Huntington's disease is a very rare, debilitating disease that affects approximately 1 in 10,000people. The disease is caused by a particular type of genetic mutation (large number of CAG repeats)in a gene called huntingtin (HTT). Designate the disease-causing allele HTTP and the non-disease-causing allele HTTN. We know that individuals with genotype HTTN will not develop Huntington'sDisease, but people with either HTTD/HTTP or HTTN/HTTD will develop the disease.Which allele is dominant--HTTN or HTTP? Explain your reasoning thoroughly, using the correctdefinition of dominance.

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Description: Huntington's disease is a very rare, debilitating disease that affects approximately 1 in 10,000people. The disease is caused by a particular type of genetic mutation (large number of CAG repeats)in a gene called huntingtin (HTT). Designate the dise

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Huntington's disease is a very rare, debilitating disease that affects approximately 1 in 10,000 people. The disease is caused by a particular type of genetic mutation (large number of CAG repea n a gene called huntingtin (HTT). Designate the disease-causing allele HTTD and the non-disease- causing allele HTTN. We know that individuals with genotype HTTN will not develop Huntington's Disease, but people with either HTTP/HTTD or HTTN/HTTD will develop the disease. Which allele is dominant--HTTN or HTTD? Explain your reasoning thoroughly, using the correct definition of dominance

Huntington's disease is a very rare, debilitating disease that affects approximately 1 in 10,000 people. The disease is caused by a particular type of genetic mutation (large number of CAG repea n a gene called huntingtin (HTT). Designate the disease-causing allele HTTD and the non-disease- causing allele HTTN. We know that individuals with genotype HTTN will not develop Huntington's Disease, but people with either HTTP/HTTD or HTTN/HTTD will develop the disease. Which allele is dominant--HTTN or HTTD? Explain your reasoning thoroughly, using the correct definition of dominance

Human Heredity: Principles and Issues (MindTap Course List)

11th Edition

ISBN:9781305251052

Author:Michael Cummings

Publisher:Michael Cummings

Chapter11: Genome Alterations: Mutation And Epigenetics

Section: Chapter Questions

Problem 16QP: Familial retinoblastoma, a rare autosomal dominant defect, arose in a large family that had no prior...

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