A. Identify the most likely inheritance pattern in the pedigree below. B. What are the genotypes of individuals II-3 and Il-4? Use any letter for your example. 1 2 II 1 2 3 4 5 6 II 1 2 3 4 5 6
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- A) what are the genotypes for EB27 and EB67? B) what is the relationship between the three alleles (B,br, y)? Show evidence using the pedigreeRabbits may be classified as agouti, chinchilla, Himalayan, or albino according to coat color. A cross between CC h x C ch c produced 5 agouti, 3 chinchilla and 2 Himalayans. a. What are the phenotypes of the parent rabbits? Copy the genotypes then write the corresponding phenotype beside each. b. What are the genotypes of the F1s? c. What mode of inheritance is exhibited? d. If the two F1 agouti genotypes will be crossed, what percentage of theiroffspring will have the same phenotype? e. What will be the genotypes of the rabbits in (d)?The pedigree below is of a rare single gene disease. Given the pedigree shown below, what is the most likely pattern of inheritance for this disease? Explain your answer. Note that closed symbols are for individuals affected by the disease and open symbols are unaffected individuals (limit 3-4 sentences).
- Two albino parents have four unaffected children. If albinism in the parents is given by mutations on two different genes (A and B) and complementation is observed in all four children, what are the genotypes of the parents? A. AaBb and AABB B. AABb and AaBB C. both parents are AaBb D. AAbb and BBaa2a) Identify the pattern of Mendelian inheritance represented in the pedigree above. 2b) Explain how you made this determination.Below 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.
- Albinism causes the skin, hair, or eyes to have little or no color. It is also associated with vision problems. Albinism results from an allele a that is recessive to the allele for normal melanin production. Maya has normal skin color, but her sister has albinism. Maya’s mother has albinism, and her father has normal skin color. a)What are the genotypes of Maya, her sister, her mother, and her father. b)If Maya’s parents have another child, what is the probability that this child will have albinism? Show the Punnett square you use to help in solving. c)If Maya marries a man with albinism, what is the probability that their first child will have albinism? Show the Punnett square you use to help in solving.Circle any inheritance patterns that could explain this pedigree. Assume individuals marrying into the family do not have a mutant allele. Please refer to the image attached. A) Paternally imprinted B) Maternally imprinted C) Maternal inheritance D) Autosomal recessive E) Autosomal dominant F) X-linked recessive G) X-linked dominantConsider the pedigree below for a recessive autosomal trait caused by allele t. The dominant wild-type allele is represented by T. What is the genotype of individual 5 in generation II? A. TT or Tt B. tt C. Tt D. Tt or tt E. TT
- What is the likely mode of inheritance in the below pedigree? Select one: a. Dominant b. Recessive c. There is not enough information to determine dominant or recessive modes of inheritance.Consider the pedigree below for a recessive autosomal trait caused by allele t. The dominant wild-type allele is represented by T. What is the genotype of individual 4 in generation II?In the pedigree below what type of disease trait expression pattern is being observed? a Autosomal recessive b Autosomal dominant c Y-linked d X-linked recessive e X-linked dominant