Deck 13: Extensions of and Deviations From Mendelian Genetic Principles

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Question
Individuals with neurofibromatosis may have a range of phenotypes,from pigment spots on the skin to tumorlike growths.This is an example of

A)incomplete penetrance.
B)variable expressivity.
C)age of onset.
D)X-inactivation.
E)gene magnification.
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Question
Familial hypercholesterolemia is a genetic disease that affects approximately one in 500 people worldwide.There is more than one genetic cause of the disease.Class I is often described as an autosomal dominant disease.Affected individuals have cholesterol levels >250 as children and often >300 as adults.However,homozygotes have cholesterol levels of >600 as children and can die of heart attacks in their 20s.These individuals entirely lack a functional LDL receptor.Which of the following would be the best description of the inheritance of this form of hypercholesterolemia?

A)Dominant epistatic
B)Codominant
C)Incompletely dominant
D)Complementary
E)Recessive epistatic
Question
Two true-breeding mutant strains of Drosophila have black body color instead of the wild-type gray yellow.When the two strains are crossed,all the F1 flies have wild-type body color.How can these data be interpreted?

A)Recombination occurred.
B)Complementation occurred.
C)The mutations involved are on two different genes.
D)A new mutation occurred in all the offspring.
E)Both B and C
Question
This form of inheritance is called

A)maternal inheritance.
B)sex-limited inheritance.
C)sex-linked inheritance.
D)maternal effect.
E)partial penetrance.
Question
The distinctive fur pattern of Siamese cats results when genes that are responsible for the coat color are influenced by

A)age.
B)X-inactivation.
C)gender.
D)temperature.
E)other genes.
Question
A person with type B blood could safely receive a transfusion of blood from someone with blood type

A)B.
B)AB.
C)O.
D)Both A and C
E)Any of these
Question
Which of the following will result in modifications to the expected Mendelian ratios?

A)Epistasis
B)Incomplete dominance
C)Incomplete penetrance
D)Gene interaction
E)All of these
Question
In the multiple allelic system for eye color in Drosophila,the phenotypic expression of the alleles depends on

A)how much pigment is produced by the alleles present.
B)the interaction of alleles from two different genes.
C)the temperature at which the flies are grown.
D)the sex of the fly.
E)Both A and B
Question
Mutants that make up a complementation group complement each other.
Question
Solid black,black with tan belly,and agouti coat color in mice are all caused by alleles of the agouti gene.All three colors can be true-breeding.When using mice from true-breeding strains: (1)Black × Agouti F1s are all agouti,(2)Black × Black with Tan belly F1s are all black and tan,and (3)Black with Tan belly × Agouti F1s are all agouti.If you were to cross the F1s from (1)with the F1s from (2),what proportion of the resulting offspring would you expect to be black with a tan belly?

A)None
B) 14\frac { 1 } { 4 }
C) 316\frac { 3 } { 16 }
D) 12\frac { 1 } { 2 }
E) 116\frac { 1 } { 16 }
Question
Studies performed on identical twins separated at birth have shown that many phenotypes,such as IQ or alcoholism,are influenced by the person's genotype as well as by their environment.
Question
For a gene with complete dominance,the recessive allele has no effect on the phenotype of a heterozygote.
Question
People affected by diseases caused by mtDNA defects

A)typically have cells that are heteroplasmons.
B)show partial penetrance.
C)are sterile.
D)inherited them through maternal effect.
E)have epistatic respiration.
Question
Two persons who have recessive genetic deafness marry and have 6 children.All the children can hear.The reason they can hear is most likely due to

A)epistasis.
B)pleiotropy.
C)sex linkage.
D)complementation.
E)partial penetrance.
Question
A and B antigens in human blood are produced by the conversion of ________ by the addition of a sugar group.

A)anti-A and anti-B antibodies
B)the H antigen
C)hemoglobin
D)α-N-acetylgalactosamine
E)anti-O antibodies
Question
What were the genotypes of the sinistral female and dextral male that were initially chosen?

