Genes a and b are 20 cM apart. An a+ b+/a b individual was mated with an a b/a b individual. Which of the following is not true: Group of answer choices a and b are autosomal alleles for a and b are in the a cis configuration alleles for a and b are in the a trans configuration a and b are linked
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- Two pure-breeding lines of petunia plants are crossed. Line 1 plants grow to a height of 54 cm, and Line 2 plants grow to a height of 18 cm. Petunia plant height is controlled by three genes, A, B and C. Line 1 has the genotype A₁A₁B₁B₁C₁C₁, and line 2 has the genotype A2A2B₂B₂C₂C₂. Assume that genotype alone determines plant height under ideal growth conditions and that the alleles of the three genes are additive. If the F1 plants are self crossed, what is the expected proportion of F2 plants with the genotype A₁A₁B₁B₁C₁C₁ 1/8 1/32 1/16 1/4 1/64In roses, purple flower color is determined by the dominant P allele, while pphomozygotes are white. The presence of long stems is determined by the dominant S allele, while ss homozygotes have short stems. Both mutations are completely penetrant. A test cross was performed between a rose plant of unknown genotype with a white flowered, short stemmed rose plant (pp ss) and the following 200 progeny plants were obtained: 84 white flowers, long stems 16 purple flowers, long stems 82 purple flowers, short stems 18 white flowers, short stems Select two statements below that are TRUE. options: The P and S genes independently assort during meiosis. The map distance between P and S is 17 cM. The genotype of the progeny plants with purple flowers and short stems is PP ss. The map distance between P and S is 83 cM. The homologs in the plant with…Suppose that the wild type phenotype for tomatoes is red, round fruit with three-parted leaves and that a strain of mutant tomatoes has yellow, pear-shaped fruit with entire leaves. A and a represent the alleles for fruit color, B and b represent the alleles for fruit shape, and C and c the leaf shape. Two tomatoes with the genotypes Aa Bb cc and Aa Bb CC are crossed. The resulting Punnett square is shown. One cell has been completed with the correct tomato phenotype. Fill in the rest of the Punnett square by placing a fruit and leaf phenotype in each cell. ABC AbC aBC abC ABC Abc aBc abc Answer Bank
- Two fruit flies (Drosophila melanogaster) were crossed. The cross was between a homozygous red-eyed, wingless female and a white-eyed male heterozygous for wings. Recall that red eyes (R) is dominant over white eyes (r) and is inherited on the X chromosome (sex-linked) and as such, eye colour alleles should be written as superscript. In addition, the autosomal trait wings (W) is dominant over wingless (w). 1. List the female genotype 2. List the male genotype 3. Construct a Punnett Square for this dihybrid cross on a piece of paper, to determine what the offspring of such a cross would be with respect to sex, eye colour & wings. 4. Using the information from your Punnett Square answer the following: a. What genotypes did you get (list all genotype combinations; if you have more than one of the same kind, you do NOT have to re-list it.) b. What are the phenotypic ratios of the offspring with respect to sex, eye colour and wings?There are two genetic disorders that result from mutation in imprinted genes: Prader-Willi syndrome, Angelman syndrome. Angelman syndrome results from deletion of UBE3A, which is a gene imprinted such that only the maternal copy is expressed. In the pedigree above, individual I-1 is heterozygous for a deletion of UBE3A and does not have Angelman syndrome. Individual I-2 is homozygous wild type for UBE3A. Which individuals in the pedigree are at risk for exhibiting Angelman syndrome, if any? (Who could potentially have the syndrome, based on what alleles it is possible for them to inherit and express?) Question 8 options: Only I-1 could have been at risk. If he does not have the syndrome, no one in the pedigree could. Only III-1 is at risk I-1, II-2, and III-1 are all at risk Only II-2 is at risk No one in the pedigree is at risk Both II-2 and III-1 are at…What is the approximate percentage chance that individual V.2, shown in the pedigree diagram below will have inherited the X- linked recessive allele shown to be carried by his great-great-grandmother? Note: only type the number, not the percentage symbol. Answer: The chance that individual V.2 shown in the pedigree below has inherited the X-linked recessive allele shown to be carried by his great-great grandmother is approximately Blank 1 percent. 노 ㅍ먹이 12 I 마일 메인 de 먹어 요 58 ㅁ + ܡܐ
- please answer all subquestions as they are all related to the diagram,a like is guaranteed.In the rat, the pattern of coat color is affected by a gene with two alleles. PH is the allele for hooded, in which the animal is mostly white with color restricted to the shoulders and neck. P+ is the normal solid body color allele. These two alleles exhibit incomplete dominance, so that heterozygotes have white bellies only. A true-breeding solid strain is crossed with a true-breeding hooded strain, to produce an F₁ generation that is all white belly. The F₁ generation rats are mated with each other to produce 800 F₂ offspring. Below is a table that gives the observed number of each phenotype in the F2 and also gives you the expected number. Question: If you perform a Chi-square goodness of fit test, what is the value of Chi square X² (Express your answer to the hundredths.) solid white belly hooded Σ Observed 195 420 185 800 Expected 200 400 200 800A breeder is interested in a new coat colour in mice. This trait is controlled by a single autosomal gene (Gene T) with two alleles. The T-allele results in a yellow coat colour, while the recessive allele causes a cream coat colour. The breeder has a yellow mouse. Can you suggest how the breeder can determine the genotype (TT or Tt) of his mouse in a single cross? Describe this cross and provide details on how you would interpret the results.
- The data set attached summarizes F2 numbers from an F1 cross arising from two, true-breeding Drosophila strains (P generation), which differ with respect to two mutant traits. Here are the hypothesis: Leg length - The wild-type and mutant alleles for leg length are incomplete dominant relative to each other. Justification: The data set includes three phenotypic categories for leg length: wild type (long leg), medium leg, and truncated wings. The presence of three distinct phenotypes suggests an incomplete dominance pattern, where the heterozygous individuals exhibit an intermediate leg length phenotype (medium leg). The absence of purebred short-legged individuals supports the idea that the long leg allele is dominant over the short leg allele. This shows that mode of inheritance is incomplete dominance of the alleles relative to each other. Since the data does not mention any specific differences between males and females, we can assume that the mode of inheritance for the trait is…A test cross between a plant of genotype PpSs and the tester white plant with wrinkled seed coat (ppss) gives the following numbers of progeny in four phenotypic types. 14:87:83:16 (purple flower + smooth seed coat: purple flower + wrinkled seed coat: white flower + smooth seed coat: white flower + wrinkled seed coat). a. What is the expected ratio of progeny phenotypes assuming independent assortment of alleles? b. Explain how ratios of progeny show that the two genes are linked. c. How many map units separate the purple and smooth genes? Show your calculations. d. What is the “parental” genotype of the heterozygous parent? (i.e. Which alleles of the P and S loci are present on each of the two chromosomes of the doubly heterozygous parent of this test cross?)Which of the Pedigree diagrams below is most likely to show a family with Sickle Cell Anaemia?