M/J/20 ucles 2020 6



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18
0610/41/M/J/20
© UCLES 2020

Colour blindness is a characteristic that is inherited. Colour blindness is more common in males 
than in females.
 
Fig. 6.1 is a pedigree diagram showing the inheritance of colour blindness in a family.
1
2
3
5
6
7
8
4
male with normal
colour vision
male with colour
blindness
female with normal
colour vision
Key:
Fig. 6.1
 (a) 
Define the term 
inheritance
.
...................................................................................................................................................
...................................................................................................................................................
............................................................................................................................................. [1]
 
(b) (i)
Using the symbols 
B
and 
b
, state the genotypes of individual 
5
and individual 

in the 
pedigree diagram.
5
........................................................................................................................................
8
........................................................................................................................................
[3]
610/41 May 2020
it is the transmission of information from generation to generation
XBY
XBY


19
0610/41/M/J/20
© UCLES 2020
(ii) 
Individual 
3
is a carrier of colour blindness because she has one copy of the allele for 
colour blindness but has normal colour vision.

Describe the evidence from Fig. 6.1 that shows that individual 


3
is a carrier.
...........................................................................................................................................
...........................................................................................................................................
...........................................................................................................................................
...........................................................................................................................................
...........................................................................................................................................
...........................................................................................................................................
..................................................................................................................................... [3]
 
(iii)
There was no history of colour blindness in the parents and grandparents of individuals 
1
and 
2
.

Suggest how colour blindness first occurred in the family in Fig. 6.1.


...........................................................................................................................................
...........................................................................................................................................
...........................................................................................................................................
...........................................................................................................................................
..................................................................................................................................... [2]
[Total: 9]
to individuals 5 and 6 copied X chromosomes of their mother and 3 is their 
mother. if she is not carier 5 and 6 won't be colour blindless
They may be gave this from environment during their life

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