9.) In humans, when a dark-skinned person reproduces with a very light-skinned person, their children may range in color from dark to brown. Thisoccurs because skin color is controlled by more than one gene (the exact # ofgenes is not known). For your convenience, a table is presented below thatshows several possible genotypes & phenotypes:GenotypesPhenotypesVery dark skinDark skinAABBAABB or AaBBAаBb, AAЬЬ, or aaBBAabb or aaBbMedium brown skinLight skinVery light skinaabbIf a man with dark skin whose genotype is AABB reproduces with a womanwho has light skin (aaBb), what are the possible skin colors that theirchildren will have? Develop a Punnett square and list the possible genotypes& phenotypes.

Name: 9.) In humans, when a dark-skinned person reproduces with a very ligh
Uploaded: 2024-03-20T06:43:04.000Z
Channel: Bartleby
Description: 9.) In humans, when a dark-skinned person reproduces with a very light-skinned person, their children may range in color from dark to brown. Thisoccurs because skin color is controlled by more than one gene (the exact # ofgenes is not known). For yo

Gene is known as the unit of heredity, which is transferred from one generation to the next. In most…

Science

Biology

9.) In humans, when a dark-skinned person reproduces v skinned person, their children may range in color from d occurs because skin color is controlled by more than one genes is not known). For your convenience, a table is pr shows several possible genotypes & phenotypes: Genotypes Phenotypes

9.) In humans, when a dark-skinned person reproduces v skinned person, their children may range in color from d occurs because skin color is controlled by more than one genes is not known). For your convenience, a table is pr shows several possible genotypes & phenotypes: Genotypes Phenotypes

Human Heredity: Principles and Issues (MindTap Course List)

11th Edition

ISBN:9781305251052

Author:Michael Cummings

Publisher:Michael Cummings

Chapter5: The Inheritance Of Complex Traits

Section: Chapter Questions

Problem 5QP: As it turned out, one of the tallest Potsdam Guards had an unquenchable attraction to short women....