A)dd female and Dd male
B)Dd female and dd male
C)dd female and DD male
D)DD female and dd male
E)Dd female and Dd male
Question
Comb shape in chickens is controlled by

A)the interaction of three alleles and codominance,resulting in four different phenotypes.
B)one gene with incomplete dominance,resulting in three different phenotypes.
C)the epistatic interaction of two genes,resulting in two different phenotypes.
D)the interaction of two genes with complete dominance,resulting in four different phenotypes.
E)None of these
Question
Manx cats have no tails.When two Manx cats are bred together there is always a one third chance that a kitten will have a tail.When a Manx cat is bred to a cat with a normal tail there is a one-half chance that a kitten will have a tail.Which of the following is the best explanation for this?

A)The Manx genotype exhibits variable expression.
B)The Manx phenotype is dominant,but the allele is a recessive lethal.
C)The Manx phenotype is dominant epistatic.
D)The Manx phenotype is caused by gene interactions.
E)The Manx phenotype is a result of heteroplasmy.
Question
An allele that exhibits incomplete dominance is usually haplosufficient.
Question
Human height is a trait affected by both genes and the environment.How is this so?
Question
Sex-limited traits are caused by genes that are on sex chromosomes.
Question
What is the cause of Tay-Sachs disease?
Question
For a gene with multiple alleles,what is the maximum number of alleles that a diploid organism may have?
Question
How could a man with blood type A and a woman with blood type B produce a child with blood type O?
Question
In a dihybrid cross with independent assortment of the two genes,any deviation from the Mendelian 9:3:3:1 ratio indicates that the phenotype is the product of the interaction of two or more genes.
Question
In the human ABO blood system,the allele i is dominant to IA and IB.
Question
Explain and differentiate among the molecular bases of codominance,incomplete dominance,and complete dominance.
Question
Use a Punnett square to demonstrate a cross between two of the F1 offspring.What are the phenotypes and ratios that occur?
Question
Phenylketonuria (PKU)is an example of a phenotype that is solely influenced by genes.
Question
Recessive lethals are often mutations in essential genes.
Question
What is the number of possible genotypes in a multiple allele series with 6 alleles? How many of these are homozygous and how many are heterozygous?
Question
In a genotype with complete penetrance,less than 100% of individuals with a particular genotype exhibit the expected phenotype.
Question
Generally,blue eyes are recessive to dark brown eyes in humans.Individuals with albinism typically have blue eyes with a strong red reflection.A blue-eyed woman with albinism marries a man who is blue-eyed but does not have albinism.All their children have dark brown eyes.How can this be explained?
Question
What is the phenotype and genotype of the chicks?
Question
In chickens,there is a mutant gene called "frizzle" that results in weak,stringy,and easily broken feathers.When a frightfully frizzled fowl is bred to a normal chicken,the offspring are all mildly frizzled.If one breeds two mildly frizzled chickens to each other,the offspring have the phenotypic ratio of 1 normal: 2 mildly frizzled: 1 frightfully frizzled.What is the mode of inheritance of "frizzle"?
Question
In cats,the dominant white gene (W)may or may not also cause deafness.Homozygotes are more likely to be deaf than heterozygotes.If you breed heterozygous white cats together and produce 100 kittens,how many would you expect to be deaf if all the proportions came out perfectly? Assume that heterozygotes have an 8% chance of being deaf,and homozygotes a 60% chance of being deaf.
Question
Why is it that human males and females who are both heterozygous for the pattern-baldness gene have different phenotypes (males are bald,females are not bald)?
Question
In the ABO blood-type system,which genotypes could confer type A blood to a person?
Question
Comb shape in chickens also involves the interaction of two genes,but the F2 generation shows a typical 9:3:3:1 Mendelian ratio.How does this work?
Question
The 9:6:1 F2 ratio found in fruit shape in summer squash is a deviation from an expected Mendelian ratio.What does this represent?
Question
Match between columns
Incomplete dominance
When each allele causes a distinct phenotype,and heterozygotes exhibit both phenotypes of heterozygotes
Incomplete dominance
When the genotype at one locus generates phenotypic expression of a trait that overrides and conceals the phenotypic traits arising from one or more other genes
Incomplete dominance
When heterozygotes display a phenotype intermediate between those shown by homozygotes for that allele
Incomplete dominance
When a genotype underlies a given phenotype,but not all individuals with that genotype display the phenotype
Incomplete dominance
When a genotype gives rise to a range of phenotypes
Incomplete penetrance
When each allele causes a distinct phenotype,and heterozygotes exhibit both phenotypes of heterozygotes
Incomplete penetrance
