Human Heredity: Principles and Issues (MindTap Course List)
11th Edition
ISBN: 9781305251052
Author: Michael Cummings
Publisher: Cengage Learning
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Chapter 5, Problem 13QP
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Which of these definitions of heritability is most correct?
a)The total amount of phenotypic variation in a population.
b) The total amount of genetic variation in a population.
c) The proportion of phenotypic variation in a population that is due to genetic factors.
d) The proportion of phenotypic variation in a population that is due to environmental factors.
A given autosomal locus has three possible alleles (A1, A2, and A3). Assuming that the numbers of individuals with the six possible genotypes are as follows, what would be the frequency of the A1 allele in the population?
A1A1 = 30 A1A2 = 27 A2A2 = 12
A1A3 = 17 A2A3 = 10 A3A3 = 4
What would be the frequency of the A3A3 genotype? Assume the population is under Hardy-Weinberg equilibrium.
A.
0.182
B.
0.27
C.
0.03
D.
0.317
E.
0.107
F.
0.09
There are two types of alleles:
Type B1 and Type B2
(In total there are 10)
Type B1 has 6
Type B2 has 4
Question:
What is the probability of an individual in the offspring generation being homozygous [p^2] for B1?
What is the probability of an individual in the offspring generation being homozygous [q^2] for B2?
What is the probability of an individual in the offspring gen being heterozygous[2pq]?
Chapter 5 Solutions
Human Heredity: Principles and Issues (MindTap Course List)
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- Why are monozygotic twins who are reared apart so useful in the calculation of heritability?arrow_forwardIf there are five alleles at a locus, how many genotypes can there be at this locus? How many different kinds of homozygotes can there be? How many genotypes and homozygotes can there be with eight alleles at a locus?arrow_forwardIn human population X, consider the simple Mendelian trait for freckles. F is the dominant allele and f is the recessive allele. Individuals who are homozygous dominant (FF) or heterozygous (Ff) for the trait express freckles. Individuals who are homozygous recessive (ff) for the trait do not express freckles. In this population, 30% (0.3) of the alleles are recessive (f) and 70% (0.7) are dominant (F). Q1. Use the Hardy-Weinberg equation to determine the genotype frequencies we should expect in the next generation. Be sure to show your work. Q2. You have collected data on the observed genotype frequencies of the next generation. They are: 60% FF, 30% Ff, and 10% ff. Based on these observations and your expectations, is this trait currently evolving in this population? Why or why not? Show your work.arrow_forward
- In a population of 1000 individuals, 180 have kinky hair, 360 have wavy hairy, and the rest have straight hair. Let us assume that hair type is governed by a pair of alleles, and there are two types of alleles, S (kinky) and s (straight), with the heterozygote condition being wavy. Compute for the allelic frequencies for hair type in the population. Albinism is a rare genetic condition, occurring in only one in every 17,000 to 22,000 individuals in the world (Campbell et al. 2003; Gronskov et al. 2007). a. What can you conclude about the allelic frequency of the a allele globally? b. Where do you think the a allele would be more commonly found, among the heterozygotes (Aa) or the homozygote recessives (aa)? Why do you say so?arrow_forwardIn a population of 1000 individuals, 180 have kinky hair, 360 have wavy hairy, and the rest have straight hair. Let us assume that hair type is governed by a pair of alleles, and there are two types of alleles, S (kinky) and s (straight), with the heterozygote condition being wavy. Compute for the allelic frequencies for hair type in the population. Albinism is a rare genetic condition, occurring in only one in every 17,000 to 22,000 individuals in the world (Campbell et al. 2003; Gronskov et al. 2007). a. What happens to an individual who is albino (aa) or who has very low or lacks melanin pigments in the hair, skin and eyes? b. Based on your answer in c, how would you explain the frequency of the a allele?arrow_forwardWhich of the following choices accurately describe what makes one person different from another with regard to traits (such as height) that have a very high heritability? Choose all that apply a) What makes us different is not that we have different genes, but that we have different alleles of many of those genes b) What makes us different from each other is that we have different genes from each other c) Random factors during development is the most significant causes of differences between people d) Most of us have exactly the same genes and alleles, and it’s the environment we were raised in that makes us different e) None of the other choices are accuratearrow_forward
- Tay–Sachs disease is an autosomal recessive disorder. Among Ashkenazi Jews, the frequency of Tay–Sachs disease is 1 in 3600. Assuming the Ashkenazi population is in Hardy-Weinberg equilibrium, what proportion of the population is expected to be carriers (e.g. heterozygous) for the Tay–Sachs allele?arrow_forwardWhat is a Mendelian population? How is the gene pool of a Mendelian population usually described?arrow_forwardAssume for simplicity that height is a discrete characteristic that is affected most strongly by a single locus with two alleles, T and S. Homozygous TT are taller than average, heterozygous TS are of average height, and homozygous SS are shorter than average. a) In the Dutch population, the results of height on fertility in males is an example of? b) Would your answer above change for the Dutch women? c) What about the American men and women? d) Can you provide an explanation for the discrepancies in this phenomenon between the Dutch and American populations?arrow_forward
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