HUMAN HEREDITY (LL)-W/MINDTAP ACCESS
11th Edition
ISBN: 9781305717022
Author: Cummings
Publisher: CENGAGE L
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Chapter 4, Problem 5QP
Analysis of Autosomal Recessive and Dominant Traits
- a. What pattern of inheritance is suggested by the following pedigree?
- b. For genotype assignment, assume that the pedigree is for an autosomal dominant trait and that the affected male in the first generation is heterozygous. Assign genotypes to all other individuals in the pedigree.
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a. The pedigree follows the inheritance of a relatively common trait. Is the trait most likely autosomal dominant, autosomal recessive, X-linked dominant, or X-linked recessive? Explain your reasoning.
b. If the couple marked with a “*” had another child, what is the probability that it would be an affected daughter? (Note: this is a compound outcome.)
Examine the pedigree and answer the following questions; shaded individuals show the trait; genotypes are all unknown.
The individual marked with the question mark is of an unknown genotype but lacks the trait.
A. What mode of inheritance is the most likely, autosomal recessive or autosomal dominant? State your rationale for full credit.
B. What is the genotype of the individual designated with the question mark? (Heterozygous, homozygous, or unknown).
C. What are the genotypes of the parents in generation I? (Heterozygous, homozygous, or unknown).
D. What are the genotypes of the three children of generation IV? (Heterozygous, homozygous, or unknown).
Examine the pedigree and answer the following questions; shaded individuals show the trait; genotypes are all unknown.
The individual marked with the question mark is of an unknown genotype but does have the trait.
A. What mode of inheritance is the most likely for this trait, autosomal recessive or autosomal dominant? State your rationale for full credit.
B. What is the genotype of the individual marked with the question mark? (Heterozygous, homozygous, or unknown)
Chapter 4 Solutions
HUMAN HEREDITY (LL)-W/MINDTAP ACCESS
Ch. 4.3 - Does a pedigree drawn from the available...Ch. 4.3 - Prob. 2EGCh. 4.7 - Did the fact that Prince Albert and Queen Victoria...Ch. 4.7 - Which members of the pedigree could have been...Ch. 4 - Pedigree analysis is a fundamental tool for...Ch. 4 - Pedigree analysis is a fundamental tool for...Ch. 4 - Pedigree analysis is a fundamental tool for...Ch. 4 - Pedigree Analysis Is a Basic Method in Human...Ch. 4 - Pedigree Analysis Is a Basic Method in Human...Ch. 4 - Pedigree Analysis Is a Basic Method in Human...
Ch. 4 - Pedigree Analysis Is a Basic Method in Human...Ch. 4 - Analysis of Autosomal Recessive and Dominant...Ch. 4 - Analysis of Autosomal Recessive and Dominant...Ch. 4 - Use the following information to respond to the...Ch. 4 - Analysis of Autosomal Recessive and Dominant...Ch. 4 - Analysis of Autosomal Recessive and Dominant...Ch. 4 - A proband female with an unidentified disease...Ch. 4 - Analysis of Autosomal Recessive and Dominant...Ch. 4 - Prob. 12QPCh. 4 - Analysis of Autosomal Recessive and Dominant...Ch. 4 - Analysis of Autosomal Recessive and Dominant...Ch. 4 - Analysis of X-Linked Dominant and Recessive Traits...Ch. 4 - Prob. 16QPCh. 4 - Analysis of X-Linked Dominant and Recessive Traits...Ch. 4 - Analysis of Autosomal Recessive and Dominant...Ch. 4 - Analysis of X-Linked Dominant and Recessive Traits...Ch. 4 - Analysis of X-Linked Dominant and Recessive Traits...Ch. 4 - Analysis of X-Linked Dominant and Recessive Traits...Ch. 4 - Analysis of X-Linked Dominant and Recessive Traits...Ch. 4 - Prob. 23QPCh. 4 - Prob. 24QPCh. 4 - Variations in Phenotype Expression Define...Ch. 4 - Prob. 26QPCh. 4 - Variations in Phenotype Expression A genetic...Ch. 4 - Variations in Phenotype Expression Explain how...
