abnormality of monocarboxylic acid metabolism Gene Set
Genes
13 genes associated with the abnormality of monocarboxylic acid metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol |
Name |
|
ABCB4
|
ATP-binding cassette, sub-family B (MDR/TAP), member 4
|
|
ARG1
|
arginase 1
|
|
ASL
|
argininosuccinate lyase
|
|
ASS1
|
argininosuccinate synthase 1
|
|
ATP8B1
|
ATPase, aminophospholipid transporter, class I, type 8B, member 1
|
|
BAAT
|
bile acid CoA:amino acid N-acyltransferase
|
|
EPHX1
|
epoxide hydrolase 1, microsomal (xenobiotic)
|
|
HPD
|
4-hydroxyphenylpyruvate dioxygenase
|
|
SLC7A7
|
solute carrier family 7 (amino acid transporter light chain, y+L system), member 7
|
|
TAT
|
tyrosine aminotransferase
|
|
TJP2
|
tight junction protein 2
|
|
UMPS
|
uridine monophosphate synthetase
|
|
UROC1
|
urocanate hydratase 1
|
