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Human Disease and Mouse Model Detail
Human Disease

Term: Hypomagnesemia 5, Renal, with Ocular Involvement; HOMG5
OMIM ID: 248190

Synonyms Fhhnc with Severe Ocular Involvement; Hypomagnesemia, Familial, with Hypercalciuria, Nephrocalcinosis, and Severe Ocular Involvement; Hypomagnesemia, Renal, with Ocular Involvement; Macular Coloboma, Bilateral, with Hypercalciuria
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...
     
Cldn19 CLDN19
  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