Match the following 1-If a father is affected with X-linked dominantthat means2-If the Y-linked is recessive then the boys will beaffected3- In autosomal recessive4- In autosomal dominant5- In X-linked dominant6- In X-linked recessive7-AB blood type is8- Metaphase9- Transposon10- DNTP11-ddNTP12- Silent mutation13- Reverse transcriptase convertsD-all his daughters will be affected.F-false, because the Y chromosome is neitherdominant nor recessive.A- it can skip generation.Caffected parents can have unaffected children.S-RNA TO DNAB-the disease will never transfer to sons, but allhis daughters will be affected.E-male are more affected.N-Deaxyribonucleic acidcodominantH-incomplete dominantF-general acceptorgeneral donorL-looks like wound suturesM-is type of translocation of the gene0-Di-deoxy ribonucleic acidP-Is harmfulQ-Is not harmfulR-DNA TO RNAT-Protein to RNAK-complete dominantQ- is used in sequencing

Name: Match the following 1-If a father is affected with X-linked dominantth
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Description: Match the following 1-If a father is affected with X-linked dominantthat means2-If the Y-linked is recessive then the boys will beaffected3- In autosomal recessive4- In autosomal dominant5- In X-linked dominant6- In X-linked recessive7-AB blood type

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1-If a father is affected with X-linked dominant that means 2-If the Y-linked is recessive then the boys will be affected 3- In autosomal recessive 4- In autosomal dominant 5- In X-linked dominant 6-In X-linked recessive 2-AB blood type is 3-Metaphase - Transposon 10- UNTP 1-ddNTP 2- Silent mutation 3- Reverse transcriptase converts D- all his daughters will be affected. F-false, because the Y chromosome is neither dominant nor recessive. A- it can skip generation. Gaffected parents can have unaffected children. S-RNA TO DNA B-the disease will never transfer to sons, but all his daughters will be affected. Emale are more affected. N- Deaxy ribonucleic acid codominant H-incomplete dominant F-general acceptor general donor L-looks like wound sutures M-is type of translocation of the gene 0-Di-deoxy ribonucleic acid P- Is harmful Q-Is not harmful R-DNA TO RNA T- Protein to RNA

1-If a father is affected with X-linked dominant that means 2-If the Y-linked is recessive then the boys will be affected 3- In autosomal recessive 4- In autosomal dominant 5- In X-linked dominant 6-In X-linked recessive 2-AB blood type is 3-Metaphase - Transposon 10- UNTP 1-ddNTP 2- Silent mutation 3- Reverse transcriptase converts D- all his daughters will be affected. F-false, because the Y chromosome is neither dominant nor recessive. A- it can skip generation. Gaffected parents can have unaffected children. S-RNA TO DNA B-the disease will never transfer to sons, but all his daughters will be affected. Emale are more affected. N- Deaxy ribonucleic acid codominant H-incomplete dominant F-general acceptor general donor L-looks like wound sutures M-is type of translocation of the gene 0-Di-deoxy ribonucleic acid P- Is harmful Q-Is not harmful R-DNA TO RNA T- Protein to RNA

Biology: The Unity and Diversity of Life (MindTap Course List)

14th Edition

ISBN:9781305073951

Author:Cecie Starr, Ralph Taggart, Christine Evers, Lisa Starr

Publisher:Cecie Starr, Ralph Taggart, Christine Evers, Lisa Starr

Chapter10: Control Of Gene Expression

Section: Chapter Questions

Problem 3CT: Almost all calico cats (one is pictured in FIGURE 10.7B) are female. Why? B When this calico cat was...

