Question

A boy is born with an autosomal recessive genetic disease that is determined by a single-gene...

A boy is born with an autosomal recessive genetic disease that is determined by a single-gene defect. Both his parents are unaffected. What is the most accurate statement can we say about the parents genotypes with respect to the relevant locus?

In the following statement there are 2 fill in spots, i am providing the options given at these spots and putting them in bold, and in parentheses.

(ONE/BOTH) of his parents must be ["homozygous", "heterozygous"] for the disease-causing allele

Homework Answers

Answer #1

Answer:- Both, heterozygous

Know the answer?
Your Answer:

Post as a guest

Your Name:

What's your source?

Earn Coins

Coins can be redeemed for fabulous gifts.

Not the answer you're looking for?
Ask your own homework help question
Similar Questions
Consider a single-gene disease that has an autosomal recessive pattern of inheritance in humans. Assume that...
Consider a single-gene disease that has an autosomal recessive pattern of inheritance in humans. Assume that the disease-causing gene is in Hardy-Weinberg equilibrium within a population. Suppose that the disease affects 0.17% of the population. (A)What is the frequency of the normal allele in the population? (B)What is the frequency of the mutated (diseased) allele in the population? (C)What percent of the population is an unaffected carrier of the disease?
A widow’s peak is an autosomal dominant trait while a straight hairline is a recessive trait....
A widow’s peak is an autosomal dominant trait while a straight hairline is a recessive trait. Mike and his dad have a widow’s peak. Mike marries Bethany who has a continuous hairline like Mike’s mom. What is the probability that Mike and Bethany’s first child will have a widow’s peak? Complete Punnett Square to support your answer. Leave Blank Probability of first child: A 15-year old boy was diagnosed with a usual autosomal inherited form of diabetes. His mother was...
Cystic fibrosis is a genetic disease caused by several variants of a gene. It is autosomal...
Cystic fibrosis is a genetic disease caused by several variants of a gene. It is autosomal recessive. In other words, an individual must receive two copies of a cystic fibrosis genetic variant, one from the father and one from the mother, to manifest the condition. The probability that a child will be born with cystic fibrosis in the US is about 0.0004. a. Assuming independent inheritance from the father and mother, what is the probability that any given copy of...
Albinism is a genetic disorder where an individual is homozygous recessive for the gene producing melanin...
Albinism is a genetic disorder where an individual is homozygous recessive for the gene producing melanin (the “M” gene). Jack and Jill are both heterozygous at the “M” locus. A) What is the probability of them having two albino boys OR two albino girls in a row (consecutively)? Show your calculation One of their albino children (Sarah) meets a nice non-albino man (Sam) and has children of her own. Both of their children are non-albinos. B) Can you determine the...
HUNTINGTON’S DISEASE is an autosomal dominantly inherited, degenerative human disease of the nervous system. Individuals homozygous...
HUNTINGTON’S DISEASE is an autosomal dominantly inherited, degenerative human disease of the nervous system. Individuals homozygous for this dominant gene almost always die as a fetus. The disease has no obvious phenotypic effects in a heterozygous individual, until a person is about 35-40 years old, well into child-rearing years. There is no known cure for this genetic disease. D.    Determine the results of a mating between a person who will get Huntington’s disease and one who will not develop...
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...
the question is based on the answer of q1 that is already solved ( i will...
the question is based on the answer of q1 that is already solved ( i will post it ) Read the scenario then answer the question: When Ahmad and Amina decided to get married, they were worried that their coming children might suffer from Sickle cell disease, since Amina’s mother had the disease. But the doctor made things clear …. DOC: “Unfortunately Mr. Ahmad after tracking your family’s genetics you might be carrying the recessive allele for the disease so...
Sickle cell disease (sickle cell anemia) is a relatively common disorder in individuals of African descent...
Sickle cell disease (sickle cell anemia) is a relatively common disorder in individuals of African descent and affects approximately 1 in 500 African-Americans. Due to a mutation in an autosomal gene for hemoglobin, the homozygous recessive genotype leads to red blood cells that are relatively stiff and sticky, and deform into a sickle shape as they lose oxygen. This leads to problems in the spleen, and anemia. There are hundreds of different hemoglobin alleles. Individuals heterozygous for the sickle cell...
Part II – Genetic Basis of the Disorder As Alexander’s family and you have now discovered,...
Part II – Genetic Basis of the Disorder As Alexander’s family and you have now discovered, spondyloepiphyseal dysplasia congenita (SEDC) is a genetic disorder in which the primary deficits are abnormal growth of one or more spinal vertebrae and the growing ends of the femurs, resulting in disproportionate, short-trunk dwarfism (Parikh & Crawford, 2017). Interestingly, both of Alexander’s parents, his grandparents and an older sister are of normal height. Therefore, what do you think the mode of inheritance is for...
Sickle-cell anemia is an interesting genetic disease. Normal homozygous individuals (SS) have normal blood cells that...
Sickle-cell anemia 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 sickling...
ADVERTISEMENT
Need Online Homework Help?

Get Answers For Free
Most questions answered within 1 hours.

Ask a Question
ADVERTISEMENT