Inheritance Flashcards

1
Q

What is a gene?

A

A gene is a sequence of DNA that codes for a specific protein or functional RNA.

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2
Q

What is an allele?

A

An allele is a variant form of a gene that can produce different characteristics in an organism.

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3
Q

What is the difference between dominant and recessive alleles?

A

Dominant alleles are expressed in the phenotype even when only one copy is present (heterozygous), while recessive alleles are only expressed when two copies are present (homozygous).

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4
Q

What is a homozygous genotype?

A

A homozygous genotype has two identical alleles for a particular gene, either both dominant or both recessive (e.g., AA or aa).

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5
Q

What is a heterozygous genotype?

A

A heterozygous genotype has two different alleles for a particular gene, one dominant and one recessive (e.g., Aa).

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6
Q

What is co-dominance?

A

Co-dominance occurs when both alleles contribute equally and visibly to the phenotype in a heterozygote (e.g., AB blood type).

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7
Q

What is incomplete dominance?

A

Incomplete dominance is when the phenotype of the heterozygote is intermediate between the two homozygotes (e.g., red and white flowers producing pink flowers).

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8
Q

What is a Punnett square used for?

A

A Punnett square is a diagram used to predict the genetic outcomes of a cross between two individuals, showing the possible genotypes of offspring.

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9
Q

What is the phenotypic ratio in a monohybrid cross for two heterozygous parents?

A

The phenotypic ratio in a monohybrid cross between two heterozygous parents is 3:1, with three individuals showing the dominant phenotype and one showing the recessive phenotype.

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10
Q

What is a dihybrid cross?

A

A dihybrid cross is the genetic cross between two organisms that examines the inheritance of two traits simultaneously.

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11
Q

What is the phenotypic ratio in a dihybrid cross for two heterozygous parents?

A

The phenotypic ratio in a dihybrid cross for two heterozygous parents is 9:3:3:1, with four possible phenotypes in the offspring.

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12
Q

What is the law of segregation?

A

The law of segregation states that during gamete formation, the two alleles for each gene separate, so that each gamete only carries one allele for each gene.

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13
Q

What is the law of independent assortment?

A

The law of independent assortment states that genes for different traits segregate independently of each other during gamete formation.

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14
Q

What is genetic linkage?

A

Genetic linkage occurs when two or more genes are located close to each other on the same chromosome and are inherited together more often than expected by chance.

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15
Q

What is a test cross?

A

A test cross is a genetic cross used to determine the genotype of an individual showing the dominant phenotype by crossing it with a homozygous recessive individual.

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16
Q

What is a carrier in terms of genetic inheritance?

A

A carrier is an individual who has one copy of a recessive allele for a genetic disorder but does not show the disorder because the other allele is dominant.

17
Q

What is the difference between autosomal and sex-linked inheritance?

A

Autosomal inheritance involves genes located on non-sex chromosomes, while sex-linked inheritance involves genes located on sex chromosomes (X or Y).

18
Q

What is the significance of X-linked inheritance?

A

X-linked inheritance refers to the inheritance of genes located on the X chromosome. Males are more likely to express X-linked recessive traits because they have only one X chromosome.

19
Q

What is an example of an X-linked genetic disorder?

A

An example of an X-linked genetic disorder is hemophilia, which affects blood clotting and is more common in males due to the single X chromosome.

20
Q

What is polygenic inheritance?

A

Polygenic inheritance involves the control of a characteristic by multiple genes, often resulting in continuous variation (e.g., height, skin color).

21
Q

What is epistasis?

A

Epistasis is when one gene affects the expression of another gene, typically through the interaction between different alleles or genes.

22
Q

What is a mutation?

A

A mutation is a change in the DNA sequence that can result in a new allele. Mutations can be beneficial, neutral, or harmful to an organism.