Question

A certain disease is caused by a recessive mutant allele. (The wild-type allele is dominant.) However,...

A certain disease is caused by a recessive mutant allele. (The wild-type allele is dominant.) However, the penetrance of the disease is 75%. Two individuals known to be heterozygotes have a child. What is the probability that the child exhibits the disease?

0 0
Add a comment Improve this question Transcribed image text
Answer #1

Normal = AA, Aa

Affected = aa

Aa × Aa

Gametes A a
A AA normal Aa normal
a Aa normal aa affected

Probability of affected child = 1/4

But the disease is only 75% penetrant. So, the probability will be 75% of 1/4 = 75/100 × 1/4 = 3/4 × 1/4 = 3/16.

Answer is 3/16.

Please rate high.

Add a comment
Know the answer?
Add Answer to:
A certain disease is caused by a recessive mutant allele. (The wild-type allele is dominant.) However,...
Your Answer:

Post as a guest

Your Name:

What's your source?

Earn Coins

Coins can be redeemed for fabulous gifts.

Not the answer you're looking for? Ask your own homework help question. Our experts will answer your question WITHIN MINUTES for Free.
Similar Homework Help Questions
  • 6 A human trait that is caused by an autosomal dominant mutant allele has a penetrance...

    6 A human trait that is caused by an autosomal dominant mutant allele has a penetrance of 50%. A man who is heterozygous for this mutant allele marries a woman who is homozygous recessive for the normal allele. If they have two children then what is the probability that both children will show the normal phenotype? O 1/4 o 1/2 03/16 0 7/8 09/16

  • Huntington's disease is caused by the allele H, which is completely dominant to the normal recessive...

    Huntington's disease is caused by the allele H, which is completely dominant to the normal recessive allele h. Consider a couple where the man has the genotype Hh, and the woman has the genotype hh. What is the chance that their first child will develop Huntington's disease? A. 0% B. 25% C. 75% D. 50%

  • In humans, albinism is caused by a recessive allele (a) while normal pigmentation is caused by...

    In humans, albinism is caused by a recessive allele (a) while normal pigmentation is caused by the dominant allele (A). a) If two pigmented parents have an albino child, what must the genotypes of the parents be? b) What is the probability that if they have another child, that child will be albino? c) What is the probability that the next two children are albinos? d) What is the probability that they have one albino and one pigmented child? Be...

  • In humans, sickle-cell anemia is caused by a recessive lethal allele Hbs. A healthy allele is...

    In humans, sickle-cell anemia is caused by a recessive lethal allele Hbs. A healthy allele is denoted by Hba. Following is a table that shows the three possible genotypes, with the associated phenotypes. Genotype Phenotype Hba Hba Healthy (no sign of disease) HbaHbs Healthy (no sign of disease) Hbs Hbs Shows symptoms of sickle-cell anemia What is the probability of two heterozygous individuals giving birth to a child who has a sickle-cell allele, but shows a healthy phenotype? Enter in...

  • 6. Hemochromatosis is an inherited disease caused by a recessive allele. If a woman and her...

    6. Hemochromatosis is an inherited disease caused by a recessive allele. If a woman and her husband, who are both carriers, have three children, what is the probability of each of the following? (a) All three children are of normal phenotype. (b) One or more of the three children have the disease. (c) All three children have the disease. (d) At least one child is phenotypically normal. (Note: It will help to remember that the probabilities of all possible outcomes...

  • Albinism is a genetic disorder caused by an autosomal recessive allele. The dominant allele results in...

    Albinism is a genetic disorder caused by an autosomal recessive allele. The dominant allele results in the wildtype pigmentation. a) If an albino marries a homozygous person for the wildtype pigmentation allele, what would be the expected phenotype and genotype of their children? b) If an albino marries a person with wildtype pigmentation but that carries the albino allele, what would be the expected phenotypes and genotypes of their children? c) Two parents of wildtype pigmentation had an albino child....

  • 2. Achondroplasia is a short-limbed dwarfism that is inherited as an autosomal dominant disease. The mutant...

    2. Achondroplasia is a short-limbed dwarfism that is inherited as an autosomal dominant disease. The mutant allele that causes this form of dwarfism (D) is dominant to the normal allele at this location (d). Individuals who inherit 2 alleles for dwarfism (DD) typically have a very severe form of achondroplasia that causes extreme shortening of the bones and an underdeveloped rib cage. These individuals are usually miscarried or stillborn. Tom and Vonna both have achondroplasia (but each of them has...

  • 7. What type of trait is found the most often in nature? a. mutant trait b....

    7. What type of trait is found the most often in nature? a. mutant trait b. wild-type trait C. dominant trait d. recessive trait 8. A heterozygous person that has one disease allele and one normal allele is referred to as a 9. Tay-Sachs is an autosomal recessive disease. A couple (Jack and Jill) is worried about having a child who has Tay-Sachs, because Jack had a brother with the deadly disease. Since they wanted to have children, they sought...

  • 3. Sickle-cell disease is a genetic condition caused by an autosomal recessive allele which al- fects...

    3. Sickle-cell disease is a genetic condition caused by an autosomal recessive allele which al- fects one in every 500 African American children born in the U.S. One in every ten African Americans is a carrier for the recessive allels. Although sickle cell disease is caused by a single human gene, it is expressed through many different effects throughout the body. The presence of a recessive sickle-cell allele in humans causes the red blood cells to produce abnormal hemoglobin protein...

  • Sickle cell disease is an autosomal recessive disease. Homozygous dominant (SS) and heterozygous (Ss) individuals will...

    Sickle cell disease is an autosomal recessive disease. Homozygous dominant (SS) and heterozygous (Ss) individuals will be non-diseased, but homozygous recessive (ss) individuals will have the disease. A study of sickle cell disease in New York found that in a one year period: 1/1146 of all infants in the state were born with sickle cell disease 1/230 non-hispanic black infants were born with sickle cell disease 1/41,647 non-hispanic white infants were born with sickle cell disease 1/2,320 hispanic infants were...

ADVERTISEMENT
Free Homework Help App
Download From Google Play
Scan Your Homework
to Get Instant Free Answers
Need Online Homework Help?
Ask a Question
Get Answers For Free
Most questions answered within 3 hours.
ADVERTISEMENT
ADVERTISEMENT
ADVERTISEMENT