The following letters indicate the pairs of alleles present on a homologous chromosome pair within an individual organism. Match each gene and determine whether it is homozygous dominant, homozygous recessive, or heterozygous... Dd jj RR Jj
Q: In humans, as well as in many other animals and some plants, the sex of the individual is determined…
A: Haemophilia is an inherited bleeding disorder where blood doesn't clot properly. It is caused when…
Q: Albinism is an autosomal (not sex-linked) recessive trait. A man and woman are both of normal…
A: Introduction Albinism Is A Genetic Condition That Causes A Person's Skin, Hair, And Eyes To Be…
Q: For each of the following chromosome complements, what is the phenotypic sex of a person who has a.…
A: Hi! Since you have posted a question with multiple sub-parts, we will solve the first three…
Q: The most common form of colorblindness is a recessive, sex-linked hereditary con dition caused by a…
A: Color blindness is a genetic disorder which is caused by the inheritance of the mutated genes. The…
Q: Hemophilia is a disease caused by a gene found on the X chromosome. Therefore, it is a sex-linked…
A: If the woman gets the X chromosome with the hemophilia gene, she will have hemophilia . A man who…
Q: Male pattern baldness is inherited on the X chromosome. The allele for baldness is designated Xb,…
A: Baldness refers to the complete loss of hairs that leads to a visible scalp. If hair loss gets…
Q: Both red/green color blindness (R=normal, r=colorblind) and Duchenne-type muscular dystrophy…
A: X-linked recessive inheritance is the genetic condition that can be passed from parent to child…
Q: Color blindness is a recessive sex-linked trait on the X chromosome. A non-color blind heterozygous…
A: The alleles are generally of dominant and recessive type and some other forms like codominant are…
Q: A woman is heterozygous for the gene that causes cystic fibrosis, an autosomal recessive disorder.…
A: A series of event that occurs in a cell to make it ready for the division is the cell cycle. There…
Q: Geneticists are concerned about three different genetic conditions present within their family.…
A: Autosomal dominant A = achondroplasia a = average height AA and Aa = affected aa = normal X…
Q: In humans, hemophilia is a sex-linked recessive disease, and the gene is located on the X…
A: Answer: HEMOPHILIA = It is the chromosomal disorder , which sex-linked recessive disease, men are…
Q: A man and both his parents are affected with a disease. His older sister is unaffected. This man…
A: Pedigree is a family tree drown by a genetic councillor uses some special symbol to identity a…
Q: Colorblindness is inherited as an X-linked recessive trait while pattern baldness is controlled by…
A: Colourblindness is X linked recessive condition in which recessive allele h is present on X…
Q: Which of the following genotype(s) must a female child have in order to be color blind? XNXN…
A: Colorblindness is a X-linked recessive disorder which doesn't allow the individual to differentiate…
Q: Two parents who do not have color blindness have a daughter who has only one X chromosome and is…
A: The event of nondisjunction occurs when the chromosomes fail to separate during the process of…
Q: In the following pedigree, is the disorder’s mode of inheritanceautosomal dominant, autosomal…
A: In this pedigree, affected individuals appear in every generation. There are no carriers shown in…
Q: Hemophilia is an X-linked recessive disorder and blood type is autosomal. If two healthy parents,…
A: Introduction X linked inheritance is based on the sex chromosome (X chromosome). This inheritance…
Q: A type of red-green colorblindness is inherited recessively on the X chromosome. A woman who is…
A: Color blindness is sex-linked recessive disorder. A person is said to be color blind if he is not…
Q: ABO Blood Type The following pedigree shows the incidence of ABO blood types in a family. dentify…
A: ABO Blood TypeThe following pedigree shows the incidence of ABO blood types in a family. Parents: AB…
Q: Which of the following is the most common type of chromosomal disorder? O a. Kleinfelter's Syndrome…
A: Any syndrome produced by an aberrant chromosome number or constitution, marked by deformities or…
Q: refers to the following pedigree of albinism (an autosomal recessive trait): What are the genotypes…
A: Sir Gregor Mendel was a priest and a teacher who did the famous hybridization experiment on garden…
Q: Match the following terms in column A with the correct description in column B. Column A Column B A)…
A:
Q: A couple seeks advice from a genetic counselor because they know that they are both carriers for…
A: There are 2 diseases one is the cystic fibrosis which is autosomal recessive and the other is the…
Q: Fill in the blanks to complete the Punnett Square using the following information. For blank #7,…
A: Given - Cystic fibrosis is a hereditary illness which is inherited due to the recessive allele (c)…
Q: Suppose gene B is X-linked and is embryonically lethal when homozygous or hemizygous recessive. A…
A: Let us first discuss the terms used in the question, Homozygous:- A condition when two copies of an…
Q: On average, what proportion of the genome in the following pairs of humans would be exactly the same…
A: Chromosomes are thread-like structures comprised of two strands of DNA. Humans contain 23 pairs of…
Q: Assume that color blindness is a recessive character on the X chromosome. A man and woman with…
A: Introduction Inheritance referred to the transmission of character/traits in the form of gene from…
Q: A woman with blonde hair and blues eyes, which are recessive genes, marries a heterozygous man who…
A: Traits are characteristic features that are unique to particular individual . As per the question ,…
Q: f the following patterns of transmission is consistent with this pedigree? Select one: a. Autosomal…
A: To know whether a genetic disease is there in family or not ,we generally go through each and…
Q: An individual comes into your genetics clinic to be tested for any anomalies. When looking at their…
A: Given: An individual come to your genetics clinic to be tested for any anomalies.When looking at…
Q: A recessive allele on the X chromosome is responsible for red-green color blindness in humans. A…
A: The colorblindness is encoded by the genes present on the X chromosome.
