Please double check the information is done correctly. And, using the information and data, answer the question at the bottom of the second page which asks: “Did your results from the coin tosses support your prediction from the Punnett Square? Specifythe data you used.” Write the answer in detail Autosomal Recessive Disorder: Cystic Fibrosis2. Cystic fibrosis is lethal autosomal recessive disorder in humans. It is the most common fataldisorder in the United States. Its hallmark is bacterial infections of the lungs and intestine. Awoman who is a carrier of cystic fibrosis (Cc) has children with a man who is also a carrier(Cc). What are the chances that a particular child will have cystic fibrosis? What are thechances that a particular child will be a carrier?a. Phenotypes of the parents:Mother:b. Genotypes of the parents:C.Gamete genotypes:d. Punnett Square:(egg)Mother:СсEgg: CcCFсCCCc/ Cc(sperm)сCcссFather:CFFather: CCSperm : CCe. List all possible genotypes of offspring of these parents: CC, Cc, and cc1. Which of these genotypes are heterozygous? Cc2. Which of these genotypes are homozygous? CC and cc60f. List all the possible phenotypes of offspring of these parents:carrier of cystic fibrosis, affected i.e. cystic fibrosis andnonaffectedg. Calculate the probability of each genotype and phenotype as listed. Fill in table on thefollowing page. Table 3: Expected Probabilities for Cystic FibrosisGenotypeprobability as apercentGenotype GenotypeCCCcCCCCprobability as afraction114214114Ccсс25%50%.25%.PhenotypeNormalCFTable 4. Data for Cystic FibrosisGenotype Total #(Total #genotype genotypeafter 24/24) X100tossesin %20.8% 25% Normal54.2% 50%25% 25%5136h. What are the chances a child will have cystic fibrosis?Report data as a percentage: 25% as a fraction: 4Phenotypeprobability as afraction2/4i. What are the chances a child will be a carrier of cystic fibrosis?Report data as a percentage:50%.as a fraction:We are going to test the ratio of offspring given the parental genotypes above for Cystic Fibrosisby using a coin toss. Obtain the appropriate coins for the mother and father. Follow the previouscoin toss procedure.3141/4CFProbability Phenotype Total #fromphenotypeafter 24PunnettSquare intosses%61Phenotypeprobability asa percent75%.1825%.(total #phenotype/ 24) x100in %75%.ProbabilityfromPunnettSquare in%75%625%.25%Did your results from the coin tosses support your prediction from the Punnett Square? Specifythe data you used.

Please double check the information is done correctly. And, using the information and data, answer the question at the bottom of the second page which asks: “Did your results from the coin tosses support your prediction from the Punnett Square? Specify the data you used.” Write the answer in detail

Please double check the information is done correctly. And, using the information and data, answer the question at the bottom of the second page which asks: “Did your results from the coin tosses support your prediction from the Punnett Square? Specify the data you used.” Write the answer in detail

Biology (MindTap Course List)

11th Edition

ISBN:9781337392938

Author:Eldra Solomon, Charles Martin, Diana W. Martin, Linda R. Berg

Publisher:Eldra Solomon, Charles Martin, Diana W. Martin, Linda R. Berg

Chapter16: Human Genetics And The Human Genome

Section16.3: Genetic Diseases Caused By Single-gene Mutations

Problem 7LO: State whether each of the following genetic defects is inherited as an autosomal recessive,...

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AaBbCcDc AaBbCcD Ac Heading 1 Heading 2 Title Subtitle Subtle Em.. Emphasis Intense E... Strong Quote Int Paragraph Styles 4 Genetic Inheritance Patterns Retinitis pigmentosa (RP) can be autosomal recessive, autosomal dominant, or x-linked. Apparently the dominant forms are often less severe. Eric's form of RP is Usher's Syndrome, which is an autosomal recessive inheritance (i.e., you must get a copy of the defective carried on one of the chromosomes that determines sex. Usher's Type II is recessive, so for Eric this means that both his Mom and Dad are carriers of this condition. His brother, Dirk, does not have any symptoms of RP. gene from your Mom and one from your Dad). Autosomal means it is not Question below short answer approach image you are the genetics counselor, should Eric have children? Imagine he has a daughter (he has two, but both are adopted). What advice would you give Eric if his wife was a carrier from a genetics counseling viewpoint? Describe all the possibilities,…
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Genetic Inheritance Patterms Retinitis pigmentosa (RP) can be autosomal recessive, autosomal dominant, or x-linked. Apparently the dominant forms are often less severe. Eric's form of RP is Usher's Syndrome, which is an autosomal recessive inheritance (i.e., you must get a copy of the defective gene from your Mom and one from your Dad). Autosomal means it is not carried on one of the chromosomes that determines sex. Usher's Type II is recessive, so for Eric this means that both his Mom and Dad are carriers of this condition. His brother, Dirk, does not have any symptoms of RP. Draw a pedigree of Eric's family showing possible genotypes and chances of having RP. Your pedigree must include his parents, Eric, his brother Dirk, and a potential daughter of Eric's. Draws a pedigree that shows the correct genotypes and chances of having retinitis pigmentosa for Eric and his family. D.Focus (United States) a S W 37 F 八口

Genetic Inheritance Patterms Retinitis pigmnentosa (RP) can be autosomal recessive, autosomal dominant, or x-linked. Apparently the dominant forms are often less severe. Eric's form of RP is Usher's Syndrome, which is an autosomal recessive inheritance (i.e., you must get a copy of the defective gene from your Mom and one from your Dad). Autosomal means it is not carried on one of the chromosomes that determines sex. Usher's Type II is recessive, so for Eric this means that both his Mom and Dad are carriers of this condition. His brother, Dirk, does not have any symptoms of RP. Question below - short answer approach Imagine you are a genetics counselor, and Dirk, Erik's brother, comes in to see you. Based on his parents, what are Dirk's possible genotypes for RP? What advice would you give Dirk about the chances of Dirk's children having retinitis pigmentosa if his wife is not a carrier? How would your advice change if his wife fully has the disease? Describe all the possibilities,…
young couple is planning to have children. The male is heterozygous for Huntington’s disease and homozygous dominant for Tay-Sachs. The female is homozygous recessive for Huntington’s disease and heterozygous for Tay-Sachs. The couple is curious about the possibility and probability of their offspring inheriting Tay-Sachs and/or Huntington’s. For humans, Huntington’s disease is dominant (H) over the “normal” condition (h), and the “normal” condition is dominant (T) over Tay-Sachs (t). Complete a Punnett square for this cross and record the percent probabilities for genotypes and phenotypes of the offspring.
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