Q: How can the same phenotype stem from many different genotypes
A: Sir Gregor Mendel was a priest and a teacher who did the famous hybridization experiment on garden…
Q: If an WwxxyyZz individual is crossed to an WwXXYYZZ individual, what is the probability that the…
A: Various phenotypic characters can be controlled by more than one gene and such cases are called…
Q: Explain the difference between epistasis and dominance. How many loci are involved in each case?
A: The structural and functional unit of inheritance is the gene. These are composed of DNA and act as…
Q: assuming independent assortment, what phenotypic ratio would you see if an individual with the…
A: In the given case, the allele 'R' is dominant over 'r' and allele 'G' is dominant over 'g'. If an…
Q: At which level is incomplete dominance more likely to beobserved—at the molecular/cellular level or…
A: Incomplete dominance is a phenomenon in which neither of the two alleles is completely dominant in a…
Q: 1 2 3 4 5 6 7 8 10 11 12 13 14
A: Sex limited inheritance: It is a trait that is limited to a single sex . It is mostly seen in the…
Q: How many unique gametes could be produced through independent assortment by an individual with the…
A: ANSWER;- 8 unique gametes could be produced through independent assortment by an individual with the…
Q: With the help of an example differentiate between incomplete and co-dominance?
A: The genotype is the genetic constitution of the organism while the phenotype is the external…
Q: What is cross-matching?
A: The cross-match procedure determines whether donor blood is compatible with recipient blood.…
Q: Distinguish the following terms . A complete dominance and co - dominance B. genotype and phenotype
A: Inheritance patterns are of different type’s Mendelian inheritance, incomplete dominance,…
Q: How can there be more than one possible genotype for an observed phenotype
A: A genotype is a set of heritable genes in an organism that are transferred from parents to…
Q: Define what is the Karyotype ?
A: The process in which the chromosomes of an organism are paired and ordered is known as Karyotyping.…
Q: Differentiate between complete and incomplete dominance with examples?
A: A gene is a unit of hereditary present in thousands on the strands of DNA(deoxyribonucleic acid).…
Q: Use the foil method To determine the genotypes For a cross between TtTt x TtTt. Assume that T (tall)…
A: The FOIL method used in genetics stands for First, Outside, Inside, and Last. The method is used to…
Q: explain the Phenotypic effects of duplications
A: Duplication of chromosome refers to an addition of an extra chromosomal arm attached to a…
Q: Is it possible to determine the genotype of an individual having a dominant phenotype? How?
A: Phenotype refers to the set of observable characteristics in an organism. Although it is dependent…
Q: Explain how a testcross can reveal the genotype of an individualwith a dominant trait.
A: The test cross is a tool devised by Gregor Mendel that involves crossing of an individual of unknown…
Q: Is it possible to determine the genotype of an individual expressing a dominant phenotype? Provide…
A: We determine the unknown genotype of a dominant organism by crossing it with a homozygous recessive…
Q: What is meant by test cross and how is it significant to genetics?
A: The branch of biology that deals with the study of genes, heredity and genetic variations are termed…
Q: What ratio of genotypes to phenotypes is observed in a two-point test cross if genes are unlinked?
A: A test cross is performed between a dominant and a recessive phenotype to determine the zygosity,…
Q: what are the reasons for the occurence of codominance and incomplete dominance traits?
A: Codominance is a term that refers to the link between two variants of a gene. Individuals inherit…
Q: What is a change in phenotype due to chemical/environmental agent exposure?
A: The DNA (deoxyribonucleic acid) is the genetic material of the body that is passed on from the…
Q: What are the causes of phenotypic variation
A: DNA is the genetic material in most living organisms. It is the information hub of the cell that…
Q: How to determine the genotype frequencies ?
A: Introduction Hardy Weinberg equilibrium: this states that the sum of genotypic and allelic…
Q: Is it possible for an unaffected female to havefemale offspring with red–green color blindness?
A: When the mutation is on the gene of the X chromosome, it is called the X-linked inheritance. As…
Q: How to determine unknown genotype
A: The genetic constitution of an organism for a particular trait is known as its genotype.
Q: What are factors that alter the phenotypic expression of genotype?
A: Genotype The genotype can be defined as the genetic make-up of an individual organism. Our genotype…
Q: Explain the following terms: Heterozygous: Genotype: Phenotype: Dominant allele: Recessive…
A: All these terms described in the question are related to the genetics which is the study of the…
Q: in the the dihybrid cross of Mendel how many genotype and phenotype?
