abnormality of lysine metabolism Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of a lysine metabolic process. (Human Phenotype Ontology, HP_0010908)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0010908
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Genes

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

Symbol Name
AASS aminoadipate-semialdehyde synthase
DECR1 2,4-dienoyl CoA reductase 1, mitochondrial
SLC3A1 solute carrier family 3 (amino acid transporter heavy chain), member 1
SLC7A9 solute carrier family 7 (amino acid transporter light chain, bo,+ system), member 9