GENETIC ANALYSIS: INTEGRATED - ACCESS
GENETIC ANALYSIS: INTEGRATED - ACCESS
3rd Edition
ISBN: 9780135349298
Author: Sanders
Publisher: PEARSON
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Chapter 4, Problem 31P

Human ABO blood type is determined by three alleles, two of which (IA and IB) produce gene products that modify the antigen produced by protein activity of an independently assorting H gene. A rare abnormality known as the Bombay phenotype” is the result of epistatic interaction etween the gene for the ABO blood group and the H gene. ndividuals with the Bombay henotype appear to have lood type O based on the inability of both anti-A antibody nd anti-B antibody to detect an antigen. The apparent lood type O in Bombay phenotype is due to the absence of antigen as a result of homozygous recessive mutations of he H gene. Individuals with the Bombay phenotype have he hh genotype. Use the information above to make predictions bout the outcome of the cross shown below.

I A I B Hh×I A I B Hh

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Several genes in humans in addition to the ABO gene(I) give rise to recognizable antigens on the surface ofred blood cells. The MN and Rh genes are two examples. The Rh locus can contain either a positive or anegative allele, with positive being dominant to negative. M and N are codominant alleles of the MN gene.The following chart shows several mothers and theirchildren. For each mother-child pair, choose the fatherof the child from among the males in the right column, assuming one child per male.Mother Child Malesa. O M Rh(pos) B MN Rh(neg) O M Rh(neg)b. B MN Rh(neg) O N Rh(neg) A M Rh(pos)c. O M Rh(pos) A M Rh(neg) O MN Rh(pos)d. AB N Rh(neg) B MN Rh(neg) B MN Rh(pos)
y 301 Amelogenesis imperfecta is X-linked dominant. Affected XY individuals have extremely thin enamel on the teeth while XX carriers have grooved teeth from uneven deposition of enamel. If an unaffected XY individual were to produce children with a XX carrier partner, a. what would be the expected chance of a XY child being affected with the disease? b. what would be the expected chance of a XY child being affected with the disease?
In humans, the Rh factor genetic information is inherited from our parents, but it is inherited independently of the ABO blood type alleles. In humans, Rh+ individuals have the Rh antigen on their red blood cells, while Rh- individuals do not. There are two different alleles for the Rh factor known as Rh+ and rh. Assume that a dominant gene Rh produces the Rh+ phenotype, and that the recessive rh allele produces the Rh- phenotype. In a population that is in Hardy-Weinberg equilibrium, if 160 out of 200 individuals are Rh+, calculate the frequencies of both alleles.

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GENETIC ANALYSIS: INTEGRATED - ACCESS

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