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ZDHHC17 Gene Huntington Disease ZDHHC17 Related Genetic Test

Original price was: 5,600 د.إ.Current price is: 4,400 د.إ.

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The ZDHHC17 gene, also known as Huntington Interacting Protein 14 (HIP14), plays a crucial role in the neuropathology of Huntington’s Disease (HD), a progressive brain disorder that affects movement, behavior, and cognition. The ZDHHC17 gene encodes an enzyme involved in palmitoylation, a post-translational modification essential for the proper functioning and localization of proteins within cells. Mutations or dysfunctions in this gene have been linked to the development and progression of Huntington’s Disease, making it a significant focus for genetic testing and research.

Genetic testing for Huntington’s Disease related to the ZDHHC17 gene provides critical information for individuals with a family history of the disease or those showing symptoms, enabling them to make informed decisions about their health and future. The test typically involves analyzing DNA to identify mutations in the ZDHHC17 gene that might increase the risk or confirm the diagnosis of Huntington’s Disease.

In the United Arab Emirates, DNA Labs UAE offers this specialized genetic test for individuals concerned about their risk of Huntington’s Disease. The test cost is set at 4400 AED, reflecting the comprehensive analysis and detailed report provided by the lab. Conducting the test at DNA Labs UAE ensures that individuals receive accurate and reliable results, benefiting from the lab’s expertise in genetic diagnostics and its use of advanced testing technologies. This service not only aids in early diagnosis and intervention but also supports families in understanding their genetic health, potentially guiding them towards appropriate counseling and management strategies for Huntington’s Disease.

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ZDHHC17 Gene Huntington Disease Genetic Test

About the ZDHHC17 Gene

The ZDHHC17 gene codes for a protein called palmitoyltransferase ZDHHC17. This protein is involved in the process of palmitoylation, which is the addition of a fatty acid called palmitate to proteins. Palmitoylation plays a crucial role in the proper functioning of proteins and is involved in various cellular processes.

About Huntington’s Disease

Huntington’s disease is a neurodegenerative disorder characterized by progressive loss of motor control, cognitive decline, and psychiatric symptoms. It is primarily caused by a mutation in the huntingtin gene. However, there is evidence suggesting that other genes, such as ZDHHC17, may also contribute to the development and progression of the disease.

About the ZDHHC17 Related Genetic Test

The ZDHHC17 related genetic test is a type of genetic test that utilizes next-generation sequencing (NGS) technology to analyze the ZDHHC17 gene. The test aims to identify any variants or mutations present in the gene that may be associated with Huntington’s disease or other neurological conditions.

Test Details:

  • Test Name: ZDHHC17 Gene Huntington Disease ZDHHC17 related Genetic Test
  • Components: ZDHHC17 gene analysis
  • Price: 4400.0 AED
  • Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
  • Report Delivery: 3 to 4 Weeks
  • Method: NGS Technology
  • Test Type: Neurological Disorders
  • Doctor: Neurologist
  • Test Department: Genetics
  • Pre Test Information: Clinical history of the patient, Genetic Counselling session to draw a pedigree chart of affected family members

Importance and Limitations

While the ZDHHC17 gene has been identified as a potential modifier gene for Huntington’s disease, further research is needed to fully understand its role in the disease and its potential diagnostic or therapeutic applications. Genetic testing for ZDHHC17 variants is not currently a standard diagnostic test for Huntington’s disease, but it may be used in research studies or specific clinical settings.

Conclusion

The ZDHHC17 related genetic test using NGS technology offers the opportunity to analyze the ZDHHC17 gene and identify any variants or mutations associated with Huntington’s disease or other neurological conditions. While it is not a standard diagnostic test at present, it holds promise for future research and potential clinical applications.

Test Name ZDHHC17 Gene Huntington disease ZDHHC17 related Genetic Test
Components
Price 4400.0 AED
Sample Condition Blood or Extracted DNA or One drop Blood on FTA Card o
Report Delivery 3 to 4 Weeks
Method NGS Technology
Test type Neurological Disorders
Doctor Neurologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for ZDHHC17 Gene Huntington disease, ZDHHC17 related NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with ZDHHC17 Gene Huntington disease, ZDHHC17 related
Test Details

The ZDHHC17 gene is a gene that codes for a protein called palmitoyltransferase ZDHHC17. This protein is involved in the process of palmitoylation, which is the addition of a fatty acid called palmitate to proteins. Palmitoylation is important for the proper functioning of proteins and is involved in various cellular processes.

Huntington’s disease is a neurodegenerative disorder characterized by progressive loss of motor control, cognitive decline, and psychiatric symptoms. It is caused by a mutation in the huntingtin gene, but there is evidence to suggest that other genes may also play a role in the development and progression of the disease.

The ZDHHC17 gene has been identified as a potential modifier gene for Huntington’s disease. Modifier genes are genes that can influence the severity or age of onset of a disease in individuals with a specific genetic mutation.

A ZDHHC17 related NGS genetic test is a type of genetic test that uses next-generation sequencing (NGS) technology to analyze the ZDHHC17 gene and identify any variants or mutations that may be present. This test can help determine if an individual has any genetic variants in the ZDHHC17 gene that may be associated with Huntington’s disease or other neurological conditions.

It is important to note that while the ZDHHC17 gene has been implicated in Huntington’s disease, further research is needed to fully understand its role in the disease and how it may be used for diagnostic or therapeutic purposes. Genetic testing for ZDHHC17 variants is not currently a standard diagnostic test for Huntington’s disease, but it may be used in research studies or in certain clinical settings.

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