See similar textbooks

Similar questions

The XG locus on the human X chromosome has twoalleles, XG+ and XG. The XG+ allele causes the presence of the Xg surface antigen on red blood cells,while the recessive XG allele does not allow antigento appear. The XG locus is 10 m.u. from the STSlocus. The STS+ allele produces normal activity ofthe enzyme steroid sulfatase, while the recessive STSallele results in the lack of steroid sulfatase activityand the disease ichthyosis (scaly skin). A man withichthyosis and no Xg antigen has a normal daughterwith Xg antigen. This daughter is expecting a child.a. If the child is a son, what is the probability he willlack Xg antigen and have ichthyosis?b. What is the probability that a son would have boththe antigen and ichthyosis?c. If the child is a son with ichthyosis, what is theprobability he will have Xg antigen?
A woman who sought genetic counseling is found to be heterozygousfor a chromosomal rearrangement between the second andthird chromosomes. Her chromosomes, compared to those in anormal karyotype, are diagrammed on the next page:(a) This woman is phenotypically normal. Does thissurprise you? Why or why not? Under what circumstancesmight you expect a phenotypic effect of such arearrangement?
An individual comes into your genetics clinic to be tested for any anomalies. When looking at their karyotype, you notice they have three X chromosomes and a Y chromosome. What information would you be able to relay to this individual? O They have Turner syndrome, are genetically female, and have two Barr bodies per cell. O They have Klinefelter syndrome, are genetically female, and have two Barr bodies per cell. O They have Klinefelter syndrome, are genetically male, and have two Barr bodies per cell. O They have Klinefelter syndrome, are genetically male, and have three Barr bodies per cell. O They have Turner syndrome, are genetically male, and have three Barr bodies per cell.
A woman who sought genetic counseling is found to be heterozygousfor a chromosomal rearrangement between the second andthird chromosomes. Her chromosomes, compared to those in anormal karyotype, are diagrammed on the next page:(a) What kind of chromosomal aberration is shown?
In individuals affected by cystic fibrosis, salt crystals may appear afterperspiration dries up. In addition, the disease causes respiratory disorderswhich can be both debilitating and lethal. It occurs in individuals homozygousfor the recessive gene. Two normal parents had a daughter with thesymptoms of this disease, and a normal son who marries a normal womanwith an afflicted A test (salt concentration in perspiration of heterozygotes ishigher than normal) disclosed that both are indeed carriers of the gene. If thefirst child born to the mating in (b) was defective, what is the probability thatthe 2nd child would also be defective?Express answer in fraction form
9. Make a pedigree for each of the following situations. For each individual, write the individual's genotype (when possible) next to the individual's symbol (e.g. O xty, I Gg): a. Two parents do not have cystic fibrosis and they have a daughter with cystic fibrosis and a son who does not have cystic fibrosis. The daughter grows up and she mates with a male who does not have cystic fibrosis. Their only child is a boy and he has cystic fibrosis. b. A man with hemophilia mates with a female without hemophilia. They have one son and one daughter. The daughter has hemophilia and the son does not have hemophilia. The son grows up, and he marries and mates with a female. Their only child is a boy, and he has hemophilia.
The maternal-effect mutation bicoid (bcd) is recessive. Inthe absence of the bicoid protein product, embryogenesis isnot completed. Consider a cross between a female heterozygousfor the bicoid mutation (bcd+/ bcd-) and a homozygousmale(bcd-/ bcd-). How is it possible for a male homozygous for the mutationto exist?
In individuals affected by cystic fibrosis, salt crystals may appear afterperspiration dries up. In addition, the disease causes respiratory disorderswhich can be both debilitating and lethal. It occurs in individuals homozygousfor recessive gene. If 2 normal parents had a daughter with the symptoms ofthis disease, and a normal son, what is the probability that he might be acarrier of the recessive gene?Express answer in fraction form.
You have spent two decades studying a muscular dystrophy disorder. All previous pedigree data indicate this is an X-linked dominant trait, you notice that in one instance the trait skips one daughter coming from an effected father. If this disease is truly X-linked dominant, what is a likely explanation as to why it was not seen in this single female? O Only environmental conditions actually cause the disease O This disease may not be 100% penetrant for the disease O Skipping generations is common for X-linked dominant traits O The definition for X-linked dominant no longer means what it did when this disease was first discovered O This disease must not actually be X-linked dominant
For this problem, use the information given in problem 15. A young woman with blood type O gave birth to a baby with blood type O. In a court case, she claims that a certain young man is the father of her child. The man has type A blood. Could he be the father? Can it be proven on this evidence alone that he is the father? ^Need answers to that one, including genotype, phenotype gametes and punnett square. This is question 15 as a little background dont need this solved . In humans, there are three alleles for blood type: A, B, and O. The allele for blood type A and the allele for blood type B show incomplete dominance. A person with both alleles has blood type AB. Both A and B dominate type O. A person with alleles for blood types A and O marries someone with alleles for blood types B and O. List the types of blood their offspring could have and the probability for each blood type in the offspring
Duchenne muscular dystrophy is a recessive disorder caused by a rare,loss-of-function allele that is located on the X chromosome in humans. Anunaffected woman (i.e., without disease symptoms) who is heterozygousfor the X-linked allele causing Duchenne muscular dystrophy has childrenwith a man with a functional (non-disease-causing) allele. What is theprobability that this couple will have an unaffected son?
1. The pedigree below shows the incidence of rare, autosomal dominant disorder called Ehlers-Danlos disease. The pedigree covers three generations of a particular family and also shows individual genotypes at a potential marker locus (M). a) Indicate the phase of all gen II and III individuals. DdM1M3 ddM2M6 II DDM3M6 ddM4M5 III DdMзM4 DdMЗМ5 DDM3M4 ddM3M5 DDM3M4 ddM5M6 DDM3M4 ddM4M6 ddM5M6 ddM5M6 b) Which, if any, of the gen III individuals are recombinants? c) Calculate the LOD score as a test of physical linkage between the marker (M) and the disease locus. d) What do you conclude about linkage between D and M?