Dominant trait -- it is expressed when it is either in Homozygous or heterozygous condition.
Example -- here trait is represented by A and a. If dominant can be AA and Aa.
Recessive trait -- it is expressed only in Homozygous condition.
Example -- aa.
Ans a) the trait expressed in the Pedigree is recessive because the parents of individual IV-4 are unaffected with the trait. As parents are unaffected so they can be Homozygous dominant( AA) or heterozygous dominant (Aa). If either of parent is Homozygous dominant so they can't have an affected child. That means IV-4 individual parents are heterozygous dominant (Aa). The trait is recessive as parents aren't affected but are carrier of the recessive allele.
Ans b) the relationship between III-1 and III-2 is that they both have a common ancestor. The II-2 and II-3 are the children or progeny of I-1 and I-2. And I-1 and I-2 are the common ancestor of III-1 and III-2.
Ans c) the genotypes of all the individuals in the Pedigree are as follows:
As the trait is recessive in nature; recessive allele=a and dominant allele=A. Individual with recessive trait=aa; dominant trait = AA or Aa.
The likely genotypes of all individuals are in the image below :
Generation I,II and III will have genotype Aa. IV have aa, A_. _ can be A or a.
Thank you...
Expect a ???....
4. Assume that the trait in the accompanying pedigree is due to simple Mendelian inheritance. ....
The pedigree above shows the inheritance history of a trait that is known to be due to a sex- linked allele. a) is the allele responsible for the trait recessive or dominant? Explain your reasoning. (2 marks b) What is the chance that the fifth (5) child born to III-11 and 111-12 will be affected? (1 mark) c) What is the chance that the sixth (6) child born to III-11 and III-12 will be a female carrier? (1 mark) Display...
Question 20 This pedigree (Pedigree #1) illustrates the inheritance of a simple Mendelian disorder. What is the likely mode of inheritance A autosomal dominant B. autosomal recessive C. cannot be determined from the information given D. (This is not a choice.) A Moving to another question will save this response.
In simple Mendelian inheritance alleles display a simple dominant/recessive relationship. There are many exceptions to Mendelian laws of inheritance. Most genes have more than two allelic forms and do not exhibit simple Mendelian inheritance. The human ABO antigens are an example of a multiple allelic trait. There are three ABO blood group antigens, IA, IB and i. The i allele is recessive to both IA and IB. A person who is homozygous ii has type O blood and does not...
Question 24 This pedigree (Pedigree #2) illustrates the inheritance of a simple Mendelian trait. What is the genotype of individual I-17 Lo- O AAA B. Aa ос. аа ODA
Part B Determining genotypes in pedigrees of X-linked conditions The pedigree from Part A is shown below. Fill in the most likely genotypes of the indicated individuals in the pedigree. Note that a dominant allele followed by an underscore (_) indicates that either the dominant or the recessive allele may be present at the second position. Drag one pink label (for condition A, autosomal recessive) to each pink target. Drag one blue label (for condition B, X-linked recessive) to each...
Question 25 4 points Save This pedigree (Pedigree #2) illustrates the inheritance of a simple Mendelian trait. If individual II-4 marries a woman who is M. what are the chances that they would have a child with this disorder? To A 1004 B.0% C.25% 0.75 E SOM
In the pedigree below, what is the most likely mode of inheritance for this condition?: X-linked recessive, autosomal dominant, or autosomal recessive? Affected individuals are shown as black symbols. Based on your prediction, give the genotypes of the following individuals: I-1, I-2, II-1, II-3, II-4, III-1, III-2, III-4, IV-2, and IV-3. If you choose autosomal, use A or a; if you choose X-linked, use X^A, X^a, or Y List the proposed genotypes of the designated individuals along the side:
3. The accompanying pedigree shows the inheritance of deaf-mutism. I OOOO II doodoo III a. Provide an explanation for the inheritance of the rare condition in the two families in generation I and II. (1 mark) b. Provide an explanation for the production of only normal individuals in generation III, making sure that your answer is compatible with the answer to part a. (1 mark) c. Give the genotypes of the following individuals, using symbols of your own choosing: (3.5...
QUESTION 9 5 pe If the characteristic depicted in the pedigree below is rare and subject to complete penetrance, it is likely to be X-linked recessive? 5 6 7 -OOO No, because individuals ll-2 and 11-4 are not affected No, because individuals 111-4 and III-6 are not affected Yes, because individuals III-4 and III-6 are not affected Yes, because only females are affected in generation 11 1. The gene for cystic fibrosis (normal dominant allele CF and abnormal recessive allele...
Procedure 8.5 PEDIGREE CHARTS Pedigree charts are diagrams that illustrate how a trait is inherited through generations of a family. They can help us determine genotypes and patterns of inheritance for a trait. HOW TO READ A PEDIGREE CHART 1. Look at the sample pedigree chart in Figure 8.7. 2. Square boxes represent males and circles represent females. 3. A filled-in figure means that the trait is present in that individual. An empty figure means the trait is not present....