abnormality of glycine metabolism Gene Set
Genes
18 genes associated with the abnormality of glycine 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
|
