**Question:**What is the mode of inheritance for the Spider Curse? (Hint: compare the children of individual II-2 and II-5)- a. X-Linked Dominant- b. X-Linked Recessive- c. Autosomal Dominant- d. Autosomal Recessive**Follow-Up Question:**What evidence supports your hypothesis about the spider curse? Give at least 2 pieces of information from the pedigree that support your answer to 3c.**Answer:** [Blank space for response] The image is a pedigree chart that illustrates the inheritance patterns of two fictional conditions: "Jekyll-Hyde Afflicted" and "Spider Curse Afflicted."**Legend:**- Red Square: Jekyll-Hyde Afflicted- Black Circle: Spider Curse Afflicted- Half Black/Red Circle: Jekyll-Hyde/Spider Curse Afflicted- White Circle/Square: Human (unafflicted)**Generation I:**- Individual 1 (red square): Jekyll-Hyde Afflicted- Individual 2 (black circle): Spider Curse Afflicted**Generation II:**- Individuals 1 and 3 (white squares): Human- Individual 2 (black circle): Spider Curse Afflicted- Individual 4 (white circle): Human- Individual 5 (black square): Spider Curse Afflicted- Individual 6 (white circle): Human**Generation III:**- Individual 1 (half black/red circle): Jekyll-Hyde/Spider Curse Afflicted- Individual 2 (black square): Spider Curse Afflicted- Individual 3 (red square): Jekyll-Hyde Afflicted- Individuals 4 and 5 (white squares): HumanThe chart demonstrates the transmission of these fictional traits across three generations, using standard symbols for pedigree analysis.

Inheritance or heredity is passing on one trait from the parents to the progeny by either asexual or…

What is the mode of inheritance for the Spider Curse? (Hint: compare the children of individual Il-2 and Il-5) a. X-Linked Dominant O b. X-Linked Recessive O c. Autosomal Dominant O d. Autosomal Recessive What evidence supports your hypothesis about the spider curse? Give at least 2 pieces of information from the pedigree that support your answer to 3c. Answer:

What is the mode of inheritance for the Spider Curse? (Hint: compare the children of individual Il-2 and Il-5) a. X-Linked Dominant O b. X-Linked Recessive O c. Autosomal Dominant O d. Autosomal Recessive What evidence supports your hypothesis about the spider curse? Give at least 2 pieces of information from the pedigree that support your answer to 3c. Answer:

Human Anatomy & Physiology (11th Edition)

11th Edition

ISBN:9780134580999

Author:Elaine N. Marieb, Katja N. Hoehn

Publisher:Elaine N. Marieb, Katja N. Hoehn

Chapter1: The Human Body: An Orientation

Section: Chapter Questions

Problem 1RQ: The correct sequence of levels forming the structural hierarchy is A. (a) organ, organ system,...

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A. Look at the pedigree, and DISREGARD individual II-8 for the moment. Is the pattern of inheritance of Unetan syndrome dominant or recessive? You may assume that the gene is FULLY-PENETRANT in this family. Please give two specific reasons that support your conclusion. B. Now, looking at BOTH the pedigree AND at the Southern blot, is this trait autosomal, X-linked, or Y-linked? Please give two specific reasons that support your conclusion. Once again, disregard II-8 for the moment. One of your two reasons must refer specifically to evidence present in the Southern blot. C. Define the gene alleles associated with Unetan syndrome. Your alleles MUST be consistent with the pattern of inheritance, AND your genetic notation must be consistent with that used throughout the course. Unetan syndrome allele: ________ Normal allele: ________
Below is a pedigree chart for a family that has a history of Alkaptonuria. Individuals infected with this condition can have darkened skin, brown urine, and can suffer from joint damage and other complications. Given this pedigree answer the following questions. Given the data in the pedigree chart is this genetic condition autosomal dominant or autosomal recessive? What are the genotypes for #1, #2, and #3? If either of the 4th generation "aa" females were to mate with a homozygous dominant male would any of their offspring illustrate the phenotype? Why or why not?
What is the most likely mode of inheritance for the trait shown in the following pedigree? Select one: O a. Autosomal dominant O b. Autosomal recessive O c. X-linked dominant O d. X-linked recessive Oe. Mitochondrial 80
please make sure to read the question (THERE ARE OTHER VARIATIONS OF THE QUESTION ON DIFFERNT WEBSITES THAT ARE DIFFERENT THAN MINE)
In the example below, crossing you left thumb over your right thumb is dominant T to crossing your right over left recessive t. Identify the genotype of the individual shown below: OShutterstock / robynleig O A. homozygous dominant (TT) O B. heterozygous dominant (Tt) or homozygous dominant (TT) OC. homozygous recessive (tt) O D. Cannot be determined from information provided
36. Look at this pedigree and circle each row yes/no. Any assumption (that is not outrageous) can be made), for example, can assume someone is a carrier. a. Could this trait be inherited as a simple autosomal recessive? YES oo 8995 ON b. Could this trait be inherited as a simple autosomal dominant? YES ON C. Could this trait be inherited as a simple x linked recessive? YES ON d. Could this trait be inherited as a simple x linked dominant? YES ON e. Could this trait be inherited as a Y linked? YES ON
4. In this pedigree of another family with hemophilia A. If the woman Il-2 has a son, what is the chance that he is affected? II B. If the woman Il-2 has a daughter, what is the chance 1 2 3 4 III that she is affected? -1 C. If the woman Il-2 has 2 sons, what is the chance that neither will be affected? D. What are the chances that the child of II-4 and Il-5 will be affected?
the pedigree below shows the inheritance of a newly identified eye color gene. Assume 100% penetrance and expressivity. Use the pedigree to find: 1. Identify the mode of inheritance (either autosomal dominant, or autosomal recessive) 2. Argue why your mode of inheritance must be correct. Your argument should cite specific individuals from the pedigree. (For example, the top left individual is person I-1).
Examine the pedigree and answer the following questions; shaded individuals show the trait; genotypes are all unknown. The individual marked with the question mark is of an unknown genotype but does have the trait. A. What mode of inheritance is the most likely for this trait, autosomal recessive or autosomal dominant? State your rationale for full credit. B. What is the genotype of the individual marked with the question mark? (Heterozygous, homozygous, or unknown)
Blood types in humans are Codominant. a. What are the possible genotypes of someone with type O blood? b. What are the possible genotypes of someone with type B blood? c. What is the phenotype of someone’s whose genotype is AO? d. A man with AB blood is married to a woman with AB blood. What blood types will their children be and in what proportion?
Pompe disease is a glycogen storage disorder caused by a lack of ⍺-glucosidase, the enzyme that converts glycogen to glucose in the muscles. Babies born with this disorder die by the age of two. pope disease is a genetic disorder caused by the presence of two recessive autosomal alleles. A. A man and a woman heterozygous for the condition have two female unaffected children. Determine, using a Punnett square, the probability, expressed as a whole number percentage, of a fourth baby being born a male with Pompe disease. B. Iftheman,fromthepreviousquestion,hadtypeAbloodandthewomanhadtypeO blood, what would be probability of them having a daughter with type O blood and affected with Pompe disease? (Show clearly your calculations and express your answer as a frequency between 0 - 1 and rounded to 2 decimal places)