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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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What is caused by chromosomal translocation?
A translocation chromosomal mutation will result when two non-homologous chromosomes each broken by some sort of clastogen and then are swapped.
Is color blindness a result of translocation or deletion?
none. its a slight mutation in 23rd x chromosome
What is significance of translocation?
Translocations can result into gene dysregulation, thus leading to diseases like cancer.
Royal hemophilia is the result of inheritance?
Royal Hemophilia is a reference to Hemophilia B, also known as Factor IX (9) deficiency. This is a genetic disorder that can be inherited. Also near 30% of the Hemophilia B cases result from spontaneous mutations and are not inherited at all. That being said, once the mutation has occurred, that individual can pass the mutation on.
What is it called when one chromosome breaks off and is added to a different chromosome?
translocation i'm doing the same worksheet for my finals study guide, and in my book it discussed this.
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 is caused by chromosomal translocation?
A translocation chromosomal mutation will result when two non-homologous chromosomes each broken by some sort of clastogen and then are swapped.
What whoud be the result of a normal women having a child with a hemophilia men?
All Girls will be carriers of Hemophilia and all Males will be unaffected (they won't have Hemophilia).
When part of the one chromosome breaks off and is added to a different chromosome the result is a?
Translocation
What genotype will result in Hemophilia?
XA Xa
Is color blindness a result of translocation or deletion?
none. its a slight mutation in 23rd x chromosome
Is sickle-cell disease a result of a translocation?
No. It arises due to point mutations (like A -> T).
What is significance of translocation?
Translocations can result into gene dysregulation, thus leading to diseases like cancer.
Royal hemophilia is the result of what inheritance?
Hemophilia is broken into three subcategories; Hemophilia A, Hemophilia B, and Hemophilia C. These subcategories designate a person as having a deficiency of one of three specific clotting proteins. Hemophilia A is the deficiency of the protein called Clotting Factor VIII. Hemophilia B is the deficiency of Clotting Factor IX. Hemophilia C is the deficiency of Clotting Factor XI. "Royal" hemophilia is simply a reference to Hemophilia B and is therefore a result of a deficiency in the Clotting Factor IX protein. It is sometimes called the royal disease because it has been known to have been passed through some royal families throughout history.
Is hemophilia a hereditary disease or acquired from microorganisms?
Hemophilia is not acquired from microorganisms. Hemophilia is typically a genetic disorder that can either be inherited or result from a random mutation. In rare cases non genetic forms (that can not be inherited or passed on) of hemophilia can be acquired due to liver impairment, and certain medications.
What is another word for translocation?
Leaching is another word for translocation.
What is transfer of genes between nonhomologous chromosomes?
translocation!
