abnormality of pyrimidine metabolism Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of a pyrimidine base metabolic process. (Human Phenotype Ontology, HP_0004353)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0004353
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Genes

11 genes associated with the abnormality of pyrimidine 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
DPYD dihydropyrimidine dehydrogenase
DPYS dihydropyrimidinase
FANCA Fanconi anemia, complementation group A
FANCC Fanconi anemia, complementation group C
FANCD2 Fanconi anemia, complementation group D2
FANCE Fanconi anemia, complementation group E
SLC7A7 solute carrier family 7 (amino acid transporter light chain, y+L system), member 7
UMPS uridine monophosphate synthetase