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. Author manuscript; available in PMC: 2018 Nov 29.
Published in final edited form as: Curr Mol Med. 2010 Dec;10(9):851–863. doi: 10.2174/156652410793937750

Table 3.

Connexin Mutation Identified in Cataracts of Mouse and Rat

Mutation Location Cataract Types Inheritary Origin References
Mouse Cx50
G22R M1 Microphthalmia & dense
cataract
Autosomal semidominant Lop10 mutation cataract
mouse
[91]
D47A E1 Nuclear Autosomal dominant No2 cataract mouse [89]
S50P E1 Whole cataract & small eye Autosomal dominant ENU mutagenesis [92]
V64A E1/M2 Nuclear and zonular cataract &
microphthalmia
Autosomal dominant Mouse Aey5 generated
by ENU mutagenesis
[90]
Rat Cx50
R340W CT Cataract Autosomal semidominant UPL rat strain [93]
L7Q NT Cataract & microphthalmia Autosomal semidominant [95]
Rat Cx46
E42K E1/M1 Nuclear Autosomal recessive Cataract rat strain [94]