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No. It arises due to point mutations (like A -> T).

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16y ago

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Is prader-willi syndrome a result of translocation?

According to the research I've done, Prader-Willi Syndrome is rarely a result of translocation, but it is a possibility. Translocation in this syndrome results in an inactivation of genes on the paternal chromosome 15.


What ethnic group is greatly affected by sicklecell?

African American and Hispanic are greatly affect by sicklecell.


Can you go into the Navy with sicklecell?

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What is transfer of genes between nonhomologous chromosomes?

Transfer of genes between nonhomologous chromosomes is known as chromosomal translocation. It can result in the fusion of two chromosomes or the exchange of genetic material between them. This process can lead to genetic abnormalities and diseases.


When part of the one chromosome breaks off and is added to a different chromosome the result is a?

Translocation


What is significance of translocation?

Translocations can result into gene dysregulation, thus leading to diseases like cancer.


What occurs when a segment breaks of chromosome breaks off and reattaches to another chromosome?

This is known as a chromosomal translocation, which can result in genetic material being exchanged between chromosomes. Translocations can lead to disruptions in gene expression and potential genetic disorders. Depending on the specific genes involved, translocations can have diverse effects on an individual's health.


What is caused by chromosomal translocation?

Chromosomal translocation can lead to genetic disorders and cancer. It can result in the fusion of genes from different chromosomes, creating abnormal gene products that may interfere with normal cellular functions. This can disrupt gene expression and lead to the development of various health conditions.


What is another word for translocation?

Leaching is another word for translocation.


What disease is the result of hyperthyroidism?

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Is hemophilia a result of translocation?

It can be. Basically most mutations (regardless of type; translocation, reversal, transcription, etc...) can cause hemophilia if they occur within a specific part of the genetic sequencing that codes for the production of the clotting factor proteins. This genetic sequence if found in a segment of the X chromosome.


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