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The simplest answer is variation or death. If the mutation is abberant enough it renders the organism nonviable...a continum of lesser effects that potentially result in deformity, disorder, pigment variation, behavioral change all the way to some fabulous modification that creates a great adaptation that makes an

organism more successful.

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What is a change in a gene due to damage or being copied incorrectly called?

A change in a gene due to damage or being copied incorrectly is called a mutation. This alteration can result in changes to the gene's function or produce new traits in an organism.


Is gene mutation and mutation is same?

Yes, gene mutation and mutation are often used interchangeably in biological contexts. Gene mutation specifically refers to a change in the sequence of DNA in a particular gene, whereas mutation can refer to changes in DNA sequences more broadly, including those not within a specific gene.


If Rett syndrome is a chromosomal abnormality what is the abnormality?

Rett syndrome is not primarily caused by a chromosomal abnormality, but rather a genetic mutation in the MECP2 gene located on the X chromosome. This gene provides instructions for making a protein that is important for brain development. Mutations in the MECP2 gene disrupt the production of this protein, leading to the characteristic features of Rett syndrome.


Which types of mutation causes sickle cell anemia?

Sickle cell anemia is caused by a point mutation in the HBB gene, specifically a substitution of adenine for thymine in the sixth codon of the gene, resulting in the production of abnormal hemoglobin known as hemoglobin S.


Does Fibrodysplasia Ossificans Progressiva have a bad chromosome?

The gene that is mutated in a person who has Fibrodysplasia Ossificans Progressiva is called the ACVR1 gene. A small mutation in one of the two copies of the ACVR1 gene modifies the meaning of its genetic message, so a defective protein is made.

Related Questions

Diseases that result from an abnormality in or a mutation of a gene are termed what type of disease?

Genetic diseases


Is cystic fibrosis chromosomal abnormality?

Yes, it is caused by a mutation in the gene for the protein CFTR.


What does briste geine mean in english?

"Briste geine" is Irish Gaelic for "broken gene." It likely refers to a genetic mutation or abnormality.


What organism is born with a genetic abnormality not present in any of its ancestors this abnormality is most likely the result of?

mutation


Is marfan syndrome a chromosomal abnormality?

No, Marfan syndrome is not a chromosomal abnormality. It is a genetic disorder caused by a mutation in the fibrillin-1 (FBN1) gene, which affects the body's connective tissue. This gene is located on chromosome 15.


What is a change in a gene due to damage or being copied incorrectly called?

A change in a gene due to damage or being copied incorrectly is called a mutation. This alteration can result in changes to the gene's function or produce new traits in an organism.


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.


Is gene mutation and mutation is same?

Yes, gene mutation and mutation are often used interchangeably in biological contexts. Gene mutation specifically refers to a change in the sequence of DNA in a particular gene, whereas mutation can refer to changes in DNA sequences more broadly, including those not within a specific 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)?

Point Mutation- a type of gene mutation in which only a single nucleotide in a gene has been changed.