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AP Biology Exam Review Put Your Knowledge to the Test
Enter the Game How to play
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How This Works Read the Question
Click on the button of the right answer If you are wrong you go back to the start, if you answer correctly, you move on. **Click on the buttons only, not the page*** Enter the Game
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Genetics 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24
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Genetics Continued 25 26 27 28 29 35 30 31 32 33 34
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A B C 1. What are Mendel’s Laws? Law of Segregation
Law of Independent assortment C Both Law of Segregation and Law of Independent Assortment
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Nope! Try Again BACK TO QUESTION
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Right!!!!!!!! Both the Law of Segregation and the Law of Independent Assortment are included in Mendel’s Law The Law of Segregation states that each allele segregates separately. One of each homologous chromosomes goes to each new cell. The Law of Independent Assortment states that in a dihybrid cross, each trait is independent of the other. BACK TO GENETICS PAGE
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A B C 2. What is a Locus? The copied strand of the chromosome.
Exact location on a chromosome where a gene is located. C The offspring generation
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Wrong! Try Again BACK TO QUESTION
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Right!!!!!!!! A locus is the exact location on a chromosome where a gene is located BACK TO GENETICS PAGE
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A B C 3. What is progeny? The offspring generation
The parent generation C A sex influenced trait
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SORRY, Try again! BACK TO QUESTION
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Progeny is the offspring generation of a test cross
RIGHT! Progeny is the offspring generation of a test cross BACK TO GENETICS PAGE
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4. What is a homologous pair?
Every cell contains two copies of each chromosome B The chromosome and its copy C The original pair of chromosomes
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Wrong Answer! BACK TO QUESTION
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***RIGHT*** In a homologous pair, every cell contains two copies of each chromosome BACK TO GENETICS PAGE
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5. Define an x-inactivation
A genetic defect on the x chromosome B The x chromosome replicates uncontrollable C One of the x chromosomes does not uncoil into chromatin, it becomes a barr body instead.
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TRY AGAIN BACK TO QUESTION
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CORRECT X-inactivation is when one of the x chromosomes does not uncoil into chromatin and becomes a barr body instead BACK TO GENETICS PAGE
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6. What is a test cross? A A cross between any two pair of alleles to find the progeny When you are trying to figure out what the make up of the allele is, A_ (either A or a), and you cross it with a pure recessive allele B C A test between progeny to find the parent generation
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Sorry, try again BACK TO QUESTION
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Yeah!! A test cross is when you are trying to figure out what the make up of the allele is, A_ (either A or a), and you cross it with a pure recessive allele BACK TO GENETICS PAGE
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7. In the genus Homo sapien, who is the heterogametic sex?
Female B Either sex could be the heterogametic sex C Male
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WRONG! BACK TO QUESTION
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~RIGHT~ In the genus Homo sapien, the male is the heterogametic sex
BACK TO GENETICS PAGE
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8. In the genus Homo sapien, who is the homogametic sex?
Female B Male C Either sex could be the homogametic sex
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NOPE, TRY AGAIN! BACK TO QUESTION
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ALRIGHT! In the genus Homo sapien, the female is the homogametic sex
BACK TO GENETICS PAGE
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9. What is the genotype of the blood type A?
AA and AB B AB and AO C AA and AO
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Sorry, wrong answer BACK TO QUESTION
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RIGHT!! The genotype of blood type A is AA or AO BACK TO GENETICS PAGE
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10. What is the genotype of the blood type B?
BB and BO B BB and AB C AB and BO
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WRONG BACK TO QUESTION
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YEP! The genotype for blood type B is BO or BB BACK TO GENETICS PAGE
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11. What is the genotype of the blood type AB?
AB and AO B AB C AA and AB
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~TRY AGAIN~ BACK TO QUESTION
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***RIGHT*** The genotype for blood type AB is AB BACK TO GENETICS PAGE
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12. What is the genotype of the blood type O?
OO and BO B OO C AO and OO
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Try Again! BACK TO QUESTION
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CORRECT!!!! The Genotype for blood type O is OO BACK TO GENETICS PAGE
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A B C 13. What is pleiotrophy? An inactive gene
A single gene which has multiple effects C A recessive gene that shows in the phenotype
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Wrong, try again BACK TO QUESTION
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RIGHT Pleiotrophy is a single gene which has multiple effects
An example would be Siamese cats BACK TO GENETICS PAGE
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14. What is epistasis? A A gene that expressed in the genotype but not shown in the phenotype B A gene which effects multiple characteristics C Two recessive genes which cause dominance not to show
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Go Back and Try Again! BACK TO QUESTION
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You’re Right!!! An epistasis is two recessive genes that cause dominance not to show An example would be snapdragons BACK TO GENETICS PAGE
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15. What is polygenic inheritance?
A single gene which has multiple effects B A gene which shows no characteristics C A dominant trait that is not expressed
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Nope, try again BACK TO QUESTION
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RIGHT!!! Polygenic Inheritance is a single gene which has multiple effects An example would be in skin color and height BACK TO GENETICS PAGE
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16. An environmentally produced phenotype that stimulates the effects of a particular gene is called: A Genetic Drift B Industrial Melanism C A Phenocopy
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SORRY, GO BACK !!! BACK TO QUESTION
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Correct!!!! An environmentally produced phenotype that stimulates the effects of a particular gene is called a phenotype Examples are tranquilizer BACK TO GENETICS PAGE
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17. Which genetic defect is the inability to break down phenylalanine?
