Deck 10: Patterns of Inheritance
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Deck 10: Patterns of Inheritance
1
When two alleles of the same gene are identical, the individual carrying those alleles is said to be ____.
A) dominant
B) heterozygous
C) recessive
D) genotypical
E) homozygous
A) dominant
B) heterozygous
C) recessive
D) genotypical
E) homozygous
E
2
An allele is ____ if its effect masks that of a ____ allele paired with it.
A) recessive; codominant
B) codominant; recessive
C) recessive; dominant
D) dominant; recessive
E) incompletely recessive; dominant
A) recessive; codominant
B) codominant; recessive
C) recessive; dominant
D) dominant; recessive
E) incompletely recessive; dominant
D
3
Observable traits are known in genetics as ____.
A) phenotypes
B) genotypes
C) homozygous
D) heterozygous
E) homozygous genotypes
A) phenotypes
B) genotypes
C) homozygous
D) heterozygous
E) homozygous genotypes
A
4
In cats, short hair ( L ) is dominant to long hair ( l ). If a short-haired cat of unknown genotype is crossed with a long-haired animal, and they produce one long-haired kitten and one short-haired kitten, this would indicate that ____.
A) the short-haired cat was true-breeding
B) the short-haired cat was not true-breeding
C) the long-haired cat was not true-breeding
D) the long-haired cat was heterozygous
E) neither parent was true-breeding
A) the short-haired cat was true-breeding
B) the short-haired cat was not true-breeding
C) the long-haired cat was not true-breeding
D) the long-haired cat was heterozygous
E) neither parent was true-breeding
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5
In a person with cystic fibrosis, the CFTR mutation causes the protein to be ____.
A) embedded in the plasma membrane
B) destroyed in the endoplasmic reticulum
C) shuttled to the nuclear membrane instead of the plasma membrane
D) shuttled to the plasma membrane instead of the nuclear membrane
E) expelled from the cell by exocytosis before it can do its job
A) embedded in the plasma membrane
B) destroyed in the endoplasmic reticulum
C) shuttled to the nuclear membrane instead of the plasma membrane
D) shuttled to the plasma membrane instead of the nuclear membrane
E) expelled from the cell by exocytosis before it can do its job
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6
Various forms of the same gene are called ____.
A) genotypes
B) alleles
C) somatic
D) recessive
E) phenotypes
A) genotypes
B) alleles
C) somatic
D) recessive
E) phenotypes
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7
Red coat is dominant in horses and white coat is recessive. In a cross between a homozygous dominant red-coated horse and a white-coated horse, what genotype(s) would be observed in the offspring?
A) all homozygous recessive
B) all homozygous dominant
C) half homozygous dominant and half homozygous recessive
D) all heterozygous
E) half heterozygous and half homozygous dominant
A) all homozygous recessive
B) all homozygous dominant
C) half homozygous dominant and half homozygous recessive
D) all heterozygous
E) half heterozygous and half homozygous dominant
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8
____ raises miscarriage risks by 2-10 percent and is rarely performed.
A) Conventional ultrasound
B) Fetoscopy
C) 4D ultrasound
D) Amniocentesis
E) CVS
A) Conventional ultrasound
B) Fetoscopy
C) 4D ultrasound
D) Amniocentesis
E) CVS
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9
The mutated gene that causes cystic fibrosis is ____.
A) CFTR
B) CRFT
C) CTFR
D) CRTF
E) CFRT
A) CFTR
B) CRFT
C) CTFR
D) CRTF
E) CFRT
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10
When Gregor Mendel first started his genetics experiments, he ____.
A) knew about the existence of genes
B) knew that some plants "breed true"
C) knew that genes were responsible for observable traits
D) allowed the pea plants to self-fertilize
E) expected all true breeding crosses to produce offspring with intermediate phenotypes
A) knew about the existence of genes
B) knew that some plants "breed true"
C) knew that genes were responsible for observable traits
D) allowed the pea plants to self-fertilize
E) expected all true breeding crosses to produce offspring with intermediate phenotypes
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11
When two alleles of the same gene are different, the individual carrying those alleles is said to be ____.