Q: Cystic fibrosis is an autosomal recessive disorder that affects 1 in 3 000 newborns with Caucasian…
A: Cystic fibrosis (CF) is an inherited disorder that causes severe damage to the lungs, digestive…
Q: A woman homozygous dominant for albinism marries a man who is homozygous recessive for albinism.…
A: Albinism is a disorder common in several organisms that occurs as the mutation of TYR gene. TYR gene…
Q: Using the same information listed above for hair and eye color, (E = dominant brown eyes with e =…
A:
Q: Below is a pedigree chart of a certain family with a genetic disorder. Shaded individuals show…
A: The pedigree analysis deals with the study of the inheritance of genetic disorders. Genetic…
Q: What is the mode of inheritance for the genes controlling maniac and shiny? autosomal dominant for…
A: Mutation A kind of alteration in the DNA base pairs either by chemical or physical or by some error…
Q: How can NF1 be spontaneous? Include the following terms: -genotype - phenotype - homozygous -…
A: NF1 or neurofibromatosis I is a Mendelian genetic disorder that results due to mutation in the NF1…
Q: A man and woman are both of normal pigmentation, but both have one parent who is albino (without…
A: Answer - 1/4 Albinism is an autosomal recessive trait. Normal pigmentation = AA, Aa (heterozygous)…
Q: One form of red-green color blindness is an X-linked recessive trait. A heterozygote woman has…
A: Color blindness is a deficiency of color vision and the individual with color blindness have…
Q: Make a pedigree for each of the following situations. For each individual, write the individual…
A: The cystic fibrosis transmembrane conductance regulator (CFTR) gene mutation causes this hereditary…
Q: What is the chance the parents would have a color-blind boy? A color-blind girl? What about a girl…
A: Colour Blindness It is a kind of disability which involves the inability to distinguish between…
Q: The next three questions go together. Duchenne's muscular dystrophy (DMD) is a disease caused by a…
A: DMD trait is present on X chromosome that means DMD is an x-linked disorder. In this case males have…
Q: In humans, as well as in many other animals and some plants, the sex of the individual is determined…
A: Haemophilia is X-linked recessive disorder. It is generally caused by a mutation in the genes which…
Q: Cystic fibrosis is a genetic disease that causes an abnormal production of mucus which in turn can…
A: Cystic fibrosis (CF) is a disease caused by a mutation in a protein in the body. Cystic fibrosis is…
Q: Propose the most likely mode of inheritance (autosomal dominant, autosomal recessive, or X-linked…
A: In humans, there are 23 pairs of chromosomes in which the 23rd pair is the sex chromosome which…
Q: Given that a human normally contains 46 chromosomes, give the chromosome number for each of the…
A: DNA molecule is the genetic material present in the animals. Genetic material is present in the…
Q: In human beings, the gene for red‑green colorblindness (r) is sex‑linked and recessive to its allele…
A: Given that colorblindness is a recessive X-linked trait. Hence in females, both X chromosomes should…
Q: A newly-married couple is thinking of having children. They are worried about their child having…
A: CYSTIC FIBROSIS It is an inherited disorder that caused due to defect in chloride transport.…
Q: Albinism is a recessive disorder where there is a lack of melanin. Andrea and her husband Claude…
A: Albinism is autosomal recessive disorder. Claude's parents are carrier ( Aa) however they do not…
Q: Change in chromosome numbers will lead to abnormalities. Which of the following is a correct match…
A: Introduction A karyotype is a preparation of the entire set of metaphase chromosomes in the cells of…
- Dd
- jj
- RR
- Jj
Trending now
This is a popular solution!