When the genotype at one locus generates phenotypic expression of a trait that overrides and conceals the phenotypic traits arising from one or more other genes
Incomplete penetrance
When heterozygotes display a phenotype intermediate between those shown by homozygotes for that allele
Incomplete penetrance
When a genotype underlies a given phenotype,but not all individuals with that genotype display the phenotype
Incomplete penetrance
When a genotype gives rise to a range of phenotypes
Variable expressivity
When each allele causes a distinct phenotype,and heterozygotes exhibit both phenotypes of heterozygotes
Variable expressivity
When the genotype at one locus generates phenotypic expression of a trait that overrides and conceals the phenotypic traits arising from one or more other genes
Variable expressivity
When heterozygotes display a phenotype intermediate between those shown by homozygotes for that allele
Variable expressivity
When a genotype underlies a given phenotype,but not all individuals with that genotype display the phenotype
Variable expressivity
When a genotype gives rise to a range of phenotypes
Codominance
When each allele causes a distinct phenotype,and heterozygotes exhibit both phenotypes of heterozygotes
Codominance
When the genotype at one locus generates phenotypic expression of a trait that overrides and conceals the phenotypic traits arising from one or more other genes
Codominance
When heterozygotes display a phenotype intermediate between those shown by homozygotes for that allele
Codominance
When a genotype underlies a given phenotype,but not all individuals with that genotype display the phenotype
Codominance
When a genotype gives rise to a range of phenotypes
Epistasis
When each allele causes a distinct phenotype,and heterozygotes exhibit both phenotypes of heterozygotes
Epistasis
When the genotype at one locus generates phenotypic expression of a trait that overrides and conceals the phenotypic traits arising from one or more other genes
Epistasis
When heterozygotes display a phenotype intermediate between those shown by homozygotes for that allele
Epistasis
When a genotype underlies a given phenotype,but not all individuals with that genotype display the phenotype
Epistasis
When a genotype gives rise to a range of phenotypes
Question
Match between columns
Heteroplasmon
When a cell or individual has more than one mitochondrial genome type
Heteroplasmon
A phenotype caused by a maternal nuclear genotype that affects eggs prior to fertilization,and is therefore expressed in all offspring,regardless of paternal genes
Heteroplasmon
When a genotype and phenotype are only inherited from the mother
Heteroplasmon
When a genotype causes a phenotype in only one sex
Heteroplasmon
When either the frequency or amount of a phenotype depends on the sex of the individual
Maternal inheritance
When a cell or individual has more than one mitochondrial genome type
Maternal inheritance
A phenotype caused by a maternal nuclear genotype that affects eggs prior to fertilization,and is therefore expressed in all offspring,regardless of paternal genes
Maternal inheritance
When a genotype and phenotype are only inherited from the mother
Maternal inheritance
When a genotype causes a phenotype in only one sex
Maternal inheritance
When either the frequency or amount of a phenotype depends on the sex of the individual
Sex-influenced
When a cell or individual has more than one mitochondrial genome type
Sex-influenced
A phenotype caused by a maternal nuclear genotype that affects eggs prior to fertilization,and is therefore expressed in all offspring,regardless of paternal genes
Sex-influenced
When a genotype and phenotype are only inherited from the mother
Sex-influenced
When a genotype causes a phenotype in only one sex
Sex-influenced
When either the frequency or amount of a phenotype depends on the sex of the individual
Sex-limited
When a cell or individual has more than one mitochondrial genome type
Sex-limited
A phenotype caused by a maternal nuclear genotype that affects eggs prior to fertilization,and is therefore expressed in all offspring,regardless of paternal genes
Sex-limited
When a genotype and phenotype are only inherited from the mother
Sex-limited
When a genotype causes a phenotype in only one sex
Sex-limited
When either the frequency or amount of a phenotype depends on the sex of the individual
Maternal effect
When a cell or individual has more than one mitochondrial genome type
Maternal effect
A phenotype caused by a maternal nuclear genotype that affects eggs prior to fertilization,and is therefore expressed in all offspring,regardless of paternal genes
Maternal effect
When a genotype and phenotype are only inherited from the mother
Maternal effect
When a genotype causes a phenotype in only one sex
Maternal effect
When either the frequency or amount of a phenotype depends on the sex of the individual
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Deck 13: Extensions of and Deviations From Mendelian Genetic Principles
1
Individuals with neurofibromatosis may have a range of phenotypes,from pigment spots on the skin to tumorlike growths.This is an example of

