| Symbol |
Name |
|
ABCD4
|
ATP-binding cassette, sub-family D (ALD), member 4
|
|
ACADM
|
acyl-CoA dehydrogenase, C-4 to C-12 straight chain
|
|
ALDH4A1
|
aldehyde dehydrogenase 4 family, member A1
|
|
AMN
|
amnion associated transmembrane protein
|
|
AMT
|
aminomethyltransferase
|
|
BAAT
|
bile acid CoA:amino acid N-acyltransferase
|
|
CUBN
|
cubilin (intrinsic factor-cobalamin receptor)
|
|
EPHX1
|
epoxide hydrolase 1, microsomal (xenobiotic)
|
|
GCSH
|
glycine cleavage system protein H (aminomethyl carrier)
|
|
GIF
|
gastric intrinsic factor (vitamin B synthesis)
|
|
GLDC
|
glycine dehydrogenase (decarboxylating)
|
|
GLYCTK
|
glycerate kinase
|
|
GUCY2C
|
guanylate cyclase 2C
|
|
HCFC1
|
host cell factor C1
|
|
IVD
|
isovaleryl-CoA dehydrogenase
|
|
LMBRD1
|
LMBR1 domain containing 1
|
|
MCCC2
|
methylcrotonoyl-CoA carboxylase 2 (beta)
|
|
MCEE
|
methylmalonyl CoA epimerase
|
|
MMAA
|
methylmalonic aciduria (cobalamin deficiency) cblA type
|
|
MMAB
|
methylmalonic aciduria (cobalamin deficiency) cblB type
|
|
MMACHC
|
methylmalonic aciduria (cobalamin deficiency) cblC type, with homocystinuria
|
|
MMADHC
|
methylmalonic aciduria (cobalamin deficiency) cblD type, with homocystinuria
|
|
MTR
|
5-methyltetrahydrofolate-homocysteine methyltransferase
|
|
MTRR
|
5-methyltetrahydrofolate-homocysteine methyltransferase reductase
|
|
MUT
|
methylmalonyl CoA mutase
|
|
OCRL
|
oculocerebrorenal syndrome of Lowe
|
|
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
|
|
SUCLA2
|
succinate-CoA ligase, ADP-forming, beta subunit
|
|
TJP2
|
tight junction protein 2
|
|
TTPA
|
tocopherol (alpha) transfer protein
|
|
TTR
|
transthyretin
|
