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Human Disease and Mouse Model Detail
Human Disease

Term: Hyperglycinuria
OMIM ID: 138500

Synonyms Glycinuria with or without Oxalate Nephrolithiasis; Glycinuria with or without Oxalate Urolithiasis; Iminoglycinuria Type II
Associated Genes

Orthologous mouse and human markers where mutations in one or both species have been associated with phenotypes characteristic of this disease.

Mouse Gene
Human Gene
 
Characteristics of this human disease are associated with mutations in...
     
Slc36a2 SLC36A2
Slc6a19 SLC6A19
Slc6a20a SLC6A20
  human...the human gene.
     MGI data currently do not associate this disease with mutations in the orthologous mouse gene.
     
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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Send questions and comments to User Support. 		last database update
04/03/2013
MGI 5.12 		The Jackson Laboratory