Title: AP Biology Exam Review Put Your Knowledge to the Test
1AP Biology Exam ReviewPut Your Knowledge to the
Test
Enter the Game
How to play
2How 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
3Genetics
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4Genetics Continued
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51. What are Mendels Laws?
A
Law of Segregation
B
Law of Independent assortment
C
Both Law of Segregation and Law of Independent
Assortment
6Nope! Try Again
BACK TO QUESTION
7Right!!!!!!!!
- Both the Law of Segregation and the Law of
Independent Assortment are included in Mendels
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
82. What is a Locus?
A
The copied strand of the chromosome.
B
Exact location on a chromosome where a gene is
located.
C
The offspring generation
9Wrong! Try Again
BACK TO QUESTION
10Right!!!!!!!!
- A locus is the exact location on a chromosome
where a gene is located
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113. What is progeny?
A
The offspring generation
B
The parent generation
C
A sex influenced trait
12SORRY, Try again!
BACK TO QUESTION
13RIGHT!
- Progeny is the offspring generation of a test
cross
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144. What is a homologous pair?
A
Every cell contains two copies of each chromosome
B
- The chromosome and its copy
C
The original pair of chromosomes
15Wrong Answer!
BACK TO QUESTION
16RIGHT
- In a homologous pair, every cell contains two
copies of each chromosome
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175. Define an x-inactivation
A
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.
18TRY AGAIN
BACK TO QUESTION
19CORRECT
- X-inactivation is when one of the x chromosomes
does not uncoil into chromatin and becomes a barr
body instead
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206. 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
21Sorry, try again
BACK TO QUESTION
22Yeah!!
- 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
237. In the genus Homo sapien, who is the
heterogametic sex?
A
Female
B
Either sex could be the heterogametic sex
C
Male
24WRONG!
BACK TO QUESTION
25RIGHT
- In the genus Homo sapien, the male is the
heterogametic sex
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268. In the genus Homo sapien, who is the
homogametic sex?
A
Female
B
Male
C
Either sex could be the homogametic sex
27NOPE, TRY AGAIN!
BACK TO QUESTION
28ALRIGHT!
- In the genus Homo sapien, the female is the
homogametic sex
BACK TO GENETICS PAGE
299. What is the genotype of the blood type A?
A
AA and AB
B
AB and AO
C
AA and AO
30Sorry, wrong answer
BACK TO QUESTION
31RIGHT!!
- The genotype of blood type A is AA or AO
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3210. What is the genotype of the blood type B?
A
BB and BO
B
BB and AB
C
AB and BO
33WRONG
BACK TO QUESTION
34YEP!
- The genotype for blood type B is BO or BB
BACK TO GENETICS PAGE
3511. What is the genotype of the blood type AB?
A
B
AB
C
AA and AB
36TRY AGAIN
BACK TO QUESTION
37RIGHT
- The genotype for blood type AB is AB
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3812. What is the genotype of the blood type O?
A
OO and BO
B
OO
C
AO and OO
39Try Again!
BACK TO QUESTION
40CORRECT!!!!
- The Genotype for blood type O is OO
BACK TO GENETICS PAGE
4113. What is pleiotrophy?
A
B
A single gene which has multiple effects
C
A recessive gene that shows in the phenotype
42Wrong, try again
BACK TO QUESTION
43RIGHT
- Pleiotrophy is a single gene which has multiple
effects - An example would be Siamese cats
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4414. 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
45Go Back and Try Again!
BACK TO QUESTION
46Youre Right!!!
- An epistasis is two recessive genes that cause
dominance not to show - An example would be snapdragons
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4715. What is polygenic inheritance?
A
A single gene which has multiple effects
B
- A gene which shows no characteristics
C
- A dominant trait that is not expressed
48Nope, try again
BACK TO QUESTION
49RIGHT!!!
- Polygenic Inheritance is a single gene which has
multiple effects - An example would be in skin color and height
BACK TO GENETICS PAGE
5016. An environmentally produced phenotype that
stimulates the effects of a particular gene is
called
A
Genetic Drift
B
Industrial Melanism
C
A Phenocopy
51SORRY, GO BACK !!!
BACK TO QUESTION
52Correct!!!!
- An environmentally produced phenotype that
stimulates the effects of a particular gene is
called a phenotype - Examples are tranquilizer
BACK TO GENETICS PAGE
5317. Which genetic defect is the inability to
break down phenylalanine?
A
Tay-Sachs Syndrome
B
C
Huntington Disease
54WRONG
BACK TO QUESTION
55RIGHT
- The genetic disease that effects the inability to
break down phenylalanine is phenylketonuria.
BACK TO GENETICS PAGE
5618. Which genetic defect is characterized by
lipids causing nervous system disorder?
A
Tay-Sachs Syndrome
B
Phenylketonuria
C
Huntington Disease
57Go Back and Try Again!