A: Mendel's law of independent assortment states that the alleles of two (or more) different genes get…
Q: Recognize progeny ratios that imply the existence ofrecessive lethal alleles.
A: Genes are the fundamental unit of inheritance. They are the governing factors which determines the…
Q: What is the differencebetween dominant allele andrecessive allele?
A: Genetics is a study of genes, heredity, and genetic variation in an organism. Living organisms…
Q: What is the reason for doing a test cross? to determine which allele is dominant to the genotype of…
A: In the field of genetics, a test cross is a genetic cross performed to determine whether an organism…
Q: Canphenotype change without a change in genotype?
A: Epigenetics: It is study of heritable changes / phenotypes which are caused due to no changes in…
Q: Assuming brown eyes (B) are dominant over blue eyes (b), determine the genotypes of all the…
A: Chromosomes are the unit of inheritance. The transfer characteristics from one generation to…
Q: offspring with Given the cross AaBbCc x Aabbcc, what is the probability of obtaining the genotype…
A: Trihybrid cross follows all laws postulated by Mendel a, law of segregation, law of dominance and…
Q: Describe the difference between genotype and phenotype. Give three examples. Is it possible for two…
A: Genetics is the branch of biology which deals with genes, heredity, and genome in the organism.…
Q: What is the difference between codominance and incomplete dominance?
A:
Q: Discuss the factors that can cause different individualswith the same genotype to be phenotypically…
A: Phenotype in genetics refers to the morphological appearance of the organism that is controlled by…
Q: Explain the following features of the Mendelian traits and fill the Punnet Squares. a)The…
A: Genetics is a study of genes, heredity, and genetic variation in an organism. Living organisms…
Q: What is the probability that parents AaBb and AaBb will have offspring with genotype AaBb
A: A dihybrid cross is a cross given by Mendel . It involves two traits . A ) First trait have two…
Q: Identify the phenotype for each number represented in the 3:1 ratio.
A: The cross is a mono hybrid cross where only one character is considered. Dominant character is…
Q: What is the purpose of a testcross? To determine the genotype of offspring from a cross. To…
A: The allele combination is called "genotype" while the observable traits are called "phenotype". The…
Q: In dogs, rough hair (R) is dominant to smooth hair (r). If you crossed a homozygous, rough hair dog…
A: Answer - Option A - Rr only
Q: What genotypic and phenotypic probabilities would be expected regarding a mating of an Ss/RR…
A: The genotype is a set of genes in DNA that are responsible for a specific trait or characteristic,…
Q: Is this pedigree consistent with extranuclear inheritance of the shaded characteristic?
A: Answer: Extranuclear inheritance : Extranuclear genes are the genes which found outside the nucleus…
Q: had a karyotype prepared for her baby before birth, would it be more useful in predicting the risk…
A: Down`s syndrome, also known as trisomy 21 is a genetic disorder caused when abnormal cell division…
Q: Is it possible to determine the genotype of an individual who has a dominant phenotype? Why or Why…
A: The genetic makeup of an individual is known as genotype. The genotype reflects the alleles or the…
Q: Pedigrees indicate that color blindness and which two forms of hemophilia are X-linked traits?
A: Introduction Pedigree Analysis: this is the new approach to study the inheritance pattern in the…
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- Piebald spotting is a condition found in humans inwhich there are patches of skin that lack pigmentation. The condition results from the inability ofpigment-producing cells to migrate properly duringdevelopment. Two adults with piebald spotting haveone child who has this trait and a second child withnormal skin pigmentation.a. Is the piebald spotting trait dominant or recessive?What information led you to this answer?b. What are the genotypes of the parents?.Certain forms of human color blindness are inherited as X-linkedrecessive traits. Hemizygous males are color-blind, but heterozygous females are not. However, heterozygous females sometimeshave partial color blindness.A. Discuss why heterozygous females may have partial color blindness.B. Doctors identified an unusual case in which a heterozygousfemale was color-blind in her right eye but had normal colorvision in her left eye. Explain how this might have occurred.In individuals affected by cystic fibrosis, salt crystals may appear afterperspiration dries up. In addition, the disease causes respiratory disorderswhich can be both debilitating and lethal. It occurs in individuals homozygousfor recessive gene. If 2 normal parents had a daughter with the symptoms ofthis disease, and a normal son, what is the probability that he might be acarrier of the recessive gene?Express answer in fraction form.
