Human Anatomy & Physiology (11th Edition)
11th Edition
ISBN: 9780134580999
Author: Elaine N. Marieb, Katja N. Hoehn
Publisher: PEARSON
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- . BRCA1 is a bi-allelic gene (let's call the two alleles as C and c) that is inherited on an autosome. The C allele is completely dominant over c, expressing breast cancer as a phenotype. Eye color is determined by two independently assorting bi-allelic genes, B (alleles B and b) and G (alleles G and g), such that the Ballele shows dominant epistasis over the G and g alleles. Brown-eyed individuals have at least one copy of the B allele, green eyed individuals have at least one G allele, while blue eyed individuals have neither B nor G. A blue-eyed person whą is a heterozygote carrier for the BRCA1 gene has 3 children with a brown-eyed person (heterozygote for both B and G genes) who does not have breast cancer. (a) What are the possible genotypes and phenotypes of all their possible children? What are their respective probabilities of being observed (please write all genotype and phenotype probabilities)? (b) What is the probability that all three children will be blue-eyed and not…arrow_forwardExplain the ABO blood system as an example of multiple alleles and codominance; be sure to discuss blood phenotype as an expression of surface proteins, “markers” on the red blood cellsarrow_forwardTEST goo.g/CUYGKD 2.) A man with type A blood marries a woman with type B blood. Their child has type O blood. What are the genotypes of these three individuals? What genotypes, and in what frequencies, would you expect in future offspring from this marriage? 3. A man has six fingers on each hand and six toes on each foot. His wife and their daughter have the normal number of digits. Remember that extra digits is a dominant trait. What fraction of this couple's children would be expected to have extra digits?arrow_forward
- How many (%) of their daughters will have hemophilia? 8. Beta thalassemia is a blood disorder caused by a mutation in the HBB gene on chromosome 11 which codes for the beta subunit of the hemoglobin protein. This changes the shape and functioning of the protein and causes it to misshapen and unable to carry oxygen efficiently. The disorder is recessive. Normal Beta thalassemia If two parents are carriers for the disorder, what percentage of their children will have Beta Thalassemia? How many (%) of their children will have beta thalassemia? Are males and females affected equally? How do you know?arrow_forwardplz fill this out 4 me tooarrow_forwardDominant Traits. A couple is going to have a baby. They are concerned about Huntington's Diseases, which results from having a dominant copy of the Huntington allele ("H"). Homozygous recessive individuals ("hh") are not affected. Thus, having one dominant version of the gene results in an affected phenotype. The woman is not affected, but the man is. What alleles does mom have? What alleles does that have? Make a punnett squarearrow_forward
- n5NtidRw TWUZCDKDPI5Z9P_SHPZ9İA-XH-pfftLbhNc/edit Add-ons Help Last edit was 4 minutes ago Calibri 12 BIUA + 16. The characteristic of albinism (lack of pigment in skin and hair), can be caused by a single gene. The following pedigree shows a family in which some people are affected by albinism. 3 4 I3D 4 7 8 II 1. 3 4 IV 1 2 3 4 5 6 7 a. Using just the information on this pedigree, is albinism caused by a dominant allele or recessive alleles? b. What are the genotypes of the great-grandparents (generation I)? !!!arrow_forwardHelp. Got it wrong.arrow_forwardGive typed full explanationarrow_forward
- Please show all your work.arrow_forwardasap please.arrow_forwardpeatles Feather 2. Tim and Stephanie are devastated when they find out their newborn son has hemophilia - a sex-linked recessive disease. Tim is shocked becaused he doesn't have hemophilia, and figures if his son has it he would have gotten it from him. Is Tim correct in his thinking? Explain. Also explain what their genotypes must be in order for neither of them to have the disease but have a son who does. Χ 비 H HMM X" X"X" X"Y Father (TIM): хну XH X ts itter Stephanie: не No atim provide the Y, which is not a Carrier for the disease.tle wire movise the x which is a carrier for disewer. to make a time with a baby girl. They are nervous that she bay 3. Tim and Stephanie (from #2) are pregnant again! This too may get hemophilia. Based on what you know about Tim and Stephanie, what is the probability that they do have a daughter with the disease? Show a Punnett square to support your answer. Y XHXH XHY +4 th フェ× X X X X Y 0% Jaughters will have hemophilia 4. In carnations, red and white…arrow_forward
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