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Results 1 - 5 of 5 for "3-methylcrotonyl-coa"
  1. 3-methylcrotonyl-CoA carboxylase deficiency 
    3-methylcrotonyl-CoA carboxylase deficiency (also called MCC deficiency) is an inherited disorder in which the body is unable to process certain proteins. ...
    https://medlineplus.gov/...methylcrotonyl-coa-carboxylase-deficiency - Genetics
  2. MCCC1 gene 
    ... many proteins. This step converts a molecule called 3-methylcrotonyl-CoA to a molecule called 3-methylglutaconyl-CoA. Additional ... MCCC1 gene have been identified in people with 3-methylcrotonyl-CoA carboxylase deficiency (also called MCC deficiency). MCC deficiency ...
    https://medlineplus.gov/genetics/gene/mccc1 - Genetics
  3. MCCC2 gene 
    ... many proteins. This step converts a molecule called 3-methylcrotonyl-CoA to a molecule called 3-methylglutaconyl-CoA. Additional ... MCCC2 gene have been identified in people with 3-methylcrotonyl-CoA carboxylase deficiency (also called MCC deficiency). MCC deficiency ...
    https://medlineplus.gov/genetics/gene/mccc2 - Genetics
  4. IVD gene 
    ... a molecule called isovaleryl-CoA to another molecule, 3-methylcrotonyl-CoA. Additional chemical reactions convert 3-methylcrotonyl-CoA into molecules that are used for energy. Nearly ...
    https://medlineplus.gov/genetics/gene/ivd - Genetics
  5. CA5A gene 
    ... synthetase-1, pyruvate carboxylase, propionyl-CoA carboxylase, and 3-methylcrotonyl-CoA carboxylase. These enzymes help control the amount of ... gluconeogenesis) in the liver. Propionyl-CoA carboxylase and 3-methylcrotonyl-CoA carboxylase help break down certain protein building blocks ( ...
    https://medlineplus.gov/genetics/gene/ca5a - Genetics