Question

If the d and e genes are 24cM apart in humans, and a DE/de woman mates...

If the d and e genes are 24cM apart in humans, and a DE/de woman mates with a de/de man, what is the probability that their first child will have the genotype DdEe?

Homework Answers

Answer #1

Question:

Answer:

Male : de/de

Female: DE/de

Alleles

de

de

DE

DdEe

DdEe

de

ddee

ddee

Probability of getting DdEe offspring in absence of linkage =2/4 = 0.5

But in presence of linkage, map distance between d and e = 24cM

Probability of getting DdEe offspring = (Probability of getting DdEe offspring in absence of linkage – probability of conversion DE into De or dE

= (0.5- (0.24/2)

= (0.5-0.12)

= 0.38          

Know the answer?
Your Answer:

Post as a guest

Your Name:

What's your source?

Earn Coins

Coins can be redeemed for fabulous gifts.

Not the answer you're looking for?
Ask your own homework help question
Similar Questions
1.) Two linked genes, A and B, are separated by 20cM. A man with genotype AB/ab...
1.) Two linked genes, A and B, are separated by 20cM. A man with genotype AB/ab marries a woman who is ab/ab. What is the probability that their first child will be Ab/ab? 2.) An individual has genotype Ab/aB. Gene loci A and B are 20cM apart. What is the proportion of expected progeny Ab/ab if a testcross is performed on this individual?
Hemophilia is a sex-linked recessive disorder. If an unaffected woman mates with an unaffected man, and...
Hemophilia is a sex-linked recessive disorder. If an unaffected woman mates with an unaffected man, and they have 2 children with hemophilia, and 2 children who are unaffected What are the chances that the couple will have a child with hemophilia?
a.) There are genes C and D that are 16 map units apart. The cross parent...
a.) There are genes C and D that are 16 map units apart. The cross parent genotypes are: CC:DD x cc:dd. What would be the proportion of gametes C:D in the F1 generation? b.) There are genes C and D that are 20 map units apart. The parental cross was CC:dd x cc:DD and F1 individuals were crossed, Cc:Dd x Cc:Dd. What is the proportion of the F2 offspring that have the CC:DD genotype?
There is a gene in humans that causes dimples to form on the face. The allele...
There is a gene in humans that causes dimples to form on the face. The allele that causes facial dimples (D) is completely dominant to the allele (d) that does not cause dimples. Let’s say there is a man and woman who are both heterozygous at this locus. The predicted phenotypic ratio of their F1 is: a. 1:1 b. 1:2 c. 1:2:1 d. 3:1 There is a gene in humans that causes dimples to form on the face. The allele...
Complete a punnett square for the cross between a human female (XX) and a human male...
Complete a punnett square for the cross between a human female (XX) and a human male (XY). What is the chance that the parents will have a girl? If the same parents have four boys, what is the probability their fifth child will be a girl? Hemophilia is a recessive sex-linked disease carried on the X chromosome in humans. Write the genotype of a woman who does not have hemophilia. ______ Write the genotype of a woman with hemophilia. ________...
(5 pts) Genes D and E are located in the Drosophila genome. DE·DE females are crossed...
(5 pts) Genes D and E are located in the Drosophila genome. DE·DE females are crossed with de·de males to produce F1 flies that are heterozygous for both traits. What gametes do each of these parents make? F1 females were crossed with de·de males, and 2000 flies were examined. What gametes do each of these parents make? What are the possible genotypes of the offspring produced from the cross in part B? If the genes were sorting independently (not linked),...
Hemophilia is a sex-linked recessive disorder. If an unaffected woman mates with an unaffected man, and...
Hemophilia is a sex-linked recessive disorder. If an unaffected woman mates with an unaffected man, and they have 2 children with hemophilia, and 2 children who are unaffected What are the chances that the couple will have a boy who has hemophilia?
In humans, the disease galactosemia is inherited as a rare autosomal recessive trait in a simple...
In humans, the disease galactosemia is inherited as a rare autosomal recessive trait in a simple Mendelian manner. A normal woman whose father had galactosemia intends to marry a normal man whose grandfather had galactosemia. What is the probability that their first child will have galactosemia? A. 1/2 B. 1/8 C. 1/16 D. 1/4 E. 0 Correct Answer: B. 1/8 Can you explain why?
A and B genes are linked at 20 cM apart. A genotype with known linkage phase...
A and B genes are linked at 20 cM apart. A genotype with known linkage phase AB/ab is testcrossed to aa bb. What proportion of the offspring is expected to be dominant for both genes? Select one: A. 80% B. 40% C. 10% D. 20% E. 0%
A man and woman both have one parent who has albinism but both (man and woman...
A man and woman both have one parent who has albinism but both (man and woman ) have normal skin pigmentation. What is the probability that their first child will have albinism if albinism is a recessive trait?
ADVERTISEMENT
Need Online Homework Help?

Get Answers For Free
Most questions answered within 1 hours.

Ask a Question
ADVERTISEMENT