abnormality of monocarboxylic acid metabolism Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of monocarboxylic acid metabolism. (Human Phenotype Ontology, HP_0010996)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0010996
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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