abnormality of glutamine family amino acid metabolism Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of a glutamine family amino acid metabolic process. (Human Phenotype Ontology, HP_0010902)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0010902
Similar Terms
Downloads & Tools

Genes

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

Symbol Name
ALDH4A1 aldehyde dehydrogenase 4 family, member A1
ASL argininosuccinate lyase
ASS1 argininosuccinate synthase 1
CPS1 carbamoyl-phosphate synthase 1, mitochondrial
OTC ornithine carbamoyltransferase
PLOD2 procollagen-lysine, 2-oxoglutarate 5-dioxygenase 2
PRODH proline dehydrogenase (oxidase) 1
SLC36A2 solute carrier family 36 (proton/amino acid symporter), member 2
SLC3A1 solute carrier family 3 (amino acid transporter heavy chain), member 1
SLC6A19 solute carrier family 6 (neutral amino acid transporter), member 19
SLC6A20 solute carrier family 6 (proline IMINO transporter), member 20
SLC7A9 solute carrier family 7 (amino acid transporter light chain, bo,+ system), member 9
SQSTM1 sequestosome 1
TNFRSF11A tumor necrosis factor receptor superfamily, member 11a, NFKB activator
TNFRSF11B tumor necrosis factor receptor superfamily, member 11b