Concepts of Genetics Plus Mastering Genetics with Pearson eText -- Access Card Package (12th Edition) (What's New in Genetics)
12th Edition
ISBN: 9780134811390
Author: William S. Klug, Michael R. Cummings, Charlotte A. Spencer, Michael A. Palladino, Darrell Killian
Publisher: PEARSON
expand_more
expand_more
format_list_bulleted
Concept explainers
Videos
Textbook Question
Chapter 26, Problem 16PDQ
Achondroplasia is a dominant trait that causes a characteristic form of dwarfism. In a survey of 50,000 births, five infants with achondroplasia were identified. Three of the affected infants had affected parents, while two had normal parents. Calculate the mutation rate for achondroplasia and express the rate as the number of mutant genes per given number of gametes.
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solution
Students have asked these similar questions
Uniparental disomy (UPD) occurs when both chromosomes of a pair or areas from one chromosome in any individual have been inherited from a single parent. Since chromosomal numbers remain the same, cytogenetic analysis will not detect them. Hence, UPD disorders were not described until recently since molecular analysis is required to show that the two chromosomes originated from the same parent.
Read recently published literature regarding UPD, and answer the following questions:
What are the mechanisms that lead to UPD?
Give at least 3 examples of UPD disorders and their clinical consequences:
UPD Disorder
OMIM #
Locus
Type of UPD
Phenotype (include images)
1
2
3
In C. elegans, lon-2 and unc-2 are recessive mutations that are 8 map units apart on the X chromosome. An hermaphrodite who is Lon and Unc is mated to a wild-type male. An F1 hermaphrodite is mated to a wild-type male. What are the expected percentages of the different phenotypes among the male progeny?
Cystic fibrosis in humans is caused by mutations in a single gene and is inherited as an autosomal
(non-sex chromosome) recessive trait. An unaffected couple has two children. The first child has
cystic fibrosis, and the second child is unaffected. What is the probability that the second child is a
carrier (heterozygous) for the mutation that causes the disease?
2/3
1
1/2
3/4
Chapter 26 Solutions
Concepts of Genetics Plus Mastering Genetics with Pearson eText -- Access Card Package (12th Edition) (What's New in Genetics)
Ch. 26 - The ability to taste the compound...Ch. 26 - Determine whether the following two sets of data...Ch. 26 - If the albino phenotype occurs in 1/10,000...Ch. 26 - A prospective groom, who is unaffected, has a...Ch. 26 - In a region of Quebec, Canada, 1 in 22 people are...Ch. 26 - Critics argue that a uniform panel of disorders...Ch. 26 - Others argue that the current testing system...Ch. 26 - HOW DO WE KNOW? Population geneticists study...Ch. 26 - CONCEPT QUESTION Read the Chapter Concepts list on...Ch. 26 - Price et al. [(1999).J. Bacteriol181:2358-2362)...
Ch. 26 - The genetic difference between two Drosophila...Ch. 26 - The use of nucleotide sequence data to measure...Ch. 26 - Prob. 6PDQCh. 26 - What must be assumed in order to validate the...Ch. 26 - In a population where only the total number of...Ch. 26 - If 4 percent of a population in equilibrium...Ch. 26 - Consider a population in which the frequency of...Ch. 26 - If the initial allele frequencies are p = 0.5 and...Ch. 26 - Under what circumstances might a lethal dominant...Ch. 26 - Assume that a recessive autosomal disorder occurs...Ch. 26 - One of the first Mendelian traits identified in...Ch. 26 - Describe how populations with substantial genetic...Ch. 26 - Achondroplasia is a dominant trait that causes a...Ch. 26 - Prob. 17PDQCh. 26 - Prob. 18PDQCh. 26 - A botanist studying water lilies in an isolated...Ch. 26 - A farmer plants transgenic Bt corn that is...Ch. 26 - In an isolated population of 50 desert bighorn...Ch. 26 - To increase genetic diversity in the bighorn sheep...Ch. 26 - What genetic changes take place during speciation?Ch. 26 - Some critics have warned that the use of gene...Ch. 26 - Prob. 25PDQCh. 26 - What are the two groups of reproductive isolating...Ch. 26 - A form of dwarfism known as Ellisvan Creveld...Ch. 26 - The original source of new alleles, upon which...Ch. 26 - A number of comparisons of nucleotide sequences...Ch. 26 - Shown below are two homologous lengths of the...Ch. 26 - Recent reconstructions of evolutionary history are...
