SLC26A1 Gene Renal Dysfunction – Genetic Test
Welcome to DNA Labs UAE, your trusted genetic testing laboratory. In this blog post, we will discuss the SLC26A1 gene and its association with renal dysfunction. We offer a comprehensive genetic test to diagnose SLC26A1 deficiency and provide valuable insights for personalized treatment strategies.
Test Name: SLC26A1 Gene Renal Dysfunction due to SLC26A1 Deficiency Genetic Test
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: Hepatology, Nephrology, Endocrinology Disorders
- Doctor: General Physician
- Test Department: Genetics
Pre Test Information:
Before undergoing the SLC26A1 Gene Renal Dysfunction Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected by SLC26A1 Gene Renal Dysfunction.
Test Details:
The SLC26A1 gene is responsible for encoding a protein called sulfate anion transporter (SAT1), which plays a crucial role in transporting sulfate ions across cell membranes. Deficiencies or mutations in this gene can lead to renal dysfunction, indicating impaired kidney function.
Our NGS (Next-Generation Sequencing) genetic testing method allows for the simultaneous analysis of multiple genes, providing a comprehensive assessment of an individual’s genetic makeup. In the context of SLC26A1 deficiency and renal dysfunction, NGS genetic testing can identify any mutations or variations in the SLC26A1 gene that may contribute to the condition.
By detecting these genetic abnormalities, NGS genetic testing aids in diagnosing the underlying cause of renal dysfunction and guides appropriate treatment strategies. Additionally, it provides valuable information for genetic counseling, helping determine the risk of passing on the genetic mutation to future generations.
At DNA Labs UAE, we are committed to providing accurate and reliable genetic testing services. Our SLC26A1 Gene Renal Dysfunction Genetic Test is conducted using state-of-the-art NGS technology, ensuring the highest level of precision in your results. For more information or to schedule an appointment, please contact our Genetics Test Department.
| Test Name | SLC26A1 Gene Renal dysfunction due to SLC26A1 deficiency 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 | Hepatology Nephrology Endocrinology Disorders |
| Doctor | General Physician |
| Test Department: | Genetics |
| Pre Test Information | Clinical History of Patient who is going for SLC26A1 Gene Renal dysfunction due to SLC26A1 deficiency NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SLC26A1 Gene Renal dysfunction due to SLC26A1 deficiency NGS Genetic DNA Test gene SLC26A1 |
| Test Details | The SLC26A1 gene is responsible for encoding a protein called sulfate anion transporter (SAT1), which plays a crucial role in transporting sulfate ions across cell membranes. Deficiencies or mutations in this gene can lead to renal dysfunction, which refers to impaired kidney function. NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze multiple genes simultaneously, providing a comprehensive assessment of an individual’s genetic makeup. In the context of SLC26A1 deficiency and renal dysfunction, NGS genetic testing can identify any mutations or variations in the SLC26A1 gene that may be contributing to the renal dysfunction. By detecting these genetic abnormalities, NGS genetic testing can help in diagnosing the underlying cause of renal dysfunction and guide appropriate treatment strategies. It can also provide valuable information for genetic counseling, as it can help determine the risk of passing on the genetic mutation to future generations. |
