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Amiraneli [1.4K]
3 years ago
8

Some individuals have defective genes for LDL receptor receptors rendering them nonfunctional. Individuals with these mutations

typically have
Biology
2 answers:
deff fn [24]3 years ago
6 0
Individuals with these mutations typically have familial hypercholesterolemia.
These genes provide information for the formation of the low-density lipoprotein receptor, a receptor that binds to low-density lipoproteins (LDLs). LDLs carry the cholesterol in the blood and regulate the amount of cholesterol in the circulation. Mutations to these genes either reduce the number of receptors or cause several disruptions to their function. This results in high blood cholesterol levels and in a higher risk for heart disease.
babymother [125]3 years ago
6 0
<span>People who have defective genes for LDL receptors often have familial hypercholesterolemia. This is a genetic disorder that is caused in chromosome 19. It makes the body unable to remove lipoprotein that is low density, or LDL, which is type of protein that creates cholesterol in the blood. It will result in high amounts of LDL in the blood.</span>
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The genotypes found in the F2 offspring will be An1An1, An1An2 and An2An2.

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In the example given in the question, the color of the petals of snapdragon flowers are given with the An1 allele having full activity and the An2 allele being the null allele. For the F1 offspring, two snapdragon flowers are crossed, one with red petals which is An1An1 and one with ivory petals which is An2An2. All the genotypes for the F1 offspring will result in An1An2.

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