abnormality of proline metabolism Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of a proline metabolic process. (Human Phenotype Ontology, HP_0010907)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0010907
Similar Terms
Downloads & Tools

Genes

9 genes associated with the abnormality of proline 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
PLOD2 procollagen-lysine, 2-oxoglutarate 5-dioxygenase 2
PRODH proline dehydrogenase (oxidase) 1
SLC36A2 solute carrier family 36 (proton/amino acid symporter), member 2
SLC6A19 solute carrier family 6 (neutral amino acid transporter), member 19
SLC6A20 solute carrier family 6 (proline IMINO transporter), member 20
SQSTM1 sequestosome 1
TNFRSF11A tumor necrosis factor receptor superfamily, member 11a, NFKB activator
TNFRSF11B tumor necrosis factor receptor superfamily, member 11b