Name ______Date ______Hour ______
Genetics Test Study Guide
Define the following vocabulary words:
- Punnett Square (p. 182) –
- Heredity (p. 173) -
- Gregor Mendel (p. 173) –
- Alleles (p. 178) –
- Dominant (p. 177) –
- Recessive (p. 177)–
- Genotype (p. 180) –
- Phenotype (p. 180) –
- Heterozygous (p. 181) –
- Incomplete Dominance (p. 184)–
- Codominance (p. 184)–
- Sex-Linked Traits (p. 237)–
- Polygenic Traits (p. 242) –
- Can a mother and father with brown eyes have a child with blue eyes? Create a Punnett Square as proof that this is possible and explain your answer.
- Explain the difference between homozygous dominant, homozygous recessive and heterozygous. Give an example of each. (p. 181)
- Explain the difference between chromosome and gene mutations. Give an example of each. (p. 239-240)
- In humans, having freckles (F) is dominant over not having freckles (f). Cross a girl and boy who are both heterozygous for freckles. List the genotype and phenotype percentages.
- From the cross in #17, what is the probability their children would have freckles? Would NOT have freckles?
- Cross a homozygous recessive individual with a heterozygous individual using the letter B. List the genotype percentages from the cross.
- Tallness (T) is dominant over shortness (t) in pea plants. How would you write the genotype of a plant that is heterozygous for tallness?
- In rabbits, black fur (B) is dominant over brown fur (b). Cross a homozygous dominant rabbit with a homozygous recessive rabbit. List the genotype and phenotype percentages.
- What fur color would a homozygous dominant rabbit have?
- What fur color would a homozygous recessive rabbit have?
- If the trait for coat color in cows is codominant, what color would offspring cows be if their parents are a red cow and a white cow?
- What kind of traits determine skin color? (p. 242 near the bottom)
- A mother is heterozygous for blood type A and the father is heterozygous for blood type B. What is the probability that their child will be blood type O? Show the cross.
- The genes for hemophilia are located on the X chromosome. It is a recessive disorder in which the blood does not clot. The mother is a carrier for hemophilia and the father is normal for blood clotting. What is the probability that a son will have hemophilia?
- Within the skin cells of a child, a mutation occurs that causes skin cancer. Who will this mutation affect?
- What is nondisjunction? How can it cause Down syndrome? Explain.
- If a red flower and white flower are crossed to make pink flowers, what is this an example of?
- Using the letter B, write the genotype for a heterozygous organism.