What are the genotypes and phenotypes of the offspring? What are the genotypes and phenotypes of the parents? Please answer no need explanations only answer thank you!
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- 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.Steven has the dominant tongue rolling phenotype but does not know his genotype. His wife has the recessive non-tongue rolling trait. If their son CANNOT roll his tongue this means: O Steven has a heterozygous genotype Steven has a homozygous dominant genotype Steven has a homozygous recessive genotype o it is impossible to tell Steven's genotype from this information aloneRolly's APPLE ACK Free stu X O Leaming Lab Varsity Tutors + tutors.com/learning-lab/assessment/2eb9c784-88d7-4224-91d8-87c72f8edeb1 r rr rr Which best describes the parent genotypes in the punnet square provided? A Homozygous dominant and heterozygous B Two heterozygous C| Homozygous recessive and homozygous dominant D Homozygous recessive and heterozygous I don't know Next Question
- the Mode of Inheritance (MOI) exercises. Focus on determining the values in the colored cells. Your solutions should read as prose, not simply computations. I have provided values for two MOIs discussed in the lecture, Autosomal Dominant MOI, and X-linked Recessive where the father is affected and the mother is homozygous unaffected. Sometimes, there is confusion regarding defining the disease allele and wild-type allele for a specific mode of inheritance. In this worksheet, you'll note that the D allele is the disease allele for the Autosomal Dominant mode of inheritance. However, it is also the disease allele for the Sex-Linked Recessive mode of inheritance, where the father is affected. The point is, any letter or symbol can represent a disease allele or wild-type allele as long as you define its meaning. For example, I may use r to be the disease allele in an Autosomal Recessive mode of inheritance, and R to be the wild-type allele, or vice versa, as long as I write something like:…Parents Genotype : Bb/bb – Eye Color - (brown eyes dominant , blue eyes recessive) Dd- Dimples ( dominant) Cc/cc- Cleft chin (Dominant) Sarah BbDdcc James bbDdCc What is the probability that Sarah and James will have a baby girl with blue eyes and dimplesG Describe Muller's Ratchet-Googl x nooreps.owschools.com/owsoo/studentAssignment/index?eh=310247513 Asslgnment -6. Mendelian Genetics Attempt 1 of 2 ASSIGNMENTS COURSES SECTION 7 OF 8 « < 4 5 8. 9. 10 11 12 13 14 Click an item in the list or group of pictures at the bottom of the problem and, holding the button down, drag it into correct position in the answer box. Release your mouse button when the item is place. If you change your mind, dra the item to the trashcan. Click the trashcan to clear all your answers. Make a Punnett Square for two smooth seed hybrid pea plants (Ss) Click once to select an item at the bottom of the problem. Click again to drop the item in its correct place. S SS Ss SS S
- a. 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?Having a widows peak is dominant W to not having one (ww)Having attached earlobes is a recessive trait (ee)- Jack and Jill are heterozygous for both traits.What's the probability of them having a child with a widow's peak and attachedearlobes?the Mode of Inheritance (MOI) exercises. Focus on determining the values in the colored cells. Your solutions should read as prose, not simply computations. I have provided values for two MOIs discussed in the lecture, Autosomal Dominant MOI, and X-linked Recessive where the father is affected and the mother is homozygous unaffected. Sometimes, there is confusion regarding defining the disease allele and wild-type allele for a specific mode of inheritance. In this worksheet, you'll note that the D allele is the disease allele for the Autosomal Dominant mode of inheritance. However, it is also the disease allele for the Sex-Linked Recessive mode of inheritance, where the father is affected. The point is, any letter or symbol can represent a disease allele or wild-type allele as long as you define its meaning. For example, I may use r to be the disease allele in an Autosomal Recessive mode of inheritance, and R to be the wild-type allele, or vice versa, as long as I write something like:…
- 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? _____________________T Aa v In pea plants, tall (T) is dominant to short (t). If an offspring pea plant is "tt", what are its PARENT's possible genotypes? (Choose two correct answers) O TTx tt Tt x tt OTt x Tt O TTX TT Support | Schoology Blog | PRIVACY POLICY | Terms ofMuscular Dystrophy is an X linked recessive disease. Maria and Nick are getting genetic counseling by you to determine thier risk of the disease on their new born child.If Maria is a carrier and Nick is healthy. What is the probability of a daugther with muscular dystrophy ? A son?