hyperglycinuria Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An increased concentration of glycine in the urine. (Human Phenotype Ontology, HP_0003108)
External Link http://www.omim.org/entry/138500
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Genes

3 genes associated with the hyperglycinuria phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
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