_3. It is a Non-Mendelian pattern of inheritance that occurs when twodominant alleles of a contrasting pair fully expressed at the same time in theheterozygous individual._4. It is a Non-Mendelian pattern of inheritance that occurs when thephenotype of the offspring is somewhere in between the phenotypes of bothparents.5. It is when more than 2 alleles control the inheritance of acharacter.

Non-Mendelian inheritance is any pattern of inheritance in which traits do not segregate in…

Answered: _3. It is a Non-Mendelian pattern of…

Human Anatomy & Physiology (11th Edition)

11th Edition

ISBN:9780134580999

Author:Elaine N. Marieb, Katja N. Hoehn

Publisher:Elaine N. Marieb, Katja N. Hoehn

Chapter1: The Human Body: An Orientation

Section: Chapter Questions

Problem 1RQ: The correct sequence of levels forming the structural hierarchy is A. (a) organ, organ system,...

See similar textbooks

Similar questions

A certain type of deafness in humans is inherited as an X-linked recessive trait. A man with this type of deafness married a normal woman, and they are expecting a child. They find out that they are distantly related. Part of the family tree is shown here.How would you advise the parents about the probability of their child being a deaf boy, a deaf girl, a normal boy, or a normal girl? Be sure to state any assumptions that you make.
Could the trait presented in the pedigree shown be caused by an X-linked recessive allele? Why or why not? 11 ||| IV ■ 5 6 Yes, with individual 2 of generation I being heterozygous. No, the offspring of 7 and 8 contradict an X-linked recessive inheritance. No, the offspring of 3 and 4 of generation II contradict an X-linked recessive inheritance. No, the offspring of 1 and 2 of generation I contradict an X-linked recessive inheritance.
LO19 Analyze a cross and identify non-Mendelian pattern of inheritance in non-allelic genes (normal interaction vs epistasis) Hair color is determined in Labrador retrievers by alleles at the B and E loci. A dominant allele B encodes black pigment, whereas a recessive allele b encodes brown pigment. Alleles at a second locus affect the deposition of the pigment in the shaft of the hair; dominant allele E allows dark pigment (black or brown) to be deposited, whereas recessive allele e prevents the deposition of dark pigment, causing the hair to be yellow. What type of gene interaction does this represent? duplicate recessive epistasis normal non-allelic gene interaction Orecessive epistasis Odominant epistasis normal allelic gene interaction
6) Duchenne muscular dystrophy (DMD) is a muscle wasting disease and is an X-linked recessive disorder. A man with this disease has children with a woman who does not have the disease, but her father did. If they had a ason, what would be the chance that he would have DMD? If they had a daughter? Any child? Construct a Punnett square to determine the answers. 10) In cats, coat color is completely dominant to albino (Mendelian genetics) and is an autosomal trait. Playa is a female albino cat and is crossed with Azul, a black-coated male. In their first litter, they have 4 black kittens and 2 albino kittens. If in the second litter, they have 8 kittens, how many of the kittens are expected to be albino? Construct a Punnett Square to determine the answer.
8. Huntington’s disease is a degenerative disease of the nervous system that strikes in middle age. The allele that causes the disease (H) is dominant to the allele that results in the normal condition (h). Answer the following questions about the inheritance of this disease. A. What is the genotype of a man who is normal but whose father had Huntington’s disease? B. What is the genotype of a woman who has Huntington’s disease if both of her parents had Huntington’s disease? C. If a man who is heterozygous for Huntington’s disease marries a woman who is normal, what would you expect for the genotypes and phenotypes of their children? D. If a normal man marries a woman who is homozygous for Huntington’s disease, what do you expect for the genotypes and phenotypes of their children?
One family is shown in both pedigrees below. Each pedigree focuses on a different monogenic, fully penetrant phenotype. Shaded individuals affected by Phenotype 1: 3 Shaded individuals affected by Phenotype 2: a. Phenotype 1: Which modes of inheritance can be ruled out, base don't this pedigree? For each mode of inheritance listed below, either state that it is not ruled out, or describe a detail of the pedigree that allows you to rule it out. Autosomal recessive Autosomal dominant X-linked recessive X-linked dominant Y-linked b. Phenotype 2: Which modes of inheritance can be ruled out, base don't this pedigree? For each mode of inheritance listed below, either state that it is not ruled out, or describe a detail of the pedigree that allows you to rule it out. Autosomal recessive Autosomal dominant X-linked recessive X-linked dominant
Adenike and her partner, Debare, are expecting their first child. Adenike is healthy as are her two sisters but her brother has PKU, a recessive disorder of the PAH gene. Genotypically he must be pah-/pah-. Neither of Adenike's parents has PKU but both of her grandmothers did. Debare is a carrier of Sickle Cell trait, which means he has one allele for wildtype hemoglobin (HbA) and one allele for Sickle Cell (HbS), making him HgA/HbS. More importantly, he has two alleles for Marfan Syndrome, a pleiotropic dominant disorder that can affect up to 30 different traits (M+/M+). No one in Debare's family has ever had PKU and no one in Adenike’s family has ever had Sickle Cell or Marfan Syndrome. They consult a genetics counselor over concern of the health of their baby. The genetics counselor collects the medical histories of three generations; their grandparents, their parents, and them. In her calculations, she produces a phenotypic key that indicates M = Marfan, Hb = sickle cell, and pah-…
Additional problems (Chapter 4 (Extension of Mendelian Inheritance): 1. In rabbits, coloration of the fur depends on alleles of the gene c. From information given in the chapter, what phenotypes and proportions would be expected from the following crosses: a) CC X cc b) Cc x Cc c) Cc x Ccch d) cc x cc 2. From the information given in the chapter about the ABO blood types, what phenotypes and ratios are expected from the following matings: a) type AB x type O b) Type AB x type B individual whose mother is type O c) Type O x Type A individual whose father is type O d) Type Ox type O 3. A woman with type AB blood type gave birth to a baby with type B blood. Two different men claim to be the father. One has type A blood and the other type B blood. Can the genetic evidence decide in favor of either? 4. You have been studying a trait that seems to be present in every generation within a particular family. Further, you have observed that every affected offspring has at least affected parent…
What is the approximate percentage chance that individual V.2, shown in the pedigree diagram below will have inherited the X- linked recessive allele shown to be carried by his great-great-grandmother? Note: only type the number, not the percentage symbol. Answer: The chance that individual V.2 shown in the pedigree below has inherited the X-linked recessive allele shown to be carried by his great-great grandmother is approximately Blank 1 percent. 노 ㅍ먹이 12 I 마일 메인 de 먹어 요 58 ㅁ + ܡܐ
5. The pedigree below traces the inheritance of Albinism, a genetic disorder. Affected individuals, indicated here by the coloured circles and squares, are unable to make a normal amount of melanin, the chemical that is responsible for eye, skin, and hair colour. Does Albinism appear to be caused by a dominant allele or by a recessive allele? Fill in the genotypes of the individuals whose genotypes can be deduced. What genotypes are possible for each of the other individuals? Explain! Naruto Hinata Reiner Asta Hange Mikasa Eren Historia Luffy Nezuko Zenitsu Tanjiro Son Goku
Adenike and her partner, Debare, are expecting their first child. Adenike is healthy as are her two sisters but her brother has PKU, a recessive disorder of the PAH gene. Genotypically he must be pah-/pah-. Neither of Adenike's parents has PKU but both of her grandmothers did. Debare is a carrier of Sickle Cell trait, which means he has one allele for wildtype hemoglobin (HbA) and one allele for Sickle Cell (HbS), making him HgA/HbS. More importantly, he has two alleles for Marfan Syndrome, a pleiotropic dominant disorder that can affect up to 30 different traits (M+/M+). No one in Debare's family has ever had PKU and no one in Adenike’s family has ever had Sickle Cell or Marfan Syndrome. They consult a genetics counselor over concern of the health of their baby. The genetics counselor collects the medical histories of three generations; their grandparents, their parents, and them. In her calculations, she produces a phenotypic key that indicates M = Marfan, Hb = sickle cell, and pah-…
3) You have sought a job at a human genetic counseling clinic. They gave you an aptitude test shown below. Answer the yes/no questions concerning each of the following pedigrees. Pedigree A: YES or NO Could this trait be inherited as a simple autosomal recessive? Could this trait be inherited as a simple autosomal dominant? Could this trait be inherited as a simple X-linked recessive? Could this trait be inherited as a simple X-linked dominant? Pedigree B: YES or NO Could this trait be inherited as a simple autosomal recessive? Could this trait be inherited as a simple autosomal dominant? Could this trait be inherited as a simple X-linked recessive? Could this trait be inherited as a simple X-linked dominant?

