Refer to the pedigree autosomal recessive disorder. Those who are not shaded have the dominant Thenotype. Let "A" and "a" represent the dominant and recessive alleles, respectively. Fill in the probability functions below to indicate the genotype or probability function or the genotype of each individual. Give all probabilities as fractions that are simplified to the lowest value. Type your fractions in #/# format without spaces. For example, one-half should be typed as 1/2. Place a zero in each space that does not have a number. Failure to follow these instructions will result in your answer being marked as incorrect. Note that two of the individuals have been completed for you as examples. 멍ㅇ Individual 1-5 is genotype ㅁㅇ ㅇ ㄹㅇ Individual 1-3 is genotype 0 AA+ 1 Aa + 0 aa Individual ||-4 is genotype 1/3 AA + 2/3 Aa + O aa Aa + AA+ 많 aa

Refer to the pedigree autosomal recessive disorder. Those who are not shaded have the dominant Thenotype. Let "A" and "a" represent the dominant and recessive alleles, respectively. Fill in the probability functions below to indicate the genotype or probability function or the genotype of each individual. Give all probabilities as fractions that are simplified to the lowest value. Type your fractions in #/# format without spaces. For example, one-half should be typed as 1/2. Place a zero in each space that does not have a number. Failure to follow these instructions will result in your answer being marked as incorrect. Note that two of the individuals have been completed for you as examples. 멍ㅇ Individual 1-5 is genotype ㅁㅇ ㅇ ㄹㅇ Individual 1-3 is genotype 0 AA+ 1 Aa + 0 aa Individual ||-4 is genotype 1/3 AA + 2/3 Aa + O aa Aa + AA+ 많 aa

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Description: Someone please help with each question, they are all about the same pedigree Refer to the pedigree below for this question. Individuals who are shaded have a rareautosomal recessive disorder. Those who are not shaded have the dominantphenotype. Let "

Human Heredity: Principles and Issues (MindTap Course List)

11th Edition

ISBN:9781305251052

Author:Michael Cummings

Publisher:Michael Cummings

Chapter18: Genetics Of Behavior

Section: Chapter Questions

Problem 14QP: A pedigree analysis was performed on the family of a man with schizophrenia. Based on the known...