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Almost all calico cats (one is pictured in FIGURE 10.7B) are female. Why? B When this calico cat was an embryo, one of the two X chromosomes was inactivated in each of her cells. The descendants of the cells formed her adult body, which is a mosaic for expression of X chromosome genes. Black fur arises in patches where genes on the X chromosome inherited from one parent are expressed; orange fur arises in patches where genes on the X chromosome inherited from the other parent are expressed. FIGURE 10.7 Animated X chromosome inactivation.
Redgreen color blindness is an X-linked recessive disorder in humans. Your friend is the daughter of a color-blind father. Her mother had normal color vision, but her maternal grandfather was color-blind. What is the probability that your friend is color-blind? (a) 1 (b) (c) (d) (e) 0
5. Woody Guthrie, who wrote This Land is Your Land, was heterozygous for Huntington’s disease (Hh). His wife was homozygous recessive and perfectly normal (hh). Huntington’s disease is caused by a latent dominant gene, meaning that it is not phenotypically (physically) expressed until later in life. Dominant disease genes are expressed in homozygous dominant and heterozygous people (HH or Hh). Draw a Punnett square for Woody ad his wife.
1. Hemophilia is due to a sex-linked gene. It is recessive and found on the X chromosome. A woman who is a carrier for hemophilia marries a normal man. What will be the possible phenotypes of their children? Use a punnet square. 2. A phenotypically normal man, who has a hemophiliac brother, marries a normal woman, who is not a carrier. What is the probability that any of their children will be hemophiliac? Use a punnet square. 3. Color-blindness is an X-linked, recessive trait. If a normal-sighted woman, whose father was color-blind, marries a colorblind man, what is the probability that they will have a son who is color-blind? Use a punnet square. 4. A man and woman, both of normal vision, have: 1) a color-blind son (#1) who has a daughter of normal vision 2) a daughter (#1) of normal vision who has one color-blind son and one normal vision son 3) another daughter (#2) of normal vision who has five sons, all with normal vision What are the probable genotypes of the…
13. A dominant x-linked allele (B) gives normal color vision but the recessive allele (b) causes red-green color blindness.A. What is the genotype of a man with normal color vision whose father was color- blind? B. What is the genotype of a woman with normal color vision whose father was color-blind? C. If a woman who is colorblind marries a man with normal vision, what would you expect for the genotypes and phenotypes of their children? D. If a man is color-blind, which parent did he inherit the gene from? Explain your answer. E. Which parent does a man get all his x-linked genes from? F. If a woman is color-blind, what do you know about the genotypes and phenotypes of her parents? G. Are men more likely than women to get a genetic disease which is x-linked and dominant? Are they more likely to get a disease that is x-linked and recessive? Explain your answers. H. Can a man with normal color vision have a colorblind daughter? Explain your answer.…
13. Which of the following is true regarding X linked recessive traits? More males are affected than females because they have nothing to maska recessive allele carried on the X chromosome More females are affected than males because they have nothing to mask a recessive allele carried on the X chromosome. More females are affected than males because they have an extra X More males are affected than females because they have an extra X
4. In the pedigree shown, the trait is most likely caused by what type of inheritance? X-linked dominant autosomal recessive autosomal dominant X-linked recessive
15.Hemophilia is a sex-linked recessive condition that results in deficient blood clotting. The disease causes excessive bleeding which occurs spontaneously or upon slight injury. In dogs (as in humans) hemophilia is caused by a defect in a gene on the X chromosome. What will be the results of mating between a normal, noncarrier female dog and a male dog with hemophilia? All of the offspring will be normal, but all females will be carriers. B. All female offspring will be normal and half the male offspring will have hemophilia. C. Half the male offspring will be normal and half will have hemophilia; all females will be carriers. D. Half the female offspring will have hemophilia and half will be carriers, all male offspring will be normal.
man who is a dwarf due to achondroplasia and has normal vision marries a color-blind woman of normal height. The man's father was 6 feet tall, and both the woman's parents were of average height. Achondroplasia is autosomal dominant, and red-green color blindness is X-linked recessive. What are the possible genotypes and phenotypes of their children? What are the ratios for each? you must show all work.
1) Perception of a bitter taste from phenylthiocarbamide (PTC) is dominant (T) to not being able to taste PTC. Albinism is recessive to normal pigmentation (A). The genes controlling these traits are on separate chromosomes. a. A normally pigmented woman who cannot taste PTC has a father who is an albino taster, marries a many homozygous for normal pigmentation who is a PTC taster, but whose mother did not taste PTC. What are the genotypes of the woman and man listed here? b. Assuming the man and woman in the above section have children, what percentage of these children will be albino? c. What percentage of these children will have the same phenotype as their mother?
Both hemophilia (h) and favism (gd) are inherited as X-linked recessive traits. Hemophilia is an inherited disorder of blood clotting, and favism is an inherited hemolytic anemia caused by absence of the enzyme glucose-6-phosphate dehydrogenase. A phenotypically normal woman is known to have the X chromosome genotype h + / + gd. The frequency of recombination between h and gd is 16%. What proportion of sons born to this woman are expected to be phenotypically normal with respect to both hemophilia and favism?
1-Polydactyly is an example of what type of allele? a-X-linked Dominant b-Dominant Lethal c-Autosomal Dominant d-Autosomal Recessive 2-Achondroplasia is an example of what type of allele? a-X-linked Dominant b-Dominant Lethal c-Autosomal Dominant d-Autosomal Recessive