what is an example of a trait determined by incomplete dominance inheritance. Then, include a model, such as a Punnet Square, to demonstrate this pattern of inheritance.
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A: a incomplete dominance is correct answer.
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what is an example of a trait determined by incomplete dominance inheritance. Then, include a model, such as a Punnet Square, to demonstrate this pattern of inheritance.
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- The dominance pattern of a gene can be determined from the phenotypes of the parents and offspring. In the examples below, assume that each parent is homozygous for the specific allele and that the progeny are heterozygous. Classify each example as either complete dominance, incomplete dominance, or codominance. Complete dominance Incomplete dominance Codominance Answer Bank A black sheep and a white sheep produce a gray lamb. A white cow and a red bull have a calf that is white with red spots (roan colored). A mother with type A blood and a father with type B blood have a daughter with type AB blood. A pea plant with all purple flowers and a pea plant with all white flowers produce a pea plant with all purple flowers. A moth with red wings and a moth with yellow wings produce a moth with orange wings.Shown in the pictures below are the degrees of dominance in the inheritance of flower color in some plants. *Based on the phenotypes (or maybe genotype), differentiate between complete dominance, incomplete dominance, and codominance. Be able to discuss the difference briefly but concisely. You may also refer to the definition.Pedigree analysis is a fundamental tool for investigating whether or not a trait is following a Mendelian pattern of inheritance. It can also be used to help identify individuals within a family who may be at risk for the trait. Adam and Sarah, a young couple of Eastern European Jewish ancestry, went to a genetic counselor because they were planning a family and wanted to know what their chances were for having a child with a genetic condition. The genetic counselor took a detailed family history from both of them and discovered several traits in their respective families. Sarahs maternal family history is suggestive of an autosomal dominant pattern of cancer predisposition to breast and ovarian cancer because of the young ages at which her mother and grandmother were diagnosed with their cancers. If a mutant allele that predisposed to breast and ovarian cancer was inherited in Sarahs family, she, her sister, and any of her own future children could be at risk for inheriting this mutation. The counselor told her that genetic testing is available that may help determine if this mutant allele is present in her family members. Adams paternal family history has a very strong pattern of early onset heart disease. An autosomal dominant condition known as familial hypercholesterolemia may be responsible for the large number of deaths from heart disease. As with hereditary breast and ovarian cancer, genetic testing is available to see if Adam carries the mutant allele. Testing will give the couple more information about the chances that their children could inherit this mutation. Adam had a first cousin who died from Tay-Sachs disease (TSD), a fatal autosomal recessive condition most commonly found in people of Eastern European Jewish descent. Because TSD is a recessively inherited disorder, both of his cousins parents must have been heterozygous carriers of the mutant allele. If that is the case, Adams father could be a carrier as well. If Adams father carries the mutant TSD allele, it is possible that Adam inherited this mutation. Because Sarah is also of Eastern European Jewish ancestry, she could also be a carrier of the gene, even though no one in her family has been affected with TSD. If Adam and Sarah are both carriers, each of their children would have a 25% chance of being afflicted with TSD. A simple blood test performed on both Sarah and Adam could determine whether they are carriers of this mutation. Would you decide to have a child if the test results said that you carry the mutation for breast and ovarian cancer? The heart disease mutation? The TSD mutation? The heart disease and the mutant alleles?
- Pedigree analysis is a fundamental tool for investigating whether or not a trait is following a Mendelian pattern of inheritance. It can also be used to help identify individuals within a family who may be at risk for the trait. Adam and Sarah, a young couple of Eastern European Jewish ancestry, went to a genetic counselor because they were planning a family and wanted to know what their chances were for having a child with a genetic condition. The genetic counselor took a detailed family history from both of them and discovered several traits in their respective families. Sarahs maternal family history is suggestive of an autosomal dominant pattern of cancer predisposition to breast and ovarian cancer because of the young ages at which her mother and grandmother were diagnosed with their cancers. If a mutant allele that predisposed to breast and ovarian cancer was inherited in Sarahs family, she, her sister, and any of her own future children could be at risk for inheriting this mutation. The counselor told her that genetic testing is available that may help determine if this mutant allele is present in her family members. Adams paternal family history has a very strong pattern of early onset heart disease. An autosomal dominant condition known as familial hypercholesterolemia may be responsible for the large number of deaths from heart disease. As with hereditary breast and ovarian cancer, genetic testing is available to see if Adam carries the mutant allele. Testing will give the couple more information about the chances that their children could inherit this mutation. Adam had a first cousin who died from Tay-Sachs disease (TSD), a fatal autosomal recessive condition most commonly found in people of Eastern European Jewish descent. Because TSD is a recessively inherited disorder, both of his cousins parents must have been heterozygous carriers of the mutant allele. If that is the case, Adams father could be a carrier as well. If Adams father carries the mutant TSD allele, it is possible that Adam inherited this mutation. Because Sarah is also of Eastern European Jewish ancestry, she could also be a carrier of the gene, even though no one in her family has been affected with TSD. If Adam and Sarah are both carriers, each of their children would have a 25% chance of being afflicted with TSD. A simple blood test performed on both Sarah and Adam could determine whether they are carriers of this