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- A. Identify the pattern of inheritance in the pedigree below. B. Provide two pieces of evidence that you used to come to this conclusion. C. Identify the genotypes of individuals II-1 and III-2 (at the arrows)arrow_forwarda. On the basis of this pedigree, what is the most likely mode of inheritance for the disease? Explain your reasoning. b. Based your answer to part a, give the most likely genotypes for all family members in the pedigree.arrow_forwardthe pedigree below shows the inheritance of a newly identified eye color gene. Assume 100% penetrance and expressivity. Use the pedigree to find: 1. Identify the mode of inheritance (either autosomal dominant, or autosomal recessive) 2. Argue why your mode of inheritance must be correct. Your argument should cite specific individuals from the pedigree. (For example, the top left individual is person I-1).arrow_forward
- Background Information: Autosomal Dominant/Recessive- The trait is encoded by a single genetic locus with two segregating alleles: One dominant (A) and one recessive (a). The locus is not on a sex chromosome, and is not linked to any other trait unless specified.Autosomal Codominance- This mode is the same as Autosomal Dominant/Recessive, except that neither allele isdominant or recessive and heterozygous individuals have a distinct phenotype. X-linked Dominant/Recessive - The trait is encoded by a single genetic locus with two segregating alleles: One dominant (A) and one recessive (a). The locus is located on the X-chromosome, and is not linked to any other trait unless specified.X-linked Codominance- This is the same as X-linked dominant/recessive, except that heterozygous females (twocopies of the X-chromosome) experience a distinct phenotype relative to females that are homozygous for either of the two alleles. Males will be segregating with two phenotypes (because they only have…arrow_forwardUsing the pedigree chart attached: Above is a pedigree for colorblindness. Based on the pedigree, is the disease dominant or recessive and is it sex-linked or autosomal? Why? Furthermore, what is the probability that 18 on this chart is affected but the condition, and what is the probability that 18 is a carrier? Why? Are the probability of being a carrier and an affected individual different? Why?arrow_forwardPlease consider the following pedigree. Assume that people who marry in to the family do not carry the allele unless otherwise indicated. Assume complete penetrance. image attached a. Is it possible for the inheritance pattern for the trait illustrated in this pedigree to be as a result of each of the following? Answer yes or no. (i) an autosomal recessive allele (AR)(ii) an autosomal dominant allele (AD)(iii) a X-linked recessive allele (XR)(iv) a X-linked dominant allele (XD) b. Provide a set of parents that definitively supports your answers in (a).arrow_forward
- a. Determine if the pedigree below can be for a trait that is X-linked traits. Write the genotype of each individual next to the symbol. b. Is it possible that this pedigree is for an X-linked recessive trait? c. What can you conclude about the children if both parents are affected with an X-linked recessive trait?arrow_forwardPlease consider the following pedigree. Assume that people who marry in to the family do not carry the allele. Assume complete penetrance. I II III 3 IV 1 2 a. Is it possible for the inheritance pattern for the trait illustrated in this pedigree to be as a result of each of the following? Answer yes or no. (i) an autosomal recessive allele (AR) (ii) an autosomal dominant allele (AD) (iii) a X-linked recessive allele (XR) (iv) a X-linked dominant allele (XD) b. Based strictly on the characteristic patterns of inheritance that define the four different options in (a), give a definitive motivation for the most likely mode of inhertance.arrow_forward. The pedigree below was obtained for a rare kidney disease.a. Deduce the inheritance of this condition, stating your reasons. b. If persons 1 and 2 marry, what is the probability that their first child will have the kidney disease?arrow_forward
- Working with the definitions of penetrance and expressivity, analyze the following pedigree and assume that the father of the proband is homozygous for a rare trait. (Consider a rare trait here to be less than 1 in 30,000.) What pattern of inheritance other than autosomal recessive could explain this pedigree? In particular, explain the genotype and phenotype of the proband (arrow).arrow_forward15. The following pedigree shows inheritance of Huntington's disease, a fatal genetic disorder that causes neurodegeneration. Since signs and symptoms usually do not appear until adulthood, many who are carriers may not realize their risk of passing on the disease-causing allele. The following pedigree represents a family in which some people are affected by Huntington's disease. Reeessive Trit er btmnt be Mec yplicalty Hinheteearrow_forwardSickle cell anemia is an inherited red blood cell disorder in which there are not enough healthy red blood cells to carry oxygen throughout the body. The allele that causes sickle-cell anemia is autosomal recessive (s), and the dominant allele can be represented by S. How many offspring will be affected by the disorder if the mother is a carrier, and the father appears to be normal? (Include the gender) a. b. How many will become carriers? (include the gender) A- 三三三 四 四 II !!arrow_forward
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