BACK TO QUESTION
58RIGHT
- Tay-Sachs syndrome is characterized by lipids
causing a nervous system disorder.
BACK TO GENETICS PAGE
5919. Which genetic disease starts at middle age
with mild mental illness?
A
Tay-Sachs Syndrome
B
Cystic Fibrosis
C
Huntington disease
60Nope, try again
BACK TO QUESTION
61RIGHT
- Huntington disease is a genetic disease which
starts at middle age with mild mental illness.
BACK TO GENETICS PAGE
6220. Which genetic defect has sickle shaped cells
and abnormal hemoglobin?
A
Down Syndrome
B
Cystic Fibrosis
C
Sickle cell anemia
63Sorry, wrong answer
BACK TO QUESTION
64Correct!!!!
- Sickle cell anemia is characterized by sickle
shaped cells and abnormal hemoglobin.
BACK TO GENETICS PAGE
6521. Which genetic disease causes problems with
blood clotting?
A
Sickle Cell Anemia
B
Hemophilia
C
Cystic Fibrosis
66NO WAY!!
BACK TO QUESTION
67RIGHT
- Hemophilia is a genetic disease which causes
problems with blood clotting.
BACK TO GENETICS PAGE
6822. What is the inability to distinguish red from
green?
A
Sickle Cell Anemia
B
Hemophilia
C
Red-green colorblindness
69SORRY, TRY AGAIN
BACK TO QUESTION
70CORRECT
- Red-green colorblindness is a genetic disorder
which is characterized by the inability to
distinguish red from green.
BACK TO GENETICS PAGE
7123. What genetic disease is known as trisomy21?
A
Downs Syndrome
B
Tay-Sachs Syndrome
C
Red-Green Colorblindness
72TRY AGAIN
BACK TO QUESTION
73GOOD JOB
- The genetic disease also know as trisomy 21 is
Downs Syndrome.
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7424. Which genetic disease causes the
deteriorating of muscles?
A
Cystic Fibrosis
B
Duchenes Muscular Dystrophy
C
Downs Syndrome
75NOPE
BACK TO QUESTION
76RIGHT!!!
- Duchenes Muscular Dystrophy is a genetic disease
which causes the deteriorating of muscles.
BACK TO GENETICS PAGE
7725. Which genetic disease is caused by an X, X,
and Y chromosome?
A
Klinefelton syndrome
B
Downs Syndrome
C
Criduchat
78WRONG ANSWER
BACK TO QUESTION
79CORRECT
- The genetic disease caused by an XXY chromosome
is Klinefelton syndrome
BACK TO GENETICS PAGE
8026. Which genetic disease is characterized by a
cat-like cry?
A
Criduchat
B
Downs Syndrome
C
Hemophilia
81TRY AGAIN
BACK TO QUESTION
82ALRIGHT!
- The genetic disease characterized by a cat-like
cry is Criduchat.
BACK TO GENETICS PAGE
8327. What is deletion?
A
Sections of the chromosome are inverted
B
Sections of the chromosome are duplicated
C
Sections of the chromosome are deleted
84Try again
BACK TO QUESTION
85RIGHT!!!!
- Deletion happens when sections of the chromosomes
are deleted.
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8628. What is inversion?
A
Sections of the chromosome are switched
B
Sections of the chromosome are duplicated
C
Sections of the chromosome are deleted
87Sorry, Wrong Answer
BACK TO QUESTION
88Yep!
- Inversion is when sections of the chromosome are
switched.
BACK TO GENETICS PAGE
8929. What is translocation?
A
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
90Try again
BACK TO QUESTION
91Good answer
- Translocation is when a section of one chromosome
switches with another chromosome.
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9230. What is duplication?
A
Sections of the chromosome are deleted
B
Sections of the chromosome are switched
C
Sections of a chromosome replicate more than once
93Wrong Answer
BACK TO QUESTION
94Alright!
- Duplication is when sections of a chromosome are
duplicated more than once.
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9531. What is nondisjunction?
A
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
96SORRY, TRY AGAIN
BACK TO QUESTION
97GOOD JOB
- Nondisjunction is when the homologous chromosomes
do not separate at interphase.
BACK TO GENETICS PAGE
9832. What is expressivity?
A
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
99Go back and try again
BACK TO QUESTION
100RIGHT!!!
- Expressivity is the degree to which a particular
gene is expressed. - An example would be sickle cells
BACK TO GENETICS PAGE
10133. What is polyploidy?
A
Chromosome 21 duplicates more than once
B
There are more than two complete sets of
chromosomes
C
The X chromosome is expressed twice along with a
Y chromosome
102NOPE, GO BACK
BACK TO QUESTION
103RIGHT!!!
- Polyploidy is when there are more than two
complete sets of chromosomes.
BACK TO GENETICS PAGE