Sickle cell disease is an autosomal recessive disease. Homozygous dominant (SS) and heterozygous (Ss) individuals will be non-diseased, but homozygous recessive (ss) individuals will have the disease. A study of sickle cell disease in New York found that in a one year period:
Based on this information:
1) You would estimate that the frequency of the dominant allele in the total population of New York, based on all infants born in the state, would be approximately:
0
0.03
0.29
0.67
0.97
2) You would estimate that the frequency of the recessive allele in a population of non-hispanic whites would be approximately:
0
0.03
0.00002
0.004
0.99998
0.996
3) You would estimate that the frequency of carriers for the disease (Ss) in a population of non-hispanic black individuals would be approximately:
0
1/4
1/8
1/100
1/8000
4) You would estimate that the frequency of homozygous dominant (SS) in a population of hispanic individuals would be approximately:
0
0.959
0.041
0.783
0.061
5) You would estimate that the frequency of heterozygotes (Ss) in a population of hispanic individuals would be approximately:
0
1/24
1/4
1/150
1/900
Sickle cell disease is an autosomal recessive disease. Homozygous dominant (SS) and heterozygous (Ss) individuals will...
5. Sickle-cell disease is an interesting genetic disease. Normal homozygous individuals (SS) have normal blood cells that are easily infected with the malarial parasite. Thus, many of these individuals become very ill from the parasite and many die. Individuals homozygous for the sickle-cell trait (ss) have red blood cells that readily collapse when deoxygenated. Although malaria cannot grow in these red blood cells, individuals often die because of the genetic defect. However, individuals with the heterozygous condition (Ss) have some...
30) In Tanzania, 4% of the population are homozygous recessive for a condition called sickle cell anemia. From this data, a) Calculate the frequency of the dominant and recessive alleles. 1-04-06 b) Calculate the genotype frequencies for individuals not carrying a sickle cell allele, carriers and individuals who have the disease.
Hardy-Weinberg Practice Problems: You need to list equations used and provide steps of problem solving. Providing answer itself is not enough for full grade. 1. You have sampled a population in which you know that the percentage of the homozygous recessive genotype (aa) is 36%. Calculate the frequency of the heterozygous genotype, homozygous dominant genotype and homozygous recessive genotype. 2. You have sampled a population in which you know that the percentage of the homozygous recessive genotype (aa) is 49%....
Even though sickle-cell anemia is usually fatal to homozygous individuals, the disease persists because: Gene therapy has alleviated the condition The disease is carried on the dominant allele Individuals with one allele for sickle-cell anemia are resistant to malaria None of the above
If individuals with the sickle-cell hemoglobin are selected against, how is it that the mutated hemoglobin gene persists in the human population? Choose the best answer. Individuals with sickle-cell disease (recessive homozygous) are best able to fight off malaria, so the gene persists in malarious areas. The monkey bread tree is not sensitive to temperature. When a non-sickle cell individual (dominant homozygous) mates with an individual with sickle-cell disease (recessive homozygous) the produce heterozygotes and that is how the mutated...
6. Sickle cell anemia (disease) is described as an autosomal recessive condition (individuals must have two copies of the recessive allele to display “sickle cell disease”). However, sickle cell trait (the heterozygous condition) has a unique phenotype. a. How would you classify/describe sickle cell trait at the organismal level (complete, incomplete, or co-dominance)? Explain your reasoning. b. How would you classify/describe sickle cell trait at the molecular level (complete, incomplete, or co-dominance)? Explain your reasoning. (HINT: think about the hemoglobin...
. In a population of 200 individuals, 72 are homozygous recessive for the character of eye color (cc). One hundred individuals from this population die from a fatal disease. Thirty-six of the survivors are homozygous recessive. In the original population, the frequency of the dominant allele is ???
2. Hardy-Weinberg Equilibrium; chi-square test Sickle cell anemia is a recessive disorder caused by a recessive mutation (S) in the b-hemoglobin gene. 80% of affected SS individuals die before reproducing. Heterozygotes (AS) and homozygous dominant (AA) individuals do not have sickle cell anemia. The table below shows the number of people of each genotype in a population of 100 people in population of Cameroon. Observed # individuals in a Cameroon population AA AS SS 62 32 6 What are the...
In a population, you observe 300 homozygous dominant (AA) individuals, 400 heterozygous (Aa) individuals, and 300 homozygous recessive (aa) individuals. Please show all your work while answer the following questions. What are the observed allele frequencies for this population? • observed dominant allele (A) frequency: • observed recessive allele (a) frequency: What are the observed genotype frequencies for this population? • observed homozygous dominant (AA) genotype frequency: • observed heterozygous (Aa) genotype frequency: • observed homozygous recessive (aa) genotype frequency:...
3. Sickle-cell disease is a genetic condition caused by an autosomal recessive allele which al- fects one in every 500 African American children born in the U.S. One in every ten African Americans is a carrier for the recessive allels. Although sickle cell disease is caused by a single human gene, it is expressed through many different effects throughout the body. The presence of a recessive sickle-cell allele in humans causes the red blood cells to produce abnormal hemoglobin protein...