1. In this family, Noonan’s Syndrome is being caused by allele (a)______ in gene (b)______; specifically the Mutation with letter (leave off the “Mutation” and just give the letter) (c)______.
2. In this family, deafness is caused by a mutation in the (a)__________ gene; specifically the mutation with letter (leave off the “mutation” and just give the letter) (b)__________.
*No answer choices. Plain thinking and guessing.
IGF1R,PTPN11,RAF
1. (a) Alpaca; (b) Yodel; (c) B
2. (a) Kazoo; (b) M
1. In this family, Noonan's Syndrome is being caused by allele (a) present in gene (b) with Mutation (c).
2. In this family, deafness is caused by a mutation in the (a) gene; specifically the mutation with letter (b).
To answer these questions, we need to know the specific alleles and genes associated with Noonan's Syndrome and deafness in this family. Since no answer choices are provided, we'll use our knowledge and reasoning skills to make an educated guess.
1. Noonan's Syndrome is a genetic disorder that can be caused by various mutations in different genes. One well-known gene associated with Noonan's Syndrome is the PTPN11 gene. So, let's assume that gene (b) refers to the PTPN11 gene. Regarding the specific mutation, I'm sorry, but without any additional information, I cannot determine the specific mutation letter (c). It would be helpful to have more details or context about the family's medical history or the specific mutation involved.
2. Deafness can be caused by mutations in different genes, but one common gene associated with hereditary deafness is the GJB2 gene. Let's assume that gene (a) refers to the GJB2 gene. Similar to the previous question, without more information, it's not possible to determine the exact mutation letter (b). Understanding the specific mutation would require additional context or knowledge of the family's medical history.
Remember, based on the given information, these answers are educated guesses, and you may need more specific data to provide a definitive answer.