The information in pedigrees that is useful for mapping disease genes is sometimes limited. This pedigree shows segregation of neurofibromatosis, which is a fully-penetrant, autosomal dominant condition, and a single nucleotide polymorphism, SNP1, which has alleles G or T. Why is the cross in generation I not useful for determining the degree of linkage between the disease-causing gene NF and SNP1?

Since neurofibromatosis is an autosomal dominant condition, the cross between individuals with genotypes carrying the same SNP type is not useful to show the degree of linkage between the disease-causing gene NF and SNP1. This occurs because it is necessary to observe segregation for the trait in order to determine its effects

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explanation:

it has to be understood that the sea water contains a huge amount of sodium and chlorine ions and if they enter the cell of the atlantic cod fish, the cell will shrivel and the fish will die. to avoid such a condition, the fish uses active transport for the purpose of removing the ions against the gradient.

explanation:

the atlantic cod is not a maritime osmoconformer. its native application of salts is less than that of the seawater it lives in. it is continually falling water from the gills to the ocean via osmosis.

countering that, the fish is going to be swallowing seawater. but since its internal collection of salts is lower than seawater, the fish will want to go free of excess salt, and since that's going upon a gradient, then active transport, requiring energy, must be used to pump out the salt. much marine fish use the organs to filter out the salt and these fish discharge very straight urine.