A) recessive
B) heterozygous
C) phenotypic
D) somatic
E) homozygous
A) recessive
B) heterozygous
C) phenotypic
D) somatic
E) homozygous
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12
The most common type of mutation that causes cystic fibrosis is a(n) ____.
A) deletion
B) insertion
C) base-pair substitution
D) gene duplication
E) transformation
A) deletion
B) insertion
C) base-pair substitution
D) gene duplication
E) transformation
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13
The failure of which organ affected by a defective CFTR protein is likely to cause death in cystic fibrosis patients?
A) lungs
B) intestines
C) heart
D) liver
E) reproductive system
A) lungs
B) intestines
C) heart
D) liver
E) reproductive system
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14
If R is dominant to r , the offspring of the cross of RR with rr will ____.
A) have a unique phenotype
B) have the same phenotype as the RR parents
C) have the same phenotype as the rr parents
D) have the same genotype as the RR parents
E) have the same genotype as the rr parents
A) have a unique phenotype
B) have the same phenotype as the RR parents
C) have the same phenotype as the rr parents
D) have the same genotype as the RR parents
E) have the same genotype as the rr parents
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15
An individual's ____ determines its observable ____.
A) phenotype; genotype
B) genotype; phenotype
C) gene location; allele
D) heterozygote; homozygote
E) homozygote; heterozygote
A) phenotype; genotype
B) genotype; phenotype
C) gene location; allele
D) heterozygote; homozygote
E) homozygote; heterozygote
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16
If tall ( D ) is dominant to dwarf ( d ), and two homozygous varieties DD and dd are crossed, the progeny produced will be____.
A) all intermediate forms
B) all tall
C) all dwarf
D) 1/2 tall and 1/2 dwarf
E) 3/4 tall and 1/4 dwarf
A) all intermediate forms
B) all tall
C) all dwarf
D) 1/2 tall and 1/2 dwarf
E) 3/4 tall and 1/4 dwarf
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17
____ is the most fatal genetic disorder in the United States.
A) Cystic fibrosis
B) Huntington's disease
C) Sickle-cell anemia
D) Anhidrotic dysplasia
E) Color blindness
A) Cystic fibrosis
B) Huntington's disease
C) Sickle-cell anemia
D) Anhidrotic dysplasia
E) Color blindness
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18
In the lungs of cystic fibrosis patients, ____.
A) chloride ions are stuck inside epithelial cells
B) water is excessively abundant on epithelial surfaces
C) epithelial surfaces are coated with slippery mucus
D) excess water and chloride ions are pumped out of epithelial cells
E) chloride ions are not transported out of epithelial cells, and epithelial surfaces are dry
A) chloride ions are stuck inside epithelial cells
B) water is excessively abundant on epithelial surfaces
C) epithelial surfaces are coated with slippery mucus
D) excess water and chloride ions are pumped out of epithelial cells
E) chloride ions are not transported out of epithelial cells, and epithelial surfaces are dry
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19
The main problem for those with cystic fibrosis involves ____.
A) mucus sticking to dry surfaces
B) jerky muscle contractions
C) constant thirst
D) salt accumulations between tissues
E) low pH in tissues preventing proper enzymatic activity
A) mucus sticking to dry surfaces
B) jerky muscle contractions
C) constant thirst
D) salt accumulations between tissues
E) low pH in tissues preventing proper enzymatic activity
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20
A(n) ____ is an offspring of a cross between two individuals that breed true for different forms of a given trait.
A) homozygote
B) recessive
C) hybrid
D) phenotype
E) genotype
A) homozygote
B) recessive
C) hybrid
D) phenotype
E) genotype
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21
The mutation that causes the lighter skin color of all people of European descent was the result of a ____ in the gene for a melanin transport protein.
