abnormality of serine family amino acid metabolism Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of a serine family amino acid metabolic process. (Human Phenotype Ontology, HP_0010894)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0010894
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Genes

18 genes associated with the abnormality of serine family amino acid metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ACADM acyl-CoA dehydrogenase, C-4 to C-12 straight chain
ALDH4A1 aldehyde dehydrogenase 4 family, member A1
AMT aminomethyltransferase
GCSH glycine cleavage system protein H (aminomethyl carrier)
GLDC glycine dehydrogenase (decarboxylating)
GLYCTK glycerate kinase
IVD isovaleryl-CoA dehydrogenase
MCCC2 methylcrotonoyl-CoA carboxylase 2 (beta)
MMAA methylmalonic aciduria (cobalamin deficiency) cblA type
MMAB methylmalonic aciduria (cobalamin deficiency) cblB type
MUT methylmalonyl CoA mutase
PCCA propionyl CoA carboxylase, alpha polypeptide
PCCB propionyl CoA carboxylase, beta polypeptide
PRODH proline dehydrogenase (oxidase) 1
PSAT1 phosphoserine aminotransferase 1
SLC36A2 solute carrier family 36 (proton/amino acid symporter), member 2
SLC6A19 solute carrier family 6 (neutral amino acid transporter), member 19
SLC6A20 solute carrier family 6 (proline IMINO transporter), member 20