Knowledge Booster
Learn more about
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
- An abnormality of the large intestine called intestinal polyposis (IP) is dependent on dominant gene A. A nervous disorder called Huntington’s chorea (HC) is determined by dominant gene H, a lethal gene the effects of which appear on a mean age of 40 years. A and H are on nonhomologous chromosomes. A man carrying the gene A marries a woman carrying the gene H. If this couple had 7 children, what is the chance that at least 2 of their children will survive up to old age? What are the genotypes of the man and his wife?arrow_forwardIn elegans, lon-2 and unc-2 are recessive mutations that are 8 map units apart on the X chromosome. An hermaphrodite who is Lon and Unc is mated to a wild-type male. An F1 hermaphrodite is mated to a wild-type male. What are the expected percentages of the different recombinant phenotypes among the male progeny?arrow_forwardIn man, muscular dystrophy is a condition in which the muscles waste away during early life and may result in a shorter life expectancy. It is due to a sex-linked, recessive gene. A certain couple has five children – three boys (ages 1yr, 3yrs, and 10yrs old) and two girls (ages 5yrs and 7yrs old). The oldest boy shows the symptoms of this disease. You are their family physician and they come to you for advice. What would you tell them about the chances of their other children developing the disease?arrow_forward
- Consider a Droscophilia fly with a genotype of Nn XqYY. The dominant allele of the sex-linked gene specifies a black body and the recessive a white body. The recessive autosomal allele specifies hairy bristles while the dominant allele specifies smooth bristles. i)What is the ploidy of this fly? ii) What would the sex of this fly be? iii)What would the phenotype of this fly be with respect to these two loci?arrow_forwardOculocutaneous Albinism is an inherited autosomal recessive condition caused by a mutation in the tyrosinase (TYR) gene. A male and female who are phenotypically normal, discover through genetic testing that they are both carriers of a TYR mutant allele. What is the probability that their first child will be biologically male and have Oculocutaneous Albinism? Select one: а. 1/8 b. 3/4 c. 1/4 d. 1/16 e. 1/2arrow_forwardConsider an autosomal recessive disease in which an individual must inherit two recessive alleles to display the disease phenotype. What is the probability that a woman who is a heterozygous for the trait and a man who is homozygous for the dominant allele will produce an offspring with the autosomal recessive phenotype? Assume no new mutations occur. Select one 1.) 100% 2.)25% 3.) 0% 4.)50% 5.) More information is neededarrow_forward
- THE MOST COMMON FORM OF ALBINISM, A TOTAL LACK OF SKIN PIGMENT, IS DUE TO A RARE RECESSIVE GENE LOCATED ON CHROMOSOME 11. TWO PARENTS ARE NORMALLY PIGMENTED, BUT EACH PARENT HAS AN ALBINO SIBLING. NO ONE ELSE IN THEIR FAMILY IS ALBINO GOING BACK AT LEAST TWO GENERATIONS. ASSUMING NO MUTATION, WHAT IS THE PROBABILITY THAT THIS COUPLE WILL HAVE AN ALBINO CHILD? (HINT: WHAT IS THE PROBABILITY THAT 1: THEY ARE BOTH CARRIERS AND 2: THEY BOTH PASS ON A RECESSIVE ALLELE TO THEIR CHILD?)arrow_forwardPiebaldism is a skin condition that causes an infant to be born with white birthmarks due to a genetic mutation. It is an autosomal dominant trait. A woman with piebaldism married a man without it. They have three daughters, two of whom also have piebaldism. One of their piebald daughters married a man who also has piebaldism and they have two sons with piebaldism, one son without it and one daughter with it. Draw the pedigree for this family and fill in as many of their genotypes as you can.arrow_forwardIn the fruit fly Drosophila melanogaster, a recessive condition called eyeless (ey) significantly interferes with normal eye development. Eyes are either very small or absent. The ey gene is found on chromosome 4, which is the smallest of the four chromosomes in the organism. Individuals with a single copy or three copies of chromosome 4 are viable and can reproduce. A trisomic wild-type male is crossed with a disomic wild-type female: see attached image Determine the chromosome constitution and phenotypic ratios in the offspring. Assume random segregation of chromosomes into gametes.arrow_forward
- The gene causing Coffin-Lowry syndrome (OMIM 303600) was recently identified and mapped on the human X chromosome. Coffin-Lowry syndrome is a rare disorder affecting brain morphology and development. It also produces skeletal and growth abnormalities, as well as abnormalities of motor control. Coffin-Lowry syndrome affects males who inherit a mutation of the X-linked gene. Most carrier females show no symptoms of the disease but a few carriers do. These carrier females are always less severely affected than males. Offer an explanation for this finding.arrow_forwardAnalyze the karyotype shown. Indicate if it is a chromosomal male or achromosomal female. If the karyotype is normal, write the word normal under name or description. If the karyotype is abnormal, name or describethe disorder.arrow_forwardTable 8.1 shows that Turner syndrome occurs when an individual inherits one X chromosome but lacks a second sex chromosome. Can Turner syndrome be due to nondisjunction during oogenesis, spermatogenesis, or both? If a phenotypically normal couple has a color-blind child (due to a recessive X-linked allele) with Turner syndrome, did nondisjunction occur duringoogenesis or spermatogenesis in this child’s parents? Explain your answer.arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
Human Biology (MindTap Course List)BiologyISBN:9781305112100Author:Cecie Starr, Beverly McMillanPublisher:Cengage Learning
Human Biology (MindTap Course List)
Biology
ISBN:9781305112100
Author:Cecie Starr, Beverly McMillan
Publisher:Cengage Learning
Mitochondrial mutations; Author: Useful Genetics;https://www.youtube.com/watch?v=GvgXe-3RJeU;License: CC-BY