2024_ProblemSet_1(1)

1-Gigantism is being traced in a family through a pedigree. Its mode of inheritance is thought to be autosomal recessive. You examine the pedigree and decide that the mode of inheritance is not correct. What is the correct mode of inheritance? 2-Provide 2 pieces of evidence for the mode of inheritance selected for Gigantism. (i.e.- Individual 45 is afflicted and passed it on to all of her offspring, indicating that it is dominant. Or there is a gendered pattern of inheritance seen when Individual 99 passed it on to only his female offspring.)

tion 8: below is the pedigree of inheritance of phenylketonuria (PKU). We will designate the letter Caven for the dominant allele and "p" for the recessive allele. 4 The pedigree shows that the pattern of inheritance for the allele for phenylk ylketonuria is: I. II. 1 III. IV. Autosomal dominant Autosomal recessive X-linked dominant X-linked recessive b. The parents in generation I have how many children: I. 3 Boys II. 3 Girls III. IV. 3 Boys and 1 Girl 3 Girls and 1 Boy c. What is the genotype of individual 1 in generation III: I. PP II. pp III. Pp " O 1 III. 50% E III 1 ▬ 2 2 IV. 25% 1 3 IV. Can be PP or Pp ii. Suppose that a man having type AB blood marries a woman having type O blood. What is the probability that their child will have type A blood? I. 100% II. 75% 2 4 3

What is the probability that III-j has Huntington's?

PEDIGREES: Problem 7 This pedigree shows the inheritance of atype of X-linked color blindness. It is a recessive trait. Carriers have NOT been half-shaded in this pedigree. • QUESTIONS • • • I ODO0 I. Work out who is definitely a carrier & drag the correct shape onto them. 1 2 3 4 II 1 3 2. Is it possible to work out the geno- type of individual II-I? Explain III your reasoning. 1 2 3 IV 1

40 Below is a pedigree of a family, some of whom have the autosomal dominant condition Huntington's disease. Affected individuals are indicated by a dark square or circle. The male in generation I (indicated by the arrow) is heterozygous for the Huntington's disease mutation. The following two questions relate to this pedigree. Generation II II If H represents the disease allele, and h the wild type allele, what is the genotype of the individual indicated by the *? Select one alternative: O hh O Hh O hH O HH

11 please answer all with complete explanation/solution

age 105 of 114 3 5 € BUD > D Q Autosomal Genes 1. Parental Cross: It is possible that your mutation is autosomal (dominant or recessive). In this case, you only need one Punnett square to make predictions for the F1 generation that will result from the parental cross, as it does not matter if the female or male in the parental generation is the true breeding mutant. a. Provide a Punnett square to predict the genotype of the F1 generation. b. Q Search If the mutant allele is dominant, predict the phenotype of the F1 generation. Make sure to also summarize the prediction as a ratio, comparing Wild-type : Mutant. c. If your mutant allele is recessive, predict the phenotype of the F1 generation. Make sure to also summarize the prediction as a ratio, comparing Wild-type : Mutant. 2. F1 Self-Cross: Take the F1 results from question #1 to create a Punnett square predicting the F2 generation genotypes. 104 a. What are the predicted F2 phenotypes if the mutant allele is dominant? Make sure to…

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Please draw it out so I understand how it's suppose to be drawn

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8-9. White eyes (w) is sex-linked and recessive in Drosophila. Cruved wings(cu) and black body (b) are autosomal recessive alleles on the same chromosome, separated by 20 map units. If one breeds a homozygous white, curved winged female fly to a homozygous black male fly to produce an F1, and inbreeds the F1 males and females, at what frequency is a phenotypically wild-type male expected? (note: male flies do not cross over) A. 0.25 es B.0.05 C.0.10 D. 0.20 E.0.125

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70 T 꿈 ㅁ ㅁ 이어어어어어어 In the pedigree shown, indicate whether each of the following inheritance patterns is possible by selecting YES or NO from the appropriate drop down menu. Y-linked Autosomal Recessive Autosomal Dominant X-linked Recessive X-linked Dominant ()

Show your solution please. 4.

Consider the following pedigree. 하 3 10 (5 3 2 (a) What pattern of transmission is most consistent with this pedigree? (1) autosomal recessive, (2) autosomal dominant, (3) X-linked recessive, (4) X-linked dominant. (b) If individual V-2 marries a normal individual, and if the condition has a pene-trance of 85 percent, what is the probability that their second child will express the trait? (c) On the third line, what does the diamond with a 10 in the middle mean?

solve only a4 and a5

AKS 7b/7e Mendelian Inheritance In pea plants the allele for round seeds (R) is dominant to the allele for oval seeds (r). In a cross between the two heterozygous plants what percentage of the offspring will have round seeds? * O 75% O 50% O 25% O 100% This is a required question In pigeons, the allele for normal feathers (F) is dominant to the allele for frizzy feathers (f). If a purebred, normal feathered bird (FF) is crossed with a frizzy

BIU A- == 三E 12 - Match each of the following examples to the appropriate type of non-Mendelian inheritance. 1. A homozygous recessive genotype for the gene that encodes phenylalanine hydroxylase (which breaks down the amino acid phenylalanine) causes lighter skin color, a musty odor, differences in intellectual development, and seizures. 2. In pea plants, alleles of Gene W control flower color, with the dominant allele (W) leading to purple flower.color, and the recessive allele (w) leading to white flower color. Usually, a genotype of WW or Ww leads to purple flowers. However, when Gene C is homozygous recessive, WW or Ww plants always have white flowers. 3. In mallard ducks, feather coloring is controlled by Gene F. A dominant allele (F) leads to green head feathers, while a recessive allele (f) leads to brown head feathers. In male mallards, inheritance of one or more F alleles always leads to the green head feather trait. But female mallards always have brown head feathers,…