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
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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