- Let’s suppose a gene exists as a functional wild-type allele and anonfunctional mutant allele. At the organism level (i.e., at the levelof visible traits), the wild-type allele is dominant. In a heterozygote,discuss whether dominance occurs at the cellular or molecularlevel. Discuss examples in which the issue of dominance dependson the level of examination.In 1995, doctors reported a Chinese family in whichretinitis pigmentosa (progressive degeneration of theretina leading to blindness) affected only males. Allsix sons of affected males were affected, but all of thefive daughters of affected males (and all of thechildren of these daughters) were unaffected.a. What is the likelihood that this form of retinitispigmentosa is due to an autosomal mutationshowing complete dominance?b. What other possibilities could explain the inheritance of retinitis pigmentosa in this family? Whichof these possibilities do you think is most likely?In rabbits, fur colour can be either grey, black or blotchy. Blotchy is present as grey and black spotspresent in no specific pattern. Males are almost always either grey or black, while females can begrey, black or blotchy. However, a male individual is found that shows the blotchy pattern, and youexpect a non-disjunction event might be to blame. Explain the inheritance of coat colour in rabbits,and also provide an explanation for the blotchy male.
- Let’s look at hair texture. Some people have curly hair, some have straight hair and some express a traitthat is in-between (Incomplete Dominance), or wavy hair. Therefore curly and straight are bothhomozygous and wavy is the expression of the heterozygous condition. Instead of using capital and lowercase letters, we’ll add a prime (`) to the letter. This is because one is not dominant over the other, andthey will both contribute to the phenotype. We can use H to indicate curly hair and H` to indicate straighthair.Given this information, complete the square: Parent Phenotype(appearance) Genotype(alleles) 1 Curly hair HH 2 Straight hair H'H' Do you remember where the alleles of each parent go?Parents: Offspring: Genotypes: Phenotypes: What are the potential phenotypes and genotypes of the offspring?There is an autosomal gene in cats that controls whether or not they also have white patches of fur (W = white spots, w= no white spots). Considering this along with the Orange gene (O0 and OB) from the previous question, and how it works, how many possible genotypes (using these 4 alleles) are there for cats that are orange, black, and white (in other words, calico)?Color blindness in humans is controlled by an X-linked completely recessive allele (Xc), while breast cancer is controlled by an autosomal completely dominant allele, B. A color blind male, who is a heterozygote carrier for breast cancer has three children/n with a normal eyed female (whose mother was color blind), who is homozygote recessive for the breast cancer allele. What is the probability that out of three children, 2 will be color blind males, and not show breast cancer, and one will be a color blind female, who shows breast cancer?
- Rabbits may be classified as agouti, chinchilla, Himalayan, or albino according to coat color. A crossbetween CC^h x C^ch c produced 5 agouti, 3 chinchilla and 2 Himalayans. a. What are the phenotypes of the parent rabbits? b. What are the genotypes of the F1s? c. What mode of inheritance is exhibited? d. If the two F1 agouti genotypes will be crossed, what percentage of their offspring will have the same phenotype? e. What will be the genotypes of the rabbits in (d)?Some heterozygotes express a phenotype that is intermediate between the dominant and recessive phenotype. For example, in 4 o’clock flowers the gene for red pigmentation is dominant and the gene for white pigmentation is recessive. However, heterozygotes are pink. The dominant allele does not completely mask expression of the recessive allele: it is incompletely dominant. a. By observing flower color in 4 o’clock flowers, is it possible to unambiguously determine the genotype? YES/NO. Explain your answer. b. Is the same true for flower color in snow peas? YES/NO Why or why not?Finger mid-digital hair (M) is dominant over the recessive trait of no mid-digital hair (m). Freckles (F) is dominant over the recessive trait of no freckles (f). (It is important to note that this example of mid-digital hair and freckles cannot be explained with simple genetics, but for the purpose of this question, assume that it can.)A woman that is heterozygous for freckles and has no mid-digital hair is married to a man with no freckles that is heterozygous for mid-digital hair. The couple is expecting a child. Draw a Punnett square of this cross. What is the probability that their offspring will have mid-digital hair? What is the probability that two offspring in a row will have no freckles? What is the probability of two offspring in a row having mid-digital hair and freckles?