A) base-pair substitution
B) insertion
C) deletion
D) whole chromosome duplication
E) multiple gene mutations involving several mechanisms
A) base-pair substitution
B) insertion
C) deletion
D) whole chromosome duplication
E) multiple gene mutations involving several mechanisms
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22
Genetic recombination as a result of crossing over occurs more readily between genes that are ____.
A) on the sex chromosomes
B) near the centromere
C) located close together on the same chromosome
D) located far apart on the same chromosome
E) located on different chromosomes
A) on the sex chromosomes
B) near the centromere
C) located close together on the same chromosome
D) located far apart on the same chromosome
E) located on different chromosomes
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23

In the figure above, how many plants would have white flowers and short stems?
A) 1
B) 3
C) 5
D) 9
E) 16
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24

In the figure above, how many plants would have purple flowers and tall stems?
A) 1
B) 3
C) 5
D) 9
E) 16
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25

In the figure above, what would be the genotype of plant #7?
A) AaBb
B) AABb
C) AaBB
D) AABB
E) aaBB
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26
For this problem, you may want to create a Punnett Square on a separate piece of paper. Manuel has cystic fibrosis, a recessive disorder, and sickle-cell anemia, which is also a recessive disorder. Manuel's partner, Lucretia, is normal for both conditions. What is the probability that Manuel and Lucretia will have a normal child without either of the conditions Manuel has?
A) 0 percent
B) 25 percent
C) 75 percent
D) 100 percent
E) It is not possible to solve this problem with the information provided.
A) 0 percent
B) 25 percent
C) 75 percent
D) 100 percent
E) It is not possible to solve this problem with the information provided.
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27
In cats, short hair L is dominant to long hair l and black hair B is dominant to brown hair b . If you found a black, short-haired cat, you could determine his genotype by crossing it to an animal with a genotype of ____.
A) LLBB
B) llBB
C) llBb
D) llbb
E) LLbb
A) LLBB
B) llBB
C) llBb
D) llbb
E) LLbb
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28
If two individuals who are heterozygous for two traits that display incomplete dominance (e.g., AaBb) mate and have offspring, how many different phenotypes are possible?
A) 1
B) 3
C) 6
D) 9
E) 16
A) 1
B) 3
C) 6
D) 9
E) 16
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29
Cystic fibrosis is a recessive disorder. If a couple, each of whom is heterozygous for the CFTR mutation, have children, what is the probability that they will have a child with cystic fibrosis?
A) 0 percent
B) 25 percent
C) 50 percent
D) 75 percent
E) 100 percent
A) 0 percent
B) 25 percent
C) 50 percent
D) 75 percent
E) 100 percent
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30

In the figure above, what would be the genotype of plant #9?
A) Aabb
B) aaBb
C) AaBB
D) AABB
E) aaBB
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31
The ease of detecting and treating ____ is a good example of the advantages of genetic screening.
A) PKU
B) Tay-Sachs
C) Marfan syndrome
D) color blindness
E) Down syndrome
A) PKU
B) Tay-Sachs
C) Marfan syndrome
D) color blindness
E) Down syndrome
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32
The discarded theory of blending inheritance most closely resembles ____.
A) X-linked inheritance
B) dihybridization
C) codominance
D) incomplete dominance
E) complete dominance
A) X-linked inheritance
B) dihybridization
C) codominance
D) incomplete dominance
E) complete dominance
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33
If a child has an AB blood type, ____.
A) both parents must have different blood types
B) neither parent can have blood type AB
C) both parents must have blood type AB
D) both parents can be any blood type
E) one parent can have blood type O
A) both parents must have different blood types
B) neither parent can have blood type AB
C) both parents must have blood type AB
D) both parents can be any blood type
E) one parent can have blood type O
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34
In a Punnett square, the letters on top of the square and on the side of the square represent ____.
A) offspring genotypes
B) zygote genotypes
C) parental gametes
D) offspring phenotypes
E) parental phenotypes
A) offspring genotypes
B) zygote genotypes
C) parental gametes
D) offspring phenotypes
E) parental phenotypes
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35
For this problem, you may want to create a Punnett Square on a separate piece of paper. Assume brown eyes are dominant to blue eyes and dimples are dominant to no dimples. John has brown eyes, and his mother has blue eyes. John does not have dimples. Zena has blue eyes and also has no dimples. What are the chances if this couple have children, they will produce a child with blue eyes and no dimples?
