The pedigree below shows the inheritance of red-green colorblindness, an X-linked recessive trait (XD = normal vision, Xd = colorblindness allele). For all of the questions below, assume that there is no abnormal event or new mutation; also, ignore X-inactivation for this problem. - Genotype II 1 2 3 II What are the genotypes of the following individuals for color vision. Use "?" to indicate any allele about which you are uncertain. 1-1 = 1-2 = Il-1 = Il-2= Il-3 = (a) What is the probability that III-1 will be colorblind? Explain your reasoning to show how
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- Does the phenotype indicated by the red circles and squares in this pedigree show an inheritance pattern that is autosomal dominant, autosomal recessive, or X-linked?The following pedigree describes the inheritance of Lesch-Nyhan syndrome, an x-linked recessive disease. Affected individuals are shaded. what is the probability, that the indicated child (IV.1) will be affected by Lesch-Nyhan syndrome? show solutionIn the pedigree attached, the shaded symbols represent people affected with a neurological disorder caused by an X-linked recessive allele. The normal allele is D and the recessive allele is d. What are the genotypes of every person in this pedigree? Please explain in as much detail as possible.
- Using the pedigree chart attached: Above is a pedigree for colorblindness. Based on the pedigree, is the disease dominant or recessive and is it sex-linked or autosomal? Why? Furthermore, what is the probability that 18 on this chart is affected but the condition, and what is the probability that 18 is a carrier? Why? Are the probability of being a carrier and an affected individual different? Why?Red-green color blindness is inherited as an X-linked recessive (Xc). If a color-blind man marries a woman who is heterozygous for normal vision, what would be the expected phenotypes of their children with reference to this character? In your answer, specify in your phenotype descriptions the gender of the children. (For example, don’t just say 75% of the children would be colorblind – you would instead say 100 % of the daughters would be colorblind and 50% of the sons would be colorblind. Note that this is not a correct answer; it is just to give you an idea of how to explain the correct phenotypes of the cross.)___The pedigree below represents the inheritance of a rare genetic disorder (members joining the pedigree are not carriers). Consider the following pedigree and answer questions (i) to (vii) below. The allele descriptors are B/b. What is the mode of inheritance in this pedigree ? Y-linked inheritance X-linked recessive inheritance X-linked dominant inheritance Autosomal recessive inheritance Autosomal dominant inheritance What is the genotype of individual III-2 ? a) XbXb b) XBXB c) XBXb d) Bb e) bb What is the genotype of individual IV-3 ? a) XbXb b) XBXB c) XBXb d) Bb e) bb Individual IV-4 and an unaffected woman is planning a family. What is the probability that their first child will be phenotypically normal ? a) chance that the first child will be phenotypically normal. b) chance that the first child will be phenotypically normal. c) chance that the first female child will be phenotypically normal; all male children will be phenotypically normal. d) chance that the…
- Duchenne muscular dystrophy is a recessive disorder caused by a rare,loss-of-function allele that is located on the X chromosome in humans. Anunaffected woman (i.e., without disease symptoms) who is heterozygousfor the X-linked allele causing Duchenne muscular dystrophy has childrenwith a man with a functional (non-disease-causing) allele. What is theprobability that this couple will have an unaffected son?Suppose gene B is X-linked and is embryonically lethal when homozygous or hemizygous recessive. A man marries a woman who is heterozygous for this gene. They want to have three kids – one girl and two boys. Using a Punnett square, answer the following: What is the probability that they will have a son that dies before birth? _______________________ What is the probability that they will have a daughter who has the same genotype as her mother? _________________ One of their daughters eventually has a child with a man. One of their sons dies before birth. What was the genotype of this daughter? _______________________________ please show me how to get the answer and explain how you got and use a punnet squareIn the following pedigree, is the disorder’s mode of inheritanceautosomal dominant, autosomal recessive, or X-linked recessive?Explain your reasoning.
- Figure 5.1 presented abbreviated pedigrees looking at the inheritance of X-linked human conditions. El Figure 5.1a initiated with a male who was color blind and had hemophilia A. The grandsons and great-grandsons of this male were either color blind and had hemophilia A, or they had neither condition. a. Which if any individuals in the G Fig. 5.1a pedigree is a double heterozygote? b. Are any of the grandsons or great-grandsons shown in the pedigree the product of recombinant type gametes? c. Do the genes responsible for color blindness and hemophilia A segregate independently? d. If you examined many pedigrees, each starting with a man who was simultaneously color blind and had hemophilia A, do you think any grandsons or great-grandsons would ever have one condition but not the other? L Figure 5.1b initiated with a male who was color blind and had hemophilia B. The grandsons of this male were either only color blind, only had hemophilia B, had both conditions, or they had neither…The following X-linked recessive traits are found in fruit flies:vermilion eyes are recessive to red eyes, miniature wings are recessiveto long wings, and sable body is recessive to gray body. A cross wasmade between wild-type males with red eyes, long wings, and graybodies and females with vermilion eyes, miniature wings, and sablebodies. The heterozygous female offspring from this cross, whichhad red eyes, long wings, and gray bodies, were then crossed tomales with vermilion eyes, miniature wings, and sable bodies. Thefollowing data were obtained for the F2 generation (including bothmales and females):1320 vermilion eyes, miniature wings, sable body1346 red eyes, long wings, gray body102 vermilion eyes, miniature wings, gray body90 red eyes, long wings, sable body42 vermilion eyes, long wings, gray body48 red eyes, miniature wings, sable body2 vermilion eyes, long wings, sable body1 red eyes, miniature wings, gray bodyA. Calculate the map distances separating the three genes.B. Is…The following X-linked recessive traits are found in fruit flies:vermilion eyes are recessive to red eyes, miniature wings are recessiveto long wings, and sable body is recessive to gray body. A cross wasmade between wild-type males with red eyes, long wings, and graybodies and females with vermilion eyes, miniature wings, and sablebodies. The heterozygous female offspring from this cross, whichhad red eyes, long wings, and gray bodies, were then crossed tomales with vermilion eyes, miniature wings, and sable bodies. Thefollowing data were obtained for the F2 generation (including bothmales and females):1320 vermilion eyes, miniature wings, sable body1346 red eyes, long wings, gray body102 vermilion eyes, miniature wings, gray body90 red eyes, long wings, sable body42 vermilion eyes, long wings, gray body48 red eyes, miniature wings, sable body2 vermilion eyes, long wings, sable body1 red eyes, miniature wings, gray bodyWhat information do you know based on the question and your…