A)incomplete penetrance.
B)variable expressivity.
C)age of onset.
D)X-inactivation.
E)gene magnification.
B
2
Familial hypercholesterolemia is a genetic disease that affects approximately one in 500 people worldwide.There is more than one genetic cause of the disease.Class I is often described as an autosomal dominant disease.Affected individuals have cholesterol levels >250 as children and often >300 as adults.However,homozygotes have cholesterol levels of >600 as children and can die of heart attacks in their 20s.These individuals entirely lack a functional LDL receptor.Which of the following would be the best description of the inheritance of this form of hypercholesterolemia?

A)Dominant epistatic
B)Codominant
C)Incompletely dominant
D)Complementary
E)Recessive epistatic
C
3
Two true-breeding mutant strains of Drosophila have black body color instead of the wild-type gray yellow.When the two strains are crossed,all the F1 flies have wild-type body color.How can these data be interpreted?

A)Recombination occurred.
B)Complementation occurred.
C)The mutations involved are on two different genes.
D)A new mutation occurred in all the offspring.
E)Both B and C
E
4
This form of inheritance is called

A)maternal inheritance.
B)sex-limited inheritance.
C)sex-linked inheritance.
D)maternal effect.
E)partial penetrance.
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5
The distinctive fur pattern of Siamese cats results when genes that are responsible for the coat color are influenced by

A)age.
B)X-inactivation.
C)gender.
D)temperature.
E)other genes.
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6
A person with type B blood could safely receive a transfusion of blood from someone with blood type

A)B.
B)AB.
C)O.
D)Both A and C
E)Any of these
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7
Which of the following will result in modifications to the expected Mendelian ratios?

A)Epistasis
B)Incomplete dominance
C)Incomplete penetrance
D)Gene interaction
E)All of these
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8
In the multiple allelic system for eye color in Drosophila,the phenotypic expression of the alleles depends on

A)how much pigment is produced by the alleles present.
B)the interaction of alleles from two different genes.
C)the temperature at which the flies are grown.
D)the sex of the fly.
E)Both A and B
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9
Mutants that make up a complementation group complement each other.
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10
Solid black,black with tan belly,and agouti coat color in mice are all caused by alleles of the agouti gene.All three colors can be true-breeding.When using mice from true-breeding strains: (1)Black × Agouti F1s are all agouti,(2)Black × Black with Tan belly F1s are all black and tan,and (3)Black with Tan belly × Agouti F1s are all agouti.If you were to cross the F1s from (1)with the F1s from (2),what proportion of the resulting offspring would you expect to be black with a tan belly?

A)None
B) 14\frac { 1 } { 4 }
C) 316\frac { 3 } { 16 }
D) 12\frac { 1 } { 2 }
E) 116\frac { 1 } { 16 }
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11
Studies performed on identical twins separated at birth have shown that many phenotypes,such as IQ or alcoholism,are influenced by the person's genotype as well as by their environment.
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k this deck
12
For a gene with complete dominance,the recessive allele has no effect on the phenotype of a heterozygote.
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13
People affected by diseases caused by mtDNA defects

A)typically have cells that are heteroplasmons.
B)show partial penetrance.
C)are sterile.
D)inherited them through maternal effect.
E)have epistatic respiration.
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14
Two persons who have recessive genetic deafness marry and have 6 children.All the children can hear.The reason they can hear is most likely due to

A)epistasis.
B)pleiotropy.
C)sex linkage.
D)complementation.
E)partial penetrance.
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15
A and B antigens in human blood are produced by the conversion of ________ by the addition of a sugar group.

A)anti-A and anti-B antibodies
B)the H antigen
C)hemoglobin
D)α-N-acetylgalactosamine
E)anti-O antibodies
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16
What were the genotypes of the sinistral female and dextral male that were initially chosen?

