a. What are the ABO blood group genotypes of individuals I-1 and I-2? b. Which child/ren of individual I-4 can donate blood to him? c. Which individual in the pedigree can donate blood to all the other individuals in the pedigree?
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Q: TTGG ttgg F1 TG tg F2 TtGg Which types of genotypes are represented in F1 and F2 in the above…
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Q: óa. In a pedigree, a square represents a male. If it is darkened he has hemophilia; if clear, he had…
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A: Introduction Genotype for Blood group A - Either lAlA (homogygous) or, lAlo (heterozygous)…
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A: The ABO blood group are determined by the presence of antigens. They are encoded by the ABO locus…
Q: b) Figure 2 shows a family tree in which the blood group of certain individuals have been…
A: Alleles are the alternative forms of a gene that occupies the same locus of homologous chromosome…
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A: ABO blood group was first discovered by the Carl Landsteiner. This system is used to denote the…
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A: Possible genotypes of father can be- IAIA , IAIO , IBIB, IBIO, IAIB
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A:
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A: Blood group is controlled by three alleles IA, IB, i alleles. It is the case of multiple allelism.
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A: Answer. Grace Grace has type O blood is adopted Explanation:-
Q: n the genetically inherited disease called hemophilia. From the information in he pedigree chart…
A: Haemophilia follows X linked recessive pattern. The genes associated with this condition are located…
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Q: Blood types in humans are Codominant. a. What are the possible genotypes of someone with type O…
A: Answer: CO-DOMINANCE = It is the cross between those alleles that lacks the dominant and recessive…
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A: The ABO blood group system is present in human beings. There are four blood groups in the system,…
Q: In this pedigree chart, what is the genotype of individual III-1? (It's circled in blue.)
A: A pedigree is a diagrammatic representation of genetic traits passed on from one generation to…
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- The mother of a family with 10 children has blood typeRh+. She also has a very rare condition (elliptocytosis,phenotype E) that causes red blood cells to be oval rather than round in shape but that produces no adverseclinical effects. The father is Rh− (lacks the Rh+ antigen)and has normal red blood cells (phenotype e). The children are 1 Rh+ e, 4 Rh+ E, and 5 Rh− e. Information isavailable on the mother’s parents, who are Rh+ E andRh− e. One of the 10 children (who is Rh+ E) marriessomeone who is Rh+ e, and they have an Rh+ E child.a. Draw the pedigree of this whole family.b. Is the pedigree in agreement with the hypothesisthat the Rh+ allele is dominant and Rh− is recessive?c. What is the mechanism of transmission ofelliptocytosis?d. Could the genes governing the E and Rh phenotypesbe on the same chromosome? If so, estimate the mapdistance between them, and comment on your resultHemophilia A is caused by a sex-linked recessive gene in human and in dogs. a. What proportions (and sexes), among their offspring will be hemophiliacs if a hemophilic male is mated to a homozygous nonhemophilic female?b. If a daughter produced by the mating in (a) is mated to a normal male, what proportions and (sexes) will be hemophilic among their offspring?my widows peak phenotype is aa. what is my widows peak genotype.
- Hemophilia is an X-linked disease associated with the inability to produce specific proteins in the blood-clotting pathway. Shown above is a family pedigree tree in which family members afflicted with the disease are shown with filled-in squares (male) or circles (females). A couple is trying to determine the likelihood of passing on the disease to their future children (represented by the ? symbol above) because the hemophilia runs in the woman’s family 4.Assuming that the woman in the couple is a carrier, what is the probability that the couple’s first son will have hemophilia?Consider three genes L, U, and W, for which the count of F2 phenotypes after a 3-point cross is as follows: Phenotype F2 count: L U w 19 L u W 1 l u W 21 L U W 33 l U W 274 l u w 41 l U w 2 L u w 259 Which of the following statements about genes L, U, and W are TRUE? (may be more than one correct ans) A. L, U, and W are each on a different chromosome B. Only U and L are on the same chromosome C. Only U and W are on the same chromosome D. Only W and L are on the same chromosome E. L, U, and W are all on the same chromosomeSeveral genes in humans in addition to the ABO gene () give rise to recognizable antigens on the surface of the red blood cells. The Rh marker is determined by positive (R) and negative alleles () of gene R, where R is completely dominant to r. The presence of M and N surface proteins are controlled by two codominant alleles of gene L (LM and LM. For each mother-child pair, choose the father of the child from among the males in the right column. (Assume that all mothers and fathers are HH; there is no involvement of the Bombay phenotype.) Paternal genotypes maybe used once, more than once, or not at all. Each mother-child pair matches with one or more than one paternal genotype. Maternal phenotype: Child phenotype: Paternal genotype: Reset A, M, Rh(neg) O, M, Rh(pos) B, N, Rh(neg) O, N, Rh(pos) O, M, Rh(neg) A, MN, Rh(pos) A, N, Rh(pos) AB, MN, Rh(pos) B, N, Rh(pos) A, MN, Rh(neg) Genotypes of possible fathers AiLMLN rr BiLMLN RR ii LNLN rr ii LMLM rr AALMLN RR
- Explain why it is possible for the proband in the following pedigree to have children of blood types A, B, and AB. Considering epistatic genes, what are the possible genotypes of II-2?Please consider the pedigree below. There are no cases of false paternity. I II III IV в 1 a. Which individual/s definitely has/have Bombay phenotype in the descendants of I-1 and I-2? b. What are the genotypes of individuals II-2 and III-2 at the AB0 and H loci? Please label your answers a and b, Il-2: and Ill-2:.The genotype of EB27 and EB67 are unknown. Based on pedigree, what are the most likely genotype of each individual?
- An experimental assay for the blood-clotting protein called factorIX is available. A blood sample was obtained from each individual in the following pedigree. The amount of factor IX protein, shown within each symbol on the pedigree, is expressed as a percentage of the average amount observed in individuals who do not carry a mutant copy of the gene.You've been having trouble sleeping because of your obsession with understanding the Rh factor (+ positive or - negative) in blood typing. Your blood type is O-. You know both of your parents phenotypes so you decide to visit a famous genetic counselor, Dr. Jean Etix. After she bills you $300, she tells you to take your parents' genotypes and "stick them in a punnet square!" Your Dad is B- and your Mom is A+. What are their possible genotypic combinations? O Pi++ and^i +- Oi+- and Ai +- O IPi+- and IAA+ +- and Ai+- O Pi -- and IAi +-The following results are derived from crosses between Neurospora strain xy and strain ++: Tetrad Class 3 4 ху x+ x+ xy ++ ++ ++ +y +y ху +y 25 ++ 3 124 4 (i) Name the ascus type of each class from 1 to 4 as P, NP or T. (ii) Are genes x and y linked? Explain your answer. (iii) If they are linked, determine the map distance between the two genes. If they are unlinked, provide all the information you can about why you draw this conclusion.