A tortoiseshell cat, such as the cat pictured, is likely to be female.Why do tortoiseshell coats occur primarily in female cats?Testosterone suppresses the tortoiseshell gene in males, so tortoiseshell coats appear more often in females, who haveless testosterone than males.Tortoiseshell coloring is an X-linked recessive trait, so females with two X chromosomes are more likely to express thetrait than males.One of a female's two X chromosomes is randomly inactivated in each cell, so each cell may express different alleles.O The X chromosome is disabled in males, so a tortoiseshell coat, which is an X-linked recessive trait, does not occurin males.

Tortoiseshell is a cat coat color that is named for the tortoiseshell material it resembles.…

Answered: Why do tortoiseshell coats occur…

Human Heredity: Principles and Issues (MindTap Course List)

11th Edition

ISBN:9781305251052

Author:Michael Cummings

Publisher:Michael Cummings

Chapter7: Development And Sex Determination

Section: Chapter Questions

Problem 9QP

See similar textbooks

Similar questions

Analysis of X-Linked Dominant and Recessive Traits In the eighteenth century, a young boy with a skin condition known as ichthyosis hystrix gravior was identified. The phenotype of this disorder includes thickening of skin and the formation of loose spines that are sloughed off periodically. This man married and had six sons, all of whom had the same condition. He also had several daughters, all of whom were unaffected. In all succeeding generations, the condition was passed on from father to son. What can you theorize about the location of the gene that causes ichthyosis hystrix gravior?
Note: Don't copy from internet, Also answer correctly in terms of diploid, hemizygous, and carrier!! Thanks Explain why genetic disorders caused by recessive alleles of X-linked genes appear more frequently in males than in females? In your explanation, please include explanations of the following terms: diploid, hemizygous, carrier.
What is a Barr body? How many Barr bodies in a person with genotype XXXXX? How is the structure of a Barr body different from that of other chromosomes in the cell? How does the structure of a Barr body affect gene expression? Color-blindness is an X-linked recessive trait. Heterozygous females are not color blind but they can sometimes have partial color blindness. Explain how this can occur.
In grasshoppers, rosy body color is caused by a recessive mutation; the wild-type body color is green. If the gene for body color is on the X chromosome, what kind of progeny would be obtained from a mating between a homozygous rosy female and a hemizygous wild-type male? (In grasshoppers, females are XX and males are XO
In humans color vision is X-linked, the gene for color vision is located on the X chromosome but is absent on the Y chromosome. Normal color vision (XN) is dominant over colorblindness (Xn). Suppose a colorblind man fathers the children of a woman with genotype XNXN. What is the genotype of the father? What proportion of daughters will be colorblind? What proportion of the sons will be colorblind?
A type of baldness is sex –limited such that the allele that causes it is dominant in men and recessive in women. Thus baldness is much more common in men than women even though the locus is on an autosome. How is the pattern of inheritance in this example different from X-linked inheritance of a recessive allele? Group of answer choices A. the trait can be passed from fathers to sons B. the trait can be passed from fathers to daughters C. the trait can be passed from mothers to sons D. the trait can be passed from mothers to daughters
Red-green colorblindness is inherited in an X-linked recessive pattern in humans. A colorblind man and a woman with normal vision have four children, and one of them is a colorblind male. Does the mother have to be a carrier in this case? (Yes or No) What is the probability of the next child in this family being both colorblind and male? No, 25% Yes, 25% No, 50% Yes, 50%
In humans, an X-linked disorder called coloboma iridia (a fissure in the iris_ is a recessive trait. A normal couple has an afflicted daughter. What would be the most plausible scenario for this situation? the female is not the biological mother, but the male is the biological father the father carries one recessive allele, and the mother carries one recessive allele the mother carries two recessive alleles the male is not the biological father, but the female is the biological mother both parents are heterozygous for the trait
Let’s suppose that two different X-linked genes exist in mice,designated with the letters N and L. Gene N exists in a dominant,normal allele and in a recessive allele, n, that is lethal. Similarly,gene L exists in a dominant, normal allele and in a recessive allele,l, that is lethal. Heterozygous females are normal, but males thatcarry either recessive allele are born dead. Explain whether or notit would be possible to map the distance between these two genesby making crosses and analyzing the number of living and deadoffspring. You may assume that you have strains of mice in whichfemales are heterozygous for one or both genes.
Duchenne muscular dystrophy is an X-linked, recessive disorder in which muscles waste away early in life, resulting in death in the teens or twenties. A man and woman in their late thirties have five children—three boys (ages 1, 3, and 10 years) and two girls (ages 5 and 7 years). The oldest, boy shows symptoms of the disease. What are the probabilities that their other children will develop the disease? Give only typing answer with explanation and conclusion
Red-green colorblindness in humans is recessive and x-linked. if a woman, heterozygous for colorblindness marries a colorblind man, what is the probability that they will have colorblind daughter?
Which of the following statements is false? Dosage compensation is accomplished in humans by stimulation of gene expression from the single X chromosome. Dosage compensation is accomplished in humans by inactivating a female X chomosome. An individual with Turner Syndrome has no Barr bodies. An individual with Klinefelter syndrome generally has one Barr body. A typical XX human female has one Barr body.

SEE MORE QUESTIONS

Recommended textbooks for you

Human Heredity: Principles and Issues (MindTap Co…

Biology

ISBN:

9781305251052

Author:

Michael Cummings

Publisher:

Cengage Learning