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I'm assuming you need an explanation:
Females have XX, males have XY. Since the disease is X-linked recessive, females require two X chromosomes with the same mutation to have the disease, but males require only one X chromosome with the mutation.
Disease frequency in females is 1/1,000,000. In that case, the frequency at which the mutation is present in each X chromosome is 1/1,000 (1/1,000 x 1/1,000 = 1,000,000)
Males have XY, then their disease frequency has to be the same as that of a single X chromosome: 1/1,000
I was a teaching assistant for genetics and I think it is just the convention in genetics. Think about pedigree analysis, "affected" will always mean individuals who express the phenotype and you wouldn't call a carrier individual "affected" in a pedigree analysis.
Your explanation is great. However, by the word affected in the question, couldn't the female be only a carrier and thus one X chromosome needs to be mutated to be affected. The question is lacking a clearance a bit. The word affected could mean expressing the disease (two X chromosomes are affected for the female) or just a carrier (just one X chromosome is affected and thus the dominant is healthy overall). If however they meant the disease in the question, then I agree with you 100 %.
I would agree with you, but the question states that the disease is X linked recessive. A female with only one mutation would be a carrier, thus she would not be affected. Her male offsprings have a 50% chance inheriting the mutated X chromosome and the disease.
I hope that clears things up!
jsut curious, so lets say the disease is X-link dominant, if the female affected is 1/x, what is the ratio of male affected...
I was thinking if female have XX, they have double the chances of being affected (can get it both from mom and dad), so male ratio (can only get it from mom) would be 1/2x...
or should I solve it using the frequency of the allele, which probaly impossible to solve since this is a dominant disease...
Or...is this problem can not be solved using these information...
jsut curious, so lets say the disease is X-link dominant, if the female affected is 1/x, what is the ratio of male affected...
I was thinking if female have XX, they have double the chances of being affected (can get it both from mom and dad), so male ratio (can only get it from mom) would be 1/2x...
or should I solve it using the frequency of the allele, which probaly impossible to solve since this is a dominant disease...
Or...is this problem can not be solved using these information...
how can this be related to mutation, I was taught you get X from mom and, either X or Y from your dad, purely hereditary...