Genetics: From Genes to Genomes, 5th edition
5th Edition
ISBN: 9780073525310
Author: Leland H. Hartwell, Michael L. Goldberg, Janice A. Fischer, Leroy Hood, Charles F. Aquadro
Publisher: McGraw-Hill Education
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Chapter 2, Problem 33P
For each of the following human pedigrees, indicate whether the inheritance pattern is recessive or dominant. What feature(s) of the pedigree did you use to determine the mode of inheritance? Give the genotypes of affected individuals and of individuals who carry the disease allele but are not affected.
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Cystic fibrosis (CF) is an autosomal recessive trait. A three-generation pedigree is shown below for a family that carries the mutant allele for cystic fibrosis. Note that carriers are not colored in to allow you to figure out their genotypes. Normal allele = F CF mutant allele = f
What is the genotype of individual #13?
A) ff
B) FF
C) Ff
D) it is impossible to tell
This pedigree (below) shows inheritance of a genetic disorder in a family. Assume the trait is
rare.
What is the mode of inheritance for this trait? [Select]
You know this because that mode of inheritance is characterized by:
[Select]
individuals who have the allele express it and
• An affected male parent passes the allele to [Select]
and [Select]
of his daughters.
• An affected female parent passes the allele to
sons and [Select]
[Select]
of her daughters.
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This pedigree (below) shows inheritance of a genetic disorder in a family. Assume the trait is
rare.
What is the mode of inheritance for this trait? [Select]
You know this because that mode of inheritance is characterized by:
[ Select]
• An affected male parent passes the allele to [Select]
and [Select]
individuals who have the allele express it and
and [Select]
of his daughters.
• An affected female parent passes the allele to [Select]
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Chapter 2 Solutions
Genetics: From Genes to Genomes, 5th edition
Ch. 2 - For each of the terms in the left column, choose...Ch. 2 - During the millennia in which selective breeding...Ch. 2 - Describe the characteristics of the garden pea...Ch. 2 - An albino corn snake is crossed with a...Ch. 2 - Two short-haired cats mate and produce six...Ch. 2 - Piebald spotting is a condition found in humans in...Ch. 2 - As a Drosophila research geneticist, you keep...Ch. 2 - A mutant cucumber plant has flowers that fail to...Ch. 2 - In a particular population of mice, certain...Ch. 2 - In humans, a dimple in the chin is a dominant...
Ch. 2 - Among Native Americans, two types of earwax...Ch. 2 - Imagine you have just purchased a black stallion...Ch. 2 - If you roll a die singular of dice, what is the...Ch. 2 - Prob. 14PCh. 2 - How many genetically different eggs could be...Ch. 2 - What is the probability of producing a child that...Ch. 2 - Prob. 17PCh. 2 - Galactosemia is a recessive human disease that is...Ch. 2 - Albinism is a condition in which pigmentation is...Ch. 2 - A cross between two pea plants, both of which grew...Ch. 2 - A third-grader decided to breed guinea pigs for...Ch. 2 - The self-fertilization of an pea plant produced...Ch. 2 - Prob. 23PCh. 2 - A pea plant from a pure-breeding strain that is...Ch. 2 - Prob. 25PCh. 2 - A pea plant heterozygous for plant height, pod...Ch. 2 - In the fruit fly Drosophila melanogaster, the...Ch. 2 - Prob. 28PCh. 2 - Considering the yellow and green pea color...Ch. 2 - Prob. 30PCh. 2 - Prob. 31PCh. 2 - Prob. 32PCh. 2 - For each of the following human pedigrees,...Ch. 2 - Consider the pedigree that follows for cutis laxa,...Ch. 2 - A young couple went to see a genetic counselor...Ch. 2 - Huntington disease is a rare fatal, degenerative...Ch. 2 - Is the disease shown in the following pedigree...Ch. 2 - Figure 2.22 shows the inheritance of Huntington...Ch. 2 - Prob. 39PCh. 2 - People with nail-patella syndrome have poorly...Ch. 2 - Midphalangeal hair hair on top of the middle...Ch. 2 - A man with Huntington disease he is heterozygous...Ch. 2 - Explain why disease alleles for cystic fibrosis CF...