Recommended textbooks for you

Human Anatomy & Physiology (11th Edition)

Biology

ISBN:

9780134580999

Author:

Elaine N. Marieb, Katja N. Hoehn

Publisher:

PEARSON

Biology 2e

Biology

ISBN:

9781947172517

Author:

Matthew Douglas, Jung Choi, Mary Ann Clark

Publisher:

OpenStax

Anatomy & Physiology

Biology

ISBN:

9781259398629

Author:

McKinley, Michael P., O'loughlin, Valerie Dean, Bidle, Theresa Stouter

Publisher:

Mcgraw Hill Education,

Human Anatomy & Physiology (11th Edition)

Biology

ISBN:

9780134580999

Author:

Elaine N. Marieb, Katja N. Hoehn

Publisher:

PEARSON

Biology 2e

Biology

ISBN:

9781947172517

Author:

Matthew Douglas, Jung Choi, Mary Ann Clark

Publisher:

OpenStax

Anatomy & Physiology

Biology

ISBN:

9781259398629

Author:

McKinley, Michael P., O'loughlin, Valerie Dean, Bidle, Theresa Stouter

Publisher:

Mcgraw Hill Education,

Molecular Biology of the Cell (Sixth Edition)

Biology

ISBN:

9780815344322

Author:

Bruce Alberts, Alexander D. Johnson, Julian Lewis, David Morgan, Martin Raff, Keith Roberts, Peter Walter

Publisher:

W. W. Norton & Company

Laboratory Manual For Human Anatomy & Physiology

Biology

ISBN:

9781260159363

Author:

Martin, Terry R., Prentice-craver, Cynthia

Publisher:

McGraw-Hill Publishing Co.

Inquiry Into Life (16th Edition)

Biology

ISBN:

9781260231700

Author:

Sylvia S. Mader, Michael Windelspecht

Publisher:

McGraw Hill Education

SEE MORE TEXTBOOKS