The A & B antigens in humans may be found in water-soluble forms in secretions, including saliva of individuals with the genotypes E/E& E/e, but not individuals with the genotype e/e. Thus, the population contains ‘secretors’ & ‘nonsecretors’. A cross was performed between 2 heterozygous secretors, one with type O blood and the second with type AB blood. What phenotypic ratios are expected in their offspring? A) 1/4 type A : 1/4 type B : 1/2 non-secretor B) 3/8 type A : 3/8 type B : 2/8 non-secretor C) 1/2 type A : 1/2 type B D) 3/4 type AB : 1/4 non-secretor

The A & B antigens in humans may be found in water-soluble forms in secretions, including saliva of individuals with the genotypes E/E& E/e, but not individuals with the genotype e/e. Thus, the population contains ‘secretors’ & ‘nonsecretors’. A cross was performed between 2 heterozygous secretors, one with type O blood and the second with type AB blood. What phenotypic ratios are expected in their offspring? A) 1/4 type A : 1/4 type B : 1/2 non-secretor B) 3/8 type A : 3/8 type B : 2/8 non-secretor C) 1/2 type A : 1/2 type B D) 3/4 type AB : 1/4 non-secretor

Human Heredity: Principles and Issues (MindTap Course List)

11th Edition

ISBN:9781305251052

Author:Michael Cummings

Publisher:Michael Cummings

Chapter15: Genomes And Genomics

Section: Chapter Questions

Problem 1QP: The gene controlling ABO blood type and the gene underlying nail-patella syndrome are said to show...

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In humans, four different blood types (A, B, AB, and O) are encoded by three alleles 1, 1, and i Individuals with both I and I alleles have blood type AB (red blood cells with both A and B antigens). Two copies of the i allele are required for an individual to have blood type O (red blood cells with no antigens). Which of the following correctly indicates the relationship between the I and / alleles for the blood type gene? Select one: OA. I is dominant to / OB. I is recessive to i OC. I and I are co-dominant OD. I and/exemplify incomplete dominance
While sitting at home during Movement Control Order (MCO) because of pandemic covid19, observe two different traits of a couple in your family (eg. your mom & dad or your sister & her husband or your brother & his wife, etc). Draw a genetic cross that involves cross of the parents with the chosen 2 pairs of their contracting traits. Imagine that the cross obeys the Mendelian Laws, show the cross and gametes production for each generation (P, F1 and F2). By Using a Punnet square as symbolic representation of the results for the cross, determine the phenotypes, genotypes, phenotypic ratio and genotypic ratio of F2 generation in the family.
Rabbits may be classified as agouti, chinchilla, Himalayan, or albino according to coat color. A cross between CCh x Cchc produced 5 agouti, 3 chinchilla and 2 Himalayans. a. What are the genotypes of the F1s? b. If the two F1 agouti genotypes will be crossed, what percentage of their offspring will have the same phenotype? c. What will be the genotypes of the rabbits in (d)?
Spherocytosis is an inherited blood disease in whichthe erythrocytes (red blood cells) are spherical insteadof biconcave. This condition can be inherited in adominant fashion, with ANK1 (the nonfunctional mutant allele) dominant to ANK1+. In people with spherocytosis, the spleen recognizes the spherical redblood cells as defective and removes them from thebloodstream, leading to anemia. The spleen in different people removes the spherical erythrocytes withdifferent efficiencies. Some people with sphericalerythrocytes suffer severe anemia and some mild anemia, yet others have spleens that function so poorly nosymptoms of anemia exist at all. When 2400 peoplewith the genotype ANK1 ANK1+ were examined, itwas found that all of them had spherical erythrocytes,2250 had anemia of varying severity, and 150 had nosymptoms. (Assume that ANK1 ANK1 homozygotesdo not exist.)a. Does this description of people with spherocytosisrepresent incomplete penetrance, variable expressivity, or both? Explain…
α-thalassemia is another blood disorder in which abnormal hemoglobin molecules are formed, leading to anemia. One mutant allele known to cause α-thalassemia occurs in α-hemoglobin and is called Constant Spring. Normal α-hemoglobin is 141 amino acids long, while the Constant Spring protein is 172 amino acids long. Include answers to both A and B in your response. A maximum of 2 sentences per part. A) Explain how a frameshift mutation in the coding region of α-hemoglobin could result in the Constant Spring protein. B) Explain how a single base-substitution mutation in the coding region of α-hemoglobin could result in the Constant Spring protein.
Consider three genes L, U, and W, for which the count of F2 phenotypes after a 3-point cross is as follows: Phenotype F2 count: L U w 19 L u W 1 l u W 21 L U W 33 l U W 274 l u w 41 l U w 2 L u w 259 Which of the following statements about genes L, U, and W are TRUE? (may be more than one correct ans) A. L, U, and W are each on a different chromosome B. Only U and L are on the same chromosome C. Only U and W are on the same chromosome D. Only W and L are on the same chromosome E. L, U, and W are all on the same chromosome
Given the karyotype shown at right, is this a male or a female? Normal or abnormal? What would the phenotype of this individual be?
The gene controlling ABO blood type and the gene underlying nail-patella syndrome are said to show linkage. What does that mean in terms of their relative locations in the genome? What does it mean in terms of how the two traits are inherited with respect to each other?
Spherocytosis is an inherited blood disease in which erythrocytes (red blood cells) are spherical instead of biconcave. This condition is inherited in a dominant fashion, with ANK1 (the nonfunctional mutant allele) dominant to ANK1+. In people with spherocytosis, the spleen recognizes the spherical red blood cells as defective and removes them from the bloodstream, leading to anemia; this removal occurs with different efficiency in different people. Some people with spherical erythrocytes suffer severe anemia, some have mild anemia, and others do not have any symptoms of anemia. When 2400 people with the genotype ANK1/ANK1+ were examined, it was found that all of them had spherical erythrocytes, 2250 had anemia of varying severity, and 150 had no anemia symptoms. The ANK1/ANK1 genotype is never observed. Which evidence suggests that spherocytosis is incompletely penetrant?
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An experimental assay for the blood-clotting protein called factorIX is available. A blood sample was obtained from each individual in the following pedigree. The amount of factor IX protein, shown within each symbol on the pedigree, is expressed as a percentage of the average amount observed in individuals who do not carry a mutant copy of the gene.