A) 0
B) ¼
C) ½
D) ¾
E) There is not enough information provided to solve this problem.
A) 0
B) ¼
C) ½
D) ¾
E) There is not enough information provided to solve this problem.
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36
In codominance, ____.
A) one allele is dominant to another allele
B) the genotype is determined by the phenotype
C) the heterozygous phenotype is intermediate to the homozygous phenotypes
D) the intermediate phenotype may be the result of enzyme insufficiency
E) two alleles may be equally expressed
A) one allele is dominant to another allele
B) the genotype is determined by the phenotype
C) the heterozygous phenotype is intermediate to the homozygous phenotypes
D) the intermediate phenotype may be the result of enzyme insufficiency
E) two alleles may be equally expressed
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37
Approximately how many gene products are involved in the synthesis of melanin in humans?
A) 10
B) 25
C) 50
D) 100
E) 1000
A) 10
B) 25
C) 50
D) 100
E) 1000
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38

In the figure above, how many plants would have the genotype AaBb ?
A) 1
B) 3
C) 4
D) 6
E) 9
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39
In a cross of a DDRR individual with a ddrr individual, the genotype of all offspring will ____.
A) DDRR
B) DdRR
C) DdRr
D) ddRR
E) ddRr
A) DDRR
B) DdRR
C) DdRr
D) ddRR
E) ddRr
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40
If a pure-breeding wired-hair terrier ( WW ) is crossed with a pure-breeding smooth-hair terrier (ww), and a puppy with a wavy hair is produced, the simplest explanation is ____.
A) a mutation has occurred
B) hair texture is an X-linked trait
C) incomplete dominance
D) hair texture is a lethal trait
E) codominance
A) a mutation has occurred
B) hair texture is an X-linked trait
C) incomplete dominance
D) hair texture is a lethal trait
E) codominance
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41
When genes are located very close together on the same chromosome, ____.
A) gametes usually end up with the same combination of alleles as parental cells
B) gametes usually end up with unique combination of alleles
C) they are inherited separately
D) they often recombine during crossing over
E) offspring will look just like one parent
A) gametes usually end up with the same combination of alleles as parental cells
B) gametes usually end up with unique combination of alleles
C) they are inherited separately
D) they often recombine during crossing over
E) offspring will look just like one parent
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42
The switching between asexual and sexual reproduction by water fleas is controlled by ____.
A) epistasis
B) pleiotropy
C) incomplete dominance
D) codominant inheritance
E) environmental effects
A) epistasis
B) pleiotropy
C) incomplete dominance
D) codominant inheritance
E) environmental effects
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43
In an autosomal dominant disorder such as Huntington's disease, two carrier parents have the probability of passing the gene onto ____ of their children.
A) 0 percent
B) 25 percent
C) 50 percent
D) 75 percent
E) 100 percent
A) 0 percent
B) 25 percent
C) 50 percent
D) 75 percent
E) 100 percent
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44
Narrative:
Achondroplasia, a hereditary form of dwarfism, is an autosomal dominant disorder; however homozygous dominant individuals either die before birth or very shortly thereafter. The homozygous recessive condition is normal. A dwarf couple decide to have children. Use this information to answer the following question:
Of the children of this couple who survive, what is the probability that they will be normal?
A) 0
B) ¼
C) 1/3
D) 2/3
E) ½
Achondroplasia, a hereditary form of dwarfism, is an autosomal dominant disorder; however homozygous dominant individuals either die before birth or very shortly thereafter. The homozygous recessive condition is normal. A dwarf couple decide to have children. Use this information to answer the following question:
Of the children of this couple who survive, what is the probability that they will be normal?
A) 0
B) ¼
C) 1/3
D) 2/3
E) ½
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45
In a pedigree chart, a male who demonstrates the trait being studied is represented by a ____.
