Biology: Life on Earth with Physiology (11th Edition)
11th Edition
ISBN: 9780133923001
Author: Gerald Audesirk, Teresa Audesirk, Bruce E. Byers
Publisher: PEARSON
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Chapter 11, Problem 2MC
Summary Introduction
Introduction:
An organism’s genotype is the number of different alleles for a particular trait present in it. If the organism carries the same type of allele for a particular type of gene, it is homozygous for that particular gene. If it carries two different type of allele, it is heterozygous for that gene.
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Color blindness in men is controlled by a recessive gene located on the X chromosome. Can a brother and sister with color blindness have another normal brother?
A. Yes, if the mother is a carrier.
B.Yes, if the mother is homozygous.
C.Yes, if the father is heterogametic.
D.Yes, if the father is a carrier.
Which of the following statements accurately represents the difference between a gene and a locus?
a. A gene is dominant, and a locus is recessive.
b. A locus and a gene are essentially the same - there is no difference.
c. A locus occurs in diploid cells, and a gene occurs in a haploid cell.
d. A locus is a phenotype and a gene is a genotype.
Phenylketonuria (PKU) is a disease that results from a recessive gene. Suppose that two unaffected parents produce a child with PKU. a. What is the probability that a sperm from the father will contain the PKU allele? b. What is the probability that an egg from the mother will contain the PKU allele? c. What is the probability that their next child will have PKU? d. What is the probability that their next child will be heterozygous for the PKU gene?
Chapter 11 Solutions
Biology: Life on Earth with Physiology (11th Edition)
Ch. 11.1 - describe the relationships among chromosomes, DNA,...Ch. 11.1 - Prob. 2CYLCh. 11.2 - distinguish between self-fertilization and...Ch. 11.2 - Prob. 2CYLCh. 11.3 - Sudden Death on the court Many traits, in humans...Ch. 11.3 - describe the pattern of inheritance of a trait...Ch. 11.3 - Prob. 1TCCh. 11.3 - Prob. 2CYLCh. 11.3 - Prob. 3CYLCh. 11.4 - Prob. 1CYL
Ch. 11.4 - Prob. 1TCCh. 11.4 - Prob. 2CYLCh. 11.4 - Prob. 2TCCh. 11.4 - Prob. 3CYLCh. 11.5 - Prob. 1CSCCh. 11.5 - Prob. 1CYLCh. 11.5 - Prob. 1HYEWCh. 11.5 - Prob. 1TCCh. 11.5 - explain how polygenic inheritance and...Ch. 11.6 - describe how the patterns of inheritance differ...Ch. 11.7 - Prob. 1CYLCh. 11.7 - explain why most sex-linked traits are controlled...Ch. 11.7 - describe the pattern of inheritance of sex-linked...Ch. 11.8 - Prob. 1CSRCh. 11.8 - use pedigrees to determine the pattern of...Ch. 11.8 - Prob. 1ETCh. 11.8 - Prob. 1TCCh. 11.8 - Prob. 2CYLCh. 11.8 - Prob. 2ETCh. 11 - Prob. 1ACCh. 11 - An organism is described as Rr, with red coloring....Ch. 11 - In certain cattle, hair color can be red...Ch. 11 - Prob. 1MCCh. 11 - Define the following terms: gene, allele,...Ch. 11 - Prob. 2ACCh. 11 - Prob. 2FIBCh. 11 - Prob. 2GPCh. 11 - Prob. 2MCCh. 11 - Prob. 2RQCh. 11 - Prob. 3FIBCh. 11 - Prob. 3GPCh. 11 - Prob. 3MCCh. 11 - Prob. 3RQCh. 11 - Genes that are present on one sex chromosome but...Ch. 11 - Prob. 4GPCh. 11 - Prob. 4MCCh. 11 - Prob. 4RQCh. 11 - Prob. 5FIBCh. 11 - Prob. 5GPCh. 11 - Prob. 5MCCh. 11 - Prob. 5RQCh. 11 - Prob. 6GPCh. 11 - Prob. 6RQCh. 11 - In the couple described in Problem 6, the woman...
