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Unit 4: Inheritance and Variation Test

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Last updated 2 months ago
39 questions
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Question 1
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Question 2
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Read the scenario and use the information to help you answer the questions.
Disease Possibilities
A man and woman have decided to have children but are worried about possible genetic diseases. The couple visits a geneticist to determine what the possible risks are for their future children. The couple learns that they are both carriers (heterozygous) for Sickle Cell Disease. Each of them has one recessive allele. In order to have Sickle Cell Disease, you have to have two recessive alleles. The following year, the parents are blessed with a bouncing baby boy!
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Question 29
29.

Fill in the missing information for the Punnett square below

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Question 31
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Question 33
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How many males are there?

Question 34
34.

How many males have hemophilia?

Question 35
35.

How many children did the couple in generation 3 (III) have?

Question 36
36.

This pedigree tracks hemophelia in a family. How many of II-2's grandsons have hemophelia?

Question 37
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Question 38
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Question 39
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Compared with normal hemoglobin, the hemoglobin of a person with sickle cell disease
has no mutation in the gene for hemoglobin
transports oxygen more efficiently
has a mutation in the gene for hemoglobin
is broken down quickly
The following cross shows two people who are carriers for sickle cell anemia. In this cross, R is the allele for a normal red blood cell, while r is the allele for a sickle, mutated blood cell.
​​What is the chance that an offspring from this cross will be fully affected with sickle cell anemia?
Their offspring has a 25% chance of being fully affected with sickle cell anemia.
Their offspring has a 75% chance of being fully affected with sickle cell anemia.
Their offspring has a 50% chance of being fully affected with sickle cell anemia.
Their offspring has a 100% chance of being fully affected with sickle cell anemia.
Which of the following is the correct genotype of the parents?
aA
AA
aa
Aa
What is the probability (percent chance) that the child will have the same genotype as the parents?
25%
100%
50%
75%
What is the probability (percent chance) that the child will have Sickle Cell Disease?
25%
100%
50%
75%
The baby boy goes through his newborn tests and the doctors discover that the boy does have Sickle Cell Disease. What is the child's genotype?
Aa
aA
AA
aa
At the end of Meiosis, how many gametes are produced?
6
3
4
1
How many chromosomes does a diploid human cell have?
46
43
19
23
Which three of the following may lead to genetic variations?
the need to have a trait
independent assortment/random alignment
crossing over
mutations
The gametes produced at the end of Meiosis are different in chromosome number than other cells in that they have fewer chromosomes. After going through the process of Meiosis, gametes are referred to as
diploid
haploid
triploid
Based on the pedigree shown below, how is it possible for the daughter to have a curved thumb while the rest of the family has straight thumbs? Straight thumbs are dominant, curved thumbs are recessive.
The father must be homozygous and the mother must be heterozygous.
Both parents must be heterozygous.
The mother must be homozygous and the father must be heterozygous.
Both parents must be homozygous.
The allele for the presence of a white forelock is dominant in Figure 14–1. What is the probability of the couple labeled 2 of having a child with the trait?
25%
100%
75%
50%
Carefully review the entire image above before answering the question.

Epigenetics has the ability to change phenotypes. Epigenetics is not considered a mutation because
it does not change the DNA sequence
it changes the phenotype
it changes where genes are located on the chromosome
Mendel's law of segregation occurs during which phase of meiosis?
Prophase I
Cytokenesis
Anaphase I
Metaphase II
What is the role of meiosis in sexual reproduction?
Cuts the chromosome number in half
Forms genetically identical daughter cells
Increases the chromosome number
Forms somatic cells with identical genetic material
Gametes are produced by the process of
mitosis
replication
crossing over
meiosis
Gametes have
two sets of chromosomes
twice the number of chromosomes found in body cells
homologous chromosomes
one copy of each chromosome
What is shown in the image below?
anaphase I of meiosis
crossing over
replication
independent assortment
If a eukaryotic cell has 20 chromosomes and it undergoes meiosis, how many cells will result, and how many chromosomes will they contain?
2 cells, each with 10 chromosomes
2 cells, each with 20 chromosomes
4 cells, each with 20 chromosomes
4 cells, each with 10 chromosomes
Match the number of each phase in the diagram to the phase of meiosis that is shown.
Prophase I
Anaphase II
Metaphase I
Metaphase II
Telophase/cytokinesis II
Anaphase I
Interphase
Prophase II
What is the process in which DNA makes a copy of itself?
Translation
Mutation
Transcription
DNA replication
What is the function of DNA polymerase during replication?
Builds new DNA strand
Repairs DNA damage
Unzips DNA
Carries genetic code
Why is DNA replication considered semi-conservative?
Results in DNA mutations
Produces entirely new DNA
Each new DNA molecule has one half of the original strand
Occurs only in prokaryotes
True or false: ALL mutations effect the resulting protein
True
False
Which of the following explains why mutations may have no affect on a protein?
There is redundancy in the genetic code, several different codon's can equal the same amino acid
There are at least 3 copies of every gene, so if one is mutated, the other's are used instead
The RNA that is made can be destroyed and a new copy made.
Which of the following mutations is most likely going to have large affects on any proteins made from the gene(s) involved?
Frameshift mutations
Base pair substitution within a single gene
Insertion or deletion within a single gene
silent mutations
In humans the ability to taste Phenylthiocarbamide (PTC) is dominant. “Tasters” (TT) or (Tt) taste an extremely bitter taste from PTC, while “non-tasters” (tt) do not taste anything.

What are the genotypes of Mr. and Mrs. Jones if they can taste PTC but have a child who is a non-taster?
TT
tt
There is not enough information to determine this
Tt
In pigs, having erect ears that stick up (E) is dominant to having droopy ears (e).


If a pig has droopy ears what must its genotype be?
Ee
can't be determined
EE
ee
What is the expected genotype ratio of a monohybrid cross (Tt x Tt)?
2 TT : 2 tt
4 TT : 0 Tt : 0 tt
1 TT : 1 Tt : 1 tt
1 TT : 2 Tt : 1 tt
What are the possible genotypes of offspring from a cross between two heterozygous parents?
AA:aa
Aa:aa
Aa:AA
AA:Aa:aa
In horses, having black hair is dominant (B) to having chesnut colored hair (b).



If a homozygous dominant horse is crossed with a chesnut colored horse, then what are the chances they will have a foal (a baby horse) with chesnut colored hair?
0%
25%
50%
75%
100%
The pedigree below tracks the appearance of a recessive trait:
Match each individual on the left with the correct genotype on the right.
Brother 1
Sister
Brother 2
Mom
Dad
Definitely homozygous dominant
Definitely heterozygous
Definitely homozygous recessive
Could be homozygous dominant or heterozygous
How does the end result of mitosis compare to meiosis? Select ALL that apply.
Meiosis produces cells that are genetically different
Mitosis produces cells that are genetically exact copies
Mitosis produces cells that are genetically different
Meiosis produces cells that are genetically exact copies
Compare the mutated DNA sequence to the original. Identify the mutation as either an insertion, deletion, or substitution, and whether it is a frameshift, missense, nonsense, or silent mutation.

Original DNA Sequence: T A C A C C T T G G C G A C G A C T

Mutated DNA Sequence: T A C A T C T T G G C G A C G A C T
substitution
insertion
deletion