Amino Acid Metabolism, Inborn Errors Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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Genes

5 genes associated with the Amino Acid Metabolism, Inborn Errors phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
ACADSB acyl-CoA dehydrogenase, short/branched chain
ACAT1 acetyl-CoA acetyltransferase 1
MMACHC methylmalonic aciduria (cobalamin deficiency) cblC type, with homocystinuria
MUT methylmalonyl CoA mutase
PRODH proline dehydrogenase (oxidase) 1