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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
- Phenylketonuria (PKU) is a disease that results from a recessive gene.Suppose that two unaffected parents produce a child with PKU. a. What is the probability that a sperm from the father will contain the PKU allele?b. What is the probability that an egg from the mother will contain the PKU allele?c. What is the probability that their next child will have PKU?d. What is the probability that their next child will be heterozygous for the PKU gene?arrow_forwardEdward was found to be heterozygous (Ss) for the sickle-cell trait. The alleles represented by the letters S and s are a. on the X and Y chromosomes. b. linked. c. on homologous chromosomes. d. both present in each of Edward’s sperm cells.arrow_forwardIn humans, the ability to roll one's tongue is a dominant trait (R). A woman who can roll her tongue is married to a man who cannot roll his tongue. The couple's daughter, Brie, can roll her tongue, but their son, Michael, cannot. What gametes does the mother produce? а. R b.r c. R and r d. Rr e. RR QUESTION 67 Please read the scenario below; then, answer the question (in bold) that follows. In humans, the ability to roll one's tongue is a dominant trait (R). A woman who can roll her tongue is married to a man who cannot roll his tongue. The couple's daughter, Brie, can roll her tongue, but their son, Michael, cannot. What gametes does the father produce? а. R Ob.r c. R and r d. Rr e. RRarrow_forward
- An organism that has two different alleles for a single trait is said to be for that trait. Select one: O O O a. heterologous b. heterozygous c. homozygous d. haploid e. diploidarrow_forwardThe father has curly hair; the mother has also curly hair. Will it be possible for their offspring to have straight hair since both parents are curly? a. No, it is very impossible to have a child with straight hair. b. Yes, it is possible for their offspring to have straight hair if the mother also has black hair. c. Yes, all of their offspring will have straight hair. d. Yes, the parents will have offspring with straight hair if the parents are heterozygous for traits. e. Yes, the parents will have offspring with straight hair if the parents are homozygous for the trait.arrow_forwardHoney Bees are unusual in that male bees (drones) have only one copy of each gene, while female bees have two copies of each gene. That is because drones develop from eggs that have not been fertilised by sperm cels. In bees, the trait of long wings is dominant over short wings, and the trait of black eyes is dominant over white eyes. If a drone with short wings and black eyes was mated to a queen bee that is heterozygous for both genes, what are the predicted genotypes and phenotypes of male and female offspring. What are the phenotypic ratios if we assume an equal number of male and female offspring?arrow_forward
- The chart below is showing 4 generations of a family that is affected by a hereditary disease. a. Is the disorder being tracked dominant or recessive? How do you know? b. There is only one possible genotype for person C. True or False? c. What are the possible genotypes for person A? d. What are the possible genotypes for person B?, e. If two people with the same genotypes as person C's spouse and person A's spouse had a child, what is the probability that the child will be affected by this genetic disorder? (draw a Punnett square using the correct genotypes to help you). % chance offspring will be affected % chance offspring will not be affectedarrow_forwardHemophilia is a disease caused by a gene found on the X chromosome. Therefore, it is a sex-linked disease which is caused by the recessive allele. Suppose, a man with hemophilia marries a woman who is homozygous dominant for the trait. Predict the genotype of the man. (XH = normal; Xh= hemophiliac) * a. XH Y b. XHXh c. XhXh d. Xh Yarrow_forwardWhich statement about an individual that is homozygous for an allele is FALSE? Select one: a. Its parents were necessarily homozygous for that allele. b. Each of the gametes it produces will contain one copy of that allele. c. It will pass that allele to its offspring. d. It is true-breeding with respect to that allele. e. Each of its cells possesses two copies of that allele.arrow_forward
- Fragile X is a disorder which causes mental impairment in affected individuals. The trait which is due to a mutation in the FMR1 gene on the X chromosome is inherited in a recessive manner. An unaffected son was born to an affected man and an unaffected woman. The woman’s mother was affected while the father was normal. a. Indicate the gene notation. b. Give the genotype of the son. c. Is it possible for the couple to have an affected daughter? affected son? Derive the genotypic and phenotypic ratios for the offspring. Show and label your solutions properly. d. If the couple has four children, what is the probability that they will have three normal daughters and one normal son?arrow_forwardIn a certain breed of dogs, a gene (L) codes for hair length. The dominant trait is short hair and the recessive is long hair. Suppose a heterozygous female dog and a homozygous recessive male dog mate. What is the male dog’s genotype and the female dog’s genotype? What is the male dog’s phenotype and the female dog’s phenotype? What will be the genotypic ratio for the offspring from these dogs? What will be the phenotypic ratio for the offspring from these dogs?arrow_forwardWhich statement about the pattern of inheritance for a recessive X-linked allele is true? A. Unaffected parents can produce daughters who are affected. B. Unaffected parents can have sons who are affected and daughters who are carriers. C. Unaffected fathers can be carriers. D. Affected parents do not produce affected children. E. Every affected person has an affected parent.arrow_forward
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