether glycerolipids and other potential sources such as sphingolipids. | Leukotriene B4 | aldehyde dehydrogenase 3 family member A2 | Homo sapiens |
| 9 | FALDH oxidizes fatty aldehyde substrates arising from metabolism of fatty alcohols, leukotriene B4, ether glycerolipids and other potential sources such as sphingolipids. | ether glycerolipids | aldehyde dehydrogenase 3 family member A2 | Homo sapiens |
| 10 | FALDH oxidizes fatty aldehyde substrates arising from metabolism of fatty alcohols, leukotriene B4, ether glycerolipids and other potential sources such as sphingolipids. | Sphingolipids | aldehyde dehydrogenase 3 family member A2 | Homo sapiens |