In the family's pedigree shown below, a horizontal pink bar indicates that an individual is affected with hypercholesterolemia (high blood cholesterol levels). A vertical blue bar indicates that an individual is affected with Hunter's syndrome (a lysosomal storage disease). Individuals I-1 and I-2 have no family history of Hunter's syndrome, but individuals I-3 and I-4 do.
What is the mode of inheritance for Hunter's syndrome? For hypercholesterolemia?
a. Autosomal dominant
b. Autosomal recessive
c. X-linked dominant
d. X-linked recessive
e.More than one of the above are possible
Homework Answers
The mode of inheritance for Hunter's syndrome is X linked recessive disease. The women carry the defective X chromosome which can cause the disease and they can pass it on to the next generation
Hypercholesterolemia is autosomal dominat condition. The parent who carries the altered genes has 50% chance to pass it on to the child or next generation.
Add Answer to:
In the family's pedigree shown below, a horizontal pink bar
indicates that an individual is affected...
What is the mode of inheritance for hypercholesterolemia? a. Autosomal dominant b. Autosomal recessive c. X-linked...
What is the mode of inheritance for hypercholesterolemia?
a.
Autosomal dominant
b.
Autosomal recessive
c.
X-linked dominant
d.
X-linked recessive
e.
More than one of the above are possible
----------------------------------------------------------------
What is the mode of inheritance for Hunter's syndrome?
a.
Autosomal dominant
b.
Autosomal recessive
c.
X-linked dominant
d.
X-linked recessive
e.
More than one of the above are possible.
------------------------------------------------------------
What is the genotype for individual II-3 at the
hypercholesterolemia locus (dominant allele is denoted by H,
recessive allele...
Part B Determining genotypes in pedigrees of X-linked conditions The pedigree from Part A is shown...
Part B Determining genotypes in pedigrees of X-linked
conditions
The pedigree from Part A is shown below. Fill in the most likely
genotypes of the indicated individuals in the pedigree. Note that a
dominant allele followed by an underscore (_) indicates that either
the dominant or the recessive allele may be present at the second
position. Drag one pink label (for condition A, autosomal
recessive) to each pink target. Drag one blue label (for condition
B, X-linked recessive) to each...
Question 3 The following human pedigree shows a family affected by a specific disease. Assume that...
Question 3 The following human pedigree shows a family affected by a specific disease. Assume that the individuals marked with an asterisk () do not carry any allele associated with the affected phenotype and that no other mutation spontaneously occurs. Also assume complete penetrance a) State the most likely mode of inheritance for this disease. Choose from: autosomal dominant, autosomal recessive, X-linked dominant, X-linked recessive b) Write all possible genotypes of the following individuals in the pedigree. Use the uppercase...
A B C D 1. Consider the pedigree below where affected individuals are in dark blue...
A B C D 1. Consider the pedigree below where affected individuals are in dark blue and carriers are in lightblue._-ig.^ 3 4 5 A. (1 pts) Select the mode of inheritance shown in this pedigree and explain your reasoning: Autosomal dominant Autosomal recessive X-linked Y-linked B. (1 pts) Predict whether each of the great-grandparents (labeled A-D) are affected, carriers, or unaffected noncarriers and explain your reasoning 2. In Jabberwocks, flame eyes (F) are dominant to blue eyes ( and...
this is all that im given Question 3: (4 points) Consider the following pedigree: O O...
this is all that im given
Question 3: (4 points) Consider the following pedigree: O O 1 2 3 4 5 Characterize each of the following modes of inheritance as: Impossible, Possible, or Most likely. Justify your answers. a. Autosomal dominant b. Autosomal recessive X-linked dominant d. X-linked recessive e. Y-linked f. Going with the most likely mode of inheritance .... Assume individual V-1 marries a phenotypically normal male. What is the likelihood that their first child is affected with...
For each pedigree below determine the most likely mode of inheritance and label each individual with...
For each pedigree below determine the most likely mode of
inheritance and label each individual with a genotype. If you know
they have a dominant phenotype, but don’t know the genotype, then
label them with both possibilities. Please use the alleles A and a
for autosomal modes of inheritance and XA, Xa and Ya for any types
of sex-linkage (note: an “a” is only on the Y if the trait is
Y-linked). Modes of inheritance are autosomal dominant, autosomal
recessive,...
please help me!!! best will be rated 1. (20 points) a. The short pedigree below shows...
please help me!!! best will be rated
1. (20 points) a. The short pedigree below shows affected individuals in this family in red. Which modes of inheritance (X-linked recessive, X-linked dominant, Y-linked, autosomal recessive, autosomal dominant) can be ruled out, and which mode is most likely? b. (10 points) What is the likelihood that child A will be affected? Child B? O ■ ● Co
In the pedigree below, what is the most likely mode of inheritance for this condition?: X-linked...
In the pedigree below, what is the most likely mode of inheritance for this condition?: X-linked recessive, autosomal dominant, or autosomal recessive? Affected individuals are shown as black symbols. Based on your prediction, give the genotypes of the following individuals: I-1, I-2, II-1, II-3, II-4, III-1, III-2, III-4, IV-2, and IV-3. If you choose autosomal, use A or a; if you choose X-linked, use X^A, X^a, or Y List the proposed genotypes of the designated individuals along the side:
The conclusions about inheritance (above) can be used to help analyze pedigrees. For each pedigree below,...