A) darkened square
B) darkened diamond
C) clear circle
D) clear square
E) darkened circle
A) darkened square
B) darkened diamond
C) clear circle
D) clear square
E) darkened circle
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46
Narrative:
Achondroplasia, a hereditary form of dwarfism, is an autosomal dominant disorder; however homozygous dominant individuals either die before birth or very shortly thereafter. The homozygous recessive condition is normal. A dwarf couple decide to have children. Use this information to answer the following question:
Of the children of this couple who survive, what is probability that they will be affected by achondroplasia?
A) 0
B) ¼
C) 1/3
D) 2/3
E) ½
Achondroplasia, a hereditary form of dwarfism, is an autosomal dominant disorder; however homozygous dominant individuals either die before birth or very shortly thereafter. The homozygous recessive condition is normal. A dwarf couple decide to have children. Use this information to answer the following question:
Of the children of this couple who survive, what is probability that they will be affected by achondroplasia?
A) 0
B) ¼
C) 1/3
D) 2/3
E) ½
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47
In the Bombay phenotype, a gene in the recessive condition blocks the expression of A and B red blood cell antigens. Thus, all A, B, and AB genotypes are expressed as the O phenotype. This is an example of ____.
A) complete dominance
B) polygeny
C) incomplete dominance
D) codominance
E) pleiotropy
A) complete dominance
B) polygeny
C) incomplete dominance
D) codominance
E) pleiotropy
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48
A gene that produces multiple effects is called a(n) ____.
A) codominant gene
B) X-linked gene
C) epistatic gene
D) pleiotropic gene
E) incompletely dominant gene
A) codominant gene
B) X-linked gene
C) epistatic gene
D) pleiotropic gene
E) incompletely dominant gene
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49
A pleiotropic gene ____.
A) acts on secondary sexual characteristics
B) influences multiple traits
C) is additive
D) produces lethal effects when homozygous
E) produces epigenetic effects
A) acts on secondary sexual characteristics
B) influences multiple traits
C) is additive
D) produces lethal effects when homozygous
E) produces epigenetic effects
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50
The probability of producing a normal child by two parents who are carriers for an autosomal recessive disorder is ____.
A) 0 percent
B) 25 percent
C) 50 percent
D) 75 percent
E) 100 percent
A) 0 percent
B) 25 percent
C) 50 percent
D) 75 percent
E) 100 percent
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51
An X-linked carrier is a ____.
A) homozygous dominant female
B) heterozygous female
C) homozygous recessive female
D) homozygous male
E) heterozygous male
A) homozygous dominant female
B) heterozygous female
C) homozygous recessive female
D) homozygous male
E) heterozygous male
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52
Geneticists use ____ to study the genetics of families through generations.
A) Punnett squares
B) pedigrees
C) karyotypes
D) DNA profiles
E) fossil analyses
A) Punnett squares
B) pedigrees
C) karyotypes
D) DNA profiles
E) fossil analyses
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53
The ABO blood types have ____ different genotypes.
A) 4
B) 6
C) 8
D) 12
E) 16
A) 4
B) 6
C) 8
D) 12
E) 16
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54
An autosomal recessive disorder ____.
A) requires that only one parent be a carrier
B) displays its symptoms in heterozygotes
C) is more frequent in males than females
D) requires that both parents are carriers
E) only affects females
A) requires that only one parent be a carrier
B) displays its symptoms in heterozygotes
C) is more frequent in males than females
D) requires that both parents are carriers
E) only affects females
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55
Human eye color is an example of a trait that varies ____.
A) according to the geographical area
B) periodically
C) according to humidity
D) continuously
E) according to seasons
A) according to the geographical area
B) periodically
C) according to humidity
D) continuously
E) according to seasons
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56
In humans, skin color is controlled by several genes. Thus, skin color is a(n) ____ characteristic.
A) dominant
B) codominant
C) polygenic
D) pleiotropic
E) recessive
A) dominant
B) codominant
C) polygenic
D) pleiotropic
E) recessive
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57
In a pedigree chart, a female showing the specific trait being studied is indicated by a ____.
