Which statement below defines epistasis? proportion of individuals with an abnormal genotype that exhibit its associated phenotype when a single gene affects several phenotypes when one gene influences or masks the effect of another gene when a heterozygote displays a phenotype intermediate between its two alleles
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Q: genotypes of parents
A: Answer :
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A: Answer : Option (2) is correct. - blending inheritance.
![Which statement below defines epistasis?
O proportion of individuals with an abnormal genotype that exhibit its associated phenotype
when a single gene affects several phenotypes
when one gene influences or masks the effect of another
gene
when a heterozygote displays a phenotype intermediate between its two alleles](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F392ed7d0-c4af-4524-abc3-d3ba3f8ce1c1%2F50b6bb96-f183-4ea6-9fa2-b2ac9bffe621%2Fff19oy_processed.png&w=3840&q=75)
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- Pseudohypertrophic muscular dystrophy is an inheriteddisorder that causes gradual deterioration of the muscles. It isseen almost exclusively in boys born to apparently unaffectedparents and usually results in death in the early teens. Isthis disorder caused by a dominant or a recessive allele?Is its inheritance sex-linked or autosomal? How do youknow? Explain why this disorder is almost never seen in girls.The part that is missing is where the traits for things like colorblindness and hemophilia exist. This meansthat if you have XY chromosomes, you are missing alleles on one of the chromosomes. So whatever alleleis on your X is expressed regardless of if being dominant or recessive. These X-Linked Traits have a specialway to note the alleles.X-Linked alleles use X and Y as their base and then the allele that notates the trait is in the top, rightcorner. For instance: Phenotype(appearance) Genotype(alleles) XY with Hemophilia XhY XX withouth Hemophilia XHXh Notice that the female has two X’s so has 2 alleles. She is not a hemophiliac, but is carrying the trait.That means she can pass the trait to her offspring.Why don’t you cross those two parents here and find the outcome:Parents: Offspring: Genotypes:Phenotypes: Is there a chance of producing an XY offspring with hemophilia? Explain your answer Will…The X-linked gene responsible for DMD encodes a protein called dystrophin that is required for muscle function. Dystrophin protein is not secreted—it remains inthe cells that produce it. Given what you know aboutBarr body formation, do you think that females heterozygous for the recessive DMD disease allele could havethe disease in some parts of their bodies and not others?
- All of the following statements aboutinheritance are true, except one. Which one of the following statements is INCORRECT ? O All genes have two alleles: one dominant and one recessive. Some phenotypes arise from the interaction of more than one gene. O Incomplete dominance is when heterozygotes express a phenotype that appears to be a blend between the phenotypes of homozygotes. O Even If you know the genotypes of both parents, you cannot always know with certainty the genotype their child will have.What explains how the parents in a family both have the same eye color, but some of their children have a different eye color? Assume for this example that eye color is determined by a single gene. ● One parent is homozygous dominant, and the other homozygous recessive for a gene that controls eye color allowing some of the children to express a different trait. O The parents are both heterozygous for a gene that controls eye color allowing some of the children to get two recessive alleles. O The parents are both homozygous dominant for a gene that controls eye color allowing some of the children to get two recessive alleles. O One parent is homozygous dominant, and the other heterozygous for a gene that controls eye color allowing some of the children to express a different trait.TTGG ttgg F1 TG tg F2 TtGg Which types of genotypes are represented in F1 and F2 in the above figure, respectively? heterozygous and heterozygous heterozygous and homozygous homozygous and heterozygous homozygous and homozygous
- If a gene shows classic dominance (one allele is dominant, one is allele is recessive), what is the phenotype of a heterozygote? O Recessive phenotype O Unable to determine without more information Mixed phenotype O Dominant phenotypeAlbinism 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? _____________________What mode of inheritance does dark blue skin color in Gunguns show? The Ankura race of Gunguns on the planet Naboo have a an inherited genetic disorder which results in afiete ididuas haveing dark blue skin color.The pedigree belowis from anafected faniy Gunguns are dpid wih females being homoazygous and males being hemizygous. Answer questions 3-6 based on the pedigre below: 2 3 9 10 00 5 6 89 1 12 13 14
- In rabbits, fur colour can be either grey, black or blotchy. Blotchy is present as grey and black spotspresent in no specific pattern. Males are almost always either grey or black, while females can begrey, black or blotchy. However, a male individual is found that shows the blotchy pattern, and youexpect a non-disjunction event might be to blame. Explain the inheritance of coat colour in rabbits,and also provide an explanation for the blotchy male.If a genotype has two identical alleles that are always expressed, how would it be described as? O Homozygous recessive O Heterozygous O Nullizygous O Homozygous dominantHuntington’s disease, is an incurable neurodegenerative genetic disorder that affectsmuscle coordination and some cognitive functions, typically becoming noticeable inmiddle age. It results from an autosomal dominant gene (H) and there are no carriers ofthe disease. Two parents with Huntington’s disease have an affected child. What is theprobability that their next child will be an unaffected girl if they are not double-dominant?
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