Below is a pedigree for a particular rare genetic disorder. It could be autosomal dominant, autosomal recessive, limited expression in females, limited expression in males, mitochondrial, reduced penetrance, sex- sex-linked dominant, or sex-linked recessive. • Recall this is a rare disorder. Propose the best fitting mechanism of inheritance. Justify your answer. • What are the genotypes of the individuals who marry into this family? Explain your answer.
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- Discuss inheritance. Think broadly on inheritance patterns through generations. What impact do modifications, such as those offered by CRISPR and genetic testing, have on the generational lineage of these traits? Are some traits (e.g., susceptibility to Sickle Cell Anemia) worth removing from our genome? List plus and minuses for gene removal (include facts and references). Support your position.PEDIGREES: Problem (continued) This pedigree shows the inheritance of cystic fibrosis in this family. I • QUESTIONS ••. 5. What is the genotype of individual II-3? Use the letter "f" to 1 2 represent the disease allele. II 1 2 3 6. Individuals II-I and II-2 are sisters. Explain how it is possible for one sister to have cystic fibrosis but NOT the other. III 1 2 3Question: The disorder: Red-Green color blindness Explain the mode of inheritance of the disorder (recessive, dominant, x-linked, etc.) . Can a person be a carrier of this disorder? • Describe the probability of having a child with the disorder -- give a specific scenario (ex. both parents are heterozygous for the trait) • Describe the symptoms associated with this disorder Explain the prognosis of a person born with this disorder
- Homozygous mice are better able to adapt to their environment. O Heterozygous mice live shorter lives since they do not have the lethal allele. Is it possible to determine the genotype of an individual expressing a dominant phenotype? Provide evidence to support your claim * Provide at least 3 COMPLETE SENTENCES Your answer This is a required question Is it possible to determine the genotype of an individual expressing a recessive phenotype? Provide evidence to support your claim Provide at least 3 COMPLETE SENTENCES a phenotype is a personality's noticeable traits. Eye color, height and, evident. The genetic contribution to the constitution is named the genotype, So basically phenotypes are on the surfacel Yes it is possibleSaved Gene linkage Complete the following statements about gene linkage. Not all choices will be used. independent A chromosome contains a long series of different are in a definite assortment that sequence linkage group Their position, or on the chromosome is fixed. locus alleles All of the alleles on a chromosome form a(n) they tend to be inherited together. because gametes Because they reside so close together on the chromosome, there is a reduced chance that not follow the traditional Mendelian genotypic ratios. will occur and therefore they do 30 acerGive typed full explanation Two parents who are each known to be carriers of an autosomal recessive alleles have four children. None of the children has the recessive condition. What is the probability that one or more of the children is a carrier of the recessive allele?
- O StompOnStep1.com a. Assume this pedigree represents inheritance of a human disease. What is the most likely mode of inheritance for this disease? b. What is the most likely genotype person III-IV if we use A and a as the alleles for this disease? a. Autosomal dominant, b. Aa a. Y linked, b. Aa a. Autosomal dominant, b. AA a. Autosomal recessive, b. aa. The human IGF2 gene is autosomal and maternallyimprinted. Copies of the gene received from themother are not expressed, but copies received fromthe father are expressed. You have found two allelesof this gene that encode two different forms of theIGF2 protein distinguishable by gel electrophoresis.One allele encodes a 60K (Kilodalton) blood protein;the other allele encodes a 50K blood protein. In ananalysis of blood proteins from a couple named Billand Joan, you find only the 60K protein in Joan’sblood and only the 50K protein in Bill’s blood. Youthen look at their children: Jill is producing only the50K protein, while Bill Jr. is producing only the 60Kprotein.a. With these data alone, what can you say about theIGF2 genotype of Bill Sr. and Joan?b. Bill Jr. and a woman named Sara have two children, Pat and Tim. Pat produces only the 60K protein and Tim produces only the 50K protein. Withthe accumulated data, what can you now say aboutthe genotypes of Joan and Bill Sr.?Provide the required information. Show the COMPLETE 7-step method of gene-interaction and epistasis Dog ears may either be drooping or erect. In terms of their barking, some always bark, otherssometimes bark, and still other are non-barking. Two dogs from the same species but of differentphenotypes were used in the cross: (See attached Image)