A)dd female and Dd male
B)Dd female and dd male
C)dd female and DD male
D)DD female and dd male
E)Dd female and Dd male
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17
Comb shape in chickens is controlled by

A)the interaction of three alleles and codominance,resulting in four different phenotypes.
B)one gene with incomplete dominance,resulting in three different phenotypes.
C)the epistatic interaction of two genes,resulting in two different phenotypes.
D)the interaction of two genes with complete dominance,resulting in four different phenotypes.
E)None of these
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18
Manx cats have no tails.When two Manx cats are bred together there is always a one third chance that a kitten will have a tail.When a Manx cat is bred to a cat with a normal tail there is a one-half chance that a kitten will have a tail.Which of the following is the best explanation for this?

A)The Manx genotype exhibits variable expression.
B)The Manx phenotype is dominant,but the allele is a recessive lethal.
C)The Manx phenotype is dominant epistatic.
D)The Manx phenotype is caused by gene interactions.
E)The Manx phenotype is a result of heteroplasmy.
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19
An allele that exhibits incomplete dominance is usually haplosufficient.
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20
Human height is a trait affected by both genes and the environment.How is this so?
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21
Sex-limited traits are caused by genes that are on sex chromosomes.
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22
What is the cause of Tay-Sachs disease?
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23
For a gene with multiple alleles,what is the maximum number of alleles that a diploid organism may have?
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24
How could a man with blood type A and a woman with blood type B produce a child with blood type O?
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25
In a dihybrid cross with independent assortment of the two genes,any deviation from the Mendelian 9:3:3:1 ratio indicates that the phenotype is the product of the interaction of two or more genes.
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26
In the human ABO blood system,the allele i is dominant to IA and IB.
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27
Explain and differentiate among the molecular bases of codominance,incomplete dominance,and complete dominance.
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28
Use a Punnett square to demonstrate a cross between two of the F1 offspring.What are the phenotypes and ratios that occur?
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29
Phenylketonuria (PKU)is an example of a phenotype that is solely influenced by genes.
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30
Recessive lethals are often mutations in essential genes.
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31
What is the number of possible genotypes in a multiple allele series with 6 alleles? How many of these are homozygous and how many are heterozygous?
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32
In a genotype with complete penetrance,less than 100% of individuals with a particular genotype exhibit the expected phenotype.
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33
Generally,blue eyes are recessive to dark brown eyes in humans.Individuals with albinism typically have blue eyes with a strong red reflection.A blue-eyed woman with albinism marries a man who is blue-eyed but does not have albinism.All their children have dark brown eyes.How can this be explained?
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34
What is the phenotype and genotype of the chicks?
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35
In chickens,there is a mutant gene called "frizzle" that results in weak,stringy,and easily broken feathers.When a frightfully frizzled fowl is bred to a normal chicken,the offspring are all mildly frizzled.If one breeds two mildly frizzled chickens to each other,the offspring have the phenotypic ratio of 1 normal: 2 mildly frizzled: 1 frightfully frizzled.What is the mode of inheritance of "frizzle"?
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36
In cats,the dominant white gene (W)may or may not also cause deafness.Homozygotes are more likely to be deaf than heterozygotes.If you breed heterozygous white cats together and produce 100 kittens,how many would you expect to be deaf if all the proportions came out perfectly? Assume that heterozygotes have an 8% chance of being deaf,and homozygotes a 60% chance of being deaf.
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37
Why is it that human males and females who are both heterozygous for the pattern-baldness gene have different phenotypes (males are bald,females are not bald)?
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38
In the ABO blood-type system,which genotypes could confer type A blood to a person?
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39
Comb shape in chickens also involves the interaction of two genes,but the F2 generation shows a typical 9:3:3:1 Mendelian ratio.How does this work?
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40
The 9:6:1 F2 ratio found in fruit shape in summer squash is a deviation from an expected Mendelian ratio.What does this represent?
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41
Match between columns
Incomplete dominance
When each allele causes a distinct phenotype,and heterozygotes exhibit both phenotypes of heterozygotes
