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When a mutation occurs outside a gene, it is referred to as a "regulatory mutation" or "non-coding mutation." These mutations can affect gene expression by altering regulatory elements such as promoters, enhancers, or silencers, which control when and how much a gene is expressed. Although they do not change the protein-coding sequence, they can still have significant effects on an organism's phenotype.
What else can I help you with?
What type of mutation results when bases are added to the gene?
This is called an insertion mutation.Some repeats, such as the repeats in the Huntington's gene, can be repeated too many times and then you have the deleterious mutation in this gene.
What describes a mutation that occurs within a gene?
A mutation that occurs within a gene is known as a gene mutation. This type of mutation can involve changes in the DNA sequence, such as substitutions, insertions, or deletions of nucleotides. These alterations can affect the protein encoded by the gene, potentially altering its function, stability, or expression levels. Depending on the nature of the mutation, it may lead to neutral, beneficial, or harmful effects on the organism.
What is isogenic mutation?
Isogenic mutation refers to a genetic mutation that occurs in an organism's DNA, resulting in a change in a specific gene or genes. It is called isogenic because it affects only a specific gene in an otherwise identical genetic background. This type of mutation is often used in research to study the effects of a single gene mutation without any additional genetic variability.
What is the mutation caused by the addition of a nucleotide to an already existing gene sequence called deletion duplication insertion inversionWhat is the mutation caused by the addition of a nucleot?
The mutation caused by the addition of a nucleotide to an existing gene sequence is called an "insertion." This type of mutation can disrupt the reading frame of the gene, potentially leading to significant changes in the resulting protein. If the insertion occurs within a coding region, it can alter the amino acid sequence and affect the protein's function.
What is any permanent change in a gene called?
A Mutation
What type of mutation results when bases are added to the gene?
This is called an insertion mutation.Some repeats, such as the repeats in the Huntington's gene, can be repeated too many times and then you have the deleterious mutation in this gene.
A change in a gene is called?
A mutation
A mutation that involves a single nucleotide is called a(an)?
Point Mutation- a type of gene mutation in which only a single nucleotide in a gene has been changed.
What describes a mutation that occurs within a gene?
A mutation that occurs within a gene is known as a gene mutation. This type of mutation can involve changes in the DNA sequence, such as substitutions, insertions, or deletions of nucleotides. These alterations can affect the protein encoded by the gene, potentially altering its function, stability, or expression levels. Depending on the nature of the mutation, it may lead to neutral, beneficial, or harmful effects on the organism.
What is damage to a gene called?
mutation
Whats a change in gene or chromosome?
A change in a gene could involve a mutation that alters the DNA sequence, affecting the function of the protein it codes for. A change in a chromosome could involve alterations in the structure, number, or distribution of genetic material, leading to genetic disorders or diseases.
A change in the nucleotide base sequence of gene or DNA molecule is called a what?
this is called a mutation
When there is a change in the information in a gene it is called a?
Mutation
What is any change in a gene called?
A Mutation
What is isogenic mutation?
Isogenic mutation refers to a genetic mutation that occurs in an organism's DNA, resulting in a change in a specific gene or genes. It is called isogenic because it affects only a specific gene in an otherwise identical genetic background. This type of mutation is often used in research to study the effects of a single gene mutation without any additional genetic variability.
What is the mutation caused by the addition of a nucleotide to an already existing gene sequence called deletion duplication insertion inversionWhat is the mutation caused by the addition of a nucleot?
The mutation caused by the addition of a nucleotide to an existing gene sequence is called an "insertion." This type of mutation can disrupt the reading frame of the gene, potentially leading to significant changes in the resulting protein. If the insertion occurs within a coding region, it can alter the amino acid sequence and affect the protein's function.
Can a point mutation result in a frameshift mutation?
Yes, a point mutation can result in a frameshift mutation if it occurs in a coding region of a gene and disrupts the reading frame of the genetic code.
