3. Calvin is colorblind which is a sex linked recessive condition. Which of his family members could have passed the color-blindness allele to him. List all that are possible His father His mother His mother's father His mother's mother His father's father His father's mother
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Genetics Q3
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- 5. A woman who is a carrier for colorblindness marries a colorblind man. The woman nas 5 nngers on each hand and the man, whose father had father had 5 fingers, has 6 fingers. (Polydactyly-have 6 fingers on each hand-is inherited as an autosomal dominant trait. What percent of their children do you expect to be colorblind with 5 fingers? man with type AB blood is married to a woman with type O blood. They have 2 natural children 01one adopted child. 'One child has type A blood, one has type B blood and the other has type O blood. Whi s adopted?1. Mary and Joe are both healthy individuals. Joe has a mother who suffered from cystic fibrosis, an autosomal recessive disorder. Mary has been genetically tested in order to find out if she has the allele responsible for this disease and her tests came out positive. They are planning on having two children together in the near future. What is the probability that she and Joe will have either 2 boys who have the disorder, OR that they have one boy who has the disorder and one boy who does not? (in other words, what is the probability that any of these two outcomes takes place? a) 1/8 b) 1/16 c) 3/32 d) 1/64 e) 9/641. Red-green colorblindness is caused by a recessive allele (x) at an X-linked gene, and albinism is caused by a recessive allele (a) at an autosomal gene. A phenotypically normal woman (Sara) has a father who is colorblind, and she knows that she is a carrier for albinism. She plans to have a child with a colorblind man (Abdul) who is also a carrier for albinism. What is the probability that Sara and Abdul's child will have one of the conditions, but not both? (C. Follow the steps below to answer this question. a) What is the cross? b) What are the target genotypes? Note: it might be useful to come back to this one and double- check it after you have completed step c, below. Break this down to the single gene level by answering the following questions: a. What is the proportion of normal to albino offspring? Show the Punnett square: b. What is the proportion of normal to colorblind offspring? Show the Punnett square: d) What is the probability that Sara and Abdul's child will have one…
- YOUR SISTER DIED FROM TAY-SACHS DISEASE, INHERITED AS A RECESSIVE ALLELE (t). you're married and planning to start your family. you're worried about the disease and decide to have genetic testing to see if you or your spouse is a carrier of the tay-sachs allele. the test results show that you're a carrier of the allele, but your spouse isn't. what is the probability that you and your spouse will have a child with tay-sachs disease? show your work.Albinism is a recessive autosomal trait for skin pigmentation. Hemophilia is a sex-linked recessivedisorder of the blood. assign alleles to the traitsA – normal skin pigmentation X H – normal blooda – albino X h - hemophilia A double heterozygous woman marries a non-hemophilic man and heterozygous for skinpigmentation. Double heterozygous means heterozygous for both traits. Aa for skin pigmentation andX H X h for blood trait. Therefore, the genotype of the woman is AaX H X h . Non-hemophilic man is X H Y and heterozygous for skin pigmentation is Aa. The genotype,therefore, of the man is AaX H Y. What is the probability that they will have:a. a child with normal skin? _____________________b. a child with normal blood? _____________________c. an albino girl? _____________________d. A hemophilic boy? _____________________X-linked recessive, carrier mother Unaffected. Carrier mother father X Y XX |Unaffected |Affected I Carrier XY Unaffected Unaffected Carrier daughter Affected son daughter U.S. National Library of Medicine son Color blindedness is a sex-linked trait. If we could see the pedigree chart for several more generations of the family illustrated here, we would expect A) more males to be color blind. B) móre females to be color blind. no females to ever be color blind. D) an equal number of males and females that are color blind.
- 6 Huntington's disease causes damage to the nervous system. It is an inherited condition caused by a dominant allele (H). Only individuals who are homozygous for the recessive allele (h) are protected from the disease. The diagram shows the inheritance of Huntington's disease in a family. A F G H K M N Male Female Male with Female with Huntington's disease Huntington's disease (a) Complete the table to show how many people in the diagram fit each description. The first one has been done for you. Number of people who fit the description Description male 7 female with Huntington's disease homozygous recessive heterozygous homozygous dominant.Hemophilia is a blood-clotting disorder in humans that followsan X-linked recessive pattern of inheritance. A man with hemophilia and a woman without hemophilia have a daughter withhemophilia. If you let H represent the normal allele and h thehemophilia allele, what are the genotypes of the parents?a. Mother is XHXhand father is XhY.b. Mother is XhXhand father is XhY.c. Mother is XhXhand father is XHY.d. Mother is XHXhand father is XHYRed-green color blindness is inherited through an X-linked, recessive allele (b). Two parents, Fred and Ginger, have normal vision. They have two daughters, Takiyah and Kelly, who also have normal vision, and a color-blind son, David. 3. Daughter Kelly has a color-blind son, Kevin. Daughter Takiyah has five sons, all with normal vision. What are the genotypes of all the individuals? Show all your work! Fred Ginger David Takiyah Kelly Kevin Takiyah's five sons If Kelly marries a man with normal vision, what is the probability that she'll have a color-blind son? a color-blind daughter?
- Clark's eyes are brown in color. However, both his parents have eyes that are blue in color. According to the dominant-recessive genes principle, the most likely reason for Clark's eyes being brown in color is thata. The ability to taste the chemical phenylthiocarbamideis an autosomal dominant phenotype, and the inabilityto taste it is recessive. If a taster woman with a nontasterfather marries a taster man who in a previous marriagehad a nontaster daughter, what is the probability thattheir first child will be(1) A nontaster girl(2) A taster girl(3) A taster boyb. What is the probability that their first two childrenwill be tasters of either sex?4. Mr. Salazar has Type A blood while Mrs. Salazar has Type B. They have four children. Bobbie has Type A, Gabbie has Type B, Alex has Type AB, and Teddie has Type O. What are the genotypes of all six people in this family? NOTE: The ABO blood type gene has three alleles. IA and IB are codominant; i (for Type O) is recessive to both.