Question

Explain how the expected F1 results differ depending on whether the genes are x-linked or autosomal.

Explain how the expected F1 results differ depending on whether the genes are x-linked or autosomal.

Homework Answers

Answer #1

If a disease is showing sex linked inheritance it defiantly differ in its way of transmitting to the next generations from the autosomal diseases. In autosomal diseases receprocal crosses would give the similar offspring. But in sex linked inheritance receprocal crosses resulted in different progeny.

For example let's considera gene-A responsible for enzyme for which nonfunctional form causes disease if we consider a cross

(Female) aa. X. AA (male)

Progeny all Aa having no disease irrespective of the gender.

But in x linked cromosomal disease's

If female effected

(Female) xx. X. XY(male)

Progeny Xx (female) and xY (male) male effected and female are not effected but all female are carriers

If male effected

XX. X. xY

Progeny Xx all female are carrier's and XY male not effected but xY male are effected.

  

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
. (4 pts.) The mouse autosomal genes B and S are linked and 38 map units...
. (4 pts.) The mouse autosomal genes B and S are linked and 38 map units apart. We cross mouse strains BBSS and bbss to produce an F1. That F1 is the test crossed to bbss. Predict the number of progeny from the test cross in each of the following phenotype groups: B_S_ = B_ss = bbS_ = bbss =
Assume that genes X and Y are linked and are 20 cM apart. Also assume that...
Assume that genes X and Y are linked and are 20 cM apart. Also assume that an individual homozygous for X and y is cross to an individual homozygous for x and Y to produce an F1 individual. True/False: 40% of the gametes produced by this F1 individual should be x Y gametes. Assume that this F1 individual is crossed with an xx yy homozygote. True/False: 10% of the progeny should be heterozygous for both genes.
1. Describe how Sex-linked inheritance works 2.Explain how linked genes are inherited
1. Describe how Sex-linked inheritance works 2.Explain how linked genes are inherited
Morgan found that the genes pr and vg were closely linked. In a incross of F1...
Morgan found that the genes pr and vg were closely linked. In a incross of F1 in the cis dihybrid configuration for these genes, what phenotypic classes would be in the minority? A. pr and vg B. WT and pr vg C. WT and vg pr and pr vg D. pr pr and vg vg *Please show how you found the answer.
The cross EEFF X eeff is made, and a testcross is then performed with the f1...
The cross EEFF X eeff is made, and a testcross is then performed with the f1 individuals. The testcross yield the following proportion of offspring. 2/6 EeFf, 1/6 Eeff, 1/6 eeFf, 2/6 eeff a) if the two genes are unliked, them what should the proportion of offspring be? b) Do the testcross results suggestion suggestion that the gene are linked or unlinked? c) if the two genes are linked, then how far apart are they?
In the snail Cepaea nemoralis, an autosomal allele causing a banded shell (BB) is recessive to...
In the snail Cepaea nemoralis, an autosomal allele causing a banded shell (BB) is recessive to the allele for unbanded shell (BO). Genes at a different locus determine the background color of the shell; yellow (CY) is recessive to brown (CB). A banded, yellow snail is crossed with a homozygous brown, unbanded snail. The F1 are crossed with a banded, yellow snail (a testcross). a. What will be the results of the testcross if the loci assort independently? b. What...
Linkage studies in individuals heterozygous for an inversion show that genes appear more closely linked than...
Linkage studies in individuals heterozygous for an inversion show that genes appear more closely linked than expected. Explain how an inversion might “suppress” meiotic recombination.
(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),...
Three Drosophila genes on the X chromosome occupy three different loci. The mutant versions of these...
Three Drosophila genes on the X chromosome occupy three different loci. The mutant versions of these genes are y for yellow body ct for cut wing ec for echinus (spiky eyes) When a cross is between female X, and male Y flies, the P and F1 have the following genotype + + +/y ct ec When the F1 is selfed to create the F2, most wild type genes remain linked on the same chromosome, as do the mutant genes on...
15) Colorblindness is an X-linked recessive trait (“D” results in normal vision, whereas “d” results in...
15) Colorblindness is an X-linked recessive trait (“D” results in normal vision, whereas “d” results in colorblindness). A man has normal color vision. In addition, he is heterozygous (Bb) for an autosomal gene that causes extreme sensitivity to strep throat when homozygous recessive. a) What proportion of his sperm will be “bD”? b) If he marries a woman who is heterozygous for both traits, what proportion of their children will be daughters that are colorblind and sensitive to strep throat?...
ADVERTISEMENT
Need Online Homework Help?

Get Answers For Free
Most questions answered within 1 hours.

Ask a Question
ADVERTISEMENT