A man with a specific unusual genetic trait (leading to
heterozygosity) is
house with an unaffected and non-carrying woman, and they have four
children. The pedigrees of
this family is shown in graphs a-e. For each inheritance mode
indicate
how many children of each sex will express the trait (color those
affected in each tree
genealogical according to the type of inheritance).
a) Autosomal recessive trait:
b) Autosomal dominant trait:
c) X-linked recessive trait:
d) X-linked dominant trait:
e) Trait linked to Y:

Answer a) The man is heterozygous for this unusual genetic trait hence it can not be an autosomal recessive trait, as autosomal recessive trait can be expressed only in homozygous condition.
Answer b) If the trait is autosomal dominant then there are chances that 50% of the children will be affected out of 4
If the genotype of the man is considered as “Aa”(A is disorder causing allele)
And genotype of the woman is “aa”
Then the outcome of mating will be
|
gamates |
A |
a |
|
a |
Aa affected |
aa Not affected |
|
a |
Aa affected |
aa Not affected |
The chances of a male or a female being affected are 50%
Answer c) If the trait is X-linked recessive
then let the genotype of man be XaY (Xa is disorder causing allele)
And the genotype of woman be XX
Then the outcome of mating will be
|
gamates |
Xa |
Y |
|
X |
XXa Not affected(carrier) |
XY Not affected |
|
X |
XXa Not affected(carrier) |
XY Not affected |
In this case the females will be carriers(as the disorder is recessive) and the males will not be affected as the disorder is X linked and males get only Y chromosome from the father.
Answer d) If the trait is X-linked dominant
then let the genotype of man be XAY(XAis disorder causing allele)
And the genotype of woman be XX
Then the outcome of mating will be
|
gamates |
XA |
Y |
|
X |
XXA affected |
XY Not affected |
|
X |
XXA affected |
XY Not affected |
In this case all the females will be affected(as the trait is dominant) and the males will be not affected as the disorder is X linked and males get only Y chromosome from the father.
Answer e) If the trait is Y linked
Then then let the genotype of man be XYA(YA is disorder causing allele)
And the genotype of woman be XX
|
gamates |
X |
YA |
|
X |
XX Not affected |
X YA affected |
|
X |
XX Not affected |
X YA affected |
In this case all the females will not be affected and all the males will be affected as the disorder is Y linked and males get only Y chromosome from the father.
Note in answer a the condition is not possible as the recessive character is not expressed in the heterozygous condition, if the father would have been homozygous for the trait and the trait was recessive then none of the children would have been affected.
A man with a specific unusual genetic trait (leading to heterozygosity) is house with an unaffected...
모모모 < 모 2 1 | 미모 모 오 or lo III = - - genetic disorder is segregating. 3. Each of the pedigrees shown represents a human family within which a genetic disorder is se Assume the two traits are extremely rare in the population and completely penetrant. Part 1. For the first pedigree. lisorder: autosomal recessive, autosomal a. Determine the most probable inheritance pattern of the disorder: autosomal recessive dominant, X-linked recessive or X-linked dominant. b. Indicate the...
In general, the following characteristics suggest (but do not prove) specific inheritance patterns: Autosomal recessive inheritance: -affected individuals can be born to unaffected parents -if both parents are affected, all children are affected -observable effect of relatedness (consanguinity) -horizontal" inheritance: trait appears at once among several members of one generation (siblings) *** Autosomal dominant inheritance each affected individual has an affected parent -when one parent is affected, transmission to the offspring (on average) *** -two unaffected parents do not transmit...
Look carefully at the pedigrees below and:
1) indicate whether the transmission appears autosomal or
sex-linked
2) indicate whether the transmission appears dominant or
recessive
3) provide at least two characteristics for each that support
your conclusion.
In general, the following characteristics suggest (but do not prove) specific inheritance patterns: Autosomal recessive inheritance: -affected individuals can be born to unaffected parents -if both parents are affected, all children are affected -observable effect of relatedness (consanguinity) -horizontal" inheritance: trait appears at...
NAME: 6. Red-green color deficiency is an X-linked recessive trait. A woman with normal color vision has a father who is color-deficient. The woman has a child with a man with normal color vision. Which phenotype is NOT expected as a possibility for that child? a) a color-deficient male b) a color deficient female c) a male with normal color vision d) a female with normal color vision 7. Which of the individuals in the human pedigree shown below allow...
<Mendellen Genetics Problem 3.22 99 of 103 > Review Submit Drow all possible conclusions concerning the mode of inheritance of the trait expressed in each of the folowing limhed pedigrees. Each case is based on a different trait) Part D O o Select the two correct statements. - the trail is sex-linked and dominant, then it is heterozygous and 1-2 is homozygous. If the traitis sex-linked and recessive, then 1-1 and 1-2 are heterozygous -If the traitis sex-linked and dominant,...
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...
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QUESTION 3 When first presented with a pedigree, you should initially look for general trends. For example: Are there affected individuals in each generation? Are both males and females equally affected? Are traits from a father or mother passed on to all their children? Or only to their sons or daughters? Based on these general observations, you can usually make a fairly reasonable guess...
#7a, b, c, d
Look at the following pedigree for a sex-linked trait to answer the questions below. a) Is the allele for this trait found on the X or the Y chromosome? __________ b) Is this a dominant or a recessive trait? ___________ c) Give the genotype of all the individuals d) If individual A has children with an unaffected male, what are the chances that her children will have the trait? e) Individual B marries an unaffected woman....
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...
need help with pedigrees
You are a genetic counselor. The data: Henry has a double row of eyelashes, which h is a dominant trait. Both his maternal grandfather and his mother have double eyelashes. Their spouses are normal. Henry is married to Isabella and their first child, Polly, has normal eyelashes. The couple wants to know the chances of any child having a double row of eyelashes. Construct two blank pedigrees. Begin with the maternal grandparents and end with Polly...