All diseases

OMIM ID
138500
OMIM term:
HYPERGLYCINURIA
Alternative terms:
GLYCINURIA WITH OR WITHOUT OXALATE UROLITHIASIS
GLYCINURIA WITH OR WITHOUT OXALATE NEPHROLITHIASIS
IMINOGLYCINURIA TYPE II
(∗) Location:
3p21.31   5p15.33   5q33.1  
(†) Associated OMIM genes:
SLC36A2   SLC6A19   SLC6A20  
(‡) Associated MGI genes:

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/fniyjlka