SLC25A3 Gene Mitochondrial Phosphate Carrier Deficiency Genetic Test
Welcome to DNA Labs UAE, where we offer the SLC25A3 gene mitochondrial phosphate carrier deficiency genetic test. This blog post will provide you with all the information you need to know about this test.
Test Components and Price
The SLC25A3 gene mitochondrial phosphate carrier deficiency genetic test is priced at 4400.0 AED. The test requires a blood sample, extracted DNA, or one drop of blood on an FTA card.
Report Delivery and Method
After the sample is collected, the report will be delivered within 3 to 4 weeks. The test utilizes NGS (Next-Generation Sequencing) technology to analyze the DNA sequence of the SLC25A3 gene.
Test Type and Doctor
The SLC25A3 gene mitochondrial phosphate carrier deficiency genetic test falls under the category of cardiovascular pneumology disorders. It is performed by a cardiologist.
Test Department and Pre-Test Information
The test is conducted in the genetics department. Before undergoing the SLC25A3 gene mitochondrial phosphate carrier deficiency genetic test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session is recommended to draw a pedigree chart of family members affected by the gene SLC25A3.
Test Details
The SLC25A3 gene is responsible for encoding a protein called the mitochondrial phosphate carrier (PiC). This protein plays a crucial role in transporting phosphate ions across the inner mitochondrial membrane, which is essential for energy production in the mitochondria.
Deficiency in the SLC25A3 gene can result in mitochondrial phosphate carrier deficiency, a rare genetic disorder. This condition impairs the transport of phosphate ions into the mitochondria, leading to decreased ATP production and dysfunction in energy metabolism.
NGS genetic testing is a method used to analyze the DNA sequence of an individual’s genes. It can identify mutations or variations in the SLC25A3 gene that may be associated with mitochondrial phosphate carrier deficiency. NGS allows for the simultaneous analysis of multiple genes, providing a comprehensive evaluation of genetic variations that may contribute to the disorder.
NGS genetic testing for SLC25A3 gene mutations can help diagnose mitochondrial phosphate carrier deficiency and guide appropriate treatment and management strategies. It is also useful for carrier testing in individuals with a family history of the disorder or for prenatal testing in at-risk pregnancies.
Thank you for choosing DNA Labs UAE for your genetic testing needs. If you have any further questions or would like to schedule an appointment, please contact us.
| Test Name | SLC25A3 Gene Mitochondrial phosphate carrier 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 | Cardiovascular Pneumology Disorders |
| Doctor | Cardiologist |
| Test Department: | Genetics |
| Pre Test Information | Clinical History of Patient who is going for SLC25A3 Gene Mitochondrial phosphate carrier deficiency NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SLC25A3 Gene Mitochondrial phosphate carrier deficiency NGS Genetic DNA Test gene SLC25A3 |
| Test Details |
The SLC25A3 gene is responsible for encoding a protein called the mitochondrial phosphate carrier (PiC). This protein is involved in the transport of phosphate ions across the inner mitochondrial membrane, which is necessary for energy production in the mitochondria. Deficiency in the SLC25A3 gene can lead to mitochondrial phosphate carrier deficiency, which is a rare genetic disorder. This condition impairs the transport of phosphate ions into the mitochondria, resulting in decreased ATP production and energy metabolism dysfunction. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of an individual’s genes. It can identify mutations or variations in the SLC25A3 gene that may be associated with mitochondrial phosphate carrier deficiency. NGS allows for the analysis of multiple genes simultaneously, providing a comprehensive evaluation of genetic variations that may contribute to the disorder. NGS genetic testing for SLC25A3 gene mutations can help diagnose mitochondrial phosphate carrier deficiency and guide appropriate treatment and management strategies. It can also be used for carrier testing in individuals with a family history of the disorder or for prenatal testing in at-risk pregnancies. |
