Question

In: Biology

An autosomal locus has alleles A and a. The frequency of individuals with the autosomal recessive...

An autosomal locus has alleles A and a.

The frequency of individuals with the autosomal recessive phenotype is given. Which statements are true? (pick all that are true)

HWE= Hardy-Weinberg equilibrium

1. We can calculate q=Freq(a) even if we don't assume Hardy-Weinberg Equilibrium

2. Even if we don't assume HWE, we can calculate the genotype frequencies that we weren't given

3. If we assume HWE, we can calculate the genotype frequencies that we weren't given

4. If we assume HWE, we can calculate both allele frequencies

5. We can calculate both allele frequencies even if we don't assume HWE.

Solutions

Expert Solution

Hardy Weinberg equilibrium (HWE) states that the frequency of alleles and genotype remain the same in successive generations, if no evolutionary force acts on the population.

The given statement is that there are two alleles, A and a, and the phenotypic frequency of recessive individuals is known.

Let us consider an example, out of 100 individuals, 36 express the recessive phenotype. This means, the frequency of aa individuals is 36/100. In other words, taking frequency of A = p, and frequency of allele a = q, we get,

q2 = 36/100

q = √ (36/100)

q = 0.6

Now since there are only two alleles in a population for this trait (A, a) , thus the sum of their frequencies will be 1, even in the absence of HWE. The frequency of allele A, i.e.

p = (1-0.6)

p = 0.4

Now, we can calculate the genotypic frequencies of other classes using the above two results. Hence, the correct statements should be:

  • We can calculate q=Freq(a) even if we don't assume Hardy-Weinberg Equilibrium.
  • Even if we don't assume HWE, we can calculate the genotype frequencies that we weren't given.
  • We can calculate both allele frequencies even if we don't assume HWE..

Related Solutions

IA and IB are codominant alleles at the ABO locus, whereas IO is recessive. Individuals with...
IA and IB are codominant alleles at the ABO locus, whereas IO is recessive. Individuals with hh genotypes at another locus called FUT1 (which involves the Bombay phenotype) do not express antigens encoded by the ABO locus at all. This examplifies A. pleitotropy B. dominant epistasis C. recessive epsistasis D. incomplete dominance E. epigentics
1. you are evaluating autosomal recessive condition A (alleles A and a) and B (alleles B...
1. you are evaluating autosomal recessive condition A (alleles A and a) and B (alleles B and b) which you hypothesize are on different chromosomes. You are given 7 wildtype (homozygous dominant) female flies and 7 male flies that are homozygous recessive. What genotypic ratio would you expect in the F1 generation produced? 2. you mate the F1 females with males that are homozygous recessive for both disease A and B to produce an F2 generation. What phenotypic ratio would...
The agouti locus in mice has three alleles: a is recessive and confers a black coat,...
The agouti locus in mice has three alleles: a is recessive and confers a black coat, A is dominant to a and confers an agouti coat, and AY is dominant to both and confers a yellow coat. AY is also a recessive lethal. In addition, the independently assorting c allele is recessive (to C) and prevents the mice from making any fur pigments at all, resulting in albinos. Two mice are crossed, and produce offspring in a ratio of 2...
Locus A has two alleles (A and a) while locus B has two alleles (B and...
Locus A has two alleles (A and a) while locus B has two alleles (B and b). The recombination frequency between locus A and locus B is 11%. A F1 heterozygote in trans configuration is mated with an aabb individual. What are the expected phenotypic percentages in the resulting progeny? Report your percentages to the tenths place and in the following format, replacing the "0.0" with your percentages.
CF is an autosomal recessive condition. A population of 387 individuals has 7 people with CF....
CF is an autosomal recessive condition. A population of 387 individuals has 7 people with CF. If we assume that the CF gene is in Hardy-Weinberg equilibrium what is the estimated frequency of the CF allele? Give answer in decimal places
The frequency of carriers for a rare autosomal recessive genetic condition is 0.04 in a population....
The frequency of carriers for a rare autosomal recessive genetic condition is 0.04 in a population. Assuming this population is in Hardy-Weinberg equilibrium, what is the allele frequency of the recessive allele? 0.2 0.4 0.64 0.8 Not enough information is provided.
Among 40 individuals, 4 are heterozygous for a particular locus with two alleles (A1 and A2),...
Among 40 individuals, 4 are heterozygous for a particular locus with two alleles (A1 and A2), 16 are homozygous for allele A1, and 20 are homozygous for allele A2. 1. What is the frequency of allele A1? 2.What is chi-squared for your observed/expected genotypes? 3.Does the population depart significantly from Hardy-Weinberg expectations? (For 1 degree of freedom χ,> 3.84 is significant)
5pts) Gaucher’s Disease displays an autosomal recessive pattern of inheritance and occurs more frequently in individuals...
5pts) Gaucher’s Disease displays an autosomal recessive pattern of inheritance and occurs more frequently in individuals of Ashkenazi Jewish heritage. Gaucher’s Disease is the result of the loss of an enzyme (encoded by the GBA gene) that catalyzes the breakdown of glucocerebroside. You have gathered data from a local population and estimate that approximately 7 in 1000 newborns are affected by Gaucher’s Disease. (Answer the following questions using 3 significant digits). a. Assuming there are only two alleles, wildtype GBA...
5. If 1/1000 individuals with your genetic background are carriers for a certain autosomal, recessive disease...
5. If 1/1000 individuals with your genetic background are carriers for a certain autosomal, recessive disease allele, what is the chance that both you and your spouse will be carriers? 6. (Related to 5) What is the chance that you will both be carriers and have an affected child? 7. (Related to 5 and 6) If you are a carrier for this disease allele and your spouse’s status is unknown, what is you chance of having a child with the...
Sickle cell anemia is inherited as an autosomal, recessive disorder. Individuals who inherit the mutated gene...
Sickle cell anemia is inherited as an autosomal, recessive disorder. Individuals who inherit the mutated gene from both parents will show symptoms of sickle cell, including a stiffening of the red blood cells when the individual is under conditions with low oxygen levels in the air (e.g. on top of a mountain). This can lead to low red blood cell count (anemia), shortness of breath, fatigue, jaundice, and joint pain. Most critically, the stiffened red blood cells can clog small...
ADVERTISEMENT
ADVERTISEMENT
ADVERTISEMENT