A) clear square
B) darkened square
C) clear circle
D) darkened diamond
E) darkened circle
A) clear square
B) darkened square
C) clear circle
D) darkened diamond
E) darkened circle
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58
Six fingers on one hand would be classified as a(n) ____.
A) genetic disorder
B) disease
C) syndrome
D) genetic abnormality
E) illness
A) genetic disorder
B) disease
C) syndrome
D) genetic abnormality
E) illness
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59
In Siamese cats, enzymes that code for dark fur color are only active in cooler temperatures. Thus, the tips of a Siamese cat's ears, feet, and tail are dark but not the warmer regions of its body core. This is an example of ____.
A) p leiotropy
B) environmental effects
C) epistasis
D) incomplete dominance
E) codominance
A) p leiotropy
B) environmental effects
C) epistasis
D) incomplete dominance
E) codominance
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60
Males are more commonly affected by X-linked recessive genetic disorders than females because ____.
A) females have two X chromosomes; therefore, they do not inherit recessive alleles
B) males have only one X chromosome; therefore, they express all recessive X-linked traits
C) males have only one X chromosome; therefore, they have multiple alleles for each X-linked gene
D) Y chromosomes cause X-linked gene mutations
E) males are genetically weaker than females
A) females have two X chromosomes; therefore, they do not inherit recessive alleles
B) males have only one X chromosome; therefore, they express all recessive X-linked traits
C) males have only one X chromosome; therefore, they have multiple alleles for each X-linked gene
D) Y chromosomes cause X-linked gene mutations
E) males are genetically weaker than females
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61
Match between columns
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62
Suppose a single nondisjunction event occurs during anaphase II of meiosis in a normal male cell from meiosis I. Of the resulting sperm, ____.
A) three would be normal and one would have an extra chromosome
B) two would be normal, one would have an extra chromosome, and one would be missing a chromosome
C) two would have an extra chromosome and two would be missing a chromosome
D) all four sperm would have an extra chromosome
E) three would have an extra chromosome and one would be normal
A) three would be normal and one would have an extra chromosome
B) two would be normal, one would have an extra chromosome, and one would be missing a chromosome
C) two would have an extra chromosome and two would be missing a chromosome
D) all four sperm would have an extra chromosome
E) three would have an extra chromosome and one would be normal
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63
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64
Face length in dogs is controlled by ____.
A) a dozen alleles
B) a dozen genes
C) multiple chromosomes
D) sex-linked alleles
E) trisomies
A) a dozen alleles
B) a dozen genes
C) multiple chromosomes
D) sex-linked alleles
E) trisomies
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65
The process by which chromosomes fail to separate during meiosis is called ____.
A) aneuploidy
B) trisomy
C) monosomy
D) nondisjunction
E) polyploidy
A) aneuploidy
B) trisomy
C) monosomy
D) nondisjunction
E) polyploidy
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66
Amniocentesis involves sampling ____.
A) the embryo at the eight-cell stage
B) fetal cells in the amniotic fluid
C) sperm or egg cells
D) fetal skin tissue
E) placental cells
A) the embryo at the eight-cell stage
B) fetal cells in the amniotic fluid
C) sperm or egg cells
D) fetal skin tissue
E) placental cells
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67
Match between columns
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68
____ is an example of a genetic disorder with little impact on the individual.
A) XXX syndrome
B) Turner syndrome
C) Hemophilia
D) XYY syndrome
E) Down syndrome
A) XXX syndrome
B) Turner syndrome
C) Hemophilia
D) XYY syndrome
E) Down syndrome
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69
Genetic testing by ____ can be performed earliest in pregnancy.
A) amniocentesis
B) obstetric sonography
C) fetoscopy
D) chorionic villus sampling
E) preimplantation genetic diagnosis
A) amniocentesis
B) obstetric sonography
C) fetoscopy
D) chorionic villus sampling
E) preimplantation genetic diagnosis
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