mutation. If Sarah carries the mutant cancer allele and Adam carries the mutant heart disease allele, what is the chance that they would have a child who is free of both diseases? Are these good odds?Pedigree analysis is a fundamental tool for investigating whether or not a trait is following a Mendelian pattern of inheritance. It can also be used to help identify individuals within a family who may be at risk for the trait. Adam and Sarah, a young couple of Eastern European Jewish ancestry, went to a genetic counselor because they were planning a family and wanted to know what their chances were for having a child with a genetic condition. The genetic counselor took a detailed family history from both of them and discovered several traits in their respective families. Sarahs maternal family history is suggestive of an autosomal dominant pattern of cancer predisposition to breast and ovarian cancer because of the young ages at which her mother and grandmother were diagnosed with their cancers. If a mutant allele that predisposed to breast and ovarian cancer was inherited in Sarahs family, she, her sister, and any of her own future children could be at risk for inheriting this mutation. The counselor told her that genetic testing is available that may help determine if this mutant allele is present in her family members. Adams paternal family history has a very strong pattern of early onset heart disease. An autosomal dominant condition known as familial hypercholesterolemia may be responsible for the large number of deaths from heart disease. As with hereditary breast and ovarian cancer, genetic testing is available to see if Adam carries the mutant allele. Testing will give the couple more information about the chances that their children could inherit this mutation. Adam had a first cousin who died from Tay-Sachs disease (TSD), a fatal autosomal recessive condition most commonly found in people of Eastern European Jewish descent. Because TSD is a recessively inherited disorder, both of his cousins parents must have been heterozygous carriers of the mutant allele. If that is the case, Adams father could be a carrier as well. If Adams father carries the mutant TSD allele, it is possible that Adam inherited this mutation. Because Sarah is also of Eastern European Jewish ancestry, she could also be a carrier of the gene, even though no one in her family has been affected with TSD. If Adam and Sarah are both carriers, each of their children would have a 25% chance of being afflicted with TSD. A simple blood test performed on both Sarah and Adam could determine whether they are carriers of this mutation. Would you want to know the results of the cancer, heart disease, and TSD tests if you were Sarah and Adam? Is it their responsibility as potential parents to gather this type of information before they decide to have a child?Referring to the pattern of inheritance of comb type and feathering in chicken, consider the cross between the following: a hen heterozygous for hen feathering and walnut comb and a cock feathered roster with single comb. What are the genotypes and phenotypes of their male and female offspring? Please use Punnett square.
- In oats, the color of the chaff is determined by a two-gene interaction. When a true-breeding black chaff plant was crossed to a truebreeding white chaff plant, the F1 generation was composed of allblack chaff plants. When the F1 offspring were crossed to eachother, the ratio produced was 12 black to 3 gray to 1 white. First,construct a Punnett square that accounts for this pattern of inheritance. Which genotypes produce the gray chaff phenotype? Second,at the level of protein function, how would you explain this type ofinheritance?raccoons may have wide, medium-sized, or narrow bands around their tails. They may also havethe habit of washing all, or some of their food, or do not wash their food at all. a) assign genotypes to the phenotypes mentioned (see attached table) b. What mode of inheritance would most likely be exhibited by these traits if crosses were made? c. If two raccoons with medium-sized tail bands and have the habit of washing some of theirfoods will be crossed, what is the probability of having F1 raccoons with: c.1 wide tail bands that won’t wash any of their food? c.2 the same genotype as the parent raccoons? d. If a raccoon with a wide tail band that washes only some of its food is crossed with a raccoonwith a narrow tail band that doesn’t wash any food, what percentage of their offspring wouldbe medium-tailed and washes all its food? Show COMPLETE cross.What is the pattern of inheritance shown by the following example? A brown guinea pig mated with a white guinea pig, their offspring are tan.
- Mendel's concept of dominance states that in a genotype where two different alleles of a locus are present, only the trait encoded by the dominant allele is observed. Give a molecular explanation for dominance, i.e. explain intracellular molecular events that can result in what we observe as dominance on a phenotypic level. Use the gene that encodes seed shape in peas as an example, where roun(R) is dominant over wrinkled(r), to explain how RR and Rr plants can have the same phenotype.Hair texture is determined by gene c in an incomplete dominance inheritance pattern, where the heterozygous condition (c1c2) results in wavy hair. Hairline is controlled by gene H, where a widow's peak is dominant to a straight hairline. If a woman with curly hair and a straight hairline has a child with a man with a widow's peak and straight hair (his mom had a straight hairline), what is the chance they would have a kid that has exactly the same hair as mom? Draw the Punnett square and demonstrate the possible genotypes and phenotypes that could result from these two parents' mating.Consider a situation where you have a parental cross with the mother and father phenotypes listed below. Remember that the genotype for the wild-type parent is always homozygous. The counts of the F1offspring are listed in Table 1. Two randomly selected individuals are selected and mated to produce a set of F2individuals. If you test the F2counts to determine whether they are consistent with an autosomal dominant mode of inheritance, what is your decision? Use a 0.05 significance level. PARENTAL CROSS Parental cross: Mother with disease phenotype, Father with wild-type phenotype. Table 1. F1 DATA Gender Phenotype Disease Wild-type Male 0 23 Female 0 34 Table 2. F2 DATA Gender Phenotype Disease Wild-type Male 7 25 Female 0 25 A. Do not reject the null hypothesis that the F2 data are consistent with an autosomal dominant mode of inheritance; chi-square goodness of fit test p-value is greater than 0.05. B. Reject the null hypothesis that the F2…