HYPERGLYCINURIA Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An increased concentration of glycine in the urine. (Human Phenotype Ontology, HP_0003108)
External Link http://ctdbase.org/detail.go?type=disease&acc=OMIM:138500
Similar Terms
Downloads & Tools

Genes

3 genes/proteins associated with the disease HYPERGLYCINURIA from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
SLC36A2 solute carrier family 36 (proton/amino acid symporter), member 2 2.88009
SLC6A20 solute carrier family 6 (proline IMINO transporter), member 20 2.88009
SLC6A19 solute carrier family 6 (neutral amino acid transporter), member 19 2.88009