If our hemoglobin gene is normal, the hemoglobin protein works fine. But if the instuctions in that gene are changed, or "mutated,"changes in the hemoglobin protein could result. One such mutation causes a disorder called sickle cell anemia.
6th amino acid is changed in haemoglobin chain due to a recessive mutation on beta haemoglobin producing gene
The dangerous mutation in sickle cell anemia is a point mutation in the HBB gene that results in the substitution of glutamic acid with valine in the beta-globin chain of hemoglobin. This leads to the production of abnormal hemoglobin known as hemoglobin S, which causes red blood cells to take on a sickle shape, leading to various complications such as vaso-occlusive crises, anemia, and organ damage.
In a point mutation, a change in a single nucleotide can lead to a specific mutation. For example, a substitution mutation occurs when one nucleotide is swapped for another, such as A to T or C to G. This change can result in different amino acids being coded for in the protein sequence.
The sickle cell allele can have a point mutation where a single nucleotide is changed, resulting in the substitution of glutamic acid with valine in the beta-globin chain of hemoglobin. This leads to the characteristic sickle-shaped red blood cells in individuals with sickle cell disease.
The most common type of mutation is a point mutation, where a single nucleotide base is changed, inserted, or deleted in the DNA sequence. This can result in a different amino acid being incorporated into the protein during translation, leading to potential changes in the protein's function.
6th amino acid is changed in haemoglobin chain due to a recessive mutation on beta haemoglobin producing gene
Only one or two nucleotides are changed in a certain mutation. This is an example of a(n)
The dangerous mutation in sickle cell anemia is a point mutation in the HBB gene that results in the substitution of glutamic acid with valine in the beta-globin chain of hemoglobin. This leads to the production of abnormal hemoglobin known as hemoglobin S, which causes red blood cells to take on a sickle shape, leading to various complications such as vaso-occlusive crises, anemia, and organ damage.
mutation
a point mutation
mutation
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A mutation.
The answer is MUTATION
A mutation that involves a single nucleotide is called a point mutation. This type of mutation can include substitutions, insertions, or deletions of a single nucleotide in the DNA sequence.
In a point mutation, a change in a single nucleotide can lead to a specific mutation. For example, a substitution mutation occurs when one nucleotide is swapped for another, such as A to T or C to G. This change can result in different amino acids being coded for in the protein sequence.
one that changed the triplet grouping of the genetic message