answersLogoWhite

0

yup

User Avatar

Wiki User

12y ago

What else can I help you with?

Continue Learning about Natural Sciences

Mutation is any change in a gene or chromosome?

mutations


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.


As a result of the incorrect sequence of amino acids will be translated into a protein-resulting in a mutation?

Missence mutation


How is it possible for gene with a mutation in coding region to encode a polypeptide with the same amino acid sequence as the nonmutant gene?

A mutation in the third position of a codon (silent mutation) can result in the same amino acid being encoded due to the redundancy of the genetic code. Since multiple codons can code for the same amino acid, a mutation may not change the amino acid sequence despite occurring in the coding region of the gene.


What is it called when a mutation occurs outside a gene?

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.

Related Questions

A change in a gene is called?

A mutation


Is Huntington's Disease a gene mutation?

No, it's caused by a single point mutation of a gene.


What is the effects of mutation?

A mutation is a permenent in DNA sequence of a gene,mutation in a gene's DNA sequence can alterthe aminoacid sequence of the protein encodedby the gene.


Is Huntington's disease caused by a gene mutation or a chromosomal mutation?

Huntington's disease is caused by a gene mutation, specifically in the HTT gene on chromosome 4.


A mutation that involves a single nucleotide is called a(an)?

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.


Is achondroplastic dwarfism a gene malfunction or mutation?

it is a mutation of the gene FRG3 in chromosome 4


Mutation is any change in a gene or chromosome?

mutations


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.


Which mutation would not change the remainder of the reading frame of a gene sequence that follows the mutation?

A silent mutation, where a nucleotide substitution results in a codon that codes for the same amino acid, would not change the remainder of the reading frame of a gene sequence. This is because the amino acid sequence produced by the altered codon remains the same.


What can gene mutations be caused by?

A gene mutation can be caused by radiation. A gene mutation can also be inherited from family members, such as grandparents and parents.


What is a gene mutation what is a chromosomal mutation?

a gene is passed on from generations and a chromosome is just found in certain cells


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.