The conclusions about inheritance (above) can be used to help analyze pedigrees. For each pedigree below, tell if the trait can be autosomal dominant, autosomal recessive, and X-linked recessive. If the pedigree cannot fit a mode of inheritance, tell why. Record your answers in the table on the next page. Pedigree A 2 3 o.a. 9 10 12 (13 14 ad ada 15 16 Xx 20 aa ia ha Pedigree B 910 11 12 14 a ta da Enter either...
For each pedigree below determine the most likely mode of inheritance and label each individual with...
For each pedigree below determine the most likely mode of
inheritance and label each individual with a genotype. If you know
they have a dominant phenotype, but don’t know the genotype, then
label them with both possibilities. Please use the alleles A and a.
Modes of inheritance for these pedigrees are autosomal dominant or
autosomal recessive. For each pedigree determine if the alternative
mode (not the one you chose) is also possible.
to100 0 KEY Affected Male Affected Female Unaffected...
What is the mode of inheritance for hypercholesterolemia?
a.
Autosomal dominant
b.
Autosomal recessive
c.
X-linked dominant
d.
X-linked recessive
e.
More than one of the above are possible
----------------------------------------------------------------
What is the mode of inheritance for Hunter's syndrome?
a.
Autosomal dominant
b.
Autosomal recessive
c.
X-linked dominant
d.
X-linked recessive
e.
More than one of the above are possible.
------------------------------------------------------------
What is the genotype for individual II-3 at the
hypercholesterolemia locus (dominant allele is denoted by H,
recessive allele...
Part B Determining genotypes in pedigrees of X-linked
conditions
The pedigree from Part A is shown below. Fill in the most likely
genotypes of the indicated individuals in the pedigree. Note that a
dominant allele followed by an underscore (_) indicates that either
the dominant or the recessive allele may be present at the second
position. Drag one pink label (for condition A, autosomal
recessive) to each pink target. Drag one blue label (for condition
B, X-linked recessive) to each...
Question 3 The following human pedigree shows a family affected by a specific disease. Assume that the individuals marked with an asterisk () do not carry any allele associated with the affected phenotype and that no other mutation spontaneously occurs. Also assume complete penetrance a) State the most likely mode of inheritance for this disease. Choose from: autosomal dominant, autosomal recessive, X-linked dominant, X-linked recessive b) Write all possible genotypes of the following individuals in the pedigree. Use the uppercase...
A B C D 1. Consider the pedigree below where affected individuals are in dark blue and carriers are in lightblue._-ig.^ 3 4 5 A. (1 pts) Select the mode of inheritance shown in this pedigree and explain your reasoning: Autosomal dominant Autosomal recessive X-linked Y-linked B. (1 pts) Predict whether each of the great-grandparents (labeled A-D) are affected, carriers, or unaffected noncarriers and explain your reasoning 2. In Jabberwocks, flame eyes (F) are dominant to blue eyes ( and...
this is all that im given
Question 3: (4 points) Consider the following pedigree: O O 1 2 3 4 5 Characterize each of the following modes of inheritance as: Impossible, Possible, or Most likely. Justify your answers. a. Autosomal dominant b. Autosomal recessive X-linked dominant d. X-linked recessive e. Y-linked f. Going with the most likely mode of inheritance .... Assume individual V-1 marries a phenotypically normal male. What is the likelihood that their first child is affected with...
For each pedigree below determine the most likely mode of
inheritance and label each individual with a genotype. If you know
they have a dominant phenotype, but don’t know the genotype, then
label them with both possibilities. Please use the alleles A and a
for autosomal modes of inheritance and XA, Xa and Ya for any types
of sex-linkage (note: an “a” is only on the Y if the trait is
Y-linked). Modes of inheritance are autosomal dominant, autosomal
recessive,...
please help me!!! best will be rated
1. (20 points) a. The short pedigree below shows affected individuals in this family in red. Which modes of inheritance (X-linked recessive, X-linked dominant, Y-linked, autosomal recessive, autosomal dominant) can be ruled out, and which mode is most likely? b. (10 points) What is the likelihood that child A will be affected? Child B? O ■ ● Co
In the pedigree below, what is the most likely mode of inheritance for this condition?: X-linked recessive, autosomal dominant, or autosomal recessive? Affected individuals are shown as black symbols. Based on your prediction, give the genotypes of the following individuals: I-1, I-2, II-1, II-3, II-4, III-1, III-2, III-4, IV-2, and IV-3. If you choose autosomal, use A or a; if you choose X-linked, use X^A, X^a, or Y List the proposed genotypes of the designated individuals along the side:
The conclusions about inheritance (above) can be used to help analyze pedigrees. For each pedigree below, tell if the trait can be autosomal dominant, autosomal recessive, and X-linked recessive. If the pedigree cannot fit a mode of inheritance, tell why. Record your answers in the table on the next page. Pedigree A 2 3 o.a. 9 10 12 (13 14 ad ada 15 16 Xx 20 aa ia ha Pedigree B 910 11 12 14 a ta da Enter either...
For each pedigree below determine the most likely mode of
inheritance and label each individual with a genotype. If you know
they have a dominant phenotype, but don’t know the genotype, then
label them with both possibilities. Please use the alleles A and a.
Modes of inheritance for these pedigrees are autosomal dominant or
autosomal recessive. For each pedigree determine if the alternative
mode (not the one you chose) is also possible.
to100 0 KEY Affected Male Affected Female Unaffected...
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