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- The following pedigree shows the pattern of inheritance of red green color blindness in a family. Females are shown as circles and males as squares; the squares or circles of individuals affected by the trait are filled in red. What is the chance that a son of the third-generation female indicated by the arrow will be color-blind if the father is a normal man? If the father is color-blind?Individuals affected by a condition known as polydactyly have extra fingers or toes. The following pedigree shows the pattern of inheritance of this trait in one family: From the pedigree, can you tell if polydactyly comes from a dominant or recessive allele? Is the trait sex-linked? As far as you can determine, what is the genotype of each person in the pedigree with respect to the trait?Hi, I'm having trouble with my study guide for my upcoming genetics exam. If someone could please help with work shown and an explanation it would help so much! Thank you!! 2a. The pedigree below represents inheritance of rare condition. What pattern of inheritance is most consistent with the data? Assign alleles to all individuals to support your answer. If an allele is unknown, assign it a ? symbol. NOTE: Individuals whose phenotype or genotype cannot be determined are assumed to be unaffected and homozygous, unless otherwise indicated. 2b. In addition to the alleles you’ve indicated, describe 2 overall features of the pedigree that make it consistent with your chosen form of inheritance. 2c. Based on your mode of inheritance, what is the probability that the child of couple IV-4 x IV-5 will be affected? Show your work. attached is the pedigree
- Can someone help me with these genetics questions about Punnett squares and pedigrees?A corn geneticist wants to obtain a corn plant that hasthe three dominant phenotypes: anthocyanin (A), longtassels (L), and dwarf plant (D). In her collection ofpure lines, the only lines that bear these alleles are AALL dd and aa ll DD. She also has the fully recessive lineaa ll dd. She decides to intercross the first two and testcross the resulting hybrid to obtain in the progeny aplant of the desired phenotype (which would have to beAa Ll Dd in this case). She knows that the three genesare linked in the order written, that the distance between the A/a and the L/l loci is 16 m.u., and that thedistance between the L/l and the D/d loci is 24 m.u.a. Draw a diagram of the chromosomes of the parents,the hybrid, and the tester.b. Draw a diagram of the crossover(s) necessary toproduce the desired genotype.c. What percentage of the testcross progeny will be ofthe phenotype that she needs?d. What assumptions did you make (if any)?1. The pedigree shown below illustrates the inheritance pattern for a trait controlled by a single fully penetrant gene with complete dominance. Based on the pedigree do the following: a. List one mode of inheritance consistent with the pedigree.
- 1. You have a line of rice that is true breeding for the recessive traits fo white rice (r) and dwarfisim (d). You cross a member of this line with an individual that is heterozygous at both loci and shows the dominant phenotypes of red grains (R) and tall height (D) yeilding the following progeny. 417 white grains-dwarf 403 red grains-tall 95 white grains-tall 85 red grains-dwarf a) what is the allelic configuration of the heterozygote? b) how far are the genes controlling grain color and plant height in (cM) c) what are the non cross over gametes d) what are the cross over gametes e) what genotype will result in white grains and tall heights (multplie answers) f) if you cross a heterozygote with the same allelic configuration as above, what is the probability that the offspring will have white grain and trall height? Give your answer to number to THREE decimal places not as a percentage (e.g 0.044Tay-Sachs is a recessive lethal disease in which thereis neurological deterioration early in life. This diseaseis rare in the population overall but is found at relatively high frequency in Ashkenazi Jews from EasternEurope. A woman whose maternal uncle had the disease is trying to determine the probability that sheand her husband could have an affected child. Her father does not come from a high-risk population. Herhusband’s sister died of the disease at an early age.a. Draw the pedigree of the individuals described.Include the genotypes where possible.b. Determine the probability that the couple’s firstchild will be affected.1. Construct a pedigree chart of the trait traced in the situation below.2. The pedigree chart must be constructed with the names and genotypes at the bottom of every individual in the chart.If it is autosomal: Always use the first letter of the dominant trait to represent the dominant allele. For example, if the dominant trait is red, so the allele R-red, while r-yellow. For example, if the person is homozygous dominant for curly hair, we write CC as his genotype. If sex-linked, do not forget to write the parents’ chromosomes (XX-female, XY-male), with their corresponding superscripts (dominant or recessive). The superscript must be based on the first letter of the disorder. For example, the mother is a carrier of hemophilia (which is x-linked recessive), so we write XHXh. If the father has hemophilia, we write XhY. Put the pedigree chart using code properly. The situation is given below: Trait: NeurofibromatosisThe dominant form is neurofibromatosis, caused by the production of…
- 1. Construct a pedigree chart of the trait traced in the situation below.2. The pedigree chart must be constructed with the names and genotypes at the bottom of every individual in the chart.If it is autosomal: Always use the first letter of the dominant trait to represent the dominant allele. For example, if the dominant trait is red, so the allele R-red, while r-yellow. For example, if the person is homozygous dominant for curly hair, we write CC as his genotype. If sex-linked, do not forget to write the parents’ chromosomes (XX-female, XY-male), with their corresponding superscripts (dominant or recessive). The superscript must be based on the first letter of the disorder. For example, the mother is a carrier of hemophilia (which is x-linked recessive), so we write XHXh. If the father has hemophilia, we write XhY. Put the pedigree chart using code properly. The situation is given below: Trait: NeurofibromatosisThe dominant form is neurofibromatosis, caused by the production of…4.) A man and a woman have a child. The father is blood type A, and one of his parents was blood type A and the other was blood type O. The mother is blood type B, and one of her parents was blood type B, the other type O. Both the father and the mother are carriers of the Bombay allele. (Neither of the type-O grandparents were type O because of the Bombay allele – they had the regular type O genotype.) WhataretheoddsthattheirbabywillhavebloodtypeO? WhataretheoddsthattheirbabywillhavebloodtypeAB? (Hint – for this question, you should draw out a pedigree and fill in as much as you can for the genotypes of BOTH genes that are involved.)Two mothers give birth to sons at the same time at a busy urbanhospital. The son of mother 1 has hemophilia, a disease causedby an X-linked recessive allele. Neither parent has the disease.Mother 2 has a son without hemophilia, despite the fact thatthe father has hemophilia. Several years later, couple 1 suesthe hospital, claiming that these two newborns were swappedin the nursery following their birth. As a genetic counselor, youare called to testify. What information can you provide the juryconcerning the allegation?