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Table 1 Phenotypic changes in wild type (WT), WT/R49Cneo heterozygous, and R49Cneo/R49Cneo homozygous mice.

From: αA-crystallin R49Cneomutation influences the architecture of lens fiber cell membranes and causes posterior and nuclear cataracts in mice

A. Slit lamp analysis*

Genotype

Phenotype

Age Group

Total

 

Nuclear and posterior changes by slit lamp biomicroscopy

<2 month

2–3 months

>4 months

 

WT

 

0/4

0/4

2/9

2/17 (0.12)

WT/R49Cneo

 

3/6

14/22

7/7

24/35 (0.68)

R49Cneo/R49Cneo

 

4/5

5/7

13/14

22/26 (0.85)

B. Histological analysis*

Genotype

Phenotype

Age Group

Total

 

Swollen cells and/or posterior changes by histology

<1 month

2–3 months

>4 months

 

WT

 

0/5

1/4

1/7

2/16 (0.13)

WT/R49Cneo

 

4/11

2/4

2/3

8/18 (0.44)

R49Cneo/R49Cneo

 

4/5

3/4

6/8

13/17 (0.76)

  1. * For each age group, the total number of mice analyzed is shown in the denominator, and the number of mice demonstrating the phenotype is shown in the numerator. The final columns show the total number of mice of each genotype that demonstrate a phenotype, with the proportion given in parentheses.