Question

= = = 6 7 7 8 2. Individual IV-1 is expecting a child with individual IV-7. Assuming a fully penetrant trait, what is the lik

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

d) 1/8 is correct.

Since II-4 and II-5 are both normal but have affected children, and the disease affects both males and females, the disease is inherited as an Autosomal Recessive disorder.

This means that affected individuals are Homozygous recessive. If A allele leads to normal phenotype and the a allele leads to the mutant phenotype, affected individuals have the genotype aa.

So,

Probability of child of IV-4 and IV-7 developing the disorder
    = Probability of inheriting the a allele from IV-4 * Probability of inheriting the a allele from IV-7

Individual IV-7 has the genotype aa, and he will transmit the a allele to all progeny.

Probability of inheriting the a allele from IV-7 = 1

Now,

Individual I-2 is affected. Thus, they will pass on the a allele to all their progeny, including II-2, who is an ancestor of IV-4. Since II-2 is normal, their genotype is Aa.

Now,
Probability of II-2 passing on the a allele to III-2 (IV-4's mother) = 1/2

Probability of III-2 passing on the a allele to IV-4 = 1/2

Probability of IV-4 passing on the a allele to her child = 1/2.

The child of IV-4 and IV-7 will be affected only if they inherit the a allele from both IV-4 and IV-7. That probability is a product of the probability of the child inheriting the a allele from IV-4, the probability of IV-4 inheriting the a allele from III-2, and the probability of III-2 inheriting the a allele from II-2; or:

Pr(Child inheriting a from IV-4) = Pr(a allele from IV-4 --> Child) * Pr(a allele from III-2 --> IV-4) * Pr(a allele from II2-2 --> III-2) = 1/2 * 1/2 * 1/2 = 1/8

Therefore,
Probability of child of IV-4 and IV-7 developing the disorder
    = 1/8 * 1 = 1/8

Add a comment
Know the answer?
Add Answer to:
= = = 6 7 7 8 2. Individual IV-1 is expecting a child with individual...
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
  • Caculating probabilities with human pedigree charts Homework Unanswered If individuals IV.4 and IV.5 have a child...

    Caculating probabilities with human pedigree charts Homework Unanswered If individuals IV.4 and IV.5 have a child that is unaffected, what is the probability that the child is still a carrier for the recessive allele? 1 2 2 3 4 5 6 7 1 II 12 3 10 4 5 6 7 8 9 11 IV 1 2 3 4 5 6 7 8 100% В 50% 75% C 25% E 0%

  • (a) What is the genotype of individual I-1? (b) What is the genotype of individual I-2?...

    (a) What is the genotype of individual I-1? (b) What is the genotype of individual I-2? (c) What is the genotype of individual IV-3? (d) What is the genotype of individual IV-6? PART B If individuals IV-3 and IV-6 were to have children: (e) What is the probability that these children will express this X-linked dominant trait?   % (f) If they only have sons, what is the probability that these sons will express this X-linked dominant trait?   % (g) If...

  • 1. What is the risk of Fabry disease in Mary's unborn child (IV.2 in the pedigree),...

    1. What is the risk of Fabry disease in Mary's unborn child (IV.2 in the pedigree), provided that her nephew (IV.1) does have Fabry disease, and how is it calculated? 2 II III IV 1 A. The risk is 1/8: 7 that III.7 is a heterozygous carrier, reduced by 50% to the next generation, and with a 50% chance of a boy = /*/*/ -1/8 B The risk is 1/4: 7 that III.7 is a heterozygous carrier, reduced by 50%...

  • please provide an explanation for both questions! Thank You! 9. Consider the pedigree to the right,...

    please provide an explanation for both questions! Thank You! 9. Consider the pedigree to the right, displaying the inheritance of a rare recessive autosomal disease which is fully penetrant. What is the likelihood that the child will be affected? a. 1/2 b. 27/81 c. 1/4 d. 1/36 e. 1/64 10. Consider the following pedigree from a human family containing a male with Klinefelter syndrome (a set of abnormalities seen in XXY individuals; indicated with a shaded box). In each, A...

  • QUESTION 9 5 pe If the characteristic depicted in the pedigree below is rare and subject...

    QUESTION 9 5 pe If the characteristic depicted in the pedigree below is rare and subject to complete penetrance, it is likely to be X-linked recessive? 5 6 7 -OOO No, because individuals ll-2 and 11-4 are not affected No, because individuals 111-4 and III-6 are not affected Yes, because individuals III-4 and III-6 are not affected Yes, because only females are affected in generation 11 1. The gene for cystic fibrosis (normal dominant allele CF and abnormal recessive allele...

  • this is all that im given Question 3: (4 points) Consider the following pedigree: O O...

    this is all that im given Question 3: (4 points) Consider the following pedigree: O O 1 2 3 4 5 Characterize each of the following modes of inheritance as: Impossible, Possible, or Most likely. Justify your answers. a. Autosomal dominant b. Autosomal recessive X-linked dominant d. X-linked recessive e. Y-linked f. Going with the most likely mode of inheritance .... Assume individual V-1 marries a phenotypically normal male. What is the likelihood that their first child is affected with...

  • 2. (a) Consider the following matrices: A = [ 8 −6, 7 1] , B =...

    2. (a) Consider the following matrices: A = [ 8 −6, 7 1] , B = [ 3 −5, 4 −7] C = [ 3 2 −1 ,−3 3 2, 5 −4 −3 ] (i) Calculate A + B, (ii) Calculate AB (iii) Calculate the inverse of B, (iv) Calculate the determinant of C. (b) The points P, Q and R have co-ordinates (2, 2, 1), (4, 1, 2) and (5, −1, 4) respectively. (i) Show that P Q~ =...

  • 4. What is the chance of the next child of individuals 1-3 and II-4 is affected?...

    4. What is the chance of the next child of individuals 1-3 and II-4 is affected? 5. (More Challenging) II-5 marries someone with the trait, what is the chance of their child affected? Example 3 ho OD DO 00 m OOO 1. Is this a dominant or recessive trait? Explain why. 2. What are the genotypes of l-1 and 1-2? 3. What is the chance of the next child of individuals 11-5 and Il-6 is affected? 4. If unaffected cousins...

  • Paragraph - Individual 5 The 2 alleles at the ALK locus are denoted ALK+ and ALK....

    Paragraph - Individual 5 The 2 alleles at the ALK locus are denoted ALK+ and ALK. The 3 alleles at the ABO blood group locus are A, B (co-dominant) and 0 (the 0 allele is recessive to A and B). Example: Individual 5 has a genotype of ALK-ALK- for alkaptonuria and 00 for blood type Genotype Individual 5 ALK-ALK-00 (both mutant ALK alleles and Type O blood) Questions 1. What is the genotype of individual 1 at the ALK and...

  • Problem 3. (7 minutes individual, 8 minutes in group) For the following cash flows, with 1-5%...

    Problem 3. (7 minutes individual, 8 minutes in group) For the following cash flows, with 1-5% per ar a. Draw a fully labeled cash flow diagram b. Calculate the equivalent single cash flow EOY 0 c. Calculate the equivalent single cash flow EOY 6 d. Calculate the equivalent annuity cash flov for EOY 1 to 6 EOCash Flow, s 300 2150 4150 5300

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