abnormality of orotic acid metabolism Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the metabolism of orotic acid. (Human Phenotype Ontology, HP_0010928)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0010928
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Genes

5 genes associated with the abnormality of orotic acid metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ARG1 arginase 1
ASL argininosuccinate lyase
ASS1 argininosuccinate synthase 1
SLC7A7 solute carrier family 7 (amino acid transporter light chain, y+L system), member 7
UMPS uridine monophosphate synthetase