Hyperglycinuria, also known as glycinuria with or without oxalate nephrolithiasis, is related to iminoglycinuria and nephrolithiasis, calcium oxalate, 1. An important gene associated with Hyperglycinuria is SLC36A2 (Solute Carrier Family 36 Member 2), and among its related pathways/superpathways are Infectious disease and Transport of inorganic cations/anions and amino acids/oligopeptides. Affiliated tissues include kidney and liver, and related phenotypes are calcium oxalate nephrolithiasis and hyperglycinuria