Incomplete dominance
When the genotype at one locus generates phenotypic expression of a trait that overrides and conceals the phenotypic traits arising from one or more other genes
Incomplete dominance
When heterozygotes display a phenotype intermediate between those shown by homozygotes for that allele
Incomplete dominance
When a genotype underlies a given phenotype,but not all individuals with that genotype display the phenotype
Incomplete dominance
When a genotype gives rise to a range of phenotypes
Incomplete penetrance
When each allele causes a distinct phenotype,and heterozygotes exhibit both phenotypes of heterozygotes
Incomplete penetrance
When the genotype at one locus generates phenotypic expression of a trait that overrides and conceals the phenotypic traits arising from one or more other genes
Incomplete penetrance
When heterozygotes display a phenotype intermediate between those shown by homozygotes for that allele
Incomplete penetrance
When a genotype underlies a given phenotype,but not all individuals with that genotype display the phenotype
Incomplete penetrance
When a genotype gives rise to a range of phenotypes
Variable expressivity
When each allele causes a distinct phenotype,and heterozygotes exhibit both phenotypes of heterozygotes
Variable expressivity
When the genotype at one locus generates phenotypic expression of a trait that overrides and conceals the phenotypic traits arising from one or more other genes
Variable expressivity
When heterozygotes display a phenotype intermediate between those shown by homozygotes for that allele
Variable expressivity
When a genotype underlies a given phenotype,but not all individuals with that genotype display the phenotype
Variable expressivity
When a genotype gives rise to a range of phenotypes
Codominance
When each allele causes a distinct phenotype,and heterozygotes exhibit both phenotypes of heterozygotes
Codominance
When the genotype at one locus generates phenotypic expression of a trait that overrides and conceals the phenotypic traits arising from one or more other genes
Codominance
When heterozygotes display a phenotype intermediate between those shown by homozygotes for that allele
Codominance
When a genotype underlies a given phenotype,but not all individuals with that genotype display the phenotype
Codominance
When a genotype gives rise to a range of phenotypes
Epistasis
When each allele causes a distinct phenotype,and heterozygotes exhibit both phenotypes of heterozygotes
Epistasis
When the genotype at one locus generates phenotypic expression of a trait that overrides and conceals the phenotypic traits arising from one or more other genes
Epistasis
When heterozygotes display a phenotype intermediate between those shown by homozygotes for that allele
Epistasis
When a genotype underlies a given phenotype,but not all individuals with that genotype display the phenotype
Epistasis
When a genotype gives rise to a range of phenotypes
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42
Match between columns
Heteroplasmon
When a cell or individual has more than one mitochondrial genome type
Heteroplasmon
A phenotype caused by a maternal nuclear genotype that affects eggs prior to fertilization,and is therefore expressed in all offspring,regardless of paternal genes
Heteroplasmon
When a genotype and phenotype are only inherited from the mother
Heteroplasmon
When a genotype causes a phenotype in only one sex
Heteroplasmon
When either the frequency or amount of a phenotype depends on the sex of the individual
Maternal inheritance
When a cell or individual has more than one mitochondrial genome type
Maternal inheritance
A phenotype caused by a maternal nuclear genotype that affects eggs prior to fertilization,and is therefore expressed in all offspring,regardless of paternal genes
Maternal inheritance
When a genotype and phenotype are only inherited from the mother
Maternal inheritance
When a genotype causes a phenotype in only one sex
Maternal inheritance
When either the frequency or amount of a phenotype depends on the sex of the individual
Sex-influenced
When a cell or individual has more than one mitochondrial genome type
Sex-influenced
A phenotype caused by a maternal nuclear genotype that affects eggs prior to fertilization,and is therefore expressed in all offspring,regardless of paternal genes
Sex-influenced
When a genotype and phenotype are only inherited from the mother
Sex-influenced
When a genotype causes a phenotype in only one sex
Sex-influenced
When either the frequency or amount of a phenotype depends on the sex of the individual
Sex-limited
When a cell or individual has more than one mitochondrial genome type
Sex-limited
A phenotype caused by a maternal nuclear genotype that affects eggs prior to fertilization,and is therefore expressed in all offspring,regardless of paternal genes
Sex-limited
When a genotype and phenotype are only inherited from the mother
Sex-limited
When a genotype causes a phenotype in only one sex
Sex-limited
When either the frequency or amount of a phenotype depends on the sex of the individual
Maternal effect
When a cell or individual has more than one mitochondrial genome type
Maternal effect
A phenotype caused by a maternal nuclear genotype that affects eggs prior to fertilization,and is therefore expressed in all offspring,regardless of paternal genes
Maternal effect
When a genotype and phenotype are only inherited from the mother
Maternal effect
When a genotype causes a phenotype in only one sex
Maternal effect
When either the frequency or amount of a phenotype depends on the sex of the individual
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