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3. What is the name of the protein involved in DMD? Why does a gene mutation affect a protein?
5. What are the chances a woman (XDXd) with DMD on one of her X chromosomes and a man (XdY)
without DMD have children with the disease? Complete the punnett square. (Use Ctrl + . to format the
exponent).
Xd
3. How is it possible that a woman can carry the mutated gene and not be color blind but if a man
carries the mutated gene he is always color blind?
4. What is the name of the cell that senses light in your eye? Which type allows us to see color?
2. What is hemophilia?
4. Did more royal men or royal women have hemophilia? Why does this make sense?
3. Are female carriers of the disease completely symptom free? Why do you think this is?
4. Based on what we learned about DNA replication, why do you think the chances of sporadic
hemophilia are so low? (Hint: What are DNA Polymerases 2 jobs?)
2. Do both genders express and/or inherit sex-linked traits equally? Why or why not?
3. When making a pedigree that traces a sex-linked trait, we show the X chromosome carrying the
alleles, e.g. XA Xa or XE XE or Xh Y. Why is it important to trace the X and Y chromosomes in a pedigree
in addition to the alleles?