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SLC2A9 Gene Hypouricemia Renal Type 2 Genetic Test Cost

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

-21%

The SLC2A9 Gene Hypouricemia Renal Type 2 Genetic Test is a specialized diagnostic procedure offered at DNA Labs UAE, designed to identify mutations in the SLC2A9 gene. These mutations are associated with renal hypouricemia type 2, a rare genetic disorder characterized by abnormally low levels of uric acid in the blood due to impaired renal urate reabsorption. The condition can lead to various complications, including kidney stones and exercise-induced acute kidney injury.

This genetic test is crucial for individuals with a clinical history suggestive of renal hypouricemia or those with a family history of the condition, as it provides definitive confirmation of the diagnosis. The test involves collecting a DNA sample, typically through a blood draw or a cheek swab, which is then analyzed for specific mutations in the SLC2A9 gene.

Offered at a cost of 4400 AED, the test at DNA Labs UAE employs advanced genetic sequencing technologies to ensure accurate and reliable results. Understanding one’s genetic status regarding the SLC2A9 gene can be vital for making informed decisions about treatment and management options, as well as for genetic counseling purposes.

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SLC2A9 Gene Hypouricemia renal type 2 Genetic Test

Test Name: SLC2A9 Gene Hypouricemia renal type 2 Genetic Test

Components: DNA Labs UAE

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 SLC2A9 Gene Hypouricemia, renal type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with Hypouricemia, renal type 2

Test Details

The SLC2A9 gene is responsible for encoding a protein called glucose transporter 9 (GLUT9), which is primarily found in the kidneys and plays a crucial role in uric acid reabsorption. Hypouricemia refers to a condition characterized by abnormally low levels of uric acid in the blood. Renal hypouricemia type 2 specifically refers to a genetic form of hypouricemia that is caused by mutations in the SLC2A9 gene.

NGS (Next-Generation Sequencing) is a high-throughput DNA sequencing technology that allows for the simultaneous sequencing of multiple genes or even the entire genome. In the context of genetic testing for hypouricemia, NGS can be used to identify mutations or variations in the SLC2A9 gene that may be responsible for the condition.

A genetic test for SLC2A9 gene hypouricemia, renal type 2 using NGS would involve obtaining a DNA sample, typically through a blood sample or buccal swab. The DNA would then be sequenced using NGS technology to analyze the SLC2A9 gene for any mutations or variations. The results of the genetic test can help diagnose the specific genetic cause of hypouricemia in an individual and guide treatment decisions.

It is important to note that genetic testing for hypouricemia, including SLC2A9 gene testing, is typically performed in individuals with symptoms or a family history of the condition. The results of the genetic test can provide valuable information for both diagnosis and genetic counseling.

Test Name SLC2A9 Gene Hypouricemia renal type 2 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 SLC2A9 Gene Hypouricemia, renal type 2 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Hypouricemia, renal type 2
Test Details

The SLC2A9 gene is responsible for encoding a protein called glucose transporter 9 (GLUT9), which is primarily found in the kidneys and plays a crucial role in uric acid reabsorption.

Hypouricemia refers to a condition characterized by abnormally low levels of uric acid in the blood. Renal hypouricemia type 2 specifically refers to a genetic form of hypouricemia that is caused by mutations in the SLC2A9 gene.

NGS (Next-Generation Sequencing) is a high-throughput DNA sequencing technology that allows for the simultaneous sequencing of multiple genes or even the entire genome. In the context of genetic testing for hypouricemia, NGS can be used to identify mutations or variations in the SLC2A9 gene that may be responsible for the condition.

A genetic test for SLC2A9 gene hypouricemia, renal type 2 using NGS would involve obtaining a DNA sample, typically through a blood sample or buccal swab. The DNA would then be sequenced using NGS technology to analyze the SLC2A9 gene for any mutations or variations. The results of the genetic test can help diagnose the specific genetic cause of hypouricemia in an individual and guide treatment decisions.

It is important to note that genetic testing for hypouricemia, including SLC2A9 gene testing, is typically performed in individuals with symptoms or a family history of the condition. The results of the genetic test can provide valuable information for both diagnosis and genetic counseling.

SKU: TEST-2482 Category:

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