2
answers
0
watching
38
views

Cystic fibrosis is a genetic disease caused by mutations in the gene for a chloride ion transport protein. The gene is on chromosome seven. Alleles that cause the disease are recessive in comparison to the normal allele. The phenotype includes effects on the lungs, liver, small intestine and pancreas. Females are infertile. Mucus accumulates in the lungs, making the patients subject to chronic bacterial infections. Cystic fibrosis is one of the most common genetic diseases in Caucasians, with a prevalence of about 1 in 400 people being carriers for a mutant allele.

Suppose a man and a woman are both carriers. What are the possible genotypes of their gametes? Draw a Punnett square. What are the possible genotypes of their children? What are the probabilities these genotypes will appear? What are the corresponding phenotypes?

Now suppose a man is a carrier, but the woman is not. Answer the same questions as above.

For unlimited access to Homework Help, a Homework+ subscription is required.

Unlock all answers

Get 1 free homework help answer.
Get unlimited access
Already have an account? Log in
Keith Leannon
Keith LeannonLv2
17 Jun 2019
Get unlimited access
Already have an account? Log in

Related textbook solutions

Related questions

Weekly leaderboard

Start filling in the gaps now
Log in