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The position of the mutation is what determines how severe it is, the ATP7A gene is what is effected. My son has menkes, does yours? is that why you are asking? you can email me at huntermommy08@hotmail.com or catch me on twitter @missusmommy08

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Is Parkinson disease on chromosome 6?

No, Parkinson's disease is not caused by a mutation on chromosome 6. The exact cause of Parkinson's disease is not fully understood, but it is believed to involve a combination of genetic and environmental factors. Some rare forms of Parkinson's disease are linked to specific gene mutations, but these are not located on chromosome 6.


What chromosome is affected in fabry disease?

The allele that is responsible of Fabry Disorder/Disease is located on the X chromosome and is the only lipid storage disorder identified as being sex linked.


What chromosome does tay-sachs disease affect?

Tay-Sachs disease is caused by mutations in the HEXA gene located on chromosome 15. These mutations result in the absence or deficiency of the enzyme hexosaminidase A, leading to the accumulation of harmful substances in the brain and nervous system.


The rare genetic disorders Menkes disease and Wilson's disease result from abnormal utilization of?

Menkes disease results from abnormal utilization of copper, leading to a copper deficiency that affects various body functions. In contrast, Wilson's disease results from abnormal utilization of copper, causing a buildup of copper in the body, particularly in the liver and brain, which can lead to various symptoms and complications.


What chromosome is affected during Wilson's disease?

Wilson's disease is caused by a mutation in the ATP7B gene, which is located on chromosome 13. This gene encodes a copper-transporting enzyme involved in copper metabolism. Mutations in this gene lead to impaired copper transport and accumulation of copper in various tissues, causing the symptoms of Wilson's disease.

Related Questions

Who discovered or first announced Menkes disease or Menkes syndrome?

Menkes disease was first described by the pediatrician John Menkes in 1962. He noticed a distinct set of symptoms in a group of patients, which later led to the identification of the genetic disorder now known as Menkes disease.


Is gaucher disease-sex linked?

Gaucher's disease is located on chromosome 1, which is not the sex chromosome, so no. It is not a sex linked disease.


Is there any famous people that have or had Menkes disease?

No, nobody that has been famous had this particular disease


What chromosome is polycystic kidney disease found?

It is a mutated gene called PKD1 located on chromosome 16.


Is Parkinson disease on chromosome 6?

No, Parkinson's disease is not caused by a mutation on chromosome 6. The exact cause of Parkinson's disease is not fully understood, but it is believed to involve a combination of genetic and environmental factors. Some rare forms of Parkinson's disease are linked to specific gene mutations, but these are not located on chromosome 6.


What chromosome number is affected by alzheimer's disease?

Chromosome numbers: 1, 14, 19, and 21 are affected by Alzheimer's disease.


Has anyone done research on menkes disease?

my son has the disease, if you would like to know more about it email me at huntermommy08@hotmail.com


What chromosome is affected in fabry disease?

The allele that is responsible of Fabry Disorder/Disease is located on the X chromosome and is the only lipid storage disorder identified as being sex linked.


What is the birth name of Suzy Menkes?

Suzy Menkes's birth name is Suzy Peta Menkes.


What chromosome does tay-sachs disease affect?

Tay-Sachs disease is caused by mutations in the HEXA gene located on chromosome 15. These mutations result in the absence or deficiency of the enzyme hexosaminidase A, leading to the accumulation of harmful substances in the brain and nervous system.


What chromosome is Parkinson's disease on?

Chromosome 4


The rare genetic disorders Menkes disease and Wilson's disease result from abnormal utilization of?

Menkes disease results from abnormal utilization of copper, leading to a copper deficiency that affects various body functions. In contrast, Wilson's disease results from abnormal utilization of copper, causing a buildup of copper in the body, particularly in the liver and brain, which can lead to various symptoms and complications.