Tay-Sach’s Syndrome B Phenylketonuria C Huntington Disease
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WRONG BACK TO QUESTION
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RIGHT The genetic disease that effects the inability to break down phenylalanine is phenylketonuria. BACK TO GENETICS PAGE
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18. Which genetic defect is characterized by lipids causing nervous system disorder?
Tay-Sachs Syndrome B Phenylketonuria C Huntington Disease
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Go Back and Try Again! BACK TO QUESTION
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***RIGHT*** Tay-Sachs syndrome is characterized by lipids causing a nervous system disorder. BACK TO GENETICS PAGE
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19. Which genetic disease starts at middle age with mild mental illness?
Tay-Sach’s Syndrome B Cystic Fibrosis C Huntington disease
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Nope, try again BACK TO QUESTION
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~RIGHT~ Huntington disease is a genetic disease which starts at middle age with mild mental illness. BACK TO GENETICS PAGE
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20. Which genetic defect has sickle shaped cells and abnormal hemoglobin?
Down Syndrome B Cystic Fibrosis C Sickle cell anemia
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Sorry, wrong answer BACK TO QUESTION
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Correct!!!! Sickle cell anemia is characterized by sickle shaped cells and abnormal hemoglobin. BACK TO GENETICS PAGE
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21. Which genetic disease causes problems with blood clotting?
Sickle Cell Anemia B Hemophilia C Cystic Fibrosis
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NO WAY!! BACK TO QUESTION
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RIGHT Hemophilia is a genetic disease which causes problems with blood clotting. BACK TO GENETICS PAGE
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22. What is the inability to distinguish red from green?
Sickle Cell Anemia B Hemophilia C Red-green colorblindness
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SORRY, TRY AGAIN BACK TO QUESTION
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CORRECT Red-green colorblindness is a genetic disorder which is characterized by the inability to distinguish red from green. BACK TO GENETICS PAGE
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23. What genetic disease is known as trisomy21?
Down’s Syndrome B Tay-Sach’s Syndrome C Red-Green Colorblindness
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**TRY AGAIN** BACK TO QUESTION
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GOOD JOB The genetic disease also know as trisomy 21 is Down’s Syndrome. BACK TO GENETICS PAGE
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24. Which genetic disease causes the deteriorating of muscles?
Cystic Fibrosis B Duchene’s Muscular Dystrophy C Down’s Syndrome
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NOPE BACK TO QUESTION
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RIGHT!!! Duchene’s Muscular Dystrophy is a genetic disease which causes the deteriorating of muscles. BACK TO GENETICS PAGE
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25. Which genetic disease is caused by an X, X, and Y chromosome?
Klinefelton syndrome B Down’s Syndrome C Criduchat
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WRONG ANSWER BACK TO QUESTION
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CORRECT The genetic disease caused by an XXY chromosome is Klinefelton syndrome BACK TO GENETICS PAGE
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26. Which genetic disease is characterized by a cat-like cry?
Criduchat B Down’s Syndrome C Hemophilia
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**TRY AGAIN** BACK TO QUESTION
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ALRIGHT! The genetic disease characterized by a cat-like cry is Criduchat. BACK TO GENETICS PAGE
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A B C 27. What is deletion? Sections of the chromosome are inverted
Sections of the chromosome are duplicated C Sections of the chromosome are deleted
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Try again BACK TO QUESTION
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RIGHT!!!! Deletion happens when sections of the chromosomes are deleted. BACK TO GENETICS PAGE
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A B C 28. What is inversion? Sections of the chromosome are switched
Sections of the chromosome are duplicated C Sections of the chromosome are deleted
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Sorry, Wrong Answer BACK TO QUESTION
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Yep! Inversion is when sections of the chromosome are switched.
BACK TO GENETICS PAGE
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A B C 29. What is translocation?
A section of one chromosome switches with a section of another chromosome B Sections of the chromosome are switched C A section of the chromosome is deleted
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Try again BACK TO QUESTION
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Good answer Translocation is when a section of one chromosome switches with another chromosome. BACK TO GENETICS PAGE
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A B C 30. What is duplication? Sections of the chromosome are deleted
Sections of the chromosome are switched C Sections of a chromosome replicate more than once
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Wrong Answer BACK TO QUESTION
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Alright! Duplication is when sections of a chromosome are duplicated more than once. BACK TO GENETICS PAGE
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31. What is nondisjunction?
There is a duplication of the chromosome B The homologous chromosomes do not separate at interphase C One X chromosome is duplicated in chromosome 23
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SORRY, TRY AGAIN BACK TO QUESTION
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GOOD JOB Nondisjunction is when the homologous chromosomes do not separate at interphase. BACK TO GENETICS PAGE
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A B C 32. What is expressivity?
The degree to which a particular gene is expressed B There is a duplication of chromosome 21 C Recessive genes are expressed instead of dominant genes
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Go back and try again BACK TO QUESTION
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RIGHT!!! Expressivity is the degree to which a particular gene is expressed. An example would be sickle cells BACK TO GENETICS PAGE
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A B C 33. What is polyploidy? Chromosome 21 duplicates more than once
There are more than two complete sets of chromosomes C The X chromosome is expressed twice along with a Y chromosome
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NOPE, GO BACK BACK TO QUESTION
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RIGHT!!! Polyploidy is when there are more than two complete sets of chromosomes. BACK TO GENETICS PAGE
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