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Is tay-sachs disease caused by a mutation?
deletion
Is the William syndrome a mutation?
Yes, Williams syndrome is a genetic condition caused by a deletion of genetic material on chromosome 7. This deletion is not usually inherited, but occurs randomly. It is not considered a mutation in the traditional sense, but rather a genetic anomaly.
what type of mutation occurs when a nucleotide is left out?
deletion mutation
Genetic mutation caused by the loss of a chromosomal segment?
Deletion
What type of mutation occurs when part of a chromosome is missing after replication?
Deletion
A frame shift mutation occurs any time a gene mutation results in the insertion or deletion of a number of nucleotides that is not a multiple of three?
false
What type of mutation when a nucleotide is dropped from a DNA sequence?
A deletion mutation occurs when a nucleotide is dropped from a DNA sequence. This can cause a shift in the reading frame, leading to a non-functional protein being produced.
What causes Deletion Syndrome?
deletion syndrome is a disorder caused by the deletion of a small piece of chromosome 22. The deletion occurs near the middle of the chromosome at a location designated q11.2.
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.
Is the deletion mutation dominant or recessive?
A deletion mutation can be dominant or recessive, depending on the specific gene affected and the consequences of the deletion on the protein encoded by that gene. In general, the impact of a deletion mutation on an individual's phenotype will determine whether it is dominant or recessive.
Is angel-man syndrome caused by a mutation?
Yes, Angelman syndrome is caused by a mutation in a gene called UBE3A. This gene is responsible for producing a protein that is vital for normal brain function. The mutation leads to the characteristic symptoms of Angelman syndrome.
Deletion is when a whole segment of a gene is?
Deletion occurs when a whole segment of a gene is lost.
