Eyelash length is an inherited trait. In the human population, there is an eyelash length gene. There are two possible variants of this gene-an allele for long eyelashes (> lcm) and an allele for short eyelashes (1 cm or less). The allele for long eyelashes is dominant (L) and the allele for short eyelashes is recessive (I). An individual who is heterozygous for eyelash length would have which of the following genotypes? O L OLI

Eyelash length is an inherited trait. In the human population, there is an eyelash length gene. There are two possible variants of this gene-an allele for long eyelashes (> lcm) and an allele for short eyelashes (1 cm or less). The allele for long eyelashes is dominant (L) and the allele for short eyelashes is recessive (I). An individual who is heterozygous for eyelash length would have which of the following genotypes? O L OLI

Human Biology (MindTap Course List)

11th Edition

ISBN:9781305112100

Author:Cecie Starr, Beverly McMillan

Publisher:Cecie Starr, Beverly McMillan

Chapter19: Introduction To Genetics

Section: Chapter Questions

Problem 9CT

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The young woman shown at right has albinismvery pale skin, white hair, and pale blue eyes. This phenotype is due to the absence of melanin, which imparts color to the skin, hair, and eyes. It typically is caused by a recessive allele. In the following situations, what are the probable genotypes of the father, the mother, and their children? a. Both parents have normal phenotypes; some of their children are albino and others are not. b. Both parents and all their children are albino. c. The mother is not albino, the father is albino, and one of their four children is albino.
Cystic fibrosis is an autosomal disease that mainly affects the white population, and 1 in 20 whites are heterozygotes. Genetic testing can diagnose heterozygotes. Should a genetic screening program for cystic fibrosis be instituted? Should the federal government fund it? Should the program be voluntary or mandatory, and why?
When you decide to breed your Labrador retriever Molly and sell the puppies, you discover that two of Mollys four siblings have developed a hip disorder that is traceable to the action of a single recessive allele. Molly herself shows no sign of the disorder. If you breed Molly to a male Labrador that does not carry the recessive allele, can you assure a purchaser that the puppies will also be free of the condition? Explain your answer.
In humans, the genetic disease cystic fibrosis is caused by a recessive allele (a). The normal (healthy) allele is dominant (A). What is the genotype of someone who has cystic fibrosis? What are the two different genotypes that a healthy person could have? If two people were both heterozygous for the cystic fibrosis gene, what fraction of their children would be likely to have this disease? Hint: Draw a Punnett square to figure it out.
Albinism is a recessive genetic condition in which a person lacks pigment that gives color to the skin. If the allele for albinism is represented as "a," and the functional allele is represented as "A," what will be the genotype of a person with albinism? Aa or AA Aa or aa AA aa
Color blindness is typically an inherited genetic condition in which individuals have a decreased ability to see color or differences in color. Color blindness only occurs in individuals who have two recessive alleles for the condition. Normal color vision is due to a dominant allele (C) Color blindness is due to the recessive allele (c) a) If Susan is homozygous for normal vision, and Matt is homozygous for color blindness, what is the likelihood (in percentage) that their son Alex will have color blindness? Perform a Punnett Square (either below or by hand on paper) to find the probability. Provide your answer in a full sentence. If you did the Punnett Square by hand, attach your photo to the next question.
Albinism is a recessive disorder where there is a lack of melanin. Andrea and her husband Claude both have normal skin pigmentation. Andrea’s mother has the albino phenotype, but her father and her brother do not (normal pigmentation). Claude’s parents are both normal, but he has a sister who has the condition (is albino). Answer the following questions If Andrea and Claude are carriers for the albino allele, what is the probability that they have an albino child? If Andrea and Claude have a second child, what is the probability this child be normal (non-albino)? NOTE: Draw a punnet square or show your work.
In human beings, the gene for red‑green colorblindness (r) is sex‑linked and recessive to its allele for normal vision (R), while the gene for freckles (F) is autosomal and dominant over its allele for nonfreckled (f). A nonfreckled, normal‑visioned woman whose father was freckled and colorblind, marries a freckled, colorblind man whose mother was nonfreckled. What is the genotype of the woman's father? What is the probability that the couple's first child will be a non-freckled, normal visioned girl? What is the probability that the first two children born to the couple will be freckled and colorblind girls?
In genetics, the dash symbol (–) is a “wild card” that stands for either the dominant allele or the recessive allele; for example, A– means the individual has either the genotype AA or Aa. Two genes that undergo independent assortment affect coat color in Duroc pigs. Each gene has two alleles, one of which is dominant for coat color. Genotypes of the form A– B– are red, those of the form A– bb and aa B– are sandy, and genotype aa bb is white. What ratio of red:sandy:white is expected from the cross Aa Bb x Aa Bb?
In humans, the gene for albinism (a) is recessive to the gene for normal skin pigmentation (A). If two heterozygous persons have children, what is the probability they will have a child who is an albino? What is the probability they will have a child that is a carrier of the recessive gene?
The allele for albinism is recessive to the allele for normal skin pigmentation. All individuals who are homozygous for this recessive allele (m) are unable to produce the enzyme needed for melanin production and are referred to as albinos. In the following statements, determine the correct genotypes: An albino male (genotype A) whose parents both have normal skin pigmentation (genotype B) marries a woman who does not have albinism (genotype C). This woman’s father is an albino (genotype D). The married couple has three children, two with normal skin pigmentation (genotype E) and one exhibiting albinism (genotype F)
In humans, cystic fibrosis and albinism are both inherited as independently assorting autosomal recessive traits. Use f to represent the recessive allele for cystic fibrosis and F for the allele for the unaffected condition. Use A to represent the dominant allele for normal melanin and a for the recessive allele for albinism. A man is albino and heterozygous for cystic fibrosis. His wife has the unaffected phenotype for both traits, although her father had cystic fibrosis and her mother is albino. 4a. What is the genotype of the wife 4b.What is the probability that a child of this couple is albino and has cystic fibrosis? 4c.What is the probability that a child of this couple is a girl who is albino and has cystic fibrosis? 4d.What is the probability that a child of this couple is normal for both traits?