|Dataset||MPO Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||anomaly in the process that results in the complete oxidation of a long-chain fatty acid, beginning with the addition of coenzyme A to a fatty acid, with successive cycles of reactions during each of which the fatty acid is shortened by a two-carbon fragment removed as acetyl coenzyme A; the cycle continues until only two or three carbons remain (as acetyl-CoA or propionyl-CoA respectively) (Mammalian Phenotype Ontology, MP_0010952)|
|Downloads & Tools|
2 gene mutations causing the abnormal fatty acid beta-oxidation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.