Ans. a
Allele is X-linked recessive for trait because the two normal parents i.e. 1 and 2 or 4 and 5 are having affacted offspring which is only possible when Male is healthy and female is carrier.
Ans. b
III - 12 will be carrier because their son (IV-6) is affacted which is only possible when mother having mutant allele.
Now 5th child may be male or female but the it will decided by the X gene from mother that child is affacted or not. 1/2 chances will there to be affacted child.
Ans. c
6th child to be born girl child will be 1/4
1/2 chances to be girl child and further 1/2 chances will there that gamete with X chromosome having normal gene will fuse with fathers X chromosome bearing gamete.
The pedigree above shows the inheritance history of a trait that is known to be due...
4. Assume that the trait in the accompanying pedigree is due to simple Mendelian inheritance. . Co to odno a) Is it likely to be due to a dominant allele or a recessive allele? Explain. b) What is the biological relationship between Ill1 and 1112 c) If the allele responsible for the condition is rare, what are the most likely genotypes of all the people in the pedigree in generations I, II and III? (Use A and a for the...
Makimiy PILUILLIUM THE PROBLEM This pedigree shows the inheritance of a recessive trait in humans. Indi- viduals that have the trait are homozygous for a recessive allele a. If Handl, who happen to be first cousins, marry and have a child, what is the chance that this child will have the recessive trait?
11. (8 m) Refer to the following pedigree, which traces the inheritance of a biochemical disorder. female not affected female affected 0 male not affected male affected a. (2 m) Does this disorder appear to be caused by an autosomal or sex-linked gene? Does this disorder appear to be caused by a dominant allele or by a recessive allele? Explain how you know this. b. (2 m) Fill in the genotypes of all affected individuals. Use A and a to...
QUESTION 11 In this human pedigree, what is the most likely mode of inheritance of the trait? Autosomal dominant. Autosomal recessive. Sex-linked recessive. Sex-linked dominant.
Part B - Identify the mode of inheritance Look over the pedigree you constructed in Part A. Based on the inheritance pattern, which mode of inheritance must be the cause of galactosemia? Based on the inheritance pattern, which mode of inheritance must be the cause of galactosemia? sex-linked dominant autosomal dominant sex-linked recessive autosomal recessive SubmitHintsMy AnswersGive UpReview Part Part C - Predicting the probability of inheritance Jane and John are considering having another child. Given the pedigree you constructed...
For each pedigree below determine the most likely mode of inheritance and label each individual with a genotype. If you know they have a dominant phenotype, but don’t know the genotype, then label them with both possibilities. Please use the alleles A and a for autosomal modes of inheritance and XA, Xa and Ya for any types of sex-linkage (note: an “a” is only on the Y if the trait is Y-linked). Modes of inheritance are autosomal dominant, autosomal recessive,...
The conclusions about inheritance (above) can be used to help analyze pedigrees. For each pedigree below, tell if the trait can be autosomal dominant, autosomal recessive, and X-linked recessive. If the pedigree cannot fit a mode of inheritance, tell why. Record your answers in the table on the next page. Pedigree A 2 3 o.a. 9 10 12 (13 14 ad ada 15 16 Xx 20 aa ia ha Pedigree B 910 11 12 14 a ta da Enter either...
The mode of inheritance for the following pedigree is X-linked recessive. If individuals III-1 and III-2 were to have another child, what is the probability that they would express the trait? Explain your reasoning.
The pedigree below shows the inheritance pattern of a sex-linked allele for one family. What is true about the genotype of individuall-2? 1-1 1-2 II-1 II-2 II-3 II-4 III-1 III-2 The disease is caused by a dominant allele (D) and his genotype is dd He must have the genotype X'Y The disease is caused by having two recessive alleles (dd) and his genotype is He has the recessive disease allele on his X chromosome XY He has the dominant disease...
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...