MPDU1 Gene Glycosylation Disorder Type 1F Genetic Test
Welcome to DNA Labs UAE, where we offer comprehensive genetic testing services. In this blog, we will discuss the MPDU1 Gene Glycosylation Disorder Type 1F Genetic Test, including its cost, symptoms, diagnosis, and other relevant information.
Test Name: MPDU1 Gene Glycosylation Disorder Type 1F Genetic Test
Components:
- 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:
Metabolic Disorders
Doctor:
General Physician
Test Department:
Genetics
Pre Test Information:
Clinical History of Patient who is going for MPDU1 Gene Glycosylation Disorder Type 1F NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with Glycosylation Disorder Type 1F.
Test Details:
The MPDU1 gene is responsible for encoding the enzyme mannosyl-oligosaccharide glucosidase, which is involved in the glycosylation process. Glycosylation disorders, such as type 1F, result from mutations in the MPDU1 gene, leading to impaired glycosylation of proteins.
NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses high-throughput sequencing technologies to analyze multiple genes simultaneously. In the case of MPDU1 gene glycosylation disorder type 1F, NGS genetic testing can be used to identify mutations or variants in the MPDU1 gene that may be causing the glycosylation disorder.
This type of genetic testing can provide valuable information for diagnosis, prognosis, and potential treatment options for individuals with MPDU1 gene glycosylation disorder type 1F. It can also help in identifying carriers of the mutation and provide information for family planning and genetic counseling.
Test Name | MPDU1 Gene Glycosylation disorder type 1F Genetic Test |
---|---|
Components | |
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 | Metabolic Disorders |
Doctor | General Physician |
Test Department: | Genetics |
Pre Test Information | Clinical History of Patient who is going for MPDU1 Gene Glycosylation disorder type 1F NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Glycosylation disorder type 1F |
Test Details |
The MPDU1 gene is responsible for encoding the enzyme mannosyl-oligosaccharide glucosidase, which is involved in the glycosylation process. Glycosylation disorders, such as type 1F, result from mutations in the MPDU1 gene, leading to impaired glycosylation of proteins. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses high-throughput sequencing technologies to analyze multiple genes simultaneously. In the case of MPDU1 gene glycosylation disorder type 1F, NGS genetic testing can be used to identify mutations or variants in the MPDU1 gene that may be causing the glycosylation disorder. This type of genetic testing can provide valuable information for diagnosis, prognosis, and potential treatment options for individuals with MPDU1 gene glycosylation disorder type 1F. It can also help in identifying carriers of the mutation and provide information for family planning and genetic counseling. |