Due to dosage compensation by X inactivation, females can exhibit a mosaic pattern of sweat glands on only some portions of their body if they carry a particular loss of function allele. Could any of the following genotypes result in males with such a mosaic pattern of sweat glands? Explain. A. X^AY B. X^AX^AY C. X^AX^aY D. Not possible

Due to dosage compensation by X inactivation, females can exhibit a mosaic pattern of sweat glands on only some portions of their body if they carry a particular loss of function allele. Could any of the following genotypes result in males with such a mosaic pattern of sweat glands? Explain. A. X^AY B. X^AX^AY C. X^AX^aY D. Not possible

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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Red-green colorblindness is determined in humans by a single X-linked locus. Colorblind males are XbY, and males with normal vision are XBY. XB is dominant, so XBXB and XBXb females have normal vision, while XbXb females are colorblind. Typically, 8% of males are red-green colorblind. Assuming H-W equilibrium, what percentage of females is typically colorblind?
Consider a couple: a woman who is homozygous for a recessive mutation that causes X-linked colorblindness, and a man with full color vision (he does not carry a copy of the mutation). a) What is the probability that a son of this couple will be colorblind? b) What is the probability that a daughter of the couple will be colorblind?
Duchenne muscular dystrophy is sex linked and usuallyaffects only males. Victims of the disease become progressively weaker, starting early in life.a. What is the probability that a woman whose brotherhas Duchenne’s disease will have an affected child?b. If your mother’s brother (your uncle) had Duchenne’sdisease, what is the probability that you have receivedthe allele?c. If your father’s brother had the disease, what is theprobability that you have received the allele?
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.
In guinea pigs, a black coat is dominant to an albino coat, and short hair is dominant to long hair. A BbHh ginea pig is crossed with a bbHH ginea pig. If 30 offspirng are produced, how many would be expeted to be a) black with short hair, b) albino with short hair, and c)albino with long hair?
In mice, the wild-type coat color, agouti (AA) [left mouse], is dominant to solid-colored, black fur (aa) [middle mouse]. However, a separate gene (C) is necessary for pigment production. A mouse that is homozygous for a recessive c allele at this locus is unable to produce pigment and is albino [right mouse] regardless of the allele present at locus A. Thus, the following genotypes are listed with their associated phenotypes: ~ A/A; C/C or A/A; C/c or A/a; C/C or A/a; C/c ==> "agouti" ~ a/a; C/C or a/a; C/c ==> "black" ~ A/A; c/c or A/a; c/c or a/a; c/c or a/a; c/c ==> "albino" This is an example of recessive epistasis, in which the recessive c allele "stands upon" the possible genotypes for the A gene (A/A, A/a, or a/a). If two agouti mice with the A/a; C/c genotype are mated, what is the expected phenotypic ratio in their offspring? A.9 albino, 4 agouti, 3 black B. 9 agouti, 4 albino, 3 black C.9 black, 4 albino, 3 agouti D.9 agouti, 4 black, 3 albino
Skin color in humans is determined by polygenic inheritance, which means the more dominant alleles there are, the darker the skin color will be. A medium-toned skinned woman (AaBb) has a child with another medium-toned skinned man (AaBb). What is the probability of them having a very dark-toned skinned child? (Hint: the genotype is homozygous dominant)
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?
A pedigree analysis was performed on the family of a man with schizophrenia. Based on the known concordance statistics, would his MZ twin be at high risk for the disease? Would the twins risk decrease if he were raised in an environment different from that of his schizophrenic brother?
.Certain forms of human color blindness are inherited as X-linkedrecessive traits. Hemizygous males are color-blind, but heterozygous females are not. However, heterozygous females sometimeshave partial color blindness.A. Discuss why heterozygous females may have partial color blindness.B. Doctors identified an unusual case in which a heterozygousfemale was color-blind in her right eye but had normal colorvision in her left eye. Explain how this might have occurred.
The father of two children is type O+, and the mother is type A+. The children are O- and A+. Given this information, what are the genotypes of the father vs. the mother at both the “I” and “Rh” alleles? Explain your rationale.
In a woman who is a carrier of a mutant OTC deficiency allele, her sons who receive the mutant allele will be affected and her daughters will be carriers who may or may not be symptomatic, depending on random X inactivation in the liver. 1) Is this a single gene inheritance or multifactorial disease? 2) Is there a strong genetic or environmental cause to the development of this disease? If both genetic and environmental causes are implicated, you have to indicate each of them separately.