abnormality of glutamine metabolism Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of a glutamine metabolic process. (Human Phenotype Ontology, HP_0010903)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0010903
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Genes

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

Symbol Name
ASL argininosuccinate lyase
ASS1 argininosuccinate synthase 1
OTC ornithine carbamoyltransferase