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Given the karyotype shown at right, is this a male or a female? Normal or abnormal? What would the phenotype of this individual be?
Pedigree Analysis Is a Basic Method in Human Genetics Using the pedigree provided, answer the following questions. a. Is the proband male or female? b. Is the grandfather of the proband affected? c. How many siblings does the proband have, and where is he or she in the birth order?
Refer to the pedigree below for this question. Individuals who are shaded have a rare autosomal recessive disorder. Those who are not shaded have the dominant phenotype. Let "A' and a represent the dominant and recessive alleles, respectively. Fill in the probability functions below to indicate the genotype or probability function for the genotype af each individual. Give all probabilities as fractions that are simplified to the lowest value. Type your fractions in ## format without spaces. For example, one-half should be typed as 1/2. Place a zero in each space that does not have a number. Individual 3 is genotype 0 AA + 1 Aa + 0 aa Individual Il-4 is genotype 1/3 AA + 2/3 Aa + 0 aa Individual -1 is genotype AA + Aa + aa Individual Il-1 is genotype AA + Aa + aa Individual Il-7 is genotype AA + Aa + aa Individual I-1 is notype AA + aa Individual lII-5 is genotype AA + Aa + aa Individual IV-3 is genotype AA + Aa + aa For the next question, give the probability as a fraction that is…
Refer to the pedigree below for this question. Individuals who are shaded have a rare autosomal recessive disorder. Those who are not shaded have the dominant phenotype. Let "A' and "a" represent the dominant and recessive alleles, respectively. Fill in the probability functions below to indicate the genotype or probability function for the genotype of each individual. Give all probabilities as fractions that are simplified to the lowest value. Type your fractions in ## format without spaces. For example, one-half should be typed as 1/2. Place a zero in each space that does not have a number. Failure to follow these instructions will result in your answer being marked as incorrect. Note that two of the individuals have been completed for you as examples. Individual 1-3 is genotype O AA + 1 Aa +0 aa Individual II-4 is genotype 1/3 AA + 2/3 Aa + 0 aa Individual 1-6 is genotype AA + Aa + aa Individual II-1 is genotype Aa + AA + aa Individual II-5 is genotype AA + Aa + aa Individual II-7…
Refer to the pedignee below for this question, Individuals who are shaded have a rare autosamal recessive disorder. Those who are not shaded have the dominant phenotype. Let "A" and "a' represent the dominant and recessive alleles, respectively. Fill in the probability functions below to indicate the genotype or probability function far the genotype of each individual. Give all probabilities as fractions that are simplified to the lowest value. Type your fractione in ## format without spaces. For axample, one-half should be typed as 1/2. Place a zero in each space that does not have a number. inst lure Individual 1-3 is genotype 0 AA + 1 Aa + 0 aa Individual Il-4 is genotype 1/3 AA + 2/3 Aa + O aa Individual -5 is genotype AA + Aa + aa Individual Il-1 is genotype AA + Aa + aa Individual Il-5 is genotype AA + Aa + aa Individual Il-6 is genotype AA + Aa + aa Individual III-1 is genotype AA + Aa + aa Individual ill-2 is genotype AA + Aa + aa For the next question, give the probability as…
Refer to the pedigree below for this question. Individuals who are shaded have an X-inked disorder. Those who are not shaded have the normal phenotype. Let "A" and "a" represent the dominant and recessive alleles, respectively. The disorder represented by the shaded symbol to the normal phenotype. Recessive Dominant A list of possible genotypes is given below. Derermine the appropriate genotype for each individual. Type in the number for the correct answer in the space provided. Do not type arything else in the space. It is ok to use an answer more than one time. 6. 1/2 x^ x^ + 1/2 x^ x 7. 1/4 X x^ +3/4 x^x 8. 3/4 X^ x^ + 1/4 x^ x 9. 1/3 x^ x^ + 2/3 x^ X" 10. 2/3 x^ x^ + 1/3 X^ x* 1. X^ Y 2. X Y 3. X^ xA 4. X^ X 5. X* х The genotype of individual I-1 is The genotype of individual II-5 is The genotype of individual I1-6 is The genotype of individual ill-6 is For the next question, give the probability as a fraction that is simplified to the lowest value. Type your fraction in # format…
Refer to the pedigree below for this question. Individuals who are shaded have an X-linked disorder. Those wha are not shaded have the normal phenotype. Let "A" and "a" represent the dominant and recessive alleles, respectively. The disorder represented by the shaded symbol to the normal phenotype. Recessive Daminant A list of possible genotypes is given below. Determine the appropriate genotype for each individual. Type in the number for the correct answer in the space provided. Do not type anything else in the space. It is ok to use an answer more than one time. 1. XАY 6. 1/2 x^ x^ + 1/2 x^ x* 7. 1/4 X^ x* + 3/4 x^ x° 8. 3/4 X^ x^ + 1/4 x^ x 9. 1/3 x^ x* + 2/3 X^ x 10. 2/3 х* х* + 1/3 х^ х 2. X Y 3. ХА ХА 4. X^ X 5. X X The genotype of individual -2 is The genotype of individual -3 is The genotype of individual Il-5 is The genotype of individual II-7 is The genotype of individual lll-3 is
Using the pedigree below, determine whether the alleles B or C have a dominant or recessive relationship, which allele is dominant, and the genotype for individuals I-1, I-2, I-3, I-4, II-4, and II-5. Use B or C for the alleles and X for unknown alleles. Note: White squares/circle indicate normal phenotypes. Dark squares/circles indicate the individual has the condition. The B allele is associated with the condition. Label the pedigree chart with genotypes as needed.
Given the pedigree below, answer the following questions. Note that filled symbols represent affected individuals. You assume that the allele carrying the disease is rare and therefore individuals marrying into the family are unlikely to have defective alleles. Also, assume complete penetrance. Q2) What are the genotypes of the following individuals listed in the table below? Use the uppercase “A” to represent the dominant allele and lowercase “a” for the recessive allele. Individual Genotype II-7 III-5 IV-1 IV-3 I-2 III-7
Using the pedigree chart attached: Above is a pedigree for colorblindness. Based on the pedigree, is the disease dominant or recessive and is it sex-linked or autosomal? Why? Furthermore, what is the probability that 18 on this chart is affected but the condition, and what is the probability that 18 is a carrier? Why? Are the probability of being a carrier and an affected individual different? Why?
A typical pedigree for a family that carries neurofibromatosis is shown below. Note that carriers are not indicated with half-colored shapes in this chart. Use the letter "N" to indicate the dominant neurofibromatosis allele, and the letter "n" for the normal allele. Use the below pedigree chart and your knowledge on how to interpret a pedigree chart to answer questions # 7-9. 1 Nn nn nn 3 nn 7. Is individual #1 most likely homozygous dominant or heterozygous? Explain how you can tell. 8. What is the genotype of individual #2? Explain how you can tell. 9. What is the genotype of individual #3? Explain how you can tell. 2)
The pedigree below shows a family affected by a disease. Assume that the individuals marked with an asterisk (*) do not carry any allele associated with the affected phenotype, no other mutation spontaneously occurred, and complete penetrance. Answer the following questions below. Use the notation XR for the allele associated with the dominant phenotype and Xr for the allele associated with the recessive phenotype. Q1) Give the genotypes for as many individuals in the pedigree as possible.