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PMID:11062307
| Citation |
Lyon, MF, Bogani, D, Boyd, Y, Guillot, P and Favor, J (2000) Further genetic analysis of two autosomal dominant mouse eye defects, Ccw and Pax6(coop). Mol. Vis. 6:199-203 |
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| Abstract |
The work forms part of a major project to study the genetics of mouse cataract mutants found during the course of mutagenesis experiments. The long-term aim is to find the underlying gene mutation in each cataract mutant. Here we report further studies of the mutant cataract and curly whiskers (Ccw), previously mapped to Chromosome 4, and also investigations of the corneal opacity (Coop) mutant, which is shown to involve a mutation in the Pax6 gene. |
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| Keywords |
Animals; Base Sequence; Cataract/genetics; Cataract/pathology; Chromosome Mapping; Chromosomes/genetics; Consensus Sequence; Corneal Opacity/genetics; Corneal Opacity/pathology; DNA Mutational Analysis; DNA-Binding Proteins/genetics; Eye Diseases, Hereditary/genetics; Eye Diseases, Hereditary/pathology; Eye Proteins/genetics; Female; Homeodomain Proteins; Lens, Crystalline/pathology; Male; Mice; Mice, Inbred C3H; Mice, Inbred DBA; Mice, Mutant Strains; Microsatellite Repeats/genetics; Molecular Sequence Data; Paired Box Transcription Factors; Repressor Proteins; Vibrissae/abnormalities |
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Significance
Annotations
| Gene product | Qualifier | GO ID | GO term name | Evidence Code | with/from | Aspect | Notes | Status |
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See also
References
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