Step by step
Solved in 2 steps
- Two people are planning to have children together. Each person is heterozygous for the gene “G”. Using this letter, first list all the possible gametes that the two people can produce. Next, write all the possible genotypes and phenotypes for their offspring, using the correct genetic terminology (e.g., “genotype is homozygous dominant” “phenotype is dominant”). HINT: Use the gametes to construct a Punnett square and predict the possible offspring (you do not need to include the Punnett square in your answerCystic fibrosis in humans is caused by mutations in a single gene and is inherited as an autosomal (non-sex chromosome) recessive trait. An unaffected couple has two children. The first child has cystic fibrosis, and the second child is unaffected. What is the probability that the second child is a carrier (heterozygous) for the mutation that causes the disease? 2/3 1 1/2 3/4Two people are planning to have children together. Each person is heterozygous for the gene “A”. Using this letter, first list all the possible gametes that the two people can produce. Next, write all the possible genotypes and phenotypes for their offspring, using the correct genetic terminology (e.g., “genotype is homozygous dominant” “phenotype is dominant”). HINT: Use the gametes to construct a Punnett square and predict the possible offspring (you do not need to include the Punnett square in your answer).
- A woman who sought genetic counseling is found to be heterozygousfor a chromosomal rearrangement between the second andthird chromosomes. Her chromosomes, compared to those in anormal karyotype, are diagrammed on the next page:(a) What kind of chromosomal aberration is shown?The most common form of colorblindness is a recessive, sex-linked hereditary con dition caused by a defect on the X chromosome. Females are XX, while males are XY. Individuals inherit one chromosome from each parent, with equal probability; for example, an individual has a 50% chance of inheriting their father's X chromosome, and a 50% chance of inheriting their father's Y chromosome. If a male has an X chromosome with the defect, he is colorblind. However, a female with only one defective X chromo some will not be colorblind. Thus, colorblindness is more common in males than females; 7% of males are colorblind but only 0.5% of females are colorblind. (a) Assume that the X chromosome with the wild-type allele is X+ and the one with the disease allele is X. What is the expected frequency of each possible female genotype: X+X+, X+X¯, and X-X-? What is the expected frequency of each possible male genotype: X+ Y and X-Y? (b) Suppose that two parents are not colorblind. What is the…Albinism, lack of pigmentation in humans, results from an autosomal recessive gene designated a. Two parents with normal pigmentation have an albino child. What is the probability that their next child will be albino? What is the probability that the next child will be an albino girl? If the child is normal, what is the probability that it will be a carrier (heterozygous) for the albino gene?
- Albinism is an autosomal (not sex-linked) recessive trait. A man and woman are both of normal pigmentation and have one child out of three who is albino (without melanin pigmentation). What are the genotypes of the albino's parents? Both parents must be homozygous dominant. Both parents must be heterozygous. One parent must be homozygous dominant; the other parent must be heterozygous. One parent must be heterozygous; the other parent can be homozygous dominant, homozygous recessive, or heterozygous. One parent must be homozygous for the recessive allele; the other parent can be homozygous dominant, homozygous recessive, or heterozygous. O O O O OAn individual that is heterozygous for an inversion has the following chromosomes(∗ is the centromere):M N O P Q • R S T Um n o t s r • q p u Assume that a crossover occurred between P and Q. Starting with “M” allele, list the remaining genes in order (NO spaces between the letters) of the chromosome resulting from crossing over. You must use upper and lower-case letters correctly and the * symbol for the centromere(s).X‑linked, recessive diseases, such as hemophilia, are extremely rare in the population. However, many women are carriers and show no sign of the disease. The pedigree illustrates the inheritance of an X‑linked, recessive disease. Determine whether the unknown individuals are affected by the disease, unaffected by the disease, or carriers of the X‑linked recessive allele. Unaffected individuals are not carriers of the X‑linked recessive allele.
- A WOMAN IS HETEROZYGOUS FOR TWO HARMFUL RECESSIVE ALLELES IN DIFFERENT CHROMOSOMES, ONE FOR PHENYLKETONURIA (PKU) AND THE OTHER FOR CYSTIC FIBROSIS (CF). SHE MARRIES AN UNAFFECTED MAN WHO IS A CARRIER FOR NEITHER DISEASE. IF SHE HAS A DAUGHTER, WHAT IS THE PROBABILITY THAT THE CHILD WILL CARRY NEITHER OF THE RECESSIVE ALLELES? EXACTLY ONE? BOTH?A phenotypically normal individual has the following combinations of normal and abnormal chromosomes:The normal chromosomes are shown on the left in each pair.Suggest a series of events (breaks, translocations, crossovers, etc.)that may have produced this combination of chromosomes.Albinism is an autosomal (not sex-linked) recessive trait. A man and woman are both of normal pigmentation and have one child out of three who is albino (without melanin pigmentation). What are the genotypes of the albino's parents? One parent must be homozygous for the recessive allele; the other parent can be homozygous dominant, homozygous recessive, or heterozygous. Both parents must be homozygous dominant. One parent must be heterozygous; the other parent can be homozygous dominant, homozygous recessive, or heterozygous. Both parents must be heterozygous. One parent must be homozygous dominant; the other parent must be heterozygous. O000