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- 1. Multiple Choice
A change in a gene, group of genes or chromosome that results in a change in the proteins
Replication
Mutations
Translation
Transcription
- 2. Multiple Choice
Mutations that effect gametes and that will be passed on
to the next generation
Genetic change
Protein synthesis
Apoptosis
Cell membrane
- 3. Multiple Choice
A permanent change in the DNA sequence
which can affect a single gene or group of genes
Homeostasis
Somatic Cell
Chromosomal Mutation
Gene Mutation
- 4. Multiple Choice
One nucleotide base is changed so only one amino acid
is affected
Substitution Mutation
Point Mutation
Translocation
Inverse Mutation
- 5. Multiple Choice
A point mutation where one nucleotide base replaces an original nucleotide base
Inversion Mutation
Chromosomal Mutation
Translocation
Substitution Mutation
- 6. Multiple Choice
A substitution mutation that has no effect
on amino acids sequence
Insertion Mutation
Translocation
Silent Mutation
Deletion Mutation
- 7. Multiple Choice
A mutation that results in an amino acid change
Translocation
Homeostasis
Silent Mutation
Expressed Mutation
- 8. Multiple Choice
A nucleotide base is inserted or deleted shifting the entire DNA sequence. Entire protein will be changed.
Substitution Mutation
Silent Mutation
Frameshift Mutation
Translocation
- 9. Multiple Choice
A frameshift mutation where a nucleotide base
is removed from the DNA sequence.
Deletion Mutation
Substitution Mutation
Translocation
Silent Mutation
- 10. Multiple Choice
A frameshift mutation where a nucleotide base is added
to the DNA sequence
Insertion Mutation
Deletion Mutation
Substitution Mutation
Chromosomal Mutation
- 11. Multiple Choice
Mutations that involve parts of or all of
a chromosome
Replication
Deletion Mutation
Chromosomal Mutation
Transcription
- 12. Multiple Choice
Part of a chromosome
is deleted
Deletion Mutation-Gene
Translocation
Deletion Mutation -Chromosomal
Crossing Over
- 13. Multiple Choice
Part of a chromosome is repeated
Gene Mutation
Point Mutation
Deletion Mutation
Duplication Mutation
- 14. Multiple Choice
Part of a chromosome is reversed.
Inversion Mutation
Deletion Mutation
Translocation
Point Mutation
- 15. Multiple Choice
Part of one chromosome is transported and attached
to a non-homologous chromosome
Inversion Mutation
Translocation Mutation
Duplication Mutation
Point Mutation
- 16. Multiple Choice
Failure of homologous chromosomes
to separate during meiosis.
Results in gametes with either one extra or one missing chromosome.
Translocation
Nondisjunction
Replication
Transcription
- 17. Multiple Choice
Condition caused by nondisjunction at pair 21 during meiosis.
Individuals have an extra chromosome
at pair 21, or a total of 47 chromosomes.
Also called Trisomy 21.
Cystic Fibrosis
Translocation
Hemophilia
Down Syndrome
- 18. Multiple Choice
A point mutation where DNA adenine (A)
is replaced by thymine (T) resulting in a single amino acid change during translation(affects blood cell
shape and function)
Encephelitis
Hemophilia
Sickle Cell Anemia
Influenza
- 19. Multiple Choice
Analyzes the inheritability of Sickle Cell Anemia,
a recessive trait that must be passed on
from both parents.
Nondisjunction Punnett Square
Hemophilia Punnett Sqaure
Cyctic Fibrosis Punnett Square
Sickle Cell Anemia Punnett Square
- Answer choicesTagsAnswer choicesTags