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- The pedigree below shows three generations of a family that carries albinism, an autosomal recessive genetic disease. In the third generation, a child was born with albinism but the genotypes of the rest of the family are unknown. No other family members have the disease. Assume normal, Mendelian genetics with no new mutations. What are the genotypes of the parents of the affected child? A) There is not enough information to determine their genotypes B) Both are homozygous for albinism C) One is hemizygous and one is heterozygous for albinism D) Both are heterozygous for albinism E) One is homozygous and one is heterozygous for abinismarrow_forwardIn pedigrees, individuals are usually specified by using a Roman numeral for their generation in the chart and an Arabic number for their position (reading left to right) within that generation. If we use the letter c for the allele that causes cystic fibrosis, what are the genotypes of individuals III-3 and III-4 (the third and fourth individuals shown in generation III) in the pedigree that shows this disease?arrow_forwardEctrodactyly is a rare condition in which the fingers are absent and the hand is split. This condition is usually inherited as an autosomal dominant trait. Ademar Freire-Maia reported the appearance of ectrodactyly in a family in São Paulo, Brazil, whose pedigree is shown here. Is this pedigree consistent with autosomal dominant inheritance? If not, what mode of inheritance is most likely? Explain your reasoning.arrow_forward
- For the pedigrees below, name the inheritance pattern of the depicted disorder: If more than one pattern is possible, name all possibilities. For any recessive disorder, clearly mark all individuals who must be carriers by placing a dot inside the corresponding circle or square. Assume that each disorder is rare (i.e. any individual "marrying into" the pedigree is normal and not carrying a mutant allele). A) I II III IV C) I II III IV 1 2 E) 몽 I II III IV B) D) I II III IV II III IV 3E% 2arrow_forwardThe following pedigree shows the pattern of inheritance for an uncommon human disease. Filled symbols indicate individuals with the disease: open symbols indicate normal individuals. Using the symbols A and a, answer the following questions about this pedigree. 1. What are the most probable genotypes of individuals II-9 and II-10 2. If individuals II-1 and II-2 have another child, what is the probability that it will have the disease?arrow_forwardUsing the pedigree chart, explain: a) The number of generations seen. b) If all blue-coloured shapes are affected with disease X- how many males are affected? how many females are affected? c) Does this disease have a dominant or recessive inheritance pattern? Justify your answer.arrow_forward
- The pedigree below traces the inheritance of Albinism, a genetic disorder. Affected individuals, indicated here by the colored gray circles and squares, are unable to make a normal amount of melanin, the chemical that is responsible for eye, skin, and hair color. Does Albinism appear to be caused by a dominant allele or by a recessive allele? Fill in the genotypes of the individuals whose genotypes can be deduced. What genotypes are possible for each of the other individuals? Explain!arrow_forwarda) Which of the four modes of inheritance are consistent with the disease shown in this human pedigrees below? (List the compatible mode or modes) Give an answer for a, b and c b) If the parents in pedigree c have 2 other children, what is the probability that they will carry the disease?arrow_forwardThe pedigree below tracks the inheritance of a genetic disorder through a family's generation. Determine the probable inheritance mode for the trait shown in the affected individual (the shaded symbols) by answering the following questions. I II 2 3 4 5 7 III 2 3 6 7 8 5 (i) Based on the pedigree, Y-linked inheritance can be excluded at a glance. Give your reason. (ii) What TWO (2) other modes of inheritance can be definitely excluded? Explain your answer. Of the remaining modes of inheritance, which is the most likely? Which is less likely? Explain your answers. (ii)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_forwardWhat is the most likely pattern of inheritance for this disorder? (Is it autosomal dominant? Autosomal recessive? X-linked dominant? X-linked recessive? Y-linked? Mitochondrial?) Please include two specific pieces of evidence, present within the pedigree, that indicate that this pattern is most likely, as opposed to any other potential pattern. You may assume that the gene responsible for the trait is fully penetrant.arrow_forwardBelow is a pedigree of a human genetic disease in which solid color indicates affected individuals. Assume that the disease is caused by a gene that can have the alleles A or a. a) Based on this pedigree, what is the most likely mode of inheritance? b) What is/are the possible genotype/s of person 1? c) What is/are the possible genotype (s) of person 4 ? Explain your answers.arrow_forward
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