Term: Cataract, Autosomal Dominant
OMIM ID: 604219

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...
Acc none identified Alm none identified Apo none identified Apoca none identified Cat2 none identified Cat4 none identified Ccw none identified Coc none identified Cryga CRYGA Crygb CRYGB Cryge none identified Crygs CRYGS Enc none identified Iac none identified Idc none identified Lim2 LIM2 Mip MIP Nuca none identified Pax6 PAX6 Tcm none identified			...the mouse gene.      OMIM data currently do not associate this disease with the orthologous human gene.