EBK BIOLOGY
10th Edition
ISBN: 9780133556209
Author: *BYERS
Publisher: PEARSON CUSTOM PUB.(CONSIGNMENT)
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Chapter 10, Problem 7GP
In humans, one of the genes determining color vision is located on the X chromosome. The dominant form (C) produces normal color vision; red-green color deficiency (c) is recessive. If a man with normal color vision marries a color-deficient woman, what is the probability of them having a color-deficient son? A color-deficient daughter?
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In humans, one of the genes determining color vision islocated on the X chromosome. The dominant form (C )produces normal color vision; red-green color deficiency(c) is recessive. If a man with normal color visionmarries a color-deficient woman, what is the probabilityof them having a color-deficient son? A color-deficientdaughter?
A common kind of red-green blindness in humans is caused by the presence of a sex-linked recessive gene c, whose normal allele is c+. Using these genes, what are the possible genotypes and their corresponding phenotypes in males and females? Can two colorblind parents produce a normal son? (b) A normal daughter? (c) Can two normal parents produce a colorblind son? (d) a colorblind daughter?
Consider a couple: a woman who is homozygous for a recessive mutation that causes X-linked colorblindness, and a man with full color vision (he does not carry a copy of the mutation).
a) What is the probability that a son of this couple will be colorblind?
b) What is the probability that a daughter of the couple will be colorblind?
Chapter 10 Solutions
EBK BIOLOGY
Ch. 10 - Fill-in-the-Blank The physical position of a gene...Ch. 10 - Define nondisjunction, and describe common...Ch. 10 - In certain cattle, hair color can be red...Ch. 10 - Prob. 2GPCh. 10 - In the edible pea, tall (T) is dominant to short...Ch. 10 - In tomatoes, round fruit (R) is dominant to long...Ch. 10 - In the tomatoes of Problem 4, an F1 offspring...Ch. 10 - Prob. 6GPCh. 10 - In humans, one of the genes determining color...Ch. 10 - In the couple described in Problem 7, the woman...
Ch. 10 - An organism is described as Rr, with red coloring....Ch. 10 - 2. The inheritance of multiple traits depends on...Ch. 10 - Fill-in-the-Blank Many organisms, including...Ch. 10 - 4. Genes that are present on one sex chromosome...Ch. 10 - 5. When the phenotype of heterozygotes is...Ch. 10 - 1. Define the following terms: gene, allele,...Ch. 10 - 2. Explain why genes located on the same...Ch. 10 - 3. Define polygenic inheritance. Why does...Ch. 10 - What is sex linkage? In mammals, which sex would...Ch. 10 - What is the difference between a phenotype and a...Ch. 10 - 6. In the pedigree of part (a) of Figure 11–22, do...Ch. 10 - Sometimes the term gene is used rather casually....Ch. 10 - In an alternate universe, all the genes in all...Ch. 10 - Prob. 3AC
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Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, biology and related others by exploring similar questions and additional content below.Similar questions
- Human sex chromosomes are XX for females and XY for males. a. With respect to an X-linked gene, how many different types of gametes can a male produce? b. If a female is homozygous for an X-linked allele, how many different types of gametes can she produce with respect to this allele? c. If a female is heterozygous for an X-linked allele, how many different types of gametes can she produce with respect to this allele?arrow_forwardThe following pedigree shows the pattern of inheritance of red-green color blindness in a family. Females are shown as circles and males as squares; the squares or circles of individuals affected by the trait are filled in black. What is the chance that a son of the third-generation female indicated by the arrow will be color blind if the father is not color blind? If he is color blind?arrow_forwardIn humans, color vision depends on genes encoding three pigments. The R (red pigment) and G (green pigment) genes are close together on the X chromosome, whereas the B (blue pigment) gene is autosomal. A recessive mutation in any one of these genes can cause color blindness. Suppose that a color-blind man married a woman with normal color vision. The four sons from this marriage were color-blind, and the five daughters were normal. Specify the most likely genotypes of both parents and their children, explaining your reasoning. (A pedigree drawing will probably be helpful.) (Problem 50 is by Rosemary Redfield.)arrow_forward
- Duchenne muscular dystrophy (DMD), marked by muscular degeneration, results from an X- linked recessive gene. Thus, a female who is heterozygous for this gene and does not have the disease can be a carrier. What kind of offspring can you expect from a DMD-affected male and a carrier female? Can there be a carrier male?arrow_forwardColour-blindness is the result of an X-linked recessive allele, Xc. The allele for normal eyesight is XC. (a) A woman with normal colour vision whose father was colour-blind marries a colour-blind man. Give the genotypes and phenotypes of their children. What ratio of their children can be expected to be colour-blind? (b) A man with normal colour vision whose father was colour-blind marries a woman carrier of the colour-blind allele. What is the likelihood that their children will be colour-blind? Carriers of the trait?arrow_forwardIn humans color vision is X-linked, the gene for color vision is located on the X chromosome but is absent on the Y chromosome. Normal color vision (XN) is dominant over colorblindness (Xn). Suppose a colorblind man fathers the children of a woman with genotype XNXN. What is the genotype of the father? What proportion of daughters will be colorblind? What proportion of the sons will be colorblind?arrow_forward
- In humans, blue eyes are inherited as a recessive autosomal trait and color blindness is an X-linked recessive trait. A woman with blue eyes and normal color vision (her father was colorblind) marries a man who has normal color vision. The man has brown eyes, but his mother had blue eyes. What is the probability that this couple will have a child with normal vision and blue eyes?arrow_forwardA color-blind man marries a woman with normal vision whose father was color-blind. Remember that color-blindness is an X-linked recessive trait. Hint: see figure 12.7 in book. A) What is the probability that their first child will be a color-blind daughter? B) What is the probability that their first son will be color-blind?arrow_forwardGlucose-6-phosphate dehydrogenase deficiency (G6PD) is inherited as an X-linked recessive gene in humans. A woman whose father suffered from G6PD marries a normal man. What proportion of their sons is expected to be G6PD? If the husband were not normal but G6PD deficient, would you change your answer to part (a)?arrow_forward
- Red-green color blindness is inherited as an X-linked recessive (Xc). If a color-blind man marries a woman who is heterozygous for normal vision, what would be the expected phenotypes of their children with reference to this character? In your answer, specify in your phenotype descriptions the gender of the children. (For example, don’t just say 75% of the children would be colorblind – you would instead say 100 % of the daughters would be colorblind and 50% of the sons would be colorblind. Note that this is not a correct answer; it is just to give you an idea of how to explain the correct phenotypes of the cross.)___arrow_forwardA man who is an achondroplastic dwarf with normal vision marries a color-blind woman of normal height. The man's father was 6 feet tall, and both the woman's parents were of average height. Achondroplastic dwarfism is autosomal dominant, and red-green color blindness is X-linked recessive. a) How many of their daughters might be expected to be color-blind dwarfs? b)What proportion of their sons would be color-blind and of normal height? c)They have a daughter who is a dwarf with normal color vision. What is the probability that she is heterozygous for both genes?arrow_forwardGlucose-6-phosphate dehydrogenase deficiency (G6PD) is inherited as a recessive allele of an X-linked gene in humans. A woman whose father suffered from G6PD marries a normal man.(a) What proportion of their sons is expected to be G6PD?(b) If the husband was not normal but was G6PD deficient, would you change your answer in part (a)arrow_forward
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